TW201841458A - Magnetohydrodynamic electric power generator - Google Patents

Magnetohydrodynamic electric power generator Download PDF

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TW201841458A
TW201841458A TW107105863A TW107105863A TW201841458A TW 201841458 A TW201841458 A TW 201841458A TW 107105863 A TW107105863 A TW 107105863A TW 107105863 A TW107105863 A TW 107105863A TW 201841458 A TW201841458 A TW 201841458A
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power
hydrogen
molten metal
converter
source
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TW107105863A
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Chinese (zh)
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雷戴爾 李 米爾斯
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美商明亮光源能源公司
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Abstract

A power generator that provides at least one of electrical and thermal power comprising (i) at least one reaction cell for the catalysis of atomic hydrogen to form hydrinos identifiable by unique analytical and spectroscopic signatures, (ii) a reaction mixture comprising at least two components chosen from: a source of H2O catalyst or H2O catalyst; a source of atomic hydrogen or atomic hydrogen; reactants to form the source of H2O catalyst or H2O catalyst and a source of atomic hydrogen or atomic hydrogen; and a molten metal to cause the reaction mixture to be highly conductive, (iii) a molten metal injection system comprising at least one pump such as an electromagnetic pump that causes a plurality of molten metal streams to intersect, (iv) an ignition system comprising an electrical power source that provides low-voltage, high-current electrical energy to the plurality of intersected molten metal streams to ignite a plasma to initiate rapid kinetics of the hydrino reaction and an energy gain due to forming hydrinos, (v) a source of H2and O2supplied to the plasma, (vi) a molten metal recovery system, and (vii) a power converter capable of (a) converting the high-power light output from a blackbody radiator of the cell into electricity using concentrator thermophotovoltaic cells or (b) converting the energetic plasma into electricity using a magnetohydrodynamic converter.

Description

磁流體動力發電機Magnetic fluid power generator

本發明係關於電力產生領域,且特定言之,係關於用於產生電力之系統、裝置及方法。更具體言之,本發明之實施例係針對經由磁流體動力功率轉換器、光-電功率轉換器、電漿-電功率轉換器。光子-電功率轉換器或熱-電功率轉換器產生光功率、電漿及熱功率並產生電功率的發電裝置及系統以及相關方法。此外,本發明之實施例描述使用光伏打功率轉換器,使用水或基於水之燃料來源之點火來產生光功率、機械功率、電功率及/或熱功率之系統、裝置及方法。此等及其他相關實施例詳細描述於本發明中。The present invention relates to the field of power generation and, in particular, to systems, devices and methods for generating electrical power. More specifically, embodiments of the present invention are directed to a magnetic fluid power converter, an opto-electric power converter, a plasma-electric power converter. Photonic-electric power converters or thermo-electric power converters generate power, plasma and thermal power and generate electrical power, and related methods. Moreover, embodiments of the present invention describe systems, devices, and methods for generating optical power, mechanical power, electrical power, and/or thermal power using a photovoltaic power converter using water or a source of water based fuel. These and other related embodiments are described in detail in the present invention.

相關申請案之交叉參考 本申請案主張2017年2月12日提交之美國臨時申請案第62/457,935號、2017年2月21日提交之第62/461,768號、2017年2月26日提交之第62/463,684號、2017年4月04日提交之第62/481,571號、2017年5月31日之提交第62/513,284號、2017年5月31日提交之第62/513,324號、2017年6月23日提交之第62/524,307號、2017年7月14日提交之第62/532,986號、2017年7月26日提交之第62/537,353號、2017年8月14日提交之第62/545,463號、2017年9月11日提交之第62/556,941號、2017年10月17日提交之第62/573,453號、2017年11月10日提交之第62/584,632號、2017年11月04日提交之第62/594,511號、2017年11月29日提交之第62/612,304號及2017年1月17日提交之第62/618,444號之權益,該等申請案全部均以引用之方式併入本文中。 電力產生可採取許多形式,利用來自電漿之功率。電漿之成功商業化可視能夠有效形成電漿且隨後捕捉所產生之電漿之功率的電力產生系統而定。 電漿可以在某些燃料之點火期間形成。此等燃料可以包括水或基於水之燃料來源。在點火期間,形成剝除電子之原子之電漿雲,且可釋放出高光功率。電漿之高光功率可藉由本發明之功率轉換器利用。離子及激發態原子可以再結合且經歷電子弛豫,發射光功率。光功率可藉由光伏打裝置轉換成電。 本發明之某些實施例係針對電力產生系統,其包含:經組態以將功率傳送至燃料以點火燃料並產生電漿之複數個電極,諸如固體或熔融金屬電極;經組態以將電能傳送至該複數個電極之電源;及經定位以接收高溫及高壓電漿之至少一個磁流體動力功率轉換器或經定位以接收至少複數個電漿光子之至少一個光伏打(「PV」)功率轉換器。 在實施例中,產生電能及熱能中之至少一者之SunCell®電力系統包含:至少一個容器,其能夠保持壓力低於、處於或高於大氣壓;反應物,其包含:(i) 至少一種包含初生H2 O之催化劑來源或催化劑、(ii)至少一種H2 O來源或H2 O、(iii)至少一種原子氫來源或原子氫及(iv)熔融金屬;熔融金屬噴射系統,其包含至少兩個各自包含泵及噴射管之熔融金屬儲集器;至少一個反應物供應系統,其用以補充在反應物發生反應以產生電能及熱能中之至少一者的過程中消耗之反應物;至少一個點火系統,其包含用以向至少兩個各自包含電磁泵之熔融金屬儲集器供應相反電壓之電源;及光及熱輸出中之至少一者至電功率及/或熱功率的至少一個功率轉換器或輸出系統。 在實施例中,熔融金屬可包含此項技術中已知之任何導電金屬或合金。熔融金屬或合金可具有低熔點。例示性金屬及合金為鎵、銦、錫、鋅及鎵銦錫合金,其中典型共晶混合物之實例為68% Ga、22% In及10% Sn (按重量計),但比例可在62至95% Ga、5至22% In、0至16% Sn (按重量計)之間變化。在金屬可與氧及水中之至少一者反應以形成相對應的金屬氧化物的實施例中,低能量氫反應混合物可包含熔融金屬、金屬氧化物及氫。金屬氧化物可充當氧來源以形成HOH催化劑。可在金屬氧化物與HOH催化劑之間回收氧,其中可再供應經消耗以形成低能量氫之氫。 熔融金屬噴射系統可包含至少兩個熔融金屬儲集器,其各自包含噴射在容器內部相交之熔融金屬流之電磁泵,其中每一儲集器可包含熔融金屬位準控制器,其包含進水升管。點火系統可包含用以向至少兩個各自包含電磁泵之熔融金屬儲集器供應相反電壓之電源,其供應流動穿過相交之熔融金屬流之電流及功率,引起反應物之反應(包含點火)以在容器內部形成電漿。點火系統可包含:(i)用以向至少兩個各自包含電磁泵之熔融金屬儲集器供應相反電壓之電源及(ii)自該至少兩個各自包含電磁泵之熔融金屬儲集器噴出之至少兩個相交的熔融金屬流,其中電源能夠遞送足以引起反應物反應形成電漿之短脈衝高電流電能。傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源可包含至少一個超級電容器。每一電磁泵可包含以下中之一者:(i) DC或AC導電型,其包含經由電極供應至熔融金屬之DC或AC電流源及恆定或同相交變向量交叉磁場之來源;或(ii)感應型,其包含穿過熔融金屬之短路迴路之交變磁場來源,其在金屬中誘導交流電;及同相交變向量交叉磁場來源。泵與相對應的儲集器之至少一個活接(union)及包含容器、噴射系統及轉換器之部件之間的另一活接可包含濕封、凸緣及墊片密封、黏著密封及滑動螺母密封中之至少一者,其中墊片可包含碳。熔融金屬點火系統之DC或AC電流可在10 A至50,000 A之範圍內。熔融金屬點火系統之電路可由熔融金屬流之相交而閉合以引起點火,從而進一步引起在0 Hz至10,000 Hz之範圍內的點火頻率。感應型電磁泵可包含形成熔融金屬之短路迴路之陶瓷溝道。電力系統可進一步包含用以由相對應的固體金屬形成熔融金屬之電感耦合加熱器,其中該熔融金屬可包含銀、銀銅合金及銅中之至少一者。電力系統可進一步包含真空泵及至少一個急冷器。電力系統可包含反應功率輸出之至少一個功率轉換器或輸出系統,諸如以下各者之群組中之至少一者:熱光伏打轉換器、光伏打轉換器、光電轉換器、磁流體動力轉換器、電漿動力轉換器、熱離子轉換器、熱電轉換器、斯特林引擎(Sterling engine)、布累登循環引擎(Brayton cycle engine)、朗肯循環引擎(Rankine cycle engine)及熱機、加熱器及鍋爐。鍋爐可包含輻射鍋爐。反應容器之一部分可包含黑體輻射器,其可保持在1000 K至3700 K之範圍內之溫度下。電力系統之儲集器可包含氮化硼,容器之包含黑體輻射器之部分可包含碳,且與熔融金屬接觸之電磁泵部件可包含抗氧化金屬或陶瓷。低能量氫反應的反應物可包含甲烷、一氧化碳、二氧化碳、氫、氧及水中之至少一者。反應物供應器可將甲烷、一氧化碳、二氧化碳、氫、氧及水中之每一者保持在0.01 Torr至1 Torr範圍內之壓力下。由電力系統之黑體輻射器發射並引向熱光伏打轉換器或光伏打轉換器的光可主要為黑體輻射,包含可見光及近紅外光,且光伏打電池可為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)、銻化砷磷銦(InPAsSb)、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge。由反應電漿發射且引向熱光伏打轉換器或光伏打轉換器的光可主要為紫外光,且光伏打電池可為聚光電池,其包含至少一種選自III族氮化物、GaN、AlN、GaAlN及InGaN之化合物。 在實施例中,PV轉換器可進一步包含至PV電池之UV窗。PV窗可替換黑體輻射器之至少一部分。該窗可實質上透過UV。該窗可抗用熔融金屬潤濕。該窗可在係高於熔融金屬之熔點及高於熔融金屬之沸點中之至少一者的溫度下操作。例示性窗為藍寶石、石英、MgF2 及熔融矽石。窗可經冷卻且可包含用於在操作期間或在維護期間清潔的構件。SunCell®可進一步包含電場及磁場中之至少一者的來源以將電漿約束於避免與窗及PV電池中之至少一者接觸的區域中。來源可包含靜電沈澱系統。來源可包含磁性約束系統。電漿可由重力約束,其中窗及PV電池中之至少一者處於關於電漿產生之位置的合適高度處。 或者,磁流體動力功率轉換器可包含連接至反應容器之噴嘴、磁流體動力通道、電極、磁體、金屬採集系統、金屬再循環系統、熱交換器及視情況選用之氣體再循環系統,其中反應物可包含H2 O蒸氣、氧氣及氫氣中之至少一者。反應物供應器可將O2 、H2 及反應產物H2 O保持在0.01 Torr至1 Torr之範圍內之壓力下。用以補充在反應物發生反應以產生電能及熱能中之至少一者的過程中消耗之反應物的反應物供應系統可包含以下中之至少一者:O2 及H2 氣體供應器、氣體殼體、在反應容器、磁流體動力通道、金屬採集系統及金屬再循環系統中之至少一者的壁中之選擇性透氣膜、用以保持O2 及H2 壓力中之至少一者的O2 、H2 及H2 O分壓感測器、流量控制器、至少一個閥門及電腦。在實施例中,電力系統之至少一個組件可包含陶瓷,其中陶瓷可包含金屬氧化物、氧化鋁、氧化鋯、氧化鎂、氧化鉿、碳化矽、碳化鋯、二硼化鋯及氮化矽中之至少一者。熔融金屬可包含銀且磁流體動力轉換器可進一步包含氧源以形成供應至儲集器、反應容器、磁流體動力噴嘴及磁流體動力通道中之至少一者的銀粒子之氣溶膠,其中反應物供應系統可另外供應及控制氧源以形成銀氣溶膠。熔融金屬可包含銀。磁流體動力轉換器可進一步包含電解槽氣體(cell gas),其包含環境氣體,與儲集器及容器中之至少一者中的銀接觸。電力系統可進一步包含保持與熔融銀接觸之電解槽氣體的流動以形成銀氣溶膠之構件,其中電解槽氣體流動可包含強制氣體流動及對流氣體流動中之至少一者。電解槽氣體可包含稀有氣體、氧、水蒸氣、H2 及O2 中之至少一者。保持電解槽氣體流動之構件可包含氣泵或壓縮機中之至少一者,諸如磁流體動力氣泵或壓縮機、磁流體動力轉換器及由熔融金屬噴射系統及電漿中之至少一者引起的擾流。 電力系統之感應型電磁泵可包含雙級泵,其包含第一級,該第一級包含金屬再循環系統之泵,及第二級,該第二級包含金屬噴射系統之泵以噴射與容器內部之另一熔融金屬流相交之熔融金屬流。點火系統之電源包含感應點火系統,該感應點火系統可包含穿過熔融金屬之短路迴路之交變磁場來源,其在金屬中產生包含點火電流之交流電。交變磁場來源可包含初級變壓器繞組,其包含變壓器電磁體及變壓器磁軛,且銀可至少部分地充當次級變壓器繞組,諸如單匝短路繞組,其圍封初級變壓器繞組且包含感應型電流迴路。儲集器可包含熔融金屬交接通道,其連接兩個儲集器以使得電流迴路圍封變壓器磁軛,其中感應電流迴路包含在儲集器、交接通道中所含之熔融銀、噴射管中之銀及相交以接通感應電流迴路之所噴射熔融銀流中產生的電流。 在實施例中,發射器產生電能及熱能中之至少一者,其中發射器包含:至少一個容器,其能夠保持壓力低於、處於或高於大氣壓;反應物,該等反應物包含:a)至少一種包含初生H2 O之催化劑來源或催化劑;b)至少一種H2 O來源或H2 O;c)至少一種原子氫來源或可滲透穿過容器壁之原子氫;d)熔融金屬,諸如銀、銅或銀銅合金;及e)氧化物,諸如CO2 、B2 O3 、LiVO3 及不與H2 反應之穩定氧化物中之至少一者; 至少一個熔融金屬噴射系統,其包含熔融金屬儲集器及電磁泵;至少一個包含電源之反應物點火系統,其用以引起反應物形成發光電漿及發熱電漿中之至少一者,其中電源自功率轉換器接收電功率;用以回收熔融金屬及氧化物之系統;光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統; 其中熔融金屬點火系統包含以下中之至少一者:點火系統,其包含i)來自以下之群組的電極:a)至少一組用以約束熔融金屬之耐火金屬或碳電極;b)耐火金屬或碳電極及藉由電磁泵自電隔離熔融金屬儲集器傳送之熔融金屬流,及c)藉由至少兩個電磁泵自複數個電隔離熔融金屬儲集器傳送之至少兩個熔融金屬流; 及ii)電源,其用以傳送足以引起反應物反應形成電漿之高電流電能,其中熔融金屬點火系統電流在50 A至50,000 A之範圍內; 其中熔融金屬噴射系統包含電磁泵,其包含提供磁場之至少一個磁體及用以提供向量交叉電流分量之電流源; 其中熔融金屬儲集器包含電感耦合加熱器; 發射器,其進一步包含回收熔融金屬及氧化物之系統,諸如包含能夠在重力下提供熔體流動之壁之容器及與該容器連通之儲集器中之至少一者,且其進一步包含冷卻系統,該冷卻系統用以將儲集器保持在比容器低的溫度下以使金屬採集在儲集器中; 其中能夠保持壓力低於、處於或高於大氣壓之容器包含:內部反應電解槽,其包含高溫黑體輻射器;及外部腔室,其能夠保持壓力低於、處於或高於大氣壓; 其中黑體輻射器經保持在1000 K至3700 K之範圍內之溫度下;其中包含黑體輻射器之內部反應電解槽包含耐火材料,諸如碳或W;其中自池外部發射之黑體輻射入射於光-電功率轉換器上;其中反應功率輸出之至少一個功率轉換器包含熱光伏打轉換器及光伏打轉換器中之至少一者; 其中由該池發射之光主要為黑體輻射,包含可見光及近紅外光,且光伏打電池為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)及銻化砷磷銦(InPAsSb)、III族/V族半導體、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge,且電力系統進一步包含真空泵及至少一個排熱系統,且黑體輻射器進一步包含黑體溫度感測器及控制器。視情況地,發射器可包含至少一個額外反應物噴射系統,其中該等額外反應物包含:a)至少一種包含初生H2 O之催化劑來源或催化劑;b)至少一種H2 O來源或H2 O;及c)至少一種原子氫來源或原子氫。額外反應物噴射系統可進一步包含電腦、H2 O及H2 壓力感測器及流量控制器中之至少一者,該等流量控制器包含質量流量控制器、泵、注射泵及高精度電子可控閥之群組中之至少一或多者;該閥門包含針閥、比例電子閥及步進馬達閥中之至少一者,其中該閥門由壓力感測器及電腦控制以保持H2 O及H2 壓力中之至少一者處於所需值;其中額外反應物噴射系統將H2 O蒸氣壓保持在0.1 Torr至1 Torr之範圍內。 在實施例中,藉由將H轉換為低能量氫發電之產生器可由氫產生以下產物中之至少一者: a)具有為0.23至0.25 cm- 1 整數倍之拉曼峰值加在0至2000 cm- 1 範圍內之基質位移的氫產物; b) 具有為0.23至0.25 cm- 1 整數倍之紅外峰值加在0至2000 cm- 1 範圍內之基質位移的氫產物; c)具有在500至525 eV範圍內之能量處之X射線光電子光譜加在0至10 eV範圍內之基質位移的氫產物; d)引起高磁場MAS NMR基質位移的氫產物; e)相對於TMS具有大於-5 ppm之高磁場MAS NMR或液體NMR位移之氫產物; f)具有在200至300 nm範圍內之至少兩個電子束發射光譜峰之氫產物,其具有為0.23 to 0.3 cm- 1 整數倍之間距加在0至5000 cm- 1 範圍內之基質位移;及 g)具有在200至300 nm範圍內之至少兩個UV螢光發射光譜峰之氫產物,其具有為0.23 to 0.3 cm- 1 整數倍之間距加在0至5000 cm- 1 範圍內之基質位移。 在一個實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個容器,其能夠保持壓力低於、處於或高於大氣壓; 反應物,該等反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)熔融金屬; 至少一個熔融金屬噴射系統,其包含熔融金屬儲集器及電磁泵; 至少一個額外反應物噴射系統,其中該等額外反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O,及 c)至少一種原子氫來源或原子氫; 至少一個包含電源之反應物點火系統,其中電源自功率轉換器接收電功率; 用以回收熔融金屬之系統; 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統。 在實施例中,熔融金屬點火系統包含: a)至少一組用以約束熔融金屬之電極;及 b)用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能之電源。 電極可包含耐火金屬。 在實施例中,傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源包含至少一個超級電容器。 熔融金屬噴射系統可包含電磁泵,其包含提供磁場之至少一個磁體及用以提供向量交叉電流分量之電流源。 熔融金屬儲集器可包含電感耦合加熱器。 熔融金屬點火系統可包含至少一組分離以形成開路的電極,其中該開路藉由噴射熔融金屬閉合以使高電流流動而達成點火。 熔融金屬點火系統電流可在500 A至50,000 A之範圍內。熔融金屬點火系統之電路可藉由金屬噴射閉合,以使點火頻率在1 Hz至10,000 Hz之範圍內,其中熔融金屬包含銀、銀銅合金及銅中之至少一者,且加成反應物可包含H2 O蒸氣及氫氣中之至少一者。 在實施例中,額外反應物噴射系統可包含電腦、H2 O及H2 壓力感測器及流量控制器中之至少一者,該等流量控制器包含質量流量控制器、泵、注射泵及高精度電子可控閥之群組中之至少一或多者;該閥門包含針閥、比例電子閥及步進電動閥中之至少一者,其中該閥門由壓力感測器及電腦控制以保持H2 O及H2 壓力中之至少一者處於所需值。 額外反應物噴射系統可將H2 O蒸氣壓保持在0.1 Torr至1 Torr之範圍內。 在實施例中,回收反應物產物之系統包含以下中之至少一者:包含能夠在重力下提供熔體流動之壁之容器、電極電磁泵及與該容器連通之儲集器,且該系統進一步包含冷卻系統,其用以將儲集器保持在比容器之另一部分低的溫度下以使熔融金屬之金屬蒸氣凝結在儲集器中 其中回收系統可包含電極電磁泵,其包含提供磁場之至少一個磁體及向量交叉點火電流分量。 在實施例中,電力系統包含能夠保持壓力低於、處於或高於大氣壓之容器,該容器包含內部反應電解槽、包含黑體輻射器之頂蓋及能夠保持壓力低於、處於或高於大氣壓的外部腔室。 其中包含黑體輻射器之頂蓋經保持在1000 K至3700 K之範圍內之溫度下 其中內部反應電解槽及包含黑體輻射器之頂蓋中之至少一者包含具有高輻射率之耐火金屬。 電力系統可包含反應功率輸出之至少一個功率轉換器,其包含以下各者之群組中之至少一者:熱光伏打轉換器、光伏打轉換器、光電轉換器、電漿動力轉換器、熱離子轉換器、熱電轉換器、斯特林引擎、布累登循環引擎、朗肯循環引擎及熱機,以及加熱器。在實施例中,由該池發射之光主要為黑體輻射,包含可見光及近紅外光,且光伏打電池為聚光電池,其包含至少一種選自以下之化合物:鈣鈦礦、結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)、銻化砷磷銦(InPAsSb)、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge。在實施例中,由該池發射之光主要為紫外光,且光伏打電池為聚光電池,其包含至少一種選自III族氮化物、GaN、AlN、 GaAlN及InGaN之化合物。 電力系統可進一步包含真空泵及至少一個急冷器。 在一個實施例中,本發明係針對產生電能及熱能中之至少一者的電力系統,其包含: 至少一個容器,其能夠保持壓力低於、處於或高於大氣壓; 反應物,該等反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)熔融金屬; 至少一個熔融金屬噴射系統,其包含熔融金屬儲集器及電磁泵; 至少一個額外反應物噴射系統,其中該等額外反應物包含: a) 至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O,及 c)至少一種原子氫來源或原子氫; 至少一個包含電源之反應物點火系統,其用以引起反應物形成發光電漿及發熱電漿中之至少一者,其中電源自功率轉換器接收電功率; 用以回收熔融金屬之系統; 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統; 其中熔融金屬點火系統包含: a)至少一組用以約束熔融金屬之電極;及 b)用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源; 其中電極包含耐火金屬; 其中用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源包含至少一個超級電容器; 其中熔融金屬噴射系統包含電磁泵,其包含提供磁場之至少一個磁體及用以提供向量交叉電流分量之電流源; 其中熔融金屬儲集器包含電感耦合加熱器; 其中熔融金屬點火系統包含至少一組分離以形成開路的電極,其中該開路藉由噴射熔融金屬閉合以使高電流流動而達成點火; 其中熔融金屬點火系統電流在500 A至50,000 A之範圍內; 其中熔融金屬點火系統之電路閉合以使點火頻率在1 Hz至10,000 Hz之範圍內; 其中熔融金屬包含銀、銀銅合金及銅中之至少一者; 其中加成反應物包含H2 O蒸氣及氫氣中之至少一者;其中額外反應物噴射系統包含電腦、H2 O及H2 壓力感測器及流量控制器中之至少一者,該等流量控制器包含質量流量控制器、泵、注射泵及高精度電子可控閥之群組中之至少一或多者;該閥門包含針閥、比例電子閥及步進電動閥中之至少一者,其中該閥門由壓力感測器及電腦控制以保持H2 O及H2 壓力中之至少一者處於所需值; 其中額外反應物噴射系統將H2 O蒸氣壓保持在0.1 Torr至1 Torr之範圍內; 其中回收反應物產物之系統包含以下中之至少一者:包含能夠在重力下提供熔體流動之壁之容器、電極電磁泵及與該容器連通之儲集器,且該系統進一步包含冷卻系統,其用以將儲集器保持在比容器之另一部分低的溫度下以使熔融金屬之金屬蒸氣凝結在儲集器中; 其中回收系統包含電極電磁泵,其包含提供磁場之至少一個磁體及向量交叉點火電流分量; 其中能夠保持壓力低於、處於或高於大氣壓之容器包含內部反應電解槽,包含黑體輻射器之頂蓋及能夠保持壓力低於、處於或高於大氣壓的外部腔室; 其中包含黑體輻射器之頂蓋經保持在1000 K至3700 K之範圍內之溫度下; 其中內部反應電解槽及包含黑體輻射器之頂蓋中之至少一者包含具有高輻射率之耐火金屬; 其中黑體輻射器進一步包含黑體溫度感測器及控制器; 其中反應功率輸出之至少一個功率轉換器包含熱光伏打轉換器及光伏打轉換器之群組中之至少一者; 其中由該池發射之光主要為黑體輻射,包含可見光及近紅外光,且光伏打電池為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)及銻化砷磷銦(InPAsSb)、III族/V族半導體、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge;且電力系統進一步包含真空泵及至少一個急冷器。 在一個實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個容器,其能夠保持壓力低於、處於或高於大氣壓; 反應物,該等反應物包含: a)至少一種H2 O來源或H2 O; b) H2 氣體;及 c)熔融金屬; 至少一個熔融金屬噴射系統,其包含熔融金屬儲集器及電磁泵; 至少一個額外反應物噴射系統,其中該等額外反應物包含: a)至少一種H2 O來源或H2 O,及 b) H2 ; 至少一個包含電源之反應物點火系統,其用以引起反應物形成發光電漿及發熱電漿中之至少一者,其中電源自功率轉換器接收電功率; 回收熔融金屬之系統; 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統; 其中熔融金屬點火系統包含: a)至少一組用以約束熔融金屬之電極;及 b) 用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源,其中電極包含耐火金屬; 其中用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源包含至少一個超級電容器; 其中熔融金屬噴射系統包含電磁泵,其包含提供磁場之至少一個磁體及用以提供向量交叉電流分量之電流源; 其中熔融金屬儲集器包含用以至少首先加熱金屬而形成熔融金屬之電感耦合加熱器; 其中熔融金屬點火系統包含至少一組分離以形成開路的電極,其中該開路藉由噴射熔融金屬閉合以使高電流流動而達成點火;其中熔融金屬點火系統電流在500 A至50,000 A之範圍內; 其中熔融金屬點火系統之電路閉合以使點火頻率在1 Hz至10,000 Hz之範圍內; 其中熔融金屬包含銀、銀銅合金及銅中之至少一者; 其中額外反應物噴射系統包含電腦、H2 O及H2 壓力感測器及流量控制器中之至少一者,該等流量控制器包含質量流量控制器、泵、注射泵及高精度電子可控閥之群組中之至少一或多者;該閥門包含針閥、比例電子閥及步進電動閥中之至少一者,其中該閥門由壓力感測器及電腦控制以保持H2 O及H2 壓力中之至少一者處於所需值; 其中額外反應物噴射系統將H2 O蒸氣壓保持在0.1 Torr至1 Torr之範圍內; 其中回收反應物產物之系統包含以下中之至少一者:包含能夠在重力下提供熔體流動之壁之容器、電極電磁泵及與該容器連通之儲集器,且該系統進一步包含冷卻系統,其用以將儲集器保持在比容器之另一部分低的溫度下以使熔融金屬之金屬蒸氣凝結在儲集器中; 其中回收系統包含電極電磁泵,其包含提供磁場之至少一個磁體及向量交叉點火電流分量; 其中能夠保持壓力低於、處於或高於大氣壓之容器包含內部反應電解槽,包含高溫黑體輻射器之頂蓋及能夠保持壓力低於、處於或高於大氣壓的外部腔室; 其中包含黑體輻射器之頂蓋經保持在1000 K至3700 K之範圍內之溫度下; 其中內部反應電解槽及包含黑體輻射器之頂蓋中之至少一者包含具有高輻射率之耐火金屬; 其中黑體輻射器進一步包含黑體溫度感測器及控制器; 其中反應功率輸出之至少一個功率轉換器包含熱光伏打轉換器及光伏打轉換器中之至少一者; 其中由該池發射之光主要為黑體輻射,包含可見光及近紅外光,且光伏打電池為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)及銻化砷磷銦(InPAsSb)、III族/V族半導體、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge;且電力系統進一步包含真空泵及至少一個急冷器。 在一個實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個容器,其能夠保持壓力低於、處於或高於大氣壓; 反應物,該等反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d) 熔融金屬; 至少一個熔融金屬噴射系統,其包含熔融金屬儲集器及電磁泵; 至少一個額外反應物噴射系統,其中該等額外反應物包含: a) 至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O,及 c)至少一種原子氫來源或原子氫; 至少一個包含電源之反應物點火系統,其用以引起反應物形成發光電漿及發熱電漿中之至少一者,其中電源自功率轉換器接收電功率; 用以回收熔融金屬之系統; 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統; 其中熔融金屬點火系統包含: a)至少一組用以約束熔融金屬之電極;及 b)用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能之電源; 其中電極包含耐火金屬; 其中用以傳送足以引起反應物反應形成電漿之短脈衝高電流電能的電源包含至少一個超級電容器; 其中熔融金屬噴射系統包含電磁泵,其包含提供磁場之至少一個磁體及用以提供向量交叉電流分量之電流源; 其中熔融金屬儲集器包含用以至少首先加熱金屬而形成熔融金屬之電感耦合加熱器; 其中熔融金屬點火系統包含至少一組分離以形成開路的電極,其中該開路藉由噴射熔融金屬閉合以使高電流流動而達成點火; 其中熔融金屬點火系統電流在500 A至50,000 A之範圍內; 其中熔融金屬點火系統之電路閉合以使點火頻率在1 Hz至10,000 Hz之範圍內; 其中熔融金屬包含銀、銀銅合金及銅中之至少一者; 其中加成反應物包含H2 O蒸氣及氫氣中之至少一者; 其中額外反應物噴射系統包含電腦、H2 O及H2 壓力感測器及流量控制器中之至少一者,該等流量控制器包含質量流量控制器、泵、注射泵及高精度電子可控閥之群組中之至少一或多者;該閥門包含針閥、比例電子閥及步進電動閥中之至少一者,其中該閥門由壓力感測器及電腦控制以保持H2 O及H2 壓力中之至少一者處於所需值; 其中額外反應物噴射系統將H2 O蒸氣壓保持在0.1 Torr至1 Torr之範圍內; 其中回收反應物產物之系統包含以下中之至少一者:包含能夠在重力下提供熔體流動之壁之容器、電極電磁泵及與該容器連通之儲集器,且該系統進一步包含冷卻系統,其用以將儲集器保持在比容器之另一部分低的溫度下以使熔融金屬之金屬蒸氣凝結在儲集器中; 其中回收系統包含電極電磁泵,其包含提供磁場之至少一個磁體及向量交叉點火電流分量; 其中能夠保持壓力低於、處於或高於大氣壓之容器包含內部反應電解槽,包含黑體輻射器之頂蓋及能夠保持壓力低於、處於或高於大氣壓的外部腔室; 其中包含黑體輻射器之頂蓋經保持在1000 K至3700 K之範圍內之溫度下; 其中內部反應電解槽及包含黑體輻射器之頂蓋中之至少一者包含具有高輻射率之耐火金屬; 其中黑體輻射器進一步包含黑體溫度感測器及控制器; 其中反應功率輸出之至少一個功率轉換器包含熱光伏打轉換器及光伏打轉換器之群組中之至少一者; 其中由該池發射之光主要為黑體輻射,包含可見光及近紅外光,且光伏打電池為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)及銻化砷磷銦(InPAsSb)、III族/V族半導體、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge;且電力系統進一步包含真空泵及至少一個急冷器。 在另一實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個能夠具有低於大氣壓之壓力的容器; 包含反應物之丸粒,該等反應物包含: a) 至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者; 至少一個包含至少一個強化軌道炮之丸粒噴射系統,其中該強化軌道炮包含分離之帶電軌道及產生垂直於軌道平面之磁場的磁體,且軌道之間的電路為開路,直至藉由丸粒與軌道接觸而閉合為止。 至少一個用以引起丸粒形成發光電漿及發熱電漿中之至少一者之點火系統,至少一個點火系統包含: a)至少一組用以約束丸粒之電極;及 b)用以傳送短脈衝高電流電能之電源; 其中該至少一組電極形成開路,其中該開路藉由噴射丸粒而閉合,以使高電流流動而達成點火,且用以傳送短脈衝高電流電能之電源包含以下中之至少一者: 經選擇以引起在100 A至1,000,000 A、1 kA至100,000 A、10 kA至50 kA中之至少一者之範圍內的電流之高AC、DC或AC-DC混合之電壓; 在以下中之至少一者之範圍內的DC或峰值AC電流密度:100 A/cm2 至1,000,000 A/cm2 、1000 A/cm2 至100,000 A/cm2 及2000 A/cm2 至50,000 A/cm2 ; 該電壓由固體燃料之導電性確定,或其中該電壓由所需電流乘以固體燃料樣品之電阻而得到; DC或峰值AC電壓在0.1 V至500 kV、0.1 V至100 kV及1 V至50 kV中之至少一者之範圍內,以及 AC頻率在0.1 Hz至10 GHz、1 Hz至1 MHz、10 Hz至100 kHz及100 Hz至10 kHz中之至少一者之範圍內; 用以回收反應物之反應產物之系統,其包含重力及強化電漿軌道炮回收系統中之至少一者,該強化電漿軌道炮回收系統包含至少一個提供磁場之磁體及點火電極之向量交叉電流分量; 至少一個用以自反應產物再生額外反應物且形成額外丸粒之再生系統,其包含粒化機,該粒化機包含用以形成熔融反應物之熔爐、用以將H2 及H2 O添加至熔融反應物之系統、熔體滴落器及用以形成丸粒之蓄水器, 其中額外反應物包含: a) 至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者;及 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統,其包含以下各者之群組中之一或多者:光伏打轉換器、光電轉換器、電漿動力轉換器、熱離子轉換器、熱電轉換器、斯特林引擎、布累登循環引擎、朗肯循環引擎及熱引擎以及加熱器。 在另一實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個能夠具有低於大氣壓之壓力的容器; 包含反應物之丸粒,該等反應物包含銀、銅、所吸收之氫氣及水中之至少一者; 至少一個包含至少一個強化軌道炮之丸粒噴射系統,其中該強化軌道炮包含分離之帶電軌道及產生垂直於軌道平面之磁場的磁體,且軌道之間的電路為開路,直至藉由丸粒與軌道接觸而閉合為止; 至少一個用以引起丸粒形成發光電漿及發熱電漿中之至少一者之點火系統,至少一個點火系統包含: a)至少一組用以約束丸粒之電極;及 b)用以傳送短脈衝高電流電能之電源; 其中該至少一組電極經分離以形成開路,其中該開路藉由噴射丸粒而閉合,以使高電流流動而達成點火,且用以傳送短脈衝高電流電能之電源包含以下中之至少一者: 經選擇以引起在100 A至1,000,000 A、1 kA至100,000 A、10 kA至50 kA中之至少一者之範圍內的電流之高AC、DC或AC-DC混合之電壓; 在以下中之至少一者之範圍內的DC或峰值AC電流密度:100 A/cm2 至1,000,000 A/cm2 、1000 A/cm2 至100,000 A/cm2 及2000 A/cm2 至50,000 A/cm2 ; 該電壓由固體燃料之導電性確定,其中該電壓由所需電流乘以固體燃料樣品之電阻而得到; DC或峰值AC電壓在0.1 V至500 kV、0.1 V至100 kV及1 V至50 kV中之至少一者之範圍內,以及 AC頻率在0.1 Hz至10 GHz、1 Hz至1 MHz、10 Hz至100 kHz及100 Hz至10 kHz中之至少一者之範圍內;用以回收反應物之反應產物之系統,其包含重力及強化電漿軌道炮回收系統中之至少一者,該強化電漿軌道炮回收系統包含至少一個提供磁場之磁體及點火電極之向量交叉電流分量; 至少一個用以自反應產物再生額外反應物且形成額外丸粒之再生系統,其包含粒化機,該粒化機包含用以形成熔融反應物之熔爐、用以將H2 及H2 O添加至熔融反應物之系統、熔體滴落器及用以形成丸粒之蓄水器, 其中額外反應物包含銀、銅、所吸收之氫氣及水中之至少一者; 至少一個功率轉換器或輸出系統,其包含聚光型紫外光伏打轉換器,其中該等光伏打電池包含至少一種選自III族氮化物、GaAlN、GaN及InGaN之化合物。 在另一實施例中,本發明係針對一種產生電能及熱能中之至少一者之電力系統,其包含: 至少一個容器; 包含反應物之丸粒,該等反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者; 至少一個丸粒噴射系統; 至少一個丸粒點火系統,其用以引起丸粒形成發光電漿及發熱電漿中之至少一者; 用以回收反應物之反應產物之系統; 至少一個再生系統,其用以自反應產物再生額外反應物且形成額外丸粒, 其中額外反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者; 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統。 本發明之某些實施例係針對一種電力產生系統,其包含:複數個經組態以將功率傳送至燃料以對該燃料點火且產生電漿之電極;經組態以將電能傳送至複數個電極之電源;以及至少一個定位成用於接收至少複數個電漿光子之光伏打功率轉換器。 在一個實施例中,本發明係針對一種產生直流電能及熱能中之至少一者之電力系統,其包含: 至少一個容器; 反應物,其包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種原子氫來源或原子氫; c) 導體及導電基質中之至少一者;及 至少一組用以約束低能量氫反應物之電極, 用以傳送短脈衝高電流電能之電源; 重載系統; 至少一個用以自反應產物再生初始反應物之系統,及 至少一個電漿動力轉換器或至少一個光伏打轉換器。 在一個例示性實施例中,產生電力之方法可包含向複數個電極之間的區域供應燃料;為複數個電極供能以對該燃料點火,形成電漿;用光伏打功率轉換器將複數個電漿光子轉換成電功率;以及輸出至少一部分電功率。 在另一例示性實施例中,產生電功率之方法可包含向複數個電極之間的區域供應燃料;為複數個電極供能以對該燃料點火,形成電漿;用光伏打功率轉換器將複數個電漿光子轉換成熱功率;以及輸出至少一部分電功率。 在本發明之實施例中,產生功率之方法可包含:將一定量之燃料傳送至燃料裝載區,其中該燃料裝載區位於複數個電極間;藉由向複數個電極施加至少約100 A/cm2 之電流,使該電流流過燃料來對該燃料點火,從而產生電漿、光及熱中之至少一者;在光伏打功率轉換器中接收光之至少一部分;使用光伏打功率轉換器將光轉換成不同形式之功率;以及輸出不同形式之功率。 在另一實施例中,本發明係針對一種水電弧電漿電力系統,其包含:至少一個封閉之反應容器;包含H2 O來源及H2 O中之至少一者之反應物;至少一組電極;用以傳送該H2 O之初始高擊穿電壓且提供後續高電流之電源;及熱交換器系統,其中該電力系統產生電弧電漿、光及熱能;及至少一個光伏打功率轉換器。可在電極上或跨電極供應呈蒸氣形式之水。可准許電漿擴展至電漿電池之低壓區域中,以防止由於約束而抑制低能量氫反應。電弧電極可包含火花塞設計。電極可包含銅、鎳、鍍有鉻酸銀及鋅以供抗腐蝕之鎳、鐵、鎳鐵、鉻、貴金屬、鎢、鉬、釔、銥及鈀中之至少一者。在實施例中,水電弧經保持處於低水壓,諸如在約0.01 Torr至10 Torr及0.1 Torr至1 Torr中之至少一個範圍中。 壓力範圍可藉助於針對SF-CIHT電池之揭示內容而保持在本發明之一個範圍中。用以供應水蒸氣之例示性構件係質量流量控制器及包含H2 O之儲集器中之至少一者,該儲集器諸如為水合沸石或鹽浴,諸如在所需壓力範圍下排出氣體H2 O之KOH溶液。水可由注射泵供應,其中傳送至真空中導致水之汽化。 本發明之某些實施例係針對一種電力產生系統,其包含:至少約100 A/cm2 或至少約5,000 kW之電源;電耦接至該電源之複數個電極;經組態以接收固體燃料之燃料裝載區,其中該複數個電極經組態以將電功率傳送至該固體燃料,從而產生電漿;及經定位以接收由反應產生之電漿、光子及/或熱之至少一部分的電漿功率轉換器、光伏打功率轉換器及熱-電功率轉換器中之至少一者。其他實施例係針對一種電力產生系統,其包含:複數個電極;位於該複數個電極之間且經組態以接收導電燃料之燃料裝載區,其中該複數個電極經組態以將足以對該導電燃料點火且產生電漿及熱功率中至少一者之電流施加至該導電燃料;用於將該導電燃料移至該燃料裝載區中之傳送機構;及用以將電漿光子轉換成某一形式之功率之光伏打功率轉換器或用以將熱功率轉換成非熱形式之功率(包含電力或機械功率)之熱-電功率轉換器中之至少一者。其他實施例係針對一種產生電力之方法,其包含:將一定量燃料傳送至燃料裝載區,其中該燃料裝載區係位於複數個電極間;藉由向複數個電極施加至少約2,000 A/cm2 之電流,使該電流流過該燃料來對該燃料點火,從而產生電漿、光及熱中至少一者;在光伏打功率轉換器中接收該光之至少一部分;使用光伏打功率轉換器將該光轉換成不同形式之功率;及輸出該不同形式之功率。 額外實施例係針對一種電力產生系統,其包含:至少約5,000 kW之電源;複數個間隔開之電極,其中該複數個電極至少部分地包圍燃料,電連接至該電源,經組態以接收電流從而對該燃料點火,且該複數個電極中至少一者為可移動的;用於移動該燃料之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的光伏打功率轉換器。本發明另外提供一種電力產生系統,其包含:至少約2,000 A/cm2 之電源;複數個間隔開之電極,其中該複數個電極至少部分地包圍燃料,電連接至該電源,經組態以接收電流從而對該燃料點火,且該複數個電極中至少一者為可移動的;用於移動該燃料之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的光伏打功率轉換器。 另一實施例係針對一種電力產生系統,其包含:至少約5,000 kW或至少約2,000 A/cm2 之電源;複數個間隔開之電極,其中該複數個電極中之至少一者包括壓縮機構;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,使得該至少一個電極之壓縮機構朝向該燃料裝載區定向,且其中該複數個電極電連接至該電源且經組態以向該燃料裝載區中所接收之燃料供電,從而對該燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之光子轉換成非光子形式之功率的光伏打功率轉換器。本發明之其他實施例係針對一種電力產生系統,其包含:至少約2,000 A/cm2 之電源;複數個間隔開之電極,其中該複數個電極中之至少一者包括壓縮機構;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,使得該至少一個電極之壓縮機構朝向該燃料裝載區定向,且其中該複數個電極電連接至該電源且經組態以向該燃料裝載區中所接收之燃料供電從而對該燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的電漿功率轉換器。 本發明之實施例亦針對電力產生系統,其包含:複數個電極;由該複數個電極包圍且經組態以接收燃料之燃料裝載區,其中該複數個電極經組態以對位於該燃料裝載區中之燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;經組態以將由該燃料點火產生之光子轉換成非光子形式之功率之光伏打功率轉換器;用於移除經點火之燃料之副產物的移除系統;及可操作地耦接至該移除系統之再生系統,其用於將移除的經點火之燃料之副產物再循環至再循環之燃料中。本發明之某些實施例亦針對一種電力產生系統,其包含:經組態以輸出至少約2,000 A/cm2 或至少約5,000 kW之電流的電源;電連接至該電源之複數個間隔開之電極;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,且其中該複數個電極經組態以在該燃料接收於該燃料裝載區中時向該燃料供電以對該燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之複數個光子轉換成非光子形式之功率的光伏打功率轉換器。某些實施例可進一步包括以下中之一或多者:可操作地耦接至光伏打功率轉換器之輸出功率端子;功率儲存裝置;經組態以量測與該電力產生系統相關之至少一個參數之感測器;及經組態以控制與該電力產生系統相關之至少一個製程的控制器。本發明之某些實施例亦針對一種電力產生系統,其包含:經組態以輸出至少約2,000 A/cm2 或至少約5,000 kW之電流之電源;複數個間隔開之電極,其中該複數個電極至少部分地包圍燃料,電連接至該電源,經組態以接收電流從而對該燃料點火,且該複數個電極中之至少一者為可移動的;用於移動該燃料之傳送機構;及經組態以將由該燃料點火產生之光子轉換成不同形式之功率之光伏打功率轉換器。 本發明之額外實施例係針對一種電力產生系統,其包含:至少約5,000 kW或至少約2,000 A/cm2 之電源;電連接至該電源之複數個間隔開之電極;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,且其中該複數個電極經組態以在該燃料接收於該燃料裝載區中時向該燃料供電以對該燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;經組態以將由該燃料點火產生之複數個光子轉換成非光子形式之功率的光伏打功率轉換器;經組態以量測與該電力產生系統相關之至少一個參數之感測器;及經組態以控制與該電力產生系統相關之至少一個製程的控制器。另外的實施例係針對一種電力產生系統,其包含:至少約2,000 A/cm2 之電源;電連接至該電源之複數個間隔開之電極;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,且其中該複數個電極經組態以在該燃料接收於該燃料裝載區中時向該燃料供電以對該燃料點火;用於將該燃料移至該燃料裝載區中之傳送機構;經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的電漿功率轉換器;經組態以量測與該電力產生系統相關之至少一個參數之感測器;及經組態以控制與該電力產生系統相關之至少一個製程的控制器。 本發明之某些實施例係針對一種電力產生系統,其包含:至少約5,000 kW或至少約2,000 A/cm2 之電源;電連接至該電源之複數個間隔開之電極;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,且其中該複數個電極經組態以在該燃料接收於該燃料裝載區中時向該燃料供電以對該燃料點火,且其中該燃料裝載區中之壓力為部分真空;用於將該燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的光伏打功率轉換器。一些實施例可包括以下額外特徵中之一或多者:光伏打功率轉換器可位於真空單元內;該光伏打功率轉換器可包括抗反射塗層、光阻抗匹配塗層或保護塗層中之至少一者;該光伏打功率轉換器可以可操作地耦接至經組態以清潔該光伏打功率轉換器之至少一部分的清潔系統;該電力產生系統可包括光學濾光片;該光伏打功率轉換器可包含單晶電池、多晶電池、非晶電池、串狀/帶狀矽電池、多接面電池、同質接面電池、異質接面電池、p-i-n裝置、薄膜電池、染料敏化電池及有機光伏打電池中之至少一者;且該光伏打功率轉換器可包含多接面電池,其中該多接面電池包含倒置式電池、立式電池、晶格失配電池、晶格匹配電池及包含III-V族半導體材料之電池中之至少一者。 額外例示性實施例係針對一種經組態以生成電力之系統,其包含:經組態以供應燃料之燃料供應器;經組態以供應電功率之電力供應器;及至少一對經組態以接收燃料及電功率之電極,其中該等電極選擇性地將電功率引向圍繞電極之局部區域,以對該局部區域內之燃料點火。一些實施例係針對一種生成電功率之方法,其包含:向電極供應燃料;向電極供應電流以對經定位之燃料點火從而生成能量;及將由點火生成之至少一些能量轉換成電功率。 其他實施例係針對一種電力產生系統,其包含:至少約2,000 A/cm2 之電源;電連接至該電源之複數個間隔開之電極;經組態以接收燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,且其中該複數個電極經組態以在該燃料接收於該燃料裝載區中時向該燃料供電以對該燃料點火,且其中該燃料裝載區中之壓力為部分真空;用於將該燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的光伏打功率轉換器。 另外的實施例係針對一種電力產生單元,其包含:耦接至真空泵之出口孔;電耦接至至少約5,000 kW之電源的複數個電極;經組態以接收主要包含H2 O之基於水之燃料的燃料裝載區,其中該複數個電極經組態以將功率傳送至該基於水之燃料,從而產生電弧電漿及熱功率中之至少一者;及經組態以將該電弧電漿及該熱功率中之至少一者的至少一部分轉換成電功率的功率轉換器。亦揭示一種電力產生系統,其包含:至少約5,000 A/cm2 之電源;電耦接至該電源之複數個電極;經組態以接收主要包含H2 O之基於水之燃料的燃料裝載區,其中該複數個電極經組態以將功率傳送至該基於水之燃料,從而產生電弧電漿及熱功率中之至少一者;及經組態以將該電弧電漿及該熱功率中之至少一者的至少一部分轉換成電功率的功率轉換器。在一實施例中,該功率轉換器包含將光功率轉換成電之光伏打轉換器。 額外實施例係針對一種產生電力之方法,其包含:將燃料裝載至燃料裝載區中,其中該燃料裝載區包括複數個電極;將至少約2,000 A/cm2 之電流施加至該複數個電極以對該燃料點火,從而產生電弧電漿及熱功率中之至少一者;執行以下至少一者:使該電弧電漿通過光伏打轉換器以產生電功率,及使該熱功率通過熱-電轉換器以產生電功率;及輸出所產生之電功率之至少一部分。亦揭示一種電力產生系統,其包含:至少約5,000 kW之電源;電耦接至該電源之複數個電極,其中該複數個電極經組態以將電功率傳送至主要包含H2 O之基於水之燃料,從而產生熱功率;及經組態以將該該熱功率之至少一部分轉換成電功率之熱交換器;及經組態以將光之至少一部分轉換成電功率之光伏打功率轉換器。另外,另一發實施例係針對一種電力產生系統,其包含:至少約5,000 A/cm2 之電源;複數個間隔開之電極,其中該複數個電極中之至少一者包括壓縮機構;經組態以接收主要包含H2 O之基於水之燃料之燃料裝載區,其中該燃料裝載區由該複數個電極包圍,使得該至少一個電極之壓縮機構朝向該燃料裝載區定向,且其中該複數個電極電連接至該電源且經組態以向該燃料裝載區中所接收之基於水之燃料供電從而對該燃料點火;用於將該基於水之燃料移至該燃料裝載區中之傳送機構;及經組態以將由該燃料點火產生之電漿轉換成非電漿形式之功率的光伏打功率轉換器。 本文中揭示用以釋放來自原子氫之能量以形成較低能態之催化劑系統,其中電子外殼處於相對於核較接近之位置。 所釋放之功率用於發電,且另外,新型氫物質及化合物為所需產物。該等能態係由經典物理定律所預測的,且需要催化劑來接受來自氫的能量以便進行相對應的能量釋放躍遷。 經典物理學給出氫原子、氫陰離子、氫分子離子及氫分子的閉型解,且預測具有分數主量子數之相對應的物質。原子氫可經歷與某些物質(包括其本身)之催化反應,其可接受原子氫之位能之整數倍的能量m·27.2 eV,其中m為整數。所預測之反應涉及諧振非輻射能量自原本穩定之原子氫傳遞至能夠接受該能量之催化劑。產物為H(1/p),原子氫之分數芮得伯態(fractional Rydberg state),稱作「低能量氫原子」,其中在用於氫激發態之芮得伯方程式中,n=1/2、1/3、1/4、...、1/p(p≤137,為整數)替換熟知參數n=整數。各低能量氫態亦包含電子、質子及光子,但來自光子之場份額增加結合能而非減小結合能,其對應於能量解吸而非吸收。因為原子氫之位能為27.2 eV,所以mH 原子充當針對另一第(m + 1)個H原子之具有m·27.2 eV之催化劑[1]。舉例而言,H原子可藉由經由跨空間能量傳遞(諸如藉由磁或所感應之電偶極-偶極耦合)自另一個H接受27.2 eV而充當其催化劑,從而形成隨連續譜帶之發射衰變之中間物,其具有短波長截止及能量。除原子H以外,自原子H接受m · 27.2 eV且分子位能量值減少相同能量之分子亦可充當催化劑。H2 O之位能為81.6 eV。隨後,藉由相同機制,預測藉由金屬氧化物之熱力學有利的還原形成之初生H2 O分子(並非以固態、液態或氣態鍵合之氫)充當催化劑,以形成釋放204 eV能量(包含81.6 eV傳遞至HOH)及釋放在10.1 nm處具有截止之連續輻射(122.4 eV)的H (1/4)。 在涉及躍遷至態之H 原子催化劑反應中,mH 原子充當另外第(m + 1 )個H原子之具有m · 27.2eV 之催化劑。隨後,m 個原子藉以自第(m +1 )個氫原子以諧振及非輻射方式接受m · 27.2eV 而使得mH 充當催化劑之m +1個氫原子之間的反應藉由以下給出: 且,總反應為關於新生H2 O [1]之位能,催化反應(m =3)為且,總反應為在能量傳遞至催化劑(方程式(1)及(5))之後,形成具有H原子半徑及為質子中心場之m + 1倍的中心場的中間物。預測半徑隨著電子經歷徑向加速度而減小,直至半徑為未催化氫原子之半徑的1/(m + 1)的穩定狀態,且釋放出m2 · 13.6 eV能量。預測歸因於中間物(例如方程式(2)及方程式(6)之遠紫外連續輻射譜帶具有短波長截止及藉由以下給出之能量且延伸至比對應的截止長之波長。此處,由於H*[aH /4]中間物之衰減而引起之遠紫外連續輻射譜帶經預測為在 E = m2 ·13.6 = 9·13.6 = 122.4 eV (10.1 nm)處具有短波長截止[其中在方程式(9)中, p = m + 1 = 4且m = 3]並延伸至更長的波長。觀察到10.1 nm處之連續輻射譜帶,且對於理論上預測之H至較低能量(所謂的「低能量氫」狀態H(1/4))之躍遷到達較長波長,其僅由包含一些氫之脈衝捏縮氣體放電引起。藉由方程式(1)及(5)預測之另一觀察結果為自快H+ 之再結合形成快速激發態H原子。該等快原子產生展寬之巴耳麥α發射。 揭露了在某些混合氫電漿中具有非常高的動能能量氫原子之群體的大於50 eV之巴耳麥α線展寬係一種熟知現象,其中其原因係由於在低能量氫之形成中所釋放的能量。在連續發射氫捏縮電漿中觀察到快H。 形成低能量氫之額外催化劑及反應係可能的。基於已知電子能級可鑑別的具體物質(例如,He+ 、Ar+ 、Sr+ 、K、Li、HCl及NaH、OH、SH、SeH、初生H2 O、nH (n=整數))需要與原子氫一起存在以催化該過程。該反應涉及非輻射性能量傳遞,接著為q·13.6 eV連續發射或q·13.6 eV傳遞至H以形成極熱的激發態H及氫原子,該氫原子之能量低於對應於分數主量子數的未反應之原子氫。亦即,在氫原子之主能級之式中:其中aH 為氫原子之波爾半徑(Bohr radius) (52.947 pm),e 為電子電荷之量值,且ε o 為真空電容率,分數量子數:;其中p ≤ 137為整數 (12) 替換氫激發態之芮得伯方程式(Rydberg equation)中之熟知參數n =整數且表示稱為「低能量氫」之較低能態氫原子。氫之狀態及氫之狀態為非輻射性的,但兩種非輻射狀態之間的躍遷,比如n = 1至n = 1/2,係可能經由非輻射性能量傳遞發生的。氫為由方程式(10)及(12)給出之穩定狀態的特例,其中氫或低能量氫原子之相對應半徑係由以下給出:, (13) 其中p = 1、2、3、...。為使能量守恆,能量必須以處於普通n = 1 狀態中之氫原子的位能之整數為單位自氫原子傳遞至催化劑,且半徑躍遷至。藉由使普通氫原子與具有以下之反應淨焓之合適的催化劑反應而形成低能量氫: m • 27.2 eV (14) 其中m 為整數。據信,隨著反應淨焓更緊密地匹配m • 27.2eV ,催化之速率增加。已發現反應,反應淨焓在m • 27.2eV 之±10% (較佳±5%)內之催化劑適合於大多數應用。 催化反應涉及兩步能量釋放:非輻射性能量傳遞至催化劑,接著隨著半徑減小,進行另外的能量釋放,直至相對應的穩定最終狀態。因此,藉由以下給出總體反應: 及 (17) 整體反應為 qrmp 為整數。具有氫原子之半徑(對應於分母中之1)及等於質子之中心場的(m +p )倍的中心場,且係半徑為H的對應穩態。 催化劑產物H (l/p )亦可與電子反應,形成低能量氫氫陰離子H - (l/p ),或兩個H (l/p ) 可發生反應,形成相對應的分子低能量氫H2 (l/p )。具體而言,催化劑產物H (l/p )亦可與電子反應,形成具有結合能EB 之新穎氫陰離子H - (l/p )。其中p = 整數 > 1,s = 1/2,為普朗克常量項(Planck's constant bar),為真空之磁導率,me 為電子之質量,為由給出之約化之電子質量,其中mp 為質子之質量,ao 為波爾半徑,且離子半徑為。根據方程式(19),經計算之氫陰離子之電離能量為0.75418eV ,且實驗值為6082.99 ± 0.15cm - 1 (0.75418 eV)。低能量氫氫陰離子之結合能可藉由X射線光電子光譜(XPS)量測。 往高磁場位移之NMR峰係存在相對於普通氫陰離子半徑減小且質子之反磁性屏蔽增大的較低能態氫的直接證據。藉由兩個電子之反磁性及幅度為p之光子場的作用之總和給出位移(Mills GUTCP方程式(7.87)):其中第一項適用於H - ,其中對於H - (l /p ),p = 1且p =整數 >1,且α 為精細結構常量。所預測之低能量氫氫陰離子峰相對於普通氫陰離子異常地往高磁場位移。在實施例中,峰為TMS的高磁場。相對於TMS之NMR位移可大於對於單獨或構成化合物之普通H- 、H、H2 或H+ 中之至少一者已知的NMR位移。該位移可大於以下中之至少一者:0、-1、-2、-3、-4、 -5、-6、-7、-8、-9、-10、-11、-12、-13、-14、-15、-16、-17、-18、 -19、-20、-21、- 22、-23、-24、-25、-26、-27、-28、-29、-30、-31、-32、-33、-34、-35、-36、-37、-38、-39及-40 ppm。相對於裸質子之絕對位移之範圍(其中TMS之位移相對於裸質子為約-31.5)可為-(p29.9 + p2 2.74) ppm (方程式(20)),其約在以下之至少一者中的範圍內:± 5 ppm、± 10 ppm、± 20 ppm、± 30 ppm、± 40 ppm、± 50 ppm、± 60 ppm、± 70 ppm、± 80 ppm、± 90 ppm及± 100 ppm。相對於裸質子之絕對位移之範圍可為-(p29.9 + p2 1.59 × 10- 3 ) ppm (方程式(20)),其約在以下之至少一者中的範圍內:0.1%至99%、1%至50%及1%至10%。在另一個實施例中,低能量氫物質(諸如,低能量氫原子、氫陰離子或分子)在固體基質(諸如,如NaOH或KOH之氫氧化物之基質)中之存在引起基質質子往高磁場位移。基質質子(諸如NaOH或KOH之基質質子)可交換。在實施例中,位移可引起基質峰在相對於TMS的約-0.1 ppm至-5 ppm之範圍內。NMR測定可包含魔角旋轉 1 H 核磁諧振光譜(MAS 1 H NMR)。H (l/p )可與質子反應且兩個H (l/p )可發生反應以分別形成H 2 (l / p)+H2 (l/p )。在非輻射之約束下,根據橢圓座標中之拉普拉斯算子(Laplacian)來求解氫分子離子及分子電荷與電流密度函數、鍵距離以及能量。在長球體分子軌道之各焦點處具有+pe 之中心場的氫分子離子之總能量ET 為:其中p 為整數,c 為真空中之光速,且μ 為經約化之核質量。在長球體分子軌道之各焦點處具有+pe 之中心場的氫分子之總能量為:氫分子H2 (1/p ) 之鍵解離能量ED 係對應氫原子之總能量與ET 之間的差。其中 ED 由方程式(23-25)給出: H2 (1/p )可由X射線光電子光譜(XPS)識別,其中除經電離電子之外的電離產物可為諸如包含兩個質子及電子(氫(H)原子、低能量氫原子、分子離子、氫分子離子及H2 (1/ p)+ )之可能物中的至少一者,其中能量可因基質而位移。 催化產物氣體之NMR提供H2 (1/p )之理論上預測的化學位移的決定性測試。大體而言,歸因於橢圓座標中之分數半徑,H2 (1/p )之1 H NMR諧振經預測為自H2 1 H NMR諧振朝向高磁場,其中電子明顯更靠近原子核。藉由兩個電子之反磁性及幅度為p之光子場的作用之總和給出H2 (1/p )之經預測位移(Mills GUTCP方程式(11.415-11.416)):其中第一項適用於H 2 ,其中對於H2 (1/p ),p = 1且p = 整數 >1。實驗絕對H2 氣相諧振位移-28.0 ppm與經預測之絕對氣相位移-28.01 ppm相符(方程式(28))。所預測之分子低能量氫的峰相對於普通H2 異常地往高磁場位移。在實施例中,峰為TMS的高磁場。相對於TMS之NMR位移可大於對於單獨或構成化合物之普通H- 、H、H2 或H+ 中之至少一者已知的NMR位移。該位移可大於以下中之至少一者:0、-1、-2、-3、-4、-5、 -6、-7、-8、-9、-10、-11、-12、-13、-14、-15、-16、-17、-18、-19、-20、-21、- 22、-23、-24、-25、-26、-27、-28、-29、-30、-31、-32、-33、-34、-35、-36、-37、-38、-39及-40 ppm。相對於裸質子之絕對位移之範圍(其中TMS之位移相對於裸質子為約-31.5 ppm)可為-(p28.01 + p2 2.56) ppm (方程式(28)),其約在以下之至少一者中的範圍內:± 5 ppm、± 10 ppm、± 20 ppm、± 30 ppm、± 40 ppm、± 50 ppm、± 60 ppm、± 70 ppm、± 80 ppm、± 90 ppm及± 100 ppm。相對於裸質子之絕對位移之範圍可為-(p28.01 + p2 1.49 × 10- 3 ) ppm (方程式(28)),其約在以下之至少一者中的範圍內:0.1%至99%、1%至50%及1%至10%。 供氫型分子H2 (1/p )自v = 0躍遷至v = 1的振動能量E vib 為:其中p 為整數。 供氫型分子H2 (1/p )自J 躍遷至J +1的旋轉能量Era t 為:其中p 為整數且I 為慣性力矩。對氣體中及捕集於固體基質中之電子束激發分子觀察到H2 (1/4)之振轉發射。 由核間距離之反向p 相關性及對慣性力矩I 之對應影響得到旋轉能量之p2 相關性。H2 (1/p )之經預測之核間距離2c '為H2 (1/p)之旋轉及振動能量中之至少一者可藉由激勵發射光譜分析、拉曼光譜分析及傅立葉變換紅外(FTIR)光譜分析來量測。H2 (1/p)可捕集於基質中(諸如MOH、MX及M2 CO3 (M = 鹼金屬;X = 鹵化物)基質中之至少一者中),以便進行量測。 在實施例中,觀察到作為大約1950 cm- 1 處之逆拉曼效應(IRE)峰的分子低能量氫產物。藉由使用包含與支援表面增強型拉曼散射(SERS)之拉曼雷射波長相當的粗糙度特徵或粒度的導電材料來增強峰,以展示IRE峰。I . 催化劑 在本發明中,諸如低能量氫反應、H催化作用、H催化反應、當提及氫時的催化、形成低能量氫之氫反應及低能量氫形成反應均係指例如以下之反應:由方程式(14)定義之催化劑的方程式(15)至(18)與原子H反應以形成具有由方程式(10)及(12)給出的能級之氫狀態。當提及執行將H催化至具有由方程式(10)及(12)給出之能級的H狀態或低能量氫狀態的反應混合物時,諸如低能量氫反應物、低能量氫反應混合物、催化劑混合、用於低能量氫形成之反應物、產生或形成低能態氫或低能量氫的反應物的對應術語亦可互換地使用。 本發明之催化性低能量氫躍遷需要自原子H接受能量以引起躍遷的催化劑,該催化劑可呈未經催化之原子氫之位能27.2eV 的整數m 倍的吸熱化學反應的形式。吸熱催化劑反應可為自諸如原子或離子之物質電離一或多個電子(例如,對於m = 3),且可進一步包含鍵斷裂與自一或多種初始鍵搭配物電離一或多個電子的協同反應(例如,對於m = 2) He + 因為以54.417eV (為2 • 27.2eV )電離,所以其滿足催化劑準則——焓變等於27.2eV 之整數倍的化學或物理過程。整數數目個氫原子亦可充當27.2eV 焓之整數倍的催化劑。催化劑能夠自原子氫接受呈約27.2 eV ± 0.5 eV及中之一者的整數單位的能量。 在實施例中,催化劑包含原子或離子M,其中t 個電子自原子或離子M各自電離至連續能級,以使得t 個電子之電離能量的總和大致為m • 27.2eV中之一者,其中m 為整數。 在實施例中,催化劑包含雙原子分子MH,其中M-H鍵之斷裂加上t 個電子自原子M各自電離至連續能級使得t 個電子之鍵能及電離能量的總和大致為m • 27.2eV中之一者,其中m 為整數。 在實施例中,催化劑包含原子、離子及/或選自分子AlH、AsH、BaH、BiH、CdH、ClH、CoH、GeH、InH、NaH、NbH、OH、RhH、RuH、SH、SbH、SeH、SiH、SnH、SrH、TlH、C2 N2 O2 C O2 N O2 NO3 之分子及以下之原子或離子:Li、Be、K、Ca、Ti、V、Cr、Mn、Fe、Co、Ni、Cu、Zn、As、Se、Kr、Rb、Sr、Nb、Mo、Pd、Sn、Te、Cs、Ce、Pr、Sm、Gd、Dy、Pb、Pt、Kr、2K +He +Ti 2+Na +Rb + Sr +Fe 3+M o 2+Mo4+ In3+ He + Ar +Xe + Ar 2+H + ,及Ne + 以及H + 。在其他實施例中,藉由以下提供用以產生低能量氫之MH- 型氫催化劑:將電子傳遞至受體A、M-H鍵斷裂加t 個電子自原子M各自電離至連續能級,使得包含MH與A之電子親和力(EA)之差異的電子傳遞能量、M-H鍵能及t 個電子自M電離的電離能量之總和為約m• 27.2eV ,其中m 為整數。能夠提供約m• 27.2eV 之反應淨焓的MH- 型氫催化劑為 OH- 、SiH- 、CoH- 、NiH- 及SeH- 。 在其他實施例中,藉由以下提供用以產生低能量氫之MH+ 型氫催化劑:自可帶負電之供體A傳遞電子、M-H鍵斷裂加t 個電子自原子M各自電離至連續能級,使得包含MH與A之電離能量之差異的電子傳遞能量、M-H鍵能及t 個電子自M電離的電離能量之總和為約m• 27.2eV ,其中m 為整數。在實施例中,分子或帶正電或帶負電分子離子中之至少一者充當自原子H接受約m27.2 eV之催化劑,其中分子或帶正電或帶負電分子離子之位能的量值減小約m27.2 eV。例示性催化劑為H2 O、OH、醯胺基NH2 及H2 S。 O2 可充當催化劑或催化劑來源。氧分子之鍵能為5.165 eV,且氧原子之第一、第二及第三電離能量分別為13.61806eV 35.11730eV 及54.9355eV 。反應分別提供為Eh 約2倍、4倍及1倍之淨焓且包含藉由自H接受此等能量以使低能量氫形成的用以形成低能量氫的催化劑反應。II . 低能量氫 具有由給出之結合能之氫原子(其中p為大於1,較佳為2至137之整數)係本發明之H催化反應的產物。原子、離子或分子之結合能(亦被稱作電離能量)係自原子、離子或分子移除一個電子所需的能量。具有方程式(10)及(12)中給出之結合能的氫原子在下文被稱作「低能量氫原子」或「低能量氫」。具有半徑之低能量氫的標識為,其中aH 為普通氫原子之半徑且p 為整數。具有半徑aH 之氫原子在下文中被稱作「普通氫原子」或「正常氫原子」。普通原子氫之特徵在於其結合能為13.6 eV。 根據本發明,提供一種具有根據方程式(19)之結合能的低能量氫氫陰離子(H- ),該結合能對於p = 2直至23大於且對於p = 24 (H- )小於普通氫陰離子之結合能(約0.75 eV)。對於方程式(19)之p = 2至p = 24,氫陰離子結合能分別為3、6.6、11.2、16.7、22.8、29.3、36.1、42.8、49.4、55.5、61.0、65.6、69.2、71.6、72.4、71.6、68.8、64.0、56.8、47.1、34.7、19.3及0.69 eV。本文亦提供包含新穎氫陰離子之例示性組合物。 亦提供包含一或多種低能量氫氫陰離子及一或多種其他元素的例示性複合物。此類化合物被稱為「低能量氫氫化物」。 普通氫物質之特徵在於以下結合能:(a)氫陰離子,0.754 eV (「普通氫陰離子」);(b)氫原子(「普通氫原子」),13.6 eV;(c)雙原子氫分子,15.3 eV (「普通氫分子」);(d)氫分子離子,16.3 eV (「普通氫分子離子」);及(e),22.6 eV (「普通三氫分子離子」)。本文中,關於氫之形式,「正常」與「普通」同義。 根據本發明之另一實施例,提供一種化合物,其包含至少一種結合能增加的氫物質,諸如:(a)氫原子,其具有約(諸如,在之約0.9倍至1.1倍的範圍內)之結合能,其中p為自2至137之整數;(b)氫陰離子(H - ),其具有約(諸如,在之約0.9倍至1.1倍的範圍內)之結合能,其中p為自2至24之整數;(c);(d)三低能量氫分子離子,其具有約 eV (諸如,在 eV 之約0.9倍至1.1倍的範圍內)之結合能,其中p為自2至137之整數;(e)二低能量氫,其具有約 eV (諸如,在 eV 的約0.9倍至1.1倍的範圍內)之結合能,其中p為自2至137之整數;(f)二低能量氫分子離子,其具有約 eV (諸如在 eV 之約0.9倍至1.1倍的範圍內)之結合能,其中p為整數,較佳為自2至137之整數。 根據本發明之另一實施例,提供一種化合物,其包含至少一種結合能增加之氫物質,諸如:(a)二低能量氫分子離子,其具有約(諸如在的約0.9倍至1.1倍的範圍內)之總能量,其中p 為整數,為普朗克常量項,me 為電子之質量,c 為真空中之光速,且μ 為經約化之核質量, 及(b)二低能量氫分子,其具有約(諸如,在之約0.9至1.1倍的範圍內)之總能量,其中p 為整數且ao 為波爾半徑。 根據本發明之一個實施例(其中化合物包含帶負電之結合能增加的氫物質),該化合物進一步包含一或多種陽離子,諸如質子、普通或普通。 本文提供一種用於製備包含至少一種低能量氫氫陰離子之化合物的方法。此類化合物在下文被稱作「低能量氫氫化物」。該方法包含使原子氫與反應淨焓為約之催化劑反應,其中m為大於1之整數,較佳為小於400之整數,從而產生結合能為約之結合能增加的氫原子,其中p 為整數,較佳為自2至137的整數。另一催化產物為能量。結合能增加之氫原子可與電子來源反應以產生結合能增加之氫陰離子。結合能增加之氫陰離子可與一或多種陽離子反應以產生包含至少一種結合能增加之氫陰離子的化合物。 新穎的氫組成物質可包含: (a)至少一種具有以下結合能之中性、正或負的氫物質(在下文中為「結合能增加之氫物質」) (i)大於對應普通氫物質之結合能,或 (ii)大於任何氫物質在對應普通氫物質因為普通氫物質之結合能小於環境條件(標準溫度及壓力,STP)下之熱能或為負而不穩定或觀察不到時的結合能;及 (b)至少一種其他元素。本發明之化合物在下文中被稱作「結合能增加之氫化合物」。 在此上下文中,「其他元素」意謂除結合能增加之氫物質以外的元素。因此,其他元素可為普通氫物質,或除氫以外之任何元素。在一組化合物中,其他元素及結合能增加之氫物質為中性。在另一組化合物中,其他元素及結合能增加之氫物質帶電,使得其他元素提供平衡電荷以形成中性化合物。前一組化合物之特徵在於分子及配位鍵合;後一組之特徵在於離子鍵合。 亦提供新穎化合物及分子離子,其包含: (a)至少一種具有以下總能量之中性、正或負的氫物質(在下文中為「結合能增加之氫物質」) (i)大於對應普通氫物質之總能量,或 (ii)大於任何氫物質在對應普通氫物質因為普通氫物質之總能量小於環境條件下之熱能或為負而不穩定或觀察不到時的總能量;及 (b)至少一種其他元素。 氫物質之總能量為自氫物質移除所有電子的能量之總和。根據本發明之氫物質的總能量大於對應普通氫物質之總能量。根據本發明之總能量增加之氫物質亦被稱作「結合能增加之氫物質」,即使總能量增加之氫物質之一些實施例可具有比對應普通氫物質之第一電子結合能小的第一電子結合能。舉例而言,p = 24之方程式(19)之氫陰離子的第一結合能小於普通氫陰離子之第一結合能,而p = 24之方程式(19)之氫陰離子的總能量遠遠大於對應普通氫陰離子之總能量。 本文亦提供新穎化合物及分子離子,其包含: (a)複數種具有以下結合能之中性、正或負的氫物質(在下文中為「結合能增加之氫物質」) (i)大於對應普通氫物質之結合能,或 (ii)大於任何氫物質在對應普通氫物質因為普通氫物質之結合能小於環境條件下之熱能或為負而不穩定或觀察不到時的結合能;及 (b)視情況選用之一種其他元素。本發明之化合物在下文中被稱作「結合能增加之氫化合物」。 可藉由使一或多種低能量氫原子與電子、低能量氫原子、含有該等結合能增加之氫物質中之至少一者及除結合能增加之氫物質以外的至少一種其他原子、分子或離子的化合物中之一或多者反應來形成結合能增加之氫物質。 亦提供新穎化合物及分子離子,其包含: (a)複數種具有以下總能量之中性、正或負的氫物質(在下文中為「結合能增加之氫物質」 (i)大於普通分子氫之總能量,或 (ii)大於任何氫物質在對應普通氫物質因為普通氫物質之總能量小於環境條件下之熱能或為負而不穩定或觀察不到時的總能量;及 (b)視情況選用之一種其他元素。本發明之化合物在下文中被稱作「結合能增加之氫化合物」。 在實施例中,提供一種化合物,其包含至少一種選自以下之結合能增加之氫物質:(a)根據方程式(19)之結合能對於p = 2直至23大於且對於p = 24小於普通氫陰離子之結合能(約0.8 eV)的氫陰離子(「結合能增加之氫陰離子」或「低能量氫氫陰離子」);(b)結合能大於普通氫原子之結合能(約13.6 eV)的氫原子(「結合能增加之氫原子」或「低能量氫」);(c)具有大於約15.3 eV之第一結合能的氫分子(「結合能增加之氫分子」或「二低能量氫」) ;或(d)具有大於約16.3 eV之結合能的分子氫離子(「結合能增加之分子氫離子」或「二低能量氫分子離子」)。在本發明中,結合能增加之氫物質及化合物亦被稱作低能氫物質及化合物。低能量氫包含結合能增加之氫物質或等同地較低能量之氫物質。III . 化學反應器 本發明亦係針對用於產生本發明之結合能增加之氫物質及化合物(諸如二低能量氫分子及低能量氫氫化物)的其他反應器。取決於電池類型,其他催化產物為功率及(可選地)電漿及光。此類反應器在下文中被稱作「氫反應器」或「氫電池」。氫反應器包含用於製作低能量氫之電池。用於製作低能量氫之電池可採用以下形式:化學反應器或氣體燃料電池(諸如氣體放電電池)、電漿炬電池或微波功率電池及電化電池。在實施例中,催化劑為HOH且HOH及H中之至少一者的來源為冰。在實施例中,電池包含電弧放電電池,該電弧放電電池包含冰及至少一個電極,以使得放電涉及冰之至少一部分。 在實施例中,電弧放電電池包含容器、兩個電極、高電壓電源(諸如能夠具有在約100 V至1 MV之範圍內的電壓及在約1 A至100 kA之範圍內的電流的電源),及水源(諸如儲集器及形成並供應H2 O液滴之構件)。液滴可在電極之間傳送。在實施例中,液滴引發電弧電漿之點火。在實施例中,水電弧電漿包含可發生反應以形成低能量氫之H及HOH。可藉由控制液滴尺寸及將液滴供應至電極之速率來控制點火速率及對應功率比。高電壓源可包含至少一個可由高電壓電源充電的高電壓電容器。在實施例中,電弧放電電池進一步包含諸如功率轉換器的構件,諸如本發明之功率轉換器,諸如PV轉換器及用以將來自低能量氫製程之功率(諸如光及熱)轉換成電的熱機中之至少一者。 用於製作低能量氫之電池的例示性實施例可採用以下形式:液體燃料電池、固體燃料電池、異質燃料電池、CIHT電池及SF-CIHT或SunCell®電池。此等電池中之每一者包含:(i)原子氫來源;(ii)至少一種用於製作低能量氫之催化劑,其選自固體催化劑、熔融催化劑、液體催化劑、氣態催化劑或其混合物;及(iii)用於使氫與用於製作低能量氫之催化劑反應之容器。如本文所使用及如本發明如預期,除非另外規定,否則術語「氫」不僅包括氕(1 H ),而且包括氘(2 H )及氚(3 H )。例示性化學反應混合物及反應器可包含本發明之SF-CIHT、CIHT或熱電池實施例。在此化學反應器部分中給出額外例示性實施例。在本發明中給出在混合物反應期間形成之用H2 O作為催化劑的反應混合物的實例。其他催化劑可用於形成結合能增加及氫物質及化合物。可在諸如反應物、反應物之wt%、H2 壓力及反應溫度之參數方面根據此等例示性情況調節反應及條件。合適的反應物、條件及參數範圍係本發明之反應物、條件及參數範圍。藉由經預測之13.6 eV之整數倍的連續輻射譜帶、由H線之多普勒線展寬所量測之在其他方面無法解釋的超高H動能、H線反轉、在無擊穿電場之情況下形成電漿及如在Mills先前公開案中所報導的不規則電漿餘暉持續時間顯示低能量氫及分子低能量氫係本發明之反應器的產物。資料(諸如關於CIHT電池及固體燃料的資料)已由其他研究人員在場外獨立驗證。由本發明之電池形成低能量氫亦藉由在較長持續時間內連續輸出之電能所證實,該等電能係電輸入之多倍,其在大多數情況下超過在無替代來源情況下的輸入的10倍以上。所預測之分子低能量氫H2 (1/4)藉由以下各者而鑑別為CIHT電池與固體燃料之產物:MAS H NMR,其展示經預測之約-4.4 ppm之往高磁場移位之基質峰;ToF-SIMS及ESI-ToFMS,其展示H2 (1/4)與集氣劑基質複合成為m/e=M+n2峰,其中M為母離子之質量且n為整數;電子束激發發射光譜分析及光致發光發射光譜分析,其展示經預測之具有H2 能量之16倍或量子數p=4的平方倍數的H2 (1/4)的旋轉及振動光譜;拉曼及FTIR光譜分析,其展示1950 cm- 1 之H2 (1/4)的旋轉能量,其為H2 之旋轉能量之16倍或量子數p=4的平方倍數;XPS,其展示經預測之500 eV的H2 (1/4)之總結合能;及到達時間在m/e=1峰之前的ToF-SIMS峰,該m/e=1峰對應於動能約204 eV之H,其將所預測之H至H(1/4)之能量釋放與傳遞至第三體H之能量相匹配,如以下中所報導:Mills先前公開案及R. Mills X Yu、Y. Lu、G Chu、J. He、J. Lotoski的「Catalyst Induced Hydrino Transition (CIHT) Electrochemical Cell」,International Journal of Energy Research, (2013)以及R. Mills、J. Lotoski、J. Kong、G Chu、J. He、J. Trevey的「High-Power-Density Catalyst Induced Hydrino Transition (CIHT) Electrochemical Cell」(2014),其以全文引用之方式併入本文中。 使用水流量熱計及Setaram DSC 131差示掃描量熱計 (DSC)兩者,藉由觀察到來自形成低能量氫之固體燃料的超過最大理論能量60倍的熱能,證實藉由本發明之電池(諸如包含用以產生熱功率之固體燃料之電池)形成低能量氫。MAS H NMR展示出約-4.4 ppm之經預測H2 (1/4)高磁場基質位移。始於1950 cm- 1 之拉曼峰匹配H2 (1/4)之自由空間旋轉能量(0.2414 eV)。此等結果報導於Mills先前公開案及R. Mills、J. Lotoski、W. Good、J. He的「Solid Fuels that Form HOH Catalyst」(2014)中,其以全文引用之方式併入本文中。IV . 固體燃料催化劑誘導之低能量氫躍遷 ( SF - CIHT ) 電池及功率轉換器 在實施例中,產生直接電能及熱能中之至少一者的電力系統包含:至少一個容器;反應物,其包含:(a)至少一種包含初生H2 O之催化劑來源或催化劑;(b)至少一種原子氫來源或原子氫;及(c)導體及導電基質中之至少一者;及至少一組用以約束低能量氫反應物之電極;用以傳送短脈衝高電流電能的電源;重載系統;至少一個用以自反應產物再生初始反應物的系統;及至少一個直接轉換器,諸如以下中之至少一者:電漿-電力轉換器(如PDC);磁流體動力轉換器;光伏打轉換器;光學整流天線(optical rectenna),諸如A. Sharma、V. Singh、T. L. Bougher、B. A. Cola的「A carbon nanotube optical rectenna」。Nature Nanotechnology,第10卷,(2015),第1027-1032頁,doi:10.1038/nnano.2015.220中所報導之光學整流天線,該參考文獻以全文引用之方式併入;及至少一個熱-電功率轉換器。在另一實施例中,容器能夠具有大氣壓、高於大氣壓及低於大氣壓中之至少一者的壓力。在實施例中,再生系統可包含水合、熱學、化學及電化學系統中之至少一者。在另一實施例中,至少一個直接電漿-電轉換器可包含以下之群組中的至少一者:電漿動力功率轉換器、直接轉換器、磁流體動力功率轉換器、磁鏡磁流體動力功率轉換器、電荷漂移轉換器、桿式或百葉窗式功率轉換器、磁旋管、光子聚束微波功率轉換器及光電轉換器。在另一實施例中,至少一個熱-電轉換器可包含以下之群組中的至少一者:熱機、蒸汽機、蒸汽渦輪機及發電機、燃氣渦輪機及發電機、朗肯循環引擎、布累登循環引擎、史特林引擎、熱離子功率轉換器及熱電功率轉換器。 SunCell®可包含複數個電極。在實施例中,低能量氫反應選擇性地在諸如正極化電極之極化電極處發生。該反應選擇率可歸因於在正偏壓電極處之低能量氫反應的更高動力學。在實施例中,SunCell®之至少一個組件(諸如反應電解槽腔室5b31壁)可正偏壓以增加低能量氫反應速率。SunCell®可包含連接至黑體輻射器之下部半球5b41之導電儲集器5c,其中該儲集器經正偏壓。偏壓可藉由儲集器5c中之熔融金屬與經正偏壓之EM泵管5k6及5k61中之至少一者之間的接觸來達成。EM可經由點火電磁泵匯流排5k2a至電源2之正極端子的連接而正偏壓。 點火可引起高功率EUV光的釋放,該高功率EUV光可對光電活性電極進行電離,以在該電極處產生電壓。點火電漿對於EUV光可為光厚的,以使得EUV光可經選擇性地約束於正電極,以進一步引起在正電極處對光電子效應的選擇性侷限。SunCell®可進一步包含橫越電負載連接以利用由光電子效應引起之電壓及基於低能量氫之功率的外部電路。在實施例中,形成低能量氫之點火事件引起可在複數個電極處作為電功率捕獲的電磁脈衝,其中整流器可對電磁功率進行整流。 除本發明之UV光伏打及熱光伏打之外,SunCell®可包含此項技術中已知之其他電轉換構件,諸如熱離子、磁流體動力、渦輪機、微型渦輪機、朗肯或布累登循環渦輪機、化學及電化學功率轉換系統。朗肯循環渦輪機可包含超臨界CO2 、有機物(諸如氫氟碳化物或碳氟化合物)或蒸氣工作流體。在朗肯或布累登循環渦輪機中,SunCell®可向渦輪機系統之預熱器、復熱器、鍋爐及外部燃燒器型熱交換器平台中之至少一者提供熱功率。在實施例中,布累登循環渦輪機包含整合於渦輪機之燃燒區段中之SunCell®渦輪機加熱器。SunCell®渦輪機加熱器可包含自壓縮機及復熱器中之至少一者接收氣流之導管,其中空氣受熱且導管將加熱之壓縮流引導至渦輪機之入口,以執行壓力體積功。SunCell®渦輪機加熱器可替換或補充燃氣渦輪機之燃燒室。朗肯或布累登循環可關閉,其中功率轉換器進一步包含冷凝器及冷卻器中之至少一者。 轉換器可為Mills先前公開案及Mills先前申請案中給出之轉換器。低能量氫反應物(諸如H來源及HOH來源)及SunCell®系統可包含本發明或諸如以下之先前美國專利申請案中之低能量氫反應物及SunCell®系統:Hydrogen Catalyst Reactor,PCT/US08/61455;2008年4月24日提交之PCT;Heterogeneous Hydrogen Catalyst Reactor,PCT/US09/052072,2009年7月29日提交之PCT;Heterogeneous Hydrogen Catalyst Power System,PCT/US10/27828,2010年3月18日提交之PCT;Electrochemical Hydrogen Catalyst Power System,PCT/US11/28889,2011年3月17日提交之PCT;H2 O-Based Electrochemical Hydrogen-Catalyst Power System,2012年3月30日提交之PCT/US12/31369;CIHT Power System,2013年5月21日提交之PCT/US13/041938;Power Generation Systems and Methods Regarding Same,PCT/IB2014/058177,2014年1月10日提交之PCT;Photovoltaic Power Generation Systems and Methods Regarding Same,PCT/US14/32584,2014年4月1日提交之PCT;Electrical Power Generation Systems and Methods Regarding Same,PCT/US2015/033165,2015年5月29日提交之PCT;Ultraviolet Electrical Generation System Methods Regarding Same,PCT/US2015/065826,2015年12月15日提交之PCT;及Thermophotovoltaic Electrical Power Generator,PCT/US16/12620,2016年1月8日提交之PCT (「Mills先前申請案」),其以全文引用之方式併入本文中。 在實施例中,在以熱、電漿及電磁(光)功率中之至少一者的形式釋放高能量的情況下,點火H2 O以形成低能量氫。(本發明中之「點火」表示H至低能量氫之極高反應速率,其可表現為爆發、脈衝或其他形式之高功率釋放)。H2 O可包含可利用施加高電流(諸如,在約100 A至100,000 A之範圍內的高電流)點火的燃料。此可藉由施加諸如約5,000至100,000 V之高電壓以首先形成高導電電漿(諸如電弧)而達成。或者,可使高電流通過包含H2 O之化合物或混合物,其中所得燃料(諸如固體燃料)之導電性高。(在本發明中,使用固體燃料來指代形成進一步反應而形成低能量氫的諸如HOH及H之催化劑的反應物。電漿電壓可較低,諸如在約1 V至100 V之範圍內。然而,反應混合物可包含除固體以外的其他物理狀態。在實施例中,反應混合物可為以下中之至少一種狀態:氣態、液體、熔融基質(諸如熔融導電基質,諸如熔融金屬,諸如熔融銀、銀銅合金及銅中之至少一者)、固體、漿液、溶膠凝膠、溶液、混合物、氣態懸浮液、氣動流及熟習此項技術者已知之其他狀態)。在實施例中,具有極低電阻之固體燃料包含含H2 O之反應混合物。低電阻可係由反應混合物之導體組分所導致的。在實施例中,固體燃料之電阻為在以下範圍內中之至少一者:約10-9 歐姆至100歐姆、10-8 歐姆至10歐姆、10-3 歐姆至1歐姆、10-4 歐姆至10-1 歐姆及10-4 歐姆至10-2 歐姆。在另一實施例中,具有高電阻之燃料包含含痕量或微量莫耳百分比之經添加化合物或材料的H2 O。在後一種情況下,可使高電流流過燃料,以藉由引起擊穿而達成點火,從而形成高度導電狀態(諸如電弧或電弧電漿)。 在實施例中,反應物可包含H2 O來源及導電基質,以形成催化劑來源、催化劑、原子氫來源及原子氫中之至少一者。在另一實施例中,包含H2 O來源之反應物可包含以下中之至少一者:體相H2 O、除體相H2 O以外的狀態、經歷用以形成H2 O及釋放結合之H2 O的反應中之至少一者的一或多種化合物。另外,經結合H2 O可包含與H2 O相互作用之化合物,其中H2 O處於經吸收H2 O、經結合H2 O、物理吸附之H2 O及水合水中之至少一者的狀態。在實施例中,反應物可包含導體及一或多種化合物或材料,該一或多種化合物或材料經歷體相H2 O、經吸收H2 O、經結合H2 O、物理吸附之H2 O及水合水之釋放中之至少一者且其反應產物為H2 O。在其他實施例中,初生H2 O催化劑來源及原子氫來源中之至少一者可包含以下中之至少一者:(a)至少一種H2 O來源;(b)至少一種氧來源;及(c)至少一種氫來源。 在實施例中,低能量氫反應速率取決於高電流之施加或形成。在SF-CIHT電池之實施例中,形成低能量氫之反應物經受引起極快反應速率及能量釋放的低電壓、高電流、高功率脈衝。在例示性實施例中,60 Hz電壓小於15 V峰值,電流在100 A/cm2 與50,000 A/cm2 峰值之間的範圍內,且功率在1000 W/cm2 與750,000 W/cm2 之間的範圍內。在此等參數之約1/100倍至100倍之範圍內之其他頻率、電壓、電流及功率係合適的。在實施例中,低能量氫反應速率取決於高電流之施加或形成。在實施例中,電壓經選擇為引起具有在以下至少一個範圍內的電流之高AC、DC或AC-DC混合:100 A至1,000,000 A、1 kA至100,000 A、10 kA至50 kA。DC或峰值AC電流密度可在以下中之至少一者的範圍內: 100 A/cm2 至1,000,000 A/cm2 、1000 A/cm2 至100,000 A/cm2 及2000 A/cm2 至 50,000 A/cm2 。DC或峰值AC電壓可在選自以下之至少一個範圍內:約0.1 V至1000 V、0.1 V至100 V、0.1 V至15 V及1 V 至15 V。AC頻率可在以下範圍內:約0.1 Hz至10 GHz、1 Hz至1 MHz、10 Hz至100 kHz及100 Hz至10 kHz。脈衝時間可在選自以下之至少一個範圍內:約10- 6 s至10 s、10- 5 s至1 s、10- 4 s至0.1 s及10- 3 s至0.01 s。 在實施例中,傳遞來自經催化為低能量氫狀態之原子氫的能量導致對催化劑之電離。自催化劑電離之電子可積聚在反應混合物及容器中並引起空間電荷堆積。該空間電荷可改變用於自原子氫至催化劑之後續能量傳遞的能級,同時降低反應速率。在實施例中,施加高電流會移除空間電荷,以引起低能量氫反應速率之增加。在另一實施例中,諸如電弧電流之高電流使得可充當H來源及HOH催化劑之反應物(諸如水)的溫度極快提高。高溫可引起水熱解為H及HOH催化劑中之至少一者。在實施例中,SF-CIHT電池之反應混合物包含H來源及催化劑(諸如nH (n為整數)及HOH中之至少一者)的來源。nH 及HOH中之至少一者可藉由至少一種物相之水(諸如,固體、液體及氣態水中之至少一者)的熱解或熱分解形成。熱解可在高溫(諸如,在約500K至10,000K、1000K至7000K及1000K至5000K之至少一個範圍內的溫度)下發生。在例示性實施例中,反應溫度為約3500至4000K,使得原子H之莫耳分數較高,如由J. Lede、F. Lapicque及J Villermaux所展示: [J. Lédé、F. Lapicque、J. Villermaux,「Production of hydrogen by direct thermal decomposition of water」, International Journal of Hydrogen Energy, 1983,V8 , 1983,第675-679頁;H. H. G. Jellinek、H. Kachi,「The catalytic thermal decomposition of water and the production of hydrogen」, International Journal of Hydrogen Energy, 1984,V9 ,第 677-688頁;S. Z. Baykara,「Hydrogen production by direct solar thermal decomposition of water, possibilities for improvement of process efficiency」,International Journal of Hydrogen Energy, 2004,V29 ,第1451-1458頁;S. Z. Baykara,「Experimental solar water thermolysis」,International Journal of Hydrogen Energy, 2004,V29 ,第1459-1469 頁,其以引用之方式併入本文中]。熱解可由固體表面(諸如電池組分中之一者)協助。可藉由輸入功率及藉由低能量氫反應所保持之電漿將固體表面加熱至高溫。熱解氣體(諸如點火區域之彼等向下的氣體流)可經冷卻以防止再結合或產物至初始水含量之逆反應。反應混合物可包含處於比產物氣體之溫度低的溫度下的冷卻劑,諸如固相、液體相氣相中之至少一者。熱解反應產物氣體之冷卻可藉由使產物與冷卻劑接觸而達成。冷卻劑可包含低溫蒸汽、水及冰中之至少一者。 SunCell®可包含熱解氫發生器,其包含SunCell®輻射器、金屬氧化物、水源、噴水器及氫氣及氧氣採集系統。來自黑體輻射器5b4之黑體輻射可入射於在加熱時分解成氧氣及金屬的金屬氧化物。氫發生器可包含水源及噴塗金屬之噴水器。金屬可與水反應以形成金屬氧化物及氫氣。可使用此項技術中已知之分離器及採集系統來採集氣體。反應可由下者表示:金屬及氧化物可為此項技術中已知的支援H2 O熱解以形成氫的金屬及氧化物,諸如ZnO/Zn及SnO/Sn。其他例示性氧化物為氧化錳、氧化鈷、氧化鐵及其混合物,如此項技術中已知及在以全文引用的方式併入本文中的https :// www . stage - ste . eu / documents / SF % 201 % 202011 % 20solar _ fuels % 20by % 20SolarPACES . pdf 中給出。 在實施例中,SF-CIHT或SunCell®發電機包含產生電能及熱能中之至少一者的電力系統,其包含: 至少一個容器; 反應物,其包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者; 至少一個反應物噴射系統; 至少一個反應物點火系統,其用以引起反應物形成發光電漿及發熱電漿中之至少一者; 用以回收反應物之反應產物之系統; 至少一個再生系統,其用以自反應產物再生額外反應物, 其中該等額外反應物包含: a)至少一種包含初生H2 O之催化劑來源或催化劑; b)至少一種H2 O來源或H2 O; c)至少一種原子氫來源或原子氫;以及 d)導體及導電基質中之至少一者;及 該光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統,諸如以下之群組中之一或多者:光伏打轉換器、光電轉換器、電漿動力轉換器、熱離子轉換器、熱電轉換器、斯特林引擎、布累登循環引擎、朗肯循環引擎,及熱機及加熱器。 在一實施例中,丸粒燃料可包含H來源、H2 、催化劑來源、H2 O來源及H2 O中之至少一者。合適的丸粒包含導電金屬基質及水合物,諸如鹼性水合物、鹼土水合物及過渡金屬水合物中之至少一者。水合物可包含MgCl2 ·6H2 O、BaI2 2·H2 O及ZnCl2 ·4H2 O中之至少一者。或者,丸粒可包含銀、銅、所吸收之氫氣及水中之至少一者。 點火系統可包含: a)至少一組用以約束反應物之電極;及 b)用以傳送短脈衝高電流電能的電源,其中該短脈衝高電流電能足以引起反應物反應以形成電漿。電源可自功率轉換器接收電功率。在實施例中,反應物點火系統包含至少一組分離以形成開路的電極,其中該開路藉由噴射反應物閉合以使高電流流動而達成點火。在一實施例中,點火系統包含用於進行以下中之至少一者的開關:起始電流及在達成點火之後中斷電流。電流之流動可藉由完成電極之間的間隙之反應物起始。開關可藉由諸如以下中之至少一者之構件以電子方式執行:絕緣閘極雙極電晶體(IGBT)、矽控整流器(SCR)及至少一個金屬氧化物半導體場效電晶體(MOSFET)。或者,可以機械方式對點火進行開關。在點火之後可中斷電流以便使輸出低能量氫產生之能量相對於輸入點火能量達到最佳。點火系統可包含在其中產生電漿之階段期間允許可控量之能量流入燃料中以引起爆震並關掉電源的開關。在實施例中,用以傳送短脈衝高電流電能之電源包含以下中之至少一者: 經選擇用於產生高AC、DC或AC-DC電流混合物之電壓,該電流在100 A至1,000,000 A、1 kA至100,000 A、10 kA至50 kA中之至少一者之範圍內; 在以下中之至少一者之範圍內的DC或峰值AC電流密度:100 A/cm2 至1,000,000 A/cm2 、1000 A/cm2 至100,000 A/cm2 及2000 A/cm2 至50,000 A/cm2 ; 其中該電壓由固體燃料之導電性確定,其中該電壓由所需電流乘以固體燃料樣品之電阻而得到; DC或峰值AC電壓在0.1 V至500 kV、0.1 V至100 kV及1 V至50kV中之至少一者之範圍內,以及 AC頻率在0.1 Hz至10 GHz、1 Hz至1 MHz、10 Hz至100 kHz及100 Hz至10 kHz中之至少一者之範圍內, SF-CIHT電池之輸出功率可包含熱及光伏打可轉換之光功率。在一實施例中,光-電轉換器可包含利用光伏打效應、熱離子效應及光電子效應中之至少一者的轉換器。功率轉換器可為將高動能電子之動能轉換成電之直接功率轉換器。在一實施例中,SF-CIHT電池之功率可至少部分地呈熱能形式或可至少部分地轉換成熱能。電力轉換器可包含熱離子功率轉換器。例示性熱離子陰極可包含摻鈧之鎢。該電池可利用光子增強熱離子發射(PETE),其中光效應藉由使半導體發射器中之電子能量跨越帶隙,提昇至熱發射電子之傳導帶中來增強電子發射。在一實施例中,SF-CIHT電池可包含光吸收劑,該光諸如遠紫外(EUV)、紫外(UV)、可見及近紅外光中之至少一者。該吸收劑可在電池外部。舉例而言,其可在PV轉換器26a之窗外部。吸收劑之溫度可由於吸收而升高。吸收劑溫度可在約500℃至4000℃之範圍內。該熱量可輸入至熱光伏打或熱離子電池。諸如史特林、朗肯、布累登及此項技術中已知之其他熱機之熱電及熱機在本發明之範疇內。 複數個轉換器之至少一個第一光-電轉換器(諸如利用光伏打效應、熱離子效應及光電子效應中之至少一者的光-電轉換器)可具有對電磁波譜之第一部分之選擇性且可透過電磁波譜之至少第二部分。第一部分可在對應的第一轉換器中轉換成電,且第一轉換器不具有選擇性之第二部分可傳播至另一個對電磁波譜所傳播之第二部分之至少一部分具有選擇性的第二轉換器。 在實施例中,圖2I28、2I69、及圖2I80至圖2I149中所示之SF-CIHT電池或發電機(亦被稱作SunCell®® )包含六個基本易維護系統,一些系統不具有活動部件且能夠長時間操作: (i)啟動電感耦合加熱器,其包含電力供應器5m、引線5p及天線線圈5f,用以首先熔化銀或銀銅合金以構成熔融金屬或熔體;及視情況選用之電極電磁泵,其包含磁體,用以在最初引導點火電漿流;(ii)燃料噴射器,諸如包含氫供應器(諸如,貫穿黑體輻射器之滲氫供應器)的燃料噴射器,其中可藉由電解或熱解自水中得到氫;及噴射系統,其包含用以噴射熔融銀或熔融銀銅合金之電磁泵5ka及氧來源(諸如氧化物,諸如LiVO3 或本發明之另一氧化物);及替代地,用以噴射水蒸氣及氫氣中之至少一者的氣體噴射器5z1;(iii)點火系統,其用以產生跨越一對電極8之低電壓高電流流動,熔融金屬、氫及氧化物、或熔融金屬及H2 O及氫氣中之至少一者經噴射至該對電極中以形成發亮光電漿;(iv)藉由電漿加熱至白熾溫度之黑體輻射器; (v)光-電轉換器26a,其包含所謂的聚光型光伏打電池15,該等聚光型光伏打電池自黑體輻射器接收光並在諸如超過一千suns之高光強度下操作; 及(vi)燃料回收及熱管理系統31,其致使熔融金屬在點火後返回至噴射系統。在另一實施例中,來自點火電漿之光可直接輻射PV轉換器26a以轉換為電。 在一實施例中,電漿以EUV及UV光形式發射出光功率及能量之顯著部分。可藉由在反應腔室電池1中維持真空來降低壓力,從而將電漿維持在光學上不太厚之條件下,從而減少短波長光之衰減。在一實施例中,光-電轉換器包含本發明之光伏打轉換器,其包含光伏打(PV)電池,該等伏打(PV)電池回應於自該電池發射之光之實質性波長區域,諸如對應於至少10%之光功率輸出之波長範圍。在一實施例中,燃料可包含具有經捕集之氫及經捕集之H2 O中之至少一者的銀。光發射可主要包含紫外光,諸如在約120 nm至300 nm之波長區域內之光。PV電池可回應於約120 nm至300 nm之波長區域之至少一部分。PV電池可包含III族氮化物,諸如InGaN、GaN及AlGaN中之至少一者。在實施例中,PV電池包含SiC。在一實施例中,PV電池可包含複數個接面。該等接面可串聯分層。在另一實施例中,該等接面為獨立的或電並聯。獨立接面可以機械方式堆疊或經晶圓接合。多接面電池及串聯連接之電池之層中的至少一者可包含旁通二極體,其用以將由電池各層之間的電流錯配導致的電流及功率損失降至最低, 例示性多接面PV電池包含至少兩個接面,包含經n-p摻雜之半導體,諸如InGaN、GaN及AlGaN之群組中之複數者。GaN之n型摻雜劑可包含氧,且p型摻雜劑可包含Mg。例示性三重接面電池可包含InGaN//GaN//AlGaN,其中//可指隔離性透明晶圓接合層或機械堆疊。PV可在等於聚光型光伏打裝置(CPV)之高光強度下操作。基板可為藍寶石、Si、SiC及GaN中之至少一者,其中後兩者提供CPV應用之最佳晶格匹配。各層可使用此項技術中已知之有機金屬氣相磊晶(MOVPE)法沈積。該等電池可藉由冷板冷卻,諸如CPV或二極體雷射(諸如商用GaN二極體雷射)中所用之彼等冷板。如在CPV電池的情況下,柵格接觸點可安裝在電池之正表面及背表面上。在一實施例中,PV轉換器可具有對於其所回應之光實質上可透過之保護性窗。該窗可至少10%透過回應光。該窗可透過UV光。該窗可在PV電池上包含塗層,諸如UV透明塗層。該塗層可包含本發明之UV窗之材料,諸如藍寶石或MgF2 窗。其他合適之窗包含LiF及CaF2 。該塗層可藉由沈積、諸如氣相沈積來施加。 PV轉換器26a之電池可包含光子設計,其迫使發射器及電池單一模式僅在半導體帶隙上方進行交叉諧振耦合及阻抗匹配,從而在此處產生『擠壓』窄帶近場發射光譜。具體而言,例示性PV電池可包含表面電漿極化聲子熱發射器及銀敷層半導體薄膜光伏打電池。 EM泵5ka (圖2I28、2I69及圖2I80至圖2I163)可包含EM泵熱交換器5k1、電磁泵冷卻劑管線饋通組合件5kb、磁體5k4、磁軛及視情況選用之可包含具有任選輻射屏蔽之氣體或真空間隙的熱障5k5、泵管5k6、匯流排5k2及具有可由來自PV轉換器之電流供應之饋通件5k31的匯流排電流源連接件5k3。磁性電路之磁體5k4及磁軛5k5中至少一者可藉由EM泵熱交換器5k1冷卻,諸如利用冷卻劑(諸如水)冷卻之EM泵熱交換器,其具有至急冷器31a之冷卻劑入口管線31d及冷卻劑出口管線31e。例示性EM泵磁體5k4包含鈷釤(諸如SmCo-30MGOe及釹鐵硼(N44SH))磁體中之至少一者。磁體可包含回復磁通量電路。 在實施例中,極高功率及能量中之至少一者可藉由氫在本文中被稱作歧化之過程中經歷至具有方程式(18)中之高p值的低能量氫的躍遷而達成,如Mills GUT Chp. 5中所給出,其以引用之方式併入。氫原子H (1/p )p = 1、2、3、...137可經歷由方程式(10)及(12)所給出之至較低能態的進一步躍遷,其中一個原子之躍遷係藉由以諧振及非輻射方式接受m • 27.2eV 且伴隨有其位能之相反變化的另一個原子來催化。由方程式(35)所給出之由m • 27.2eV 諧振傳遞至H (1/p ')而誘導之H (l/p)躍遷至H (1/(p +m )的一般總方程式由以下表示:來自低能量氫製程之EUV光可解離低能量氫分子且所得低能量氫原子可充當催化劑以躍遷至較低能態。例示性反應包含藉由H(1/4)將H催化為H(1/17),其中H(1/4)可為藉由HOH對另一H進行催化的反應產物。預測低能量氫之歧化反應產生X射線區域中之特徵。如由方程式(5)至(8)所示,HOH催化劑之反應產物為。考慮在含H2 O氣體之氫雲中很可能有躍遷反應,其中第一氫型原子為H原子,且充當催化劑之第二受體氫型原子。由於之位能為42 • 27.2eV = 16• 27.2eV = 435.2eV ,故躍遷反應由以下表示:且,總反應為預測歸因於中間物(例如方程式(16)及方程式(37))之遠紫外連續輻射譜帶具有短波長截止及藉由以下給出之能量且延伸至比對應的截止長之波長。此處,預測歸因於中間物之衰減的遠紫外連續輻射譜帶在E = 3481.6eV ;0.35625nm 處具有短波長截止並延伸至更長波長。NASA之錢德拉X射線天文台(Chandra X-ray Observatory)及XMM-Newton [E. Bulbul、M. Markevitch、A. Foster、R. K. Smith、M. Loewenstein、S. W. Randall, 「Detection of an unidentified emission line in the stacked X-Ray spectrum of galaxy clusters」, The Astrophysical Journal, 第789卷, 第1期, (2014);A. Boyarsky、O. Ruchayskiy、D. Iakubovskyi、J. Franse, 「An unidentified line in X-ray spectra of the Andromeda galaxy and Perseus galaxy cluster」, (2014),arXiv: 1402.4119 [astro-ph.CO]]近來在英仙座星團中觀察到具有3.48 keV截止之寬X射線峰,其不匹配任何已知原子躍遷。BulBul等人之分佈給具有未知身分之黑暗物質的3.48 keV特徵匹配躍遷且進一步證實低能量氫為黑暗物質之身分。 在實施例中,發電機可利用低壓H2 O產生高功率及能量。水蒸氣壓力可在以下中之至少一個範圍內:約0.001 Torr至100 Torr、0.1 mTorr至50 Torr、1 mTorr及5 Torr、10 mTorr至1 Torr及100 mTorr至800 Torr。低H2 O蒸氣壓可為以下情況中之至少一者:由水蒸氣來源及用以控制流動速率及壓力中之至少一者的構件供應及保持。供水可足以保持所需點火速率。水蒸氣壓力可由穩態或動態控制及平衡控制中之至少一者控制。發電機可包含保持所需區域中之較低水蒸氣壓力的泵13a。水可藉由差分泵抽移除,使得電池中在電極區域之外的區域可具有較低壓力,諸如水之較低分壓。 電池水蒸氣壓力可由與電池連接之蓄水器/捕集器(trap)保持。電池水蒸氣壓力可處於穩態或與蓄水器/捕集器之水面上方的水蒸氣壓力平衡中之至少一者。蓄水器/捕集器可包含用以降低蒸氣壓之構件,諸如保持對比溫度(諸如低溫溫度)之急冷器及諸如活性木炭或乾燥劑及溶質之H2 O吸收材料中之至少一者。水蒸氣壓力可為利用可經過冷之冰在平衡或穩態下確立的低壓。冷卻可包含低溫急冷器或浴,諸如二氧化碳、液氮或液氦浴。可將溶質添加至蓄水器/捕集器以降低水蒸氣壓力。蒸氣壓可根據勞氏定律降低。溶質可為高度可溶且高濃度的。例示性溶質為糖及離子化合物,諸如鹼金屬、鹼土金屬及鹵化銨、氫氧化銨、硝酸銨、硫酸銨、重鉻酸銨、碳酸銨及乙酸銨中之至少一者,諸如K2 SO4 、KNO3 、KCl、NH4 SO4 、NaCl、NaNO2 、Na2 Cr2 O7 、Mg(NO3 )2 、K2 CO3 、MgCl2 、KC2 H3 O2 、LiCl及KOH。捕集器乾燥劑可包含分子篩,諸如例示性分子篩13X、4-8目集結粒。 在移除過量水之實施例中,可密封及加熱捕集器;隨後,可泵抽出液體水或可將其作為蒸汽排出。捕集器可經再冷卻及再運行。在實施例中,將H2 添加至諸如電極處之此類區域中,以與O2 反應產物反應,從而將其轉換為利用蓄水器/捕集器控制的水。H2 可藉由在滲氫陰極(諸如PdAg陰極)處之電解提供。可利用向氫供應控制器(諸如電解控制器)提供回饋信號之感測器來監測氫壓力。 在例示性實施例中,藉由含水分子篩(諸如13X)將水分壓保持在所要壓力(諸如在約50 mTorr至500 mTorr之範圍中之壓力)下。任何自分子篩釋放之水可經水供應(諸如由相對應的歧管及管線供應之來自貯槽31l的水供應)替換。分子篩之面積可足以至少按保持所要分壓所需之速率來供水。分子篩之廢氣率可與低能量氫製程之消耗率與泵出率的總和相匹配。釋放速率與分壓中之至少一者可藉由控制分子篩之溫度來控制。電池可包含連接至電池26之分子篩的控制器。貯藏器(container)可進一步包含用以保持分子篩之溫度的構件,諸如加熱器及急冷器及溫度控制器。 在替代性穩態實施例中,水蒸氣壓力由流量控制器(諸如控制電池中之質量流量及水蒸氣壓力中之至少一者的流量控制器)保持。供水速率可經調節以匹配在低能量氫及任何其他電池反應中消耗的速率及藉由諸如泵抽之手段移除之速率。泵可包含蓄水器/捕集器、低溫泵、真空泵、機械真空泵、渦卷泵及渦輪泵中之至少一者。供應速率及移除速率中之至少一者可經調節以達成所要電池水蒸氣壓力。此外,可增添所要之氫分壓。H2 O及H2 壓力中之至少一者可由感測器及控制器(諸如壓力計,如Baratron量規及質量流量控制器)感測及控制。水可由流量控制器經由EM泵管5k4噴射,該流量控制器可進一步包含壓力捕捉器及防止熔融金屬流回至供水器(諸如質量流量控制器)中的反流止回閥。氣體可由注射泵供應。作為質量流量控制器之替代,水蒸氣壓力可由高精度電子可控閥(諸如針閥、比例電子閥及步進馬達閥中之至少一者)保持。該閥門可由水蒸氣壓力感測器及電腦控制以將電池水蒸氣壓力保持在所要值,諸如在約0.5 Torr至2 Torr之範圍內,其中該控制可達到小公差,諸如在20%內。閥門在電池中之水蒸氣壓快速變化的情況下可具有保持公差的快速回應。穿過閥門的流動之動態範圍可經調節以藉由改變在閥門之供應側上之水蒸氣壓力來適應不同最小及最大範圍。供應側壓力可藉由分別提高或減小蓄水器31l之溫度而提高或減小。水可經由EM泵管5k6供應。 在另一實施例中,水(諸如蒸汽)及氫中之至少一者可同時隨著熔融金屬(諸如熔融銀金屬)噴射。水、蒸汽及氫噴射器中之至少一者可包含端接於快速螺線管閥中的傳送管。螺線管閥可以串聯及並聯中之至少一種形式與電極電連接,使得在電流流經電極時,電流流經該閥門。在此情況下,水(諸如蒸汽)及氫中之至少一者可同時隨著熔融金屬噴射。在另一實施例中,噴射器系統包含光學感測器及引起噴射之控制器。在感測到金屬噴射或點火時,控制器可打開及關閉快速閥門(諸如螺線管閥)。在實施例中,用於噴射熔體(諸如銀熔體)、水(諸如蒸汽)及氫中之至少兩者的管線可為重合的。重合可係經由共同管線。在實施例中,噴射器包含噴射噴嘴。噴射器之噴嘴可包含氣體歧管,諸如與包含電極8之金屬流對準之氣體歧管。噴嘴可進一步包含來自歧管之複數個針孔,其傳送H2 O及H2 中之至少一者的多種氣體噴流。在實施例中,在大於電池之壓力的壓力下使H2 鼓泡通過H2 O儲集器,且H2 O經夾帶於H2 載氣中。高壓氣體混合物流經針孔進入熔體中以保持氣體噴流。在電極處,可為混合物之氣體可與導電基質(金屬熔體)組合。在施加高電流之情況下,相對應的燃料混合物可點火以形成低能量氫。 在改良發電機之能量平衡的實施例中,諸如31之急冷器可由包含電池所產生之熱量的熱功率驅動。熱功率可來自內部耗散及來自低能量氫反應。急冷器可包含熟習此項技術者已知的吸收急冷器。在實施例中,藉由冷卻劑製冷劑(諸如可汽化之水)來吸收將排出之熱量。吸收急冷器可用熱來使製冷劑凝結。在實施例中,將水蒸氣吸收於吸收材料(吸附劑)(諸如矽膠、沸石)或奈米結構材料(諸如Pacific Northwest Laboratory之P. McGrail之奈米結構材料)中。將所吸收水加熱以使其在腔室中釋放,其中壓力的增加足以使水凝結。 SF-CIHT發電機包含其參數諸如本發明中經感測及控制之參數的組件。在實施例中,具有感測器及控制系統之電腦可感測及控制:(i)每一經冷卻系統(諸如PV轉換器、EM泵磁體及電感耦合加熱器中之至少一者)之每一急冷器之入口及出口溫度及冷卻劑壓力及流動速率,(ii)點火系統電壓、電流、功率、頻率及工作循環,(iii)使用諸如光學、都卜勒、勞侖茲或電極電阻感測器之感測器及控制器之EM泵噴射流動速率,(iv)電感耦合加熱器及電磁泵5k之電壓、電流及功率,(v)電池中之壓力,(vi)電池組件之壁溫,(vii)每一區段中之加熱器功率,(viii)電磁泵之電流及磁通量,(ix)銀熔化溫度、流動速率及壓力,(xi)藉由調節器形成之可經由共同氣體噴射歧管傳送的每一滲透或噴射氣體(諸如H2 及H2 O及混合物)的壓力、溫度及流動速率,(xi)入射至PV轉換器的光之強度,(xii) PV轉換器之電壓、電流及功率輸出,(xiii)任何功率調節設備之電壓、電流、功率及其他參數,及(xiv)至寄生負載及外部負載中之至少一者的SF-CIHT發電機輸出電壓、電流及功率,(xv)至任何寄生負載(諸如電感耦合加熱器、電磁泵、急冷器及感測器及控件中之至少一者)的電壓、電流及功率輸入,及(xvi)具有能量儲存之起動電路之電壓、電流及電荷狀態。在實施例中,待量測參數可與系統中具有將在其量測期間損害感測器的高溫的區域分離。舉例而言,諸如H2 及H2 O中之至少一者的氣體的壓力可藉由使用連接氣體管線來量測,該連接氣體管線諸如係連接至電池(如5b或5c)及在進入壓力換能器(諸如Baratron電容壓力計)之前冷卻氣體的冷卻塔。在參數超出所需範圍的情況下(諸如經歷超溫),發電機可包含安全關閉機構,諸如此項技術中已知之機構。關閉機構可包含電腦及向發電機之至少一個組件提供功率的開關,其可斷開以引起關閉。 在實施例中,電池可包含至少一種集氣劑,諸如至少一種用於空氣、氧、氫、CO2 及水之集氣劑。氧氣集氣劑(諸如,氧反應性材料,諸如可細微粉碎之碳或金屬)可清除電池中形成之任何氧。至於碳,可利用可逆的CO2 洗滌劑將產物二氧化碳抽出。二氧化碳洗滌劑為此項技術中已知的,諸如有機化合物,諸如胺(如單乙醇胺)、礦物及沸石、氫氧化鈉、氫氧化鋰及基於金屬氧化物之系統。細微粉碎之碳的集氣劑亦可用於清除氧以保護電池,諸如包含氧敏材料(諸如Mo、W、石墨及Ta之容器或泵管)中之氧敏材料的目的。在此情況下,二氧化碳可利用CO2 洗滌劑移除或可利用真空泵泵出,其中細微粉碎之碳僅僅用於組件保護。 金屬集氣劑可選擇性與H2 O上的氧反應,使得其可利用氫再生。具有低水反應性之例示性金屬包含以下之群組之金屬:Cu、Ni、Pb、Sb、Bi、Co、Cd、Ge、Au、Ir、Fe、Hg、Mo、Os、Pd、Re、Rh、Ru、Se、Ag、Tc、Te、Tl、Sn、W及Zn。可自SF-CIHT電池移除集氣劑或氧氣洗滌劑且再生。該移除可為週期性的或間歇的。該再生可藉由氫還原而達成。該再生可就地發生。就地再生可為間歇的或連續的。熟習此項技術者已知其他氧氣集氣劑及其再生,諸如沸石及形成含氧可逆配位體鍵之化合物,諸如鹽,諸如與2-胺基對苯二甲酸根基相關之去氧系統之硝酸鹽,[{(bpbp)Co2 II (NO3 )}2 (NH2 bdc)] (NO3 )2 .2H2 O (bpbp- = 2,6-雙(N,N-雙(2-吡啶基甲基)胺甲基)-4-第三丁基酚根基,NH2 bdc2 - = 2-胺基-1,4-苯二羧根基)。高度可燃的金屬(諸如例示性金屬:鹼金屬、鹼土金屬、鋁及稀土金屬)亦可用作氧氣集氣劑。高度可燃的金屬亦可用作水清除劑。氫儲存材料可用於清除氫。例示性氫儲存材料包含金屬氫化物、米許合金(諸如M1: La-rich米許合金,諸如M1Ni3 . 65 Al0 . 3 Mn0 . 3 或M1(NiCoMnCu)5 、Ni、R-Ni、R-Ni + 約8 wt% Vulcan XC-72、LaNi5 、Cu或Ni-Al、Ni-Cr (諸如約10% Cr)、Ce-Ni-Cr (諸如約3/90/7 wt%)、Cu-Al或Cu-Ni-Al合金)、M-N-H系統之物質(諸如LiNH2 、Li2 NH或Li3 N),及鹼金屬氫化物,其進一步包含硼(諸如硼氫化物)或鋁(諸如鋁氫化物)。另外的合適的氫儲存材料為:金屬氫化物,諸如鹼土金屬氫化物(諸如MgH2 );金屬合金氫化物(諸如BaReH9 、LaNi5 H6 、FeTiH17 及MgNiH4 );金屬硼氫化物(諸如Be(BH4 )2 、Mg(BH4 )2 、Ca(BH4 )2 、Zn(BH4 )2 、Sc(BH4 )3 、Ti(BH4 )3 、Mn(BH4 )2 、Zr(BH4 )4 、NaBH4 、LiBH4 、KBH4 及Al(BH4 )3 、AlH3 、NaAlH4 、Na3 AlH6 、LiAlH4 、Li3 AlH6 、LiH、LaNi5 H6 、La2 Co1Ni9 H6 及TiFeH2 、NH3 BH3 、聚胺基硼烷、胺硼烷錯合物(諸如胺硼烷、硼烷氨合物、肼-硼烷錯合物、二硼烷二氨合物、硼氮炔及八氫三硼銨或四氫硼酸銨;咪唑鎓離子液體(諸如烷基(芳基)-3-甲基咪唑鎓N -雙(三氟甲磺醯基)醯亞胺鹽、硼酸鏻及草酸鹽物質)。另外的例示性化合物為氨硼烷、鹼氨硼烷(諸如鋰氨硼烷)及硼烷烷基胺錯合物(諸如硼烷二甲胺錯合物、硼烷三甲胺錯合物)及胺基硼烷及硼烷胺(諸如胺基二硼烷、正二甲基胺基二硼烷、三(二甲胺基)硼烷、二正丁基硼胺、二甲基胺基硼烷、三甲基胺基硼烷、氨-三甲基硼烷及三乙基胺基硼烷)。另外的合適的氫儲存材料為氫經吸收之有機液體,諸如咔唑及衍生物,諸如9-(2-乙基己基)咔唑、9-乙基咔唑、9-苯基咔唑、9-甲基咔唑及4,4'-雙(N-咔唑基)-1,1'-聯二苯。集氣劑可包含能夠儲存氫之合金,諸如AB5 (LaCePrNdNiCoMnAl)或AB2 (VTiZrNiCrCoMnAlSn)型中之一者,其中「ABX 」標識係指A型元素(LaCePrNd或TiZr)與B型元素(VNiCrCoMnAlSn)之比率。額外合適的氫氣集氣劑係金屬氫化物電池組(諸如熟習此項技術者中所知之鎳-金屬氫化物電池組)中所使用的氫氣集氣劑。氫化物陽極之例示性合適的集氣劑材料包含R-Ni、LaNi5 H6 、La2 Co1 Ni9 H6 、ZrCr2 H3 . 8 、LaNi3 . 55 Mn0 . 4 Al0 . 3 Co0 . 75 、ZrMn0 . 5 Cr0 . 2 V0 . 1 Ni1 . 2 之群組中的氫化物及其他能儲存氫之合金,諸如AB5 (LaCePrNdNiCoMnAl)或AB2 (VTiZrNiCrCoMnAlSn)類型中之一者,其中「ABX 」標識係指A型元素(LaCePrNd或TiZr)與B型元素(VNiCrCoMnAlSn)之比率。在其他實施例中,氫化物陽極集氣劑材料包含以下中之至少一者:MmNi5 (Mm = 米許合金),諸如:MmNi3.5 Co0.7 Al0.8 ,AB5 -類型:MmNi3.2 Co1.0 Mn0.6 Al0.11 Mo0.09 (Mm = 米許合金:25 wt% La、50 wt% Ce、7 wt% Pr、18 wt% Nd);La1-y Ry Ni5-x Mx ,AB2 -類型:Ti0.51 Zr0.49 V0.70 Ni1.18 Cr0.12 合金;鎂基合金,諸如Mg1.9 Al0.1 Ni0.8 Co0.1 Mn0.1 合金、Mg0.72 Sc0.28 (Pd0.012 + Rh0.012 )及Mg80 Ti20 、Mg80 V20 、La0.8 Nd0.2 Ni2.4 CO2 .5 Si0.1 、LaNi5-x Mx (M= Mn、Al)、(M= Al、Si、Cu)、(M= Sn)、(M= Al、Mn、Cu)及LaNi4 Co、MmNi3.55 Mn0.44 Al0.3 Co0.75 、LaNi3.55 Mn0.44 Al0.3 Co0.75 、MgCu2 、MgZn2 、MgNi2 、AB化合物,諸如TiFe、TiCo及TiNi、ABn 化合物 (n = 5、2或1)、AB3-4 化合物及ABx (A = La、Ce、Mn、Mg;B = Ni、Mn、Co、Al)。其他合適的氫化物集氣劑為ZrFe2 、Zr0 . 5 Cs0 . 5 Fe2 、Zr0 . 8 Sc0 . 2 Fe2 、YNi5 、LaNi5 、LaNi4 . 5 Co0 . 5 、(Ce、La、Nd、Pr)Ni5 、米許合金-鎳合金、Ti0 . 98 Zr0 . 02 V0 . 43 Fe0 . 09 Cr0 . 05 Mn1 . 5 、La2 Co1Ni9 、FeNi及TiMn2 。本發明之集氣劑及熟習此項技術者已知之其他集氣劑可包含超過一個種類之電解槽氣體的集氣劑。額外集氣劑可為熟習此項技術者所知之集氣劑。例示性多氣體集氣劑包含鹼金屬或鹼土金屬(諸如鋰),其可去除O2 、H2 O及H2 中之至少兩者。集氣劑可藉由此項技術中已知之方法(諸如藉由還原、分解及電解)再生。在實施例中,集氣劑可包含進行以下中之至少一者的低溫捕集器:凝結諸如水蒸氣、氧氣及氫氣中之至少一者的氣體;及將氣體捕獲於呈冷卻狀態之吸收材料中。氣體可釋放自處於較高溫度之吸收材料,使得隨著加熱及泵抽廢氣,集氣劑可再生。吸收水蒸氣、氧氣及氫氣中之至少一者的可藉由加熱及泵抽再生的例示性材料為碳,諸如活性木炭及沸石。在對應氣體位準增加至如藉由相對應的電解槽氣體含量之感測器感測的不容許位準時,可確定氧氣、氫氣及及水洗滌劑再生之時序。在實施例中,電池產生之氫氣及氧氣中之至少一者可藉由熟習此項技術者所知的系統及方法採集及作為商用氣體出售。或者,所採集氫氣可用於SunCell®中。 併入至熔體中之氫氣及水可在由諸如機械泵之對應泵產生的壓力下自貯槽5u及311流經歧管及供料管線。或者,水泵可藉由加熱水槽31l形成蒸汽壓力而替換,且氫氣泵可藉由電解產生使氫氣流動的壓力而替換。或者,藉由H2 O貯槽31l、蒸汽產生器及蒸汽關係提供成蒸汽形式之H2 O。氫氣可滲透與由電解或熱解加壓之氫貯槽連接的中空陰極。此等替換系統可消除具有活動部件之對應系統。 在實施例中,SF-CIHT電池組件及系統為以下中之至少一者:經組合、微型化及在其他方面經最佳化為重量及尺寸減小、成本減小及維護減少中之至少一者。在實施例中,SF-CIHT電池包含用於急冷器及及電池真空泵之共同壓縮機。用於排熱之急冷器亦可充當低溫泵以充當真空泵。H2 O及O2 可藉由低溫泵凝結。在實施例中,藉由儘可能靠近電極使用數目減少之電容器(諸如例示性單一2.75 V、3400 3400 Maxwell超級電容器)來微型化包含一組電容器之點火系統。在實施例中,至少一個電容器之正極端子可直接連接至正母線條或正電極且至少一個電容器之負極端子可直接連接至負母線條或負電極,其中電容器之具有相反極性的其他端子可藉由母線條連接,使得在熔融金屬藉由橋接可包含熔融金屬噴射器之電極來閉合電路時,電流流經包含電容器之電路。若需要,則跨越電極串聯連接之該組電容器可複製整數倍,以提供約整數倍以上的電流。在實施例中,可藉由利用來自PV轉換器之功率充電而將電容器上之電壓保持在所需範圍內。 SF-CIHT發電機之功率調節可藉由使用內部負載之所有DC功率簡化,其中DC功率由PV轉換器供應。在實施例中,來自PV轉換器之DC功率可供應以下中之至少一者:(i)至電極8的包含電源2的點火系統之電容器的DC充電功率;(ii)至少一個電磁泵之DC電流;(iii)電阻式或電感耦合加熱器之DC功率;(iv)包含DC電馬達之急冷器之DC功率;(v)包含DC電馬達之真空泵的DC功率;及(vi)至電腦及感測器之DC功率。輸出功率調節可包含來自PV轉換器之DC功率或來自使用反相器將來自PV轉換器之DC功率轉換為AC之過程的AC功率。 在一實施例中,光-電轉換器包含本發明之光伏打轉換器,其包含光伏打(PV)電池,其回應於自該電池發射之光之實質性波長區域,諸如對應於至少10%之光功率輸出之波長範圍。在一實施例中,PV電池為可接受大於日光強度之高強度光之聚光電池,該強度諸如在約1.5 suns至75,000 suns、10 suns至10,000 suns及100 suns至2000 suns中之至少一者之強度範圍內。聚光PV電池可包含可在約1至1000 suns範圍內操作之c-Si。矽PV電池可在進行以下中之至少一個功能的溫度下操作:改良帶隙以更好地匹配黑體光譜及改良排熱從而降低冷卻系統之複雜度。在例示性實施例中,聚光矽PV電池在約130℃下以200至500 Suns操作,以提供約0.84 V的帶隙,從而匹配3000℃黑體輻射器的光譜。PV電池可包含複數個接面,諸如三重接面。聚光PV電池可包含複數個層,諸如III/V族半導體之層,諸如以下各者之群組中之至少一者:InGaP/InGaAs/Ge;InAlGaP/AlGaAs/GaInNAsSb/Ge;GaInP/GaAsP/SiGe;GaInP/GaAsP/Si;GaInP/GaAsP/Ge;GaInP/GaAsP/Si/SiGe;GaInP/GaAs/InGaAs;GaInP/GaAs/GaInNAs;GaInP/GaAs/InGaAs/InGaAs;GaInP/Ga(In)As/InGaAs;GaInP-GaAs-晶圓-InGaAs;GaInP-Ga(In)As-Ge;以及GaInP-GaInAs-Ge。諸如三重或雙重接面之複數個接面可串聯連接。在另一實施例中,該等接面可並聯連接。該等接面可以機械方式堆疊。該等接面可經晶圓接合。在一實施例中,接面之間的隧道二極體可用晶圓接合替換。晶圓接合對於藉由後續或較深接面轉換之波長區域而言可為電絕緣及透明的。各接面可連接至獨立電連接或匯流排。獨立匯流排可串聯或並聯連接。各電獨立接面之電接觸可包含柵格導線。由於電流在用於獨立接面或接面組之多個並聯電路或互連中之分佈,可使導線陰影面積降至最低。可側向移除電流。晶圓接合層可包含透明導電層。例示性透明導體為透明導電氧化物(TCO),諸如氧化銦錫(ITO)、摻氟氧化錫(FTO)及經摻雜之氧化鋅;及導電聚合物、石墨烯及碳奈米管及熟習此項技術者已知之其他導體。苯并環丁烯(BCB)可包含中間接合層。接合可介於諸如玻璃(諸如硼矽酸鹽玻璃)之透明材料與PV半導體材料之間。例示性雙接面電池為包含接合至GaAs底層之GaInP晶圓頂層之電池(GaInP//GaAs)。例示性四接面電池包含InP基板上之GaInP/GaAs/GaInAsP/GaInAs,其中各接面可藉由隧道二極體(/)或隔離的透明晶圓接合層(//)單獨隔開,諸如藉由InP上之GaInP//GaAs//GaInAsP//GaInAs給出之電池。PV電池可包含InGaP//GaAs//InGaAsNSb//導電層//導電層//GaSb//InGaAsSb。基板可為GaAs或Ge。PV電池可包含Si-Ge-Sn及合金。二極體與晶圓接合之所有組合在本發明之範疇內。在AM1.5d光譜之297倍濃度下具有44.7%轉換功效之例示性四接面電池藉由SOITEC, France製備。PV電池可包含單一接面。例示性單一接面PV電池可包含單晶矽電池,諸如Sater等人(B. L. Sater, N. D. Sater, 「High voltage silicon VMJ solar cells for up to 1000 suns intensities」, 光伏打專家會議(Photovoltaic Specialists Conference), 2002. 第二十九屆IEEE之會議記錄(Conference Record of the Twenty-Ninth IEEE), 2002年5月19-24日, 第1019-1022頁)所給出之彼等電池中之一者,其以全文引用的方式併入本文中。或者,單接面電池可包含摻雜有其他元素之GaAs或GaAs,該等其他元素諸如III族及V族之元素。在一例示性實施例中,PV電池包含在約1000 suns下操作之三重接面聚光PV電池或GaAs PV電池。在另一例示性實施例中,PV電池包含在250 suns下操作之c-Si。在一例示性實施例中,PV可包含可選擇性地對小於900 nm之波長反應之GaAs及在InP、GaAs及Ge中之至少一者上之InGaAs,其可選擇性地回應於在900 nm與1800 nm之間的區域中之波長。可以組合形式使用包含在InP上之GaAs及InGaAs之兩種類型之PV電池來提高效率。兩個單接面型電池可用於獲得雙重接面電池之效應。該組合可藉由使用二向色鏡、二向色濾光片及單獨或與鏡子組合之電池架構中之至少一者以達成如本發明中所給出之光之多次反彈或反射來實施。在一實施例中,各PV電池包含對入射光進行分離及分類,使其重新定向以照在多接面電池中之特定層上之複光層。在一例示性實施例中,該電池包含用於可見光之磷化銦鎵層及用於紅外光之砷化鎵層,其中對應的光經定向。PV電池可包含GaAs1 - x - y Nx Biy 合金。 PV電池可包含矽。矽PV電池可包含可在約5至2000 Suns之強度範圍內操作的聚光電池。矽PV電池可包含結晶矽且至少一個表面可進一步包含可具有與結晶Si層不同之帶隙的非晶矽。非晶矽可具有比結晶矽寬的帶隙。非晶矽層可進行以下中之至少一個功能:致使電池為電透明的及防止電子-電洞對在表面處再結合。矽電池可包含多接面電池。該等層可包含個別電池。至少一個電池(諸如頂部電池,諸如包含Ga、As、InP、Al及In中之至少一者的電池)可經離子分片且機械堆疊於Si電池(諸如Si底部電池)上。多接面電池及串聯連接之電池之層中的每一者可包含旁通二極體,其用以將由電池各層之間的電流錯配導致的電流及功率損失降至最低。電池表面可有紋理以便於光穿透至電池中。電池可包含抗反射塗層以增強光穿透至電池中。抗反射塗層可進一步反射低於帶隙能量的波長。該塗層可包含複數個層,諸如約兩個至20個層。數目增加之層可增強帶通所要波長範圍(諸如高於帶隙能量之光)並反射另一範圍(諸如低於帶隙能量之波長)的的選擇率。反射自電池表面之光可反彈至可吸收光之至少一個其他電池。PV轉換器26a可包含閉合結構,諸如測地圓頂,其提供反射光之多次反彈以增加用於PV吸收及轉換之橫截面。該測地線圓頂可包含複數個接收器單元,諸如覆蓋有PV電池之三角形單元。該圓頂可充當積分球。未經轉換之光可經再循環。光再循環可經由在部件接收器單元(諸如測地圓頂之接收器單元)之間的反射而發生。表面可包含可反射低於電池之帶隙能量之波長的濾光片。電池可包含底部反射鏡(諸如銀或金底層),以將未經吸收之光反射回電池。此外,未經吸收之光及由電池表面濾光片反射之光可由黑體輻射器吸收並再發射至PV電池。在實施例中,PV基板可包含對自底部電池傳輸至基板背面上之反射器的光透明的材料。具有透明基板之例示性三重接面電池為InGaAsP (1.3 eV)、InGaAsP (0.96 eV)、InGaAs (0.73 eV)、InP基板及銅或金IR反射器。在一實施例中,PV電池可包含聚光矽電池。多接面III-V電池可因較高電壓而選擇,或Si電池可因較低成本而選擇。匯流排陰影可藉由使用諸如透明導電氧化物(TCO)之透明導體來減少。 PV電池可包含鈣鈦礦電池。例示性鈣鈦礦電池包含自上而下為Au、Al、Ti、GaN、CH3 NH3 SnI3 、單層h-BN、CH3 NH3 PbI3 - x Brx 、HTM/GA、底部接點(Au)之各層。 電池可包含多p-n接面電池,諸如包含分別轉換EUV及UV之AlN頂層及GaN底層的電池。在實施例中,光伏打電池可包含GaN p層電池,其在表面附近具有重p摻雜以避免短波長光(諸如UV及EUV)的過度衰減。n型底層可包含AlGaN或AlN。在實施例中,PV電池包含GaN及在p-n接面之頂層中經重度p摻雜之Alx Ga1 - x N,其中p摻雜層包含二維電洞氣體。在實施例中,PV電池可包含具有半導體接面之GaN、AlGaN及AlN中之至少一者。在實施例中,PV電池可包含具有金屬接面之n型AlGaN或AlN。在實施例中,PV電池利用多個電子-電洞對對高於PV材料之帶隙的高能光作出回應。光強度可足以充滿再結合機構以改良效率。 轉換器可包含(i) GaN、(ii) AlGaN或AlN p-n接面及(iii)較淺超薄p-n異質接面光伏打電池中之至少一者的複數個,其各自包含n型AlGaN或AlN基底區域上之GaN中的p型二維電洞氣體。每一電池可包含至金屬膜層(諸如Al薄膜層、n型層、耗盡層、p型層)之引線及至金屬膜層(諸如Al薄膜層且歸因於短波長光及真空操作而無鈍化層)的引線。在包含AlGaN或AlN n型層之光伏打電池的實施例中,具有適當功函數之金屬可替換p層以構成肖特基整流障壁以構成肖特基障壁金屬/半導體光伏打電池。 在另一個實施例,轉換器可包含光伏打(PV)電池、光電(PE)電池及PV電池與PE電池之混合物中之至少一者。PE電池可包含固態電池,諸如GaN PE電池。PE電池可各自包含光電陰極、間隙層及陽極。例示性PE電池包含中止之GaN (陰極)/AlN (分離器或間隙)/可經中止之Al、Yb或Eu (陽極)。PV電池可各自包含本發明之GaN、AlGaN及AlN PV電池中之至少一者。PE電池可為頂層且PV電池可為混合物之底層。PE電池可轉換最短波長光。在實施例中,PE電池之陰極及陽極層及PV電池之p層及n層中之至少一者可完全顛倒。架構可改變以改良集電。在實施例中,將自燃料點火之光發射偏振且將轉換器最佳化以使用光偏振選擇性材料以使光穿透至電池之活性層中達到最佳。可藉由用相對應的電極或磁體施加諸如電場或磁場之場來使光偏振。 在實施例中,燃料可包含銀、銅或Ag-Cu合金熔體,其可進一步包含經捕集氫及經捕集H2 O中之至少一者。光發射可主要包含紫外光及遠紫外光,諸如在約10 nm至300 nm之波長區域中的光。PV電池可回應於約10 nm至300 nm之波長區域之至少一部分。PV電池可包含聚光型UV電池。電池可回應於黑體輻射。黑體輻射可對應於約1000K至6000K之至少一個溫度範圍。入射光強度可在約2至100,000 suns及10至10,000 suns之至少一個範圍內。電池可在此項技術中已知之溫度範圍(諸如約小於300℃及小於150℃中之至少一個溫度範圍)下操作。PV電池可包含III族氮化物,諸如InGaN、GaN及AlGaN中之至少一者。在一實施例中,PV電池可包含複數個接面。該等接面可串聯分層。在另一實施例中,該等接面為獨立的或電並聯。獨立接面可以機械方式堆疊或經晶圓接合。例示性多接面PV電池包含至少兩個接面,包含經n-p摻雜之半導體,諸如InGaN、GaN及AlGaN之群組中之複數者。GaN之n型摻雜劑可包含氧,且p型摻雜劑可包含Mg。例示性三重接面電池可包含InGaN//GaN//AlGaN,其中//可指隔離性透明晶圓接合層或機械堆疊。PV可在等於聚光型光伏打裝置(CPV)之高光強度下操作。基板可為藍寶石、Si、SiC及GaN中之至少一者,其中後兩者提供CPV應用之最佳晶格匹配。各層可使用此項技術中已知之有機金屬氣相磊晶(MOVPE)法沈積。該等電池可藉由冷板冷卻,諸如CPV或二極體雷射(諸如商用GaN二極體雷射)中所用之彼等冷板。如在CPV電池的情況下,柵格觸點可安裝在電池之正表面及背表面上。在實施例中,PV電池(諸如包含GaN、AlN及GaAlN中之至少一者的PV電池)之表面可終止。終止層可包含H及F中之至少一者。終止可減小缺陷之載波再結合效應。表面可用諸如AlN之窗終止。 在實施例中,光伏打(PV)及光電(PE)轉換器中之至少一者可具有對其回應之光實質上透明的保護性窗。該窗可至少10%透過回應光。該窗可透過UV光。該窗可在PV或PE電池上包含塗層,諸如UV透明塗層。塗層可藉由諸如氣相沈積之沈積塗覆。該塗層可包含本發明之UV窗之材料,諸如藍寶石或MgF2 窗。其他合適窗包含LiF及CaF2 。諸如MgF2 窗之任何窗可製得較薄以限制EUV衰減。在實施例中,PV或PE材料(諸如硬的玻璃類材料,諸如GaN)充當可清潔表面。PV材料(諸如GaN)充當窗。在實施例中,PV或PE電池之表面電極可包含窗。電極及窗可包含鋁。窗可包含鋁、碳、石墨、氧化鋯、石墨烯、MgF2 、鹼土氟化物、鹼土鹵化物、Al2 O3 及藍寶石中之至少一者。窗可極薄,諸如約1 Å至100 Å厚,使得其對來自電池之UV及EUV發射透明。例示性較薄透明薄膜為Al、Yb及Eu薄膜。薄膜可藉由MOCVD、氣相沈積、濺鍍及此項技術中已知之其他方法塗覆。 在實施例中,電池可藉由至少一種機構將入射光轉換為電,該至少一種機構諸如係來自光伏打效應、光電效應、熱離子效應及熱電效應之群組的至少一種機構。轉換器可包含雙層電池,其各自在光伏打層之頂部上具有光電層。諸如遠紫外光之較高能量光可選擇性地藉由頂層吸收及轉換。複數個層中之一層可包含UV窗,諸如MgF2 窗。UV窗可保護紫外(UV) PV免於由於電離輻射而受損,諸如由於軟X射線輻射而受損。在實施例中,可添加低壓電解槽氣體以選擇性地使將損害(UV) PV之輻射衰減。或者,此輻射可藉由光電轉換器頂層至少部分地轉換為電且至少部分地自UV PV被阻擋。在另一個實施例中,諸如GaN之UV PV材料亦可使用光伏打效應及光電效應中之至少一者將來自電池之遠紫外發射的至少一部分轉換為電。 光伏打轉換器可包含將紫外光轉換成電之PV電池。例示性紫外PV電池包含以下中之至少一者:經沈積於Nb摻雜之氧化鈦上之聚(4-苯乙烯磺酸酯)膜(SrTiO3:Nb)摻雜之p型半導體聚合物PEDOT-PSS:(聚(3,4-伸乙二氧基噻吩)) (PEDOT-PSS/SrTiO3:Nb異質結構)、GaN、摻雜有諸如錳之過渡金屬之GaN、SiC、金剛石、Si及TiO2 。其他例示性PV光伏打電池包含n-ZnO/p-GaN異質接面電池。 為將高強度光轉換為電,發電機可包含光分佈系統及光伏打轉換器26a (諸如圖2I132中所示之光分佈系統及光伏打轉換器)。光分佈系統可包含沿自電池發射之光的傳播軸線佈置成遮光堆疊之複數個半透明反射鏡,其中在堆疊之每一個反射鏡部件23處,光至少部分地反射至PC電池15 (諸如與光傳播方向平行對準的電池)上以接收橫向反射光。光-電面板15可包含PE、PV及熱離子電池中之至少一者。至轉換器的窗可對電池發射的光(諸如短波長光)或黑體輻射(諸如對應於約2800K至4000K之溫度的黑體輻射)透明,其中功率轉換器可包含熱光伏打(TPV)功率轉換器。至PV轉換器之窗可包含以下中之之一者:藍寶石、LiF、MgF2 及CaF2 、其他鹼土鹵化物(諸如氟化物,諸如BaF2 、CdF2 )、石英、熔融石英、UV玻璃、硼矽酸鹽及紅外矽(ThorLabs)。半透明反射鏡23可對短波長光透明。材料可與PV轉換器窗之材料相同,部分覆蓋反射性材料,諸如反射鏡,諸如UV反射鏡。半透明反射鏡23可包含反射性材料之格紋圖案,該反射性材料諸如UV反射鏡,諸如以下中之至少一者:經MgF2 塗佈之Al及鋁上之氟化物薄膜,諸如MgF2 或LiF膜,或SiC膜。 在實施例中,TPV轉換效率可藉由使用選擇性發射器(諸如黑體發射器5b4之表面上的鐿)而增加。鐿為一類稀土金屬之例示性成員,其代替發射類似線路輻射光譜之光譜的正常黑體光譜。此允許相對較窄發射之能量頻譜與TPV電池之帶隙極為接近地匹配。 在實施例中,發電機進一步包含開關(諸如本發明或此項技術中已知之IGBT或另一種開關),以在低能量氫反應自身藉由熱解傳播的情況下斷開點火電流。該反應自身可維持升高之電池及電漿溫度中之至少一者,諸如支援以足以保持此該溫度及低能量氫反應速率之速率進行熱解的溫度。該電漿可包含光厚電漿。電漿可包含黑體。光厚電漿可藉由保持高氣體壓力而達成。在例示性實施例中,在利用100 A至1000 A之範圍內之連續點火電流在鎢電極處噴射熔融銀及熔融銀銅(28 wt%)合金時發生熱解,其中疊加脈衝在約2 kA至10 kA之範圍內、電漿黑體溫度為5000 K且電極溫度在約3000K至3700K之範圍。熱解可發生在電漿及與電漿接觸之電池組件(諸如反應電解槽腔室5b31之壁)中之至少一者的高溫下。該溫度可在約500K至10,000K、1000K至7000K及1000K至5000K之至少一個範圍內。在另一實施例中,電池組件中之至少一者(諸如儲集器5c)可充當冷卻劑以冷卻熱解H以防止其恢復成H2 O。 所保持黑體溫度可為發射出可利用光伏打電池轉換為電之輻射的溫度。在例示性實施例中,黑體溫度可經保持在約1000 K至4000 K中之至少一個範圍內。光伏打電池可包含熱光伏打(TPV)電池。用於熱光伏打轉換之例示性光伏打電池包含結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)及銻化砷磷銦(InPAsSb)電池。其他例示性電池為InGaAsP (1.3 eV)/InGaAsP (0.96 eV)/InGaAs (0.73 eV)/InP基板/銅或金IR發射器及InAlGaAs (1.3 eV)/InGaAs (0.96 eV)/分級緩衝層/Ge子電池/銅或金IR反射體。PV電池可包含在多接面GaSb電池上之多接面GaAs電池堆疊,諸如在2J GaSb電池上之3J GaAs電池。轉換器可包含至直接及重定向輻射至熱光伏打轉換器上中之至少一者的反射鏡。在實施例中,反向反射鏡將未經轉換之輻射反射回至來源以促成經重輻射至轉換器之功率。例示性反射鏡包含以下中之至少一者:椎體材料,諸如鋁及陽極化鋁、經MgF2 塗佈之Al;及氟化物薄膜,諸如在鋁及藍寶石上之MgF2 或LiF薄膜或SiC薄膜;氧化鋁,諸如α-氧化鋁,其可經濺射塗佈於基板上,諸如不鏽鋼、經MgF2 塗佈之藍寶石、硼矽石玻璃、鹼鋁矽酸鹽玻璃(諸如Gorilla玻璃);LiF、MgF2 及CaF2 、其他鹼土鹵化物,諸如氟化物,諸如BaF2 、CdF2 石英、熔融石英、UV玻璃、硼矽酸鹽、紅外矽(ThorLabs)及陶瓷玻璃,其可在透明時在外表面上成鏡像。諸如陽極化鋁反射鏡之反射鏡可使光擴散以均一地輻射PV轉換器。透明材料(諸如藍寶石、氧化鋁、硼矽石玻璃、LiF、MgF2 及CaF2 、其他鹼土鹵化物(諸如氟化物,諸如BaF2 、CdF2 )、石英、熔融石英、UV玻璃、硼矽酸鹽、紅外矽(ThorLabs)及陶瓷玻璃中之至少一者)可充當用於TPV轉換器之窗。TPV轉換器之另一實施例包含黑體發射器濾光片以傳送與PV之帶隙匹配的波長並將失配之波長反射回至發射器,其中該發射器可包含熱電池組件作為電極。黑體輻射器5b4可經塗佈有選擇性發射器(諸如,稀土金屬(諸如鐿)),其發射對於熱光伏打轉換更有利之光譜,諸如類似線路輻射光譜之光譜。 電池之帶隙經選擇以使用於給定黑體操作溫度及對應光譜之電輸出效率達到最佳。在於約3000K或3500K下操作的例示性實施例中,TPV電池接面之帶隙於表1中給出。 表1. 用於具有n =1、2、3或4個接面(J)之電池的最佳帶隙組合. 為使包含多接面電池之熱光伏打轉換器之效能達到最佳,自電池發射之光的黑體溫度可經保持為約在諸如10%內的常量。隨後,可利用功率調節設備來控制功率輸出,其中盈餘功率儲存於諸如電池或電容器之裝置中或經排出(諸如作為熱量排出)。在另一實施例中,可藉由用本發明降低反應速率(諸如改變點火頻率及電流、金屬噴射速率及H2 O及H2 中之至少一者的噴射速率)來保持來自電漿之功率,其中黑體溫度可藉由控制電漿之發射率來保持。可藉由添加諸如稀有氣體之電解槽氣體改變電池氛圍(諸如最初包含金屬蒸氣之電池氛圍)來改變電漿之發射率。 在實施例中,利用對應感測器或量規來感測電解槽氣體(諸如水蒸氣、氫及氧之壓力)之壓力。在實施例中,藉由監測電池之至少一個參數來感測至少一種氣體壓力(諸如水壓及氫壓中之至少一者),該至少一個參數回應於此等電解槽氣體中之至少一者的壓力變化而變化。可藉由隨著氣體的供應改變一或多種壓力同時監測改變之效應來達成合乎需要之水壓及氫壓中之至少一者。藉由氣體改變之例示性經監測參數包含點火電路之電行為及電池之光輸出。點火電流及光輸出中之至少一者可在氫壓及水蒸氣壓中之至少一者的所要壓力下達到最大。光偵測器(諸如二極體)及PV轉換器之輸出中之至少一者可量測電池之光輸出。電壓及電流計中之至少一者可監測點火電路之電行為。發電機可包含壓力控制系統(諸如包含軟體之壓力控制系統)、處理器(諸如電腦)及自對參數之監測中接收輸入資料及調節氣體壓力以達成發電機之所要功率輸出的最佳化的控制器。在包含燃料金屬(包含銅)之實施例中,氫可保持在一定壓力下以自H2 O與低能量氫及氧之反應達成對來自銅與氧之反應的氧化銅的還原,其中調節水蒸氣壓以藉由監測參數來使發電機輸出達到最佳。在實施例中,可藉由電解藉由供應H2 將氫壓控制在約恆定壓力下。可將電解電流保持在約恆定電流下。可以一定速率供應氫以與大約全部低能量氫反應氧產物反應。盈餘氫可經由電池壁擴散,以保持低能量氫反應及與氧產物反應所消耗之氫上方的恆定壓力。氫可滲透過中空陰極至反應電解槽腔室5b31。在實施例中,壓力控制系統回應於點火電流及頻率與光輸出來控制H2 及H2 O壓力以使至少一者達到最佳。可利用二極體、功率計或光譜儀監測光。可利用萬用錶或數位示波器來監測點火電流。亦可控制電磁泵5k之熔融金屬的噴射速率以使點火電路之電行為及電池之光輸出中之至少一者達到最佳。 在另一個實施例中,感測器可量測多個組件。在例示性實施例中,利用質譜儀(諸如四極質譜儀,諸如殘氣分析儀)來量測電解槽氣體及總壓力。質譜儀可以分批或趨向模式進行感測。水或濕度感測器可包含絕對、電容及電阻濕度感測器中之至少一者。能夠分析複數種氣體之感測器包含電漿源,諸如微波腔室及發生器,其中電漿激發電解槽氣體發射諸如可見及紅外光的光。藉由光譜發射(諸如氣態組分之特徵線及強度)來測定氣體及濃度。氣體可在取樣之前冷卻。在分析電解槽氣體之氣體組成之前,自電解槽氣體移除金屬蒸氣。電池(諸如包含銀及銅中之至少一者的電池)中之金屬蒸氣可經冷卻以凝結金屬蒸氣,使得電解槽氣體可在金屬蒸氣不存在時流動至感測器中。SF-CIHT電池在本文中亦被稱作SF-CIHT發電機或發電機可包含通道(諸如氣體自電池流動之管),其中該管包含電池入口及經凝結金屬蒸氣流動之出口及不可凝結氣體至至少一個氣體感測器的輸出。管可經冷卻。冷卻可藉由傳導達成,其中管經散熱至經冷卻電池組件(諸如電極電磁泵之磁體)。可藉由諸如水冷之方式及諸如散熱管之被動構件來有效冷卻管。包含金屬蒸氣之電解槽氣體可進入管,其中金屬蒸氣由於管之低溫而凝結。經凝結金屬可藉由諸如重力流動及泵抽中之至少一者的方式流動至椎體儲集器,使得待感測之氣體在金屬蒸氣不存在時流動至感測器中。或者,可在外部腔室5b3a中量測氣體壓力,其中氣體可滲透至反應電解槽腔室5b31中。滲透可經由黑體輻射器5b4。 在實施例中,發電機包含黑體輻射器5b4,其可充電包含反應電解槽腔室5b31之容器。在實施例中,PV轉換器26a包含在金屬罩殼之內部上之PV電池15,該金屬罩殼包含含有黑體輻射器5b4之電池腔室5b3。PV冷卻板可在電池腔室外部。腔室5b3、5b3a及5b31中之至少一者能夠將壓力保持為以下中之至少一者:低於大氣壓、為大氣壓及高於大氣壓。PV轉換器可進一步包含至少一組電饋通件以將來自電池腔室之內表面內之PV電池的電功率傳送至電池腔室外部。饋通件可為具有氣密及真空或壓力能力中之至少一者。 在實施例中,諸如儲集器5c之至少一個電池組件可經絕緣。絕緣件可包含熱屏蔽,亦可包含其他形式之熱絕緣,諸如陶瓷絕緣材料(諸如MgO、火磚、Al2 O3 、氧化鋯(諸如Zicar))、氧化鋁增強型熱障(AETB) (諸如AETB 12絕緣件、ZAL-45及SiC-碳氣凝膠(AFSiC))。例示性AETB 12絕緣厚度為約0.5至5 cm。絕緣件可囊封於兩個層(諸如,可包含相同或不同材料(諸如不鏽鋼)的內部耐火金屬或材料電池組件壁及外部絕緣壁)之間。電池組件可經冷卻。外部絕緣囊封壁可包含冷卻系統,諸如將熱量傳遞急冷器或輻射器31的冷卻系統。 在實施例中,急冷器可包含輻射器31且可進一步包含至少一個風扇31j1及至少一個冷卻劑泵31k來冷卻輻射器並使冷卻劑循環。輻射器可經空氣冷卻。例示性輻射器包含汽車或卡車輻射器。急冷器可進一步包含冷卻劑儲集器或貯槽31l。貯槽31l可充當流動緩衝器。冷卻系統可包含旁通閥以將來自貯槽之流動返回至輻射器。在實施例中,冷卻系統包含以下中之至少一者:用以在輻射器入口管線壓力由於冷卻管線中之泵抽之降低或中止而較低時使冷卻劑在貯槽與輻射器之間再循環的旁通迴路;及在輻射器與貯槽之間的輻射器過壓或溢流管線。冷卻系統可進一步包含在旁通迴路中之至少一個止回閥。冷卻系統可進一步包含輻射器溢流閥(諸如止回閥)及自輻射器至溢流貯槽31l之溢流管線。輻射器可充當貯槽。急冷器(諸如輻射器31及風扇31j1)可具有往返貯槽31l的流動。 冷卻系統可包含自輻射器至貯槽31l之用以傳送已冷卻之冷卻劑的貯槽入口管線。冷卻劑可自貯槽31l泵抽至可向待冷卻之每一組件供應降溫冷卻劑的共同貯槽出口歧管。輻射器31可充當貯槽,其中輻射器出口提供降溫冷卻劑。或者,待冷卻之每一組件(諸如電感耦合加熱器、EM泵磁體5k4及PV轉換器26a)可具有單獨冷卻劑流動迴路,其具有藉由急冷器(諸如輻射器及風扇)冷卻之貯槽。每一迴路可包含複數個泵31k中之獨立泵或泵及複數個閥門31m中之閥門。每一迴路可接收來自調節迴路中之流動的獨立泵31k的流動。或者,每一迴路可接收來自向複數個迴路提供流動之泵31k的流動,其中每一迴路包含閥門31m,諸如調節迴路中之流動的螺線管閥門。穿過每一迴路之流動可獨立地藉由其控制器(諸如熱感測器,諸如熱電偶、流量計、可控制值、泵控制器及電腦中之至少一者)控制。 在實施例中,反應電解槽腔室5b31經密封以約束以下中之至少一者:燃料氣體,諸如水蒸氣及氫及氧來源(諸如氧化物)中之至少一者;及燃料熔體之金屬蒸氣,諸如Ag或Ag-Cu合金蒸氣。反應電解槽腔室5b31之外表面可包含黑體輻射器5b4,其可包含能夠在極高溫(諸如在約1000℃至4000℃之範圍內)下操作的材料。在實施例中,黑體輻射器5b4可包含熔點比熔融金屬(諸如銀)之熔點高的材料。例示性材料為來自以下各者之群組的金屬及合金中之至少一者:WC、TaW、CuNi、赫史特合金C、赫史特合金X、英高鎳(Inconel)、英高合金(Incoloy)、碳鋼、不鏽鋼、鉻-鉬鋼(諸如,經改質之9Cr-1Mo-V (P91)、21/4Cr -1Mo鋼(P22))、Nd、Ac、Au、Sm、Cu、Pm、U、Mn、經摻雜Be、Gd、Cm、Tb、經摻雜Si、Dy、Ni、Ho、Co、Er、Y、Fe、Sc、Tm、Pd、Pa、Lu、Ti、Pt、Zr、Cr、V、Rh、Hf、Tc、Ru、經摻雜B、Ir、Nb、Mo、Ta、Os、Re、W、碳、陶瓷(諸如SiC、MgO、氧化鋁、Hf-Ta-C、氮化硼)及此項技術中已知之可充當黑體的其他高溫材料。黑體輻射器自電漿吸收功率以加熱至其高操作溫度。在熱光伏打實施例中,黑體輻射器5b4提供入射至PV轉換器26a之光。黑體輻射器可具有諸如接近一之發射率的發射率。在實施例中,可調節發射率以產生匹配PV轉換器之能力的黑體功率。在例示性實施例中,可藉助於本發明增加或減小發射率。在金屬黑體輻射器5b4之例示性情況下,表面可為經氧化及經粗化中之至少一者,以增加發射率。發射率可與波長成非線性(諸如與波長成反比),以使得短波長發射自其外表面係有利的。在黑體輻射器5b4與PV轉換器26a之間的間隙中之濾光片、透鏡及反射鏡中之至少一者可對於將短波長光傳送至PV轉換器同時將紅外光返回至輻射器5b4具有選擇性。在例示性實施例中,W或碳黑體輻射器5b4之操作溫度係W白熾電燈泡之操作溫度,諸如至多3700 K。在發射率為1的情況下,根據斯蒂芬波茲曼方程式,黑體輻射器功率為至多10.6 MW/m2 。在實施例中,使黑體輻射入射PV轉換器26a,該PV轉換器包含回應對應輻射之聚光型光伏打電池15 (諸如本發明之聚光型光伏打電池),諸如回應可見及近紅外光之聚光型光伏打電池。電池可包含多接面電池,諸如包含III/V半導體之雙或三接面電池,諸如本發明之電池。 SF-CIHT發電機可進一步包含黑體溫度感測器及黑體溫度控制器。黑體輻射器5b4之黑體溫度可經保持及調節以使黑體光至電的轉換達到最佳。可利用諸如以下中之至少一者的感測器來感測黑體輻射器5b4之黑體溫度:光譜儀、光學高溫計、PV轉換器26a及使用發射率來測定黑體溫度的功率計。藉助於本發明,控制器(諸如包含電腦之控制器及低能量氫反應參數感測器及控制器)可控制來自低能量氫反應之功率。在例示性實施例中,為控制溫度及黑體溫度之穩定性,藉由控制水蒸氣壓、氫壓、燃料噴射速率、點火頻率及點火電壓及電流中之至少一者來控制低能量氫反應速率。對於來自加熱黑體輻射器5b4之反應電解槽腔室5b31的給定低能量氫反應功率,可藉由以下中之至少一者來達成黑體輻射器5b4的所要操作黑體溫度:選擇及控制黑體輻射器5b4之內及外表面中之至少一者的發射率。在實施例中,自黑體輻射器5b4輻射之功率大約為與PV轉換器26a匹配的光譜及功率。在實施例中,外表面之發射率經選擇(諸如在約0.1至1之範圍內的發射率),以便使頂蓋5b4在所要黑體溫度下將功率輻射至PV轉換器,該功率並未超出其最大可接受入射功率。黑體溫度可經選擇以較好地匹配PV電池之光伏打轉換反應,使得轉換效率可最大化。可藉由修改黑體輻射器5b4的外表面來改變發射率。可藉由塗覆發射率增加或減小之塗層來增加或減小發射率。在例示性實施例中,可將熱解碳塗層施加至黑體輻射器5b4以增加其發射率。發射率亦可藉由氧化及粗化W表面中之至少一者來增加,且發射率可藉由還原經氧化表面及拋光粗糙W表面中之至少一者來減小。發電機可包含氧化氣體(諸如氧及H2 O中之至少一者)的來源及還原氣體(諸如氫)的來源以及用以控制電池腔室中之氛圍的組成及壓力的構件。發電機可包含氣體感測器(諸如壓力計)、泵、氣體供應器及用以控制氣體組成及壓力以控制黑體輻射器5b4的發射率的氣體供應控制器。 黑體輻射器5b4及PV轉換器26a可藉由間隙(諸如氣體或真空間隙)分隔,以防止PV轉換器由於熱傳導至PV轉換器而過熱。黑體輻射器5b4可包含多個合適的形狀,諸如包含扁平板或圓頂之形狀。可針對結構完整性及將光傳輸至PV區域的最佳化中之至少一者來選擇形狀。例示性形狀為立方體形、直圓柱形、多邊形及測地線球。黑體輻射器5b4 (諸如碳)可包含零件,諸如可膠合在一起之板。例示性立方體反應電解槽腔室5b31及可包含碳之黑體輻射器5b4可包含自碳之固體立方體機械加工並膠合在一起的兩個半立方體。 空腔之基底可包含諸如圓錐通道之幾何結構,以准許熔融金屬流回至儲集器中。基底可比上壁厚,以充當絕緣件,使得功率優先自非基底表面輻射。 空腔可包含壁,其厚度沿周界變化,以便產生沿包含黑體輻射器5b4之外表面的所要溫度分佈。在例示性實施例中,立方體形反應電解槽腔室5b31可包含壁,其包含在各壁上居中之球面區段以產生外表面之均一黑體溫度。球面區段可經機械加工成壁形式,或其可膠合成平面內壁表面。球面區段之球面半徑可經選擇以達成所要黑體表面溫度分佈。 為增強電池電輸出及效率,黑體發射器5b4之面積與接收PV轉換器26a可最佳匹配。在實施例中,其他電池組件(諸如儲集器5c)可包含材料(諸如耐火材料,諸如碳、BN、SiC或W)以充當黑體輻射器至沿圓周佈置至組件以接收黑體輻射之PV轉換器。電池組件(諸如黑體輻射器5b4及儲集器5c)中之至少一者可包含使PV電池15之堆疊最佳以接受來自組件的光的幾何結構。 在例示性實施例中,電池組件可包含多面體表面,諸如多邊形,諸如三角形、五邊形、六邊形、正方形及矩形中之至少一者,與PV電池15之幾何結構相匹配。考慮到諸如照明光子之入射角及對PV效率之對應影響的參數,黑體輻射器及PV轉換器之幾何結構可經選擇以使自該黑體輻射器至該PV轉換器的光子傳遞最佳。在實施例中,PV轉換器26a可包含用以移動PV電池(諸如PV回轉料架)以引起入射於電池上之時間平均輻射的更多均一性的構件。PV回轉料架可使軸向對稱PC轉換器(諸如包含橫向多邊形環之PC轉換器)繞對稱軸或z軸旋轉。多邊形可包含六邊形。旋轉可由機械驅動連接、氣動馬達、電磁驅動裝置或熟習此項技術者所知之其他驅動裝置引起。 可更改黑體輻射器5b4表面以利用關於自黑體輻射器輻射之功率的對應改變來更改發射率。黑體輻射器發射率可藉由(i)更改表面之拋光、粗糙度或紋理、(ii)向碳添加塗層(諸如碳化物,諸如碳化鎢、碳化鉭及碳化鉿中之至少一者)或熱解塗層及(iii)向碳黑體輻射器添加包層(諸如W包層)來改變。在後一種情況下,可藉由扣件(諸如具有膨脹構件(諸如狹槽)之螺釘)以機械方式將W附接至碳。在例示性實施例中,相對於碳的約1之發射率,在碳黑體輻射器5b4上之TaC (諸如TaC塗層、平鋪或包層)的發射率為約0.2。 黑體輻射器5b4可包含具有第一幾何結構之空腔,諸如在具有第二幾何結構(諸如立方體)的實心形狀內的球面空腔5b31 (圖2I134至圖2I138)。在另一個實施例中,具有第一幾何結構之第一空腔5b31可在具有第二幾何結構之第二空腔5b4a1內部。例示性實施例包含在中空立方體空腔中之球殼空腔。相對應的第二空腔5b4a1可包含黑體空腔,其包含黑體輻射器外表面5b4a。第二空腔之內部可藉由具有第一幾何結構之內部第一空腔加熱至黑體溫度。來自相對應的第二黑體輻射器5b4a之黑體輻射可入射至PV電池15,其可以匹配幾何結構組織。電池可佈置在具有匹配幾何結構之陣列中。在實施例中,可藉由以下中之至少一者將接收至PV電池中之光功率降低至在黑體輻射器之操作溫度下發射之光的可容許強度:增加第二空腔與PV電池之間的間距;使用在表面上包含半反射鏡的PV電池以反射一部分入射光;使用次級輻射器(諸如鎢而非碳,發射率降低之輻射器);及使用在PV電池前方之具有針孔的反射器,該等針孔僅將來自初級或次級黑體輻射器之黑體輻射部分地透射至PV電池並理想地反射非透射光。在實施例中,次級輻射器5b4a及具有匹配幾何結構之PV轉換器26a之幾何結構可經選擇以降低PV冷板、PV冷卻器或PV熱交換器26b的複雜度。例示性立方幾何結構可將PV冷板之數目降至最低,將PV冷板之尺寸最大,且導致電互連及冷卻劑管線連接(諸如至PV冷卻劑系統之入口31b及出口31c的電互連及冷卻劑管線連接)的複雜度較低。 可藉由支援鹵素循環之構件保護W次級黑體輻射器免受昇華影響。在實施例中,圍封W黑體輻射器之腔室(諸如腔室5b3 (圖2I80))的氣體可包含鹵素來源(諸如I2 或Br2 )或與昇華鎢形成錯合物的烴溴化合物。錯合物可在熱鎢表面上分解以將鎢再沈積於黑體輻射器5b4上。可為多層之PV電池15上的窗可支援溫度梯度以支援鎢-鹵素物質的揮發從而支援鹵素循環。 在實施例中,可藉由施加外部壓力保護碳電池組件(諸如碳黑體輻射器5b4)免受昇華影響。在例示性實施例中,藉由施加約100大氣壓之壓力使碳穩定昇華至4500 K。可如藉由高壓氣體(諸如惰性氣體、氫及熔融金屬蒸氣(諸如銀蒸氣)中之至少一者)施加壓力。 在實施例中,黑體輻射器5b4包含可連接至儲集器5c之球面圓頂。黑體輻射器可為除球面(諸如立方體)以外的形狀且可進一步經塗佈或包覆有材料以改變其發射率,從而較好地將經輻射功率與PV電池之能力匹配。例示性包覆黑體輻射器5b4包含具有耐火材料之碳立方體包覆,該耐火材料之發射率比在黑體操作溫度下具有自氣化或昇華之低蒸氣壓的碳低。至少一個電池組件(諸如儲集器5c、黑體輻射器5b4及黑體輻射器包層中之至少一者)可包含以下中之至少一者:石墨(昇華點=3642℃);耐火金屬(諸如鎢(M.P.=3422℃)或鉭(M.P.=3020℃));陶瓷;超高溫陶瓷;及陶瓷基質複合物(諸如硼化物、碳化物、氮化物及氧化物中之至少一者,該等硼化物、碳化物、氮化物及氧化物諸如係早期過渡金屬之彼等者,諸如硼化物(HfB2 )、二硼化鋯(ZrB2 )、氮化鉿(HfN)、氮化鋯(ZrN)、碳化鈦(TIC)、氮化鈦(TiN)、二氧化釷(ThO2 )、硼化鈮(NbB2 )及碳化鉭(TaC)及其相關聯複合物)。具有所需高熔點之例示性陶瓷為氧化鎂(MgO) (M.P.=2852℃)、氧化鋯(ZrO) (M.P.=2715℃)、氮化硼(BN) (M.P.=2973℃)、二氧化鋯(ZrO2 ) (M.P.=2715℃)、硼化鉿(HfB2 ) (M.P.=3380℃)、碳化鉿(HfC) (M.P.=3900℃)、Ta4 HfC5 (M.P.=4000℃)、Ta4 HfC5 TaX4 HfCX5 (4215℃)、氮化鉿 (HfN) (M.P.=3385℃)、二硼化鋯(ZrB2 ) (M.P.=3246℃)、碳化鋯(ZrC) (M.P.=3400℃)、氮化鋯(ZrN)(M.P.=2950℃)、硼化鈦(TiB2 )(M.P.=3225℃)、碳化鈦(TIC) (M.P.=3100℃)、氮化鈦(TiN)(M.P.=2950℃)、碳化矽(SiC) (M.P.=2820℃)、硼化鉭(TaB2 )(M.P.=3040℃)、碳化鉭(TaC) (M.P.=3800℃)、氮化鉭(TaN) (M.P.=2700℃)、碳化鈮(NbC) (M.P.=3490℃)、氮化鈮(NbN) (M.P.=2573℃)、碳化釩(VC) (M.P.=2810℃)及氮化釩(M.P.=2050℃)及渦輪葉片材料(諸如來自以下各者之群組中之一或多者:超合金、包含鉻、鈷及錸之鎳基超合金、包含陶瓷基質複合物之超合金、U-500、Rene 77、Rene N5、Rene N6、PWA 1484、CMSX-4、CMSX-10、英高鎳、IN-738、GTD-111、EPM-102及PWA 1497)。諸如MgO及ZrO之陶瓷可對與H2 反應有抗性。在例示性實施例中,相對於碳的約1之發射率,在碳黑體輻射器5b4上之TaC (諸如TaC塗層、平鋪或包層)的發射率為約0.2。例示性電池組件(諸如儲集器)包含MgO、氧化鋁、ZrO、ZrB2 、SiC或BN。例示性黑體輻射器5b4可包含碳或鎢。電池組件材料(諸如石墨)可經塗佈有另一種高溫或耐火材料(諸如耐火金屬(諸如鎢)或陶瓷(諸如ZrB2 、TaC、HfC、WC))或本發明或此項技術中已知之另一種材料。另一石墨表面塗層包含類金剛石碳,其可藉由對椎體之電漿處理形成於表面上。處理方法可包含此項技術中已知之用於將類金剛石碳沈積於基板上之處理方法。在實施例中,銀蒸氣可藉由預塗覆或在操作期間沈積於表面上以保護錐面免受侵蝕。在實施例中,反應電解槽腔室5b31可包含碳與電解槽氣體(諸如H2 O、H2 、CO及CO2 中之至少一者)的反應產物以遏制碳之進一步反應。在一實施例中,至少一個組件(諸如泵管5k6之下部及EM泵組合件5kk)可包含高溫鋼,諸如海恩斯230。在實施例中,藉由低能量氫反應保持之稀有氣體-H2 電漿(諸如氬-H2 (3至5%))可將石墨形式之碳轉換為類金剛石或金剛石形式中之至少一者。 電池組件(諸如儲集器5c或黑體輻射器5b4)可經鑄造、研磨、熱壓、燒結、電漿燒結、浸潤、火花電漿燒結、藉由粉末床雷射熔化3D打印及藉由熟習此項技術者已知之其他方法形成。在實施例中,至少一個組件(諸如外殼5b3a)可藉由衝壓或印模按壓組成材料(諸如金屬)來製造。 在熱離子及熱電實施例中,熱離子或或熱電轉換器可與熱黑體輻射器5b4直接接觸。黑體輻射器5b4亦可將熱量傳遞至熱機(諸如朗肯、布累登或史特林熱機)或可充當熱至電轉換器之加熱器。在實施例中,除標準介質(諸如水或空氣)以外的介質可用作熱機之工作介質。在例示性實施例中,烴或超臨界二氧化碳可置換渦輪發電機之朗肯循環中之水,且關於外部燃燒器設計之空氣可用作渦輪發電機之布累登循環之工作介質。例示性超臨界二氧化碳循環發電機包含Echogen電力系統之發電機(https://www.dresser-rand.com/products-solutions/systems-solutions/waste - heat - recovery - system /http://www.echogen.com/_CE/pagecontent/Documents/News/Echogen_brochure_2016.pdf)。或者,熱蓋5b4可充當熱源或加熱器或光源。至熱機或加熱器之熱流可為直接或間接的,其中SF-CIHT發電機可進一步包含熱交換器或熱傳遞構件(諸如本發明中之一者)。在另一實施例中,SunCell®可包含磁流體動力(MHD)或電漿流體動力(PHD)發電機,其中在反應電解槽腔室5b31中產生之高壓電漿流動至MHD或PHD發電機中並轉換為電。回流可進入反應電解槽腔室中。 電池腔室5b3或5b3a1及反應電解槽腔室3b31中之至少一者可利用泵13a經由諸如13b之泵管線抽空。相對應的泵管線閥門可用於選擇經泵抽容器。電池可進一步包含一或多個用於氧、氫、水蒸氣、金屬蒸氣、氣態氧化物(諸如CO2 、CO)中之至少一者及總壓力的具有高溫能力之感測器。藉助於本發明,水及氫壓力可經控制至所要壓力,諸如本發明之壓力,諸如在0.1 Torr至1 Torr之範圍內的水蒸氣壓。在例示性實施例中,閥門及其中閥門開口經控制以利用使用氣體之經量測壓力的回饋供應保持氣體之所要壓力的流動的氣體供應器保持所要氣體壓力。H2 O及H2 可藉由氫氣貯槽及管線31l供應,該氫氣貯槽及管線31l可包含提供H2 之電解系統、H2 O/蒸汽貯槽及管線31l、氫進料管線5ua、氬貯槽5u1及進料管線5u1a及氣體噴射器(諸如可穿過EM泵管之H2 、氬氣及H2 O/蒸汽噴射器中之至少一者)。作為泵抽出氧氣或吸除氧氣之替代,電池中產生之氧氣可與經供應之氫氣反應以形成水。低能量氫氣體可經由電池之壁及接合點擴散或流出選擇性氣體閥門。 在另一實施例中,反應電解槽腔室5b31在惰性氛圍下操作。SF-CIHT發電機可包含惰性氣體來源(諸如貯槽)及以下中之至少一者:壓力計、壓力調節器、流量調節器、至少一個閥門、泵及用以讀取壓力及控制壓力之電腦。惰性氣體壓力可在約1 Torr至10 atm之範圍內。 在實施例中,在啟動後,可卸除加熱器,且可進行冷卻以將電池組件(諸如儲集器5c、EM泵及PV轉換器26a)保持在其操作溫度(諸如本發明中所給出之操作溫度)下。在實施例中,圖2I28、2I69、及圖2I80至圖2I149中所示之SF-CIHT電池或發電機(亦被稱作SunCell®® )包含六個基本易維護系統,一些系統不具有活動部件且能夠長時間操作:(i)啟動電感耦合加熱器,其包含電力供應器5m、引線5p及天線線圈5f,用以首先熔化銀或銀銅合金以構成熔融金屬或熔體;及視情況選用之電極電磁泵,其包含磁體,用以在最初引導點火電漿流;(ii)燃料噴射器,諸如包含氫供應器(諸如,貫穿黑體輻射器之滲氫供應器)的燃料噴射器,其中可藉由電解或熱解自水中得到氫;及噴射系統,其包含用以噴射熔融銀或熔融銀銅合金之電磁泵5ka及氧來源(諸如氧化物,諸如CO2 、CO、LiVO3 或本發明之另一氧化物);及替代地,氣體噴射器,其可包含用以噴射水蒸氣及氫氣中之至少一者的穿過EM泵管5k6的埠;(iii)點火系統,其用以產生跨越一對電極8之低電壓高電流流動,熔融金屬、氫及氧化物、或熔融金屬及H2 O及氫氣中之至少一者經噴射至該對電極中以形成發亮光電漿;(iv)藉由電漿加熱至白熾溫度之黑體輻射器5b4;(v)光-電轉換器26a,其包含所謂的聚光型光伏打電池15,該等聚光型光伏打電池自黑體輻射器接收光並在諸如超過一千個Suns之高光強度下操作;及(vi)燃料回收及熱管理系統,其致使熔融金屬在點火後返回至噴射系統並冷卻至少一個電池組件(諸如電感加熱器天線5f、EM泵磁體5k4及PV轉換器26a)。在另一實施例中,來自點火電漿之光可直接輻射PV轉換器26a以轉換為電。在另一實施例中,EM泵5ka可包含熱電泵、機械泵(諸如齒輪泵,諸如陶瓷齒輪泵)或此項技術中已知之另一種泵(諸如包含葉輪的能夠進行高溫(諸如在約900℃至2000℃之溫度範圍內)操作的泵)。 在實施例中,至PV轉換器26a之黑體輻射器可包含高溫材料(諸如碳)、耐火金屬(諸如W、Re)或陶瓷(諸如過渡元素(諸如鉿、鋯鉭及鈦)的硼化物、碳化物及氮化物)、Ta4 HfC5 (M.P. = 4000℃)、TaB2 、HfC、BN、 HfB2 、HfN、ZrC、TaC、ZrB2 、TiC、TaN、NbC、ThO2 、氧化物(諸如MgO)、MoSi2 、W-Re-Hf-C合金及本發明之其他材料。黑體輻射器可包含有效地將光傳遞至PV且使PV電池填充最佳的幾何結構,其中光之功率自反應電解槽腔室5b31流動。例示性黑體輻射器可包含多邊形或球面圓頂。黑體輻射器可藉由氣體或真空間隙與PV轉換器26a分離,其中PV電池經定位以自黑體輻射器接收黑體光。 發電機可進一步包含能夠密封至該氛圍並進一步能夠保持壓力低於、等於及大於大氣壓中之至少一者的周邊腔室。發電機可包含在圓頂周邊之球面壓力或真空容器,其包含電池腔室5b3,其中PV轉換器包含殼體或壓力容器。電池腔室可包含熟習此項技術者已知之合適材料,其提供結構強度、密封及熱傳遞。在例示性實施例中,電池腔室包含不鏽鋼及銅中之至少一者。PV電池可覆蓋電池腔室之內部,且PV冷卻系統(諸如熱交換器87)可覆蓋電池腔室之外表面。在熱光伏打實施例中,PV轉換器26a可包含用於至PV轉換器26a之可見波長的選擇性濾光片(諸如光子晶體)。 在實施例中,黑體輻射器包含球面圓頂5b4。在實施例中,石墨球之內表面經塗佈有具有高溫能力之碳化物,諸如Ta4 HfC5 (M.P. = 4000℃)、碳化鎢、碳化鈮、碳化鉭、碳化鋯、碳化鈦或碳化鉿。相對應的金屬可與石墨表面之碳反應以形成相對應的金屬碳化物表面。圓頂5b4可藉由氣體或真空間隙與PV轉換器26a分離。在一實施例中,為減小入射於PV電池上之光強度,PV電池可經定位為更遠離黑體輻射器。舉例而言,周邊球面腔室之半徑可增加以減小自內部球面黑體輻射器發射之光的強度,其中PV電池安裝在周邊球面腔室之內表面上(圖2I143)。PV轉換器可包含由複數個PV電池構成之密集型接收器陣列(DRA)。DRA可包含鑲花形狀。個別PV電池可包含三角形、五邊形、六邊形及其他多邊形中之至少一者。形成圓頂或球形之電池可按測地線圖案組織。在於諸如3500 K之高溫下操作的次級黑體輻射器之例示性實施例中,輻射發射率為發射率的約8.5 MW/m2 倍。在此情況下,可藉由塗覆碳化鎢塗層來將發射率約為1之碳圓頂5b4之發射率減小至約0.35。黑體輻射器5b4可包含不同材料之包層26c (圖2I143)以將發射率變為更合乎需要的發射率。在例示性實施例中,相對於碳的約1之發射率,在碳黑體輻射器5b4上之TaC (諸如TaC塗層、平鋪或包層)的發射率為約0.2。在另一實施例中,PV電池(諸如包含外部測地線圓頂之PV電池)可為以下情況之至少一者:成角及包含反射塗層以將由PV電池吸收之光減少至在PV電池之強度容量之內的位準。至少一個PV電路元件(諸如PV電池電極、互連件及匯流排之群組中之至少一者)可包含具有高發射率之材料,諸如經拋光導體,諸如經拋光鋁、銀、金或銅。PV電路元件可將來自黑體輻射器5b4之輻射反射回至黑體輻射器5b4,使得PV電路元件並不會顯著促成遮蔽PV功率轉換損失。 在實施例中,黑體輻射器5b4可包含複數個可分離之區段,諸如可分離的頂部及底部半球。該兩個半球可在凸緣處結合。W圓頂可藉由此項技術中已知之技術(諸如熔結W粉末、活化電漿熔結、鑄造及藉由雷射熔化之3D打印)製造。下部腔室5b5可在半球凸緣處結合。電池腔室可藉由能夠具有真空、大氣壓及高於真空之壓力中之至少一者的凸緣附接至下部腔室。下部腔室可與電池腔室及反應電解槽腔室中之至少一者密封隔離。氣體可滲透在電池腔室與反應電解槽腔室之間。氣體交換可平衡兩個腔室中之壓力。氣體(諸如氫及稀有氣體(諸如氬)中之至少一者)可添加至電池腔室以藉由滲透或流動向電池反應腔室供應氣體。滲透及流動可對於所要氣體(諸如氬-H2 )有選擇性。金屬蒸氣(諸如銀金屬蒸氣)可為不可滲透的或可為流動受限的,以使得其選擇性地僅保留在電池反應腔室中。可藉由將儲集器5c保持在凝結金屬蒸氣及保持其蒸氣壓處於所要位準的溫度下來控制金屬蒸氣壓。發電機可利用氣體壓力(諸如低於操作壓力(諸如大氣壓)之氬-H2 氣體壓力)啟動,使得不會隨著電池加熱及氣體膨脹而形成超壓。氣體壓力可利用本發明之控制器(諸如電腦、壓力感測器、閥門、流量計及真空泵)來控制。 在實施例中,藉由充當導電基質之銀蒸氣來保持低能量氫反應。其中至少一部分變為蒸氣的連續噴射及來自儲集器5c之銀的直接沸騰中之至少一者可提供銀蒸氣。電極可向反應提供高電流以移除電子並引發低能量氫反應。來自低能量氫反應之熱量可幫助向反應電解槽腔室提供金屬蒸氣(諸如銀金屬蒸氣)。 點火電力供應器可包含電容器及電感器中之至少一者。點火電路可包含變壓器。變壓器可輸出高電流。發電機可包含自PV轉換器接收DC功率並輸出AC的反相器。發電機可包含DC至DC電壓及電流調節器,以改變來自PV轉換器的可輸入至反相器的電壓及電流。輸入至變壓器之AC可來自反相器。反相器可在所要頻率(諸如在約一至10,000 Hz之範圍內的頻率)下操作。在實施例中,PV轉換器26a輸出DC功率,其可直接饋送至反相器或可在輸入至反相器之前進行調節。經反相功率(諸如60 Hz AC)可直接為電極供電或可輸入至變壓器以增加電流。在實施例中,電源2向電極提供連續DC或AC電流。電極及電磁泵可支援經噴射熔體(諸如熔融Ag,其可進一步包含氧來源(諸如氧化物))的連續點火。氫可藉由滲透過黑體輻射器來添加。 可藉助於本發明達成負載追蹤。在實施例中,當向下調節來自反應電解槽腔室5b31之功率時,至PV轉換器26a之黑體輻射器5b4可極快速地輻射掉其儲存能量。在實施例中,輻射器表現為白熾長絲,其在中斷功率自反應腔室5b31流動至輻射器5b4的情況下具有類似光中止時間。在另一實施例中,電負載追蹤可藉由在對應於約恆定操作溫度之約恆定功率流動下操作輻射器來達成,其中至負載之非所需功率耗散或堆積至電阻性元件(諸如電阻器,諸如SiC電阻器或本發明之其他加熱元件)中。 在實施例中,發電機可包含智慧型控制系統,其智慧型地啟動及撤銷啟動複數個負載中之負載以控制波峰聚集負載。發電機可包含複數個發電機,其可連軸以獲得穩定性及提供峰值功率中之至少一者。智慧型計量及控制中之至少一者可藉由遙測(諸如藉由使用具有WiFi之蜂巢式電話或個人電腦)而達成。 在實施例中,來自黑體輻射器5b4之黑體光經隨機引導。該光可為經反射、經吸收及在輻射器黑體輻射器5b4與PV電池15之間來回再輻射中之至少一者。PV電池可最佳成角以達成所要PV吸收及光至電轉換。PV防護玻璃罩之反射率可隨位置而變化。反射率之變化可利用具有空間可變反射率之PV窗達成。可變性可利用塗層達成。例示性塗層為MgF2 -ZnS抗反射塗層。PV電池可在幾何學上經佈置以達成所要PV電池吸收及反射,其涉及在黑體輻射器5b4與PV電池中之至少兩者之間、在複數個PV電池之間及在複數個PV電池與黑體輻射器5b4之間的功率流動相互作用。在實施例中,PC電池可經佈置至一表面中,該表面具有隨表面角度(諸如摺疊表面,諸如摺疊測地線圓頂)變化之可變半徑。在實施例中,黑體輻射器5b4可具有相對於彼此成角度之元件,以進行以下中之至少一者:定向地發射、吸收及反射輻射至PV電池或自PV電池定向地發射、吸收及反射輻射。在實施例中,黑體輻射器5b4可包含在黑體輻射器表面上之元件發射器板以匹配PV定向,從而達成功率至PV電池的所要傳遞。黑體輻射器、反射器或吸收器表面中之至少一者可具有以下中之至少一者:發射率、反射率、吸收係數及表面積,該表面積經選擇以達成至涉及輻射器及PV電池之PV轉換器的所要功率流動。功率流動可涉及在PV電池與黑體輻射器之間的輻射反彈。在實施例中,黑體輻射器5b4之內對外表面之發射率及表面積中之至少一者經選擇以達成所要的功率流動至PV電池對功率流回至反應電解槽腔室5b31。 在實施例中,高能量光(諸如UV及EUV中之至少一者)可解離反應電解槽腔室5b31中之H2 O及H2 中之至少一者,以增加低能量氫反應之速率。解離可為熱解效應之替代。 在另一實施例中,操作發電機以保持反應電解槽腔室5b31中之高金屬蒸氣壓。高金屬蒸氣壓可為以下中之至少一者:形成光厚電漿以將來自低能量氫反應之UV及EUV發射轉換為黑體輻射;及充當低能量氫反應之反應物(諸如導電基質)以增加其反應速率。低能量氫反應可在藉由水之熱解支援的反應電解槽腔室中傳播。金屬蒸氣及黑體溫度中之至少一者可較高(諸如,在1000K至10,000K之範圍內)以支援水之熱解,從而增加低能量氫反應速率。低能量氫反應可在氣相及電漿相中之至少一者中發生。金屬可藉由電磁泵噴射且藉由點火電流及來自低能量氫反應之熱量中之至少一者汽化。反應條件、電流及金屬噴射速率可經調節以達成所要金屬蒸氣壓。 在高於金屬蒸氣之金屬來源之沸點的溫度下操作發電機可引起大於大氣壓之反應電解槽腔室壓力。金屬蒸氣壓可藉由以下中之至少一者控制:控制由電磁(EM)泵供應至腔室之金屬蒸氣的量;及控制電池組件(諸如電池儲集器)之溫度。在實施例中,反應電解槽腔室5b31及儲集器5c中之至少一者可包含至少一個擋板,其引起熱蒸氣自反應電解槽腔室之一個區域對流流動至儲集器5c之較冷液體金屬表面,在該區域中,蒸氣在諸如其中發生低能量氫反應之區域中具有最高溫度。熱循環可藉由凝結蒸氣來控制銀蒸氣壓,其中蒸氣壓可藉由輸送速率及對可控制之液體銀溫度的蒸氣壓依賴性中之至少一者來測定。儲集器可足夠深以保持液體銀位準。儲集器可藉由熱交換器冷卻以保持液體銀。該溫度可使用冷卻(諸如水冷)來控制。在例示性實施例中,自儲集器延伸至反應電解槽腔室中之筆直擋板可將外部冷卻流與內部熱流分離。在另一實施例中,可控制EM泵以在達成所要金屬蒸氣壓時停止泵抽。或者,電池腔室5b3或5b3a1之壓力可與反應電解槽腔室5b31之壓力匹配,使得存在跨越腔室之所要可容許壓力梯度。可藉由自由閥門、調節器、控制器及壓力感測器控制之氣體供應件添加氣體(諸如稀有氣體)至電池腔室來減小或等化或平衡腔室壓力之間的差。在實施例中,氣體可在電池腔室5b3或5b3a1與反應電解槽腔室5b31之間滲透。腔室氣體而非金屬蒸氣可移動及平衡兩個腔室之壓力。可利用氣體(諸如稀有氣體)將兩個腔室加壓至高壓。壓力可高於金屬蒸氣之最高操作分壓。最高金屬蒸氣分壓可對應於最高操作溫度。在操作期間,金屬蒸氣壓可增加反應電解槽壓力,使得氣體選擇性地自反應電解槽5b3流動至電池腔室5b3或5b3a1直至壓力平衡,且反之亦然。在實施例中,兩個腔室之間的氣體壓力自動平衡。平衡可藉由氣體在腔室之間的選擇性移動性而達成。在實施例中,避免壓力偏移,以便避免大壓差。 電池腔室中之壓力可經保持為大於反應電解槽腔室中之壓力。外部電池腔室中之較大壓力可用來以機械方式將電池組件(黑體輻射器56b4及儲集器5c)固持在一起。 在實施例中,將金屬蒸氣保持在穩態壓力下,其中將蒸氣之凝結降至最少。電磁泵可在所要金屬蒸氣壓下停止。可間歇地啟動EM泵進行泵抽以便保持所要穩態壓力。金屬蒸氣壓可經保持在0.01 Torr至200 atm、0.1 Torr至100 atm及1 Torr至50 atm之至少一個範圍內。 在一實施例中,為達成高低能量氫功率,控制電極電磁泵抽動作以控制點火電流參數,諸如波形、峰值電流、峰值電壓、恆定電流及恆定電壓。在實施例中,波形可為任何所要波形,其使所要功率輸出及效率最佳。波形可為恆定電流、恆定電壓、恆定功率、鋸齒、方波、正弦、梯形、三角形、具有截止之斜升、斜升-斜降及此項技術中已知之其他波形。在其中波形具有約為零之電壓或電流的一部分的情況下,工作循環可在約1%至99%之範圍內。頻率可為任何所要的,諸如在約0.001至1 MHz、0.01 Hz至100 kHz及0.1 Hz至10 kHz之至少一個範圍內。波形之峰值電流可在約10 A至1 MA、100 A至100 kA及1 kA至20 kA之至少一個範圍內。電壓可藉由電阻與電流之乘積給出。在實施例中,電源2可包含點火電容器組90。在實施例中,電源2 (諸如電容器組)可經冷卻。冷卻系統可包含本發明之冷卻系統,諸如輻射器。 在實施例中,電源2包含具有不同數目個串聯及並聯電容器的電容器組以提供最佳電極電壓及電流。PV轉換器可將電容器組充當至所要最佳電壓並保持最佳電流。點火電壓可藉由使跨越電極之電阻增加而增加。電極電阻可藉由在更高溫下(諸如在約1000K至3700K之溫度範圍內)操作電極而增加。可控制電極溫度以藉由控制點火過程及電極冷卻來保持所要溫度。電壓可在約1 V至500 V、1 V至100 V、1 V至50 V及1 V至20 V之至少一個範圍內。電流可在約10 A至100 kA、100 A至10 kA及100 A至5 kA之至少一個範圍內。在例示性實施例中,在150 A與250 A之間的恆定電流下,電壓為約16 V。在實施例中,歸因於低能量氫反應之功率由於較高低能量氫反應速率而在正電極處較高。較高速率可歸因於藉由正電極更有效地自反應電漿移除電子。在實施例中,低能量氫反應取決於電子之移除,其在所施加之較高電極電壓下係有利的。電子之移除亦可藉由使與反應電漿接觸之電池組件接地來增強。發電機可包含額外接地或正偏壓電極。電容器包含於點火電容器殼體90中(圖2I89)。 點火電壓可較高,諸如在約1 V至100 V、1 V至50 V及1 V至25 V之至少一個範圍內。電流可為脈衝式或連續的。電流可在約50 A至100 kA、100 A至10 kA及300 A至5 kA之至少一個範圍內。汽化熔體可提供自低能量氫催化反應移除電子以增加反應速率的導電路徑。在例示性實施例中,歸因於在約2162℃至4000℃之溫度範圍中的汽化,銀蒸氣壓較高,諸如在約0.5 atm至100 atm之範圍內。 在實施例中,SunCell®可包含液體電極。電極可包含液體金屬。液體金屬可包含燃料之熔融金屬。噴射系統可包含至少兩個儲集器5c及至少兩個可實質上彼此電隔離之電磁泵。複數個噴射系統中之每一者的噴嘴5q可經定向以致使複數個熔融金屬流相交。每一流可具有至電源2之端子的連接,以向相交流提供電壓及電流。電流可自一個噴嘴5q經由其熔融金屬流流動至其他流及噴嘴5q且返回至電源2的相對應端子。電池包含熔融金屬返回系統以便於將所噴射之熔融金屬傳回至複數個儲集器。在實施例中,熔融金屬返回系統將穿過熔融金屬之點火電流及噴射電流中之至少一者的短接降到最少。反應電解槽腔室5b31可包含底層,其將所噴射熔融金屬之回流引至單獨儲集器5c中,使得銀實質上在單獨儲集器5c中隔離,以將在銀連接儲集器中的電氣短路降至最少。用於電傳導之電阻在儲集器之間的銀回流中實質上比在相交銀中高,使得大部分電流流經相交流。電池可包含儲集器電隔離器或分離器,其可包含電絕緣體,諸如陶瓷或具有低導電性之耐火材料(諸如石墨)。 低能量氫反應可引起高濃度電子的產生,其可減緩其他低能量氫產生且由此抑制低能量氫反應速率。點火電極8處之電流可移除電子。在實施例中,歸因於在陽極處優先移除電子從而引起高低能量氫反應速率及局部加熱,固體電極(諸如固體耐火金屬電極)在為正電極或陽極時易於熔化。在實施例中,電極包含液體電極與固體電極之混合物。陽極可包含液體金屬電極且陰極可包含固體電極,諸如W電極,且反之亦然。液體金屬陽極可包含至少一個EM泵及噴嘴,其中噴射液體金屬以與陰極接觸從而接通點火電路。 在實施例中,當低能量氫反應在不存在電功率輸入的情況下傳播時,終止點火功率。低能量氫反應可在藉由水之熱解支援的反應電解槽腔室中傳播。與點火功率無關之反應自身可在合適的反應條件下傳播。反應條件可包含高溫及合適的反應物濃度中之至少一者。可控制低能量氫反應條件及電流中之至少一者以達成在電極之至少一部分上的高溫從而達成熱解。反應溫度及電極之一部分之溫度中之至少一者可較高,諸如在約1000℃至20,000℃、1000℃至15,000℃及1000℃至10,000℃之至少一個範圍內。合適的反應濃度可包含在以下之至少一個範圍內的水蒸氣壓:約0.1 Torr至10,000 Torr、0.2 Torr至1000 Torr、0.5 Torr至100 Torr及0.5 Torr至10 Torr。合適的反應濃度可包含在以下之至少一個範圍內的氫壓:約0.1 Torr至10,000 Torr、0.2 Torr至1000 Torr、0.5 Torr至100 Torr及0.5 Torr至10 Torr。合適的反應濃度可包含在以下之至少一個範圍內的金屬蒸氣壓:約1 Torr至100,000 Torr、10 Torr至10,000 Torr及1 Torr至760 Torr。反應電解槽腔室可經保持在一溫度下,該溫度保持使低能量氫反應速率最佳的金屬蒸氣壓。 在實施例中,可將化合物添加至熔融金屬(諸如熔融Ag或AgCu合金)以便進行以下中之至少一者:降低其熔點及黏度。化合物可包含助熔劑,諸如硼砂。在實施例中,固體燃料(諸如本發明之固體燃料)可添加至熔融金屬。在實施例中,熔融金屬(諸如熔融銀、銅或AgCu合金)包含用於將水結合或分散於熔體(諸如助熔劑)中之組成物,該助熔劑可經水合,諸如硼砂,其可經水合至各種程度,諸如無水硼砂、五水合硼砂及十水合硼砂。熔體可包含助熔劑以自泵管之內部移除氧化物。移除可在電磁泵母線5k2之區域處保持熔融金屬與泵管5k6之間的良好電接觸。 在實施例中,包含氧來源之化合物可添加至熔融金屬,諸如熔融銀、銅或AgCu合金。在實施例中,金屬熔體包含並不黏附於電池組件(諸如錐形儲集器及椎體或圓頂)的金屬。金屬可包含合金,諸如Ag-Cu (諸如AgCu (28 wt%))或Ag-Cu-Ni合金。化合物可在儲集器5c及電磁泵之操作溫度下熔化,使得其進行以下中之至少一者:溶解及與熔融金屬混合。化合物可在低於熔點之溫度下進行以下中之至少一者:在熔融金屬中溶解及混合。包含氧來源之例示性化合物包含氧化物,諸如金屬氧化物或13、14、15、16或17族氧化物。金屬氧化物之例示性金屬為具有低水反應率之金屬中之至少一者,該等金屬係諸如以下各者之群組之彼等金屬:Cu、Ni、Pb、Sb、Bi、Co、Cd、Ge、Au、Ir、Fe、Hg、Mo、Os、Pd、Re、Rh、Ru、Se、Ag、Tc、Te、Tl、Sn、W及Zn。相對應的氧化物可以熱力方式有利地與氫反應形成HOH催化劑。例示性金屬氧化物及其相對應的熔點為十水合四硼酸鈉(M.P. = 743℃,無水)、CuO (M.P. = 1326℃)、NiO (M.P. = 1955℃)、PbO (M.P. = 888℃)、Sb2 O2 (M.P. = 656℃)、Bi2 O3 (M.P. = 817℃)、CO2 O3 (M.P. = 1900℃)、CdO (M.P. = 900-1000℃)、GeO2 (M.P. = 1115℃)、Fe2 O3 (M.P. = 1539-1565℃)、MoO3 (M.P. = 795℃)、TeO2 (M.P. = 732℃)、SnO2 (M.P. = 1630℃)、WO3 (M.P. = 1473℃)、WO2 (M.P. = 1700℃)、ZnO (M.P. = 1975℃)、TiO2 (M.P. = 1843℃)、Al2 O3 (M.P. = 2072℃)、鹼土金屬氧化物、稀土金屬氧化物、過渡金屬氧化物、內部過渡金屬氧化物、鹼金屬氧化物(諸如Li2 O (M.P. = 1438℃)、Na2 O (M.P. = 1132℃)、K2 O (M.P. = 740℃)、Rb2 O (M.P. = >500℃)、Cs2 O (M.P. = 490℃))、氧化硼(諸如B2 O3 (M.P.=450℃))、V2 O5 (M.P. = 690℃)、VO (M.P. = 1789℃)、Nb2 O5 (M.P. = 1512℃)、NbO2 (M.P. = 1915℃)、SiO2 (M.P. = 1713℃)、Ga2 O3 (M.P. = 1900℃)、In2 O5 (M.P. = 1910℃)、Li2 WO4 (M.P. = 740℃)、Li2 B4 O7 (M.P. = 917℃)、Na2 MoO4 (M.P. = 687℃)、LiVO3 (M.P. = 605℃)、Li2 VO3 、Mn2 O5 (M.P. = 1567℃)及 Ag2 WO4 (M.P. = 620℃)。另外的例示性氧化物包含氧化物之混合物,諸如包含鹼型氧化物(諸如Li2 O及Na2 O及Al2 O3 、B2 O3 及VO2 )中之至少兩者的混合物。該混合物可引起更合乎需要之物理性質,諸如較低熔點或較高沸點。氧化物可經乾燥。在氧來源(諸如Bi2 O3 或Li2 WO4 )之例示性實施例中,氧來源之氫還原反應在熱力學上係有利的,且還原產物與水反應形成氧來源可在操作條件下(諸如在赤熱條件下)發生。在例示性實施例中,在赤熱下,鉍與水反應形成三氧化物(三氧化二鉍(III))(2Bi(s) + 3H2 O(g) →Bi2 O3 (s) + 3H2 (g))。在實施例中,氧化物經汽化為氣相或電漿。反應電解槽腔室5b31中之氧化物的莫耳數可限制其蒸氣壓。在實施例中,形成HOH催化劑之氧來源可包含多種氧化物。複數個氧化物中之每一者可揮發以在某些溫度範圍內充當HOH催化劑之來源。舉例而言,LiVO3 可充當高於以上其熔點及低於第二氧來源(諸如第二氧化物)之熔點的主氧源。第二氧化物在較高溫度(諸如高於其熔點)下充當氧源。例示性第二氧化物為Al2 O3 、ZrO、MgO、鹼土金屬氧化物及稀土金屬氧化物。氧化物在諸如3000K之操作溫度下基本上可全部為氣態。壓力可藉由添加至反應電解槽腔室5b31之莫耳數來調節。氧化物與銀蒸氣壓之比率可經調節以使低能量氫反應條件及速率最佳。 在實施例中,氧來源可包含無機化合物,諸如以下中之至少一者:H2 O、CO、CO2 、N2 O、NO、NO2 、N2 O3 、N2 O4 、N2 O5 、SO、SO2 、SO3 、PO、PO2 、P2 O3 、P2 O5 。氧來源(諸如CO2 及CO中之至少一者)可為處於室溫下之氣體。氧源(諸如氣體)可處於外部壓力容器腔室5b31a中。氧源可包含氣體。氣體可進行以下中之至少一者:自外部壓力容器腔室5b31a擴散或滲透至反應電解槽腔室5b31;及自反應電解槽腔室5b31擴散或滲透至外部壓力容器腔室5b31a。反應電解槽腔室5b31內部之氧源氣體濃度可藉由控制其在外部壓力容器腔室5b31a中之壓力來控制。氧源氣體可藉由供應管線添加至反應電解槽腔室作為在反應電解槽腔室內部之氣體。供應管線可進入較冷區域中,諸如進入在儲集器之底部處之EM泵管中。氧源氣體可藉由分解或汽化固體或液體(諸如凍結CO2 、碳酸鹽或碳酸)而供應。可利用壓力計(諸如本發明之壓力計)來量測外部壓力容器腔室5b31a及反應電解槽腔室5b31中之至少一者中的壓力。可利用控制器及氣體源控制氣體壓力。 反應電解槽腔室5b31氣體可進一步包含H2 ,其可滲透黑體輻射器5b4或經由EM泵管或另一入口供應。另一種氣體(諸如CO2 、CO及H2 O中之至少一者)可藉由滲透及流經入口(諸如EM泵管)中之至少一者供應。H2 O可包含水蒸氣及氣態水或蒸氣中之至少一者。外部腔室中之氣體可包含H2 、H2 O、CO及CO2 中之至少一者,該氣體滲透黑體輻射器(諸如碳黑體輻射器5b4)以供應反應電解槽腔室5b31。氣體可進行以下中之至少一者:自外部壓力容器腔室5b31a擴散或滲透至反應電解槽腔室5b31;及自反應電解槽腔室5b31擴散或滲透至外部壓力容器腔室5b31a。控制外部腔室中之相對應的氣體壓力可控制每種氣體之反應電解槽腔室5b31濃度。可用相對應的感測器來感測每種氣體之反應電解槽腔室5b31壓力或濃度。CO、CO2 及H2 在反應電解槽腔室5b31中之存在可遏制H2 O與由碳構成之任何電池組件(諸如碳反應電解槽腔室)反應。在實施例中,H2 O與低能量氫(諸如H2 (1/4))之反應的氧產物可有益於低能量氫反應。氧產物與電池組件之氧化副反應可由氫之存在來遏制。可在操作期間形成之熔融金屬塗層亦可保護電池組件免於與H2 O及氧中之至少一者反應。在實施例中,壁(諸如反應電解槽腔室之內壁)可經塗佈有塗層(諸如在反應電解槽腔室之情況下為熱解石墨),其中該塗層對於所要氣體係選擇性可滲透的。在例示性實施例中,黑體輻射器5b4包含碳,且反應電解槽腔室5b31之內壁包含熱解石墨,其對H2 係可滲透的,同時對O2 、CO、CO2 及H2 O中之至少一者係不可滲透的。內壁可經塗佈有熔融金屬(諸如銀)以避免壁與氧化物質(諸如O2 及H2 O)反應。 氧來源可包含化合物,該化合物包含氧陰離子。該化合物可包含金屬。該化合物可選自以下中之一者:氧化物、氫氧化物、碳酸鹽、碳酸氫鹽、硫酸鹽、硫酸氫鹽、磷酸鹽、磷酸氫鹽、磷酸二氫鹽、硝酸鹽、亞硝酸鹽、高錳酸鹽、氯酸鹽、過氯酸鹽、亞氯酸鹽、過亞氯酸鹽、次亞氯酸鹽、溴酸鹽、過溴酸鹽、亞溴酸鹽、過亞溴酸鹽、碘酸鹽、過碘酸鹽、亞碘酸鹽、過亞碘酸鹽、鉻酸鹽、重鉻酸鹽、碲酸鹽、硒酸鹽、砷酸鹽、矽酸鹽、硼酸鹽、氧化鈷、氧化碲及其他氧陰離子,諸如以下各者之氧陰離子:鹵素、P、B、Si、N、As、S、Te、Sb、C、S、P、Mn、Cr、Co及Te,其中金屬可包含以下中之一或多者:鹼金屬、鹼土金屬、過渡金屬、內過渡金屬或稀土金屬、Al、Ga、In、Ge、Sn、Pb、Sb、Bi、Se及Te。氧來源可包含MNO3 、MClO4 、MOx 、Mx O及Mx Oy 中之至少一者,其中M為金屬,諸如過渡金屬、內過渡金屬、稀土金屬、Sn、Ga、In、鉛、鍺、鹼金屬或鹼土金屬,且x及y為整數。氧來源可包含以下中之至少一者:SO2 、SO3 、S2 O5 O2 、F5 SOF、M2 S2 O8 、SOx Xy (諸如SOCl2 、SOF2 、SO2 F2 或SOBr2 )、Xx X'y Oz (其中X及X'為鹵素(諸如ClO2 F、ClO2 F2 、ClOF3 、ClO3 F,及ClO2 F3 )、氧化碲(諸如TeOx ,諸如TeO2 或TeO3 、Te(OH)6 )、SeOx (諸如SeO2 或SeO3 )、氧化硒(諸如 SeO2 、SeO3 、SeOBr2 、SeOCl2 、SeOF2 或SeO2 F2 )、P2 O5 、POx Xy (其中X為鹵素,諸如POBr3 、POI3 、POCl3 或POF3 )、氧化砷(諸如As2 O3 或As2 O5 )、氧化銻(諸如Sb2 O3 、Sb2 O4 或Sb2 O5 、或SbOCl、Sb2 (SO4)3 )、氧化鉍、另一種鉍化合物(諸如BiAsO4 、Bi(OH)3 、Bi2 O3 、BiOBr、BiOCl、BiOI、Bi2 O4 )、金屬氧化物或氫氧化物(諸如Y2 O3 、GeO、FeO、Fe2 O3 、或NbO、NiO、Ni2 O3 、SnO、SnO2 、Ag2 O、AgO、Ga2 O、As2 O3 、SeO2 、TeO2 、In(OH)3 、Sn(OH)2 、In(OH)3 、Ga(OH)3 或Bi(OH)3 )、CO2 、CO、高錳酸鹽(諸如KMnO4 及NaMnO4 )、P2 O5 、硝酸鹽(諸如 LiNO3 、NaNO3 及KNO3 )、過渡金屬氧化物或氫氧化物(Sc、Ti、V、Cr、Mn、Fe、Co、Ni、Cu、或具有至少一個O及OH之Zn)、氧(氫氧)化物(諸如FeOOH)、第二或第三過渡系列氧化物或氫氧化物(諸如Y、Zr、Nb、Mo、Tc、Ag、Cd、Hf、Ta、W、Os之氧化物或氫氧化物)、貴金屬氧化物(諸如PdO或PtO)、金屬及氧陰離子(諸如 Na2 TeO4 或Na2 TeO3 )、CoO、含有至少兩個來自氧及不同鹵素原子之群組的原子的化合物(諸如F2 O、Cl2 O、ClO2 、Cl2 O6 、Cl2 O7 、ClOF3 、ClO2 F、ClO2 F3 、ClO3 F、I2 O5 )、在還原後可形成金屬之化合物。氧來源可包含氣體,該氣體包含氧,諸如O2 、N2 O及NO2 中之至少一者。 在實施例中,熔體包含至少一種添加劑。添加劑可包含一個氧來源及氫來源。氧來源及氫來源中之至少一者可包含以下各者之群組中之一或多者: H2 、NH3 、MNH2 、M2 NH、MOH、MAlH4 、M3 AlH6 及MBH4 、MH、MNO3 、MNO、MNO2 、M2 NH、MNH2 、NH3 、MBH4 、MAlH4 、M3 AlH6 、MHS、M2 CO3 、MHCO3 、M2 SO4 、MHSO4 、M3 PO4 、M2 HPO4 、MH2 PO4 、M2 MoO4 、M2 MoO3 、MNbO3 、M2 B4 O7 、MBO2 、M2 WO4 、M2 CrO4 、M2 Cr2 O7 、M2 TiO3 、MZrO3 、MAlO2 、M2 Al2 O2 、MCoO2 、MGaO2 、M2 GeO3 、MMnO4 、M2 MnO4 、M4 SiO4 、M2 SiO3 、MTaO3 、MVO3 、MIO3 、MFeO2 、MIO4 、MOCl、MClO2 、MClO3 、MClO4 、MClO4 、MScO3 、MScOn 、MTiOn 、MVOn 、MCrOn 、MCr2 On、MMn2 On 、MFeOn 、MxCoOn (x為整數或分數)、MNiOn、MNi2 On、MCuOn、MZnOn,其中n=1、2、3或4且M為金屬,諸如鹼金屬、Mg3 (BO3 )2 及M2 S2 O8 ;混合金屬氧化物或插層氧化物(諸如鋰離子電池插層化合物),諸如以下各者之群組中之至少一者:LiCoO2 、LiFePO4 、LiNix Mny Coz O2 、LiMn2 O4 、LiFeO2 、Li2 MnO3 、Li2 MnO4 、LiNiO2 、LiFeO2 、LiTaO3 、LiVO3 、Li2 VO3 、Li2 NbO3 、Li2 SeO3 、Li2 SeO4 、Li2 TeO3 、Li2 TeO4 、Li2 WO4 、Li2 CrO4 、Li2 Cr2 O7 、Li2 HfO3 、Li2 MoO3 或Li2 MoO4 、Li2 TiO3 、Li2 ZrO3 及LiAlO2 ; 助熔劑,諸如四硼酸鈉(M.P. = 743℃,無水)、K2 SO4 (M.P. = 1069℃)、Na2 CO3 (M.P. = 851℃)、K2 CO3 (M.P. = 891℃)、KOH (M.P. = 360℃)、MgO、(M.P. = 2852℃)、CaO、(M.P. = 2613℃)、SrO (M.P. = 2531℃)、BaO (M.P. = 1923℃)、CaCO3 (M.P. = 1339℃); 分子氧化劑,其可包含諸如以下之氣體:CO、CO2 、SO2 、SO3 、S2 O5 Cl2 、F5 SOF、SOx Xy (諸如SOCl2 、SOF2 、SO2 F2 、SOBr2 )、PO2 、P2 O3 、P2 O5 、POx Xy (諸如POBr3 、POI3 、POCl3 或POF3 )、I2 O5 、Re2 O7 、I2 O4 、I2 O5 、I2 O9 、SO2 、CO、CO2 、N2 O、NO、NO2 、N2 O3 、N2 O4 、N2 O5 、Cl2 O、ClO2 、Cl2 O3 、Cl2 O6 、Cl2 O7 、NH4 X,其中X為硝酸根離子或熟習此項技術者已知之其他合適的陰離子,諸如包含以下各者之群組中之一者: NO3-、NO2-、SO42-、HSO4-、CoO2-、IO3-、IO4-、TiO3-、CrO4-、FeO2 -、PO43-、HPO42-、H2PO4-、VO3-、ClO4-及Cr2O72; 氧陰離子,諸如以下各者之群組中之一者:NO3-、NO2-、SO42-、HSO4-、CoO2-、IO3-、IO4-、TiO3-、CrO4-、FeO2 -、PO43-、HPO42-、H2PO4-、VO3-、ClO4-及Cr2O72-; 強酸、氧化劑、分子氧化劑之氧陰離子,該分子氧化劑諸如為以下各者之群組中之一者:V2O3、I2O5、MnO2 、Re2O7、CrO3、RuO2 、AgO、PdO、PdO2 、PtO、PtO2 及NH4X,其中X為硝酸根離子或熟習此項技術者已知之其他合適的陰離子; 氫氧化物,諸如以下各者之群組中之一者:Na、K、Rb、Cs、Mg、Ca、Sr、Ba、Al、V、Zr、Ti、Mn、Zn、Cr、Sn、In、Cu、Ni、Pb、Sb、Bi、Co、Cd、Ge、Au、Ir、Fe、Hg、Mo、Os、Pd、Re、Rh、Ru、Se、Ag、Tc、Te、Tl及W、MOH、MOH、M'(OH)2,其中M為鹼金屬且M'為鹼土金屬、過渡金屬氫氧化物、Co(OH)2、Zn(OH)2、Ni(OH)2、其他過渡金屬氫氧化物、稀土金屬氫氧化物、Al(OH)3、Cd(OH)2、Sn(OH)2、Pb(OH)、In(OH)3、Ga(OH)3、Bi(OH)3、包含之化合物、錯合離子氫氧化物,諸如Li2Zn(OH)4、Na2Zn(OH)4、Li2Sn(OH)4、Na2Sn(OH)4、Li2Pb(OH)4、Na2Pb(OH)4、LiSb(OH)4、NaSb(OH)4、LiAl(OH)4、NaAl(OH)4、LiCr(OH)4、NaCr(OH)4、Li2Sn(OH)6及Na2Sn(OH)6; 酸,諸如H2SO3、H2SO4、H3PO3、H3PO4、HClO4、HNO3、HNO、HNO2 、H2CO3、H2MoO4、HNbO3、H2B4O7、HBO2 、H2WO4、H2CrO4、H2Cr2O7、H2TiO3、HZrO3、MAlO2 、HMn2O4、HIO3、HIO4、HClO4,或酸來源,諸如無水酸,諸如以下各者之群組中之至少一者:SO2 、SO3、CO、CO2 、NO2 、N2O3、N2O5、Cl207、PO2 、P2O3及 P2O5; 固體酸,諸如MHSO4、MHCO3、M2HPO4及MH2PO4之群組中之一者,其中M為金屬,諸如鹼金屬; 氧(氫氧)化物,諸如以下各者之群組中之一者:WO2(OH)、WO2(OH)2、VO(OH)、VO(OH)2、VO(OH)3、V2O2(OH)2、V2O2(OH)4、V2O2(OH)6、V2O3(OH)2、V2O3(OH)4、V2O4(OH)2、FeO(OH)、(α -MnO(OH)錳榍石及γ -MnO(OH)水錳礦)、MnO(OH)、MnO(OH)2、Mn2O3(OH)、Mn2O2(OH)3、Mn2O(OH)5、MnO3(OH)、MnO2(OH)3、MnO(OH)5、Mn2O2(OH)2、Mn2O6(OH)2、Mn2O4(OH)6、NiO(OH)、TiO(OH)、TiO(OH)2、Ti2O3(OH)、Ti2O3(OH)2、Ti2O2(OH)3、Ti2O2(OH)4、及NiO(OH)、水鈣礦(CrO(OH))、水鋁石(AlO(OH))、ScO(OH)、YO(OH)、VO(OH)、針鐵礦(α -Fe3+O(OH))、錳榍石(Mn3+O(OH))、圭亞那鐵礦(guyanaite) (CrO(OH))、黑鐵釩礦((V,Fe)O(OH))、CoO(OH)、NiO(OH)、Ni1/2Co1/2O(OH)及Ni1/3Co1/3Mn1/3O(OH)、RhO(OH)、InO(OH)、綠磷鉛銅礦(tsumgallite) (GaO(OH))、水錳礦(Mn3+O(OH))、釔鎢華-(Y)YW2O6(OH)3、釔鎢華-(Ce) ((Ce、Nd、Y)W2O6(OH)3)、未命名(釔鎢華-(Ce)之Nd-類似物) ((Nd、Ce、La)W2O6(OH)3)、弗蘭克鐵鉻鋇礦(frankhawthorneite) (Cu2[(OH)2[TeO4])、碲鉛銅石、副碲鉛銅礦及MxOyHz,其中x、y及z為整數,且M為金屬,諸如過渡金屬、內過渡金屬或稀土金屬(諸如金屬氧(氫氧)化物); 氧化物,諸如以下各者之群組中之一者:氧陰離子化合物;鋁酸鹽;鎢酸鹽;鋯酸鹽;鈦酸鹽;硫酸鹽;磷酸鹽;碳酸鹽;硝酸鹽;鉻酸鹽及錳酸鹽、氧化物;亞硝酸鹽;硼酸鹽;氧化硼(諸如B2 O3 );金屬氧化物;非金屬氧化物;以下各者之氧化物:鹼金屬、鹼土金屬、過渡金屬、內過渡金屬及稀土金屬、及Al、Ga、In、Sn、Pb、S、Te、Se、N、P、As、Sb、Bi、C、Si、Ge及B,及形成氧化物或氧陰離子之其他元素;氧化物,其包含至少一個來自鹼金屬、鹼土金屬、過渡金屬、內過渡金屬及稀土金屬之群組之陽離子、及Al、Ga、In、Sn及Pb陽離子、金屬氧化物陰離子及陽離子(諸如鹼金屬、鹼土金屬、過渡金屬、內過渡金屬及稀土金屬陽離子);及其他金屬及類金屬之氧化物(諸如Al、Ga、In、Si、Ge、Sn、Pb、As、Sb、Bi、Se及Te之氧化物,諸如:MM'2xO3x+1或MM'2xO4 (M=鹼土金屬,M'=過渡金屬,諸如Fe或Ni或Mn,x=整數)及M2M'2xO3x+1或M2M'2xO4 (M=鹼金屬,M'=過渡金屬,諸如Fe或Ni或Mn,x=整數)、M2O及MO,其中M為金屬(諸如鹼金屬,諸如Li2 O、Na2 O及K2 O))及鹼土金屬(諸如MgO、CaO、SrO及BaO)、MCoO2 (其中M為金屬,諸如鹼金屬)、CoO2 、MnO2 、Mn2 O3 、Mn3 O4 、PbO2 、Ag2 O2 、AgO、RuO2 ;化合物,其包含銀及氧、過渡金屬之氧化物(諸如NiO及CoO)、V、Zr、Ti、Mn、Zn、Cr、Sn、In、Cu、Ni、Pb、Sb、Bi、Co、Cd、Ge、Au、Ir、Fe、Hg、Mo、Os、Pd、Re、Rh、Ru、Se、Ag、Tc、Te、Tl及W過渡金屬之氧化物及Sn之氧化物(諸如SnO)、鹼金屬之氧化物(諸如Li2O、Na2O及K2O)及鹼土金屬之氧化物(諸如MgO、CaO、SrO及BaO)、MoO2 、TiO2 、ZrO2 、SiO2 、Al2O3、NiO、Ni2O3、FeO、Fe2O3、TaO2 、Ta2O5、VO、VO2 、V2O3、V2O5、B2O3、NbO、NbO2 、Nb2O5、SeO2 、SeO3、TeO2 、TeO3、WO2 、WO3、Cr3O4、Cr2O3、CrO2 、CrO3、MnO、Mn2O7、HfO2 、CO2 O3、CoO、Co3O4、PdO、PtO2 、BaZrO3、Ce2O3、LiCoO2 、Sb2O3、BaWO4、BaCrO4、BaSi2O5、Ba(BO2 )2、Ba(PO3)2、BaSiO3、BaMoO4、Ba(NbO3)2、BaTiO3、BaTi2O5、BaWO4、CoMoO4、CO2 SiO4、CoSO4、CoTiO3、CoWO4、CO2 TiO4、Nb2O5、Li2MoO4、LiNbO3、LiSiO4、Li3PO4、Li2SO4、LiTaO3、Li2B4O7、Li2TiO3、Li2WO4、LiVO3、Li2VO3、Li2ZrO3、LiFeO2 、LiMnO4、LiMn2O4、LiGaO2 、Li2GeO3、LiGaO2 ; 水合物,諸如本發明中之水合物,諸如硼砂或六水合四硼酸鈉; 過氧化物,諸如H2O2 、M2O2 (其中M為鹼金屬) (諸如Li2O2 、Na2O2 、K2O2 )、其他離子過氧化物,諸如鹼土金屬過氧化物(諸如Ca、Sr、或Ba過氧化物之離子過氧化物、其他正電性金屬之離子過氧化物(諸如鑭系元素之離子過氧化物)及共價金屬過氧化物(諸如Zn、Cd及Hg之共價金屬過氧化物);超氧化物,諸如MO2 (其中M為鹼金屬),諸如NaO2 、KO2 、RbO2 及CsO2 及鹼土金屬超氧化物; 化合物,其包含OH物質及H物質中之至少一者,該等氧物質諸如O2、O3、、O、O+、H2O、H3O+、OH、OH+、OH-、HOOH、OOH-、O-、O2-、中之至少一者,該等H物質諸如H2、H、H+、H2O、H3O+、OH、OH+、OH-、HOOH及OOH-中之至少一者;能夠經歷水合反應之酐或氧化物,其包含元素、金屬、合金或混合物,諸如來自以下之群組中之一者:Mo、Ti、Zr、Si、Al、Ni、Fe、Ta、V、B、Nb、Se、Te、W、Cr、Mn、Hf、Co及 Mg、Li2MoO3、Li2MoO4、Li2TiO3、Li2ZrO3、Li2SiO3、LiAlO2 、LiNiO2 、LiFeO2 、LiTaO3、LiVO3、Li2VO3、Li2B4O7、Li2NbO3、Li2SeO3、Li2SeO4、Li2TeO3、Li2TeO4、Li2WO4、Li2CrO4、Li2Cr2O7、Li2MnO4、Li2HfO3、LiCoO2 及MO (其中M為金屬,諸如鹼土金屬,諸如MgO之Mg)、As2O3、As2O5、Sb2O3、Sb2O4、Sb2O5、Bi2O3、SO2 、SO3、CO、CO2 、NO2 、N2O3、N2O5、Cl2O7、PO2 、P2O3及P2O5; 氫化物,諸如來自以下之群組中之氫化物:R-Ni、La2Co1Ni9H6、La2Co1Ni9H6、ZrCr2H3.8、LaNi3.55Mn0.4Al0.3Co0.75、ZrMn0.5Cr0.2V0.1Ni1.2;及能夠儲存氫之其他合金,該氫諸如係選自MmNi5 (Mm = 米許合金) (諸如MmNi3.5Co0.7Al0.8、AB5 (LaCePrNdNiCoMnAl)或AB2 (VTiZrNiCrCoMnAlSn)類型)之氫,其中「ABx」標識係指A型元素(LaCePrNd或TiZr)與B型元素(VNiCrCoMnAlSn)之比率; AB5型,MmNi3.2Co1.0Mn0.6Al0.11Mo0.09 (Mm = 米許合金: 25 wt% La,50 wt% Ce,7 wt% Pr, 18 wt% Nd),La1-yRyNi5-xMx;AB2型:Ti0.51Zr0.49V0.70Ni1.18Cr0.12合金;鎂基合金;Mg1.9Al0.1Ni0.8Co0.1Mn0.1合金;Mg0.72Sc0.28(Pd0.012 + Rh0.012)及Mg80Ti20、Mg80V20、La0.8Nd0.2Ni2.4CO2 .5Si0.1、LaNi5-xMx (M= Mn、Al)、(M= Al、Si、Cu)、(M= Sn)、(M= Al、Mn、Cu)及LaNi4Co、MmNi3.55Mn0.44Al0.3Co0.75、LaNi3.55Mn0.44Al0.3Co0.75、MgCu2、MgZn2、MgNi2;AB化合物;TiFe、TiCo及TiNi、ABn化合物(n = 5、2或1)、AB3-4 化合物;ABx (A = La、Ce、Mn、Mg;B = Ni、Mn、Co、Al)、ZrFe2、Zr0.5Cs0.5Fe2、Zr0.8Sc0.2Fe2、YNi5、LaNi5、LaNi4.5Co0.5、(Ce、La、Nd、Pr)Ni5;米許合金鎳合金、Ti0.98Zr0.02V0.43Fe0.09Cr0.05Mn1.5、La2Co1Ni9、FeNi、TiMn2、TiFeH2、M-N-H 系統之物質(諸如LiNH2、Li2NH或 Li3N);及鹼金屬氫化物,其進一步包含硼(諸如硼氫化物)或鋁(諸如鋁氫化物);鹼土金屬氫化物(諸如MgH2);金屬合金氫化物(諸如BaReH9、LaNi5H6、 FeTiH1.7及MgNiH4);金屬硼氫化物(諸如Be(BH4)2、Mg(BH4)2、Ca(BH4)2、Zn(BH4)2、Sc(BH4)3、Ti(BH4)3、Mn(BH4)2、Zr(BH4)4、NaBH4、LiBH4、KBH4及Al(BH4)3、AlH3、NaAlH4、Na3AlH6、LiAlH4、Li3AlH6、LiH、LaNi5H6、La2Co1Ni9H6及TiFeH2、NH3BH3;氫化物金屬或半金屬,其包含鹼金屬(Na、K、Rb、Cs)、鹼土金屬(Mg、Ca、Ba、Sr)、來自族IIIA之元素(諸如B、Al、Ga、Sb)、來自族IVA之元素(諸如C、Si、Ge、Sn)及來自族VA之元素(諸如N、P、As)、過渡金屬合金及金屬間化合物ABn,其中A表示一或多個能夠形成穩定氫化物之元素且B為形成不穩定氫化物之元素;表2中給出之金屬間化合物;其中部位A及/或部位B之一部分經另一元素(諸如其中M表示LaNi5之元素)取代的金屬間化合物,該金屬間合金可由LaNi5-xAx表示,其中A為(例如)Al、Cu、Fe、Mn及/或Co,且La可經米許合金取代;含有30%至70%鈰、釹及極小量來自同一系列之元素的稀土金屬之混合物取代,剩餘物為鑭;形成混合氫化物(諸如MMgH3 (M=鹼金屬)之合金(諸如Li3Mg、K3Mg、Na3Mg);聚胺硼烷;胺硼烷錯合物(諸如胺硼烷、硼烷氨合物、肼-硼烷錯合物、二硼烷二氨合物、硼氮炔及八氫三硼銨或四氫硼酸銨);咪唑鎓離子液體(諸如烷基(芳基)-3-甲基咪唑鎓N-雙(三氟甲磺醯基)醯亞胺鹽、硼酸鏻及草酸鹽物質)。另外的例示性化合物為氨硼烷、鹼氨硼烷(諸如鋰氨硼烷)及硼烷烷基胺錯合物(諸如硼烷二甲胺錯合物、硼烷三甲胺錯合物)及胺基硼烷及硼烷胺(諸如胺基二硼烷、正二甲基胺基二硼烷、三(二甲胺基)硼烷、二正丁基硼胺、二甲基胺基硼烷、三甲基胺基硼烷、氨-三甲基硼烷及三乙基胺基硼烷。另外的合適的氫儲存材料為氫經吸收之有機液體,諸如咔唑及衍生物,諸如9-(2-乙基己基)咔唑、9-乙基咔唑、9-苯基咔唑、9-甲基咔唑及4,4'-雙(N-咔唑基)-1,1'-聯二苯; 表2.形成氫化物之元素及組合. 滲氫膜,諸如Ni(H2)、V(H2)、Ti(H2)、Fe(H2)或Nb(H2); 化合物,其包含氧及氫中之至少一者,諸如本發明中之化合物,其中其他金屬可置換本發明之金屬,M亦可為另一種陽離子,諸如鹼土金屬、過渡金屬、內部過渡金屬或稀土金屬陽離子或第13至第16族陽離子(諸如Al、Ga、In、Sn、Pb、Bi及Te),且金屬可為熔融金屬中之一者,諸如銀及銅中之至少一者, 及氫及氧中之至少一者的其他此類來源,諸如熟習此項技術者已知的來源。在實施例中,藉由低能量氫反應釋放之能力及跨越電極施加之電壓中之至少一者足以破壞氧來源之氧結合以釋放氧氣。該電壓可在約0.1 V至30 V、0.5 V至4 V及0.5 V至2 V中之至少一個範圍內。在實施例中,氧來源比氫還原產物(諸如水)及包含較少氧之氧來源更穩定。氫還原產物可與水反應以形成氧來源。經還原之氧來源可與水及氧中之至少一者反應以保持此等氧化劑在反應電解槽腔室5b31中之低濃度。經還原之氧來源可保持圓頂5b4。在包含W圓頂及高度穩定之氧化物(諸如Na2 O)的例示性實施例中,經還原之氧來源氧為Na金屬蒸氣,其與H2 O及O2 二者反應以自反應電解槽腔室中清除此等氣體。Na亦可使圓頂上之W氧化物還原為W以保持其不會腐蝕。 例示性氧來源(諸如具有合適的熔點及沸點之能夠溶解或混合成熔體(諸如熔融銀)之氧來源)係選自以下之群組中之至少一者:NaReO4、NaOH、NaBrO3、B2O3、PtO2 、MnO2 、Na5P3O10、NaVO3、Sb2O3、Na2MoO4、V2O5、Na2WO4、Li2MoO4、Li2CO3、TeO2 、Li2WO4、Na2B4O7、Na2CrO4、Bi2O3、LiBO2 、Li2SO4、Na2CO3、Na2SO4、K2CO3、K2MoO4、K2WO4、Li2B4O7、KBO2 、NaBO2 、Na4P2O7、CoMoO4、SrMoO4、Bi4Ge3012、K2SO4、Mn2O3、GeO2 、Na2SiO3、Na2O、Li3PO4、SrNb2O6、Cu2O、LiSiO4、LiNbO3、CuO、CO2 SiO4、BaCrO4、BaSi2O5、NaNbO3、Li2O、BaMoO4、BaNbO3、WO3、BaWO4、SrCO3、CoTiO3、CoWO4、LiVO3、Li2VO3、Li2ZrO3、LiMn2O4、LiGaO2 、Mn3O4、Ba(BO2 )2 *H2O、Na3VO4、LiMnO4、K2B4O7*4H2O及NaO2 。 在實施例中,氧來源(諸如過氧化物,諸如Na2 O2 )、氫來源(諸如氫化物或氫氣,諸如氬/H2 (3%至5%))及導電基質(諸如熔融銀)可充當固體燃料以形成低能量氫。反應可在惰性容器(諸如鹼土金屬氧化物容器,諸如MgO容器)中進行。 添加劑可進一步包含藉由氧來源之氫還原形成之化合物或元素。經還原之氧來源可藉由在反應電解槽腔室5b31中與多餘氧及水中之至少一者反應而形成氧來源(諸如氧化物)。氧來源及經還原之氧來源中之至少一者可包含一定重量百分比之經噴射熔體,其包含熔融金屬(諸如銀)、氧來源(諸如硼砂)及使低能量氫反應速率達到最大的經還原氧來源中之至少兩者。氧來源及經還原之氧來源中之至少一者的重量百分比可在以下中之至少一個重量百分比範圍內:約0.01 wt%至50 wt%、0.1 wt%至40 wt%、0.1 wt%至30 wt%、0.1 wt%至20 wt%、0.1 wt%至10 wt%、1 wt%至10 wt%及1 wt%至5 wt%。反應電解槽腔室氣體可包含氣體混合物。該混合物可包含稀有氣體,諸如氬及氫。反應電解槽腔室5b31可保持在包含氫之分壓之氛圍下。氫壓可在以下中之至少一個範圍內:約0.01 Torr至10,000 Torr、0.1 Torr至1000 Torr、1 Torr至100 Torr及1 Torr至10 Torr。稀有氣體(諸如氬)的壓力可在以下中之至少一個範圍內:約0.1 Torr至100,000 Torr、1 Torr至10,00 Torr及10 Torr至1000 Torr。氧來源可經歷與氫反應以形成H2 O。H2 O可充當HOH催化劑以形成低能量氫。氧來源可在熱力學上對氫還原不利。HOH可在點火期間(諸如在電漿中)形成。經還原產物可與在點火期間形成之水反應。水反應可將反應電解槽腔室5b31中之水保持在較低位準下。低水位可在以下中之至少一個範圍內:約小於40 Torr、小於30 Torr、小於20 Torr、小於10 Torr、小於5 Torr及小於1 Torr。反應電解槽腔室中之低水蒸氣壓可保護至少一個電池組件(諸如圓頂5b4,諸如W或石墨圓頂)免於經歷腐蝕。氧化鎢作為氧來源可參與鎢循環以保持鎢圓頂5b4免於腐蝕。氧及鎢存量之平衡可保持近乎恆定。藉由使來自氧化鎢之氧與鎢金屬反應得到的任何氧化鎢腐蝕產物可由來自氧化鎢之鎢金屬置換,該氧化鎢經還原以提供氧反應物。 添加劑可包含用以增強另一添加劑(諸如氧來源)之可溶性的化合物。化合物可包含分散劑。化合物可包含焊劑。發電機可進一步包含攪拌器,其用以將熔融金屬(諸如銀)與添加劑(諸如氧來源)混合。攪拌器可包含機械、氣動、磁性、電磁攪拌器(諸如使用勞侖茲力之攪拌器)、壓電及此項技術中已知之其他攪拌器中之至少一者。攪拌器可包含音波器,諸如超音波發生器。攪拌器可包含電磁泵。攪拌器可包含電極電磁泵及噴射電磁泵5ka中之至少一者。攪拌可發生在固持熔體之電池組件(諸如儲集器及EM泵中之至少一者)中。可調節熔體組合物以增加添加劑之可溶性。熔體可包含銀、銀銅合金及銅中之至少一者,其中熔體組合物可經調節以增加添加劑之可溶性。增加可溶性之化合物可包含氣體。氣體可具有與添加劑(諸如氧來源)的可逆反應。可逆反應可增強氧來源之可溶性。在例示性實施例中,氣體包含CO及CO2 中之至少一者。例示性可逆反應為CO2 與氧化物(諸如鹼金屬氧化物,諸如Li2 O)反應以形成碳酸鹽。在另一個實施例中,反應包含氧來源之還原產物(諸如,金屬氧化物(諸如鹼金屬氧化物,諸如Li2 O或Na2 O)、過渡金屬氧化物(諸如CuO)及氧化鉍的金屬及水)的反應。 在例示性實施例中,熔體或經噴射熔融金屬包含熔融銀及LiVO3 及M2 O (M=Li或Na)中之至少一者,其在約0.1至5 mol%、1至3 mol%及1.5至2.5 mol%之至少一個濃度範圍中。反應電解槽腔室5b31氣體包含惰性氣體,諸如氬,其中氫氣經保持在約1至10%、2至5%及3至5%之至少一個範圍內。可藉由供應氫至電池腔室5b3或5b31a同時諸如在電池腔室中監測氫分壓及總壓力中之至少一者來置換消耗之氫,其中歸因於氬氣存量之惰性本質及恆定性,可自總壓力推斷出氫壓。氫反加速率可在以下中之至少一個範圍內:約0.00001 moles/s至0.01 moles/s、0.00005 moles/s至0.001 moles/s及0.0001 moles/s至0.001 moles/s。黑體輻射器5b4可包含W或碳。黑體輻射器5b4可包含金屬布或織物(諸如包含鎢之金屬布或織物,其包含細鎢長絲),其中織物密度係可透氣的,但防止銀蒸氣自反應電解槽腔室內部滲透至電池腔室。儲集器5c及EM泵組件(諸如泵管5k6)中之至少一者可包含以下中之至少一者:鈮、鉬、鉭、鎢、錸、鈦、釩、鉻、鋯、鉿、釕、銠、鋨及銥。該等組件可藉由燒結粉末焊接、雷射焊接、電子束焊接、放電機械加工、鑄造、使用螺紋接頭、使用包含耐火材料之接頭套管、使用合金用劑(諸如用於Mo之錸、鈦及鋯(TZM))及電鍍接合之群組中之至少一種接合或製造技術接合。在包含耐火金屬之實施例中,泵管5k6在EM泵匯流排5k2處之區段可自固體塊機械加工或藉由諸如功率熔結鑄造之方式鑄造。該區段可包含用於鄰接泵管之相對應的入口及噴嘴部分的入口及出口管。接合可係藉助於本發明。鄰接導管區段可為經焊接成直立區段之電子束且隨後彎曲以形成泵迴路。自儲集器之泵管入口部分及噴嘴部分可分別經對接至儲集器之底部並穿過底部。可藉由電子束焊接將管焊接在儲集器之底部之每一穿透件處。 在實施例中,使用O形環(諸如耐火金屬或材料O形環)將螺紋耐火金屬電池組件塊密封在一起。螺紋連接塊可在扁平及刃口對處接合,其中刃口壓縮O形環。例示性耐火金屬或材料為本發明之耐火金屬或材料,諸如W、Ta、Nb、Mo及WC。在實施例中,電池之部件(諸如EM泵之部件,諸如儲集器5c之泵管噴嘴5q、泵管5k6入口及出口及儲集器5c、錐形儲集器5b及圓頂5b4中之至少一者)可藉由螺紋、O形環、VCR型配件、擴口及壓縮配件,及接頭套管配件或接頭套管型配件中之至少一者連接至連續部件。配件及O形環中之至少一者可包含耐火材料,諸如W。O形環、VCR型配件之壓縮環、接頭套管配件或接頭套管型配件中之至少一者可包含較軟的耐火材料,諸如Ta或石墨。電池組件及配件中之至少一者可包含以下中之至少一者:Ta、W、Mo、W-La2 O3 合金、Mo、TZM及鈮(Nb)。部件(諸如圓頂5b4)可自固體W或W-氧化鑭合金機械加工。部件(諸如黑體輻射器5b4,諸如W圓頂)可藉由選擇性雷射熔化(SLM)形成。 在實施例中,發電機進一步包含能夠具有低於大氣壓、為大氣壓及高於大氣壓之壓力的電池腔室,其容納圓頂5b4及相對應的反應電解槽腔室5b31。電池腔室5b3殼體及下部腔室5b5殼體可為連續的。或者,下部腔室5b5可為獨立的,具有其自有壓力控制系統,其可在與電池腔室不同之壓力(諸如大氣壓或真空)下操作。電池腔室5b3及下部腔室5b5之分離器可包含在儲集器5c之頂部5b81或底部5b8處之板。板5b8可藉由板5b81或5b8與儲集器5c之間的螺紋緊固至儲集器。螺紋黑體輻射器及具有底板之儲集器中之至少一者可經機械加工為來自經鍛造鎢的單塊。經按壓鎢電磁泵匯流排5k2可藉由塗覆在高溫下操作期間形成燒結焊之鎢粉末而燒結焊接至泵管壁凹痕。將耐火材料(諸如鎢)用於電池組件可避免在黑體輻射器與儲集器之間或在儲集器與EM泵之間具有熱障(諸如熱絕緣體,諸如SiC)的必要性。 在實施例中,反應電解槽腔室5b31可包含銀鍋爐。在實施例中,允許熔融金屬(諸如銀)之蒸氣壓約在操作溫度下達到平衡,使得金屬蒸發之過程將停止且將消除利用排熱之銀汽化及凝結的功率損失。在3000K及3500K之操作溫度下之例示性銀蒸氣壓分別為10 atm及46 atm。在電池操作溫度下保持平衡銀蒸氣壓包含在電池發電操作期間利用回流液體保持電池壓力的穩定構件。由於圓頂5b4可在高壓力及溫度下斷裂,故在實施例中,電池腔室5b3中之壓力匹配反應電解槽腔室5b31中之壓力,使得基本上不存在跨越黑體輻射器5b4之淨壓差。在實施例中,可保持反應電解槽腔室5b31中之輕微超壓(諸如在約1 mTorr至100 Torr之範圍內)以避免鎢圓頂黑體輻射器5b4之潛移,諸如針對重力之潛移。在一實施例中,可藉由添加穩定添加劑至黑體輻射器5b4之金屬來遏制潛移。在實施例中,鎢摻雜有添加劑(諸如少量的K、Re、CeO2 、HfC、Y2 O3 、HfO2 、La2 O3 、ZrO2 、Al2 O3 、SiO2 及K2 O中之至少一個者)以減少潛移。添加劑可為任何所需量,諸如在1 ppm至10 wt%之範圍內。 在作為銀鍋爐操作之反應電解槽腔室5b31的實施例中,電池組件(諸如黑體輻射器5b4及儲集器5c)分別包含諸如鎢或碳及氮化硼的耐火材料。在啟動模式下,可利用加熱器(諸如電感耦合加熱器5m)將儲集器5c可加熱至充足溫度,以使得以使得蒸氣壓(諸如銀金屬蒸氣壓)加熱黑體輻射器5b4。在啟動EM泵及電極以引起泵抽及點火時,該溫度可高於銀之熔點。在實施例中,在啟動期間,隨著金屬蒸氣在加熱期間回流,氧來源(諸如氧化物,諸如LiVO3 )可經塗佈於黑體輻射器5b4壁上以便合併成熔體。 在實施例中,藉由充當導電基質之銀蒸氣來保持低能量氫反應。其中至少一部分變為蒸氣的連續噴射及來自儲集器之銀的直接沸騰中之至少一者可提供銀蒸氣。電極可向反應提供高電流以移除電子並引發低能量氫反應。來自低能量氫反應之熱量可幫助向反應電解槽腔室提供金屬蒸氣(諸如銀金屬蒸氣)。在實施例中,穿過電極之電流可至少部分地分流至與電漿接觸之替代或補充電極。電流分流可在銀蒸氣之壓力變得足夠高而使得銀蒸氣至少部分地充當導電基質之後發生。與電漿接觸之替代或補充電極可包含一個或多個中心電極及圍繞反應電解槽腔室之周界的相對電極。電池壁可充當電極。 在實施例中,PV轉換器26a包含於具有外部腔室5b3a1之外部壓力容器5b3a中(圖2I80至圖2I94)。外部壓力容器可具有任何合乎需要的幾何形狀,其含有PV轉換器及包含照亮PV轉換器之光源的內部電池組件。外部腔室可包含具有至少一個圓頂狀端蓋之圓柱形主體。外部壓力容器可包含圓頂或球面幾何結構或其他合適的幾何結構,其能夠含有PV轉換器及圓頂5b4並能夠將壓力保持為低於、等於或大於真空中之至少一者。在實施例中,包含PV電池、冷板及冷卻系統之PV轉換器26a位於外部壓力容器內部,其中電管線及冷卻劑管線經由密封穿透件及饋通件(諸如本發明之密封穿透件及饋通件中之一者)穿透容器。在實施例中,外部壓力容器可包含圓柱形主體,其可包含至少一個圓頂頂部。在實施例中,發電機可包含圓柱形腔室,其可具有用以容納黑體輻射器5b4及PV轉換器26a之圓頂狀蓋。發電機可包含容納PV轉換器之頂部腔室及容納電磁泵之底部腔室。腔室可在相同或不同壓力下操作。 在實施例中,外部壓力容器包含PV轉換器支架,諸如PV圓頂,其形成含有圍封反應電解槽腔室5b3之圓頂5b4之電池腔室5b3。外部壓力容器可包含圓頂或球面幾何結構或其他合適的幾何結構,其能夠含有圓頂5b4並能夠將壓力保持為低於、等於或大於真空中之至少一者。在實施例中,PV電池15在外部壓力容器壁(諸如球面圓頂壁)之內部上,且冷板及冷卻系統在壁外。電連接件可經由密封穿透件及饋通件(諸如本發明之密封穿透件及饋通件中之一者)穿透容器。熱傳遞可跨越可導熱之壁發生。合適的壁材料包含金屬,諸如銅、不鏽鋼或鋁。在PV電池之內部上的PV窗可包含透明區段,其可藉由黏著劑(諸如矽黏著劑)接合以形成氣密透明窗。窗可保護PV電池免受氣體影響,該等氣體將自圓頂5b4汽化之金屬再沈積回至圓頂。氣體可包含鹵素循環之氣體。壓力容器PV容器(諸如圓頂狀容器)可藉由ConFlat或其他此類凸緣密封而密封至在上部與下部腔室或其他腔室之間的隔板5b81或5b8。上部腔室可含有黑體輻射器5b4及PV電池15,且下部腔室可含有EM泵。下部腔室可進一步包含下部腔室冷板或冷卻管線5b6a (圖2I89)。 鎢的熔點3422℃在所有金屬中係最高的且在元素中僅次於碳(3550℃)。耐火陶瓷及合金具有較高熔點,尤其係Ta4 HfC5 TaX4 HfCX5 熔點為4215℃,碳化鉿為3900℃且碳化鉭為3800℃。在實施例中,電池組件(諸如黑體輻射器5b4及儲集器5c)可包含耐火材料,諸如W、C及耐火陶瓷或合金中之至少一者。在其中黑體輻射器包含石墨之實施例中,電池腔室5b3含有高壓氣體,諸如遏制石墨昇華之高壓惰性氣體氛圍。 在實施例中,黑體輻射器可包含碳。自石墨黑體輻射器(諸如球面石墨黑體輻射器)昇華之碳可藉由靜電沈澱(ESP)自電池腔室5b3移除。ESP系統可包含陽極、陰極、電力供應器及控制器。粒子可藉由一個電極充電並藉由另一對立電極採集。所採集之煙灰可自採集電極變位且使其落入採集箱中。變位可藉由機械系統達成。在實施例中,透明容器之內部可帶負電,且圓頂可利用所施加之電壓源而帶正電。在壁與黑體輻射器5b4之間的場的影響下,自石墨黑體輻射器5b4昇華之帶負電之碳粒子可遷移回至圓頂。在實施例中,可藉由活性輸送(諸如藉由使氣體流動經過電池腔室53b且接著經過碳粒子過濾器)來移除碳, 在實施例中,圓頂5b4可包含石墨,且儲集器可包含耐火材料,諸如氮化硼。石墨可包含各向同性石墨。本發明之組件之石墨可包含玻璃碳,如Compressed glassy carbon: An ultrastrong and elastic interpenetrating graphene network, Science Advances,2017年6月09日:第3卷,第6號, e1603213 DOI: 10.1126/sciadv.1603213,http :// advances . sciencemag . org / content / 3 / 6 / e1603213 . full 中給出,其以引用之方式併入本文中。在實施例中,石墨黑體輻射器(諸如球面圓頂)可包含用以避免在反應電解槽腔室5b31內部之熔融金屬侵蝕石墨的襯墊。襯墊可包含耐火材料,諸如鎢。襯墊可包含形成至石墨圓頂之內部的網狀物或薄片。襯墊可防止流動的熔融金屬的剪切力侵蝕反應電解槽腔室之內表面。 PV轉換器可包含PV電池,其各自具有可包含至少一個熱光伏打濾光片(諸如紅外濾光片)的窗。該濾光片可優先反射具有不會藉由PV轉換器轉換為電的波長的光。 PV轉換器之電池可於背面上成鏡像以反射穿過電池返回黑體輻射器的光。反射鏡可對於不會藉由PV電池轉換為電之紅外光具有選擇性。紅外反射鏡可包含金屬。電池之背面可經金屬化。金屬可包含紅外反射器,諸如金。金屬可藉由接觸點附接至PV電池之半導體基板。該等接觸點可分佈在電池背面上。該等點可包含黏結材料,諸如Ti-Au合金或Cr-Au合金。PV電池可包含至少一個接面。在3500 K下操作之代表性電池包含在GaAs基板上之GaAs或在InP或GaAs基板上之InAlGaAs作為單接面電池及在InP或GaAs基板上之InAlGaAs作為雙接面電池。在3000 K下操作之代表性電池包含在GaAs基板上之GaAs或在InP或GaAs基板上之InAlGaAs作為單接面電池及在InP或GaAs基板上之InAlGaAs作為雙接面電池。 在實施例中,黑體輻射器5b4之測地線PV轉換器26可包含光分佈系統23 (諸如本發明之光分佈系統) (圖2I132)。光分佈系統23可將光分成不同波長區域。分離可藉由反射鏡及濾光片(諸如本發明之彼等者)中之至少一者達成。縫隙光可入射於對經分離及入射光具有選擇性的PV電池15。光分佈系統23可經佈置為自圍繞球面黑體輻射器5b4的測地線球朝外突出之柱。 發電機可包含用於電池腔室壓力及反應電解槽腔室壓力中之至少一者的精密氣體壓力感測及控制系統。本發明之系統可包含氣體貯槽及管線,諸如氫氣及稀有氣體貯槽及管線(諸如貯槽5u及管線5ua1)中之至少一者。氣體系統可進一步包含壓力感測器、歧管、入口管線、饋通件、噴射器、噴射器閥門、真空泵(諸如真空泵13a)、真空泵管線(諸如真空泵管線13b)、控制閥及管線及饋通件。稀有氣體(諸如氬或氙)可添加至電池腔室5b3或5b3a1以匹配反應電解槽腔室5b31中之壓力。反應電解槽腔室壓力可藉由量測黑體溫度及使用金屬蒸氣壓與溫度之間的關係來量測。圓頂之溫度可使用其黑體光譜發射來量測。該溫度可使用光學高溫計量測,該光學高溫計可使用光纖來將光採集及輸送至感測器。該溫度可藉由具有濾光片之複數個二極體來量測,該等濾光片對於黑體曲線之樣本部分有選擇性以確定溫度。電池組件(諸如儲集器5c)可包含耐火材料(諸如氧化鋁、藍寶石、氮化硼及碳化矽中之至少一者),其至少部分地對可見及紅外光中之至少一者透明。組件(諸如儲集器,諸如氮化硼儲集器)可包含在該組件中之凹部或變薄斑點,以更好地准許光穿過組件達到光學溫度感測器。 除稀有氣體以外,外部壓力容器腔室5b3a1、電池腔室5b3中之至少一者中的氣體亦可包含氫。藉由貯槽、管線、閥門及噴射器供應至至少一個腔室之氫可經由電池組件擴散,該電池組件在電池操作溫度下係氫可滲透的,以替換所消耗之氫,從而形成低能量氫。氫可滲透黑體輻射器5b4。低能量氫氣體產物可自腔室(諸如腔室5b3或5b3a1及5b31)擴散至環境氛圍或採集系統。或者,低能量氫氣體產物可選擇性地自至少一個腔室泵出。在另一實施例中,低能量氫氣體可以集氣劑採集,該集氣劑可定期替換或更新。 在實施例中,圍封W黑體輻射器之腔室之氣體可進一步包含鹵素來源(諸如I2 或Br2 )或與昇華的鎢形成錯合物之烴溴化合物。錯合物可在熱鎢圓頂表面上分解以將鎢再沈積於黑體輻射器5b4上。一些圓頂耐火金屬(諸如W)可經添加至熔融金屬(諸如銀)以汽化及沈積於內圓頂表面上從而替換經汽化或昇華金屬。 在實施例中,電池進一步包含至電池腔室之氫供應。該供應可經由EM泵管、儲集器及黑體輻射器中之至少一者穿透電池。該供應可包含耐火材料,諸如W及Ta中之至少一者。該供應可包含氫滲透膜,諸如包含耐火材料之氫滲透膜。氫供應可穿透電池中溫度比黑體輻射器之溫度低的區域。該供應可穿透在EM泵管或儲集器處之電池。該供應可包含氫滲透膜,其在EM泵管或儲集器中之熔融銀的操作溫度下穩定。氫滲透膜可包含Ta、Pt、Ir、Pd、Nb、Ni、Ti或具有熟習此項技術者已知之合適的熔點的其他合適的氫滲透金屬。 在實施例中,在反應電解槽腔室及黑體輻射器之操作溫度下將至少一個外部腔室或在反應電解槽腔室5b31外部之腔室加壓至約為反應電解槽腔室之內部壓力的外部壓力。外部壓力與內部壓力之匹配可在約加減0.01%至加減500%之範圍內。在例示性實施例中,在黑體輻射器及反應電解槽腔室之外的一個容器的至少一個腔室之外部壓力為約10 atm以匹配處於約3000K之操作溫度下的反應電解槽腔室的10 atm銀蒸氣壓。黑體輻射器能夠支援外部壓差,其隨著黑體輻射器溫度增加至操作溫度而減小。 在圖2I80至圖2I103中所展示之實施例中,SunCell®包含外部壓力容器5b3a,其具有含有PV轉換器26a、黑體輻射器5b4、儲集器5c及EM泵的外部壓力容器5b3a1。外部壓力容器5b3a之壁可藉由冷卻劑管線、冷板或熱交換器5b6a水冷。SunCell®組件(諸如外部壓力容器5b3a之壁)可包含熱或輻射屏蔽以幫助冷卻。該屏蔽可具有低發射率來反射熱量。外部壓力容器5b3a可包含在外部之熱交換器鰭片。鰭片可包含高熱導體,諸如銅或鋁。發電機可進一步包含用以提供自散熱片之強制對流熱傳遞的構件。該構件可包含可位於壓力容器下方的殼體中的風扇或風機。風扇或風機可迫使空氣在鰭片上朝上。外部壓力容器可包含諸如圓柱形區段之區段,其含有並安裝電池組件,諸如PV轉換器26a、黑體輻射器5b4、儲集器5c及EM泵組合件5ka。用以安裝及支撐電池組件的連接件包含用以適應組件與底座及支架之間的不同熱膨脹速率或量以避免膨脹損害的構件。底座及支架可包含膨脹接頭及可膨脹連接器或扣件(諸如墊圈及襯套)中之至少一者。連接器及扣件可包含可壓縮碳(諸如Graphoil或Perma-Foil (Toyo Tanso))或由六方氮化硼構成之碳。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之一者,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)或本發明之另一種材料。在實施例中,電、氣體、感測器、控制及冷卻管線可穿透外部壓力容器5b3a之底部。外部壓力容器可包含圓柱形及圓頂殼體及與該殼體密封之底板5b3b。殼體可包含碳纖維或不鏽鋼或經塗佈之剛。塗層可包含鎳鍍敷。殼體可為抽取式的,以便易於使用SunCell®組件。底板5b3b可包含電、氣體、感測器、控制及冷卻管線中之至少一者的饋通件。饋通件可為耐壓的且在管線可電短接至殼體的情況下係電絕緣的。在實施例中,PV轉換器冷卻系統包含歧管,其具有至密集型接收器陣列之元件(諸如三角形元件)的冷板之分支。底板饋通件可包含:i.)點火匯流排連接器10a2,其連接至電源2,諸如在殼體90中包含點火電容器組之點火匯流排連接器,該殼體可進一步包含由PV轉換器26a輸出供電之DC至DC轉換器,且該點火匯流排連接器10a2進一步連接至用於點火匯流排9及10之饋通件10a,該等點火匯流排9及10穿透在點火匯流排饋通組合件10a1之底板(例示性點火電壓及電流大約為50 V DC及50至100 A);ii.) EM泵匯流排連接器5k33,其連接至EM電力供應器5k13且進一步連接至EM泵饋通件5k31,該等EM泵饋通件穿透在EM泵匯流排饋通凸緣5k33處之底板;電力供應器5k13可包含由PV轉換器26a輸出供電之DC至DC轉換器(例示性EM泵電壓及電流大約為0.5至1 V DC及100至500 A);ⅲ.)電感耦合加熱器天線饋通組合件5mc,其中天線由電感耦合加熱器電力供應器5m供電,該電感耦合加熱器電力供應器可包含由PV轉換器26a輸出供電之DC至DC轉換器、變壓器、至少一個IGBT及射頻傳輸器(例示性電感耦合加熱器頻率、電壓、電流大約為15 kHz、250 V AC或DC等效及100至300 A),iv.)用於分別連接至氫貯槽5u及氬貯槽5u1之氫氣管線5ua及氬氣管線5ua1的穿透件5h1及5h3, v.)用於連接至熱交換器冷卻劑管線5k11之EM泵冷卻劑管線31d及31e的穿透件,其中EM泵熱交換器5k1之冷卻劑管線5k11及EM泵冷板5k12可各自包含跨越兩個熱交換器5k1之一個片件, vi.)用於PV冷卻劑管線31b及31c之穿透件,及 vii.)用於自PV轉換器26a至功率調節器或反相器110之功率流動的穿透件。入口冷卻劑管線(諸如入口冷卻劑管線31e)連接至輻射器入口管線31t且出口冷卻劑管線(諸如出口冷卻劑管線31d)連接至水泵出口31u。除輻射器31以外,發電機由風扇31j1冷卻。在實施例中,PV轉換器26a包含緊固在一起以圍繞黑體輻射器5b4安裝之下部及上部半球面零件。PV電池可各自包含在PV電池上之窗。PV轉換器可擱置於PV轉換器支撐板5b81上。支撐板可懸掛以避免與黑體輻射器或儲集器接觸且可經穿孔以允許在整個外部壓力容器之間進行氣體交換。半球(諸如下部半球)可包含圍繞區域之一部分(諸如底部)以將光反射至PV轉換器之PV電池的反射鏡。反射鏡可適應用以接收來自黑體輻射器之光的理想測地線圓頂與可由PV元件形成之測地線圓頂之間的任何失配。非理想性可歸因於繞黑體輻射器安裝PV元件之空間侷限性,該等空間侷限性由包含測地線圓頂之PV元件的幾何結構導致。 例示性PV轉換器可包含測地線圓頂,其由陣列模組三角形元件構成,該等陣列模組三角形元件各自包含複數個聚光型PC電池及背襯冷板。該等元件可咬合在一起。例示性陣列可包含五方十二面體。例示性陣列可包含6個五邊形及16個三角形。在實施例中,PV轉換器26a之基底可包含處於並未安裝測地線PV轉換器陣列之三角形PV元件之位置的反射器。反射器可進行以下中之至少一者:將入射光反射至PV轉換器之另一部分及反射回至黑體輻射器。在實施例中,來自下部半球5b41之基底的功率至少部分地經恢復成光及熱中之至少一者。在實施例中,PV轉換器26a包含在下部半球5b41之基底周圍之PV電池套環。在實施例中,藉由熱交換器(諸如散熱管)採集呈熱量形式之功率。該熱量可用於冷卻。該熱量可供應至熟習此項技術者已知之吸收急冷器以達成冷卻。 在實施例中,冷卻系統(諸如急冷器及輻射器中之至少一者)的覆蓋面積可藉由允許冷卻劑(諸如水,諸如池過濾水)經歷相變而減小。相變可包含液體至氣體。相變可發生在自PV電池移除熱量之冷板內。液體至氣體之相變可發生在微通道冷板之微通道中。冷卻劑系統可包含用以減小冷卻系統中之至少一個位置的壓力的真空泵。相變可由保持冷卻劑系統中之減壓來協助。可保持冷卻系統之冷凝器區段中之減壓。PV轉換器、冷板及PV電池中之至少一者可浸沒於經歷相變(諸如沸騰)以提高熱移除的冷卻劑中。冷卻劑可包含此項技術中已知之冷卻劑,諸如惰性冷卻劑,諸如3M全氟三丁胺。 在實施例中,冷卻劑系統可包含多個冷卻劑迴路。第一冷卻劑迴路可直接或經由冷板(諸如包含微通道板之冷板)自PV電池提取熱量。冷卻劑系統可進一步包含至少一個熱交換器。第一熱交換器可自第一冷卻劑迴路至另一冷卻劑迴路傳熱。冷卻劑相變可發生在其他冷卻劑迴路中之至少一者中。相變可為可逆的。相變可提高冷卻劑在給定流動速率下與環境交換熱量並冷卻PV轉換器的能力。另一冷卻劑迴路可包含自其冷卻劑至空氣傳熱之加熱交換器。可控制每一冷卻劑迴路中之操作參數(諸如流動條件、流動速率、壓力、溫度變化、平均溫度及其他參數),以控制所要熱傳遞速率及在第一冷卻劑迴路內之所要操作參數(諸如在冷板之微通道板內之冷卻劑的操作參數)。微通道中之例示性條件為約10℃至20℃之冷卻劑之溫度變化範圍、約50℃至70℃之平均溫度及層流從而避免擾流。 在實施例中,為減小冷卻系統之尺寸,第一冷卻劑迴路可在高溫下操作,該高溫諸如係儘可能高而不會使PV電池效能顯著降低的溫度,諸如40℃至90℃之溫度。冷卻劑之溫差在第一迴路中可比在另一冷卻劑迴路中小。在例示性實施例中,冷卻劑在第一迴路中之溫差可為約10℃;然而,冷卻劑在另一迴路(諸如次級迴路)中之溫差可較高,諸如約50℃。例示性的對應溫度溫範圍分別為80℃至90℃及40℃至90℃。相變可發生在至少一個冷卻迴路中以提高熱傳遞從而減小冷卻系統尺寸。 在實施例中,冷卻PV電池之微通道板可由熱交換器、散熱管、熱傳遞塊、冷卻劑噴口及冷卻劑浴中之至少一者替換,該冷卻劑浴諸如係包含惰性冷卻劑(諸如蒸餾或去離子水)或介電液體(諸如3M全氟三丁胺、R134a或Vertrel XF)的冷卻劑浴。就水冷卻劑而言,冷卻劑系統可進一步包含水純化或處理系統以防止水有過度腐蝕性。冷卻劑可包含抗腐蝕劑,諸如此項技術中已知的用於銅的抗腐蝕劑。輻射器可包含耐腐蝕之不鏽鋼、銅或鋁中之至少一者。冷卻劑可包含防凍劑,諸如以下中之至少一者:陶氏熱媒(Dowtherm)、乙二醇、氨及醇(諸如甲醇及乙醇中之至少一者)。電池可不斷運行以防止冷卻劑凍結。冷卻劑系統亦可包含加熱器以防止水凍結。PV電池可浸沒於冷卻劑浴中。PV電池可自未照射側面至冷卻劑浴傳熱。冷卻劑系統可包含至少一個泵,其中冷卻劑可循環以在冷卻系統中之一個位置吸收熱量並在另一位置排出該熱量。PV電池可在較高操作溫度及高溫溫度範圍中之至少一個條件下操作,由此可減小冷卻系統之尺寸。冷卻劑系統可包含冷凝器,其中相變隨著自PV電池之熱傳遞而發生。冷卻劑系統可經加壓、處於大氣壓或低於大氣壓。可控制壓力以控制冷卻劑沸點溫度。在壓力下操作之冷卻劑系統可包含泵,其具有入口及出口以及使冷卻劑返回低壓泵入口側之壓力排氣閥,其中冷卻劑經由入口泵抽至熱交換器(諸如輻射器或急冷器)。就急冷器而言,經冷凍冷卻劑可再循環以降低溫度並增加冷卻劑PV之間的溫差以提高熱傳度速率。已冷卻之冷卻劑可進一步泵抽至PV電池-冷卻劑熱傳遞介面以接收熱量,冷卻劑由此可沸騰。冷卻劑系統可在低於臨界熱流通量之熱流下操作,在形成足夠蒸氣時不再繼續潤濕經冷卻表面。冷卻劑可在過冷卻沸騰下操作。歸因於跨越對應熱交換器(諸如輻射器)之較大冷卻劑-空氣熱量梯度,PV電池可在保持過冷卻沸騰同時將至環境之熱傳遞速率最大化的溫度下操作。例示性PV操作溫度為130℃。該系統可經操作以避免薄膜沸騰。熱冷卻劑與環境空氣之間的熱交換器可包含輻射器,諸如環繞式輻射器,諸如具有汽車輻射器設計之輻射器。熱交換器可包含至少一個風扇以移動空氣。風扇可居中。電池亦可居中。 PV電池可安裝在傳熱介質(諸如散熱片,諸如銅板)上。銅板可進行以下中之至少一者:介接傳遞熱量的熱傳遞構件(諸如熱交換器、散熱管及熱傳遞塊中之至少一者)及介接冷卻劑以增加熱傳遞接觸面積。熱傳遞構件可徑向散熱。冷卻劑可經歷相變以提高熱傳遞,由此可減小冷卻劑系統尺寸。熱傳遞構件可經塗佈有銷釘以增加用於熱傳遞之表面積。冷卻劑系統可包含用以凝結冷卻劑之構件及排熱系統(諸如至少一個冷卻劑循環泵及在冷卻劑與環境(諸如可加壓之輻射器)之間的熱交換器中之至少一者)。在實施例中,PV轉換器之半徑、PV電池冷卻劑系統之半徑(諸如PV冷卻劑系統之熱交換器、散熱管或熱傳遞塊中之至少一者的半徑)中之至少一者可增加以減小待自PV電池傳遞至環境之熱流通量負載,以便有效地冷卻PV電池。PV轉換器可包含保持與黑體輻射器5b4相距相同距離的形狀。黑體輻射器可為球面的,且PV轉換器至黑體輻射器的距離可為恆定的,以達成入射至可包含均一照射強度之PV的所要光強度。 在實施例中,PV轉換器冷卻系統可包含球面歧管,其包含具有散熱片刺狀球面沸騰表面之冷卻劑儲集器,其包含在PV電池之背面上之散熱片及鍋爐板。鍋爐板可經塗佈有銷釘以增加用於熱傳遞之表面積。冷卻劑可藉由至少一個泵流動。流動可包含自在頂部處之至少一個入口及在急冷器之底部處之至少一個出口的球面流動。經加熱冷卻劑可經由待冷卻之輻射器泵抽且返回至儲集器。在另一實施例中,冷卻劑可經由鍋爐板中之通道泵抽,該等鍋爐板經接合至PC電池之背面並自PV電池接收熱量。 熱傳遞板或元件可包含多孔金屬表面塗層,諸如包含燒結金屬粒子之塗層。表面可提供多孔層結構,其特徵在於互連通路之圖案。通路經恰當地設定大小,以為蒸氣凝核提供大量穩定部位,從而針對所給出的表面與冷卻劑飽和溫度之間的溫度差而極大地增加熱流通量(多達10倍)。表面塗層亦可增加臨界熱流通量(CHF)。表面可包含形成用於凝核之微空腔的導電微多孔塗層。例示性表面包含燒結銅微多孔表面塗層(SCMPSC,cf. Jun等人,Nuclear Engineering and Technology, 2016)。表面增強方法可與短銷釘(亦為多孔式經塗佈之銷釘)結合使用以進一步增加表面積。表面積增強件(諸如多孔式經塗佈銷釘或短柱)可經鑄造。在例示性實施例中,具有多孔表面積增強件之短柱(諸如銅短柱)可鑄造於熱傳遞板(諸如銅板)之背面上。 來自輻射器之回流可經組態以在鍋爐板之表面上提供對流。複數個入口可將冷卻劑流動分成多個入口噴流,其在球面及圓柱形冷卻劑儲集器之壁上沿切線成角,以提供主體渦流運動。該運動可引起在表面處之對流沸騰,其自凝核部位移除蒸氣泡,從而抑制CHF。在實施例中,可使用除水以外的冷卻劑,係因為可在增強型凝核部位之存在下提高具有較小表面張力之流體(諸如有機液體、致冷劑及熱傳遞流體)的沸騰。可基於未加壓系統之飽和(P-T)狀態來選擇冷卻劑。在實施例中,為達成溫度均一性並解釋至跨越PV元件之冷卻劑之對流傳導的變化,可利用相同微通道散熱片來冷卻每一元件。 在實施例中,PV轉換器26a可包含複數個三角形接收器單元(TRU),其各自包含複數個光伏打電池( 諸如正面聚光型光伏打電池)、安裝板及在安裝板背面上之冷卻器。冷卻器可包含多通道板、支援冷卻劑相變之表面及散熱管中之至少一者。三角形接收器單元可連接在一起以形成至少部分測地線圓頂。TRU可進一步包含電連接件、匯流排及冷卻劑通道中之至少一者的互連。在實施例中,接收器單元及連接圖案可包含降低冷卻系統之複雜度的幾何結構。PV轉換器組件之數目(諸如測地線球面PV轉換器之三角形接收器單元的數目)可減少。PV轉換器可包含複數個區段。該等區段可接合在一起以形成圍繞黑體輻射器5b4之部分罩殼。PV轉換器及黑體輻射器中之至少一者可為多面體形的,其中黑體輻射器及接收器單元的表面在幾何學上可為匹配的。罩殼可藉由三角形、正方形、矩形、圓柱形或其他幾何單元中之至少一者形成。黑體輻射器5b4可包含正方形、球體或其他合乎需要的幾何結構中之至少一者以照射PV轉換器之各單元。在例示性實施例中,罩殼可包含圍繞可為球面或正方形之黑體輻射器5b4的五個正方形單元。罩殼可進一步包含自黑體輻射器之基底接收光的接收器單元。基底單元之幾何結構可為使光採集最佳的幾何結構。罩殼可包含正方形與三角形之組合。罩殼可包含頂部正方形,其連接至包含四個交替正方形及三角形對之上部區段,該上部區段連接至作為中段之六個正方形,該中段連接至包含四個交替正方形及三角形對之至少一部分下部區段,其連接至部分或不存在的底部正方形。 光伏打轉換器之測地線密集型接收器陣列之三角形元件的示意圖展示於圖2I133中。PV轉換器26a可包含由三角形元件200組成之密集型接收器陣列,該等三角形元件各自包含複數個能夠將來自黑體輻射器5b4之光轉換為電的聚光型光伏打電池15。PV電池15可包含在GaAs N晶圓上之GaAs P/N電池、在InP上之InAlGaAs及在GaAs上之InAlGaAs中之至少一者。電池可各自包含至少一個接面。三角形元件200可包含罩蓋主體203 (諸如包含經衝壓科伐合金薄片之罩蓋主體)、熱埠202及冷埠204 (諸如包含壓入配合管之冷埠),以及用於連接連續三角形元件200之附接凸緣203 (諸如包含經衝壓科伐合金薄片之附接凸緣)。 在包含熱功率源之實施例中,熱交換器26a包含:複數個熱交換器元件200 (諸如,圖2I133中所展示之三角形元件200),其各自包含熱冷卻劑出口202及較冷的冷卻劑入口204;及用以吸收來自黑體輻射器5b4之光並將功率作為熱量傳遞至流動穿過元件之冷卻劑中的構件。冷卻劑入口及出口中之至少一者可附接至共同水歧管。如圖2I108至2I109中所示,熱交換器系統26a進一步包含冷卻劑泵31k、冷卻劑貯槽31l及負載熱交換器(諸如輻射器31及利用經過輻射器之空氣流動向負載提供熱空氣的風扇31j1)。除測地線幾何結構之外,具有其他幾何結構之熱交換器(諸如此項技術中已知之熱交換器)在本發明之範疇內。例示性立方體幾何結構展示於圖2I134至圖2I138中,該等圖分別展示至熱負荷之熱冷卻劑入口管線31b及低溫出口管線31c,其中模組式平板熱交換器元件26b不存在於PV電池15中。熱交換器26a可具有使熱傳遞、尺寸、功率要求、簡單性及成本中之至少一者最佳之所要幾何結構。在實施例中,熱交換器系統26a之面積按比例調整為黑體輻射器5b4之面積,使得所接收之功率密度為所要的功率密度。 至少一個接收器單元可經反射鏡替換或部分替換,該等反射鏡進行以下中之至少一者:直接或間接地將黑體輻射反射至其他接收器單元或接收器單元上覆蓋有PV電池之其他位置。接收器單元可在最佳高強度照明區域(諸如在球面黑體輻射器5b4之情況下為中心圓形區域)上經填入有PV電池,其中未經PV填入之區域可由反射鏡覆蓋。接收類似量之輻射的電池可經連接以形成所要匹配電流之輸出,其中該等電池可串聯連接。包含較大面積之接收器(諸如正方形接收器單元)之罩殼可各自包含相對應的冷卻器或熱交換器26b (圖2I134至圖2I138)。每一接收器單元(諸如正方形接收器單元)之冷卻器或熱交換器26b可包含以下中之至少一者:冷卻劑殼體,其包含至少一個冷卻劑入口及一個冷卻劑出口;至少一個冷卻劑分佈結構,諸如分流器擋板(諸如具有通路之板);以及安裝至PV電池安裝板上之複數個冷卻劑鰭片。鰭片可包含高導熱材料,諸如銀、銅或鋁。鰭片之高度、間距及分佈可經選擇以達成在PV電池區域上之均一溫度。冷卻器可藉由熱環氧樹脂安裝至安裝板及PV電池中之至少一者。可藉由防護玻璃罩或窗保護PV電池之前側(發光側)。在實施例中,包含接收器單元之罩殼可包含壓力容器。壓力容器之壓力可經調節以至少部分地平衡反應電解槽腔室5b31內部之熔融金屬蒸氣壓的內部壓力。 在一實施例(圖2I143)中,PV轉換器之半徑可相對於黑體輻射器之半徑增大,以基於光功率通量之半徑平方依賴性而減小光強度。或者,可藉由光分佈系統減小光強度,該光分佈系統包含沿黑體輻射器光線路徑之一系列半透明反射鏡23 (圖2I132),該黑體輻射器光線路徑將入射光部分地反射至PV電池15並另外將一部分光傳輸至該系列之下一個部件。光分佈系統可包含用以沿徑向路徑、Z形路徑或便於堆疊一系列PV電池之其他路徑減小光強度的反射鏡及用以達成所要光強度分佈及轉換的反射鏡。在實施例中,黑體輻射器5b4可具有與光分佈及PV轉換系統相配之幾何結構,該光分佈及PV轉換系統包含一系列與相對應的PV電池組合之反射鏡、透鏡或濾光片。在例示性實施例中,黑體輻射器可為正方形且與直線光分佈及PV轉換系統幾何結構相匹配。 冷卻系統之參數可經選擇以使發電機之成本、效能及功率輸出最佳。例示性參數為冷卻劑之標識、冷卻劑之相變、冷卻劑壓力、PV溫度、冷卻劑溫度及溫度範圍、冷卻劑流動速率、PV轉換器及冷卻劑系統相對於黑體輻射器之半徑的半徑,及在PV之正面或背面的光再循環及波長帶選擇性濾光片或反射器,其用以減少無法藉由PV轉換為電之PV入射光的量或使在穿過PV電池後未能轉換的PV入射光再循環。例示性冷卻劑系統為執行以下中之至少一者的系統:i.)在PV電池處形成蒸汽、輸送蒸汽及凝結蒸汽,以利用環境在交換介面處釋放熱量;ⅱ.)在PV電池處形成蒸氣,將其凝結回液體,並利用環境(諸如輻射器)在熱交換器處自單相排熱;及ⅲ.)自具有微通道板之PV電池移除熱量並利用環境在熱交換器處排熱。在冷卻PV電池期間,冷卻劑可仍處於單相。 PV電池可安裝至冷板。可藉由至冷卻歧管的冷卻劑導管或冷卻劑導管自冷板移除熱量。歧管可包含圓周圍繞PV轉換器之複數個環形導管,其可沿PV轉換器之垂直或z軸間隔開;且該歧管包含與其分離之冷卻劑導管或冷卻劑導管。 黑體輻射器可包含密封在一起以構成反應電解槽腔室5b31的複數個零件。複數個零件可包含下部半球5b41及上部半球5b42。其他形狀在本發明之範疇內。兩個半球可在密封件5b71處緊固在一起。該密封件可包含凸緣、至少一個墊片5b71及扣件(諸如夾鉗與螺釘)中之至少一者。該密封件可包含石墨墊片(諸如Perma-Foil (Toyo Tanso))及耐火螺栓(諸如石墨或W螺栓及螺母),其中金屬螺栓及螺母(諸如W螺栓及螺母)可進一步包含石墨或Perma-Foil墊片或墊圈以補償碳與螺栓及螺母金屬(諸如W)之間的不同熱膨脹係數。黑體輻射器5b41之下部半球及儲集器5c可接合。接合可包含密封凸緣、螺紋接頭、焊接接頭、膠合接頭或另一種接頭(諸如本發明或熟習此項技術者已知之接頭)。密封可包含藉由密封劑形成之膠合或化學鍵合密封。例示性石墨膠為 Aremco Products, Inc. Graphi-Bond 551RN石墨黏著劑及具有Resbond 931黏合劑之Resbond 931粉末。膠合碳區段可經熱處理以形成化學碳鍵。該鍵可與每一片件之結構相同或類似。黏結可包含石墨化。在實施例中,兩個片件(諸如上部半球及下部半球)可為經螺紋及旋擰在一起及經膠合中之至少一者。接合區段可經舌槽式接合以增加接觸面積。 在實施例中,下部半球5b41及儲集器5c可包含單一片件。儲集器可包含藉由接頭(諸如本發明或熟習此項技術者已知之接頭)附接之底部板。或者,底部板及儲集器主體可包含整體件,其可進一步包含具有下部半球之一個片件。儲集器部底板可連接至儲集器支撐板5b8,其提供至外部壓力容器5b3a壁之連接以支撐儲集器5c。EM泵管5k6及噴嘴5q可穿透並利用接頭(諸如機械配件,諸如接頭套管型及VCR型配件5k9及接頭套管型接合O形環5k10中之至少一者)連接至儲集器5c之底部板(圖2I69)。在實施例中,頂部半球5b42、底部半球5b42、儲集器5c、儲集器5c之底部板及EM泵管5k6、噴嘴5q及連接器5k9中之至少一者包含W、Mo及碳中之至少一者。可藉由鑄造形成碳管組件(諸如具有彎管之碳管組件,諸如碳立管)或噴射器管及噴嘴。在實施例中,頂部半球5b42、底部半球5b41、儲集器5c及儲集器5c之底部板包含碳。在實施例中,碳電池部件(諸如儲集器及黑體輻射器)可包含襯墊。襯墊可防止底層表面(諸如碳表面)免受侵蝕。襯墊可包含耐火材料薄片或網狀物中之至少一者。襯墊可包含W箔或網狀物或WC薄片。箔可經退火。在實施例中,石墨電池組件之襯墊(諸如黑體輻射器、儲集器及VCR型配件之內部)可包含塗層,諸如熱解石墨、碳化矽或本發明或此項技術中已知的防止碳侵蝕的另一種塗層。塗層可在高溫下藉由在塗層上施加及維持高氣體壓力而穩定。 在包含電池組件塗層之實施例中,塗層及基板(諸如碳)中之至少一者可經選擇以使得熱膨脹係數相符。 在實施例中,一對電極中之至少一個電極包含液體電極8。在實施例中,電極可包含液體及固體電極。液體電極可包含電磁泵噴射器之熔融金屬流。點火系統可包含電磁泵,其將熔融金屬噴射至固體電極上以接通電路。點火電路之接通可歸因於來自電源2之電流流動而引起點火。固體電極可與熔融電極電隔離。電隔離可由固體電極之電絕緣塗層在其穿透處(諸如在儲集器5c側壁處)提供。固體電極可包含負電極,且液體電極可包含正電極。歸因於來自正電極處之高動力學之較高熱量,液體正電極可消除正電極熔化之可能性。固體電極可包含經鍛造W。電極可包含導電陶瓷,諸如以下中之至少一者:碳化物,諸如WC、HfC、ZrC及TaC中之一者;硼化物,諸如ZrB2 ;及複合物,諸如可逐步達到1800℃之ZrC-ZrB2 及ZrC-ZrB2 -SiC複合物。導電陶瓷電極可包含塗層或覆蓋物,諸如套筒或套環。 在實施例中,SunCell®包含至少兩個EM泵噴射器,其產生相交以構成至少兩個液體電極之至少兩個熔融金屬流。EM泵之相對應的儲集器可為垂直的,其具有偏離垂直之噴嘴以使得噴出之熔融金屬流相交。每一EM泵噴射器可連接至具有相反極性之電源,使得電流流動穿過在交點處之金屬流。電源2之正極端子可連接至一個EM泵噴射器且負極端子可連接至另一EM泵噴射器。點火電連接件可包含點火電磁泵匯流排5k2a。電源2可向點火過程供應電壓及電流,同時避免對EM泵電力供應器之實質電干擾。電源2可包含浮動電壓電力供應器及開關電力供應器中之至少一者。電氣連接可在EM泵之導電組件處,該導電組件諸如係EM泵管5k6、熱傳遞塊5k7及EM泵匯流排5k2中之至少一者。每一熱傳遞塊5k7可藉由導電膏(諸如金屬粉末,諸如W或Mo粉末)熱耦接至泵管5k6。點火功率可連接至各組熱傳遞塊5k7,使得在電源2與各組熱傳遞塊塊5k7之間建立極性相反之良好電連接。熱傳遞塊可將來自點火功率之熱量沿熱傳遞塊分佈。噴嘴可運行浸沒於液體金屬中以防止電弧及加熱損失。包含儲集器熔融金屬位準感測器及EM泵控制器(諸如EM泵電流控制器)之位準控制系統可將儲集器熔融金屬位準保持在合理的容限內,使得自浸沒噴嘴之噴射為以下中之至少一者:並未顯著由浸沒位準更改及位準控制系統控制EM泵抽以調節浸沒位準。 EM泵可自浸沒噴嘴5q中泵抽金屬,使得所噴出之熔融金屬可形成相對重力行進之流。該流可經導向以與包含雙熔融金屬噴射器之SunCell®實施例的相對流相交。SunCell®可包含至少一個熔融金屬流偏轉器。至少一個流(諸如浸沒電極流)可經導向至流偏轉器。流偏轉器可再導向流以與雙熔融金屬噴射器實施例之相對流相交。偏轉器可包含耐火材料,諸如碳、鎢或本發明之另一材料。偏轉器可包含反應電解槽腔室5b31之延伸部分,諸如黑體輻射器5b41之下部半球之延伸部分或伸出部分。偏轉器可包含電絕緣體。絕緣體可電隔離偏轉器。 在雙熔融金屬EM泵噴射器實施例(諸如包含至少一個浸沒噴嘴之實施例(圖2I139至圖2I147)中,至少一個儲集器及EM泵管5k61之相對應的噴嘴區段可傾斜,以使得相比未傾斜之情況,熔融流更多地經導向中心。傾斜儲集器可包含EM泵組合件5kk之傾斜底板。儲集器支撐板5b8可包含匹配傾角以支撐EM泵組合件5kk之傾斜底板。或者,儲集器5c、EM泵組合件5kk及包含磁體5k4及磁性冷卻5k1之EM泵5ka中之至少一者可在EM泵5ka之基底處遠離中心傾斜,以引起在儲集器5c之頂部處的朝內傾斜。儲集器支撐板5b8可包含匹配傾角以支撐傾斜儲集器及EM泵組合件5ka。儲集器管5c之頂部可以一定角度切割,以在具有黑體輻射器5b41之下部半球的扁平活接的底部相抵配合。或者,黑體輻射器5b41之下部半球可包含相對應的傾斜活接,諸如包含傾斜套環及連接器(諸如自下部半球5b41延伸之滑動螺母連接器)的傾斜套節,以允許有自黑體輻射器5b4至儲集器5c之熱量梯度。在滑動螺母接頭5k14之例示性實施例中,儲集器5c包含氮化硼,下部半球5b41滑動螺母連接器包含碳,螺母包含碳,且墊片5k14a包含碳,其中石墨及BN之熱膨脹係數經選擇以達成可熱循環之密封。在實施例中,碳及BN部件具有匹配的熱膨脹係數,或BN之熱膨脹係數略大於亦構成壓縮接頭之碳部件的熱膨脹係數。墊片可壓縮以防止熱膨脹超出碳部件之抗張強度。該壓縮可為可逆的,以允許熱循環。 進水升管之高度及位置可經選擇以在SunCell®之操作期間保持浸沒噴嘴。進水升管可包含開端式管,其中發生至管中之流動,直至熔融金屬位準大約為管開口之高度的位準。可在至熔融金屬位準的匹配傾斜下切割管端開口。管開口之尺寸可經選擇以節制或抑制朝內流動速率以保持在雙熔融金屬噴射器系統之兩個儲集器之間的位準控制的穩定性。管開口可包含多孔覆蓋物(諸如網狀物)以達成節流。EM泵速率可節制位準控制以保持相對位準穩定性。EM泵速率可藉由控制EM泵電流調節,其中針對包含一個流微傾斜於另一流略之實施例,管開口節制及動態電流調節範圍中之至少一者足以達成相對位準控制穩定性及流的對準。 進水升管可包含耐火電絕緣體,諸如BN管,其可插入附接至EM泵組合件基底之固持器中或上方。在例示性實施例中,固持器包含較短金屬管,諸如附接至EM泵組合件基底之Mo或SS。進水升管(諸如頂槽形BN管)可藉由緊線器(諸如固定螺釘)或藉由壓縮配件在固持器內固定就位。進水升管可藉由安裝在進水升管及固持器兩者之兩端上方的耦合器連接至固持器。在實施例中,進水升管可包含碳。碳進水升管與EM泵組合件5kk之連接可包含至固持器(諸如管固持器)之螺紋及壓縮配件中之至少一者,該管固持器可藉由扣件(諸如螺紋及焊縫中之至少一者)緊固至EM泵組合件的基底。固持器(諸如管固持器)可包含不與進水升管固持器反應之材料。用以固定碳進水升管之例示性固持器包含耐碳化物反應之管(諸如鎳或錸管)或耐碳化之SS管(諸如包含SS 625或Haynes 230之管)。進水升管(諸如碳管)在操作期間可變為塗佈有熔融金屬,其中熔融金屬可保護管免受反應電漿侵蝕。 在實施例中,碳進水升管5qa、EM泵管5k61之噴嘴區段及噴嘴5q中之至少一者可包含氧化穩定之耐火材料,諸如耐火貴金屬(諸如Pt、Re、Ru、Rh或Ir)或耐火氧化物(諸如MgO (M.P.2825℃)、ZrO2 (M.P.2715℃)、對H2 O穩定之氧化鎂氧化鋯、鋯酸鍶(SrZrO3 M.P.2700℃)、HfO2 (M.P.2758℃)、二氧化釷(M.P.3300℃)或本發明之另一氧化物)。陶瓷泵噴射器部件(諸如進水升管5qa、EM泵管5k61之噴嘴區段及噴嘴5q)可緊固至靠近或處於EM泵組合件5kk之金屬EM泵入口或出口。扣件可包含本發明之扣件。扣件可包含以下中之至少一者:螺紋或金屬化及螺紋陶瓷部件、螺紋泵組成部件及硬焊至靠近或處於EM泵組合件5kk之金屬EM泵入口或出口的金屬化陶瓷部件。金屬化可包含不會氧化之金屬,諸如鎳或耐火金屬。扣件可包含擴口配件。陶瓷部件可包含擴口,其可為圓錐形的或其可為扁平的。扣件之凸出部分(male portion)可附接至EM泵組合件5kk的基底。擴口配件之凸出部分可包含金屬螺紋套環及凸出導管區段以與凹形螺紋套環配合,該凹形螺紋套環在匹配螺紋經繃緊時使陶瓷部件之擴口繃緊至凸出導管區段。扣件可進一步包含墊片,諸如Graphoil或Perma-Foil (Toyo Tanso)墊片。金屬部件(諸如EM泵組合件5kk之金屬部件)可包含不與墊片反應之材料,諸如鎳。藉由配合螺紋部件形成之任何空隙可用惰性材料填充,以防止熔融金屬(諸如熔融銀)浸潤並充當用以緩解來自熱膨脹及收縮之壓力的構件。填充可包含墊片材料,諸如本發明之墊片材料,諸如Graphoil或Perma-Foil (Toyo Tanso)。在例示性實施例中,陶瓷管至EM泵組合件5kk之基底的所述可包含以下中之至少一者:(i)陶瓷部件及EM泵組合件5kk部件螺紋;(ii)陶瓷部件金屬化及將金屬螺合或硬焊至靠近或處於EM泵組合件之金屬EM泵入口或出口(氧化鋁為待金屬化及硬焊之常見材料);及(iii)擴口配件,其包含陶瓷管,其中每一陶瓷管具有圓錐形或扁平擴口端及螺紋金屬上滑凹形套環,以附接至焊接至EM泵組合件底板之螺紋套環;擴口配件可進一步包含Graphoil或Perma-Foil (Toyo Tanso)墊片,且EM泵組合件可包含鎳金屬部件以防止與碳以及水反應。材料(諸如凸出扣件部件之材料)可經選擇以匹配凹形部件之熱膨脹係數。 在一實施例中,為避免組件腐蝕,(i)反應電解槽腔室5b31 (諸如碳反應電解槽腔室)可為以下中之至少一者;經塗佈有熔融金屬(諸如銀)之保護層,包含熱解石墨或熱解石墨表面塗層,經負偏壓,其中負偏壓可由點火電壓(諸如至負極噴射器及儲集器之連接)中之至少一者提供;(ii) EM泵管之內表面可包含不與水反應之材料,諸如鎳;及(iii)儲集器、進水升管及噴射器可包含陶瓷(諸如MgO)或熟習此項技術者已知之其他耐火及穩定陶瓷。在實施例中,施加至碳下部半球5b41之負偏壓保護碳免於與氧化物儲集器(諸如MgO或ZrO2 儲集器)進行碳還原反應。偏壓可施加至碳部件而非接觸性氧化物部件。或者,氧化物與碳之間的活接可包含濕封或墊片以限制氧化物與碳之間的接觸。在實施例中,控制溫度及壓力使得其在熱力學上對於碳還原氧化物(諸如MgO)係可能的。例示性壓力(P)及溫度(T)條件大約係在T/P0.0449<1200時。碳可包含熱解碳以減小碳還原反應性。氛圍可包含CO2 以降低碳還原之自由能。碳可塗佈有保護塗層(諸如來自熔融銀之汽化的銀)或石墨Cova塗層(http :// www . graphitecova . com / files / coating 4 . pdf )。Cova塗層可包含以下複數層:鋁加化合物/鋁加合金/純鋁/金屬/石墨。在實施例中,石墨塗佈有塗層以避免與氫反應。例示性塗層包含由ZrC、Nb、Mo及/或Nb-Mo合金及/或MO2 C構成之金屬層及非金屬層。 在實施例中,儲集器5c、下部半球5b41及上部半球5b42中之至少一者包含陶瓷,諸如氧化物,諸如金屬氧化物(諸如ZrO2 、HfO2 、Al2 O3 或MgO)。下部半球5b41、上部半球5b42及儲集器5c之群組中之至少兩個部件可膠合在一起。在實施例中,下部半球5b41、上部半球5b42及儲集器5c之群組中之至少兩個部件可模製為單一組件。在實施例中,儲集器可藉由滑動螺母接頭、濕封接頭、墊片接頭及本發明之另一接頭接合至下部半球及EM泵組合件5kk中之至少一者。滑動螺母接頭可包含碳墊片。螺母、EM泵組合件5kk及下部半球中之至少一者可包含耐碳化及碳化物形成之材料(諸如鎳)、碳及耐碳化之不鏽鋼(SS) (諸如SS 625或Haynes 230 SS)。在實施例中,歸因於接合至氧化物儲集器之碳下部半球的套環之合適長度,碳下部半球與氧化物儲集器(諸如MgO儲集器)之間在其活接處的碳還原反應藉由至少一個構件避免,該至少一個構件諸如係包含經冷卻至碳還原反應溫度以下之濕封的接頭及保持低於碳還原反應溫度的滑動螺母接頭。在實施例中,藉由保持包含與碳接觸之氧化物的接頭處於非反應溫度(低於碳還原反應溫度之溫度)來避免碳還原反應。在實施例中,MgO碳還原反應溫度高於約2000℃至2300℃之範圍。可利用諸如磁流體動力之系統來達成功率轉換,該系統能夠利用接頭在非反應溫度下進行有效轉換。在實施例中,下部半球5b41、上部半球5b42及儲集器5c包含陶瓷,諸如金屬氧化物(諸如氧化鋯),其中部件為經模製及膠合在一起中之至少一者,且EM泵組合件處之接頭包含濕封。在實施例中,下部半球5b41及儲集器5c包含氧化鋯,其中部件為經模製及膠合在一起中之至少一者,且EM泵組合件處之接頭包含濕封。在實施例中,黑體輻射器5b4包含利用MgO穩定之ZrO2 、TiO2 或氧化釔。歸因於約0.2之較低ZrO2 發射率,PV圓頂之半徑可相對於具有入射功率密度相同之碳黑體輻射器的SunCell®的半徑減小。PV轉換器之更同心幾何結構可提供更有利的約正入射角之黑體輻射至PV電池上。 在包含下部半球5b41之實施例中,該下部半球包含電絕緣體,儲集器5c可包含導體,諸如金屬(諸如耐火金屬)、碳、不鏽鋼或本發明之其他導電材料, 包含電絕緣體之下部半球5b41可包含金屬氧化物(諸如ZrO2 、HfO2 、Al2 O3 或MgO)或塗佈有絕緣體(諸如富鋁紅柱石或本發明之其他電絕緣塗層)之碳。 在實施例中,黑體輻射器5b4之發射率對於高於PV電池之帶隙的光較低且對於低於PV電池帶隙之輻射較高。低於PV帶隙之光可藉由自PV電池反射再循環,藉由黑體輻射器5b4吸收,且在黑體輻射器之操作溫度(諸如在約2500 K至3000 K之範圍內)再發射為黑體輻射。在實施例中,低於帶隙之經反射輻射可對於黑體輻射器5b4透明,使得其藉由反應電解槽腔室5b31氣體及電漿吸收。經吸收反射功率可加熱黑體輻射器以有助於保持其溫度,且由此達成對經反射之低於帶隙之光的再循環。在包含具有對於低於帶隙的光的低發射率及高透射率之黑體輻射器的實施例中,黑體輻射器(諸如陶瓷黑體輻射器,諸如氧化鋯黑體輻射器)包含添加劑(諸如塗層或內部層)以吸收經反射低於帶隙的光並使其再循環至PC電池。塗層或內部層可包含高發射率,使得其吸收自PV電池反射之光。添加劑可包含碳、碳化物、硼化物、氧化物、氮化物或本發明之其他耐火材料。例示性添加劑為石墨、ZrB2 、碳化鋯及ZrC複合物(諸如ZrC-ZrB2 及ZrC-ZrB2 -SiC)。添加劑可包含粉末層。黑體輻射器5b4可包含層壓結構,諸如內表面耐火物質,諸如陶瓷/中間高發射率耐火化合物/外表面耐火物質(諸如陶瓷)。表面耐火物質(諸如陶瓷)對於水及氧氣係不可滲透的。例示性層壓結構為內表面ZrO2 /中間ZrC/外表面ZrO2 。可藉由在模具中鑄造內層,用中間層化合物噴塗經鑄造層及接著在模具中鑄造外層來製造層壓結構。 由於氧化鋯用於沈積光學塗層且其為自近UV至中間IR可用的高折射材料,歸因於其在此光譜區中之低吸收,黑體輻射器包含氧化鋯,其中低於帶隙的光經透射穿過黑體輻射器,吸收在反應電解槽腔室5b31之內部且經再循環至PV轉換器26a。在實施例中,近UV至中間IR光對於黑體輻射器5b4 (諸如氧化鋯黑體輻射器)透明。反應電解槽腔室電漿之黑體發射可直接傳輸至PV電池以及經吸收以將黑體輻射器加熱至其黑體操作溫度。 在實施例中,PV轉換器包含覆蓋PV電池並保護其免受來自黑體輻射器之汽化材料(諸如經汽化金屬氧化物,諸如MgO或ZrO2 )影響的窗。窗可包含接帚,諸如可自動清潔窗的機械接帚。在實施例中,PV窗包含自黑體輻射器5b4形成經凝結汽化金屬氧化物的透明塗層的材料及設計。在例示性實施例中,黑體輻射器5b4包含一種材料,諸如氧化鋯,其對於在約近UV至中間IR之波長範圍中之輻射透明,以使得至PV窗上的氧化鋯沈積不會明顯使窗變為不透明,達到來自黑體輻射器之黑體輻射。 在實施例中,保持在黑體輻射器上之高氣體壓力(諸如,惰性氣體(諸如稀有氣體,諸如氬)的氣體壓力)以遏制汽化。氣體壓力可在約1至500 atm、2至200 atm及2至10 atm之至少一個範圍內。可保持外部壓力容器5b3a中之氣體壓力。可在啟動期間降低外部壓力容器5b3a中之壓力以降低電感耦合加熱器所消耗之功率,其中可在電池產生超過保持所要操作溫度所需的功率的功率之後重建壓力。黑體輻射器(諸如金屬氧化物黑體輻射器)可塗佈有塗層以遏制汽化。該塗層可包含本發明之塗層。例示性金屬氧化物塗層為ThO2 (M. P. = 3390℃)。氧化釷以及氧化釔及氧化鋯可進一步充當在黑體輻射器5b4上之氣體網罩以產生較高PV轉換效率。在實施例中,金屬氧化物陶瓷組件(諸如黑體輻射器5b4)經保持在氧化氛圍中,該氧化氣氛諸如係包含H2 O及O2 中之至少一者的氧化氛圍,其增加金屬氧化物之穩定性。在實施例中,SunCell®包含經加熱金屬氧化物之來源,其為以下中之至少一者:充當沈積於藉由汽化丟失金屬氧化物之至少一個組件上的來源;及充當遏制來自至少一個金屬氧化物電池組件之汽化的經汽化金屬氧化物來源。 在實施例中,反應電解槽腔室5b31之內壁包含不與水反應之耐火材料。耐火材料可包含錸、銥、陶瓷中之至少一者,陶瓷諸如係金屬氧化物(諸如氧化鋯)、硼化物(諸如二硼化鋯)及碳化物(諸如碳化鉭、碳化鉿、碳化鋯及碳化鉭鉿)。碳反應電解槽腔室5b31之壁可包含錸,係因為其耐碳化物形成。錸塗層可藉由化學氣相沈積施加至碳壁。該方法可包以下中之方法:Yonggang Tong、Shuxin Bai、Hong Zhang、Yicong Ye, 「Rhenium coating prepared on carbon substrate by chemical vapor deposition」, Applied Surface Science, 第261卷,2012年11月15日, 第390-395頁,其以全文引用之方式併入。在碳反應電解槽腔室5b31之壁上之銥塗層可塗覆於錸夾層上,以提高黏著強度並緩解部分熱膨脹失配。錸塗層可藉由化學氣相沈積塗覆至碳壁,且銥塗層可以電化方式塗覆。方法可包含以下中之方法:Li'an Zhu、Shuxin Bai、Hong Zhang、Yicong Ye、Wei Gao, 「Rhenium used as an interlayer between carbon-carbon composites and iridium coating: Adhesion and wettability」,Surface & Coatings Technology, 第235卷, (2013), 第68-74頁,其以全文引用之方式併入。在實施例中,黑體輻射器包含陶瓷,其對與水之反應穩定,該陶瓷塗佈有在操作溫度下為非揮發性的材料,諸如ZrC、W、碳、HfC、TaC、碳化鉭鉿或本發明之其他合適的耐火材料。不與水反應之材料可包含反應電解槽腔室5b31之內壁。例示性實施例包含塗佈有石墨或ZrC之ZrO2 。 在實施例中,反應電解槽腔室5b31之碳壁經塗佈有塗層,該塗層防止碳與氧來源或催化劑(諸如Li2 O、水及HOH中之至少一者)反應。塗層可包含氟。碳反應電解槽腔室之內表面可經塗佈有末端鍵結至碳之氟。在實施例中,反應電解槽腔室包含氟來源,諸如熔融金屬氟化物(諸如氟化銀)或與熔融金屬接觸之電池組件的金屬之氟化物(諸如氟化鎳、氟化錸、氟化鉬或氟化鎢),以保持氟端碳,其保護氧化,諸如藉由氧來源或水的氧化。在實施例中,反應電解槽腔室5b31包含插入碳中之物質或物質來源。物質可包含以下中之至少一者:鹼金屬(諸如鋰);與水反應之金屬(諸如鹼金屬或鹼土金屬);及不與水反應之金屬(諸如鎳、銅、銀或錸)。鋰金屬可交換藉由經插入鋰與水反應形成之Li2 O或LiOH。 在實施例中,形成HOH催化劑之氧來源可包含氧化物。氧化物可不溶於熔融金屬(諸如銀)。氧化物可包含氧化鋰。反應電解槽腔室之壁可經塗佈有熔融金屬(諸如銀)。氧來源可與氫反應以形成HOH催化劑。銀塗層可保護反應電解槽腔室壁,諸如包含來自接觸氧來源之碳的反應電解槽腔室壁。銀塗層可保護碳壁免於與氧來源反應。碳壁可包含經插入鋰。鋰可與碳反應以將其還原。碳可藉由施加負電位至碳來還原。碳可具有鋰離子電池之碳陽極的組成。陽極組合物可保護碳免於藉由氧來源及HOH中之至少一者氧化。可相對於熔融金屬(諸如銀)、至少一個儲集器5c及至少一個熔融金屬電極(諸如正電極)中之至少一者來施加還原電位。藉由氧來源(諸如氧化鋰)對石墨壁之碳還原反應可受到銀塗層、經插入金屬離子(諸如鋰離子)及施加電壓中之至少一者妨礙。鋰化碳可以電化方式形成,如熟習此項技術者已知。鋰化可藉由使用碳作為具有鋰相對電極之電化電池之陽極來形成,其中鋰化藉由對電池充電而形成。在實施例中,熔融金屬(諸如銀)包含插層物,諸如鋰。插層物可藉由施加負電位至反應電解槽腔室5b31而插入至碳中。反應電解槽腔室可包含電化電池以形成嵌鋰碳。碳圓頂可電連接至陰性熔融金屬噴射器系統。碳圓頂可連接至負極性儲集器。負極性儲集器可包含碳。碳圓頂可藉由接頭(諸如滑動螺母)連接指示碳儲集器。碳圓頂及負極性儲集器可包含單一單元。碳儲集器可藉由濕封或本發明或此項技術中已知之另一活接而接合至EM泵組合件5kk基底。陽性熔融金屬噴射器可充當電化電池之相對電極,該電化電池進行以下中之至少一者:形成及保持嵌物質碳(諸如嵌鋰碳)。 在實施例中,黑體輻射器5b4可包含表面塗層以使高能光的選擇性發射之比例大於黑體輻射。塗層可准許黑體輻射器5b4在較低溫度(諸如在約2500 K至3000 K之範圍內之溫度)下操作,同時達成對應較高黑體溫度之PV轉換效率。黑體輻射器5b4 (諸如金屬氧化物黑體輻射器,諸如ZrO2 或HfO2 黑體輻射器)可在合適的操作溫度範圍內操作,以避免汽化,同時歸因於塗層而達成所要PV轉換效率。塗層可包含本發明或此項技術中已知之熱光伏打濾光片。該塗層可包含選擇性管線發射器,諸如網罩塗層。用以產生較高PV轉換效率之黑體輻射器5b4上之例示性網罩為氧化釷及氧化釔。 在實施例中,光可直接自低能量氫電漿直接傳播至PV轉換器26a之PV電池。歸因於反應電解槽腔室5b31之透明度,反應電解槽腔室5b31可在至PV電池之給定光學功率流動下保持處於較低黑體溫度下(圖2I146至圖2I147)。反應電解槽腔室5b31可包含透明材料,諸如透明的耐火材料,諸如陶瓷。陶瓷可包含金屬氧化物。金屬氧化物可為多晶的。反應電解槽腔室5b31可包含光學透明氧化鋁(藍寶石) Al2 O3 、氧化鋯(立方氧化鋯) ZrO2 、氧化鉿(HfO2 )、氧化釷ThO2 及其混合物中之至少一者。保持在反應電解槽腔室5b31內部之低能量氫電漿可發光,諸如黑體及對反應電解槽腔室5b31透明之線發射。透明度可用於至少具有高於PV轉換器26a之PV電池之帶隙的能量的波長。PV電池可反射未經轉換之光,該光之能量為高於帶隙及低於帶隙中之至少一者。光可反射至反射鏡、另一PV電池及可包含反應電解槽腔室5b31內部之電漿的黑體輻射器中之至少一者。歸因於電漿之散射、電離及黑體特徵,電漿可對經反射輻射有高吸收性。反射光可經循環回至PV電池以用於進一步轉換為電。反應電解槽腔室5b31可包含具有反射鏡之區段,其用以將光反射至PV電池及使光再循環中之至少一者。反應電解槽腔室5b31可包含不透明區段。不透明區段可為以下中之至少一者:不透光的或較冷的。銀反射鏡可在所要位置處形成以保持不透明度。反射鏡可藉由凝結自熔融銀形成。儲集器5c及下部半球5b41之下部中之至少一者可為不透明的。反應電解槽腔室5b31可能夠在高於熔融金屬(諸如銀)之沸點的溫度下操作以避免金屬凝結在透明區段上。圓頂5b4可能夠在高於銀之沸點(2162℃)之溫度下操作,使得其保持對電漿黑體輻射透明以照射PV電池。能夠高於銀之沸點(B.P.=2162℃)操作的例示性透明陶瓷為氧化鋯(立方氧化鋯) ZrO2 、氧化鉿 (HfO2 )、氧化釷ThO2 及其混合物。在實施例中,透明圓頂5b4 (諸如藍寶石圓頂)可低於熔融金屬之沸點操作,其中電漿過熱熔融金屬以防止其凝結在透明圓頂區段上。電池之部件(諸如下部半球5b41、上部半球5b42及儲集器5c)可包含單個部件或可包含複數個經接合之部件。接合可藉助於本發明,諸如藉由使用陶瓷膠將部件膠合在一起。在實施例中,透明圓頂5b4可包含各具有較小直徑之複數個透明圓頂。複數個圓頂可包含單一片件或膠合在一起之複合圓頂。 在實施例中,透明反應電解槽腔室5b31內部之電漿溫度經保持在對於藉由PV電池的電轉換大約最佳的溫度下,該等PV電池諸如係商用PV電池,諸如基於Si及III-V半導體之PV電池(諸如本發明之PV電池)中之至少一者,其中電池可包含聚光電池。黑體溫度可保持在太陽熱(Sun)之溫度(諸如約5600K)下。 在實施例中,輻射器5b4 (諸如可傳輸大部分電漿輻射之透明圓頂)包含用以冷卻圓頂以避免超出其最大操作溫度的冷卻系統。冷卻系統可包含保持在殼體5b3中之氣體以藉由傳導、對流及強制對流中之至少一個方式移除熱量。冷卻系統可包含具有氣體急冷器之強制氣體冷卻系統。或者,冷卻系統可包含至少一個冷卻劑管線、在可為透明之圓頂表面上之冷卻劑管線表面網狀物、可約為透明之冷卻劑、冷卻劑泵及急冷器。大約透明之冷卻劑可包含熔鹽,諸如鹼金屬或鹼土金屬熔鹽,諸如鹵鹽。在實施例中,圓頂之基底可經冷卻以防止光阻。在實施例中,圓頂可覆蓋有耐火導體帶以使熱量流動至周界以便由冷卻系統移除。在實施例中,圓頂之部分可覆蓋有高發射率耐火材料(諸如本發明之耐火材料)以增強自圓頂之輻射性熱損失以便冷卻圓頂。在包含複數個可包含單一片件或膠合在一起之複合圓頂的元件圓頂的實施例中,冷卻系統可包含沿元件圓頂之間的接縫延行之冷卻劑管線。 在實施例中,低能量氫反應電漿經保持在包含透明球體之反應電解槽腔室5b31之中心,以達成自反應電解槽腔室5b31之中心至透明圓頂5b4的熱梯度。可在空間上控制低能量氫反應速率以藉由控制低能量氫反應物之噴射及控制反應條件(諸如將導電熔融金屬基質保持至中心)以及控制點火參數(諸如電壓及電流)而定位於球體之中心。在另一個實施例中,緩衝層之非電漿氣體可沿圓頂5b4之內側壁噴射以防止低能量氫電漿與壁直接接觸。或者,SunCell®可包含充電源(諸如電電力供應器及電極)以致使壁及電漿可同樣充電以引起電漿與壁之間的電斥力,從而防止電漿與壁直接接觸。在實施例中,SunCell®可包含用於電漿磁性約束之磁場來源。電漿可藉由磁場經約束至圓頂之大致中心處。圓頂可包含磁瓶,其中電漿經約束至中心以使得透明壁不會過熱。 在實施例中,進水升管5qa及噴射器5k61管中之至少一者可包含碳或陶瓷。陶瓷可包含不與H2 O反應之陶瓷(諸如氧化物,諸如ZrO2 、HfO2 、MgO、Al2 O3 中之至少一者),本發明之陶瓷及熟習此項技術者已知之陶瓷。陶瓷可包含碳化物,其為以下中之至少一者:形成保護性氧化物塗層並抗與水發生反應,諸如ZrC。管可包含在基底端處之螺紋且可螺合至EM泵組合件5kk之基底中。 在實施例中,進水升管5qa、噴射器5k61及儲集器5c中之至少一者為至少部分導電的且經負偏壓以避免腐蝕。例示性導電耐火陶瓷為碳化矽、氧化釔穩定之氧化鋯及熟習此項技術者已知之其他。負偏壓部件(諸如進水升管5qa、噴射器5k61及儲集器5c中之至少一者)可包含耐火導體,諸如石墨。正偏壓部件可包含氧化穩定之耐火材料,諸如耐火貴金屬(諸如Pt、Re、Ru、Rh或Ir)或耐火氧化物(諸如MgO或本發明之其他氧化物)。在實施例中,電池組件可包含非反應性表面塗層以避免腐蝕,諸如因與氧化劑(諸如氧及水蒸氣)氧化而腐蝕。例示性部件(諸如EM泵管5k4、進水升管5qa及噴射器5k61中之至少一者)的塗層可包含Ni、Co、耐火貴金屬(諸如Pt、Re、Ru、Rh或Ir)或陶瓷(諸如MgO、Al2 O3 、富鋁紅柱石或本發明之另一氧化物)。與高溫H2 O接觸之部件可包含抗氧化不鏽鋼,諸如以下中之至少一者:Haynes 230、Pyromet®合金625、Carpenter L-605合金及BioDur® Carpenter CCM®合金。在高溫下操作之部件可塗佈有非反應性耐火塗層。塗佈可藉由熟習此項技術者已知之方法(諸如藉由電鍍、化學沈積、噴塗及氣相沈積)來達成。在例示性實施例中,Mo或W進水升管5qa及噴射器5k61中之至少一者可塗佈有錸(M.P. = 3180℃)、銥(M.P. = 2410℃)及相對應的合金中之至少一者。在實施例中,諸如Mo管噴射器5k61及W噴嘴5q之組件可使用羰基熱分解方法而塗佈有錸。十二羰基錸(Re2 (CO)10 )在170℃下分解,Re2 (CO)10 可經汽化及分解至保持於超過170℃之溫度下之部件上。其他合適的塗佈方法係此項技術中已知之塗佈方法,諸如電鍍、氣相沈積及化學沈積方法。燒焊或扣件(諸如擴口配件)可用於將金屬進水升管5qa及噴射器5k61 (諸如鍍Re之Mo及W噴射器中之至少一者)中之至少一者連接至EM泵組合件5kk之底板。與鎳相同,在普通條件下,錸不與水反應。不與水反應之金屬可為以下中之至少一者:受保護以免於氧化;及氧化物可藉由保持包含氫之氛圍而還原為金屬及水。氧化鎳及氧化錸可各自藉由與氧反應而形成。在例示性實施例中,保持氫氛圍可將氧化鎳及氧化錸中之至少一者還原。EM泵組合件5kk可包含用於進水升管5qa及噴射器5k61之套環。套環可焊接至底板或機械加工成底板。套環以及進水升管5qa及噴射器5k61管可包含抵抗與H2 O反應的材料。套環、進水升管5qa及噴射器5k61管可為經鎳經塗佈、經鉑塗佈、經貴金屬塗佈及經錸塗佈中之至少一者。經塗佈之進水升管5qa及噴射器5k61中之至少一者可藉由至套環之螺紋而接合至EM泵組合件5kk的底板。 熱解石墨幾乎不會與氫反應且不會插入銀;因此,碳部件(諸如反應電解槽腔室5b31)可包含可與氫氛圍及熔融銀一起使用的熱解石墨。銀亦具有有利屬性,即其不會自許多金屬(諸如鎳及錸)形成合金。 電池組件之間的活接或接合可包含硬焊接合。硬焊接合可包含熟習此項技術者已知之接合,諸如在文章R. M. do Nascimento、A. E. Martinelli、A. J. A. Buschinelli, 「Review Article: Recent advances in metal-ceramic brazing」,, 第49卷, (2003)第178-198頁中所描述之接合中一者,該文章以全文引用之方式併入本文中。硬焊件可包含商用硬焊,諸如包含S-Bond® 活性焊料(http://www.s-bond.com)之硬焊件,該等活性焊料使得能夠將陶瓷(諸如氧化物、氮化物、碳化物、碳/石墨矽化物、藍寶石及其他)接合至金屬以及彼此接合。S-鍵結合金之活性元素(諸如鈦及鈰)添加至Sn-Ag、Sn-In-Ag及Sn-Bi合金以形成可在鍵結之前直接與陶瓷及藍寶石表面反應的焊料。S-鍵結合金利用所有金屬(包括鋼、不鏽鋼。鈦、鎳合金、銅及鋁合金)產生可靠的密閉式接合,其限制條件為管理在接合溫度下之熱膨脹失配。 在實施例中,進水升管5qa、噴射器5k61管及儲集器5c中之至少一者可硬焊至EM組合件5kk底板。進水升管5qa、噴射器5k61管,儲集器5c中之至少一者可包含可硬焊至EM組合件5kk底板之陶瓷,諸如金屬氧化物(諸如ZrO2 、HfO2 Al2 O3 中之至少一者)。EM組合件5kk底板可包含金屬,諸如不鏽鋼(SS) (諸如400系列SS)、鎢、鎳、鈦、鈮、鉭、鉬、陶瓷(諸如ZrO2 或本發明之另一氧化物)。底板可包含具有與儲集器類似之熱膨脹係數的材料。硬焊件可包含熔填金屬,該熔填金屬可包含貴金屬,諸如銠、釕、鈀、錸、銥、鉑、金、銀及其合金(諸如Pd-Au合金)中之至少一者。活性金屬(諸如鉿、鋯及鈦中之至少一者)可添加至諸如貴金屬之熔填金屬。可添加呈細粉形式之活性金屬。可添加呈氫化物(諸如氫化鈦)形式之活性金屬,其在硬焊期間分解以形成精細鈦粒子。可以所要莫耳百分比(諸如在約1至2莫耳%之範圍內)添加活性金屬至熔填金屬以達成硬焊。 活性金屬可用來潤濕陶瓷。活性金屬可部分地取代陶瓷金屬以達成潤濕陶瓷及用陶瓷黏結中之至少一者。可儘可能密切地匹配經接合部件之熱係數,同時達成組件的所要操作特性。在例示性實施例中,至少一個組件(諸如進水升管5qa、噴射器5k61管及儲集器5c中之至少一者)可包含ZrO2 、HfO2 及Al2 O3 中之至少一者,其經硬焊至鉬EM組合件5kk底板。在另一例示性實施例中,至少一個組件(諸如進水升管5qa、噴射器5k61管及儲集器5c中之至少一者)可包含ZrO2 、HfO2 及Al2 O3 中之至少一者,其經硬焊至410不鏽鋼EM組合件5kk底板,其中硬焊件包含Paloro-3V鈀-金-釩合金(Morgan Advanced Materials)。合金之金屬百分比可經調節以達成所要最大操作溫度,諸如在約1150℃至1300℃之範圍內的溫度,其中硬焊件溫度可更高,諸如高100℃。 經接合電池組件之間的熱膨脹係數失配可至少部分藉由使用躍遷元件校正,該躍遷元件包含經硬焊至EM組合件5kk底板及陶瓷部件的金屬連接器。金屬連接器之熱膨脹係數可更密切地匹配陶瓷組件之熱膨脹係數。連接器可適應與EM組合件5kk底板之較大熱失配,其係歸因於底板及連接器金屬之可變形性。例示性連接器為鉬套環,其一端經硬焊至金屬氧化物部件且另一端經硬焊或焊接至不鏽鋼EM組合件5kk底板,其中鉬與陶瓷(諸如氧化鋯)之熱膨脹係數更密切地匹配,且金屬之變形適應在兩種金屬之活接處的較高熱膨脹失配應力。在另一實施例中,連接器可包含波紋管以適應差分膨脹。波紋管可經電鑄。 硬焊可在真空中進行。硬焊可在高溫真空爐中進行。熔填及活性金屬可形成為匹配接頭(諸如環)之幾何結構的幾何結構以構成硬焊材料。部件可與介入該等部件之間的硬焊材料並列。爐可在約硬焊材料之熔點的溫度下操作以使該硬焊材料熔化並形成硬焊件。經硬焊金屬部件可塗佈有抗氧化塗層(諸如鎳、貴金屬、或鉑塗層)或本發明之另一種塗層。 在例示性實施例中,EM組合件5kk底板、EM泵管5k6,EM泵匯流排5k2包含鉬。該等部件可藉由此項技術中已知之方式(諸如雷射或電子束焊接)而焊接在一起。用於進水升管5qa及噴射器5k61管之套環可經機械加工成底板,且進水升管5qa及噴射器5k61管在裝配期間可藉由螺紋連接至底板。使用具有1至2莫耳%之鈦細粉作為活性金屬之鈀填料來將包含ZrO2 、HfO2 或Al2 O3 之儲集器5c硬焊至鉬EM組合件5kk底板。利用介入在經硬焊之部件之間的硬焊材料將儲集器置放於經裝配之EM組合件5kk之底板上。硬焊在真空爐中在約1600℃下進行以熔化鈀(M. P. = 1555℃)。或者,填料可包含合金,諸如Pd-Au 90% (M. P. = 1300℃)。儲集器5c之內部之底板的表面及EM泵管5k6之內部經塗佈有氧化保護塗層,諸如鉑或鎳。塗層可藉由電鍍、氣相沈積或熟習此項技術者已知之其他方法形成。 剛性支柱(諸如金屬或陶瓷支柱)可支撐儲集器支撐板5b8。前一者可藉由將支柱安裝在諸如陽極化鋁底板之絕緣體上而電隔離,其中支柱與底板之間的連接可包含陽極化扣件,諸如螺栓或螺釘。金屬支柱可經塗佈有絕緣塗層(諸如BN、SiC、富鋁紅柱石、黑色氧化物)或本發明之其他塗層。 在另一實施例中,噴嘴5q可包含至少一個孔洞、縫隙或小開口,其在低流動速率下傳遞熔融金屬以塗佈噴嘴。流動可不斷地使因電漿汽化而損失的熔融金屬表面而非噴嘴再生。孔洞可藉由鑽孔、電極放電機器、雷射鑽孔及在諸如藉由鑄造及藉由此項技術中已知之其他方法製造期間形成。在另一實施例中,噴嘴5q可包含分流器,其引導所噴出之熔融金屬之一部分在噴嘴上方流動從而保護噴嘴免受電漿汽化影響。在另一個實施例中,包含電源2之點火電路進一步包含電弧感測器,其感測在噴嘴處而非穿過熔融金屬流的電弧;及電弧保護電路,其終止噴嘴上之電弧電流。 在實施例中,噴射管5k61可彎曲以將噴嘴5q置放在儲集器5c之頂部處的大約中心處。在實施例中,噴射管5k61可自垂直成角以使噴嘴5q在儲集器5c之頂部處居中。角度在處於儲集器5k9之底部處的連接器處固定。連接器可建立角度。連接器可包含接頭套管5k9,其具有至儲集器基底之鎖緊螺母;且進一步包含至螺紋端噴射管5k61之成角陰連接器。陰連接器可包含具有陰連接器之彎曲套環或成角螺母以使得陰螺紋之角度傾斜。或者,儲集器基底可成角度以建立噴射器管之角度。在另一實施例中,儲集器底板中之螺紋可傾斜。接頭套管配件5k9可螺合至傾斜或成角螺紋中。EM泵管5k61之已連接直式噴射部分可由於成角螺紋而成角度。該角度可將噴嘴5q置放於儲集器5c之中心。相對於儲集器之基底成角之接頭套管配件5k9可連接至在儲集器底板下方之成角套環,以准許與EM泵管5k6之約垂直連接,其中該EM泵管連接以穿透儲集器底板。泵管5k6可包含抵抗與水反應之不鏽鋼(SS),諸如用於鍋爐中之SS。泵管可焊接至EM泵管組合件(諸如傾斜的EM泵管組合件)。 在實施例中,SunCell®發電機包含兩個儲集器5c及在儲集器中之一者(噴射儲集器)中之一個熔融金屬噴射器。熔融金屬噴射器可包含EM泵噴射器。另一儲集器,即非噴射器儲集器,可用熔融金屬填充。由單一噴射器噴射之多餘熔融金屬可溢位並返回至具有噴射器之儲集器中。下部半球5b41可傾斜以使金屬流動返回至噴射儲集器。儲集器可藉由電連接至點火電源2之相對應端子而充當相反極化之端子或電極。極性可如此以防止噴射器之噴嘴5q免於受到劇烈的低能量氫反應電漿損壞。非噴射器儲集器可包含正電極且噴射器儲集器可包含負電極。 儲集器支撐板或底板5b8可包含電絕緣體,諸如SiC或氮化硼。或者,支撐板可為能夠在局部溫度下操作之金屬,諸如鈦。金屬可為非磁性及高度導電中之至少一者,以限制自電感耦合加熱器吸收之RF功率並具有高熔點。例示性金屬為W及Mo。底板可包含碳。金屬底板5b8之電隔離可由板與安裝夾具之間以及儲集器與板之間的絕緣體提供。絕緣體可包含絕緣體墊圈或襯套,諸如SiC或陶瓷墊圈或襯套。雙儲集器之支撐板可為一個或單獨支撐板。儲集器支撐板可包含具有絕緣體套環或襯套(諸如SiC或BN套環或襯套)縱向分離板以電隔離儲集器。儲集器支撐板可包含縱向分離的兩片式底板,該底板具有用於其上安放儲集器之墊片(諸如電絕緣墊片,諸如SiC或BN墊片)之狹槽。或者,每一儲集器可由獨立底板支撐,使得在底板之間存在電流中斷。底板可包含具有用於電感耦合加熱器之RF功率的低吸收截面的材料。底板可包含抗熱衝擊陶瓷,諸如碳化矽或氮化硼。底板可包含具有低RF吸收之金屬。底板可包含塗佈有可具有低RF吸收截面之塗層(諸如本發明之塗層)的金屬。 交點可為任何所要的,諸如在範圍自儲集器至在反應電解槽腔室5b31之頂部處的區域的區域中。交點可大約在反應電解槽腔室之中心。交點可藉由泵壓及噴嘴自垂直之相對彎曲或傾角中之至少一者控制。儲集器可為單獨及電隔離的。熔融金屬(諸如熔融銀)可自反應電解槽腔室流回至待再循環之每一儲集器。可藉由金屬流斷流器或分裂器防止回流銀跨越兩個儲集器電短路,以中斷原本將橋接兩個儲集器並提供導電路徑之銀的連續性。分裂器可包含不規律表面,其由致使銀成珠粒以中斷儲集器之間的電連接的材料組成。分裂器可包含每一儲集器壁在短路區域處之中斷,使得銀滴落在中斷或滴水邊緣上方從而使連續性受到破壞。分裂器可包含覆蓋兩個儲集器之交點的圓頂或半球,其中圓頂或半球之基底包含用於每一儲集器之中斷。在實施例中,兩個儲集器5c及其底部板或底板以及黑體輻射器5b41之下部半球可包含一個片件。黑體輻射器5b41之下部半球可包含在設定儲集器之底部中的凸起圓頂或橫向脊線。在實施例中,每一儲集器之頂部可包含充當回流銀在其上流動的唇部的環板或墊圈。唇部引起金屬流流動至每一儲集器的中斷,以破壞儲集器之間的可另外流動經過回流銀的任何電流路徑。每一儲集器之頂部可包含經機械加工之圓周凹槽,墊圈安放在該圓周凹槽中以形成唇部或滴水邊緣5ca,如圖2I83中所示。至少一個電池組件(諸如,分裂器(諸如圓頂或半球分裂器)、儲集器5c、黑體輻射器5b41之下部半球、黑體輻射器5b41之下部半球之凸起或圓頂底部及在每一儲集器上之唇部)可包含碳。 在實施例中,黑體輻射器之基底(諸如反應電解槽腔室5b31之底層,諸如黑體輻射器5b41之下部半球之底層)可包含凹槽或通道以將較佳路徑中之熔融金屬流動導向至儲集器5c之入口,使得兩個反向充電之儲集器之間的任何電連接受到破壞或大約受到破壞。通道可將熔融金屬導向至儲集器之正面、側面及背面中之至少一者。通道可各自包含階度(gradation)以引起至儲集器中之重力流動。通道可為以下中之至少一者:分級及傾斜的。該級別可引起相對於反應電解槽腔室之中心朝向所要儲集器位置(諸如儲集器之背面)的緯斜。將流動導向至雙噴射器實施例之兩個儲集器中之給定儲集器的傾斜分級通道可為與另一儲集器之通道相對的鏡像,以引起至相反相對位置的流動。在於具有處於位置(-1,0)及(1,0)的儲集器之反應腔室之底層的中心處具有經指定的xy座標系統的例示性實施例中,分級及相反傾斜之通道的流動將熔融金屬導向至居中在每一儲集器上的相對極角(3/2π 及1/2 π)。底層可包含在每一儲集器開口之中心及正面的至少一個伸出部分。可優選流動至儲集器之側面及背面中之至少一者。 在實施例中,發電機包含感測器及點火控制器,該點火控制器用以減小點火電壓及電流中之至少一者,以防止電池組件(諸如下部半球5b41)的短路引起對組件的損害。電氣短路感測器可包含電流或電壓感測器,其將信號饋送至控制點火電流及電壓中之至少一者的點火控制器中。 在實施例中,在自過度填充之儲集器流動至填充不足之儲集器的情況下,熔融金屬可被動地流經兩個儲集器之間的導管。電池可包含在儲集器之間的導管中的旋轉分離器以中斷熔融金屬內的電路。經過熔融金屬之點火電流的電氣短路可由包含可移動裝置之分裂器(諸如電絕緣閘極)中斷。該閘極可包含具有複數個輪葉之可移動裝置以中斷熔融金屬導電路徑。例示性設計為可包含耐火材料(諸如SiC或氮化硼)之葉輪的設計。葉輪可容納於導管中並准許金屬流動而不准許儲集器之間的電連接。 在實施例中,返回熔融金屬流可藉由至少一個系統中斷,該系統包含:(i)滴水邊緣,諸如置放於儲集器入口之頂部中的扁平墊圈;(ii)噴嘴5q、熔融金屬位準及在儲集器5c中降低的進水升管中之至少一者;(iii)下部半球5b41返回熔融金屬流道,其將流動分散以避免大型流或中斷任何連接性電流路徑;(iv)自儲集器壁之複數個電絕緣伸出部分;(iv)切割成滴水邊緣之複數個電絕緣波紋或凸起、儲集器頂部入口或儲集器壁;(v)光柵,諸如在儲集器頂部上之電絕緣光柵;及(vi)所施加磁場,其在電氣短路電流流經該流時產生勞侖茲力以使該流偏轉至珠粒中。 在實施例中,SunCell®包含儲集層銀位準均衡系統,其包含銀位準感測器、EM泵電流控制器及接收來自位準感測器之輸入並驅動電流控制器在儲集器5c中保持大約相同的金屬位準的控制器,諸如可程式化邏輯控制器(PLC)或電腦100。在實施例中,SunCell®包含熔融金屬均衡器,其用以在每一儲集器5c中保持大約相同的位準(諸如銀位準)。均衡器可包含在每一儲集器上之儲集器位準感測器及EM泵速率控制器以及用以啟動每一EM泵以保持大約相同位準的控制器。感測器可包含:基於至少一個物理參數之感測器,該至少一個物理參數諸如係放射性不透明度、電阻或電容、熱發射、溫度梯度、聲音(諸如超音波頻率、位準相關聲學諧振頻率、阻抗或速度)、光學(諸如紅外發射);或此項技術中已知的適合於藉由歸因於位準之變化或跨越位準介面之變化的參數變化偵測指示儲集器熔融金屬位準的參數的其他感測器。位準感測器可指示EM泵之啟動位準且由此指示熔融金屬流動。可藉由監測點火電流及電壓中之至少一者來監測點火狀態。 感測器可包含放射源5s1,諸如放射性核種,諸如以下中之至少一者:發射60 keV γ射線的鋂(諸如241 Am)、133 Ba、14 C、109 Cd、137 Cs、57 Co、60 Co、152 Eu、55 Fe、54 Mn、22 Na、210 Pb、210 Po、90 Sr、204 Tl或65 Zn。放射性核種輻射可經準直。準直器可產生複數個光束,諸如兩個光束,其各與中心軸線成45°,其中一個放射性同位素來源可形成兩個扇形光束以穿透兩個儲集器中之每一者並接著變為入射於一對中之相對應的偵測器。準直器可包含光閥(shutter),其用以在感測器未處於操作中時阻擋輻射。來源5s1可包含X射線及γ射線發生器,諸如制動輻射X射線源,諸如http://www.source1xray.com/index-1.html處之彼等者。感測器可進一步包含相對於放射源在儲集器之相對側面上之至少一個輻射偵測器5s2。感測器可進一步包含位置掃描儀或構件(諸如機械構件),其用以將輻射源及輻射偵測器中之至少一者沿垂直儲集器軸線移動,同時保持源與偵測器之間的對準。該移動可跨越熔融金屬位準。掃描儀可包含移動電感耦合加熱器天線5f之致動器,其中輻射源(諸如241 Am來源)及輻射偵測器中之至少一者可附接至線圈5f、線圈電容器箱90a及活動致動器機構中之至少一者。在隨著經準直輻射超越該位準後在貫穿輻射計數中之變化可識別位準。或者,掃描儀可循環地改變來源與偵測器之相對定向,以在該金屬位準上方及下方掃描以便偵測金屬位準。在另一實施例中,感測器可包含沿每一儲集器之垂直軸線佈置之複數個來源5s1。感測器可包含相對於對應來源在儲集器之相對側面上之複數個輻射偵測器5s2。在實施例中,輻射偵測器可與輻射源成對,以使得輻射沿軸向路徑自該源行進穿過儲集器,到達偵測器。輻射源可藉由儲集器金屬(若存在)衰減,以使得輻射偵測器將記錄在位準上升超過輻射路徑時的較低信號,且將記錄在位準降低至路徑以下時的較高信號。該來源可包含寬光束或具有寬輻射角範圍的光束,該輻射橫越儲集器到達空間擴展之偵測器或經擴展之偵測器陣列(諸如X射線敏感線性二極體陣列),以提供對輻射路徑中之儲集器的金屬含量的縱向或深度分佈的量測。例示性的X射線敏感線性二極體陣列(LDA)為 X-Scan Imaging Corporation XI8800 LDA。金屬位準對計數之衰減可指示位準。例示性來源可包含來自放射性或X射線管來源之擴散光束,且偵測器可包含經擴展之閃爍或蓋格計數器偵測器。偵測器可包含以下中之至少一者;蓋格計數器、CMOS偵測器、閃爍體偵測器及具有光電二極體偵測器之閃爍體(諸如碘化鈉或碘化銫)。偵測器可包含電離偵測器,諸如MOSFET偵測器,諸如煙霧偵測器中的MOSFET偵測器。電離腔室電極可包含在輻射入射側上之至少一個薄箔或線柵以及如煙霧偵測器電路中之典型的相對電極。 在實施例中,包含貫穿輻射(X射線)之來源、偵測器及控制器之感測器進一步包含用以將在偵測器處自該來源接收之信號的強度處理為儲集器熔融金屬位準讀數的演算法。感測器可包含單個廣角發射器及單個廣角偵測器。X射線或γ射線可以一角度穿透儲集器之內部到達儲集器橫向平面,以增加穿過含有熔融金屬之飛行區域至偵測器的路徑長度。該角度可對熔融金屬之較大深度取樣以提高用於判定儲集器中之熔融金屬的深度的鑑別。可針對已知熔融金屬位準來校準偵測器信號強度。隨著位準上升,偵測器強度信號減小,其中自該校準判定位準。例示性來源為放射性同位素(諸如鋂241)及X射線來源(諸如制動輻射裝置)。例示性偵測器為蓋格計數器及閃爍體及光電二極體。X射線源可包含AmeTek來源,諸如Mini-X,且偵測器可包含NaI或YSO晶體偵測器。可掃描輻射源(諸如X射線源)及偵測器中之至少一者以獲得X射線衰減之縱向分佈且由此獲得金屬位準。掃描儀可包含機械掃描儀,諸如凸輪驅動掃描儀。該凸輪可藉由旋轉軸轉動,該旋轉軸可由電動馬達驅動。掃描儀可包含機械、氣動、液壓、壓電、電磁、伺服馬達驅動掃描儀或構件或熟習此項技術者已知之其他此類掃描儀或構件,以便以可逆方式平移或重定向X射線源及偵測器中之至少一者以獲得金屬位準之深度分佈。放射性同位素(諸如鋂)可封裝於耐火材料(諸如W、Mo、Ta、Nb、氧化鋁、ZrO、MgO)或另一種耐火材料(諸如本發明之耐火材料)中,以准許在溫度高的情況下將其置放為與儲集器極接近。X射線源及發射器以及偵測器中之至少一者可安裝於可具有受控壓力及溫度中之至少一者的殼體中。殼體可安裝至外部壓力容器5b3a。可移除殼體以准許容易移除外部壓力容器5b3a。殼體可以水平方式移除以准許垂直移除外部壓力容器5b3a。殼體可具有用於傳送X射線同時保持跨越窗之壓力梯度的內窗。窗可包含碳纖維。殼體之外端可與大氣相通或封閉。 在實施例中,位準感測器包含X射線或γ射線之來源,其在儲集器5c內部之套管(well)或殼體的內部。X射線或γ射線之來源可為放射性核種,諸如41 Am、133 Ba、14 C、109 Cd、137 Cs、57 Co、60 Co、152 Eu、55 Fe、54 Mn、22 Na、210 Pb、210 Po、90 Sr、204 Tl或65 Zn。套管可緊固至EM泵組合件5kk之底板。放射性核種可囊封於耐火材料(諸如碳、W、氮化硼或碳化矽)中。放射性核種可包含耐火合金。放射性核種可包含具有高熔點之元素或化合物,諸如14 C、Ta4 Hf14 C5 (M.P. 4215℃)、133 BaO、147 Pm2 O2144 Ce2 O390 SrTiO360 Co、242 Cm2 O3144 Cm2 O3 。套管壁可包含容易由X射線或γ射線穿透的材料。例示性套管為氮化硼套管。儲集器可包含容易由X射線或γ射線穿透的材料,諸如氮化硼或碳化矽儲集器。位準感測器可包含可經校準以形成複數個光束的複數個X射線或γ射線來源。位準感測器可包含複數個X射線或γ射線偵測器,其在儲集器之壁之外並定位為在不藉由熔融金屬(諸如銀)衰減時入射X射線或γ射線。光束衰減差異位置指示如藉由處理器判定的液面的位置。在實施例中,X射線或γ射線來源(諸如在套管內的放射性核種)可並未經準直。可在儲集器外部的至少一個偵測器處偵測X射線或γ射線信號之強度。偵測器可包含閃爍體晶體及光電二極體(諸如Gadox、CsI、NaI或CdW光電二極體)。可校準隨熔融金屬位準變化的信號強度。位準感測器可包含處理器,其處理經量測信號強度及來自查找表之校準資料並判定熔融金屬位準。在實施例中,位準感測器包含粒子後向散射類型。位準感測器可包含粒子(諸如氦離子、質子、X射線或γ射線、電子及中子中之至少一者)之來源。該來源可包含經準直來源。粒子可在複數個垂直座標位置處入射儲集器5c或可隨時間掃描複數個垂直位置。當在相較於低於熔融金屬位準而在高於該位準之垂直位置處入射於儲集器上時,粒子可隨強度變化後向散射。強度變化可視粒子及其能量而增大或減小。X射線可由熔融金屬(諸如銀)吸收,以使得自遠儲集器壁之後向散射可歸因於介入熔融金屬而減少。因而,當X射線在低於位準的垂直座標位置處入射儲集器時,後向散射之X射線的強度可減小。X射線之能量可經選擇以相較於在儲集器壁中的衰減而在熔融金屬(諸如銀)中具有較高衰減。X射線能量可經選擇為剛好在電子邊緣處高於電子殼之結合能的能量。X射線來源可包含放射性同位素或X射線發生器。在實施例中,偵測經後向散射之X射線的減少以作為識別位準的方式,其中X射線能量經選擇,以使得相較於無高於位準之銀柱,經後向散射之信號藉由低於位準的銀高度衰減。具有高吸收率之能量可在邊緣處,諸如銀K邊緣之25 keV能量。 在實施例中,入射粒子可產生次級粒子或具有不同能量之相同粒子。次級粒子發射之強度變化可用於偵測位準。在例示性實施例中,具有第一能量之X射線在不同垂直位置處入射儲集器,且具有第二能量之X射線由偵測器偵測。具有第二能量之X射線或螢光X射線的強度在越過光束之間的位準時的變化指示位準。舉例而言,偵測器可處於使諸如沿著與0°或180°或90°之入射光束相同的軸線的螢光X射線信號最大的位置。在實施例中,當入射光束入射低於位準相對高於位準的儲集器時,銀之螢光X射線增加。位準感測器可包含此項技術中已知之X射線螢光(XRF)或能量色散X射線螢光(EDXRF)系統。X射線來源可包含放射性同位素或X射線發生器。EDXRF系統可包含高能粒子(諸如電子或質子)之來源。偵測器可包含矽漂移偵測器或熟習此項技術者已知之其他偵測器。 當中子自指示液面位置的銀柱後向散射時,強度可增加。中子可自241 Am及鈹金屬產生。中子來源可包含中子發生器,諸如使用電場以加速氘及氚離子中之至少一者以隨著中子產生引起D-D或D-T融合的中子發生器。可用相對應的偵測器(諸如X射線或中子偵測器)偵測經後向散射之粒子。在另一實施例中,可自在儲集器之一側上之來源發射且在儲集器之另一測上的同一軸線上偵測到粒子。經偵測作為偵測器強度下降之粒子束的衰減增加的垂直儲集器位置可識別位準之位置。本發明之例示性中子後向散射及γ射線衰減位準感測器為可購自Thermo Scientific之感測器(https://tools.thermofisher.com/content/sfs/brochures/EPM-ANCoker-0215.pdf),其針對儲集器5c之幾何結構而修改。 在實施例中,位準感測器可包含選擇性地自低於熔融金屬位準的熔融金屬反射的電磁輻射來源及經反射輻射之強度的偵測器。該位準可藉由相比高於位準之反射強度的低於位準之增強型雷射反射強度來偵測。可自沿著產生增強型反射強度的垂直儲集器軸線的入射光束的位置來判定位準之位置。輻射可包含波長,其對於儲集器壁足夠透明以使得其穿透壁並反射回至偵測器。儲集器5c壁可能夠透射光。儲集器可包含對可見及紅外光透明之氧化鋁、藍寶石、氮化硼及碳化矽中之至少一者。輻射可穿透熔融金屬之薄膜。雷射可有足夠大功率以穿透熔融金屬之薄膜。在實施例中,儲集器壁可包含氮化硼,其對於在輻射之波長範圍中(諸如在UV至紅外之範圍中)的輻射具有部分透明度。雷射可包含高功率可見或紅外光二極體雷射。電池組件(諸如儲集器)可對雷射光束透明。對紅外光透明的合適的耐火材料為MgO、藍寶石及Al2 O3 。雷射可包含紅外雷射以更好地保持焦點。在包含氮化硼之實施例中,波長可為約5微米,係因為BN在此波長下具有透射窗。在實施例中,雷射具有足夠功率以在自雷射至偵測器的軸向路徑上穿透儲集器壁(諸如氮化硼壁、任何銀壁塗層及銀蒸氣)。壁可在雷射光束-壁接觸斑點處變薄。壁可經機械加工以防止雷射光束擴散或散佈。壁可經刨平。壁可經機械加工以形成重聚焦橫越壁之光的透鏡。透鏡可與雷射波長匹配。壁可包含嵌入式透鏡。透鏡可包含抗反射塗層。透鏡可包含四分之一波片以減低反射。透射光信號指示不存在儲集器銀柱,且不存在光信號指示存在銀柱,且光信號不連續性之垂直儲集器位置可用於識別位準。雷射可包含透鏡以增加焦點及功率密度(光束強度)中之至少一者。例示性商用雷射在http :// www . freemascot . com / match - lighting - laser . htmlhttp :// www . freemascot . com / 50mw - 532nm - handheld - green - laser - pointer - 1010 - black . html ? gclid = CNu8gJ - EqtICFZmNswodZLMNQA .給出。雷射及偵測器中之至少一者可遠離儲集器以便定位於溫度不會過度升高而危害雷射或偵測器功能的區域中。雷射及偵測器(諸如光電二極體)中之至少一者可經冷卻。 熔融金屬可包含銀。銀在約300 nm之波長下具有透射窗。輻射可包含在約250至320 nm之範圍內的波長。輻射來源可包含UV二極體,諸如UVTOP310。UV二極體可包含透鏡,其可包含半球透鏡以製作定向光束。輻射來源可包含雷射,諸如二極體泵抽雷射。銀之透射窗的波長區域中之例示性雷射為KrF準分子雷射、Nd:YAF第四諧波雷射、InGaN二極體雷射、XeCl雷射、He-Cd雷射、氮雷射、XeF準分子雷射及Ne+ 雷射。偵測器可包含光電二極體。 雷射型位準感測器可包含雷射掃描儀,其隨時間垂直移動雷射及偵測器中之至少一者以截取高於、處於及低於位準的區域從而偵測位準。或者,電流輻射-照明型位準感測器可包含複數個輻射源及相對應的偵測器,其垂直間隔開以使得位準處於接近該複數個源的位置處,使得該位準之位置可藉由源與其偵測器之間的差分反射來偵測。輻射源及偵測器可相對於彼此成角,使得源輻射可自熔融金屬柱(若存在)反射並變為入射至相對應的偵測器。儲集器之壁可經機械加工為在輻射入射及反射時更薄,以准許該輻射在自熔融金屬柱反射後自來源傳播至偵測器。在另一個實施例中,當在光束路徑中不存在熔融金屬柱時,輻射可穿透儲集器之兩個壁,且在光束路徑低於位準時,該柱可阻擋該光束。可藉由偵測器偵測光束透射穿過儲集器,該偵測器可位於輻射源(諸如雷射)之相對側上。可一致地掃描輻射源及相對應的偵測器,或位準感測器可包含沿儲集器之垂直軸線間隔開的複數個輻射源及對應偵測器,以藉由在高於相對低於熔融金屬位準的光束的傳輸之差異來偵測該位準。在實施例中,RF線圈5f具有用於入射及經反射或經透射光束的開口。線圈5f可經設計為補償任何開口,以在不存在開口的情況下提供所要加熱功率分佈。 感測器可包含至少一個滴水邊緣、朝下成角管或熱源(諸如雷射,諸如二極體雷射)及振動器中之至少一者,以至少部分地消除在高於位準的可反射輻射之金屬儲集器壁上的熔融金屬膜。在實施例中,在光束路徑與儲集器壁相交時,任何熔融金屬膜可藉由在回流金屬之位置處的滴水邊緣移除。電池可包含儲集器振動器或發波器及加熱器中之至少一者。交點處之任何熔融金屬膜可藉由振動或藉由加熱該點處之壁來移除。光束可加強以藉由使用更大功率光束及透鏡中之至少一者來穿透金屬膜。 雷射光束可相對於儲集器壁以一角度定向,以引起成一角度之反射,從而提高穿過任何薄銀層之透射,使得反射在經監測時減少。在實施例中,調節雷射光束角度以產生消散波,其中反射在銀位準下方相對銀位準上方增加。在實施例中,感測器可包含套管中之光纖電纜,該套管在反射光經定量之情況下具有部分透明度。藉由偵測器(諸如光電二極體)偵測的反射強度准許藉由處理器判定位準之位置。 雷射波長可經選擇以提高穿過儲集器壁及任何銀膜塗層的傳輸。例示性波長為約315 nm,係因為銀在約315 nm下具有透射窗。光偵測器(諸如,可視情況包含光學波長帶通濾波器之光電二極體)可選擇性地回應於雷射光。在實施例中,燈可替代雷射。燈可包含大功率發光二極體(LED)陣列。位準感測器可包含短波長來源,諸如能夠發射諸如在約315至320 nm之波長區域中的UV光的來源。短波長來源可包含氘燈以照明儲集器。燈可包含可見光或紅外光燈。在實施例中,照明源(諸如高於銀位準之短波長光)可為電漿發射。 在實施例中,電漿利用對儲集器透明之強光照明熔融金屬位準上方的空間。透明儲集器可包含透明材料,諸如氮化硼、碳化矽及氧化鋁中之至少一者。可藉由使用至少一個光偵測器(諸如光電二極體)量測光在金屬位準處的不連續性來記錄熔融金屬位準。 在實施例中,儲集器5c壁能夠透射光。儲集器可包含對可見及紅外光透明的氧化鋁、藍寶石、氮化硼及碳化矽中之至少一者。在實施例中,包含透光型位準感測器之熔融金屬位準感測器偵測自儲集器5c內部透射至外部的光,且至少一個光感測器中之透射光強度的垂直變化由處理器處理以判定熔融金屬位準。處理器可自兩個儲集器接收資料並關聯資料,以移除來自熔融金屬在儲集器壁上流動的任何渾濁影響,其可另外錯誤地指示熔融金屬位準之存在。 在實施例中,藉由在反應電解槽腔室5b31中點火產生的電漿照明儲集器5c壁,且部分光選擇性地穿透在熔融金屬位準上方的區域中的壁。光感測器(諸如攝影機或光電二極體)可偵測經透射穿過儲集器壁之光。光感測器(諸如光電二極體)可經垂直掃描,或位準感測器可包含複數個垂直分離之光感測器,諸如光電二極體。在一實施例中,為判定熔融金屬位準,處理器處理以下中之至少一者:i)攝影機影像上方之光強度的差;ii)複數個光感測器之間的光強度的差;及iii)經掃描光感測器之垂直位置之間的光強度的差。 為促進經由儲集器壁將電漿光傳輸或傳送至光感測器,儲集器可包含至少一個光通路,諸如壁中之凹痕、凹部或變薄區域。至少一個光感測器(諸如攝影機)、複數個光學感測器或經掃描光學感測器(諸如二極體)可記錄隨著沿儲集器的通路高度的透射光變化可藉由光纜(諸如高溫光纜,諸如石英電纜)將光傳導至每一遠端光感測器。光纜或其他光導管可增大在背景黑體光上方的固有光信號。可藉由使用光偵測器使來自電漿光之固有信號增加超過黑體輻射,該光偵測器相對於來自外部儲集器壁之黑體輻射的光譜對於較短波長有選擇性。偵測器可包含選擇性短波長偵測器或在該偵測器上的濾波器。偵測器或濾波器可准許對藍色或UV輻射之選擇性偵測。偵測器可偵測藉由儲集器壁透射之短波長光,諸如在氮化硼壁的情況下為長於約320 nm的光。可利用具有穿透件之遮光蓋沿著光通路之視線阻擋諸如黑體輻射之背景光。位準感測器可包含至少一個靜止或經掃描反射鏡,以自至少一個壁位置將透射光反射至遠端光感測器。在例示性實施例中,為適應加熱器天線5f極為接近儲集器5c,將透射光朝下反射至發生器之基底以便入射至光偵測器。反射鏡可安裝於天線5f上。處理器可接收並處理光感測器資料來判定熔融金屬位準。 在實施例中,位準感測器包含場源(諸如電流線圈、天線或在電池內部(諸如在儲集器內部)的燈),其將場(諸如磁場及電磁輻射中之至少一者)發射至外部場偵測器。經偵測信號之強度或空間變化為熔融金屬位準之函數,且處理器使用對應資料來識別熔融金屬位準。 在實施例中,透光熔融金屬位準感測器包含光源,其照明儲集器壁以產生輸入至處理器的影像或垂直光強度變化來識別位準。光源可包含燈、雷射及電漿中之至少一者。燈可在儲集器內部。燈可包含白熾燈,諸如W燈或W鹵素燈。燈可包含裸W長絲,其連接至封裝於電絕緣體中之引線,該電絕緣體可包含耐火陶瓷,諸如SiC或BN。燈可包含可支援電漿(諸如電弧電漿)的兩個分離電極。燈可包含碳弧。絕緣件可充當支架,或燈可包含充當支架的導管。該導管可包含耐火材料,諸如本發明之耐火材料。至外部電力供應器之引線可為燈供電。電力供應器可為與EM泵電力供應器、點火電力供應器及電感耦合加熱器電力供應器中之至少一者共用的電力供應器。電力供應器可在外部電池殼體之第二腔室中。引線可在EM泵組合件5kk之基底中的饋通件處穿透儲集器。燈可容納於套管中,該套管可在EM泵組合件5kk之基底處穿透。套管壁可至少部分地對內部燈透明。套管可包含耐火材料,諸如至少部分地對光透明的氧化鋁、藍寶石、氮化硼及碳化矽中之至少一者。在實施例中,燈可照明槽內部。燈可在槽下方。套管可包含至少一個反射鏡或光擴散器,其用以使光自槽(在水平面中)徑向傳輸。 光感測器可消除來自儲集器壁之背景黑體發射的干擾。光感測器可選擇性地回應於電漿或燈光。光感測器可包含濾光片以傳送電漿或燈光之選擇性波長區域特性。光感測器可回應於電漿或燈光之複數個波長特性。光感測器可包含光學高溫計或光學溫度感測器。 在實施例中,電池經加熱至所要溫度分佈,其支援電漿形成及熔融金屬再循環並大約處於EM泵噴射熔融金屬開始時。加熱器線圈5f可在黑體輻射器5b4之至少一部分上方延伸,以將其加熱至所要溫度分佈。加熱器可藉由致動器替換。可施加點火電壓,使得點火及電漿形成在來自雙EM泵之熔融金屬流相交時發生。電漿光可直接或經由通路透射穿過儲集器壁,以准許偵測到熔融金屬位準。 感測器可包含沿儲集器之垂直軸線間隔開之一連串電觸點及用以量測電觸點之間的導電性及電容中之至少一者的導電計及電容計中之至少一者,其中導電性及電容中之至少一者跨越在儲集器內部之熔融金屬位準而可量測地變化。電觸點可各自包含圍繞內部或外部圓周或儲集器之圓周之一部分的導電環。導電計可包含歐姆錶。在實施例中,導電性或電容探測器中之至少一者可包含複數個引線,其在熔融金屬位準之所要高度範圍內的複數個空間分離位置處進入EM泵管,沿EM泵管行進,並退出EM泵管。引線出口可在感測器或探測器中終止。或者,導線可在套管中行進,該套管可焊接至EM泵組合件5kk之底部中。探測器可包含導體或電容器。可使用單獨探測器之間的導電性或單獨探測器處的相對導電性來偵測熔融金屬位準,其中導電性在探測器與熔融金屬接觸時增加。引線可包含電絕緣導線,其在諸如接頭套管之密封饋通件處穿透在儲集器之外的EM泵管。引線可經由可密封或可不密封之電絕緣穿透件離開儲集器內部之EM泵管。導線可經塗佈有耐火電絕緣體,諸如氮化硼或本發明之另一耐火塗層。導線可塗佈有經陽極化之Al。導線可包含耐火導體,諸如Mo、W或本發明之另一種耐火導體。在實施例中,導線可由耐火光纜替代,其中可以光纖方式感測位準。 在包含儲集器之實施例中,該等儲集器包含電絕緣體(諸如SiC、BN、AUO3 或ZrO2 ),複數個縱向隔開之導線可穿過儲集器之壁且橫跨熔融金屬位準的範圍。導線可為裸露的。導線可藉由壓縮密封來密封。在儲集器製造期間,導線可經燒結或鑄造在適當位置。或者,導線可經由緊密配合穿透件插入。穿透件(諸如孔)可藉由機械加工。放電研磨、噴水鑽孔、雷射鑽孔或此項技術中已知之其他方法產生。緊密配合導線之熱膨脹係數可能比儲集器材料之熱膨脹係數高,使得在加熱儲集器時形成壓縮密封。導線可感測隨著熔融金屬位準變化的導電性變化及電容變化中之至少一者。 藉由隨著熔融金屬位準變化的導電性、電感、電容及阻抗的變化中之至少一者感測熔融銀位準的位準感測器可包含參考電觸點(諸如在EM泵組合件5kk之基底上的參考電觸點)及容納在套管中之至少一個探測器導線,該套管緊固至儲集器之底部(諸如EM泵組合件5kk之底部處)。電容感測器可包含兩個板,其可取決於位準而用熔融金屬填充並對該位準作出回應。電感感測器可包含線圈,其中由線圈連接之通量取決於熔融金屬位準。套管可藉由扣件(諸如接頭套管)緊固或可焊接至EM泵組合件之底部。導線可以電氣方式及實體方式附接至每一導線末端處之套管的內壁。至少一個導線之對應電觸點可垂直隔開。例示性套管包含耐火金屬管(諸如Mo管),其在EM泵組合件5kk之底部處可用開槽不鏽鋼接頭套管緊固,其中藉由氧化鋁護套絕緣之導電性探測器導線進入底部的開口端,在管內行進,且藉由焊件附接至Mo椎體,該Mo椎體焊接在管末端處。能夠在高溫下再結晶的金屬探測器可經預加熱以在將其用作探測器時使金屬再結晶。量測探測器導線與附接至EM泵組合件5kk之基底的參考觸點之間的導電性。在另一實施例中,EM泵管5k6之出口部分充當槽。隨著銀位準上升,探測器與參考之間的導電性歸因於穿過熔融金屬之探測器電流的平行路徑而降低。可校準隨金屬位準變化之導電性。可根據套管溫度進行校準。套管可進一步含有熱電偶以量測探測器處之套管溫度,以准許選擇對應校準。或者,導電性感測器可包含在單獨儲集器中之兩個匹配探測器(諸如兩個匹配再結晶的W導管),其中控制相對EM泵抽速率以匹配兩個探測器之導電性從而控制及匹配兩個儲集器中之熔融金屬的位準。感測器可進一步包含用於探測器之間隨平均導電性及操作溫度中之至少一者變化的任何偏移導電性的校準曲線。導電性探測器可包含電絕緣護套或塗層以防止利用點火功率進行電弧擊穿,同時保持足夠電連接以感測導電性。導電性探測器可包含可經摻雜之半導體。可用高頻率探測器電流或電壓及相對應的電壓或電流信號來量測導電性,以判定導電性可進一步經濾波以移除雜訊(諸如由點火電流引起之雜訊)的效應。 藉由複數個導體之間或複數個導體處之隨熔融金屬位準變化的差分導電性或電容中之至少一者來感測熔融銀位準的位準感測器可包含複數個導體,諸如穿過儲集器壁之導線。儲集器壁可包含電絕緣體,諸如氮化硼或碳化矽。歸因於導線相對於壁材料之差分膨脹,導線可藉由壓縮密封。舉例而言,Mo、Ta及Nb各自具有有利的高於SiC之熱膨脹係數。可在室溫下藉由執行以下至少一個初始步驟達成對電池之密封:在經由儲集器壁中之孔插入在不存在壁加熱或導線冷卻的情況下緊密配合的導線之前,藉由手段(諸如藉由施加致冷劑(諸如液氮))來加熱壁及冷卻導線。在另一實施例中,導線可藉由模製、膠合或密封來密封。或者,可在製造期間藉由將導線合併至壁材料中來達成密封。可在儲集器製造期間使用黏膠或密封劑來將導線密封在適當位置。 感測器可包含位準依賴性聲學諧振頻率感測器。儲集器可包含空腔。大體而言,取決於水填充位準,空腔(諸如樂器,諸如經部分填充之水瓶)各自具有諧振頻率,諸如基音。在實施例中,儲集器空腔具有取決於熔融金屬填充位準的諧振聲學頻率。頻率可隨著熔融金屬位準變化以及儲集器空氣之氣體填充部分相對金屬填充部分的體積變化而移位。可利用取決於填充位準的頻率而支援儲集器中之至少一個諧振聲波。可在給定操作條件(諸如儲集器及電池溫度)下使用填充位準及對應頻率校準感測器。 諧振聲學感測器可包含用以激發聲波(諸如駐聲波)之構件及用以偵測位準依賴聲波之頻率的聲學頻率分析器。用以激發儲集器空腔中之聲音的構件可包含機械、氣動、液壓、壓電、電磁、伺服馬達驅動源構件以可逆地使儲集器之壁變形。用以激發及接收儲集器空腔中之聲音中的至少一者的構件可包含驅動振動膜。該振動膜可使聲音傳播至儲集器中。振動膜可包含電池之組件,諸如EM泵、上部半球及下部半球中之至少一者。聲學激發源與用於聲學激發之組件之間的接觸可經由探測器,諸如對與組件之接觸點的溫度穩定的耐火材料探測器。用以激發儲集器空腔中之聲音的構件可包含發波器,諸如聲納發波器。頻率分析器可為麥克風,其可接收儲集器之諧振頻率回應作為穿過組件周圍的氣體的聲音。用以接收及分析聲音之構件可包含麥克風、換能器、壓力換能器、可藉由聲音變形且可具有殘餘電荷之電容器板,且可包含此項技術中已知之其他聲音分析器。在實施例中,用以引起儲集器之聲學激發之構件及用以接收諧振聲學頻率之構件中之至少一者可包含麥克風。麥克風可包含用以判定填充位準之頻率分析器。激發源及接收器中之至少一者可位於外部壓力容器5b3a外部。 在實施例中,聲學感測器包含聲音頻率之壓電換能器。感測器可經由聲音引導件(諸如中空導管或實心導管)接收聲音。聲音可用儲集器發波器激發。壓電換能器可包含汽車爆震感測器。爆震感測器可匹配具有處於所要位準之銀的儲集器之聲學諧振特性。可使用加速計判定諧振特徵。聲音導管導體可直接附接至儲集器及換能器。聲音導體可包含耐火材料,諸如鎢或碳。換能器可位於熱區之外,諸如在外部壓力容器5b3a之外。在例示性實施例中,爆震感測器經螺合至連接至聲音導體之外部容器5b3a的底板5b3b中的孔,該聲音導體在另一端與儲集器接觸。導管可沿著垂直軸線行進以避免線圈5f之運動。陷波濾波器可選擇性地傳遞適合於感測儲集器中的銀位準之頻率。控制器可調節EM泵電流以將銀位準變為所要位準,如自係位準之函數之頻率所判定。 聲學感測器可包含在儲集器內部之至少一個探測器或空腔。空腔可包含槽。套管可焊接至EM泵組合件5kk之基底。套管可為中空或實心的。探測器可包含閉端管或桿,其藉由扣件(諸如接頭套管)連接至EM泵組合件5kk之基底。可藉由發波器引起探測器或空腔振動。發波器可藉由連接桿(諸如耐火材料連接桿,諸如包含Mo、W或Ta或不鏽鋼的傳輸發波器之發波動作的連接桿)而定位於高溫區域外部。定向可為在振動激發下最有效的定向。振動感測器(諸如麥克風)可感測振動頻率,其中頻率為特徵且用於判定探測器或空氣周圍的熔融金屬位準。探測器或空腔可經選擇以促進對熔融金屬位準之聲學頻率感測。可校準熔融位準之頻率依賴性。可針對可量測之操作溫度來調節校準。能夠在高溫下再結晶之金屬探測器可經預加熱以在用作探測器之前使金屬再結晶。或者,聲學感測器可包含在單獨儲集器中之兩個匹配探測器(諸如兩個匹配再結晶的W導管),其中控制相對EM泵抽速率以匹配兩個探測器之頻率從而控制及匹配兩個儲集器中之熔融金屬的位準。感測器可進一步包含用於探測器之間隨平均頻率及操作溫度中之至少一者變化的任何偏移頻率的校準曲線。 探測器或空腔可包含耐火材料,諸如以下中之至少一者:Mo、鈦-鋯-鉬(TZM)、鉬-鉿-碳(MHC)、鉬-氧化鑭(ML)、鉬-ILQ (MoILQ)、鉬-鎢(MoW)、鉬-錸(MoRe)、鉬-銅(MoCu)、鉬-氧化鋯(MoZrO2 )、W、碳、Ta、氧化鋁、氧化鋯、MgO、SiC、BN及本發明之其他耐火金屬、合金及陶瓷以及此項技術中已知之耐火金屬、合金及及陶瓷。金屬探測器可包含電絕緣蓋或護套或電絕緣塗層(諸如富鋁紅柱石、SiC或本發明之另一者)以防止利用點火功率進行電弧擊穿。陶瓷探測器可包含中空空腔,諸如末端密封之中空管。陶瓷探測器可藉由螺紋接頭(諸如EM泵管組合件之基底上之匹配螺紋焊接套環)緊固至EM泵組合件之底部。其他例示性扣件包含鎖緊套環、夾鉗、固定螺釘套環或固持器及接頭套管固持器裝置。例示性陶瓷探測器包含向外開口之氮化硼(BN)管,其一端未開孔且另一端密封,該另一端旋擰進入焊接至EM泵管組合件之基底的螺紋不鏽鋼套環。探測器可進一步包含銷釘,其穿透EM泵組合件之基底及陶瓷探測器的密封端以穿透中空部分。銷釘可為螺紋式的。銷釘可旋擰至EM泵組合件之基底與陶瓷管之密封端中之至少一者中。管可包含氮化硼。銷釘可用於以下中之至少一者:沿探測器傳輸及接收聲能。探測器可包含壓電或微機電系統(MEMS),其中可藉由施加及感測壓電電壓或MEMS信號來達成對聲學頻率、振動及加速度中之至少一者的激勵及感測。感測器可包含加速度計,其量測熔融金屬阻尼加速度或探測器振動頻率。可使用相同裝置來達成激勵及感測。發波及感測構件可組合於同一裝置中。可控制熔融金屬位準以匹配單獨儲集器中之單獨探測器的聲學回應,其中任何偏移可藉由校準判定且用於匹配控制演算法中。 在實施例中,聲學感測器可包含發波器,其在EM泵管5k6之出口部分中激勵諸如振動之運動。激勵在所要頻率(諸如EM泵管之機械諧振頻率)下可為連續的或間斷的。EM泵管之末端可包含經附接振動阻尼器。消震器可包含橫切於EM泵管之縱向軸線的葉片。振動阻尼器可包含耐火材料。材料可為電絕緣體,諸如氮化硼或SiC。阻尼器可藉由扣件緊固至噴嘴5q。緊固可使用螺紋部件達成。螺紋阻尼器及噴嘴或EM泵管之末端可旋擰在一起。阻尼器可靠近熔融金屬之表面。阻尼器可浸沒或部分地高於金屬表面。阻尼器在熔融金屬中之深度可判定減振量。減振可藉由EM泵管再發射之聲能中之頻率、加速度或振幅變化中之至少一者量測。可在EM泵管上(諸如在儲集器之外的位置)感測所發射聲能。或者,可自儲集器壁感測所發射聲能。可附接至儲集器壁之具有高溫能力之導管可傳輸聲音。附接可包含螺紋旋進式連接或圍繞儲集器的夾持式套環。在實施例中,聲學感測器包含外部聲音抑制或抵消構件,其用以改良聲學信雜比。抑制構件可包含吸聲材料,諸如此項技術中已知之吸聲材料。消聲構件可包含主動消聲系統,諸如此項技術中已知之消聲系統。或者,諸如EM泵管或探測器等之儲集器內部之振動物體可將其振動傳輸至將以同樣方式振動之儲集器壁。儲集器壁振動可由偵測最初入射至振動壁之反射光之頻率或位置變化的裝置以電磁方式量測。入射電磁輻射可在具有高反射性之波長範圍中,諸如微波可見區域中。分析器可包含量測頻率變化之外差式計或干涉計或量測位置變化之位置感測器。分析器可包含將反射光束轉換成電氣信號之構件,諸如光伏打電池、光電二極體或光電晶體管。感測器可包含將頻率或位置變化處理成為熔融位準之函數的聲學信號之信號處理器。聲學感測器可包含可見光、紅外線或微波雷射干涉計麥克風。雷射可包含二極體雷射。依賴於由儲集器壁移動所引起之傳回或反射之雷射束之頻率變化(其中頻率變化由干涉量測術偵測)的例示性雷射麥克風由普林斯頓大學給出(http://www.princeton.edu/~romalis/PHYS210/Microphone/)。依賴於由儲集器壁移動引起之傳回或反射雷射束之位置變化之例示性雷射麥克風由Lucidscience(http://www.lucidscience.com/pro-laser%20spy%20device- 1 . aspx ; hackadayhttp://hackaday.com/2010/09/25/laser-mic-makes- eavesdropping - remarkably - simple / )給出。在另一實施例中,雷射脈衝之隨時間變化的飛行時間用於量測壁位移及聲學信號之頻率及振幅。聲學感測器可包含光偵測及測距(LIDAR)系統。可附接至儲集器壁之麥克風可量測壁振動。麥克風可包含壓電裝置。 聲學分析器可為本文所揭示內容中之一者,諸如麥克風及頻率分析器。可控制熔融位準匹配獨立儲集器之獨立感測器之聲學回應,其中任何偏移可由校準判定且用於匹配控制演算法。或者,感測器可包含探測器,該探測器在其末端進一步包含振動衰減器。由於任何熔融位準變化,衰減器可增大信號。 感測器可包含兩個平行板,該等平行板在EM泵組合件5kk之基座中引入電子感測連接通孔穿透。熔融金屬可將該等板填充至熔融位準。可由發波器引起金屬板振動。由於為該等板之間熔融位準之函數的振動頻率之改變,電感及電容中之至少一者改變。在另一實施例中,對接對之磁線圈及電容器板中之至少一者嵌入於電絕緣體套管中,諸如包含氮化硼之電絕緣套管。發波器可振動槽,且線圈或板之間的電感及電容中之至少一者可經由電連接件讀取,其中彼等參數為該對對接部件之間的位準之函數。可藉由將電流及電壓中之至少一者施加至線圈及板上而實現讀取。 位準感測器可包含光偵測及測距(LIDAR)系統,其中自感測器之發射器發射、自液面反射且由感測器之偵測器偵測到之雷射脈衝的飛行時間藉由感測器來量測以獲取熔融位準之位置。在另一實施例中,位準感測器可包含導引式雷達系統。不同頻率之電磁輻射(諸如雷達)可代替LIDAR系統之光。 在另一實施例中,位準感測器可包含超音波裝置,諸如包含藉由轉換發送至儲集器內部且自儲集器內部反射回之聲能脈衝之飛行時間感測熔融位準的超音波發射器及接收器的厚度規。聲音可垂直行進以感測熔融金屬之深度。發射器及接收器可位於EM泵組合件5kk之基座處以沿垂直或儲集器縱向軸線(亦被稱作z軸)發送及接收聲音。在另一實施例中,發射器及接收器可位於儲集器之側面處。聲音可沿橫向軸線或平面發送及接收。在位準攔截聲音時,反射可自儲集器相反壁或熔融金屬表面。發射器及接收器可包含沿z軸空間分離之成像該位準之複數個裝置。發射器及接收器可包含相同裝置,諸如壓電換能器。換能器可與EM泵組合件5kk之基座或儲集器壁直接接觸。或者,可使用可能夠在高溫下操作之聲音導管傳輸聲音。例示性厚度感測器為Elcometer MTG系列規(http :// www . elcometerusa . com / ultrasonic - ndt / Material - Thickness - Gauges / )。飛行時間資料可由經校準之處理器處理以自該資料判定金屬水平並控制相對EM泵速率從而控制儲集器位準。 在另一實施例中,位準感測器可包含此項技術中已知之至少一個短線感測器,諸如微波短線感測器。可在熔融位準區域內掃描短線感測器以偵測熔融位準。可藉由致動器實現掃描,諸如本發明或此項技術中已知的機械、機電、壓電、液壓、氣動或其它類型的致動器。或者,位準感測器可包含可藉由比較複數個短線感測器之間的信號而感測位準之複數個短線感測器。 在實施例中,位準感測器可包含渦流位準量測感測器(ECLMS)。ECLMS可包含至少三個線圈,諸如一個初級及兩個二級感測線圈。ECLMS可進一步包含高頻電流源,諸如RF源。可將RF電流施加至初級線圈以產生高頻磁場,該高頻磁場因此在熔融金屬表面產生渦流。渦流可感應可定位於初級線圈之任一側面上的兩個感測線圈中之電壓。感測線圈之電壓差隨感測器到金屬表面之不同距離而變化。可將ECLMS校準到熔融位準使其可在電池操作期間讀取位準。 感測器可包含回應於儲集器銀位準之阻抗計。阻抗計可包含回應於位準之函數之電感的線圈。線圈可包含電感耦合加熱器線圈。線圈可包含高溫或耐火金屬導線,諸如塗佈有高溫絕緣體之W或Mo。線圈之導線間距可為非絕緣導線不會電短路之間距。熔融銀可包含添加物,諸如鐵磁性或順磁性金屬或化合物,諸如此項技術中已知的金屬或化合物,從而提高電感回應。電感可藉由針對交流電波形驅動線圈所量測之電流與電壓之間的相移來量測。頻率可為諸如約5 kHz至1 MHz範圍內之射頻。 在實施例中,位準感測器可包含成像感測器,該成像感測器包含複數個發射器及接收器,該複數個發射器自複數個位置發射電磁信號,且該複數個接收器在複數個位置處接收信號以成像位準。可針對位準校準成像信號。發射器及接收器可包含天線,諸如RF天線。頻率範圍可在kHz到GHz範圍中。例示性範圍為5至10 GHz RF。成像感測器可包含RF陣列以自所反射信號構建資料。感測器可包含自原始資料提供密度類型反饋以識別位準之處理器。例示性成像感測器為包含使用穿過儲集器壁之射頻技術看起來像物體之可程式化3D感測器之Walabot。Walabot使用天線陣列照射其前方區域,並且感測傳回信號。由VYYR2401 A3系統單晶片積體電路產生並記錄信號。使用USB介面將資料傳達至主機裝置,該USB介面使用Cypress控制器實施。感測器可包含自電感耦合加熱器移除RF干擾之RF濾波器。 感測器可包含量測溫度量測裝置之間的溫度的一系列溫度量測裝置,諸如沿儲集器之垂直軸線隔開的熱敏電阻或熱電偶,其中該溫度跨越儲集器內部之熔融位準可量測地變化。在實施例中,感測器包含在儲集器內以不同高度空間分離之複數個熱電偶。所感測溫度為熔融銀位準之函數。熱電偶可包覆於可焊接至EM泵組合件5kk之底部的熱套管中。熱管可包含耐火材料,諸如本發明之Mo、Ta或另一元素。熱管可藉由諸如Swagelok之緊固件緊固。諸如本發明之彼等熱電偶可能夠承受高溫。多個熱電偶可在一個熱管中垂直地隔開。EM泵管5k6之出口可充當熱管。儲集器外部之EM泵管之穿透可包含此項技術中已知的穿透,諸如進入之Swagelok或電子饋入。熱電偶可由另一溫度感測器代替,諸如光學溫度感測器。 感測器可包含紅外線攝影機。紅外線溫度標記可跨越銀位準而變化。位準感測器可包含至少一個套管及電磁輻射源及對應偵測器。套管可包含進入儲集器5c內部之封閉式導管,該封閉式導管可附接於儲集器之基座處。附接可在EM泵組合件5kk之基座處。套管可包含電磁輻射透明材料,諸如電絕緣體,諸如氧化鋁、MgO、ZrO2 氮化硼及碳化矽。感測器可使用可穿過套管之壁且反射出熔融位準之電磁輻射照射套管內部。成像熔融位準之感測器可偵測所反射電磁輻射。電磁輻射可包含可跨越位準區域掃描之波束。感測器可包含處理所反射影像以判定熔融位準之處理器。所反射電磁輻射可照射電磁輻射偵測器上之區域。區域可隨位準、入射電磁輻射及偵測器之相對位置而改變。經照射偵測器區域之大小可回應於位準及與熔融位準之交點處之逐漸變小的套管之對應橫截面而改變。舉例來說,由於位準較高,反射可包含可具有較小直徑之環。可選擇感測器之電磁輻射來減小背景電磁輻射。感測器之電磁輻射可包含經加熱套管或電解槽之黑體輻射不具有相當大背景強度之波長。電磁輻射可包含紅外線、可見光及UV輻射中之至少一者。例示性波長範圍為約250 nm至320 nm,其中銀具有透射窗以使得由於銀之行而不是薄銀膜,反射為選擇性的。 在實施例中,感測器包含壓力感測器,其中壓力隨位準增大而增大。由於儲集器5c中之熔融金屬行之額外重量,壓力增大可歸因於排出壓力增大。 在實施例中,感測器包含偵測至少一個儲集器之重量之變化或儲集器之間的重心之變化的重量感測器,其中重量隨儲集器熔融位準增大而增大。儲集器之間的差分重量分佈使所量測之重心偏移。重量感測器可位於具有回應於對應儲集器中之質量之增大的位移或壓力變化之位置處。該位置可在對應儲集器之支架上。重量感測器可在儲集器內部,其中感測器可回應於隨熔融位準之重量及壓力變化中之至少一者。感測器可在可穿透電解槽之至少一個導線上傳輸其信號。可控制熔融位準以匹配獨立儲集器中之獨立探測器之重量或壓力,其中任何偏移可由校準判定且用於匹配控制演算法。導線可自儲集器內部之感測器延行至EM泵管5k6入口,且穿透儲集器5c外部之區段上之EM泵管5k6。穿透可使用諸如Swagelok之饋入通孔或固定件密封。重量感測器可包含需要具有最小位移之壓力的感測器。感測器可包含由熟習此項技術者已知的壓電式感測器或其他此類感測器。 在實施例中,重量或壓力感測器可容納於自高溫電解槽移除同時保持壓力或重量連續性之外殼中。壓力或重量連接性可藉由來自電池組件(諸如儲集器或EM泵管(諸如儲集器外之部分管))之熔融金屬連接件實現。熔融金屬連接件可包含具有比儲集器中之熔融金屬之密度更高的密度的熔融金屬行。舉例而言,包含於連接到儲集器外之EM泵管之管中的金行可連接至含有重量或壓力感測器之外殼。在實施例中,連續性連接件可包含具有比儲集器中之金屬之密度更高的密度及比儲集器中之金屬之金屬熔點更低之金屬熔點的金屬以便有助於在低溫下操作之重量或壓力感測器之使用。 回應於熔融金屬重量之位準感測器可包含天平,其中天平之傾斜隨銀位準而變化。該天平可包含兩個剛性連接之臂。臂可在支點附接至支架。該天平可在各臂之末端包含觸點。各觸點可鄰接儲集器底部上之振動膜或波紋管。振動膜可為凹陷的,諸如朝外凹陷以提供更多移動。振動膜可為半球形的。振動膜可隨對應儲集器中之熔融金屬之重量的變化而向下移位。臂或觸點之部分中之至少一者可電絕緣以防止電流在儲集器之間流動。天平可包含天平橫桿,在橫桿之各端具有附接活塞。活塞可包含電絕緣體。各活塞可在儲集器之基座中鄰接其振動膜。傾斜感測器(諸如位移、應力或扭轉感測器中之至少一者)可感測橫桿或臂之傾斜。傾斜感測器可包含自放大由傾斜感測器感測之傾斜的橫桿的延伸部。例示性傾斜感測器可包含自臂或天平橫桿之至少一部分到應變計之連接件。例示性天平包含金屬橫桿,諸如末端具有氧化鋁或氮化硼活塞之不鏽鋼橫桿。各活塞可在EM泵組合件之基座中與其焊入薄不鏽鋼振動膜接觸,其中傾斜可藉由應變計通過到橫桿之一端的連接件來量測。該連接件可准許應變計自SunCell®之高溫區域移除。在實施例中,連接件及活塞中之至少一者可包含亦可抵抗電感耦合加熱器之加熱的耐火材料。可調整天平以所要熔融金屬儲集器位準實現橫桿末端或臂之間的平衡。可藉由將重量添加到一個橫桿端或一個臂來實現平衡。 或者,支點之位置可調整。在實施例中,平衡型感測器進一步包含接收傾斜資料且調整EM泵電流以等化儲集器之熔融位準之處理器。包含平衡型之位準感測器可進一步包含用於諸如在原動力源SunCells®之情況下平移運動引發之力的感測器。平衡型位準感測器可進一步包含加速度計、MEMS裝置及陀螺儀中之至少一者以將資料提供至修改對傾斜資料之回應的處理器從而校正在相對EM泵速率之控制下外部平移引發之力。平衡型位準感測器可進一步包含振動抑制或抵消構件,諸如抑制安裝件或襯套、減震器及主動振動抵消系統中之至少一者,諸如此項技術中已知之彼等構件,從而減小外部振動之效應。 在實施例中,重量型位準感測器包含伸長計,諸如破裂開口位移(COD)規。例示性COD規為各自被應力規束之ε模型3548COD、3448COD、3549COD及3648COD伸長計中之一者。伸長計可包含接觸EM泵管組合件5kk中之振動膜之桿,諸如氧化鋁或碳化矽桿。伸長計可包含非接觸類型,諸如包含量測距離之雷射的非接觸類型。例示性感測器為ε模型LE-05及LE-15雷射伸長計,其中各自包含判定反射點之間的間距之高速雷射掃描器,諸如兩個振動膜中之各者上的反射點。振動膜可包含用於反射雷射束之反射表面。包含具有高熔點之非氧化反射箔片之例示性反射表面為Pt箔片(MP=1768℃)。可過濾伸長計信號以移除諸如來自振動之噪音。 在實施例中,振動膜包含EM泵組合件5kk之底部區域之大體部分以將對行高度變化及對應重量變化之靈敏度增至最大。在實施例中,相較於位移規或伸長計之加壓抗性或彈簧常量,振動膜具有對變形相對低之抗性。在此情形下,位準偵測變得對可改變其對變形之抗性的振動膜溫度更不敏感。在實施例中,振動膜包含改變其回應於變形之抗性之材料。振動膜可包含感測熔融位準隨校準電阻變化而變之變形的惠斯登電橋(Wheatstone bridge)之支腳。 在實施例中,位準感測器包含當位準為所要高度時至少部分浸沒於熔融金屬中之驅動機械探測器,熔融金屬抵抗驅動探測器之運動,且量測抗性為對自抗性判定位準之處理器的輸入。探測器可為旋轉及平移中之至少一者。探測器可包含耐火材料,諸如W、SiC、碳或BN。探測器可穿透EM泵組合件5kk處之儲集器5c。機械運動可由可能夠承受諸如962℃到1200℃高溫之軸承支援。感測器可包含准許縱向平移之波紋管。隨位準而變之抗性可使用應變計量測。 在實施例中,位準感測器包含量測電磁泵之取決於電磁泵處之熔融金屬排出壓力之至少一個電子參數的時差式電子參數感測器(諸如時差式電抗、阻抗、抗性、電感、電容、電壓、電流及功率感測器)中之至少一者。可改變至少一個電子參數,且可量測EM泵及電子參數回應,其中回應為排出壓力之函數。處理器可使用回應資料及查找校準資料集判定熔融位準。 在實施例中,發電機包含感測各儲集器中之熔融銀位準及調整EM泵電流以保持儲集器中之大約匹配位準之電路控制系統。控制系統可大約連續保持各EM泵上之最小注射壓力以使得對接熔融銀流相交以點火。在實施例中,注射系統包含相同平面中之兩個金屬流,其中流衝擊具有非匹配EM泵速度以使得可不定地控制速度從而保持匹配儲集器銀位準。在實施例中,發電機可包含一個儲集器上之位準感測器而不是包含兩個位準感測器,每個儲集器各一個。諸如銀之熔融金屬之總量在封閉式反應電解槽腔室5b31情況下為恆定的。因此,藉由量測一個儲集器中之位準,可判定另一儲集器中之位準。發電機可包含用於一個儲集器之EM泵之電路控制系統而不是包含兩個電路控制系統,每個儲集器之EM泵各一個。不具有位準感測器之儲集器之EM泵之電流可為固定的。或者,用於不具有位準感測器之儲集器之EM泵可包含回應於具有位準感測器之儲集器中所感測位準之電路控制系統。 可由於對應儲集器中熔融位準升高時增大之排出壓力發生通過EM泵之熔融金屬流動速率之自發增大。排出壓力可有助於泵壓並產生對流動速率之對應貢獻。在實施例中,儲集器高度足以提高包含最低與最高所要熔融位準之極值之間的充足排出壓力差從而提供用於至少一個EM泵之控制信號從而保持大約相等熔融位準。EM泵感測器可包含流動感測器,諸如勞侖茲力(Lorentz force)感測器或此項技術中已知之其他EM泵流動感測器。流動速率可由於排出壓力之變化,由於位準之變化而變化。至少一個流動速率參數,諸如個別EM泵流動速率、組合流動速率、個別差分流動速率、組合差分流動速率、相對流動速率、個別流動速率之變化率、組合流動速率之變化率、相對流動速率之變化率、其他流動速率量測值可用於感測至少一個儲集器中之熔融位準。所感測流動速率參數可與至少一個EM泵電流相比較以判定至少一個EM泵電流之控制調整從而保持大約相等之儲集器熔融位準。 在實施例中,下半球5b41可包含鏡面成像高度分級信道以直接自一個儲集器5 c上溢至另一儲集器並且進一步有助於諸如銀之熔融金屬返回到儲集器。在另一實施例中,位準藉由導管均等化,該導管將兩個儲集器在導管之各端處與滴液邊緣連接從而防止兩個儲集器之間的短路。過度充滿之儲集器中之銀通過導管流回另一儲集器從而將位準更大程度均等化。 在實施例中,儲集器5c之間的熔融位準藉由主動與被動機制中之至少一者基本上保持相同。主動機制可包含回應於藉由感測器量測之熔融位準來調整EM泵速率。被動機制可包含由於熔融位準在對應儲集器中升高時增大之排出壓力通過EM泵之熔融金屬速率的自發增大。排出壓力可有助於固定或變化之EM泵壓從而保持大約相等之儲集器位準。在實施例中,儲集器高度足以使包含最低與最高所要熔融位準之極值之間的充足排出壓力差增大從而使得儲集器位準在操作過程中保持大約相同。可由於差分流動速率,由於對應於儲集器之間的熔融位準之差的差分排出壓力而實現該保持。 在實施例中,EM泵包含入口立管5qa (圖2I138),在該入口立管上包含複數個熔融金屬入口開口或孔隙。入口立管5qa可包含中空導管,諸如管。導管可連接到EM泵磁體5k4之入口側上之EM泵管5k6。連接件可位於EM泵組合件5kk之基座處。連接件可包含本發明中之一者,諸如匹配螺紋或Swagelok。入口立管可包含耐火材料,諸如耐火金屬、碳或陶瓷,諸如W、Mo、SiC、氮化硼及本發明之其他耐火材料中之一者。入口立管可具有比噴嘴5q之高度更小之高度從而減小或消除點火電流之勢能從而電短接到進水升管。在實施例中,到入口立管之最低入口可具有比EM泵注射器之噴嘴5q之頂部更大之高度使得噴嘴保持浸沒。浸沒噴嘴可為可浸沒以保護其形成低能量氫反應電漿之正電極。入口立管可為非導管的。入口立管可塗佈有諸如本發明之塗層的塗層。塗層可為非導體。可包含諸如Mo之耐火金屬的入口立管可覆蓋有外皮或包層。外皮或包層可包含非導體。諸如BN外皮的外皮可藉由熱壓縮固持到入口立管。在實施例中,EM泵管組合件5kk之基座與進水升管5qa及EM泵管注射器5k61中之至少一者的活接中之至少一者可包含配對之螺紋結合。管可分別在EM泵管組合件5kk之基座處螺旋至EM泵之入口及出口。具有浸沒噴嘴之儲集器之例示性入口立管包含在EM泵出口處旋入EM泵組合件基座中之BN管;入口包含管之側面上之V形槽且開放式頂部以比噴嘴之尖端之高度更大的高度具有V底部使得噴嘴保持浸沒,其中噴嘴可包含正電極。在另一實施例中,進水升管之底部可包含可在EM泵組合件之基座處螺旋入或焊接至EM泵管出口之第一材料(諸如例如不鏽鋼之金屬或諸如Mo之耐火金屬),且進一步包含上部分,該上部分包含諸如非導體或塗佈或包覆有非導體之導體的第二材料。例示性上部進水升管區段包含可為螺旋入及壓縮擬合至下管部分中之至少一者的BN。 入口開口可從入口立管之上到下逐漸變小以藉由控制到EM泵之入口流速而自動控制泵速率及銀位準。在實施例中,入口立管5qa包含垂直隔開之開口使得隨著儲集器熔融位準增大,EM泵抽速率增大,其由於以下中之至少一個效應:(i)熔融金屬更快流動到入口立管中,因為總開口橫截面隨著熔融位準高度增大;(ii)入口立管中之熔融金屬高度隨著熔融位準增大而增大,熔融位準隨著EM泵排出壓力之對應增大而增大;及(iii)流動限制之減小,由於較大總開口橫截面或區域根據歐拉(Bernoulli's)等式減小任何對應壓降且可在無流動限制情況下入口流速限制將入口立管填充到其最大高度情況下進一步增加排出壓力。相比之下雙注射器電極系統之反入口立管及注射器可由於滴液相對熔融位準而經歷相反效應及對應的減小之EM泵抽速率。在對可在開口範圍內從上到下進行限定入口流動之複數個垂直隔開開口之替代實施例中,入口立管可在入口立管之頂端包含至少一個垂直槽,該等垂直槽可跨越諸如熔融位準之所要高度範圍之高度範圍。槽可將槽之寬度從上至下逐漸減小以使得對應流動限制具有熔融金屬高度。入口立管之頂部可為開放式或封閉式。在另一實施例中,複數個垂直隔開之進入單個EM泵入口管之孔洞中之各者可由對應入口管代替。在實施例中,複數個入口管在磁體5k4之前或之後組合,或其保持獨立使得其各自充當在熔融金屬以其特有高度流動到對應入口端中時選擇性地泵抽之個別EM泵注射器。在實施例中,EM泵可包含量測總電壓及電流或個別電壓及電流中之至少一者之電壓及電流感測器中之至少一者。處理器可使用感測器資料且控制總電壓及電流或個別電壓及電流中之至少一者從而控制總泵抽速率或個別泵抽速率。可選擇儲集器高度及平均熔融金屬深度以藉由經由開口之限制流動限定件達成所需排出壓力及排出壓力降中的至少一者。熔融金屬位準歸因於隨EM泵抽驅動雙熔融金屬噴射器電極之儲集器的相對熔融金屬位準變化的自動流入及對應泵抽速率調整而趨於平衡。每一噴射器之EM泵可設定為約恆定電流。該電流可足以使得反應物單元腔室5b31之約中心處之雙噴射金屬流與至遍及泵抽速率之任一側面偏心之區間的小型變體相交,引起位準更改及對應泵流入及EM泵抽速率。由每一EM泵電力供應器5k13供應之電流可設定為所需恆定位準。可替代地,SunCell®可包含EM泵電力供應器5k13、EM泵電力供應器電流感測器及控制器、點火電流感測器及處理器。每一EM泵電流可由其電流感測器感測且由控制器調整以得到如由點火電流感測器量測且由處理器處理之所需起始點火電流。點火控制器亦可控制點火功率參數。電流可維持在一範圍內,該範圍提供熔融金屬流在反應物單元腔室之約中部中之交叉的穩定性。在一例示性實施例中,電流維持在大於該流相交之閾限且低於使得一個流無相交存在下傳播至相對儲集器的位準。例每一EM泵電流之示性電流區間為約300 A至550 A。兩個泵之電流可相等。 EM泵速可由以下中的至少一者控制:入口流動速率控制器,藉由水平高度相關進液升管流入橫截面及藉由熔融金屬位準感測器;位準處理器;及EM泵電流控制器。EM泵電力供應器5k13之電阻、電流、電壓及功率中之至少一者之變化可藉由對應感測器感測,且可控制EM泵電流以進一步控制相對EM泵抽速率以達成儲集器熔融金屬位準之間的大致平衡。在一實施例中,EM泵5ka可包含功率限制器以在EM泵管5k6電阻歸因於較低熔融金屬裝入及流動而過度增大之情況下,防止EM泵管電阻過熱及對應高溫。 在一實施例中,進液升管開口可包含諸如入口防護件之保護件,該保護件係針對諸如炭或金屬氧化物顆粒之顆粒,該等顆粒可阻塞開口或堵塞進液升管及EM泵管5k6中的至少一者。在一例示性實施例中進液升管開口在進液升管頂部跨距大致1 cm,其中所需頂部熔融金屬水準在上一開口之頂部且最小開口略微大於最大腐蝕產物,同時對相對於未受限EM泵抽速率之流動之流動提供限制。 每一EM泵可由獨立電力供應器供電。可替代地,複數個EM泵(諸如兩個EM泵)可經由並聯電連接由共同電力供應器供電。每一泵之電流可由每一並聯電路之電流調節器控制。每一並聯電路可包含絕緣二極體以使得每一電路電絕緣。電絕緣可防止EM泵噴射器之間的點火功率之短接。在一實施例中,EM泵冷卻劑管線5k11可對EM泵組合件5ka兩者係共同的。在一實施例中,至少一個EM泵噴射器之噴嘴5q可浸沒在熔融銀中。該浸沒可至少部分防止噴嘴由電漿劣化。 噴嘴5q可低於熔融金屬位準以防止噴嘴由電漿損壞。可替代地,可抬升泵管之噴嘴段5k61,且噴嘴可包含側孔以使得朝向相對匹配噴嘴側向噴射,使得該等流相交。噴嘴可成角度放置以使得雙流之相交點在所需位置處。噴嘴可包含球面管端,其中一孔在該球面上之角位處,以將熔融金屬引導至反應物單元腔室5b31中之所需位置。在一實施例中,噴嘴5q包括延伸部以引導熔融金屬流之方向。延伸部可包含短管以藉由雙熔融金屬噴射系統之相對流使流朝向相交點流動。噴嘴管段(諸如耐火者,諸如包含W或Mo者)可係垂直的。其可包含至泵管之另一段的螺紋連接。其可包含至接頭套管或VCR接頭(諸如儲集器滲透5k9處之一者)之螺紋連接。噴嘴5q (諸如耐火者,諸如W或Mo者)可具有傾斜出口。噴嘴可藉由螺紋接合而接合泵管之噴嘴區段5k61。噴嘴中之旋擰可保持在所需位置處,該位置使得熔融金屬流在諸如固定螺釘或鎖緊螺母之緊固件附近或焊接件附近相交。焊接件可包含雷射焊接件。 在一實施例中,包含兩個儲集器及兩個EM泵(充當雙液體電極)之黑體輻射器5b41之下部半球劃分為由電絕緣密封件連接之至少兩個區段。密封件可包含凸緣、墊片及緊固件。墊片可包含電絕緣體。密封件可使兩個液體電極電絕緣。在一實施例中,兩個儲集器之間的電絕緣邊界可藉由將上部半球5b41及下部半球5b42之凸緣及墊片垂直地而非水平地定向來達成,使得黑體輻射器5b4包括垂直凸緣處接合的左及右半部。每一半部可包含黑體輻射器5b4及一個儲集器5c之垂直分割之半部。 在一實施例中,黑體輻射器5b41之下部半球包含具有緊固或連接至其之兩個儲集器5c的單獨片件。連接可各自包含螺紋活接或接合。每一儲集器5c可包含頂部處外表面上與下部半球5b41之螺紋配合之螺紋。螺紋可塗佈有使每一儲集器與下部半球至少部分電隔離之糊狀物或塗層,以進一步使兩個儲集器彼此電隔離。塗層可包含本發明中的一者,諸如ZrO。在一實施例中,電絕緣表面塗層可包含本發明之塗層或高溫材料,諸如ZrO、SiC及官能化石墨中的至少一者。絕緣表面塗層可包含陶瓷,諸如基於鋯之陶瓷。例示性氧化鋯塗層包含經氧化釔穩定化之氧化鋯,諸如3 wt%氧化釔。另一可能之鋯陶瓷塗層為二硼化鋯(ZrB2 )。表面塗層可藉由熱噴塗或本領域中已知的其他技術塗覆。塗層可包含浸漬石墨塗層。塗層可為多層。例示性多層塗層包含氧化鋯及氧化鋁之交替層。官能化石墨可包含封端石墨。封端石墨可包含H、F及O封端石墨中的至少一者。在一實施例中,至少一個儲集器可係電絕緣且至少另一個可與黑體輻射器5b41之下部半球電接觸使得下部半球可包含電極。下部半球可包含負電極。在一實施例中,每一儲集器5c與黑體輻射器5b41之下部半球之間的該連接遠離反應物單元腔室5b31,將該連接之此電絕緣塗層維持在低於諸如SiC或ZrO之塗層之熔融或分解溫度的溫度。 儲集器之間的電絕緣可藉由包含電絕緣體之間隔件(諸如碳化矽間隔件)來達成。下部半球5b41可包含至間隔件之經延長連接,該連接自下部半球之主體經充分延長使得該連接處之溫度適當低於間隔件之溫度。間隔件可由螺紋連接在經延長連接處且可連接至儲集器5c。至儲集器5c之連接可包含螺紋。間隔件可包含藉由螺紋連接至下部半球5b41之延伸部之碳化矽汽缸,且藉由螺紋連接至SiC圓柱形之相對端部處之儲集器5c。活接可由螺紋直接密封且可進一步包含密封件及墊片中的至少一者,諸如間隔件與下部半球之間的連接處的一者及間隔件與儲集器之間的連接處的一者。墊片可包含石墨(諸如坡莫合金-箔(Toyo Tanso)或柔性石墨),或由六角氮化硼構成之一者。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之一者,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)或本發明之另一種材料。SiC間隔件可包含結合反應物之SiC。包含螺紋之間隔件可初始地包含經碳化以形成螺紋SiC間隔件之Si。間隔件可結合至下部半球及對應儲集器之上部部分。該結合可包含化學鍵結。結合可包含SiC。SiC間隔件可熔合至碳組分,諸如對應下部半球及儲集器。該熔合可出現在高溫下。可替代地,結合可包含黏著劑。間隔件可包含滴水簷以防止熔融金屬之返回流動電短接儲集器。滴水簷可經機器加工或澆築到諸如SiC間隔件之間隔件中。可替代地,間隔件可包含凹槽以供插入諸如環盤形滴水簷之滴水簷。間隔件可包含其他耐火材料、本發明之電絕緣材料(諸如氧化鋯)、經氧化釔穩定化之氧化鋯及MgO。在一實施例中,點火系統包含安全截斷開關以感測雙儲集器-噴射器之間的電短路且終止點火功率以防止損壞噴射器(諸如噴嘴5q)。感測器可包含經由下部半球5b41之儲集器電路之間的電流之電流感測器。 在圖2I95至圖2I147中所展示之一實施例中,減少單元之接點之數目以避免故障之風險。在一實施例中,去除(i)下部半球5b41與上部半球5b42,(ii)下部半球與不導電間隔件及(iii)不導電間隔件與儲集器之間的接點中的至少一者。接點去除可藉由形成單一片件而非接合片件來達成。舉例來說,下部及上部半球可形成為包含單一半球形5b4。(i)下部半球與不導電間隔件及(ii)不導電間隔件與儲集器之間的至少一個接點可藉由形成單一片件來去除。 下部及上部半球可包含單一片件或兩個片件,其中(i)下部半球與不導電間隔件及(ii)不導電間隔件與儲集器之間的至少一個接點可藉由形成單一片件來去除。單一片件可藉由以下中之至少一種方法形成:澆鑄、模製、熔結、衝壓、3D印刷、放電加工、雷射切除機械加工、藉由化學蝕刻(諸如在包含氧氣之氛圍中碳氧燃燒之雷射點火)之雷射切除、氣動或液體機械加工(諸如噴水器機械加工)、化學或熱蝕刻、工具機械加工及此項技術中已知之其他方法。 在一實施例中,諸如黑體輻射器5b4 (諸如半球形黑體輻射器)及至少一個儲集器5c之電池組件的至少一個區段係不導電的。包含半球形5b4或下部半球5b41及上部半球5b42的儲集器5c及黑體輻射器中的至少一者之圓周區段可係不導電的或包含非導體。黑體輻射器之不導電區段可包含橫切於雙液體噴射器實施例之兩個噴嘴之間的管線的平面。非導體可藉由將組件之區段之材料轉化為不導電而形成。非導體可包含SiC或碳化硼(諸如B4 C)。電池組件之SiC或B4 C區段可藉由使碳電池組件分別與矽源或硼源反應而形成。舉例來說,碳儲集器可與液體矽或矽聚合物(諸如聚(甲基苯胺)中的至少一者反應以形成碳化矽區段。聚合物可在組件之所需區段處形成。可加熱電池組件。電流可經過組件以使得反應物形成不導電區段。不導電區段可藉由熟習此項技術者已知之其他方法形成。儲集器5c之外部表面可包含凸起圓周帶以在碳至碳化矽或碳化硼在所需區段中之轉化期間保持熔融矽或硼。碳化矽可藉由反應物鍵結而形成。自硼與碳形成碳化硼之例示性方法在https :// www . google . com / patents / US3914371 中給出,以上內容併入參考。碳化矽或碳化硼區段可藉由如https :// www3 . nd . edu /~ amoukasi / combustion _ synthesis _ of_silicon carbide . pdf 中給出之燃燒合成及Jesse C.Margiotta之Study Of Silicon Carbide Formation By Liquid Silicon Infiltration By Porous Carbon Structures形成,以上內容併入參考。其他適合之儲集器材料為不導電石墨(諸如熱解石墨或摻雜石墨)、SiC、氮化矽、碳化硼、氮化硼、氧化鋯、氧化鋁、AlN、AlN-BN (諸如SHAPAL Hi Msoft (Tokuyama Corporation))、二硼化鈦及其他高溫陶瓷。儲集器可為複合材料,其中不導電區段形成用於父儲集器材料(諸如碳)。儲集器可包含塗佈有諸如SiC、氧化鋯或氧化鋁之耐火材料電絕緣體的材料。經塗佈材料可為由塗層電絕緣之諸如碳之電導體。在一例示性實施例中,碳儲集器包含可為各向異性之諸如Minteq Pyroid SN/CN熱解石墨之連續成核石墨,其中低電導率可在橫向平面中,且儲集器之端部可塗佈有諸如SiC之非導體以防止電流沿縱向儲集器軸線流動。在一實施例中,多孔SiC儲集器可塗佈有碳以密封孔。可藉由來自諸如電碳弧之源的碳之氣相沈積塗佈。 如圖2I95至圖2I147中所展示,半球形54b及儲集器5c可包含單一片件。單一片件可藉由就愛那個電池組件之材料機械加工為單一片件來達成。可替代地,此實例中之單一片件可初始地包含由至少一個密封件接合的多個區段、部件或組件,該至少一個密封件可包含由密封件形成之膠合或化學結合密封件。本發明之其他片件、部件或組件可類似地經膠合或化學接合。例示性石墨膠為 Aremco Products, Inc. Graphi-Bond 551RN石墨黏著劑及具有Resbond 931黏合劑之Resbond 931粉末。儲集器靠近接近半球形之頂部可包含不導電區段。儲集器可連接至底板。儲集器可擱置到凹形套環中。僅套環之頂部之遠端的套環之外表面及儲集器之端部中的至少一者可帶螺紋。緊固在螺紋上之螺母可接合儲集器及底板。螺紋可傾斜使得螺母之旋轉一起拖曳儲集器及底板。在具有配合螺母螺紋之相對區段上螺紋可具有相對間距。 儲集器在底板5b8端部處可包含滑動螺母5k14,其中滑動螺母緊固在外螺紋底板套環5k15上以形成緊固接合。在一實施例中,滑動螺母可包含凹槽及墊片。滑動螺母可在凹槽處附接至儲集器。凹槽可經澆築或機器加工成圓柱形儲集器壁。O形環或墊片可壓入至凹槽中且滑動螺母可緊固在外螺紋底板套環5k15上以形成禁錮接合。外螺紋底板套環可經進一步楔形化以容納儲集器。 滑動螺母5k14緊固件可進一步包含墊片5k14a或O形環(諸如柔性石墨或坡莫合金-箔(Toyo Tanso)),或六角氮化硼墊片或陶瓷繩O形環以將儲集器密封至底板。BN儲集器5c壁之突出部可包含六角氮化硼墊片。BN墊片可經機器加工或澆築至BN儲集器5c之壁中。 墊片可包含與儲集器之材料相同的材料。墊片可旋擰到儲集器上。墊片可包含較寬寬度,諸如約1 mm至20 mm寬之寬度範圍。EM泵組合件5kk套環及滑動螺母之螺母可包含用於BN墊片之凸緣類安放表面。墊片可填充包含螺母、儲集器壁及EM泵組合件5kk套環之墊片支座之空腔。在一例示性實施例中,寬螺紋BN墊片旋擰到BN儲集器上,其中用於墊片之套環及螺母座在寬度上匹配以產生較大墊片安放及密封面積。BN墊片可用BN膠塗佈至滑動螺母密封件之空間填充空隙。例示性膠是Cotronics Durapot 810及Cotronics Durapot 820。 為避免包含碳之墊片形成諸如碳化鐵之碳化物的反應,包含鐵或諸如碳反應之金屬的其他材料之部件可塗佈有惰性塗層,諸如富鋁紅柱石、SiC、BN、MgO、矽酸鹽、鋁酸鹽、ZrO或本發明之其他材料。塗層可包含密封劑,諸如Cotronics Resbond 920陶瓷黏著劑、Cotronics Resbond 940LE陶瓷黏著劑或本發明中的一者。塗層可包含並不形成碳化物之金屬或元素,其中該等元素可包含合金元素,諸如鋼鐵中的合金元素。並不在鋼鐵中形成碳化物之例示性元素為Al、Co、Cu、N、Ni及Si。接觸碳(諸如碳墊片)之接合部件(諸如螺紋套環及滑動螺母接頭之螺母)可包含或可電鍍有並不形成碳化物或形成在電池工作溫度下不穩定之碳化物的金屬,諸如鎳。接頭部件可包覆有耐碳化物形成材料,諸如鎳。為避免形成碳化鐵之反應,在墊片接觸鐵或部件(諸如包含鐵之螺母)情況下,墊片可為除碳以外之材料。接頭部件可包含耐滲碳之不鏽鋼,諸如Hayes 230。 在一實施例中,EM泵組合件5kk可包含碳使得其與石墨滑動螺母墊片相容,其中該螺母亦可包含碳。EM泵管5k61之注射區段及進液升管5qa中的至少一者可包含碳。碳部件可藉由3D印刷、澆鑄、模製及機械加工中的至少一者形成。 應亦避免其他此類化學不相容性。墊片或O形環可包含諸如鎳、鉭或鈮之金屬。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之一者,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)或本發明之另一種材料。儲集器(諸如包含BN之儲集器)與EM泵組合件5kk (諸如包含不鏽鋼之EM泵組合件)之套環之間的接頭可包含諸如BN與金屬(諸如不鏽鋼)之間的鍵的化學鍵。在一實施例中,EM泵組合件套環之內部經BN塗佈,且隨後BN儲集器管藉由按壓接頭及加熱中的至少一者結合至套環之內部。化學鍵可藉由此項技術中已知之其他方法形成,諸如藉由如Yoo等人之「Diffusion bonding of boron nitride on metal substrates by plasma activated sintering process」,Scripta Materialia,第34卷,第9號, (1996),第1383頁至第1386頁,以上內容以其全文引用之方式併入本文中。接合部可包含由以下之群組之至少一種形成:施加壓力下擴散結合、熱噴塗或機械結合、使用P/M技術之燒結結合(諸如在可發生陶瓷粉末之熔結及結合到金屬基板上同時熱均衡加壓(HIP))及電漿輔助熔結(PAS)製程,以在熔結陶瓷層時在BN陶瓷層與金屬基板產生良好擴散結合。BN儲集器與金屬EM泵組合件套環之間的結合可包含黏結劑、化合物或具有氮化矽-氧化鋁及氮化鈦-氧化鋁陶瓷中的至少一者的複合陶瓷(諸如包含BN之複合陶瓷)、BN強化氧化鋁及氧化鋯、硼矽酸鹽玻璃、玻璃陶瓷、搪瓷,及具有硼化鈦、硼化鈦-氮化鋁及碳化矽-氮化硼組合物之陶瓷。接合部可包含滑動螺母或本發明之填充箱體類型。塗佈有黏結劑、化合物或複合陶瓷之諸如六角BN或氧化鋁-矽酸鹽纖維墊片的墊片可使用黏結劑在諸如熱及壓力之至少一個結合反應條件下化學結合(膠合)至表面粗化陶瓷儲集器(諸如BN儲集器)。墊片可包含六角BN或布或帶(諸如包含陶瓷纖維之一者),其包含高量氧化鋁及耐火材料氧化物(諸如Cotronics Corporation Ultra Temp 391),且黏結劑可包含諸如Cotronics Resbond陶瓷黏著劑(諸如Resbond 906)之密封劑。 在一實施例中,密封件可包含接頭套管。在一實施例中,密封件可包含Gyrolok,諸如包含前部套圈、後部套圈、對接密封件、主體及螺母中的至少一者的Gyrolok,其中前部套圈、後部套圈及對接密封件中的至少一者可包含諸如本發明中之一者的墊片。套圈可為倒角。密封件部件可與墊片化學相容;舉例來說,與碳墊片接觸之部件可包含鎳。 套環可包含內部錐形以容納儲集器,從而藉由滑動螺母之緊固壓緊墊片。儲集器可包含待由套環容納之外部錐形以藉由滑動螺母之緊固壓緊墊片。套環可包含外部錐形以藉由滑動螺母之緊固將張力施加至O形環。底板可包含碳。儲集器可包含筆直壁。儲集器壁可包含針對至少一個墊片之至少一個凹槽。除容納滑動螺母之套環之外部上的螺紋以外,EM泵管組合件5kk套環可內部帶螺紋以容納諸如包含氮化硼之儲集器之儲集器的端部上之匹配螺紋。螺紋可楔形化。螺紋可包含導管螺紋。 儲集器與EM泵管組合件5kk套環之間的活接可包含套環之內部部分與儲集器之間的內部墊片,諸如套環之內部底座與儲集器之端部之間的一個。儲集器端部可楔形化以截留墊片。錐形可將墊片截留在儲集器之外部壁與套環之內部壁之間。墊片密封件可在儲集器之底座處。密封墊及螺紋中的至少一者可經諸如Cotronics Resbond 920陶瓷黏著劑或Cotronics Resbond 940LE陶瓷黏著劑之密封劑進一步密封。 在一實施例中,活接可包含配合螺紋活接。儲集器及EM泵管組合件5kk套環可旋擰在一起。密封劑可將施加至螺紋。例示性密封劑為Cotronics Resbond 920陶瓷黏著劑及Cotronics Resbond 940LE陶瓷黏著劑。此活接或本發明之其他活接之螺紋可包含與接合部件中的至少一者形成合金之軟金屬。在一例示性實施例中,軟金屬可與套環形成合金,其中合金可具有高熔點。錫金屬可充當套環至儲集器螺紋之軟金屬密封劑,其中套環可包含鎳及鐵中的至少一者,且儲集器可包含氮化硼或碳化矽。套環可藉由來自以下之群組之至少一個方法塗佈有Sn:將套環浸漬在熔融錫中、氣相沈積及電鍍。 底板可包含藉由墊片中的至少一者至EM泵管(諸如接頭套管)的緊固件,諸如柔性石墨或坡莫合金-箔(Toyo Tanso)、六角氮化硼或矽酸鹽墊片及密封劑。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之一者,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)或本發明之另一種材料。可替代地,底板可包含諸如不鏽鋼或耐火金屬之金屬。EM泵管可藉由焊接緊固至金屬底板。可選擇底板金屬以使儲集器之熱膨脹與接合部件匹配。滑動螺母及墊片可接受底板之膨脹與儲集器組件的差別。 在一實施例中,上部滑動螺母可包含接合石墨下部半球5b41上之匹配螺紋的石墨。EM泵組合件5kk可包含不鏽鋼。下部滑動螺母可包含諸如Mo、W、Ni、Ti、或不同不鏽鋼類型之金屬,該金屬之熱膨脹係數比EM泵組合件不鏽鋼(SS)低,使得滑動螺母維持壓緊在滑動螺母墊片上。例示性組合為分別具有17.3×10- 6 m/mK及9.9×10- 6 m/mK之線性溫度膨脹係數的SS奧氏體(304)及SS鐵磁體(410)。可替代地,滑動螺母可包含膨脹係數類似於儲集器之材料。在儲集器為氮化硼或碳化矽之情況下,滑動螺母可包含石墨、氮化硼或碳化矽。滑動螺母接合部之至少一個組件(諸如EM泵組合件之螺紋部分)可包含熱膨脹凹槽。熱膨脹凹槽可允許在所需方向上熱膨脹,諸如使凹槽周向性變窄與徑向膨脹。在一實施例中,橫跨EM泵管組合件5kk之整個套環切割膨脹凹槽。切割可極薄使得其藉由套環之熱膨脹密封,其中添加或多或少以達成密封組合件工作溫度諸如約1000℃。切割可藉由諸如機械加工、噴水器切割及雷射切割之方式完成。螺母可包含碳、氮化硼或SiC。可選擇諸如碳或氮化硼之類型的材料類型以允許一些螺母膨脹,從而避免其在電池工作溫度(諸如約1000℃至1200℃之溫度範圍)下破裂。可選擇凹槽或切割之數目、置放及寬度以匹配電池工作溫度下之套環金屬膨脹量。在一實施例中,膨脹凹槽可為經由套環僅部分延伸,諸如延伸套環之寬度之50%至95%以防止熔融金屬洩漏。切割可自外螺紋向內延伸以允許套環之螺紋面積處之膨脹,其中滑動螺母之相對螺母螺紋在緊固螺母時配合。切割可基本上覆蓋在緊固螺母時由螺母覆蓋之螺紋套環之部分。切割可藉由諸如焊接之方式經由具有添加之金屬裏襯之材料的整個套環以提供擠壓或殘缺區。添加之裏襯金屬可為同一或不同金屬。添加之材料或金屬可係可延展的。 在一實施例中,諸如氮化硼管儲集器之儲集器5c與EM泵管組合件5kk之間的活接可包含壓縮配件。活接可包含內部螺紋EM泵管組合件套環、雙面螺紋圓筒形插入件及螺紋端儲集器。EM泵管組合件5kk之套環可包含具有第一熱膨脹係數之材料,諸如400不鏽鋼或410不鏽鋼。雙面螺紋圓筒形可包含具有可高於套環之熱膨脹係數的第二熱膨脹係數之材料,諸如304不鏽鋼。其他材料組合係可能的,諸如具有304 SS底板之304 SS或410 SS套環,其中304焊接於EM泵管5k6中;及包含在諸如約1000℃至1200℃中之一者的操作溫度範圍下不熔融之金屬之插入件,金屬諸如Ni、Ti、Nb、Mo、Ta、Co、W、304 SS或400 SS、410 SS、鎳鋼(FeNi36)、Inovco (F333Ni4.5Co)、FeNi42或科伐合金(FeNiCo合金)。儲集器管可旋擰至插入件之內部螺紋中,且插入件可旋擰至套環之內部中。或者,插入件可僅旋擰於內部上且可焊接至EM泵組合件5kk之基底處之套環。在一實施例中,套環之內部、插入件之外部、插入件之內部及儲集器中之至少兩者之間的至少一個活接不帶螺紋。在一實施例中,插入件具有比套環更高的熱膨脹係數;因此,插入件可朝內膨脹以壓縮儲集器管從而在其中配合插入件表面及套環表面與儲集器表面中之至少一者帶螺紋的情況下形成壓縮密封以及螺紋密封。壓縮插入件可藉由膨脹形成緊密密封以避免在配合表面之間形成間隙且不在可使其故障之儲集器管上造成過大壓力。在另一實施例中,活接包含壓縮密封,其中儲集器在具有或不具有封閉劑之情況下壓入配合至套環中。在一實施例中,加熱至少一個EM泵組合件-儲集器活接組件,諸如無螺紋套環、螺紋套環、螺紋插入件及無螺紋插入件之群組中之至少一者,以在將其配合或安裝至活接之對應組件或將其按壓至對應組件中之前使其膨脹。在一實施例中,冷卻至少一個EM泵組合件-儲集器活接組件,諸如螺紋插入件、無螺紋插入件及儲集器管之群組中之至少一者,以在將其配合或安裝至活接之對應組件或將其按壓至對應組件中之前使其收縮。可冷卻至低溫溫度。冷卻可藉由將組件暴露於諸如液氮之低溫劑來達成。對應活接可包含壓縮配件、螺紋配件及密封配件中之至少一者。在一實施例中,諸如BN管之儲集器管可置於EM泵組合件基底中之凹入式凹槽中。在另一實施例中,蓄水焊接或以化學方式結合至EM泵組合件基底。BN可藉由粗化BN表面及使焊接金屬流入對應孔隙中結合至金屬基底從而形成與金屬底板之結合。 例示性EM泵組合件-儲集器活接包含410 SS、鎳鋼(FeNi36)、Inovco (F333Ni4.5Co)、FeNi42或科伐合金(FeNiCo合金)套環,其中304 SS底板具有304 SS或鈮雙邊螺紋或無螺紋插入件與配合螺紋或無螺紋套環及BN儲集器,其中無螺紋部分可包含藉由差溫加熱或冷卻所達成之壓縮配件的部分形成之壓縮配件。 滑動螺母密封可包含複數個密封。滑動螺母密封可包含背對背滑動螺母。滑動螺母密封可包含標準螺母及上下顛倒之滑動螺母及墊片。在一實施例中,滑動螺母可包含上部螺母及下部螺母及包夾於其間之墊片,其中兩個螺母可旋擰至EM泵組合件5kk之套環之外部螺紋上。藉由旋擰螺紋而施加至墊片之壓力可將墊片推動至儲集器管5c中從而形成緊密壓縮密封。儲集器5c可包含經壓縮墊片之位置處的凹槽以更好地容納墊片且改良密封。儲集器與EM泵組合件之間的密封可包含壓蓋密封或填料箱密封。墊片可包含本發明之墊片。填料箱密封可進一步包含封閉劑,諸如包含惰性耐火細粉之封閉劑(諸如本公開之封閉劑)。封閉劑可具有高熱膨脹係數以在高溫下填充填料箱。在一實施例中,EM泵組合件基底可替換填料箱密封之底部螺母,其中滑動螺母可包含上部螺母。填充可為儲集器之圓周,其中儲集器可包含填充之凹部。儲集器可進一步包含滑動螺母內部之壓縮填充之上部凸緣。 在一實施例中,活接可僅僅包含外側螺紋儲集器,諸如旋擰至內部螺紋套環(諸如304不鏽鋼套環)中之氮化硼儲集器。本發明之活接(諸如儲集器與套環之間的活接)之螺紋可包含管道螺紋。活接可進一步包含螺紋封閉劑及滑動螺母密封件中之至少一者。例示性封閉劑為Cotronics Resbond 920陶瓷黏著劑及Cotronics Resbond 940LE陶瓷黏著劑。在一實施例中,封閉劑可包含與插入件或套環形成合金之軟金屬,其中該合金可具有高熔點。錫金屬可充當插入件或套環之包含鎳及鐵中之至少一者之軟金屬封閉劑。插入件及套環中之至少一者可藉由在熔融錫中浸漬插入件、氣相沈積及電鍍之群組中之至少一個方法用Sn塗佈。 在一實施例中,活接可包含本發明之活接,諸如螺紋活接或無螺紋活接(諸如壓縮密封件)中之至少一者,且活接可進一步包含密封件,其包含齊平鄰接EM泵組合件之基底上之儲集器的底部邊緣。儲集器底部邊緣與EM泵組合件基底之間的密封件可進一步包含墊片,諸如包含Celmet、MoS2 、或布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)之墊片。活接可進一步包含滑動螺母連接。儲集器管(諸如BN儲集器管)可包含較小上部外徑(OD)及較大下部外徑。在螺紋穿過EM泵組合件套環上之滑動螺母室外情況下,滑動螺母可藉由抵靠包含兩個直徑之凸緣而繃緊來將儲集器底部邊緣緊固至EM泵組合件基底。在另一實施例中,凸緣可由扣件(諸如擰緊之栓釘)替換以緊固螺母。包含螺母、螺紋套環及儲集器管之滑動螺母接頭可進一步包含凸緣頂部與螺母內部之間的墊片。凸緣墊片可包含Celmet、MoS2 或布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)。例示性活接包含410 SS套環、410 SS基底、在包含較小上部OD及較大下部OD之套環螺紋處具有凸緣之BN儲集器、410 SS滑動螺母及Celmet墊片,其中BN儲集器之下邊緣與EM泵組合件之基底鄰接,且該鄰接藉由隨著將滑動螺母旋擰至套環上而抵靠凸緣緊固滑動螺母來緊固。 在一實施例中,在圓頂5b4處由活接接合之儲集器可包含諸如陶瓷(諸如SiC、氮化矽、碳化硼、氮化硼、氧化鋯、氧化鋁或其他高溫陶瓷)之絕緣體。具有所需高熔點之例示性陶瓷為氧化鎂(MgO) (M.P.=2852℃)、氧化鋯(ZrO) (M.P.=2715℃)、氮化硼(BN) (M.P.=2973℃)、二氧化鋯(ZrO2 ) (M.P.=2715℃)、硼化鉿(HfB2 ) (M.P.=3380℃)、碳化鉿(HfC) (M.P.=3900℃)、Ta4 HfC5 (M.P.=4000℃)、Ta4 HfC5 TaX4 HfCX5 (4215℃)、氮化鉿(HfN) (M.P.=3385℃)、二硼化鋯(ZrB2 ) (M.P.=3246℃)、碳化鋯(ZrC) (M.P.=3400℃)、氮化鋯(ZrN) (M.P.=2950℃)、硼化鈦(TiB2 ) (M.P.=3225℃)、碳化鈦(TiC) (M.P.=3100℃)、氮化鈦(TiN) (M.P.=2950℃)、碳化矽(SiC) (M.P.=2820℃)、硼化鉭(TaB2 ) (M.P.=3040℃)、碳化鉭(TaC) (M.P.=3800℃)、氮化鉭(TaN) (M.P.=2700℃)、碳化鈮(NbC) (M.P.=3490℃)、氮化鈮(NbN) (M.P.=2573℃)。絕緣體儲集器5c可包含頂部處之滴落邊緣以藉由回流熔融金屬以防止電短路。活接可包含滑動螺母活接,諸如與儲集器與底板之間的滑動螺母活接相同類型之滑動螺母活接。滑動螺母可包含耐火材料(諸如碳、SiC、W、Ta)或另一耐火金屬中之至少一者。陶瓷儲集器可藉助於諸如鑽石工具研磨來研磨從而形成適合於達成滑動螺母密封之精密表面。在陶瓷儲集器(諸如包含氧化鋁管之陶瓷儲集器)之一實施例中,儲集器之至少一端可帶螺紋。螺紋可藉由附接螺紋套環來達成。螺紋套環可藉由黏著劑、黏結劑或膠附接。膠可包含陶瓷膠。 介接墊片或O形環之接合表面可經粗化或開槽以形成有高壓能力之密封。墊片或O形環可用封閉劑進一步密封。可將矽(諸如矽粉末或液體矽)添加至包含碳之墊片或O形環中,其中形成SiC之反應可在高溫下進行以形成化學鍵作為封閉劑。另一例示性封閉劑為石墨膠,諸如本發明之石墨膠。除形成墊片或O形環密封之滑動螺母以外,接合部分可包含配合螺紋以防止該等部分由於較高反應電解槽腔室壓力而分離。活接可進一步包含黑體輻射器5b4與儲集器5c或底板之底部之間的結構支架,以防止活接在內部壓力下分離。結構支架可包含至少一個將該等部分固持在一起之夾鉗。或者,結構支架可包含具有將黑體輻射器及儲集器或底板之底部螺栓在一起之端螺母的端螺桿,其中黑體輻射器及儲集器或底板之底部包含用於桿之結構錨。桿及螺母可包含碳。 在一實施例中,活接可包含至少一個端部凸緣及O形環或墊片密封。活接可包含滑動螺母或夾鉗。滑動螺母可在凸緣形成之前置於接合零件上。或者,滑動螺母可包含圍繞儲集器及套環中之至少一者自至少兩個零件焊接在一起的金屬(諸如不鏽鋼或耐火金屬)。 在一實施例中,黑體輻射器5b4之儲集器5c及底部套環及儲集器及底板——EM泵——噴射器組合件5kk中之至少一者可藉由螺紋(其可在相反儲集器末端及滑動螺母活接上具有相反間距)中之至少一者接合。螺紋活接之螺紋、滑動螺母之螺紋及滑動螺母墊片中之至少一者可藉由本發明之膠(諸如可用碳或碳膠形成SiC之矽)膠合。 在一實施例中,導電性較小或絕緣之儲集器(諸如SiC或B4 C儲集器)可替換碳儲集器。絕緣儲集器可包含(i)在頂部之連接至下半球5b41或單件式黑體輻射器圓頂5b4之螺紋及(ii)儲集器底部中之至少一者,其中儲集器及儲集器底部係一個整體件。SiC儲集器可藉由墊片及包含矽之封閉劑中之至少一者接合至碳下半球,其中矽酮可與碳反應以形成SiC。亦可使用此項技術中已知之其他封閉劑。儲集器底部可包含用於EM泵管扣件(諸如Swagelok扣件)之螺紋穿透件。儲集器底部可為單獨零件,諸如可包含金屬之底板。金屬底板可包含EM泵管在穿透件處之焊接接頭。底板可包含連接至儲集器之配合扣件(諸如滑動螺母)之螺紋套環。套環可錐形化以容納儲集器。套環楔形可在內部。儲集器末端可楔形化。儲集器楔形可在外部以容納於套環內部。扣件可包含諸如Graphoil或Perma-Foil (Toyo Tanso)、六方氮化硼或矽酸鹽墊片之墊片。墊片或O形環可包含諸如鎳、鉭或鈮之金屬。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之Celmet™,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391),或本發明之另一種材料。滑動螺母之緊固可向墊片施加壓縮。 在一實施例中,黑體輻射器5b4可包含一個整體件(諸如圓頂)或可包含上半球5b42及下半球5b41。圓頂5b4或下半球5b41可包含基底處之至少一個螺紋套環。螺紋可與儲集器5c配合。套環之活接及儲集器可包含旋擰至套環之內部螺紋中之儲集器上的外部螺紋或反之亦然。活接可進一步包含墊片。或者,活接可包含旋擰於套環上之外部螺紋上之儲集器上的滑動螺母。套環可包含末端處容納儲集器之內部楔形。活接可包含墊片,諸如Graphoil或Perma-Foil (Toyo Tanso)、六方氮化硼或矽酸鹽墊片、經按壓之MoS2 或WS2 、Celmet™ (諸如包含Co、Ni或鈦之Celmet™,諸如多孔Ni C6NC (Sumitomo Electric))、陶瓷繩或熟習此項技術者已知之其他高溫墊片材料,諸如布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)。墊片可安放在儲集器與套環之間的活接處。儲集器可包含諸如SiC、B4 C或氧化鋁之非導體。儲集器可經鑄造或機械加工。圓頂或下半球可包含碳。滑動螺母可包含耐火材料,諸如碳、SiC、W、Ta或其他耐火金屬或材料(諸如本發明之耐火金屬或材料)。 儲集器可進一步附接至EM泵末端處之底板組合件。活接可包含與黑體輻射器末端處相同的類型。底板組合件可包含(i)可在內部或外部帶螺紋以與匹配螺紋儲集器配合之活接套環、(ii)可在末端處內部楔形化以容納儲集器且在外部帶螺紋以與滑動螺母配對之活接套環、(iii)儲集器底部及(iv)其中穿透件可藉由焊縫接合之EM泵管組件。底板組合件及滑動螺母可包含不鏽鋼。在一實施例中,滑動螺母可附接至凸緣或凹槽處之儲集器。凹槽可經鑄造或機械加工成圓筒形儲集器壁。儲集器及套環兩者皆可在至少一個末端上包含凸緣,其中活接包含在接合零件之配合凸緣與夾鉗(其繞過凸緣且在緊固時將其拖曳在一起)之間的O形環或墊片。 在另一實施例中,密封或接合(諸如儲集器與EM泵組合件5kk之間的密封或接合)可包含濕封或冷封(圖2I139)。濕封可具有熔融碳酸鹽燃料電池濕封之設計。濕封可包含待接合之零件中之各者上的經配合凸緣,其形成熔融金屬之通道以填充諸如儲集器凸緣5k17及EM泵組合件套環凸緣5k19。在圖2I140中所示之另一實施例中,EM泵組合件套環凸緣5k19可進行以下中之至少一者:(i)與儲集器支撐板5b8配合,(ii)包含儲集器支撐板5b8,及(iii)包含儲集器支撐板5b8及EM泵組合件5kk1 (其包含EM泵管5k4之入口及出口)之基底。儲集器支撐板5b8可藉由錨定至支撐基底5b83之柱5b82支撐。在一實施例中,濕封冷卻器5k18包含儲集器支撐板5b8之周界及支撐柱5b82中之至少一者之冷卻器,其可散熱儲集器支撐板5b8之周界。儲集器凸緣5k17、儲集器支撐板5b8、EM泵套環凸緣5k19、無套環EM泵凸緣5k19、EM泵組合件5kk1之基底及儲集器5c中之至少一者在傾斜儲集器設計中可為傾斜的。凸緣可與扣件(諸如鉗夾、螺栓、螺釘、本發明之扣件及熟習此項技術者已知之扣件)接合。扣件穿透件、儲集器凸緣5k17及EM泵組合件套環凸緣5k19中之至少一者可包含用於差膨脹濕封部分及座架(諸如儲集器支撐板5b8之任何座架)之構件。濕封冷卻劑迴路5k18通道可徑向延伸,使得通道之外延區可保持在低於熔融金屬之熔點(諸如在銀之情況下低於962℃)的溫度下。固化金屬之濕封區域可包含與扣件(諸如螺栓5k20)接觸以避免在扣件處洩漏之區域。螺栓可包含碳且可進一步包含碳墊圈(諸如Perma-Foil或Graphoil墊圈)來充當膨脹襯墊。 在一例示性實施例中,濕封可包含儲集器5c上之套環凸緣,諸如氮化硼管,其可為在EM泵組合件5kk之套環上膠合上之套環凸緣及旋擰上之套環凸緣及焊接上之套環凸緣中之至少一者。濕封凸緣(諸如陶瓷儲集器之凸緣)可藉由將凸緣板(諸如BN凸緣板)旋擰及膠合至圓筒形儲集器(諸如BN儲集器)上中之至少一者形成。例示性膠為Cotronics Durapot 810及Cotronics Durapot 820。或者,濕封凸緣(諸如陶瓷儲集器之凸緣)可藉由模製、熱按壓及機械加工陶瓷(諸如BN)中之至少一者形成。BN組件(諸如儲集器5c、墊圈及儲集器凸緣5k17中之至少一者)可藉由熱按壓BN粉末以及後續機械加工製造。可將氧化硼添加至由氮化硼粉末製成的部分中以更好地壓縮。將BN特性(諸如熱膨脹、可壓縮性、及抗張強度及壓縮強度)改變成彼等期望特性之其他BN添加劑為CaO、B2 O3 、SiO2 、AUO3 、SiC、ZrO2 及AlN。氮化硼薄膜可藉由化學氣相沈積自三氯化硼及氮前驅體製造。氮化硼等級HBC及HBT不含黏合劑且可在達至3000℃下使用。 通道外邊緣可包含圓周同心帶。該帶可包含BN凸緣置於其中之EM泵組合件套環凸緣之外圓周緣。通道可經冷卻以對通道之入口處的周界及熔融金屬維持固態金屬。 接頭冷卻系統可包含本發明之接頭冷卻系統,諸如包含液體或氣體冷卻劑或輻射器之接頭冷卻系統。接頭可藉由至少一個冷卻劑迴路5k18在周界處冷卻。冷卻劑迴路5k18可包含來自EM泵冷卻熱交換器5k1之管線、冷卻劑管線5k11或冷板5k12。接頭可藉由至少一個散熱片(諸如輻射器或對流或導電鰭片)在周界處冷卻。接頭可藉由至少一個散熱管在周界處冷卻。例示性濕封冷卻器包含銅管冷卻劑迴路5k18,其中冷卻劑可包含水。凸緣中之至少一者可具有充當圓周冷卻迴路之通道的圓周凹槽。冷卻迴路可相對於圓周扣件(諸如螺栓)徑向向內以使熔融金屬自螺栓徑向向內固化。在一實施例中,EM泵組合件套環凸緣5k19及儲集器凸緣5k17可足夠寬以使得密封件之周界處之溫度低於熔融金屬之熔點,使得冷卻劑迴路5k18並非係必要的。EM泵組合件套環凸緣5k19可包含儲集器支撐板5k8。儲集器可傾斜於可為水平的儲集器凸緣5k17上。在其他實施例中凸緣5k17及5k19以及儲集器5c可相對於彼此處於任何所需角度以達成密封及將熔融金屬噴射至反應電解槽腔室5b31中。在一實施例中,凸緣(諸如5k17及5k19)之材料及厚度可測定熱傳遞且藉此冷卻。在一例示性實施例中,儲集器凸緣5k17與包含儲集器支撐板5b8、EM泵凸緣5k19及EM泵組合件基底5kk之板直接配合,該EM泵組合件基底進一步包含EM泵之EM泵管5k4之入口及出口,且儲集器凸緣5k17包含具有高熱導率之BN。板5k17及配合板5k19之厚度及寬度可經選擇以提供充足冷卻以維持濕封。密封可進一步包含本發明之冷卻器,諸如嵌入於至少一個凸緣5k17及5k19之周界中的冷卻劑迴路5k18。板5k17可包含具有可傾斜之經附接儲集器5c之套環。儲集器可藉由模製機械加工、旋擰及膠合中之至少一者附接至板凸緣5k17。 在一實施例中,傾斜(slanted/tilted)儲集器可包含適合於引起濕封在儲液器之基底處之所需分離的長度。濕封可包含覆蓋固化金屬部分之法拉弟籠以減少加熱此部分。濕封之配合凸緣、扣件及任何其他組件可包含對來自電感耦合加熱器之RF具有低吸收率之材料,諸如Mo及BN。濕封之冷卻迴路可至少冷卻濕封且可包含較大冷卻系統(諸如進一步冷卻儲集器5c、EM泵磁體5k4、EM泵管5k6及另一EM泵或電池組件中之至少一者)之分支。濕封冷卻系統可包含至少一個冷卻迴路、至少一個泵、至少一個溫度感測器,及冷卻劑流量控制器。 在一實施例中,配合凸緣密封可包含墊片。墊片可在栓固凸緣之間形成密封。墊片可包含密封至凹形組件之凸形組件。BN墊片可包含BN儲集器凸緣5k17之突起,其中BN墊片可包含凸形墊片組件。墊片可包含本發明之另一墊片,諸如氧化鋁-矽酸鹽陶瓷板墊片。 在另一實施例中,儲集器陶瓷(諸如BM)可包含金屬化陶瓷或金屬EM泵組合件5kk套環之硬焊密封中之至少一者。例示性金屬化材料及硬焊包含Ag、Ag-Cu、Cu、Mo-Mn、W-Mn、Mo-W-Mn、Mo-Mn-Ti、Cu基合金、Ni基合金、Ag基合金、Au基合金、Pd基合金及活性金屬硬焊合金中之至少一者。 在滑動螺母密封之一實施例中,螺母、螺母上之螺紋塗層及螺母之填充內部之群組中之至少一者包含與儲集器熔融金屬(諸如銀)形成具有比熔融金屬更高熔點之合金的元件。填充可包含粉末或包層,諸如金屬粉末或包層。密封可包含填料箱型密封,其中封閉劑包含填充或包層。封閉劑可包含墊片,其包含元素。元素可包含Pt、稀土、Er、Gd、Dy、Ho、Pd、Si、Y及Zr中之至少一者。 在一實施例中,密封可包含反向滑動螺母設計(圖141),其中螺母5k21旋擰於EM泵組合件5kk套環內部上,儲集器管5c在EM泵組合件5kk之套環5k15之外部上方滑動,且墊片5k14a位於儲集器管5c之內部圓周上。例示性墊片及儲集器管包含氮化硼。EM泵組合件5kk可包含不鏽鋼。反向滑動螺母密封可進一步包含可抵抗套環5k15及儲集器5c之膨脹力(諸如熱膨脹力)的壓縮保持套筒5k16 (諸如包含W、Mo或C之壓縮保持套筒) 密封可進一步包含反向壓縮型密封(圖142)。在一例示性實施例中EM泵組合件套環5k15隨著溫度自室溫升高而抵靠儲集器管5c膨脹。儲集器及EM泵組合件套環之材料可經選擇以具有所需熱膨脹係數,以達成壓縮密封且不破壞儲集器管。在反向壓縮型密封之一實施例中,密封進一步包含儲集器管5c周圍之壓縮保持套筒5k16以增加管的抗張強度。壓縮保持套筒5k16可具有所需低熱膨脹係數以防止儲集器5c由於EM泵組合件套環5k15內部膨脹而破裂。例示性壓縮保持套筒5k16可包含耐火材料,諸如W、Mo或C。例示性壓縮密封可包含薄壁套環5k16中之至少一者,其包含具有低熱膨脹係數之不鏽鋼,諸如410 SS、鎳鋼(FeNi36)、Inovco (F333Ni4.5Co)、FeNi42或科伐合金(FeNiCo合金),以減少熱膨脹從而防止BN儲集器5c及石墨壓縮保持套筒5k16開裂。 密封可包含反向滑動螺母及壓縮密封中之至少一者。在一實施例中,接頭(諸如反向滑動螺母及壓縮密封中之至少一者)可進一步包含螺紋部分,諸如在壓縮密封之情況下旋擰至外部儲集器管之內部之EM泵管套環的外部。在一實施例中,螺紋冠部可相對於螺紋凹部減低高度以包含沿壓縮接頭接觸區域之膨脹接頭。 底板及EM泵部分可經裝配以包含底板-EM泵-噴射器組合件5kk (圖2I98及圖2I147)。在雙熔融金屬噴射器實施例之情況下,發電機包含兩個電隔離底板-EM泵-噴射器組合件。電隔離可藉由實體分離該兩個組合件來達成。或者,兩個組合件藉由組合件之間的電絕緣來電隔離。雙液體噴射器實施例之噴嘴可對準。儲集器可倒置置放或處於倒置位置,且充當熔融金屬之金屬可經由至少一個儲集器之開口端添加至反應電解槽腔室中。隨後,底板-EM泵-噴射器組合件可連接至儲集器。該連接可藉由本發明之連接器(諸如濕封、壓縮或滑動螺母套環連接器)達成。底板-EM泵-噴射器組合件可包含不鏽鋼或耐火金屬(諸如Mo及W中之至少一者)中之至少一者。諸如連接器之EM泵管、儲集器底部、噴嘴、底板及配合套環的部分可經焊接及緊固在一起中之至少一者。扣件可包含螺紋活接。雙熔融噴射器實施例之兩個基底板5b8可藉由電絕緣板(諸如陶瓷板,諸如SiC、SiN、BN、BN+Ca、B4 C、氧化鋁或氧化鋯板)藉助於諸如扣件(諸如螺栓)連接以形成單個儲集器結構支架,其可由柱(諸如陶瓷柱或電絕緣410 SS、鎳鋼(FeNi36)、Inovco (F333Ni4.5Co)、FeNi42或科伐合金(FeNiCo合金)柱)升高以減弱熱膨脹效應。柱可包含管以減弱熱膨脹效應。在一實施例中,儲集器支撐板5b8可包含具有支架之單個或多個零件以形成連續板從而避免熱變形。儲集器結構支架可由可包含管以減弱熱膨脹效應之柱(諸如陶瓷柱或電絕緣410 SS、鎳鋼(FeNi36)、Inovco (F333Ni4.5Co)、FeNi42或科伐合金(FeNiCo合金)柱)升高。 在一實施例中,SunCell®包含儲集器位置調整系統或儲集器調節器以控制熔融金屬噴射器之對準。在包含雙熔融金屬噴射器之一實施例中,SunCell®包含使得支撐儲集器支撐板5b8之柱的長度調整對準噴嘴5q以使得兩個熔融流相交之構件。SunCell®可包含儲集器支撐板致動器,諸如機械致動器、氣動致動器、液壓致動器、電測致動器及壓電致動器中之至少一者,諸如本發明之儲集器支撐板致動器。噴嘴可能在加熱電池時由於儲集器支撐柱之差膨脹而丟失對準。為了避免熱膨脹造成未對準,柱可包含具有低熱膨脹係數之材料,諸如耐火材料。柱可經隔熱及冷卻中之至少一者以防止其膨脹。SunCell®可包含柱冷卻器,諸如熱交換器或導電或對流冷卻構件。冷卻可藉由沿柱導熱至散熱片來達成。SunCell®可包含藉由選擇性地控制柱之長度來對準噴嘴之構件,該等柱藉由控制及導致熱差膨脹或在不同柱之間收縮中之至少一者來支撐儲集器支撐板5b8。SunCell®可包含至少一或多個柱加熱器及柱冷卻器以選擇性地及以差動方式加熱或冷卻儲集器支撐柱,使得長度藉由膨脹或收縮選擇性地變化,從而使噴射器對準。 在一實施例中,SunCell®包含儲集器位置調整系統或儲集器調節器,諸如機械調節器,諸如可穿透殼體5b3a之推挽桿調節器。作用於殼體5b3a壁處之桿的螺紋機構可提供該推挽。調節器可提供沿或圍繞至少一個軸之移動。調節器可具有垂直地或水平地推動或牽拉至少一個儲集器或圍繞x軸、y軸或z軸旋轉其之能力。可執行調整以使得雙熔融金屬噴射器之熔融金屬流最佳地相交。在其中儲集器及EM泵組合件可藉由諸如濕封之手段穩固地連接之一實施例中,儲集器可在具有下半球5b41之儲集器5c之接頭處旋轉。儲集器中心5c軸及具有噴嘴之EM泵組合件5kk中心軸可沿相同軸。准許BN儲集器旋轉之例示性連接器為包含BN儲集器5c、石墨下半球5b41、石墨墊片及石墨螺母之滑動螺母連接器。h-BN及石墨兩者皆可包含潤滑劑。EM泵之連接件(諸如電流5k2及點火5k2a匯流排之彼等連接件)可包含諸如接頭或樞軸之構件,以使儲集器充分旋轉以造成噴射熔融金屬流之對準。匯流排可至少部分地包含堆疊薄片或纜線(諸如編結纜線)以准許對準運動。在一實施例中,在由控制器控制時調整EM泵電流可控制流之垂直位置,且流之橫向位置可由儲集器調節器控制。在其中儲集器穩固地固定之一實施例中,對準可實現為服務作業,其中部分拆卸SunCell®,對準噴嘴,且重新裝配SunCell®。 在包含雙熔融金屬噴射器之實施例中,來自一個噴嘴的熔融金屬流之軌道可處於第一平面,且來自第二噴嘴的熔融金屬流之軌道之平面可處於圍繞第一平面之兩個笛卡爾(Cartesian)軸中之至少一者旋轉的第二平面。該等流可沿傾斜路徑彼此接近。在一實施例中,第一噴嘴之熔融金屬流之軌道處於yz平面,且第二噴嘴可自yz平面側向地移動且朝向yz平面旋轉,使得該等流傾斜地接近。在本發明之例示性實施例中,第一噴嘴之熔融金屬流之軌道處於yz平面,且第二噴嘴之熔融金屬流之軌道處於由yz平面圍繞z軸之旋轉定義之平面,使得第二噴嘴可自yz平面側向地移動且朝向yz平面旋轉使得該等流傾斜地接近。在一實施例中,第一流高度及第二流高度處的軌跡交叉各自經調節以引起相交。在一實施例中,第二EM泵之出口管偏離第一EM泵套管之出口管,且第二EM泵之噴嘴朝向第一EM泵之噴嘴,使得熔融流彼此傾斜地接近,且流相交可藉由調節流之相對高度來達成。流高度可由諸如控制至少一個EM泵之EM泵電流之一者的控制器來控制。 在包含最初在同一yz平面中對準的兩個噴射器之兩個噴嘴的實施例中,達成噴射流之相交的噴射熔融金屬流之相對傾斜軌道可藉由使至少一個對應的儲集器5c略微圍繞z軸旋轉及藉由朝向yz平面旋轉而略微彎曲自yz平面平移之噴嘴的操作中之至少一個操作來達成。諸如餅狀部分之電感耦合加熱器天線5f可彎曲成非平面以適應對應的EM泵套管5k6。可視需要旋轉其他組件及連接件。舉例而言,亦可旋轉EM泵磁體5k4以維持其相對於EM泵套管5k6垂直的位置。 在另一實施例中,噴射系統可包含諸如使至少一股熔融金屬流偏轉以達成噴射流之對準的磁場及電場中之至少一者之源的場源。歸因於對應的導體經由所施加磁場之移動及諸如霍爾(Hall)及點火電流之至少一種電流與所施加磁場之間的力,噴射熔融金屬流中之至少一者可由勞侖茲力偏轉。偏轉可藉由控制磁場強度、熔融金屬流動速率及點火電流中之至少一者來控制。磁場可藉由永久磁體、電磁體(其可經冷卻)及超導磁體中之至少一者提供。磁場強度可藉由控制電流來控制磁體與熔融流之間的距離及磁場強度中之至少一者來控制。 量測點火電流或電阻可判定最佳交叉點。當電流在設定電壓或電阻最小時經最大化時,可獲得最佳對準。可包含可程式化邏輯控制器及電腦中之至少一者的控制器可達成最佳化。 在一實施例中,各儲集器可包含諸如電感耦合加熱器之加熱器以將諸如銀之儲集器金屬維持在至少啟動之熔融狀態下。發電機可進一步包含圍繞黑體輻射器之加熱器以防止諸如銀之熔融金屬至少在啟動期間黏附。在不需要黑體輻射器5b4加熱器之實施例中,諸如5b41及5b42之黑體輻射器可包含其未黏附有如銀之熔融金屬的材料。非黏附可發生在藉由來自儲集器5c加熱器之熱傳遞達成的溫度下。黑體輻射器可包含碳且可加熱至處於或高於諸如銀之熔融金屬在EM泵啟動之前未黏附之溫度。在一實施例中,黑體輻射器在啟動期間由儲集器加熱器加熱。黑體輻射器5b4壁可充分地厚以允許熱量自儲集器傳遞至黑體輻射器,從而允許黑體輻射器達成熔融金屬黏附至黑體輻射器之溫度以上及大於熔融金屬之熔點中之至少一者之溫度。在一實施例中,接近加熱之電池組件的電感耦合加熱器(ICH)天線(諸如捲繞在儲集器5c周圍)與電池組件很好地熱絕緣,其中來自ICH之RF輻射穿透絕緣體。熱絕緣體可將自電池組件至ICH天線之冷卻劑的熱流減少至所要流動速率。 系統進一步包含諸如電池(諸如鋰離子電池)之啟動功率/能源。可替代地,可經由自外部電源至發電機之連接件提供用於啟動的諸如柵極電源之外部電源。連接件可包含功率輸出匯流排。 在一實施例中,在啟動期間可由諸如至少一個熱燈之外部輻射加熱器加熱黑體輻射器。熱燈可在PV轉換器26a外部且可經由移除PV轉換器中之面板來提供輻射。可替代地,可在啟動期間加熱黑體輻射器,且可在電池連續運作且產生足夠的濾網以在維持分數氫反應之足夠的溫度下維持反應電解槽腔室5b31之後移除加熱器。 在電感耦合加熱器在加熱諸如陶瓷儲集器(諸如BN或SiC儲集器)之儲集器時效率低下之情況下,儲集器可包含能夠有效地吸收電感耦合加熱器輻射之耐火覆蓋物或套筒。吸收套筒之例示性RF包含碳。 發電機可包含用以應用及伸縮加熱器線圈及儲存加熱器線圈中之至少一者的諸如機械(諸如齒條及齒輪、螺釘、線性齒輪及其他本領域中已知的)、氣動、液壓及電磁系統中之至少一者的致動器5f1。電磁致動器可包含揚聲器機構。氣動及液壓可包含活塞。加熱器天線可包含允許伸縮的可撓性區段。例示性可撓性天線係銅編織的導線編織鐵氟龍套管。在一實施例中,外部壓力容器5b3a可包含容納經收縮天線之凹形腔室。 電感耦合加熱器天線5f可包含可移動的區段。電感耦合加熱器可包含各儲集器之可伸縮的至少一個線圈5f (圖2I84至圖2I152)。線圈可包含將濾網有效地施加至儲集器之形狀或幾何結構。例示性形狀係用於圓柱狀儲集器之托架或可調節式抓鬥(clamshell)。托架可在受熱期間將RF功率施加至對應的儲集器且此後可收縮。各托架可包含餅狀線圈且附接至共同餅狀線圈,該餅狀線圈定向於平行於由EM泵裝配5kk之EM泵套管在其底座下方形成之平面的平面中。各托架餅狀線圈可藉由可撓性或可擴展天線區段附接至共同餅狀線圈。共同餅狀線圈可附接至可安裝在致動器上的電感耦合加熱器電容器箱。可替代地,各托架可附接至對應的電容器箱及電感耦合加熱器,或兩個分離的電容器箱可連接至共同電感耦合加熱器。托架餅狀線圈、共同餅狀線圈、共同電容器箱及分離電容器箱中之至少一者可安裝或附接至致動器以達成在啟動之後儲存天線之動作。 在一實施例中,諸如電感耦合加熱器之加熱器包含單個可伸縮線圈5f (圖2I93至圖2I94、圖2I134至圖2I135及圖2I148至圖2I152)。線圈可為圍繞儲集器5c中之至少一者之圓周。加熱器可包含圍繞兩個儲集器5c之單個多捲曲線圈。加熱器可包含諸如15 kHz加熱器之低頻加熱器。加熱器之頻率可在約1 kHz至100 kHz、1 kHz至25 kHz及1 kHz至20 kHz的至少一個範圍內。單個線圈可為沿儲集器之豎軸可伸縮。線圈5f可藉由諸如本發明(諸如氣動、液壓、電磁、機械)中之一者之致動器或伺服馬達驅使之致動器、齒輪馬達驅動之致動器沿豎軸移動。線圈可用熟習此項技術者已知的機械裝置(諸如螺釘、齒條及齒輪)及活塞來移動。在彼此上方以機械方式移動之諸如齒輪齒或滑移部件之致動器部件可用諸如六方氮化硼、MoS2 或石墨之高溫潤滑劑潤滑。其他係滑石、氟化鈣、氟化鈰、二硫化鎢、軟金屬(銦、鉛、銀、錫)、聚四氟乙烯、一些固體氧化物、稀土氟化物及金剛石。線圈可在允許所要運動之一或多側或末端位置或其他適宜位置處安裝至致動器,同時不會使致動器過載負重。天線可經由可撓性天線區段連接至濾網供應器以允許移動。在一實施例中,電感耦合加熱器包含具有與加熱器之其餘部分分離之傳輸器組件之分裂單元。分單獨傳輸器組件可包含電容器/RF傳輸器。電容器/RF傳輸器可安裝在致動器上。電容器/RF傳輸器可藉由外部壓力容器腔室5b3a1中之可撓性電線及冷卻管線連接至加熱器之其餘部分。此等管線可穿過外部壓力容器5b3a之壁。電容器/RF傳輸器可安裝在連接至RF天線之致動器上,其中天線亦安裝在致動器上。電容器可安裝於可經冷卻之罩殼中。箱可包含熱反射塗層。罩殼可充當安裝燈具。箱可包含導軌及其他驅動機構之安裝托架。電感耦合加熱器可包含使用諸如一個6至12米長之長加熱器的並聯諧振模型加熱器。諸如冷卻板之熱交換器可在由天線冷卻管線提供之冷卻之情況下安裝在電容器/RF傳輸器上。致動器可由受控制器控制的電動伺服馬達或齒輪馬達驅動,該控制器可回應於溫度分佈輸入來獲得諸如儲集器5c、EM泵、下半球5b41及上半球5b42之發電機組件之所要溫度分佈。 在一實施例中,諸如電感耦合加熱器之加熱器包含單個可伸縮線圈5f (圖2I93至圖2I94、圖2I134至圖2I135及圖2I148至圖2I152),其係圍繞期望被加熱之電池組件之圓周,諸如黑體輻射器5b4、儲集器5c及諸如EM泵套管5k6之EM泵組件之至少一部分中之至少一者。在一實施例中,加熱器可在加熱期間固定。幾何結構及線圈匝密度可經組態以選擇性地將所要加熱功率施加至各電池組件或各電池組件之區域以達到諸如在970℃至1200℃之範圍內的組件或區域特定所要溫度範圍。歸因於先前加熱校準及加熱器設計,對電池上有限數目個點之溫度的監測提供電池上所監測點之溫度。在一實施例中,可控制加熱器功率及加熱持續時間以達到所要溫度範圍,其中可能不需要溫度監測。控制熔融金屬泵浦至反應電解槽腔室及點火功率之施加中之至少一者可控制加熱黑體輻射器。將輸入提供至溫度控制器之諸如熱電偶或光學溫度感測器之溫度感測器可監測黑體輻射器溫度。可經掃描之例示性光學溫度感測器係Ω iR2P。可替代地,EM泵浦及點火功率以及電感耦合加熱功率之定時順序可用於實現所要電池溫度分佈,諸如其中與熔融金屬接觸之電池組件之溫度高於金屬熔點之一者。 同時加熱所要電池組件之加熱器線圈5f可允許消除熱傳遞塊5k7、粒子絕緣體、粒子絕緣體儲集器5e1及控制系統中之至少一者以進行垂直移動加熱器及當垂直移動加熱器時控制加熱器功率位準中之至少一者。電感耦合加熱器5k4之磁體可包含RF屏蔽物及由冷卻系統(諸如包含EM泵冷卻劑管線5k11及EM泵冷板5k12之冷卻系統)提供之足夠冷的水中之至少一者,以防止磁體過熱至由EM泵套管5k6水平所施加之熱量所造成的磁化損耗之點。RF屏蔽物可包含多層RF反射材料,諸如可包含金屬箔片或濾網之高度導電材料,諸如Al、Cu或Ag。 在一實施例中,電感耦合加熱器屏蔽物可包含磁性材料,以使入射於EM泵磁體上之磁通量衰減。例示性磁性材料包含坡莫合金(Permalloy)或高電阻高導磁率合金(Mu-Metal),諸如具有高磁導率之基於鎳之金屬,諸如在低飽和度水平之情況下具有約300,000之滲透率之金屬。在加熱器所施加磁場強度高之實施例中,磁性材料可包含較高飽和度材料,諸如磁性金屬,諸如碳鋼或鎳。在一實施例中,歸因於永久性磁場經屏蔽金屬吸收且永久性磁場在EM泵套管中之液態金屬中減弱,磁性材料可具有將對永久性EM泵磁體之永久性磁場線之負面影響減到最小之設計及滲透率。在另一實施例中,屏蔽物包含法拉弟籠(Faraday cage) 5k1a (圖2I115),其包含圍繞預期被屏蔽組件(諸如EM泵磁體5k4)之高導電率金屬,諸如銅。諸如面板之法拉弟籠部件5ka1可用諸如高度導電的螺釘5k1b (諸如銅螺絲釘)之緊固件固定。在一實施例中,法拉弟籠5k1a不會影響永久磁體5k4之靜態磁場,使得籠型可完全包圍磁體。法拉弟籠可經冷卻。冷卻可藉由EM泵冷板5k12及EM泵冷卻劑管線5k11來提供。在一實施例中,冷板可包含用以冷卻聚光PV電池(諸如包含微通道之聚光PV電池)之設計。在一實施例中,各磁體可包含單獨的法拉弟籠(圖2I116)。法拉弟籠之壁厚可大於電感耦合加熱器之RF發射之穿透深度。在一實施例中,感應加熱頻率之穿透深度小於0.3 mm;因此,針對增加壁厚而增加屏蔽之屏蔽物,籠壁可厚於0.3 mm。在一實施例中,EM泵磁體5k4可包含引導磁通量穿過EM泵套管5k6之磁軛5k5或梯形磁體,且可進一步包含磁性電路,其中磁體5k4及磁體冷卻系統5k1可位於諸如中心在儲集器5c外部之部分EM泵套管5k6下方的位置。磁性電路可包含在EM泵桿體5k2之位置處引導磁通量橫切電流之磁軛。在一實施例中,磁體5k4可包含錐形磁體,其在電流沿z軸且泵沿y軸流送之情況下沿x軸經由EM泵套管5k6壁使高磁場富集。在一實施例中,諸如5k2及5k3中之至少一者之EM泵匯流排可包含能夠在高溫下運作之高度導電的導體,諸如Mo。磁性電路可包含EM泵磁體5k4、包含高度可滲透材料之芯體,該高度可滲透材料可進一步包含在其區段、用於EM泵套管5k6之電路的間隙與在間隙處經由EM泵套管5k6使磁通量富集之磁軛之間的磁體。芯體可包含諸如肥粒鐵之向上C形可滲透材料,其中間隙在C之開口中。在另一實施例中,EM泵包含具有複數個繞組之定子及含有待泵浦之熔融金屬之至少一個圓柱狀導管。在例示性實施例中,具有三對螺旋狀繞組之定子產生旋轉扭轉磁場。軸向推力以及所產生的旋轉扭力作用於圓柱狀導管中之熔融金屬。 在一實施例中,電感耦合加熱器線圈5f可進一步包含聚光器,以藉由增加電池組件或電池組件之區域中之對應的電流在所要區域中強化電磁場。例示性聚光器可包含高頻肥粒鐵及低頻墊片鋼。聚光器可用於實現電池之所要溫度分佈。在包含期望被加熱但不包含易於耦接至電感耦合加熱器之RF功率之材料的電池組件之實施例中,組件可用諸如碳之RF吸收材料包覆。包層可包含分裂或膨脹間隙,以適應不同熱係數之膨脹。例示性實施例包含圓柱狀BN儲集器5c,其經被分離以適應差異性熱膨脹之圓柱狀石墨套管包覆。 在一實施例中,可水冷卻之電感耦合加熱器天線線圈5f可包含對兩個儲集器為圓周的至少一個線圈及對黑體輻射器5b4之至少一部分為圓周的線圈或線圈之一部分。線圈可進一步包含至少一個餅狀線圈。餅狀線圈之平面可平行於儲集器外部的EM泵套管之平面。餅狀線圈可沿EM泵套管之外部部分的至少一側置放。餅狀線圈可加熱兩個EM泵套管。可替代地天線5f可包含複數個餅狀線圈,其中餅狀線圈可單獨或共同地加熱各個EM泵套管。餅狀線圈可沿發電機之豎軸伸縮。餅狀線圈可與儲集器線圈一起伸縮且可為儲集器線圈之一部分。天線可包含複數個單獨組件。天線可包含各自包含一對餅狀線圈的兩個天線。兩個餅狀線圈可各自包含加熱黑體輻射器之一部分及儲集器中之至少一者的上部線圈。上部餅狀線圈可圍繞經加熱之表面配適。例示性形狀分別係圍繞球面或橢圓黑體輻射器之底部的C形及圍繞圓柱狀儲集器之U形。線圈可沿複數個軸(諸如橫軸且接著豎軸)伸縮以在啟動之後經儲存。致動器可沿此等軸移動各天線5f以達成儲存。天線之連接部分可包含可撓性引水導管線,諸如可撓性金屬套管,諸如伸縮式套管。套管可包含銅。 在一實施例中,餅狀或其他線圈5f可包含至少一個可撓性區段。可撓性區段可允許線圈圍繞諸如法拉弟籠上之EM泵磁體5k4、磁軛5k5或突出物之電池組件收縮,該電池組件容納視情況包含磁通量聚集磁軛之至少一個磁體。可替代地,EM泵可包含可移動磁軛(諸如可在法拉弟籠外部可滑動之磁軛)及可在軌道上的可移動磁體5k4中之至少一者,以有助於餅狀線圈之伸縮。在一實施例中,諸如EM泵點火匯流排5k2a之區域處的EM泵套管5k6之加熱組件之區段可由電感耦合加熱器天線5f選擇性地加熱,藉由包含其線圈之一部分緊鄰組件的天線中之至少一者且藉由包含較佳耦接至RF場之材料的組件,諸如不鏽鋼或鉬上方之磁鋼。類似材料可與磁性金屬之躍遷附接一起附接。例示性附接件係焊接及螺栓及螺母緊固件。EM泵點火匯流排5k2a可包含焊接至不鏽鋼泵套管5k6之不鏽鋼及焊接或緊固至EM泵點火匯流排5k2a之不鏽鋼部分的磁鋼。在一實施例中,點火匯流排5k2a可附接至底板5b8。 天線線圈5f可包含至少一個捲曲迴路,其中線圈迴路可逆向延伸且可伸縮,使得線圈可緊鄰電池摺疊以實現良好的RF功率耦合且接著擴展以允許伸縮且儲存天線。天線儲存可用本發明之致動器實現。線圈之各迴路可包含可伸縮式或伸縮式區段。在一實施例中,天線線圈5f之至少一個迴路可逆向地擴展及伸縮。迴路可包含可伸縮式或伸縮式區段。水冷卻可經由將套管密封在線圈迴路之可逆向擴展及伸縮區段之內部獲得。套管可包含可插入引導線圈迴路之內部以至少橋連可逆向擴展及伸縮區段的鐵氟龍或其他高溫水套管。套管可包覆有導體,諸如可撓性導體,諸如編織金屬,諸如編織銅導線。例示性可撓性天線區段係導線編織鐵氟龍套管或彈性套管,諸如手術套管。導線編帶可包含銅編帶。可替代地,可延伸區段可包含諸如聚酯薄膜之金屬化塑膠。天線線圈5f可進一步包含使至少一個迴路擴展或伸縮之致動器。在一實施例中,可伸縮迴路以達成緊鄰經加熱電池組件,諸如儲集器。接近可實現對電池組件之較大RF耦接。相同或至少一個附加致動器可擴展迴路以允許相同或另一致動器移動線圈從而將其儲存。可垂直移動。可儲存在下腔室5b5中。線圈可藉由施加至天線線圈之水及真空壓力擴展及伸縮,其中電感耦合加熱器電源供應器及電容器之冷卻迴路可經螺線管閥旁通。致動器在散佈機上方移動彈簧負載線圈之朝下線性移動可擴展線圈。 在圖2I148至圖2I152中所展示之實施例中,圍繞雙熔融金屬噴射系統之兩個儲集器5c及黑體輻射器5b4之至少一部分中之至少一者的圓周線圈可逆向擴展及伸縮。線圈可沿軸向(沿電池垂直)延伸之線圈之每一迴路的兩個位置垂直分離。諸如導線(諸如絞合漆包線)之可撓性電連接器可橋連分離的迴路區段。導線可為高度導電的,諸如銅導線。導線可為耐火的,諸如W或Mo。諸如導線之各橋連件可藉由諸如傳導、對流及輻射之方式在外部經冷卻。橋連件可經由氣體冷卻,諸如具有高熱傳遞能力之氣體,諸如氦氣。橋連件氣體冷卻系統可包含強制對流或傳導系統。橋連件冷卻系統可包含外部熱交換器,諸如外部冷卻劑熱交換器。當處於摺疊位置時,諸如導線之橋連件可捲曲。橋連線圈可包含逆向延伸及伸縮之彈簧導線。在例示性實施例中,天線可包含耐火金屬彈簧,以使電感耦合加熱器天線之可伸縮線圈區段電跨接。跨接線可由氦氣冷卻或由其他外部系統冷卻,諸如與天線導線跨接線熱接觸之單獨的捲曲系統,諸如熱交換器。可替代地,跨接線可能不經主動冷卻。 在分離橢圓螺旋狀線圈之實施例中,相對分離線圈迴路區段之間的連接件包含接觸連接件(圖2I151至圖2I152)。接觸點可包含線圈迴路端板。相對線圈迴路區段之端部上的接觸點可包含陽極連接器5f4及陰極連接器5f5或熟習此項技術者所已知的其他電接觸連接器。接觸點可在其將分離線圈區段水平移入及移出接觸點時由致動器5f1接合及脫離。各陽極插塞連接器5f4可包含圓形或指針末端,使得當兩個天線半部滑在一起時其更容易地與陰極連接器5f5對準。經連接兩個半部天線區段可形成橢圓螺旋線。當處於閉合(經插入在一起)組態時,天線可作為具有經附接垂直平面餅狀線圈之橢圓螺旋線來操作。在另一實施例中,天線包含分離橢圓線圈,其中兩個區段中之每一者包含可視情況包含用於配對之電連接器的一對餅狀線圈之附接構件。當天線處於閉合(經插入在一起)組態時,天線可作為具有包含兩個經連接或未經連接區段之垂直平面餅狀線圈的橢圓螺旋線來操作。在閉合天線包含兩件餅狀線圈之兩個未經連接構件之情況下,各構件可包含水冷卻之連接器的單獨系統。在一實施例中,可藉由致動器逆向移動可進一步包含法拉弟籠5k1a之至少一個EM泵磁體5k4以適應分離天線的接合及脫離。磁體之伸縮可允許餅狀線圈在其由致動器移動期間通過。在餅狀線圈已經移動至其運作位置之後,磁體可經移動至運作位置,諸如緊鄰EM泵套管5k6。 分離線圈之各半部之線圈迴路可包含在垂直鄰接之線圈迴路端部之間延伸的水導管5f2。導管可相反螺合以旋擰至線圈之表面或邊緣。天線之迴路可由天線間隔件分隔開及支撐件5f3支援。在一實施例中,水導管5f2及線圈迴路區段提供用於諸如水之冷卻劑的連續流動路徑。冷卻劑導管可電絕緣或包含諸如高溫聚合物、陶瓷或玻璃之電絕緣體。冷卻劑導管可包含在線圈迴路處電絕緣的導體。冷卻劑導管可經熱屏蔽。例示性鐵氟龍或縮醛樹脂(Delrin acetal)水導管將各半部線圈之鄰接迴路區段之端部分別連接至水冷卻的各半部線圈。導管可藉由擠塑、射出模製、印模、銑削、加工及3D雷射印刷來製造。導管可連接至可經焊接至天線線圈迴路之冷卻劑套管。諸如鐵氟龍導管之水導管亦可充當結構支撐件。在一實施例中,水冷卻管通道在各迴路區段內可為雙向的。在一實施例中,天線可包含諸如鐵氟龍水導管5f2之單獨冷卻劑導管及結構支撐件或間隔件5f3。結構支撐件可包含耐火絕緣體間隔件,諸如其可進一步對熱衝擊具有抗性之氮化硼或氮化矽。在一實施例中,各半部線圈經連接至天線RF電源供應器90a之電容器箱。電連接件可經冷卻且充當冷卻劑管線。各半部線圈可進一步包含另一冷卻劑管線或連接件冷卻劑管線以充當導管以形成經由對應半部天線及諸如冷卻器之熱交換器之閉合冷卻劑迴路。連接件冷卻劑管線中之每一者可僅用於冷卻,其中各者可包含電絕緣體或可與天線電隔離。 在一實施例中,SunCell®包含包覆且加熱儲集器5c及至少一個餅狀線圈之諸如兩線圈之複數個天線,該至少一個餅狀線圈加熱EM泵套管5k6。各線圈可包含其自身電容器箱及濾網供應器中之至少一者。電源可包含功率分離器。天線可包含兩個上部C形線圈及至少一個餅狀線圈,該至少一餅狀線圈可包含諸如各者包含溫度感測器之單獨電源及單獨控制器,諸如紅外線感測器,諸如光學高溫計及功率控制器。當不操作時,線圈可由至少一個致動器伸縮。在一實施例中,諸如餅狀線圈或線圈之至少一個線圈在不使用時可排出冷卻劑且保持在運作位置(未伸縮)。線圈可包含泵、冷卻劑儲集器或供應器及控制器以在操作及儲存模式中分別逆向地添加及排出冷卻劑。 在一實施例中,SunCell®包含包覆且加熱儲集器5c及至少一個餅狀線圈之諸如兩個線圈之複數個天線,該至少一個餅狀線圈加熱EM泵套管5k6,其中各天線之截斷頻率經獨立調制以防止天線之間的耦接。天線中之至少一者可伸縮。SunCell®可包含至少一個致動器以實現伸縮。可替代地,至少一個天線可經固定。固定天線可充當次級角色作為熱交換器以在SunCell®濾網產生操作期間移除過熱。熱交換器天線可包含具有高熔點之導體,諸如耐火金屬,諸如鉬或本發明之另一者。天線可包含水或另一冷卻劑,諸如熔融金屬、熔融鹽或本發明或本領域中已知的另一者。固定天線之冷卻劑可在SunCell®啟動之後排出。可替代地,當運作以產生濾網時,冷卻劑可用於移除來自SunCell®之熱量。固定天線可用於在啟動期間加熱至少一個SunCell®組件且在濾網產生期間冷卻至少一個組件。SunCell®組件可為諸如EM泵5ka、儲集器5c及反應電解槽腔室5b31中之至少一者之電池組件,及諸如MHD噴嘴區段307、MHD發電機區段308、MHD凝聚區段309、回流管310、回流儲集器311、回流EM泵312及回流EM泵套管313中之至少一者之MHD轉換器之組件之群中之至少一者。 在一實施例中,天線5f可包含可將加熱功率傳遞至儲集器之RF耦接材料。RF耦接材料可包含碳。碳可包含適配於待填充空隙且形成天線及儲集器之天線中的塊。RF耦接材料可變形以允許在電池啟動之後儲存天線。碳塊可變形。碳塊可為可疊縮式。可疊縮式碳塊可經彈簧負載以提供對儲集器之良好RF耦接及熱接觸。碳塊可伸縮使得可儲存天線。石墨塊可由致動器系統延伸及收縮,諸如氣動、液壓、電子、機械系統或本發明之其他致動器。液壓系統可應用來自由冷卻劑泵所提供之天線冷卻劑之壓力,其中電感耦合加熱器冷卻迴路可使用螺線管閥旁通。氣動系統可應用由真空泵所提供之真空或壓力。機械致動器可包含齒條及齒輪或球形螺釘致動器或本發明之其他者。 各磁體可容納於單獨的法拉弟籠中(圖2I116)。在另一實施例中,餅狀線圈可塑形以具有各EM磁體下方之區段以允許其伸縮。在由EM泵套管定義之平面之一側上的可伸縮餅狀線圈可包含倒置雙背或環回C形線圈及雙背W形線圈中之至少一者,其中線圈在彼等位置處之各磁體下方穿過。諸如餅狀線圈之線圈5f可為諸如EM泵套管之加熱部分的圓周以增加加熱效率。當減少對磁體施加RF功率時,諸如圖2I151至圖2I152中所展示之雙背W形線圈之線圈可選擇性地加熱諸如入口側及出口側之各EM泵套管之至少一部分。為實現自雙背W形線圈至EM泵套管之良好RF功率傳遞,EM泵套管可在儲集器之間的中部充分分隔開,以允許天線之各支腳在天線之倒置V形區段中之對應泵套管外部延伸。EM泵套管及天線中之至少一者可藉由使用線圈套管彎曲之系統及方法來製造,以達成在天線線圈之泵套管內部之緊密適配。在另一實施例中,雙線圈之繞組以此類路徑沿天線線圈為外部-內部-外部-內部對比外部-外部-內部-內部方式在中部上方交叉。 諸如圓周及餅狀線圈中的至少一者的線圈5f可為電絕緣的。天線的管路可包含用以覆蓋更多表面區域以將加熱功率更佳地耦合至電池組件的寬平管。並不有效地吸收射頻功率的組件,諸如氮化硼儲集器,可覆蓋有RF吸收器覆蓋物,該RF吸收器覆蓋物可包含諸如碳的具有更佳RF耦合或吸收的材料。當諸如兩個圓周蛤殼的區段可藉由諸如W夾鉗、帶材或線材的扣件保持在適當位置時,可附接用於諸如BN儲集器的儲集器的間接RF加熱的碳。在一實施例中,蛤殼被設計成防止電池的電極化部件之間的電接觸以避免電短接。為避免形成碳化鐵之反應性,碳蛤殼不應與包含鐵之部件接觸;在蛤殼接觸鐵或諸如包含鐵之螺母之部件的情況下,蛤殼可包含除碳以外的材料。亦應避免其他此類化學不相容性。在一實施例中,RF吸收器覆蓋物可包含諸如碳織物、蜂巢或泡沫之材料,其用以自電感耦合加熱器吸收RF功率且充當熱絕緣件。天線電絕緣件可包含Fibrex、Kapton帶、環氧樹脂、陶瓷、石英、玻璃及水泥中之至少一者。至少一個線圈可在啟動之後收縮及儲存。儲存器可在腔室內部之容納黑體輻射器的第二室中。諸如髮夾或餅狀線圈的其他特殊幾何形狀的線圈(諸如沿儲集器外部的EM泵管之端部、側面或底部的部分之線圈)在本發明的範圍內。線圈中之任一者可包含聚光器。在另一實施例中,發電機包含複數個線圈致動器,其中用以加熱池之天線可包含可沿複數個軸收縮的複數個線圈。在一例示性實施例中,線圈可水平地收縮且隨後垂直地收縮。在一實施例中,發電機可包含至少一個EM泵管加熱器線圈及至少一個線圈致動器及至少一個EM泵磁體致動器。一或多個加熱器線圈可在EM泵磁體收縮之情況下加熱儲集器外部之EM泵管區段,一或多個線圈可藉由一或多個線圈致動器收縮,且一或多個EM泵磁體致動器可將EM泵磁體移動至適當位置以在EM泵管冷卻至諸如銀之內部熔融金屬的熔點以下之前支援泵抽。可協調線圈收縮及磁體定位之運動。該協調可藉由機械連接或藉由控制器(諸如包含電腦及感測器之控制器)來達成。 在一實施例中,EM泵管5k6可選擇性地經加熱同時藉由以下中之至少一者維持EM泵磁體5k4冷卻:(i)使用RF屏蔽及磁性防護罩或法拉弟籠(Faraday cage)中之至少一者來減小入射EM泵磁體之RF功率,(ii)使用聚光器來選擇性地強化EM泵管處之電磁場且因此增大RF電流並加熱EM泵管,其中聚光器之磁場可沿避免干擾EM泵的方向,諸如在EM泵電流的方向上或在EM泵管的方向上,(iii)使用選擇性地加熱EM泵管5k6之RF線圈5f,(iv)使用熱傳遞構件,諸如熱傳遞塊5k7、具有較大橫截面之EM泵管或散熱管,以將熱量自經加熱上部電池組件傳遞至較少加熱的EM泵管,及(v)增大藉由諸如電磁泵熱交換器5k1之冷卻器冷卻的磁體。儲集器底板可包含諸如陶瓷之材料,該材料阻止自電感耦合加熱器吸收RF,使得更多功率可藉由在對應區中施加之加熱選擇性地由EM泵管吸收。 加熱器線圈及電容器箱可安裝至在啟動期間可移動至加熱位置且在並未使用時收縮至儲存器室中之致動器。儲存器室可包含在外部壓力容器腔室5b3a1中之亦可含有功率調節器的區段。線圈可進一步用於水冷卻可冷卻功率調節器之儲存器室。用以移動加熱器之構件可包含本發明中的一者,諸如可安裝於加熱器儲存器室中之馬達驅動的滾珠螺桿或齒條及小齒輪機構。加熱器儲存器室可包含功率調節設備腔室。 在一實施例中,致動器可包含安裝於凹進腔室(諸如在外部壓力容器5b3b之底座中的一者)中之驅動機構,諸如伺服馬達。伺服馬達或齒輪馬達可驅動諸如螺桿、活塞或齒條及小齒輪的機械移動裝置。線圈5f及用於電感耦合加熱器之電容器中之至少一者可藉由移動裝置移動,其中該運動可藉由移動附接有移動組件之導向安裝件來達成。在一實施例中,致動器可至少部分地定位於外部壓力容器5b3a外部。致動器可至少部分地定位於外部壓力容器5b3b之底座外部。提昇機構可包含氣動、液壓、電磁、機械或伺服馬達驅動之機構中之至少一者。線圈可藉由熟習此項技術者已知之機械裝置移動,該等機械裝置諸如螺桿、齒條及小齒輪,及活塞。致動器可包含具有活塞穿透件之可密封在波紋管中的至少一個提昇活塞,其中用以垂直地移動活塞之機構可在壓力容器5b3a外部,諸如外部壓力容器5b3b之底座外部。此類型的例示性致動器包含諸如Veeco系統之MBE/MOCVD系統的致動器,該系統包含例示性快門葉片波紋管。在一實施例中,致動器可包含磁耦合機構,其中外部磁場可引起外部壓力容器5b3a內部之機械運動。磁耦合機構可包含外部馬達、外部永磁體或電磁體、內部永磁體或電磁體及機械移動裝置。外部馬達可引起外部磁體的旋轉。旋轉外部磁體可耦接至內部磁體以使得該內部磁體旋轉。內部磁體可連接至諸如齒條及小齒輪或螺桿的機械移動裝置,其中旋轉使得裝置移動線圈5f及電容器中之至少一者。致動器可包含旋轉磁場之電子外部源及內部磁性耦合器。在一實施例中,耦合至內部磁體之外部旋轉磁場可以電子方式獲得。旋轉外部場可藉由定子產生,且耦合可達至諸如電動馬達之一者的內部轉子。定子可為電子整流類型。在另一實施例中,以機械方式在彼此上方移動之致動器部件,諸如齒輪齒或滑移部件,可藉由諸如MoS2 或石墨之高溫潤滑劑潤滑。 在諸如圖2I95至圖2I149中所展示的一實施例中,諸如伺服馬達或齒輪馬達之馬達93可驅動機械移動裝置,諸如具有軸承94a之滾珠螺桿94、活塞、齒條及小齒輪,或懸浮於滑輪上之緊密纜線。天線及電感耦合加熱器致動器箱中之至少一者可附接至藉由驅動滑輪移動之纜線,該驅動滑輪藉由電動馬達旋轉。馬達93及諸如滾珠螺桿機構94之機械移動裝置之間的驅動連接件可包含齒輪箱92。諸如齒輪馬達之馬達及諸如齒條及小齒輪或滾珠及螺桿94之機械移動裝置及導軌92a可在外部壓力容器5b3a的內部或外部,諸如在外部壓力容器5b3b之底板外部,且可進一步包含線性軸承95及可具有高溫及高壓中之至少一者的軸承軸。線性軸承95可包含諸如Glyon之滑移材料。軸承軸可諸如穿過外部壓力容器5b3b之底板穿透外部壓力容器腔室5b3a1且附接至加熱器線圈5f及加熱器線圈電容器箱中之至少一者,以在該軸在向上或向下方向上藉由機械移動裝置垂直地驅動時引起其垂直運動。線性軸承可安裝於凹進腔室(諸如外部壓力容器5b3b之底座中之一者)中。軸承軸可穿過一孔穿透外部壓力容器5b3b之底板。線圈5f及用於電感耦合加熱器之電容器90a中之至少一者可藉由移動裝置移動,其中該運動可藉由移動附接有移動組件之導向安裝件來達成。 在一實施例中,電池組件(諸如下部半球5b41、上部半球5b42)、儲集器5c及連接器可能夠在諸如3000 K的黑體輻射器之操作溫度下經加壓至對應於10 atm的銀蒸氣壓之壓力。黑體輻射器可覆蓋有碳纖維之網狀瓶以維持高壓。外部壓力容器腔室5b3a1可能未加壓以平衡反應電解槽腔室5b31中之壓力。外部壓力容器可具有大氣壓或低於大氣壓。外部壓力容器腔室5b3a1可維持在真空下以避免至腔室壁的熱傳遞。致動器可包含在外部容器5b3a之底板5b3b處的用於藉由外部馬達驅動的轉向或傳動軸之穿透件的密封軸承,該外部馬達諸如藉由諸如電腦之控制器的伺服或步進馬達控制器。驅動系統可包含用於增加之轉矩、編碼器及控制器的步進馬達、確動皮帶、繃緊滑輪、驅動滑輪或齒輪箱中之至少一者。驅動軸可轉動齒輪,諸如蝸輪、斜齒輪、齒條及小齒輪、滾珠螺桿及螺母、傾斜盤或其他機械構件,以移動加熱器線圈5f。用於驅動軸穿透件之軸承可能夠相對於真空、大氣壓及高壓中之至少一者密封。軸承可能夠在高溫下操作。在一實施例中,軸承可藉由套環或管及凸緣配件自底板5b3b偏移以在較低操作溫度環境中定位軸承。 已充分確定與其液相平衡之任何氣體的蒸氣壓為與其接觸且平衡之最冷液體的蒸氣壓。在一實施例中,儲集器5c中的在其表面處與反應電解槽腔室5b31氛圍接觸之熔融金屬液體的溫度比反應電解槽腔室5b31溫度低得多,使得反應電解槽腔室5b31中之金屬蒸氣壓比在黑體輻射器之溫度下的銀蒸氣壓低得多。在一例示性實施例中,在其表面處與反應電解槽腔室5b31氛圍接觸之銀液的溫度在約2200℃至2800℃範圍內,使得反應電解槽腔室5b31中之銀蒸氣壓略高於其中高於此之壓力將導致在氣液界面處至液體的凝結的一種氛圍。在一實施例中,電池包含用以在反應電解槽腔室5b31與儲集器5c的內部之間建立高溫度梯度的構件。高溫度梯度可確保熔融金屬液體-蒸氣界面在充分地低於儲集器5c之熔點的溫度下。溫度亦可提供所要金屬蒸氣壓。溫度梯度構件可包含熱量屏蔽、擋板、絕緣件及儲集器直徑之變窄且使反應電解槽腔室5b31與儲集器5c之間的開口變窄中之至少一者。另一選項為使儲集器壁厚變窄,增大儲集器壁區域,及藉由熱交換器及諸如水冷卻輻射器之排熱器增加自儲集器之熱傳遞來維持儲集器冷卻中之至少一者。 在一實施例中,為增大自反應電解槽腔室5b31至儲集器5c液體金屬界面之熱梯度,其中反應電解槽腔室5b31中之電力主要藉由輻射傳遞且諸如銀之熔融金屬具有用於熔融金屬及其蒸氣之極低發射率,基本上來自反應電解槽腔室5b31之所有電力在液體銀界面處得以反射。在一實施例中,儲集器被設計成採用電力返回至反應電解槽腔室5b31中之反射。儲集器可包含反射器及擋板中之至少一者以藉由增加反射、減少傳導及減少對流之群組的機構中之至少一者在儲集器5c處產生溫度梯度。在另一實施例中,諸如銀之熔融金屬包含添加物,該添加物包含可漂浮在液體金屬之頂部上且改變界面處之發射率以增加電力反射的較低密度材料。添加物亦可起增大金屬蒸氣之凝結速率及降低金屬蒸氣之汽化率中之至少一個作用。 在一實施例中,電力可藉由饋通件供應至外部壓力容器腔室5b3a1,至腋系統電力供應器,該腋系統電力供應器為至少一個腋系統(諸如電感耦合加熱器、至少一個電磁泵、點火系統及至少一個真空泵中之至少一者)供電。在一實施例中,用以運行至少一個腋系統之電力藉由PV轉換器26a之輸出提供。腋系統電力供應器可包含至少一個功率調節器,該至少一個功率調節器自外部壓力容器腔室5b3a1內之PV轉換器26a接收電力輸出且為至少一個輔助系統供電。腋系統電力供應器可包含足以為寄生發電機負載(諸如電感耦合加熱器、至少一個電磁泵及點火系統中之彼等)提供電力之反相器。點火系統可藉由直接來自反相器或間接地在電力調節之後的AC電力供電。點火系統可由可藉由PV轉換器26a供應之DC電力供電。PV轉換器可為能夠輸出所要電壓及電流之電容器組充電,所要電壓及電流諸如在約1 V至100 V範圍內之電壓及在約10 A至100,000 A範圍內之電流。PV的主要電力可經由饋通件輸出為DC電力。寄生負載之對應外部饋通件可由包含來自PV轉換器之內部調節電力的內部電源替換。在一實施例中,外部壓力容器腔室5b3a1可包含容納至少一個功率調節器的功率調節設備腔室。功率調節設備腔室可為經熱量屏蔽、經熱絕緣及經冷卻中之至少一者。外部壓力容器5b3a可包含可在約大氣壓,諸如在加或減100%內之大氣壓下操作的殼體。外部壓力容器5b3a可為諸如矩形的任何所需形狀。 發電機可包含加熱器系統。加熱器系統可包含用以接收感測器輸入(諸如電池組件(諸如上部半球、下部半球、儲集器及EM泵組件之彼等)之溫度)的可移動加熱器、致動器、諸如熱電偶之溫度感測器及控制器。熱電偶可包含在熱電偶套管中之一者,該熱電偶套管提供對電池內部之溫度(諸如EM泵管內部的溫度及儲集器內部的溫度)中之至少一者的存取。熱電偶可穿過EM泵管的壁穿透至EM泵管及儲集器中之至少一者中。熱電偶可量測EM泵管及儲集器之連接器的溫度,諸如接頭套管溫度,該溫度可在EM泵管內部得以量測。接頭套管溫度可藉由外部熱電偶量測,該外部熱電偶藉由諸如接合構件之構件或諸如熱膏之熱導體具有與接頭套管表面的良好熱接觸。熱電偶可安裝於熱管中,該熱管諸如焊接在EM泵組合件5kk中之一者。控制器可進行以下中之至少一者:驅動致動器以移動加熱器線圈及控制加熱器功率以將電池組件之溫度控制在所要範圍內。範圍可各自高於熔融金屬之熔點且低於電池組件之熔點或故障點。熱電偶可能夠進行高溫操作,諸如由硒化鉛、鉭及此項技術中已知之其他組成的一者。熱電偶可經電隔離或偏壓以防止干擾諸如電感耦合加熱器之外部電源。電隔離可藉由諸如陶瓷外鞘之電絕緣的、能夠經受高溫的外鞘達成。熱電偶可由紅外溫度感測器替換。光學感測器可包含光纖溫度感測器。至少一個光纖纜線可將藉由黑體輻射器5b4發射之光傳輸至光學熱感測器以量測黑體輻射器5b4的溫度。可掃描的例示性光學溫度感測器為Ω iR2P。光學感測器可經空間地掃描以量測發電機上之複數個位置的溫度。空間掃描可藉由諸如本發明或熟習此項技術者已知的電磁或其他致動器之致動器來達成。 量測下部半球溫度及上部半球溫度中之至少一者的熱電偶可為可伸縮的。反應可在所量測溫度達至其操作的上限時發生。縮回器可包含機械、氣動、液壓、壓電、電磁、伺服馬達驅動的或熟習此項技術者已知之其他此類縮回器。收縮可在冷卻的PV轉換器內或離其更遠。下部半球及上部半球中之至少一者的高於熱電偶之操作溫度的溫度可藉由諸如高溫計之光學感測器或光譜儀中之至少一者及藉由PV轉換器回應量測。 在池啟動之後可降低線圈。底板5b3b可具有用於線圈5f及安裝在致動器上之對應電容器組中之至少一者的凹進外殼。線圈可包含水冷射頻(RF)天線。線圈可進一步充當用以提供冷卻水冷的熱交換器。線圈可用於在電磁泵的操作溫度歸因於自反應電解槽腔室5b31中之低能量氫反應加熱而變得過高時水冷電磁泵,其中熱量沿儲集器5c傳導至EM泵。諸如EM泵及儲集器之電池組件可絕緣以藉由減少或終止之加熱功率維持組件的所需溫度,其中天線亦可為非絕緣組件提供冷卻。例示性所需溫度高於藉由EM泵噴射之熔融金屬的熔點。 在一實施例中,必要時,諸如在啟動期間,電感耦合加熱器可延伸至EM泵區域以熱量EM泵管從而維持熔融金屬。磁體可包含用以反射來自電感耦合加熱器之加熱功率的主要部分的電磁輻射屏蔽。屏蔽可包含諸如包含鋁或銅之一者的高度導電覆蓋物。EM泵磁體可藉由RF反射器屏蔽以允許線圈5f在磁體的水平面上。避免加熱EM泵磁體可至少部分地藉由使用帶缺口的線圈設計來達成,其中該缺口在磁體位置處。電感耦合加熱器功率可隨EM泵功率減少而增加,且反之亦然,以維持穩定溫度從而避免引起EM泵及儲集器連接器螺紋失效之快速變化。 EM磁體5k4可包含用於內部冷卻之導管。內部冷卻系統可包含兩個同心水管線。水管線可包含將水傳送至磁體之EM泵管端的內部管及外部返回水管線。水管線可包含用以准許外部壓力容器5b3a之垂直出口穿過底座5b3b的彎管或彎頭。每一磁體之兩個同心內部水管線可在磁體的中心縱向軸線上。水管線可壓入磁體中之通道中。內部冷卻系統可進一步包含用以增加冷卻管線與磁體之間的熱接觸之熱傳遞膏。內部水冷管線可減小磁體冷卻系統的大小以允許加熱器線圈5f在EM泵之區域中垂直地移動。磁體可包含用以跨泵管提供軸向磁場同時進一步提供緊密設計之非線性幾何形狀。設計可允許線圈5f在磁體上方通過。磁體可包含具有L定向之L形狀,使得冷卻管線可在所要方向上經引導以提供緊密設計。水管線可朝向外部壓力容器5b3b之底座向下引導或諸如朝向兩個儲集器之間的中心水平地引導。考慮沿兩個儲集器之四個EM泵磁體的軸之後一情況的順時針圓形路徑。磁極可定向為S-N-S-N//S-N-S-N,其中//表明兩組EM泵磁體及一個EM泵相對於另一EM泵之電流定向可為反向的。其他緊密磁體冷卻設計在本發明之此類裝配磁體的冷卻劑夾套及線圈的範圍內。 EM泵可包含用以防止磁體藉由電感耦合加熱器線圈5f加熱之在EM泵磁體5k4處的RF屏蔽。當RF線圈5f以其中電感耦合加熱器的RF斷開之冷卻模式接觸屏蔽時,該屏蔽稍後可充當熱傳遞板。在另一實施例中,冷卻劑管線可穿過每一磁體穿透冷卻劑迴路中之磁體的側面。可使用其他冷卻劑幾何結構,其有利於自磁體移除熱量同時准許加熱器線圈在垂直地移動時通過該等其他冷卻劑幾何結構。 在一實施例中,加熱器藉由加熱儲集器5c及儲集器中所含之熔融金屬間接地加熱泵管5k6。熱量轉移至泵管,諸如具有穿過諸如銀之熔融金屬、儲集器壁及熱傳遞塊5k7中之至少一者的所施磁場的區段。EM泵可進一步包含諸如熱電偶或熱敏電阻之溫度感測器。溫度讀數可輸入至諸如可程式化邏輯控制器及加熱器電力控制器的控制系統,該控制系統讀取泵管溫度且控制加熱器以在熔融銀的情況下將溫度維持在諸如高於金屬之熔點(諸如熔融金屬之熔點100℃內)及低於泵管之熔點(諸如在1000℃至1050℃的範圍內)的所要範圍內。 諸如下部半球5b41、上部半球5b42、儲集器5c、熱傳遞塊5k7及EM泵管5k6中之至少一者的電池組件可為絕緣的。絕緣件在啟動之後可為抽取式的。絕緣件可為可再用的。絕緣件可包含顆粒、珠、粒及片中之至少一者,諸如包含MgO、CaO、二氧化矽、氧化鋁、諸如雲母之矽酸鹽及諸如沸石之矽酸鋁中之至少一者的一者。絕緣件可包含砂粒。絕緣件可經乾燥以移除水。絕緣件可保持在容器5e1 (圖2I102及圖2I103)中,該容器對於來自電感耦合加熱器之輻射可為透明的。容器可經組態以准許加熱器線圈5f沿垂直軸線移動。在一例示性實施例中,包含砂粒之絕緣件含於玻璃纖維或陶瓷容器5e1中,其中加熱器線圈可沿線圈5f內部之容器垂直地移動。顆粒絕緣容器5e1可包含入口5e2及出口5e3。絕緣件可經排出或加回以改變絕緣件。絕緣件可藉由重力排出容器。移除可使得絕緣件按自儲集器之頂部至EM泵管之底部的次序移除。絕緣件可按自距產生低能量氫反應之功率最近至最遠的次序移除。所移除絕緣件可儲存在絕緣件儲集器中。絕緣件可藉由將其返回至容器而回收。絕緣件可藉由機械構件及氣動構件中之至少一者返回。絕緣件可藉由螺旋鑽或輸送帶以機械方式移動。絕緣件可藉由風機或抽吸泵以氣動方式移動。絕緣件可藉由熟習此項技術者已知之其他構件移動。在一實施例中,諸如砂粒之顆粒絕緣件可由諸如銅丸之傳熱媒介替換,該傳熱媒介可在發電機啟動之後自儲存容器添加以自儲集器及EM泵中之至少一者移除熱量。熱傳遞可達至電感耦合加熱器的水冷天線。 反應自身可維持在諸如升高的電池溫度及電漿溫度中之至少一者的有反應條件下。反應條件可以充足速率支援熱解以維持溫度及低能量氫反應速率。在其中低能量氫反應變得自持的一實施例中,可終止至少一個啟動電源,諸如加熱器功率、點火功率及熔融金屬泵抽功率中之至少一者。在一實施例中,當電池溫度充分地升高以維持熔融金屬之充足高蒸氣壓時,可終止電磁泵,使得金屬泵抽並非維持所要低能量氫反應速率所需的。升高溫度可高於熔融金屬之沸點。在一例示性實施例中,包含黑體輻射器5b4之反應電解槽腔室的壁的溫度在約2900 K至3600 K範圍內,且熔融銀蒸氣壓在約5 atm至50 atm範圍內,其中反應電解槽腔室5b31充當回流熔融銀之鍋爐,如此EM泵功率可消除。在一實施例中,熔融金屬蒸氣壓足夠高,以使得金屬蒸氣充當用以消除對電弧電漿之需要且藉此對點火電流之需要的導電基質。在一實施例中,低能量氫反應提供熱量以將諸如儲集器5c、下部半球5b41及上部半球5b42之電池組件維持在所要升高溫度下,使得加熱器功率可移除。所需溫度可高於熔融金屬之熔點。在一實施例中,電池啟動可藉由諸如抽取式加熱器、點火及EM泵電源中之至少一者的至少一個抽取式電源達成。一旦開始,則電池可在連續操作中操作。在一實施例中,啟動可藉由諸如電池組及電容器(諸如超級電容器裝置)中之至少一者的能量儲存裝置達成。裝置可藉由發電機之電力輸出或藉由獨立電源充電。在一實施例中,發電機可在使用獨立啟動電力供應器的工廠處起動且在缺乏啟動電源供應器(諸如加熱器、點火及泵抽電力供應器中之至少一者)之連續操作中運送。 在例示性實施例中,SunCell®包含在碳儲集器中藉由雙重EM泵噴射至反應電解槽腔室5b31中的熔融鋁(M.P. = 660℃, B.P. = 2470℃)或熔融銀(M.P. = 962℃, B.P. = 2162℃),該反應電解槽腔室包含碳下部半球5b41及碳上部半球5b42,該雙重EM泵包含諸如Hayes 230之不鏽鋼、Ti、Nb、W、V及Zr扣件(諸如接頭套管5k9)中之至少一者,及諸如Haynes 230或SS 316之不鏽鋼、Ti、Nb、W、V及Zr EM泵管、碳或鐵熱傳遞塊5k7中之至少一者,噴嘴泵管(具有泵管及W噴嘴之定位焊接的W末端噴嘴區段5k61)之不鏽鋼、Ti、Nb、W、V及Zr初始區段中之至少一者。每一EM泵管可進一步包含用於連接至包含與EM泵管相同的金屬之電源2的端子的點火源匯流排。在一實施例中,點火系統可進一步包含電路,該電路包含在啟動期間在閉合時使點火源EM泵管匯流排短路以加熱泵管的開關。在電池操作期間處於打開位置之開關使得電流流動穿過相交之熔融金屬流。碳熱傳遞塊可包含用以用線劃分EM泵管之凹痕的熱傳遞碳粉末。儲集器可製得較長以減低諸如扣件5k9及EM泵管5k6之EM泵組件處的溫度。具有添加氫來源(諸如氬-H2 (3%))之HOH催化劑的氧化物源可包含CO、CO2 、LiVO3 、Al2 O3 及NaAlO2 中之至少一者。HOH可形成於點火電漿中。在一實施例中,與熔融鋁接觸之電池組件可包含諸如SiC或碳的陶瓷。儲集器及EM泵管及噴嘴可包含碳。組件可包含塗佈有諸如陶瓷之保護塗層的金屬,諸如不鏽鋼。例示性陶瓷塗層為本發明之彼等,諸如石墨、鋁矽酸鹽耐火材料、AlN、Al2 O3 、Si3 N4 及鋁氧氮陶瓷。在一實施例中,與熔融鋁接觸之電池組件可包含至少一種耐腐蝕材料,諸如Nb-30Ti-20W合金、Ti、Nb、W、V、Zr;及陶瓷,諸如石墨、鋁矽酸鹽耐火材料、AlN、Al2 O3 、Si3 N4 及SiAlON。 在一實施例中,分離器包含可位於兩個儲集器之接合區域處的EM泵。EM泵可包含電磁體及永磁體中之至少一者。EM泵匯流排上之電流及電磁體電流中之至少一者的極性可週期性地反向以將返回銀引導至一個儲集器且隨後至另一儲集器從而避免儲集器之間的電短路。在一實施例中,點火電路包含迫使電流在一個方向上穿過雙重EM泵噴射器液體電極的電二極體。 在一實施例中,由碳組成之電池組件塗佈有能夠在電池組件的操作溫度下維持約零蒸氣壓的諸如碳塗層之塗層。黑體輻射器之例示性操作溫度為3000 K。在一實施例中,用以抑制應用於諸如碳電池組件(諸如黑體輻射器5b4或儲集器5c)之外部表面的表面之昇華的塗層包含熱解石墨、裂解色譜(Pyrograph)塗層(Toyo Tanso)、石墨化塗層(Poco/Entegris)、碳化矽、TaC,或本發明或此項技術中已知的抑制昇華之另一塗層。塗層可在高溫下藉由在塗層上施加及維持高氣體壓力而穩定。在一實施例中,EM泵管5k6、電流匯流排5k2、熱傳遞塊5k7、噴嘴5q及配件5k9可包含Mo及W中之至少一者。在一實施例中,接頭套管型及VCR型配件5k9可包含碳,其中儲集器可包含碳。碳配件可包含諸如耐火金屬網狀物之襯墊或諸如W的箔片。在一實施例中,電極在饋通件10a處穿透壓力容器壁及黑體輻射器5b4的下部半球5b41及儲集器5c中之至少一者。電極8可藉由電極O形環鎖定螺母8a1鎖定在適當位置。電極匯流排9及10可經由匯流排集電器9a連接至電源。電極穿透件可用諸如ZrO的電絕緣體塗佈。由於C具有低導電性,電極可在穿透件(諸如在儲集器壁處的穿透件)處藉由諸如石墨膏的密封劑直接密封。替代地,電極可在穿透件處藉由VCR或接頭套管饋通件密封。具有不同熱膨脹係數的部件(諸如EM泵管與儲集器5c的底座及電極與儲集器壁之間的VCR型或型鍛式配件中之至少一者)的機械接合可包含可壓縮密封件,諸如碳墊片或墊圈,諸如Perma-Foil或Graphoil墊片或墊圈或六方氮化硼墊片。墊片可包含經按壓MoS2 、WS2 、Celmet™ (諸如包含Co、Ni或Ti之一者,諸如多孔Ni C6NC (Sumitomo Electric))、布或鏈布(諸如包含陶瓷纖維之布或鏈布,其包含高氧化鋁及耐火氧化物,諸如Cotronics Corporation Ultra Temp 391)或本發明之另一種材料。 在一例示性實施例中,反應電解槽腔室功率為400 kW,具有6吋直徑之碳黑體輻射器的操作溫度為3000 K,EM泵之泵抽速率為約10 cc/s,用以熔融銀之電感耦合加熱器功率為約3 kW,點火功率為約3 kW,EM泵功率為約500 W,反應電解槽氣體包含Ag蒸氣及氬/H2 (3%),外部腔室氣體包含氬/H2 (3%),且反應電解槽及外部腔室壓力各自為約10 atm。 外部壓力容器可經加壓以平衡反應電解槽腔室5b31的壓力,其中後一壓力歸因於諸如銀的基質金屬之汽化隨著溫度增大。壓力容器可最初經加壓,或壓力可隨著反應電解槽腔室溫度升高而增大。氫可添加至壓力容器以滲透至反應電解槽腔室中。在其中黑體輻射為各向同性碳的一實施例中,圓頂對氣體而言至少部分地可透以平衡壓力且為反應供應氫,該等氣體為諸如氫及惰性氣體(諸如氬)中之至少一者。在一實施例中,電力可藉由控制至流動反應電解槽腔室5b31中之低能量氫反應的氫受控。低能量氫反應可藉由吹掃或排空氫而停止。吹掃可藉由流動諸如氬氣的惰性氣體來達成。 SunCell®可包含在高壓下具有水以提供高壓氫之高壓水電解劑,諸如包含質子交換薄膜(proton exchange membrane,PEM)電解劑的一者。H2 及O2 腔室中之每一者可包含用以分別消除污染物O2 及H2 之複合器。PEM可充當陽極及陰極室之分離器及鹽橋中之至少一者,以允許在陰極處產生氫且在陽極處產生氧作為分離氣體。陰極可包含二硫屬化物析氫催化劑,諸如包含鈮及鉭中之至少一者的可進一步包含硫的一者。陰極可包含此項技術中已知的一者,諸如Pt或Ni。氫可在高壓下產生且可直接地或藉由滲透,諸如滲透黑體輻射器供應至反應電解槽腔室5b31。SunCell®可包含自陰極室至將氫氣傳送至電池之點的氫氣管線。SunCell®可包含自陽極室至將氧氣傳送至儲存容器或排氣孔之點的氧氣管線。在一實施例中,SunCell®包含感測器、處理器及電解電流控制器。感測器可感測以下中之至少一者:(i)諸如電解陰極室、氫管線、外部腔室5b3a1及反應電解槽腔室5b31之至少一個腔室中的氫壓,(ii) SunCell®之電力輸出,及(iii)電解電流。在一實施例中,至電池中之氫供應藉由控制電解電流受控。氫供應可隨著增加電解電流增大,且反之亦然。氫可為在高壓下及包含低庫存中之至少一者,使得至電池之氫供應可藉由控制電解電流以快速時間回應受控。 在另一實施例中,氫可藉由使用所供應水及由SunCell®產生之熱量熱解來產生。熱解循環可包含本發明或此項技術中已知的一種中之一者,諸如基於金屬及其氧化物(諸如SnO/Sn及ZnO/Zn中之至少一者)的一者。在其中電感耦合加熱器、EM泵及點火系統僅在啟動期間消耗功率的一實施例中,氫可藉由熱解產生,使得寄生電力要求極低。SunCell®可包含用以提供電力以運行諸如氣體感測器及控制系統之系統的諸如鋰離子電池組的電池組,該等控制系統諸如用於反應電漿氣體的彼等。 反應腔室5b31之壓力可藉由量測至少一個電池組件因內部壓力所致的延伸或移位來量測。因內部壓力所致的延伸或移位可在給定反應腔室5b31溫度下藉由量測隨由給定反應腔室溫度下的不凝結氣體引起的內部壓力而變化的此等參數中之至少一者經校準。 在一實施例中,石墨電池組件的塗層,諸如黑體輻射器、儲集器及VCR型配件的表面可包含熱解石墨、碳化矽或本發明或此項技術中已知的不與氫的發生反應之另一塗層。塗層可在高溫下藉由在塗層上施加及維持高氣體壓力而穩定。 在一實施例中,負(還原)電位應用於可經受與H2 O及氧中之至少一者的氧化反應的電池組件,諸如黑體輻射器5b4、儲集器5c及泵管中之至少一者。產生器可包含用以將負電壓施加至電池組件的電壓源、至少兩個電導線、導電基質、正電極及相對電極。在一實施例中,黑體輻射器5b4、一個儲集器5c及一個EM泵5ka中之至少一者可藉由負電壓或還原電壓加偏壓。該對電極8的負電極可包含一個EM泵5ka、黑體輻射器5b4及一個儲集器5c的群組中之至少一個組件,使得組件藉由負電壓或還原電壓加偏壓。電極8可包含熔融金屬噴射器電極。導電基質可包含電漿及金屬蒸氣中之至少一者。 正熔融電極可包含第一EM泵5ka及第一儲集器5c,該第一儲集器與黑體輻射器5b4、另一或第二儲集器5c及另一或第二EM泵5ka中之至少一者電隔離。第一儲集器5c可至少部分地包含電絕緣體。第一EM泵5ka的點火功率及正偏壓中的至少一者可由電源2供應。可浸沒第一正偏壓EM泵5ka的第一噴射器噴嘴5q。浸沒可減少或防止電漿及水反應中的至少一者對噴嘴的損壞。 黑體輻射器5b4、第二儲集器5c及第二EM泵5ka中之至少一者可藉由負電壓或還原電壓加偏壓。可藉由電源2供應針對黑體輻射器5b4、第二儲集器5c及第二EM泵5ka中之至少一者之點火功率及負偏壓中之至少一者。第二儲集器可包含電導體,諸如石墨。替代地,第二儲集器可包含電絕緣體,且電池其進一步包含自負偏壓來源(諸如點火電磁匯流排5k2a)至黑體輻射器5b4的電短路。短路可包含EM泵組合件5kk之導電部分與黑體輻射器5b4之間的電導體。例示性短路包含施加至氮化硼管之石墨貝殼掀蓋,其中貝殼掀蓋接觸EM泵組合件5kk及黑體輻射器5b4。貝殼掀蓋亦可有助於自電感耦合加熱器吸收RF輻射。黑體輻射器5b4、第二儲集器5c及第二EM泵5ka可在負偏壓下電性連接。 負偏壓可足以防止黑體輻射器5b4、第二儲集器5c及第二EM泵5ka中之至少一者與H2 O及氧氣中之至少一者反應。反應電解槽腔室5b31中之熔融金屬蒸氣(諸如銀蒸氣)以及點火及低能量氫反應支援之電漿中之至少一者可充當完成正電極與不利偏壓之電池組件(諸如黑體輻射器5b4、第二儲集器5c及第二EM泵5ka中之至少一者)之間的電解電路的手段。H2 O、H2 、CO及CO2 中之至少一者可滲透穿過黑體輻射器5b4及至少一個儲集器5c中之至少一者。H2 O、H2 、CO及CO2 中之至少一者可由至反應電解槽腔室5b31 (諸如包含EM泵管5k6之反應電解槽腔室)之通路供應。H2 O可充當H及HOH催化劑中之至少一者之來源。氫氣可進行以下中之至少一者:充當H來源以形成低能量氫及與氧反應以形成水,其中氧氣可為來自作為H來源以形成低能量氫之H2 O的產物。可藉由保持氫氣、二氧化碳及一氧化碳中之至少一者之氛圍進一步抑止碳氧化反應。 在一實施例中,發電機可僅包含第一儲集器5c及包含熔融金屬噴射器電極之第一EM泵5ka。對立電極可包含黑體輻射器5b4。電極可由電源2供電。熔融金屬噴射器電極可為正的,且黑體輻射器電極為負的。可至少部分地保護不利偏壓之黑體輻射器免於與H2 O及O2 中之至少一者反應。諸如CO、CO2 、H2 及H2 O中之至少一者的氣體可由本發明之系統和方法供應。H2 O、H2 、CO及CO2 中之至少一者可滲透穿過黑體輻射器5b4及儲集器5c中之至少一者。H2 O、H2 、CO及CO2 中之至少一者可由至反應電解槽腔室5b31 (諸如包含EM泵管5k6之反應電解槽腔室)之通路供應。 在一實施例中,SunCell®包含化學上防止氧化反應或化學上減少至少一個經氧化電池組件(諸如EM泵管、黑體輻射器、進水升管及噴嘴中之至少一者)的熔融金屬添加劑。可將還原劑/保護劑添加至銀以防止EM泵管由H2 O及O2 中之至少一者氧化。添加劑可包含此項技術中已知之還原劑,諸如硫代硫酸鹽、Sn、Fe、Cr、Ni、Cu或Bi。添加劑可減少碳反應電解槽腔室與水、氧氣、二氧化碳及一氧化碳中之至少一者的反應。當正偏壓碳組件(諸如反應電解槽腔室5b31)時,添加劑可保護碳免遭氧化反應。添加劑可包含碳、烴及氫氣中之至少一者。在另一實施例中,熔融金屬及添加劑中之至少一者可塗佈或濕潤電池組件之壁以保護免遭氧化反應。可保護EM泵管5k6之內部及反應電解槽腔室5b31 (諸如碳反應電解槽腔室)中之至少一者。經供應低能量氫反應物(諸如H2 O)在由於塗層或潤濕而對應氣體對電池組件(諸如黑體輻射器5b4)或反應電解槽腔室5b31 (諸如碳反應電解槽腔室)不可滲透的情況下可經由EM泵管5k6供應。 亦可藉由應用負電位保護EM泵管。可使用點火電源2施加負電位。可將電位可逆地施加至雙熔融金屬噴射器之兩個EM泵管中之每一者。點火電源2可包含循環地逆轉點火匯流排5k2a中之每一者處之極性的開關。SunCell®可包含黑體輻射器5b4,諸如碳黑體輻射器,其進一步包括至電壓源之負極端的匯流排。電壓源可包含點火電力電源2。負匯流排可連接至頂部滑動螺母,該頂部滑動螺母連接儲集器及黑體輻射器5b4之底座。至諸如頂部滑動螺母之熱碳部件的連接器可包含碳,以避免金屬連接器之金屬碳化物形成。任何金屬碳連接可經由置放區域中之連接的擴展來進行,其中連接溫度低於將導致金屬碳化物形成的溫度。負電位可包含恆定負電位。匯流排可包含耐火電導體,諸如Mo或W。在一實施例中,提供至黑體輻射器之負偏壓的連接可包含機械式跨接線,以直接地或間接地與點火匯流排及黑體輻射器之底座可逆地形成電連接。連接可包含至少一個可逆的機械開關及包覆儲集器5c之一部分(諸如儲集器外部上(諸如BN管外部上)之碳貝殼掀蓋)的導體。應避免化學不相容性。舉例來說由於鐵及碳可反應以形成碳化鐵,故應避免包含鐵之部件與包含鐵之部件接觸。 可在藉由電解還原或藉由化學還原來還原經氧化電池組件之後再生氧化添加劑。電解還原可由施加至至少一個電池組件之負電位提供。反應電解槽腔室氛圍5b31可包含水蒸氣。反應電解槽腔室5b31可包含電解電池陰極,其中電漿完成陰極與陽極之間的電路。陽極可包含正偏壓之熔融金屬電極。在電池之負(陰極)放電電極處(諸如在反應電解槽腔室5b31壁處)形成之氫氣可保護電極(壁)免於由H2 O氧化。水還原/氧化反應可為 陰極:2H2 O + 2e- 至H2 + 2OH- (41) 陽極:4OH- 至O2 + 2H2 O + 4e- (42) 在一實施例中,EM泵管5k6之內部可用熔融金屬塗料塗佈以保護其免於由反應電解槽腔室5b31、儲集器5c及EM泵管5k6中之至少一者中之物種腐蝕,該等物種諸如水、CO2 、Co及O2 中之至少一者。銀潤濕塗層可保護SunCell®之至少一個組件。在一實施例中,可處理至少一個金屬表面(諸如EM泵管5k6之內部之金屬表面)以移除氧化物塗層以准許熔融金屬(諸如銀)潤濕表面。可移除氧化物塗層以改善穿過熔融金屬(諸如銀)之匯流排上之導電率。可藉由至少一個方法(諸如機械及化學移除中之一或多者)移除氧化物塗層。可藉由使用研磨工具(諸如鋼絲刷)或藉由噴砂移除氧化物塗層。可藉由蝕刻劑(諸如酸,諸如HCl或HNO3 或還原劑(諸如氫氣))移除氧化物塗層。諸如銀之熔融金屬可來自塗層以保護反應電解槽腔室5b31之內部、儲集器5c及EM泵管5k6。電極中之至少一者可經浸沒以保護其免於由電漿腐蝕或侵蝕。在一實施例中,反應電解槽腔室之壁可包含諸如各向同性碳之經銀塗佈之碳、熱碳及經銀塗佈之熱碳中之至少一者。鍍銀層可在電池操作期間形成或可藉由塗佈方法施加,該等塗佈方法諸如電漿噴射、電鍍、氣相沈積及由熟習此項技術者已知之其他方法。 電池之組件可包含材料及塗料中之至少一者以防止或減少氧化反應,諸如與氧氣及水蒸氣中之至少一者的氧化反應。在一實施例中,EM泵管5k4可包含鍋爐級不鏽鋼或鎳,或管可內部地經鎳塗佈。在一實施例中,耐火EM泵管5k61可包含抗水材料,諸如Mo超合金,諸如TZM。EM泵管5k61之噴嘴或噴射部分可包含碳,諸如熱碳。EM泵管之內部可用銀塗佈以防止與水反應。在一實施例中,進水升管5qa、EM泵管5k61之噴嘴部分及噴嘴5q中之至少一者可包含對氧化反應穩定之耐火材料,諸如耐火氧化物,諸如MgO (M.P. 2825℃)、ZrO2 (M.P. 2715℃)、氧化鎂、對H2 O穩定之氧化鋯、鋯酸鍶(SrZrO3 M.P. 2700℃)、HfO2 (M.P. 2758℃)、二氧化釷(M.P. 3300℃)或本發明之另一種氧化物。反應電解槽腔室5b31可包含可用保護性銀塗佈之碳,諸如熱碳。反應電解槽腔室5b31可不利地偏壓將保護其免遭氧化反應。儲集器可包含氮化硼,其可包含添加劑或表面塗料以保護其免遭氧化反應,諸如CaO、B2 O3 、SiO2 、AUO3 、SiC、ZrO2 及AlN中之至少一者,其中水及氧氣中之至少一者可包含氧化劑。氮化硼可包含對水反應具有抗性之結晶結構,諸如αBN。反應混合物可包含添加劑(諸如Hx By Oz ),其可包含氣體以抑止BN之氧化反應。在一實施例中,諸如儲集器5c之細胞組件可包含耐火氧化物,諸如MgO (M.P. 2825℃), ZrO2 (M.P. 2715℃),氧化鎂、對H2 O穩定之氧化鋯、鋯酸鍶(SrZrO3 M.P. 2700℃)、HfO2 (M.P. 2758℃)或在工作溫度下對氧化反應穩定之二氧化釷(M.P. 3300℃)。 在一實施例中,氧氣之氣態來源(諸如水蒸氣、CO2 、CO及O2 )可浮升至反應電解槽腔室5b31之頂部。除金屬蒸氣(諸如銀蒸氣)以外,反應電解槽腔室氣體包含由於水之較高浮力而使水蒸氣移位至反應電解槽腔室的頂部稠密氣體(諸如氙氣)。在一實施例中,將銀蒸氣保持在足以使水蒸氣浮升至反應電解槽腔室之頂部的壓力下。水蒸氣之上升移位可防止其免於造成電池組件(諸如EM泵管5b6)腐蝕。至少一種反應物氣體(諸如H2 O及H2 )可經由EM泵管供應。 化學還原可由還原氣體(諸如氫氣)提供。例示性還原氛圍包含Ar/H2 (3%)氣體。氫氣可滲透穿過至少一個電池組件,諸如黑體輻射器5b4及EM泵管5k6中之至少一者。EM泵管可包含氫氣可滲透金屬,諸如不鏽鋼(SS),諸如430 SS、釩、鉭、或鈮、或鎳。氫氣可滲透噴射至中噴射至正EM泵管中。在此情況下,可避免產生氧氣之氧化反應,其中氧化反應可包含: 陽極:2OH- + H2 至2H2 O + 2e- (43) 在一實施例中,SunCell®進一步包含正電極、施加正電極與至少一個電池組件之間的電位之偏壓電源及偏壓電源之控制器。正電極可包含熔融金屬電極。正電極可包含諸如銀之熔融金屬之至少一部分,諸如儲集器5c或黑體輻射器5b41之下半球中之至少一者中之熔融金屬。正電極可包含對氧化反應穩定之導體,諸如貴金屬,其亦可為耐火金屬,諸如Pt、Re、Ru、Rh或Ir。可在EM泵管外部施加正偏壓,使得管之內部不經正偏壓。泵管之內部可包含法拉弟籠。EM泵管可包含正電極,其為在表面上流動之浸沒有銀及塗佈有銀中之至少一者。流動銀可在噴嘴及EM泵管中之至少一者中形成孔。孔可選擇性地在暴露於電漿之EM泵管部分上。 可藉由在電池組件與正電極之間施加負偏壓保護至少一個電池組件(諸如黑體輻射器54b、儲集器5c及EM泵5ka中之至少一者)免受電池反應物或產物(諸如氧氣來源、CO、CO2 、H2 O及O2 中之至少一者)之氧化反應。偏壓電位可為至少造成還原電池組件之氧化物及防止電池組件之氧化中之至少一者的電位。偏壓電壓可在約0.1 V至25V、 0.5 V至10 V及0.5 V至5 V中之至少一個範圍內。正電極可為可消耗及可替換中之至少一者。正電極可包含碳。碳正電極可附接至正EM泵管及噴嘴5q,其中正電極可比噴嘴之尖端更接近反應電解槽腔室。正電極可與正EM泵管及噴嘴電接觸。氫氣及氧氣中之至少一者之來源可包含H2 O。低能量氫反應產物可包含H2 (1/p),諸如H2 (1/4)及氧氣。正電極可與氧氣產物反應。碳電極可與過多氧氣反應且形成CO2 。可自反應電解槽腔室5b31移除CO2 。可藉由經由至少一個電池組件(諸如黑體輻射器5b4)泵送及擴散中之至少一者來移除CO2 。 在圖2I80至圖2I173中所展示之一實施例中,可藉由以下中之至少一者將惰性氣體、水或蒸汽、氫氣及氧氣中之至少一者供應至反應電解槽腔室5b31:噴射至泵管5k6中(諸如在噴嘴5q末端處);及噴射至反應電解槽腔室5b31中。發電機可包含至少一種惰性氣體、水或蒸汽、氫氣及氧氣來源,諸如貯槽及傳送線。諸如流動閥或壓力閥之閥門(諸如電磁線圈閥)可控制噴射。在一實施例中,SunCell®可包含水噴射器,包含噴嘴、水位線、流量及壓力控制器、水源(諸如水之貯槽)及汽化水以形成氣態H2 O之構件中之至少一者。汽化水以形成氣態H2 O之構件可包含蒸汽發電機。流入電池之內部中之水可防止熔融金屬反流入噴嘴中。可設定噴嘴開口或孔口之大小,使得保持低能量氫反應之最小所要流速可由線路中之水壓力提供,其該線路至少為反應電解槽腔室5b31壓力之線路。增加線路中之水壓力可提供更高水供應速率。噴嘴及噴嘴孔口中之至少一者可包含由於高壓水噴射而對腐蝕及侵蝕具有抗性之材料。諸如陶瓷之材料可為極硬的且對氧化反應具有抗性,該陶瓷諸如氧化物陶瓷,諸如Al2 O3 、氧化鋯或氧化鉿。 在一實施例中,HOH催化劑之來源及H之來源包含噴射至電極中之水。施加高電流以致使點火為明亮發光電漿。水之來源可包含結合水。噴射至電極中之固體燃料可包含水及高度導電基質,諸如熔融金屬,諸如銀、銅及銀-銅合金中之至少一者。固體燃料可包含化合物,其包含結合水。可供應至點火之結合水化合物可包含水合物,諸如分解溫度為740℃之BaI2 2H2 O。可包含結合水之化合物可可與熔融金屬(諸如銀)混溶。可互溶化合物可包含焊劑,諸如水合Na2 CO3 、KCl、碳、硼砂(諸如Na2 B4 O7 ·10H2 O)、氧化鈣及PbS中之至少一者。結合水化合物可對高達熔融金屬之熔點的水損失穩定。舉例而言,結合水可對超過1000℃穩定,且在點火事件處損失水。包含結合水之化合物可包含氧氣。在釋放氧氣之情況下,熔融金屬可包含銀,此係因為銀不在其熔點處形成穩定的氧化物。包含結合水之化合物可包含:氫氧化物,諸如鹼、鹼土、過渡金屬、內部過渡金屬、稀土、13、14組、15組及16組氫氧化物;礦物,諸如滑石、由具有化學式H2 Mg3 (SiO3 )4 或Mg3 Si4 O10 (OH)2 之水合矽酸鎂組成的礦物、及白雲母或雲母、具有式KAl2 (AlSi3 O10 )(F,OH)2 或(KF)2 (Al2 O3 )3 (SiO2 )6(H2 O)之鋁及鉀的頁矽酸鹽礦物。在一實施例中,脫水化合物充當乾燥劑以保持低反應電解槽腔室壓力。舉例而言,氫氧化鋇在加熱至800℃時分解為氧化鋇及H2 O,且所得BaO之沸點為2000℃,使得其仍然針對高於2300 K之電漿溫度大體上氣化。在一實施例中,水之來源包含亦可充當H來源之氧化物及氫氣。氫來源可包含氫氣。氧化物可能夠藉由氫氣還原以形成H2 O。氧化物可包含以下中之至少一者:Cu、Ni、Pb、Sb、Bi、Co、Cd、Ge、Au、Ir、Fe、Hg、Mo、Os、Pd、Re、Rh、Ru、Se、Ag、Tc、Te、Tl、Sn、W及Zn。可控制H2 O化合物之來源、H2 O化合物之來源之濃度、反應電解槽腔室中之水蒸氣壓、工作溫度及EM泵送速率中之至少一者以控制供應至點火之水的量。H2 O化合物之來源之濃度可在約0.001莫耳%至50莫耳%、0.01莫耳%至20莫耳%及0.1莫耳%至10莫耳%之至少一個範圍內。在一實施例中,將水溶解於燃料熔化物中,諸如包含銀、銅及銀-銅合金中之至少一者的燃料熔化物。水之溶解度隨著水與熔化物接觸之分壓(諸如反應電解槽腔室之水蒸氣分壓)增加。反應電解槽腔室中之水壓力可由槽腔室中之水蒸氣壓平衡。可藉由本發明之手段(諸如用於諸如氬氣之其他氣體的彼等)來達成平衡。反應電解槽腔室水蒸氣壓可在約0.01 Torr至100 atm、0.1 Torr至10 atm及0.5 Torr至1 atm之至少一個範圍內。EM泵送速率可在約0.01 ml/s至10,000 ml/s、0.1 ml/s至1000 ml/s及0.1 ml/s至100 ml/s之至少一個範圍內。 SunCell®可包含輻射熱交換器及輻射鍋爐中之至少一者(圖2I153至圖2I160)。SunCell®可包含輻射能量吸收器,諸如圍繞黑體輻射器5b4之初級熱交換器87。輻射能量吸收器可包含黑體吸收器(諸如碳吸收器)且可進一步包含鍋爐管以接收來自黑體吸收器(其中蒸汽可在管中形成且經由熱水或蒸汽出口111離開)的熱量。可將管嵌入於黑體吸收器中。蒸汽可傳送至諸如城市蒸汽加熱系統之負載。SunCell®可包含次級熱交換器87a,其可藉由初級熱交換器87傳遞自黑體輻射器5b4或反應電解槽腔室5b31吸收之熱量且將該熱量傳遞至次級介質,諸如固體、液體或氣態介質。在一實施例中,次級熱交換器可將熱量傳遞至空氣,該空氣可藉由風扇31j1吹掃通過或吹過熱交換器87a。空氣可離開熱空氣管道112以流動至熱負載。 在圖2I156至圖2I160中所展示之熱發電機實施例中,經由水入口113將冷的冷卻劑(諸如冷水)供應至熱發電機,且經由蒸汽及熱水出口111中之至少一者輸出熱水及蒸汽中之至少一者。可將反應電解槽腔室5b31中產生之熱量輻射至上部加熱器交換器114之鍋爐管以在鍋爐腔室116中產生蒸汽。蒸汽鍋爐進一步包含具高壓上部熱交換器及鍋爐腔室殼體5b3a及底板5b3b。來自儲集器5c及下部電池組件之熱量可輻射至下部熱交換器115以形成離開出口111之熱水及蒸汽中之至少一者。在一實施例中,鍋爐管可攜載熱水而非蒸汽。 SunCell®功率可以直接輻射、熱空氣、熱水及蒸汽之形式用作熱功率。在另一實施例中,鍋爐或熱交換器可包含液體液滴輻射器,其包含夾帶於氣流或流體流中之粒子吸收劑(諸如氣溶膠或金屬蒸氣),其中粒子吸收熱通量且傳遞其以移動氣體或流體冷卻劑。液滴冷卻系統可包含液滴噴霧及收集系統,諸如包含噴墨列印機之系統。自黑體輻射器至粒子吸收劑之熱傳遞在性質上可主要為輻射的。包含耐火粒子及具有較高熱傳遞能力之氣體的一例示性實施例包含懸浮於氫氣流或氦氣流中之鎢微粒子。 在另一實施例中,鍋爐或熱交換器可包含將熱量自反應電解槽腔室5b31或黑體輻射器5b4中之至少一者傳遞至鍋爐或熱交換器之冷卻劑的傳熱介質(諸如固體、液體或氣體介質)。熱傳遞機構可包含輻射、對流及傳導中之至少一者。例示性液體傳熱介質包含水、熔融金屬及熔融鹽中之至少一者。例示性氣體傳熱介質可包含惰性氣體、氫氣、氦氣、稀有氣體及氮氣中之至少一者。鍋爐或熱交換器可包含氣體傳熱介質及調節其壓力之構件,諸如供應源,諸如貯槽、調節器、壓力計、泵及控制器,以實現所要常數或所要可變壓力以控制熱傳遞速率。 SunCell®可包含熱交換器87,諸如反應電解槽腔室5b31之外表面5b4上之凸片,以加熱流動工作介質,諸如冷卻劑(諸如熔融鹽),諸如共熔物混合物、熔融金屬、水或氣體(諸如空氣)。熱交換器亦可包含吸熱器及吸熱器上之熱傳遞凸片,其中熱傳遞可吸收來自黑體輻射器5b4之熱量。凸片可與氣體或流體冷卻劑/工作介質交換熱量。吸收器可包含較高輻射率材料,諸如碳。布累登循環系統可包含封閉式加壓氣體迴路及渦輪機及環境熱交換器,其中氣體由SunCell®加熱,在最高壓力下流動至燃氣渦輪機中,且可在藉由經由熱交換器對環境之熱損失而在渦輪機之後端處下降壓力。化學系統可包含構件,諸如熱分解系統,以使用來自低能量氫反應之熱量將水轉換為H2 。氫氣可用於已知轉換器中,諸如燃燒渦輪機或燃料電池,諸如PEM燃料電池,以產生電力。替代地,電化學循環可包含具有氫化物離子電解質、氫氣陰極及金屬氫化物陽極的燃料電池。金屬氫化物可以熱方式分解以保持使用來自低能量氫製程之熱量形成電力的可逆的金屬氫化物/金屬加氫氣循環。氫化物離子燃料電池描述於吾之先前申請中,諸如美國專利申請案,諸如Electrochemical Hydrogen Catalyst Power System,2011年3月17日申請之PCT/US11/28889;H2 O-Based Electrochemical Hydrogen-Catalyst Power System,2012年3月30日申請之PCT/US12/31369;CIHT Power System,2013年5月21日申請之PCT/US13/041938;及Power Generation Systems and Methods Regarding Same,2014年1月10日申請之PCT/IB2014/058177,其以全文引用之方式併入。 在一實施例中,複數個發電機可連軸以提供所要功率輸出。複數個發電機可以串聯及平行中之至少一者互連以實現所要功率輸出。經連軸發電機之系統可包含控制器,以控制在控制發電機之間的串聯連接及平行連接中之至少一者,該等發電機控制複數個經連軸發電機之經疊加輸出電力之功率、電壓及電流中之至少一者。複數個發電機可各自包含電力控制器,以控制功率輸出。電力控制器可控制低能量氫反應參數,以控制發電機功率輸出。各發電機可包含在PV轉換器26a之PV電池或PV電池組中之至少一者之間的開關且進一步包含控制器,以控制PV電池或之組之間的串聯連接及平行連接中之至少一者。控制器可切換互連以實現自PV轉換器輸出之所要電壓、電流及電功率中之至少一者。經連軸複數個發電機之中央控制器可控制經連軸發電機之間的串聯互連及平行互連中之至少一者、至少發電機上之低能量氫反應參數及複數個經連軸發電機之至少一個發電機之至少一個PV轉換器之PV電池或PV電池組之間的連接。中央控制器可直接地或經由個別發電機控制器控制發電機及PV連接及低能量氫反應參數中之至少一者。功率輸出可包含DC或AC功率。各發電機可包含DC至AC反相器,諸如反相器。替代地,可經由發電機之間的連接組合複數個發電機之DC功率且使用DC至AC轉換器(諸如能夠轉換經疊加DC功率之反相器)將其轉換為AC功率。PV轉換器及經連軸發電機系統中之至少一者之例示性輸出電壓為約380V DC或780V DC。約380 V輸出可轉換為二相AC。約760 V輸出可轉換為三相AC。AC功率可轉換為另一個所要電壓,諸如約120 V、240 V或480 V。可使用變壓器轉變AC電壓。在一實施例中,可使用IGBT將DC電壓改變為另一個DC電壓。在一實施例中,反相器之至少一個IGBT亦可用作電感耦合加熱器5m之IGBT。 在一實施例中,轉換器包含經連軸以包含經組合循環的複數個轉換器。經組合循環轉換器可選自以下的組:光伏打轉換器、光電轉換器、電漿動力轉換器、熱轉換器、熱電轉換器、斯特林引擎、布累登循環引擎、朗肯循環引擎及熱機以及加熱器。在一實施例中,SF-CIHT電池主要產生紫外光及極遠紫外光。轉換器可包含經組合循環,其包含光電子轉換器,接著為光電轉換器,其中光電轉換器對紫外光為透明的且可主要地回應於極遠紫外光。轉換器可進一步包含額外的經組合循環轉換器元件,諸如熱電轉換器、斯特林引擎、布累登循環引擎、朗肯循環引擎及磁流體動力轉換器中之至少一者。磁流體動力 ( MHD ) 轉換器 基於交叉磁場中之離子或導電介質之質量流量之形成的電荷分離作為磁流體動力(MHD)功率轉換為熟知的技術。陽離子和陰離子在相對的方向上流經洛倫茲方向並且在相應的MHD電極處被接收以影響其之間的電壓。形成離子之質量流量典型的MHD方法為經由噴嘴擴展接種有離子之高壓氣體以產生穿過經交叉磁場之高速流,其中一組MHD電極關於偏轉場交叉以接收經偏轉離子。在一實施例中,壓力通常大於常壓,且方向性質量流量可藉由反應來實現以形成電漿及高度導電、高壓及高溫熔融金屬蒸氣,其經擴增以產生穿過MHD轉換器之橫向磁場部分的高速流。可穿過MHD轉換器之流動可為軸向或徑向的。其他方向性流動可藉由約束性磁體,諸如赫爾姆霍茲線圈或磁瓶之彼等磁體實現。 特定言之,圖2I161至圖2I195中所展示之MHD電功率系統可包含本發明之低能量氫反應電漿源(諸如包含EM泵5ka之電漿源)、至少一個儲集器5c、至少兩個電極(諸如包含雙熔融金屬噴射器5k61之電極)、低能量氫反應物來源(諸如HOH催化劑及H之來源)、點火系統(包含將電壓及電流施加至電極以由低能量氫反應物形成電漿的電源2)及MHD電功率轉換器。包含低能量氫反應電漿源及MHD轉換器的MHD電力系統之組件可由抗氧化劑材料中之至少一者組成,該等抗氧化劑材料諸如抗氧化劑金屬、包含抗氧化劑塗料的金屬及陶瓷,使得系統可在空氣中操作。在一雙熔融金屬噴射器實施例中,藉由保持包含間歇性電流之脈衝噴射來實現高電場。藉由銀流斷開連接及重新連接脈衝電漿。可施加電壓直至連接雙熔融金屬流。脈衝可包含藉由造成金屬流之斷開-重新連接之對應高頻的高頻。連接-重新連接可自發地發生且可藉由控制藉由構件之低能量氫反應功率(諸如本發明之彼等)及藉助於本發明之熔融金屬噴射速率(諸如藉由控制EM泵電流)中之至少一者來控制。在一實施例中,點火系統可包含電壓及電流之來源,諸如DC電源及一組電容器,以用針對高電流脈衝之能力傳送脈衝點火。 圖2I161至圖2I195中所展示之磁流體動力電力轉換器可包含橫向於z軸之磁通量之來源,該z軸其MHD轉換器300之穿過軸向熔融金屬蒸氣及電漿流之方向。導電流動沿z軸可具有較佳速度,此係由於氣體沿z軸擴展。其他方向性流動可藉由約束性磁體,諸如赫爾姆霍茲線圈或磁瓶之彼等磁體實現。因此,金屬電子及離子傳播至橫向磁通量之區域中。傳播電子及離子上之洛倫茲力藉由以下給出F =e v × B (44)力橫向於電荷速度及磁場且在陽離子及陰離子之相對方向上。因此,橫向電流形成。橫向磁場之來源可包含依據沿z軸之位置提供不同強度之橫向磁場以便最佳化具有平行速度分散之流動電荷之交叉偏轉(方程式(44))的組件。 儲集器5c熔融金屬可呈液體及氣態之至少一個狀態。儲集器5c熔融金屬可定義為MHD工作介質且可同樣被稱作MHD工作介質或被稱作熔融金屬,其中其暗示熔融金屬可進一步呈液體及氣態之至少一個狀態。亦可使用諸如熔融金屬、液體金屬、金屬蒸氣或氣態金屬之特定狀態,其中亦可存在另一種物理狀態。例示性熔融金屬為可呈液體及氣態狀態中之至少一者的銀。MHD工作介質可進一步包含添加劑,其包含以下中之至少一者:添加金屬,其在工作溫度範圍處可呈液體及氣態中之至少一者;化合物,諸如本發明中之一者,其在工作溫度範圍處可呈液體及氣態中之至少一者;及氣體,諸如稀有氣體(諸如氦氣或氬氣)、水、H2 及本發明之其他電漿氣體中之至少一者。MHD工作介質添加劑可與MHD工作介質呈任何所要比率。在一實施例中,選擇介質與添加劑介質之比率以得到MHD轉換器之視情況選用之電力轉換性能。諸如銀或銀-銅合金之工作介質可在過飽和條件下操作。 在一實施例中,MHD發電機300可包含法拉第、通道霍耳及圓盤霍耳類型中之至少一者。在通道霍耳MHD實施例中,膨脹或發電機通道308可沿z軸垂直地定向,其中熔融金屬電漿(諸如銀蒸氣及電漿)流動穿過加速器部分(諸如限制或噴嘴導入口307),隨後膨脹部分308。通道可包含螺線管磁體306,諸如超導或永久磁體,諸如沿x軸橫向於流動方向之海爾貝克陣列(Halbach array)。磁體可由MHD磁體安裝托架306a固定。磁體可包含液體致冷劑或可包含具有或不具有液體致冷劑之低溫致冷機。低溫致冷機可包含乾燥稀釋致冷機。磁體可包含磁場之返回路徑,諸如磁軛,諸如C形或矩形反磁軛。一例示性永久磁體材料為SmCo,且一例示性磁軛材料為磁性CRS、冷軋鋼或鐵。發電機可包含至少一組電極,諸如沿y軸之經分段電極304,其橫向於磁場(B )以接收在MHD電極304上產生電壓之橫向地洛倫茲偏轉離子。在另一實施例中,至少一個通道(諸如發電機通道308)可包含除具有平面壁(諸如圓柱形壁通道)之幾何結構以外的幾何結構。藉由[E. M. Walsh, Energy Conversion Electromechanical, Direct, Nuclear, Ronald Press Company, NY, NY, (1967), 第221-248頁]描述磁流體動力產生,其之完整本發明以引用之方式併入本文中。 MHD磁體306可包含永久磁體及電磁體中之至少一者。電磁體306可為具有對應低溫管理之未冷卻磁體、經水冷卻磁體及超導磁體中之至少一者。例示性磁體為螺線管或鞍形物線圈,其可磁化MHD通道308及跑道線圈,其可磁化圓盤通道。超導磁體可包含低溫致冷機及致冷劑杜瓦瓶系統中之至少一者。超導磁體系統306可包含:(i)超導線圈,其可包含NbTi或NbSn之超導體線螺旋圈,其中超導體可包覆於保護免受由諸如振動之手段誘導之超導體狀態之瞬態局部淬滅的正常導體(諸如銅線)或高溫超導體(HTS)上,該高溫超導體諸如YBa2 Cu3 O7 ,通常被稱作YBCO-123或僅YBCO;(ii)液態氦杜瓦瓶,其在線圈之兩側上提供液態氦;(iii)液氮杜瓦瓶,其在螺線管磁體之內部及外部半徑上具有液氮,其中液態氦及液氮杜瓦瓶二者可包含輻射擋板及輻射護罩(可包含銅、不鏽鋼及鋁中之至少一者)及在壁處絕緣之高真空;及(iv)各磁體之入口,其可附接低溫泵及壓縮機,該低溫泵及壓縮機可經由其輸出功率端子由SunCell®發電機之功率輸出供電。 在一個實施例中,磁流體動力電力轉換器為經分段法拉第發電機。在另一實施例中,由離子流之洛倫茲偏轉形成之橫向電流在平行於離子之輸入流之方向(z軸)上經受進一步洛倫茲偏轉以在沿z軸相對地移位之至少第一MHD電極與第二MHD電極之間產生霍耳電壓。此裝置在此項技術中稱為磁流體動力電力轉換器之霍耳發電機實施例。其中MHD電極在xy平面中關於z軸成角度的類似裝置包含本發明的之另一實施例且稱為具有「窗口訊框」構造之對角發電機。在每一情況下,電壓可驅使電流流過電力負載。經分段法拉第發電機、霍耳發電機及對角發電機之實施例在Petrick [J. F. Louis, V. I. Kovbasyuk, Open-cycle Magnetohydrodynamic Electrical Power Generation, M Petrick及B. Ya Shumyatsky編者, Argonne National Laboratory, Argonne, Illinois, (1978), 第157-163頁]中給出,其之完整本發明以引用之方式併入。 在磁流體動力電力轉換器之另一實施例中,隨著沿z軸之離子流可接著進入包含增加的軸向磁場梯度之壓縮部分,其中平行於z軸之方向之電子運動分量至少部分地轉換為垂直運動,此係由於絕熱不變量=常數。由於,故在z軸周圍形成方位角電流。在運動平面中電流由於軸向磁場而徑向偏轉,在盤式產生器磁流體動力電力轉換器之內環與外環MHD電極之間產生霍爾電壓(Hall voltage)。電壓可驅使電流流過電力負載。電漿功率亦可使用本發明或此項技術中已知之電力裝置的直接轉換器或其他電漿轉換為電力。 MHD發電機可包含接收膨脹流動之冷凝器通道部分309且發電機進一步包含回流通道或管310,其中MHD工作介質(諸如銀蒸氣)冷卻,此係因為其在冷凝器部分中損失溫度、壓力及能量中之至少一者且經由通道或管310流回至儲集器。發電機可包含至少一個回流泵312及回流泵管313以將回流泵送至儲集器5c及EM泵噴射器5ka。回流泵及泵管可泵送液體、蒸氣及氣體中之至少一者。回流泵312及回流泵管313可包含電磁(EM)泵及EM泵管。至EM泵之入口可具有比出口泵管直徑更大的直徑以增加泵出口壓力。在一實施例中,回流泵可包含EM泵噴射器電極5ka之噴射器。在一雙熔融金屬噴射器實施例中,發電機包含各自藉由對應回流泵(諸如回流EM泵312)之回流儲集器311。回流儲集器311可進行以下中之至少一者:平衡回流熔融金屬(諸如熔融銀)流動且冷凝或分離與液體銀混合之銀蒸氣。儲集器311可包含冷凝銀蒸氣之熱交換器。儲集器311可包含第一級電磁泵以較佳地泵送液體銀以分離液體與氣態銀。在一實施例中,可藉由離心力將液體金屬選擇性地噴射至回流EM泵312中。回流導管或回流儲集器可包含離心部分。離心儲集器可自入口至出口為楔形的,使得離心力在頂部比在底部更大以迫使熔融金屬至底部且將其與氣體(諸如金屬蒸氣及任何工作介質氣體)分離。替代地,SunCell®可安裝於離心表上,該離心表圍繞垂直於回流熔融金屬之流動方向的軸旋轉以產生分離液體及氣態物種的離心力。 在一實施例中,經冷凝金屬蒸氣流動至兩個獨立回流儲集器311中,且各回流EM泵312將熔融金屬泵送至對應儲集器5c中。在一實施例中,兩個回流儲集器311及EM泵儲集器5c中之至少一者包含含量控制系統,諸如本發明中之一者,諸如進水升管5qa。在一實施例中,由於呈視回流儲集器中之含量而定之較高或較低速率,可將回流熔融金屬抽吸至回流儲集器311中,其中抽吸速率由對應含量控制系統(諸如進水升管)控制。 在一實施例中,MHD轉換器300可進一步包含至少一個加熱器,諸如電感耦合加熱器。加熱器可預熱與MHD工作介質接觸之組件,諸如反應電解槽腔室5b31、MHD噴嘴部分307、MHD發電機部分308、MHD冷凝部分309、回流導管310、回流儲集器311、回流EM泵312及回流EM泵管313中之至少一者。加熱器可包含接合及回縮加熱器之至少一個致動器。加熱器可包含複數個線圈及線圈部分中之至少一者。線圈可包含此項技術中已知之線圈。線圈部分可包含至少一個分離線圈,諸如本發明中之一者。在一實施例中,MHD轉換器可包含至少一個冷卻系統,諸如熱交換器316。MHD轉換器可包含用於至少一個電池及MHD組件之冷卻器,諸如以下組中之至少一者:腔室5b31、MHD噴嘴部分307、MHD磁體306、MHD電極304、MHD發電機部分308、MHD冷凝部分309、回流導管310、回流儲集器311、回流EM泵312及回流EM泵管313。冷卻器可自MHD流動通道移除熱量損失,諸如來自以下中之至少一者之熱量損失:腔室5b31、MHD噴嘴部分307、MHD發電機部分308及MHD冷凝部分309。冷卻器可自MHD工作介質回流系統移除熱量,該MHD工作介質回流系統諸如回流導管310、回流儲集器311、回流EM泵312及回流EM泵管313中之至少一者。冷卻器可包含可將熱量排出至環境氣氛的輻射熱交換器。 在一實施例中,冷卻器可包含將能量自冷凝部分309傳遞至儲集器5c、反應電解槽腔室5b31、噴嘴307及MHD通道308中之至少一者的再循環器或復熱器。經傳遞能量(諸如熱量)可包含來自剩餘熱能、壓力能及工作介質之汽化熱中之至少一者的熱量,該工作介質諸如包含氣化金屬、動力氣溶膠及氣體(諸如稀有氣體)中之至少一者的工作介質。散熱管為被動二相裝置,其能夠隨著十分之幾度溫度下降在幾米之距離內轉移大量熱通量(諸如高達20 MW/m2 );因此,顯著地降低材料上之熱應力,從而僅使用少量工作流體。鈉及鋰散熱管可傳遞大量熱通量且沿軸向方向保持幾乎等溫。鋰散熱管可傳遞高達200 MW/m2 。在一實施例中,諸如熔融金屬(諸如液體鹼金屬,諸如包覆於耐火金屬(諸如W)中之鈉或鋰)的散熱管可傳遞來自冷凝器309之熱量且將其再循環至反應電解槽腔室5b31或噴嘴307。在一實施例中,至少一個散熱管回收銀汽化熱且使其再循環,使得經回收熱量功率為輸入至MHD通道308之功率的部分。 在一實施例中,SunCell®之組件(諸如包含MHD轉換器之組件)中之至少一者可包含散熱管以進行以下中之至少一者:將熱量自SunCell®發電機之一個部分傳遞至另一部分及將熱量自加熱器(諸如電感耦合加熱器)傳遞至SunCell®組件,諸如EM泵管5k6、儲集器5c、反應電解槽腔室5b31及MHD熔融金屬回流系統,諸如MHD回流導管310、MHD回流儲集器311、MHD回流EM泵312及MHD回流EM管。替代地,可在烘箱(諸如此項技術中已知之烘箱)內加熱SunCell®或至少一個組件。在一實施例中,可加熱至少一個SunCell®組件以供至少啟動操作。加熱器可為電阻性加熱器或電感耦合加熱器。在一實施例中,可在一個SunCell®組件處加熱低能量氫反應之熱量。在一例示性實施例中,諸如電感耦合加熱器之加熱器加熱EM泵管5k6、儲集器5c及至少反應電解槽腔室5b31之底部。至少一個其他組件可藉由低能量氫反應之熱量釋放加熱,該至少一個其他組件諸如反應電解槽腔室5b31之頂部、MHD噴嘴307、MHD通道308、MHD冷凝部分309及MHD熔融金屬回流系統中之至少一者,該MHD熔融金屬回流系統諸如MHD回流導管310、MHD回流儲集器311、MHD回流EM泵312及MHD回流EM管。在一實施例中,諸如MHD回流導管310、MHD回流儲集器311、MHD回流EM泵312及MHD回流EM管的MHD熔融金屬回流系統可用高溫熔融金屬或金屬蒸氣(諸如熔融銀或蒸氣)加熱,該高溫熔融金屬或金屬蒸氣具有在約1000℃至7000℃、1100℃至6000℃、1100℃至5000℃、1100℃至4000℃、1100℃至3000℃、1100℃至2300℃、1100℃至2000℃、1100℃至1800℃及1100℃至1500℃之至少一個範圍內的溫度。高溫熔融金屬或金屬蒸氣可在旁通或停用MHD轉換為電力之情況下導致流動穿過MHD組件。停用可藉由移除電場或藉由電性地使電極短路來實現。 在一實施例中,電池及MHD轉換器之至少一個組件可經絕緣以防止熱量損失。可使以下各者之群組中之至少一者絕緣:腔室5b31、MHD噴嘴部分307、MHD發電機部分308、MHD冷凝部分309、回流導管310、回流儲集器311、回流EM泵312及回流EM泵管313。來自絕緣之熱量損失可耗散於對應冷卻器或熱交換器中。在一實施例中,諸如銀之工作流體可充當冷卻劑。可增加EM泵噴射速率以提供吸收熱量之銀,以冷卻至少一個電池或MHD組件,諸如MHD噴嘴307。銀之氣化可冷卻噴嘴MHD 307。循環器或復熱器可包含用於冷卻之工作介質。在一例示性實施例中,經由待冷卻之組件泵送銀其將其噴射至反應電解槽腔室及MHD轉換器中以回收熱量,同時提供冷卻。 至少諸如儲集器5c、反應電解槽腔室5b31及MHD轉換器307及308之高壓部分之高壓組件可保持在包含殼體5b3a及5b3b之壓力腔室5b3a1中。壓力腔室5b3a1可保持在壓力下以至少反向平衡高內反應腔室5b31及MHD噴嘴307及MHD發電機通道308之至少一部分。壓力平衡可減少發電機組件(諸如儲集器5c與EM泵組合件5kk之間的彼等)之接點上之張力。高壓容器5b3a可選擇性容納高壓組件,諸如反應電解槽腔室5b31、儲集器5c及MHD膨脹通道308中之至少一者。其他電池組件可容納在低壓力容器或殼體中。 諸如H2 O、H2 、CO2 及CO中之至少一者之低能量氫反應物的來源可滲透通過可滲透電池組件,諸如槽腔室5b31、儲集器5c、MHD膨脹通道308及MHD冷凝部分309中之至少一者。可諸如經由EM泵管5k6、MHD膨脹通道308、MHD冷凝部分309、MHD回流導管310、回流儲集器311、MHD回流泵312、MHD回流EM泵管313將低能量氫反應氣體引入至至少一個位置中之熔融金屬流中。諸如質量流量控制器之氣體噴射器可能夠諸如經由EM泵管5k6、MHD回流泵312及MHD回流EM泵管313中之至少一者在MHD轉換器之高壓側上在高壓下噴射。氣體噴射器可能夠諸如經由MHD冷凝部分309、MHD回流導管310及回流儲集器311在諸如至少一個位置之MHD轉換器之低壓側上在較低壓力下噴射低能量氫反應物。在一實施例中,可藉由流體控制器經由EM泵管5k4噴射水及水蒸氣中之至少一者,該流量控制器可進一步包含壓力捕集器及防止熔融金屬流回至供水器(諸如質量流量控制器)中的反流止回閥可經由選擇性地滲透膜(諸如陶瓷或碳膜)噴射水。在一實施例中,轉換器可包含PV轉換器,其中低能量氫反應物噴射器能夠藉由諸如藉由滲透或在傳送位置操作壓力下噴射的手段中之至少一者供應反應物。在另一實施例中,SunCell®可進一步包含氫氣來源及氧氣來源,其中兩種氣體經合併以在反應電解槽腔室5b31中提供水蒸氣。氫來源及氧來源可各自包含對應貯槽、氣體直接或間接地流動至反應電解槽腔室5b31之線路、流量調節器、流量控制器、電腦、流量感測器及至少一個閥門中之至少一者。在後者情況中,氣體可藉由反應電解槽腔室5b31以氣體連續性流動至腔室中,該反應電解槽腔室諸如EM泵5ka、儲集器5c、噴嘴307、MHD通道308及其它MHD轉換器組件(諸如任何回流線路310a、導管313a及泵312a)中之至少一者。在一實施例中,可將H2 及O2 中之至少一者噴射至EM泵管5k61之噴射部分中。可經由雙重EM泵噴射器之單獨的EM泵管噴射O2 及H2 。替代地,可在具有較低銀蒸氣壓之區域中經由噴射器將諸如氧氣及氫氣中之至少一者的氣體添加至電池內部,諸如MHD通道308或MHD冷凝部分309。可經由選擇性膜(諸如陶瓷膜,諸如奈米多孔陶瓷膜)噴射氫氣及氧氣中之至少一者。氧可經由氧氣滲透膜供應,該氧氣滲透膜諸如可經Bi26 Mo10 O69 塗佈以增加氧氣滲透率之BaCo0 . 7 Fe0 . 2 Nb0 . 1 O3 - δ (BCFN)氧氣滲透膜之本發明中之一者。氫氣可經由氫氣滲透膜供應,該氫氣滲透膜諸如鈀-銀合金膜。SunCell®可包含電解器,諸如高壓電解器。電解器可包含質子交換膜,其中純氫氣可藉由陰極區室供應。純氧氣可藉由陽極區室供應。在一實施例中,EM泵部件塗佈有非氧化塗層或氧化保護塗層,且使用兩個質量流量控制器(其中可基於藉由對應氣體感測器感測之電池濃度來控制流量)在受控制條件單獨地噴射下氫氣及氧氣。 在一實施例中,SunCell®及包含內部區室之MHD轉換器之至少一個組件(諸如儲集器5c、反應電解槽腔室5b31、噴嘴307、MHD通道308、MHD冷凝部分309及其他MHD轉換器組件(諸如任何回流線路310a、導管313a及泵312a))容納於經氣體密封之殼體或腔室中,其中藉由在對氣體可滲透且對銀蒸氣不可滲透之膜片上擴散用內部電解槽氣體平衡腔室中之氣體。氣體選擇性膜可包含半滲透陶瓷,諸如本發明中之一者。電解槽氣體可包含氫氣、氧氣及稀有氣體(諸如氬氣或氦氣)中之至少一者。外部殼體可包含用於各氣體之壓力感測器。SunCell®可包含用於各氣體之來源及控制器。諸如氬氣之稀有氣體之來源可包含貯槽。氫氣及氧氣中之至少一者的來源可包含電解器,諸如高壓電解器。氣體控制器可包含流量控制器、氣體調節器及電腦中之至少一者。可控制殼體中之氣體壓力以控制電池之內部中(諸如儲集器、反應電解槽腔室及MHD轉換器組件中)之各氣體之氣體壓力。各氣體之壓力可在約0.1 Torr至20 atm之範圍內。在圖2I179至圖2I195中所展示之一例示性實施例中,直線MHD通道308及MHD冷凝部分309包含氣體殼體309b、壓力計309c以及氣體供應及抽空組合件309e,該抽空組合件包含進氣口線、出氣口線及凸緣,其中透氣膜309d可安裝於MHD冷凝部分309之壁中。安裝件可包含經燒結接點、金屬化陶瓷接點、銅焊接點或本發明之其他。氣體殼體309b可進一步包含存取埠。氣體殼體309b可包含諸如抗氧化金屬之金屬(諸如SS 625)或金屬上之抗氧化塗層(諸如適合CTE (諸如鉬)之金屬上之銥塗層)。替代地,氣體殼體309b可包含陶瓷,諸如金屬氧化物陶瓷,諸如氧化鋯、氧化鋁、氧化鎂、氧化鉿、石英或本發明之另一者。可冷卻經由金屬氣體殼體309b (諸如MHD回流導管310之彼等)穿透之陶瓷。穿透可包含碳密封,其中密封溫度低於金屬之碳化溫度及陶瓷之碳還原溫度。可針對熱熔融金屬移除密封以使其冷卻。密封可包含冷卻,諸如被動或加壓空氣或水冷卻。 在例示性實施例中,電感耦合加熱器天線5f可包含一個線圈、如圖2I178至圖2I179中所展示之三個單獨的線圈、如圖2I182至圖2I183中所展示之三個連續的線圈、兩個經分離線圈或如圖2I180至圖2I181中所展示之兩個連續的線圈。一例示性電感耦合加熱器天線5f包含上部橢圓形線圈及下部EM泵管餅狀線圈,該下部EM泵管餅狀線圈可包含螺旋形線圈,其可包含具有連續圓周電流方向之同心箱(圖2I180至圖2I181)。反應電解槽腔室5b31及MHD噴嘴307可包含平面、多邊形、矩形、圓柱形、球形或其他所需幾何結構,如圖2I162至圖2I195中所展示。電感耦合加熱器天線5f可包含連續的一組三個匝,包含環繞各儲集器5c之兩個螺旋及平行於EM泵管之餅狀線圈,如圖2I182至圖2I183中所展示。可捲繞圍繞儲集器之相對螺旋之匝以使得電流處於相同方向以強化兩個線圈之磁場或處於相對方向以消除螺旋之間的空間中之磁場。電感耦合加熱器天線5f可進一步用於冷卻至少一個組件,諸如EM泵5kk、儲集器5c、反應電解槽腔室5b31之壁及感應點火系統之磁軛中之至少一者。至少一個冷卻組件可包含陶瓷,諸如本發明中之一者,諸如氮化矽、石英、氧化鋁、氧化鋯、氧化鎂或氧化鉿。 SunCell®可包含自MHD膨脹通道之末端至儲集器5c之一個MHD工作介質回流導管,其中儲集器5c可包含經密封頂蓋,該頂蓋將儲集器中之較低壓力與較高反應電解槽腔室5b31壓力分離。EM泵噴射器部分5k61及噴嘴5q可穿透蓋以噴射熔融金屬,諸如反應電解槽腔室5b31中之銀。穿透可包含本發明之密封,諸如壓縮密封、滑動螺母、墊片銅焊或填充箱密封。儲集器可包含進水升管5qa以控制儲集器5c之熔融金屬含量。所覆蓋儲集器及接收回流熔融金屬流量之EM泵組合件5kk可包含雙熔融金屬噴射器系統之第一噴射器。包含第二儲集器及EM泵組合件之第二噴射器可包含間接地接收來自第一噴射器之回流的開放儲集器。第二噴射器可包含正電極。第二噴射器可保持浸沒在儲集器中之熔融金屬含量以方。對應進水升管5qa可控制浸沒。 SunCell®可包含自MHD發電機通道308之末端至熔融金屬噴射器系統之至少一個儲集器5c之至少一個氣態金屬回流導管310。SunCell®可包含自MHD發電機通道308之末端至雙熔融金屬噴射器系統之兩個對應儲集器5c之兩個回流導管310。各儲集器5c可包含經密封頂蓋,該頂蓋將儲集器5c中之較低壓力與較高反應電解槽腔室5b31壓力分離。EM泵噴射器部分5ka及5k61及噴嘴5q可穿透儲集器頂蓋以噴射熔融金屬,諸如反應電解槽腔室5b31中之銀。穿透可包含本發明之密封,諸如壓縮密封、滑動螺母、墊片、銅焊或填充箱密封。各儲集器5c可包含進水升管5qa以控制儲集器5c中之熔融金屬含量。反應電解槽腔室5b31之溫度可高於熔融金屬之沸點,使得噴射至反應電解槽腔室中之液態金屬氣化且經由回流導管310回流。 SunCell®可包含自MHD冷凝器通道309之末端至熔融金屬噴射器系統之至少一個儲集器5c之至少一個MHD工作介質回流導管310。SunCell®可包含自MHD冷凝器通道309之末端至雙熔融金屬噴射器系統之兩個對應儲集器5c之兩個MHD工作介質回流導管310。各儲集器5c可包含經密封頂蓋,該頂蓋將儲集器5c中之較低壓力與較高反應電解槽腔室5b31壓力分離。EM泵噴射器部分5ka及5k61及噴嘴5q可穿透儲集器頂蓋以噴射熔融金屬,諸如反應電解槽腔室5b31中之銀。穿透可包含本發明之密封,諸如壓縮密封、滑動螺母、墊片、銅焊或填充箱密封。各儲集器5c可包含進水升管5qa以控制儲集器5c中之熔融金屬含量。反應電解槽腔室5b31之溫度可高於熔融金屬之沸點,使得噴射至反應電解槽腔室中之液態金屬氣化,蒸氣經由MHD噴嘴部分307加速,蒸氣之動能轉換為發電機通道308中之電力,蒸氣冷凝在MHD冷凝器部分309中,且熔融金屬經由回流導管310回流。 SunCell®可包含至少一個MHD工作介質回流導管310、一個回流儲集器311及對應泵312。泵312可包含電磁(EM)泵。SunCell®可包含雙熔融金屬管310、回流儲集器311及對應EM泵312。對應進水升管5qa可控制各回流儲集器311中之熔融金屬含量。回流EM泵312可將MHD工作介質自MHD冷凝器通道309之末端泵送至回流儲集器311且接著至對應噴射器儲集器5c。在另一實施例中,熔融金屬回流經由回流導管310直接地至對應回流EM泵312且接著至對應噴射器儲集器5c。在一實施例中,針對壓力梯度(諸如約10 atm)泵送MHD工作介質(諸如銀)以完成熔融金屬流電路,包含噴射、點火、膨脹及回流。為達成高壓,EM泵可包含一系列級別。SunCell®可包含雙熔融金屬噴射器系統,其包含一對儲集器5c,該對儲集器各自包含EM泵噴射器5ka及5k61及進水升管5qa,以控制對應儲集器5c中之熔融金屬含量。回流可進入對應EM泵組合件5kk之底座5kk1。 在一實施例中,工作介質在至少一個位置(包含MHD組件中之位置,諸如噴嘴之入口、噴嘴、噴嘴之出口及MHD通道之所需部分)中之速度可足夠高,使得即使在滿足金屬蒸氣飽和條件之情況下,冷凝(諸如衝擊冷凝)不發生。由於與冷凝時間相比之較短轉變時間,可不發生冷凝。可藉由控制電漿壓力、電漿溫度、噴氣速度、工作介質組合物及磁場強度來更改或選擇冷凝動力學。諸如銀蒸氣之金屬蒸氣可冷凝於可具有較高表面積之冷凝器309上,且所收集液體銀可經由回流導管及EM泵系統回流。在一實施例中,利用避免衝擊冷凝之噴嘴中之較短轉變時間以允許另外將導致衝擊冷凝之MHD通道307中之有利MHD轉換條件的產生。 在一實施例中,亦已知作為MHD通道的MHD膨脹或發電機通道包含擴口MHD通道以持續導出能力轉換,其中熱量梯度轉換為驅動動能流量之壓力梯度。來自銀冷凝之熱量可有助於MHD通道中之壓力梯度或質量流量。藉由冷凝銀釋放之汽化熱可充當噴氣式引擎中之後燃器之功能以產生更高速度流量。在一例示性實施例中,銀汽化熱充當噴氣式後燃器中之燃燒功能以增加或有助於銀噴氣式流之速度。在一實施例中,藉由冷凝銀蒸氣釋放之汽化熱增加高於無冷凝存在下之壓力的壓力。MHD通道可包含幾何結構(諸如閃焰或噴嘴幾何結構)以將壓力轉換為經導引流量或藉由MHD轉換器轉換成電力的動能。可調節由MHD磁體306提供之磁場以防止電漿在銀蒸氣藉由導電性之對應改變冷凝之情況下停滯。在一實施例中,將MHD通道308之壁保持在高溫下以防止金屬蒸氣藉由對應質量及動能損失冷凝於壁上。較高電極溫度亦可防止電漿電弧放電,該電漿電弧放電可在與相對於較熱電漿具有較少導電或更多絕緣邊界層之冷卻電極相對之情況中發生。 可藉由將熱量自反應電解槽腔室5b31傳遞至MHD通道之壁而將MHD通道308保持在所需高溫下。MHD轉換器可包含將熱量自反應電解槽腔室傳遞至MHD通道之壁的熱交換器。熱交換器可包含導電或對流熱交換器,諸如包含將熱量自反應電解槽腔室傳遞至MHD通道之壁之熱傳遞區塊的熱交換器。熱交換器可包含輻射的熱交換器,其中反應電解槽腔室之至少一部分之外壁包含黑體輻射器以發射功率且MHD通道之壁之至少一部分可包含黑體輻射器以吸收黑體輻射。熱交換器可包含可經泵送之冷卻劑。泵可包含EM泵,其中冷卻劑為熔融金屬。在另一實施例中,低能量氫反應進一步傳播且保持在MHD通道308中以保持MHD通道壁溫度高於在通道中流動之金屬蒸氣之冷凝溫度。低能量氫反應可藉由供應反應物(諸如H及HOH催化劑或其來源)來保持。由於其支援且促進低能量氫反應速率之導電性,反應可選擇性地保持在電極處。MHD轉換器可包含記錄MHD通道壁溫度之至少一個溫度感測器及控制熱傳遞構件(諸如熱交換器)中之至少一者及保持所需MHD通道壁溫度之低能量氫反應速率的控制器。可藉助於本發明控制低能量氫反應速率,諸如控制低能量氫反應物至MHD通道之流動的構件。 在另一實施例中,將電漿、金屬蒸氣及冷凝金屬蒸氣中之至少一者限制在通道中且藉由通道限制構件(諸如包含電力及磁場中之至少一者之來源的構件)防止在MHD壁上收集。限制構件可包含磁性限制構件,諸如磁瓶。限制構件可包含以感應方式耦合之場,諸如RF場。MHD轉換器可包含RF電源、至少一個天線、靜電電極及電源以及至少一個靜磁磁場源中之至少一者以實現限制。 在一實施例中,工作介質包含MHD通道308中之氣化金屬,其中工作介質之壓力及溫度藉由由沿MHD通道冷凝金屬蒸氣釋放之熱量增加,此係因為其由於MHD轉換為電力而損失動能。來自銀之冷凝的能量可增加MHD通道中之工作介質之壓力、溫度、速度及動能中之至少一者。可藉由利用文丘里效應(Venturi effect)或柏努利原理(Bernoulli principle)的通道幾何結構增加流速。在一實施例中,流動液體銀可充當蒸氣之吸引器介質以使得其在MHD通道中流動。 在一實施例中,MHD通道308直徑及容積體積中之至少一者根據沿自噴嘴307出口至MHD通道308出口的MHD通道之流動軸或z軸之距離而減小。MHD通道308可包含僅聚集z軸之通道。在另一實施例中,沿z軸之通道大小仍然相同且發散小於習知經晶種氣體MHD工作介質轉換器之通道大小。在銀冷凝且釋放熱量以保持高能電漿時,可減小通道體積以保持沿z軸之壓力及速度。藉由沿z軸之電漿流動自冷凝銀蒸氣(254 kJ/莫耳)釋放之汽化熱可增加工作介質之溫度及壓力以使得增加沿通道之z軸的任何給出位置處非冷凝銀之流動。流速之增加可由文丘里效應或柏努利原理造成。磁通量可沿MHD通道之流動軸(z軸)持久性或動態地變化以提取隨z軸位置而變之MHD功率以保持沿通道之所要壓力、溫度、速度、功率及能量存量,其中隨沿z軸之距離而變的通道大小可匹配z軸磁通量變化以至少部分地實現氣化金屬自提取汽化熱之能量作為電力。電漿氣流亦可充當經冷凝銀蒸氣之載氣。 經冷凝銀可包含薄霧或霧。由於銀在遠低於給出壓力下之其沸點的溫度下形成氣溶膠之趨勢,霧狀態可為有利的。工作介質可包含氧氣及銀,其中熔融銀具有在遠低於給出壓力下之其沸點的溫度下在氧氣存在下形成氣溶膠的趨勢,其中銀可吸收大量氧氣。工作介質可包含氣溶膠化氣體,諸如氮氣、氧氣、水蒸氣或稀有氣體(諸如氬氣),除諸如形成冷凝銀之氣溶膠之銀蒸氣的金屬蒸氣以外。在一實施例中,在整個反應電解槽腔室及MHD通道中之氣溶膠化氣體之壓力可在操作條件下保持在其穩態分佈處。MHD轉換器可進一步包含氣溶膠化氣體之供應源,諸如氣溶膠化氣體之貯槽、泵及選擇性地量測一或多個位置處之氣溶膠化氣體壓力的至少一個量規。可使用泵及氣溶膠化氣體供應器藉由添加或移除氣溶膠化氣體將氣溶膠化氣體存量保持在所需含量處。在一例示性實施例中,液體銀在僅高於熔點之溫度下形成霧或氣溶膠,使得MHD通道308中之恆定環境壓力氣溶膠化氣體(諸如氬氣)使銀蒸氣至液體轉變以氣溶膠之形式發生,該氣溶膠可攜帶有電漿流量且聚集於MHD冷凝器309上。在一實施例中,冷凝蒸氣之速度保存於冷凝物中。冷凝物之速度可自釋放汽化熱增加。MHD通道可包含將汽化熱轉換為冷凝物動能的幾何結構。在一實施例中,通道可為窄的以將汽化熱轉換為冷凝物動能。在另一實施例中,汽化熱可增加通道壓力,且壓力可藉由噴嘴轉換為動能。在一實施例中,銅或銀-銅合金可替換銀。在一實施例中,充當金屬氣溶膠之來源的熔融金屬包含銀、銅及銀-銅合金中之至少一者。氣溶膠可在氣體存在下形成,該氣體諸如氧氣、水蒸氣及稀有氣體(諸如氬氣)中之至少一者。 在一實施例中,SunCell®包含保持電解槽氣體之流量與熔融銀接觸以形成熔融金屬氣溶膠(諸如銀氣溶膠)的構件。氣流可包含加壓氣流及對流氣流中之至少一者。在一實施例中,反應電解槽腔室5b31及儲集器5c中之至少一者可包含至少一個擋扳以使得電解槽氣體循環以增加氣流。可藉由諸如由來自電漿反應之熱量梯度及壓力中之至少一者造成之彼等的對流及壓力梯度中之至少一者來驅動流動。氣體可包含稀有氣體、氧氣、水蒸氣、H2 及O2 中之至少一者。保持氣流之構件可包含氣泵或壓縮機中之至少一者,諸如MHD氣泵或壓縮機312a、MHD轉換器及由EM泵熔融金屬噴射器及低能量氫電漿反應中之至少一者引起的擾流。可控制氣體之氣流速率及組合物中之至少一者以控制氣溶膠產生速率。在一實施例中,其中水蒸氣經再循環,SunCell®進一步包含將熱化為H2 及O2 的任何H2 O重組為H2 O的複合器、將水蒸氣冷凝至液體水的冷凝器及將加壓水噴射至供應至少一個內部電池組件的線路中之液體水泵,該內部電池組件諸如儲集器5c或反應電解槽腔室5b31,其中加壓水可在路徑中轉變為蒸汽以在電池之內部噴射。複合器可為此項技術中已知之複合器,諸如包含雷尼鎳、Pd及Pt中之至少一者的複合器。水蒸氣可在包含高壓區室之迴路中(諸如在反應電解槽腔室5b31與儲集器5c之間)經再循環。 在一實施例中,儲集器5c及反應電解槽腔室5b31中之至少一者包含具有足夠低溫度以進行以下中之至少一者之氣體來源:將銀蒸氣冷凝為銀氣溶膠且冷卻銀氣溶膠。藉由高能低能量氫反應釋放之熱量可形成銀蒸氣。氣化可在低能量氫反應電漿中發生。與低能量氫反應接觸的環境氣體包含電解槽氣體。電解槽氣體及氣溶膠中之至少一者之一部分可藉由含有氣體氣溶膠及電漿中之至少一者的儲集器及反應電解槽腔室中之至少一者之區域內部中之熱交換器及急冷器冷卻。電解槽氣體及氣溶膠中之至少一者可經充分冷卻以進行以下中之至少一者:將銀蒸氣冷凝為氣溶膠且冷卻氣溶膠。可藉由控制冷卻期間之熱傳遞及冷卻電解槽氣體及氣溶膠之溫度及壓力來控制蒸氣冷凝速率及冷卻電解槽氣體-氣溶膠-蒸氣混合物之溫度及壓力中之至少一者。 在一實施例中,為避免沿通道之質量損失,銀蒸氣在蒸氣冷凝時導致形成霧。沿通道損失其電力之動能的莫耳分數可導致形成霧,其中對應汽化熱將動能賦予對應氣溶膠粒子以保持另外損失質量之恆定初速度。由於部分原子聚合為與剩餘氣體原子一起流動之氣溶膠粒子,通道可為直線彙聚以保持伴隨減小之粒子數目的速度。在一實施例中,MHD通道308壁可維持在諸如大於銀之熔點的溫度下以避免經冷凝液體藉由支援霧形成冷凝。 在一實施例中,銀電漿噴射接觸之MHD通道組件及表面可包含藉由銀液體抗潤濕之材料。MHD通道壁308及MHD電極304中之至少一者可包含抗潤濕之表面。 氣溶膠粒子可經充電及收集。收集可在MHD通道末端發生。可藉由靜電沈澱或電噴射沈澱移除氣溶膠粒子。在一實施例中,MHD轉換器可包含氣溶膠粒子充電構件(諸如至少一個粒子充電電極)、電能供應源(諸如高壓源)及經電性偏壓以收集帶電粒子帶電粒子集電極(諸如至少一個電極)。可藉由施加電場在MHD通道末端收集帶電粒子。 在一實施例中,藉由電漿流量進行金屬蒸氣液滴。液滴可形成MHD電極及MHD通道壁中之至少一者之表面上之薄膜。盈餘經冷凝液體可經機械地剝蝕且藉由電漿及質量流量運載。在一實施例,法拉第電流穿過經冷凝金屬蒸氣(諸如經冷凝銀蒸氣)且產生霍耳電流,該霍耳電流促使經冷凝銀粒子沿著來自MHD噴嘴307之電漿噴射的軌跡。霍耳電流可使經冷凝銀流出MHD通道以回流至儲集器5c。由於比金屬蒸氣更高的導電性,電流可較佳地流動穿過經冷凝銀。在另一實施例中,可藉由MHD通道之發散及彙聚中之至少一者來輔助輸送。在一實施例中,諸如圓盤發電機之MHD轉換器可包含在MHD通道之入口及出口處接觸電漿以使得改善熔融金屬在通道中之短路之效應的電極。 在一實施例中,工作介質包含可在低於其沸點之溫度下昇華以防止金屬冷凝於MHD通道之壁上以使得其流至再循環系統的金屬(諸如銀)。在一實施例中,將MHD通道之出口處之壓力保持在低壓(諸如低於常壓之壓力)處。真空可保持在MHD通道之出口處,使得工作介質金屬蒸氣不在MHD通道308中冷凝。可藉由MHD氣泵或壓縮機312a (圖2I67至圖2I73)保持真空。 在一實施例中,MHD通道可包含入口部分中之發電機及出口部分中之壓縮機。壓縮機可使得將經冷凝蒸氣泵送出MHD通道。MHD轉換器可包含電流源及電流控制器,以可控制地在所施加磁場之垂直方向上將電流施加至MHD通道之工作介質,以使得經冷凝工作介質蒸氣自通道流動,其中通道條件可經控制以使得蒸氣冷凝以實現蒸氣之汽化熱之釋放。 在另一實施例中,可藉由在諸如MHD冷凝器309的熱交換器處冷凝蒸氣來諸如銀金屬蒸氣的金屬蒸氣之汽化熱。冷凝可在高於諸如銀的金屬之沸點的溫度下發生。可藉由此項技術中已知之手段(諸如藉由對流、傳導、輻射)或藉由冷卻劑將熱量傳遞至儲集器5c之一部分。熱傳遞系統可包含藉由傳導傳遞熱量之耐火熱傳遞區塊,諸如Mo、W或碳區塊。熱量可使得儲集器中之銀汽化。熱量可保存於汽化熱中。低能量氫反應可進一步增加氣化金屬之壓力及溫度。在包含工作介質添加劑(諸如稀有氣體,諸如氬氣或氦氣)之一實施例中,MHD轉換器進一步包含氣泵或壓縮機312a (圖2I67至圖2I73)以將氣體自低壓再循環至MHD轉換器之高壓部分。氣泵或壓縮機312a可包含驅動馬達312b及刮刀或輪葉312c。MHD轉換器可包含泵入口及泵出口,該泵入口可包含自MHD冷凝部分309至泵入口的氣體通路310a,該泵出口可包含自泵或壓縮機312a至反應電解槽腔室5b31的氣體通路313a。泵可將氣體自低壓(諸如約1至2 atm)泵送至高壓(諸如約4至15 atm)。自MHD冷凝部分309至泵312a之進水管310a可包含過濾器,諸如入口處的選擇性膜或金屬冷凝器,以將氣體(諸如稀有氣體)自金屬蒸氣(諸如銀蒸氣)分離。MHD冷凝器部分309中之擋板309a可將熔融金屬(諸如在MHD冷凝部分309中冷凝之熔融金屬)導引至MHD回流導管310中。中心中之擋板之高度及MHD回流導管310之熔融金屬回流入口中之至少一者可在其中上升氣體壓力超過經冷凝或液體熔融金屬粒子上之重力之力的位置處,以促進其流入MHD回流導管310中。 SunCell®可包含可位於MHD冷凝部分309中之金屬蒸氣冷凝器(諸如恆定壓力冷凝器)且可包含熱交換器316。工作介質可包含金屬蒸氣晶種之載劑或工作氣體,諸如銀蒸氣晶種之稀有氣體,諸如氦氣或氬氣。冷凝器可冷凝金屬蒸氣以使得可單獨地泵送液態金屬及稀有氣體。可藉由以下組之方法中之至少一者來分離:重力沈積、離心分離、氣旋分離、過濾、靜電沈澱及熟習此項技術者已知之其他方法。在一例示性實施例中,自冷凝器之頂部移除經分離稀有氣體,且自冷凝器之底部移除經分離液態金屬。液體及氣體可由以下中之至少一者分離:擋板309a、過濾器、選擇性滲透膜及氣體可穿過之液體障壁。 壓縮機312a可泵送氣體或使得氣體再循環至反應電解槽腔室5b31。EM泵312可泵送液體銀以使其回流至儲集器5c,以回注至反應電解槽腔室5b31。壓縮機312a及EM泵312分別再加壓工作介質氣體(諸如氬氣或氦氣)及液態金屬(諸如液體銀)。工作介質氣體可經由導管313a回流至反應電解槽腔室,該管可連接EM泵管5k6、儲集器5c、EM泵組合件5kk之底座5kk1及反應電解槽腔室5b31中之至少一者。替代地,氣體可經由管313a回流至反應電解槽腔室5b31,該管連接至傳送管313b,諸如提供至儲集器5c或反應電解槽腔室5b31中之導引通路的傳遞管。氣體可用於將熔融金屬噴射至反應電解槽腔室中。熔融金屬可變得夾帶在氣體噴射中以替換或補充EM泵熔融金屬噴射器。可藉由控制氣體流速、氣體壓力、氣體溫度、儲集器溫度、反應電解槽溫度、噴嘴進水壓力、MHD噴嘴流速、MHD噴嘴出口壓力及低能量氫反應速率來控制經噴射熔融金屬及蒸氣(諸如液體及氣態銀蒸氣)流動速率。 用於工作介質氣體及熔融金屬中之至少一者(諸如延行穿過儲集器5c之熔融金屬的工作介質氣體及熔融金屬)的回流導管313b可包含耐火材料,諸如Mo、W、錸、經錸塗佈之Mo或W、陶瓷(諸如金屬氧化物,諸如ZrO2 、HfO2 、MgO、Al2 O3 )中之至少一者及本發明之其他者。管可包含螺紋成EM泵管組合件基座5kk1中之套環或底座的耐火材料管。回流導管313b之高度可為期望傳送氣體的同時允許其他分量之期望效能(諸如金屬噴射劑)的高度且分別藉由EM泵管5k61及進水升管5qa之噴射部分來控制含量。高度可為約儲集器熔融金屬含量。 在圖2I71至圖2I73中所展示之一實施例中,氣泵或壓縮機312a可泵送氣態工作介質物種之混合物,該氣態工作介質物種諸如稀有氣體、熔融金屬晶種及熔融金屬蒸氣(諸如銀蒸氣)中之至少兩者。在一實施例中,氣泵或壓縮機312a可泵送氣態及液體工作介質二者,諸如稀有氣體、金屬蒸氣及液體熔融金屬(諸如液體銀)中之至少一者。液體及氣體可經由管313a回流至反應電解槽腔室,該管可連接EM泵管5k6、儲集器5c、EM泵組合件5kk之底座5kk1及反應電解槽腔室5b31中之至少一者。替代地,氣體可經由管313a回流至反應電解槽腔室5b31,該管連接至傳送管313b,諸如提供至儲集器5c或反應電解槽腔室5b31中之導引通路的傳遞管。 在一實施例中,氣體及液體可流動穿過EM泵管5k6。氣體可用於將熔融金屬噴射至反應電解槽腔室中。熔融金屬可變得夾帶在氣體噴射中以進行以下中之至少一者:加強且替換EM泵以經由噴射器管5k61及噴嘴5q泵送熔融金屬。可藉由控制氣泵或壓縮機312a之流速及壓力中之至少一者及藉由本發明之其他手段來控制噴射速率。可藉由相對於成對之其他控制一個氣泵或壓縮機312a之壓力及流速中之至少一者的本發明之水平感測器及控制器來控制儲集器5c之熔融金屬含量。 在包含泵送所有工作介質(諸如銀晶種之稀有氣體)之氣泵或壓縮機的一實施例及包含僅泵送稀有氣體之氣泵或壓縮機的一實施例中,可等溫地操作壓縮。MHD轉換器可包含熱交換或冷卻器以進行中之至少一者:在壓縮之前及期間冷卻氣態工作介質。氣泵或壓縮機可包含中間冷卻器。氣泵或壓縮機可包含複數個級別,諸如多級中間冷卻器壓縮機。冷卻可增加壓縮氣體之效率以匹配反應電解槽腔室5b31之操作壓力。 在回流循環中之泵送階段之後,回流氣態工作介質可經加熱以增加其壓力。加熱可藉由自MHD轉換器接收熱量的熱交換器或可自MHD冷凝部分309或其他熱組件接收熱量的再生器實現,該其他熱組件諸如以下群組中之至少一者:反應電解槽腔室5b31、MHD噴嘴部分307、MHD發電機部分308及MHD冷凝部分309。在一實施例中,可藉由使用用於分別流入反應電解槽腔室5b31及流出MHD噴嘴之氣體的入口閥及出口閥而大量地減少氣泵功率,其中將低壓氣體泵送至反應電解槽腔室中且壓力藉由電漿反應功率增加至所要壓力,諸如10 atm。可將所得脈衝MHD功率調節為穩定DC或AC功率。回流MHD氣體管313a可包含打開以准許比峰值反應電解槽腔室操作壓力更低的壓力之氣體流動的閥門,且MHD噴嘴部分307可包含打開以允許高壓氣體在藉由反應電解槽腔室5b31電漿加熱氣體後流出噴嘴的閥門。閥門可有助於藉由氣泵或壓縮機將低壓氣體噴射至反應電解槽腔室中,其中藉由低能量氫反應電漿將氣體加熱至高壓。閥門可經同步以准許藉由電漿加熱累積之反應腔室壓力。閥門可為180°異相。閥門可包含轉動擋閘類型。MHD噴嘴可經冷卻以准許操作MHD噴嘴閥門。回流氣體管313a閥門可在EM泵組合件5kk1之底座處或靠近該EM泵組合件之底座以避免銀在對應氣體傳送管313b中冷凝。MHD轉換器可包含脈衝電力系統,包含反應電解槽腔室5b31之工作介質氣體之入口閥及出口閥的電力系統。脈衝MHD功率可水平化至藉由功率調節設備輸出恆定功率,諸如包含功率儲存之設備,諸如電池組或電容器。 在一實施例中,經再循環之熔融金屬(諸如銀)仍然呈氣態,其中包括任何回流線路310a、管313a及泵312a的MHD轉換器之溫度在MHD系統中之操作壓力或銀分壓下保持呈高於銀之沸點溫度的溫度。 泵312a可包含機械泵,諸如齒輪泵(諸如陶瓷齒輪泵),或此項技術中已知之其他泵,諸如包含葉輪之泵。泵312a可在高溫下操作,諸如在約962℃至2000℃之溫度範圍中操作。泵可包含渦輪機類型,諸如用於燃氣渦輪機之渦輪機或用作內燃引擎之渦輪增壓器之類型的渦輪機。氣泵或壓縮機312a可包含螺旋泵、軸向壓縮機及渦輪機壓縮機中之至少一者。泵可包含正排量類型。氣泵或壓縮機可將根據伯努利定律(Bernoulli's law)在固定反應電解槽腔室體積中轉換為壓力的較高氣體速度。回流氣體管313a可包含閥門(諸如背壓遏制閥)以迫使來自壓縮機之流體流入反應電解槽腔室且接著MHD轉換器。 易於由工作介質磨損之機械部件(諸如泵312a輪葉或渦輪機刮刀)可經熔融金屬(諸如熔融銀)塗佈以防止其磨耗或磨損。在一實施例中,包含氣泵或壓縮機之氣體及熔融金屬回流系統之至少一個組件(諸如MHD回流導管310a、回流儲集器311a、與回流氣體及熔融金屬接觸之MHD回流氣泵或壓縮機312a部件(諸如輪葉)及MHD泵管313a (圖2I67至圖2I73))包括執行熱保護且防止由熔融金屬潤濕之至少一個功能以促進回流金屬流動至儲集器5c。 在一實施例中,在SunCell®啟動期間,壓縮機312a可再循環工作介質(諸如氦氣或氬氣)以預熱反應電解槽腔室5b31及MHD組件中之至少一者,諸如MHD噴嘴部分307、MHD通道308、MHD冷凝部分309及包含MHD回流導管310、回流儲集器311、MHD回流EM泵312及MHD回流EM泵管313之EM回流泵系統之至少一個組件。工作介質可分流至EM回流泵系統之至少一個組件。諸如對應於天線5f之電感耦合加熱器可加熱可經再循環以使得預加熱反應電解槽腔室5b31及至少一個MHD組件中之至少一者的工作介質。 在一例示性實施例中,MHD系統包含工作介質,該工作介質包含經銀接種或經銀-銅合金接種之氬氣或氦氣,其中大部分壓力可歸因於氬氣或氦氣。銀或銀-銅合金莫耳分數隨著增加使用氬氣供應源、感測及控制系統控制之稀有氣體(諸如氬氣)分壓而下降。SunCell®可包含冷卻系統以用於反應電解槽腔室5b31及MHD組件,諸如MHD噴嘴部分307、MHD通道308及MHD冷凝部分309中之至少一者。可控制至少一個參數,諸如反應電解槽腔室5b31及MHD通道之壁溫度及反應及氣體混合條件,以確定最佳銀或銀-銅合金存量或蒸氣壓力。在一實施例中,最佳銀蒸氣壓力為最佳化金屬蒸氣之導電性及能量存量以實現最佳功率轉換密度及效率的銀蒸氣壓力。在一實施例中,一些金屬蒸氣冷凝於MHD通道中以釋放在MHD通道中轉換為額外動能且轉換為電力的熱量。泵或壓縮機312a可包含諸如用於銀及氬氣二者之機械泵,或MHD轉換器可包含兩個泵類型,氣體312a及熔融金屬312。 在一實施例中,MHD轉換器可包含複數個噴嘴以產生呈複數個級別之熔融金屬之高速傳導流。第一噴嘴可包含與反應電解槽腔室5b31結合之噴嘴307。其他噴嘴可位於冷凝部分309處,其中自冷凝銀釋放之熱量可在噴嘴之入口處產生高壓。MHD轉換器可包含在各噴嘴之下游具有交叉磁體及電極的MHD通道以將高速傳導流轉換為電力。在一實施例中,MHD轉換器可包含複數個反應電解槽腔室5b31,諸如在緊靠著前述噴嘴之位置中。 在不包含回流儲集器311之一實施例中,其中MHD通道309之末端表現得如同黑體輻射器5b41之下半球,且回流EM泵312速度較快(不限制回流速率),則銀將以與其在本發明之黑體輻射器設計中相同之方式分配回至噴射儲集器5c。可接著藉由各儲集器5c之進水升管5qa來控制相對噴射速率,如在本發明之黑體輻射器設計之情況中。 在一實施例中,SunCell®包含在僅加速噴嘴307之下游的位置處的EM泵以將經冷凝熔融金屬泵送回至熔融金屬噴射器系統之至少一個儲集器,諸如開放式雙熔融金屬噴射器系統5ka及6k61之儲集器5c。 在一實施例中,SunCell®包含可藉由熟習此項技術者選擇之回流導管310及310a、回流儲集器311及311a、回流EM泵312及壓縮機312a、開放式噴射器儲集器5c、封閉式噴射器儲集器5c、開放式EM泵噴射器截面5k61及噴嘴5q以及封閉式EM泵噴射器截面5k61及噴嘴5q之其他組合及組態,以實現MHD工作介質經由反應電解槽腔室5b31及MHD轉換器300之所要流動電路。在一實施例中,諸如回流儲集器311及噴射儲集器5c中之至少一者的任何儲集器之熔融金屬含量控制器5qa可包含進水升管5qa、本發明之其他者及熟習此項技術者已知者中之至少一者。 在一實施例中,工作介質可包含氣態及液相之混合物,諸如至少一種液態金屬及至少一種氣體,諸如金屬蒸氣及氣體(諸如稀有氣體)中之至少一者。例示性工作介質包含液體銀及氣態銀或液體銀、氣態銀及至少一種其他氣體,諸如稀有氣體或其他金屬蒸氣。 在一實施例中,MHD轉換器可包含液態金屬MHD (LMMHD)轉換器,諸如此項技術中已知之轉換器。LMMHD轉換器可包含熱交換器以使得熱量自反應電解槽腔室5b31流動至LMMHD轉換器。MHD轉換器可包含利用Rankine、Brayton、Ericsson及Allam循環中之至少一者的系統。在一實施例中,工作介質包含高密度且相對於稀有氣體保持高密度,使得工作流體之復原及再循環泵送中之至少一者藉由工作流體之較少膨脹及較多熱量保持中之至少一者來實現。工作介質可包含熔融金屬及其蒸氣,諸如銀及銀蒸氣。工作介質可進一步包含液體及蒸氣狀態中之至少一者中之額外金屬及諸如稀有氣體、蒸汽、氮氣、氟利昂(Freon)、氮氣及液態金屬MHD (LMMHD)轉換器之此項技術中已知之其他者的氣體中之至少一者。在一實施例中,MHD轉換器可包含EM泵、MHD壓縮機及機械壓縮機或泵中之至少一者以再循環工作介質。 MHD轉換器可進一步包含混合器以將液體與氣體混合,其中可在混合之前加熱至少一個相。替代地,可加熱經混合相。由於加熱在工作介質中產生之壓力,包含相之混合物的熱工作介質流動至MHD通道中以產生電力。在另一實施例中,液體可包含複數種液體,諸如充當導電基質(諸如銀)之液體及由於其在反應電解槽腔室中氣化而具有較低沸點以充當氣態工作介質之另一種液體。金屬之氣化可准許熱力學MHD循環。由二相傳導產生之電能在MHD通道中流動。可藉由熱交換器加熱工作介質以產生壓力以提供通道中之流動。反應電解槽腔室可向熱交換器之入口提供流動至熱交換器出口且接著工作介質的熱量。 在一實施例中,低能量氫電漿蒸氣在混合器中與液體銀混合以形成二相工作介質。加熱產生主要熔融銀通過其中熱量動能轉換為電力之MHD通道及冷卻器的高壓流,MHD通道之出口處之低壓工作介質藉由MHD EM泵再循環。 在包含混合循環(開放式氣體循環及封閉式金屬循環)之一實施例中,工作介質可包含用金屬蒸氣(諸如銀金屬蒸氣)接種之氧氣、氮氣及空氣中之至少一者。在反應電解槽腔室5b31中氣化以包含氣體晶種之液態金屬(諸如銀)可在離開MHD通道308後冷凝且再循環至儲集器5c。離開MHD通道之氣體(諸如空氣)可自晶種分離且可排出至大氣。可自排出氣體回收熱量。可藉由氣體泵或壓縮機312a吸入諸如空氣之環境氣體。 在一實施例中,MHD轉換器可包含均相MHD發電機,其包含經加熱以使得金屬在至MHD通道之入口處氣化的金屬或金屬混合物。轉換器可進一步包含通道入口熱交換器以將熱量自反應電解槽腔室傳遞至工作介質以使得其在進入至MHD通道之前氣化。均相MHD發電機可進一步包含MHD通道之出口處的通道熱交換器以充當再生器以在熱量流動至入口熱交換器之前將其傳遞至工作介質。入口熱交換器可包含通過反應電解槽腔室之工作介質管。金屬工作介質可在出口熱交換器之下游的冷凝熱交換器處冷凝,其中接著藉由再循環EM泵來泵送熔融金屬。 在一實施例中,工作介質包含金屬及氣體,該氣體在低溫下可溶於熔融金屬且在高溫下不可溶於熔融金屬或較不溶於熔融金屬。在一例示性實施例中,工作介質可包含銀及氧氣中之至少一者。在一實施例中,反應電解槽腔室中之氧氣壓力保持在大體上防止熔融金屬(諸如銀)經受氣化的壓力處。低能量氫反應電漿可加熱氧氣及液體銀至所需溫度,諸如3500K。包含工作介質之混合物可在諸如25 atm之壓力下流動通過楔形MHD通道,其中壓力及溫度在熱能轉換成電力時下降。由於溫度下降,熔融金屬(諸如銀)可吸收氣體(諸如氧氣)。接著,可將液體泵送回至儲集器以在反應電解槽腔室中再循環,其中電漿加熱釋放氧氣以增加保持所要反應電解槽腔室壓力及溫度條件以驅動MHD轉換。在一實施例中,MHD通道之出口處的銀之溫度為約熔融金屬之熔點,其中氧氣之溶解度在一個大氣壓O2 下為氧氣之約20 cm3 (STP)至銀之1 cm3 。包含溶解氣體之液體之再循環泵送功率可大大小於游離氣體之功率。此外,可大體上減少在熱力學功率循環期間使游離氣體之壓力及溫度下降的氣體冷卻需求及MHD轉換器體積。 在一實施例中,MHD通道可為垂直的且通道中之工作介質之壓力梯度可由於重力之力大於壓力等值,使得熔融金屬之工作介質流量保持在自反應電解槽腔室5b31至MHD通道之出口的循環中,其中將熔融金屬泵送回至儲集器5c。在一實施例中,最小壓力P為P = pgh (45) 其中p為密度(對於銀,1.05×104 kg/m3 ),g為重力常數,且h為金屬管柱之高度。對於例示性,h=0.2 m,P=0.2 atm。 噴嘴307中之膨脹可為等熵的。在一實施例中,反應電解槽腔室5b31中之低能量氫反應條件可提供且保持適合MHD噴嘴307溫度及壓力,使得噴嘴可產生高速度射流,同時避免冷凝衝擊。可在於MHD通道308中膨脹期間保持約常數速度條件及連續性條件中之至少一者(由此密度、速度及面積之乘積為約常數)。在一實施例中,在自MHD噴嘴307至MHD通道308的進入口處噴射超聲波銀蒸氣。一些銀可冷凝於通道中,但是由於等熵膨脹,冷凝可受限。包含蒸氣及任何經冷凝液體之射流中之剩餘能量以及銀之汽化熱可藉由在冷凝器309處冷凝至少部分地回收且藉由再循環器或再生器(諸如散熱管)再循環。在一實施例中,使用散熱管實現再生,其中散熱管至少回收銀汽化熱且再循環其,使得經回收熱量功率為輸入至 MHD通道的功率之部分;接著此功率平衡之分量僅降低散熱管之效率。冷凝之金屬蒸氣之百分比可為無關緊要的,諸如在約1%至15%之範圍內。在一實施例中,經冷凝蒸氣可導致形成氣溶膠。反應電解槽腔室、噴嘴及MHD通道可含有導致冷凝蒸氣來自氣溶膠的氣體,諸如氬氣。蒸氣可在冷凝器(諸如冷凝器309)處冷凝在MHD通道308之末端。液態金屬可經再循環,且汽化熱可藉由再生器(諸如包含散熱管之再生器)至少部分地回收。 在另一實施例中,蒸氣可經加壓以冷凝在所要區域中,諸如噴嘴307部分。噴嘴膨脹可為等熵的,其中純氣體(諸如銀蒸氣)之冷凝限於臨界溫度處開始之50%液體莫耳分數及對於銀分別為506.6 MPa及7480 K的重要壓力。在一實施例中,可藉由諸如移除熱量以使得熵值可減少及用至少一種其他氣體加壓冷凝區域中之至少一者的手段來克服來自經加壓蒸氣之膨脹的此冷凝侷限性。氣體壓力在其中存在氣體連續性的區域之所有部分中,諸如在反應電解槽腔室5b31、噴嘴307及MHD通道308區域中可為相等的。MHD轉換器可進一步包含其他氣體之貯槽、氣壓計、氣泵及氣體壓力控制器。可藉由壓力控制器控制至少一種其他氣體壓力。可控制氣體壓力以使得在比純金屬蒸氣之等熵膨脹更大的程度上冷凝金屬蒸氣。在一實施例中,氣體包含可溶於蒸氣金屬中之氣體。在一例示性實施例中金屬包含銀且氣體包含O2 及H2 O中之至少一者。 在一實施例中,噴嘴307及MHD通道308中之至少一者中之壓力產生藉由在金屬氣相快速地冷凝至液態金屬流上時產生冷凝衝擊來實現,產生自二相至單相流動的快速轉化,從而釋放汽化熱。能量釋放為顯現為液體流之動能。液體流之動能在MHD通道308中轉換為電力。在一實施例中,蒸氣冷凝為霧或氣溶膠。氣溶膠可在氣體環境氛圍中形成,諸如包含氣溶膠形成氣體(諸如氧氣)及視情況選用之稀有氣體(諸如氬氣)的氣體環境氣氛。MHD通道308可為直線的以保持MHD通道流動之恆定速度及壓力。氣溶膠形成氣體(諸如氧氣)及視情況選用之稀有氣體(諸如氬氣)可流動通過儲集器5c、反應電解槽腔室5b31、MHD噴嘴307、MHD通道308及其他MHD轉換器組件(諸如任何回流線路310a、管313a及泵312a)中之至少一者。可藉由MHD回流氣泵或壓縮機312a再循環氣體。 在一實施例中,噴嘴307包含冷凝噴流噴射器,該冷凝噴流噴射器包含二相噴射裝置,其中呈液態之熔融金屬與其氣相混合,產生具有壓力的液體流,該壓力高於兩個進水流中之任一者之壓力。壓力可在反應電解槽腔室5b31及噴嘴307中之至少一者中產生。噴嘴壓力可在噴嘴307之出口處轉換為流速度。在一實施例中,反應電解槽腔室電漿包含噴射裝置之一個相。來自至少一個EM泵噴射器之熔融金屬可包含噴射裝置之其他相。在一實施例中,可藉由獨立EM泵噴射器噴射諸如液相之其他相,該EM泵噴射器可包含EM泵5ka、儲集器(諸如5c)、EM泵管5k61之噴嘴部分及噴嘴5q。 在一實施例中,MHD噴嘴307包含氣溶膠噴流噴射器,該氣溶膠噴流噴射器在MHD通道308中將反應電解槽腔室5b31之高壓電漿轉換為高速度氣溶膠流或噴流。噴流之動能可來自反應電解槽腔室5b31中之電漿之壓力組之至少一個源及經冷凝以形成氣溶膠噴流之金屬蒸氣之汽化熱。在一實施例中,經冷凝蒸氣之莫耳體積為小於標準條件下之對應蒸氣的約50至500倍。蒸氣在噴嘴307中之冷凝可使得噴嘴之出口部分處的壓力減小。減小的壓力可導致增加可包含液體及氣溶膠噴流中之至少一者的經冷凝流體之速度。噴嘴可經伸展且可經彙集以將局部壓力轉換為動能。通道可包含比噴嘴出口之面積更大的橫截面積,且可為直線的以允許傳播氣溶膠流。其他噴嘴307及MHD通道308幾何結構(諸如具有彙集、發散及直線截面的幾何結構)可經選擇以實現金屬蒸氣之所要冷凝,其中在MHD通道308中將能量之至少一部分轉換為傳導流。 在一實施例中,一些殘餘氣體在MHD通道308中可保持不冷凝。未冷凝氣體可支援MHD通道中之電漿以提供導電MHD通道流動。可藉由可在MHD通道308中傳播之低能量氫反應保持電漿。可將低能量氫反應物提供至反應電解槽腔室5b31及MHD通道308中之至少一者。 在一實施例中,噴嘴307及MHD通道308中之至少一者中之壓力產生藉由金屬蒸氣(諸如銀金屬蒸氣)之冷凝與汽化熱之釋放來實現。能量釋放顯現為冷凝物之動能。流動之動能可在MHD通道308中轉換為電力。MHD通道308可為直線的以保持MHD通道流動之恆定速度及壓力。在一實施例中,蒸氣冷凝為霧或氣溶膠。氣溶膠可在包含惰性氣體(諸如包含氬氣的惰性氣體)的環境氣氛中形成。氣溶膠在包含氧氣之環境氣氛可形成。MHD轉換器可包含金屬氣溶膠(諸如銀氣溶膠)之來源。來源可包含雙熔融金屬噴射器中之至少一者。氣溶膠來源可包含獨立EM泵噴射器,該EM泵噴射器可包含EM泵5ka、儲集器(諸如5c)、EM泵管5k61之噴嘴部分及噴嘴5q,其中熔融金屬噴射劑至少部分地轉換為金屬氣溶膠。氣溶膠可流動或噴射至其中需要冷凝金屬蒸氣之區域中,諸如在MHD噴嘴307中。氣溶膠可在比對於經受等熵膨脹(諸如等熵噴嘴膨脹)之金屬蒸氣為可能的程度更大的程度上冷凝金屬蒸氣。金屬蒸氣冷凝可釋放金屬蒸氣汽化熱,該金屬蒸氣汽化熱可增加氣溶膠之溫度及壓力中之至少一者。對應能量及功率可有助於噴嘴之出口處的氣溶膠及電漿流之動能及功率。由於來自金屬蒸氣汽化熱之功率之貢獻,流動之功率可隨著效率的增加轉換為電力。MHD轉換器可包含金屬氣溶膠之來源之控制器以控制氣溶膠流速及氣溶膠質量密度中之至少一者。控制器可控制氣溶膠之EM泵來源之EM泵送的速率。可控制氣溶膠噴射速率以最佳化回收蒸氣汽化熱之蒸氣冷凝及MHD功率轉換效率。 在一實施例中,藉由蒸氣在噴嘴中冷凝釋放之汽化熱直接地或間接地至少部分地傳遞至反應電解槽腔室電漿。噴嘴可包含熱交換器以將熱量傳遞至反應電解槽腔室。可藉由輻射、傳導及對流之至少一個方法來傳遞熱量。可藉由經釋放汽化熱加熱噴嘴且可藉由傳導將熱量傳遞至反應電解槽腔室。噴嘴可包含高度導熱之材料,諸如可包含抗氧化塗層的耐火導熱體。在例示性實施例中,噴嘴可包含可用抗氧化耐火塗層(諸如ZrO2 塗層)塗佈之氮化硼或碳。材料可包含本發明之其他耐火材料及塗層。 在一實施例中,噴嘴307及MHD通道308中之至少一者中之壓力產生藉由金屬蒸氣(諸如銀金屬蒸氣)之冷凝與汽化熱之釋放來實現。能量釋放顯現為冷凝物之動能。流動之動能可在MHD通道308中轉換為電力。MHD通道308可為直線的以保持MHD通道流動之恆定速度及壓力。在一實施例中,蒸氣冷凝為霧或氣溶膠。氣溶膠可在環境氣氛中形成,諸如包含氬氣及氧氣中之至少一者的環境氣氛。可藉由氧氣及稀有氣體中之至少一者噴射、被動流動或強制流動通過液體銀來形成氣溶膠。可使用壓縮機312a再循環氣體。氣體可在高壓氣流迴路中再循環,諸如在反應電解槽腔室531處接收氣體且再循環其至儲集器5c的迴路,在該儲集器中氣體流動通過熔融銀以增加氣溶膠形成。在一實施例中,銀可包含添加劑以增加氣溶膠形成速率及程度。在一替代實施例中,高速之氣溶膠產生可由以高速循環液態金屬形成。可藉由至少一個熔融金屬噴射器(諸如包含EM泵5kk之雙熔融金屬噴射器)以高速噴射金屬。泵送速率可在約1 g/s至10 g/s、10 g/s至100 g/s、1 kg/s至10 kg/s、10 kg/s至100 kg/s及100 kg/s至1000 kg/s之至少一個範圍內。在一實施例中,藉由在經保持電池氛圍(諸如包含氧氣之所要濃度的氛圍)中泵送熔融金屬形成銀氣溶膠的能量效率可高於泵送氣體通過熔融銀。 MHD轉換器可包含金屬氣溶膠(諸如銀氣溶膠)之來源。來源可包含雙熔融金屬噴射器中之至少一者及來自至少一個儲集器之氣溶膠形成物中之一或多者,此係由於含於儲集器中之金屬之溫度高於金屬的熔點。氣溶膠來源可包含獨立EM泵噴射器,該EM泵噴射器可包含EM泵5ka、儲集器(諸如5c)、EM泵管5k61之噴嘴部分及噴嘴5q,其中熔融金屬噴射劑至少部分地轉換為金屬氣溶膠。氣溶膠可流動或噴射至其中需要冷凝金屬蒸氣之區域中,諸如在MHD噴嘴307中。氣溶膠可在比對於經受等熵膨脹(諸如等熵噴嘴膨脹)之金屬蒸氣為可能的程度更大的程度上冷凝金屬蒸氣。金屬蒸氣冷凝可釋放金屬蒸氣汽化熱,該金屬蒸氣汽化熱可增加氣溶膠之溫度及壓力中之至少一者。對應能量及功率可有助於噴嘴之出口處的氣溶膠及電漿流之動能及功率。由於來自金屬蒸氣汽化熱之功率之貢獻,流動之功率可隨著效率的增加轉換為電力。MHD轉換器可包含金屬氣溶膠之來源之控制器以控制氣溶膠流速及氣溶膠質量密度中之至少一者。控制器可控制氣溶膠之EM泵來源之EM泵送的速率。可控制氣溶膠噴射速率以最佳化回收蒸氣汽化熱之蒸氣冷凝及MHD功率轉換效率。 在另外的等熵膨脹期間造成銀蒸氣冷凝之熵值減少可藉由以下給出之銀之氣化的熵值來評估:其中為銀沸點且為氣化之銀焓。在銀蒸氣接觸具有1500 K之儲集器之例示性溫度的銀霧或氣溶膠情況下,以達到沸點之熵值變為其中為差分霧焓,為霧溫度,C p 為恆定壓力下之銀之比熱容,且為儲集器及起始霧溫度。因此,在霧之質量流量為金屬蒸氣之質量流量約8倍的情況下,金屬蒸氣將在噴嘴中冷凝以釋放其汽化熱,其中可用之對應能量顯著地轉換為動能。假定作為霧或氣溶膠之經冷凝蒸氣之例示性莫耳體積為小於對應蒸氣之約50倍,則霧流需要僅為總氣體/電漿體積流之約15%,以實現蒸氣之冷凝以產生約純霧或氣溶膠電漿流。可藉由控制儲集器溫度、霧來源噴射速率(諸如EM泵送速率)及氣溶膠-形成氣體之壓力(諸如氧氣及視情況選用之氬氣)來控制霧流速。 在一實施例中,MHD熱力學循環包含保持低能量氫反應電漿(保持過熱銀蒸氣)且藉由添加冷銀氣溶膠或液體銀金屬噴射劑將冷凝為高液滴動能氣溶膠噴流的過程。氣溶膠噴流功率存量可包含主要動能功率。電功率轉換可主要來自MHD通道308中之動能功率改變。MHD轉換器之操作模式可包含與軌道槍之操作模式相反的操作模式或與DC傳導電磁泵相反的操作模式。 形成液體銀液滴之高動能噴流的蒸氣冷凝可大體上避免在能量及功率平衡中損失汽化熱。冷銀氣溶膠可形成於儲集器中且輸送至反應電解槽腔室5b31及MHD噴嘴307中之至少一者。電池可進一步包含在穿過反應電解槽腔室至MHD轉換器的電漿流之下游側處的混合腔室。冷氣溶膠及過熱蒸氣之混合可發生於反應電解槽腔室5b31、混合腔室及MHD噴嘴307中之至少一者中。在一實施例中,SunCell®包含氧氣來源以形成發煙熔融銀以促進銀氣溶膠形成。可將氧氣供應至以下中之至少一者:儲集器5c、反應電解槽腔室5b31、MHD噴嘴307、MHD通道308、MHD冷凝部分309及SunCell®-MHD轉換器發電機之其他內部腔室。可由熔融銀吸收氧氣以形成氣溶膠。可藉由在發電機內部存在稀有氣體(諸如氬氣氛圍)來增強氣溶膠。可藉由本發明之系統在所要壓力下添加及保持氬氣氛圍,該等系統諸如氬氣貯槽、線路、閥門、控制器及噴射器。噴射器可在冷凝部分309或其他合適區域中以避免銀回流。在一實施例中,超熱銀蒸氣可經冷凝以藉由將銀直接地或間接地噴射至噴嘴中形成氣溶膠噴流。在一實施例中,可在較低溫度及較低壓力中之至少一者下操作反應電解槽腔室5b31以准許待在膨脹(諸如等熵膨脹)下液化之蒸氣之較大分數。例示性較低溫度及壓力相較於3500 K及10 atm分別為約2500 K及約1 atm。 在流速減小之情況下,霧之密度可升高以保持在通道中恆定流動。可藉由聚合銀霧液滴增加密度。通道可包含直線通道。在其他實施例中,通道可彙集或發散或具有適於最佳化MHD功率轉換的其他幾何結構。 在一實施例中,噴嘴可包含用於相對冷的金屬蒸氣氣溶膠之至少一個通道及用於銀蒸氣或超熱銀蒸氣之至少其他通道。通道可傳送待在噴嘴307中混合之對應氣溶膠。混合可減小熵值以使得銀蒸氣冷凝。冷凝及噴嘴流動可在噴嘴出口處產生快速氣溶膠噴流。可藉由控制來源之溫度(諸如儲集器溫度,其中儲集器可充當來源)來控制相對冷的氣溶膠之流速。可藉由控制低能量氫反應速率及熔融金屬噴射速率中之至少一者來控制過熱蒸氣之流速。 在一實施例中,噴嘴出口壓力及溫度為約MHD通道308出口處之彼等,且MHD通道308之入口處之輸入功率為約藉由與其速度v 處之質量流速相關聯之動能給出之輸入功率。MHD通道中之電力轉換功率藉由以下給出其中V為MHD通道電壓,I為通道電流,E為通道電場,J為通道電流密度,L該通道長度,σ 為流動導電率、v為流速,B為磁場強度,A為電流橫截面積(噴嘴出口面積),d為電極間距,且W為負載因子(跨負載之電場與斷路電場之比率)。效率η 藉由MHD通道(方程式(49))中之電力轉換功率及輸入功率(方程式(48))之比率給出:在質量流量為1 kg/s,導電率σ 為50,000 S/m,速度為1200 m/s,磁通量B 為0.25 T,負載因子W 為0.5,例示性直線正方形矩形通道之通道寬度及電極間距d 為0.05 m以及通道長度L 為0.2 m之情況下,功率及效率為:方程式(53)為當總能量存量基本上為動能時之總焓效率,其中汽化熱亦在噴嘴307中轉換為動能。 在一實施例中,差分勞侖茲力dFL 與銀電漿流速及沿MHD通道308之差分距離dx 成比例:差分勞侖茲力(方程式(54))可重新配置為:其中(i)導電率σ 及磁通量B可沿通道恆定,(ii)理想地不存在沿通道之質量損失以使得質量關於距離恆定,且通道m中之質量流速由於噴射至通道入口中之恆定速率及在穩態條件下流動之連續性而為恆定的,及(iii)速度與距離之差分在穩定流動條件下與時間無關。隨著沿通道減小速度的恆定質量流速可對應於增加氣溶膠粒子之聚合以限制MHD通道出口處之完全崩解。接著,速度關於通道距離之變化率與速度成比例:其中k 為藉由邊界條件判定之常數。方程式(57)之整合提供藉由比較方程式(57)與方程式(56),常數k藉由組合方程式(58)及方程式(59),作為通道距離之函數的速度為根據方程式(49),通道之對應功率藉由以下給出在質量流量為0.5 kg/s,導電率σ 為50,000 S/m,速度為1200 m/s,磁通量B 為0.1 T,負載因子W 為0.7,例示性直線正方形矩形通道之通道寬度及電極間距d 為0.1 m以及通道長度L 為0.25 m之情況下,功率及效率為:方程式(64)對應於轉換為供電外部負載之電力的起始通道動能之54%以及耗散在內部阻抗中之功率之46%,其中電功率密度為80 kW/公升。 電功率聚集至輸入至MHD通道之動能功率乘以MHD通道之負載因子W 。可藉由增加輸入動能功率且藉由減小通道尺寸來增加功率密度。後者可藉由增加質量流速、磁通量密度及流動導電率中之至少一者來達成。在質量流量為2 kg/s,導電率σ 為500,000 S/m,速度為1500 m/s,磁通量B 為1 T,負載因子W 為0.7,例示性直線正方形矩形通道之通道寬度及電極間距d 為0.05 m以及通道長度L 為0.1 m之情況下,功率及效率為:方程式(67)對應於轉換為供電外部負載之電力的起始通道動能之70%及耗散在內部阻抗中之功率之30%,其中電功率密度為6.3 MW/公升。 藉由方程式(61)給出之功率可表示為其中K0 為起始通道動能。可藉由獲取P 關於W 之衍生物且將其設置為等於0來判定最大功率輸出。其中則,在其中s=125之方程式(65-67)之例示性情況中,使用迭代方法,功率在W=0.96時為最佳。在此情況下,針對方程式(65-66)之條件的效率為96%。 在一實施例中,反應電解槽腔室5b31及噴嘴307中之至少一者可包含磁瓶,該磁瓶可選擇性地形成沿MHD通道308之縱軸的電漿噴流。電力轉換器可包含磁鏡,其在離子流動之所要方向上為磁場梯度之來源,其中電漿電子v || 之起始平行速度增加,此係因為根據絕熱不變量=常數,軌道速度隨著能量之守恆而減小,自軌道運動抽取線性能量。由於磁通量B減小,離子迴旋半徑將增加,使得流量πa2 B保持恆定。連接軌道之流量之不變性為「磁鏡」之機制之依據。磁鏡之原理為在初速度針對鏡之情況下帶電粒子由強磁場之區域反射且以其他方式自鏡射出。經由離子之軌道的流量之絕熱不變性為沿z軸形成離子流之手段,其中將轉換為,使得。兩個磁鏡或更多磁鏡可形成磁瓶以限制電漿,諸如形成於反應電解槽腔室5b31中之電漿。產生含於中心區域中之瓶中之離子將沿軸螺旋,但將由各端處之磁鏡反射。具有平行於所要軸之速度之高分量的更高能離子將在瓶之端部處逸出。瓶可在MHD通道末端處更大的漏泄。因此,瓶可產生自磁瓶之端部至磁流體動力轉換器之通道入口中之基本上線性離子流。 特定言之,電漿可藉由磁鏡磁化,該磁鏡使得垂直於MHD通道或z軸之方向的離子運動之分量由於絕熱不變量=常數而至少部分地轉換為平行運動。離子具有沿z軸之較佳速度且傳播至磁流體動力電力轉換器中,其中洛倫茲偏轉離子在與對應橫向偏轉場交叉之電極處形成電壓。電壓可驅使電流流過電力負載。在一實施例中,磁鏡包含產生等效於亥姆霍茲線圈(Helmholtz coil)或電磁線圈之場的電磁體或永久磁體。在電磁磁鏡之情況下,可藉由控制電磁電流以控制離子自反應電解槽腔室流出以控制功率轉換時的速率來調節磁場強度。在在至MHD通道308之入口處的情況下,藉由給出之速度可為平行於z軸之約95%。 在一實施例中,低能量氫反應混合物可包含氧氣、水蒸氣及氫氣中之至少一者。MHD組件可包含諸如陶瓷之材料,諸如金屬氧化物,諸如氧化鋯及氧化鉿中之至少一者,或在氧化氛圍下穩定的矽石或石英。在一實施例中,MHD電極304可包含可在操作期間較不易受腐蝕或降解影響的材料。在一實施例中,MHD電極304可包含導電陶瓷,諸如導電固體氧化物。在另一實施例中,MHD電極304可包含液體電極。液體電極可包含在電極工作溫度下為液體的金屬。液體金屬可包含工作介質金屬,諸如熔融銀。熔融電極金屬可包含浸漬有熔融金屬之基質。基質可包含諸如金屬之耐火材料,諸如可導電之W、碳、陶瓷或本發明之其他耐火材料。負電極可包含固體耐火金屬。負極性可保護負電極免遭氧化。正電極可包含液體電極。 液體電極可包含施加電磁限制(勞侖茲力)以保持游離表面液體金屬的構件。液體金屬電極可包含磁場源及電流源以保持電磁限制。磁場源可包含MHD磁體306及其他一組磁體(諸如永久磁體、電磁體及超導磁體)中之至少一者。電流源可包含MHD電流及來自外部電流源之所施加電流中之至少一者。 在一實施例中,導電陶瓷電極可包含本發明中之一者,諸如碳化物(諸如ZrC、HfC或WC)或硼化物(諸如ZrB2 )或具有可處理至1800℃之20% SiC組合物的組合物(諸如ZrC-ZrB2 、ZrC-ZrB2 -SiC及ZrB2 )。電極可包含碳。在一實施例中,複數個液體電極可經由歧管供應液體金屬。液體金屬可藉由EM泵泵送。液體電極可包含浸染在非反應性基質中之熔融金屬,該非反應性基質諸如陶瓷基質,諸如金屬氧化物基質。替代地,可經由基質泵送液體金屬以連續供應熔融金屬。在一實施例中,電極可包含持續噴射之熔融金屬,諸如點火電極。噴射器可包含非反應性耐火材料,諸如金屬氧化物,諸如ZrO2 。在一實施例中,液體電極中之每一者可包含暴露於MHD通道電漿之熔融金屬之流動流。 在一實施例中,可將電極配置於霍耳發電機設計中。負電極可接近MHD通道之入口且正電極可接近MHD通道之出口。可接近MHD通道之入口的電極可包含液體電極,諸如浸沒式電極。接近MHD通道之出口的電極可包含在電極工作溫度下對氧化具有抗性的導體,其中出口處之該工作溫度可比MHD通道之入口處的顯著地更低。MHD出口處之例示性抗氧化電極可包含諸如ZrC之碳化物或諸如ZrB2 之硼化物。在一實施例中,電極可包含由絕緣體部分分離之一系列電極部分,該絕緣體部分包含可包含電絕緣體之MHD通道壁之突起。凸起部分可在防止金屬蒸氣冷凝之溫度下保持。絕緣部分可包含壁帶,該等壁帶中之至少一者經加熱及絕緣以保持帶溫度在MHD通道之操作壓力下高於金屬之沸點。通道之出口處之電極可包含抗氧化電極,諸如可穩定以在出口溫度下氧化的碳化物或硼化物。在一實施例中,MHD通道可保持在低於導致壁之絕緣體部分上的金屬蒸氣冷凝及電極之腐蝕中之至少一者的溫度下,該等電極諸如碳化物或硼化物電極(諸如包含ZrC或ZrB2 之碳化物或硼化物)或可處理至1800℃之組合物(諸如ZrC-ZrB2 及ZrC-ZrB2 -SiC組合物)。在一實施例中,工作介質包含可在低於其沸點之溫度下昇華以防止金屬冷凝於MHD通道之壁上以使得其流至再循環系統的金屬(諸如銀)。 在一實施例中,MHD磁體306可包含可將正弦或交變磁場施加至MHD通道308的交變場磁體(諸如電磁體)。正弦或交變施加之場可使得MHD電力輸出為交變(AC)功率。交變電流及電壓頻率可為標準的電流及電壓頻率,諸如50 Hz或60 Hz。在一實施例中,藉由感應將MHD功率自通道傳遞出。感應發電機可消除接觸電漿之電極。 將反應電解槽腔室5b31及MHD加速通道或噴嘴307連接至MHD膨脹或發電機通道308之組件(諸如密封件314)之間的活接及密封件可包含墊片凸緣密封件或本發明之其他。其他密封件(諸如回流導管310、回流儲集器311、回流EM泵312、噴射儲集器5c及噴射EM泵組合件5kk之密封件)可包含本發明中之一者。例示性墊片包含碳(諸如石墨或Graphoil),其中經接合金屬氧化物部分(諸如包含氧化鋁、氧化鉿、氧化鋯及氧化鎂中之至少一者的金屬氧化物部分)保持低於碳還原溫度(低於約1300℃至1900℃之範圍)。分量可包含本發明之不同材料(諸如耐火材料)及基於其操作參數及需求的不鏽鋼。在一例示性實施例中,i.)EM泵組合件5kk、回流導管310、回流儲集器311及回流EM泵管312中之至少一者包含不鏽鋼,其中內部可用氧化保護塗層(諸如鎳、Pt、錸或其他貴金屬)塗佈;ii.)儲集器5c、反應電解槽腔室5b31、噴嘴307及MHD膨脹部分308中之至少一者包含電絕緣耐火材料(諸如氮化硼)或耐火氧化物(諸如MgO (M.P. 2825℃))、ZrO2 (M.P. 2715℃)、氧化鎂、對H2 O穩定之氧化鋯、鋯酸鍶(SrZrO3 M.P. 2700℃)、HfO2 (M.P. 2758℃),或在工作溫度下對氧化反應穩定之二氧化釷(M.P. 3300℃);iii.)反應電解槽腔室5b31包含石墨(諸如各向同性及熱石墨中之至少一者);及iv.)進水升管5qa、電磁泵管5k61之噴嘴部分、噴嘴5q及MHD電極304中之至少一者可包含碳、Mo、W、錸、經錸塗佈之Mo、經錸塗佈之W中之至少一者。在一例示性實施例中,EM泵組合件5kk、回流導管310a、回流儲集器311a及回流氣泵或壓縮機312a中之至少一者包含不鏽鋼,其中內部可用氧化反應保護塗層塗佈,該氧化反應保護塗層諸如鎳、Pt、錸或其他貴金屬。 電極可包含經貴重金屬塗覆之導體,諸如銅、鎳、鎳合金及鈷合金上之Pt,或此等未經塗佈之金屬,其中可藉由背襯熱交換器或冷板應用冷卻。電極可包含尖晶石類型電極,諸如0.75 MgAl2 O4 -0.25 Fe3 O4 、0.75 FeAl2 O4 -0.25 Fe3 O4 及鉻化鑭La(Mg)CrO3 。在一實施例中,MHD電極304可包含液體電極,諸如液體銀塗佈之耐火金屬電極或經冷卻金屬電極。Ni及錸塗層中之至少一者可防止經塗佈組件與H2 O反應。MHD氛圍可包含氫氣以保持金屬之還原條件,諸如EM泵管5k6、進水升管5qa、電磁泵管5k61之噴嘴部分、噴嘴5q及MHD電極304之彼等。MHD氛圍可包含水蒸氣以保持氧化物陶瓷,諸如鋯酸鍶、氧化鉿、陶瓷組件之ZrO2 或MgO,諸如反應電解槽腔室5b31、噴嘴307及MHD膨脹部分308中之至少一者。可使用陶瓷膠(諸如氧化鋯磷酸鹽膠結劑、ZrO2 膠結劑或氧化鈣-氧化鋯磷酸鹽)將金屬氧化物部分膠合或膠結在一起。例示性Al2 O3 黏著劑為Rescor 960氧化鋁(Cotronics)及Ceramabond 671。另外的例示性陶瓷膠為Resbond 989 (Cotronics)及Ceramabond 50 (Aremco)。在一實施例中,壁組件可包含可用MgO穩定之隔熱陶瓷(諸如ZrO2 或HfO2 ),且經分段電極之電極絕緣體可包含導熱陶瓷(諸如MgO)。為防止自外表面氣化的損失,陶瓷可為足夠厚以外部充分冷卻、主動或被動冷卻或包覆於絕緣中之至少一者。 可將若干氧化物添加至ZrO2 (氧化鋯)或HfO2 (氧化鉿)以使材料穩定,該等材料諸如氧化釔(Y2 O3 )、氧化鎂(MgO)、氧化鈣(CaO)、氧化鍶(SrO)、氧化鉭(Ta2 O5 )、三氧化二硼(B2 O3 )、TiO2 、氧化鈰(Ce2 O3 )、SiC、釔及銥。晶體結構可為立方相,其被稱作立方穩定之氧化鋯(氧化鉿)或穩定之氧化鋯(氧化鉿)。在一實施例中,諸如反應電解槽腔室5b31之至少一個電池組件對氧氣及氧化物離子中之至少一者為可透的。例示性氧化物可穿透材料為ZrO2 。可藉由控制通過氧化物可穿透或氧化物移動材料(諸如ZrO2 )之氧化物擴散率來控制反應電解槽腔室5b31之氧含量。電池可包含氧化物可穿透材料上之電壓及電流源及一及電流控制系統,其中氧化物離子在材料上之流動受電壓及電流控制。其他適合之耐火分量材料包含SiC (M. P. = 2830℃)、BN (M. P. = 2970℃)、HfB2 (M. P. = 3250℃)及ZrB2 (M. P. = 3250℃)中之至少一者。 為避免MHD電極藉由熔融金屬蒸氣電短路,電極304 (圖2I161)可包含導體,各自安裝於電絕緣體覆蓋之導電柱或充當隔絕引線之引線305上,該引線進一步充當電極與發電機通道308之壁的間隔物。電極304可經經分段且可包含陰極302及陽極303。除隔絕引線305以外,電極可自由地懸浮於發電機通道308中。沿垂直軸線隔開之電極可足以防止熔融金屬短路。電極可包含耐火導體,諸如W或Mo。引線305可連接至電線,該等電線可藉由耐火絕緣體(諸如BN)絕緣。電線可接合在線束中,該線束穿透可包含金屬之MHD匯流排饋通凸緣301處之通道。在MHD轉換器外,線束可連接至功率合併器及反相器。 在一例示性實施例中,MHD轉換為電力期間之黑體電漿最初及最終溫度3000K及1300K。在一實施例中,MHD發電機冷卻於低壓側上以保持電漿流動。霍耳或發電機通道308可經冷卻。冷卻手段可為本發明中之一者。MHD發電機300可包含熱交換器316 (諸如輻射熱交換器),其中熱交換器可經設計以依據其溫度輻射功率以保持所要最低通道溫度範圍,諸如在約1000℃至1500℃範圍內。輻射熱交換器可包含較高表面以最小化其大小及重量中之至少一者。輻射熱交換器316可包含複數個表面,該複數個表面可經組態呈方錐形或方形琢面以增加輻射表面積。輻射熱交換器可在空氣中操作。輻射熱交換器之表面可用具有以下組之至少一個特性之材料塗佈:(i)能夠高溫操作,諸如耐火材料,(ii)具有較高輻射率,(iii)對氧化反應穩定,且提供較高表面積,諸如具有不受阻或無阻礙排放的刻花表面。例示性材料為陶瓷,諸如氧化物,諸如MgO、ZrO2 、HfO2 、Al2 O3 及其他氧化穩定之陶瓷,諸如ZrC-ZrB2 及ZrC-ZrB2 -SiC組合物。 發電機可進一步包含再生器或再生式熱交換器。在一實施例中,流體在以逆流方式穿過之後回流至噴射系統以接收膨脹部分308或其他熱量損耗區域中之熱量以預熱噴射至電池反應腔室5b31中之金屬以保持反應電解槽腔室溫度。在一實施例中,工作介質(諸如銀及稀有氣體中之至少一者)、細胞組件(諸如儲集器5c、反應電解槽腔室5b31及MHD轉換器組件(諸如MHD冷凝部分309或其他熱組件(諸如儲集器5c、反應電解槽腔室5b31、MHD噴嘴部分307、MHD發電機部分308及MHD冷凝部分309之群組中之至少一者)中之至少一者))中之至少一者可藉由熱交換器加熱,該熱交換器自至少一個其他電池或MHD組件(諸如儲集器5c、反應電解槽腔室5b31、MHD噴嘴部分307、MHD發電機部分308及MHD冷凝部分309之群組中之至少一者)接收熱量。再生器或再生式熱交換器可將熱量自一個組件傳遞至其他組件。 在一實施例中,可控制輻射加熱器交換器316之輻射率、面積及溫度中之至少一者以控制熱傳遞速率。可藉由控制輻射器上之熱屏之覆蓋程度來控制面積。可藉由控制流動至輻射器之熱量來控制溫度。在另一實施例中,熱交換器316可包含冷卻劑迴路,其中MHD熱交換器316經由MHD冷卻劑入口317接收冷卻劑且經由MHD冷卻劑出口318移除熱量。熱量可用於再生式熱交換器中以預熱回流銀流動、電池組件或MHD組件。替代地,熱量可用於加熱及熱電共生應用。 噴嘴導入口307可包含對耗損具有抗性之耐火材料,諸如金屬氧化物(諸如ZrO2 、HfO2 、Al2 O3 或MgO)、耐火氮化物、耐火碳化物(諸如碳化鉭、碳化鎢或碳化鉭鎢)、可包含耐火覆層之熱石墨(諸如鎢)或僅本發明之其他耐火材料或可包覆耐火材料(諸如碳)上之材料。電極304可包含耐火導體,諸如W或Mo。諸如電極305之彼等的發電機通道308或電絕緣載體可為耐火絕緣體,諸如本發明中之一者,諸如陶瓷氧化物,諸如ZrO2 、氮化硼或碳化矽。在其中MHD組件經冷卻的另一實施例中,諸如噴嘴307及通道308中之至少一者的MHD組件可包含可用耐火材料(諸如Al2 O3 、ZrO2 、富鋁紅柱石或本發明之其他)塗佈之過渡金屬(諸如Cu或Ni)。電極可包含可經冷卻之過渡金屬,其中表面可用耐火導體(諸如W或Mo)塗佈。可藉由水、熔融鹽或其他冷卻劑冷卻之組件由熟習此項技術者已知,諸如熱油(諸如矽基聚合物)、熔融金屬(諸如Sn、Pb、Zn、合金)、熔融鹽(諸如鹼性鹽)及共熔鹽混合物(諸如鹼性鹵化物-鹼金屬氫氧化物混合物(MX-MOH M = Li、Na、K、Rb、Cs;X = F、Cl、Br、I))中之至少一者。熱冷卻劑可經再循環以預熱噴射至反應電解槽腔室5b31中之熔融金屬。對應熱回收系統可包含復熱器。 在一實施例中,MHD組件(諸如MHD噴嘴307、MHD通道308及MHD冷凝部分309)可包含耐火材料,諸如本發明中之一者,諸如碳化物、碳及硼化物中之至少一者,及金屬。耐火材料可易於氧化為氧氣及水中之至少一者。為抑止氧化反應,HOH催化劑之氧氣來源可包含化合物,該化合物包含氧氣,諸如CO、鹼金屬或鹼土金屬氧化物中之至少一者,或包含本發明之氧氣的其他氧化物或化合物。硼化物可包含可摻雜有SiC之ZrB2 。碳化物可包含ZrC、WC、SiC、TaC、HfC及Ta4 HfC5 中之至少一者。諸如碳化物之導電材料可在經指示之情況下(諸如在點火及MHD電極中之至少一者之電隔離之情況下)用絕緣間隔物或襯套電隔離。 例示性MHD體積轉換密度為約70 MW/m3 (70 kW/公升)。歷史上MHD之大部分問題來源於燃氣情況中及燃煤對應物中之低導電性加排渣環境中之低導電性特徵。根據12 V電壓下之10,000 A電流,銀SunCell®電漿之導電率經估計為約1 mΩ。根據弧形尺寸,與鹼接種惰性MHD工作氣體(其中功率密度與導電率成比例)之約20 S/m相比,對應導電率經估計為1×105 S/m。 在一實施例中,工作介質可包含銀蒸氣及銀蒸氣接種之稀有氣體中之至少一者,諸如He、Ne或Ar。在一實施例中,可藉由控制熔融金屬蒸氣壓力(諸如銀蒸氣壓力)及工作介質之電離中之至少一者來控制工作介質之導電率。可藉由控制低能量氫反應功率、藉由低能量氫反應發射之EUV及UV光之強度、點火電壓、點火電流、熔融金屬流之EM泵送速率及操作溫度(諸如氣體、電子、離子及黑體溫度中之至少一者)來控制工作介質之電離。可藉由控制點火及低能量氫反應條件中之至少一者來控制至少一個溫度。例示性低能量氫反應條件為氣體壓力及氣體成分,諸如H2 O、H2 及惰性氣體成分。低能量氫反應條件及對應控制可為本發明之一者或其他適合之條件。 在一實施例中,SunCell®可進一步包含熔融金屬溢出系統,諸如包含溢出貯槽、至少一個泵、電池熔融金屬存量傳感器、熔融金屬存量控制器、加熱器、溫度控制系統及熔融金屬存量之系統,以視需要存儲熔融金屬且供應至SunCell®,此可藉由至少一個感測器及控制器判定。溢流系統之熔融金屬存量控制器可包含本發明之熔融金屬含量控制器,諸如進水升管及EM泵。溢流系統可包含MHD回流導管310、回流儲集器311、回流EM泵312及回流EM泵管313中之至少一者。 在一實施例中,在確保等熵流動之條件下保持工作介質之膨脹。在一實施例中,針對將確保噴嘴之可逆膨脹及MHD通道之強力驅動壓力梯度的超聲波噴嘴膨脹選擇入口工作介質條件。由於飽和(若其發生於噴嘴中),由於快速冷卻速率(諸如約15 K/us)將導致強列的不平衡過.冷卻且此可進一步將觸發噴嘴之發散部分中之冷凝衝擊,噴嘴入口條件可高度過熱以便蒸氣不在膨脹期間變得飽和。在一實施例中,將避免冷凝衝擊,此係因為其導致與所要等熵流動條件偏離且急劇地降低噴嘴出口速度的不可逆性,夾帶在噴嘴之超聲波/發散部分中之蒸氣流中之所得高度稠密液體Ag液滴可導致噴嘴表面之經加速侵蝕。在其中勞侖茲力對流動方向不利作用以使得MHD通道中之微弱驅動壓力梯度可產生減少的穿過系統之體積流動的一實施例中,噴嘴入口溫度儘可能高以允許適當過熱,且壓力亦適當地較高以確保噴嘴之下游的MHD部分中之強烈的驅動壓力梯度。在一例示性實施例中,噴嘴入口處之反應電解槽腔室5b31壓力為約6 atm,且電漿溫度為約4000 K以引起等熵膨脹且乾蒸氣以約722 m/s速度及多於2 atm之壓力在約馬赫數目1.24下離開噴嘴。較低入口溫度亦為可能的,但此等可各自產生更小出口速度及壓力。 在其中勞侖茲力可在達成所要MHD通道308出口溫度之前停滯電漿噴射的一實施例中,電漿導電率、磁場強度、氣體溫度、電子溫度、離子溫度、通道入口壓力、噴流速度及工作介質流動參數中之至少一者經最佳化以實現所要MHD轉化效率及功率密度。在包含熔融金屬接種之稀有氣體電漿(諸如銀蒸氣接種之氬氣或氦氣電漿)的一實施例中,控制金屬蒸氣至稀有氣體之相對流動以實現所要導電率、電漿氣體溫度、反應腔室5b31壓力及MHD通道308入口噴射速度、壓力及溫度中之至少一者。在一實施例中,可藉由控制對應回流泵來控制稀有氣體及金屬蒸氣流動以實現所要相對比率。在一實施例中,可藉由控制相對稀有氣體及金屬噴射速率藉由控制接種至反應電解槽腔室5b31之量來控制導電率。在一實施例中,可藉由控制低能量氫反應速率來控制導電率。可藉助於本發明來控制低能量氫反應速率,諸如藉由控制催化劑來源、氧氣來源、氫氣來源、水蒸氣、氫氣、導電基質之流動(諸如熔融銀之噴射)及點火參數(諸如點火電壓及電流中之至少一者)中之至少一者之噴射速率。在一實施例中,MHD轉換器包含用於低能量氫反應及MHD操作參數之感測器及控制系統,諸如(i)反應條件,諸如反應物壓力、溫度及相對濃度、諸如HOH及H或其來源之彼等的反應物流動及諸如液體及氣化銀的導電基質之流動及泵送速率以及諸如點火電流及電壓的點火條件;(ii)電漿及氣體參數,諸如通過MHD轉換器之級的壓力、速度、流動速率、傳導率及溫度;(iii)回流及再循環材料參數,諸如稀有氣體及熔融金屬之泵送速率及物理參數,諸如流動速率、溫度及壓力;及(iv)反應電解槽腔室5b31、MHD噴嘴部分307、MHD通道308及MHD冷凝部分309中之至少一者中之電漿導電率感測器。 在一實施例中,可諸如氫氣(諸如H2 氣體及H2 O中之至少一者)之氣體來源供應至反應電解槽腔室5b31。SunCell®可包含至少一個質量流量控制器以供應可呈液體及氣態形式中之至少一者的氫氣來源,諸如H2 氣體及H2 O中之至少一者。供應可經由以下中之至少一者:EM泵組合件5kk1之底座、儲集器5c壁、反應電解槽腔室5b31之壁、噴射EM泵管5k6、MHD回流導管310、MHD回流儲集器311、MHD回流EM泵312之泵管及MHD回流EM泵管313。添加至電池或MHD內部之氣體可噴射在MHD冷凝機部分309中或在連接至內部之任何方便的電池或MHD轉換器組件處。在一實施例中,氫氣可經由選擇性膜(諸如氫氣滲透膜)供應。氫氣供應膜可包之Pd或Pd-Ag H2 滲透膜或熟習此項技術者已知之類似膜片。氣體至EM泵管壁的穿透可包含焊入或旋擰入的凸緣。可由氫氣貯槽供應氫氣。氫氣可由自氫化物釋放供應,其中該釋放可由熟習此項技術者已知的手段控制,諸如藉由控制氫化物之壓力及溫度中之至少一者。可藉由電解水供應氫氣。水電解器可包含高壓電解器。可藉由控制器(諸如包含電腦及對應感測器的控制器)來控制電解器及氫氣質量流量控制器中之至少一者。可基於可藉由轉換器(諸如熱量測裝置、PV轉換器或MHD轉換器)記錄之SunCell®之功率輸出控制氫氣流量。 在一實施例中,可將H2 O供應至反應電解槽腔室5b31。供應源可包含一線路,諸如通過EM泵管5k6或EM泵組合件5kk的線路。H2 O可提供H及HOH催化劑中之至少一者。低能量氫反應可產生O2 及H2 (1/p)及產物。諸如H2 (1/4)的H2 (1/p)可自反應電解槽腔室及MHD轉換器中之至少一者擴散至諸如環境氣氛的外部區域或H2 (1/p)收集系統。H2 (1/p) 可由於其較小體積而經由反應電解槽腔室及MHD轉換器中之至少一者之壁擴散。O2 產物可自反應電解槽腔室及MHD轉換器中之至少一者擴散至諸如環境氣氛的外部區域或O2 收集系統。O2 可經由選擇性膜、材料或值擴散。選擇性材料或膜可包含能夠導電氧化物(諸如氧化釔、鎳/氧化釔穩定的氧化鋯(YSZ)/矽酸鹽分層)的材料或膜或熟習此項技術者已知之其他氧氣或氧化物選擇性膜。O2 可經由可滲透壁(諸如能夠導電氧化物的壁,諸如氧化釔壁)擴散。氧氣滲透膜可包含反應電解槽及MHD轉換器之低壓組件之多孔陶瓷,諸如MHD通道308之陶瓷壁。氧氣選擇性膜可包含可用Bi26 Mo10 O69 塗佈以增加氧氣滲透率的BaCo0.7 Fe0.2 Nb0.1 O3- δ (BCFN)氧氣滲透膜。氧氣選擇性膜可包含Gd1 - x Cax CoO3 - d 及Ce1 - x Gdx O2 - d 中之至少一者。氧氣選擇性膜可包含陶瓷氧化物膜,諸如SrFeCo0 . 5 Ox 、SrFe0 . 2 Co0 . 5 Ox 、Ba0 . 5 Sr0 . 5 Co0 . 8 Fe0 . 2 Ox 、BaCo0 . 4 Fe0 . 4 Zr0 . 2 Ox 、La0 . 6 Sr0 . 4 CoOx 及Sr0 . 5 La0 . 5 Fe0 . 8 Ga0 . 2 Ox 中之至少一者。 諸如EM泵組合件5kk、EM泵5ka、EM泵管5k6、進水升管5qa及噴射EM泵管5k61中之至少一者的EM泵或組件可包含對氧氣穩定的材料或塗料,諸如陶瓷,諸如Al2 O3 、ZrC、ZrC-ZrB2 、ZrC-ZrB2 -SiC及具有20% SiC組合物的ZrB2 中之至少一者,或至少一種貴金屬,諸如白金(Pt)、鈀(Pd)、釕(Ru)、銠(Rh)及銥(Ir)中之至少一者。 在圖2I174至圖2I181中所展示之一實施例中,EM泵組合件5kk、EM泵5ka、泵管5k6、進水升管5qa及噴射EM泵管5k61中之至少一者可包含對氧化反應具有抗性的陶瓷。陶瓷可不與O2 反應。陶瓷可包含對與升高溫度下的氧氣反應穩定的電導體。例示性陶瓷為ZrC、ZrB2 、ZrC-ZrB2 、ZrC-ZrB2 -SiC及具有20%SiC組合物的ZrB2 。導電陶瓷可摻雜有SiC以提供保護免遭氧化反應。 銥(M.P. = 2446℃)不與銀形成合金或固溶體;因此,銥可充當EM泵組合件5kk及EM泵管5k6中之至少一者的適合抗氧化反應塗層以避免氧化反應。可將銥塗層施加至約匹配熱膨脹係數(CTE)的金屬。在一例示性實施例中,用銥電鍍EM泵組合件5kk及EM泵管5k6之內部,其中經電鍍組件包含具有與銥類似之CTE的不鏽鋼(SS),諸如Haynes 230、310 SS或625 SS。替代地鉬EM泵組合件5kk可用銥塗佈,其中存在CTE匹配(例如,約7 ppm/K)。在一實施例中,使用管作為陰極電鍍EM泵管之內部,且對立電極可包含具有絕緣間隔物的線,該線在對立電極上週期性地移動至由間隔物覆蓋之電鍍區域。在一實施例中,可藉由氣相沈積施加銥塗層,諸如包含化學沈積包含銥之有機分子的方法,諸如熱量分解四銥十二羰基以使得銥沈積於在升高溫度下保持之所要表面上。可藉由此項技術中已知之一或多種方法沈積銥,該等方法諸如以下中之至少一者:磁控濺鍍(直流電磁控濺鍍(DCMS)及射頻磁控濺鍍(RFMS))、化學氣相沈積(CVD)、金屬有機CVD (MOCVD)、原子層沈積(ALD)、物理氣相沈積(PVD)、雷射誘導之化學氣相沈積(LCVD)、電沈積、脈衝雷射沈積(PLD)及兩倍輝光電漿(DGP)。在一實施例中,EM泵5k6管之內部可由銥包覆。可藉由本發明之手段(諸如CVD或電鍍)用銥塗佈覆層之端部。 在另一實施例中,可用耐火抗氧化劑塗料(諸如氧化物及碳化物中之至少一者)塗佈諸如不鏽鋼EM泵組合件的EM泵組合件。塗料可包含碳化物(諸如碳化鉿/碳化矽(HfC/SiC))及氧化物(諸如HfO2 、ZrO2 、Y2 O3 、AUO3 、SiO2 、Ta2 O5 及TiO2 中之至少一者)中之至少一者。 在另一實施例中,EM泵管5k6包含抗氧化不鏽鋼(SS),諸如用於煤火箱及鍋爐管煤水壁的不鏽鋼,諸如奧氏體不鏽鋼。例示性材料為Haynes 230、SS 310及SS 625,為一種具有出色的耐腐蝕性與低溫至1800℉ (982℃)之高強度聯合之罕見組合的奧氏體鎳-鉻-鉬-鈮合金。在一實施例中,諸如Haynes 230、SS 310或SS 625的材料可經預氧化以形成保護性氧化物塗層。可藉由在包含氧氣之氛圍中加熱形成保護性氧化物塗層。可在空氣或受控制氛圍(諸如包含氧氣之氛圍)及稀有氣體(諸如氬氣)中預氧化諸如Haynes 230之SS。在例示性實施例中,在空氣中在1000℃下或在氬氣80%/氧氣20%中預氧化諸如具有W之Ni-Cr合金及Mo合金的Haynes 230持續24小時。可在所要工作溫度及氧氣濃度下形成氧化物塗層。在一實施例中,可3D打印諸如包含SS 625 (諸如EM泵組合件5kk)之彼等的金屬部件。在一實施例中,可保護EM泵組合件的外部免遭氧化反應。保護可包含藉由抗氧化劑塗層(諸如本發明中之一者)的塗層。替代地,可將EM泵組合件5kk之至少一部分嵌入於抗氧化劑材料中,該抗氧化劑材料諸如陶瓷、石英、玻璃及膠結劑。經氧化反應保護部分可在空氣中操作。在一實施例中,諸如銀之熔融金屬可包含添加劑,該添加劑可防止或減少EM泵管之內部的氧化反應。添加劑可包含還原劑(諸如硫代硫酸鹽)或EM泵管之氧化產物,使得藉由穩定管壁之保護性氧化物來抑制另外的氧化反應。替代地,熔融金屬添加劑可包含鹼,其使泵管之壁上的保護性金屬氧化物穩定。 在一實施例中,EM泵組合件可包含複數個陶瓷,諸如導電及不導電陶瓷。在一例示性實施例中,除EM泵匯流排5k2外,EM組合件5kk可包含不導電陶瓷,諸如氧化物(諸如Al2 O3 、氧化鋯或氧化鉿),且EM泵匯流排5k2可包含導電陶瓷,諸如ZrC、ZrB2 或組合物(諸如ZrC-ZrB2-SiC)。儲集器5c可包含與EM泵組合件5kk相同的不導電陶瓷。在一實施例中,陶瓷EM泵可包含至少一個銅焊或金屬化陶瓷部分以在部件之間形成活接。 電磁泵可各自包含用於液體金屬的兩個主要類型之電磁泵中之一者:AC或DC傳導泵,其中AC或DC磁場在含有液體金屬之管上建立,且將AC或DC電流分別饋入至連接至管壁的液體貫通電極;及感應泵,其中移動式場感應所需電流,如同其中電流可與所施加AC電磁場交叉的感應電動機。感應泵可包含三個主要形式:環形線性、平面線性及螺旋形。泵可包含此項技術中已知之其他泵,諸如機械及熱電泵。機械泵可包含具有電動機驅動葉輪之離心泵。 熔融金屬泵可包含移動磁體泵(MMP),諸如描述於M. G. Hvasta, W. K. Nollet, M. H. Anderson 「Designing moving magnet pumps for high-temperature, liquid-metal systems」, Nuclear Engineering and Design, 卷327, (2018), 第228-237頁中之泵,其全部內容以引用之方式併入。MMP可藉由永久磁體之自旋陣列及多相場線圈中之至少一者產生移動式磁場。在一實施例中,MMP可包含多級泵,諸如用於MHD再循環及點火噴射的二級泵。二級MMP泵可包含電動機,諸如轉動軸的電馬達。二級MMP可進一步包含兩個轉鼓,其各自包含交變在各轉鼓之表面上固定之極性的一組周向性安裝之磁體及具有容納轉鼓之U形部分的陶瓷容器,其中各轉鼓可藉由軸旋轉以使得熔融金屬在陶瓷容器中流動。在另一MMP實施例中,由在包夾條帶陶瓷容器之對置位置上之各圓盤表面上交變極性磁體之兩個盤片替換交變磁體之滾筒,該容器含有藉由旋轉盤片泵送之熔融金屬。在另一實施例中,容器可包含磁場可滲透材料,諸如非二價鐵金屬(諸如不鏽鋼)或陶瓷(諸如本發明中之一者)。可藉由諸如空氣冷卻或水冷卻之手段來冷卻磁體以准許在高溫下操作。 例示性商業AC EM泵為CMI Novacast CA15,其中加熱及冷卻系統可經修改以支援泵送熔融銀。可藉由本發明之加熱器(諸如電阻或電感耦合加熱器)加熱包含入口及出口部分之EM泵管及含有銀之容器的加熱器。諸如電阻或電感耦合加熱器之加熱器可在EM泵管外部且進一步包含熱傳遞構件以經熱量自加熱器傳遞至EM泵管(諸如散熱管)。散熱管可在高溫下操作,諸如藉由鋰工作流體。可藉由本發明之系統(諸如藉由水冷卻迴路及急冷器)冷卻EM泵之電磁體。 在一實施例(圖2I184至圖2I185)中,EM泵400可包含AC感應型,其中銀上之勞侖茲力由通過銀之時變電流及交叉同步時變磁場產生。通過銀之時變電流可由第一時變磁場之法拉弟感應產生,該第一時變磁場由EM泵變壓器繞組電路401a產生。 第一時變磁場之來源可包含初級變壓器繞組401,且銀可充當次級變壓器繞組,諸如單匝短路繞組,其包含電流迴路之EM泵套管區段405及EM泵電流迴路傳回區段406。初級繞組401可包含AC電磁體,其中第一時變磁場通過銀圓周迴路405及406、感應電流迴路藉由磁性電路或EM泵變壓器磁軛402來導電。銀可含有於諸如陶瓷容器405及406之容器中,諸如包含本發明之陶瓷的容器,諸如氮化矽(MP 1900℃)、石英、氧化鋁、氧化鋯、氧化鎂或氧化鉿。保護性SiO2 層可在亞硝酸矽上藉由受控鈍化氧化來形成。容器可包含圍封磁性電路或EM泵變壓器磁軛402之通道405及406。容器可包含扁平區段405以使得感應電流具有在垂直方向上流動至同步時變磁場及根據對應勞侖茲力之泵流動所需方向之組件。交叉同步時變磁場可藉由包含AC電磁體403及EM泵電磁磁軛404之EM泵電磁電路403c來產生。磁性磁軛404在含有銀之容器405之扁平區段處可具有間隙。EM泵變壓器繞組電路401a之電磁體401及EM泵電磁電路403c之電磁體403可由單相AC電源或此項技術中已知的其他適合之電源供電。磁體可接近於迴路彎曲部定位以使得存在所需電流向量組件。供電變壓器繞組401及電磁體繞組403之AC電流的相位可同步以保持勞侖茲泵抽力之所需方向。 在實施例(圖2I184-2I185)中,感應電流迴路可包含入口EM泵套管5k6、電流迴路之EM泵套管區段405、出口EM泵套管5k6以及通過儲集器5c中之銀的路徑,該儲集器可包含包含此等組件之實施例中之進水升管5qa及噴射器5k61的壁。EM泵可包含監測及控制系統,諸如用於初級繞組之電流及電壓及使用泵抽參數回饋控制SunCell功率產生之監測及控制系統。例示性量測回饋參數可為反應電解槽腔室5b31處之溫度及MHD轉換器處之電力。監測及控制系統可包含對應感測器、控制器及電腦。 在僅具有一對電磁泵400之MHD轉換器實施例中,每一MHD回流導管310延伸至對應電磁泵5kk之入口且連接至該入口。連接可包含諸如具有MHD回流導管310之輸入的活接(諸如Y活接)與諸如儲集器底板組合件409之凸台的儲集器之基座之凸台308。在包含具有MHD轉換器之加壓SunCell®的實施例中,EM泵之噴射側、儲集器及反應電解槽腔室5b31相對於MHD回流導管310在高壓下操作。每一EM泵之入口可僅包含MHD回流導管310。連接可包含諸如具有MHD回流導管310之輸入的活接(諸如Y活接與儲集器之基座的凸台,其中泵功率預防自來自儲集器之入口流回流至MHD回流導管310。 在MHD功率產生器實施例中,噴射EM泵及MHD傳回EM泵可包含本發明中之任一者,諸如DC或AC導電泵及AC感應泵。在例示性MHD功率產生器實施例(圖2I184)中,噴射EM泵可包含感應EM泵400,且MHD傳回EM泵312可包含感應EM泵或DC導電EM泵。 在另一實施例中,噴射泵可進一步充當MHD傳回EM泵。MHD回流導管310可在比來自儲集器之入口更低之壓力位置處輸入至EM泵。來自MHD回流導管310之入口可在適合於MHD冷凝區段309及MHD回流導管310中之低壓的位置處進入EM泵。來自儲集器5c之入口可在壓力較高之EM泵套管的位置處進入,諸如在壓力為所需反應電解槽腔室5b31操作壓力之位置處。噴射器區段5k61處之EM泵壓可至少為所需反應電解槽腔室壓力之壓力。入口可在套管及電流迴路區段5k6、405或406處附接至EM泵。 EM泵可包含多段泵(圖2I186-2I195)。多級EM泵可在各自對應於基本上僅允許向前熔融金屬流離開EM泵出口及噴射器5k61之壓力之不同泵級處接收輸入金屬流,諸如來自MHD回流導管310之輸入金屬流及來自儲集器5c之基座的輸入金屬流。在實施例中,多級EM泵組合件400a (圖2I188)包含至少一個EM泵變壓器繞組電路401a且進一步包含至少一個AC EM泵電磁電路403c,該EM泵變壓器繞組電路包含穿過感應電流迴路405及406之變壓器繞組401及變壓器磁軛402,該AC EM泵電磁電路包含AC電磁體403及EM泵電磁軛404。感應電流迴路可包含EM泵套管區段405及EM泵電流迴路傳回區段406。電磁軛404在含有諸如銀之泵送熔融金屬之電流迴路405的容器或EM泵套管區段之扁平區段處可具有間隙。 在實施例中,多級EM泵可包含供應垂直於電流及金屬流兩者之磁通量之複數個AC EM泵電磁電路403c。多級EM泵可沿電流迴路405之EM泵套管區段在入口壓力適合於局部泵壓之位置處接收入口,以實現向前泵流,其中壓力在下一AC EM泵電磁電路403c階段增大。在例示性實施例中,MHD回流導管310在包含AC電磁體403a及EM泵電磁軛404a之第一AC電磁體電路403c之前的入口處進入電流迴路,該電流迴路諸如電流迴路405之EM泵套管區段。來自儲集器5c之入口流可在第一AC電磁體電路403c之前及在第二AC電磁體電路403c之後進入,該等AC電磁體電路包含AC電磁體403b及EM泵電磁軛404b,其中泵保持電流迴路405中之熔融金屬壓力,該熔融金屬壓力保持來自每一入口之所需流至下一泵級或至泵出口及噴射器5k61。每一泵級之壓力可利用控制AC電磁體電路之對應AC電磁體的電流來控制。 在實施例中,諸如陶瓷通道之EM泵電流迴路傳回區段406可包含熔融金屬流量限制器或可用固體電導體填充以使得電流迴路之電流完整,同時防止熔融金屬自更高壓力回流至EM泵套管之更低壓力區段。固體可包含諸如本發明之不鏽鋼之金屬,諸如Haynes 230、Pyromet®合金625、Carpenter L-605合金、BioDur® Carpenter CCM®合金、Haynes 230、310 SS或625 SS。固體可包含耐火金屬。固體可包含抗氧化劑之金屬。固體可包含諸如銥之金屬或導電頂蓋層或塗層以避免固體導體之氧化。 在實施例中,轉換器及電磁體中之至少一者之磁性繞組與電流迴路之EM泵套管區段405保持距離,其含有藉由變壓器磁軛402及電磁電路磁軛404中的至少一者之延伸來流動金屬。延伸允許諸如EM泵套管405之電感耦合加熱之更高效加熱及變壓器繞組401、變壓器磁軛402以及包含AC電磁體403及EM泵電磁軛404的電磁電路403c中之至少一者之更高效冷卻中之至少一者。就二級EM泵而言,磁性電路可包含AC電磁體403a及403b以及EM泵電磁軛404a及404b。變壓器磁軛402及電磁軛404中之至少一者可包含具有較高居里溫度之鐵磁性材料,諸如鐵或鈷。EM泵變壓器繞組電路401a及EM泵電磁電路403c中之至少一者可包含諸如本發明中之一者之水冷卻系統,諸如DC導電EM泵之磁體5k4中的一者(圖2I115-2I116)。感應EM泵400b中之至少一者可包含空氣冷卻系統400b (圖2I190-2I191)。感應EM泵400c中之至少一者可包含水冷卻系統(圖2I192)。 例示性變壓器包含矽鋼層合變壓器芯。點火變壓器可包含(i)在約10至10,000匝、100至5000匝及500至25,000匝之至少一個範圍內的繞組數目;在約10 W至1 MW、100 W至500 kW、1 kW至100 kW及1 kW至20 kW之至少一個範圍內的功率,以及(iii)在約0.1 A至10,000 A、1 A至5 kA、1 A至1 kA及1 A至500 A之至少一個範圍內的初級繞組電流。在例示性實施例中,點火電流在約6 V至10 V之電壓範圍內,且電流為約1000 A;因此具有50匝之繞組在約500 V及20 A下操作以在1000 A下提供10 V之點火電流。EM泵電磁體可包含在約0.01 T至10 T、0.1 T至5 T及0.1 T至2 T之至少一個範圍內的通量。在例示性實施例中,約0.5 mm直徑磁線保持在約200℃下。 EM泵套管可使用諸如餅狀線圈天線之電感耦合加熱器天線加熱。天線可經水冷卻。在實施例中,儲集器5c可使用電感耦合加熱器加熱。加熱器天線5f可包含在儲集器5c周圍之可進一步連接至諸如餅狀線圈之線圈以加熱EM泵套管的兩個圓柱形螺旋。可捲繞儲集器周圍之相對螺旋之匝以使得電流處於相同方向以強化兩個線圈之磁場或處於相對方向以消除螺旋之間的空間中之磁場。在例示性實施例中,電感耦合加熱器天線5f可包含持續組三個匝,該等匝如圖2I182-2I183、2I186及2I190-2I192中所展示包含每一儲集器5c圓周之兩個螺旋線及平行於EM泵管之餅狀線圈,其中兩個螺旋線順時針捲繞,且電流自一個螺旋線之頂部流動至其底部,流動至餅狀線圈中,且隨後自第二螺旋線之底部流動至其頂部。電流迴路之EM泵套管區段405可藉由通量聚集器、諸如石英或氮化矽之添加劑的EM泵套管405材料之添加劑及諸如來自電感耦合加熱器之RF的吸收之碳套管之泵套管405的包層中之至少一者來選擇性加熱。在實施例中,電流迴路之EM泵套管區段405可藉由包含泵套管405周圍之螺旋線的電感耦合加熱器天線來選擇性加熱。諸如MHD回流導管310、EM泵儲集器管線416及EM泵噴射管線417中之至少一者之至少一個管線(圖2I192-2I195)可藉由電感耦合加熱器加熱,該電感耦合加熱器可包含纏繞於可水冷天線的管線周圍之天線415。纏繞有諸如5f及415之電感耦合加熱器天線的組件可包含內部絕緣層。電感耦合加熱器天線可提供雙重功能或加熱及水冷卻以保持對應組件之所需溫度。SunCell可進一步包含:固定諸如MHD磁體殼體306a、MHD噴嘴307及MHD通道308之組件之結構支架418,電輸出,感測器,及可安裝在結構支架418及諸如EM泵儲集器管線416及EM泵噴射管線417周圍之420的熱屏蔽上之控制管線419。 電流迴路之EM泵套管區段405可包含連接至對應EM泵套管5k6區段之熔融金屬入口及出口通道(圖2I185)。EM泵套管5k6之每一入口及出口可緊固至對應儲集器5c、進水升管5qa及噴射器5k61。扣件可包含本發明之接頭、扣件或密封件。密封件407a可包含陶瓷膠。接合可各自包含使用諸如石墨墊片之墊片密封的凸緣。每一儲集器5c可包含諸如金屬氧化物之連接至可為陶瓷之儲集器底板的陶瓷。底板連接可包含凸緣及墊片密封,其中墊片可包含碳。底板可包含儲集器底板組合件409(圖2I187),該儲集器底板組合件包含底板409a,該底板具有附接進水升管5qa及噴射器套管5k61,該噴射器套管具有噴嘴5q。套管可穿透儲集器底板409a之基座作為凸台408。來自儲集器5c之凸台408可藉由具有扣件及墊片之凸緣活接407中的至少一者連接至感應型EM泵400之EM泵套管之陶瓷入口及出口,該等扣件諸如螺栓,該等螺栓諸如碳、鉬或陶瓷螺栓,該墊片諸如碳墊片,其中包含至少一個陶瓷組件之活接在低於碳還原溫度下操作。在其他實施例中,活接可包含此項技術中已知其他活接,諸如Swagelok、滑動螺母或壓縮配件。在實施例中,點火電流藉由電源供應,該電源具有連接至相對泵套管、儲集器、凸台及活接中之一者之導電組件的其正極端子及負極端子。 在另一實施例中,點火系統包含感應系統(圖2I186、2I189-2I195),其中電源應用於導電熔融金屬以使得低能量氫反應之點火提供感應電流、電壓及功率。點火系統可包含無電極系統,其中點火電流藉由通過感應點火變壓器組合件410之感應來應用。感應電流可流動穿過來自藉由諸如EM泵400之泵保持之複數個噴射器之相交熔融金屬流。在實施例中,儲集器5c可進一步包含陶瓷交接通道414,諸如儲集器5c之底座之間的通道。感應點火變壓器組合件410可包含感應點火變壓器繞組411及感應點火變壓器磁軛412,該感應點火變壓器磁軛可延伸穿過由儲集器5c、來自複數個熔融金屬噴射器之相交熔融金屬流及交接通道414形成的感應電流迴路。感應點火變壓器組合件410可與EM泵變壓器繞組電路401a之感應點火變壓器組合件類似。 在實施例中,點火電流源可包含AC感應型,其中諸如銀之熔融金屬中之電流由通過銀的時變磁場之法拉弟感應產生。時變磁場之來源可包含初級變壓器繞組、感應點火變壓器繞組411,且銀可至少部分充當次級變壓器繞組,諸如單匝短路繞組。初級繞組411可包含AC電磁體,其中感應點火變壓器磁軛412通過包含熔融銀之圓周導電迴路來傳導時變磁場。變壓器電磁體可藉由單相AC電源或此項技術中已知之其他適合電源供電。可增加變壓器頻率以減小變壓器磁軛412之大小。變壓器頻率可在約1 Hz至1 MHz、1Hz至100 kHz、10 Hz至10 kHz及10 Hz至1 kHz之至少範圍內。儲集器5c可包含諸如連接兩個儲集器5c之交接通道414之熔融金屬通道。圍封變壓器磁軛412之電流迴路可包含儲集器5c、交接通道414中所含之熔融銀、噴射器套管5k61中的銀及所噴射之相交以使感應電流迴路完整之熔融銀流。感應電流迴路可進一步至少部分包含熔融銀,該熔融銀含於諸如進水升管5qa、EM泵套管5k6、凸台及噴射器5k61之EM泵組件中之至少一者中。 交接通道414可在諸如儲集器中之銀之熔融金屬之所需位準處。可替代地,交接通道414可在低於所需儲集器熔融金屬位準之位置處以使得通道在操作期間連續地用熔融金屬填充。交接通道414可朝向儲集器5c之基座定位。通道可形成感應電流迴路或電路之部分且進一步有助於熔融金屬自具有較高銀位準之一個儲集器流動至具有較低位準的另一儲集器以保持兩個儲集器5c中之所需位準。熔融金屬排出壓力中之差分可使得金屬在儲集器之間流動以保持每一儲集器中之所需位準。電流迴路可包含相交熔融金屬流、噴射器套管5k61、儲集器5c中之熔融金屬塔及連接所需熔融銀位準處之儲集器5c或低於所需位準處之儲集器的交接通道414。電流迴路可圍封藉由法拉弟感應產生電流之變壓器磁軛412。在另一實施例中,至少一個EM泵變壓器磁軛402可進一步包含感應點火變壓器磁軛412以藉由通過點火熔融金屬迴路額外供應時變磁場來產生感應點火電流,該點火熔融金屬迴路諸如由相交熔融金屬流及含於儲集器及交接通道414中之熔融金屬形成的點火熔融金屬迴路。儲集器5c及通道414可包含諸如陶瓷之電絕緣體。感應點火變壓器磁軛412可包含蓋板413,該蓋板可包含諸如陶瓷蓋板之電絕緣體及熱絕緣體中之至少一者。在儲集器之間延伸的感應點火變壓器磁軛412之區段可藉由蓋板413熱或電屏蔽,該等儲集器可包含諸如螺旋線圈之沿圓周纏繞電感耦合加熱器天線。儲集器5c、通道414及蓋板413中之至少一者之陶瓷可為本發明之陶瓷,諸如氮化矽(MP 1900℃)、諸如熔融石英的石英、氧化鋁、氧化鋯、氧化鎂或氧化鉿。保護性SiO2 層可在亞硝酸矽上藉由受控鈍化氧化來形成。 諸如石英部件之陶瓷部件可使用諸如石墨或其他耐火惰性模製之模製來澆築。在例示性實施例中,藉由諸如Hellma分析(http://www.hellmaanalytics.com/assets/adb/32/32e6a909951dc0e2.pdf)之方法的此項技術中已知之方法之熱或低溫液體澆築石英的模製包含四個部件,該等部件包含兩個鏡面對諸如儲集器5c及反應電解槽腔室5b31之電池組件之內及外表面。 在實施例中,交接通道414保持儲集器銀位準接近恆定。SunCell®可進一步包含噴射器5k61之浸沒噴嘴5q。歸因於每一儲集器5c之大約恆定之熔融金屬位準,每一浸沒噴嘴的深度且因此噴射器噴射通過之排出壓力可基本上保持恆定。在包含交接通道414之實施例中,進水升管5qa可經移除且用孔置換至儲集器凸台408或EM泵儲集器管線416中。 EM泵及點火系統中之至少一者的變壓器繞組401及411、電磁體403、磁軛402、404及412以及磁性電路401a、403a及410中之至少一者可屏蔽電感耦合加熱器之RF磁場以減小加熱效果。屏蔽可包含法拉弟籠。籠壁厚可大於電感耦合加熱器之RF場之趨膚深度。在包含感應點火系統410之實施例中,變壓器磁軛412可藉由水冷卻天線5f的鄰近而至少部分冷卻,該水冷卻天線可在操作期間進一步用於冷卻SunCell®及儲集器5c中之至少一者。 點火電流可為時變的,諸如約60 Hz AC,但可具有其他特性及波形,諸如具有在1 Hz至1 MHz、10 Hz至10 kHz、10 Hz至1 kHz及10 Hz至100 Hz之至少一個範圍內之頻率的波形,在約1 A至100 MA、10 A至10 MA、100 A至1 MA、100 A至100 kA及1 kA至100 kA之至少一個範圍內的峰值電流,以及在約1 V至1 MV、2 V至100 kV、3 V至10 kV、3 V至1 kV、2 V至100 V及3 V至30 V之至少一個範圍內的峰值電壓,其中波形可包含正弦波、方波、三角形或其他所需波形,該波形可包含諸如在1%至99%、5%至75%及10%至50%之至少一個範圍內的占空比之占空比。 在實施例中,調節點火頻率以產生反應電解槽腔室5b31及MHD通道308中之至少一者中的低能量氫發電對應頻率。諸如約60 Hz AC之電力輸出的頻率可藉由控制點火頻率來控制。點火頻率可藉由變化感應點火變壓器組合件410之時變磁場的頻率來調節。感應點火變壓器組合件410之頻率可藉由變化感應點火變壓器繞組411之電流的頻率來調節,其中可變化繞組411之功率之頻率。MHD通道308中之時變功率可防止氣溶膠噴柱流之震波形成。在另一實施例中,時變點火可驅動導致時變電功率輸出之時變低能量氫發電。MHD轉換器可輸出AC電力,該轉換器亦可包含DC組件。AC組件可用於對諸如變壓器及電磁體繞組中之一或多者中之至少一者的至少一個繞組供電,該等變壓器及電磁體繞組諸如EM泵變壓器繞組電路401a之繞組及EM泵電磁電路403c之電磁體的繞組中之至少一者。 具有MHD轉換器之加壓SunCell®可在不依賴重力之情況下操作。諸如兩級空氣冷卻EM泵400b之諸如400之EM泵可定位於使熔融金屬入口及出口管道或管線之填料及最小化中之至少一者最佳化的位置中。例示性包裝為EM泵定位在MHD冷凝區段309之末端與儲集器5c之基座之間的中間位置之包裝(圖2I193-2I195)。 在實施例中,離開MHD噴嘴307且進入MHD通道308之銀蒸氣-銀氣溶膠混合物包含大部分液體分數。為實現大部分液體分數在MHD通道308入口處,混合物可包含MHD噴嘴307之入口處的大部分液體。由低能量氫反應產生之反應電解槽腔室5b31之熱功率可藉由MHD噴嘴307大部分轉換成動能。在實現MHD噴嘴307之出口處之大部分能量庫存為動能的條件之實施例中,混合物必須為大部分液體分數,且混合物之溫度及壓力應接近熔融金屬在其熔點處之溫度及壓力。為將較大分數之混合物之熱能庫存轉換成動能,諸如de Laval噴嘴之聚合-分岔MHD噴嘴307之分岔區段的噴嘴區域必須增大。因為混合物之熱能轉換成MHD噴嘴307中之動能,混合物之溫度隨著伴隨壓降下降。低壓條件對應於較低蒸氣密度。較低蒸氣密度減小橫截面以將向前動量及動能轉移至混合物之液體分數。在實施例中,可增加噴嘴長度以產生噴嘴出口之前的更長液體加速時間。在實施例中,可減小MHD噴嘴出口處之氣溶膠噴柱之橫截面積。區域減小可藉由至少一個聚焦磁體、隔板及此項技術中已知之其他構件中之一或多者來實現。具有減小區域之聚焦氣溶膠噴柱可准許MHD通道308橫截面積更小。MHD通道功率密度可為更高。MHD磁體306歸因於磁化通道308之更小體積可為更小。 在實施例中,MHD通道308之入口處之混合物的溫度接近於熔融金屬之熔點。就銀而言,混合物溫度可在約965℃至2265℃、1000℃至2000℃、1000℃至1900℃及1000℃至1800℃之至少一個範圍內。在實施例中,銀液體可藉由EM泵400、400a、400b或400c再循環至儲集器5c以回收液體中之熱能之至少一部分。 在包含活接之實施例中,該等活接包含陶瓷部件及碳墊片,再循環銀之溫度可低於石墨以及陶瓷之碳還原溫度及諸如陶瓷組件之SunCell®組件的材料之失效溫度中之至少一者。在包含諸如傳回管道310、電流迴路之EM泵套管區段405、儲集器5c、反應電解槽腔室5b31、MHD噴嘴307、在陶瓷組件之間具有至少一個碳墊片凸緣活接407之MHD通道308及MHD冷凝區段309的氧化釔穩定氧化鋯之例示性實施例中,銀溫度低於約1800℃至2000℃。包含動能及熱能之氣溶膠的功率可轉換成MHD通道中之電力。氣溶膠動能可藉由液體MHD機制轉換成電力。諸如MHD通道308中之混合物的任何蒸氣之熱功率之一些殘餘熱功率可藉由作用於對應蒸氣之勞侖茲力轉換成電力。熱能轉換率使得混合物溫度下降。銀蒸氣壓可對應於較低混合物溫度而較低。MHD通道308可保持在較低背景壓力下,諸如在約0.001托至760托、0.01托至100托、0.1托至10托之至少一個範圍內之壓力下,以防止來自噴嘴307的氣溶膠噴柱經受震波,諸如冷凝震波或擾流,從而氣溶膠產生加壓,諸如MHD通道308中之背壓。 在實施例中,混合物之蒸氣分數在噴嘴入口處最小化以在噴嘴出口處減小其。蒸氣分數可在約0.01至0.3、0.05至0.25、0.05至0.20、0.05至0.15及0.05至0.1之至少一個範圍內。20個大氣壓、0 m/s速度、3253 K溫度、混合物之0.9液體質量分數、聲波速度137 m/s、Mach數目0及0 kJ/kg動能之給定噴嘴例示性入口參數、噴嘴出口處的混合物之例示性參數約為表3中給定之參數。 表3. 20個大氣壓之壓力、0.9液體分數及1 kg/s質量流之初始入口參數的噴嘴出口參數。 在實施例中,蒸氣可在MHD通道之末端至少部分冷凝,諸如在MHD冷凝區段309中。熱交換器316可移除熱以使得冷凝。可替代地,蒸氣壓可為足夠低以使得MHD效率藉由不冷凝蒸氣增加,其中蒸氣在MHD通道308中保持靜態平衡壓力。在實施例中,勞侖茲力大於MHD通道308中之任何未冷凝蒸氣的碰撞摩擦力。勞侖茲力可增加至增大磁場強度所需之勞侖茲力。可增加MHD磁體306之磁通量。在實施例中,磁通量可在約0.01 T至15 T、0.05 T至10 T、0.1 T至5T、0.1 T至2 T及0.1 T至1 T之至少一個範圍內。在實施例中,銀蒸氣冷凝以使得汽化熱加熱再循環至儲集器或輸出為噴射器5k61之二級EM泵的EM泵套管之銀。蒸氣可使用壓縮機312a壓縮。壓縮機可連接至諸如400c之二級EM泵。 在實施例中,銀蒸氣/氣溶膠混合物在MHD噴嘴307之出口處幾乎為純淨液體加氧。氧於銀中之溶解度隨著溫度接近熔點而增大,其中溶解度針對銀體積為至多約40至50個氧體積(圖3)。銀在MHD通道308處吸收氧,諸如在出口處,且液體銀及氧皆經再循環。氧可經再循環為熔融銀中所吸收之氣體。在實施例中,氧釋放於反應腔室5b31中以再生循環。高於熔點之銀的溫度亦充當用於熱功率再循環或再生之手段。氧氣濃度經最佳化以實現熱力學循環,其中再循環銀之溫度小於諸如1800℃的SunCell®組件之最大操作溫度。在例示性實施例中,(i)反應電解槽腔室5b31及MHD噴嘴307中之至少一者中之氧壓為1個大氣壓,(ii)MHD通道308的出口處之銀幾乎全為諸如氣溶膠之液體,(iii)氧質量流率為約0.3wt%,且(iv)MHD通道之出口處的溫度為約1000℃,其中O2 加速氣溶膠且隨後由1000℃銀吸收。液體銀氧混合物再循環至反應電解槽腔室5b31,其中氧經釋放,以形成熱力學循環。可減小或除去諸如312a之氣體壓縮機及對應寄生功率負載的需求。在實施例中,氧壓可在約0.0001個大氣壓至1000個大氣壓、0.01個大氣壓至100個大氣壓、0.1個大氣壓至10個大氣壓及0.1個大氣壓至1個大氣壓之至少一個範圍內。氧在一個電池區域中可具有較高分壓,該電池區域諸如反應電解槽腔室5b31及相對於MHD通道出口308之噴嘴307中之至少一者。SunCell®可具有可在諸如反應電解槽腔室5b31及相對於MHD通道出口308之噴嘴307中之至少一者的一個電池區域中升高之背景氧氣分壓。歸因於操作溫度下之遠遠更高氧熱容量及非冷凝力,MHD噴嘴可相對於僅使用銀蒸氣之MHD轉換器的尺寸在尺寸上減小以實現氣溶膠噴柱加速。 熱力學循環可經最佳化以最大化電轉換效率。在實施例中,最大化混合物動能同時最小化蒸氣分數。在實施例中,熱功率再循環或再生隨自MHD通道308之出口至反應電解槽腔室5b31之再循環銀的溫度而變來實現。再循環銀之溫度可小於SunCell®組件之諸如1800℃之最大操作溫度。在另一實施例中,勞侖茲力可冷卻混合物以至少部分濃縮液相,其中對應所釋放之汽化熱至少部分轉移至液相。MHD噴嘴擴展、MHD通道308擴展及MHD通道308中之勞侖茲力冷卻中之至少一者可將MHD噴嘴307出口及MHD通道308中的一或多者處之混合物之溫度降低低於銀熔點。由冷凝蒸氣所釋放之熱可隨著溫度提高而吸收至銀及銀熱容量之熔融熱。由冷凝蒸氣汽化熱加熱之銀可再循環以再生對應熱功率。在提高效率之另一個實施例中,相對低溫氣溶膠可藉由諸如來自儲集器5c之管道的構件噴射至諸如MHD噴嘴307或MHD通道308之功率轉換組件中。 SunCell®之陶瓷部件可借助於本發明接合,諸如藉由兩個或多於兩個陶瓷部件之陶瓷膠、陶瓷至金屬部件之銅焊、滑動螺母密封、墊片密封及濕封。墊片密封可包含用墊片密封之兩個凸緣。凸緣可連同諸如螺栓之扣件抽出。滑動螺母接合或墊片密封可包含碳墊片。螺母、EM泵組合件5kk、儲集器底板5b8及下部半球5b41中之至少一者可包含抗碳化及碳化物形成之材料,諸如鎳、碳及抗碳化之諸如SS 625或Haynes 230 SS的不鏽鋼(SS)。EM泵組合件與陶瓷儲集器之間的滑動螺母接合可包含EM泵組合件5kk及石墨墊片,該EM泵組合件包含螺紋軸環及螺母,該螺紋軸環及螺母包含抗碳化的諸如SS 625或Haynes 230 SS之不鏽鋼(SS),其中螺母擰在軸環上以緊固彼墊片。EM泵組合件5kk與儲集器5c之間的凸緣密封接合可包含具有螺栓孔之儲集器底板5b8、具有凸緣以及螺栓孔之陶瓷儲集器及碳墊片。具有儲集器底板之EM泵組合件可包含抗碳化之諸如SS 625或海恩斯230 SS之不鏽鋼(SS)。儲集器之凸緣可藉由緊固碳或石墨墊片之螺栓來緊固至底板5b8。在實施例中,諸如碳墊片之碳與諸如氧化物儲集器5c之包含氧化物的部件之間的碳還原反應藉由維持包含氧化之接合與碳在非反應性溫度下接觸來避免,氧化物儲集器諸如MgO、Al2 O3 或ZrO2 儲集器,該非反應性溫度低於碳還原反應溫度。在實施例中,MgO碳還原反應溫度高於約2000℃至2300℃之範圍。 在例示性實施例中,諸如氧化物陶瓷之陶瓷可用諸如Mo-Mn之合金金屬化,該氧化物陶瓷諸如氧化鋯或氧化鋁。兩個金屬化陶瓷部件可藉由銅焊接合。金屬化陶瓷部件及諸如EM泵匯流排5k2之金屬部件可藉由銅焊連接。可塗佈金屬化以保護其免於氧化。例示性塗層就水氧化劑而言包含鎳及貴金屬,且就氧而言包含貴金屬。在例示性實施例中,氧化鋁或氧化鋯EM泵套管5k6在EM泵匯流排5k2之穿透處金屬化,且EM泵匯流排5k2藉由銅焊連接至金屬化EM泵套管穿透。在另一例示性實施例中,來自EM泵組合件5kk、EM泵5ka、EM泵套管5k6、進水升管5qa、噴射EM泵套管5k61、儲集器、MHD噴嘴307及MHD通道308中之至少兩者的清單之部件可用陶瓷膠膠合在一起。陶瓷部件可使用本發明或此項技術中已知之方法來構造。陶瓷部件可經粉末模製、澆築或燒結、或膠合在一起、或擰在一起。在實施例中,組件可在陶瓷生坯中構造並燒結。在例示性實施例中,氧化鋁部件可燒結在一起。在另一實施例中,複數個部件可構造為生坯部件,裝配及燒結在一起。部件及材料之尺寸可經選擇以補償部件收縮。 在實施例中,諸如包含ZrC-ZrB2-SiC中之至少一者的陶瓷部件之陶瓷SunCell®部件可藉由球磨研磨組件粉末之化學計量混合物形成,在模製中形成為所需形狀,且藉由諸如熱均衡加壓(HIP)或火花電漿燒結(SPS)之手段燒結。陶瓷可具有相對較高密度。在實施例中,諸如EM泵套管5k6之空心部件可使用用於空心部件的氣囊澆築。氣囊可在澆鑄之後放氣且部件經燒結。可替代地,部件可藉由3D列印構造。諸如下部半球5b41及上部半球5b42中之至少一者的部件可滑動澆築,且諸如儲集器5c之部件可藉由擠出及壓製中之至少一者形成。其他構造方法包含噴霧乾燥、射出模製、加工、金屬化及塗層中之至少一者。 在實施例中,碳化物陶瓷部件可構造為分別與諸如鋯或矽之對應金屬反應之石墨製備ZrC或SiC部件。包含不同陶瓷之部件可藉由本發明之方法或此項技術中已知之方法接合在一起,諸如擰緊、膠合、濕封、銅焊及墊片密封。在實施例中,EM泵套管可包含套管區段及彎管以及膠合在一起之匯流排突片5k2。在例示性實施例中,膠合EM泵套管部件包含ZrC或與Zr金屬反應以形成ZrC之石墨。可替代地,部件可包含ZrB2 或相似非氧化導電陶瓷。 在實施例中,MHD電極304包含諸如液體銀電極之液體電極。MHD電導線305及饋入孔301中之至少一者類似於濕封可包含諸如固化銀之固化熔融金屬,其中導線或饋入孔中之至少一者可經冷卻以保持固體金屬狀態。MHD轉換器可包含圖案化結構,該圖案化結構包含MHD電極304、諸如305之電絕緣導線、絕緣電極分離器及諸如穿透諸如310之MHD匯流排饋入孔凸緣的饋入孔之饋入孔的群組之至少一個組件。包含諸如銀電極之液體電極之圖案化結構組件及絕緣分離器可包含浸潤材料以保持液態金屬呈所需形狀及諸如銀電極之液體電極與絕緣電極分離器兩者之間的間距。圖案化結構之浸潤材料及絕緣分離器中之至少一者可包含陶瓷。液體電極之浸潤材料可包含多孔陶瓷。電絕緣分離器可包含可針對銀為非濕潤之緻密陶瓷。導線可包含可諸如水冷之冷卻以保持導線之硬度的電絕緣通道及套管。例示性實施例包含經冷卻以將固化銀保持在內部以充當導電引線之電絕緣MHD電極導線305。在另一實施例中,MHD電導線305及饋入孔301中之至少一者可包含諸如塗層之銥,該塗層諸如經銥塗佈的Mo或諸如625 SS之抗氧化劑不鏽鋼。 用於具有MHD轉換器之SunCell®之例示性材料包含(i)儲集器5c、反應電解槽腔室5b31及噴嘴307:諸如穩定化氧化鋯或氧化鉿的固體氧化物;(ii)MHD通道308:MgO或Al2 O3 ;(iii)電極304:ZrC或ZrC-ZrB2 、ZrC-ZrB2 -SiC及具有可至多1800℃下工作之20%SiC複合物之ZrB2 或塗佈有貴金屬之金屬;(iv)EM泵5ka:諸如塗佈有貴金屬的不鏽鋼或塗佈有具有類似熱膨脹係數之材料諸如Paloro-3V鈀金釩合金(Morgan高級材料)的410不鏽鋼之金屬,該貴金屬諸如白金(Pt)、鈀(Pd)、釕(Ru)、銠(Rh)及銥(Ir)中之至少一者;(v)儲集器5c-EM泵組合件5kk活接:諸如釺焊至410不鏽鋼EM組合件5kk底板之ZrO2 、HfO2 或Al2 O3 的氧化物儲集器,其中銅焊包含Paloro-3V鈀金釩合金(Morgan高級材料);(vi)噴射器5k61及進水升管5qa:諸如穩定化氧化鋯或氧化鉿之固體氧化物;以及(vii)氧選擇性隔膜:可塗佈有Bi26 Mo10 O69 以增加氧滲透率之BaCo0 . 7 Fe0 . 2 Nb0 . 1 O3 - δ (BCFN)氧滲透膜。 在實施例中,SunCell®進一步包含氧氣感測器及諸如以惰性氣體稀釋氧及將惰性氣體泵離中之至少一者的手段之氧控制系統。前者可包含惰性氣體貯槽、閥門、調節器及泵中之至少一者。後者可包含閥門及泵中之至少一者。 反應電解槽腔室5b31之低能量氫反應混合物可進一步包含諸如H2 O及包含氧的化合物中之至少一者之氧來源。諸如包含氧之化合物之氧來源可呈過量形式以保持接近恆定氧來源庫存,其中在電池操作期間,較小部分可逆地與諸如H2 氣體的供應H來源反應以形成HOH催化劑。包含氧之例示性化合物為MgO、CaO、SrO、BaO、ZrO2 、HfO2 、Al2 O3 、Li2 O、LiVO3 、Bi2 O3 、Al2 O3 、WO3 及本發明之其他化合物。氧來源化合物可為用於使諸如氧化釔或氧化鉿之氧化物陶瓷穩定的氧來源化合物,該氧化物陶瓷諸如氧化釔(Y2 O3 )、氧化鎂(MgO)、氧化鈣(CaO)、氧化鍶(SrO)、氧化鉭(Ta2 O5 )、三氧化二硼(B2 O3 )、TiO2 氧化鈰(Ce2 O3 )、鋯酸鍶(SrZrO3 )、鋯酸鎂(MgZrO3 )、鋯酸鈣(CaZrO3 )及鋯酸鋇(BaZrO3 ) 在導電性大於約20 kS/m且電漿氣體溫度為約4000 K之例示性實施例中,反應腔室壓力保持在約15 MPa至25 MPa的範圍內以抗勞侖茲力保持MHD通道308中之流動。在例示性實施例中,導電性保持在約700 S/m,電漿氣體溫度為約4000 K,反應電解槽腔室5b31壓力為約0.6 MPa,噴嘴307出口速度為約Mach 1.24,噴嘴出口區域為約3.3 cm2 ,噴嘴出口直徑為約2.04 cm,噴嘴出口壓力為約213 kPa,噴嘴出口處之溫度為約2640 K,通過噴嘴的質量流為約250 g/s,MHD通道308中之磁場強度為約2 T,MHD通道308長度為約0.2 m,MHD通道出口壓力為約11 kPa,MHD通道出口溫度為約1175 K,且輸出電功率為約180 kW。在理想實施例中,效率藉由Carnot方程式確定,其中電漿溫度至環境溫度之不可避免功率損失為氣體及液態金屬泵損失。 在實施例中,用於能夠加熱銀以形成銀蒸氣及銀氣溶膠中之至少一者之諸如核或燃燒的任何電源之MHD轉換器包含本發明之MHD轉換器,該MHD轉換器進一步包含至少一個熱交換器以轉移來自電源的熱以加熱儲集器5c及反應電解槽腔室5b31中之至少一者來產生銀蒸氣及銀氣溶膠中之至少一者。MHD轉換器可進一步包含諸如晶種中之至少一者的電離源極,該晶種諸如鹼金屬,該鹼金屬諸如熱電離之銫及電離器,該ionizer諸如雷射、RF放電產生器、微波放電產生器及輝光放電產生器。 在包含加熱器電力轉換器之SunCell®電力系統之實施例中,雙重熔融金屬噴射器的EM泵可各自包含感應型電磁泵以將與另一熔融金屬之流相交的熔融金屬之流噴射於容器之內部。點火系統之電源包含電感點火系統410,其可包含穿過熔融金屬之短路迴路之交變磁場來源,其在金屬中產生包含點火電流之交流電。交變磁場來源可包含初級變壓器繞組411,其包含變壓器電磁體及變壓器磁軛412,且銀可至少部分充當次級變壓器繞組,諸如單匝短路繞組,其圍封初級變壓器繞組且包含電感型迴路。儲集器5c可包含熔融金屬交接通道414,其連接兩個儲集器以使得電流迴路圍封變壓器磁軛412,其中感應電流迴路包含在儲集器5c、交接通道414中所含之熔融銀、噴射器套管5k61中之銀及所噴射之相交以使感應電流迴路完整之熔融銀流中產生的電流。諸如氫及氧之反應氣體可通過進氣口及氣體殼體309b之排空組合件309e供應至電池。氣體殼體309e可在沿球面之頂部極點之軸線的球狀熱交換器外部。氣體殼體可包含凸緣連接處之至球狀反應電解槽腔室5b31之頂部的薄氣管連接。氣管連接可穿過將冷卻劑流動供應至球狀熱交換器之同心冷卻劑流動管道的內部。在反應電解槽側上,至氣管之凸緣連接可連接至半滲透氣體309d隔膜,諸如多孔陶瓷隔膜。 SunCell®加熱器或熱功率產生器實施例(圖2I196)包含球狀反應器電池5b31以及包含接收來自球狀反應器5b4之輻射的熱之面板或區段114a之空間分離圓周半球狀熱交換器114。每一面板可包含由通過球面之極點之兩個較大環限定的球狀表面之區段。熱交換器114可進一步包含具有來自熱交換器之面板114a中之各者的冷卻劑管線114c之環面歧管之歧管114b及歧管冷卻劑出口114f。每一冷卻劑管線114c可包含冷卻劑入口孔114d及冷卻劑出口孔114e。熱功率產生器可進一步包含具有入口及出口309e之貯氣瓶421及通過熱交換器114之頂部延伸至球狀電池5b31之頂部上的透氣膜309d之氣體供應套管422。氣體供應套管422可穿過熱交換器114之頂部處的冷卻劑收集歧管114b。在另一SunCell®加熱器實施例(圖2I156-2I160及2I196)中,反應電解槽腔室5b31可為具有圓柱形熱交換器114之圓柱形的。貯氣瓶421可在熱交換器114外部,其中氣體供應套管422藉由穿過熱交換器114連接至反應電解槽腔室5b31之頂部上的半滲透氣體隔膜309d。冷水可饋入入口113中且在熱交換器114中加熱以形成鍋爐116中收集且蒸汽出口111中存在之蒸汽。熱功率產生器可進一步包含雙重熔融金屬噴射器,該等雙重熔融金屬噴射器包含感應EM泵400、儲集器5c及反應電解槽腔室5b31。諸如儲集器5c之至少一個SunCell®加熱器組件可用電感耦合加熱器天線5f加熱。SunCell®加熱器可包含感應點火系統,該感應點火系統諸如包含感應點火變壓器繞組411及感應點火變壓器磁軛412之感應點火系統。例示性實施例 在本發明之包含PV轉換器之SunCell®發電機的例示性實施例中:(i)EM泵組合件5kk可包含不鏽鋼,其中諸如EM泵套管5k6之內部的曝露於氧化之表面可用諸如鎳塗層之抗氧化劑塗層塗佈,其中選擇諸如英高鎳之不鏽鋼以具有與鎳之熱膨脹係數類似的熱膨脹係數;(ii)儲集器5c可包含諸如BN-Ca之氮化硼,其可抗氧化穩定化;(iii)儲集器與EM泵組合件5kk之間的活接可包含濕封;(iv)熔融金屬可包含銀;(v)進水升管5qa及噴射套管5k61可包含擰至EM泵組合件底板5kk1中之軸環中的ZrO2 ;(vi)下部半球5b41可包含諸如抗與氫反應之熱碳的碳;(vii)上部半球5b42可包含諸如抗與氫反應之熱碳的碳;(viii)氧來源可包含CO,其中CO可作為氣體添加,由諸如金屬羰基(例如W(CO)6 、Ni(CO)4 、Fe(CO)5 、Cr(CO)6 、Re2 (CO)10 及Mn2 (CO)10 )之羰基之受控熱或其他分解供應,且作為CO2 來源或CO2 氣體供應,其中CO2 可在低能量氫電漿中分解以釋放CO或可與諸如供應犧牲碳粉末的碳反應,以供應CO,或O2 可通過諸如本發明中之一者之本發明的氧滲透膜添加,諸如可用Bi26 Mo10 O69 塗佈以增加氧滲透率之BaCo0.7 Fe0.2 Nb0.1 O3 - δ (BCFN)氧滲透膜,其中添加可與犧牲碳粉末反應以隨著用偵測器監測及用控制器控制來保持所需CO濃度之O2 ;(ix)氫來源可包含可通過諸如EM泵套管5k4壁中的Pd或Pd-Ag隔膜使用質量流量控制器供應氫滲透膜以控制來自高壓水電解劑之氫流之H2 氣體;(x)儲集器與下部半球5b41之間的活接可包含滑動螺母,該滑動螺母可包含碳墊片及碳螺母;以及(xi)PV轉換器可包含緻密接收器陣列,該緻密接收器陣列包含藉由冷板冷卻之多接面III-V PV電池。反應電解槽腔室5b31可包含諸如碳粉末之犧牲碳來源以清除將另外與碳反應電解槽腔室的壁反應之O2 及H2 O。水與碳之反應速率取決於與反應電解槽腔室5b31壁之表面區域相比就犧牲碳而言大多個數量級之表面區域。在實施例中,碳反應電解槽腔室之內部壁包含碳鈍化層。在實施例中,反應電解槽腔室之內壁塗佈有錸塗層以保護壁免於H2 O氧化。在實施例中,SunCell®之氧庫存保持大約恆定。在實施例中,添加氧庫存可添加為CO2 、CO、O2 及H2 O中之至少一者。在實施例中,添加H2 可與犧牲粉末狀碳反應以形成甲烷,以使得低能量氫反應物包含諸如甲烷之由O、C及H元素形成之至少一種烴及諸如CO或CO2 之由O、C及H元素形成的至少一種氧化合物。氧化合物及烴可分別充當氧來源及H來源,以形成HOH催化劑及H。 SunCell®可進一步包含諸如CO感測器、CO通風口、CO稀釋劑氣體及CO吸收劑中之至少一者的一氧化碳安全系統。CO可受濃度及總庫存中之至少一者限制以提供安全。在實施例中,CO可經限制至反應腔室5b31且視情況經限制至外部容器腔室5b3a1。在實施例中,SunCell®可包含次級腔室以限制及稀釋自反應電解槽腔室5b31漏泄之任何CO。次級腔室可包含電池腔室5b3、外部容器腔室5b3a1、下部腔室5b5及另一腔室中之至少一者,該另一腔室可接收CO以進行以下中之至少一者:含有及稀釋漏泄CO至安全位準。CO感測器可檢測任何漏泄CO。SunCell®可進一步包含稀釋氣體貯槽、稀釋劑氣體貯槽閥門、排氣閥門及CO控制器中之至少一者以接收來自CO感測器之輸入且控制閥門中之打開及流動來在速率下稀釋及釋放或拍出CO,其濃度不超過所需或安全位準。含有漏泄CO之腔室中之CO吸收劑亦可吸收漏泄CO。例示性CO吸附劑為亞銅銨鹽、溶解於HCl溶液中之氯化亞銅、氨溶液或鄰甲氧基苯胺及本領域的技術人員已知的其他吸附劑。任何排出CO可呈小於約25 ppm之濃度。在反應電解槽腔室CO濃度保持在約1000 ppm CO且反應電解槽腔室CO包含總CO庫存之例示性實施例中,外部密閉或次級腔室體積相對於反應電解槽腔室體積大超過40倍,以使得SunCell®對CO洩漏為本質上安全的。在實施例中,SunCell®進一步包含諸如氧化器之CO反應器,該氧化器諸如燃燒器或分解器,諸如電漿反應器,以將CO反應成諸如CO2 或C及O2 安全產物。例示性催化氧化器產物為包含Moleculite (Molecular,http :// www . molecularproducts . com / products / marcisorb - co - absorber )之Marcisorb CO吸收器。 在實施例中,氫可充當催化劑。將nH (n為整數)供應為催化劑及H原子以形成低能量氫之氫來源可包含可通過EM泵套管5k4壁中之諸如Pd或Pd-Ag的氫滲透膜使用質量流量控制器以控制來自高壓水電解劑之氫流來供應的H2 氣體,該氫滲透膜諸如23%Ag/77%Pd合金隔膜。使用氫作為HOH催化劑之替代的催化劑可避免諸如碳反應電解槽腔室5b31之至少一個電池組件之氧化反應。反應電解槽腔室中所保持之電漿可分解H2 以提供H原子。碳可包含熱碳以遏制碳與氫之間的反應。 在本發明之SunCell®加熱器之例示性實施例中:(i) EM泵組合件5kk可包含不鏽鋼,其中諸如EM泵套管5k6之內部的曝露於氧化之表面可用諸如鎳塗層之抗氧化劑塗層塗佈;(ii)儲集器5c可包含呈立方型藉由MgO或Y2 O3 穩定化之ZrO2 ;(iii)儲集器與EM泵組合件5kk之間的活接可包含濕封;(iv)熔融金屬可包含銀;(v)進水升管5qa及噴射套管5k61可包含擰至EM泵組合件底板5kk1中之軸環中的ZrO2 ;(vi)下部半球5b41可包含呈立方型藉由MgO或Y2 O3 穩定化之ZrO2 ;(vii)上部半球5b42可包含呈立方型藉由MgO或Y2 O3 穩定化的ZrO2 ;(viii)氧來源可包含諸如鹼金屬氧化物或鹼土金屬氧化物或其混合物之金屬氧化物;(ix)氫來源可包含可通過EM泵套管5k4壁中之氫滲透膜使用質量流量控制器供應以控制來自高壓水電解劑的氫流之H2 氣體;(x)儲集器與下部半球5b41之間的活接可包含陶瓷膠;(xi)下部半球5b41與上部半球5b42之間的活接可包含陶瓷膠;以及(xii)熱交換器可包含輻射鍋爐。在實施例中,下部半球5b41及上部半球5b42中之至少一者可包含具有熱導率之材料,諸如導電陶瓷,諸如本發明中之一者,諸如在1800℃對氧化穩定之ZrC、ZrB2 及ZrC-ZrB2 及ZrC-ZrB2 -SiC複合物中之至少一者,以改良自電池之內部至外部的熱傳遞。 在包含磁流體動力(MHD)轉換器之本發明之SunCell®發電機的例示性實施例中:(i)EM泵組合件5kk可包含不鏽鋼,其中諸如EM泵套管5k6之內部的曝露於氧化之表面可用諸如鎳塗層之抗氧化劑塗層塗佈;(ii)儲集器5c可包含呈立方型藉由MgO或Y2 O3 穩定化的ZrO2 ;(iii)儲集器與EM泵組合件5kk之間的活接可包含濕封;(iv)熔融金屬可包含銀;(v)進水升管5qa及噴射套管5k61可包含擰至EM泵組合件底板5kk1中之軸環中的ZrO2 ;(vi)下部半球5b41可包含呈立方型藉由MgO或Y2 O3 穩定化之ZrO2 ;(vii)上部半球5b42可包含呈立方型藉由MgO或Y2 O3 穩定化之ZrO2 ;(viii)氧來源可包含諸如鹼金屬氧化物或鹼土金屬氧化物或其混合物之金屬氧化物;(ix)氫來源可包含可通過EM泵套管5k4壁中之氫滲透膜使用質量流量控制器供應以控制來自高壓水電解劑之氫流的H2 氣體;(x)儲集器與下部半球5b41之間的活接可包含陶瓷膠;(xi)下部半球5b41與上部半球5b42之間的活接可包含陶瓷膠;(xii)MHD噴嘴307、通道308及冷凝309區段可包含呈立方型藉由MgO或Y2 O3 穩定化之ZrO2 ;(xiii) MHD電極304可包含諸如經Pt塗佈Mo或W的經Pt塗佈之耐火金屬、在700℃對水反應穩定的碳、在1800℃對氧化穩定之ZrC-ZrB2 及ZrC-ZrB2 -SiC複合物、或銀液體電極;以及(xiv)MHD回流導管310、傳回EM泵312、傳回EM泵套管313可包含不鏽鋼,其中諸如套管及管道之內部的曝露於氧化之表面可用諸如鎳塗層之抗氧化劑塗層塗佈。MHD磁體306可包含諸如具有1 T磁通量密度之鈷釤磁體之永久磁體。 在包含磁流體動力(MHD)轉換器之本發明之SunCell®發電機的例示性實施例中:(i)EM泵可包含二級感應型,其中第1級充當MHD傳回泵切第2級充當噴射泵;(ii)電流迴路之EM泵套管區段405、EM泵電流迴路406、接合部凸緣407、儲集器底板組合件409及MHD回流導管310可包含諸如熔融石英之石英、氮化矽、氧化鋁、氧化鋯、氧化鎂或氧化鉿;(iii)變壓器繞組401、變壓器磁軛404a及404b以及電磁體403a及403b可為水冷式;(iv)儲集器5c、反應電解槽腔室5b31、MHD噴嘴307、MHD通道308、MHD冷凝區段309及氣體殼體309b可包含諸如熔融石英之石英、氮化矽、氧化鋁、氧化鋯、氧化鎂或氧化鉿,其中ZrO2 呈立方型藉由MgO或Y2 O3 穩定化;(v)氣體殼體309b及MHD冷凝區段309中之至少一者可包含諸如625 SS或經銥塗佈Mo之不鏽鋼;(vi) (a)組件之間的活接可包含具有諸如碳墊片之墊片之凸緣密封、膠合密封或濕封,其中濕封可接合相異陶瓷或諸如不鏽鋼部件的陶瓷及金屬部件,(b)具有石墨墊片之凸緣密封可接合金屬部件或在低於金屬之碳化溫度下操作之陶瓷至金屬部件,以及(c)具有墊片的凸緣密封可接合金屬部件或陶瓷至金屬部件,其中石墨墊片接觸包含不具碳化傾向之諸如鎳之金屬或塗層的密封之金屬部分,或另一高溫墊片在適合操作溫度下使用;(vii)熔融金屬可包含銀;(viii)進水升管5qa及噴射套管5k61可包含擰至儲集器底板組合件409中之軸環中的ZrO2 ;(ix)氧來源及氫來源可分別包含可通過MHD冷凝區段309壁中之透氣膜309d使用質量流量控制器供應以控制來自高壓水電解劑之每一氣流的O2 氣體及H2 氣體;(x)MHD電極304可包含諸如經Pt塗佈Mo或W的經Pt塗佈之耐火金屬、在700℃對水反應穩定的碳、在1800℃對氧化穩定之ZrC-ZrB2 及ZrC-ZrB2 -SiC複合物、或銀液體電極;以及(xi)MHD磁體306可包含諸如具有在約0.1至1 T的範圍內之磁通量密度之鈷釤磁體的永久磁體。 在實施例中,SunCell®電源可包含諸如可穿透黑體輻射器5b4之壁之包含諸如鎢的耐火金屬之陰極之電極及熔融金屬噴射器對立電極。可浸沒諸如EM泵套管噴射器5k61及噴嘴5q之對立電極。可替代地,對立電極可包括諸如立方ZrO2 或氧化鉿之電絕緣耐火材料。鎢電極可在黑體輻射器5b4之穿透處密封。電極可藉由儲集器5c與黑體輻射器5b4之間的電絕緣體襯套或間隔物電絕緣。電絕緣體襯套或間隔物可包含BN或諸如ZrO2 、HfO2 、MgO或Al2 O3 之金屬氧化物。在另一實施例中,黑體輻射器5b4可包含諸如耐火陶瓷之電絕緣體,該耐火陶瓷諸如BN或諸如ZrO2 、HfO2 、MgO或Al2 O3 之金屬氧化物。其他實施例 在實施例中,SunCell®可包含可逆地鍵合來自大氣之水的水吸收器、將熱自諸如熱交換器26a的SunCell®之熱組件轉移至水負載吸收器之構件、冷凝所釋放的水之冷凝器及接收待用於SunCell®之冷凝水的收集容器。在實施例中,提供HOH催化劑及H反應物以形成低能量氫之HOH催化劑來源及H來源中之至少一者可位大氣水。 水可使用水吸收材料收集且隨後脫水以釋放經吸收水。水可藉由使用由SunCell®提供之熱來脫水或解吸附。水吸收材料可包含結合水蒸氣且在加熱時將其釋放至冷凝器之諸如鋯金屬及己二酸或M2 Cl2 (BTDD) (M = Mn (1)、CO (2)、Ni (3);BTDD =雙(1H-1,2,3-三唑并[4,5-b],[4',5'-l]二苯并[1,4]二氧雜環己烯)之組合的金屬有機框架。 在實施例中,SunCell®包含將低能量氫形成為反應產物之反應混合物。反應可形成能量電漿。反應混合物可進一步包含諸如石墨及烴中之至少一者的碳來源。能量電漿可轟擊固體碳或來自碳來源的沈積於基板上之碳。在實施例中,轟擊將石墨碳轉換成鑽石形式碳。在以引用之方式併入的Mills公開案R. L. Mills, J. Sankar, A. Voigt, J. He, B. Dhandapani, 「Synthesis of HDLC Films from Solid Carbon」, J. Materials Science, J. Mater. Sci. 39 (2004) 3309-3318及R. L. Mills, J. Sankar, A. Voigt, J. He, B. Dhandapani,「Spectroscopic Characterization of the Atomic Hydrogen Energies and Densities and Carbon Species During Helium-Hydrogen-Methane Plasma CVD Synthesis of Diamond Films」, Chemistry of Materials, 第15卷, (2003),第1313-1321頁中所描述之例示性實施例中,SunCell®包含能量電漿源以使得自非鑽石形式碳形成鑽石。鑽石之產生可藉由1333 cm- 1 拉曼峰值之存在來量測。 分子低能量氫氣體可藉由電離普通氫來純化及分離。電離氫可藉由電及磁場中之至少一者單獨移除。可替代地,普通氫可藉由與形成可冷凝反應產物之反應物反應來移除,其中反應藉由電漿條件而有利進行。例示性反應物為形成在低溫冷阱中移除以產生純化分子低能量氫氣體之可冷凝氨之氮。可替代地,分子低能量氫氣體可使用基於分子低能量氫氣體之較高擴散而將普通氫與分子低能量氫氣體分離之分子篩來純化及分離。例示性分離分子篩為Na8 (Al6 Si6 O24 )Cl2 。 在實施例中,來自黑體輻射器之熱能可用於加熱與CO2 及H2 O之混合物反應的諸如CeO2 之催化劑以形成合成氣(CO + H2 )。合成氣可用於形成烴燃料。燃料反應器可包含費歇爾托普希反應器。 在實施例中,包含水蒸氣之低能量氫反應電漿可進一步包含氬。氬可至少起一下中之一種作用:藉由增大H2 分子再結合時間而增大H原子濃度,藉由干擾水氫鍵而增大新生HOH濃度,以及提供諸如Ar+ 催化劑之額外催化劑來源。 低能量氫反應可在包含呈諸如晶格之經組織或重複結構之水的固體燃料中傳播。固體燃料可包含可為結晶之水合物。固體燃料可包含諸如冰之結晶形式水,諸如I型冰。冰固體燃料可具有能量,其中能量釋放可包含脈衝。脈衝可以依序方式實施以諸如就內燃發動機中之空氣燃料之點火而言在延伸至無限之持續時間中提供功率。冰燃料系統包含在在冰水中產生衝擊波之構件。冰燃料系統可包含衝擊波限制構件。限制構件可包含冰套子。套子可包含諸如金屬外殼之外殼。衝擊波及限制中之至少一者可產生衝擊波以破壞冰水分子之間的氫鍵中的一些中之至少一者及水分子中的一些之至少一個氧氫鍵。冰燃料系統可包含爆炸物以在諸如冰之包含H2 O的結晶結構中產生衝擊波。爆炸物可包含C-N-O-H型之爆炸物、諸如氫氧爆炸物之另一爆炸物或熟習此項技術者已知之另一爆炸物。爆炸物可非常接近於諸如冰之結晶結構以將衝擊波有效耦合至結晶結構中。爆炸物可嵌入於諸如冰之結晶結構中之至少一個通道中。 可替代地,冰燃料系統可包含在冰水中產生衝擊波之電構件,諸如至少一個爆炸線。爆炸線可包含諸如高電壓及電流中之至少一者之電源的大功率電源。較高電功率電源可包含至少一個電容器。電容器可具有高電壓及電流。至少一個電容器通過至少一個電線放電可使其爆炸。電線爆炸物系統可包含薄導電電線及電容器。例示性電線為包含金、鋁、鐵或白金之電線。在例示性實施例中,電線可具有小於0.5 mm之直徑,且電容器可具有約25 kWh/kg之能量消耗且放出104 - 106 A/mm2 之電荷密度的脈衝,導致溫度至多為100,000 K,其中標誌可在約10- 5 - 10- 8 秒之時段中出現。具體而言,100μ F油填充之電容器可使用DC電源充電至3 kV,且電容器可通過12英吋長之30標準尺寸(gauge)裸鐵電線使用刀口開關或氣體電弧開關,其中電線嵌入於限制在鋼殼體中之冰中。冰燃料系統可進一步包含諸如電池、燃料電池中之至少一者處的電源及諸如SunCell®之產生器以對電容器充電。例示性能量材料包含藉由可包含Ti、Al及另一金屬中之至少一者的爆炸電線點火之Ti + Al + H2 O (冰)。 在實施例中,能量反應混合物及系統可包含諸如本發明及先前申請案中之低能量氫燃料混合物中之一者的低能量氫燃料混合物,該等申請案以引用之方式併入。反應混合物可包含呈諸如冷凍固態、液體、及氣態之至少一種物理狀態的水。能量反應可藉由應用諸如在約20 A至50,000 A的範圍內之電流的高電流來引發。電壓可較低,諸如在約1 V至100 V之範圍內。電流可通過諸如金屬基質之導電基質運載,該金屬基質諸如Al、Cu或Ag金屬粉末。可替代地,導電基質可包含諸如金屬容器之容器,其中容器可圍封或包覆反應混合物。例示性金屬容器包含Al、Cu或Ag DSC盤。例示性能量反應混合物包含冷凍水(冰)或液體水包含以下中之至少一者:Al坩堝Ti + H2 O;Al坩堝Al + H2 O;Cu坩堝Ti + H2 O;Cu坩堝Cu + H2 O;Ag坩堝Ti + H2 O;Ag坩堝Al + H2 O;Ag坩堝Ag + H2 O;Ag坩堝Cu + H2 O;Ag坩堝Ag + H2 O O + NH4 NO3 (莫耳50:25:25);Al坩堝Al + H2 O + NH4 NO3 (莫耳50:25:25)。 除呈如冰之冷凍狀態之外,水亦可包含諸如呈水合物形式之呈鍵結形式之固態。反應混合物可包含:(i)諸如過氧化物之氧來源,(ii)諸如金屬氫化物、水及諸如還原劑之水反應物以及諸如燃油的烴中之至少一者的氫來源,該還原劑諸如金屬,該金屬諸如金屬粉末,以及(iii)諸如金屬粉末之導電基質。例示性反應混合物包含Al坩堝Ti或TiH + Na2 O2 或諸如Na2 O2 ·2H2 O2 ·4H2 O、Na2 O2 ·2H2 O、Na2 O2 ·2H2 O2 及Na2 O2 ·8H2 O中之至少一者之水合Na2 O2 。反應混合物可分別使用諸如約15 V及27,000 A之低電壓高電流點火。 在實施例中,低能量氫反應混合物可包含諸如可具有較高表面積之鹼或鹼土金屬之水反應性金屬,諸如粒子金屬。金屬粒子可包含諸如氧化物塗層之保護性塗層。例示性低能量氫反應物包含具有氧化物塗層之粒子Li金屬。反應混合物可進一步包含水或冰。在實施例中,粒子金屬添加至諸如1℃水之冷水且快速冷凍。快速凍結可使用液氮達成以避免金屬反應。反應混合物可包含諸如本發明中之導電基質的導電基質。 爆炸電線可接近諸如冰之結晶結構以使得衝擊波在冰中傳播。電線可嵌入於冰中以使得衝擊波有效耦合至冰。在實施例中,嵌入於冰中之複數個電線爆震以使得衝擊波及壓縮通過冰傳播,使結晶冰結構碎裂以形成H及HOH催化劑來形成低能量氫。爆炸電線可產生歸因於導電電弧電流而支撐較高動力學之導電電漿路徑,該等導電電弧電流歸因於在催化期間催化劑之電離而重組離子且減小空間變化中之至少一者以增加反應速率。諸如冰之結晶結構可進一步包含諸如嵌入金屬之導體以歸因於其導電性而增加動力學,該嵌入金屬諸如金屬線、金屬功率或金屬柵格。金屬可為對水高度導電及化學穩定的,諸如銀或銅。在實施例中,冰嵌入於諸如金屬網狀物之導電基質中,該金屬網狀物諸如銅、鎳、銀或鋁網狀物,諸如Celmet(Sumitomo Electric Industries,Ltd.)型網狀物。 在實施例中,冰燃料系統可包含釋放熱且產生與氧爆震以在冰水中產生衝擊波之氫的反應物,其中反應物可嵌入且限制於冰中。反應物可包含諸如至少部分嵌入及包覆在冰水中之Fe2 O3 /Al金屬粉末混合物之鋁熱劑。套子可包含金屬貯藏器。鋁熱劑可包含莫耳過量之鋁以與水反應以形成H2 氣體來使用大氣氧充當爆炸物。過量金屬亦可充當導體以增加反應速率。 在實施例中,補充諸如包含諸如冰之呈適合形式之水的能量材料之能量材料及視情況諸如包含氫來源及諸如金屬之導電性中之至少一者的此類添加劑的添加劑,該金屬諸如較高表面積金屬,諸如Al粉末或鹼金屬粉末,諸如鋰粉末。可限制能量材料以使得限制由能量材料之點火產生之衝擊波。衝擊波之限制可有助於破壞H2 O之鍵合以供應H及HOH。能量材料可包覆於諸如金屬容器之密封容器中以提供限制。在實施例中,點火可藉由使高電流穿過至少一個電線來執行,電線穿過能量材料或非常接近於能量材料,其中高電流可致使一或多個電線爆炸。電線爆炸可在能量材料中產生衝擊波。電線可經佈置以增強能量材料中之衝擊波。在例示性實施例中,電線可彼此平行延伸以自複數個方向壓縮能量材料。在另一實施例中,內爆可產生於能量材料中,其中能量材料中之衝擊波朝內導向。朝內衝擊波可為球形地朝內。內爆可藉由一或多個電線爆震及諸如TNT之習知爆炸物之爆震中之至少一者來產生。爆炸物可經成形以產生內爆。爆炸物可包含球形地成形之電荷。冰水中之內爆及衝擊波可致使冰爆震。例示性能量材料裝置可包含諸如用爆炸電線點火之習知爆炸物的具有包圍球狀衝擊波源之冰。涉及能量材料之限制及內爆中之至少一者可產生額外能量材料的爆震補充。在實施例中,爆震電線可包含包圍諸如水之HOH及H來源之諸如螺線管或環面的圍封結構以使得其內爆來更有效地形成HOH及H以反應以形成低能量氫,該水諸如冰。 在另一實施例中,結晶固體燃料使用諸如液體水之對應液體置換。 在實施例中,能量反應系統包含HOH催化劑及諸如呈諸如氣體、液體或諸如I型冰之固體之任何物理狀態的水之H中之至少一者的來源及爆炸來源,以產生衝擊波。在實施例中,能量反應系統包含複數個衝擊波來源。衝擊波之來源可包含諸如本發明之爆炸電線之一或多個爆炸電線及諸如TNT或本發明的另一習知能量材料之一或多個電荷中之至少一者。能量反應系統可包含習知能量材料之至少一個雷管。能量反應系統可進一步包含諸如延遲線之依序觸發器構件或至少一種定時開關以使得形成在至少第一及另一衝擊波之間具有時間延遲的複數個衝擊波。依序觸發器可在爆炸中產生延遲以在第一及至少一個其他爆震之間產生延遲,其中每一爆震形成衝擊波。觸發器可延遲應用於爆炸電線及習知能量材料之雷管中之至少一者的功率。延遲時間可在約1飛秒至1秒、1奈秒至1秒、1微秒至1秒及10微秒至10毫秒之至少一個範圍內。 在實施例中,SunCell®可包含化學反應器,其中除低能量氫反應物外,反應可供應至反應器以形成所需化學產物,或除低能量氫反應物之外,反應亦可供應至反應器以形成所需化學產物。反應物可通過EM泵套管供應。產物可通過EM泵套管提取。反應物可在反應器閉合且反應引發之前添加於物料中。可藉由在反應器操作之後打開反應器來移除物料中之產物。反應產物可藉由通過諸如反應電解槽腔室壁之反應器壁之滲透來提取。反應器可在1250 K至10,000 K之範圍內的黑體溫度下提供持續電漿。反應器壓力可在1大氣壓至25大氣壓的範圍內。壁溫度可在1250 K至4000 K的範圍內。熔融金屬可包含支撐所需化學反應之熔融金屬,諸如銀、銅及銀銅合金中之至少一者。 在實施例中,封裝在冰水中之爆炸電線可包含過渡金屬,諸如Sc、Ti、V、Cr、Mn、Fe、Co、Ni、Cu及Zn中之至少一者。電線可進一步包含鋁。爆震電壓可為諸如在1000 V至100,000 V及3000 V至10,000 V之至少一個範圍內的電壓之高電壓。包含過渡金屬及低能量氫氫之薄膜可形成諸如低能量氫氫化鐵、鉻或錳、分子低能量氫錯合物或原子低能量氫錯合物。H包含低能量氫之FeH由使用4000 V及千安培來爆震包含Fe、Cr及Al合金之電線形成。FeH藉由ToF-SIM來識別。包含低能量氫及諸如另一金屬之另一元素之其他化合物可藉由使用包含諸如另一金屬的對應元素之爆炸電線來形成。 在實施例中,形成包含諸如分子低能量氫之較低能量氫物種之大型聚集體或聚合物的構件包含HOH來源及諸如呈諸如氣體、液體及冰中之至少一者的任何物理狀態之水之H來源,且可進一步包含諸如爆震電線之高電流來源。形成包含諸如分子低能量氫之較低能量氫物種之大型聚集體或聚合物的構件進一步包含反應腔室以限制低能量氫反應產物。例示性低能量氫反應物為空氣或諸如惰性氣體之另一氣體中之水蒸氣。水蒸氣壓可在1毫托至1000托的範圍內。低能量氫反應可藉由電線利用電功率之爆震來引發。在例示性實施例中,本發明之電線藉由使用本發明之爆震構件在包含空氣中之環境水蒸氣之空腔中爆震。環境水蒸氣壓可在約1至50托的範圍內。例示性產物為諸如FeH2 (1/4)之鐵低能量氫聚合物及諸如MoH(1/4)16 之鉬低能量氫聚合物。產物可藉由諸如新穎組合物之獨特物理特性來識別,諸如包含諸如鐵氫、鋅氫、鉻氫或鉬氫之金屬及氫的新穎組合物。若獨特組合物存在,則獨特組合物在不存在已知之包含普通氫的對應組合物磁性之情況下可為磁性的。在例示性實施例中,獨特組合物聚合鐵氫、鉻氫、鈦氫、鋅氫、鉬氫及鎢氫為磁性的。包含諸如分子低能量氫之較低能量氫物種之大型聚集體或聚合物可藉由以下識別:(i)可基於金屬及氫化物離子及諸如H16 及H24 的較高質量片段之較高質量片段之較高質量消解而明確地記錄諸如FeH及MoH16 的獨特金屬及氫組合物之飛行時間次級離子質譜分析(ToF-SIMS);(ii)可記錄約1940 cm- 1 處之H2 (1/4)旋轉能量及指紋區域中的吸收帶中之至少一者的傅里葉變換紅外光譜分析(FTIR),其中可不存在已知官能團之其他較高能量特徵;(iii)可記錄諸如-4 ppm至-6 ppm區域中之高場矩陣峰值的高場矩陣峰值之質子魔角旋轉核磁諧振光譜(1 H MAS NMR);(iv)可記錄歸因於可包含聚合結構之獨特組合物的新穎峰值之X射線繞射(XRD);(v)可記錄氫聚合物在諸如200℃至900℃之區域中的極低溫度下分解且提供獨特氫化學計量或諸如FeH或MoH16 之組合物之熱解重量分析(TGA);(vi)可記錄包含以0.25 eV間隔開的峰值之260 nm區域中之H2 (1/4)振轉帶的電子束激發發射光譜分析;(vii)可記錄包含以0.25 eV間隔開之峰值之260 nm區域中的H2 (1/4)振轉帶之第二級之光致發光拉曼光譜分析;(viii)可記錄約1940 cm- 1 處的H2 (1/4)旋轉峰值之拉曼光譜法;以及(ix)可記錄約500 eV處之H2 (1/4)的總能量之X射線光電子光譜分析(XPS)。 在實施例中,收集呈氣態、物理吸收、液化或呈其他狀態之分子低能量氫的設備包含:包含較低能量氫物種之大型聚集體或聚合物之來源,含有包含較低能量氫物種的大型聚集體或聚合物之腔室,熱分解腔室中之包含較低能量氫物種的大型聚集體或聚合物之構件,及收集自包含較低能量氫物種之大型聚集體或聚合物所釋放的氣體之構件。分解構件可包含加熱器。加熱器可將第一腔室加熱至比包含較低能量氫物種之大型聚集體或聚合物之分解溫度更大的溫度,諸如在約10℃至3000℃、100℃至2000℃及100℃至1000℃之至少一個範圍內之溫度。收集來自包含較低能量氫物種之大型聚集體或聚合物之分解的氣體之構件可包含第二腔室。第二腔室可包含氣泵、氣體閥門、壓力計及質量流量控制器中之至少一者以進行以下中之至少一者:儲存及轉移經收集分子低能量氫氣體。第二腔室可進一步包含吸氣劑以吸收分子低能量氫氣體或諸如低溫系統之冷卻器以液化分子低能量氫。冷卻器可包含低溫泵或杜瓦瓶,該低溫泵或杜瓦瓶含有諸如液氦或液氮之低溫液體。 形成包含較低能量氫物種之大型聚集體或聚合物之構件可進一步包含場源,諸如電場或磁場中之至少一者之來源。電場之來源可包含至少兩個電極及電壓源以將電場應用至反應腔室,其中形成聚集體或聚合物。可替代地,電場之來源可包含靜電充電材料。靜電充電材料可包含諸如包含碳之腔室之反應電解槽腔室,諸如塑膠玻璃腔室。本發明之爆震可對反應電解槽腔室靜電充電。磁場之來源可包含諸如永久性電磁體或超導磁體之至少一個磁體以將磁場應用至反應腔室,其中形成聚集或聚合物。 諸如H2 (1/4)之分子低能量氫可具有非零及對應於具有對應磁矩之軌道角動量的量子數。分子低能量氫之磁性特徵藉由質子魔角旋轉核磁諧振光譜(1 H MAS NMR)證明。可進一步包含一些水合水之諸如鹼金屬氫氧化物-鹼金屬鹵化物矩陣之固體矩陣中的分子低能量氫之存在歸因於分子低能量氫之順磁矩陣效果而產生高場1 H MAS NMR峰值,通常在-4至-5 ppm。產生呈非零角動量狀態之分子低能量氫之便利方法為在H2 O存在的情況下藉由電線爆震以充當低能量氫催化劑及H來源。包含水蒸氣之大氣中之電線爆震產生包含諸如具有非零及具有可聚集以形成腹板的金屬原子或離子之量子狀態的分子低能量氫之低能量氫的磁性線性鏈。自裝配可包含磁性次序或自裝配機制。吾人熟知,外部磁場之應用產生懸置於諸如甲苯之溶劑中的諸如磁鐵(Fe2 O3 )之膠態磁性奈米顆粒以裝配至線性結構中。歸因於較小質量及較高磁矩,分子低能量氫甚至在不存在磁場之情況下磁性地自裝配。在增強自裝配且控制形成低能量氫產物之替代結構之實施例中,外部磁場應用於低能量氫反應,諸如電線爆震。磁場可藉由將至少一個永久磁體置放在反應腔室中來應用。可替代地,爆震電線可包含充當諸如磁鐵之磁性粒子來源以驅動分子低能量氫之磁性自裝配的金屬,其中來源可為水蒸氣中之電線爆震或另一來源。 在實施例中,分子低能量氫可包含非零角動量量子數。分子低能量氫可為磁性的,其中磁性可歸因於非零角動量量子數。歸因於分子低能量氫之固有磁矩,其可自裝配至大型聚集體中。在實施例中,諸如H2 (1/4)之分子低能量氫可裝配至受磁偶極子力束縛之線性鏈中。在另一實施例中,分子低能量氫可裝配至諸如在八個頂點中之各者處具有諸如H2 (1/4)之H2 (1/p)的立方體之三維結構中。在實施例中,八個諸如H2 (1/4)分子之H2 (1/p)分子磁性鍵結至立方體中,其中每一分子之中心在立方體的八個頂點中之一者處,且每一間核軸線平行於頂點上定中心之立方體的邊緣。磁性對準為以使得每一分子偶極之每一北及南極點與立方體之其三個最接近相鄰者中之各者相對地定向。H16 可充當由自裝配形成之更複雜宏觀結構的單元或部分。在另一實施例中,在方形之四頂點中之各者處包含諸如H2 (1/4)之H2 (1/p)的H8 單元可添加至長方體H16 以包含H 16 + 8n ,其中n為整數。例示性額外大型聚集體為H16 、H24 及H32 。氫大型聚集體中性物及離子可與諸如O、OH、C及N之其他物種組合為中性物或離子。在實施例中,所得結構產生飛行時間次級離子質譜(ToF-SIMS)中之H16 峰值,其中片段可為對應於自H16 之整數H損失的觀測到之質量,諸如H16 、H14 、H13 及H12 。歸因於1.00794 u之H之質量,對應+1或-1離子峰值具有以下質量:16.125、15.119、14.111、13.103、12.095……諸如H - 16或H + 16之氫大型聚集體離子可包含介穩態物。具有寬峰值之介穩定特徵之氫大型聚集體H - 16及H + 16藉由ToF-SIMS在正及負光譜中的16.125處觀測到。H - 15在15.119處之負ToF-SIMS頻譜中觀測到。H24 介穩定物種H+ 23H- 25 分別在正及負ToF-SIMS光譜中觀測到。 在實施例中,諸如H16 之分子低能量氫大型聚集體或諸如H2 (1/4)之諸如H2 (1/p)的分解產物可包含磁諧振成像(MRI)造影劑,諸如旋轉極化Xeon。分子低能量氫可歸因於成像之其NMR主動質子或其在普通質子上之效果中的至少一者而吸入及用於MRI成像,該等普通質子諸如經成像人、動物或物件之主體的水分子之質子,其中分子低能量氫之順磁性影響對應NMR位移或諸如T1T2 中之至少一者的弛緩時間中之至少一者。在實施例中,分子低能量氫之對形式可藉由旋轉交換轉換成NMR主動鄰形式。旋轉交換可使用諸如磁性物種之旋轉交換試劑達成,諸如磁鐵(Fe2 O3 )粒子。氣體可與旋轉交換試劑一起培育以達成H2 (1/p)之鄰形式之轉換。體內鄰形式之生存期可用作MRI造影劑之基礎。 在實施例中,諸如原子低能量氫、分子低能量氫或低能量氫氫化物離子之低能量氫物種藉由H與OH及H2 O催化劑中之至少一者反應來合成。在實施例中,諸如包含本發明之丸粒或電線點火以形成低能量氫的SunCell®反應及能量反應中之至少一者的產物為包含與以下中之至少一者錯合的諸如H2 (1/p)之低能量氫物種的低能量氫化合物或物種:(i)除氫外之元素;(ii)諸如H+ 、普通H2 、普通H- 及普通H+ 3 中之至少一者的普通氫物種,諸如有機離子或有機分子之有機分子物種;以及(iv)諸如無機離子或無機化合物之無機物種。低能量氫化合物可包含諸如鹼或鹼土碳酸酯或氫氧化物之氧陰離子化合物或本發明的其他此類化合物。在實施例中,產物包含M 2 CO 3H 2 (l / 4)及MOHH 2 (/ 4) (M =本發明之鹼或其他陽離子)錯合物中之至少一者。產物可藉由ToF-SIMS分別識別為包含M(M2 CO3 • H2 (l/ 4))+ n及M ( MOH H2 (l/ 4))+ n之正波譜中之一系列離子,其中n為整數,且整數P > 1可用4替代。在實施例中,包含諸如SiO2 或石英之矽及氧之化合物可充當H2 (1/4)的吸氣劑。H2 (1/4)之吸氣劑可包含過渡金屬、鹼金屬、鹼土金屬、內過渡金屬、稀土金金屬組合、諸如MoCu的諸如Mo合金之合金、以及諸如本發明之材料的氫儲存材料。 包含藉由本發明之方法合成之低能量氫物種的化合物可具有式MH、MH2 或M2 H2 ,其中M為鹼陽離子,且H為低能量氫物種。化合物可具有式MHn ,其中n為1或2,M為鹼土陽離子,且H為低能量氫物種。化合物可具有式MHX,其中M為鹼陽離子,X為諸如鹵素原子之中性原子、分子或諸如鹵素陰離子的單帶負電陰離子中之一者,且H為低能量氫物種。化合物可具有式MHX,其中M為鹼土陽離子,X為單帶負電陰離子,且H為低能量氫物種。化合物可具有式MHX,其中M為鹼土陽離子,X為雙帶負電陰離子,且H為低能量氫物種。化合物可具有式M2 HX,其中M為鹼陽離子,X為單帶負電陰離子,且H為低能量氫物種。化合物可具有式MHn ,其中n為整數,M為鹼性陽離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式M2 Hn ,其中n為整數,M為鹼土陽離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式M2 XHn ,其中n為整數,M為鹼土陽離子,X為單帶負電陰離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式M2 X2 Hn ,其中n為1或2,M為鹼土陽離子,X為單帶負電陰離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式M2 X3 H,其中M為鹼土陽離子,X為單帶負電陰離子,且H為低能量氫物種。化合物可具有式M2 XHn ,其中n為1或2,M為鹼土陽離子,X為雙帶負電陰離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式M2 XX'H,其中M為鹼土陽離子,X為單帶負電陰離子,X'為雙帶負電陰離子,且H為低能量氫物種。化合物可具有式MM'Hn ,其中n為1至3之整數,M為鹼土陽離子,M'為鹼金屬陽離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式MM'XHn ,其中n為1或2,M為鹼土陽離子,M'為鹼金屬陽離子,X為單帶負電陰離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式MM'XH,其中M為鹼土陽離子,M'為鹼金屬陽離子,X為雙帶負電陰離子,且H為低能量氫物種。化合物可具有式MM'XX'H,其中M為鹼土陽離子,M'為鹼金屬陽離子,X及X'為單帶負電陰離子,且H為低能量氫物種。化合物可具有式MXX'Hn ,其中n為1至5之整數,M為鹼或鹼土陽離子,X為單或雙帶負電陰離子,X'為金屬或類金屬、過渡元素、內過渡元素或稀土元素,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式MHn ,其中n為整數,M為諸如過渡元素、內過渡元素或稀土元素之陽離子,且化合物之氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式MXHn ,其中n為整數,M為諸如鹼陽離子、鹼土陽離子之陽離子,X為諸如過渡元素、內過渡元素或稀土元素陽離子之另一陽離子,且化合物的氫內容物Hn 包含至少一種低能量氫物種。化合物可具有式(MHm MCO3 )n ,其中M為鹼陽離子或其他+1陽離子,m及n皆為整數,且化合物之氫內容物Hm 包含至少一種低能量氫物種。化合物可具有式(MHm MNO 3 )+ nnX - ,其中M為鹼陽離子或其他+1陽離子,m及n皆為整數,X為單帶負電陰離子,且化合物之氫內容物Hm 包含至少一種低能量氫物種。化合物可具有式(MHMNO 3 )n ,其中M為鹼陽離子或其他+1陽離子,n為整數,且化合物之氫內容物H包含至少一種低能量氫物種。化合物可具有式(MHMOH )n ,其中M為鹼陽離子或其他+1陽離子,n為整數,且化合物之氫內容物H包含至少一種低能量氫物種。包括陰離子或陽離子之化合物可具有式( MH m M 'X )n ,其中m及n皆為整數,M及M'皆為鹼或鹼土陽離子,X為單或雙帶負電陰離子,且化合物之氫內容物Hm 包含至少一種低能量氫物種。包括陰離子或陽離子之化合物可具有式(MHm M ' X')+ nnX- ,其中m及n皆為整數,M及M'皆為鹼或鹼土陽離子,X及X'為單或雙帶負電陰離子,且化合物之氫內容物Hm 包含至少一種低能量氫物種。陰離子可包含本發明之陰離子中之一者。適合例示性單帶負電陰離子為鹵離子、氫氧根離子、碳酸氫根離子或硝酸根離子。適合例示性雙帶負電陰離子為碳酸根離子、氧化物或硫酸根離子。 在實施例中,低能量氫化合物或混合物包含諸如低能量氫原子、低能量氫氫化物離子之至少一種低能量氫物種及嵌入於諸如金屬或離子晶格中的諸如晶格之晶格中之二低能量氫分子。在實施例中,晶格不與低能量氫物種反應。矩陣諸如就經嵌入低能量氫氫化物離子而言可為非質子。化合物或混合物可包含嵌入於鹽晶格中之H(1/p)、H2 (1/p)及H- (1/p)中之至少一者,鹽晶格諸如鹼或鹼土鹽,諸如鹵化物。例示性鹼鹵化物為KCl及KI。鹽就經嵌入H- (1/p)而言可不存在任何H2 O。其他適合之鹽晶格包含本發明之鹽晶格。 本發明之低能量氫化合物較佳地超過0.1原子%純。更佳地,化合物超過1原子%純。甚至更佳地,化合物超過10原子%純。最佳地,化合物超過50原子%純。在另一實施例中,化合物超過90原子%純。在另一實施例中,化合物超過95原子%純。實驗 SF-CIHT電池電力產生系統包括經組態以採集由燃料點火反應產生之電漿光子且將其轉換成可使用的能量之光伏打電力轉換器。在一些實施例中,高轉換效率可為所要。反應器可沿多個方向排出電漿,例如,至少兩個方向,且反應之半徑可在約若干毫米至若干米之規模,例如,半徑為約1 mm至約25 cm。此外,藉由燃料點火產生之電漿光譜可類似於藉由太陽產生之電漿光譜及/或可包括附加短波長輻射。圖4展示對包含經吸收之H2 及H2 O之80 mg丸粒點火的處於5 nm至450 nm區域之絕對光譜之例示性實施例,該經吸收H2 O來自隨著銀冷卻成丸粒添加至熔融銀之水,其展示基本上全部處於紫外及遠紫外光譜區中的1.3 MW之平均光功率。該點火使用Taylor-Winfield型號ND-24-75點焊機以低電壓高電流達成。丸粒內之電壓降小於1 V且電流為約25 kA。較高強度UV發射之持續時間約為1 ms。控制光譜在UV區域中為扁平的。固體燃料之輻射諸如譜線及黑體發射中之至少一者,可具有在約2至200,000 suns、10至100,000 suns、100至75,000 suns之至少一個範圍內之強度。在實施例中,可增加焊機點火電路之電感以增加點火之後的電流衰減時間。更長衰減時間可保持低能量氫電漿反應以增加能量產生。 UV及EUV光譜可轉換成黑體輻射。轉換可藉由使電池大氣對於UV及EUV光子中之至少一者的傳播而言為光學不透明來達成。光學厚度可藉由使諸如燃料金屬之金屬在電池中汽化來增加。光學厚電漿可包含黑體。黑體溫度歸因於低能量氫反應之極大功率密度容量及藉由低能量氫反應發射的光子之高能量可為較高的。在具有約1 Torr之環境H2 O蒸氣壓的大氣氬中對泵送至W個電極中之熔融銀點火的光譜(歸因於藍寶石光譜儀窗口,在180 nm處具有截止之100 nm至500 nm區域)展示於圖5中。電源2包含兩組串聯之兩個電容器(馬克士威技術K2超電容器(Maxwell Technologies K2 Ultracapacitor) 2.85V/3400F),該等電容器並聯連接以提供約5至6 V及300 A之恆定電流,其中在約1 kHz至2 kHz之頻率下,疊加電流脈衝為5kA。W個電極(1 cm × 4 cm)之平均輸入功率為約75 W。當大氣隨著銀之汽化而變得對於UV輻射光學不透明時,初始UV管線發射藉由低能量氫反應功率轉變為5000K黑體輻射。具有0.15之氣化銀輻射率的5000K黑體輻射器之功率密度為5.3 MW/m2 。觀測到之電漿之區域為約1 m2 。黑體輻射可加熱可充當本發明之熱光伏實施例中之PV轉換器26a的黑體輻射器之諸如頂蓋5b4之電池26的組件。 包含氧來源之熔融物的例示性測試包含在具有藉由絕對光譜分析確定之光功率之氬/5莫耳% H2 大氣中點火80 mg銀/1 wt%硼砂脫水丸粒。觀測使用焊機(Acme 75 KVA點焊機)以在約1 V之電壓降250 kW功率時應用約12 kA之高電流持續約1 ms。在包含氧來源之熔融物的另一例示性測試中,包含在具有藉由絕對光譜分析確定之光功率之氬/5莫耳% H2 大氣中點火80 mg銀/2 mol%Na2 O脫水丸粒。觀測使用焊機(Acme 75 KVA點焊機)以在約1 V之電壓降370 kW功率時應用約12 kA之高電流持續約1 ms。在包含氧來源之熔融物的另一例示性測試中,包含在具有藉由絕對光譜分析確定之光功率之氬/5莫耳% H2 大氣中點火80 mg銀/2 mol%Li2 O脫水丸粒。觀測使用焊機(Acme 75 KVA點焊機)以在約1 V之電壓降500 kW功率時應用約12 kA之高電流持續約1 ms。 基於使用Edgertronics高速視訊攝影機記錄之電漿之大小,低能量氫反應及功率視反應體積而定。體積可能需要為最小值供用於最佳化反應功率及能量,諸如約0.5至10公升,用於點火諸如銀丸粒及諸如水合之H及HOH催化劑來源之約30至100 mg的丸粒。自丸粒點火,低能量氫反應速率在極高銀壓力下較高。在實施例中,低能量氫反應在較高電漿壓力之情況下可具有較高動力學。基於高速光譜及Edgertronics數據,低能量氫反應速率在電漿體積最低且Ag蒸氣壓最高之初始時最高。1 mm直徑Ag丸粒當熔融時(T = 1235 K)點火。80 mg (7.4 × 10- 4 莫耳)丸粒之初始體積為5.2 × 10- 7 公升。對應最大壓力為約1.4 × 105 個大氣壓。在例示性實施例中,觀測到反應以約聲音速度(343 m/s)擴展持續反應約0.5 ms。最終半徑為約17 cm。在無任何背壓之情況下之最終體積為約20公升。最終Ag分壓為約3.7E-3個大氣壓。因為反應在更高壓力下可具有較高動力學,所以反應速率可藉由通過應用電極壓力及允許電漿垂直於間電極軸線擴展之電極限制來增加。 量測在存在97%氬/3%氫氣氛圍之情況下由低能量氫反應所釋放的功率,該低能量氫反應由將一mol%或0.5 mol%氧化鉍以2.5 ml/s添加至噴射至SunCell®之點火電極中的熔融銀造成。在添加對應於氧化物添加的低能量氫反應功率比重之前及之後的暫態反應電解槽水冷卻劑溫度之斜率中之相對變化乘以充當內標的恆定初始輸入功率。針對重複延伸,具有在氧來源添加之後的低能量氫功率比重之總電池輸出功率藉由對應於7540 W、8300 W、8400 W、9700 W、8660 W、8020 W及10,450 W之總輸入功率的97、119、15、538、181、54及27之暫態冷卻劑溫度回應的斜率之比率的產物確定。熱峰值功率分別為731,000 W、987,700 W、126,000 W、5,220,000 W、1,567,000 W、433,100 W及282,150 W。 量測在存在97%氬/3%氫氣氛圍之情況下由低能量氫反應所釋放的功率,該低能量氫反應由將一mol%氧化鉍(Bi2 O3 )、一mol%釩酸鋰(LiVO3 )或0.5 mol%釩酸鋰以2.5 ml/s添加至噴射至SunCell®之點火電極中的熔融銀造成。在添加對應於氧化物添加的低能量氫反應功率比重之前及之後的暫態反應電解槽水冷卻劑溫度之斜率中之相對變化乘以充當內標的恆定初始輸入功率。針對重複延伸,具有在氧來源添加之後的低能量氫功率比重之總電池輸出功率藉由對應於6420 W、9000 W及8790 W之總輸入功率的497、200及26之暫態冷卻劑溫度回應的斜率之比率的產物確定。熱峰值功率分別為3.2 MW、1.8 MW及230,000 W。 在例示性實施例中,點火電流對應於電壓在約0.5中自約0 V增加至1 V而自約0 A逐漸上升至2000 A,在該電壓處電漿點火。電壓隨後以一步增加至約16 V且保持約0.25 s,其中約1 kA流動通過熔融物且1.5 kA通過除電極8外之另一接地迴路串聯流動通過大多數電漿。在以9公升/s之流動速率約25 kW之輸入功率至包含Ag (0.5莫耳% LiVO3 )及氬-H2 (3%)的SunCell®之情況下,電力輸出高於1 MW。點火序列在約1.3 Hz重複。 在例示性實施例中,點火電流為約500 A恆定電流,且電壓為約20 V。在以9公升/s之流動速率約15 kW之輸入功率至包含Ag(0.5莫耳% LiVO3 )及氬-H2 (3%)的SunCell® 之情況下,電力輸出為高於1 MW。 在圖6中所展示之實施例中,形成包含較低能量氫物種之大型聚集體或聚合物的系統500包含諸如塑膠玻璃腔室之腔室507、金屬導線506、具有可藉由高電壓DC電源503充電的接地連接504之高電壓電容器505及諸如12 V電開關502及觸發電花隙開關501之開關,該開關將電路自電容器閉合至腔室507之內部的金屬導線506,以使得電線爆震。腔室可包含水蒸氣及諸如大氣空氣或惰性氣體之氣體。 形成包含較低能量氫物種之大型聚集體或聚合物的例示性系統包含:具有46 cm之長度及12.7 cm之寬度及高度的閉合矩形長方體塑膠玻璃腔室;10.2 cm長、0.22~0.5 mm直徑金屬導線,其使用不鏽鋼螺母以距腔室底層9 cm之距離安裝在兩個不鏽鋼極點之間;15 kV電容器(Westinghouse模型5PH349001AAA,55 uF),其對應於557 J充電至約4.5 kV;充電電容器的35 kV DC電源;以及12 V開關及觸發電花隙開關(Information Unlimited,模型Trigatron10,3 kJ),其將電路自電容器閉合至腔室之內部的金屬導線,以使得電線爆震。電線可包含Mo (鉬金屬網,來自0.305 mm直徑電線之20目,99.95%,Alpha Aesar)、Zn (0.25 mm直徑,99.993%,Alpha Aesar)、Fe-Cr-Al合金(73%-22%-4.8%,31標準尺寸,0.226 mm直徑,KD Cr-Al-Fe合金電線部件第#1231201848號,Hyndman Industrial Products Inc.)或Ti(0.25 mm直徑,99.99%,Alpha Aesar)電線。在例示性延伸中,腔室包含空氣,空氣包含約20托水蒸氣。高電壓DC電源在閉合觸發器開關之前關閉。約4.5 kV之峰值電壓在5 kA之峰值電流下以高於約300 us之阻尼諧波振盪器放電。包含較低能量氫物種之大型聚集體或聚合物在電線爆震之後約3-10分鐘內形成。自腔室底層及壁以及在置放在腔室中之Si晶圓上收集分析樣本。分析結果匹配本發明之低能量氫標記。 在實施例中,低能量氫振轉光譜藉由包含諸如氬氣之惰性氣體及充當HOH催化劑及原子氫之來源的水蒸氣之反應混合物氣體之電子束激發來觀測到。氬可在約100托至10個大氣壓之壓力範圍內。水蒸氣壓可在約1微托至10托的範圍內。電子束能量可在約1 keV至100 keV的範圍內。旋轉管線在來自包含藉由通過氮化矽窗口入射腔室中之氣體的12 keV至16 keV電子束激發之約100毫托水蒸氣之大氣壓氬電漿的145-300 nm區域中觀測到。觀測通過反應氣體腔室之MgF2 另一窗口的發射。氫之能量間距42 倍的能量間距將核間距離確定為H2 之核間距離之1/4且識別H2 (1/4) (方程式(29-31))。該系列匹配用於H2 (1/4)振動躍遷v = 1 → v = 0之H2 (1/4)之P分支,該分支分別包含在154.94、159.74、165.54、171.24、178.14及183.14 nm處觀測到的P(1)、P(2)、P(3)、P(4)、P(5)及P(6)。 在另一實施例中,包含諸如本發明中之低能量氫的低能量氫之物質組合物經熱分解,且包含諸如H2 (1/4)之低能量氫的分解氣體引入至反應氣體腔室中,其中低能量氫氣體使用電子束激發,且記錄振轉發射光譜。 在另一實施例中,諸如H2 (1/4)之低能量氫氣體吸收於諸如鹼鹵化物或鹼鹵化物鹼金屬氫氧化物矩陣之吸氣劑中。旋轉振動光譜可藉由在真空中電子束激發吸氣劑來觀測到。電子束能量可在約1 keV至100 keV的範圍內。峰值之間的旋轉能量間距可藉由方程式(30)給定。藉由方程式(29)給定之振動能量歸因於由結晶矩陣造成之較高有效質量而可位移至較低能量。在例示性實驗實例中,吸氣劑之晶格中捕獲之H 2 (1/ 4)之振轉發射藉由在5 × 10- 6 托的壓力範圍內具有10-20μA 之光束電流之入射6 KeV電子槍激發,且藉由無窗UV光譜分析記錄。充當Mills等人(R. Mills, X Yu, Y. Lu, G Chu, J. He, J. Lotoski, 「Catalyst induced hydrino transition (CIHT) electrochemical cell」, (2012), Int. J. Energy Res., (2013), DOI: 10.1002/er.3142,其以引用之方式併入)之5 W CIHT電池堆疊中之吸氣劑的UV透明矩陣KCl中之H2 (1/4)(所謂260 nm帶)之經解決振轉光譜包含258 nm處之峰值最大值,其中峰值之代表性位置在222.7、233.9、245.4、258.0、272.2及287.6 nm處,具有0.2491 eV的相等間距。大體而言,能量相對於峰值數目之曲線產生在與用於躍遷及Q(0)、R(0)、R(1)、R(2)、P(1)、P(2)、P(3)及P(4)之H2 (1/4)的經預測值極為一致之R2 = 0.999或更好處藉由y = -0.249 eV + 5.8 eV給定之管線,其中Q(0)可識別為該系列的最強峰值。 此外,具有經吸收低能量氫反應產物氣體之吸氣劑之正離子ToF-SIMS光譜展示矩陣化合物之多聚體群,其中二氫作為結構之部分,M:H2 (M = KOH或K2 CO3 )。具體而言,包含KOH及K2 CO3 [26-27]或具有此等化合物作為低能量氫反應產物氣體之吸氣劑的先前低能量氫反應產物之正離子光譜展示與作為結構中之錯合物的H2 (1/p)一致之。 在另一實施例中,低能量氫振轉光譜藉由電子束激發包含諸如諸如H16 之分子低能量氫化合物或大型聚集體或諸如H2 (1/p)之分解產物的低能量氫之組合物物質來觀測到。包含低能量氫之物質組合物可包含本發明之低能量氫化合物。電子束能量可在約1 keV至100 keV的範圍內。發射光譜可藉由EUV光譜分析在真空中記錄。最早例示性實驗實施例中,H2 (1/4)振轉管線藉由12 keV至16 keV電子束激發自低能量氫氫化鋅在145-300 nm區域中觀測到。光束在真空中入射化合物。低能量氫氫化鋅由在空氣中存在水蒸氣之情況下根據本發明之方法的鋅電線爆震形成。氫之能量間距42 倍的能量間距將核間距離確定為H2 之核間距離之1/4且識別H2 (1/4) (方程式(29-31))。該系列匹配用於H2 (1/4)振動躍遷v = 1 → v = 0之H2 (1/4)之P分支,該分支分別包含P(1)、P(2)、P(3)、P(4)、P(5)、P(6)及P(7)。 Cross-reference to related applications This application claims US Provisional Application No. 62/457,935 filed on February 12, 2017, No. 62/461,768 filed on February 21, 2017, and No. 62/463,684 filed on February 26, 2017, Submitted on April 4, 2017, No. 62/481,571, May 31, 2017, No. 62/513,284, May 31, 2017, No. 62/513,324, submitted on June 23, 2017 No. 62/524, 307, No. 62/532,986, submitted on July 14, 2017, No. 62/537,353, filed on July 26, 2017, No. 62/545,463, submitted on August 14, 2017, 2017 No. 62/556,941 filed on September 11th, No. 62/573,453 submitted on October 17, 2017, No. 62/584,632 submitted on November 10, 2017, and No. 62 submitted on November 4, 2017 / 594, 511, the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit of the benefit. Power generation can take many forms, utilizing power from the plasma. The successful commercialization of plasma can be determined by a power generation system that is capable of efficiently forming a plasma and then capturing the power of the generated plasma. The plasma can be formed during ignition of certain fuels. Such fuels may include water or a source of water based fuel. During ignition, a plasma cloud of electron-extracting atoms is formed and high optical power is released. The high optical power of the plasma can be utilized by the power converter of the present invention. The ions and excited state atoms can recombine and undergo electron relaxation, emitting optical power. The optical power can be converted to electricity by the photovoltaic device. Certain embodiments of the present invention are directed to a power generation system comprising: a plurality of electrodes configured to transfer power to a fuel to ignite fuel and produce plasma, such as a solid or molten metal electrode; configured to energize a power source transmitted to the plurality of electrodes; and at least one magneto-hydrodynamic power converter positioned to receive high temperature and high voltage plasma or at least one photovoltaic ("PV") positioned to receive at least a plurality of plasma photons Power converter. In an embodiment, a SunCell® power system that produces at least one of electrical energy and thermal energy includes: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; and a reactant comprising: (i) at least one inclusion Newborn H2 O catalyst source or catalyst, (ii) at least one H2 O source or H2 O, (iii) at least one atomic hydrogen source or atomic hydrogen and (iv) molten metal; a molten metal injection system comprising at least two molten metal reservoirs each comprising a pump and a spray tube; at least one reactant supply system, a reactant for consuming in a process in which the reactant reacts to generate at least one of electrical energy and thermal energy; at least one ignition system comprising a molten metal reservoir for containing at least two electromagnetic pumps each At least one power converter or output system that supplies at least one of light and heat output to electrical power and/or thermal power. In embodiments, the molten metal may comprise any electrically conductive metal or alloy known in the art. The molten metal or alloy may have a low melting point. Exemplary metals and alloys are gallium, indium, tin, zinc, and gallium indium tin alloys, of which examples of typical eutectic mixtures are 68% Ga, 22% In, and 10% Sn (by weight), but the ratio can range from 62 to 95% Ga, 5 to 22% In, 0 to 16% Sn (by weight) vary. In embodiments in which the metal can react with at least one of oxygen and water to form a corresponding metal oxide, the low energy hydrogen reaction mixture can comprise a molten metal, a metal oxide, and hydrogen. The metal oxide can act as a source of oxygen to form a HOH catalyst. Oxygen may be recovered between the metal oxide and the HOH catalyst, wherein hydrogen consumed to form low energy hydrogen may be replenished. The molten metal injection system can include at least two molten metal reservoirs each comprising an electromagnetic pump that injects a flow of molten metal intersecting within the interior of the vessel, wherein each reservoir can include a molten metal level controller that includes the influent water Lift pipe. The ignition system can include a power supply for supplying opposite voltages to at least two molten metal reservoirs each comprising an electromagnetic pump that supplies current and power flowing through the intersecting molten metal stream, causing reaction of the reactants (including ignition) To form a plasma inside the container. The ignition system can include: (i) a power supply for supplying opposite voltages to at least two molten metal reservoirs each containing an electromagnetic pump and (ii) a molten metal reservoir from the at least two respective electromagnetic pumps At least two intersecting streams of molten metal, wherein the power source is capable of delivering short pulsed high current electrical energy sufficient to cause the reactants to react to form a plasma. The power source that delivers short pulsed high current electrical energy sufficient to cause the reactants to react to form a plasma may comprise at least one supercapacitor. Each electromagnetic pump may comprise one of: (i) a DC or AC conductivity type comprising a DC or AC current source supplied to the molten metal via the electrode and a source of a constant or in-phase alternating vector cross magnetic field; or (ii) An inductive type comprising an alternating magnetic field source passing through a short circuit of molten metal, which induces alternating current in the metal; and an in-phase alternating vector cross-magnetic field source. The at least one union of the pump and the corresponding reservoir and another joint between the container, the injection system and the components of the converter may include a wet seal, a flange and gasket seal, an adhesive seal and a slip At least one of the nut seals, wherein the gasket can comprise carbon. The DC or AC current of the molten metal ignition system can range from 10 A to 50,000 A. The circuit of the molten metal ignition system can be closed by the intersection of the molten metal streams to cause ignition, further causing an ignition frequency in the range of 0 Hz to 10,000 Hz. The inductive electromagnetic pump may include a ceramic channel that forms a short circuit of molten metal. The power system can further include an inductively coupled heater for forming a molten metal from the corresponding solid metal, wherein the molten metal can comprise at least one of silver, silver copper alloy, and copper. The power system can further include a vacuum pump and at least one chiller. The power system can include at least one power converter or output system that reflects the power output, such as at least one of the group of: a thermal photovoltaic converter, a photovoltaic converter, a photoelectric converter, a magnetohydrodynamic converter , plasma power converter, thermoelectric converter, thermoelectric converter, Sterling engine, Brayton cycle engine, Rankine cycle engine and heat engine, heater And the boiler. The boiler can contain a radiant boiler. A portion of the reaction vessel may comprise a black body radiator that is maintained at a temperature in the range of 1000 K to 3700 K. The reservoir of the power system may comprise boron nitride, the portion of the container containing the black body radiator may comprise carbon, and the electromagnetic pump component in contact with the molten metal may comprise an oxidation resistant metal or ceramic. The reactant of the low energy hydrogen reaction may comprise at least one of methane, carbon monoxide, carbon dioxide, hydrogen, oxygen, and water. The reactant supply maintains each of methane, carbon monoxide, carbon dioxide, hydrogen, oxygen, and water at a pressure in the range of 0.01 Torr to 1 Torr. The light emitted by the black body radiator of the power system and directed to the thermal photovoltaic converter or the photovoltaic converter may be mainly black body radiation, including visible light and near infrared light, and the photovoltaic battery may be a concentrating battery, which includes at least one selected From the following compounds: crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), indium gallium arsenide (InGaAsSb), indium phosphide indium (InPAsSb), InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/Ge, GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/ GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-wafer-InGaAs, GaInP-Ga(In)As-Ge, and GaInP-GaInAs-Ge. The light emitted by the reactive plasma and directed to the thermal photovoltaic converter or the photovoltaic converter may be mainly ultraviolet light, and the photovoltaic cell may be a concentrating battery comprising at least one selected from the group consisting of a group III nitride, GaN, AlN, A compound of GaAlN and InGaN. In an embodiment, the PV converter can further comprise a UV window to the PV cell. The PV window can replace at least a portion of the black body radiator. The window can be substantially transparent to UV. The window is resistant to wetting with molten metal. The window can be operated at a temperature above at least one of the melting point of the molten metal and above the boiling point of the molten metal. Exemplary windows are sapphire, quartz, MgF2 And molten vermiculite. The window can be cooled and can include components for cleaning during operation or during maintenance. The SunCell® can further include a source of at least one of an electric field and a magnetic field to confine the plasma to regions that avoid contact with at least one of the window and the PV cell. The source can include an electrostatic precipitation system. The source can include a magnetic restraint system. The plasma may be constrained by gravity, wherein at least one of the window and the PV cell is at a suitable height relative to the location at which the plasma is generated. Alternatively, the magnetohydrodynamic power converter can include a nozzle connected to the reaction vessel, a magnetic fluid power channel, an electrode, a magnet, a metal acquisition system, a metal recirculation system, a heat exchanger, and optionally a gas recirculation system, wherein the reaction May contain H2 At least one of O vapor, oxygen, and hydrogen. Reactant supply can be O2 , H2 And reaction product H2 O is maintained at a pressure in the range of 0.01 Torr to 1 Torr. The reactant supply system for replenishing the reactants consumed in the process of reacting at least one of the reactants to generate electrical energy and thermal energy may comprise at least one of the following:2 And H2 a gas permeable membrane, a gas housing, a selective gas permeable membrane in the wall of at least one of the reaction vessel, the magnetic fluid power channel, the metal collection system, and the metal recycling system for maintaining O2 And H2 O of at least one of the pressures2 , H2 And H2 O partial pressure sensor, flow controller, at least one valve and computer. In an embodiment, at least one component of the power system may comprise a ceramic, wherein the ceramic may comprise metal oxide, aluminum oxide, zirconium oxide, magnesium oxide, cerium oxide, lanthanum carbide, zirconium carbide, zirconium diboride, and tantalum nitride. At least one of them. The molten metal may comprise silver and the magnetic fluid power converter may further comprise an oxygen source to form an aerosol of silver particles supplied to at least one of the reservoir, the reaction vessel, the magnetohydrodynamic nozzle, and the magnetohydrodynamic channel, wherein the reaction The material supply system can additionally supply and control the oxygen source to form a silver aerosol. The molten metal may comprise silver. The magnetohydrodynamic converter may further comprise a cell gas comprising an ambient gas in contact with silver in at least one of the reservoir and the vessel. The power system can further include a member that maintains a flow of the cell gas in contact with the molten silver to form a silver aerosol, wherein the cell gas flow can include at least one of a forced gas flow and a convective gas flow. The cell gas can contain rare gases, oxygen, water vapor, H2 And O2 At least one of them. The means for maintaining the flow of the gas in the electrolytic cell may comprise at least one of a gas pump or a compressor, such as a magnetic fluid power pump or compressor, a magnetohydrodynamic converter, and a disturbance caused by at least one of the molten metal injection system and the plasma. flow. The inductive electromagnetic pump of the power system may comprise a two-stage pump comprising a first stage, the first stage comprising a pump of a metal recirculation system, and a second stage comprising a pump of the metal injection system for spraying and the container A stream of molten metal intersecting another molten metal stream inside. The power source of the ignition system includes an inductive ignition system that can include an alternating magnetic field source that passes through a short circuit of molten metal that produces an alternating current containing ignition current in the metal. The alternating magnetic field source may comprise a primary transformer winding comprising a transformer electromagnet and a transformer yoke, and the silver may at least partially act as a secondary transformer winding, such as a single turn short winding, enclosing the primary transformer winding and including an inductive current loop . The reservoir may comprise a molten metal interface, which connects the two reservoirs such that the current loop encloses the transformer yoke, wherein the induced current loop is contained in the reservoir, the molten silver contained in the transfer channel, and the injection tube Silver and intersect to turn on the current generated in the jet of molten silver that is injected into the induced current loop. In an embodiment, the emitter generates at least one of electrical energy and thermal energy, wherein the emitter comprises: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; and a reactant comprising: a) At least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen permeable to the wall of the vessel; d) molten metal such as silver, copper or silver-copper alloy; and e) oxide such as CO2 , B2 O3 LiVO3 And not with H2 At least one of the stable oxides of the reaction; at least one molten metal injection system comprising a molten metal reservoir and an electromagnetic pump; at least one reactant ignition system comprising a power source for causing the reactant to form a luminescent plasma and At least one of the pyroelectric plasma, wherein the power source receives electrical power from the power converter; the system for recovering molten metal and oxide; at least one of the optical and thermal outputs to at least one of the electrical power and/or the thermal power Or an output system; wherein the molten metal ignition system comprises at least one of: an ignition system comprising i) electrodes from the group: a) at least one set of refractory metal or carbon electrodes for constraining the molten metal; b) a refractory metal or carbon electrode and a molten metal stream transported from the electrically isolated molten metal reservoir by an electromagnetic pump, and c) at least two of the plurality of electrically isolated molten metal reservoirs transported by at least two electromagnetic pumps a molten metal stream; and ii) a power source for delivering high current electrical energy sufficient to cause a reactant reaction to form a plasma, wherein the molten metal ignition system current The range of 50 A to 50,000 A; wherein the molten metal injection system comprises an electromagnetic pump comprising at least one magnet providing a magnetic field and a current source for providing a vector cross current component; wherein the molten metal reservoir comprises an inductively coupled heater; a transmitter further comprising a system for recovering molten metal and oxide, such as at least one of a vessel containing a wall capable of providing melt flow under gravity and a reservoir in communication with the vessel, and further comprising a cooling system The cooling system is configured to maintain the reservoir at a lower temperature than the vessel to collect the metal in the reservoir; wherein the vessel capable of maintaining a pressure below, at or above atmospheric pressure comprises: an internal reaction cell, a high temperature black body radiator; and an external chamber capable of maintaining a pressure below, at or above atmospheric pressure; wherein the black body radiator is maintained at a temperature in the range of 1000 K to 3700 K; wherein the interior of the black body radiator is included The reaction cell contains a refractory material such as carbon or W; wherein the black body radiation emitted from the outside of the cell is incident on the light-electric power The at least one power converter of the reactive power output includes at least one of a thermal photovoltaic converter and a photovoltaic converter; wherein the light emitted by the pool is mainly black body radiation, including visible light and near infrared light, and The photovoltaic cell is a concentrating cell comprising at least one compound selected from the group consisting of crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), and gallium indium arsenide (indium gallium arsenide) InGaAsSb) and arsenic indium phosphide indium (InPAsSb), Group III/V semiconductor, InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/Ge , GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-Wafer-InGaAs, GaInP- Ga(In)As-Ge and GaInP-GaInAs-Ge, and the power system further includes a vacuum pump and at least one heat rejection system, and the black body radiator further includes a black body temperature sensor and a controller. Optionally, the emitter may comprise at least one additional reactant injection system, wherein the additional reactants comprise: a) at least one comprising a primary H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; and c) at least one atomic hydrogen source or atomic hydrogen. The additional reactant injection system can further include a computer, H2 O and H2 At least one of a pressure sensor and a flow controller comprising at least one or more of a mass flow controller, a pump, a syringe pump, and a high precision electronically controllable valve; the valve includes At least one of a needle valve, a proportional electronic valve, and a stepper motor valve, wherein the valve is controlled by a pressure sensor and a computer to maintain H2 O and H2 At least one of the pressures is at a desired value; wherein the additional reactant injection system will H2 O vapor pressure is maintained in the range of 0.1 Torr to 1 Torr. In an embodiment, at least one of the following products may be produced from hydrogen by a generator that converts H to low energy hydrogen: a) having a polarity of 0.23 to 0.25 cm- 1 Integer multiple Raman peak is added from 0 to 2000 cm- 1 a hydrogen product in the range of matrix displacement; b) having a range of 0.23 to 0.25 cm- 1 Integer multiple of the infrared peak is added to 0 to 2000 cm- 1 The hydrogen product of the matrix displacement within the range; c) the X-ray photoelectron spectrum at the energy in the range of 500 to 525 eV plus the hydrogen product of the matrix displacement in the range of 0 to 10 eV; d) the high magnetic field MAS NMR matrix a displaced hydrogen product; e) a hydrogen product having a high magnetic field MAS NMR or liquid NMR shift of greater than -5 ppm relative to TMS; f) a hydrogen product having at least two electron beam emission peaks in the range of 200 to 300 nm, It has a range of 0.23 to 0.3 cm- 1 Integer multiples are added between 0 and 5000 cm- 1 a matrix displacement within the range; and g) a hydrogen product having at least two peaks of UV fluorescence emission in the range of 200 to 300 nm, having a purity of 0.23 to 0.3 cm- 1 Integer multiples are added between 0 and 5000 cm- 1 Matrix displacement within the range. In one embodiment, the present invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; reactants, such reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) molten metal; at least one molten metal injection system comprising a molten metal reservoir and an electromagnetic pump; at least one additional reactant injection system, wherein the additional reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O, and c) at least one atomic hydrogen source or atomic hydrogen; at least one reactant ignition system comprising a power source, wherein the power source receives electrical power from the power converter; a system for recovering molten metal; at least one of light and heat output At least one power converter or output system to electrical power and/or thermal power. In an embodiment, the molten metal ignition system comprises: a) at least one set of electrodes for constraining the molten metal; and b) a power source for delivering short pulsed high current electrical energy sufficient to cause the reactants to react to form a plasma. The electrode may comprise a refractory metal. In an embodiment, the power source that delivers short pulsed high current electrical energy sufficient to cause the reactants to react to form a plasma comprises at least one supercapacitor. The molten metal injection system can include an electromagnetic pump that includes at least one magnet that provides a magnetic field and a current source that provides a vector cross current component. The molten metal reservoir can include an inductively coupled heater. The molten metal ignition system can include at least one set of electrodes that are separated to form an open circuit, wherein the open circuit is ignited by spraying the molten metal to close the high current flow. The molten metal ignition system current can range from 500 A to 50,000 A. The circuit of the molten metal ignition system can be closed by metal spraying such that the ignition frequency is in the range of 1 Hz to 10,000 Hz, wherein the molten metal comprises at least one of silver, silver copper alloy and copper, and the addition reactant can be Contains H2 At least one of O vapor and hydrogen. In an embodiment, the additional reactant injection system can include a computer, H2 O and H2 At least one of a pressure sensor and a flow controller comprising at least one or more of a mass flow controller, a pump, a syringe pump, and a high precision electronically controllable valve; the valve includes At least one of a needle valve, a proportional electronic valve, and a stepping electric valve, wherein the valve is controlled by a pressure sensor and a computer to maintain H2 O and H2 At least one of the pressures is at the desired value. Additional reactant injection system for H2 O vapor pressure is maintained in the range of 0.1 Torr to 1 Torr. In an embodiment, the system for recovering the reactant product comprises at least one of: a vessel comprising a wall capable of providing melt flow under gravity, an electrode electromagnetic pump, and a reservoir in communication with the vessel, and the system further A cooling system is included for maintaining the reservoir at a lower temperature than another portion of the vessel to condense metal vapor of molten metal in the reservoir, wherein the recovery system can include an electrode electromagnetic pump that includes at least a magnetic field A magnet and vector cross-ignition current component. In an embodiment, the power system includes a container capable of maintaining a pressure below, at or above atmospheric pressure, the container comprising an internal reaction cell, a cap comprising a blackbody radiator, and capable of maintaining a pressure below, at or above atmospheric pressure External chamber. The top cover including the black body radiator is maintained at a temperature in the range of 1000 K to 3700 K, wherein at least one of the internal reaction cell and the top cover including the black body radiator comprises a refractory metal having a high emissivity. The power system can include at least one power converter that reflects the power output, including at least one of the group consisting of: a thermal photovoltaic converter, a photovoltaic converter, a photoelectric converter, a plasma power converter, and a heat Ion converters, thermoelectric converters, Stirling engines, Braden cycle engines, Rankine cycle engines and heat engines, and heaters. In an embodiment, the light emitted by the cell is mainly black body radiation, comprising visible light and near-infrared light, and the photovoltaic cell is a concentrating battery comprising at least one compound selected from the group consisting of perovskites, crystalline ruthenium, osmium, GaAs, GaAs, Gab, InGaAs, InGaAsSb GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/Ge, GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-wafer-InGaAs, GaInP-Ga(In)As-Ge, and GaInP-GaInAs-Ge. In an embodiment, the light emitted by the cell is primarily ultraviolet light, and the photovoltaic cell is a concentrating cell comprising at least one compound selected from the group consisting of Group III nitride, GaN, AlN, GaAlN, and InGaN. The power system can further include a vacuum pump and at least one chiller. In one embodiment, the invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; reactants, such reactants Contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) molten metal; at least one molten metal injection system comprising a molten metal reservoir and an electromagnetic pump; at least one additional reactant injection system, wherein the additional reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O, and c) at least one atomic hydrogen source or atomic hydrogen; at least one reactant ignition system comprising a power source for causing the reactant to form at least one of a luminescent plasma and a pyroelectric plasma, wherein the power source is a self-power converter At least one power converter or output system for receiving electrical power; a system for recovering molten metal; at least one of optical and thermal output to electrical power and/or thermal power; wherein the molten metal ignition system comprises: a) at least one group An electric source for confining the molten metal; and b) a power source for transmitting short-pulse high-current electric energy sufficient to cause the reactant to react to form a plasma; wherein the electrode comprises a refractory metal; wherein the transport is sufficient to cause the reactant to react to form a plasma The power source for pulsed high current electrical energy comprises at least one supercapacitor; wherein the molten metal injection system comprises an electromagnetic pump comprising at least one magnet providing a magnetic field and a current source for providing a vector cross current component; wherein the molten metal reservoir comprises an inductive coupling a heater; wherein the molten metal ignition system comprises at least one set of separations to form an opening An electrode, wherein the open circuit is ignited by spraying molten metal to cause high current flow to achieve ignition; wherein the molten metal ignition system current is in the range of 500 A to 50,000 A; wherein the circuit of the molten metal ignition system is closed so that the ignition frequency is The range of 1 Hz to 10,000 Hz; wherein the molten metal comprises at least one of silver, silver copper alloy and copper; wherein the addition reactant comprises H2 At least one of O vapor and hydrogen; wherein the additional reactant injection system comprises a computer, H2 O and H2 At least one of a pressure sensor and a flow controller comprising at least one or more of a mass flow controller, a pump, a syringe pump, and a high precision electronically controllable valve; the valve includes At least one of a needle valve, a proportional electronic valve, and a stepping electric valve, wherein the valve is controlled by a pressure sensor and a computer to maintain H2 O and H2 At least one of the pressures is at a desired value; wherein the additional reactant injection system will be H2 O vapor pressure is maintained in the range of 0.1 Torr to 1 Torr; wherein the system for recovering the reactant product comprises at least one of: a vessel comprising a wall capable of providing melt flow under gravity, an electrode electromagnetic pump, and the container a connected reservoir, and the system further includes a cooling system for maintaining the reservoir at a lower temperature than another portion of the vessel to condense metal vapor of the molten metal in the reservoir; wherein the recovery system comprises An electrode electromagnetic pump comprising at least one magnet and a vector cross-ignition current component providing a magnetic field; wherein the container capable of maintaining a pressure below, at or above atmospheric pressure comprises an internal reaction cell comprising a black body radiator cap and capable of maintaining pressure An outer chamber below, at or above atmospheric pressure; wherein the top cover comprising the black body radiator is maintained at a temperature in the range of 1000 K to 3700 K; wherein the inner reaction cell and the top cover including the black body radiator At least one of the refractory metals having a high emissivity; wherein the black body radiator further comprises a black body temperature sensor and control The at least one power converter of the reactive power output comprises at least one of a group of a thermal photovoltaic converter and a photovoltaic converter; wherein the light emitted by the pool is mainly black body radiation, including visible light and near infrared light, The photovoltaic cell is a concentrating cell comprising at least one compound selected from the group consisting of crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), and gallium indium arsenide. (InGaAsSb) and antimony phosphide indium (InPAsSb), group III/V semiconductor, InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/ Ge, GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-Wafer-InGaAs, GaInP -Ga(In)As-Ge and GaInP-GaInAs-Ge; and the power system further comprises a vacuum pump and at least one chiller. In one embodiment, the present invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; reactants, such reactions Contains: a) at least one H2 O source or H2 O; b) H2 a gas; and c) a molten metal; at least one molten metal injection system comprising a molten metal reservoir and an electromagnetic pump; at least one additional reactant injection system, wherein the additional reactants comprise: a) at least one H2 O source or H2 O, and b) H2 At least one reactant ignition system comprising a power source for causing the reactant to form at least one of a light-emitting plasma and a heat-generating plasma, wherein the power source receives electrical power from the power converter; a system for recovering molten metal; and an optical output At least one of the at least one power converter or output system to electrical power and/or thermal power; wherein the molten metal ignition system comprises: a) at least one set of electrodes for constraining the molten metal; and b) for transmitting sufficient to cause The reactant reacts to form a short pulse high current electrical energy source of the plasma, wherein the electrode comprises a refractory metal; wherein the power source for delivering short pulse high current electrical energy sufficient to cause the reactant to react to form a plasma comprises at least one supercapacitor; wherein the molten metal The injection system includes an electromagnetic pump including at least one magnet that provides a magnetic field and a current source for providing a vector cross current component; wherein the molten metal reservoir includes an inductively coupled heater for at least first heating the metal to form a molten metal; The molten metal ignition system includes at least one set of separations to form an open circuit An electrode, wherein the open circuit is ignited by spraying molten metal to cause high current flow to achieve ignition; wherein the molten metal ignition system current is in the range of 500 A to 50,000 A; wherein the circuit of the molten metal ignition system is closed so that the ignition frequency is In the range of 1 Hz to 10,000 Hz; wherein the molten metal comprises at least one of silver, silver-copper alloy and copper; wherein the additional reactant injection system comprises a computer, H2 O and H2 At least one of a pressure sensor and a flow controller comprising at least one or more of a mass flow controller, a pump, a syringe pump, and a high precision electronically controllable valve; the valve includes At least one of a needle valve, a proportional electronic valve, and a stepping electric valve, wherein the valve is controlled by a pressure sensor and a computer to maintain H2 O and H2 At least one of the pressures is at a desired value; wherein the additional reactant injection system will be H2 O vapor pressure is maintained in the range of 0.1 Torr to 1 Torr; wherein the system for recovering the reactant product comprises at least one of: a vessel comprising a wall capable of providing melt flow under gravity, an electrode electromagnetic pump, and the container a connected reservoir, and the system further includes a cooling system for maintaining the reservoir at a lower temperature than another portion of the vessel to condense metal vapor of the molten metal in the reservoir; wherein the recovery system comprises An electrode electromagnetic pump comprising at least one magnet and a vector cross-ignition current component providing a magnetic field; wherein the container capable of maintaining a pressure below, at or above atmospheric pressure comprises an internal reaction cell, a top cover comprising a high temperature black body radiator and capable of being maintained An external chamber having a pressure lower than, at or above atmospheric pressure; wherein the top cover including the black body radiator is maintained at a temperature in the range of 1000 K to 3700 K; wherein the internal reaction electrolytic cell and the top cover including the black body radiator At least one of the refractory metals having a high emissivity; wherein the blackbody radiator further comprises a black body temperature sensor and The at least one power converter of the reactive power output includes at least one of a thermal photovoltaic converter and a photovoltaic converter; wherein the light emitted by the pool is mainly black body radiation, including visible light and near infrared light, and The photovoltaic cell is a concentrating cell comprising at least one compound selected from the group consisting of crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), and gallium indium arsenide (indium gallium arsenide) InGaAsSb) and arsenic indium phosphide indium (InPAsSb), Group III/V semiconductor, InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/Ge , GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-Wafer-InGaAs, GaInP- Ga(In)As-Ge and GaInP-GaInAs-Ge; and the power system further includes a vacuum pump and at least one chiller. In one embodiment, the present invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; reactants, such reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) molten metal; at least one molten metal injection system comprising a molten metal reservoir and an electromagnetic pump; at least one additional reactant injection system, wherein the additional reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O, and c) at least one atomic hydrogen source or atomic hydrogen; at least one reactant ignition system comprising a power source for causing the reactant to form at least one of a luminescent plasma and a pyroelectric plasma, wherein the power source is a self-power converter At least one power converter or output system for receiving electrical power; a system for recovering molten metal; at least one of optical and thermal output to electrical power and/or thermal power; wherein the molten metal ignition system comprises: a) at least one group An electric source for constraining the molten metal; and b) a power source for transmitting short-pulse high-current electric energy sufficient to cause the reactant to react to form a plasma; wherein the electrode comprises a refractory metal; wherein the transport is sufficient to cause the reactant to react to form a plasma The power source for pulsed high current electrical energy includes at least one supercapacitor; wherein the molten metal injection system includes an electromagnetic pump including at least one magnet that provides a magnetic field and a current source for providing a vector cross current component; wherein the molten metal reservoir is included An inductively coupled heater that at least first heats the metal to form a molten metal; The ignition system includes at least one set of electrodes separated to form an open circuit, wherein the open circuit is ignited by spraying molten metal to cause high current flow to achieve ignition; wherein the molten metal ignition system current is in the range of 500 A to 50,000 A; wherein melting The circuit of the metal ignition system is closed such that the ignition frequency is in the range of 1 Hz to 10,000 Hz; wherein the molten metal comprises at least one of silver, silver copper alloy, and copper; wherein the addition reactant comprises H2 At least one of O vapor and hydrogen; wherein the additional reactant injection system comprises a computer, H2 O and H2 At least one of a pressure sensor and a flow controller comprising at least one or more of a mass flow controller, a pump, a syringe pump, and a high precision electronically controllable valve; the valve includes At least one of a needle valve, a proportional electronic valve, and a stepping electric valve, wherein the valve is controlled by a pressure sensor and a computer to maintain H2 O and H2 At least one of the pressures is at a desired value; wherein the additional reactant injection system will be H2 O vapor pressure is maintained in the range of 0.1 Torr to 1 Torr; wherein the system for recovering the reactant product comprises at least one of: a vessel comprising a wall capable of providing melt flow under gravity, an electrode electromagnetic pump, and the container a connected reservoir, and the system further includes a cooling system for maintaining the reservoir at a lower temperature than another portion of the vessel to condense metal vapor of the molten metal in the reservoir; wherein the recovery system comprises An electrode electromagnetic pump comprising at least one magnet and a vector cross-ignition current component providing a magnetic field; wherein the container capable of maintaining a pressure below, at or above atmospheric pressure comprises an internal reaction cell comprising a black body radiator cap and capable of maintaining pressure An outer chamber below, at or above atmospheric pressure; wherein the top cover comprising the black body radiator is maintained at a temperature in the range of 1000 K to 3700 K; wherein the inner reaction cell and the top cover including the black body radiator At least one of the refractory metals having a high emissivity; wherein the black body radiator further comprises a black body temperature sensor and control The at least one power converter of the reactive power output comprises at least one of a group of a thermal photovoltaic converter and a photovoltaic converter; wherein the light emitted by the pool is mainly black body radiation, including visible light and near infrared light, The photovoltaic cell is a concentrating cell comprising at least one compound selected from the group consisting of crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), and gallium indium arsenide. (InGaAsSb) and antimony phosphide indium (InPAsSb), group III/V semiconductor, InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/ Ge, GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-Wafer-InGaAs, GaInP -Ga(In)As-Ge and GaInP-GaInAs-Ge; and the power system further comprises a vacuum pump and at least one chiller. In another embodiment, the present invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one vessel capable of having a pressure below atmospheric pressure; pellets comprising reactants, the reactions The object contains: a) at least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; at least one pellet injection system comprising at least one enhanced railgun, wherein the enhanced railgun comprises a separate charged orbit And a magnet that produces a magnetic field perpendicular to the plane of the orbit, and the circuit between the tracks is open until closed by contact of the pellets with the track. At least one ignition system for causing the pellet to form at least one of a luminescent plasma and a pyroelectric plasma, the at least one ignition system comprising: a) at least one set of electrodes for constraining the pellets; and b) for transmitting short a power source for pulsing high current electrical energy; wherein the at least one set of electrodes forms an open circuit, wherein the open circuit is closed by spraying the pellets to cause high current to flow to achieve ignition, and the power source for transmitting short pulse high current electrical energy includes the following At least one of: a voltage of a high AC, DC or AC-DC mixture that is selected to cause a current in a range of at least one of 100 A to 1,000,000 A, 1 kA to 100,000 A, 10 kA to 50 kA; DC or peak AC current density in the range of at least one of: 100 A/cm2 Up to 1,000,000 A/cm2 , 1000 A/cm2 Up to 100,000 A/cm2 And 2000 A/cm2 Up to 50,000 A/cm2 The voltage is determined by the conductivity of the solid fuel, or where the voltage is obtained by multiplying the required current by the resistance of the solid fuel sample; DC or peak AC voltage is between 0.1 V and 500 kV, 0.1 V to 100 kV and 1 V to Within a range of at least one of 50 kV, and an AC frequency in the range of 0.1 Hz to 10 GHz, 1 Hz to 1 MHz, 10 Hz to 100 kHz, and 100 Hz to 10 kHz; a system of reaction products of reactants comprising at least one of a gravity and enhanced plasma orbital gun recovery system comprising at least one vector cross current component of a magnet providing a magnetic field and an ignition electrode; A regeneration system for regenerating additional reactants from a reaction product and forming additional pellets, comprising a granulator comprising a furnace for forming a molten reactant for H2 And H2 O is added to the system of molten reactants, a melt dripper, and a reservoir for forming pellets, wherein the additional reactants comprise: a) at least one comprising primary H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; and at least one of light and heat output to at least one power converter of electrical power and/or thermal power or An output system comprising one or more of the following groups: photovoltaic converter, photoelectric converter, plasma power converter, thermionic converter, thermoelectric converter, Stirling engine, Breiden Cycle engine, Rankine cycle engine and heat engine and heater. In another embodiment, the present invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one vessel capable of having a pressure below atmospheric pressure; pellets comprising reactants, the reactions The object comprises at least one of silver, copper, absorbed hydrogen and water; at least one pellet injection system comprising at least one enhanced railgun, wherein the enhanced railgun comprises a separate charged orbit and produces a magnetic field perpendicular to the plane of the orbit. a magnet, and the circuit between the tracks is open until closed by contact of the pellets with the track; at least one ignition system for causing the pellet to form at least one of the luminescent plasma and the heated plasma, at least one ignition The system comprises: a) at least one set of electrodes for constraining the pellets; and b) a power source for delivering short pulses of high current electrical energy; wherein the at least one set of electrodes are separated to form an open circuit, wherein the open circuit is by jetting pellets And a power source that is closed to cause a high current to flow to ignite, and a power source for transmitting short-pulse high-current power includes at least one of the following: Selecting a voltage that causes a high AC, DC, or AC-DC mixture of currents in a range of at least one of 100 A to 1,000,000 A, 1 kA to 100,000 A, 10 kA to 50 kA; at least one of DC or peak AC current density in the range of 100 A/cm2 Up to 1,000,000 A/cm2 , 1000 A/cm2 Up to 100,000 A/cm2 And 2000 A/cm2 Up to 50,000 A/cm2 The voltage is determined by the conductivity of the solid fuel, which is obtained by multiplying the required current by the resistance of the solid fuel sample; DC or peak AC voltage is between 0.1 V and 500 kV, 0.1 V to 100 kV, and 1 V to 50. Within the range of at least one of kV, and the AC frequency is in the range of at least one of 0.1 Hz to 10 GHz, 1 Hz to 1 MHz, 10 Hz to 100 kHz, and 100 Hz to 10 kHz; a system of reaction products comprising at least one of a gravity and enhanced plasma orbital gun recovery system comprising at least one vector cross current component of a magnetic field providing a magnetic field and an ignition electrode; at least one a regeneration system for regenerating additional reactants from a reaction product and forming additional pellets, comprising a granulator comprising a furnace for forming a molten reactant for H2 And H2 O is added to the system of molten reactants, a melt dripper, and a reservoir for forming pellets, wherein the additional reactants comprise at least one of silver, copper, absorbed hydrogen, and water; at least one power converter Or an output system comprising a concentrating ultraviolet photovoltaic converter, wherein the photovoltaic cells comprise at least one compound selected from the group consisting of Group III nitrides, GaAlN, GaN, and InGaN. In another embodiment, the invention is directed to a power system for generating at least one of electrical energy and thermal energy, comprising: at least one container; pellets comprising reactants, the reactants comprising: a) at least one inclusion Newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; at least one pellet injection system; at least one pellet ignition system for causing the pellet to form a luminescent plasma And at least one of the pyroelectric plasma; a system for recovering the reaction product of the reactant; at least one regeneration system for regenerating the additional reactant from the reaction product and forming additional pellets, wherein the additional reactant comprises: a) At least one containing newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; at least one of light and heat output to at least one power converter or output of electrical power and/or thermal power system. Certain embodiments of the present invention are directed to a power generation system including: a plurality of electrodes configured to transfer power to a fuel to ignite the fuel and generate plasma; configured to transfer electrical energy to a plurality of a power source for the electrode; and at least one photovoltaic power converter positioned to receive at least a plurality of plasma photons. In one embodiment, the invention is directed to a power system for generating at least one of direct current electrical energy and thermal energy, comprising: at least one container; a reactant comprising: a) at least one comprising a nascent H2 a catalyst source or catalyst of O; b) at least one atomic hydrogen source or atomic hydrogen; c) at least one of a conductor and a conductive matrix; and at least one set of electrodes for constraining the low energy hydrogen reactant for transmitting short pulses a high current electrical energy source; a heavy duty system; at least one system for regenerating the initial reactant from the reaction product, and at least one plasma power converter or at least one photovoltaic converter. In an exemplary embodiment, a method of generating electrical power can include supplying fuel to a region between a plurality of electrodes; energizing a plurality of electrodes to ignite the fuel to form a plasma; and using a photovoltaic power converter to convert the plurality of electrodes The plasma photons are converted to electrical power; and at least a portion of the electrical power is output. In another exemplary embodiment, a method of generating electrical power can include supplying fuel to a region between a plurality of electrodes; energizing a plurality of electrodes to ignite the fuel to form a plasma; and using a photovoltaic power converter to convert the plurality A plasma photon is converted to thermal power; and at least a portion of the electrical power is output. In an embodiment of the invention, a method of generating power may include: delivering a quantity of fuel to a fuel loading zone, wherein the fuel loading zone is between a plurality of electrodes; by applying at least about 100 A/cm to the plurality of electrodes2 a current that causes the current to flow through the fuel to ignite the fuel, thereby producing at least one of plasma, light, and heat; receiving at least a portion of the light in the photovoltaic power converter; and converting the light using a photovoltaic power converter Different forms of power; and output different forms of power. In another embodiment, the present invention is directed to a water arc plasma power system comprising: at least one closed reaction vessel; comprising H2 O source and H2 a reactant of at least one of O; at least one set of electrodes; for conveying the H2 An initial high breakdown voltage of O and providing a subsequent high current power source; and a heat exchanger system, wherein the power system generates arc plasma, light, and thermal energy; and at least one photovoltaic power converter. Water in the form of a vapor can be supplied on or across the electrodes. The plasma may be permitted to expand into the low pressure region of the plasma battery to prevent suppression of low energy hydrogen reactions due to constraints. The arc electrode can include a spark plug design. The electrode may comprise at least one of copper, nickel, silver chromate and zinc for corrosion resistance, nickel, iron, nickel iron, chromium, precious metals, tungsten, molybdenum, niobium, tantalum and palladium. In an embodiment, the water arc is maintained at a low water pressure, such as in at least one of about 0.01 Torr to 10 Torr and 0.1 Torr to 1 Torr. The pressure range can be maintained within a scope of the invention by means of the disclosure for the SF-CIHT battery. An exemplary component for supplying water vapor is a mass flow controller and includes H2 At least one of the reservoirs of O, such as a hydrated zeolite or salt bath, such as venting gas H at a desired pressure range2 O KOH solution. Water can be supplied by a syringe pump where delivery to a vacuum results in vaporization of the water. Certain embodiments of the present invention are directed to a power generation system comprising: at least about 100 A/cm2 Or a power source of at least about 5,000 kW; a plurality of electrodes electrically coupled to the power source; a fuel loading zone configured to receive solid fuel, wherein the plurality of electrodes are configured to deliver electrical power to the solid fuel, thereby producing a plasma; and at least one of a plasma power converter, a photovoltaic power converter, and a thermoelectric power converter positioned to receive at least a portion of the plasma, photons, and/or heat generated by the reaction. Other embodiments are directed to a power generation system comprising: a plurality of electrodes; a fuel loading zone located between the plurality of electrodes and configured to receive a conductive fuel, wherein the plurality of electrodes are configured to be sufficient to A conductive fuel is ignited and a current that produces at least one of plasma and thermal power is applied to the conductive fuel; a transfer mechanism for moving the conductive fuel into the fuel loading zone; and a photon to convert the plasma photon to a certain A form of power photovoltaic power converter or at least one of a thermo-electric power converter for converting thermal power into a non-thermal form of power, including electrical or mechanical power. Other embodiments are directed to a method of generating electrical power comprising: delivering a quantity of fuel to a fuel loading zone, wherein the fuel loading zone is between a plurality of electrodes; by applying at least about 2,000 A/cm to the plurality of electrodes2 a current that causes the current to flow through the fuel to ignite the fuel, thereby producing at least one of plasma, light, and heat; receiving at least a portion of the light in the photovoltaic power converter; using a photovoltaic power converter The light is converted into different forms of power; and the different forms of power are output. Additional embodiments are directed to a power generation system comprising: a power source of at least about 5,000 kW; a plurality of spaced apart electrodes, wherein the plurality of electrodes at least partially surround the fuel, electrically coupled to the power source, configured to receive current Thereby igniting the fuel, and at least one of the plurality of electrodes is movable; a transport mechanism for moving the fuel; and configured to convert the plasma generated by the ignition of the fuel into a non-plasma form of power Photovoltaic power converter. The invention further provides a power generation system comprising: at least about 2,000 A/cm2 a plurality of spaced apart electrodes, wherein the plurality of electrodes at least partially surround the fuel, electrically coupled to the power source, configured to receive current to ignite the fuel, and at least one of the plurality of electrodes is Mobile; a transport mechanism for moving the fuel; and a photovoltaic power converter configured to convert plasma generated by ignition of the fuel into power in a non-plasma form. Another embodiment is directed to a power generation system comprising: at least about 5,000 kW or at least about 2,000 A/cm2 a plurality of spaced apart electrodes, wherein at least one of the plurality of electrodes includes a compression mechanism; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes such that the at least An electrode compression mechanism is oriented toward the fuel loading zone, and wherein the plurality of electrodes are electrically coupled to the power source and configured to power the fuel received in the fuel loading zone to ignite the fuel; A transfer mechanism in which fuel is moved into the fuel loading zone; and a photovoltaic power converter configured to convert photons produced by the ignition of the fuel into power in the form of non-photons. Other embodiments of the present invention are directed to a power generation system comprising: at least about 2,000 A/cm2 a plurality of spaced apart electrodes, wherein at least one of the plurality of electrodes includes a compression mechanism; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes such that the at least An electrode compression mechanism is oriented toward the fuel loading zone, and wherein the plurality of electrodes are electrically coupled to the power source and configured to power the fuel received in the fuel loading zone to ignite the fuel; for the fuel a transfer mechanism moved into the fuel loading zone; and a plasma power converter configured to convert the plasma generated by the ignition of the fuel into a power in a non-plasma form. Embodiments of the present invention are also directed to a power generation system including: a plurality of electrodes; a fuel loading zone surrounded by the plurality of electrodes and configured to receive fuel, wherein the plurality of electrodes are configured to be located at the fuel loading Fuel ignition in the zone; a transfer mechanism for moving the fuel into the fuel loading zone; a photovoltaic power converter configured to convert photons generated by the ignition of the fuel into power in the form of non-photons; a removal system in addition to the by-product of the ignited fuel; and a regeneration system operatively coupled to the removal system for recycling the by-product of the removed ignited fuel to the recirculated fuel . Certain embodiments of the present invention are also directed to a power generation system comprising: configured to output at least about 2,000 A/cm2 a power source having a current of at least about 5,000 kW; a plurality of spaced apart electrodes electrically coupled to the power source; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes, and wherein the plurality Electrodes are configured to energize the fuel as it is received in the fuel loading zone to ignite the fuel; a transfer mechanism for moving the fuel into the fuel loading zone; and configured to be A photovoltaic power converter that converts a plurality of photons generated by fuel ignition into a power in the form of non-photons. Some embodiments may further include one or more of: an output power terminal operatively coupled to the photovoltaic power converter; a power storage device; configured to measure at least one associated with the power generation system a sensor of the parameter; and a controller configured to control at least one process associated with the power generation system. Certain embodiments of the present invention are also directed to a power generation system comprising: configured to output at least about 2,000 A/cm2 a power source having a current of at least about 5,000 kW; a plurality of spaced apart electrodes, wherein the plurality of electrodes at least partially surround the fuel, electrically coupled to the power source, configured to receive current to ignite the fuel, and the plurality of At least one of the electrodes is moveable; a transport mechanism for moving the fuel; and a photovoltaic power converter configured to convert photons generated by the ignition of the fuel into different forms of power. Additional embodiments of the present invention are directed to a power generation system comprising: at least about 5,000 kW or at least about 2,000 A/cm2 a plurality of spaced apart electrodes electrically coupled to the power source; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes, and wherein the plurality of electrodes are configured to The fuel is ignited to the fuel as it is received in the fuel loading zone; a transfer mechanism for moving the fuel into the fuel loading zone; configured to convert a plurality of photons generated by the ignition of the fuel a photovoltaic power converter in the form of a non-photon form; a sensor configured to measure at least one parameter associated with the power generation system; and configured to control at least one process associated with the power generation system Controller. Further embodiments are directed to a power generation system comprising: at least about 2,000 A/cm2 a plurality of spaced apart electrodes electrically coupled to the power source; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes, and wherein the plurality of electrodes are configured to The fuel is ignited to the fuel as it is received in the fuel loading zone; a transfer mechanism for moving the fuel into the fuel loading zone; configured to convert the plasma generated by the ignition of the fuel into a plasma power converter of non-plasma form power; a sensor configured to measure at least one parameter associated with the power generation system; and configured to control at least one process associated with the power generation system Controller. Certain embodiments of the present invention are directed to a power generation system comprising: at least about 5,000 kW or at least about 2,000 A/cm2 a plurality of spaced apart electrodes electrically coupled to the power source; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes, and wherein the plurality of electrodes are configured to The fuel is ignited to the fuel as it is received in the fuel loading zone, and wherein the pressure in the fuel loading zone is a partial vacuum; a transfer mechanism for moving the fuel into the fuel loading zone; A photovoltaic power converter configured to convert the plasma produced by the ignition of the fuel into a power in the form of a non-plasma. Some embodiments may include one or more of the following additional features: a photovoltaic power converter may be located within the vacuum unit; the photovoltaic power converter may include an anti-reflective coating, an optical impedance matching coating, or a protective coating At least one; the photovoltaic power converter can be operatively coupled to a cleaning system configured to clean at least a portion of the photovoltaic power converter; the power generation system can include an optical filter; the photovoltaic power The converter may include a single crystal battery, a polycrystalline battery, an amorphous battery, a string/belt battery, a multi-junction battery, a homojunction battery, a heterojunction battery, a pin device, a thin film battery, a dye-sensitized battery, and At least one of the organic photovoltaic cells; and the photovoltaic power converter may comprise a multi-junction battery, wherein the multi-junction battery comprises an inverted battery, a vertical battery, a lattice mismatch battery, a lattice matching battery, and At least one of the batteries comprising the III-V semiconductor material. Additional exemplary embodiments are directed to a system configured to generate electrical power, comprising: a fuel supply configured to supply fuel; a power supply configured to supply electrical power; and at least one pair configured An electrode that receives fuel and electrical power, wherein the electrodes selectively direct electrical power to a localized region surrounding the electrode to ignite fuel within the localized region. Some embodiments are directed to a method of generating electrical power comprising: supplying fuel to an electrode; supplying current to the electrode to ignite the positioned fuel to generate energy; and converting at least some of the energy generated by the ignition to electrical power. Other embodiments are directed to a power generation system comprising: at least about 2,000 A/cm2 a plurality of spaced apart electrodes electrically coupled to the power source; a fuel loading zone configured to receive fuel, wherein the fuel loading zone is surrounded by the plurality of electrodes, and wherein the plurality of electrodes are configured to The fuel is ignited to the fuel as it is received in the fuel loading zone, and wherein the pressure in the fuel loading zone is a partial vacuum; a transfer mechanism for moving the fuel into the fuel loading zone; A photovoltaic power converter configured to convert the plasma produced by the ignition of the fuel into a power in the form of a non-plasma. A further embodiment is directed to a power generation unit comprising: an exit aperture coupled to a vacuum pump; a plurality of electrodes electrically coupled to a power source of at least about 5,000 kW; configured to receive primarily H2 a water-based fuel-loading zone of O, wherein the plurality of electrodes are configured to deliver power to the water-based fuel to produce at least one of arc plasma and thermal power; and configured to A portion of the arc plasma and at least a portion of the thermal power is converted to a power converter of electrical power. Also disclosed is a power generation system comprising: at least about 5,000 A/cm2 a power source; a plurality of electrodes electrically coupled to the power source; configured to receive primarily H2 a water-based fuel-loading zone of O, wherein the plurality of electrodes are configured to deliver power to the water-based fuel to produce at least one of arc plasma and thermal power; and configured to A portion of the arc plasma and at least a portion of the thermal power is converted to a power converter of electrical power. In an embodiment, the power converter includes a photovoltaic converter that converts optical power into electricity. Additional embodiments are directed to a method of producing electrical power comprising: loading fuel into a fuel loading zone, wherein the fuel loading zone includes a plurality of electrodes; at least about 2,000 A/cm2 Applying a current to the plurality of electrodes to ignite the fuel to produce at least one of arc plasma and thermal power; performing at least one of: passing the arc plasma through a photovoltaic converter to generate electrical power, and The thermal power is passed through a thermo-electric converter to generate electrical power; and at least a portion of the generated electrical power is output. Also disclosed is a power generation system comprising: a power source of at least about 5,000 kW; a plurality of electrodes electrically coupled to the power source, wherein the plurality of electrodes are configured to deliver electrical power to primarily include H2 a water-based fuel, thereby generating thermal power; and a heat exchanger configured to convert at least a portion of the thermal power to electrical power; and photovoltaic power configured to convert at least a portion of the light into electrical power converter. Additionally, another embodiment is directed to a power generation system comprising: at least about 5,000 A/cm2 Power supply; a plurality of spaced apart electrodes, wherein at least one of the plurality of electrodes includes a compression mechanism; configured to receive primarily H2 a fuel-loading zone of water-based fuel, wherein the fuel-loading zone is surrounded by the plurality of electrodes such that a compression mechanism of the at least one electrode is oriented toward the fuel-loading zone, and wherein the plurality of electrodes are electrically connected to the power source and Configuring to ignite water-based fuel received in the fuel-loading zone to ignite the fuel; transfer mechanism for moving the water-based fuel into the fuel-loading zone; and configured to be A plasma-powered power converter that converts plasma generated by fuel ignition into power in a non-plasma form. A catalyst system for releasing energy from atomic hydrogen to form a lower energy state is disclosed herein, wherein the electronic housing is in a relatively close position relative to the core. The released power is used to generate electricity, and in addition, the novel hydrogen species and compounds are the desired products. These energy states are predicted by classical laws of physics and require a catalyst to accept energy from hydrogen for a corresponding energy release transition. Classical physics gives a closed-form solution for a hydrogen atom, a hydrogen anion, a hydrogen molecular ion, and a hydrogen molecule, and predicts a corresponding substance having a fractional primary quantum number. Atomic hydrogen can undergo a catalytic reaction with certain substances, including itself, which accepts an integral multiple of the energy of the atomic hydrogen m·27.2 eV, where m is an integer. The predicted reaction involves the transfer of resonant non-radiative energy from the originally stabilized atomic hydrogen to a catalyst capable of accepting this energy. The product is H(1/p), and the fraction of atomic hydrogen is obtained from the fractional Rydberg state, which is called "low-energy hydrogen atom". Among the equations used in the excited state of hydrogen, n=1/ 2. 1/3, 1/4, ..., 1/p (p ≤ 137, an integer) replace the well-known parameter n = integer. Each low-energy hydrogen state also contains electrons, protons, and photons, but the field fraction from photons increases binding energy rather than reducing binding energy, which corresponds to energy desorption rather than absorption. Because the atomic hydrogen can be 27.2 eV, som OneH The atom acts as the otherm + 1) A catalyst having a H atom of m·27.2 eV [1]. For example, a H atom can act as a catalyst by accepting 27.2 eV from another H via energy transfer across space (such as by magnetic or induced electric dipole-dipole coupling), thereby forming a continuum band. A decaying intermediate that has a short wavelength cutoff and energy. In addition to the atom H, a molecule that accepts m · 27.2 eV from the atom H and the molecular energy value decreases by the same energy can also act as a catalyst. H2 The position of O can be 81.6 eV. Subsequently, by the same mechanism, the nascent H formed by the thermodynamically favorable reduction of the metal oxide is predicted.2 O molecules (not hydrogen bonded in a solid, liquid or gaseous state) act as a catalyst to form 204 eV energy (containing 81.6 eV to HOH) and release continuous radiation (122.4 eV) with a cutoff at 10.1 nm.H (1/4). Involving the transition toStateH In the atomic catalyst reaction,m OneH The atom acts as anotherm + 1 ) H atoms have m · 27.2eV Catalyst. Subsequently,m Atom borrowed from the firstm +1 ) A hydrogen atom accepts m · 27.2 in a resonant and non-radiative mannereV Makem OneH Acting as a catalystm The reaction between +1 hydrogen atoms is given by: And the total response isAbout New Life H2 O [1] potential energy, catalytic reaction (m =3) isAnd the total response isAfter the energy is transferred to the catalyst (equations (1) and (5)), an intermediate having a central radius of the H atom radius and m + 1 times the proton center field is formed.. The predicted radius decreases as the electron undergoes radial acceleration until the radius is a steady state of 1/(m + 1) of the radius of the uncatalyzed hydrogen atom, and m is released2 · 13.6 eV energy. Forecast is attributed toIntermediates (eg, the far ultraviolet continuous radiation bands of equations (2) and (6) have short wavelength cutoffs and are given by the energy given below:And extending to a longer wavelength than the corresponding cutoff. Here, due to H*[aH /4] The far-ultraviolet continuous radiation band caused by the attenuation of the intermediate is predicted to be at E = m2 · 13.6 = 9·13.6 = 122.4 eV (10.1 nm) has a short wavelength cutoff [where in equation (9), p = m + 1 = 4 and m = 3] and extends to longer wavelengths. A continuous radiation band at 10.1 nm is observed, and for a theoretically predicted transition from H to lower energy (the so-called "low energy hydrogen" state H (1/4)) reaches a longer wavelength, which consists only of some Hydrogen pulse pinch gas discharge caused. Another observation predicted by equations (1) and (5) is self-fast H+ The recombination forms a fast excited state H atom. These fast atoms produce a broadened Baal alpha emission. A well-known phenomenon of Barley alpha line broadening of more than 50 eV with a population of very high kinetic energy hydrogen atoms in certain mixed hydrogen plasmas is disclosed, the reason for which is due to the release in the formation of low energy hydrogen. energy. A fast H was observed in the continuous emission of hydrogen pinch plasma. Additional catalysts and reaction systems that form low energy hydrogen are possible. Specific substances that can be identified based on known electron energy levels (eg, He+ , Ar+ , Sr+ , K, Li, HCl and NaH, OH, SH, SeH, nascent H2 O, nH (n = integer)) need to be present together with atomic hydrogen to catalyze the process. The reaction involves non-radiative energy transfer followed by a continuous emission of q·13.6 eV or q·13.6 eV to H to form an extremely hot excited state H and a hydrogen atom whose energy is lower than the fractional main quantum number Unreacted atomic hydrogen. That is, in the formula of the main energy level of a hydrogen atom:among thema H Is the Bohr radius of the hydrogen atom (52.947 pm),e Is the magnitude of the electrical charge, andε o For vacuum permittivity, fractional quantum number:Where p ≤ 137 is an integer (12) a well-known parameter in the Rydberg equation that replaces the excited state of hydrogenn = integer and represents a lower energy hydrogen atom called "low energy hydrogen". HydrogenState and hydrogenThe state is non-radiative, but the transition between the two non-radiative states, such asn = 1 ton = 1/2, which may occur via non-radiative energy transfer. Hydrogen is a special case of the steady state given by equations (10) and (12), wherein the corresponding radius of hydrogen or low-energy hydrogen atoms is given by:, (13) wherep = 1, 2, 3, .... In order to conserve energy, energy must be in the ordinaryn = 1 The integer energy of the hydrogen atom in the state is transmitted from the hydrogen atom to the catalyst, and the radius transitions to. Low energy hydrogen is formed by reacting a common hydrogen atom with a suitable catalyst having the following reaction: m • 27.2 eV (14)m Is an integer. It is believed that as the reaction nets match more closelym • 27.2eV The rate of catalysis increases. The reaction has been found and the reaction is netm • 27.2eV The catalyst within ±10% (preferably ±5%) is suitable for most applications. The catalytic reaction involves two steps of energy release: non-radiative energy is transferred to the catalyst, and then as the radius decreases, additional energy is released until the corresponding stable final state is reached. Therefore, the overall response is given by: And (17) the overall response is q ,r ,m andp Is an integer.Has a radius of hydrogen atoms (corresponding to 1 in the denominator) and is equal to the central field of the proton (m +p ) times the center field, andRadius isH ItCorresponding to steady state. Catalyst productH (l/p ) can also react with electrons to form low-energy hydrogen hydride anionsH - (l/p ), or twoH (l/p ) Reaction can occur to form a corresponding molecular low-energy hydrogen H2 (l/p ). Specifically, the catalyst productH (l/p ) can also react with electrons to form binding energyE B Novel hydrogen anionH - (l/p ).among themp = Integer > 1,s = 1/2,For Planck's constant bar,Is the permeability of the vacuum,m e For the quality of electronics,ForGiven the electronic quality of the reduction,m p For the quality of protons,a o Is the Bohr radius and the ionic radius is. According to equation (19), the calculated ionization energy of the hydrogen anion is 0.75418eV And the experimental value is 6082.99 ± 0.15Cm - 1 (0.75418 eV). The binding energy of the low energy hydrino hydride ion can be measured by X-ray photoelectron spectroscopy (XPS). The NMR peaks to high magnetic field shifts have direct evidence of lower energy states of hydrogen with decreasing cation radius and increased diamagnetic shielding of protons. The displacement is given by the sum of the kinetics of the two electrons and the photon field of amplitude p (Mills GUTCP equation (7.87)):The first of these applies toH - Which forH - (l /p ),p = 1 andp = integer >1, andα For fine structure constants. The predicted low energy hydrino hydride peak is abnormally displaced to a high magnetic field relative to a common hydride anion. In an embodiment, the peak is a high magnetic field of TMS. The NMR shift relative to TMS can be greater than the normal H for individual or constituent compounds.- , H, H2 Or H+ At least one of the known NMR shifts. The displacement may be greater than at least one of: 0, -1, -2, -3, -4, -5, -6, -7, -8, -9, -10, -11, -12, - 13,-14, -15, -16, -17, -18, -19, -20, -21, - 22, -23, -24, -25, -26, -27, -28, -29, -30, -31, -32, -33, -34, -35, -36, -37, -38, -39, and -40 ppm. The range of absolute displacement relative to bare protons (where the displacement of TMS is about -31.5 relative to bare protons) can be -(p29.9 + p2 2.74) ppm (Equation (20)), which is in the range of at least one of the following: ± 5 ppm, ± 10 ppm, ± 20 ppm, ± 30 ppm, ± 40 ppm, ± 50 ppm, ± 60 ppm ± 70 ppm, ± 80 ppm, ± 90 ppm and ± 100 ppm. The absolute displacement relative to the bare proton can be -(p29.9 + p2 1.59 × 10- 3 ) ppm (equation (20)), which is in the range of at least one of: 0.1% to 99%, 1% to 50%, and 1% to 10%. In another embodiment, the presence of a low energy hydrogen species (such as a low energy hydrogen atom, a hydrogen anion or a molecule) in a solid substrate, such as a substrate such as a hydroxide of NaOH or KOH, causes the matrix protons to go to a high magnetic field. Displacement. Matrix protons (such as matrix protons of NaOH or KOH) can be exchanged. In an embodiment, the displacement can cause the matrix peak to be in the range of about -0.1 ppm to -5 ppm relative to TMS. NMR measurements can include magic angle rotation 1 H Nuclear magnetic resonance spectroscopy 1 H NMR).H (l/p ) can react with protons and twoH (l/p Can react to form separatelyH 2 (l / p)+ andH 2 (l/p ). Under the non-radiation constraint, the hydrogen molecule ion and molecular charge and current density function, bond distance and energy are solved according to the Laplacian in the elliptic coordinates.+ at each focus of the long sphere molecular orbitalPe The total energy of the hydrogen molecular ions in the central fieldE T for:among themp As an integer,c Is the speed of light in a vacuum, andμ The nuclear quality for the contract. + at each focus of the long sphere molecular orbitalPe The total energy of the hydrogen molecules in the central field is:Hydrogen moleculeH 2 (1/p ) Key dissociation energyE D Corresponding to the total energy of the hydrogen atomE T The difference between.among them E D Given by equation (23-25): H 2 (1/p ) can be identified by X-ray photoelectron spectroscopy (XPS), wherein the ionization product other than ionized electrons can be, for example, comprising two protons and electrons (hydrogen (H) atoms, low energy hydrogen atoms, molecular ions, hydrogen molecular ions, andH 2 (1/p)+ At least one of the possibilities, wherein the energy can be displaced by the matrix. NMR of catalytic product gasH 2 (1/p Deterministic test of theoretically predicted chemical shifts. In general, due to the fractional radius in the elliptical coordinates,H 2 (1/p )1 H NMR resonance is predicted to be selfH 2 of1 H The NMR resonance is directed towards a high magnetic field where the electrons are significantly closer to the nucleus. Given by the sum of the diamagnetic properties of two electrons and the photon field of amplitude pH 2 (1/p Predicted displacement(Mills GUTCP equation (11.415-11.416)):The first of these applies toH 2 Which forH 2 (1/p ),p = 1 andp = integer >1. Experimental absoluteH 2 The gas phase resonance displacement of -28.0 ppm is consistent with the predicted absolute gas phase shift of -2.801 ppm (Equation (28)). The predicted molecular low-energy hydrogen peak relative to normal H2 Abnormally displaced to a high magnetic field. In an embodiment, the peak is a high magnetic field of TMS. The NMR shift relative to TMS can be greater than the normal H for individual or constituent compounds.- , H, H2 Or H+ At least one of the known NMR shifts. The displacement may be greater than at least one of: 0, -1, -2, -3, -4, -5, -6, -7, -8, -9, -10, -11, -12, - 13,-14, -15, -16, -17, -18, -19, -20, -21, - 22, -23, -24, -25, -26, -27, -28, -29, -30, -31, -32, -33, -34, -35, -36, -37, -38, -39, and -40 ppm. The range of absolute displacement relative to bare protons (where the displacement of TMS is about -31.5 ppm relative to bare protons) can be -(p28.01 + p2 2.56) ppm (Equation (28)), which is in the range of at least one of: ± 5 ppm, ± 10 ppm, ± 20 ppm, ± 30 ppm, ± 40 ppm, ± 50 ppm, ± 60 ppm ± 70 ppm, ± 80 ppm, ± 90 ppm and ± 100 ppm. The absolute displacement relative to the bare proton can be -(p28.01 + p2 1.49 × 10- 3 Ppm (equation (28)), which is in the range of at least one of: 0.1% to 99%, 1% to 50%, and 1% to 10%. Hydrogen donorH 2 (1/p )fromv = 0 transition tov = 1 vibration energyE Vib for:among themp Is an integer. Hydrogen donorH 2 (1/p )fromJ Transition toJ +1 rotation energyE ra t for:among themp Is an integer andI It is the moment of inertia. Observed for electron beam excitation molecules in gas and trapped in a solid matrixH 2 (1/4) of the vibration transmission. Inverse by the distance between the coresp Correlation and inertia momentI Corresponding influencep 2 Correlation.H 2 (1/p Predicted internuclear distance2c 'forH2 At least one of the rotational and vibrational energy of (1/p) can be measured by excitation emission spectroscopy, Raman spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. H2 (1/p) can be trapped in the matrix (such as MOH, MX and M2 CO3 (M = alkali metal; X = halide) in at least one of the matrices) for measurement. In the examples, observed as approximately 1950 cm- 1 The molecular low-energy hydrogen product of the inverse Raman effect (IRE) peak. The peak is enhanced by using a conductive material comprising a roughness characteristic or particle size comparable to the Raman laser wavelength supporting surface enhanced Raman scattering (SERS) to exhibit an IRE peak.I . catalyst In the present invention, such as low-energy hydrogen reaction, H-catalysis, H-catalyzed reaction, catalysis when hydrogen is mentioned, hydrogen reaction for forming low-energy hydrogen, and low-energy hydrogen formation reaction all mean, for example, the following reaction: by the equation (14) Equations (15) to (18) of the defined catalyst are reacted with the atom H to form a hydrogen state having the energy levels given by the equations (10) and (12). When referring to performing a reaction mixture that catalyzes H to an H state or a low energy hydrogen state having the energy levels given by equations (10) and (12), such as a low energy hydrogen reactant, a low energy hydrogen reaction mixture, a catalyst Corresponding terms for mixing, reactants for low energy hydrogen formation, reactants for generating or forming low energy hydrogen or low energy hydrogen are also used interchangeably. The catalytic low energy hydrogen transition of the present invention requires a catalyst that receives energy from atom H to cause a transition, which can be an uncatalyzed atomic hydrogen potential of 27.2.eV Integerm The form of the endothermic chemical reaction. An endothermic catalyst reaction can ionize one or more electrons from a substance such as an atom or an ion (eg, for,m = 3), and may further comprise a bond cleavage and a synergistic reaction of ionizing one or more electrons from one or more initial bond mate (eg, for,m = 2). He + Because with 54.417eV (for 2 • 27.2eV ) ionization, so it meets the catalyst criterion - 焓 is equal to 27.2eV An integral multiple of a chemical or physical process. An integer number of hydrogen atoms can also act as 27.2eV An integer multiple of the catalyst. The catalyst is capable of accepting about 27.2 eV ± 0.5 eV from atomic hydrogen andThe energy of an integer unit of one of them. In an embodiment, the catalyst comprises an atom or an ion M, whereint Electrons from ions or ions M are each ionized to a continuous energy level such thatt The sum of the ionization energies of the electrons is roughlym • 27.2eV andOne of them, of whichm Is an integer. In an embodiment, the catalyst comprises a diatomic molecule MH wherein the M-H bond is brokent Electrons from the atom M respectively ionize to a continuous energy levelt The sum of the bond energy and the ionization energy of an electron is roughlym • 27.2eV andOne of them, of whichm Is an integer. In an embodiment, the catalyst comprises atoms, ions, and/or is selected from the group consisting of molecules AlH, AsH, BaH, BiH, CdH, ClH, CoH, GeH, InH, NaH, NbH, OH, RhH, RuH, SH, SbH, SeH, SiH, SnH, SrH, TlH,C 2 ,N 2 ,O 2 ,C O 2 ,N O 2 andNO 3 Molecules and the following atoms or ions: Li, Be, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Kr, Rb, Sr, Nb, Mo, Pd , Sn, Te, Cs, Ce, Pr, Sm, Gd, Dy, Pb, Pt, Kr, 2K + ,He + ,Ti 2+ ,Na + ,Rb + ,Sr + ,Fe 3+ ,M o 2+ ,Mo 4+ ,In 3+ ,He + ,Ar + ,Xe + ,Ar 2+ andH + ,andNe + as well asH + . In other embodiments, the MH for producing low energy hydrogen is provided by- Type hydrogen catalyst: transfer electrons to the receptor A, M-H bond break plust Electrons are ionized to a continuous level, such that the electron transfer energy, M-H bond energy, and the difference in electron affinity (EA) between MH and A aret The sum of the ionization energies of electrons from M ionization is aboutm• 27.2eV ,among themm Is an integer. Able to providem• 27.2eV Reactive MH- Type hydrogen catalyst is OH- , SiH- CoH- NiH- And SeH- . In other embodiments, the MH for producing low energy hydrogen is provided by+ Type hydrogen catalyst: electrons are transferred from donor A with negative charge, and M-H bond is broken.t Each electron is ionized to a continuous energy level from the atom M, such that the electron transfer energy, M-H bond energy, and the difference between the ionization energies of MH and A aret The sum of the ionization energies of electrons from M ionization is aboutm• 27.2eV ,among themm Is an integer. In an embodiment, at least one of a molecule or a positively or negatively charged molecular ion acts as a catalyst for accepting about m27.2 eV from atom H, wherein the molecular or positively charged or negatively charged molecular ion has a potential energy value. Reduce it by about m27.2 eV. An exemplary catalyst is H2 O, OH, guanamine NH2 And H2 S. O2 Can act as a catalyst or source of catalyst. The bond energy of oxygen molecules is 5.165 eV, and the first, second and third ionization energies of oxygen atoms are 13.61806, respectively.eV , 35.11730eV And 54.9355eV . reactionandProvided separatelyE h About 2 times, 4 times, and 1 times the net enthalpy and contains a catalyst reaction to form low energy hydrogen by accepting such energy from H to form low energy hydrogen.II . Low energy hydrogen HaveThe hydrogen atom giving the binding energy (where p is greater than 1, preferably from 2 to 137) is the product of the H catalytic reaction of the present invention. The binding energy of atoms, ions, or molecules (also known as ionizing energy) is the energy required to remove an electron from an atom, ion, or molecule. The hydrogen atoms having the binding energies given in equations (10) and (12) are hereinafter referred to as "low-energy hydrogen atoms" or "low-energy hydrogens". With radiusThe low energy hydrogen is identified as,among thema H Is the radius of a common hydrogen atom andp Is an integer. With radiusa H The hydrogen atom is hereinafter referred to as "ordinary hydrogen atom" or "normal hydrogen atom". Ordinary atomic hydrogen is characterized by a binding energy of 13.6 eV. According to the present invention, there is provided a low energy hydrino hydride (H) having a binding energy according to equation (19)- ), the binding energy forp = 2 up to 23 is greater than and forp = 24 (H- ) is less than the binding energy of an ordinary hydrogen anion (about 0.75 eV). For equation (19)p = 2 top = 24, the hydrogen anion binding energy is 3, 6.6, 11.2, 16.7, 22.8, 29.3, 36.1, 42.8, 49.4, 55.5, 61.0, 65.6, 69.2, 71.6, 72.4, 71.6, 68.8, 64.0, 56.8, 47.1, 34.7, 19.3 and 0.69 eV. Exemplary compositions comprising novel hydrogen anions are also provided herein. Exemplary complexes comprising one or more low energy hydrino hydride ions and one or more other elements are also provided. Such compounds are known as "low energy hydrogen hydrides". Ordinary hydrogen species are characterized by the following binding energies: (a) a hydrogen anion, 0.754 eV ("ordinary hydrogen anion"); (b) a hydrogen atom ("ordinary hydrogen atom"), 13.6 eV; (c) a diatomic hydrogen molecule, 15.3 eV ("ordinary hydrogen molecule"); (d) hydrogen molecular ion, 16.3 eV ("normal hydrogen molecular ion"); and (e), 22.6 eV ("Ordinary trihydrogen molecular ion"). In this paper, "normal" is synonymous with "ordinary" with respect to the form of hydrogen. According to another embodiment of the present invention, there is provided a compound comprising at least one hydrogen species having increased binding energy, such as: (a) a hydrogen atom having about(such as ina binding energy in the range of about 0.9 to 1.1 times, wherein p is an integer from 2 to 137; (b) a hydride anion (H - ), it has about(such as ina binding energy in the range of about 0.9 to 1.1 times, wherein p is an integer from 2 to 24; (c)(d) three low energy hydrogen molecular ionsIt has about eV (such as in eV a binding energy in the range of about 0.9 to 1.1 times, wherein p is an integer from 2 to 137; (e) a di-low energy hydrogen having about eV (such as in eV a binding energy in the range of about 0.9 to 1.1 times, wherein p is an integer from 2 to 137; (f) a di-low energy hydrogen molecular ion having about eV (such as in eV The binding energy in the range of about 0.9 to 1.1 times, wherein p is an integer, preferably an integer from 2 to 137. According to another embodiment of the present invention, there is provided a compound comprising at least one hydrogen species having increased binding energy, such as: (a) a di-low energy hydrogen molecular ion having about(such as inTotal energy in the range of about 0.9 times to 1.1 times, wherep As an integer,For the Planck constant term,m e For the quality of electronics,c Is the speed of light in a vacuum, andμ a reduced nuclear mass, and (b) a two-low energy hydrogen molecule having about(such as inTotal energy in the range of about 0.9 to 1.1 times, of whichp Is an integer anda o For the Bohr radius. According to an embodiment of the invention wherein the compound comprises a negatively charged binding energy, the compound further comprises one or more cations, such as protons,Or ordinary. Provided herein is a method for preparing a compound comprising at least one low energy hydrino hydride anion. Such compounds are referred to below as "low energy hydrogen hydrides". The method comprises causing atomic hydrogen to react with the reactionCatalyst reaction wherein m is an integer greater than 1, preferably less than 400, such that the binding energy is abouta combination of increased hydrogen atoms, of whichp It is an integer, preferably an integer from 2 to 137. Another catalytic product is energy. A hydrogen atom with increased binding energy can react with an electron source to produce a hydrogen anion with increased binding energy. The hydride anion which is increased in binding energy can react with one or more cations to produce a compound comprising at least one hydrogen anion having increased binding energy. The novel hydrogen composition material may comprise: (a) at least one hydrogen species having a neutral, positive or negative binding energy (hereinafter referred to as "hydrogen species with increased binding energy") (i) greater than a combination of corresponding ordinary hydrogen species Energy, or (ii) greater than any hydrogen species in the corresponding ordinary hydrogen species because the binding energy of ordinary hydrogen species is less than the environmental conditions (standard temperature and pressure, STP), the thermal energy is negative or unstable or not observed And (b) at least one other element. The compound of the present invention is hereinafter referred to as "a hydrogen compound having an increased binding energy". In this context, "other elements" means elements other than hydrogen species that can be combined with increased energy. Therefore, other elements may be ordinary hydrogen species, or any element other than hydrogen. In a group of compounds, other elements and hydrogen species with increased binding energy are neutral. In another group of compounds, other elements and hydrogen species with increased binding energy are charged such that other elements provide an equilibrium charge to form a neutral compound. The former group of compounds is characterized by molecular and coordinate bonding; the latter group is characterized by ionic bonding. Novel compounds and molecular ions are also provided, which comprise: (a) at least one hydrogen species having a neutral, positive or negative total energy (hereinafter referred to as "hydrogen species with increased binding energy") (i) greater than the corresponding ordinary hydrogen The total energy of the substance, or (ii) greater than the total energy of any hydrogen species in the corresponding ordinary hydrogen species because the total energy of the ordinary hydrogen species is less than the thermal energy under ambient conditions or is unstable or unobservable; and (b) At least one other element. The total energy of the hydrogen species is the sum of the energy of all electrons removed from the hydrogen species. The total energy of the hydrogen species according to the invention is greater than the total energy of the corresponding normal hydrogen species. The hydrogen species having an increased total energy according to the present invention is also referred to as "a hydrogen species having increased binding energy", and even some embodiments of the hydrogen species having a total energy increase may have a smaller binding energy than the first electron of the corresponding ordinary hydrogen species. An electron binding energy. For example,p = The first binding energy of the hydride anion of Equation (19) of 24 is smaller than the first binding energy of the common hydride anion, andp The total energy of the hydride anion of equation (19) = 24 is much greater than the total energy of the corresponding common hydride anion. Also provided herein are novel compounds and molecular ions comprising: (a) a plurality of hydrogen species having a neutral, positive or negative binding energy (hereinafter referred to as "hydrogen species with increased binding energy") (i) greater than corresponding The binding energy of the hydrogen species, or (ii) the binding energy of any hydrogen species when the binding energy of the corresponding hydrogen species is less than or equal to the thermal energy under ambient conditions; and (b) ) Another element chosen as appropriate. The compound of the present invention is hereinafter referred to as "a hydrogen compound having an increased binding energy". By at least one of one or more low-energy hydrogen atoms and electrons, low-energy hydrogen atoms, hydrogen species having increased binding energy, and at least one other atom, molecule or One or more of the ionic compounds react to form a hydrogen species with increased binding energy. Novel compounds and molecular ions are also provided, which comprise: (a) a plurality of hydrogen species having a neutral, positive or negative total energy (hereinafter referred to as "hydrogen species with increased binding energy" (i) greater than ordinary molecular hydrogen The total energy, or (ii) greater than the total energy of any hydrogen species in the corresponding ordinary hydrogen species because the total energy of the ordinary hydrogen species is less than or less than the thermal energy under ambient conditions; and (b) as appropriate A further element selected. The compound of the present invention is hereinafter referred to as "a hydrogen compound having an increased binding energy." In the examples, there is provided a compound comprising at least one hydrogen species having an increased binding energy selected from the group consisting of: (a According to the combination of equation (19)p = 2 until 23 is greater than and forp = 24 is less than the binding energy of the common hydrogen anion (about 0.8 eV) of hydrogen anion ("hydrogen anion with increased binding energy" or "low energy hydrogen hydride anion"); (b) binding energy is greater than the binding energy of ordinary hydrogen atoms (about 13.6 eV) hydrogen atom ("hydrogen atom with increased binding energy" or "low energy hydrogen"); (c) hydrogen molecule having a first binding energy greater than about 15.3 eV ("hydrogen molecule with increased binding energy" or " Two low-energy hydrogens) or (d) molecular hydrogen ions ("molecular hydrogen ions with increased binding energy" or "two low-energy hydrogen molecular ions") having a binding energy greater than about 16.3 eV. In the present invention, hydrogen species and compounds which are combined with increased energy are also referred to as low energy hydrogen species and compounds. Low energy hydrogen contains a hydrogen species that binds to an increased hydrogen species or an equivalent lower energy.III . Chemical reactor The present invention is also directed to other reactors for producing hydrogen species and compounds having increased binding energy of the present invention, such as two low energy hydrogen molecules and low energy hydrogen hydrides. Other catalytic products are power and (optionally) plasma and light depending on the type of battery. Such a reactor is hereinafter referred to as a "hydrogen reactor" or a "hydrogen battery." The hydrogen reactor contains a battery for making low energy hydrogen. The battery for making low-energy hydrogen may take the form of a chemical reactor or a gas fuel cell (such as a gas discharge battery), a plasma torch battery or a microwave power battery, and an electrochemical battery. In an embodiment, the catalyst is HOH and the source of at least one of HOH and H is ice. In an embodiment, the battery comprises an arc discharge battery comprising ice and at least one electrode such that the discharge involves at least a portion of the ice. In an embodiment, the arc discharge battery comprises a vessel, two electrodes, a high voltage power source (such as a power source capable of having a voltage in the range of about 100 V to 1 MV and a current in the range of about 1 A to 100 kA) And water sources (such as reservoirs and forming and supplying H2 O droplet component). Droplets can be transported between the electrodes. In an embodiment, the droplets initiate ignition of the arc plasma. In an embodiment, the water arc plasma comprises H and HOH that can react to form low energy hydrogen. The firing rate and corresponding power ratio can be controlled by controlling the droplet size and the rate at which the droplets are supplied to the electrodes. The high voltage source can include at least one high voltage capacitor that can be charged by a high voltage power supply. In an embodiment, the arc discharge cell further comprises components such as a power converter, such as the power converter of the present invention, such as a PV converter and to convert power from low energy hydrogen processes, such as light and heat, into electricity. At least one of the heat engines. An exemplary embodiment of a battery for making low energy hydrogen can take the form of a liquid fuel cell, a solid fuel cell, a heterogeneous fuel cell, a CIHT battery, and an SF-CIHT or SunCell® battery. Each of the batteries comprises: (i) an atomic hydrogen source; (ii) at least one catalyst for making low energy hydrogen selected from the group consisting of a solid catalyst, a molten catalyst, a liquid catalyst, a gaseous catalyst, or a mixture thereof; (iii) a vessel for reacting hydrogen with a catalyst for producing low energy hydrogen. As used herein and as intended by the present invention, unless otherwise specified, the term "hydrogen" includes not only 氕 (1 H ), and including 氘 (2 H ) and 氚 (3 H ). Exemplary chemical reaction mixtures and reactors can comprise the SF-CIHT, CIHT or thermal battery embodiments of the present invention. Additional illustrative examples are given in this chemical reactor section. In the present invention, H is formed during the reaction of the mixture.2 An example of a reaction mixture of O as a catalyst. Other catalysts can be used to form binding energy and hydrogen species and compounds. Can be in, for example, reactants, wt% of reactants, H2 The parameters of the pressure and reaction temperature are adjusted according to these exemplary conditions. Suitable reactants, conditions and ranges of parameters are within the scope of the reactants, conditions and parameters of the invention. Ultra-high H kinetic energy, H-line reversal, and no breakdown electric field, which cannot be explained by the continuous radiation band of an integer multiple of the predicted 13.6 eV, which is measured by the Doppler line broadening of the H line. The formation of a plasma and the duration of the irregular plasma afterglow as reported in the previous publication of Mills shows that the low energy hydrogen and molecular low energy hydrogen are the products of the reactor of the present invention. Information such as data on CIHT batteries and solid fuels has been independently verified by other researchers on the field. The formation of low-energy hydrogen from the battery of the present invention is also evidenced by the continuous output of electrical energy over a longer duration, which is a multiple of the electrical input, which in most cases exceeds the input without the alternative source. 10 times or more. Molecular low energy hydrogen H2 (1/4) identified as a product of a CIHT cell and a solid fuel by MAS H NMR, which exhibits a predicted matrix peak of about -4.4 ppm to a high magnetic field shift; ToF-SIMS and ESI- ToFMS, which shows H2 (1/4) is combined with the gas-gathering agent matrix to become m/e=M+n2 peak, where M is the mass of the parent ion and n is an integer; electron beam excitation emission spectroscopy and photoluminescence emission spectroscopy analysis Forecasted with H2 H times the energy 16 times or the quantum number p=4 square multiple2 (1/4) rotation and vibrational spectra; Raman and FTIR spectroscopy, showing 1950 cm- 1 H2 (1/4) of the rotational energy, which is H2 16 times the rotational energy or squared multiple of the quantum number p=4; XPS, which shows the predicted 500 eV of H2 (1/4) of the total binding energy; and the ToF-SIMS peak of the arrival time before the m/e=1 peak, the m/e=1 peak corresponding to a kinetic energy of about 204 eV H, which will predict the H to The energy release of H(1/4) matches the energy delivered to the third body H, as reported below: Mills' previous publication and R. Mills X Yu, Y. Lu, G Chu, J. He, J Lotoski's "Catalyst Induced Hydrino Transition (CIHT) Electrochemical Cell", International Journal of Energy Research, (2013) and R. Mills, J. Lotoski, J. Kong, G Chu, J. He, J. Trevey - Power-Density Catalyst Induced Hydrino Transition (CIHT) Electrochemical Cell" (2014), which is incorporated herein by reference in its entirety. Using the water flow meter and the Setaram DSC 131 Differential Scanning Calorimeter (DSC), the battery of the present invention was confirmed by observing thermal energy exceeding 60 times the maximum theoretical energy from the solid fuel forming low energy hydrogen ( A low energy hydrogen is formed, such as a battery containing a solid fuel for generating thermal power. MAS H NMR exhibited a predicted H of about -4.4 ppm2 (1/4) High magnetic field matrix displacement. Starting at 1950 cm- 1 Raman peak matching H2 (1/4) free space rotation energy (0.2414 eV). These results are reported in the previous publication by Mills and in "Solid Fuels that Form HOH Catalyst" (2014) by R. Mills, J. Lotoski, W. Good, J. He, which is incorporated herein by reference in its entirety.IV . Solid fuel catalyst induced low energy hydrogen transition ( SF - CIHT ) Battery and power converter In an embodiment, the power system generating at least one of direct electrical energy and thermal energy comprises: at least one container; a reactant comprising: (a) at least one comprising a nascent H2 a catalyst source or catalyst of O; (b) at least one atomic hydrogen source or atomic hydrogen; and (c) at least one of a conductor and a conductive matrix; and at least one electrode for constraining the low energy hydrogen reactant; a power supply for transmitting short pulses of high current electrical energy; a heavy duty system; at least one system for regenerating the initial reactants from the reaction product; and at least one direct converter, such as at least one of the following: a plasma-to-electrical converter (eg, PDC); magnetic fluid power converter; photovoltaic converter; optical rectenna, such as A. Sharma, V. Singh, TL Bougher, BA Cola "A carbon nanotube optical rectenna". Optical rectifying antennas as reported in Nature Nanotechnology, Vol. 10, (2015), pp. 1027-1032, doi: 10.1038/nnano. 2015.220, which is incorporated by reference in its entirety; and at least one thermo-electrical power conversion Device. In another embodiment, the container can have a pressure of at least one of atmospheric pressure, above atmospheric pressure, and below atmospheric pressure. In an embodiment, the regeneration system can include at least one of a hydration, thermal, chemical, and electrochemical system. In another embodiment, the at least one direct plasma-to-electric converter may comprise at least one of the group consisting of: a plasma power converter,Direct converters, magnetohydrodynamic power converters, magnetic mirror magnetic fluid power converters, charge drift converters, rod or louvered power converters, magnetic coils, photon bunched microwave power converters, and opto-electrical converters. In another embodiment, the at least one thermo-electric converter may comprise at least one of the group consisting of: a heat engine, a steam engine, a steam turbine and a generator, a gas turbine and a generator, a Rankine cycle engine, and a brake The cycle engine, the Stirling engine, the thermionic power converter and the thermoelectric power converter. SunCell® can contain multiple electrodes. In an embodiment, the low energy hydrogen reaction occurs selectively at a polarized electrode such as a positive electrode. This reaction selectivity can be attributed to the higher kinetics of the low energy hydrogen reaction at the positive bias electrode. In an embodiment, at least one component of the SunCell®, such as the wall of the reaction cell chamber 5b31, can be positively biased to increase the rate of low energy hydrogen reaction. The SunCell® can include a conductive reservoir 5c coupled to the lower hemisphere 5b41 of the blackbody radiator, wherein the reservoir is positively biased. The bias voltage can be achieved by contact between the molten metal in the reservoir 5c and at least one of the positively biased EM pump tubes 5k6 and 5k61. The EM can be positively biased via the connection of the ignition solenoid pump busbar 5k2a to the positive terminal of the power source 2. Ignition can cause the release of high power EUV light that ionizes the photoactive electrode to generate a voltage at the electrode. The ignition plasma can be light thick for EUV light such that EUV light can be selectively confined to the positive electrode to further cause selective limitations on the photoelectron effect at the positive electrode. SunCell® may further include external circuitry that traverses the electrical load connection to utilize the voltage induced by the optoelectronic effect and the power based on low energy hydrogen. In an embodiment, an ignition event that forms a low energy hydrogen causes an electromagnetic pulse that can be captured as electrical power at a plurality of electrodes, wherein the rectifier can rectify the electromagnetic power. In addition to the UV photovoltaic and thermal photovoltaics of the present invention, SunCell® may include other electrical conversion components known in the art, such as thermionic, magnetohydrodynamic, turbine, microturbine, Rankine or Breiden cycle turbines. , chemical and electrochemical power conversion systems. Rankine cycle turbines can contain supercritical CO2 , organic matter (such as hydrofluorocarbons or fluorocarbons) or a vapor working fluid. In a Rankine or Breiden cycle turbine, SunCell® provides thermal power to at least one of the turbine system's preheater, reheater, boiler, and external burner heat exchanger platforms. In an embodiment, the Breiden cycle turbine includes a SunCell® turbine heater integrated into a combustion section of the turbine. The SunCell® turbine heater can include a conduit for receiving a flow of gas from at least one of a compressor and a reheater, wherein the air is heated and the conduit directs the heated compressed stream to an inlet of the turbine to perform pressure volumetric work. The SunCell® Turbine Heater replaces or supplements the combustion chamber of a gas turbine. The Rankine or Breiden cycle can be turned off, wherein the power converter further includes at least one of a condenser and a cooler. The converter can be a converter given in Mills' previous publication and in Mills' previous application. Low energy hydrogen reactants (such as H source and HOH sources) and SunCell® systems may comprise the invention or a low energy hydrogen reactant such as the following prior US patent application and the SunCell® system: Hydrogen Catalyst Reactor, PCT/US08/ 61455; PCT filed April 24, 2008; Heterogeneous Hydrogen Catalyst Reactor, PCT/US09/052072, PCT filed July 29, 2009; Heterogeneous Hydrogen Catalyst Power System, PCT/US10/27828, March 18, 2010 PCT submitted by Japan; Electrochemical Hydrogen Catalyst Power System, PCT/US11/28889, PCT filed March 17, 2011; H2 O-Based Electrochemical Hydrogen-Catalyst Power System, PCT/US12/31369, filed March 30, 2012; CIHT Power System, PCT/US13/041938, May 21, 2013; Power Generation Systems and Methods Regarding Same, PCT/IB2014/058177, PCT filed on January 10, 2014; Photovoltaic Power Generation Systems and Methods Regarding Same, PCT/US14/32584, PCT filed April 1, 2014; Electrical Power Generation Systems and Methods Regarding Same, PCT/US2015/033165, PCT filed May 29, 2015; Ultraviolet Electrical Generation System Methods Regarding Same, PCT/US2015/065826, PCT filed on December 15, 2015; and Thermophotovoltaic Electrical Power Generator, PCT/US16/ 12620, PCT filed on January 8, 2016 ("Mills Prior Application"), which is incorporated herein by reference in its entirety. In an embodiment, in the case of releasing high energy in the form of at least one of heat, plasma, and electromagnetic (optical) power, ignition H2 O to form low energy hydrogen. ("Ignition" in the present invention means an extremely high reaction rate of H to low energy hydrogen, which may be manifested as an explosion, pulse or other form of high power release). H2 O may comprise a fuel that can be ignited with the application of a high current, such as a high current in the range of about 100 A to 100,000 A. This can be achieved by applying a high voltage, such as about 5,000 to 100,000 V, to first form a highly conductive plasma, such as an electric arc. Or, can make high current through H2 A compound or mixture of O, wherein the resulting fuel, such as a solid fuel, is highly conductive. (In the present invention, a solid fuel is used to refer to a reactant that forms a catalyst that further reacts to form low energy hydrogen such as HOH and H. The plasma voltage can be lower, such as in the range of about 1 V to 100 V. However, the reaction mixture may comprise other physical states than solids. In embodiments, the reaction mixture may be in at least one of the following: a gaseous, liquid, molten matrix (such as a molten conductive substrate such as molten metal, such as molten silver, At least one of silver-copper alloy and copper), solids, slurries, sol-gels, solutions, mixtures, gaseous suspensions, aerodynamic streams, and other conditions known to those skilled in the art). In an embodiment, the solid fuel having very low electrical resistance comprises H2 O reaction mixture. Low electrical resistance can be caused by the conductor component of the reaction mixture. In an embodiment, the electrical resistance of the solid fuel is at least one of the following: about 10-9 Ohm to 100 ohms, 10-8 Ohm to 10 ohms, 10-3 Ohm to 1 ohm, 10-4 Ohm to 10-1 Ohm and 10-4 Ohm to 10-2 ohm. In another embodiment, the fuel having a high electrical resistance comprises H added compound or material having a trace or trace molar percentage2 O. In the latter case, a high current can be passed through the fuel to achieve ignition by causing a breakdown, thereby forming a highly conductive state (such as an electric arc or arc plasma). In an embodiment, the reactants may comprise H2 O source and a conductive substrate to form at least one of a catalyst source, a catalyst, an atomic hydrogen source, and an atomic hydrogen. In another embodiment, H is included2 The O source reactant may comprise at least one of the following: bulk phase H2 O, in addition to body phase H2 State other than O, experience to form H2 O and release combined with H2 One or more compounds of at least one of the reactions of O. In addition, combined with H2 O can be included with H2 O-interacting compound, where H2 O is in absorption H2 O, combined with H2 O, physical adsorption of H2 The state of at least one of O and hydrated water. In embodiments, the reactants may comprise a conductor and one or more compounds or materials that undergo a bulk phase H2 O, absorbed H2 O, combined with H2 O, physical adsorption of H2 At least one of O and the release of water of hydration and the reaction product thereof is H2 O. In other embodiments, the newborn H2 At least one of the O catalyst source and the atomic hydrogen source may comprise at least one of: (a) at least one H2 O source; (b) at least one source of oxygen; and (c) at least one source of hydrogen. In an embodiment, the rate of low energy hydrogen reaction depends on the application or formation of a high current. In an embodiment of the SF-CIHT cell, the reactants that form low energy hydrogen are subjected to low voltage, high current, high power pulses that cause very fast reaction rates and energy release. In an exemplary embodiment, the 60 Hz voltage is less than 15 V peak and the current is at 100 A/cm.2 With 50,000 A/cm2 Within the range between peaks and power at 1000 W/cm2 With 750,000 W/cm2 Between the limits. Other frequencies, voltages, currents, and powers within the range of about 1/100 to 100 times of these parameters are suitable. In an embodiment, the rate of low energy hydrogen reaction depends on the application or formation of a high current. In an embodiment, the voltage is selected to cause a high AC, DC or AC-DC mixture having a current in at least one of: 100 A to 1,000,000 A, 1 kA to 100,000 A, 10 kA to 50 kA. The DC or peak AC current density can be in the range of at least one of: 100 A/cm2 Up to 1,000,000 A/cm2 , 1000 A/cm2 Up to 100,000 A/cm2 And 2000 A/cm2 To 50,000 A/cm2 . The DC or peak AC voltage may be in a range selected from at least one of: about 0.1 V to 1000 V, 0.1 V to 100 V, 0.1 V to 15 V, and 1 V to 15 V. The AC frequency can be in the range of approximately 0.1 Hz to 10 GHz, 1 Hz to 1 MHz, 10 Hz to 100 kHz, and 100 Hz to 10 kHz. The pulse time can be in at least one selected from the group consisting of: about 10- 6 s to 10 s, 10- 5 s to 1 s, 10- 4 s to 0.1 s and 10- 3 s to 0.01 s. In an embodiment, the transfer of energy from atomic hydrogen catalyzed to a low energy hydrogen state results in ionization of the catalyst. Electrons ionized from the catalyst can accumulate in the reaction mixture and vessel and cause space charge buildup. This space charge can change the energy level used for subsequent energy transfer from atomic hydrogen to the catalyst while reducing the rate of reaction. In an embodiment, applying a high current removes space charge to cause an increase in the rate of low energy hydrogen reaction. In another embodiment, a high current such as an arc current causes an extremely rapid increase in the temperature of a reactant (such as water) that can act as an H source and a HOH catalyst. High temperatures can cause water to be pyrolyzed into at least one of the H and HOH catalysts. In an embodiment, the reaction mixture of the SF-CIHT battery comprises a source of H and a catalyst (such asnH The source of (n is an integer) and at least one of HOHs.nH At least one of the HOH and the HOH may be formed by pyrolysis or thermal decomposition of at least one phase of water, such as at least one of solid, liquid, and gaseous water. Pyrolysis can occur at elevated temperatures, such as temperatures in at least one of about 500K to 10,000K, 1000K to 7000K, and 1000K to 5000K. In an exemplary embodiment, the reaction temperature is from about 3,500 to about 4,000 K, such that the mole fraction of atom H is higher, as shown by J. Lede, F. Lapicque, and J Villermaux: [J. Lédé, F. Lapicque, J Villermaux, "Production of hydrogen by direct thermal decomposition of water", International Journal of Hydrogen Energy, 1983,V8 , 1983, pp. 675-679; H. H. G. Jellinek, H. Kachi, "The catalytic thermal decomposition of water and the production of hydrogen", International Journal of Hydrogen Energy, 1984,V9 , pp. 677-688; S. Z. Baykara, "Hydrogen production by direct solar thermal decomposition of water, possibilities for improvement of process efficiency", International Journal of Hydrogen Energy, 2004,V29 , pp. 1451-1458; S. Z. Baykara, "Experimental solar water thermolysis", International Journal of Hydrogen Energy, 2004,V29 , pp. 1459-1469, which is incorporated herein by reference. Pyrolysis can be assisted by a solid surface, such as one of the battery components. The solid surface can be heated to a high temperature by input power and a plasma maintained by a low energy hydrogen reaction. Pyrolysis gases, such as their downward gas flow in the ignition zone, may be cooled to prevent recombination or reverse reaction of the product to the initial water content. The reaction mixture can comprise a coolant at a temperature that is lower than the temperature of the product gas, such as at least one of a solid phase, a liquid phase gas phase. Cooling of the pyrolysis reaction product gas can be achieved by contacting the product with a coolant. The coolant may comprise at least one of low temperature steam, water, and ice. SunCell® can include a pyrolysis hydrogen generator that includes a SunCell® radiator, metal oxide, water source, water spray, and hydrogen and oxygen collection systems. The black body radiation from the black body radiator 5b4 can be incident on a metal oxide which decomposes into oxygen and metal upon heating. The hydrogen generator can include a water source and a spray metal sprayer. The metal can react with water to form metal oxides and hydrogen. Gases can be collected using separators and acquisition systems known in the art. The reaction can be expressed by the following:Metals and oxides can be supported in the art as H2 O Metals and oxides that pyrolyze to form hydrogen, such as ZnO/Zn and SnO/Sn. Other exemplary oxides are manganese oxide, cobalt oxide, iron oxide, and mixtures thereof, as is known in the art and incorporated herein by reference in its entirety.Https :// Wwww . Stage - Ste . Eu / Documents / SF % 201 % 202011 % 20solar _ Fuels % 20by % 20SolarPACES . Pdf Given in . In an embodiment, the SF-CIHT or SunCell® generator includes a power system that produces at least one of electrical energy and thermal energy, comprising: at least one container; a reactant comprising: a) at least one comprising a nascent H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; at least one reactant injection system; at least one reactant ignition system for causing a reactant to form a luminescent plasma And at least one of the pyroelectric plasma; a system for recovering the reaction product of the reactant; at least one regeneration system for regenerating the additional reactant from the reaction product, wherein the additional reactants comprise: a) at least one inclusion Newborn H2 O catalyst source or catalyst; b) at least one H2 O source or H2 O; c) at least one atomic hydrogen source or atomic hydrogen; and d) at least one of a conductor and a conductive substrate; and at least one of the light and heat output to at least one power converter of electrical power and/or thermal power Or an output system, such as one or more of the following groups: photovoltaic converter, photoelectric converter, plasma power converter, thermionic converter, thermoelectric converter, Stirling engine, Breiden cycle engine , Rankine cycle engine, and heat engine and heater. In an embodiment, the pellet fuel may comprise H source, H2 , catalyst source, H2 O source and H2 At least one of O. Suitable pellets comprise a conductive metal matrix and a hydrate, such as at least one of a basic hydrate, an alkaline earth hydrate, and a transition metal hydrate. Hydrate can contain MgCl2 ·6H2 O, BaI2 2·H2 O and ZnCl2 ·4H2 At least one of O. Alternatively, the pellets may comprise at least one of silver, copper, hydrogen absorbed, and water. The ignition system can comprise: a) at least one set of electrodes for constraining the reactants; and b) a power source for delivering short pulses of high current electrical energy, wherein the short pulsed high current electrical energy is sufficient to cause the reactants to react to form a plasma. The power source can receive electrical power from the power converter. In an embodiment, the reactant ignition system includes at least one set of electrodes that are separated to form an open circuit, wherein the open circuit is closed by injecting reactants to cause high current flow to achieve ignition. In an embodiment, the ignition system includes a switch for performing at least one of: initiating current and interrupting current after ignition is achieved. The flow of current can be initiated by the reactants that complete the gap between the electrodes. The switch can be electronically implemented by a member such as at least one of: an insulated gate bipolar transistor (IGBT), a controlled voltage rectifier (SCR), and at least one metal oxide semiconductor field effect transistor (MOSFET). Alternatively, the ignition can be switched mechanically. The current can be interrupted after ignition to optimize the energy produced by the output low energy hydrogen relative to the input ignition energy. The ignition system can include a switch that allows a controlled amount of energy to flow into the fuel during the phase in which the plasma is generated to cause knocking and turn off the power. In an embodiment, the power supply for transmitting the short pulse high current electrical energy comprises at least one of: a voltage selected to generate a high AC, DC or AC-DC current mixture, the current being between 100 A and 1,000,000 A, a range of at least one of 1 kA to 100,000 A, 10 kA to 50 kA; DC or peak AC current density in the range of at least one of: 100 A/cm2 Up to 1,000,000 A/cm2 , 1000 A/cm2 Up to 100,000 A/cm2 And 2000 A/cm2 Up to 50,000 A/cm2 Where the voltage is determined by the conductivity of the solid fuel, wherein the voltage is obtained by multiplying the required current by the resistance of the solid fuel sample; DC or peak AC voltage is between 0.1 V and 500 kV, 0.1 V to 100 kV and 1 V to SF-CIHT battery in the range of at least one of 50 kV and AC frequency in the range of 0.1 Hz to 10 GHz, 1 Hz to 1 MHz, 10 Hz to 100 kHz, and 100 Hz to 10 kHz The output power can include thermal and photovoltaic to convert the optical power. In an embodiment, the opto-electrical converter can include a converter that utilizes at least one of a photovoltaic effect, a thermionic effect, and a photoelectron effect. The power converter can be a direct power converter that converts the kinetic energy of high kinetic energy into electricity. In an embodiment, the power of the SF-CIHT battery may be at least partially in the form of thermal energy or may be at least partially converted to thermal energy. The power converter can include a thermionic power converter. An exemplary thermionic cathode can comprise erbium-doped tungsten. The cell can utilize photon enhanced thermionic emission (PETE), wherein the optical effect enhances electron emission by causing electron energy in the semiconductor emitter to rise across the band gap and into the conduction band of the thermally emitted electrons. In an embodiment, the SF-CIHT battery can include a light absorber such as at least one of extreme ultraviolet (EUV), ultraviolet (UV), visible, and near infrared light. The absorbent can be external to the battery. For example, it can be external to the window of PV converter 26a. The temperature of the absorbent can be increased by absorption. The absorbent temperature can range from about 500 °C to 4000 °C. This heat can be input to a thermal photovoltaic or thermo-ionic battery. Thermoelectric and heat engines such as Stirling, Rankine, Braden and other heat engines known in the art are within the scope of the present invention. At least one first optical-to-electrical converter of a plurality of converters, such as an optical-to-electrical converter utilizing at least one of a photovoltaic effect, a thermionic effect, and a photoelectron effect, may have a selectivity to a first portion of the electromagnetic spectrum And through at least the second part of the electromagnetic spectrum. The first portion can be converted to electricity in the corresponding first converter, and the second portion of the first converter that is not selective can be propagated to another one that is selective to at least a portion of the second portion of the electromagnetic spectrum propagation Two converters. In an embodiment, the SF-CIHT battery or generator (also referred to as SunCell®) shown in Figures 2I28, 2I69, and 2I80 through 2I149® Contains six basic easy-to-maintain systems, some with no moving parts and capable of long-term operation: (i) Inductively coupled heaters, which include a power supply 5m, leads 5p and antenna coils 5f to melt the silver first or Silver-copper alloy to form a molten metal or melt; and optionally an electrode electromagnetic pump comprising a magnet for initially directing the ignition plasma flow; (ii) a fuel injector, such as comprising a hydrogen supply (such as a fuel injector of a black body radiator, wherein hydrogen can be obtained from water by electrolysis or pyrolysis; and an injection system comprising an electromagnetic pump 5ka for spraying molten silver or molten silver-copper alloy and an oxygen source (such as oxides, such as LiVO3 Or another oxide of the present invention; and, alternatively, a gas injector 5z1 for injecting at least one of water vapor and hydrogen; (iii) an ignition system for generating a low voltage across a pair of electrodes 8. High current flow, molten metal, hydrogen and oxide, or molten metal and H2 At least one of O and hydrogen is injected into the pair of electrodes to form a brightened photo-plasma; (iv) a black body radiator heated by plasma to an incandescent temperature; (v) an optical-to-electrical converter 26a comprising So-called concentrating photovoltaic cells 15 that receive light from a black body radiator and operate at high light intensity, such as over one thousand suns; and (vi) a fuel recovery and thermal management system 31, The molten metal is returned to the injection system after ignition. In another embodiment, light from the ignition plasma can be directly radiated to the PV converter 26a for conversion to electricity. In one embodiment, the plasma emits a significant portion of the optical power and energy in the form of EUV and UV light. The pressure can be lowered by maintaining a vacuum in the reaction chamber cell 1 to maintain the plasma under optically less thick conditions, thereby reducing the attenuation of short-wavelength light. In one embodiment, an opto-electrical converter comprises a photovoltaic converter of the present invention comprising a photovoltaic (PV) cell responsive to a substantial wavelength region of light emitted from the cell , such as a wavelength range corresponding to at least 10% of the optical power output. In an embodiment, the fuel may comprise having trapped hydrogen and trapped H2 Silver of at least one of O. The light emission may mainly comprise ultraviolet light, such as light in a wavelength region of about 120 nm to 300 nm. The PV cell can respond to at least a portion of the wavelength region from about 120 nm to 300 nm. The PV cell may comprise a Group III nitride, such as at least one of InGaN, GaN, and AlGaN. In an embodiment, the PV cell comprises SiC. In an embodiment, the PV cell can include a plurality of junctions. The junctions can be layered in series. In another embodiment, the junctions are independent or electrically connected in parallel. The individual junctions can be mechanically stacked or wafer bonded. At least one of the multi-junction cells and the layers of the series connected cells may include a bypass diode to minimize current and power losses caused by current mismatch between the various layers of the battery, illustratively multi-connected The face PV cell comprises at least two junctions comprising an np-doped semiconductor, such as a plurality of groups of InGaN, GaN, and AlGaN. The n-type dopant of GaN may comprise oxygen, and the p-type dopant may comprise Mg. An exemplary triple junction cell can comprise InGaN//GaN//AlGaN, where // can refer to an isolating transparent wafer bonding layer or mechanical stack. The PV can operate at a high light intensity equal to that of a concentrating photovoltaic device (CPV). The substrate can be at least one of sapphire, Si, SiC, and GaN, with the latter two providing optimal lattice matching for CPV applications. The layers can be deposited using the organometallic vapor phase epitaxy (MOVPE) process known in the art. The cells can be cooled by cold plates, such as those used in CPV or diode lasers, such as commercial GaN diode lasers. As in the case of a CPV battery, the grid contacts can be mounted on the front and back surfaces of the battery. In an embodiment, the PV converter can have a protective window that is substantially permeable to the light it is responsive to. The window can transmit at least 10% of the response light. The window is transparent to UV light. The window can include a coating, such as a UV clear coating, on the PV cell. The coating may comprise a material of the UV window of the invention, such as sapphire or MgF2 window. Other suitable windows include LiF and CaF2 . The coating can be applied by deposition, such as vapor deposition. The battery of PV converter 26a may include a photonic design that forces the emitter and battery single mode to perform cross-resonant coupling and impedance matching only over the semiconductor bandgap, thereby creating a "squeezed" narrowband near-field emission spectrum. In particular, exemplary PV cells can include surface plasma polarized phonon thermal emitters and silver blanket semiconductor thin film photovoltaic cells. The EM pump 5ka (Fig. 2I28, 2I69 and Fig. 2I80 to Fig. 2I163) may comprise an EM pump heat exchanger 5k1, an electromagnetic pump coolant line feedthrough assembly 5kb, a magnet 5k4, a yoke and optionally may optionally have A radiation barrier gas or vacuum gap thermal barrier 5k5, a pump tube 5k6, a busbar 5k2 and a busbar current source connection 5k3 having a feedthrough 5k31 that can be supplied by current from the PV converter. At least one of the magnet 5k4 and the yoke 5k5 of the magnetic circuit may be cooled by the EM pump heat exchanger 5k1, such as an EM pump heat exchanger cooled with a coolant such as water, having a coolant inlet to the chiller 31a The line 31d and the coolant outlet line 31e. The exemplary EM pump magnet 5k4 includes at least one of cobalt ruthenium (such as SmCo-30MGOe and neodymium iron boron (N44SH)) magnets. The magnet can include a return magnetic flux circuit. In an embodiment, at least one of very high power and energy may be achieved by a transition of hydrogen to a low energy hydrogen having a high p value in equation (18) during a process referred to herein as disproportionation. As given in Mills GUT Chp. 5, it is incorporated by reference. A hydrogen atomH (1/p )p = 1, 2, 3, ... 137 may undergo further transitions from the equations (10) and (12) to the lower energy states, where the transition of one atom is accepted by resonance and non-radiationm • 27.2eV And catalyzed by another atom whose opposite change in potential energy. Given by equation (35)m • 27.2eV Resonance transfer toH (1/p ') inducedH (l/p) transition toH (1/(p +m The general general equation is expressed as follows:EUV light from a low energy hydrogen process can dissociate low energy hydrogen molecules and the resulting low energy hydrogen atoms can act as a catalyst to transition to a lower energy state. An exemplary reaction involves catalyzing H to H(1/17) by H(1/4), where H(1/4) can be the reaction product that catalyzes another H by HOH. The disproportionation reaction of low energy hydrogen is predicted to produce features in the X-ray region. As shown by equations (5) to (8), the reaction product of the HOH catalyst is. Considering H2 It is likely that there is a transition reaction in the hydrogen cloud of O gas, in which the first hydrogen atomIs a H atom and acts as a second acceptor hydrogen atom of the catalystfor. due toThe position can be 42 • 27.2eV = 16• 27.2eV = 435.2eV Therefore, the transition response is represented by the following:And the total response isForecast is attributed toThe far ultraviolet continuous radiation band of the intermediate (eg, equations (16) and (37)) has a short wavelength cutoff and is given by the energy given below:And extending to a longer wavelength than the corresponding cutoff. Here, the prediction is attributed toThe far-ultraviolet continuous radiation spectrum of the decay of the intermediateE = 3481.6eV ;0.35625Nm It has a short wavelength cutoff and extends to longer wavelengths. NASA's Chandra X-ray Observatory and XMM-Newton [E. Bulbul, M. Markevitch, A. Foster, RK Smith, M. Loewenstein, SW Randall, "Detection of an unidentified emission line in The stacked X-Ray spectrum of galaxy clusters", The Astrophysical Journal, Vol. 789, No. 1, (2014); A. Boyarsky, O. Ruchayskiy, D. Iakubovskyi, J. Franse, "An unidentified line in X- Ray spectra of the Andromeda galaxy and Perseus galaxy cluster", (2014), arXiv: 1402.4119 [astro-ph.CO]] Recently observed a wide X-ray peak with a 3.48 keV cutoff in the constellation of Perseus, which does not match any Atomic transitions are known. The distribution of BulBul et al. gives a 3.48 keV feature match for dark matter with unknown identityThe transition further confirms that low-energy hydrogen is the identity of dark matter. In an embodiment, the generator can utilize a low pressure H2 O produces high power and energy. The water vapor pressure may be in at least one of the following: about 0.001 Torr to 100 Torr, 0.1 mTorr to 50 Torr, 1 mTorr and 5 Torr, 10 mTorr to 1 Torr, and 100 mTorr to 800 Torr. Low H2 The O vapor pressure may be at least one of the following: supply and maintenance of a component from a source of water vapor and at least one of a flow rate and a pressure. The water supply can be sufficient to maintain the desired ignition rate. The water vapor pressure can be controlled by at least one of steady state or dynamic control and balance control. The generator may include a pump 13a that maintains a lower water vapor pressure in the desired zone. Water can be removed by differential pumping such that the area of the cell outside of the electrode area can have a lower pressure, such as a lower partial pressure of water. The battery water vapor pressure can be maintained by a reservoir/trap connected to the battery. The battery water vapor pressure may be at least one of a steady state or a water vapor pressure balance above the water level of the reservoir/trap. The water reservoir/trap may contain components to reduce vapor pressure, such as a chiller that maintains a contrast temperature (such as a cryogenic temperature) and a H such as activated charcoal or desiccant and solute.2 At least one of the O absorbing materials. The water vapor pressure can be a low pressure established by equilibrium or steady state through cold ice. Cooling may include a low temperature chiller or bath such as carbon dioxide, liquid nitrogen or a liquid bath. Solutes can be added to the reservoir/trap to reduce water vapor pressure. The vapor pressure can be lowered according to Law Law. The solute can be highly soluble and highly concentrated. Exemplary solutes are sugars and ionic compounds such as alkali metals, alkaline earth metals and at least one of ammonium halides, ammonium hydroxide, ammonium nitrate, ammonium sulfate, ammonium dichromate, ammonium carbonate and ammonium acetate, such as K.2 SO4 KNO3 , KCl, NH4 SO4 , NaCl, NaNO2 Na2 Cr2 O7 , Mg (NO3 )2 , K2 CO3 MgCl2 KC2 H3 O2 , LiCl and KOH. The trap desiccant may comprise a molecular sieve such as an exemplary molecular sieve 13X, 4-8 mesh agglomerated. In embodiments where excess water is removed, the trap can be sealed and heated; subsequently, the liquid water can be pumped out or it can be discharged as steam. The trap can be recooled and re-run. In an embodiment, H will be2 Add to such an area as the electrode, with O2 The reaction product reacts to convert it to water controlled by a water reservoir/trap. H2 It can be provided by electrolysis at a hydrogen absorbing cathode such as a PdAg cathode. The hydrogen pressure can be monitored using a sensor that provides a feedback signal to a hydrogen supply controller, such as an electrolysis controller. In an exemplary embodiment, the moisture pressure is maintained at a desired pressure (such as at a pressure in the range of about 50 mTorr to 500 mTorr) by an aqueous molecular sieve such as 13X. Any water released from the molecular sieve can be replaced by a water supply, such as a supply of water from a storage tank 31l supplied by a corresponding manifold and line. The area of the molecular sieve may be sufficient to supply water at least at the rate required to maintain the desired partial pressure. The exhaust gas rate of the molecular sieve can be matched with the sum of the consumption rate of the low energy hydrogen process and the pumping rate. At least one of the release rate and the partial pressure can be controlled by controlling the temperature of the molecular sieve. The battery can include a controller that is coupled to the molecular sieve of battery 26. The container may further comprise means for maintaining the temperature of the molecular sieve, such as a heater and chiller and a temperature controller. In an alternative steady state embodiment, the water vapor pressure is maintained by a flow controller, such as a flow controller that controls at least one of mass flow and water vapor pressure in the battery. The water supply rate can be adjusted to match the rate of consumption in low energy hydrogen and any other battery reaction and the rate of removal by means such as pumping. The pump may include at least one of a water reservoir/trap, a cryopump, a vacuum pump, a mechanical vacuum pump, a scroll pump, and a turbo pump. At least one of the supply rate and the removal rate can be adjusted to achieve the desired battery water vapor pressure. In addition, the desired partial pressure of hydrogen can be added. H2 O and H2 At least one of the pressures can be sensed and controlled by sensors and controllers such as pressure gauges such as Baratron gauges and mass flow controllers. Water may be injected by the flow controller via the EM pump tube 5k4, which may further include a pressure trap and a backflow check valve that prevents molten metal from flowing back into the water supply, such as a mass flow controller. The gas can be supplied by a syringe pump. As an alternative to the mass flow controller, the water vapor pressure may be maintained by a high precision electronically controllable valve, such as at least one of a needle valve, a proportional electronic valve, and a stepper motor valve. The valve can be controlled by a water vapor pressure sensor and computer to maintain the battery water vapor pressure at a desired value, such as in the range of about 0.5 Torr to 2 Torr, wherein the control can achieve a small tolerance, such as within 20%. The valve can have a quick response to maintain tolerances if the water vapor pressure in the battery changes rapidly. The dynamic range of flow through the valve can be adjusted to accommodate different minimum and maximum ranges by varying the water vapor pressure on the supply side of the valve. The supply side pressure can be increased or decreased by increasing or decreasing the temperature of the accumulator 31l, respectively. Water can be supplied via the EM pump tube 5k6. In another embodiment, at least one of water (such as steam) and hydrogen may be simultaneously sprayed with molten metal, such as molten silver metal. At least one of the water, steam, and hydrogen injectors can include a transfer tube that terminates in a fast solenoid valve. The solenoid valve may be electrically coupled to the electrode in at least one of series and parallel such that current flows through the valve as current flows through the electrode. In this case, at least one of water (such as steam) and hydrogen may be simultaneously sprayed with the molten metal. In another embodiment, the injector system includes an optical sensor and a controller that causes the injection. The controller can open and close a quick valve (such as a solenoid valve) when metal injection or ignition is sensed. In an embodiment, the lines used to inject at least two of a melt (such as a silver melt), water (such as steam), and hydrogen may be coincident. Coincidence can be via a common pipeline. In an embodiment, the injector comprises an injection nozzle. The nozzle of the injector may comprise a gas manifold, such as a gas manifold aligned with the flow of metal comprising electrode 8. The nozzle may further comprise a plurality of pinholes from the manifold, which deliver H2 O and H2 Multiple gas jets of at least one of them. In an embodiment, H is made at a pressure greater than the pressure of the battery2 Bubbling through H2 O reservoir, and H2 O is entrained in H2 In the carrier gas. The high pressure gas mixture flows through the pinholes into the melt to maintain a gas jet. At the electrode, a gas which can be a mixture can be combined with a conductive substrate (metal melt). With high current applied, the corresponding fuel mixture can be ignited to form low energy hydrogen. In embodiments that improve the energy balance of the generator, a chiller such as 31 can be driven by thermal power that includes the heat generated by the battery. Thermal power can come from internal dissipation and from low energy hydrogen reactions. The chiller may comprise an absorption chiller known to those skilled in the art. In an embodiment, the heat to be discharged is absorbed by a coolant refrigerant such as vaporizable water. The absorption chiller can use heat to condense the refrigerant. In the examples, water vapor is absorbed into an absorbent material (adsorbent) such as silicone, zeolite or a nanostructure material such as the nanostructured material of P. McGrail of Pacific Northwest Laboratory. The absorbed water is heated to release it in the chamber, wherein an increase in pressure is sufficient to cause the water to condense. The SF-CIHT generator contains components whose parameters are such as sensed and controlled parameters in the present invention. In an embodiment, a computer having a sensor and control system can sense and control: (i) each of each cooled system (such as at least one of a PV converter, an EM pump magnet, and an inductively coupled heater) Quench cooler inlet and outlet temperatures and coolant pressure and flow rate, (ii) ignition system voltage, current, power, frequency and duty cycle, (iii) using optical, Doppler, Lorentz or electrode resistance sensing EM pump injection flow rate of the sensor and controller, (iv) voltage, current and power of the inductively coupled heater and electromagnetic pump 5k, (v) pressure in the battery, (vi) wall temperature of the battery component, (vii) heater power in each zone, (viii) current and flux of the electromagnetic pump, (ix) silver melting temperature, flow rate and pressure, (xi) formed by the regulator via common gas injection Each permeated or injected gas (such as H) delivered by the tube2 And H2 O and mixture) pressure, temperature and flow rate, (xi) intensity of light incident on the PV converter, (xii) voltage, current and power output of the PV converter, (xiii) voltage and current of any power conditioning equipment , power and other parameters, and (xiv) to SF-CIHT generator output voltage, current and power to at least one of parasitic load and external load, (xv) to any parasitic load (such as inductively coupled heater, electromagnetic pump The voltage, current, and power inputs of the chiller and at least one of the sensors and controls, and (xvi) the voltage, current, and state of charge of the starting circuit with energy storage. In an embodiment, the parameter to be measured may be separated from a region of the system that will damage the high temperature of the sensor during its measurement. For example, such as H2 And H2 The pressure of the gas of at least one of O can be measured by using a connecting gas line, such as a battery (e.g., 5b or 5c) and a pressure transducer (such as a Baratron capacitive pressure gauge). Cooling tower before cooling the gas. Where the parameters are outside the desired range (such as undergoing over-temperature), the generator may include a safety shut-off mechanism, such as a mechanism known in the art. The shutdown mechanism can include a computer and a switch that provides power to at least one component of the generator that can be disconnected to cause a shutdown. In an embodiment, the battery may comprise at least one gas collector, such as at least one for air, oxygen, hydrogen, CO2 And the gas collector of water. An oxygen gassing agent such as an oxygen reactive material such as finely pulverized carbon or metal can remove any oxygen formed in the battery. As for carbon, reversible CO can be utilized2 The detergent extracts the product carbon dioxide. Carbon dioxide detergents are known in the art, such as organic compounds such as amines (e.g., monoethanolamine), minerals and zeolites, sodium hydroxide, lithium hydroxide, and metal oxide based systems. The finely pulverized carbon gas collector can also be used to remove oxygen to protect the battery, such as the purpose of an oxygen sensitive material in an oxygen sensitive material such as a container or pump tube of Mo, W, graphite, and Ta. In this case, carbon dioxide can use CO2 The detergent is removed or pumped out using a vacuum pump where the finely pulverized carbon is used only for component protection. Metal gas collector can be selectively selected with H2 The oxygen reaction on O allows it to be regenerated using hydrogen. Exemplary metals having low water reactivity include metals of the group: Cu, Ni, Pb, Sb, Bi, Co, Cd, Ge, Au, Ir, Fe, Hg, Mo, Os, Pd, Re, Rh , Ru, Se, Ag, Tc, Te, Tl, Sn, W, and Zn. The gassing agent or oxygen detergent can be removed from the SF-CIHT battery and regenerated. This removal can be periodic or intermittent. This regeneration can be achieved by hydrogen reduction. This regeneration can occur in situ. In situ regeneration can be intermittent or continuous. Other oxygen gas collectors and their regeneration are known to those skilled in the art, such as zeolites and compounds that form oxygen-containing reversible ligand bonds, such as salts, such as those associated with 2-aminoterephthalate. Nitrate, [{(bpbp)Co2 II (NO3 )}2 (NH2 Bdc)] (NO3 )2 .2H2 O (bpbp- = 2,6-bis(N,N-bis(2-pyridylmethyl)aminemethyl)-4-t-butylphenolate, NH2 Bdc2 - = 2-Amino-1,4-phenyldicarboxylate). Highly flammable metals such as the exemplified metals: alkali metals, alkaline earth metals, aluminum and rare earth metals can also be used as oxygen gas collectors. Highly flammable metals can also be used as water scavengers. Hydrogen storage materials can be used to scavenge hydrogen. Exemplary hydrogen storage materials include metal hydrides, Mickey alloys (such as M1: La-rich Mickey alloys, such as M1Ni)3 . 65 Al0 . 3 Mn0 . 3 Or M1 (NiCoMnCu)5 , Ni, R-Ni, R-Ni + about 8 wt% Vulcan XC-72, LaNi5 , Cu or Ni-Al, Ni-Cr (such as about 10% Cr), Ce-Ni-Cr (such as about 3/90/7 wt%), Cu-Al or Cu-Ni-Al alloy), MNH system Substance (such as LiNH2 Li2 NH or Li3 N), and an alkali metal hydride further comprising boron (such as borohydride) or aluminum (such as aluminum hydride). Further suitable hydrogen storage materials are: metal hydrides such as alkaline earth metal hydrides (such as MgH)2 ); metal alloy hydride (such as BaReH)9 LaNi5 H6 , FeTiH17 And MgNiH4 ); metal borohydride (such as Be (BH)4 )2 ,Mg(BH4 )2 , Ca (BH4 )2 Zn(BH4 )2 , Sc (BH4 )3 , Ti (BH4 )3 , Mn (BH4 )2 , Zr (BH4 )4 NaBH4 LiBH4 , KBH4 And Al (BH4 )3 AlH3 NaAlH4 Na3 AlH6 LiAlH4 Li3 AlH6 , LiH, LaNi5 H6 La2 Co1Ni9 H6 And TiFeH2 NH3 BH3 , polyaminoborane, amine borane complex (such as amine borane, borane ammine, hydrazine-borane complex, diborane diammine, boron azide and octahydrotriboronium Or ammonium tetrahydroborate; imidazolium ionic liquid (such as alkyl (aryl)-3-methylimidazolium N-bis(trifluoromethanesulfonyl) sulfinium salt, barium borate and oxalate material). Further exemplary compounds are ammonia borane, alkali ammonia borane (such as lithium ammonia borane) and borane alkylamine complex (such as borane dimethylamine complex, borane trimethylamine complex) and Aminoborane and borane amine (such as aminodiborane, n-dimethylaminodiborane, tris(dimethylamino)borane, di-n-butylboronamine, dimethylaminoborane, Trimethylaminoborane, ammonia-trimethylborane and triethylaminoborane. Other suitable hydrogen storage materials are hydrogen-absorbing organic liquids such as oxazoles and derivatives such as 9- (2-ethylhexyl)carbazole, 9-ethylcarbazole, 9-phenyloxazole, 9-methylcarbazole and 4,4'-bis(N-carbazolyl)-1,1'- Biphenyl. The gas collector may comprise an alloy capable of storing hydrogen, such as AB5 (LaCePrNdNiCoMnAl) or AB2 One of the (VTiZrNiCrCoMnAlSn) types, of which "ABX The mark refers to the ratio of the A-type element (LaCePrNd or TiZr) to the B-type element (VNiCrCoMnAlSn). An additional suitable hydrogen gas collector is a hydrogen gas collector used in a metal hydride battery, such as a nickel-metal hydride battery known to those skilled in the art. An exemplary suitable gas collector material for a hydride anode comprises R-Ni, LaNi5 H6 La2 Co1 Ni9 H6 , ZrCr2 H3 . 8 LaNi3 . 55 Mn0 . 4 Al0 . 3 Co0 . 75 ZrMn0 . 5 Cr0 . 2 V0 . 1 Ni1 . 2 Hydrides in the group and other alloys that can store hydrogen, such as AB5 (LaCePrNdNiCoMnAl) or AB2 One of the (VTiZrNiCrCoMnAlSn) types, of which "ABX The mark refers to the ratio of the A-type element (LaCePrNd or TiZr) to the B-type element (VNiCrCoMnAlSn). In other embodiments, the hydride anode gas generant material comprises at least one of the following: MmNi5 (Mm = Michao alloy), such as: MmNi3.5 Co0.7 Al0.8 , AB5 - Type: MmNi3.2 Co1.0 Mn0.6 Al0.11 Mo0.09 (Mm = Mickey alloy: 25 wt% La, 50 wt% Ce, 7 wt% Pr, 18 wt% Nd); La1-y Ry Ni5-x Mx , AB2 - Type: Ti0.51 Zr0.49 V0.70 Ni1.18 Cr0.12 Alloy; magnesium-based alloy, such as Mg1.9 Al0.1 Ni0.8 Co0.1 Mn0.1 Alloy, Mg0.72 Sc0.28 (Pd0.012 + Rh0.012 ) and Mg80 Ti20 , Mg80 V20 La0.8 Nd0.2 Ni2.4 CO2 .5 Si0.1 LaNi5-x Mx (M = Mn, Al), (M = Al, Si, Cu), (M = Sn), (M = Al, Mn, Cu) and LaNi4 Co, MmNi3.55 Mn0.44 Al0.3 Co0.75 LaNi3.55 Mn0.44 Al0.3 Co0.75 ,McCu2 MgZn2 MgNi2 , AB compounds such as TiFe, TiCo and TiNi, ABn Compound (n = 5, 2 or 1), AB3-4 Compound and ABx (A = La, Ce, Mn, Mg; B = Ni, Mn, Co, Al). Other suitable hydride gas collectors are ZrFe2 Zr0 . 5 Cs0 . 5 Fe2 Zr0 . 8 Sc0 . 2 Fe2 YNi5 LaNi5 LaNi4 . 5 Co0 . 5 , (Ce, La, Nd, Pr) Ni5 , Mi Xu alloy - nickel alloy, Ti0 . 98 Zr0 . 02 V0 . 43 Fe0 . 09 Cr0 . 05 Mn1 . 5 La2 Co1Ni9 , FeNi and TiMn2 . The gas accumulating agent of the present invention and other gas accumulating agents known to those skilled in the art may comprise more than one type of gas collector gas. The additional gassing agent can be a gassing agent known to those skilled in the art. An exemplary multi-gas entrainer comprises an alkali metal or alkaline earth metal such as lithium, which can remove O2 , H2 O and H2 At least two of them. The gassing agent can be regenerated by methods known in the art, such as by reduction, decomposition, and electrolysis. In an embodiment, the gas-collecting agent may include a cryogenic trap that performs at least one of: condensing a gas such as at least one of water vapor, oxygen, and hydrogen; and trapping the gas in an absorbing material in a cooled state in. The gas can be released from the absorbent material at a higher temperature so that the gas accumulating agent can be regenerated as it is heated and pumped. Exemplary materials that can be regenerated by heating and pumping, which absorb at least one of water vapor, oxygen, and hydrogen, are carbon, such as activated charcoal and zeolite. The timing of oxygen, hydrogen, and water detergent regeneration can be determined when the corresponding gas level is increased to an unacceptable level sensed by a sensor of the corresponding cell gas content. In an embodiment, at least one of hydrogen and oxygen produced by the battery can be collected and sold as a commercial gas by systems and methods known to those skilled in the art. Alternatively, the hydrogen collected can be used in SunCell®. The hydrogen and water incorporated into the melt can flow from the storage tanks 5u and 311 through the manifold and the feed line under pressure generated by a corresponding pump such as a mechanical pump. Alternatively, the water pump may be replaced by heating the water tank 31l to form a vapor pressure, and the hydrogen pump may be replaced by electrolysis to generate a pressure for flowing the hydrogen gas. Or by H2 O storage tank 31l, steam generator and steam relationship are provided in the form of steam H2 O. Hydrogen is permeable to the hollow cathode connected to the hydrogen storage tank pressurized by electrolysis or pyrolysis. Such replacement systems eliminate corresponding systems with moving parts. In an embodiment, the SF-CIHT battery assembly and system is at least one of: combined, miniaturized, and otherwise optimized for at least one of weight and size reduction, cost reduction, and maintenance reduction. By. In an embodiment, the SF-CIHT battery includes a common compressor for the chiller and the battery vacuum pump. The chiller for heat rejection can also act as a cryopump to act as a vacuum pump. H2 O and O2 It can be condensed by a cryopump. In an embodiment, the ignition system comprising a set of capacitors is miniaturized by using a reduced number of capacitors, such as an exemplary single 2.75 V, 3400 3400 Maxwell supercapacitor, as close as possible to the electrodes. In an embodiment, the positive terminal of the at least one capacitor may be directly connected to the positive bus bar or the positive electrode and the negative terminal of the at least one capacitor may be directly connected to the negative bus bar or the negative electrode, wherein other terminals of the capacitor having opposite polarities may be borrowed Connected by the bus bars such that when the molten metal closes the circuit by bridging the electrodes that may include the molten metal injector, current flows through the circuit containing the capacitor. If desired, the set of capacitors connected in series across the electrodes can be replicated an integer multiple to provide approximately an integer multiple of current. In an embodiment, the voltage across the capacitor can be maintained within a desired range by utilizing power charging from the PV converter. The power regulation of the SF-CIHT generator can be simplified by using all DC power of the internal load, where the DC power is supplied by the PV converter. In an embodiment, the DC power from the PV converter can be supplied to at least one of: (i) DC charging power to a capacitor of the ignition system of the electrode 8 including the power source 2; (ii) DC of at least one electromagnetic pump Current; (iii) DC power of a resistive or inductively coupled heater; (iv) DC power of a chiller comprising a DC electric motor; (v) DC power of a vacuum pump comprising a DC electric motor; and (vi) to a computer and The DC power of the sensor. The output power adjustment can include DC power from the PV converter or AC power from a process that uses an inverter to convert DC power from the PV converter to AC. In an embodiment, the opto-electrical converter comprises a photovoltaic converter of the invention comprising a photovoltaic (PV) cell responsive to a substantial wavelength region of light emitted from the battery, such as corresponding to at least 10% The wavelength range of the optical power output. In one embodiment, the PV cell is a concentrating cell that can accept high intensity light greater than daylight intensity, such as at least one of about 1.5 suns to 75,000 suns, 10 suns to 10,000 suns, and 100 suns to 2000 suns. Within the strength range. The concentrating PV cell can comprise c-Si that can operate in the range of about 1 to 1000 suns. The 矽PV cell can operate at a temperature that performs at least one of the following functions: improved bandgap to better match the blackbody spectrum and improved heat rejection to reduce the complexity of the cooling system. In an exemplary embodiment, the concentrating PV cell is operated at 200 to 500 Suns at about 130 ° C to provide a band gap of about 0.84 V to match the spectrum of the 3000 ° C blackbody radiator. A PV cell can include a plurality of junctions, such as triple junctions. The concentrating PV cell can comprise a plurality of layers, such as a layer of a III/V semiconductor, such as at least one of the group of: InGaP/InGaAs/Ge; InAlGaP/AlGaAs/GaInNAsSb/Ge; GaInP/GaAsP/ SiGe; GaInP/GaAsP/Si; GaInP/GaAsP/Ge; GaInP/GaAsP/Si/SiGe; GaInP/GaAs/InGaAs; GaInP/GaAs/GaInNAs; GaInP/GaAs/InGaAs/InGaAs; GaInP/Ga(In)As/ InGaAs; GaInP-GaAs-wafer-InGaAs; GaInP-Ga(In)As-Ge; and GaInP-GaInAs-Ge. A plurality of junctions, such as triple or double junctions, may be connected in series. In another embodiment, the junctions can be connected in parallel. The junctions can be stacked mechanically. The junctions can be bonded via a wafer. In an embodiment, the tunnel diodes between the junctions may be replaced with wafer bonds. Wafer bonding can be electrically insulating and transparent for wavelength regions that are converted by subsequent or deeper junctions. Each junction can be connected to an independent electrical connection or busbar. Independent busbars can be connected in series or in parallel. The electrical contacts of the respective electrical junctions may comprise grid wires. The wire shadow area is minimized due to the distribution of current in a plurality of parallel circuits or interconnects for separate junctions or junction sets. The current can be removed laterally. The wafer bonding layer may comprise a transparent conductive layer. Exemplary transparent conductors are transparent conductive oxides (TCO) such as indium tin oxide (ITO), fluorine-doped tin oxide (FTO), and doped zinc oxide; and conductive polymers, graphene and carbon nanotubes and familiarity Other conductors known to the skilled artisan. Benzocyclobutene (BCB) may comprise an intermediate tie layer. The bond may be between a transparent material such as glass (such as borosilicate glass) and a PV semiconductor material. An exemplary dual junction cell is a cell (GaInP//GaAs) comprising a top layer of a GaInP wafer bonded to a GaAs underlayer. An exemplary four-junction cell includes GaInP/GaAs/GaInAsP/GaInAs on an InP substrate, wherein the junctions can be individually separated by a tunnel diode (/) or an isolated transparent wafer bonding layer (//), such as A battery given by GaInP//GaAs//GaInAsP//GaInAs on InP. The PV cell may comprise an InGaP//GaAs//InGaAsNSb//conductive layer//conductive layer//GaSb//InGaAsSb. The substrate can be GaAs or Ge. The PV cell can comprise Si-Ge-Sn and an alloy. All combinations of diode and wafer bonding are within the scope of the present invention. An exemplary four-junction cell having a conversion efficiency of 44.7% at a 297-fold concentration of the AM 1.5d spectrum was prepared by SOITEC, France. A PV cell can contain a single junction. An exemplary single junction PV cell can comprise a single crystal germanium cell, such as Sater et al. (BL Sater, ND Sater, "High voltage silicon VMJ solar cells for up to 1000 suns intensities", Photovoltaic Specialists Conference, 2002. One of the batteries given in the Conference Record of the Twenty-Ninth IEEE, May 19-24, pages 1019-1022, This is incorporated herein by reference in its entirety. Alternatively, a single junction cell may comprise GaAs or GaAs doped with other elements such as Group III and Group V elements. In an exemplary embodiment, the PV cell comprises a triple junction concentrating PV cell or a GaAs PV cell operating at about 1000 suns. In another exemplary embodiment, the PV cell comprises c-Si operated at 250 suns. In an exemplary embodiment, the PV can include GaAs that selectively reacts to wavelengths less than 900 nm and InGaAs on at least one of InP, GaAs, and Ge, which can selectively respond to at 900 nm The wavelength in the region between 1800 nm. Two types of PV cells, GaAs and InGaAs, included on InP, can be used in combination to increase efficiency. Two single junction batteries can be used to achieve the effect of a double junction battery. The combination can be implemented by using at least one of a dichroic mirror, a dichroic filter, and a battery architecture, either alone or in combination with a mirror, to achieve multiple bounces or reflections of light as given in the present invention. . In one embodiment, each PV cell includes a complexing layer that separates and sorts the incident light to redirect it to illuminate a particular layer in the multi-junction cell. In an exemplary embodiment, the battery includes an indium gallium phosphide layer for visible light and a gallium arsenide layer for infrared light, wherein the corresponding light is oriented. PV cells can contain GaAs1 - x - y Nx Biy alloy. PV cells can contain helium. The 矽PV cell can include a concentrating cell that can operate over an intensity range of about 5 to 2000 Suns. The 矽PV cell may comprise crystalline ruthenium and at least one surface may further comprise an amorphous ruthenium which may have a different band gap than the crystalline Si layer. The amorphous germanium may have a band gap wider than the crystalline germanium. The amorphous germanium layer can perform at least one of the following functions: rendering the battery electrically transparent and preventing electron-hole pairs from recombining at the surface. The 矽 battery can contain multiple junction batteries. The layers can include individual batteries. At least one battery, such as a top cell, such as a battery comprising at least one of Ga, As, InP, Al, and In, may be ionically sliced and mechanically stacked on a Si cell, such as a Si bottom cell. Each of the multi-junction cells and the layers of the series connected cells may include a bypass diode to minimize current and power losses caused by current mismatch between the various layers of the battery. The surface of the battery can be textured to facilitate light penetration into the battery. The battery can include an anti-reflective coating to enhance light penetration into the battery. The anti-reflective coating can further reflect wavelengths below the band gap energy. The coating can comprise a plurality of layers, such as from about two to twenty layers. The increased number of layers may enhance the selectivity of the desired wavelength range of the bandpass (such as light above the bandgap energy) and reflect another range (such as a wavelength below the bandgap energy). Light reflected from the surface of the battery can bounce back to at least one other battery that can absorb light. The PV converter 26a can include a closed structure, such as a geodetic dome, that provides multiple bounces of reflected light to increase the cross section for PV absorption and conversion. The geodesic dome may comprise a plurality of receiver units, such as triangular units covered with PV cells. This dome can act as an integrating sphere. Unconverted light can be recycled. Light recycling can occur via reflection between component receiver units, such as a receiver unit of a geodetic dome. The surface can include a filter that reflects a wavelength below the band gap energy of the cell. The battery can include a bottom mirror (such as a silver or gold underlayer) to reflect unabsorbed light back to the battery. In addition, unabsorbed light and light reflected by the cell surface filter can be absorbed by the black body radiator and re-emitted to the PV cell. In an embodiment, the PV substrate can comprise a material that is transparent to light transmitted from the bottom cell to the reflector on the back side of the substrate. Exemplary triple junction cells having a transparent substrate are InGaAsP (1.3 eV), InGaAsP (0.96 eV), InGaAs (0.73 eV), InP substrates, and copper or gold IR reflectors. In an embodiment, the PV cell can comprise a concentrating cell. Multi-junction III-V batteries can be selected for higher voltages, or Si batteries can be selected for lower cost. Busbar shading can be reduced by using a transparent conductor such as a transparent conductive oxide (TCO). The PV cell can comprise a perovskite cell. An exemplary perovskite battery comprises Au, Al, Ti, GaN, CH from top to bottom3 NH3 SnI3 Single layer h-BN, CH3 NH3 PbI3 - x Brx , HTM/GA, bottom layer (Au) layers. The battery may comprise a multi-p-n junction cell, such as a cell comprising an AlN top layer and a GaN underlayer that convert EUV and UV, respectively. In an embodiment, the photovoltaic cell can comprise a GaN p-layer cell with heavy p-doping near the surface to avoid excessive attenuation of short-wavelength light such as UV and EUV. The n-type underlayer may comprise AlGaN or AlN. In an embodiment, the PV cell comprises GaN and heavily p-doped Al in the top layer of the p-n junctionx Ga1 - x N, wherein the p-doped layer comprises a two-dimensional hole gas. In an embodiment, the PV cell can include at least one of GaN, AlGaN, and AlN having a semiconductor junction. In an embodiment, the PV cell can comprise n-type AlGaN or AlN having a metal junction. In an embodiment, the PV cell utilizes multiple electron-hole pairs to respond to high energy light above the bandgap of the PV material. The light intensity can be sufficient to fill the recombination mechanism to improve efficiency. The converter may comprise a plurality of (i) GaN, (ii) AlGaN or AlN pn junctions, and (iii) at least one of the shallower ultra-thin pn heterojunction photovoltaic cells, each comprising n-type AlGaN or AlN A p-type two-dimensional hole gas in GaN on the base region. Each cell may include leads to a metal film layer (such as an Al film layer, an n-type layer, a depletion layer, a p-type layer) and a metal film layer (such as an Al film layer and is not due to short-wavelength light and vacuum operation) Lead wire of the passivation layer). In an embodiment of a photovoltaic cell comprising an AlGaN or AlN n type layer, a metal having a suitable work function replaces the p layer to form a Schottky rectifying barrier to form a Schottky barrier metal/semiconductor photovoltaic cell. In another embodiment, the converter can include at least one of a photovoltaic (PV) battery, a photovoltaic (PE) battery, and a mixture of a PV cell and a PE battery. The PE battery can include a solid state battery, such as a GaN PE battery. The PE cells can each comprise a photocathode, a gap layer, and an anode. An exemplary PE cell contains a discontinued GaN (cathode) / AlN (separator or gap) / a discontinuous Al, Yb or Eu (anode). The PV cells may each comprise at least one of the GaN, AlGaN, and AlN PV cells of the present invention. The PE cell can be the top layer and the PV cell can be the bottom layer of the mixture. PE batteries convert the shortest wavelength light. In an embodiment, at least one of the p- and n-layers of the PE cell and the p-layer and n-layer of the PV cell may be completely inverted. The architecture can be changed to improve power collection. In an embodiment, the polarization of the light ignited from the fuel is emitted and the converter is optimized to use light polarization selective material to achieve light penetration into the active layer of the cell. The light can be polarized by applying a field such as an electric or magnetic field with a corresponding electrode or magnet. In an embodiment, the fuel may comprise a silver, copper or Ag-Cu alloy melt, which may further comprise trapped hydrogen and trapped H2 At least one of O. The light emission may mainly comprise ultraviolet light and far ultraviolet light, such as light in a wavelength region of about 10 nm to 300 nm. The PV cell can respond to at least a portion of the wavelength region from about 10 nm to 300 nm. The PV cell can include a concentrating UV cell. The battery responds to blackbody radiation. The black body radiation may correspond to at least one temperature range of about 1000K to 6000K. The incident light intensity can be in the range of at least about 2 to 100,000 suns and 10 to 10,000 suns. The battery can be operated at a temperature range known in the art, such as at least one of a temperature range of less than about 300 ° C and less than 150 ° C. The PV cell may comprise a Group III nitride, such as at least one of InGaN, GaN, and AlGaN. In an embodiment, the PV cell can include a plurality of junctions. The junctions can be layered in series. In another embodiment, the junctions are independent or electrically connected in parallel. The individual junctions can be mechanically stacked or wafer bonded. An exemplary multi-junction PV cell includes at least two junctions comprising an n-p doped semiconductor, such as a plurality of groups of InGaN, GaN, and AlGaN. The n-type dopant of GaN may comprise oxygen, and the p-type dopant may comprise Mg. An exemplary triple junction cell can comprise InGaN//GaN//AlGaN, where // can refer to an isolating transparent wafer bonding layer or mechanical stack. The PV can operate at a high light intensity equal to that of a concentrating photovoltaic device (CPV). The substrate can be at least one of sapphire, Si, SiC, and GaN, with the latter two providing optimal lattice matching for CPV applications. The layers can be deposited using the organometallic vapor phase epitaxy (MOVPE) process known in the art. The cells can be cooled by cold plates, such as those used in CPV or diode lasers, such as commercial GaN diode lasers. As in the case of a CPV battery, the grid contacts can be mounted on the front and back surfaces of the battery. In an embodiment, the surface of a PV cell, such as a PV cell comprising at least one of GaN, AlN, and GaAlN, may terminate. The termination layer can include at least one of H and F. Termination can reduce the carrier recombination effect of defects. The surface can be terminated with a window such as AlN. In an embodiment, at least one of a photovoltaic (PV) and optoelectronic (PE) converter may have a protective window that is substantially transparent to the light it responds to. The window can transmit at least 10% of the response light. The window is transparent to UV light. The window can include a coating, such as a UV clear coating, on the PV or PE cell. The coating can be applied by deposition such as vapor deposition. The coating may comprise a material of the UV window of the invention, such as sapphire or MgF2 window. Other suitable windows include LiF and CaF2 . Such as MgF2 Any window of the window can be made thinner to limit EUV attenuation. In an embodiment, a PV or PE material, such as a hard glass-like material, such as GaN, acts as a cleanable surface. A PV material such as GaN acts as a window. In an embodiment, the surface electrode of the PV or PE cell can comprise a window. The electrodes and windows may comprise aluminum. The window may contain aluminum, carbon, graphite, zirconia, graphene, MgF2 , alkaline earth fluoride, alkaline earth halide, Al2 O3 And at least one of the sapphires. The window can be extremely thin, such as about 1 Å to 100 Å thick, making it transparent to UV and EUV emissions from the battery. Exemplary thinner transparent films are Al, Yb, and Eu films. The film can be applied by MOCVD, vapor deposition, sputtering, and other methods known in the art. In an embodiment, the battery can convert incident light into electricity by at least one mechanism, such as at least one mechanism from the group of photovoltaic effects, photoelectric effects, thermionic effects, and thermoelectric effects. The converter can comprise a double layer battery each having a photovoltaic layer on top of the photovoltaic layer. Higher energy light, such as far ultraviolet light, can be selectively absorbed and converted by the top layer. One of the plurality of layers may contain a UV window, such as MgF2 window. The UV window protects the ultraviolet (UV) PV from damage due to ionizing radiation, such as damage due to soft X-ray radiation. In an embodiment, a low pressure cell gas may be added to selectively attenuate radiation that would damage (UV) PV. Alternatively, the radiation can be at least partially converted to electricity by the top layer of the photoelectric converter and at least partially blocked from the UV PV. In another embodiment, a UV PV material such as GaN can also convert at least a portion of the far ultraviolet emission from the battery to electricity using at least one of a photovoltaic effect and a photoelectric effect. A photovoltaic converter can include a PV cell that converts ultraviolet light into electricity. An exemplary ultraviolet PV cell comprises at least one of the following: a poly(4-styrenesulfonate) film (SrTiO3:Nb) doped p-type semiconductor polymer PEDOT- deposited on Nb-doped titanium oxide. PSS: (poly(3,4-extended ethylenedioxythiophene)) (PEDOT-PSS/SrTiO3: Nb heterostructure), GaN, GaN, SiC, diamond, Si, and TiO doped with a transition metal such as manganese2 . Other exemplary PV photovoltaic cells include n-ZnO/p-GaN heterojunction cells. To convert high intensity light to electricity, the generator can include a light distribution system and a photovoltaic converter 26a (such as the light distribution system and photovoltaic converter shown in Figure 2I132). The light distribution system can include a plurality of semi-transparent mirrors arranged in a light-shielding stack along a propagation axis of light emitted from the battery, wherein at each of the mirror members 23 of the stack, the light is at least partially reflected to the PC battery 15 (such as with The light is propagating in a direction parallel to the battery) to receive laterally reflected light. The light-electric panel 15 can comprise at least one of a PE, a PV, and a thermionic battery. The window to the converter may be transparent to light emitted by the battery (such as short wavelength light) or black body radiation (such as black body radiation corresponding to a temperature of about 2800K to 4000K), wherein the power converter may include thermal photovoltaic (TPV) power conversion Device. The window to the PV converter can include one of the following: sapphire, LiF, MgF2 And CaF2 Other alkaline earth halides (such as fluorides, such as BaF2 , CdF2 ), quartz, fused silica, UV glass, borosilicate and infrared ray (ThorLabs). The semi-transparent mirror 23 is transparent to short-wavelength light. The material may be the same material as the PV converter window, partially covering a reflective material, such as a mirror, such as a UV mirror. The semi-transparent mirror 23 can comprise a checkered pattern of reflective material, such as a UV mirror, such as at least one of: via MgF2 Fluoride film on coated Al and aluminum, such as MgF2 Or LiF film, or SiC film. In an embodiment, the TPV conversion efficiency may be increased by using a selective emitter such as germanium on the surface of the blackbody emitter 5b4.镱 is an exemplary member of a class of rare earth metals that replaces the normal blackbody spectrum that emits a spectrum of the radiation spectrum of a similar line. This allows the energy spectrum of the relatively narrow emission to closely match the band gap of the TPV battery. In an embodiment, the generator further includes a switch (such as the present invention or an IGBT or another switch known in the art) to disconnect the ignition current in the event that the low energy hydrogen reaction itself propagates by pyrolysis. The reaction itself can maintain at least one of elevated battery and plasma temperatures, such as a temperature that supports pyrolysis at a rate sufficient to maintain this temperature and the rate of low energy hydrogen reaction. The plasma can comprise a light thick plasma. The plasma can comprise a black body. Light thick plasma can be achieved by maintaining high gas pressure. In an exemplary embodiment, pyrolysis occurs when a continuous ignition current in the range of 100 A to 1000 A is used to spray molten silver and molten silver copper (28 wt%) alloy at the tungsten electrode, wherein the superimposed pulse is at about 2 kA. In the range of up to 10 kA, the plasma blackbody temperature is 5000 K and the electrode temperature is in the range of about 3000K to 3700K. Pyrolysis can occur at a high temperature of at least one of the plasma and the battery component in contact with the plasma, such as the wall of the reaction cell chamber 5b31. The temperature may be in at least one of about 500K to 10,000K, 1000K to 7000K, and 1000K to 5000K. In another embodiment, at least one of the battery components, such as the reservoir 5c, can act as a coolant to cool the pyrolysis H to prevent it from returning to H.2 O. The maintained blackbody temperature can be a temperature that emits radiation that can be converted to electricity using photovoltaic cells. In an exemplary embodiment, the black body temperature may be maintained within at least one of about 1000 K to 4000 K. Photovoltaic cells can include thermal photovoltaic (TPV) cells. Exemplary photovoltaic cells for thermal photovoltaic conversion include crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), indium gallium arsenide (InGaAsSb), and germanium. Indium arsenate (InPAsSb) battery. Other exemplary cells are InGaAsP (1.3 eV) / InGaAsP (0.96 eV) / InGaAs (0.73 eV) / InP substrate / copper or gold IR emitter and InAlGaAs (1.3 eV) / InGaAs (0.96 eV) / graded buffer layer / Ge Subcell/copper or gold IR reflector. PV cells can include multi-junction GaAs cell stacks on multi-junction GaSb cells, such as 3J GaAs cells on 2J GaSb cells. The converter can include a mirror to direct and redirect radiation to at least one of the thermal photovoltaic converters. In an embodiment, the retroreflector reflects unconverted radiation back to the source to contribute to the power radiated to the converter. An exemplary mirror comprises at least one of: a vertebral material, such as aluminum and anodized aluminum, via MgF2 Coated Al; and fluoride film, such as MgF on aluminum and sapphire2 Or LiF film or SiC film; alumina, such as alpha-alumina, which can be sputter coated onto a substrate, such as stainless steel, via MgF2 Coated sapphire, borosilicate glass, alkali aluminosilicate glass (such as Gorilla glass); LiF, MgF2 And CaF2 Other alkaline earth halides, such as fluorides, such as BaF2 , CdF2 Quartz, fused silica, UV glass, borosilicate, ThorLabs, and ceramic glass, which can be mirrored on the outer surface when transparent. A mirror such as an anodized aluminum mirror can diffuse the light to uniformly radiate the PV converter. Transparent materials (such as sapphire, alumina, borosilicate glass, LiF, MgF2 And CaF2 Other alkaline earth halides (such as fluorides, such as BaF2 , CdF2 ), quartz, fused silica, UV glass, borosilicate, ThorLabs, and ceramic glass can serve as a window for the TPV converter. Another embodiment of a TPV converter includes a blackbody emitter filter to transmit a wavelength that matches the bandgap of the PV and reflect the mismatched wavelength back to the emitter, wherein the emitter can include a thermal battery component as an electrode. The black body radiator 5b4 may be coated with a selective emitter such as a rare earth metal such as helium, which emits a spectrum that is more favorable for thermal photovoltaic conversion, such as a spectrum similar to the line radiation spectrum. The bandgap of the cell is selected to optimize the electrical output efficiency for a given blackbody operating temperature and corresponding spectrum. In an exemplary embodiment operating at about 3000K or 3500K, the band gap of the TPV battery junction is given in Table 1. Table 1. Optimal bandgap combinations for batteries with n =1, 2, 3 or 4 junctions (J). To optimize the performance of a thermal photovoltaic converter comprising a multi-junction cell, the black body temperature of the light emitted from the cell can be maintained at a constant of about 10%, for example. The power output device can then be utilized to control the power output, wherein the surplus power is stored in a device such as a battery or capacitor or discharged (such as as heat is exhausted). In another embodiment, the reaction rate can be reduced by using the present invention (such as changing the ignition frequency and current, metal ejection rate, and H).2 O and H2 The injection rate of at least one of them is to maintain power from the plasma, wherein the black body temperature can be maintained by controlling the emissivity of the plasma. The emissivity of the plasma can be varied by adding a cell gas such as a rare gas to change the cell atmosphere, such as the cell atmosphere initially containing the metal vapor. In an embodiment, a corresponding sensor or gauge is used to sense the pressure of the electrolysis cell gases, such as the pressure of water vapor, hydrogen, and oxygen. In an embodiment, sensing at least one gas pressure (such as at least one of water pressure and hydrogen pressure) by monitoring at least one parameter of the battery, the at least one parameter responsive to at least one of the cell gases The pressure changes and changes. At least one of the desired water pressure and hydrogen pressure can be achieved by varying one or more pressures as the gas supply simultaneously monitors the effects of the changes. Exemplary monitored parameters by gas changes include the electrical behavior of the ignition circuit and the light output of the battery. At least one of the ignition current and the light output may be maximized at a desired pressure of at least one of a hydrogen pressure and a water vapor pressure. At least one of a photodetector (such as a diode) and an output of the PV converter can measure the light output of the battery. At least one of the voltage and current meters can monitor the electrical behavior of the ignition circuit. The generator may include a pressure control system (such as a pressure control system including a software), a processor (such as a computer), and monitoring of input parameters and adjusting gas pressure to achieve optimal power output of the generator. Controller. In embodiments containing a fuel metal (including copper), hydrogen can be maintained at a certain pressure from H2 The reaction of O with low energy hydrogen and oxygen achieves reduction of copper oxide from the reaction of copper with oxygen, wherein the water vapor pressure is adjusted to optimize the generator output by monitoring parameters. In an embodiment, H can be supplied by electrolysis2 The hydrogen pressure is controlled at about a constant pressure. The electrolysis current can be maintained at about a constant current. Hydrogen can be supplied at a rate to react with approximately all of the low energy hydrogen reactive oxygen products. The surplus hydrogen can diffuse through the cell wall to maintain a constant pressure above the hydrogen consumed by the low energy hydrogen reaction and reaction with the oxygen product. Hydrogen can permeate through the hollow cathode to the reaction cell chamber 5b31. In an embodiment, the pressure control system controls H in response to the ignition current and frequency and light output.2 And H2 O pressure to optimize at least one of them. Light can be monitored using a diode, power meter or spectrometer. The ignition current can be monitored using a multimeter or digital oscilloscope. The injection rate of the molten metal of the electromagnetic pump 5k can also be controlled to optimize at least one of the electrical behavior of the ignition circuit and the light output of the battery. In another embodiment, the sensor can measure multiple components. In an exemplary embodiment, the cell gas and total pressure are measured using a mass spectrometer, such as a quadrupole mass spectrometer, such as a residual gas analyzer. The mass spectrometer can be sensed in batch or trend mode. The water or humidity sensor can include at least one of an absolute, a capacitive, and a resistance humidity sensor. A sensor capable of analyzing a plurality of gases includes a plasma source, such as a microwave chamber and a generator, wherein the plasma excites the cell gas to emit light such as visible and infrared light. Gas and concentration are determined by spectral emission, such as the characteristic line and intensity of gaseous components. The gas can be cooled prior to sampling. The metal vapor is removed from the cell gas prior to analyzing the gas composition of the cell gas. The metal vapor in the battery, such as a battery comprising at least one of silver and copper, can be cooled to condense the metal vapor such that the cell gas can flow into the sensor in the absence of metal vapor. An SF-CIHT battery, also referred to herein as an SF-CIHT generator or generator, may include a passage (such as a tube from which a gas flows from a battery), wherein the tube includes a battery inlet and an outlet for condensed metal vapor flow and a non-condensable gas To the output of at least one gas sensor. The tube can be cooled. Cooling can be achieved by conduction, wherein the tube is cooled to a cooled battery assembly (such as a magnet of an electrode electromagnetic pump). The tube can be effectively cooled by means such as water cooling and passive components such as heat pipes. The cell gas containing metal vapor can enter the tube where the metal vapor condenses due to the low temperature of the tube. The condensed metal can flow to the vertebral body reservoir by at least one of gravity flow and pumping such that the gas to be sensed flows into the sensor in the absence of metal vapor. Alternatively, the gas pressure may be measured in the outer chamber 5b3a, wherein the gas may penetrate into the reaction cell chamber 5b31. The infiltration can be via the black body radiator 5b4. In an embodiment, the generator comprises a black body radiator 5b4 that can charge a vessel containing the reaction cell chamber 5b31. In an embodiment, PV converter 26a includes a PV cell 15 on the interior of a metal enclosure that includes a battery chamber 5b3 containing a blackbody radiator 5b4. The PV cooling plate can be outside the battery compartment. At least one of the chambers 5b3, 5b3a, and 5b31 is capable of maintaining the pressure at least one of: subatmospheric pressure, atmospheric pressure, and superatmospheric pressure. The PV converter can further include at least one set of electrical feedthroughs to transfer electrical power from the PV cells within the inner surface of the battery chamber to the exterior of the battery chamber. The feedthrough can be at least one of airtight and vacuum or pressure capable. In an embodiment, at least one battery component, such as reservoir 5c, may be insulated. The insulating member may comprise a heat shield and may also comprise other forms of thermal insulation, such as ceramic insulating materials (such as MgO, fire brick, Al).2 O3 Zirconium oxide (such as Zicar), alumina enhanced thermal barrier (AETB) (such as AETB 12 insulation, ZAL-45 and SiC-carbon aerogel (AFSiC)). The exemplary AETB 12 insulation thickness is about 0.5 to 5 cm. The insulator may be encapsulated between two layers, such as an inner refractory metal or material battery component wall and an outer insulating wall that may comprise the same or different materials, such as stainless steel. The battery assembly can be cooled. The outer insulating envelope can include a cooling system, such as a cooling system that transfers heat to the chiller or radiator 31. In an embodiment, the chiller may include a radiator 31 and may further include at least one fan 31j1 and at least one coolant pump 31k to cool the radiator and circulate the coolant. The radiator can be cooled by air. An exemplary radiator includes a car or truck radiator. The chiller may further comprise a coolant reservoir or sump 31l. The sump 31l can function as a flow damper. The cooling system can include a bypass valve to return flow from the sump to the radiator. In an embodiment, the cooling system comprises at least one of: recirculating the coolant between the sump and the radiator when the radiator inlet line pressure is lower due to a lowering or suspension of pumping in the cooling line a bypass circuit; and a radiator overpressure or overflow line between the radiator and the sump. The cooling system can further include at least one check valve in the bypass circuit. The cooling system may further comprise a radiator relief valve (such as a check valve) and an overflow line from the radiator to the overflow sump 31l. The radiator can act as a sump. The chiller (such as the radiator 31 and the fan 31j1) may have a flow to and from the sump 31l. The cooling system can include a sump inlet line from the radiator to the sump 31l for conveying the cooled coolant. The coolant may be pumped from the storage tank 31l to a common sump outlet manifold that supplies a cooling coolant to each of the components to be cooled. The radiator 31 can act as a sump wherein the radiator outlet provides a cooling coolant. Alternatively, each component to be cooled, such as an inductively coupled heater, EM pump magnet 5k4, and PV converter 26a, may have a separate coolant flow circuit with a sump cooled by a chiller such as a radiator and a fan. Each circuit may include a separate pump or pump of a plurality of pumps 31k and a plurality of valves 31m. Each circuit can receive the flow of a separate pump 31k from the flow in the conditioning circuit. Alternatively, each circuit may receive a flow from a pump 31k that provides flow to a plurality of circuits, wherein each circuit includes a valve 31m, such as a solenoid valve that regulates flow in the circuit. The flow through each loop can be independently controlled by its controller, such as a thermal sensor, such as a thermocouple, flow meter, controllable value, pump controller, and computer. In an embodiment, the reaction cell chamber 5b31 is sealed to constrain at least one of: a fuel gas, such as water vapor and at least one of a source of hydrogen and oxygen (such as an oxide); and a metal of the fuel melt Vapor, such as Ag or Ag-Cu alloy vapor. The outer surface of the reaction cell chamber 5b31 may comprise a black body radiator 5b4, which may comprise a material that is capable of operating at very high temperatures, such as in the range of about 1000 °C to 4000 °C. In an embodiment, the black body radiator 5b4 may comprise a material having a melting point higher than a melting point of a molten metal such as silver. An exemplary material is at least one of a group of metals and alloys from the group consisting of: WC, TaW, CuNi, Herstite C, Herstite X, Inconel, and Incoal ( Incoloy), carbon steel, stainless steel, chrome-molybdenum steel (such as modified 9Cr-1Mo-V (P91), 21/4Cr -1Mo steel (P22)), Nd, Ac, Au, Sm, Cu, Pm , U, Mn, doped Be, Gd, Cm, Tb, doped Si, Dy, Ni, Ho, Co, Er, Y, Fe, Sc, Tm, Pd, Pa, Lu, Ti, Pt, Zr , Cr, V, Rh, Hf, Tc, Ru, doped with B, Ir, Nb, Mo, Ta, Os, Re, W, carbon, ceramics (such as SiC, MgO, alumina, Hf-Ta-C, Boron nitride) and other high temperature materials known in the art to act as black bodies. The black body radiator absorbs power from the plasma to heat it to its high operating temperature. In a thermal photovoltaic embodiment, the black body radiator 5b4 provides light incident on the PV converter 26a. The black body radiator may have an emissivity such as an emissivity close to one. In an embodiment, the emissivity can be adjusted to produce black body power that matches the capabilities of the PV converter. In an exemplary embodiment, the emissivity can be increased or decreased by means of the present invention. In the illustrative case of the metal blackbody radiator 5b4, the surface may be at least one of oxidized and roughened to increase emissivity. The emissivity can be non-linear with the wavelength (such as inversely proportional to the wavelength) such that short wavelength emission is advantageous from its outer surface. At least one of a filter, a lens, and a mirror in a gap between the black body radiator 5b4 and the PV converter 26a may have a function of transmitting short-wavelength light to the PV converter while returning the infrared light to the radiator 5b4 Selectivity. In an exemplary embodiment, the operating temperature of the W or carbon blackbody radiator 5b4 is the operating temperature of the incandescent bulb, such as up to 3700 K. In the case of an emissivity of 1, the blackbody radiator power is at most 10.6 MW/m according to the Stephen Bozemann equation.2 . In an embodiment, the black body radiation is incident on a PV converter 26a that includes a concentrating photovoltaic cell 15 (such as a concentrating photovoltaic cell of the present invention) that responds to corresponding radiation, such as in response to visible and near-infrared light. The concentrating photovoltaic battery. The battery may comprise a multi-junction cell, such as a dual or triple junction cell comprising a III/V semiconductor, such as a battery of the invention. The SF-CIHT generator may further include a black body temperature sensor and a black body temperature controller. The black body temperature of the black body radiator 5b4 can be maintained and adjusted to optimize the light-to-electric conversion of the black body. The black body temperature of the black body radiator 5b4 can be sensed using a sensor such as at least one of: a spectrometer, an optical pyrometer, a PV converter 26a, and a power meter that uses emissivity to determine the black body temperature. By means of the present invention, a controller, such as a controller including a computer and a low energy hydrogen reaction parameter sensor and controller, can control the power from the low energy hydrogen reaction. In an exemplary embodiment, to control the stability of temperature and blackbody temperature, the low energy hydrogen reaction rate is controlled by controlling at least one of water vapor pressure, hydrogen pressure, fuel injection rate, ignition frequency, and ignition voltage and current. . For a given low energy hydrogen reaction power from the reaction cell chamber 5b31 of the heated black body radiator 5b4, the desired operating black body temperature of the black body radiator 5b4 can be achieved by at least one of: selecting and controlling the black body radiator The emissivity of at least one of the inner and outer surfaces of 5b4. In an embodiment, the power radiated from the black body radiator 5b4 is approximately the spectrum and power matched to the PV converter 26a. In an embodiment, the emissivity of the outer surface is selected (such as an emissivity in the range of about 0.1 to 1) to cause the cap 5b4 to radiate power to the PV converter at the desired blackbody temperature, the power not exceeding Its maximum acceptable incident power. The blackbody temperature can be selected to better match the photovoltaic switching reaction of the PV cell so that conversion efficiency can be maximized. The emissivity can be changed by modifying the outer surface of the black body radiator 5b4. The emissivity can be increased or decreased by coating a coating having an increased or decreased emissivity. In an exemplary embodiment, a pyrolytic carbon coating may be applied to the black body radiator 5b4 to increase its emissivity. The emissivity can also be increased by oxidizing and roughening at least one of the W surfaces, and the emissivity can be reduced by reducing at least one of the oxidized surface and the polished rough W surface. The generator can contain oxidizing gases (such as oxygen and H2 The source of at least one of O and the source of the reducing gas (such as hydrogen) and the means for controlling the composition and pressure of the atmosphere in the battery chamber. The generator may include a gas sensor (such as a pressure gauge), a pump, a gas supply, and a gas supply controller to control the gas composition and pressure to control the emissivity of the blackbody radiator 5b4. The black body radiator 5b4 and the PV converter 26a may be separated by a gap such as a gas or vacuum gap to prevent the PV converter from overheating due to heat conduction to the PV converter. The black body radiator 5b4 may comprise a plurality of suitable shapes, such as a shape comprising a flat plate or a dome. The shape may be selected for at least one of structural integrity and optimization of transmission of light to the PV region. Exemplary shapes are cubes, straight cylinders, polygons, and geodesic balls. The black body radiator 5b4 (such as carbon) may comprise parts such as plates that can be glued together. The exemplary cube-reaction cell chamber 5b31 and the black body radiator 5b4, which may comprise carbon, may comprise two half-cubes machined and glued together from a solid cube of carbon. The base of the cavity may contain a geometry such as a conical channel to permit the molten metal to flow back into the reservoir. The substrate can be thicker than the upper wall to act as an insulator such that power is preferentially radiated from the non-substrate surface. The cavity may comprise a wall whose thickness varies along the perimeter to produce a desired temperature profile along the outer surface comprising the black body radiator 5b4. In an exemplary embodiment, the cubic reaction cell chamber 5b31 can include a wall that includes a spherical segment centered on each wall to create a uniform black body temperature of the outer surface. The spherical section can be machined into a wall form, or it can be glued into a planar inner wall surface. The spherical radius of the spherical section can be selected to achieve the desired blackbody surface temperature profile. To enhance battery output and efficiency, the area of the black body emitter 5b4 is optimally matched to the receiving PV converter 26a. In an embodiment, other battery components (such as reservoir 5c) may comprise a material (such as a refractory material such as carbon, BN, SiC or W) to act as a black body radiator to a PV arrangement that is circumferentially arranged to the assembly to receive black body radiation. Device. At least one of the battery components, such as blackbody radiator 5b4 and reservoir 5c, can include a geometry that optimizes the stacking of PV cells 15 to accept light from the components. In an exemplary embodiment, the battery assembly can include a polyhedral surface, such as a polygon, such as at least one of a triangle, a pentagon, a hexagon, a square, and a rectangle, that matches the geometry of the PV cell 15. The geometry of the blackbody radiator and PV converter can be selected to optimize photon transfer from the blackbody radiator to the PV converter, taking into account parameters such as the angle of incidence of the illumination photons and the corresponding effects on PV efficiency. In an embodiment, PV converter 26a may include components to move a PV cell, such as a PV rotating rack, to cause more uniformity of time-averaged radiation incident on the battery. The PV rotating rack can rotate an axially symmetric PC converter, such as a PC converter including a lateral polygonal ring, about an axis of symmetry or a z-axis. Polygons can contain hexagons. Rotation may be caused by a mechanical drive connection, a pneumatic motor, an electromagnetic drive, or other drive known to those skilled in the art. The surface of the black body radiator 5b4 can be modified to change the emissivity with a corresponding change in power radiated from the black body radiator. The blackbody radiator emissivity can be achieved by (i) modifying the polishing, roughness or texture of the surface, (ii) adding a coating to the carbon (such as carbides, such as at least one of tungsten carbide, tantalum carbide, and tantalum carbide) or The pyrolytic coating and (iii) are modified by adding a cladding, such as a W cladding, to the carbon blackbody radiator. In the latter case, W can be mechanically attached to the carbon by a fastener such as a screw having an expansion member such as a slot. In an exemplary embodiment, the emissivity of the TaC (such as TaC coating, tile or cladding) on the carbon black body radiator 5b4 is about 0.2 with respect to the emissivity of carbon. The blackbody radiator 5b4 may comprise a cavity having a first geometry, such as a spherical cavity 5b31 (Fig. 2I134 to Fig. 2I138) within a solid shape having a second geometry, such as a cube. In another embodiment, the first cavity 5b31 having the first geometry may be internal to the second cavity 5b4a1 having the second geometry. The illustrative embodiment includes a spherical shell cavity in a hollow cube cavity. The corresponding second cavity 5b4a1 may comprise a black body cavity comprising a black body radiator outer surface 5b4a. The interior of the second cavity can be heated to the black body temperature by the internal first cavity having the first geometry. Black body radiation from the corresponding second black body radiator 5b4a can be incident on the PV cell 15, which can match the geometric structure. The cells can be arranged in an array with matching geometries. In an embodiment, the optical power received into the PV cell can be reduced to an allowable intensity of light emitted at the operating temperature of the blackbody radiator by at least one of: increasing the second cavity and the PV cell Spacing interval; using a PV cell containing a half mirror on the surface to reflect a portion of the incident light; using a secondary radiator (such as tungsten instead of carbon, a radiator with reduced emissivity); and having a needle in front of the PV cell The reflectors of the apertures that only partially transmit blackbody radiation from the primary or secondary blackbody radiator to the PV cell and desirably reflect the non-transmitted light. In an embodiment, the geometry of the secondary radiator 5b4a and the PV converter 26a with matching geometry can be selected to reduce the complexity of the PV cold plate, PV cooler or PV heat exchanger 26b. An exemplary cubic geometry minimizes the number of PV cold plates, maximizes the size of the PV cold plates, and results in electrical interconnects and coolant line connections (such as electrical connections to the inlet 31b and outlet 31c of the PV coolant system). The complexity of connecting the coolant line is low. The secondary black body radiator can be protected from sublimation by means of a component that supports the halogen cycle. In an embodiment, the gas enclosing the chamber of the blackbody radiator, such as chamber 5b3 (Fig. 2I80), may comprise a source of halogen (such as I)2 Or Br2 Or a hydrocarbon bromine compound that forms a complex with sublimed tungsten. The complex compound can be decomposed on the surface of the hot tungsten to redeposit the tungsten on the black body radiator 5b4. The window on the multi-layer PV cell 15 can support a temperature gradient to support the volatilization of the tungsten-halogen species to support the halogen cycle. In an embodiment, the carbon battery component (such as the carbon black body radiator 5b4) can be protected from sublimation by applying external pressure. In an exemplary embodiment, the carbon is stably sublimed to 4500 K by applying a pressure of about 100 atmospheres. The pressure can be applied, for example, by a high pressure gas such as at least one of an inert gas, hydrogen, and a molten metal vapor such as silver vapor. In an embodiment, the blackbody radiator 5b4 comprises a spherical dome connectable to the reservoir 5c. The blackbody radiator can be shaped other than a spherical surface (such as a cube) and can be further coated or coated with a material to change its emissivity to better match the radiated power to the capabilities of the PV cell. The exemplary coated blackbody radiator 5b4 comprises a carbon cube coating having a refractory material having a lower emissivity than carbon having a self-vaporizing or sublimating low vapor pressure at the black body operating temperature. At least one battery component (such as at least one of the reservoir 5c, the blackbody radiator 5b4, and the blackbody radiator cladding) may comprise at least one of: graphite (sublimation point = 3642 ° C); refractory metal (such as tungsten) (MP = 3422 ° C) or 钽 (MP = 3020 ° C)); ceramics; ultra-high temperature ceramics; and ceramic matrix composites (such as at least one of boride, carbide, nitride and oxide, such boride , carbides, nitrides and oxides such as those of early transition metals, such as boride (HfB2 ), zirconium diboride (ZrB)2 ), tantalum nitride (HfN), zirconium nitride (ZrN), titanium carbide (TIC), titanium nitride (TiN), germanium dioxide (ThO)2 ), lanthanum boride (NbB)2 ) and tantalum carbide (TaC) and its associated complexes). Exemplary ceramics having the desired high melting point are magnesium oxide (MgO) (MP = 2852 ° C), zirconia (ZrO) (MP = 2715 ° C), boron nitride (BN) (MP = 2973 ° C), zirconium dioxide (ZrO2 ) (M.P.=2715°C), lanthanum boride (HfB)2 (M.P.=3380°C), niobium carbide (HfC) (M.P.=3900°C), Ta4 HfC5 (M.P.=4000°C), Ta4 HfC5 TaX4 HfCX5 (4215 ° C), tantalum nitride (HfN) (M.P. = 3385 ° C), zirconium diboride (ZrB2 (M.P.=3246°C), zirconium carbide (ZrC) (M.P.=3400°C), zirconium nitride (ZrN) (M.P.=2950°C), titanium boride (TiB)2 (M.P.=3225°C), titanium carbide (TIC) (M.P.=3100°C), titanium nitride (TiN) (M.P.=2950°C), niobium carbide (SiC) (M.P.=2820°C), tantalum boride (TaB)2 (MP=3040°C), tantalum carbide (TaC) (MP=3800°C), tantalum nitride (TaN) (MP=2700°C), niobium carbide (NbC) (MP=3490°C), tantalum nitride (NbN) (MP = 2573 ° C), vanadium carbide (VC) (MP = 2810 ° C) and vanadium nitride (MP = 2050 ° C) and turbine blade material (such as one or more of the following groups: super Alloys, nickel-based superalloys containing chromium, cobalt and niobium, superalloys containing ceramic matrix composites, U-500, Rene 77, Rene N5, Rene N6, PWA 1484, CMSX-4, CMSX-10, Inch Nickel , IN-738, GTD-111, EPM-102 and PWA 1497). Ceramics such as MgO and ZrO can be paired with H2 The reaction is resistant. In an exemplary embodiment, the emissivity of the TaC (such as TaC coating, tile or cladding) on the carbon black body radiator 5b4 is about 0.2 with respect to the emissivity of carbon. An exemplary battery assembly (such as a reservoir) comprising MgO, alumina, ZrO, ZrB2 , SiC or BN. The exemplary blackbody radiator 5b4 can comprise carbon or tungsten. The battery component material (such as graphite) can be coated with another high temperature or refractory material (such as refractory metal (such as tungsten) or ceramic (such as ZrB)2 , TaC, HfC, WC)) or another material known in the invention or in the art. Another graphite surface coating comprises diamond-like carbon that can be formed on the surface by plasma treatment of the vertebral body. Processing methods can include processing methods known in the art for depositing diamond-like carbon onto a substrate. In an embodiment, the silver vapor may be deposited on the surface by pre-coating or during operation to protect the cone from erosion. In an embodiment, the reaction cell chamber 5b31 may comprise carbon and an electrolysis cell gas (such as H2 O, H2 , CO and CO2 The reaction product of at least one of them to suppress further reaction of carbon. In an embodiment, at least one component, such as the lower portion of pump tube 5k6 and EM pump assembly 5kk, may comprise high temperature steel, such as Haines 230. In the embodiment, the rare gas held by the low energy hydrogen reaction -H2 Plasma (such as argon-H2 (3 to 5%)) The carbon in the form of graphite can be converted to at least one of a diamond-like or diamond-like form. The battery assembly (such as the reservoir 5c or the black body radiator 5b4) can be cast, ground, hot pressed, sintered, plasma sintered, wetted, spark plasma sintered, melted by laser bed 3D printing, and by familiarizing itself with Other methods known to those skilled in the art are formed. In an embodiment, at least one component, such as the outer casing 5b3a, may be fabricated by stamping or stamping a constituent material, such as a metal. In the thermionic and thermoelectric embodiments, the thermionic or thermoelectric converter can be in direct contact with the thermal blackbody radiator 5b4. The blackbody radiator 5b4 can also transfer heat to a heat engine (such as a Rankine, Brendon or Stirling heat engine) or can act as a heater for the heat to electrical converter. In an embodiment, a medium other than a standard medium such as water or air can be used as the working medium of the heat engine. In an exemplary embodiment, the hydrocarbon or supercritical carbon dioxide can replace the water in the Rankine cycle of the turbine generator, and the air with respect to the external burner design can be used as the working medium for the Braden cycle of the turbine generator. An exemplary supercritical carbon dioxide cycle generator comprising a generator of the Echogen power system (https://www.dresser-rand.com/products-solutions/systems-solutions/Waste - Heat - Recovery - System /http://www.echogen.com/_CE/pagecontent/Documents/News/Echogen_brochure_2016.pdf). Alternatively, the heat cover 5b4 can act as a heat source or heater or light source. The heat flow to the heat engine or heater may be direct or indirect, wherein the SF-CIHT generator may further comprise a heat exchanger or heat transfer member (such as one of the present invention). In another embodiment, the SunCell® may comprise a magnetohydrodynamic (MHD) or plasma fluid power (PHD) generator, wherein the high pressure plasma generated in the reaction cell chamber 5b31 flows to the MHD or PHD generator And converted to electricity. The reflux can enter the chamber of the reaction cell. At least one of the battery chamber 5b3 or 5b3a1 and the reaction electrolytic cell chamber 3b31 may be evacuated via a pump line such as 13b using the pump 13a. A corresponding pump line valve can be used to select the pumped container. The battery may further comprise one or more components for oxygen, hydrogen, water vapor, metal vapor, gaseous oxides (such as CO2 At least one of, CO) and a high temperature capable sensor with a total pressure. By means of the invention, the water and hydrogen pressure can be controlled to a desired pressure, such as the pressure of the invention, such as a water vapor pressure in the range of from 0.1 Torr to 1 Torr. In an exemplary embodiment, the valve and its valve opening are controlled to maintain a desired gas pressure using a feedback gas supply that uses a measured pressure of the gas to maintain a desired pressure of the gas. H2 O and H2 It can be supplied by a hydrogen storage tank and a pipeline 31l, and the hydrogen storage tank and the pipeline 31l can include H2 Electrolysis system, H2 O/steam storage tank and line 31l, hydrogen feed line 5ua, argon storage tank 5u1 and feed line 5u1a and gas injectors (such as H that can pass through the EM pump tube)2 , argon and H2 At least one of the O/steam injectors). As an alternative to pumping out oxygen or absorbing oxygen, the oxygen produced in the battery can react with the supplied hydrogen to form water. The low energy hydrogen gas can diffuse or flow out of the selective gas valve via the walls and junctions of the battery. In another embodiment, the reaction cell chamber 5b31 is operated under an inert atmosphere. The SF-CIHT generator may comprise an inert gas source (such as a sump) and at least one of: a pressure gauge, a pressure regulator, a flow regulator, at least one valve, a pump, and a computer for reading pressure and controlling pressure. The inert gas pressure can range from about 1 Torr to 10 atm. In an embodiment, after startup, the heater can be removed and cooling can be performed to maintain the battery components (such as reservoir 5c, EM pump, and PV converter 26a) at their operating temperatures (such as given in the present invention) Out of operating temperature). In an embodiment, the SF-CIHT battery or generator (also referred to as SunCell®) shown in Figures 2I28, 2I69, and 2I80 through 2I149® Contains six basic easy-to-maintain systems, some of which do not have moving parts and can operate for long periods of time: (i) start an inductively coupled heater that includes a power supply 5m, leads 5p, and antenna coils 5f to melt the silver first or Silver-copper alloy to form a molten metal or melt; and optionally an electrode electromagnetic pump comprising a magnet for initially directing the ignition plasma flow; (ii) a fuel injector, such as comprising a hydrogen supply (such as a fuel injector of a black body radiator, wherein hydrogen can be obtained from water by electrolysis or pyrolysis; and an injection system comprising an electromagnetic pump 5ka for spraying molten silver or molten silver-copper alloy and an oxygen source (such as oxides, such as CO2 , CO, LiVO3 Or another oxide of the present invention; and alternatively, a gas injector, which may include a crucible passing through the EM pump tube 5k6 for injecting at least one of water vapor and hydrogen; (iii) an ignition system, Used to generate low voltage and high current flow across a pair of electrodes 8, molten metal, hydrogen and oxide, or molten metal and H2 At least one of O and hydrogen is injected into the pair of electrodes to form a brightened photo-plasma; (iv) a black body radiator 5b4 heated by plasma to an incandescent temperature; (v) an optical-to-electrical converter 26a, Included are so-called concentrating photovoltaic cells 15 that receive light from a black body radiator and operate at high light intensities such as more than one thousand Suns; and (vi) a fuel recovery and thermal management system, It causes the molten metal to return to the injection system after ignition and cool at least one of the battery components (such as the inductive heater antenna 5f, the EM pump magnet 5k4, and the PV converter 26a). In another embodiment, light from the ignition plasma can be directly radiated to the PV converter 26a for conversion to electricity. In another embodiment, the EM pump 5ka may comprise a thermoelectric pump, a mechanical pump (such as a gear pump, such as a ceramic gear pump) or another pump known in the art (such as comprising an impeller capable of high temperatures (such as at about 900) Pump operated in the temperature range of °C to 2000 °C). In an embodiment, the black body radiator to PV converter 26a may comprise a high temperature material (such as carbon), a refractory metal (such as W, Re), or a ceramic (such as boride of transition elements such as lanthanum, zirconium and titanium), Carbide and nitride), Ta4 HfC5 (M.P. = 4000 °C), TaB2 , HfC, BN, HfB2 , HfN, ZrC, TaC, ZrB2 , TiC, TaN, NbC, ThO2 , oxides (such as MgO), MoSi2 , W-Re-Hf-C alloy and other materials of the invention. The blackbody radiator can include an efficient geometry that effectively transfers light to the PV and fills the PV cell with power of light flowing from the reactive cell chamber 5b31. An exemplary blackbody radiator can include a polygonal or spherical dome. The black body radiator can be separated from the PV converter 26a by a gas or vacuum gap, wherein the PV cell is positioned to receive black body light from the black body radiator. The generator may further include a peripheral chamber that is sealable to the atmosphere and further capable of maintaining a pressure below, equal to, and greater than at least one of atmospheric pressures. The generator may comprise a spherical pressure or vacuum vessel around the dome comprising a battery chamber 5b3, wherein the PV converter comprises a housing or a pressure vessel. The battery chamber can comprise suitable materials known to those skilled in the art that provide structural strength, sealing and heat transfer. In an exemplary embodiment, the battery chamber comprises at least one of stainless steel and copper. The PV cell can cover the interior of the cell chamber, and a PV cooling system, such as heat exchanger 87, can cover the outer surface of the cell chamber. In a thermally photovoltaic embodiment, PV converter 26a may include a selective filter (such as a photonic crystal) for the visible wavelength to PV converter 26a. In an embodiment, the black body radiator comprises a spherical dome 5b4. In an embodiment, the inner surface of the graphite sphere is coated with a carbide having a high temperature capability, such as Ta4 HfC5 (M.P. = 4000 ° C), tungsten carbide, tantalum carbide, tantalum carbide, zirconium carbide, titanium carbide or tantalum carbide. The corresponding metal can react with the carbon of the graphite surface to form a corresponding metal carbide surface. The dome 5b4 can be separated from the PV converter 26a by a gas or vacuum gap. In one embodiment, to reduce the intensity of light incident on the PV cell, the PV cell can be positioned further away from the black body radiator. For example, the radius of the peripheral spherical chamber can be increased to reduce the intensity of light emitted from the internal spherical blackbody radiator, which is mounted on the inner surface of the peripheral spherical chamber (Fig. 2I 143). The PV converter can include a dense receiver array (DRA) comprised of a plurality of PV cells. The DRA can contain a mosaic shape. Individual PV cells can include at least one of a triangle, a pentagon, a hexagon, and other polygons. The cells forming the dome or sphere can be organized in a geodesic pattern. In an exemplary embodiment of a secondary blackbody radiator operating at a high temperature such as 3500 K, the emissivity is about 8.5 MW/m of emissivity.2 Times. In this case, the emissivity of the carbon dome 5b4 having an emissivity of about 1 can be reduced to about 0.35 by coating a tungsten carbide coating. The black body radiator 5b4 may comprise a cladding 26c of different materials (Fig. 2I 143) to change the emissivity to a more desirable emissivity. In an exemplary embodiment, the emissivity of the TaC (such as TaC coating, tile or cladding) on the carbon black body radiator 5b4 is about 0.2 with respect to the emissivity of carbon. In another embodiment, a PV cell, such as a PV cell including an external geodesic dome, can be at least one of: angled and includes a reflective coating to reduce light absorbed by the PV cell to a PV cell The level within the strength capacity. At least one PV circuit component (such as at least one of a group of PV cell electrodes, interconnects, and busbars) can comprise a material having a high emissivity, such as a polished conductor, such as polished aluminum, silver, gold, or copper. . The PV circuit elements can reflect the radiation from the black body radiator 5b4 back to the black body radiator 5b4 such that the PV circuit elements do not significantly contribute to the shadow PV power conversion losses. In an embodiment, the black body radiator 5b4 may comprise a plurality of separable segments, such as separable top and bottom hemispheres. The two hemispheres can be joined at the flange. The W dome can be fabricated by techniques known in the art such as sintering W powder, activated plasma sintering, casting, and 3D printing by laser melting. The lower chamber 5b5 can be joined at the hemispherical flange. The battery chamber can be attached to the lower chamber by a flange that can have at least one of vacuum, atmospheric pressure, and pressure above vacuum. The lower chamber can be hermetically sealed from at least one of the battery chamber and the reaction cell chamber. Gas can penetrate between the cell chamber and the reaction cell chamber. Gas exchange balances the pressure in the two chambers. A gas, such as at least one of hydrogen and a noble gas such as argon, may be added to the battery chamber to supply gas to the battery reaction chamber by permeation or flow. Permeation and flow can be for the desired gas (such as argon-H2 ) is selective. Metal vapors, such as silver metal vapors, may be impermeable or may be flow limited such that they selectively remain only in the cell reaction chamber. The metal vapor pressure can be controlled by maintaining the reservoir 5c at a temperature that condenses the metal vapor and maintains its vapor pressure at a desired level. The generator can utilize gas pressure (such as argon-H below operating pressure (such as atmospheric pressure)2 The gas pressure is activated so that no overpressure is formed as the battery heats up and the gas expands. Gas pressure can be controlled using the controllers of the present invention, such as computers, pressure sensors, valves, flow meters, and vacuum pumps. In an embodiment, the low energy hydrogen reaction is maintained by acting as a silver vapor for the conductive substrate. At least one of a continuous jet of at least a portion that becomes vapor and a direct boiling of silver from the reservoir 5c can provide silver vapor. The electrode can provide a high current to the reaction to remove electrons and initiate a low energy hydrogen reaction. The heat from the low energy hydrogen reaction can help provide metal vapor (such as silver metal vapor) to the reaction cell chamber. The ignition power supply can include at least one of a capacitor and an inductor. The ignition circuit can include a transformer. The transformer can output high current. The generator may include an inverter that receives DC power from the PV converter and outputs AC. The generator can include a DC to DC voltage and current regulator to vary the voltage and current from the PV converter that can be input to the inverter. The AC input to the transformer can come from the inverter. The inverter can operate at a desired frequency, such as a frequency in the range of about one to 10,000 Hz. In an embodiment, PV converter 26a outputs DC power, which may be fed directly to the inverter or may be adjusted prior to input to the inverter. The reverse phase power (such as 60 Hz AC) can be used to power the electrodes directly or can be input to the transformer to increase the current. In an embodiment, the power source 2 provides continuous DC or AC current to the electrodes. The electrodes and electromagnetic pump can support continuous firing of a sprayed melt, such as molten Ag, which can further comprise an oxygen source such as an oxide. Hydrogen can be added by infiltration through a black body radiator. Load tracking can be achieved by means of the present invention. In the embodiment, when the power from the reaction cell chamber 5b31 is adjusted downward, the black body radiator 5b4 to the PV converter 26a can radiate its stored energy extremely quickly. In an embodiment, the radiator appears as an incandescent filament having a similar light-off time in the event that the interruption of power flows from the reaction chamber 5b31 to the radiator 5b4. In another embodiment, electrical load tracking can be achieved by operating the radiator at approximately constant power flow corresponding to about a constant operating temperature, wherein undesired power to the load is dissipated or accumulated to the resistive element (such as A resistor, such as a SiC resistor or other heating element of the invention. In an embodiment, the generator may include a smart control system that intelligently activates and deactivates loads in a plurality of loads to control peak aggregation loads. The generator can include a plurality of generators that can be coupled to obtain at least one of stability and provide peak power. At least one of smart metering and control can be achieved by telemetry (such as by using a cellular phone or a personal computer with WiFi). In an embodiment, the black body light from the black body radiator 5b4 is randomly guided. The light may be at least one of reflected, absorbed, and re-radiated back and forth between the radiator blackbody radiator 5b4 and the PV cell 15. PV cells are optimally angled to achieve desired PV absorption and light to electrical conversion. The reflectivity of the PV cover glass can vary with position. The change in reflectivity can be achieved using a PV window with spatially variable reflectivity. The variability can be achieved with a coating. An exemplary coating is MgF2 - ZnS anti-reflective coating. The PV cells can be geometrically arranged to achieve absorption and reflection of the desired PV cells, involving at least two of the black body radiator 5b4 and the PV cells, between the plurality of PV cells, and between the plurality of PV cells The power flow interaction between the black body radiators 5b4. In an embodiment, the PC battery can be arranged into a surface having a variable radius that varies with surface angle, such as a folded surface, such as a folded geodesic dome. In an embodiment, the black body radiator 5b4 may have elements that are angled relative to each other to perform at least one of: directionally emitting, absorbing, and reflecting radiation to or from the PV cell, directionally emitting, absorbing, and reflecting radiation. In an embodiment, the black body radiator 5b4 may include an element emitter plate on the surface of the black body radiator to match the PV orientation to achieve the desired delivery of power to the PV cell. At least one of a blackbody radiator, reflector or absorber surface can have at least one of emissivity, reflectivity, absorption coefficient, and surface area selected to achieve PV to the radiator and PV cell. The desired power flow of the converter. Power flow can involve radiation bounce between the PV cell and the blackbody radiator. In an embodiment, at least one of the emissivity and surface area of the outer surface within the black body radiator 5b4 is selected to achieve the desired power flow to the PV cell to return power to the reaction cell chamber 5b31. In an embodiment, high energy light (such as at least one of UV and EUV) can be dissociated from the H in the reaction cell chamber 5b312 O and H2 At least one of them to increase the rate of low energy hydrogen reaction. Dissociation can be an alternative to pyrolysis effects. In another embodiment, the generator is operated to maintain a high metal vapor pressure in the reaction cell chamber 5b31. The high metal vapor pressure can be at least one of: forming a thick plasma to convert UV and EUV emissions from low energy hydrogen reactions to blackbody radiation; and acting as a reactant for low energy hydrogen reactions (such as a conductive substrate) Increase the rate of reaction. The low energy hydrogen reaction can propagate in the reaction cell chamber supported by pyrolysis of water. At least one of the metal vapor and blackbody temperatures can be higher (such as in the range of 1000K to 10,000K) to support the pyrolysis of water, thereby increasing the rate of low energy hydrogen reaction. The low energy hydrogen reaction can occur in at least one of the gas phase and the plasma phase. The metal may be ejected by an electromagnetic pump and vaporized by at least one of an ignition current and heat from a low energy hydrogen reaction. The reaction conditions, current, and metal spray rate can be adjusted to achieve the desired metal vapor pressure. Operating the generator at a temperature above the boiling point of the metal source of the metal vapor can cause a reaction cell chamber pressure greater than atmospheric pressure. The metal vapor pressure can be controlled by at least one of controlling the amount of metal vapor supplied to the chamber by an electromagnetic (EM) pump; and controlling the temperature of the battery component, such as a battery reservoir. In an embodiment, at least one of the reaction cell chamber 5b31 and the reservoir 5c may comprise at least one baffle that causes convection of hot vapor from a region of the reaction cell chamber to the reservoir 5c. A cold liquid metal surface in which the vapor has the highest temperature in a region such as where a low energy hydrogen reaction occurs. Thermal cycling can control the silver vapor pressure by condensing vapor, wherein the vapor pressure can be determined by at least one of a delivery rate and a vapor pressure dependence on a controllable liquid silver temperature. The reservoir can be deep enough to maintain liquid silver levels. The reservoir can be cooled by a heat exchanger to maintain liquid silver. This temperature can be controlled using cooling, such as water cooling. In an exemplary embodiment, a straight baffle extending from the reservoir into the reaction cell chamber separates the external cooling stream from the internal heat flow. In another embodiment, the EM pump can be controlled to stop pumping when the desired metal vapor pressure is achieved. Alternatively, the pressure of the cell chamber 5b3 or 5b3a1 can be matched to the pressure of the reaction cell chamber 5b31 such that there is a desired allowable pressure gradient across the chamber. A gas, such as a rare gas, may be added to the battery chamber by a free valve, regulator, controller, and pressure sensor controlled gas supply to reduce or equalize or balance the difference between chamber pressures. In an embodiment, gas may permeate between the cell chamber 5b3 or 5b3a1 and the reaction cell chamber 5b31. Chamber gases, rather than metal vapors, can move and balance the pressure of the two chambers. The two chambers can be pressurized to a high pressure using a gas such as a rare gas. The pressure can be higher than the highest operating partial pressure of the metal vapor. The highest metal vapor partial pressure can correspond to the highest operating temperature. During operation, the metal vapor pressure can increase the pressure of the reaction cell such that gas selectively flows from the reaction cell 5b3 to the cell chamber 5b3 or 5b3a1 until pressure equalization, and vice versa. In an embodiment, the gas pressure between the two chambers is automatically balanced. The balance can be achieved by the selective mobility of the gas between the chambers. In an embodiment, pressure offset is avoided in order to avoid large pressure differences. The pressure in the cell chamber can be maintained to be greater than the pressure in the chamber of the reaction cell. The greater pressure in the external battery chamber can be used to mechanically hold the battery components (black body radiator 56b4 and reservoir 5c) together. In an embodiment, the metal vapor is maintained at a steady state pressure wherein condensation of the vapor is minimized. The electromagnetic pump can be stopped under the desired metal vapor pressure. The EM pump can be started intermittently for pumping to maintain the desired steady state pressure. The metal vapor pressure may be maintained in at least one of 0.01 Torr to 200 atm, 0.1 Torr to 100 atm, and 1 Torr to 50 atm. In one embodiment, to achieve high and low energy hydrogen power, the control electrode is electromagnetically pumped to control ignition current parameters such as waveform, peak current, peak voltage, constant current, and constant voltage. In an embodiment, the waveform can be any desired waveform that optimizes the desired power output and efficiency. The waveforms can be constant current, constant voltage, constant power, sawtooth, square wave, sinusoidal, trapezoidal, triangular, ramped off, ramp-slope, and other waveforms known in the art. In the case where the waveform has a voltage or a portion of the current of about zero, the duty cycle can be in the range of about 1% to 99%. The frequency can be any desired, such as in at least one of about 0.001 to 1 MHz, 0.01 Hz to 100 kHz, and 0.1 Hz to 10 kHz. The peak current of the waveform can be in the range of about 10 A to 1 MA, 100 A to 100 kA, and 1 kA to 20 kA. The voltage can be given by the product of the resistance and the current. In an embodiment, the power source 2 can include an ignition capacitor bank 90. In an embodiment, the power source 2, such as a capacitor bank, can be cooled. The cooling system can include a cooling system of the present invention, such as a radiator. In an embodiment, power supply 2 includes a capacitor bank having a different number of series and parallel capacitors to provide optimum electrode voltage and current. The PV converter can act as a capacitor bank to the optimum voltage and maintain the optimum current. The ignition voltage can be increased by increasing the resistance across the electrodes. The electrode resistance can be increased by operating the electrode at a higher temperature, such as in the temperature range of about 1000K to 3700K. The electrode temperature can be controlled to maintain the desired temperature by controlling the ignition process and electrode cooling. The voltage can be in the range of about 1 V to 500 V, 1 V to 100 V, 1 V to 50 V, and 1 V to 20 V. The current may be in a range of at least about 10 A to 100 kA, 100 A to 10 kA, and 100 A to 5 kA. In an exemplary embodiment, the voltage is about 16 V at a constant current between 150 A and 250 A. In an embodiment, the power attributed to the low energy hydrogen reaction is higher at the positive electrode due to the higher low energy hydrogen reaction rate. The higher rate can be attributed to the more efficient removal of electrons from the reactive plasma by the positive electrode. In an embodiment, the low energy hydrogen reaction is dependent on the removal of electrons, which is advantageous at the higher electrode voltages applied. Electron removal can also be enhanced by grounding the battery assembly in contact with the reactive plasma. The generator can include additional ground or positive bias electrodes. The capacitor is included in the ignition capacitor housing 90 (Fig. 2I89). The ignition voltage can be high, such as in at least one of about 1 V to 100 V, 1 V to 50 V, and 1 V to 25 V. The current can be pulsed or continuous. The current may be in a range of at least about 50 A to 100 kA, 100 A to 10 kA, and 300 A to 5 kA. The vaporized melt can provide a conductive path that removes electrons from a low energy hydrogen catalyzed reaction to increase the rate of reaction. In an exemplary embodiment, the silver vapor pressure is higher due to vaporization in a temperature range of about 2162 ° C to 4000 ° C, such as in the range of about 0.5 atm to 100 atm. In an embodiment, the SunCell® can comprise a liquid electrode. The electrode can comprise a liquid metal. The liquid metal may comprise a molten metal of fuel. The injection system can include at least two reservoirs 5c and at least two electromagnetic pumps that can be substantially electrically isolated from each other. The nozzles 5q of each of the plurality of injection systems can be oriented to cause a plurality of molten metal streams to intersect. Each class can have a connection to the terminals of the power source 2 to provide voltage and current to the phase AC. Current can flow from one nozzle 5q via its molten metal stream to the other streams and nozzles 5q and back to the corresponding terminals of the power source 2. The battery includes a molten metal return system to facilitate returning the injected molten metal to a plurality of reservoirs. In an embodiment, the molten metal return system minimizes shorting of at least one of the ignition current and the injection current through the molten metal. The reaction cell chamber 5b31 may comprise a bottom layer that directs the reflux of the injected molten metal into a separate reservoir 5c such that the silver is substantially isolated in a separate reservoir 5c to be in the silver-connected reservoir Electrical shorts are minimized. The resistance for electrical conduction is substantially higher in the silver reflow between the reservoirs than in the intersecting silver such that most of the current flows through the phase. The battery may comprise a reservoir electrical isolator or separator, which may comprise an electrical insulator such as ceramic or a refractory material having low electrical conductivity such as graphite. The low energy hydrogen reaction can cause the production of high concentrations of electrons, which can slow down other low energy hydrogen production and thereby inhibit the low energy hydrogen reaction rate. The current at the ignition electrode 8 removes electrons. In an embodiment, a solid electrode, such as a solid refractory metal electrode, tends to melt when it is a positive electrode or an anode due to preferential removal of electrons at the anode to cause high and low energy hydrogen reaction rates and localized heating. In an embodiment, the electrode comprises a mixture of a liquid electrode and a solid electrode. The anode can comprise a liquid metal electrode and the cathode can comprise a solid electrode, such as a W electrode, and vice versa. The liquid metal anode can include at least one EM pump and a nozzle, wherein the liquid metal is injected to contact the cathode to turn the ignition circuit on. In an embodiment, the ignition power is terminated when the low energy hydrogen reaction propagates in the absence of electrical power input. The low energy hydrogen reaction can propagate in the reaction cell chamber supported by pyrolysis of water. The reaction independent of the ignition power itself can be propagated under suitable reaction conditions. The reaction conditions can include at least one of a high temperature and a suitable reactant concentration. At least one of low energy hydrogen reaction conditions and current can be controlled to achieve a high temperature on at least a portion of the electrode to achieve pyrolysis. At least one of the reaction temperature and the temperature of a portion of the electrode may be higher, such as at least one of about 1000 ° C to 20,000 ° C, 1000 ° C to 15,000 ° C, and 1000 ° C to 10,000 ° C. Suitable reaction concentrations can include water vapor pressures in at least one of the following ranges: about 0.1 Torr to 10,000 Torr, 0.2 Torr to 1000 Torr, 0.5 Torr to 100 Torr, and 0.5 Torr to 10 Torr. Suitable reaction concentrations can include hydrogen pressure in at least one of the following ranges: about 0.1 Torr to 10,000 Torr, 0.2 Torr to 1000 Torr, 0.5 Torr to 100 Torr, and 0.5 Torr to 10 Torr. Suitable reaction concentrations can include metal vapor pressures in at least one of the following ranges: from about 1 Torr to 100,000 Torr, from 10 Torr to 10,000 Torr, and from 1 Torr to 760 Torr. The reaction cell chamber can be maintained at a temperature that maintains a metal vapor pressure that optimizes the rate of low energy hydrogen reaction. In an embodiment, the compound may be added to a molten metal such as molten Ag or an AgCu alloy to perform at least one of: lowering its melting point and viscosity. The compound may contain a flux such as borax. In an embodiment, a solid fuel, such as the solid fuel of the present invention, may be added to the molten metal. In an embodiment, the molten metal (such as molten silver, copper or AgCu alloy) comprises a composition for binding or dispersing water in a melt, such as a flux, which may be hydrated, such as borax, which may It is hydrated to various degrees such as anhydrous borax, borax pentahydrate and borax decahydrate. The melt may contain a flux to remove oxide from the interior of the pump tube. Removal can maintain good electrical contact between the molten metal and the pump tube 5k6 at the area of the electromagnetic pump bus 5k2. In an embodiment, a compound comprising an oxygen source may be added to the molten metal, such as molten silver, copper or an AgCu alloy. In an embodiment, the metal melt comprises a metal that does not adhere to a battery component, such as a tapered reservoir and a vertebral body or dome. The metal may comprise an alloy such as Ag-Cu (such as AgCu (28 wt%)) or an Ag-Cu-Ni alloy. The compound can be melted at the operating temperature of the reservoir 5c and the electromagnetic pump such that it performs at least one of: dissolving and mixing with the molten metal. The compound can be subjected to at least one of the following: at a temperature below the melting point: dissolved and mixed in the molten metal. Exemplary compounds comprising a source of oxygen comprise an oxide such as a metal oxide or a Group 13, 14, 15, 16 or 17 oxide. An exemplary metal of a metal oxide is at least one of metals having a low water reaction rate, such as a group of the following: Cu, Ni, Pb, Sb, Bi, Co, Cd , Ge, Au, Ir, Fe, Hg, Mo, Os, Pd, Re, Rh, Ru, Se, Ag, Tc, Te, Tl, Sn, W, and Zn. The corresponding oxide can thermally react with hydrogen to form a HOH catalyst. Exemplary metal oxides and their corresponding melting points are sodium tetraborate decahydrate (MP = 743 ° C, anhydrous), CuO (MP = 1326 ° C), NiO (MP = 1955 ° C), PbO (MP = 888 ° C), Sb2 O2 (M.P. = 656 °C), Bi2 O3 (M.P. = 817 ° C), CO2 O3 (M.P. = 1900 ° C), CdO (M.P. = 900-1000 ° C), GeO2 (M.P. = 1115 ° C), Fe2 O3 (M.P. = 1539-1565 ° C), MoO3 (M.P. = 795 °C), TeO2 (M.P. = 732 ° C), SnO2 (M.P. = 1630 ° C), WO3 (M.P. = 1473 °C), WO2 (M.P. = 1700 ° C), ZnO (M.P. = 1975 ° C), TiO2 (M.P. = 1843 ° C), Al2 O3 (M.P. = 2072 ° C), alkaline earth metal oxides, rare earth metal oxides, transition metal oxides, internal transition metal oxides, alkali metal oxides (such as Li2 O (M.P. = 1438°C), Na2 O (M.P. = 1132°C), K2 O (M.P. = 740 °C), Rb2 O (M.P. = >500°C), Cs2 O (M.P. = 490 ° C)), boron oxide (such as B2 O3 (M.P.=450°C)), V2 O5 (M.P. = 690 °C), VO (M.P. = 1789 °C), Nb2 O5 (M.P. = 1512 ° C), NbO2 (M.P. = 1915 ° C), SiO2 (M.P. = 1713 ° C), Ga2 O3 (M.P. = 1900 °C), In2 O5 (M.P. = 1910 ° C), Li2 WO4 (M.P. = 740 ° C), Li2 B4 O7 (M.P. = 917 °C), Na2 MoO4 (M.P. = 687 °C), LiVO3 (M.P. = 605 ° C), Li2 VO3 Mn2 O5 (M.P. = 1567°C) and Ag2 WO4 (M.P. = 620 ° C). Further exemplary oxides comprise a mixture of oxides, such as comprising a base type oxide such as Li2 O and Na2 O and Al2 O3 , B2 O3 And VO2 a mixture of at least two of them. The mixture can cause more desirable physical properties, such as a lower melting point or a higher boiling point. The oxide can be dried. At the source of oxygen (such as Bi2 O3 Or Li2 WO4 In an exemplary embodiment, the hydrogen-derived hydrogen reduction reaction is thermodynamically advantageous, and the reduction product reacts with water to form an oxygen source that can occur under operating conditions, such as under red heat conditions. In an exemplary embodiment, under red heat, hydrazine reacts with water to form a trioxide (bismuth(III) oxide) (2Bi(s) + 3H2 O(g) →Bi2 O3 (s) + 3H2 (g)). In an embodiment, the oxide is vaporized into a gas phase or a plasma. The number of moles of oxide in the reaction cell chamber 5b31 can limit its vapor pressure. In embodiments, the source of oxygen forming the HOH catalyst can comprise a plurality of oxides. Each of the plurality of oxides can be volatilized to act as a source of HOH catalyst over certain temperature ranges. For example, LiVO3 It can serve as a primary oxygen source above its melting point and below the melting point of a second source of oxygen, such as a second oxide. The second oxide acts as a source of oxygen at higher temperatures, such as above its melting point. An exemplary second oxide is Al2 O3 , ZrO, MgO, alkaline earth metal oxides and rare earth metal oxides. The oxide may be substantially all gaseous at an operating temperature such as 3000K. The pressure can be adjusted by the number of moles added to the reaction cell chamber 5b31. The ratio of oxide to silver vapor pressure can be adjusted to optimize low energy hydrogen reaction conditions and rates. In an embodiment, the source of oxygen may comprise an inorganic compound, such as at least one of the following: H2 O, CO, CO2 , N2 O, NO, NO2 , N2 O3 , N2 O4 , N2 O5 , SO, SO2 , SO3 , PO, PO2 , P2 O3 , P2 O5 . Oxygen source (such as CO2 At least one of CO and CO can be a gas at room temperature. An oxygen source, such as a gas, can be in the outer pressure vessel chamber 5b31a. The oxygen source can comprise a gas. The gas may be at least one of: diffused or permeated from the external pressure vessel chamber 5b31a to the reaction electrolytic cell chamber 5b31; and diffused or permeated from the reaction electrolytic cell chamber 5b31 to the external pressure vessel chamber 5b31a. The concentration of the oxygen source gas inside the reaction cell chamber 5b31 can be controlled by controlling the pressure in the external pressure vessel chamber 5b31a. The oxygen source gas can be added to the reaction cell chamber as a gas inside the reaction cell chamber through a supply line. The supply line can enter a cooler region, such as into an EM pump tube at the bottom of the reservoir. Oxygen source gas can be decomposed or vaporized by solid or liquid (such as freezing CO2 , carbonate or carbonic acid). The pressure in at least one of the outer pressure vessel chamber 5b31a and the reaction cell chamber 5b31 can be measured using a pressure gauge such as the pressure gauge of the present invention. The controller and gas source can be used to control the gas pressure. The reaction cell chamber 5b31 gas may further comprise H2 It is permeable to the black body radiator 5b4 or supplied via an EM pump tube or another inlet. Another gas (such as CO2 , CO and H2 At least one of O can be supplied by at least one of permeating and flowing through an inlet, such as an EM pump tube. H2 O may comprise at least one of water vapor and gaseous water or steam. The gas in the external chamber can contain H2 , H2 O, CO and CO2 In at least one of the gases, the gas permeates a black body radiator (such as the carbon black body radiator 5b4) to supply the reaction cell chamber 5b31. The gas may be at least one of: diffused or permeated from the external pressure vessel chamber 5b31a to the reaction electrolytic cell chamber 5b31; and diffused or permeated from the reaction electrolytic cell chamber 5b31 to the external pressure vessel chamber 5b31a. Controlling the corresponding gas pressure in the external chamber controls the concentration of the reaction cell chamber 5b31 for each gas. A corresponding sensor can be used to sense the pressure or concentration of the reaction cell chamber 5b31 for each gas. CO, CO2 And H2 The presence in the reaction cell chamber 5b31 can contain H2 O reacts with any battery component consisting of carbon, such as a carbon reaction cell chamber. In an embodiment, H2 O with low energy hydrogen (such as H2 The oxygen product of the reaction of (1/4)) can be beneficial for low energy hydrogen reactions. The oxidative side reaction of the oxygen product with the battery component can be contained by the presence of hydrogen. The molten metal coating that can be formed during operation also protects the battery assembly from H2 At least one of O and oxygen reacts. In an embodiment, the wall (such as the inner wall of the reaction cell chamber) may be coated with a coating (such as pyrolytic graphite in the case of a reaction cell chamber), wherein the coating is selected for the desired gas system Sexually permeable. In an exemplary embodiment, the blackbody radiator 5b4 contains carbon, and the inner wall of the reaction cell chamber 5b31 contains pyrolytic graphite, which is H2 System permeable, at the same time O2 , CO, CO2 And H2 At least one of O is impermeable. The inner wall may be coated with a molten metal such as silver to avoid walls and oxidizing substances such as O2 And H2 O) Reaction. The source of oxygen can comprise a compound comprising an oxyanion. The compound can comprise a metal. The compound may be selected from one of the group consisting of oxides, hydroxides, carbonates, hydrogencarbonates, sulfates, hydrogen sulfates, phosphates, hydrogen phosphates, dihydrogen phosphates, nitrates, nitrites. , permanganate, chlorate, perchlorate, chlorite, perchlorate, hypochlorite, bromate, perbromate, bromate, perbromic acid Salt, iodate, periodate, iodate, periodate, chromate, dichromate, citrate, selenate, arsenate, citrate, borate, Cobalt oxide, ruthenium oxide and other oxygen anions, such as oxygen anions of the following: halogen, P, B, Si, N, As, S, Te, Sb, C, S, P, Mn, Cr, Co and Te, The metal may comprise one or more of the following: an alkali metal, an alkaline earth metal, a transition metal, an internal transition metal or a rare earth metal, Al, Ga, In, Ge, Sn, Pb, Sb, Bi, Se, and Te. Oxygen source can include MNO3 , MClO4 MOx , Mx O and Mx Oy At least one of them, wherein M is a metal such as a transition metal, an internal transition metal, a rare earth metal, Sn, Ga, In, lead, bismuth, an alkali metal or an alkaline earth metal, and x and y are integers. The oxygen source can include at least one of the following: SO2 , SO3 , S2 O5 O2 , F5 SOF, M2 S2 O8 , SOx Xy (such as SOCl2 , SOF2 , SO2 F2 Or SOBr2 ), Xx X'y Oz (where X and X' are halogens (such as ClO)2 F, ClO2 F2 , ClOF3 , ClO3 F, and ClO2 F3 ), yttrium oxide (such as TeO)x , such as TeO2 Or TeO3 Te(OH)6 ), SeOx (such as SeO2 Or SeO3 ), selenium oxide (such as SeO)2 SeO3 SeOBr2 SeOCl2 SeOF2 Or SeO2 F2 ), P2 O5 POx Xy (where X is a halogen, such as POBr3 POI3 POCl3 Or POF3 ), arsenic oxide (such as As2 O3 Or As2 O5 ), yttrium oxide (such as Sb)2 O3 , Sb2 O4 Or Sb2 O5 , or SbOCl, Sb2 (SO4)3 ), cerium oxide, another cerium compound (such as BiAsO)4 Bi(OH)3 Bi2 O3 , BiOBr, BiOCl, BiOI, Bi2 O4 ), metal oxides or hydroxides (such as Y2 O3 , GeO, FeO, Fe2 O3 , or NbO, NiO, Ni2 O3 , SnO, SnO2 , Ag2 O, AgO, Ga2 O, As2 O3 SeO2 TeO2 In(OH)3 ,Sn(OH)2 In(OH)3 Ga(OH)3 Or Bi(OH)3 ), CO2 , CO, permanganate (such as KMnO4 And NaMnO4 ), P2 O5 Nitrate (such as LiNO3 NaNO3 And KNO3 ), a transition metal oxide or hydroxide (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, or Zn having at least one O and OH), oxygen (oxygen) (such as FeOOH) , a second or third transition series of oxides or hydroxides (such as oxides or hydroxides of Y, Zr, Nb, Mo, Tc, Ag, Cd, Hf, Ta, W, Os), noble metal oxides ( Such as PdO or PtO), metals and oxyanions (such as Na2 TeO4 Or Na2 TeO3 ), CoO, a compound containing at least two atoms from oxygen and a group of different halogen atoms (such as F)2 O, Cl2 O, ClO2 Cl2 O6 Cl2 O7 , ClOF3 , ClO2 F, ClO2 F3 , ClO3 F, I2 O5 ), a metal compound can be formed after reduction. The source of oxygen may comprise a gas comprising oxygen, such as O2 , N2 O and NO2 At least one of them. In an embodiment, the melt comprises at least one additive. The additive may comprise an oxygen source and a hydrogen source. At least one of the oxygen source and the hydrogen source may comprise one or more of the following groups: H2 NH3 MNH2 , M2 NH, MOH, MAlH4 , M3 AlH6 And MBH4 , MH, MNO3 , MNO, MNO2 , M2 NH, MNH2 NH3 , MBH4 MAlH4 , M3 AlH6 , MHS, M2 CO3 MHCO3 , M2 SO4 MHSO4 , M3 PO4 , M2 HPO4 MH2 PO4 , M2 MoO4 , M2 MoO3 MNbO3 , M2 B4 O7 MBO2 , M2 WO4 , M2 CrO4 , M2 Cr2 O7 , M2 TiO3 MZrO3 MAlO2 , M2 Al2 O2 , MCoO2 , MGaO2 , M2 GeO3 MMnO4 , M2 MnO4 , M4 SiO4 , M2 SiO3 MTaO3 MVO3 MIO3 , MFeO2 MIO4 , MOCl, MClO2 , MClO3 , MClO4 , MClO4 MScO3 MScOn MTiOn MVOn , MCrOn , MCr2 On, MMn2 On , MFeOn , MxCoOn (x is an integer or fraction), MNiOn, MNi2 On, MCuOn, MZnOn, where n = 1, 2, 3 or 4 and M is a metal such as alkali metal, Mg3 (BO3 )2 And M2 S2 O8 a mixed metal oxide or intercalated oxide (such as a lithium ion battery intercalation compound), such as at least one of the group of: LiCoO2 LiFePO4 LiNix Mny Coz O2 LiMn2 O4 LiFeO2 Li2 MnO3 Li2 MnO4 LiNiO2 LiFeO2 LiTaO3 LiVO3 Li2 VO3 Li2 NbO3 Li2 SeO3 Li2 SeO4 Li2 TeO3 Li2 TeO4 Li2 WO4 Li2 CrO4 Li2 Cr2 O7 Li2 HfO3 Li2 MoO3 Or Li2 MoO4 Li2 TiO3 Li2 ZrO3 And LiAlO2 Flux, such as sodium tetraborate (M.P. = 743 ° C, anhydrous), K2 SO4 (M.P. = 1069 ° C), Na2 CO3 (M.P. = 851 °C), K2 CO3 (M.P. = 891 °C), KOH (M.P. = 360 °C), MgO, (M.P. = 2852 °C), CaO, (M.P. = 2613 °C), SrO (M.P. = 2531 °C), BaO (M.P. = 1923 °C), CaCO3 (M.P. = 1339 ° C); a molecular oxidant, which may contain gases such as CO, CO2 , SO2 , SO3 , S2 O5 Cl2 , F5 SOF, SOx Xy (such as SOCl2 , SOF2 , SO2 F2 , SOBr2 ), PO2 , P2 O3 , P2 O5 POx Xy (such as POBr3 POI3 POCl3 Or POF3 ), I2 O5 , Re2 O7 , I2 O4 , I2 O5 , I2 O9 , SO2 , CO, CO2 , N2 O, NO, NO2 , N2 O3 , N2 O4 , N2 O5 Cl2 O, ClO2 Cl2 O3 Cl2 O6 Cl2 O7 NH4 X, wherein X is a nitrate ion or other suitable anion known to those skilled in the art, such as one of the group consisting of: NO3-, NO2-, SO42-, HSO4-, CoO2-, IO3 -, IO4-, TiO3-, CrO4-, FeO2 -, PO43-, HPO42-, H2PO4-, VO3-, ClO4- and Cr2O72; oxyanions, such as one of the following groups: NO3-, NO2-, SO42-, HSO4-, CoO2-, IO3 -, IO4-, TiO3-, CrO4-, FeO2 -, PO43-, HPO42-, H2PO4-, VO3-, ClO4- and Cr2O72-; strong acid, oxidant, oxyanion of molecular oxidant, such as one of the following groups: V2O3, I2O5, MnO2 , Re2O7, CrO3, RuO2 , AgO, PdO, PdO2 , PtO, PtO2 And NH4X, wherein X is a nitrate ion or other suitable anion known to those skilled in the art; a hydroxide, such as one of the group of: Na, K, Rb, Cs, Mg, Ca, Sr, Ba, Al, V, Zr, Ti, Mn, Zn, Cr, Sn, In, Cu, Ni, Pb, Sb, Bi, Co, Cd, Ge, Au, Ir, Fe, Hg, Mo, Os, Pd, Re, Rh, Ru, Se, Ag, Tc, Te, Tl and W, MOH, MOH, M'(OH)2, wherein M is an alkali metal and M' is an alkaline earth metal, a transition metal hydroxide, Co (OH)2, Zn(OH)2, Ni(OH)2, other transition metal hydroxides, rare earth metal hydroxides, Al(OH)3, Cd(OH)2, Sn(OH)2, Pb ( OH), In(OH)3, Ga(OH)3, Bi(OH)3, including,,,,,anda compound, a complex ion hydroxide such as Li2Zn(OH)4, Na2Zn(OH)4, Li2Sn(OH)4, Na2Sn(OH)4, Li2Pb(OH)4, Na2Pb(OH)4, LiSb(OH 4) NaSb(OH)4, LiAl(OH)4, NaAl(OH)4, LiCr(OH)4, NaCr(OH)4, Li2Sn(OH)6 and Na2Sn(OH)6; acids such as H2SO3, H2SO4, H3PO3, H3PO4, HClO4, HNO3, HNO, HNO2 , H2CO3, H2MoO4, HNbO3, H2B4O7, HBO2 , H2WO4, H2CrO4, H2Cr2O7, H2TiO3, HZrO3, MAlO2 , HMn2O4, HIO3, HIO4, HClO4, or an acid source, such as an anhydrous acid, such as at least one of the group of: SO2 , SO3, CO, CO2 NO2 , N2O3, N2O5, Cl207, PO2 And P2O3 and P2O5; a solid acid, such as one of the group of MHSO4, MHCO3, M2HPO4, and MH2PO4, wherein M is a metal, such as an alkali metal; an oxygen (hydrogen) compound, such as one of the group of the following: : WO2(OH), WO2(OH)2, VO(OH), VO(OH)2, VO(OH)3, V2O2(OH)2, V2O2(OH)4, V2O2(OH)6, V2O3( OH)2, V2O3(OH)4, V2O4(OH)2, FeO(OH), (α -MnO(OH) manganese vermiculite andγ -MnO(OH) Manganese ore), MnO(OH), MnO(OH)2, Mn2O3(OH), Mn2O2(OH)3, Mn2O(OH)5, MnO3(OH), MnO2(OH)3, MnO( OH)5, Mn2O2(OH)2, Mn2O6(OH)2, Mn2O4(OH)6, NiO(OH), TiO(OH), TiO(OH)2, Ti2O3(OH), Ti2O3(OH)2, Ti2O2 (OH)3, Ti2O2(OH)4, and NiO(OH), hydrous calcium ore (CrO(OH)), diaspore (AlO(OH)), ScO(OH), YO(OH), VO(OH ), goethite (α -Fe3+O(OH)), manganese vermiculite (Mn3+O(OH)), Guyanaite (CrO(OH)), black iron vanadium ore ((V,Fe)O(OH)), CoO(OH), NiO(OH), Ni1/2Co1/2O(OH) and Ni1/3Co1/3Mn1/3O(OH), RhO(OH), InO(OH), green phosphorus lead copper ore (tsumgallite) (GaO (OH)), Manganese ore (Mn3+O(OH)), Tungsten Tungsten-(Y)YW2O6(OH)3, Tungsten Tungsten-(Ce) ((Ce, Nd, Y) W2O6(OH)3) Untitled (Nd-analog of Tungsten Tungsten-(Ce)) ((Nd, Ce, La) W2O6(OH)3), Frankish chromite ore (frankhawthorneite) (Cu2[(OH)2[TeO4] ), lead and copperDeputy lead copper oreAnd MxOyHz, wherein x, y and z are integers, and M is a metal such as a transition metal, an internal transition metal or a rare earth metal such as a metal oxyhydroxide; an oxide such as in the group of the following One: oxyanion compound; aluminate; tungstate; zirconate; titanate; sulfate; phosphate; carbonate; nitrate; chromate and manganate, oxide; nitrite; Borate; boron oxide (such as B2 O3 Metal oxides; non-metal oxides; oxides of the following: alkali metals, alkaline earth metals, transition metals, internal transition metals and rare earth metals, and Al, Ga, In, Sn, Pb, S, Te, Se , N, P, As, Sb, Bi, C, Si, Ge and B, and other elements forming oxides or oxyanions; oxides comprising at least one from alkali metals, alkaline earth metals, transition metals, internal transition metals And cations of rare earth metals, and Al, Ga, In, Sn, and Pb cations, metal oxide anions and cations (such as alkali metals, alkaline earth metals, transition metals, internal transition metals, and rare earth metal cations); and other metals And metal-like oxides (such as oxides of Al, Ga, In, Si, Ge, Sn, Pb, As, Sb, Bi, Se, and Te, such as: MM'2xO3x+1 or MM'2xO4 (M = alkaline earth) Metal, M' = transition metal such as Fe or Ni or Mn, x = integer) and M2M'2xO3x+1 or M2M'2xO4 (M = alkali metal, M' = transition metal such as Fe or Ni or Mn, x = Integer), M2O and MO, where M is a metal (such as an alkali metal such as Li2 O, Na2 O and K2 O)) and alkaline earth metals (such as MgO, CaO, SrO and BaO), MCoO2 (where M is a metal, such as an alkali metal), CoO2 MnO2 Mn2 O3 Mn3 O4 , PbO2 , Ag2 O2 , AgO, RuO2 a compound comprising silver and oxygen, an oxide of a transition metal (such as NiO and CoO), V, Zr, Ti, Mn, Zn, Cr, Sn, In, Cu, Ni, Pb, Sb, Bi, Co, Cd , oxides of Ge, Au, Ir, P, Hg, Mo, Os, Pd, Re, Rh, Ru, Se, Ag, Tc, Te, Tl and W transition metals and oxides of Sn (such as SnO), alkali Metal oxides (such as Li2O, Na2O and K2O) and alkaline earth metal oxides (such as MgO, CaO, SrO and BaO), MoO2 TiO2 ZrO2 SiO2 , Al2O3, NiO, Ni2O3, FeO, Fe2O3, TaO2 , Ta2O5, VO, VO2 , V2O3, V2O5, B2O3, NbO, NbO2 , Nb2O5, SeO2 , SeO3, TeO2 , TeO3, WO2 , WO3, Cr3O4, Cr2O3, CrO2 , CrO3, MnO, Mn2O7, HfO2 CO2 O3, CoO, Co3O4, PdO, PtO2 , BaZrO3, Ce2O3, LiCoO2 , Sb2O3, BaWO4, BaCrO4, BaSi2O5, Ba (BO2 2, Ba(PO3)2, BaSiO3, BaMoO4, Ba(NbO3)2, BaTiO3, BaTi2O5, BaWO4, CoMoO4, CO2 SiO4, CoSO4, CoTiO3, CoWO4, CO2 TiO4, Nb2O5, Li2MoO4, LiNbO3, LiSiO4, Li3PO4, Li2SO4, LiTaO3, Li2B4O7, Li2TiO3, Li2WO4, LiVO3, Li2VO3, Li2ZrO3, LiFeO2 , LiMnO4, LiMn2O4, LiGaO2 , Li2GeO3, LiGaO2 a hydrate, such as a hydrate of the present invention, such as borax or sodium tetraborate hexahydrate; a peroxide such as H2O;2 M2O2 (where M is an alkali metal) (such as Li2O2 Na2O2 K2O2 ), other ionic peroxides, such as alkaline earth metal peroxides (such as Ca, Sr, or Ba peroxide ionic peroxides, other positively charged metal ionic peroxides (such as lanthanide ion peroxidation) And covalent metal peroxides (such as covalent metal peroxides of Zn, Cd and Hg); superoxides such as MO2 (where M is an alkali metal), such as NaO2 , KO2 RbO2 And CsO2 And an alkaline earth metal superoxide; a compound comprising at least one of an OH species and an H species, such as O2, O3,,, O, O+, H2O, H3O+, OH, OH+, OH-, HOOH, OOH-, O-, O2-,andAt least one of the H substances such as H2, H, H+, H2O, H3O+, OH, OH+, OH-, HOOH, and OOH-; an anhydride or oxide capable of undergoing a hydration reaction, comprising An element, a metal, an alloy, or a mixture, such as one of the following groups: Mo, Ti, Zr, Si, Al, Ni, Fe, Ta, V, B, Nb, Se, Te, W, Cr, Mn , Hf, Co and Mg, Li2MoO3, Li2MoO4, Li2TiO3, Li2ZrO3, Li2SiO3, LiAlO2 LiNiO2 LiFeO2 , LiTaO3, LiVO3, Li2VO3, Li2B4O7, Li2NbO3, Li2SeO3, Li2SeO4, Li2TeO3, Li2TeO4, Li2WO4, Li2CrO4, Li2Cr2O7, Li2MnO4, Li2HfO3, LiCoO2 And MO (where M is a metal such as an alkaline earth metal such as Mg of MgO), As2O3, As2O5, Sb2O3, Sb2O4, Sb2O5, Bi2O3, SO2 , SO3, CO, CO2 NO2 , N2O3, N2O5, Cl2O7, PO2 , P2O3 and P2O5; hydrides, such as hydrides from the group: R-Ni, La2Co1Ni9H6, La2Co1Ni9H6, ZrCr2H3.8, LaNi3.55Mn0.4Al0.3Co0.75, ZrMn0.5Cr0.2V0.1Ni1.2 And other alloys capable of storing hydrogen, such as hydrogen selected from the group consisting of MmNi5 (Mm = Mex alloy) (such as MmNi3.5Co0.7Al0.8, AB5 (LaCePrNdNiCoMnAl) or AB2 (VTiZrNiCrCoMnAlSn) type), wherein "ABx "Marker" refers to the ratio of element A (LaCePrNd or TiZr) to element B (VNiCrCoMnAlSn); AB5 type, MmNi3.2Co1.0Mn0.6Al0.11Mo0.09 (Mm = Michao alloy: 25 wt% La, 50 wt % Ce, 7 wt% Pr, 18 wt% Nd), La1-yRyNi5-xMx; AB2 type: Ti0.51Zr0.49V0.70Ni1.18Cr0.12 alloy; magnesium-based alloy; Mg1.9Al0.1Ni0.8Co0.1Mn0. 1 alloy; Mg0.72Sc0.28 (Pd0.012 + Rh0.012) and Mg80Ti20, Mg80V20, La0.8Nd0.2Ni2.4CO2 .5Si0.1, LaNi5-xMx (M= Mn, Al), (M=Al, Si, Cu), (M=Sn), (M=Al, Mn, Cu) and LaNi4Co, MmNi3.55Mn0.44Al0. 3Co0.75, LaNi3.55Mn0.44Al0.3Co0.75, MgCu2, MgZn2, MgNi2; AB compound; TiFe, TiCo and TiNi, ABn compound (n = 5, 2 or 1), AB3-4 compound; ABx (A = La, Ce, Mn, Mg; B = Ni, Mn, Co, Al), ZrFe2, Zr0.5Cs0.5Fe2, Zr0.8Sc0.2Fe2, YNi5, LaNi5, LaNi4.5Co0.5, (Ce, La, Nd, Pr)Ni5; Mickey alloy nickel alloy, Ti0.98Zr0.02V0.43Fe0.09Cr0.05Mn1.5, La2Co1Ni9, FeNi, TiMn2, TiFeH2, MNH system substances (such as LiNH2, Li2NH or Li3N); and alkali metal hydride Further comprising boron (such as borohydride) or aluminum (such as aluminum hydride); alkaline earth metal hydride (such as MgH2); metal alloy hydride (such as BaReH9, LaNi5H6, FeTiH1.7 and MgNiH4); metal borohydride (such as Be(BH4)2, Mg(BH4)2, Ca(BH4)2, Zn(BH4)2, Sc(BH4)3, Ti(BH4)3, Mn(BH4)2, Zr(BH4)4, NaBH4, LiBH4, KBH4 and Al(BH4)3, AlH3, NaAlH4, Na3AlH6, LiAlH4, Li3AlH6, LiH, LaNi5H6, La2Co1Ni9H6 and TiFeH2, NH3BH3; hydrogen Metal or semi-metal, which comprises alkali metals (Na, K, Rb, Cs), alkaline earth metals (Mg, Ca, Ba, Sr), elements from Group IIIA (such as B, Al, Ga, Sb), from the family Elements of IVA (such as C, Si, Ge, Sn) and elements from the family VA (such as N, P, As), transition metal alloys and intermetallic compounds ABn, where A represents one or more capable of forming a stable hydride The element and B are elements forming an unstable hydride; the intermetallic compound given in Table 2; wherein the part A and/or part B is replaced by another element such as an element in which M represents an element of LaNi5. The intermetallic alloy may be represented by LaNi5-xAx, wherein A is, for example, Al, Cu, Fe, Mn, and/or Co, and La may be substituted by a Michael alloy; 30% to 70% lanthanum, cerium, and a very small amount. Substituting a mixture of rare earth metals from the same series of elements, the remainder being ruthenium; forming a mixed hydride (such as an alloy of MMgH3 (M = alkali metal) (such as Li3Mg, K3Mg, Na3Mg); polyamine borane; amine borane Compounds such as amine borane, borane ammine, bismuth-borane complex, diborane diammine, boron azide and eight Triammonium or ammonium tetrahydroborate); imidazolium ionic liquids (such as alkyl (aryl)-3-methylimidazolium N-bis(trifluoromethanesulfonyl) sulfinium imide, barium borate and oxalic acid Salt material). Further exemplary compounds are ammonia borane, alkali ammonia borane (such as lithium ammonia borane) and borane alkylamine complex (such as borane dimethylamine complex, borane trimethylamine complex) and Aminoborane and borane amine (such as aminodiborane, n-dimethylaminodiborane, tris(dimethylamino)borane, di-n-butylboronamine, dimethylaminoborane, Trimethylaminoborane, ammonia-trimethylborane and triethylaminoborane. Further suitable hydrogen storage materials are hydrogen-absorbing organic liquids such as oxazoles and derivatives such as 9-( 2-ethylhexyl)carbazole, 9-ethylcarbazole, 9-phenyloxazole, 9-methylcarbazole and 4,4'-bis(N-carbazolyl)-1,1'-linked Diphenyl; Table 2. Elements and combinations of hydride formation. a hydrogen permeable membrane such as Ni(H2), V(H2), Ti(H2), Fe(H2) or Nb(H2); a compound comprising at least one of oxygen and hydrogen, such as a compound of the present invention, Wherein other metals may be substituted for the metal of the invention, and M may be another cation such as an alkaline earth metal, a transition metal, an internal transition metal or a rare earth metal cation or a 13th to 16th cation (such as Al, Ga, In, Sn, Pb, Bi and Te), and the metal may be one of molten metals, such as at least one of silver and copper, and other such sources of at least one of hydrogen and oxygen, such as those skilled in the art The source of knowledge. In an embodiment, at least one of the ability to release by a low energy hydrogen reaction and the voltage applied across the electrodes is sufficient to destroy oxygen binding from the oxygen source to release oxygen. The voltage can be in a range of at least one of about 0.1 V to 30 V, 0.5 V to 4 V, and 0.5 V to 2 V. In an embodiment, the source of oxygen is more stable than the hydrogen reduction product (such as water) and the source of oxygen containing less oxygen. The hydrogen reduction product can react with water to form a source of oxygen. The reduced oxygen source can be reacted with at least one of water and oxygen to maintain a low concentration of such oxidants in the reaction cell chamber 5b31. The reduced oxygen source maintains the dome 5b4. Contains W domes and highly stable oxides such as Na2 In an exemplary embodiment of O), the reduced oxygen source oxygen is Na metal vapor, which is associated with H2 O and O2 The two react to remove these gases from the chamber of the reaction cell. Na also reduces the W oxide on the dome to W to keep it from corroding. An exemplary source of oxygen, such as an oxygen source capable of dissolving or mixing into a melt, such as molten silver, having a suitable melting point and boiling point, is selected from at least one of the group consisting of NaReO4, NaOH, NaBrO3, B2O3, PtO2 MnO2 , Na5P3O10, NaVO3, Sb2O3, Na2MoO4, V2O5, Na2WO4, Li2MoO4, Li2CO3, TeO2 , Li2WO4, Na2B4O7, Na2CrO4, Bi2O3, LiBO2 , Li2SO4, Na2CO3, Na2SO4, K2CO3, K2MoO4, K2WO4, Li2B4O7, KBO2 NaBO2 , Na4P2O7, CoMoO4, SrMoO4, Bi4Ge3012, K2SO4, Mn2O3, GeO2 , Na2SiO3, Na2O, Li3PO4, SrNb2O6, Cu2O, LiSiO4, LiNbO3, CuO, CO2 SiO4, BaCrO4, BaSi2O5, NaNbO3, Li2O, BaMoO4, BaNbO3, WO3, BaWO4, SrCO3, CoTiO3, CoWO4, LiVO3, Li2VO3, Li2ZrO3, LiMn2O4, LiGaO2 , Mn3O4, Ba (BO2 ) 2 *H2O, Na3VO4, LiMnO4, K2B4O7*4H2O and NaO2 . In an embodiment, a source of oxygen (such as a peroxide such as Na)2 O2 ), hydrogen source (such as hydride or hydrogen, such as argon / H2 (3% to 5%) and a conductive substrate such as molten silver can act as a solid fuel to form low energy hydrogen. The reaction can be carried out in an inert vessel such as an alkaline earth metal oxide vessel such as a MgO vessel. The additive may further comprise a compound or element formed by reduction of hydrogen from an oxygen source. The reduced oxygen source can form an oxygen source (such as an oxide) by reacting with at least one of excess oxygen and water in the reaction cell chamber 5b31. At least one of the source of oxygen and the source of reduced oxygen may comprise a weight percent of the sprayed melt comprising a molten metal (such as silver), an oxygen source (such as borax), and a process for maximizing the rate of low energy hydrogen reaction. Reducing at least two of the sources of oxygen. The weight percentage of at least one of the oxygen source and the reduced oxygen source may be in the range of at least one weight percent from about 0.01 wt% to 50 wt%, from 0.1 wt% to 40 wt%, from 0.1 wt% to 30. Wt%, 0.1 wt% to 20 wt%, 0.1 wt% to 10 wt%, 1 wt% to 10 wt%, and 1 wt% to 5 wt%. The reaction cell chamber gas may comprise a gas mixture. The mixture may contain noble gases such as argon and hydrogen. The reaction cell chamber 5b31 can be maintained in an atmosphere containing a partial pressure of hydrogen. The hydrogen pressure may be in at least one of the following ranges: about 0.01 Torr to 10,000 Torr, 0.1 Torr to 1000 Torr, 1 Torr to 100 Torr, and 1 Torr to 10 Torr. The pressure of the rare gas such as argon may be in at least one of the following: about 0.1 Torr to 100,000 Torr, 1 Torr to 10,00 Torr, and 10 Torr to 1000 Torr. The oxygen source can undergo a reaction with hydrogen to form H2 O. H2 O can act as a HOH catalyst to form low energy hydrogen. The source of oxygen can be thermodynamically detrimental to hydrogen reduction. The HOH can be formed during ignition, such as in plasma. The reduced product can react with water formed during ignition. The water reaction maintains the water in the reaction cell chamber 5b31 at a lower level. The low water level may be in at least one of the following: less than about 40 Torr, less than 30 Torr, less than 20 Torr, less than 10 Torr, less than 5 Torr, and less than 1 Torr. The low water vapor pressure in the reaction cell chamber protects at least one of the battery components, such as the dome 5b4, such as a W or graphite dome, from corrosion. Tungsten oxide, as a source of oxygen, can participate in the tungsten cycle to keep the tungsten dome 5b4 from corrosion. The balance of oxygen and tungsten stocks can be kept nearly constant. Any tungsten oxide corrosion product obtained by reacting oxygen from tungsten oxide with tungsten metal may be replaced by a tungsten metal from tungsten oxide which is reduced to provide an oxygen reactant. The additive may comprise a compound to enhance the solubility of another additive, such as a source of oxygen. The compound may comprise a dispersing agent. The compound can comprise a flux. The generator may further comprise a stirrer for mixing molten metal, such as silver, with an additive such as an oxygen source. The agitator can comprise at least one of a mechanical, pneumatic, magnetic, electromagnetic stirrer (such as a stirrer using Lorentz force), piezoelectric, and other agitators known in the art. The agitator can include an acoustic waver, such as an ultrasonic generator. The agitator can include an electromagnetic pump. The agitator may include at least one of an electrode electromagnetic pump and a jet electromagnetic pump 5ka. Stirring can occur in a battery assembly that holds the melt, such as at least one of a reservoir and an EM pump. The melt composition can be adjusted to increase the solubility of the additive. The melt may comprise at least one of silver, a silver-copper alloy, and copper, wherein the melt composition can be adjusted to increase the solubility of the additive. Compounds that increase solubility may contain gases. The gas can have a reversible reaction with an additive such as a source of oxygen. The reversible reaction enhances the solubility of the oxygen source. In an exemplary embodiment, the gas comprises CO and CO2 At least one of them. An exemplary reversible reaction is CO2 And an oxide such as an alkali metal oxide such as Li2 O) react to form a carbonate. In another embodiment, the reaction comprises a reduction product of oxygen source (such as a metal oxide (such as an alkali metal oxide such as Li)2 O or Na2 O), the reaction of a transition metal oxide (such as CuO) and a metal of cerium oxide and water). In an exemplary embodiment, the melt or sprayed molten metal comprises molten silver and LiVO3 And M2 At least one of O (M = Li or Na) is in at least one concentration range of about 0.1 to 5 mol%, 1 to 3 mol%, and 1.5 to 2.5 mol%. The reaction cell chamber 5b31 gas contains an inert gas such as argon, wherein the hydrogen gas is maintained in at least one of about 1 to 10%, 2 to 5%, and 3 to 5%. The hydrogen consumed may be replaced by supplying hydrogen to the battery chamber 5b3 or 5b31a while monitoring at least one of the hydrogen partial pressure and the total pressure, such as in the battery chamber, due to the inert nature and constancy of the argon inventory. Hydrogen pressure can be inferred from the total pressure. The hydrogen re-acceleration rate can be in at least one of the following: about 0.00001 moles/s to 0.01 moles/s, 0.00005 moles/s to 0.001 moles/s, and 0.0001 moles/s to 0.001 moles/s. The black body radiator 5b4 may contain W or carbon. The blackbody radiator 5b4 may comprise a metal cloth or fabric (such as a metal cloth or fabric comprising tungsten comprising fine tungsten filaments), wherein the fabric density is breathable, but prevents silver vapor from penetrating into the cell from inside the chamber of the reaction cell Chamber. At least one of the reservoir 5c and the EM pump assembly (such as the pump tube 5k6) may comprise at least one of: bismuth, molybdenum, niobium, tungsten, tantalum, titanium, vanadium, chromium, zirconium, hafnium, tantalum,铑, 锇 and 铱. These components can be used for sintering powder welding, laser welding, electron beam welding, electrical discharge machining, casting, use of threaded joints, use of joint sleeves containing refractory materials, use of alloying agents (such as for the use of Mo, titanium). Bonded or fabricated by at least one of zirconium (TZM) and electroplated bonding. In embodiments comprising a refractory metal, the section of pump tube 5k6 at EM pump busbar 5k2 may be machined from a solid block or by means such as power fusion casting. The section may include inlet and outlet tubes for abutting the corresponding inlet and nozzle portions of the pump tube. Engagement can be by means of the invention. The adjacent conduit section can be an electron beam that is welded into an upright section and then bent to form a pump circuit. The pump tube inlet portion and the nozzle portion of the reservoir may be docked to the bottom of the reservoir and through the bottom, respectively. The tube can be welded to each of the penetrating members at the bottom of the reservoir by electron beam welding. In an embodiment, the threaded refractory metal battery assembly blocks are sealed together using an O-ring such as a refractory metal or a material O-ring. The threaded connection block can be joined at the flat and edge pairs, wherein the cutting edge compresses the O-ring. Exemplary refractory metals or materials are the refractory metals or materials of the present invention, such as W, Ta, Nb, Mo, and WC. In an embodiment, components of the battery (such as components of an EM pump, such as pump tube nozzle 5q of reservoir 5c, inlet and outlet of pump tube 5k6 and reservoir 5c, tapered reservoir 5b, and dome 5b4) At least one of the two may be coupled to the continuous member by at least one of a thread, an O-ring, a VCR-type fitting, a flared and compression fitting, and a joint sleeve fitting or a joint sleeve fitting. At least one of the fitting and the O-ring may comprise a refractory material such as W. At least one of the O-ring, the compression ring of the VCR type fitting, the joint bushing fitting or the joint bushing fitting may comprise a softer refractory material such as Ta or graphite. At least one of the battery component and the accessory may include at least one of the following: Ta, W, Mo, W-La2 O3 Alloy, Mo, TZM and niobium (Nb). Components such as dome 5b4 can be machined from solid W or W-yttria alloys. Components such as black body radiator 5b4, such as the W dome, may be formed by selective laser melting (SLM). In an embodiment, the generator further includes a battery chamber capable of having a subatmospheric pressure, an atmospheric pressure, and a pressure above atmospheric pressure that houses the dome 5b4 and the corresponding reaction cell chamber 5b31. The housing of the battery chamber 5b3 and the housing of the lower chamber 5b5 may be continuous. Alternatively, the lower chamber 5b5 can be self-contained with its own pressure control system that can operate at a different pressure (such as atmospheric pressure or vacuum) than the battery chamber. The separator of the battery chamber 5b3 and the lower chamber 5b5 may include a plate at the top 5b81 or the bottom 5b8 of the reservoir 5c. The plate 5b8 can be fastened to the reservoir by the thread between the plate 5b81 or 5b8 and the reservoir 5c. At least one of the threaded black body radiator and the reservoir having the bottom plate can be machined into a single piece from forged tungsten. The pressed tungsten electromagnetic pump bus bar 5k2 can be sintered and welded to the pump tube wall dent by forming a sintered tungsten powder during operation at a high temperature. The use of a refractory material, such as tungsten, for the battery assembly can avoid the need for a thermal barrier (such as a thermal insulator, such as SiC) between the blackbody radiator and the reservoir or between the reservoir and the EM pump. In an embodiment, the reaction cell chamber 5b31 may comprise a silver boiler. In an embodiment, the vapor pressure of the molten metal, such as silver, is allowed to equilibrate at about the operating temperature such that the metal evaporation process will cease and the power loss of the vaporization and condensation of the silver utilizing the exhaust heat will be eliminated. Exemplary silver vapor pressures at operating temperatures of 3000K and 3500K are 10 atm and 46 atm, respectively. Maintaining a Balanced Silver Vapor Pressure at Battery Operating Temperature A stabilizing member that maintains cell pressure with a reflux liquid during battery power generation operations. Since the dome 5b4 can be broken at high pressure and temperature, in the embodiment, the pressure in the battery chamber 5b3 matches the pressure in the reaction cell chamber 5b31 so that there is substantially no net pressure across the black body radiator 5b4. difference. In an embodiment, a slight overpressure in the reaction cell chamber 5b31 (such as in the range of about 1 mTorr to 100 Torr) may be maintained to avoid migration of the tungsten dome blackbody radiator 5b4, such as for gravity migration. . In one embodiment, the migration can be suppressed by adding a stabilizing additive to the metal of the black body radiator 5b4. In an embodiment, the tungsten is doped with an additive (such as a small amount of K, Re, CeO)2 , HfC, Y2 O3 HfO2 La2 O3 ZrO2 Al2 O3 SiO2 And K2 At least one of O) to reduce the potential. The additive can be in any desired amount, such as in the range of from 1 ppm to 10 wt%. In an embodiment of the reaction cell chamber 5b31 operating as a silver boiler, the battery components (such as the black body radiator 5b4 and the reservoir 5c) respectively contain a refractory material such as tungsten or carbon and boron nitride. In the startup mode, the reservoir 5c can be heated to a sufficient temperature using a heater such as an inductively coupled heater 5m such that the vapor pressure (such as silver metal vapor pressure) heats the black body radiator 5b4. This temperature can be higher than the melting point of silver when the EM pump and electrodes are activated to cause pumping and ignition. In an embodiment, during startup, as the metal vapor reflows during heating, a source of oxygen (such as an oxide such as LiVO)3 ) can be applied to the walls of the black body radiator 5b4 to be combined into a melt. In an embodiment, the low energy hydrogen reaction is maintained by acting as a silver vapor for the conductive substrate. At least one of a continuous jet of at least a portion that becomes vapor and a direct boiling of silver from the reservoir provides silver vapor. The electrode can provide a high current to the reaction to remove electrons and initiate a low energy hydrogen reaction. The heat from the low energy hydrogen reaction can help provide metal vapor (such as silver metal vapor) to the reaction cell chamber. In an embodiment, the current through the electrode can be at least partially shunted to an alternate or supplemental electrode in contact with the plasma. Current shunting can occur after the pressure of the silver vapor becomes sufficiently high that the silver vapor at least partially acts as a conductive matrix. The replacement or supplemental electrode in contact with the plasma may comprise one or more center electrodes and opposing electrodes surrounding the perimeter of the reaction cell chamber. The battery wall can act as an electrode. In the embodiment, the PV converter 26a is included in the external pressure vessel 5b3a having the outer chamber 5b3a1 (Fig. 2I80 to Fig. 2I94). The external pressure vessel can have any desirable geometry that includes a PV converter and an internal battery assembly that includes a light source that illuminates the PV converter. The outer chamber can include a cylindrical body having at least one dome-shaped end cap. The outer pressure vessel can comprise a dome or spherical geometry or other suitable geometry that can contain the PV converter and dome 5b4 and can maintain the pressure at least one of less than, equal to, or greater than the vacuum. In an embodiment, a PV converter 26a comprising a PV cell, a cold plate, and a cooling system is located inside the external pressure vessel, wherein the electrical and coolant lines are passed through the seal penetrating member and the feedthrough (such as the seal penetrating member of the present invention) And one of the feedthroughs) penetrates the container. In an embodiment, the outer pressure vessel can comprise a cylindrical body that can include at least one dome top. In an embodiment, the generator may include a cylindrical chamber that may have a dome-shaped cover for receiving the black body radiator 5b4 and the PV converter 26a. The generator can include a top chamber that houses the PV converter and a bottom chamber that houses the electromagnetic pump. The chambers can be operated at the same or different pressures. In an embodiment, the external pressure vessel comprises a PV converter support, such as a PV dome, which forms a battery chamber 5b3 containing a dome 5b4 enclosing the reaction cell chamber 5b3. The outer pressure vessel can comprise a dome or spherical geometry or other suitable geometry that can contain the dome 5b4 and can maintain the pressure at least one of less than, equal to, or greater than the vacuum. In an embodiment, the PV cell 15 is on the interior of an external pressure vessel wall, such as a spherical dome wall, and the cold plate and cooling system are outside the wall. The electrical connector can penetrate the container via a seal penetrating member and a feedthrough such as one of the seal penetrating member and the feedthrough of the present invention. Heat transfer can occur across a thermally conductive wall. Suitable wall materials include metals such as copper, stainless steel or aluminum. The PV window on the interior of the PV cell can include a transparent section that can be joined by an adhesive such as a ruthenium adhesive to form a hermetic transparent window. The window protects the PV cells from gases that redeposit the metal vaporized from the dome 5b4 back to the dome. The gas may comprise a gas of a halogen cycle. The pressure vessel PV vessel (such as a dome-shaped vessel) can be sealed to the partition 5b81 or 5b8 between the upper and lower chambers or other chambers by ConFlat or other such flange seals. The upper chamber may contain a black body radiator 5b4 and a PV battery 15, and the lower chamber may contain an EM pump. The lower chamber may further comprise a lower chamber cold plate or cooling line 5b6a (Fig. 2I89). The melting point of tungsten at 3422 ° C is the highest among all metals and is second only to carbon (3550 ° C) in the elements. Refractory ceramics and alloys have a higher melting point, especially Ta4 HfC5 TaX4 HfCX5 The melting point was 4,215 ° C, the cerium carbide was 3,900 ° C and the cerium carbide was 3,800 ° C. In an embodiment, the battery components, such as blackbody radiator 5b4 and reservoir 5c, may comprise at least one of a refractory material, such as W, C, and a refractory ceramic or alloy. In embodiments in which the black body radiator comprises graphite, the battery chamber 5b3 contains a high pressure gas, such as a high pressure inert gas atmosphere that suppresses the sublimation of the graphite. In an embodiment, the black body radiator may comprise carbon. The carbon sublimated from the graphite black body radiator (such as a spherical graphite black body radiator) can be removed from the battery chamber 5b3 by electrostatic precipitation (ESP). The ESP system can include an anode, a cathode, a power supply, and a controller. The particles can be charged by one electrode and collected by another pair of electrodes. The collected soot can be displaced from the collection electrode and allowed to fall into the collection box. The displacement can be achieved by a mechanical system. In an embodiment, the interior of the transparent container can be negatively charged and the dome can be positively charged using the applied voltage source. Under the influence of the field between the wall and the black body radiator 5b4, the negatively charged carbon particles sublimated from the graphite black body radiator 5b4 can migrate back to the dome. In an embodiment, the carbon may be removed by active transport (such as by flowing a gas through the cell chamber 53b and then through a carbon particle filter). In an embodiment, the dome 5b4 may comprise graphite and the reservoir The device may comprise a refractory material such as boron nitride. Graphite may comprise isotropic graphite. The graphite of the assembly of the present invention may comprise glassy carbon, such as Compressed glassy carbon: An ultrastrong and elastic interpenetrating graphene network, Science Advances, June 09, 2017: Vol. 3, No. 6, e1603213 DOI: 10.1126/sciadv. 1603213 ,Http :// Advances . Sciencemag . Org / Content / 3 / 6 / E1603213 . Full It is given, which is incorporated herein by reference. In an embodiment, a graphite blackbody radiator (such as a spherical dome) may include a liner to avoid erosion of graphite by molten metal inside the reaction cell chamber 5b31. The liner may comprise a refractory material such as tungsten. The liner may comprise a mesh or sheet formed into the interior of the graphite dome. The gasket prevents the shearing force of the flowing molten metal from attacking the inner surface of the reaction cell chamber. The PV converter can comprise PV cells each having a window that can include at least one thermal photovoltaic filter, such as an infrared filter. The filter preferentially reflects light having a wavelength that is not converted to electricity by the PV converter. The battery of the PV converter can be mirrored on the back side to reflect light that passes back through the battery to the black body radiator. The mirror can be selective for infrared light that is not converted to electricity by the PV cell. The infrared mirror can comprise a metal. The back of the battery can be metallized. The metal may comprise an infrared reflector such as gold. Metal can be attached to the semiconductor substrate of the PV cell by contact points. These contacts can be distributed on the back of the battery. The points may comprise a bonding material such as a Ti-Au alloy or a Cr-Au alloy. The PV cell can include at least one junction. A representative battery operating at 3500 K comprises GaAs on a GaAs substrate or InAlGaAs on an InP or GaAs substrate as a single junction cell and InAlGaAs on an InP or GaAs substrate as a double junction cell. A representative battery operating at 3000 K comprises GaAs on a GaAs substrate or InAlGaAs on an InP or GaAs substrate as a single junction cell and InAlGaAs on an InP or GaAs substrate as a double junction cell. In an embodiment, the geodesic PV converter 26 of the blackbody radiator 5b4 may include a light distribution system 23 (such as the light distribution system of the present invention) (Fig. 2I132). Light distribution system 23 can split the light into regions of different wavelengths. Separation can be achieved by at least one of a mirror and a filter, such as the ones of the present invention. The slit light can be incident on the PV cell 15 that is selective for the separated and incident light. The light distribution system 23 may be arranged as a column projecting outward from the geodesic ball surrounding the spherical black body radiator 5b4. The generator can include a precision gas pressure sensing and control system for at least one of battery chamber pressure and reaction cell chamber pressure. The system of the present invention may comprise a gas sump and a line, such as at least one of hydrogen and a rare gas sump and a line such as a sump 5u and a line 5ua1. The gas system may further comprise a pressure sensor, a manifold, an inlet line, a feedthrough, an injector, an injector valve, a vacuum pump (such as a vacuum pump 13a), a vacuum pump line (such as a vacuum pump line 13b), a control valve and a line, and a feedthrough Pieces. A rare gas such as argon or helium may be added to the battery chamber 5b3 or 5b3a1 to match the pressure in the reaction cell chamber 5b31. The reaction cell chamber pressure can be measured by measuring the blackbody temperature and using the relationship between metal vapor pressure and temperature. The temperature of the dome can be measured using its blackbody spectral emission. This temperature can be measured using optical high temperature meters that use optical fibers to collect and deliver light to the sensor. The temperature can be measured by a plurality of diodes having filters that are selective to the sample portion of the black body curve to determine the temperature. A battery assembly, such as reservoir 5c, can comprise a refractory material (such as at least one of alumina, sapphire, boron nitride, and tantalum carbide) that is at least partially transparent to at least one of visible and infrared light. A component, such as a reservoir, such as a boron nitride reservoir, can include recesses or thin spots in the assembly to better permit light to pass through the assembly to the optical temperature sensor. In addition to the rare gas, the gas in at least one of the outer pressure vessel chamber 5b3a1 and the battery chamber 5b3 may also contain hydrogen. Hydrogen supplied to the at least one chamber by the sump, line, valve, and ejector may be diffused via a battery assembly that is hydrogen permeable at the battery operating temperature to replace the consumed hydrogen to form a low energy hydrogen . The hydrogen permeable black body radiator 5b4. The low energy hydrogen gas product can diffuse from the chamber (such as chamber 5b3 or 5b3a1 and 5b31) to an ambient atmosphere or collection system. Alternatively, the low energy hydrogen gas product can be selectively pumped from at least one chamber. In another embodiment, the low energy hydrogen gas may be collected by a gas collector that may be periodically replaced or renewed. In an embodiment, the gas enclosing the chamber of the W black body radiator may further comprise a source of halogen (such as I2 Or Br2 Or a hydrocarbon bromine compound that forms a complex with sublimed tungsten. The complex compound can be decomposed on the surface of the hot tungsten dome to redeposit tungsten on the black body radiator 5b4. Some dome refractory metals, such as W, may be added to the molten metal (such as silver) to vaporize and deposit on the inner dome surface to replace the vaporized or sublimed metal. In an embodiment, the battery further includes a supply of hydrogen to the battery chamber. The supply can penetrate the battery via at least one of an EM pump tube, a reservoir, and a black body radiator. The supply may comprise a refractory material such as at least one of W and Ta. The supply may comprise a hydrogen permeable membrane, such as a hydrogen permeable membrane comprising a refractory material. The hydrogen supply can penetrate a region of the battery that has a lower temperature than the blackbody radiator. This supply can penetrate the battery at the EM pump tube or reservoir. The supply may comprise a hydrogen permeable membrane that is stable at the operating temperature of the molten silver in the EM pump tube or reservoir. The hydrogen permeable membrane may comprise Ta, Pt, Ir, Pd, Nb, Ni, Ti or other suitable hydrogen permeating metal having a suitable melting point known to those skilled in the art. In an embodiment, the at least one external chamber or the chamber outside the reaction cell chamber 5b31 is pressurized to an internal pressure of the reaction cell chamber at the operating temperature of the reaction cell chamber and the black body radiator. External pressure. The matching of the external pressure to the internal pressure can be in the range of approximately plus or minus 0.01% to plus or minus 500%. In an exemplary embodiment, the external pressure of at least one chamber of a container outside the blackbody radiator and the reaction cell chamber is about 10 atm to match the reaction cell chamber at an operating temperature of about 3000K. 10 atm silver vapor pressure. The blackbody radiator is capable of supporting an external differential pressure that decreases as the blackbody radiator temperature increases to the operating temperature. In the embodiment shown in Figures 2I80 through 2I103, the SunCell® comprises an external pressure vessel 5b3a having an external pressure vessel 5b3a1 containing a PV converter 26a, a blackbody radiator 5b4, a reservoir 5c and an EM pump. The wall of the external pressure vessel 5b3a can be water-cooled by a coolant line, a cold plate or a heat exchanger 5b6a. The SunCell® component, such as the wall of the external pressure vessel 5b3a, may contain a thermal or radiation shield to aid in cooling. The shield can have a low emissivity to reflect heat. The outer pressure vessel 5b3a may contain heat exchanger fins on the outside. The fins may comprise a high thermal conductor such as copper or aluminum. The generator may further comprise means for providing forced convective heat transfer from the heat sink. The member can include a fan or fan that can be located in a housing below the pressure vessel. A fan or fan can force air up on the fins. The external pressure vessel may comprise a section such as a cylindrical section containing and mounting battery components such as PV converter 26a, black body radiator 5b4, reservoir 5c and EM pump assembly 5ka. The connector for mounting and supporting the battery assembly includes means for accommodating different rates of thermal expansion or amount between the assembly and the base and the bracket to avoid damage to the expansion. The base and bracket may include at least one of an expansion joint and an expandable connector or fastener such as a gasket and a bushing. The connector and fastener may comprise carbon that is compressible carbon (such as Grapho or Perma-Foil (Toyo Tanso)) or composed of hexagonal boron nitride. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as one containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391) or another material of the invention. In an embodiment, the electricity, gas, sensor, control, and cooling lines may penetrate the bottom of the outer pressure vessel 5b3a. The outer pressure vessel may comprise a cylindrical and dome housing and a bottom plate 5b3b sealed to the housing. The housing may comprise carbon fiber or stainless steel or coated wrap. The coating may comprise nickel plating. The housing can be removable for easy access to SunCell® components. The bottom plate 5b3b can include feedthroughs for at least one of electricity, gas, sensors, control, and cooling lines. The feedthrough may be pressure resistant and electrically insulated if the pipeline is electrically shortable to the housing. In an embodiment, the PV converter cooling system includes a manifold having branches to a cold plate of elements of a dense receiver array, such as triangular elements. The backplane feedthrough may comprise: i.) an ignition busbar connector 10a2 coupled to a power source 2, such as an ignition busbar connector including an ignition capacitor bank in the housing 90, the housing may further comprise a PV converter 26a outputs a powered DC to DC converter, and the ignition busbar connector 10a2 is further connected to feedthroughs 10a for ignition busbars 9 and 10 that penetrate the ignition busbar feed The bottom plate of the assembly 10a1 (exemplary ignition voltage and current is approximately 50 V DC and 50 to 100 A); ii.) EM pump bus bar connector 5k33, which is connected to the EM power supply 5k13 and further connected to the EM pump Feedthrough 5k31, the EM pump feedthrough penetrates the bottom plate at the EM pump bus feedthrough flange 5k33; the power supply 5k13 can include a DC to DC converter powered by the PV converter 26a output (exemplary EM pump voltage and current are approximately 0.5 to 1 V DC and 100 to 500 A); iii.) Inductively coupled heater antenna feedthrough assembly 5mc, where the antenna is powered by an inductively coupled heater power supply 5m, which is coupled to the heating The power supply can include D powered by the output of the PV converter 26a C to DC converter, transformer, at least one IGBT and RF transmitter (exact inductively coupled heater frequency, voltage, current is approximately 15 kHz, 250 V AC or DC equivalent and 100 to 300 A), iv.) The gas line 5ua connected to the hydrogen storage tank 5u and the argon storage tank 5u1 and the penetrating members 5h1 and 5h3 of the argon gas line 5ua1, v.) are used for the EM pump coolant line 31d connected to the heat exchanger coolant line 5k11 and a penetrating member of 31e, wherein the coolant line 5k11 of the EM pump heat exchanger 5k1 and the EM pump cold plate 5k12 may each comprise a sheet member spanning the two heat exchangers 5k1, vi.) for the PV coolant line 31b and A penetrating member of 31c, and vii.) a penetrating member for power flow from the PV converter 26a to the power regulator or inverter 110. An inlet coolant line (such as an inlet coolant line 31e) is connected to the radiator inlet line 31t and an outlet coolant line (such as an outlet coolant line 31d) is connected to the water pump outlet 31u. In addition to the radiator 31, the generator is cooled by the fan 31j1. In an embodiment, the PV converter 26a includes fastening together to mount the lower and upper hemispherical parts around the black body radiator 5b4. The PV cells can each contain a window on the PV cell. The PV converter can be placed on the PV converter support plate 5b81. The support plate can be suspended to avoid contact with the black body radiator or reservoir and can be perforated to allow gas exchange between the entire external pressure vessel. The hemisphere (such as the lower hemisphere) may include a mirror that surrounds one portion of the region, such as the bottom, to reflect light to the PV cells of the PV converter. The mirror can accommodate any mismatch between the ideal geodesic dome to receive light from the blackbody radiator and the geodesic dome that can be formed from the PV elements. The non-ideality can be attributed to the spatial limitations of installing PV elements around the black body radiator, which are caused by the geometry of the PV elements that comprise the geodesic dome. An exemplary PV converter can include a geodesic dome that is comprised of array module delta elements, each of which includes a plurality of concentrating PC cells and a backing cold plate. These components can be snapped together. An exemplary array can include a five-party dodecahedron. An exemplary array can include 6 pentagons and 16 triangles. In an embodiment, the substrate of PV converter 26a can include a reflector at a location where the triangular PV elements of the geodesic PV converter array are not mounted. The reflector can perform at least one of: reflecting incident light to another portion of the PV converter and reflecting back to the black body radiator. In an embodiment, the power from the substrate of the lower hemisphere 5b41 is at least partially restored to at least one of light and heat. In an embodiment, PV converter 26a includes a PV cell collar around the base of lower hemisphere 5b41. In an embodiment, the power in the form of heat is collected by a heat exchanger such as a heat pipe. This heat can be used for cooling. This heat can be supplied to an absorption chiller known to those skilled in the art for cooling. In an embodiment, the coverage area of the cooling system, such as at least one of the chiller and the radiator, may be reduced by allowing a coolant, such as water, such as pool filtered water, to undergo a phase change. The phase change can include a liquid to a gas. Phase changes can occur in cold plates that remove heat from the PV cells. The liquid to gas phase change can occur in the microchannels of the microchannel cold plate. The coolant system can include a vacuum pump to reduce the pressure of at least one location in the cooling system. The phase change can be assisted by maintaining a reduced pressure in the coolant system. The reduced pressure in the condenser section of the cooling system can be maintained. At least one of the PV converter, the cold plate, and the PV cell can be immersed in a coolant that undergoes a phase change, such as boiling, to enhance heat removal. The coolant may comprise a coolant known in the art, such as an inert coolant such as 3M perfluorotributylamine. In an embodiment, the coolant system can include multiple coolant circuits. The first coolant loop can extract heat from the PV cells either directly or via a cold plate, such as a cold plate containing a microchannel plate. The coolant system can further comprise at least one heat exchanger. The first heat exchanger can transfer heat from the first coolant circuit to the other coolant circuit. The coolant phase change can occur in at least one of the other coolant circuits. The phase change can be reversible. The phase change increases the ability of the coolant to exchange heat with the environment and cool the PV converter at a given flow rate. Another coolant circuit may include a heat exchanger that transfers heat from its coolant to the air. Operating parameters (such as flow conditions, flow rates, pressures, temperature changes, average temperatures, and other parameters) in each coolant circuit can be controlled to control the desired heat transfer rate and desired operating parameters within the first coolant loop ( Operating parameters of the coolant such as in the microchannel plate of the cold plate). Exemplary conditions in the microchannel are a temperature range of the coolant of about 10 ° C to 20 ° C, an average temperature of about 50 ° C to 70 ° C, and laminar flow to avoid turbulence. In an embodiment, to reduce the size of the cooling system, the first coolant circuit can be operated at a high temperature, such as a temperature that is as high as possible without significantly degrading the performance of the PV cell, such as 40 ° C to 90 ° C. temperature. The temperature difference of the coolant can be smaller in the first loop than in the other coolant loop. In an exemplary embodiment, the temperature difference of the coolant in the first circuit may be about 10 °C; however, the temperature difference of the coolant in another circuit, such as the secondary circuit, may be higher, such as about 50 °C. Exemplary corresponding temperature ranges are from 80 ° C to 90 ° C and from 40 ° C to 90 ° C, respectively. A phase change can occur in at least one of the cooling circuits to increase heat transfer to reduce the size of the cooling system. In an embodiment, the microchannel plate that cools the PV cell can be replaced by at least one of a heat exchanger, a heat pipe, a heat transfer block, a coolant jet, and a coolant bath, such as an inert coolant (such as A coolant bath of distilled or deionized water) or a dielectric liquid such as 3M perfluorotributylamine, R134a or Vertrel XF. In the case of a water coolant, the coolant system may further comprise a water purification or treatment system to prevent excessive corrosiveness of the water. The coolant may comprise an anti-corrosion agent such as an anti-corrosion agent for copper known in the art. The radiator may comprise at least one of corrosion resistant stainless steel, copper or aluminum. The coolant may comprise an antifreeze, such as at least one of the following: Dowtherm, ethylene glycol, ammonia, and an alcohol (such as at least one of methanol and ethanol). The battery can be operated continuously to prevent the coolant from freezing. The coolant system may also include a heater to prevent water from freezing. The PV cell can be immersed in the coolant bath. The PV cell can transfer heat from the unirradiated side to the coolant bath. The coolant system can include at least one pump, wherein the coolant can be circulated to absorb heat at one location in the cooling system and to dissipate the heat at another location. The PV cell can be operated under at least one of a higher operating temperature and a high temperature range, thereby reducing the size of the cooling system. The coolant system can include a condenser wherein the phase change occurs with heat transfer from the PV cell. The coolant system can be pressurized, at atmospheric pressure or below atmospheric pressure. The pressure can be controlled to control the coolant boiling temperature. The coolant system operating under pressure may include a pump having an inlet and an outlet and a pressure venting valve that returns coolant to the inlet side of the low pressure pump, wherein the coolant is pumped through an inlet to a heat exchanger (such as a radiator or chiller) ). In the case of a chiller, the chilled coolant can be recycled to lower the temperature and increase the temperature difference between the coolants PV to increase the heat transfer rate. The cooled coolant can be further pumped to the PV cell-coolant heat transfer interface to receive heat, which can thereby boil. The coolant system can operate at a heat flow below the critical heat flux and no longer wet the cooled surface when sufficient vapor is formed. The coolant can be operated under subcooled boiling. Due to the large coolant-air heat gradient across the corresponding heat exchanger (such as a radiator), the PV cell can operate at a temperature that maintains a subcooled boiling while maximizing the rate of heat transfer to the environment. An exemplary PV operating temperature is 130 °C. The system can be operated to avoid film boiling. The heat exchanger between the hot coolant and the ambient air may comprise a radiator, such as a wraparound radiator, such as a radiator having an automotive radiator design. The heat exchanger can include at least one fan to move the air. The fan can be centered. The battery can also be centered. The PV cell can be mounted on a heat transfer medium such as a heat sink such as a copper plate. The copper plate can be at least one of: a heat transfer member that transfers heat (such as at least one of a heat exchanger, a heat pipe, and a heat transfer block) and a coolant to increase the heat transfer contact area. The heat transfer member can dissipate heat radially. The coolant can undergo a phase change to increase heat transfer, thereby reducing the size of the coolant system. The heat transfer member can be coated with a pin to increase the surface area for heat transfer. The coolant system may include at least one of a member for condensing the coolant and a heat rejection system such as at least one coolant circulation pump and a heat exchanger between the coolant and the environment, such as a pressurizable radiator. ). In an embodiment, at least one of a radius of the PV converter, a radius of the PV cell coolant system (such as a radius of at least one of a heat exchanger of the PV coolant system, a heat pipe, or a heat transfer block) may be increased To reduce the heat flux load to be transferred from the PV cell to the environment in order to effectively cool the PV cell. The PV converter can include a shape that remains at the same distance from the black body radiator 5b4. The blackbody radiator can be spherical and the distance from the PV converter to the blackbody radiator can be constant to achieve the desired light intensity incident on the PV that can include a uniform illumination intensity. In an embodiment, the PV converter cooling system can include a spherical manifold that includes a coolant reservoir having a finned spherical surface boiling surface that includes a heat sink and a boiler plate on the back side of the PV cell. The boiler plate can be coated with pins to increase the surface area for heat transfer. The coolant can be flowed by at least one pump. The flow may comprise a spherical flow from at least one inlet at the top and at least one outlet at the bottom of the chiller. The heated coolant can be pumped through the radiator to be cooled and returned to the reservoir. In another embodiment, the coolant may be pumped through a passage in the boiler plate that is joined to the back of the PC battery and receives heat from the PV cell. The heat transfer plate or element may comprise a porous metal surface coating such as a coating comprising sintered metal particles. The surface may provide a porous layer structure characterized by a pattern of interconnected vias. The passages are appropriately sized to provide a large number of stable locations for the vapor condensate to greatly increase the heat flux (up to 10 times) for the temperature difference between the given surface and the coolant saturation temperature. The surface coating can also increase the critical heat flux (CHF). The surface can comprise a conductive microporous coating that forms a microcavity for coagulating. An exemplary surface comprises a sintered copper microporous surface coating (SCMPSC, cf. Jun et al, Nuclear Engineering and Technology, 2016). Surface enhancement methods can be used in conjunction with short pins (also porous coated pins) to further increase surface area. Surface area enhancers, such as porous coated pins or studs, can be cast. In an exemplary embodiment, a short post (such as a copper stub) having a porous surface area reinforcement can be cast onto the back side of a heat transfer plate, such as a copper plate. The reflow from the radiator can be configured to provide convection on the surface of the boiler plate. A plurality of inlets divide the coolant flow into a plurality of inlet jets that are angled tangentially on the walls of the spherical and cylindrical coolant reservoirs to provide bulk vortex motion. This movement can cause convective boiling at the surface, which removes vapor bubbles from the nucleation site, thereby inhibiting CHF. In embodiments, coolants other than water may be used because of the boiling of fluids having less surface tension, such as organic liquids, refrigerants, and heat transfer fluids, in the presence of enhanced condensate sites. The coolant can be selected based on the saturated (P-T) state of the unpressurized system. In an embodiment, to achieve temperature uniformity and to account for variations in convective conduction across the coolant of the PV element, the same microchannel heat sink can be utilized to cool each element. In an embodiment, PV converter 26a may include a plurality of triangular receiver units (TRUs) each including a plurality of photovoltaic cells( Such as front concentrating photovoltaic cells, mounting plates and coolers on the back of the mounting plate. The cooler may include at least one of a multi-channel plate, a surface supporting a coolant phase change, and a heat pipe. The triangular receiver units can be coupled together to form at least a portion of the geodesic dome. The TRU can further include an interconnection of at least one of an electrical connector, a bus bar, and a coolant channel. In an embodiment, the receiver unit and the connection pattern may comprise a geometry that reduces the complexity of the cooling system. The number of PV converter components, such as the number of triangular receiver units of the geodesic spherical PV converter, can be reduced. The PV converter can include a plurality of segments. The segments can be joined together to form a portion of the casing surrounding the black body radiator 5b4. At least one of the PV converter and the black body radiator may be polyhedral, wherein the surfaces of the black body radiator and the receiver unit are geometrically matched. The casing may be formed by at least one of a triangle, a square, a rectangle, a cylinder, or other geometric unit. The blackbody radiator 5b4 can comprise at least one of a square, a sphere, or other desirable geometry to illuminate each unit of the PV converter. In an exemplary embodiment, the casing may comprise five square cells surrounding a black body radiator 5b4 that may be spherical or square. The casing may further comprise a receiver unit that receives light from a substrate of the blackbody radiator. The geometry of the base unit can be the geometry that optimizes light collection. The casing may comprise a combination of squares and triangles. The casing may comprise a top square connected to the upper section comprising four alternating squares and a pair of triangles connected to the six squares as the middle section, the middle section being connected to at least four alternating squares and at least four pairs of triangles A portion of the lower section that is connected to a partially or non-existing bottom square. A schematic of the triangular elements of the geodesic dense receiver array of the photovoltaic converter is shown in Figure 2I133. The PV converter 26a may comprise a dense array of receivers consisting of triangular elements 200, each of which comprises a plurality of concentrating photovoltaic cells 15 capable of converting light from the black body radiator 5b4 into electricity. The PV cell 15 may comprise at least one of a GaAs P/N cell on a GaAs N wafer, InAlGaAs on InP, and InAlGaAs on GaAs. The batteries may each include at least one junction. The triangular element 200 can include a cover body 203 (such as a cover body comprising stamped Kovar sheets), a heat sink 202 and a cold head 204 (such as a cold head comprising a press-fit tube), and a connecting continuous triangular element Attachment flange 203 of 200 (such as an attachment flange comprising a stamped Kovar sheet). In an embodiment comprising a source of thermal power, the heat exchanger 26a includes a plurality of heat exchanger elements 200 (such as the triangular elements 200 shown in FIG. 2I 133) each including a hot coolant outlet 202 and cooler cooling a reagent inlet 204; and means for absorbing light from the black body radiator 5b4 and transferring the power as heat to the coolant flowing through the element. At least one of a coolant inlet and an outlet may be attached to a common water manifold. As shown in FIGS. 2I108 to 2I109, the heat exchanger system 26a further includes a coolant pump 31k, a coolant sump 31l, and a load heat exchanger (such as the radiator 31 and a fan that supplies hot air to the load by the flow of air through the radiator) 31j1). In addition to the geodesic geometry, heat exchangers having other geometries, such as those known in the art, are within the scope of the present invention. An exemplary cube geometry is shown in Figures 2I134 through 2I138, which respectively show a thermal load inlet line 31b and a low temperature outlet line 31c to a heat load, wherein the modular plate heat exchanger element 26b is not present in the PV cell 15 in. The heat exchanger 26a can have a desired geometry that optimizes at least one of heat transfer, size, power requirements, simplicity, and cost. In an embodiment, the area of the heat exchanger system 26a is scaled to the area of the black body radiator 5b4 such that the received power density is the desired power density. At least one receiver unit may be replaced or partially replaced by a mirror that performs at least one of: direct or indirect reflection of blackbody radiation to other receiver units or other receiver cells covered with PV cells position. The receiver unit may be filled with a PV cell in an optimal high intensity illumination region, such as a central circular region in the case of a spherical blackbody radiator 5b4, wherein the region not filled with PV may be covered by a mirror. Batteries that receive a similar amount of radiation can be connected to form an output of the desired matching current, wherein the batteries can be connected in series. The enclosures containing larger areas of receivers (such as square receiver units) may each include a corresponding cooler or heat exchanger 26b (Fig. 2I134 to Fig. 2I138). The cooler or heat exchanger 26b of each receiver unit (such as a square receiver unit) may comprise at least one of: a coolant housing comprising at least one coolant inlet and one coolant outlet; at least one cooling A distribution structure, such as a shunt baffle (such as a plate having a passage); and a plurality of coolant fins mounted to the PV cell mounting plate. The fins may comprise a highly thermally conductive material such as silver, copper or aluminum. The height, spacing and distribution of the fins can be selected to achieve a uniform temperature across the PV cell area. The cooler may be mounted to at least one of the mounting plate and the PV cell by a thermal epoxy. The front side (lighting side) of the PV cell can be protected by a cover glass or window. In an embodiment, the housing containing the receiver unit may comprise a pressure vessel. The pressure of the pressure vessel can be adjusted to at least partially balance the internal pressure of the molten metal vapor pressure inside the reaction cell chamber 5b31. In an embodiment (Fig. 2I 143), the radius of the PV converter can be increased relative to the radius of the black body radiator to reduce the light intensity based on the radius dependence of the radius of the optical power flux. Alternatively, the light intensity can be reduced by a light distribution system comprising a series of semi-transparent mirrors 23 (Fig. 2I132) along a path of the black body radiator, the black body radiator light path partially reflecting the incident light to The PV cell 15 additionally transmits a portion of the light to the next component of the series. The light distribution system can include mirrors for reducing light intensity along a radial path, a Z-shaped path, or other paths that facilitate stacking a series of PV cells, and a mirror to achieve desired light intensity distribution and conversion. In an embodiment, the black body radiator 5b4 can have a geometry that is compatible with the light distribution and PV conversion system, the light distribution and PV conversion system comprising a series of mirrors, lenses or filters in combination with corresponding PV cells. In an exemplary embodiment, the blackbody radiator can be square and match the linear light distribution and PV conversion system geometry. The parameters of the cooling system can be selected to optimize the cost, performance and power output of the generator. Exemplary parameters are coolant identification, coolant phase change, coolant pressure, PV temperature, coolant temperature and temperature range, coolant flow rate, radius of the PV converter and coolant system relative to the radius of the blackbody radiator. And a light recycling and wavelength selective filter or reflector on the front or back of the PV to reduce the amount of PV incident light that cannot be converted to electricity by PV or to pass through the PV cell Convertible PV incident light is recirculated. An exemplary coolant system is a system that performs at least one of: i.) forming steam, delivering steam, and condensing steam at the PV cell to release heat at the exchange interface using the environment; ii.) forming at the PV cell Vapor, condenses it back into the liquid, and exhausts heat from the single phase at the heat exchanger using an environment (such as a radiator); and iii.) removes heat from the PV cell with the microchannel plate and utilizes the environment at the heat exchanger Exhaust heat. The coolant may still be in a single phase during cooling of the PV cell. The PV battery can be mounted to a cold plate. Heat can be removed from the cold plate by a coolant conduit or coolant conduit to the cooling manifold. The manifold can include a plurality of annular conduits circumferentially surrounding the PV converter, which can be spaced apart along the vertical or z-axis of the PV converter; and the manifold includes a coolant conduit or coolant conduit separate therefrom. The black body radiator may comprise a plurality of parts that are sealed together to form a reaction cell chamber 5b31. The plurality of parts may include a lower hemisphere 5b41 and an upper hemisphere 5b42. Other shapes are within the scope of the invention. The two hemispheres can be fastened together at the seal 5b71. The seal can include a flange, at least one spacer 5b71, and at least one of a fastener such as a clamp and a screw. The seal may comprise a graphite gasket (such as Perma-Foil (Toyo Tanso)) and a fire resistant bolt (such as graphite or W bolt and nut), wherein the metal bolt and nut (such as W bolt and nut) may further comprise graphite or Perma- Foil gaskets or gaskets to compensate for the different coefficients of thermal expansion between carbon and bolt and nut metal (such as W). The lower hemisphere of the black body radiator 5b41 and the reservoir 5c are engageable. The joint may comprise a sealing flange, a threaded joint, a welded joint, a glue joint or another joint such as a joint known to the present invention or known to those skilled in the art. The seal may comprise a glue or chemical bond seal formed by a sealant. Exemplary graphite gums are Aremco Products, Inc. Graphi-Bond 551RN graphite adhesive and Resbond 931 powder with Resbond 931 adhesive. The cemented carbon segments can be heat treated to form chemical carbon bonds. The key can be the same or similar to the structure of each piece. The bond can include graphitization. In an embodiment, two sheets, such as an upper hemisphere and a lower hemisphere, can be at least one of threaded and screwed together and glued. The engagement section can be tongue and grooved to increase the contact area. In an embodiment, the lower hemisphere 5b41 and the reservoir 5c may comprise a single piece. The reservoir may comprise a bottom plate attached by a joint such as a joint known to the present invention or known to those skilled in the art. Alternatively, the bottom panel and the reservoir body can comprise a unitary piece that can further comprise a sheet member having a lower hemisphere. The reservoir portion bottom plate may be coupled to a reservoir support plate 5b8 that provides a connection to the wall of the outer pressure vessel 5b3a to support the reservoir 5c. The EM pump tube 5k6 and the nozzle 5q can penetrate and connect to the reservoir 5c using a joint such as a mechanical fitting such as a joint sleeve type and a VCR type fitting 5k9 and a joint sleeve type engaging O-ring 5k10. The bottom plate (Fig. 2I69). In an embodiment, at least one of the top hemisphere 5b42, the bottom hemisphere 5b42, the reservoir 5c, the bottom plate of the reservoir 5c, the EM pump tube 5k6, the nozzle 5q, and the connector 5k9 includes W, Mo, and carbon. At least one. A carbon tube assembly (such as a carbon tube assembly having a bend, such as a carbon riser) or an ejector tube and nozzle can be formed by casting. In an embodiment, the bottom plates of the top hemisphere 5b42, the bottom hemisphere 5b41, the reservoir 5c, and the reservoir 5c contain carbon. In an embodiment, carbon battery components, such as reservoirs and blackbody radiators, may comprise a gasket. The liner prevents the underlying surface, such as the carbon surface, from being eroded. The liner may comprise at least one of a refractory sheet or web. The liner may comprise a W foil or a mesh or a WC sheet. The foil can be annealed. In embodiments, liners of graphite battery components, such as blackbody radiators, reservoirs, and interiors of VCR-type fittings, may include coatings, such as pyrolytic graphite, tantalum carbide, or the invention or known in the art. Another coating to prevent carbon attack. The coating can be stabilized at high temperatures by applying and maintaining a high gas pressure on the coating. In embodiments comprising a coating of a battery component, at least one of the coating and the substrate (such as carbon) can be selected such that the coefficient of thermal expansion matches. In an embodiment, at least one of the pair of electrodes comprises a liquid electrode 8. In an embodiment, the electrodes can comprise liquid and solid electrodes. The liquid electrode can comprise a stream of molten metal from an electromagnetic pump injector. The ignition system can include an electromagnetic pump that sprays molten metal onto the solid electrode to turn on the circuit. The turn-on of the ignition circuit can be caused by the flow of current from the power source 2 causing ignition. The solid electrode can be electrically isolated from the molten electrode. Electrical isolation may be provided by an electrically insulating coating of the solid electrode at its penetration, such as at the sidewall of the reservoir 5c. The solid electrode may comprise a negative electrode and the liquid electrode may comprise a positive electrode. Due to the higher heat from the high kinetics at the positive electrode, the liquid positive electrode eliminates the possibility of positive electrode melting. The solid electrode can comprise forged W. The electrode may comprise a conductive ceramic, such as at least one of: a carbide, such as one of WC, HfC, ZrC, and TaC; a boride such as ZrB2 And complexes such as ZrC-ZrB which can gradually reach 1800 °C2 And ZrC-ZrB2 - SiC composite. The electrically conductive ceramic electrode can comprise a coating or covering such as a sleeve or collar. In an embodiment, the SunCell® comprises at least two EM pump injectors that produce at least two streams of molten metal that intersect to form at least two liquid electrodes. The corresponding reservoir of the EM pump can be vertical with a nozzle that is offset from vertical so that the molten metal streams that are ejected intersect. Each EM pump injector can be connected to a source of opposite polarity such that current flows through the metal stream at the intersection. The positive terminal of the power source 2 can be connected to one EM pump injector and the negative terminal can be connected to another EM pump injector. The ignition electrical connection may comprise an ignition solenoid pump busbar 5k2a. The power source 2 supplies voltage and current to the ignition process while avoiding substantial electrical interference to the EM pump power supply. The power source 2 can include at least one of a floating voltage power supply and a switching power supply. The electrical connection may be at a conductive component of the EM pump, such as at least one of an EM pump tube 5k6, a heat transfer block 5k7, and an EM pump bus 5k2. Each of the heat transfer blocks 5k7 may be thermally coupled to the pump tube 5k6 by a conductive paste such as a metal powder such as W or Mo powder. The ignition power can be coupled to each set of heat transfer blocks 5k7 such that a good electrical connection of opposite polarity is established between the power source 2 and each set of heat transfer blocks 5k7. The heat transfer block distributes heat from the ignition power along the heat transfer block. The nozzle can be operated to be immersed in liquid metal to prevent arcing and heating losses. A level control system including a reservoir molten metal level sensor and an EM pump controller (such as an EM pump current controller) maintains the reservoir molten metal level within a reasonable tolerance, allowing the self-immersion nozzle The injection is at least one of the following: the EM pump is not significantly controlled by the immersion level change and the level control system to adjust the immersion level. The EM pump can pump metal from the immersion nozzle 5q such that the molten metal that is ejected can form a flow that travels relative to gravity. The stream can be directed to intersect the relative flow of the SunCell® embodiment comprising a dual molten metal injector. The SunCell® can contain at least one molten metal flow deflector. At least one stream, such as a submerged electrode stream, can be directed to the flow deflector. The flow deflector can redirect the flow to intersect the opposing flow of the dual molten metal injector embodiment. The deflector may comprise a refractory material such as carbon, tungsten or another material of the invention. The deflector may comprise an extension of the reaction cell chamber 5b31, such as an extension or extension of the lower hemisphere of the black body radiator 5b41. The deflector can comprise an electrical insulator. The insulator can electrically isolate the deflector. In a dual molten metal EM pump injector embodiment, such as an embodiment comprising at least one submerged nozzle (Fig. 2I139 to Fig. 2I147), at least one of the reservoir and the corresponding nozzle section of the EM pump tube 5k61 can be tilted to The molten stream is more directed through the center than the untilted condition. The inclined reservoir may comprise a sloping floor of the EM pump assembly 5kk. The reservoir support plate 5b8 may comprise a matching inclination to support the EM pump assembly 5kk Inclining the bottom plate. Alternatively, at least one of the accumulator 5c, the EM pump assembly 5kk, and the EM pump 5ka including the magnet 5k4 and the magnetic cooling 5k1 may be inclined away from the center at the base of the EM pump 5ka to cause the reservoir The top of the 5c is inclined inwardly. The reservoir support plate 5b8 may include a matching inclination to support the inclined reservoir and the EM pump assembly 5ka. The top of the reservoir tube 5c may be cut at an angle to have a black body radiator The bottom of the flat joint of the lower hemisphere of 5b41 is matched. Alternatively, the lower hemisphere of the black body radiator 5b41 may include a corresponding inclined joint, such as a tilt collar and a connector (such as a sliding nut extending from the lower hemisphere 5b41). The slanted sleeve of the connector) allows for a thermal gradient from the black body radiator 5b4 to the reservoir 5c. In an exemplary embodiment of the sliding nut joint 5k14, the reservoir 5c comprises boron nitride and the lower hemisphere 5b41 slides The nut connector comprises carbon, the nut comprises carbon, and the spacer 5k14a comprises carbon, wherein the coefficients of thermal expansion of the graphite and BN are selected to achieve a heat cycleable seal. In an embodiment, the carbon and BN components have a matching coefficient of thermal expansion, or The coefficient of thermal expansion of BN is slightly greater than the coefficient of thermal expansion of the carbon component that also constitutes the compression joint. The gasket can be compressed to prevent thermal expansion beyond the tensile strength of the carbon component. The compression can be reversible to allow for thermal cycling. The location can be selected to maintain the immersion nozzle during operation of the SunCell®. The inlet riser can include an open-ended tube in which flow into the tube occurs until the molten metal level is approximately the level of the tube opening. The tube end opening is cut at a matching tilt to the molten metal level. The tube opening can be sized to throttle or inhibit the inward flow rate to maintain the double molten metal spray Stability of level control between the two reservoirs of the system. The tube opening may contain a porous covering such as a mesh to achieve throttling. The EM pump rate can be throttled to maintain relative position stability The EM pump rate can be adjusted by controlling the EM pump current, wherein at least one of the tube opening control and the dynamic current adjustment range is sufficient for achieving relative level control stability for embodiments including one flow slightly tilted to the other. Alignment of the flow. The inlet riser may comprise a refractory electrical insulator, such as a BN tube, that may be inserted into or over the holder attached to the substrate of the EM pump assembly. In an exemplary embodiment, the holder comprises a shorter one. Metal tube, such as Mo or SS attached to the EM pump assembly base. The inlet riser (such as a top slotted BN tube) can be secured in the holder by a wire tensioner (such as a set screw) or by a compression fitting In place. The inlet riser can be connected to the holder by a coupler mounted above both ends of the inlet riser and the retainer. In an embodiment, the inlet riser may comprise carbon. The connection of the carbon inlet riser tube to the EM pump assembly 5kk can include at least one of a thread and a compression fitting to a retainer (such as a tube holder) that can be secured by fasteners (such as threads and welds) At least one of the) is fastened to the base of the EM pump assembly. A holder, such as a tube holder, can comprise a material that does not react with the inlet riser holder. An exemplary holder for securing a carbon inlet riser comprises a carbide resistant tube (such as a nickel or neon tube) or a carbonized SS tube (such as a tube comprising SS 625 or Haynes 230). The inlet riser (such as a carbon tube) can be changed to be coated with molten metal during operation, wherein the molten metal can protect the tube from reactive plasma attack. In an embodiment, at least one of the carbon inlet riser 5qa, the nozzle section of the EM pump tube 5k61, and the nozzle 5q may comprise an oxidatively stabilized refractory material, such as a refractory precious metal (such as Pt, Re, Ru, Rh, or Ir) ) or refractory oxides (such as MgO (MP2825 ° C), ZrO2 (M.P.2715 ° C), for H2 O-stabilized magnesia zirconia, yttrium zirconate (SrZrO3 M.P. 2700 ° C), HfO2 (M.P. 2758 ° C), cerium oxide (M.P. 3300 ° C) or another oxide of the invention). The ceramic pump injector components (such as the inlet riser 5qa, the nozzle section of the EM pump tubing 5k61, and the nozzle 5q) can be secured to the metal EM pump inlet or outlet near or in the EM pump assembly 5kk. The fastener may comprise a fastener of the invention. The fastener can comprise at least one of: a threaded or metallized and threaded ceramic component, a threaded pump component, and a metallized ceramic component that is brazed to the metal EM pump inlet or outlet near or in the EM pump assembly 5kk. Metallization can include metals that do not oxidize, such as nickel or refractory metals. The fasteners can include flared fittings. The ceramic component can comprise a flare, which can be conical or it can be flat. A male portion of the fastener can be attached to the base of the EM pump assembly 5kk. The raised portion of the flared fitting can include a metal threaded collar and a raised conduit section to mate with a female threaded collar that tightens the flare of the ceramic component when the mating thread is tightened to Projecting the conduit section. The fastener may further comprise a gasket such as a Graphoil or Perma-Foil (Toyo Tanso) gasket. The metal component, such as the metal component of the EM pump assembly 5kk, may comprise a material that does not react with the gasket, such as nickel. Any void formed by the mating threaded member may be filled with an inert material to prevent the molten metal (such as molten silver) from wetting and acting as a member to relieve pressure from thermal expansion and contraction. The filling may comprise a gasket material, such as a gasket material of the invention, such as Graphi or Perma-Foil (Toyo Tanso). In an exemplary embodiment, the ceramic tube to the base of the EM pump assembly 5kk may comprise at least one of: (i) a ceramic component and an EM pump assembly 5kk component thread; (ii) a ceramic component metallization And screwing or brazing the metal to the metal EM pump inlet or outlet near or in the EM pump assembly (alumina is a common material to be metallized and brazed); and (iii) flare fittings comprising ceramic tubes Each of the ceramic tubes has a conical or flat flared end and a threaded metal upper sliding collar for attachment to a threaded collar welded to the bottom of the EM pump assembly; the flared fitting may further comprise Graphi or Perma- Foil (Toyo Tanso) gaskets, and the EM pump assembly may contain nickel metal components to prevent reaction with carbon and water. Material, such as the material of the male fastener component, can be selected to match the coefficient of thermal expansion of the female component. In an embodiment, to avoid component corrosion, (i) the reaction cell chamber 5b31 (such as a carbon reaction cell chamber) may be at least one of the following; protected by a molten metal such as silver. a layer comprising a pyrolytic graphite or pyrolytic graphite surface coating, negatively biased, wherein the negative bias voltage is provided by at least one of an ignition voltage (such as a connection to a negative electrode injector and a reservoir); (ii) EM The inner surface of the pump tube may comprise a material that does not react with water, such as nickel; and (iii) the reservoir, the inlet riser, and the ejector may comprise ceramic (such as MgO) or other fire resistant materials known to those skilled in the art. Stable ceramics. In an embodiment, the negative bias applied to the lower carbon hemisphere 5b41 protects the carbon from the oxide reservoir (such as MgO or ZrO)2 The reservoir) performs a carbon reduction reaction. A bias voltage can be applied to the carbon component rather than the contact oxide component. Alternatively, the bond between the oxide and carbon can include a wet seal or gasket to limit contact between the oxide and carbon. In an embodiment, the temperature and pressure are controlled such that it is thermodynamically possible for carbon reduction oxides (such as MgO). Exemplary pressure (P) and temperature (T) conditions are approximately at T/P 0.0449 < 1200. The carbon may comprise pyrolytic carbon to reduce carbon reduction reactivity. The atmosphere can contain CO2 To reduce the free energy of carbon reduction. The carbon may be coated with a protective coating (such as vaporized silver from molten silver) or a graphite Cova coating (Http :// Wwww . Graphitecova . Com / Files / Coating 4 . Pdf ). The Cova coating can comprise the following multiple layers: aluminum plus compound / aluminum plus alloy / pure aluminum / metal / graphite. In an embodiment, the graphite is coated with a coating to avoid reaction with hydrogen. Exemplary coatings include ZrC, Nb, Mo, and/or Nb-Mo alloys and/or MO2 C consists of a metal layer and a non-metal layer. In an embodiment, at least one of the reservoir 5c, the lower hemisphere 5b41, and the upper hemisphere 5b42 comprises a ceramic, such as an oxide, such as a metal oxide (such as ZrO)2 HfO2 Al2 O3 Or MgO). At least two of the lower hemisphere 5b41, the upper hemisphere 5b42, and the reservoir 5c may be glued together. In an embodiment, at least two of the lower hemisphere 5b41, the upper hemisphere 5b42, and the reservoir 5c can be molded as a single component. In an embodiment, the reservoir can be coupled to at least one of the lower hemisphere and the EM pump assembly 5kk by a sliding nut joint, a wet seal joint, a gasket joint, and another joint of the present invention. The sliding nut joint can include a carbon gasket. At least one of the nut, EM pump assembly 5kk, and lower hemisphere may comprise carbonization and carbide forming materials (such as nickel), carbon, and carbonized stainless steel (SS) (such as SS 625 or Haynes 230 SS). In an embodiment, the carbon lower hemisphere is at the joint between the carbon lower hemisphere and the oxide reservoir (such as the MgO reservoir) due to the proper length of the collar bonded to the carbon lower hemisphere of the oxide reservoir. The carbon reduction reaction is avoided by at least one member, such as a wet-sealed joint cooled to below the carbon reduction reaction temperature and a slip nut joint maintained below the carbon reduction reaction temperature. In an embodiment, the carbon reduction reaction is avoided by maintaining the linker comprising the oxide in contact with the carbon at a non-reaction temperature (temperature below the carbon reduction reaction temperature). In an embodiment, the MgO carbon reduction reaction temperature is in the range of from about 2000 °C to 2300 °C. Power conversion can be achieved using systems such as magnetohydrodynamics, which are capable of efficient conversion at non-reactive temperatures using joints. In an embodiment, the lower hemisphere 5b41, the upper hemisphere 5b42, and the reservoir 5c comprise ceramic, such as a metal oxide (such as zirconia), wherein the component is at least one of molded and glued together, and the EM pump combination The joint at the part contains a wet seal. In an embodiment, the lower hemisphere 5b41 and the reservoir 5c comprise zirconia, wherein the component is at least one of molded and glued together, and the joint at the EM pump assembly comprises a wet seal. In an embodiment, the blackbody radiator 5b4 comprises ZrO stabilized with MgO2 TiO2 Or bismuth oxide. Attributable to a lower ZrO of about 0.22 Emissivity, the radius of the PV dome can be reduced relative to the radius of the SunCell® with the same carbon blackbody radiator of incident power density. The more concentric geometry of the PV converter provides a more favorable black body radiation to the PV cell at approximately a positive incidence angle. In an embodiment comprising a lower hemisphere 5b41, the lower hemisphere comprises an electrical insulator, and the reservoir 5c may comprise a conductor, such as a metal (such as a refractory metal), carbon, stainless steel or other electrically conductive material of the invention, comprising an underlying hemisphere of the electrical insulator 5b41 may contain a metal oxide such as ZrO2 HfO2 Al2 O3 Or MgO) or carbon coated with an insulator such as mullite or other electrically insulating coating of the present invention. In an embodiment, the emissivity of the black body radiator 5b4 is lower for light above the band gap of the PV cell and higher for radiation below the band gap of the PV cell. Light below the PV bandgap can be re-emitted into blackbody by reflection from the PV cell, by the blackbody radiator 5b4, and at the operating temperature of the blackbody radiator (such as in the range of about 2500 K to 3000 K). radiation. In an embodiment, the reflected radiation below the band gap may be transparent to the black body radiator 5b4 such that it is absorbed by the reaction cell chamber 5b31 by gas and plasma. The black body radiator can be heated by the absorbed reflected power to help maintain its temperature and thereby achieve recirculation of the reflected lower bandgap light. In embodiments comprising a black body radiator having a low emissivity and a high transmittance for light below the band gap, the black body radiator (such as a ceramic black body radiator, such as a zirconia black body radiator) contains an additive (such as a coating) Or an inner layer) to absorb light that is reflected below the band gap and recycle it to the PC battery. The coating or inner layer may contain a high emissivity such that it absorbs light reflected from the PV cell. The additive may comprise carbon, carbides, borides, oxides, nitrides or other refractory materials of the invention. An exemplary additive is graphite, ZrB2 , zirconium carbide and ZrC composites (such as ZrC-ZrB2 And ZrC-ZrB2 -SiC). The additive may comprise a powder layer. The black body radiator 5b4 may comprise a laminate structure such as an inner surface refractory such as a ceramic/intermediate high emissivity refractory compound/outer surface refractory material such as ceramic. Surface refractory materials such as ceramics are impermeable to water and oxygen. An exemplary laminate structure is the inner surface ZrO2 /Intermediate ZrC/outer surface ZrO2 . The laminate structure can be fabricated by casting an inner layer in a mold, spraying the cast layer with an intermediate layer compound, and then casting the outer layer in the mold. Since zirconia is used to deposit an optical coating and it is a high refractive material available from near UV to intermediate IR, the black body radiator contains zirconia, which is below the band gap due to its low absorption in this spectral region. Light is transmitted through the black body radiator, absorbed inside the reaction cell chamber 5b31 and recycled to the PV converter 26a. In an embodiment, the near UV to intermediate IR light is transparent to the black body radiator 5b4, such as a zirconia black body radiator. The black body emission of the plasma of the reaction cell chamber can be directly transmitted to the PV cell and absorbed to heat the black body radiator to its black body operating temperature. In an embodiment, the PV converter comprises a vaporized material that covers the PV cell and protects it from a blackbody radiator (such as a vaporized metal oxide such as MgO or ZrO)2 The window of influence. The window may include an interface, such as a mechanical interface that automatically cleans the window. In an embodiment, the PV window comprises a material and design that forms a clear coating of the condensed vaporized metal oxide from the black body radiator 5b4. In an exemplary embodiment, the black body radiator 5b4 comprises a material, such as zirconia, which is transparent to radiation in the wavelength range from about UV to intermediate IR such that zirconia deposition onto the PV window does not significantly The window becomes opaque and reaches the black body radiation from the black body radiator. In an embodiment, a high gas pressure (such as a gas pressure of an inert gas such as a rare gas such as argon) is maintained on the black body radiator to suppress vaporization. The gas pressure may be in the range of at least about 1 to 500 atm, 2 to 200 atm, and 2 to 10 atm. The gas pressure in the external pressure vessel 5b3a can be maintained. The pressure in the external pressure vessel 5b3a can be reduced during startup to reduce the power consumed by the inductively coupled heater, wherein the pressure can be reestablished after the battery produces power that exceeds the power required to maintain the desired operating temperature. Blackbody radiators, such as metal oxide blackbody radiators, may be coated with a coating to contain vaporization. The coating may comprise a coating of the invention. An exemplary metal oxide coating is ThO2 (M. P. = 3390 ° C). Cerium oxide as well as yttria and zirconia can further act as a gas grid on the black body radiator 5b4 to produce higher PV conversion efficiency. In an embodiment, the metal oxide ceramic component (such as the black body radiator 5b4) is maintained in an oxidizing atmosphere, such as a system comprising H2 O and O2 An oxidizing atmosphere of at least one of which increases the stability of the metal oxide. In an embodiment, the SunCell® comprises a source of heated metal oxide, at least one of: acting as a source deposited on at least one component of the lost metal oxide by vaporization; and acting as a containment from at least one metal A source of vaporized vaporized metal oxide of an oxide cell assembly. In the embodiment, the inner wall of the reaction cell chamber 5b31 contains a refractory material that does not react with water. The refractory material may comprise at least one of cerium, lanthanum, and ceramics, such as a metal oxide (such as zirconia), a boride (such as zirconium diboride), and a carbide (such as tantalum carbide, tantalum carbide, zirconium carbide, and Carbide). The wall of the carbon reaction cell chamber 5b31 may contain niobium because it is resistant to carbide formation. The ruthenium coating can be applied to the carbon walls by chemical vapor deposition. The method may include the following methods: Yonggang Tong, Shuxin Bai, Hong Zhang, Yicong Ye, "Rhenium coating prepared on carbon substrate by chemical vapor deposition", Applied Surface Science, Vol. 261, November 15, 2012, Pp. 390-395, which is incorporated by reference in its entirety. A ruthenium coating on the wall of the carbon reaction cell chamber 5b31 can be applied to the ruthenium interlayer to increase the adhesion strength and mitigate some of the thermal expansion mismatch. The ruthenium coating can be applied to the carbon wall by chemical vapor deposition, and the ruthenium coating can be applied electrochemically. The method may include the following methods: Li'an Zhu, Shuxin Bai, Hong Zhang, Yicon Ye, Wei Gao, "Rhenium used as an interlayer between carbon-carbon composites and iridium coating: Adhesion and wettability", Surface & Coatings Technology, Vol. 235, (2013), pp. 68-74, which is incorporated by reference in its entirety. In an embodiment, the blackbody radiator comprises a ceramic that is stable to reaction with water coated with a material that is non-volatile at the operating temperature, such as ZrC, W, carbon, HfC, TaC, tantalum carbide or Other suitable refractory materials of the invention. The material that does not react with water may include the inner wall of the reaction cell chamber 5b31. Illustrative examples include ZrO coated with graphite or ZrC2 . In an embodiment, the carbon wall of the reaction cell chamber 5b31 is coated with a coating that prevents carbon and oxygen sources or catalysts such as Li2 O, at least one of water and HOH) reacts. The coating may comprise fluorine. The inner surface of the carbon reaction cell chamber may be coated with fluorine that is end bonded to carbon. In an embodiment, the reaction cell chamber contains a source of fluorine, such as a molten metal fluoride (such as silver fluoride) or a metal fluoride of a battery component in contact with the molten metal (such as nickel fluoride, cesium fluoride, fluorinated) Molybdenum or tungsten fluoride) to maintain fluorine-terminated carbon, which protects oxidation, such as by oxidation of oxygen sources or water. In an embodiment, the reaction cell chamber 5b31 contains a source of material or material that is inserted into the carbon. The substance may comprise at least one of an alkali metal (such as lithium); a metal that reacts with water (such as an alkali or alkaline earth metal); and a metal that does not react with water (such as nickel, copper, silver or ruthenium). Lithium metal exchangeable Li formed by the reaction of intercalating lithium with water2 O or LiOH. In an embodiment, the source of oxygen forming the HOH catalyst can comprise an oxide. The oxide may be insoluble in molten metal such as silver. The oxide may comprise lithium oxide. The walls of the reaction cell chamber may be coated with a molten metal such as silver. The source of oxygen can react with hydrogen to form a HOH catalyst. The silver coating protects the walls of the reaction cell chamber, such as the walls of the reaction cell chamber containing carbon from a source of oxygen. The silver coating protects the carbon walls from reaction with oxygen sources. The carbon wall can include intercalated lithium. Lithium can react with carbon to reduce it. Carbon can be reduced by applying a negative potential to carbon. The carbon may have the composition of a carbon anode of a lithium ion battery. The anode composition protects the carbon from oxidation by at least one of an oxygen source and HOH. The reduction potential may be applied with respect to at least one of a molten metal such as silver, at least one reservoir 5c, and at least one molten metal electrode such as a positive electrode. The carbon reduction reaction of the graphite wall by an oxygen source such as lithium oxide can be hampered by at least one of a silver coating, an intercalating metal ion such as lithium ion, and an applied voltage. Lithium carbide can be formed electrochemically, as is known to those skilled in the art. Lithiation can be formed by using carbon as an anode of an electrochemical cell having a lithium opposite electrode, wherein lithiation is formed by charging a battery. In an embodiment, the molten metal, such as silver, comprises an intercalation such as lithium. The intercalate can be inserted into the carbon by applying a negative potential to the reaction cell chamber 5b31. The reaction cell chamber can include an electrochemical cell to form lithium intercalated carbon. The carbon dome can be electrically connected to the negative molten metal injector system. The carbon dome can be connected to a negative polarity reservoir. The negative polarity reservoir can contain carbon. The carbon dome can be connected to the carbon reservoir by a joint such as a sliding nut. The carbon dome and negative polarity reservoir can comprise a single unit. The carbon reservoir can be joined to the EM pump assembly 5kk substrate by wet sealing or another joint known in the art or in the art. The positive molten metal injector can serve as the opposite electrode of an electrochemical cell that performs at least one of: forming and maintaining embedded carbon (such as lithium intercalated carbon). In an embodiment, the black body radiator 5b4 may comprise a surface coating such that the ratio of selective emission of high energy light is greater than that of black body radiation. The coating may permit the black body radiator 5b4 to operate at a lower temperature, such as a temperature in the range of about 2500 K to 3000 K, while achieving a PV conversion efficiency corresponding to a higher blackbody temperature. Black body radiator 5b4 (such as a metal oxide black body radiator, such as ZrO2 Or HfO2 The blackbody radiator can be operated at a suitable operating temperature range to avoid vaporization while achieving the desired PV conversion efficiency due to the coating. The coating may comprise a thermal photovoltaic filter known in the art or in the art. The coating may comprise a selective line emitter such as a mesh coating. Exemplary mesh covers on black body radiator 5b4 for producing higher PV conversion efficiencies are ruthenium oxide and ruthenium oxide. In an embodiment, light can be directly propagated directly from the low energy hydrogen plasma to the PV cells of PV converter 26a. Due to the transparency of the reaction cell chamber 5b31, the reaction cell chamber 5b31 can be maintained at a lower blackbody temperature for a given optical power flow to the PV cell (Fig. 2I146 to Fig. 2I147). The reaction cell chamber 5b31 may comprise a transparent material such as a transparent refractory material such as ceramic. The ceramic may comprise a metal oxide. The metal oxide can be polycrystalline. The reaction cell chamber 5b31 may comprise optically transparent alumina (sapphire) Al2 O3 Zirconium oxide (cubic zirconia) ZrO2 , yttrium oxide (HfO2 ), yttrium oxide ThO2 At least one of its mixture. The low-energy hydrogen plasma held inside the reaction cell chamber 5b31 can emit light, such as a black body and a line that is transparent to the reaction cell chamber 5b31. Transparency can be used for wavelengths having at least an energy higher than the band gap of the PV cells of PV converter 26a. The PV cell can reflect unconverted light having an energy above at least one of a band gap and a lower band gap. Light may be reflected to the mirror, at least one of the other PV cell and the black body radiator that may include the plasma inside the reaction cell chamber 5b31. Due to the scattering, ionization, and blackbody characteristics of the plasma, the plasma can be highly absorptive to reflected radiation. The reflected light can be recycled back to the PV cell for further conversion to electricity. The reaction cell chamber 5b31 can include a section having a mirror for reflecting light to at least one of the PV cell and recycling the light. The reaction cell chamber 5b31 may comprise an opaque section. The opaque section can be at least one of: opaque or cooler. A silver mirror can be formed at the desired location to maintain opacity. The mirror can be formed by condensing from molten silver. At least one of the lower portion of the reservoir 5c and the lower hemisphere 5b41 may be opaque. The reaction cell chamber 5b31 can be operated at a temperature above the boiling point of the molten metal, such as silver, to avoid condensation of the metal on the transparent section. The dome 5b4 can be capable of operating at a temperature above the boiling point of silver (2162 °C) such that it remains transparent to the plasma blackbody radiation to illuminate the PV cell. An exemplary transparent ceramic capable of operating above the boiling point of silver (B.P. = 2162 ° C) is zirconia (cubic zirconia) ZrO2 , yttrium oxide (HfO2 ), yttrium oxide ThO2 And mixtures thereof. In an embodiment, the transparent dome 5b4 (such as a sapphire dome) can operate below the boiling point of the molten metal, wherein the plasma overheats the molten metal to prevent it from condensing on the transparent dome section. Components of the battery, such as the lower hemisphere 5b41, the upper hemisphere 5b42, and the reservoir 5c, may comprise a single component or may comprise a plurality of bonded components. Bonding can be by means of the invention, such as by gluing the components together using ceramic glue. In an embodiment, the transparent dome 5b4 can comprise a plurality of transparent domes each having a smaller diameter. The plurality of domes may comprise a single piece or a composite dome glued together. In an embodiment, the plasma temperature inside the transparent reaction cell chamber 5b31 is maintained at a temperature that is about optimal for electrical conversion by the PV cell, such as a commercial PV cell, such as based on Si and III. At least one of a PV cell of the V semiconductor, such as a PV cell of the invention, wherein the battery can comprise a concentrating cell. The blackbody temperature can be maintained at a temperature of the sun (such as about 5600K). In an embodiment, the radiator 5b4 (such as a transparent dome that transmits most of the plasma radiation) includes a cooling system to cool the dome to avoid exceeding its maximum operating temperature. The cooling system can include gas held in the housing 5b3 to remove heat by at least one of conduction, convection, and forced convection. The cooling system can include a forced gas cooling system with a gas chiller. Alternatively, the cooling system can include at least one coolant line, a coolant line surface mesh on a transparent dome surface, a substantially transparent coolant, a coolant pump, and a chiller. The substantially transparent coolant may comprise a molten salt such as an alkali metal or alkaline earth metal molten salt such as a halide salt. In an embodiment, the base of the dome can be cooled to prevent photoresist. In an embodiment, the dome may be covered with a fire resistant conductor strip to allow heat to flow to the perimeter for removal by the cooling system. In an embodiment, portions of the dome may be covered with a high emissivity refractory material, such as the refractory material of the present invention, to enhance the radiative heat loss from the dome to cool the dome. In embodiments including a plurality of element domes that may comprise a single piece or a composite dome glued together, the cooling system may include a coolant line extending along the seam between the element domes. In an embodiment, the low energy hydrogen reactive plasma is maintained in the center of the reaction cell chamber 5b31 containing the transparent spheres to achieve a thermal gradient from the center of the reaction cell chamber 5b31 to the transparent dome 5b4. The low energy hydrogen reaction rate can be spatially controlled to be localized to the sphere by controlling the injection of low energy hydrogen reactants and controlling reaction conditions, such as maintaining the conductive molten metal matrix to the center, and controlling ignition parameters such as voltage and current. The center. In another embodiment, the non-plasma gas of the buffer layer can be sprayed along the inner sidewall of the dome 5b4 to prevent direct contact of the low energy hydrogen plasma with the wall. Alternatively, the SunCell® can include a source of charge (such as an electrical power supply and electrodes) such that the walls and plasma can be equally charged to cause an electrical repulsion between the plasma and the wall to prevent direct contact of the plasma with the walls. In an embodiment, SunCell® may contain a source of magnetic field for plasma magnetic confinement. The plasma can be bound to the approximate center of the dome by a magnetic field. The dome may comprise a magnetic bottle in which the plasma is constrained to the center such that the transparent wall does not overheat. In an embodiment, at least one of the inlet riser 5qa and the injector 5k61 tube may comprise carbon or ceramic. Ceramics can contain not with H2 O-reactive ceramics (such as oxides such as ZrO2 HfO2 , MgO, Al2 O3 At least one of the ceramics of the present invention and ceramics known to those skilled in the art. The ceramic may comprise a carbide which is at least one of: forming a protective oxide coating and resisting reaction with water, such as ZrC. The tube can include threads at the base end and can be threaded into the base of the EM pump assembly 5kk. In an embodiment, at least one of the inlet riser 5qa, the injector 5k61, and the reservoir 5c is at least partially electrically conductive and negatively biased to avoid corrosion. Exemplary electrically conductive refractory ceramics are niobium carbide, yttria stabilized zirconia and others known to those skilled in the art. A negative biasing member, such as at least one of the inlet riser 5qa, the injector 5k61, and the reservoir 5c, may comprise a refractory conductor, such as graphite. The positively biased component can comprise an oxidatively stable refractory material such as a refractory precious metal such as Pt, Re, Ru, Rh or Ir or a refractory oxide such as MgO or other oxides of the invention. In embodiments, the battery assembly may include a non-reactive surface coating to avoid corrosion, such as corrosion due to oxidation with oxidants such as oxygen and water vapor. The coating of exemplary components, such as at least one of EM pump tube 5k4, inlet riser 5qa, and injector 5k61, may comprise Ni, Co, refractory precious metals (such as Pt, Re, Ru, Rh, or Ir) or ceramics (such as MgO, Al2 O3 , mullite or another oxide of the invention). With high temperature H2 The O-contact component may comprise an oxidation resistant stainless steel, such as at least one of the following: Haynes 230, Pyromet® Alloy 625, Carpenter L-605 alloy, and BioDur® Carpenter CCM® alloy. Parts that operate at elevated temperatures may be coated with a non-reactive refractory coating. Coating can be accomplished by methods known to those skilled in the art, such as by electroplating, chemical deposition, spray coating, and vapor deposition. In an exemplary embodiment, at least one of the Mo or W inlet riser 5qa and the injector 5k61 may be coated with ruthenium (MP = 3180 ° C), ruthenium (MP = 2410 ° C), and corresponding alloys. At least one. In an embodiment, components such as Mo tube injector 5k61 and W nozzle 5q may be coated with tantalum using a carbonyl thermal decomposition process. Twelve carbonyl ruthenium (Re2 (CO)10 ) Decompose at 170 ° C, Re2 (CO)10 It can be vaporized and decomposed to parts that are maintained at temperatures in excess of 170 °C. Other suitable coating methods are those known in the art, such as electroplating, vapor deposition, and chemical deposition methods. A weld or fastener (such as a flared fitting) can be used to connect at least one of the metal inlet riser 5qa and the injector 5k61 (such as at least one of the Re-plated Mo and W injectors) to the EM pump combination The bottom plate of 5kk. Like nickel, under normal conditions, hydrazine does not react with water. The metal that does not react with water can be at least one of: protected from oxidation; and the oxide can be reduced to metal and water by maintaining an atmosphere containing hydrogen. Nickel oxide and ruthenium oxide can each be formed by reacting with oxygen. In an exemplary embodiment, at least one of nickel oxide and cerium oxide may be reduced by maintaining a hydrogen atmosphere. The EM pump assembly 5kk may include a collar for the inlet riser 5qa and the injector 5k61. The collar can be welded to the base plate or machined to a base plate. The collar and the inlet riser 5qa and the injector 5k61 tube can contain resistance and H2 O-reactive material. The collar, the inlet riser 5qa, and the ejector 5k61 tube may be at least one of nickel coated, platinum coated, precious metal coated, and tantalum coated. At least one of the coated inlet riser 5qa and the injector 5k61 can be joined to the bottom plate of the EM pump assembly 5kk by threading to the collar. The pyrolytic graphite hardly reacts with hydrogen and does not insert silver; therefore, the carbon member (such as the reaction electrolytic cell chamber 5b31) may contain pyrolytic graphite which can be used together with a hydrogen atmosphere and molten silver. Silver also has the advantageous property that it does not form alloys from many metals, such as nickel and niobium. The joining or joining between the battery components can include a hard weld. The hard solder joint may comprise joints known to those skilled in the art, such as in the article R. M. do Nascimento, A. E. Martinelli, A. J. A. Buschinelli, "Review Article: Recent advances in metal-ceramic brazing",One of the joints described in vol. 49, (2003) pp. 178-198, which is incorporated herein by reference in its entirety. Brazing parts can include commercial brazing, such as including S-Bond® Hard soldering of reactive solder (http://www.s-bond.com) that enables the bonding of ceramics (such as oxides, nitrides, carbides, carbon/graphite tellurides, sapphire, and others) To the metal and to each other. S-bonded gold active elements such as titanium and tantalum are added to the Sn-Ag, Sn-In-Ag, and Sn-Bi alloys to form a solder that directly reacts with the ceramic and sapphire surfaces prior to bonding. S-bonded gold utilizes all metals (including steel, stainless steel, titanium, nickel alloys, copper, and aluminum alloys) to produce a reliable hermetic bond with the constraint of managing thermal expansion mismatch at the joint temperature. In an embodiment, at least one of the inlet riser 5qa, the injector 5k61 tube, and the reservoir 5c may be brazed to the EM assembly 5kk floor. At least one of the inlet riser 5qa, the ejector 5k61, and the reservoir 5c may comprise a ceramic that can be brazed to the bottom of the EM assembly 5kk, such as a metal oxide (such as ZrO)2 HfO2 Al2 O3 At least one of them). The EM assembly 5kk bottom plate may comprise a metal such as stainless steel (SS) (such as 400 series SS), tungsten, nickel, titanium, tantalum, niobium, molybdenum, ceramic (such as ZrO)2 Or another oxide of the invention). The bottom plate may comprise a material having a coefficient of thermal expansion similar to that of a reservoir. The braze may comprise a filler metal, which may comprise a noble metal such as at least one of ruthenium, rhodium, palladium, iridium, iridium, platinum, gold, silver, and alloys thereof such as Pd-Au alloys. An active metal such as at least one of cerium, zirconium and titanium may be added to a filler metal such as a noble metal. An active metal in the form of a fine powder can be added. An active metal in the form of a hydride such as titanium hydride may be added which decomposes during brazing to form fine titanium particles. The active metal can be added to the filler metal to achieve brazing at a desired percentage of moles, such as in the range of about 1 to 2 mole percent. Active metals can be used to wet the ceramic. The active metal may partially replace the ceramic metal to achieve at least one of wetting the ceramic and bonding with the ceramic. The thermal coefficient of the joined component can be matched as closely as possible while achieving the desired operational characteristics of the component. In an exemplary embodiment, at least one component, such as at least one of the inlet riser 5qa, the injector 5k61 tube, and the reservoir 5c, may comprise ZrO2 HfO2 And Al2 O3 At least one of them is brazed to the 5kk bottom plate of the molybdenum EM assembly. In another exemplary embodiment, at least one component, such as at least one of the inlet riser 5qa, the injector 5k61 tube, and the reservoir 5c, may comprise ZrO2 HfO2 And Al2 O3 At least one of them is brazed to a base of a 410 stainless steel EM assembly 5kk, wherein the braze comprises a Paloro-3V palladium-gold-vanadium alloy (Morgan Advanced Materials). The metal percentage of the alloy can be adjusted to achieve the desired maximum operating temperature, such as a temperature in the range of from about 1150 °C to 1300 °C, wherein the braze temperature can be higher, such as 100 °C higher. The thermal expansion coefficient mismatch between the bonded battery components can be at least partially corrected by the use of a transition element comprising a metal connector that is brazed to the EM assembly 5kk backplane and the ceramic component. The coefficient of thermal expansion of the metal connector can more closely match the coefficient of thermal expansion of the ceramic component. The connector accommodates a large thermal mismatch with the EM assembly 5kk backplane due to the deformability of the backplane and connector metal. An exemplary connector is a molybdenum collar having one end brazed to a metal oxide component and the other end brazed or welded to a stainless steel EM assembly 5kk bottom plate, wherein the thermal expansion coefficients of molybdenum and ceramic (such as zirconia) are more closely Matching, and the deformation of the metal accommodates the higher thermal expansion mismatch stress at the joint of the two metals. In another embodiment, the connector can include a bellows to accommodate differential expansion. The bellows can be electroformed. Brazing can be carried out in a vacuum. Brazing can be carried out in a high temperature vacuum furnace. The melt fill and active metal can be formed into a geometry that matches the geometry of the joint (such as a ring) to form a braze material. The components can be juxtaposed with the brazing material intervening between the components. The furnace can be operated at a temperature that is about the melting point of the brazing material to melt the brazing material and form a braze. The brazed metal part may be coated with an oxidation resistant coating such as nickel, a precious metal, or a platinum coating or another coating of the present invention. In an exemplary embodiment, the EM assembly 5kk bottom plate, the EM pump tube 5k6, and the EM pump bus bar 5k2 contain molybdenum. The components can be welded together by means known in the art, such as laser or electron beam welding. The collar for the inlet riser 5qa and the ejector 5k61 can be machined into a bottom plate, and the inlet riser 5qa and the ejector 5k61 can be threaded to the bottom plate during assembly. ZrO is contained using a palladium filler having 1 to 2 mol% of titanium fine powder as an active metal2 HfO2 Or Al2 O3 The reservoir 5c is brazed to the molybdenum EM assembly 5kk bottom plate. The reservoir is placed on the bottom plate of the assembled EM assembly 5kk using a brazing material interposed between the brazed components. Brazing was carried out in a vacuum oven at about 1600 ° C to melt the palladium (M. P. = 1555 ° C). Alternatively, the filler may comprise an alloy such as Pd-Au 90% (M. P. = 1300 ° C). The surface of the bottom plate of the interior of the reservoir 5c and the interior of the EM pump tube 5k6 are coated with an oxidative protective coating such as platinum or nickel. The coating can be formed by electroplating, vapor deposition, or other methods known to those skilled in the art. A rigid struts, such as metal or ceramic struts, can support the reservoir support plate 5b8. The former may be electrically isolated by mounting the struts on an insulator such as an anodized aluminum backing, wherein the connection between the struts and the bottom plate may comprise an anodized fastener such as a bolt or a screw. The metal pillars may be coated with an insulating coating such as BN, SiC, mullite, black oxide or other coatings of the invention. In another embodiment, the nozzle 5q can include at least one hole, slit or small opening that transfers molten metal at a low flow rate to coat the nozzle. The flow continuously regenerates the surface of the molten metal lost by vaporization of the plasma rather than the nozzle. The holes can be formed by drilling, electrode discharge machines, laser drilling, and during fabrication, such as by casting and by other methods known in the art. In another embodiment, the nozzle 5q can include a flow splitter that directs a portion of the molten metal that is ejected to flow over the nozzle to protect the nozzle from plasma vaporization. In another embodiment, the ignition circuit including the power source 2 further includes an arc sensor that senses an arc at the nozzle rather than through the flow of molten metal; and an arc protection circuit that terminates the arc current on the nozzle. In an embodiment, the injection tube 5k61 can be bent to place the nozzle 5q at approximately the center at the top of the reservoir 5c. In an embodiment, the spray tube 5k61 can be angled from vertical to center the nozzle 5q at the top of the reservoir 5c. The angle is fixed at the connector at the bottom of the reservoir 5k9. The connector establishes an angle. The connector may include a joint sleeve 5k9 having a lock nut to the reservoir base; and further comprising an angled female connector to the threaded end spray tube 5k61. The female connector can include a curved collar or angled nut with a female connector to tilt the angle of the female thread. Alternatively, the reservoir substrate can be angled to establish the angle of the injector tube. In another embodiment, the threads in the reservoir floor can be tilted. The joint bushing fitting 5k9 can be screwed into a slanted or angled thread. The connected straight spray portion of the EM pump tube 5k61 can be angled due to the angled threads. This angle places the nozzle 5q in the center of the reservoir 5c. An adapter sleeve fitting 5k9 angled relative to the base of the reservoir can be coupled to an angled collar below the reservoir floor to permit approximately perpendicular connection to the EM pump tube 5k6, wherein the EM pump tube is connected for wear Through the reservoir bottom plate. The pump tube 5k6 may contain stainless steel (SS) that resists reaction with water, such as SS used in boilers. The pump tubing can be welded to an EM pump tubing assembly (such as a tilted EM pump tubing assembly). In an embodiment, the SunCell® generator includes two reservoirs 5c and one molten metal injector in one of the reservoirs (jet reservoirs). The molten metal injector can include an EM pump injector. Another reservoir, a non-injector reservoir, can be filled with molten metal. Excess molten metal injected by a single injector can overflow and return to the reservoir with the injector. The lower hemisphere 5b41 can be tilted to return the metal flow to the jet reservoir. The reservoir can act as a terminal or electrode of opposite polarization by being electrically connected to the corresponding terminal of the ignition source 2. The polarity can be such as to prevent the nozzle 5q of the injector from being damaged by the violent low energy hydrogen reaction plasma. The non-injector reservoir can include a positive electrode and the injector reservoir can include a negative electrode. The reservoir support plate or bottom plate 5b8 may comprise an electrical insulator such as SiC or boron nitride. Alternatively, the support plate can be a metal that can be operated at local temperatures, such as titanium. The metal can be at least one of non-magnetic and highly conductive to limit the RF power absorbed by the inductively coupled heater and have a high melting point. Exemplary metals are W and Mo. The bottom plate can contain carbon. The electrical isolation of the metal backplane 5b8 can be provided by an insulator between the board and the mounting fixture and between the reservoir and the board. The insulator may comprise an insulator gasket or bushing such as a SiC or ceramic gasket or bushing. The support plates of the dual reservoirs can be one or a separate support plate. The reservoir support plate can include a longitudinal splitter plate with an insulator collar or bushing (such as a SiC or BN collar or bushing) to electrically isolate the reservoir. The reservoir support plate can comprise a longitudinally separated two-piece base plate having a slot for a gasket on which the reservoir is placed, such as an electrically insulating gasket, such as a SiC or BN gasket. Alternatively, each reservoir can be supported by a separate backplane such that there is a current interruption between the backplanes. The backplane may comprise a material having a low absorption cross section for the RF power of the inductively coupled heater. The bottom plate may comprise a thermal shock resistant ceramic such as tantalum carbide or boron nitride. The backplane can comprise a metal with low RF absorption. The bottom plate may comprise a metal coated with a coating that may have a low RF absorption cross section, such as a coating of the present invention. The intersection can be any desired, such as in the region ranging from the reservoir to the region at the top of the reaction cell chamber 5b31. The intersection point can be approximately at the center of the reaction cell chamber. The intersection can be controlled by pumping and at least one of the nozzles from a relative curvature or inclination of the vertical. The reservoirs can be individually and electrically isolated. Molten metal, such as molten silver, can flow back from the reaction cell chamber to each reservoir to be recycled. The return flow of silver can be prevented from electrically shorting across the two reservoirs by a metal flow interrupter or splitter to interrupt the continuity of the silver that would otherwise bridge the two reservoirs and provide a conductive path. The splitter can comprise an irregular surface consisting of a material that causes the silver to beaded to interrupt the electrical connection between the reservoirs. The splitter can include an interruption of each reservoir wall at the shorted region such that the silver drops fall over the interrupted or dripping edge to disrupt continuity. The splitter may comprise a dome or hemisphere covering the intersection of the two reservoirs, wherein the base of the dome or hemisphere contains an interruption for each reservoir. In an embodiment, the two reservoirs 5c and their bottom or bottom plates and the lower hemisphere of the blackbody radiator 5b41 may comprise a sheet. The lower hemisphere of the blackbody radiator 5b41 may include a raised dome or a transverse ridge in the bottom of the set reservoir. In an embodiment, the top of each reservoir may contain a ring plate or gasket that acts as a lip on which the returning silver flows. The lip causes an interruption in the flow of metal to each reservoir to destroy any current path between the reservoirs that can otherwise flow through the returning silver. The top of each reservoir may include a machined circumferential groove in which a gasket is placed to form a lip or drip edge 5ca, as shown in Figure 2I83. At least one battery component (such as a splitter (such as a dome or hemisphere splitter), a reservoir 5c, a lower hemisphere of the blackbody radiator 5b41, a convex or dome bottom of the lower hemisphere of the blackbody radiator 5b41 and each The lip on the reservoir can contain carbon. In an embodiment, the substrate of the blackbody radiator, such as the bottom layer of the reaction cell chamber 5b31, such as the bottom layer of the lower hemisphere of the blackbody radiator 5b41, may include grooves or channels to direct the flow of molten metal in the preferred path to The inlet of the reservoir 5c causes any electrical connection between the two reversely charged reservoirs to be destroyed or substantially destroyed. The passage directs the molten metal to at least one of a front side, a side surface, and a back side of the reservoir. The channels may each include a gradation to cause gravity flow into the reservoir. The channel can be at least one of: graded and tilted. This level can cause a weft to the desired reservoir position (such as the back of the reservoir) relative to the center of the reaction cell chamber. The inclined grading channel that directs the flow to a given one of the two reservoirs of the dual injector embodiment may be a mirror image opposite the channel of the other reservoir to cause flow to the opposite relative position. In an exemplary embodiment having a designated xy coordinate system at the center of the bottom layer of the reaction chamber of the reservoir at positions (-1, 0) and (1, 0), the grading and oppositely inclined channels The flow directs the molten metal to a relative polar angle centered on each reservoir (3/2π And 1/2 π). The bottom layer can include at least one extension at the center and front of each reservoir opening. It may preferably flow to at least one of the side and the back of the reservoir. In an embodiment, the generator includes a sensor and an ignition controller for reducing at least one of an ignition voltage and a current to prevent damage to the component caused by a short circuit of the battery component (such as the lower hemisphere 5b41) . The electrical shorting sensor can include a current or voltage sensor that feeds the signal into an ignition controller that controls at least one of the ignition current and the voltage. In an embodiment, in the case of flow from an overfilled reservoir to an underfilled reservoir, the molten metal may passively flow through the conduit between the two reservoirs. The battery can include a rotary separator in the conduit between the reservoirs to interrupt circuitry within the molten metal. An electrical short through the ignition current of the molten metal may be interrupted by a splitter (such as an electrically insulating gate) that includes a movable device. The gate can include a movable device having a plurality of vanes to interrupt the molten metal conductive path. An exemplary design is an impeller design that can include a refractory material such as SiC or boron nitride. The impeller can be housed in the conduit and permit metal flow without permitting electrical connection between the reservoirs. In an embodiment, the returning molten metal stream may be interrupted by at least one system comprising: (i) a drip edge, such as a flat gasket placed in the top of the reservoir inlet; (ii) a nozzle 5q, molten metal Level and at least one of the reduced riser tubes in the reservoir 5c; (iii) the lower hemisphere 5b41 returns to the molten metal flow path, which disperses the flow to avoid large flows or interrupt any connected current path; Iv) a plurality of electrically insulating projections from the wall of the reservoir; (iv) a plurality of electrically insulating corrugations or projections cut into the edge of the drip, a reservoir inlet or reservoir wall; (v) a grating, such as An electrically insulating grating on top of the reservoir; and (vi) an applied magnetic field that generates a Lorentz force as the electrical short circuit current flows through the flow to deflect the flow into the bead. In an embodiment, the SunCell® includes a reservoir silver level quasi-equalization system that includes a silver level quasi-sensor, an EM pump current controller, and receives input from a level sensor and drives the current controller in the reservoir. A controller that maintains approximately the same metal level in 5c, such as a programmable logic controller (PLC) or computer 100. In an embodiment, the SunCell® comprises a molten metal equalizer that is maintained at approximately the same level (such as a silver level) in each reservoir 5c. The equalizer can include a reservoir level sensor and an EM pump rate controller on each of the reservoirs and a controller to activate each of the EM pumps to maintain approximately the same level. The sensor can include a sensor based on at least one physical parameter such as radioactive opacity, resistance or capacitance, thermal emission, temperature gradient, sound (such as ultrasonic frequency, level-dependent acoustic resonance frequency) , impedance or velocity), optics (such as infrared emission); or parameter changes known in the art that are suitable for detecting the change of the reservoir by a parameter change due to a change in level or a change in the level interface. Other sensors for the level of parameters. The level sensor can indicate the activation level of the EM pump and thereby indicate the flow of molten metal. The ignition state can be monitored by monitoring at least one of the ignition current and the voltage. The sensor may comprise a source 5s1, such as a radioactive nucleus, such as at least one of: a sputum that emits 60 keV gamma rays (such as241 Am),133 Ba,14 C,109 Cd,137 Cs,57 Co,60 Co,152 Eu,55 Fe,54 Mn,twenty two Na,210 Pb,210 Po,90 Sr,204 Tl or65 Zn. Radioactive nuclear radiation can be collimated. The collimator can generate a plurality of beams, such as two beams, each at 45[deg.] to the central axis, wherein one source of radioisotope can form two fan beams to penetrate each of the two reservoirs and then change It is the corresponding detector that is incident on a pair. The collimator can include a shutter to block radiation when the sensor is not in operation. Source 5s1 may comprise X-ray and gamma ray generators, such as brake radiation X-ray sources, such as those at http://www.source1xray.com/index-1.html. The sensor can further include at least one radiation detector 5s2 on the opposite side of the reservoir relative to the source. The sensor can further include a position scanner or member (such as a mechanical member) for moving at least one of the radiation source and the radiation detector along the vertical reservoir axis while maintaining the source and the detector Alignment. This movement can span the molten metal level. The scanner can include an actuator that moves the inductively coupled heater antenna 5f, where the radiation source (such as241 At least one of the Am source and the radiation detector can be attached to at least one of the coil 5f, the coil capacitor box 90a, and the movable actuator mechanism. The level can be identified as the change in the through-radiation count as the collimated radiation exceeds the level. Alternatively, the scanner can cyclically change the relative orientation of the source and detector to scan above and below the metal level to detect metal levels. In another embodiment, the sensor can include a plurality of sources 5s1 arranged along the vertical axis of each reservoir. The sensor can include a plurality of radiation detectors 5s2 on opposite sides of the reservoir relative to the corresponding source. In an embodiment, the radiation detector can be paired with the radiation source such that the radiation travels from the source through the reservoir along the axial path to the detector. The radiation source can be attenuated by the reservoir metal (if present) such that the radiation detector will record a lower signal when the level rises above the radiation path and will record a higher level when the level is below the path. signal. The source may comprise a wide beam or a beam having a wide range of radiation angles that traverse the reservoir to a spatially extended detector or an expanded detector array (such as an X-ray sensitive linear diode array) to A measure of the longitudinal or depth distribution of the metal content of the reservoir in the radiation path is provided. An exemplary X-ray sensitive linear diode array (LDA) is X-Scan Imaging Corporation XI8800 LDA. The attenuation of the metal level pair count can indicate the level. An exemplary source can include a diffused beam from a radioactive or X-ray tube source, and the detector can include an expanded scintillation or gate counter detector. The detector can include at least one of the following: a Geiger counter, a CMOS detector, a scintillator detector, and a scintillator having a photodiode detector (such as sodium iodide or cesium iodide). The detector can include an ionization detector, such as a MOSFET detector, such as a MOSFET detector in a smoke detector. The ionization chamber electrode can comprise at least one thin foil or wire grid on the incident side of the radiation and a typical opposing electrode as in a smoke detector circuit. In an embodiment, the sensor including the source of the radiation (X-ray), the detector, and the controller further includes processing the intensity of the signal received from the source at the detector as a reservoir molten metal The algorithm for level readings. The sensor can include a single wide-angle emitter and a single wide-angle detector. X-rays or gamma rays can penetrate the interior of the reservoir at an angle to the lateral plane of the reservoir to increase the length of the path through the flight region containing the molten metal to the detector. This angle can sample a larger depth of molten metal to enhance the identification of the depth of the molten metal used to determine the reservoir. The detector signal strength can be calibrated for known molten metal levels. As the level rises, the detector intensity signal decreases, with the level determined from the calibration. Exemplary sources are radioisotopes (such as 鋂241) and X-ray sources (such as brake radiation devices). Exemplary detectors are a Geiger counter and a scintillator and a photodiode. The X-ray source can include an AmeTek source, such as a Mini-X, and the detector can include a NaI or YSO crystal detector. At least one of a radiation source (such as an X-ray source) and a detector can be scanned to obtain a longitudinal distribution of X-ray attenuation and thereby obtain a metal level. The scanner can include a mechanical scanner, such as a cam driven scanner. The cam is rotatable by a rotating shaft that can be driven by an electric motor. The scanner may include mechanical, pneumatic, hydraulic, piezoelectric, electromagnetic, servo motor driven scanners or components or other such scanners or components known to those skilled in the art to reversibly shift or redirect the X-ray source and At least one of the detectors obtains a depth profile of the metal level. The radioisotope (such as ruthenium) may be encapsulated in a refractory material (such as W, Mo, Ta, Nb, alumina, ZrO, MgO) or another refractory material (such as the refractory material of the present invention) to permit high temperatures Place it in close proximity to the reservoir. At least one of the X-ray source and the emitter and the detector can be mounted in a housing that can have at least one of controlled pressure and temperature. The housing can be mounted to the external pressure vessel 5b3a. The housing can be removed to permit easy removal of the external pressure vessel 5b3a. The housing can be removed in a horizontal manner to permit vertical removal of the outer pressure vessel 5b3a. The housing may have an inner window for transmitting X-rays while maintaining a pressure gradient across the window. The window can comprise carbon fiber. The outer end of the housing can be open or closed to the atmosphere. In an embodiment, the level sensor comprises a source of X-rays or gamma rays that are inside the casing or housing inside the reservoir 5c. The source of X-rays or gamma rays can be a radioactive nucleus, such as41 Am,133 Ba,14 C,109 Cd,137 Cs,57 Co,60 Co,152 Eu,55 Fe,54 Mn,twenty two Na,210 Pb,210 Po,90 Sr,204 Tl or65 Zn. The sleeve can be fastened to the bottom plate of the EM pump assembly 5kk. The radioactive nucleus can be encapsulated in a refractory material such as carbon, W, boron nitride or tantalum carbide. The radioactive nucleus may comprise a refractory alloy. The radionuclide species may comprise an element or compound having a high melting point, such as14 C, Ta4 Hf14 C5 (M.P. 4215 ° C),133 BaO,147 Pm2 O2 ,144 Ce2 O3 ,90 SrTiO3 ,60 Co,242 Cm2 O3 or144 Cm2 O3 . The casing wall may comprise a material that is easily penetrated by X-rays or gamma rays. An exemplary sleeve is a boron nitride sleeve. The reservoir may comprise a material that is easily penetrated by X-rays or gamma rays, such as a boron nitride or tantalum carbide reservoir. The level sensor can include a plurality of X-ray or gamma-ray sources that can be calibrated to form a plurality of beams. The level sensor can include a plurality of X-ray or gamma ray detectors that are outside the walls of the reservoir and are positioned to incident X-rays or gamma rays when not attenuated by molten metal, such as silver. The beam attenuation difference position indicates the position of the liquid level as determined by the processor. In an embodiment, the source of X-rays or gamma rays, such as radionuclides within the cannula, may not be collimated. The intensity of the X-ray or gamma ray signal can be detected at at least one detector external to the reservoir. The detector may comprise a scintillator crystal and a photodiode (such as a Gadox, CsI, NaI or CdW photodiode). The signal strength as a function of the level of the molten metal can be calibrated. The level sensor can include a processor that processes the measured signal strength and calibration data from the lookup table and determines the molten metal level. In an embodiment, the level sensor comprises a particle backscatter type. The level sensor can comprise a source of particles, such as at least one of erbium ions, protons, X-rays or gamma rays, electrons, and neutrons. The source may include a collimated source. The particles may be incident on the reservoir 5c at a plurality of vertical coordinate positions or may scan a plurality of vertical positions over time. When incident on the reservoir at a position above the level of the molten metal below the level of the molten metal, the particles may be backscattered as a function of intensity. The change in intensity can be increased or decreased depending on the particle and its energy. The X-rays may be absorbed by a molten metal, such as silver, such that the backscatter from the far reservoir wall is reduced by the intervention of the molten metal. Thus, when the X-rays are incident on the reservoir at a lower coordinate position below the level, the intensity of the backscattered X-rays can be reduced. The energy of the X-rays can be selected to have a higher attenuation in the molten metal, such as silver, as compared to the attenuation in the reservoir walls. The X-ray energy can be selected to be energy that is higher than the binding energy of the electron shell just at the edge of the electron. The X-ray source can comprise a radioisotope or an X-ray generator. In an embodiment, the reduction of backscattered X-rays is detected as a means of identifying levels, wherein the X-ray energy is selected such that it is backscattered compared to a column of silver that is not above the level. The signal is attenuated by a lower level of silver. Energy with a high absorption rate can be at the edge, such as 25 keV energy at the edge of the silver K. In an embodiment, the incident particles may produce secondary particles or the same particles having different energies. The intensity change of the secondary particle emission can be used to detect the level. In an exemplary embodiment, X-rays having a first energy are incident on the reservoir at different vertical positions, and X-rays having a second energy are detected by the detector. The change in the intensity of the X-ray or fluorescent X-ray having the second energy as it passes over the level between the beams indicates the level. For example, the detector can be at a position that maximizes the fluorescent X-ray signal, such as along the same axis as the incident beam of 0° or 180° or 90°. In an embodiment, the fluorescent X-rays of the silver increase as the incident beam enters a reservoir that is lower than the level above the level. The level sensor can include an X-ray fluorescence (XRF) or energy dispersive X-ray fluorescence (EDXRF) system as is known in the art. The X-ray source can comprise a radioisotope or an X-ray generator. The EDXRF system can contain sources of energetic particles such as electrons or protons. The detector can include a 矽 drift detector or other detectors known to those skilled in the art. The intensity can be increased when the neutrons are backscattered from the silver column indicating the liquid level position. Neutron can be self241 Am and base metals are produced. The neutron source can include a neutron generator, such as a neutron generator that uses an electric field to accelerate at least one of the erbium and erbium ions to cause D-D or D-T fusion with neutron production. The backscattered particles can be detected by a corresponding detector, such as an X-ray or neutron detector. In another embodiment, particles may be detected from a source on one side of the reservoir and on the same axis on another of the reservoirs. The position of the vertical reservoir that is detected as an increase in the attenuation of the particle beam as the detector is reduced in intensity can identify the position of the level. An exemplary neutron backscatter and gamma ray attenuation level sensor of the present invention is a sensor available from Thermo Scientific (https://tools.thermofisher.com/content/sfs/brochures/EPM-ANCoker- 0215.pdf), which is modified for the geometry of the reservoir 5c. In an embodiment, the level sensor can include a detector of electromagnetic radiation source and intensity of the reflected radiation that is selectively reflected from the molten metal below the molten metal level. This level can be detected by an enhanced laser reflection intensity below the level of the reflected intensity above the level. The position of the level can be determined from the position of the incident beam along the vertical reservoir axis that produces the enhanced reflection intensity. The radiation can include a wavelength that is sufficiently transparent to the reservoir wall such that it penetrates the wall and is reflected back to the detector. The wall of the reservoir 5c may be capable of transmitting light. The reservoir may comprise at least one of alumina, sapphire, boron nitride, and tantalum carbide that are transparent to visible and infrared light. Radiation can penetrate a thin film of molten metal. The laser can have sufficient power to penetrate the thin film of molten metal. In an embodiment, the reservoir wall may comprise boron nitride that has partial transparency to radiation in the range of wavelengths of radiation, such as in the UV to infrared range. The laser can include a high power visible or infrared light source laser. A battery component, such as a reservoir, can be transparent to the laser beam. Suitable refractory materials that are transparent to infrared light are MgO, sapphire and Al.2 O3 . The laser can include an infrared laser to better maintain focus. In embodiments comprising boron nitride, the wavelength can be about 5 microns because BN has a transmission window at this wavelength. In an embodiment, the laser has sufficient power to penetrate the reservoir wall (such as a boron nitride wall, any silver wall coating, and silver vapor) in an axial path from the laser to the detector. The wall can be thinned at the laser beam-wall contact spot. The walls can be machined to prevent the laser beam from spreading or spreading. The wall can be planed. The walls can be machined to form a lens that focuses light across the wall. The lens can be matched to the laser wavelength. The wall can include an embedded lens. The lens can comprise an anti-reflective coating. The lens can include a quarter wave plate to reduce reflection. The transmitted light signal indicates the absence of a reservoir silver column, and there is no optical signal indicating the presence of a silver column, and the vertical reservoir position of the optical signal discontinuity can be used to identify the level. The laser may include a lens to increase at least one of focus and power density (beam intensity). An exemplary commercial laser atHttp :// Wwww . Freemascot . Com / Match - Lighting - Laser . Html orHttp :// Wwww . Freemascot . Com / 50mw - 532nm - Handheld - Green - Laser - Pointer - 1010 - Black . Html ? Gclid = CNu8gJ - EqtICFZmNswodZLMNQA Give it. At least one of the laser and the detector can be remote from the reservoir for positioning in an area where the temperature does not rise excessively and compromises the function of the laser or detector. At least one of the laser and the detector (such as a photodiode) can be cooled. The molten metal may comprise silver. Silver has a transmission window at a wavelength of about 300 nm. The radiation can comprise a wavelength in the range of about 250 to 320 nm. The source of radiation may comprise a UV diode such as UVTOP 310. The UV diode may comprise a lens, which may comprise a hemispherical lens to make a directional beam. The source of radiation may include a laser, such as a diode pumped laser. Exemplary lasers in the wavelength region of the transmission window of silver are KrF excimer laser, Nd:YAF fourth harmonic laser, InGaN diode laser, XeCl laser, He-Cd laser, nitrogen laser , XeF excimer laser and Ne+ Laser. The detector can include a photodiode. The laser level level sensor can include a laser scanner that vertically moves at least one of the laser and the detector over time to intercept regions above, below, and below the level to detect the level. Alternatively, the current-radiation-type level sensor may comprise a plurality of radiation sources and corresponding detectors vertically spaced such that the level is at a position close to the plurality of sources such that the position of the level It can be detected by differential reflection between the source and its detector. The radiation source and detector can be angled relative to one another such that source radiation can be reflected from the molten metal column (if present) and become incident on the corresponding detector. The walls of the reservoir can be machined to be thinner when the radiation is incident and reflected to permit the radiation to propagate from the source to the detector after being reflected from the molten metal column. In another embodiment, the radiation can penetrate the two walls of the reservoir when there is no molten metal column in the beam path, and the column can block the beam when the beam path is below the level. The detector can be detected to transmit light through the reservoir, which can be located on the opposite side of the radiation source, such as a laser. The radiation source and the corresponding detector may be uniformly scanned, or the level sensor may include a plurality of radiation sources and corresponding detectors spaced along the vertical axis of the reservoir to be higher than relatively low This level is detected by the difference in the transmission of the beam at the molten metal level. In an embodiment, the RF coil 5f has openings for incident and reflected or transmitted beams. The coil 5f can be designed to compensate for any opening to provide the desired heating power distribution in the absence of an opening. The sensor may include at least one drip edge, a downward angled tube or a heat source (such as a laser, such as a diode laser) and a vibrator to at least partially eliminate the above-level A molten metal film on the wall of the metal reservoir that reflects radiation. In an embodiment, any molten metal film may be removed by a drip edge at the location of the reflow metal when the beam path intersects the reservoir wall. The battery can include at least one of a reservoir shaker or a waver and a heater. Any molten metal film at the intersection can be removed by vibration or by heating the wall at that point. The beam can be reinforced to penetrate the metal film by using at least one of a larger power beam and a lens. The laser beam can be oriented at an angle relative to the reservoir wall to cause an angled reflection to increase transmission through any thin silver layer such that reflection is reduced upon monitoring. In an embodiment, the laser beam angle is adjusted to produce a dissipative wave, wherein the reflection increases above the silver level below the silver level. In an embodiment, the sensor can comprise a fiber optic cable in the sleeve that has partial transparency if the reflected light is quantified. The intensity of the reflection detected by the detector (such as a photodiode) permits the position of the level to be determined by the processor. The laser wavelength can be selected to enhance transmission through the reservoir wall and any silver film coating. An exemplary wavelength is about 315 nm because silver has a transmission window at about 315 nm. A photodetector, such as a photodiode that optionally includes an optical wavelength bandpass filter, can selectively respond to the laser light. In an embodiment, the lamp can be used in place of a laser. The lamp can include a high power light emitting diode (LED) array. The level sensor can comprise a source of short wavelengths, such as a source capable of emitting UV light, such as in a region of wavelengths between about 315 and 320 nm. Short wavelength sources can include xenon lamps to illuminate the reservoir. The light can comprise a visible light or an infrared light. In an embodiment, the illumination source (such as short wavelength light above the silver level) may be a plasma emission. In an embodiment, the plasma illuminates the space above the molten metal level with strong light that is transparent to the reservoir. The transparent reservoir may comprise a transparent material such as at least one of boron nitride, tantalum carbide, and aluminum oxide. The molten metal level can be recorded by measuring the discontinuity of the light at the metal level using at least one photodetector, such as a photodiode. In an embodiment, the wall of the reservoir 5c is capable of transmitting light. The reservoir may comprise at least one of alumina, sapphire, boron nitride, and tantalum carbide that are transparent to visible and infrared light. In an embodiment, the molten metal level sensor including the light transmissive level sensor detects light transmitted from the inside of the accumulator 5c to the outside, and the vertical of the transmitted light intensity in the at least one photo sensor The change is processed by the processor to determine the level of molten metal. The processor can receive data from two reservoirs and correlate the data to remove any turbid effects from the flow of molten metal on the walls of the reservoir, which can additionally erroneously indicate the presence of molten metal levels. In the embodiment, the plasma generated by the ignition in the reaction cell chamber 5b31 illuminates the wall of the reservoir 5c, and a portion of the light selectively penetrates the wall in the region above the molten metal level. A light sensor, such as a camera or photodiode, can detect light that is transmitted through the walls of the reservoir. A light sensor (such as a photodiode) can be scanned vertically, or a level sensor can include a plurality of vertically separated light sensors, such as a photodiode. In one embodiment, to determine the level of molten metal, the processor processes at least one of: i) a difference in light intensity above the camera image; ii) a difference in light intensity between the plurality of light sensors; And iii) the difference in light intensity between the vertical positions of the scanned photosensor. To facilitate the transmission or transmission of plasma light through the reservoir walls to the light sensor, the reservoir may comprise at least one light path, such as a dimple, recess or thinned region in the wall. At least one light sensor (such as a camera), a plurality of optical sensors, or a scanned optical sensor (such as a diode) can record a change in transmitted light along the path height of the reservoir via a fiber optic cable ( Light, such as a high temperature fiber optic cable, such as a quartz cable, is conducted to each of the remote light sensors. A fiber optic cable or other light pipe can increase the intrinsic light signal above the background black body light. The intrinsic signal from the plasma light can be increased beyond the blackbody radiation by using a photodetector whose spectrum relative to the black body radiation from the outer reservoir wall is selective for shorter wavelengths. The detector can include a selective short wavelength detector or a filter on the detector. A detector or filter can permit selective detection of blue or UV radiation. The detector can detect short wavelength light transmitted through the reservoir wall, such as light longer than about 320 nm in the case of a boron nitride wall. The light-shielding cover with the penetrating member can be used to block background light such as black body radiation along the line of sight of the light path. The level sensor can include at least one stationary or scanned mirror to reflect transmitted light from at least one wall location to the distal light sensor. In an exemplary embodiment, to accommodate the heater antenna 5f in close proximity to the reservoir 5c, the transmitted light is reflected downwardly to the base of the generator for incidence to the photodetector. The mirror can be mounted on the antenna 5f. The processor can receive and process the photosensor data to determine the level of molten metal. In an embodiment, the level sensor comprises a field source (such as a current coil, an antenna, or a light inside the battery (such as inside a reservoir) that carries a field (such as at least one of a magnetic field and electromagnetic radiation) Transmit to an external field detector. The intensity or spatial variation of the detected signal is a function of the level of the molten metal, and the processor uses the corresponding data to identify the molten metal level. In an embodiment, the light transmissive molten metal level sensor includes a light source that illuminates the reservoir wall to produce an image or vertical light intensity change input to the processor to identify the level. The light source can include at least one of a lamp, a laser, and a plasma. The light can be inside the reservoir. The lamp may comprise an incandescent lamp, such as a W lamp or a W halogen lamp. The lamp may comprise bare W filaments that are connected to leads encapsulated in an electrical insulator, which may comprise a refractory ceramic such as SiC or BN. The lamp can include two separate electrodes that can support a plasma, such as an arc plasma. The lamp can contain a carbon arc. The insulator can act as a bracket or the lamp can include a conduit that acts as a bracket. The conduit may comprise a refractory material such as the refractory material of the present invention. Leads to an external power supply can power the lamp. The power supply can be a power supply that is shared with at least one of an EM pump power supply, an ignition power supply, and an inductively coupled heater power supply. The power supply can be in the second chamber of the outer battery housing. The leads may penetrate the reservoir at the feedthrough in the base of the EM pump assembly 5kk. The lamp can be housed in a sleeve that can penetrate at the base of the EM pump assembly 5kk. The casing wall can be at least partially transparent to the interior light. The sleeve can comprise a refractory material, such as at least one of alumina, sapphire, boron nitride, and tantalum carbide that are at least partially transparent to light. In an embodiment, the lamp can illuminate the interior of the tank. The light can be below the slot. The sleeve can include at least one mirror or light diffuser for radially transmitting light from the slot (in the horizontal plane). The light sensor eliminates interference from background blackbody emissions from the reservoir wall. The light sensor can selectively respond to plasma or light. The light sensor can include a filter to deliver selective wavelength region characteristics of the plasma or light. The light sensor can respond to a plurality of wavelength characteristics of the plasma or light. The light sensor can include an optical pyrometer or an optical temperature sensor. In an embodiment, the battery is heated to a desired temperature profile that supports plasma formation and molten metal recirculation and is approximately at the beginning of the EM pump injection of molten metal. The heater coil 5f can extend over at least a portion of the blackbody radiator 5b4 to heat it to a desired temperature profile. The heater can be replaced by an actuator. An ignition voltage can be applied such that ignition and plasma formation occurs when the molten metal streams from the dual EM pumps intersect. The plasma light can be transmitted through the reservoir wall either directly or via a via to permit detection of molten metal levels. The sensor can include at least one of a series of electrical contacts spaced along a vertical axis of the reservoir and a conductivity meter and a capacitance meter for measuring at least one of electrical conductivity and capacitance between the electrical contacts Where at least one of conductivity and capacitance varies measurably across the level of molten metal within the reservoir. The electrical contacts may each comprise a conductive ring that surrounds an inner or outer circumference or a portion of the circumference of the reservoir. The conductivity meter can include an ohmmeter. In an embodiment, at least one of the conductive or capacitive detectors can include a plurality of leads that enter the EM pump tube at a plurality of spatially separated locations within a desired height range of molten metal levels, traveling along the EM pump tube And exit the EM pump tube. The lead outlet can be terminated in the sensor or detector. Alternatively, the wire can travel in a sleeve that can be welded into the bottom of the EM pump assembly 5kk. The detector can contain a conductor or a capacitor. The level of molten metal can be detected using conductivity between individual detectors or relative conductivity at individual detectors, where conductivity increases as the detector contacts the molten metal. The lead wires may comprise electrically insulated wires that penetrate the EM pump tube outside the reservoir at a sealed feedthrough such as a joint sleeve. The leads may exit the EM pump tube inside the reservoir via an electrically insulating penetration that may or may not be sealed. The wire may be coated with a refractory electrical insulator such as boron nitride or another refractory coating of the present invention. The wire can be coated with an anodized Al. The wire may comprise a refractory conductor such as Mo, W or another refractory conductor of the present invention. In an embodiment, the wires may be replaced by a refractory fiber optic cable, wherein the level may be sensed in an optical fiber manner. In embodiments including a reservoir, the reservoirs comprise electrical insulators (such as SiC, BN, AUO)3 Or ZrO2 A plurality of longitudinally spaced wires may pass through the wall of the reservoir and span the extent of the molten metal level. The wires can be bare. The wire can be sealed by a compression seal. During manufacture of the reservoir, the wires can be sintered or cast in place. Alternatively, the wires can be inserted through a tight fit penetration. Penetrating members, such as holes, can be machined. Discharge grinding, water jet drilling, laser drilling or other methods known in the art are produced. The coefficient of thermal expansion of the tight fit wire may be higher than the coefficient of thermal expansion of the reservoir material such that a compression seal is formed when the reservoir is heated. The wire can sense at least one of a change in conductivity and a change in capacitance as a function of the level of molten metal. A level sensor that senses the level of molten silver by at least one of changes in conductivity, inductance, capacitance, and impedance as a function of molten metal level can include a reference electrical contact (such as in an EM pump assembly) A reference electrical contact on the base of 5kk) and at least one detector wire housed in the sleeve secured to the bottom of the reservoir (such as at the bottom of the EM pump assembly 5kk). The capacitive sensor can include two plates that can be filled with molten metal and respond to the level depending on the level. The inductive sensor can comprise a coil, wherein the flux connected by the coil depends on the level of molten metal. The sleeve can be fastened by a fastener, such as a joint sleeve, or can be welded to the bottom of the EM pump assembly. The wires can be attached electrically and physically to the inner wall of the sleeve at the end of each wire. The corresponding electrical contacts of the at least one wire may be vertically spaced apart. An exemplary sleeve includes a refractory metal tube (such as a Mo tube) that can be fastened at the bottom of the EM pump assembly 5kk with a slotted stainless steel joint sleeve with a conductive detector wire insulated by an alumina sheath entering the bottom The open end travels within the tube and is attached to the Mo vertebral body by a weldment that is welded at the end of the tube. A metal detector capable of recrystallization at high temperatures can be preheated to recrystallize the metal when it is used as a detector. The conductivity between the detector wires and the reference contacts attached to the base of the EM pump assembly 5kk is measured. In another embodiment, the outlet portion of the EM pump tube 5k6 acts as a slot. As the silver level rises, the conductivity between the detector and the reference decreases due to the parallel path of the detector current through the molten metal. Conductivity can be calibrated as a function of metal level. Calibration can be done according to the casing temperature. The cannula may further contain a thermocouple to measure the cannula temperature at the detector to permit selection of a corresponding calibration. Alternatively, the conductive sensor can include two matched detectors in a separate reservoir (such as two matched recrystallized W conduits), wherein the relative EM pumping rate is controlled to match the conductivity of the two detectors to control And matching the level of molten metal in the two reservoirs. The sensor can further include a calibration curve for any offset conductivity between the detectors that varies with at least one of average conductivity and operating temperature. The conductivity detector may comprise an electrically insulating sheath or coating to prevent arc breakdown with ignition power while maintaining sufficient electrical connection to sense electrical conductivity. The conductivity detector can comprise a semiconductor that can be doped. Conductivity can be measured using a high frequency detector current or voltage and a corresponding voltage or current signal to determine that the conductivity can be further filtered to remove the effects of noise, such as noise caused by the ignition current. A level sensor that senses a level of molten silver by at least one of a plurality of conductors or a plurality of differential conductances or capacitances at a plurality of conductors that vary with the level of molten metal may comprise a plurality of conductors, such as A wire that passes through the wall of the reservoir. The reservoir wall can comprise an electrical insulator such as boron nitride or tantalum carbide. Due to the differential expansion of the wire relative to the wall material, the wire can be sealed by compression. For example, Mo, Ta, and Nb each have an advantageous thermal expansion coefficient higher than that of SiC. The sealing of the battery can be achieved at room temperature by performing at least one of the following initial steps: by inserting a tightly fitting wire through the hole in the wall of the reservoir in the absence of wall heating or wire cooling, by means of The wall and the cooling wire are heated, such as by application of a refrigerant such as liquid nitrogen. In another embodiment, the wires can be sealed by molding, gluing or sealing. Alternatively, the seal can be achieved by incorporating the wires into the wall material during manufacture. Adhesives or sealants can be used during the manufacture of the reservoir to seal the wires in place. The sensor can include a level dependent acoustic resonant frequency sensor. The reservoir can contain a cavity. In general, cavities, such as musical instruments, such as partially filled water bottles, each have a resonant frequency, such as a pitch, depending on the level of water filling. In an embodiment, the reservoir cavity has a resonant acoustic frequency that depends on the level of molten metal filling. The frequency may shift as the molten metal level changes and the volume of the gas filled portion of the reservoir air changes relative to the metal filled portion. At least one resonant sound wave in the reservoir can be supported with a frequency that depends on the fill level. The fill level and corresponding frequency calibration sensor can be used for given operating conditions (such as reservoir and battery temperature). The resonant acoustic sensor can include a member for exciting an acoustic wave, such as a standing acoustic wave, and an acoustic frequency analyzer for detecting the frequency of the level dependent acoustic wave. The means for exciting the sound in the reservoir cavity may comprise mechanical, pneumatic, hydraulic, piezoelectric, electromagnetic, servo motor drive source members to reversibly deform the walls of the reservoir. A member for exciting and receiving at least one of sounds in the reservoir cavity may include a drive diaphragm. The diaphragm allows sound to propagate into the reservoir. The diaphragm may comprise a component of a battery, such as at least one of an EM pump, an upper hemisphere, and a lower hemisphere. The contact between the acoustic excitation source and the component for acoustic excitation can be via a detector, such as a refractory detector that is temperature stable to the point of contact with the component. The means for exciting the sound in the reservoir cavity may comprise a waver, such as a sonar waver. The frequency analyzer can be a microphone that can receive the resonant frequency response of the reservoir as a sound that passes through the gas surrounding the assembly. Components for receiving and analyzing sound may include a microphone, a transducer, a pressure transducer, a capacitor plate that is deformable by sound and may have residual charge, and may include other sound analyzers known in the art. In an embodiment, at least one of the means for causing acoustic excitation of the reservoir and the means for receiving the resonant acoustic frequency may comprise a microphone. The microphone can include a frequency analyzer to determine the fill level. At least one of the excitation source and the receiver may be located outside of the external pressure vessel 5b3a. In an embodiment, the acoustic sensor comprises a piezoelectric transducer of sound frequency. The sensor can receive sound via a sound guide such as a hollow catheter or a solid catheter. The sound can be excited by the reservoir waver. Piezoelectric transducers can include automotive knock sensors. The knock sensor can match the acoustic resonance characteristics of a reservoir having silver at the desired level. Accelerometers can be used to determine resonance characteristics. The sound conduit conductor can be attached directly to the reservoir and the transducer. The sound conductor may comprise a refractory material such as tungsten or carbon. The transducer can be located outside of the hot zone, such as outside of the external pressure vessel 5b3a. In an exemplary embodiment, the knock sensor is screwed into a hole in the bottom plate 5b3b of the outer container 5b3a connected to the sound conductor, the sound conductor being in contact with the reservoir at the other end. The conduit can travel along the vertical axis to avoid movement of the coil 5f. The notch filter can selectively pass a frequency suitable for sensing the level of silver in the reservoir. The controller can adjust the EM pump current to change the silver level to the desired level, as determined by the frequency of the self-leveling function. The acoustic sensor can include at least one detector or cavity inside the reservoir. The cavity can include a slot. The sleeve can be welded to the base of the EM pump assembly 5kk. The sleeve can be hollow or solid. The detector may comprise a closed end tube or rod that is coupled to the base of the EM pump assembly 5kk by a fastener, such as a joint sleeve. The detector or cavity can be caused to vibrate by the waver. The wave generator can be positioned outside of the high temperature region by a connecting rod such as a refractory connecting rod such as a connecting rod for a wave-transmitting action of a transmission waver comprising Mo, W or Ta or stainless steel. Orientation can be the most efficient orientation under vibration excitation. A vibration sensor, such as a microphone, can sense the frequency of the vibration, where the frequency is characteristic and is used to determine the level of molten metal around the detector or air. The detector or cavity can be selected to facilitate acoustic frequency sensing of the molten metal level. The frequency dependence of the melting level can be calibrated. The calibration can be adjusted for the measurable operating temperature. A metal detector capable of recrystallization at elevated temperatures can be preheated to recrystallize the metal prior to use as a detector. Alternatively, the acoustic sensor can include two matched detectors in a separate reservoir (such as two W-tubes that match recrystallization), wherein the relative EM pumping rate is controlled to match the frequency of the two detectors to control and Matches the level of molten metal in the two reservoirs. The sensor can further include a calibration curve for any offset frequency between the detectors that varies with at least one of an average frequency and an operating temperature. The detector or cavity may comprise a refractory material such as at least one of: Mo, titanium-zirconium-molybdenum (TZM), molybdenum-niobium-carbon (MHC), molybdenum-niobium oxide (ML), molybdenum-ILQ ( MoILQ), molybdenum-tungsten (MoW), molybdenum-niobium (MoRe), molybdenum-copper (MoCu), molybdenum-zirconia (MoZrO)2 ), W, carbon, Ta, alumina, zirconia, MgO, SiC, BN, and other refractory metals, alloys, and ceramics of the present invention, as well as refractory metals, alloys, and ceramics known in the art. The metal detector may comprise an electrically insulating cover or sheath or an electrically insulating coating such as mullite, SiC or the other of the invention to prevent arc breakdown using ignition power. The ceramic detector can comprise a hollow cavity, such as a hollow tube that is end sealed. The ceramic detector can be secured to the bottom of the EM pump assembly by a threaded joint, such as a mating threaded weld collar on the base of the EM pump tube assembly. Other exemplary fasteners include a locking collar, a clamp, a set screw collar or retainer, and a joint sleeve retainer device. An exemplary ceramic detector includes an outwardly opening boron nitride (BN) tube having one end unopened and the other end sealed, the other end being screwed into a threaded stainless steel collar welded to the base of the EM pump tube assembly. The detector can further include a pin that penetrates the base of the EM pump assembly and the sealed end of the ceramic detector to penetrate the hollow portion. The pins can be threaded. The pin can be screwed into at least one of the base of the EM pump assembly and the sealed end of the ceramic tube. The tube can comprise boron nitride. The pin can be used in at least one of the following: transmitting and receiving acoustic energy along the detector. The detector can include a piezoelectric or microelectromechanical system (MEMS) in which excitation and sensing of at least one of acoustic frequency, vibration, and acceleration can be achieved by applying and sensing a piezoelectric voltage or MEMS signal. The sensor can include an accelerometer that measures the molten metal damping acceleration or the detector vibration frequency. The same device can be used to achieve excitation and sensing. The wave-sensing sensing members can be combined in the same device. The molten metal level can be controlled to match the acoustic response of individual detectors in a separate reservoir, where any offset can be determined by calibration and used in matching control algorithms. In an embodiment, the acoustic sensor may comprise a waver that excites a motion such as vibration in an exit portion of the EM pump tube 5k6. The excitation can be continuous or discontinuous at the desired frequency, such as the mechanical resonant frequency of the EM pump tube. The end of the EM pump tube can include an attached vibration damper. The shock absorber can include blades that are transverse to the longitudinal axis of the EM pump tube. The vibration damper may comprise a refractory material. The material can be an electrical insulator such as boron nitride or SiC. The damper can be fastened to the nozzle 5q by a fastener. Fastening can be achieved using threaded parts. The thread damper and the end of the nozzle or EM pump tube can be screwed together. The damper can be close to the surface of the molten metal. The damper can be submerged or partially above the metal surface. The depth of the damper in the molten metal determines the amount of damping. The damping can be measured by at least one of a change in frequency, acceleration or amplitude in the acoustic energy re-emitted by the EM pump tube. The emitted acoustic energy can be sensed on the EM pump tube, such as at a location other than the reservoir. Alternatively, the emitted acoustic energy can be sensed from the reservoir wall. A high temperature capable catheter that can be attached to the reservoir wall can transmit sound. The attachment may include a threaded screw-on connection or a clamped collar that surrounds the reservoir. In an embodiment, the acoustic sensor includes an external sound suppression or cancellation component to improve the acoustic signal to noise ratio. The restraining member may comprise a sound absorbing material such as a sound absorbing material known in the art. The muffling member can include an active noise cancellation system, such as a muffling system known in the art. Alternatively, a vibrating object inside the reservoir, such as an EM pump tube or detector, can transmit its vibrations to the reservoir wall that will vibrate in the same manner. The reservoir wall vibration can be electromagnetically measured by means for detecting a change in the frequency or position of the reflected light initially incident on the vibrating wall. Incident electromagnetic radiation can be in a range of wavelengths with high reflectivity, such as in the visible region of the microwave. The analyzer may include a position sensor that measures a change in frequency other than a differential meter or an interferometer or a measurement position change. The analyzer can include components that convert the reflected beam into an electrical signal, such as a photovoltaic cell, a photodiode, or a phototransistor. The sensor can include a signal processor that processes the frequency or positional changes as an acoustic signal as a function of the melting level. The acoustic sensor can include a visible, infrared or microwave laser interferometer microphone. The laser can include a diode laser. An exemplary laser microphone that relies on the frequency variation of the transmitted or reflected laser beam caused by the movement of the reservoir wall (where the frequency change is detected by the interferometry) is given by Princeton University (http:// Www.princeton.edu/~romalis/PHYS210/Microphone/). An exemplary laser microphone that relies on a change in position of a reflected or reflected laser beam caused by movement of the reservoir wall by Lucidscience (Http://www.lucidscience.com/pro-laser%20spy%20device- 1 . Aspx HackadayHttp://hackaday.com/2010/09/25/laser-mic-makes- Eavesdropping - Remarkably - Simple / ) given. In another embodiment, the time-varying time of flight of the laser pulse is used to measure the wall displacement and the frequency and amplitude of the acoustic signal. The acoustic sensor can include a Light Detection and Ranging (LIDAR) system. A microphone that can be attached to the wall of the reservoir can measure wall vibration. The microphone can include a piezoelectric device. The acoustic analyzer can be one of the ones disclosed herein, such as a microphone and a frequency analyzer. The acoustic level of the independent sensor of the independent reservoir can be controlled by the fusion level, where any offset can be determined by calibration and used to match the control algorithm. Alternatively, the sensor can include a detector that further includes a vibration attenuator at its end. The attenuator can increase the signal due to any change in the melting level. The sensor can include two parallel plates that introduce an electronic sensing connection through hole penetration in the base of the EM pump assembly 5kk. The molten metal can fill the plates to a melting level. The metal plate can be caused to vibrate by the wave generator. At least one of the inductance and the capacitance changes due to a change in the vibration frequency as a function of the melting level between the plates. In another embodiment, at least one of the magnetic coil and the capacitor plate of the docking pair is embedded in an electrical insulator sleeve, such as an electrically insulating sleeve comprising boron nitride. The waver can vibrate the slot and at least one of the inductance and capacitance between the coils or plates can be read via an electrical connector, wherein the parameters are a function of the level between the pair of docking components. Reading can be achieved by applying at least one of current and voltage to the coil and the board. The level sensor may include a Light Detection and Ranging (LIDAR) system in which the laser of the self-sensor is emitted, reflected from the liquid surface, and detected by the detector of the sensor. The time is measured by a sensor to obtain the position of the melting level. In another embodiment, the level sensor can include a guided radar system. Different frequencies of electromagnetic radiation (such as radar) can replace the light of the LIDAR system. In another embodiment, the level sensor may comprise an ultrasonic device, such as a time-of-flight sensing melting level comprising a sonic energy pulse that is transmitted to the interior of the reservoir and reflected back from the interior of the reservoir. Thickness gauge for ultrasonic transmitters and receivers. The sound can travel vertically to sense the depth of the molten metal. The transmitter and receiver may be located at the base of the EM pump assembly 5kk to transmit and receive sound along a vertical or reservoir longitudinal axis (also referred to as the z-axis). In another embodiment, the transmitter and receiver can be located at the side of the reservoir. Sound can be sent and received along a lateral axis or plane. When the position is intercepted, the reflection may be from the opposite wall of the reservoir or the molten metal surface. The transmitter and receiver may comprise a plurality of devices that spatially separate along the z-axis to image the level. The transmitter and receiver may comprise the same device, such as a piezoelectric transducer. The transducer can be in direct contact with the base or reservoir wall of the EM pump assembly 5kk. Alternatively, sound can be transmitted using a sound conduit that can operate at high temperatures. An exemplary thickness sensor is the Elcometer MTG series gauge (Http :// Wwww . Elcometerusa . Com / High speed - Ndt / Material - Thickness - Gauges / ). Time-of-flight data can be processed by a calibrated processor to determine metal levels from the data and control the relative EM pump rate to control the reservoir level. In another embodiment, the level sensor can include at least one stub sensor known in the art, such as a microwave stub sensor. A short line sensor can be scanned in the melting level region to detect the melting level. Scanning can be accomplished by an actuator, such as a mechanical, electromechanical, piezoelectric, hydraulic, pneumatic or other type of actuator known in the art or in the art. Alternatively, the level sensor can include a plurality of short line sensors that can sense levels by comparing signals between the plurality of short line sensors. In an embodiment, the level sensor can include an eddy current level measurement sensor (ECLMS). The ECLMS can include at least three coils, such as one primary and two secondary sensing coils. The ECLMS can further comprise a high frequency current source, such as an RF source. An RF current can be applied to the primary coil to generate a high frequency magnetic field that thus creates eddy currents on the surface of the molten metal. The eddy currents sense the voltages in the two sensing coils that can be positioned on either side of the primary coil. The voltage difference of the sense coil varies with the different distances from the sensor to the metal surface. The ECLMS can be calibrated to a melting level to allow it to read levels during battery operation. The sensor can include an impedance meter that is responsive to the silver level of the reservoir. The impedance meter can include a coil that is responsive to the inductance of the level. The coil can include an inductively coupled heater coil. The coil may comprise a high temperature or refractory metal wire such as W or Mo coated with a high temperature insulator. The wire spacing of the coils can be such that the non-insulated wires do not electrically short. The molten silver may comprise additives such as ferromagnetic or paramagnetic metals or compounds, such as metals or compounds known in the art, to increase the inductive response. The inductance can be measured by the phase shift between the current and voltage measured by the AC waveform drive coil. The frequency can be a radio frequency such as in the range of about 5 kHz to 1 MHz. In an embodiment, the level sensor can include an imaging sensor, the imaging sensor including a plurality of transmitters and receivers, the plurality of transmitters transmitting electromagnetic signals from a plurality of locations, and the plurality of receivers A signal is received at a plurality of locations to image the level. The imaging signal can be calibrated for level. The transmitter and receiver may comprise an antenna, such as an RF antenna. The frequency range is in the kHz to GHz range. An exemplary range is 5 to 10 GHz RF. The imaging sensor can include an RF array to construct data from the reflected signals. The sensor can include a processor that provides density type feedback from the original data to identify the level. An exemplary imaging sensor is a Walabot that includes a programmable 3D sensor that looks like an object using radio frequency technology that passes through the walls of the reservoir. Walabot uses an antenna array to illuminate its front area and senses the return signal. The signal is generated and recorded by the VYYR2401 A3 system single-chip integrated circuit. The data is communicated to the host device using a USB interface implemented using a Cypress controller. The sensor can include an RF filter that removes RF interference from the inductively coupled heater. The sensor can include a series of temperature measuring devices that measure the temperature between the temperature measuring devices, such as a thermistor or thermocouple spaced along the vertical axis of the reservoir, wherein the temperature spans the interior of the reservoir The melting level can be measured quantitatively. In an embodiment, the sensor includes a plurality of thermocouples that are spatially separated at different heights within the reservoir. The sensed temperature is a function of the level of molten silver. The thermocouple can be wrapped in a thermowell that can be soldered to the bottom of the EM pump assembly 5kk. The heat pipe may comprise a refractory material such as Mo, Ta or another element of the invention. The heat pipe can be fastened by fasteners such as Swagelok. Thermocouples such as the present invention can withstand high temperatures. Multiple thermocouples can be vertically spaced apart in a single heat pipe. The outlet of the EM pump tube 5k6 can serve as a heat pipe. The penetration of the EM pump tube outside of the reservoir can include penetrations known in the art, such as entering a Swagelok or an electronic feed. The thermocouple can be replaced by another temperature sensor, such as an optical temperature sensor. The sensor can include an infrared camera. Infrared temperature markers can vary across the silver level. The level sensor can include at least one bushing and a source of electromagnetic radiation and a corresponding detector. The cannula can include a closed conduit that enters the interior of the reservoir 5c, which can be attached to the base of the reservoir. Attachment can be at the base of the EM pump assembly 5kk. The sleeve may comprise electromagnetically transparent material such as an electrical insulator such as alumina, MgO, ZrO2 , Boron nitride and tantalum carbide. The sensor can illuminate the inside of the cannula with electromagnetic radiation that can pass through the wall of the cannula and reflect the melting level. The sensor for imaging the melting level detects the reflected electromagnetic radiation. Electromagnetic radiation can include beams that can be scanned across a level region. The sensor can include a processor that processes the reflected image to determine the level of melting. The reflected electromagnetic radiation can illuminate the area on the electromagnetic radiation detector. The area can vary with the level, the incident electromagnetic radiation, and the relative position of the detector. The size of the illuminated detector region can be varied in response to the level and the corresponding cross-section of the tapered sleeve at the intersection with the melting level. For example, due to the higher level, the reflection can include a ring that can have a smaller diameter. The electromagnetic radiation of the sensor can be selected to reduce background electromagnetic radiation. The electromagnetic radiation of the sensor may comprise a wavelength that does not have a substantial background intensity by the black body radiation of the heated jacket or cell. The electromagnetic radiation can include at least one of infrared, visible, and UV radiation. An exemplary wavelength range is from about 250 nm to 320 nm, with silver having a transmission window such that the reflection is selective due to the silver line rather than the thin silver film. In an embodiment, the sensor comprises a pressure sensor, wherein the pressure increases as the level increases. Due to the extra weight of the molten metal rows in the reservoir 5c, the increase in pressure can be attributed to an increase in discharge pressure. In an embodiment, the sensor includes a weight sensor that detects a change in the weight of the at least one reservoir or a change in the center of gravity between the reservoirs, wherein the weight increases as the reservoir melting level increases . The differential weight distribution between the reservoirs shifts the center of gravity of the measurements. The weight sensor can be located at a position having an increased displacement or pressure change in response to a mass in the corresponding reservoir. This position can be on the bracket of the corresponding reservoir. The weight sensor can be internal to the reservoir, wherein the sensor can be responsive to at least one of a weight and a pressure change with the melting level. The sensor can transmit its signal on at least one of the wires that can penetrate the cell. The melt level can be controlled to match the weight or pressure of an independent detector in an independent reservoir, where any offset can be determined by calibration and used to match the control algorithm. The wire may extend from the sensor inside the reservoir to the inlet of the EM pump tube 5k6 and through the EM pump tube 5k6 on the section outside the reservoir 5c. Penetration can be sealed using a feedthrough through hole or fastener such as Swagelok. The weight sensor can include a sensor that requires a pressure with minimal displacement. The sensor can include a piezoelectric sensor or other such sensor known to those skilled in the art. In an embodiment, the weight or pressure sensor can be housed in a housing that is removed from the high temperature electrolysis cell while maintaining pressure or weight continuity. Pressure or weight connectivity can be achieved by a molten metal connection from a battery assembly such as a reservoir or EM pump tube (such as a portion of the tube outside of the reservoir). The molten metal joint may comprise a row of molten metal having a higher density than the density of the molten metal in the reservoir. For example, a gold row contained in a tube connected to an EM pump tube outside the reservoir can be connected to a housing containing a weight or pressure sensor. In an embodiment, the continuous connector may comprise a metal having a higher density than the metal in the reservoir and a metal melting point lower than the metal melting point of the metal in the reservoir to facilitate at low temperatures Operational weight or pressure sensor use. The level sensor responsive to the weight of the molten metal may comprise a balance, wherein the tilt of the balance varies with the silver level. The balance can contain two rigidly connected arms. The arm can be attached to the bracket at the fulcrum. The balance can include contacts at the ends of each arm. Each contact can abut a diaphragm or bellows on the bottom of the reservoir. The diaphragm may be recessed, such as recessed outward to provide more movement. The diaphragm can be hemispherical. The diaphragm can be displaced downward as the weight of the molten metal in the corresponding reservoir changes. At least one of the arms or portions of the contacts can be electrically insulated to prevent current from flowing between the reservoirs. The balance may comprise a balance rail with an attached piston at each end of the crossbar. The piston can comprise an electrical insulator. Each piston can abut its diaphragm in the base of the reservoir. A tilt sensor, such as at least one of a displacement, stress or torsion sensor, can sense the tilt of the crossbar or arm. The tilt sensor can include an extension from a magnifying crossbar that is sensed by the tilt sensor. An exemplary tilt sensor can include a connector from at least a portion of the arm or balance rail to the strain gauge. An exemplary balance includes a metal crossbar, such as a stainless steel crossbar with an alumina or boron nitride piston at the end. Each piston can be contacted with a thin stainless steel diaphragm in the base of the EM pump assembly, wherein the tilt can be measured by a strain gauge through a connector to one end of the crossbar. This connector allows the strain gage to be removed from the high temperature area of SunCell®. In an embodiment, at least one of the connector and the piston may comprise a refractory material that is also resistant to heating by the inductively coupled heater. The adjustable balance achieves the balance between the ends or arms of the crossbar at the desired level of molten metal reservoir. Balance can be achieved by adding weight to one rail end or one arm. Alternatively, the position of the fulcrum can be adjusted. In an embodiment, the balanced sensor further includes a processor that receives the tilt data and adjusts the EM pump current to equalize the melting level of the reservoir. The level-integrated sensor including the balance type may further include a sensor for a force caused by a translational motion such as in the case of a prosthetic source SunCells®. The balanced level sensor can further include at least one of an accelerometer, a MEMS device, and a gyroscope to provide data to a processor that modifies the response to the tilted data to correct for external translational triggering under control of the relative EM pump rate Power. The balanced level sensor may further comprise a vibration suppression or counteracting member, such as at least one of a restraining mount or bushing, a shock absorber, and an active vibration cancellation system, such as those known in the art, such that Reduce the effects of external vibrations. In an embodiment, the gravimetric level sensor includes an extensometer, such as a rupture opening displacement (COD) gauge. Exemplary COD gauges are one of the ε model 3548 COD, 3448 COD, 3549 COD, and 3648 COD extensometers each of which is stress-regulated. The extensometer can include a rod that contacts the diaphragm in the EM pump tube assembly 5kk, such as alumina or a carbonized mast. The extensometer can include a non-contact type, such as a non-contact type that includes a laser that measures the distance. Exemplary sensors are ε model LE-05 and LE-15 laser extensometers, each of which includes a high speed laser scanner that determines the spacing between reflection points, such as reflection points on each of the two diaphragms. The diaphragm may include a reflective surface for reflecting the laser beam. An exemplary reflective surface comprising a non-oxidized reflective foil having a high melting point is a Pt foil (MP = 1768 ° C). The extensometer signal can be filtered to remove noise such as from vibration. In an embodiment, the diaphragm includes a substantial portion of the bottom region of the EM pump assembly 5kk to maximize sensitivity to line height variations and corresponding weight changes. In an embodiment, the diaphragm has a relatively low resistance to deformation compared to the compression resistance or spring constant of the displacement gauge or extensometer. In this case, the level detection becomes less sensitive to the temperature of the diaphragm that can change its resistance to deformation. In an embodiment, the diaphragm comprises a material that changes its resistance to deformation. The diaphragm may include a foot of a Wheatstone bridge that senses deformation of the melt level as a function of calibration resistance. In an embodiment, the level sensor comprises a driven mechanical detector that is at least partially submerged in the molten metal when the level is at a desired height, the molten metal resists movement of the driven detector, and the resistance is measured as self-resistance The input of the processor that determines the level. The detector can be at least one of a rotation and a translation. The detector may comprise a refractory material such as W, SiC, carbon or BN. The detector can penetrate the reservoir 5c at the EM pump assembly 5kk. Mechanical motion can be supported by bearings that can withstand temperatures such as 962 ° C to 1200 ° C. The sensor can include a bellows that permits longitudinal translation. Resistance to position can be measured using strain measurement. In an embodiment, the level sensor includes a time difference electronic parameter sensor (such as time difference reactance, impedance, resistance, etc.) that measures at least one electronic parameter of the electromagnetic pump depending on the molten metal discharge pressure at the electromagnetic pump At least one of an inductor, a capacitor, a voltage, a current, and a power sensor. At least one electronic parameter can be varied and the EM pump and electronic parameter response can be measured, wherein the response is a function of the discharge pressure. The processor can use the response data and the search calibration data set to determine the melting level. In an embodiment, the generator includes a circuit control system that senses the level of molten silver in each of the reservoirs and adjusts the EM pump current to maintain an approximately matched level in the reservoir. The control system can continuously maintain a minimum injection pressure on each of the EM pumps such that the butted molten silver streams intersect to ignite. In an embodiment, the injection system includes two metal streams in the same plane, wherein the flow impingement has a non-matching EM pump speed such that the speed can be controlled indefinitely to maintain a matching reservoir silver level. In an embodiment, the generator may include a level sensor on the reservoir instead of including two level sensors, one for each reservoir. The total amount of molten metal such as silver is constant in the case of the closed reaction electrolytic cell chamber 5b31. Therefore, by measuring the level in one of the reservoirs, the level in the other reservoir can be determined. The generator may contain a circuit control system for the EM pump of one reservoir instead of two circuit control systems, one for each reservoir. The current of the EM pump without the reservoir of the level sensor can be fixed. Alternatively, an EM pump for a reservoir without a level sensor may include a circuit control system responsive to the sensed level in a reservoir having a level sensor. The spontaneous increase in the flow rate of molten metal through the EM pump may occur due to the increased discharge pressure at which the melting level in the corresponding reservoir increases. The discharge pressure can help pump pressure and produce a corresponding contribution to the flow rate. In an embodiment, the reservoir height is sufficient to increase a sufficient discharge pressure difference between the extreme values including the lowest and highest desired melting levels to provide a control signal for the at least one EM pump to maintain an approximately equal melting level. The EM pump sensor can include a flow sensor, such as a Lorentz force sensor or other EM pump flow sensor known in the art. The flow rate can vary due to changes in discharge pressure due to changes in the level of discharge. At least one flow rate parameter, such as individual EM pump flow rate, combined flow rate, individual differential flow rate, combined differential flow rate, relative flow rate, rate of change of individual flow rates, rate of change of combined flow rate, change in relative flow rate Rate, other flow rate measurements can be used to sense the melting level in at least one of the reservoirs. The sensed flow rate parameter can be compared to at least one EM pump current to determine a control adjustment of the at least one EM pump current to maintain approximately equal reservoir melt levels. In an embodiment, the lower hemisphere 5b41 may include a specularly imaged highly graded channel to overflow directly from one reservoir 5c to another reservoir and further facilitate the return of molten metal, such as silver, to the reservoir. In another embodiment, the level is equalized by a conduit that connects the two reservoirs to the drip edge at each end of the conduit to prevent shorting between the two reservoirs. The silver in the overfilled reservoir flows back through the conduit to another reservoir to equalize the level to a greater extent. In an embodiment, the level of melting between the reservoirs 5c is substantially the same by at least one of the active and passive mechanisms. The active mechanism can include adjusting the EM pump rate in response to the melting level measured by the sensor. The passive mechanism may include a spontaneous increase in the rate of molten metal passing through the EM pump due to increased discharge pressure as the melting level increases in the corresponding reservoir. The discharge pressure can contribute to a fixed or varying EM pump pressure to maintain approximately equal reservoir levels. In an embodiment, the reservoir height is sufficient to increase the sufficient discharge pressure difference between the extreme values including the lowest and highest desired melting levels such that the reservoir levels remain approximately the same during operation. This retention can be achieved due to the differential flow rate, due to the differential discharge pressure corresponding to the difference in the melting level between the reservoirs. In an embodiment, the EM pump includes an inlet riser 5qa (Fig. 2I138) on which a plurality of molten metal inlet openings or apertures are included. The inlet riser 5qa may comprise a hollow conduit, such as a tube. The conduit can be connected to the EM pump tube 5k6 on the inlet side of the EM pump magnet 5k4. The connector can be located at the base of the EM pump assembly 5kk. The connector may comprise one of the inventions, such as a matching thread or Swagelok. The inlet riser may comprise a refractory material such as refractory metal, carbon or ceramic, such as one of W, Mo, SiC, boron nitride, and other refractory materials of the present invention. The inlet riser can have a height that is less than the height of the nozzle 5q to reduce or eliminate the potential energy of the ignition current to electrically short the inlet riser. In an embodiment, the lowest inlet to the inlet riser may have a greater height than the top of the nozzle 5q of the EM pump injector such that the nozzle remains submerged. The immersion nozzle can be a positive electrode that can be submerged to protect it from forming a low energy hydrogen reactive plasma. The inlet riser can be non-catheter. The inlet riser can be coated with a coating such as the coating of the present invention. The coating can be a non-conductor. An inlet riser that may contain a refractory metal such as Mo may be covered with a skin or cladding. The sheath or cladding may comprise a non-conductor. A skin such as a BN skin can be held to the inlet riser by thermal compression. In an embodiment, at least one of the base of the EM pump tube assembly 5kk and the union of at least one of the inlet riser 5qa and the EM pump injector 5k61 may comprise a mating threaded bond. The tubes may be screwed to the inlet and outlet of the EM pump at the base of the EM pump tube assembly 5kk, respectively. An exemplary inlet riser having a reservoir of submerged nozzles includes a BN tube that is screwed into the EM pump assembly base at the EM pump outlet; the inlet includes a V-shaped groove on the side of the tube and the open top is more than the nozzle The height of the tip is greater and the height has a V bottom such that the nozzle remains submerged, wherein the nozzle can comprise a positive electrode. In another embodiment, the bottom of the inlet riser tube may comprise a first material that can be screwed or welded to the EM pump tube outlet at the base of the EM pump assembly (such as, for example, a metal such as stainless steel or a refractory metal such as Mo) And further comprising an upper portion comprising a second material such as a non-conductor or a conductor coated or coated with a non-conductor. The exemplary upper inlet riser section includes a BN that can be screwed in and compressed to at least one of the lower tube sections. The inlet opening can be tapered from above to below the inlet riser to automatically control the pump rate and silver level by controlling the inlet flow rate to the EM pump. In an embodiment, the inlet riser 5qa includes vertically spaced openings such that as the reservoir melting level increases, the EM pumping rate increases due to at least one of the following effects: (i) molten metal is faster Flow into the inlet riser because the total opening cross-section increases with the melting level; (ii) the height of the molten metal in the inlet riser increases as the melting level increases, and the melting level follows the EM pump The discharge pressure is increased correspondingly to increase; and (iii) the flow restriction is reduced, since the larger total opening cross section or region reduces any corresponding pressure drop according to Bernoulli's equation and can be in the absence of flow restriction The lower inlet flow rate limit further increases the discharge pressure when the inlet riser is filled to its maximum height. In contrast, the reverse inlet riser and syringe of the dual injector electrode system can experience the opposite effect and corresponding reduced EM pumping rate due to the relatively molten level of the drop. In an alternative embodiment to a plurality of vertically spaced openings that define an inlet flow from top to bottom within the opening range, the inlet riser may include at least one vertical slot at the top end of the inlet riser, the vertical slots may span The height range of the desired height range, such as the melting level. The trough can gradually reduce the width of the trough from top to bottom such that the corresponding flow restriction has a molten metal height. The top of the inlet riser can be open or closed. In another embodiment, a plurality of vertically spaced holes entering a single EM pump inlet tube may be replaced by corresponding inlet tubes. In an embodiment, the plurality of inlet tubes are combined before or after the magnets 5k4, or they remain independent such that they each act as an individual EM pump injector that is selectively pumped as the molten metal flows into its corresponding inlet end at its characteristic height. In an embodiment, the EM pump can include at least one of a voltage and current sensor that measures a total voltage and current or at least one of an individual voltage and current. The processor can control the total pumping rate or the individual pumping rate using sensor data and controlling at least one of a total voltage and current or individual voltages and currents. The reservoir height and the average molten metal depth may be selected to achieve at least one of a desired discharge pressure and a discharge pressure drop by restricting the flow restriction through the opening. The level of molten metal tends to balance due to the automatic influx of relative molten metal level changes with the EM pumping drive of the reservoir of the dual molten metal injector electrodes and the corresponding pumping rate adjustment. The EM pump of each injector can be set to approximately constant current. The current may be sufficient to intersect the dual jet metal stream at about the center of the reactant unit chamber 5b31 with a small variant that is eccentric to either side of the pumping rate, causing level changes and corresponding pump inflow and EM pump Pumping rate. The current supplied by each EM pump power supply 5k13 can be set to a desired constant level. Alternatively, the SunCell® can include an EM pump power supply 5k13, an EM pump power supply current sensor and controller, an ignition current sensor, and a processor. Each EM pump current can be sensed by its current sensor and adjusted by the controller to obtain the desired initial firing current as measured by the ignition current sensor and processed by the processor. The ignition controller can also control the ignition power parameters. The current can be maintained within a range that provides stability of the intersection of the molten metal stream in about the middle of the reactant unit chamber. In an exemplary embodiment, the current is maintained at a level greater than a threshold of the flow intersection and below a level that causes one flow to be non-intersecting to propagate to the relative reservoir. For example, the EM pump current has an indicative current interval of about 300 A to 550 A. The currents of the two pumps can be equal. The EM pump speed may be controlled by at least one of: an inlet flow rate controller, a horizontally correlated inlet riser tube flowing into the cross section and by a molten metal level sensor; a level processor; and an EM pump current Controller. A change in at least one of the resistance, current, voltage, and power of the EM pump power supply 5k13 can be sensed by a corresponding sensor, and the EM pump current can be controlled to further control the relative EM pumping rate to achieve a reservoir A rough balance between the levels of molten metal. In an embodiment, the EM pump 5ka may include a power limiter to prevent overheating of the EM pump tube resistance and corresponding high temperatures in the event that the EM pump tube 5k6 resistance is excessively increased due to lower molten metal loading and flow. In an embodiment, the inlet riser opening may comprise a protective member such as an inlet guard for particles such as charcoal or metal oxide particles that can block openings or block the riser riser and EM At least one of the pump tubes 5k6. In an exemplary embodiment, the inlet riser opening has a span of approximately 1 cm at the top of the inlet riser, wherein the desired top molten metal level is at the top of the upper opening and the minimum opening is slightly larger than the maximum corrosion product, while The flow of unrestricted EM pumping rate flow provides a limit. Each EM pump can be powered by an independent power supply. Alternatively, a plurality of EM pumps (such as two EM pumps) may be powered by a common power supply via parallel electrical connections. The current of each pump can be controlled by the current regulator of each parallel circuit. Each parallel circuit can include an insulating diode to electrically insulate each circuit. Electrical insulation prevents shorting of the ignition power between the EM pump injectors. In an embodiment, the EM pump coolant line 5k11 may be common to both EM pump assemblies 5ka. In an embodiment, the nozzle 5q of at least one EM pump injector may be submerged in molten silver. This immersion can at least partially prevent the nozzle from being deteriorated by the plasma. The nozzle 5q can be lower than the molten metal level to prevent the nozzle from being damaged by the plasma. Alternatively, the nozzle section 5k61 of the pump tube can be raised and the nozzle can include side holes to cause lateral injection toward the opposite matching nozzle such that the equal flows intersect. The nozzles can be placed at an angle such that the intersection of the dual streams is at the desired location. The nozzle may include a spherical tube end with a hole at the angular position on the spherical surface to direct the molten metal to a desired location in the reactant unit chamber 5b31. In an embodiment, the nozzle 5q includes an extension to direct the direction of the flow of molten metal. The extension may include a short tube to flow the flow toward the point of intersection by the relative flow of the dual molten metal injection system. Nozzle tube segments (such as fire resistant, such as those containing W or Mo) can be vertical. It may comprise a threaded connection to another section of the pump tube. It may comprise a threaded connection to a joint sleeve or a VCR joint, such as one of the reservoir penetrations 5k9. The nozzle 5q (such as a fire resistant person such as W or Mo) may have a slanted outlet. The nozzle can engage the nozzle section 5k61 of the pump tube by threaded engagement. The screw in the nozzle can be maintained at a desired location that causes the flow of molten metal to intersect near or near the fastener such as a set screw or lock nut. The weldment can include a laser weldment. In one embodiment, the lower hemisphere of the black body radiator 5b41 comprising two reservoirs and two EM pumps (serving as two liquid electrodes) is divided into at least two sections joined by an electrically insulating seal. The seal can include flanges, gaskets, and fasteners. The gasket can comprise an electrical insulator. The seal electrically insulates the two liquid electrodes. In an embodiment, the electrically insulating boundary between the two reservoirs can be achieved by orienting the flanges and spacers of the upper hemisphere 5b41 and the lower hemisphere 5b42 vertically rather than horizontally such that the blackbody radiator 5b4 comprises The left and right halves of the joint at the vertical flange. Each half may include a black body radiator 5b4 and a vertically divided half of a reservoir 5c. In an embodiment, the lower hemisphere of the blackbody radiator 5b41 comprises a separate piece having two reservoirs 5c fastened or connected thereto. The connections may each comprise a threaded joint or joint. Each of the reservoirs 5c may include threads that cooperate with the threads of the lower hemispheres 5b41 on the outer surface at the top. The threads may be coated with a paste or coating that at least partially electrically isolates each reservoir from the lower hemisphere to further electrically isolate the two reservoirs from each other. The coating may comprise one of the inventions, such as ZrO. In an embodiment, the electrically insulating surface coating may comprise at least one of the coating of the present invention or a high temperature material, such as ZrO, SiC, and functionalized graphite. The insulating surface coating may comprise a ceramic such as a zirconium based ceramic. An exemplary zirconia coating comprises yttria stabilized zirconia, such as 3 wt% yttria. Another possible zirconium ceramic coating is zirconium diboride (ZrB)2 ). The surface coating can be applied by thermal spraying or other techniques known in the art. The coating may comprise an impregnated graphite coating. The coating can be multiple layers. An exemplary multilayer coating comprises alternating layers of zirconia and alumina. The functionalized graphite can comprise blocked graphite. The capped graphite may comprise at least one of H, F, and O capped graphite. In an embodiment, at least one of the reservoirs may be electrically insulated and at least one other may be in electrical contact with the lower hemisphere of the blackbody radiator 5b41 such that the lower hemisphere may comprise an electrode. The lower hemisphere may comprise a negative electrode. In one embodiment, the connection between each reservoir 5c and the lower hemisphere of the blackbody radiator 5b41 is remote from the reactant unit chamber 5b31, maintaining the electrically insulating coating of the connection below, such as SiC or ZrO. The temperature at which the coating melts or decomposes. Electrical insulation between the reservoirs can be achieved by spacers comprising electrical insulators, such as tantalum carbide spacers. The lower hemisphere 5b41 can include an elongated connection to the spacer that is sufficiently extended from the body of the lower hemisphere such that the temperature of the joint is suitably below the temperature of the spacer. The spacer may be threaded at the extended connection and connectable to the reservoir 5c. The connection to the reservoir 5c can include threads. The spacer may comprise a tantalum carbide cylinder threaded to an extension of the lower hemisphere 5b41 and threaded to the reservoir 5c at the opposite end of the SiC cylinder. The union may be directly sealed by a thread and may further comprise at least one of a seal and a gasket, such as one of a joint between the spacer and the lower hemisphere and one of a joint between the spacer and the reservoir . The gasket may comprise graphite (such as Toyo Tanso or flexible graphite) or one of hexagonal boron nitride. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as one containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391) or another material of the invention. The SiC spacer can comprise SiC that combines the reactants. The spacer comprising the threads may initially comprise Si that is carbonized to form a threaded SiC spacer. The spacer may be coupled to the lower hemisphere and the upper portion of the corresponding reservoir. The bond can comprise a chemical bond. The bond may comprise SiC. The SiC spacers can be fused to a carbon component, such as a corresponding lower hemisphere and a reservoir. This fusion can occur at high temperatures. Alternatively, the bond may comprise an adhesive. The spacer may comprise a drip sputum to prevent the return flow of molten metal from electrically shorting the reservoir. The drip can be machined or cast into a spacer such as a SiC spacer. Alternatively, the spacer may include a recess for insertion of a drip, such as a ring-shaped drip. The spacer may comprise other refractory materials, electrically insulating materials of the invention (such as zirconia), yttria stabilized zirconia, and MgO. In an embodiment, the ignition system includes a safety cutoff switch to sense an electrical short between the dual reservoir-injector and terminate the ignition power to prevent damage to the injector (such as nozzle 5q). The sensor can include a current sensor that passes current between the collector circuits of the lower hemisphere 5b41. In one of the embodiments shown in Figures 2I95 through 2I147, the number of contacts of the unit is reduced to avoid the risk of failure. In one embodiment, at least one of (i) the lower hemisphere 5b41 and the upper hemisphere 5b42, (ii) the lower hemisphere and the non-conductive spacer, and (iii) the contact between the non-conductive spacer and the reservoir are removed. . Contact removal can be achieved by forming a single piece rather than joining the pieces. For example, the lower and upper hemispheres may be formed to include a single halves 5b4. (i) at least one contact between the lower hemisphere and the non-conductive spacer and (ii) the non-conductive spacer and the reservoir can be removed by forming a single piece. The lower and upper hemispheres may comprise a single piece or two pieces, wherein (i) at least one contact between the lower hemisphere and the non-conductive spacer and (ii) the non-conductive spacer and the reservoir may be formed by One piece to remove. A single piece can be formed by at least one of the following methods: casting, molding, sintering, stamping, 3D printing, electrical discharge machining, laser ablation machining, by chemical etching (such as carbon and oxygen in an atmosphere containing oxygen) Laser ablation of combustion, laser or liquid machining (such as water jet machining), chemical or thermal etching, tool machining, and other methods known in the art. In an embodiment, at least one section of the battery assembly, such as blackbody radiator 5b4 (such as a hemispherical blackbody radiator) and at least one reservoir 5c, is electrically non-conductive. The circumferential section of at least one of the reservoir 5c and the blackbody radiator comprising the hemispherical 5b4 or the lower hemisphere 5b41 and the upper hemisphere 5b42 may be non-conductive or comprise a non-conductor. The non-conducting section of the blackbody radiator may comprise a plane transverse to the line between the two nozzles of the dual liquid ejector embodiment. The non-conductor can be formed by converting the material of the sections of the assembly to be non-conductive. The non-conductor may comprise SiC or boron carbide (such as B)4 C). SiC or B of battery assembly4 The C segment can be formed by reacting a carbon battery module with a helium source or a boron source, respectively. For example, the carbon reservoir can be reacted with at least one of a liquid helium or neodymium polymer, such as poly(methylaniline) to form a niobium carbide segment. The polymer can be formed at a desired section of the assembly. The battery assembly can be heated. The current can pass through the assembly to cause the reactant to form a non-conducting section. The non-conducting section can be formed by other methods known to those skilled in the art. The outer surface of the reservoir 5c can include a raised circumferential band. To maintain molten niobium or boron during the conversion of carbon to niobium carbide or boron carbide in the desired section. Tantalum carbide can be formed by reactant bonding. An exemplary method of forming boron carbide from boron and carbon isHttps :// Wwww . Google . Com / Patents / US3914371 Given above, the above is incorporated by reference. The niobium carbide or boron carbide segment can be obtained byHttps :// Www3 . Nd . Edu /~ Amoukasi / Burning _ Synthesis _ Of_silicon Carbo . Pdf The combustion synthesis given in and the Study Of Silicon Carbide Formation By Liquid Silicon Infiltration By Porous Carbon Structures by Jesse C. Margiotta is incorporated by reference. Other suitable reservoir materials are non-conductive graphite (such as pyrolytic graphite or doped graphite), SiC, tantalum nitride, boron carbide, boron nitride, zirconia, alumina, AlN, AlN-BN (such as SHAPAL Hi Msoft (Tokuyama Corporation), titanium diboride and other high temperature ceramics. The reservoir can be a composite material in which the non-conducting segments are formed for a parent reservoir material such as carbon. The reservoir may comprise a material coated with a refractory electrical insulator such as SiC, zirconia or alumina. The coated material can be an electrical conductor such as carbon that is electrically insulated by the coating. In an exemplary embodiment, the carbon reservoir comprises a continuous nucleated graphite, such as Minteq Pyroid SN/CN pyrolytic graphite, which may be anisotropic, wherein the low conductivity may be in a transverse plane and the end of the reservoir The portion may be coated with a non-conductor such as SiC to prevent current from flowing along the longitudinal reservoir axis. In an embodiment, the porous SiC reservoir may be coated with carbon to seal the pores. It can be applied by vapor deposition from carbon from a source such as an electric carbon arc. As shown in Figures 2I95 through 2I147, the hemisphere 54b and the reservoir 5c can comprise a single piece. A single piece can be achieved by machining a material that loves that battery assembly into a single piece. Alternatively, a single piece in this example may initially comprise a plurality of sections, components or assemblies joined by at least one seal, which may comprise a glued or chemically bonded seal formed by a seal. Other sheets, components or components of the invention may similarly be glued or chemically bonded. Exemplary graphite gums are Aremco Products, Inc. Graphi-Bond 551RN graphite adhesive and Resbond 931 powder with Resbond 931 adhesive. The reservoir may contain a non-conducting section near the top of the hemisphere. The reservoir can be connected to the base plate. The reservoir can rest in a concave collar. At least one of the outer surface of the collar at the distal end of the top of the collar and the end of the reservoir may be threaded. A nut fastened to the thread engages the reservoir and the bottom plate. The threads can be tilted such that the rotation of the nut drags the reservoir and the bottom plate together. The threads may have opposing spacing on opposing sections having mating nut threads. The reservoir may include a sliding nut 5k14 at the end of the bottom plate 5b8, wherein the sliding nut is fastened to the externally threaded bottom ring 5k15 to form a secure joint. In an embodiment, the sliding nut can include a groove and a gasket. A sliding nut can be attached to the reservoir at the groove. The grooves can be cast or machined into cylindrical reservoir walls. An O-ring or gasket can be pressed into the groove and the sliding nut can be fastened to the externally threaded floor collar 5k15 to form a forbidden engagement. The externally threaded bottom collar can be further wedged to accommodate the reservoir. The sliding nut 5k14 fastener may further comprise a gasket 5k14a or an O-ring (such as a flexible graphite or Toyo Tanso), or a hexagonal boron nitride spacer or a ceramic rope O-ring to seal the reservoir To the bottom plate. The protrusion of the wall of the BN reservoir 5c may comprise a hexagonal boron nitride spacer. The BN gasket can be machined or poured into the wall of the BN reservoir 5c. The gasket may comprise the same material as the material of the reservoir. The gasket can be screwed onto the reservoir. The gasket can comprise a wider width, such as a width ranging from about 1 mm to 20 mm wide. The EM pump assembly 5kk collar and the nut of the slip nut may include a flange-like mounting surface for the BN gasket. The gasket can fill a cavity containing a nut, a reservoir wall, and a gasket holder for the 5kk collar of the EM pump assembly. In an exemplary embodiment, the wide threaded BN gasket is screwed onto the BN reservoir, wherein the collar and nut seat for the gasket are matched in width to create a larger gasket placement and sealing area. The BN gasket can be applied to the space filled void of the sliding nut seal with BN glue. Exemplary glues are Cotronics Durapot 810 and Cotronics Durapot 820. In order to avoid the formation of carbon-containing gaskets to form carbides such as iron carbide, parts comprising iron or other materials such as carbon-reactive metals may be coated with an inert coating such as mullite, SiC, BN, MgO, Tellurate, aluminate, ZrO or other materials of the invention. The coating may comprise a sealant such as Cotronics Resbond 920 ceramic adhesive, Cotronics Resbond 940LE ceramic adhesive or one of the present invention. The coating may comprise metals or elements that do not form carbides, wherein the elements may comprise alloying elements such as alloying elements in steel. Exemplary elements that do not form carbides in steel are Al, Co, Cu, N, Ni, and Si. Engagement members that contact carbon, such as carbon gaskets, such as nuts for threaded collars and slip nut joints, may or may be plated with a metal that does not form carbides or forms carbides that are unstable at the operating temperature of the battery, such as nickel. The joint member may be coated with a carbide-resistant forming material such as nickel. To avoid the formation of iron carbide reactions, the gasket may be a material other than carbon in the case where the gasket contacts iron or a component such as a nut containing iron. The joint component can comprise a carburized stainless steel such as Hayes 230. In an embodiment, the EM pump assembly 5kk may comprise carbon such that it is compatible with a graphite sliding nut gasket, wherein the nut may also comprise carbon. At least one of the injection section of the EM pump tube 5k61 and the inlet riser 5qa may contain carbon. The carbon component can be formed by at least one of 3D printing, casting, molding, and machining. Other such chemical incompatibility should also be avoided. The gasket or O-ring may comprise a metal such as nickel, niobium or tantalum. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as one containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391) or another material of the invention. The joint between the reservoir (such as a reservoir containing BN) and the collar of the EM pump assembly 5kk (such as an EM pump assembly comprising stainless steel) may comprise a bond between the BN and a metal such as stainless steel. Chemical bond. In one embodiment, the interior of the EM pump assembly collar is BN coated, and then the BN reservoir tube is bonded to the interior of the collar by at least one of a compression joint and heating. The chemical bond can be formed by other methods known in the art, such as by "Diffusion bonding of boron nitride on metal substrates by plasma activated sintering process", Scripta Materialia, Vol. 34, No. 9, ( 1996), pages 1383 to 1386, the above is incorporated herein by reference in its entirety. The joint may comprise at least one of the group consisting of: diffusion bonding under applied pressure, thermal spraying or mechanical bonding, sintering bonding using P/M technology (such as sintering of ceramic powder and bonding to a metal substrate) At the same time, a thermal equilibrium pressurization (HIP) and a plasma assisted sintering (PAS) process are used to produce a good diffusion bond between the BN ceramic layer and the metal substrate when the ceramic layer is sintered. The bond between the BN reservoir and the metal EM pump assembly collar may comprise a binder, a compound or a composite ceramic having at least one of tantalum nitride-alumina and titanium nitride-alumina ceramics (such as comprising BN) Composite ceramics), BN reinforced alumina and zirconia, borosilicate glass, glass ceramics, enamel, and ceramics having titanium boride, titanium boride-aluminum nitride and tantalum carbide-boron nitride compositions. The joint may comprise a sliding nut or a filling box type of the invention. A gasket coated with a binder, compound or composite ceramic such as a hexagonal BN or alumina-phthalate fiber gasket may be chemically bonded (glued) to the surface using at least one bonding reaction condition such as heat and pressure. Roughened ceramic reservoirs (such as BN reservoirs). The gasket may comprise a hexagonal BN or cloth or tape (such as one comprising ceramic fibers) comprising a high amount of alumina and a refractory oxide (such as Cotronics Corporation Ultra Temp 391), and the binder may comprise a ceramic bond such as Cotronics Resbond. A sealant for agents such as Resbond 906. In an embodiment, the seal may comprise a joint sleeve. In an embodiment, the seal may comprise Gyrolok, such as Gyrolok comprising at least one of a front ferrule, a rear ferrule, a butt seal, a body and a nut, wherein the front ferrule, the rear ferrule and the butt seal At least one of the pieces may comprise a gasket such as one of the present invention. The ferrule can be chamfered. The seal component can be chemically compatible with the gasket; for example, the component in contact with the carbon gasket can comprise nickel. The collar may include an internal taper to accommodate the reservoir to compress the gasket by the tightening of the sliding nut. The reservoir may include an outer taper to be received by the collar to compress the gasket by the tightening of the sliding nut. The collar may include an outer taper to apply tension to the O-ring by fastening of the sliding nut. The bottom plate can contain carbon. The reservoir can contain straight walls. The reservoir wall can include at least one groove for the at least one spacer. In addition to the threads on the exterior of the collar that receives the sliding nut, the EM pump tube assembly 5kk collar can be internally threaded to accommodate matching threads on the ends of a reservoir such as a reservoir containing boron nitride. The thread can be wedged. The thread can include a conduit thread. The union between the reservoir and the EM pump tube assembly 5kk collar may include an internal gasket between the inner portion of the collar and the reservoir, such as between the inner base of the collar and the end of the reservoir one of. The end of the reservoir can be wedged to retain the gasket. The taper traps the gasket between the outer wall of the reservoir and the inner wall of the collar. The gasket seal can be at the base of the reservoir. At least one of the gasket and the thread may be further sealed by a sealant such as Cotronics Resbond 920 ceramic adhesive or Cotronics Resbond 940LE ceramic adhesive. In an embodiment, the union may include a mating threaded joint. The 5kk collar of the reservoir and EM pump tube assembly can be screwed together. The sealant can be applied to the threads. Exemplary sealants are Cotronics Resbond 920 ceramic adhesive and Cotronics Resbond 940LE ceramic adhesive. The abutment or other abutting threads of the present invention can comprise a soft metal alloyed with at least one of the joined components. In an exemplary embodiment, the soft metal may form an alloy with the collar, wherein the alloy may have a high melting point. The tin metal can act as a soft metal sealant for the collar to the reservoir threads, wherein the collar can comprise at least one of nickel and iron, and the reservoir can comprise boron nitride or tantalum carbide. The collar may be coated with Sn by at least one of the following methods: immersing the collar in molten tin, vapor deposition, and electroplating. The bottom plate may include fasteners by at least one of the shims to the EM pump tube (such as a joint sleeve), such as flexible graphite or Toyo Tanso, hexagonal boron nitride or niobate shims And sealant. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as one containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391) or another material of the invention. Alternatively, the bottom plate may comprise a metal such as stainless steel or a refractory metal. The EM pump tube can be fastened to the metal base plate by welding. The base metal can be selected to match the thermal expansion of the reservoir to the joint components. The sliding nut and washer accept the difference between the expansion of the base plate and the reservoir assembly. In an embodiment, the upper slide nut may comprise graphite that engages matching threads on the graphite lower hemisphere 5b41. The EM pump assembly 5kk can comprise stainless steel. The lower sliding nut may comprise a metal such as Mo, W, Ni, Ti, or a different stainless steel type having a lower coefficient of thermal expansion than the EM pump assembly stainless steel (SS) such that the sliding nut remains pressed against the sliding nut spacer. An exemplary combination is 17.3×10, respectively- 6 m/mK and 9.9×10- 6 SS austenite (304) and SS ferromagnet (410) with a linear temperature expansion coefficient of m/mK. Alternatively, the sliding nut may comprise a material having a coefficient of expansion similar to that of the reservoir. In the case where the reservoir is boron nitride or tantalum carbide, the sliding nut may comprise graphite, boron nitride or tantalum carbide. At least one component of the sliding nut engagement portion, such as the threaded portion of the EM pump assembly, can include a thermally expandable groove. The thermally expandable grooves may allow for thermal expansion in a desired direction, such as narrowing the groove circumferentially and radially expanding. In one embodiment, the expansion groove is cut across the entire collar of the EM pump tube assembly 5kk. The cut can be extremely thin such that it is sealed by thermal expansion of the collar where more or less is added to achieve a seal assembly operating temperature such as about 1000 °C. Cutting can be accomplished by means such as machining, water jet cutting and laser cutting. The nut may comprise carbon, boron nitride or SiC. A type of material such as carbon or boron nitride may be selected to allow some of the nut to expand to avoid cracking at battery operating temperatures, such as temperatures ranging from about 1000 °C to 1200 °C. The number, placement and width of the grooves or cuts can be selected to match the amount of collar metal expansion at the battery operating temperature. In an embodiment, the expansion groove may be only partially extended via the collar, such as 50% to 95% of the width of the extension collar to prevent leakage of molten metal. The cutting may extend inwardly from the external thread to allow expansion of the threaded area of the collar, wherein the opposing nut threads of the sliding nut cooperate when the nut is tightened. The cutting can substantially cover a portion of the threaded collar that is covered by the nut when the nut is tightened. The cutting may be provided by pressing the entire collar of the material with the added metal liner, such as by welding, to provide an extruded or incomplete area. The metal lining added may be the same or different metals. The added material or metal can be extensible. In an embodiment, the abutment between the reservoir 5c of the boron nitride tube reservoir and the EM pump tube assembly 5kk may comprise a compression fitting. The union can include an internal threaded EM pump tube assembly collar, a double-sided threaded cylindrical insert, and a threaded end reservoir. The collar of the EM pump tube assembly 5kk may comprise a material having a first coefficient of thermal expansion, such as 400 stainless steel or 410 stainless steel. The double-sided threaded cylindrical shape may comprise a material having a second coefficient of thermal expansion that may be higher than the coefficient of thermal expansion of the collar, such as 304 stainless steel. Other material combinations are possible, such as a 304 SS or 410 SS collar with a 304 SS backplane, wherein 304 is welded in the EM pump tube 5k6; and is included in an operating temperature range such as one of about 1000 ° C to 1200 ° C Inserts of non-melting metals, metals such as Ni, Ti, Nb, Mo, Ta, Co, W, 304 SS or 400 SS, 410 SS, nickel steel (FeNi36), Inovco (F333Ni4.5Co), FeNi42 or Kovar Alloy (FeNiCo alloy). The reservoir tube can be screwed into the internal threads of the insert and the insert can be screwed into the interior of the collar. Alternatively, the insert can be screwed only to the inside and can be welded to the collar at the base of the EM pump assembly 5kk. In an embodiment, at least one of the interior of the collar, the exterior of the insert, the interior of the insert, and at least two of the reservoirs is unthreaded. In an embodiment, the insert has a higher coefficient of thermal expansion than the collar; therefore, the insert can expand inwardly to compress the reservoir tube for mating the insert surface and the collar surface with the reservoir surface therein At least one of the threads forms a compression seal and a thread seal. The compression insert can be formed into a tight seal by expansion to avoid creating a gap between the mating surfaces and not causing excessive pressure on the reservoir tube that can cause it to fail. In another embodiment, the union comprises a compression seal wherein the reservoir is press fit into the collar with or without a sealant. In an embodiment, at least one of the EM pump assembly-reservoir union assembly, such as at least one of a group of unthreaded collars, threaded collars, threaded inserts, and unthreaded inserts, is heated to Fit it or fit it to the corresponding component of the joint or inflate it before pressing it into the corresponding component. In an embodiment, at least one of the EM pump assembly-reservoir union assembly, such as at least one of a threaded insert, a threadless insert, and a reservoir tube, is cooled to fit or Mount it to the corresponding component of the joint or shrink it before pressing it into the corresponding component. It can be cooled to a low temperature. Cooling can be achieved by exposing the assembly to a cryogenic agent such as liquid nitrogen. The corresponding joint may include at least one of a compression fitting, a threaded fitting, and a sealing fitting. In an embodiment, a reservoir tube, such as a BN tube, can be placed in a recessed recess in the base of the EM pump assembly. In another embodiment, the water reservoir is welded or chemically bonded to the EM pump assembly substrate. BN can be bonded to the metal substrate by roughening the BN surface and allowing the weld metal to flow into the corresponding pores to bond to the metal substrate. An exemplary EM pump assembly-reservoir joint includes 410 SS, nickel steel (FeNi36), Inovco (F333Ni4.5Co), FeNi42 or Kovar alloy (FeNiCo alloy) collars, where the 304 SS backplane has 304 SS or 铌A bilaterally threaded or unthreaded insert and a mating threaded or unthreaded collar and BN reservoir, wherein the unthreaded portion may comprise a compression fitting formed by a portion of the compression fitting achieved by differential heating or cooling. The sliding nut seal can include a plurality of seals. The sliding nut seal can include a back-to-back sliding nut. The sliding nut seal can include a standard nut and a sliding nut and washer that are turned upside down. In an embodiment, the sliding nut can include an upper nut and a lower nut and a gasket sandwiched therebetween, wherein the two nuts can be screwed onto the external threads of the collar of the EM pump assembly 5kk. The pressure applied to the gasket by screwing the threads can push the gasket into the reservoir tube 5c to form a tight compression seal. The reservoir 5c can include a groove at the location of the compression pad to better accommodate the gasket and improve the seal. The seal between the reservoir and the EM pump assembly can include a gland seal or a stuffing box seal. The gasket can comprise the gasket of the present invention. The stuffing box seal may further comprise a sealer, such as a sealer comprising an inert refractory fines (such as a sealer of the present disclosure). The sealer can have a high coefficient of thermal expansion to fill the stuffing box at elevated temperatures. In an embodiment, the EM pump assembly base can replace the bottom nut of the stuffing box seal, wherein the slip nut can include an upper nut. The fill can be the circumference of the reservoir, wherein the reservoir can include a filled recess. The reservoir may further comprise a compression-filled upper flange inside the sliding nut. In an embodiment, the abutment may only include an outer threaded reservoir, such as a boron nitride reservoir that is screwed into an inner threaded collar, such as a 304 stainless steel collar. The threads of the abutment of the present invention, such as the union between the reservoir and the collar, may comprise pipe threads. The union may further comprise at least one of a thread sealant and a slip nut seal. Exemplary sealers are Cotronics Resbond 920 ceramic adhesive and Cotronics Resbond 940LE ceramic adhesive. In an embodiment, the encapsulant may comprise a soft metal alloyed with the insert or collar, wherein the alloy may have a high melting point. The tin metal can act as a soft metal sealant for the insert or collar comprising at least one of nickel and iron. At least one of the insert and the collar may be coated with Sn by at least one of a group of immersion inserts, vapor deposition, and electroplating in molten tin. In an embodiment, the union may comprise at least one of a union of the present invention, such as a threaded or a non-threaded union (such as a compression seal), and the union may further comprise a seal that includes flush Adjacent to the bottom edge of the reservoir on the substrate of the EM pump assembly. The seal between the bottom edge of the reservoir and the EM pump assembly base may further comprise a gasket, such as comprising Celmet, MoS2 Or a cloth or chain cloth (such as a cloth or chain cloth comprising ceramic fibers comprising a high alumina and refractory oxide such as Cotronics Corporation Ultra Temp 391). The union may further comprise a sliding nut connection. The reservoir tube (such as a BN reservoir tube) can include a smaller upper outer diameter (OD) and a larger lower outer diameter. In the case of a sliding nut that is threaded through the EM pump assembly collar, the sliding nut can be tightened to the EM pump assembly base by tightening against a flange containing two diameters to tighten the bottom edge of the reservoir . In another embodiment, the flange may be replaced with a fastener such as a stud that is tightened to secure the nut. The sliding nut joint including the nut, the threaded collar, and the reservoir tube may further include a gasket between the top of the flange and the interior of the nut. Flange gaskets can include Celmet, MoS2 Or a cloth or chain cloth (such as a cloth or chain cloth comprising ceramic fibers comprising high alumina and refractory oxides such as Cotronics Corporation Ultra Temp 391). An exemplary joint includes a 410 SS collar, a 410 SS substrate, a BN reservoir with flanges at the collar threads containing the smaller upper OD and a larger lower OD, a 410 SS sliding nut, and a Celmet gasket, where BN The lower edge of the reservoir abuts the base of the EM pump assembly and the abutment is secured by tightening the sliding nut against the flange as the sliding nut is screwed onto the collar. In an embodiment, the reservoir bonded by the joint at the dome 5b4 may comprise an insulator such as ceramic (such as SiC, tantalum nitride, boron carbide, boron nitride, zirconia, alumina or other high temperature ceramic). . Exemplary ceramics having the desired high melting point are magnesium oxide (MgO) (MP = 2852 ° C), zirconia (ZrO) (MP = 2715 ° C), boron nitride (BN) (MP = 2973 ° C), zirconium dioxide (ZrO2 ) (M.P.=2715°C), lanthanum boride (HfB)2 (M.P.=3380°C), niobium carbide (HfC) (M.P.=3900°C), Ta4 HfC5 (M.P.=4000°C), Ta4 HfC5 TaX4 HfCX5 (4215 ° C), tantalum nitride (HfN) (M.P. = 3385 ° C), zirconium diboride (ZrB2 (M.P.=3246°C), zirconium carbide (ZrC) (M.P.=3400°C), zirconium nitride (ZrN) (M.P.=2950°C), titanium boride (TiB)2 (M.P.=3225°C), titanium carbide (TiC) (M.P.=3100°C), titanium nitride (TiN) (M.P.=2950°C), niobium carbide (SiC) (M.P.=2820°C), tantalum boride (TaB)2 (MP=3040°C), tantalum carbide (TaC) (MP=3800°C), tantalum nitride (TaN) (MP=2700°C), niobium carbide (NbC) (MP=3490°C), tantalum nitride (NbN) ) (MP = 2573 ° C). The insulator reservoir 5c may include a drip edge at the top to prevent metal shorting by reflowing the molten metal. The union may include a sliding nut abutment, such as a sliding nut union of the same type as a sliding nut joint between the reservoir and the bottom plate. The sliding nut may comprise at least one of a refractory material (such as carbon, SiC, W, Ta) or another refractory metal. The ceramic reservoir can be ground by means of, for example, diamond tool grinding to form a precision surface suitable for achieving a sliding nut seal. In one embodiment of a ceramic reservoir, such as a ceramic reservoir comprising an alumina tube, at least one end of the reservoir can be threaded. Threads can be achieved by attaching a threaded collar. The threaded collar can be attached by an adhesive, adhesive or glue. The glue may comprise a ceramic glue. The joint surface of the intervening gasket or O-ring can be roughened or grooved to form a high pressure capable seal. The gasket or O-ring can be further sealed with a sealer. Niobium (such as tantalum powder or liquid helium) may be added to a gasket or O-ring containing carbon, wherein the reaction to form SiC may be carried out at a high temperature to form a chemical bond as a blocking agent. Another exemplary blocking agent is graphite gum, such as the graphite gum of the present invention. In addition to forming a shim or O-ring seal slip nut, the engagement portion can include mating threads to prevent separation of the portions due to higher reaction cell chamber pressure. The joint may further comprise a structural support between the black body radiator 5b4 and the reservoir 5c or the bottom of the bottom plate to prevent the abutment from separating under internal pressure. The structural support can include at least one clamp that holds the portions together. Alternatively, the structural support can include an end screw having an end nut that bolts the blackbody radiator and the bottom of the reservoir or base plate, wherein the blackbody radiator and the bottom of the reservoir or base plate contain structural anchors for the rod. The rod and nut may contain carbon. In an embodiment, the union may comprise at least one end flange and an O-ring or gasket seal. The union can include a sliding nut or a clamp. The sliding nut can be placed on the jointed part before the flange is formed. Alternatively, the sliding nut can comprise a metal (such as stainless steel or refractory metal) welded together from at least two parts around at least one of the reservoir and the collar. In one embodiment, at least one of the reservoir 5c of the blackbody radiator 5b4 and the bottom collar and the reservoir and the bottom plate - the EM pump - the injector assembly 5kk can be threaded (which can be reversed At least one of the ends of the reservoir and the sliding nut are coupled to each other with an opposite pitch. At least one of the threaded thread, the nut of the sliding nut, and the nut runner can be glued by the glue of the present invention, such as SiC which can be formed from carbon or carbon glue. In one embodiment, a less conductive or insulating reservoir (such as SiC or B)4 C reservoir) replaceable carbon reservoir. The insulating reservoir may comprise (i) at least one of a top connection to the lower hemisphere 5b41 or the one-piece black body radiator dome 5b4 and (ii) a reservoir bottom, wherein the reservoir and the reservoir The bottom of the unit is a one-piece piece. The SiC reservoir can be bonded to the lower carbon hemisphere by at least one of a gasket and a sealant comprising ruthenium, wherein the fluorenone can react with carbon to form SiC. Other blocking agents known in the art can also be used. The bottom of the reservoir may contain threaded penetrations for EM pump tube fasteners, such as Swagelok fasteners. The bottom of the reservoir can be a separate part, such as a base plate that can contain metal. The metal base plate may comprise a welded joint of the EM pump tube at the penetration. The bottom plate may include a threaded collar that is coupled to a mating fastener of the reservoir, such as a sliding nut. The collar can be tapered to accommodate the reservoir. The collar wedge can be inside. The end of the reservoir can be wedged. The reservoir wedge can be externally received within the collar. The fastener may comprise a gasket such as Grapho or Perma-Foil (Toyo Tanso), hexagonal boron nitride or niobate gasket. The gasket or O-ring may comprise a metal such as nickel, niobium or tantalum. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as CelmetTM containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391), or another material of the invention. The fastening of the sliding nut applies compression to the gasket. In an embodiment, the blackbody radiator 5b4 may comprise a unitary piece (such as a dome) or may comprise an upper hemisphere 5b42 and a lower hemisphere 5b41. The dome 5b4 or the lower hemisphere 5b41 may comprise at least one threaded collar at the base. The threads can cooperate with the reservoir 5c. The union and reservoir of the collar may include external threads that are screwed onto the reservoir in the internal threads of the collar or vice versa. The joint may further comprise a gasket. Alternatively, the union may include a sliding nut that is threaded onto the reservoir on the outer thread on the collar. The collar may include an inner wedge that receives the reservoir at the end. The joint may comprise a gasket such as Grapho or Perma-Foil (Toyo Tanso), hexagonal boron nitride or niobate gasket, pressed MoS2 Or WS2 , CelmetTM (such as CelmetTM containing Co, Ni or Titanium, such as porous Ni C6NC (Sumitomo Electric)), ceramic rope or other high temperature gasket materials known to those skilled in the art, such as cloth or chain cloth (such as containing ceramics) A cloth or chain of fibers comprising high alumina and refractory oxides such as Cotronics Corporation Ultra Temp 391). The gasket can be placed at the joint between the reservoir and the collar. The reservoir can contain such as SiC, B4 C or a non-conductor of alumina. The reservoir can be cast or machined. The dome or lower hemisphere may contain carbon. The sliding nut may comprise a refractory material such as carbon, SiC, W, Ta or other refractory metal or material such as the refractory metal or material of the present invention. The reservoir can be further attached to the floor assembly at the end of the EM pump. The union can comprise the same type as at the end of the blackbody radiator. The base plate assembly can include (i) a union collar that can be internally or externally threaded to mate with a mating threaded reservoir, (ii) can be internally wedged at the end to accommodate the reservoir and threaded externally to a union collar mated with a sliding nut, (iii) a bottom of the reservoir, and (iv) an EM pump tube assembly in which the penetrating member can be joined by a weld. The base plate assembly and the sliding nut may comprise stainless steel. In an embodiment, a sliding nut can be attached to the reservoir at the flange or groove. The grooves can be cast or machined into a cylindrical reservoir wall. Both the reservoir and the collar may include a flange on at least one end, wherein the union includes a mating flange of the engagement part and the clamp (which bypasses the flange and drags it together when tightened) O-ring or gasket between. In another embodiment, the sealing or engagement, such as sealing or engagement between the reservoir and the EM pump assembly 5kk, may comprise a wet or cold seal (Fig. 2I139). The wet seal can have a wet seal design of a molten carbonate fuel cell. The wet seal can include a mating flange on each of the parts to be joined that forms a passage for the molten metal to fill such as the reservoir flange 5k17 and the EM pump assembly collar flange 5k19. In another embodiment illustrated in FIG. 2I140, the EM pump assembly collar flange 5k19 can be at least one of: (i) mated with the reservoir support plate 5b8, (ii) including a reservoir The support plates 5b8, and (iii) comprise a base of the reservoir support plate 5b8 and the EM pump assembly 5kk1 (which includes the inlet and outlet of the EM pump tube 5k4). The reservoir support plate 5b8 can be supported by a post 5b82 anchored to the support substrate 5b83. In one embodiment, the wet seal cooler 5k18 includes a cooler of at least one of the perimeter of the reservoir support plate 5b8 and the support column 5b82 that can dissipate the perimeter of the reservoir support plate 5b8. At least one of the reservoir flange 5k17, the reservoir support plate 5b8, the EM pump collar flange 5k19, the collarless EM pump flange 5k19, the base of the EM pump assembly 5kk1, and the reservoir 5c are inclined The reservoir design can be tilted. The flange can be engaged with fasteners such as jaws, bolts, screws, fasteners of the present invention, and fasteners known to those skilled in the art. At least one of the fastener penetration member, the reservoir flange 5k17, and the EM pump assembly collar flange 5k19 may include any seat for the differential expansion wet seal portion and the mount (such as the reservoir support plate 5b8) The structure of the frame. The wet seal coolant loop 5k18 passage can be radially extended such that the passage extension zone can be maintained at a temperature below the melting point of the molten metal, such as below 962 ° C in the case of silver. The wet seal region of the cured metal may include areas that contact the fastener (such as the bolt 5k20) to avoid leakage at the fastener. The bolt may comprise carbon and may further comprise a carbon gasket (such as a Perma-Foil or Graphoil gasket) to act as an expansion liner. In an exemplary embodiment, the wet seal may comprise a collar flange on the reservoir 5c, such as a boron nitride tube, which may be a collar flange glued onto the collar of the EM pump assembly 5kk and Screw on at least one of the collar flange and the welded collar flange. A wet seal flange (such as a flange of a ceramic reservoir) can be at least screwed and glued to a cylindrical reservoir (such as a BN reservoir) by at least a flange plate (such as a BN flange plate) One is formed. Exemplary glues are Cotronics Durapot 810 and Cotronics Durapot 820. Alternatively, a wet seal flange (such as a flange of a ceramic reservoir) can be formed by at least one of molding, hot pressing, and machining a ceramic such as BN. BN components, such as at least one of the reservoir 5c, the gasket, and the reservoir flange 5k17, can be fabricated by hot pressing of the BN powder and subsequent machining. Boron oxide can be added to the portion made of boron nitride powder for better compression. Other BN additives that change BN characteristics (such as thermal expansion, compressibility, and tensile strength and compressive strength) to their desired properties are CaO, B2 O3 SiO2 AUO3 , SiC, ZrO2 And AlN. The boron nitride film can be produced by chemical vapor deposition from boron trichloride and a nitrogen precursor. Boron nitride grades HBC and HBT contain no binder and can be used up to 3000 °C. The outer edge of the channel may comprise a circumferential concentric band. The belt may include a circumferential edge of the EM pump assembly collar flange in which the BN flange is placed. The channel can be cooled to maintain a solid metal to the perimeter of the inlet of the channel and the molten metal. The joint cooling system can include a joint cooling system of the present invention, such as a joint cooling system that includes a liquid or gas coolant or radiator. The joint can be cooled at the perimeter by at least one coolant circuit 5k18. The coolant circuit 5k18 may include a line from the EM pump cooling heat exchanger 5k1, a coolant line 5k11 or a cold plate 5k12. The joint can be cooled at the perimeter by at least one heat sink, such as a radiator or convection or conductive fins. The joint can be cooled at the perimeter by at least one heat pipe. An exemplary wet seal cooler includes a copper tube coolant loop 5k18, wherein the coolant can comprise water. At least one of the flanges can have a circumferential groove that acts as a passage for the circumferential cooling circuit. The cooling circuit can be radially inward relative to a circumferential fastener, such as a bolt, to solidify the molten metal radially inward from the bolt. In an embodiment, the EM pump assembly collar flange 5k19 and the reservoir flange 5k17 may be wide enough such that the temperature at the perimeter of the seal is lower than the melting point of the molten metal, such that the coolant circuit 5k18 is not necessary of. The EM pump assembly collar flange 5k19 can include a reservoir support plate 5k8. The reservoir can be tilted to a horizontal reservoir flange 5k17. In other embodiments the flanges 5k17 and 5k19 and the reservoir 5c can be at any desired angle relative to each other to achieve sealing and to spray molten metal into the reaction cell chamber 5b31. In one embodiment, the material and thickness of the flanges (such as 5k17 and 5k19) can be measured for heat transfer and thereby cooled. In an exemplary embodiment, the reservoir flange 5k17 is directly mated with a plate comprising a reservoir support plate 5b8, an EM pump flange 5k19 and an EM pump assembly base 5kk, the EM pump assembly base further comprising an EM pump The inlet and outlet of the EM pump tube 5k4, and the reservoir flange 5k17 contains a BN having a high thermal conductivity. The thickness and width of the plate 5k17 and the mating plate 5k19 can be selected to provide sufficient cooling to maintain a wet seal. The seal may further comprise a cooler of the invention, such as a coolant circuit 5k18 embedded in the perimeter of at least one of the flanges 5k17 and 5k19. The plate 5k17 may comprise a collar with a tiltable attached reservoir 5c. The reservoir may be attached to the plate flange 5k17 by at least one of molding machining, screwing, and gluing. In an embodiment, the slanted/tilted reservoir may comprise a length suitable to cause a desired separation of the wet seal at the base of the reservoir. The wet seal can include a Faraday cage that covers the solidified metal portion to reduce heating of the portion. The wet-sealed mating flanges, fasteners, and any other components may include materials having low absorbance for RF from inductively coupled heaters, such as Mo and BN. The wet-sealed cooling circuit can at least cool the wet seal and can include a larger cooling system (such as further cooling the reservoir 5c, the EM pump magnet 5k4, the EM pump tube 5k6, and at least one of the other EM pumps or battery assemblies) Branch. The wet seal cooling system can include at least one cooling circuit, at least one pump, at least one temperature sensor, and a coolant flow controller. In an embodiment, the mating flange seal may comprise a gasket. The gasket forms a seal between the bolting flanges. The gasket can include a male component that is sealed to the female component. The BN gasket can include a protrusion of the BN reservoir flange 5k17, wherein the BN gasket can include a male gasket assembly. The gasket may comprise another gasket of the invention, such as an alumina-tantalate ceramic plate gasket. In another embodiment, the reservoir ceramic (such as BM) can comprise at least one of a metallized ceramic or a hardened seal of a metal EM pump assembly 5kk collar. Exemplary metallization materials and brazing include Ag, Ag-Cu, Cu, Mo-Mn, W-Mn, Mo-W-Mn, Mo-Mn-Ti, Cu-based alloys, Ni-based alloys, Ag-based alloys, Au At least one of a base alloy, a Pd-based alloy, and an active metal brazing alloy. In one embodiment of the sliding nut seal, at least one of the nut, the threaded coating on the nut, and the inner portion of the filler of the nut comprises a higher melting point than the molten metal formed by the reservoir molten metal (such as silver). The components of the alloy. The filling may comprise a powder or a cladding, such as a metal powder or a cladding. The seal may comprise a stuffing box type seal wherein the sealant comprises a fill or cladding. The blocking agent can comprise a gasket comprising an element. The element may include at least one of Pt, rare earth, Er, Gd, Dy, Ho, Pd, Si, Y, and Zr. In an embodiment, the seal may comprise a reverse slip nut design (Fig. 141), wherein the nut 5k21 is screwed onto the inside of the EM pump assembly 5kk collar, and the reservoir tube 5c is in the collar 5k15 of the EM pump assembly 5kk The outer portion slides upward, and the spacer 5k14a is located on the inner circumference of the reservoir tube 5c. Exemplary gaskets and reservoir tubes contain boron nitride. The EM pump assembly 5kk can comprise stainless steel. The reverse sliding nut seal may further comprise a compression retaining sleeve 5k16 (such as a compression retaining sleeve comprising W, Mo or C) that resists the expansion force (such as thermal expansion force) of the collar 5k15 and the reservoir 5c. The seal may further comprise Reverse compression type seal (Figure 142). In an exemplary embodiment, the EM pump assembly collar 5k15 expands against the reservoir tube 5c as the temperature increases from room temperature. The material of the reservoir and EM pump assembly collar can be selected to have a desired coefficient of thermal expansion to achieve a compression seal without damaging the reservoir tube. In one embodiment of the reverse compression type seal, the seal further includes a compression retaining sleeve 5k16 around the reservoir tube 5c to increase the tensile strength of the tube. The compression retaining sleeve 5k16 can have a desired low coefficient of thermal expansion to prevent the reservoir 5c from rupturing due to internal expansion of the EM pump assembly collar 5k15. The exemplary compression retaining sleeve 5k16 can comprise a refractory material such as W, Mo or C. An exemplary compression seal can comprise at least one of thin walled collars 5k16 comprising stainless steel having a low coefficient of thermal expansion, such as 410 SS, nickel steel (FeNi36), Inovco (F333Ni4.5Co), FeNi42 or Kovar (FeNiCo) Alloy) to reduce thermal expansion to prevent cracking of the BN reservoir 5c and the graphite compression retaining sleeve 5k16. The seal can include at least one of a reverse slip nut and a compression seal. In an embodiment, the joint (such as at least one of a reverse sliding nut and a compression seal) may further comprise a threaded portion, such as an EM pump sleeve that is screwed into the interior of the outer reservoir tube with a compression seal The outside of the ring. In an embodiment, the threaded crown can be lowered in height relative to the threaded recess to include an expansion joint along the compression joint contact area. The bottom plate and EM pump portion can be assembled to include a bottom plate-EM pump-injector assembly 5kk (Fig. 2I98 and Fig. 2I147). In the case of a dual molten metal injector embodiment, the generator includes two electrically isolated backplane-EM pump-injector assemblies. Electrical isolation can be achieved by physically separating the two assemblies. Alternatively, the two assemblies are electrically isolated by electrical insulation between the assemblies. The nozzles of the dual liquid ejector embodiment can be aligned. The reservoir can be placed upside down or in an inverted position, and the metal acting as a molten metal can be added to the reaction cell chamber via the open end of at least one of the reservoirs. The bottom plate-EM pump-injector assembly can then be connected to a reservoir. This connection can be achieved by the connector of the present invention, such as a wet seal, compression or slip nut collar connector. The bottom plate-EM pump-injector assembly can comprise at least one of stainless steel or a refractory metal such as at least one of Mo and W. Portions of the EM pump tube, such as the connector, the bottom of the reservoir, the nozzle, the bottom plate, and the mating collar, may be welded and fastened together. The fastener can include a threaded joint. The two substrate plates 5b8 of the dual melt ejector embodiment may be fabricated by electrically insulating plates (such as ceramic plates such as SiC, SiN, BN, BN+Ca, B).4 C, alumina or zirconia plates) are joined by means of fasteners such as bolts to form a single reservoir structural support which can be made of columns (such as ceramic columns or electrically insulated 410 SS, nickel steel (FeNi36), Inovco (F333Ni4) .5Co), FeNi42 or Kovar (FeNiCo alloy) column is raised to attenuate the thermal expansion effect. The column can contain tubes to attenuate thermal expansion effects. In an embodiment, the reservoir support plate 5b8 may include a single or multiple pieces with brackets to form a continuous plate to avoid thermal deformation. The reservoir structural support may be a column that may include a tube to attenuate the thermal expansion effect (such as a ceramic column or an electrically insulating 410 SS, a nickel steel (FeNi36), an Inovco (F333Ni4.5Co), a FeNi42 or a Kovar alloy (FeNiCo alloy) column). high. In an embodiment, the SunCell® includes a reservoir position adjustment system or a reservoir regulator to control the alignment of the molten metal injector. In one embodiment comprising a dual molten metal injector, the SunCell® comprises means for aligning the length of the column supporting the reservoir support plate 5b8 with the nozzle 5q such that the two melt streams intersect. The SunCell® can include a reservoir support plate actuator, such as at least one of a mechanical actuator, a pneumatic actuator, a hydraulic actuator, an electrical actuator, and a piezoelectric actuator, such as the present invention. Reservoir support plate actuator. The nozzle may lose alignment due to the differential expansion of the reservoir support post when the battery is heated. In order to avoid misalignment caused by thermal expansion, the column may comprise a material having a low coefficient of thermal expansion, such as a refractory material. The column may be insulated and cooled to prevent it from expanding. The SunCell® can include a column cooler such as a heat exchanger or a conductive or convection cooling component. Cooling can be achieved by conducting heat along the column to the heat sink. The SunCell® can include members that align the nozzles by selectively controlling the length of the columns that support the reservoir support plate by at least one of controlling and causing thermal differential expansion or contraction between different columns. 5b8. The SunCell® may include at least one or more column heaters and column coolers to selectively and differentially heat or cool the reservoir support column such that the length is selectively varied by expansion or contraction such that the injector alignment. In an embodiment, the SunCell® includes a reservoir position adjustment system or a reservoir regulator, such as a mechanical regulator, such as a push rod adjuster that can penetrate the housing 5b3a. The push-pull can be provided by a threaded mechanism acting on the rod at the wall of the housing 5b3a. The adjuster can provide movement along or around at least one axis. The adjuster can have the ability to push or pull at least one of the reservoirs vertically or horizontally or to rotate them about the x-axis, the y-axis, or the z-axis. Adjustments can be made to optimally intersect the molten metal flow of the dual molten metal injectors. In one embodiment where the reservoir and EM pump assembly can be securely coupled by means such as a wet seal, the reservoir can be rotated at the joint of the reservoir 5c having the lower hemisphere 5b41. The center axis of the reservoir 5c and the central axis of the EM pump assembly 5kk with the nozzles can be along the same axis. An exemplary connector that permits rotation of the BN reservoir is a sliding nut connector that includes a BN reservoir 5c, a graphite lower hemisphere 5b41, a graphite gasket, and a graphite nut. Both h-BN and graphite may contain a lubricant. The connections of the EM pump (such as the current 5k2 and the junction of the ignition 5k2a busbar) may include components such as joints or pivots to cause the reservoir to rotate sufficiently to cause alignment of the jetted molten metal stream. The bus bar can at least partially include stacked sheets or cables (such as braided cables) to permit alignment motion. In an embodiment, adjusting the EM pump current while controlled by the controller controls the vertical position of the flow, and the lateral position of the flow can be controlled by the reservoir regulator. In one embodiment in which the reservoir is securely fixed, the alignment can be implemented as a service operation in which the SunCell® is partially disassembled, the nozzles are aligned, and the SunCell® is reassembled. In embodiments including a dual molten metal injector, the track of the molten metal stream from one nozzle may be in a first plane, and the plane of the orbit of the molten metal stream from the second nozzle may be in two flutes surrounding the first plane A second plane in which at least one of the Cartesian axes rotates. The streams can approach each other along an inclined path. In an embodiment, the track of the molten metal flow of the first nozzle is in the yz plane, and the second nozzle is movable laterally from the yz plane and rotated toward the yz plane such that the streams are obliquely approaching. In an exemplary embodiment of the invention, the track of the molten metal flow of the first nozzle is in the yz plane, and the orbit of the molten metal flow of the second nozzle is in a plane defined by the rotation of the yz plane about the z-axis such that the second nozzle It can be moved laterally from the yz plane and rotated towards the yz plane such that the streams are obliquely close. In an embodiment, the trajectory intersections at the first flow height and the second flow height are each adjusted to cause intersection. In one embodiment, the outlet tube of the second EM pump is offset from the outlet tube of the first EM pump sleeve, and the nozzle of the second EM pump is directed toward the nozzle of the first EM pump such that the melt streams are obliquely close to each other and the flows intersect. This is achieved by adjusting the relative height of the flow. The flow height can be controlled by a controller such as one of the EM pump currents that control at least one EM pump. In an embodiment comprising two nozzles of two injectors initially aligned in the same yz plane, the relative tilting trajectory of the jet molten metal stream that intersects the jets is achieved by at least one corresponding reservoir 5c This is achieved by at least one of a slight rotation about the z-axis and an operation of slightly bending the nozzle translated from the yz plane by rotating towards the yz plane. The inductively coupled heater antenna 5f, such as a pie portion, can be bent non-planar to accommodate the corresponding EM pump sleeve 5k6. Rotate other components and connectors as needed. For example, the EM pump magnet 5k4 can also be rotated to maintain its vertical position relative to the EM pump sleeve 5k6. In another embodiment, the injection system can include a field source such as a source of at least one of a magnetic field and an electric field that deflects at least one stream of molten metal to achieve alignment of the jets. At least one of the injected molten metal streams may be deflected by Lorentz force due to movement of the corresponding conductor via the applied magnetic field and a force between at least one of a current such as a Hall and an ignition current and the applied magnetic field. . The deflection can be controlled by controlling at least one of magnetic field strength, molten metal flow rate, and ignition current. The magnetic field may be provided by at least one of a permanent magnet, an electromagnet (which may be cooled), and a superconducting magnet. The magnetic field strength can be controlled by controlling the current to control at least one of a distance between the magnet and the melt stream and a magnetic field strength. Measuring the ignition current or resistance determines the best intersection. Optimal alignment is achieved when the current is maximized at a set voltage or minimum resistance. A controller that can include at least one of a programmable logic controller and a computer can be optimized. In an embodiment, each of the reservoirs may include a heater such as an inductively coupled heater to maintain a reservoir metal such as silver in at least the activated molten state. The generator may further comprise a heater surrounding the black body radiator to prevent the molten metal, such as silver, from adhering at least during startup. In embodiments where the black body radiator 5b4 heater is not required, black body radiators such as 5b41 and 5b42 may comprise materials to which they are not adhered with molten metal such as silver. Non-adhesion can occur at temperatures reached by heat transfer from the heater of the reservoir 5c. The black body radiator may contain carbon and may be heated to a temperature at or above the molten metal such as silver that did not adhere before the EM pump was started. In an embodiment, the blackbody radiator is heated by the reservoir heater during startup. The black body radiator 5b4 wall may be sufficiently thick to allow heat transfer from the reservoir to the black body radiator, thereby allowing the black body radiator to achieve at least one of a temperature above the molten metal adhered to the black body radiator and greater than a melting point of the molten metal. temperature. In one embodiment, an inductively coupled heater (ICH) antenna that is proximate to the heated battery assembly (such as wound around the reservoir 5c) is well thermally insulated from the battery assembly, with RF radiation from the ICH penetrating the insulator. The thermal insulator reduces the heat flow from the battery assembly to the coolant of the ICH antenna to the desired flow rate. The system further includes a startup power/energy source such as a battery such as a lithium ion battery. Alternatively, an external power source such as a gate power source for startup may be provided via a connection from an external power source to the generator. The connector can include a power output bus. In an embodiment, the black body radiator may be heated by an external radiant heater such as at least one heat lamp during startup. The heat lamp can be external to the PV converter 26a and can provide radiation via removal of a panel in the PV converter. Alternatively, the blackbody radiator can be heated during startup and the heater can be removed after the battery is continuously operated and sufficient screen is created to maintain the reaction cell chamber 5b31 at a sufficient temperature to maintain the hydrino reaction. In the case where the inductively coupled heater is inefficient in heating a reservoir such as a ceramic reservoir (such as a BN or SiC reservoir), the reservoir may comprise a refractory covering capable of effectively absorbing radiation from the inductively coupled heater Or sleeve. An exemplary RF of the absorbing sleeve contains carbon. The generator may include, for example, a machine (such as a rack and pinion, a screw, a linear gear, and others known in the art) for applying and retracting at least one of a heater coil and a storage heater coil, pneumatically, hydraulically, and An actuator 5f1 of at least one of the electromagnetic systems. The electromagnetic actuator can include a speaker mechanism. Pneumatic and hydraulic can include pistons. The heater antenna can include a flexible section that allows for telescoping. An exemplary flexible antenna is a copper braided wire braided Teflon sleeve. In an embodiment, the outer pressure vessel 5b3a can include a concave chamber that houses the retracted antenna. The inductively coupled heater antenna 5f can include a movable section. The inductively coupled heater may include at least one coil 5f (Fig. 2I84 to Fig. 2I152) that is retractable by each of the reservoirs. The coil may comprise a shape or geometry that effectively applies the screen to the reservoir. The exemplary shape is for a bracket of a cylindrical reservoir or an adjustable clamshell. The carrier can apply RF power to the corresponding reservoir during heating and thereafter can contract. Each of the brackets may comprise a pie-shaped coil and is attached to a common pie-shaped coil oriented in a plane parallel to the plane formed by the EM pump sleeve of the EM pump 5kk under its base. Each of the tray pie coils can be attached to the common pie coil by a flexible or expandable antenna segment. A common pie coil can be attached to an inductively coupled heater capacitor box mountable on the actuator. Alternatively, each of the brackets can be attached to a corresponding capacitor box and an inductively coupled heater, or two separate capacitor boxes can be connected to a common inductively coupled heater. At least one of the tray pie coil, the common pie coil, the common capacitor box, and the split capacitor box can be mounted or attached to the actuator to achieve the act of storing the antenna after startup. In an embodiment, a heater such as an inductively coupled heater includes a single retractable coil 5f (Fig. 2I93 to Fig. 2I94, Fig. 2I134 to Fig. 2I135, and Fig. 2I148 to Fig. 2I152). The coil may be around the circumference of at least one of the reservoirs 5c. The heater may comprise a single multi-crimp coil around the two reservoirs 5c. The heater can contain a low frequency heater such as a 15 kHz heater. The frequency of the heater can be in at least one of about 1 kHz to 100 kHz, 1 kHz to 25 kHz, and 1 kHz to 20 kHz. A single coil can be telescopic along the vertical axis of the reservoir. The coil 5f can be moved along the vertical axis by an actuator driven by an actuator such as one of the present invention (such as pneumatic, hydraulic, electromagnetic, mechanical) or a servo motor. The coils can be moved by mechanical means known to those skilled in the art, such as screws, racks and gears, and pistons. Actuator components such as gear teeth or glide members that are mechanically moved above each other can be used, for example, hexagonal boron nitride, MoS2 Or graphite high temperature lubricant lubrication. Others are talc, calcium fluoride, barium fluoride, tungsten disulfide, soft metals (indium, lead, silver, tin), polytetrafluoroethylene, some solid oxides, rare earth fluorides and diamonds. The coil can be mounted to the actuator at one or more side or end positions or other suitable locations that permit the desired movement without overloading the actuator. The antenna can be connected to the screen feeder via a flexible antenna section to allow for movement. In an embodiment, the inductively coupled heater includes a splitting unit having a transmitter assembly separate from the remainder of the heater. The separate transmitter component can include a capacitor/RF transmitter. The capacitor/RF transmitter can be mounted on the actuator. The capacitor/RF transmitter can be connected to the remainder of the heater by flexible wires and cooling lines in the outer pressure vessel chamber 5b3a1. These lines can pass through the wall of the outer pressure vessel 5b3a. The capacitor/RF transmitter can be mounted on an actuator connected to the RF antenna, wherein the antenna is also mounted on the actuator. The capacitor can be mounted in a cooled enclosure. The box may contain a heat reflective coating. The enclosure can act as a mounting fixture. The box can contain mounting brackets for rails and other drive mechanisms. Inductively coupled heaters may include parallel resonant model heaters that use a long heater such as a 6 to 12 meter long heater. A heat exchanger such as a cooling plate can be mounted on the capacitor/RF transmitter with cooling provided by the antenna cooling line. The actuator may be driven by an electric servo motor or a gear motor controlled by a controller that is responsive to a temperature distribution input to obtain a desired generator assembly such as a reservoir 5c, an EM pump, a lower hemisphere 5b41, and an upper hemisphere 5b42. Temperature Distribution. In one embodiment, a heater such as an inductively coupled heater comprises a single retractable coil 5f (Fig. 2I93 to Fig. 2I94, Fig. 2I134 to Fig. 2I135, and Fig. 2I148 to Fig. 2I152) surrounding a battery assembly that is desired to be heated A circumference, such as at least one of a black body radiator 5b4, a reservoir 5c, and at least a portion of an EM pump assembly such as an EM pump sleeve 5k6. In an embodiment, the heater can be fixed during heating. The geometry and coil turns density can be configured to selectively apply the desired heating power to each battery component or region of each battery component to achieve a desired temperature range of components or zones, such as in the range of 970 °C to 1200 °C. Due to previous heating calibration and heater design, monitoring of the temperature of a limited number of points on the battery provides the temperature of the point monitored on the battery. In an embodiment, heater power and heating duration may be controlled to achieve a desired temperature range, where temperature monitoring may not be required. Controlling at least one of the molten metal pumping to the reaction cell chamber and the application of ignition power can control the heating of the black body radiator. A temperature sensor such as a thermocouple or optical temperature sensor that provides input to a temperature controller can monitor the black body radiator temperature. An exemplary optical temperature sensor that can be scanned is Ω iR2P. Alternatively, the timing sequence of EM pumping and ignition power and inductively coupled heating power can be used to achieve a desired battery temperature profile, such as where the temperature of the battery component in contact with the molten metal is above one of the melting points of the metal. Simultaneously heating the heater coil 5f of the desired battery assembly may allow elimination of at least one of the heat transfer block 5k7, the particle insulator, the particle insulator reservoir 5e1, and the control system to perform vertical movement of the heater and control heating when the heater is vertically moved. At least one of the power levels. The magnet of the inductively coupled heater 5k4 may include an RF shield and at least one of sufficiently cool water provided by a cooling system, such as a cooling system including an EM pump coolant line 5k11 and an EM pump cold plate 5k12, to prevent the magnet from overheating The point of magnetization loss caused by the heat applied by the level of the EM pump casing 5k6. The RF shield can comprise a multilayer RF reflective material such as a highly conductive material, such as Al, Cu or Ag, which can comprise a metal foil or screen. In an embodiment, the inductively coupled heater shield may comprise a magnetic material to attenuate magnetic flux incident on the EM pump magnet. Exemplary magnetic materials include Permalloy or high-resistance high-permeability alloys (Mu-Metal), such as nickel-based metals with high magnetic permeability, such as about 300,000 permeation at low saturation levels. The rate of metal. In embodiments where the applied magnetic field strength of the heater is high, the magnetic material may comprise a relatively high saturation material such as a magnetic metal such as carbon steel or nickel. In one embodiment, the magnetic material may have a negative for the permanent magnetic field lines of the permanent EM pump magnet due to the permanent magnetic field being absorbed by the shield metal and the permanent magnetic field being attenuated in the liquid metal in the EM pump casing. Minimize the design and penetration rate of the impact. In another embodiment, the shield comprises a Faraday cage 5k1a (Fig. 2I115) comprising a high conductivity metal, such as copper, surrounding the intended shielded component, such as the EM pump magnet 5k4. A Faraday cage member 5ka1 such as a panel may be secured with a fastener such as a highly conductive screw 5k1b (such as a copper screw). In an embodiment, the Faraday cage 5k1a does not affect the static magnetic field of the permanent magnet 5k4 so that the cage can completely enclose the magnet. The Faraday cage can be cooled. Cooling can be provided by EM pump cold plate 5k12 and EM pump coolant line 5k11. In an embodiment, the cold plate may comprise a design to cool a concentrating PV cell, such as a concentrating PV cell comprising a microchannel. In an embodiment, each magnet may comprise a separate Faraday cage (Fig. 2I116). The wall thickness of the Faraday cage may be greater than the penetration depth of the RF emission of the inductively coupled heater. In one embodiment, the inductive heating frequency has a penetration depth of less than 0.3 mm; therefore, the cage wall may be thicker than 0.3 mm for increasing the wall thickness and increasing the shielding of the shield. In an embodiment, the EM pump magnet 5k4 may include a yoke 5k5 or a trapezoidal magnet that directs magnetic flux through the EM pump sleeve 5k6, and may further comprise a magnetic circuit, wherein the magnet 5k4 and the magnet cooling system 5k1 may be located at a center such as The position of the portion of the EM pump casing 5k6 outside the collector 5c. The magnetic circuit may include a yoke that directs the magnetic flux across the current at the location of the EM pump rod body 5k2. In an embodiment, the magnet 5k4 may comprise a conical magnet that enriches the high magnetic field along the x-axis via the wall of the EM pump casing 5k6 with current flowing along the z-axis and the pump flowing along the y-axis. In an embodiment, an EM pump busbar such as at least one of 5k2 and 5k3 may comprise a highly conductive conductor, such as Mo, capable of operating at high temperatures. The magnetic circuit may comprise an EM pump magnet 5k4, a core comprising a highly permeable material, which may further comprise a gap in its section, a circuit for the EM pump sleeve 5k6 and an EM pump sleeve at the gap The tube 5k6 causes the magnetic flux to enrich the magnet between the yokes. The core may comprise an upward C-shaped permeable material such as ferrite iron, wherein the gap is in the opening of C. In another embodiment, the EM pump includes a stator having a plurality of windings and at least one cylindrical conduit containing molten metal to be pumped. In an exemplary embodiment, a stator having three pairs of helical windings produces a rotating torsional magnetic field. The axial thrust and the resulting rotational torque act on the molten metal in the cylindrical conduit. In an embodiment, the inductively coupled heater coil 5f may further include a concentrator to enhance the electromagnetic field in the desired region by increasing the corresponding current in the region of the battery assembly or battery assembly. Exemplary concentrators can include high frequency ferrite iron and low frequency gasket steel. A concentrator can be used to achieve the desired temperature distribution of the battery. In embodiments that include a battery assembly that is desired to be heated but does not include materials that are easily coupled to the RF power of the inductively coupled heater, the assembly may be coated with an RF absorbing material such as carbon. The cladding may contain split or expanded gaps to accommodate expansion of different thermal coefficients. The exemplary embodiment includes a cylindrical BN reservoir 5c that is coated with a cylindrical graphite sleeve that is separated to accommodate differential thermal expansion. In an embodiment, the water-coolable inductively coupled heater antenna coil 5f may comprise a portion of a coil or coil that is circumferential for at least one of the two reservoirs and a circumference of at least a portion of the blackbody radiator 5b4. The coil may further comprise at least one pie coil. The plane of the pie coil can be parallel to the plane of the EM pump casing outside the reservoir. The pie coil can be placed along at least one side of the outer portion of the EM pump sleeve. The pie coil can heat the two EM pump sleeves. Alternatively, the antenna 5f may comprise a plurality of pie coils, wherein the pie coils may individually or collectively heat the respective EM pump sleeves. The pie coil can be stretched along the vertical axis of the generator. The pie coil can be telescoped with the reservoir coil and can be part of the reservoir coil. The antenna can include a plurality of separate components. The antenna may comprise two antennas each comprising a pair of pie coils. The two pie coils may each comprise an upper coil that heats a portion of the blackbody radiator and at least one of the reservoirs. The upper pie coil can be fitted around the heated surface. The exemplary shapes are respectively a C-shape surrounding the bottom of the spherical or elliptical black body radiator and a U-shape surrounding the cylindrical reservoir. The coil can be telescoped along a plurality of axes, such as the horizontal axis and then the vertical axis, for storage after startup. The actuator can move each antenna 5f along such an axis to achieve storage. The connecting portion of the antenna may comprise a flexible water conduit line, such as a flexible metal sleeve, such as a telescoping sleeve. The sleeve can comprise copper. In an embodiment, the pie or other coil 5f can comprise at least one flexible section. The flexible section may allow the coil to contract around a battery assembly such as an EM pump magnet 5k4, a yoke 5k5 or a protrusion on a Faraday cage that houses at least one magnet that optionally includes a magnetic flux concentrating yoke. Alternatively, the EM pump may comprise at least one of a movable yoke (such as a yoke slidable outside the Faraday cage) and a movable magnet 5k4 on the track to facilitate the pie coil Telescopic. In an embodiment, a section of the heating assembly of the EM pump sleeve 5k6 at the region of the EM pump ignition busbar 5k2a may be selectively heated by the inductively coupled heater antenna 5f by including a portion of its coil proximate the component At least one of the antennas and by a component comprising a material that is preferably coupled to the RF field, such as stainless steel or a magnetic steel above the molybdenum. Similar materials can be attached with the transition of the magnetic metal. Exemplary attachments are welds and bolt and nut fasteners. The EM pump ignition busbar 5k2a may comprise stainless steel welded to a stainless steel pump casing 5k6 and a magnetic steel welded or fastened to the stainless steel portion of the EM pump ignition busbar 5k2a. In an embodiment, the ignition bus bar 5k2a can be attached to the bottom plate 5b8. The antenna coil 5f can include at least one coiled loop, wherein the coil loop can be reversibly extended and telescopic such that the coil can be folded in close proximity to the battery to achieve good RF power coupling and then expanded to allow for telescoping and storage of the antenna. Antenna storage can be accomplished with the actuator of the present invention. Each loop of the coil can include a telescoping or telescoping section. In an embodiment, at least one loop of the antenna coil 5f is reversibly expandable and expandable. The loop can include a retractable or telescoping section. Water cooling can be obtained by sealing the sleeve within the reversible expansion of the coil loop and the interior of the telescoping section. The sleeve can include a Teflon or other high temperature water jacket that can be inserted into the interior of the lead coil loop to bridge at least the reversibly expandable and telescoping sections. The sleeve may be coated with a conductor, such as a flexible conductor, such as a braided metal, such as a braided copper wire. An exemplary flexible antenna segment is a wire braided Teflon sleeve or an elastomeric sleeve, such as a surgical cannula. The wire braid can include a copper braid. Alternatively, the extendable section may comprise a metallized plastic such as a polyester film. The antenna coil 5f may further include an actuator that expands or expands at least one loop. In an embodiment, the retractable loop is to achieve immediate proximity to a heated battery assembly, such as a reservoir. Proximity can achieve a large RF coupling to the battery assembly. The same or at least one additional actuator expands the loop to allow the same or another actuator to move the coil to store it. Can be moved vertically. It can be stored in the lower chamber 5b5. The coil can be expanded and expanded by the water and vacuum pressure applied to the antenna coil, wherein the inductively coupled heater power supply and the capacitor's cooling circuit can be bypassed by the solenoid valve. The actuator linearly moves the expandable coil downwardly moving the spring loaded coil over the spreader. In the embodiment illustrated in Figures 2I148 through 2I152, the circumferential coils surrounding at least one of the two reservoirs 5c and at least a portion of the blackbody radiator 5b4 of the dual molten metal injection system are reversibly expandable and expandable. The coil can be vertically separated at two locations of each loop of the coil extending axially (perpendicular to the cell). A flexible electrical connector such as a wire (such as a stranded enameled wire) can bridge separate circuit sections. The wires can be highly conductive, such as copper wires. The wire can be refractory, such as W or Mo. The bridges, such as wires, can be cooled externally by means such as conduction, convection, and radiation. The bridging member can be cooled via a gas, such as a gas having a high heat transfer capability, such as helium. The bridge gas cooling system can include a forced convection or conduction system. The bridge cooling system can include an external heat exchanger, such as an external coolant heat exchanger. When in the folded position, a bridge such as a wire can be crimped. The bridging coil can include a spring wire that extends in a reverse direction and telescopes. In an exemplary embodiment, the antenna may include a refractory metal spring to electrically bridge the retractable coil segments of the inductively coupled heater antenna. The jumper may be cooled by helium or cooled by other external systems, such as a separate crimping system that is in thermal contact with the antenna wire jumper, such as a heat exchanger. Alternatively, the jumper wires may not be actively cooled. In an embodiment in which the elliptical helical coil is separated, the connector between the opposing split coil loop sections includes a contact connector (Fig. 2I151 to Fig. 2I152). The contact point can include a coil loop end plate. The contact points on the ends of the opposing coil loop sections may include an anode connector 5f4 and a cathode connector 5f5 or other electrical contact connectors known to those skilled in the art. The contact point can be engaged and disengaged by the actuator 5f1 as it moves the split coil section horizontally into and out of the contact point. Each of the anode plug connectors 5f4 may include a circular or pointed end such that it is more easily aligned with the cathode connector 5f5 when the two antenna halves slide together. An elliptical spiral can be formed by connecting two half antenna segments. When in a closed (inserted together) configuration, the antenna can operate as an elliptical helix with attached vertical planar pie coils. In another embodiment, the antenna includes a separate elliptical coil, wherein each of the two segments includes an attachment member that optionally includes a pair of pie coils for the mating electrical connectors. When the antenna is configured to be closed (plugged together), the antenna can operate as an elliptical helix with a vertical planar pie coil containing two connected or unconnected segments. Where the closed antenna comprises two unconnected members of two pie-shaped coils, each member may comprise a separate system of water-cooled connectors. In an embodiment, at least one EM pump magnet 5k4 of the Faraday cage 5k1a may be further included by the reverse movement of the actuator to accommodate engagement and disengagement of the split antenna. The expansion and contraction of the magnet may allow the pie coil to pass during its movement by the actuator. After the pie coil has moved to its operational position, the magnet can be moved to an operational position, such as in close proximity to the EM pump sleeve 5k6. The coil circuit of each half of the split coil may comprise a water conduit 5f2 extending between the ends of the vertically adjacent coil loops. The catheter can be screwed in the opposite direction to screw to the surface or edge of the coil. The loop of the antenna can be separated by the antenna spacer and supported by the support 5f3. In an embodiment, the water conduit 5f2 and the coil circuit section provide a continuous flow path for a coolant such as water. The coolant conduit can be electrically insulated or comprise an electrical insulator such as a high temperature polymer, ceramic or glass. The coolant conduit can include a conductor that is electrically insulated at the coil loop. The coolant conduit can be thermally shielded. An exemplary Teflon or Delrin acetal water conduit connects the ends of the adjacent loop sections of each of the half coils to each of the water cooled half coils. The catheter can be manufactured by extrusion, injection molding, stamping, milling, machining, and 3D laser printing. The conduit can be connected to a coolant jacket that can be soldered to the antenna coil loop. A water conduit such as a Teflon conduit can also serve as a structural support. In an embodiment, the water cooling tube passages may be bidirectional within each circuit section. In an embodiment, the antenna may comprise a separate coolant conduit such as a Teflon water conduit 5f2 and a structural support or spacer 5f3. The structural support can comprise a refractory insulator spacer such as boron nitride or tantalum nitride which can be further resistant to thermal shock. In one embodiment, each of the half coils is connected to a capacitor box of the antenna RF power supply 90a. The electrical connector can be cooled and act as a coolant line. Each of the half coils may further comprise another coolant line or a connector coolant line to act as a conduit to form a closed coolant loop via a corresponding half antenna and a heat exchanger such as a chiller. Each of the connector coolant lines may be used only for cooling, where each may include or be electrically isolated from the antenna. In one embodiment, the SunCell® includes a plurality of antennas, such as two coils, encasing and heating the reservoir 5c and at least one pie coil, the at least one pie coil heating the EM pump sleeve 5k6. Each coil may include at least one of its own capacitor box and screen feeder. The power supply can include a power splitter. The antenna may comprise two upper C-shaped coils and at least one pie-shaped coil, the at least one pie-shaped coil may comprise separate power sources, each comprising a temperature sensor, and a separate controller, such as an infrared sensor, such as an optical pyrometer And power controller. When not in operation, the coil can be telescoped by at least one actuator. In an embodiment, at least one coil, such as a pie coil or coil, can vent coolant and remain in an operational position (not telescoping) when not in use. The coil may include a pump, a coolant reservoir or a supply and a controller to add and discharge the coolant in a reverse direction in the operating and storage modes, respectively. In one embodiment, the SunCell® comprises a plurality of antennas, such as two coils, encasing and heating the reservoir 5c and at least one pie coil, the at least one pie coil heating the EM pump sleeve 5k6, wherein each antenna The cutoff frequency is independently modulated to prevent coupling between the antennas. At least one of the antennas is expandable and contractible. The SunCell® can include at least one actuator for telescoping. Alternatively, at least one antenna may be fixed. The fixed antenna can act as a secondary role as a heat exchanger to remove overheating during the SunCell® filter generation operation. The heat exchanger antenna may comprise a conductor having a high melting point, such as a refractory metal such as molybdenum or the other of the present invention. The antenna may comprise water or another coolant such as molten metal, molten salt or the other of the invention or known in the art. The fixed antenna coolant can be drained after SunCell® is turned on. Alternatively, the coolant can be used to remove heat from the SunCell® when operating to create a screen. The fixed antenna can be used to heat at least one SunCell® component during startup and to cool at least one component during filter generation. The SunCell® component can be a battery component such as at least one of an EM pump 5ka, a reservoir 5c, and a reaction cell chamber 5b31, and such as an MHD nozzle section 307, an MHD generator section 308, an MHD condensation section 309. At least one of the group of components of the MHD converter of at least one of the return conduit 310, the return reservoir 311, the return EM pump 312, and the return EM pump sleeve 313. In an embodiment, the antenna 5f can include an RF coupling material that can transfer heating power to the reservoir. The RF coupling material can comprise carbon. The carbon may comprise blocks that are adapted into the antenna to be filled and form the antenna and the reservoir. The RF coupling material can be deformed to allow the antenna to be stored after battery startup. The carbon block can be deformed. The carbon block can be collapsible. The collapsible carbon block can be spring loaded to provide good RF coupling and thermal contact to the reservoir. The carbon block is telescopic so that the antenna can be stored. The graphite block can be extended and contracted by an actuator system, such as a pneumatic, hydraulic, electronic, mechanical system, or other actuator of the present invention. The hydraulic system can apply pressure from the antenna coolant provided by the coolant pump, where the inductively coupled heater cooling circuit can be bypassed using a solenoid valve. The pneumatic system can apply the vacuum or pressure provided by the vacuum pump. Mechanical actuators can include rack and pinion or ball screw actuators or others of the present invention. Each magnet can be housed in a separate Faraday cage (Fig. 2I116). In another embodiment, the pie coil can be shaped to have sections below each EM magnet to allow it to expand and contract. The retractable cake coil on one side of the plane defined by the EM pump sleeve may comprise at least one of an inverted double back or loopback C-shaped coil and a double back W-shaped coil, wherein the coils are at their positions Each magnet passes underneath. The coil 5f such as a pie coil may be a circumference such as a heating portion of the EM pump sleeve to increase heating efficiency. When reducing the application of RF power to the magnet, coils of the double-back W-shaped coils such as those shown in Figures 2I151 through 2I152 can selectively heat at least a portion of each of the EM pump sleeves, such as the inlet side and the outlet side. To achieve good RF power transfer from the double-back W-coil to the EM pump casing, the EM pump casing can be sufficiently spaced apart in the middle between the reservoirs to allow the legs of the antenna to be inverted V-shaped at the antenna. The corresponding pump sleeve in the section extends outside. At least one of the EM pump bushing and the antenna can be fabricated by a system and method that uses a coil bushing to achieve a tight fit within the pump casing of the antenna coil. In another embodiment, the windings of the dual coils cross the antenna coil in an outer-inner-outer-inside-outer-outer-inner-inner manner in such a path. The coil 5f, such as at least one of a circumference and a pie coil, may be electrically insulating. The conduit of the antenna may include a wide flat tube to cover more surface area to better couple heating power to the battery assembly. Components that do not effectively absorb RF power, such as boron nitride reservoirs, may be covered with an RF absorber cover that may contain materials such as carbon that have better RF coupling or absorption. When indirect RF heating for a reservoir such as a BN reservoir can be attached when a segment such as two circumferential clamshells can be held in place by a fastener such as a W clamp, strip or wire carbon. In an embodiment, the clamshell is designed to prevent electrical contact between the electrodeized components of the battery to avoid electrical shorting. In order to avoid the formation of iron carbide reactivity, the carbon shell should not be in contact with the component containing iron; in the case where the shell contacts iron or a component such as a nut containing iron, the shell may contain materials other than carbon. Other such chemical incompatibility should also be avoided. In an embodiment, the RF absorber cover may comprise a material such as a carbon fabric, honeycomb or foam for absorbing RF power from an inductively coupled heater and acting as a thermal insulator. The antenna electrical insulation may comprise at least one of Fibrex, Kapton tape, epoxy, ceramic, quartz, glass, and cement. At least one coil can be shrunk and stored after activation. The reservoir may be in a second chamber within the chamber that houses the blackbody radiator. Other special geometry coils such as hairpins or pie coils, such as coils along portions of the ends, sides or bottom of the EM pump tube outside the reservoir, are within the scope of the present invention. Any of the coils can include a concentrator. In another embodiment, the generator includes a plurality of coil actuators, wherein the antenna for heating the pool can include a plurality of coils that can be contracted along a plurality of axes. In an exemplary embodiment, the coils may contract horizontally and then contract vertically. In an embodiment, the generator can include at least one EM pump tube heater coil and at least one coil actuator and at least one EM pump magnet actuator. One or more heater coils may heat the EM pump tube section external to the reservoir with the EM pump magnet contracted, one or more coils may be contracted by one or more coil actuators, and one or more The EM pump magnet actuator can move the EM pump magnet to position to support pumping before the EM pump tube cools below the melting point of the internal molten metal, such as silver. Coordinates coil contraction and magnet positioning motion. This coordination can be achieved by mechanical connection or by a controller such as a controller including a computer and a sensor. In an embodiment, the EM pump tube 5k6 is selectively heated while maintaining the EM pump magnet 5k4 cooling by at least one of: (i) using an RF shield and a magnetic shield or a Faraday cage. At least one of which reduces the RF power of the incident EM pump magnet, (ii) uses a concentrator to selectively enhance the electromagnetic field at the EM pump tube and thus increases the RF current and heats the EM pump tube, where the concentrator The magnetic field can be along to avoid interference with the direction of the EM pump, such as in the direction of the EM pump current or in the direction of the EM pump tube, (iii) using the RF coil 5f that selectively heats the EM pump tube 5k6, (iv) using heat a transfer member, such as a heat transfer block 5k7, an EM pump tube or a heat pipe having a larger cross section to transfer heat from the heated upper battery assembly to the less heated EM pump tube, and (v) increase by such as The cooler cooled by the electromagnetic pump heat exchanger 5k1. The reservoir floor may contain a material such as ceramic that prevents absorption of RF from the inductively coupled heater such that more power can be selectively absorbed by the EM pump tube by heating applied in the corresponding zone. The heater coil and capacitor box can be mounted to an actuator that can be moved to a heated position during startup and retracted into the reservoir chamber when not in use. The reservoir chamber may comprise a section in the outer pressure vessel chamber 5b3a1 that may also contain a power conditioner. The coil can be further used for water cooling to cool the reservoir of the power conditioner. The means for moving the heater may comprise one of the present invention, such as a motor-driven ball screw or rack and pinion mechanism mountable in a heater reservoir chamber. The heater reservoir chamber can include a power conditioning device chamber. In an embodiment, the actuator may include a drive mechanism, such as a servo motor, mounted in a recessed chamber, such as one of the bases of the outer pressure vessel 5b3b. A servo motor or gear motor can drive a mechanical moving device such as a screw, piston or rack and pinion. At least one of the coil 5f and the capacitor for the inductively coupled heater can be moved by the mobile device, wherein the movement can be achieved by moving the guide mount to which the moving assembly is attached. In an embodiment, the actuator can be at least partially positioned outside of the outer pressure vessel 5b3a. The actuator can be at least partially positioned outside of the base of the outer pressure vessel 5b3b. The lifting mechanism can include at least one of a pneumatic, hydraulic, electromagnetic, mechanical or servo motor driven mechanism. The coils can be moved by mechanical means known to those skilled in the art, such as screws, racks and pinions, and pistons. The actuator may comprise at least one lift piston having a piston penetrating member sealable in the bellows, wherein the mechanism for vertically moving the piston may be external to the pressure vessel 5b3a, such as the base of the outer pressure vessel 5b3b. An exemplary actuator of this type includes an actuator such as the MBE/MOCVD system of the Veeco system, which system includes an exemplary shutter blade bellows. In an embodiment, the actuator may comprise a magnetic coupling mechanism, wherein the external magnetic field may cause mechanical movement inside the outer pressure vessel 5b3a. The magnetic coupling mechanism can include an external motor, an external permanent magnet or electromagnet, an internal permanent magnet or electromagnet, and a mechanical moving device. An external motor can cause rotation of the external magnet. A rotating outer magnet can be coupled to the inner magnet to cause the inner magnet to rotate. The inner magnet can be coupled to a mechanical moving device such as a rack and pinion or a screw, wherein rotation causes the device to move at least one of the coil 5f and the capacitor. The actuator can include an electronic external source of rotating magnetic field and an internal magnetic coupler. In an embodiment, the external rotating magnetic field coupled to the internal magnet can be obtained electronically. The rotating external field can be generated by the stator and coupled to an internal rotor such as one of the electric motors. The stator can be of the electronic rectification type. In another embodiment, actuator components that are mechanically moved above each other, such as gear teeth or glide components, may be by, for example, MoS2 Or graphite high temperature lubricant lubrication. In an embodiment such as that shown in Figures 2I95 through 2I149, a motor 93, such as a servo motor or gear motor, can drive a mechanical moving device, such as a ball screw 94 with a bearing 94a, a piston, a rack and pinion, or a suspension. a tight cable on the pulley. At least one of the antenna and the inductively coupled heater actuator housing can be attached to a cable that is moved by a drive pulley that is rotated by an electric motor. A drive connection between the motor 93 and a mechanical moving device such as the ball screw mechanism 94 can include a gearbox 92. A motor such as a gear motor and a mechanical moving device such as a rack and pinion or ball and screw 94 and a guide rail 92a may be internal or external to the outer pressure vessel 5b3a, such as outside the bottom plate of the outer pressure vessel 5b3b, and may further comprise a linear Bearing 95 and a bearing shaft that can have at least one of high temperature and high pressure. The linear bearing 95 can comprise a slip material such as Glyon. The bearing shaft may penetrate the outer pressure vessel chamber 5b3a1, such as through the bottom plate of the outer pressure vessel 5b3b, and be attached to at least one of the heater coil 5f and the heater coil capacitor box to be in the upward or downward direction of the shaft It causes vertical movement when it is driven vertically by a mechanical moving device. The linear bearing can be mounted in a recessed chamber, such as one of the bases of the outer pressure vessel 5b3b. The bearing shaft can penetrate the bottom plate of the outer pressure vessel 5b3b through a hole. At least one of the coil 5f and the capacitor 90a for the inductively coupled heater can be moved by the mobile device, wherein the movement can be achieved by moving the guide mount to which the moving assembly is attached. In an embodiment, the battery components (such as the lower hemisphere 5b41, the upper hemisphere 5b42), the reservoir 5c, and the connector may be capable of being pressurized to a silver corresponding to 10 atm at an operating temperature of a blackbody radiator such as 3000 K. The pressure of the vapor pressure. The black body radiator can be covered with a mesh bottle of carbon fiber to maintain high pressure. The outer pressure vessel chamber 5b3a1 may not be pressurized to balance the pressure in the reaction cell chamber 5b31. The external pressure vessel can have an atmospheric pressure or a subatmospheric pressure. The outer pressure vessel chamber 5b3a1 can be maintained under vacuum to avoid heat transfer to the chamber walls. The actuator may comprise a sealed bearing at the bottom plate 5b3b of the outer container 5b3a for a penetrating member of a steering or drive shaft driven by an external motor, such as by servo or stepping of a controller such as a computer Motor controller. The drive system can include at least one of a stepper motor for increasing torque, an encoder and a controller, a positive belt, a tension pulley, a drive pulley, or a gearbox. The drive shaft can rotate gears such as worm gears, helical gears, rack and pinion gears, ball screws and nuts, swashplates or other mechanical components to move the heater coil 5f. The bearing for driving the shaft penetration member can be sealed with respect to at least one of vacuum, atmospheric pressure, and high pressure. The bearings can be operated at high temperatures. In an embodiment, the bearing can be offset from the bottom plate 5b3b by a collar or tube and flange fitting to position the bearing in a lower operating temperature environment. It has been well established that the vapor pressure of any gas that is in equilibrium with its liquid phase is the vapor pressure of the coldest liquid that it contacts and balances. In one embodiment, the temperature of the molten metal liquid in the reservoir 5c at ambient contact with the reaction cell chamber 5b31 is much lower than the temperature of the reaction cell chamber 5b31, such that the reaction cell chamber 5b31 The metal vapor pressure is much lower than the silver vapor pressure at the temperature of the black body radiator. In an exemplary embodiment, the temperature of the silver liquid in contact with the reaction cell chamber 5b31 at its surface is in the range of about 2200 ° C to 2800 ° C, so that the silver vapor pressure in the reaction cell chamber 5b31 is slightly higher. Pressure above which this will result in an atmosphere of condensation to the liquid at the gas-liquid interface. In an embodiment, the battery includes means for establishing a high temperature gradient between the reaction cell chamber 5b31 and the interior of the reservoir 5c. The high temperature gradient ensures that the molten metal liquid-vapor interface is at a temperature sufficiently below the melting point of the reservoir 5c. The temperature also provides the desired vapor pressure of the metal. The temperature gradient member may include at least one of a heat shield, a baffle, an insulator, and a narrower diameter of the reservoir and narrowing an opening between the reaction cell chamber 5b31 and the reservoir 5c. Another option is to narrow the wall thickness of the reservoir, increase the reservoir wall area, and maintain the reservoir by heat exchangers and heat exchangers such as water-cooled radiators that increase heat transfer from the reservoir. At least one of cooling. In one embodiment, to increase the thermal gradient from the liquid metal interface of the reaction cell chamber 5b31 to the reservoir 5c, wherein the electricity in the reaction cell chamber 5b31 is primarily transmitted by radiation and the molten metal such as silver has For very low emissivity of molten metal and its vapor, substantially all of the electricity from the reaction cell chamber 5b31 is reflected at the liquid silver interface. In an embodiment, the reservoir is designed to return to the reflection in the reaction cell chamber 5b31 using electrical power. The reservoir can include at least one of a reflector and a baffle to create a temperature gradient at the reservoir 5c by at least one of a mechanism that increases reflection, reduces conduction, and reduces convection. In another embodiment, a molten metal such as silver comprises an additive comprising a lower density material that floats on top of the liquid metal and changes the emissivity at the interface to increase electrical reflection. The additive may also function to increase the condensation rate of the metal vapor and reduce the vaporization rate of the metal vapor. In an embodiment, the power may be supplied to the external pressure vessel chamber 5b3a1 through the feedthrough to the system power supply, the power system of the system being at least one system (such as an inductively coupled heater, at least one electromagnetic Power is supplied to at least one of a pump, an ignition system, and at least one vacuum pump. In one embodiment, power to operate at least one of the helium systems is provided by the output of PV converter 26a. The system power supply can include at least one power conditioner that receives power output from the PV converter 26a within the external pressure vessel chamber 5b3a1 and powers at least one auxiliary system. The helium system power supply may include an inverter sufficient to provide power to parasitic generator loads, such as inductively coupled heaters, at least one of the electromagnetic pumps, and the ignition system. The ignition system can be powered by AC power directly from the inverter or indirectly after power conditioning. The ignition system can be powered by DC power that can be supplied by the PV converter 26a. The PV converter can charge a capacitor bank capable of outputting a desired voltage and current, such as a voltage in the range of about 1 V to 100 V and a current in the range of about 10 A to 100,000 A. The main power of the PV can be output as DC power via the feedthrough. The corresponding external feedthrough of the parasitic load can be replaced by an internal power supply that includes internal regulated power from the PV converter. In an embodiment, the external pressure vessel chamber 5b3a1 may include a power conditioning device chamber that houses at least one power conditioner. The power conditioning device chamber can be at least one of thermally shielded, thermally insulated, and cooled. The outer pressure vessel 5b3a can comprise a housing that can be operated at about atmospheric pressure, such as atmospheric pressure within plus or minus 100%. The outer pressure vessel 5b3a can be any desired shape such as a rectangle. The generator can include a heater system. The heater system can include a moveable heater, actuator, such as thermoelectric to receive sensor inputs such as the temperature of battery components such as the upper hemisphere, the lower hemisphere, the reservoir, and the EM pump assembly. Even temperature sensors and controllers. The thermocouple can be included in one of a thermowell that provides access to at least one of a temperature inside the battery, such as a temperature inside the EM pump tube and a temperature inside the reservoir. The thermocouple can penetrate through the wall of the EM pump tube into at least one of the EM pump tube and the reservoir. The thermocouple measures the temperature of the EM pump tube and the connector of the reservoir, such as the joint casing temperature, which can be measured inside the EM pump tube. The joint sleeve temperature can be measured by an external thermocouple having good thermal contact with the surface of the joint sleeve by a member such as a joint member or a heat conductor such as a hot paste. The thermocouple can be mounted in a heat pipe, such as one of the EM pump assemblies 5kk. The controller can perform at least one of: driving the actuator to move the heater coil and controlling heater power to control the temperature of the battery assembly within a desired range. The ranges may each be above the melting point of the molten metal and below the melting point or point of failure of the battery component. The thermocouple can be capable of high temperature operation, such as one of lead selenide, tellurium, and other compositions known in the art. Thermocouples can be electrically isolated or biased to prevent interference with external power sources such as inductively coupled heaters. Electrical isolation can be achieved by an outer sheath that is electrically insulating, such as a ceramic sheath, that can withstand high temperatures. The thermocouple can be replaced by an infrared temperature sensor. The optical sensor can include a fiber optic temperature sensor. At least one fiber optic cable can transmit light emitted by the black body radiator 5b4 to the optical thermal sensor to measure the temperature of the black body radiator 5b4. An exemplary optical temperature sensor that can be scanned is Ω iR2P. The optical sensor can be spatially scanned to measure the temperature of a plurality of locations on the generator. Spatial scanning can be accomplished by actuators such as the present invention or electromagnetic or other actuators known to those skilled in the art. A thermocouple that measures at least one of a lower hemisphere temperature and an upper hemisphere temperature may be telescopic. The reaction can take place when the measured temperature reaches the upper limit of its operation. The retractor can include mechanical, pneumatic, hydraulic, piezoelectric, electromagnetic, servo motor driven or other such retractors known to those skilled in the art. The shrinkage can be within or further from the cooled PV converter. A temperature above the operating temperature of the thermocouple of at least one of the lower hemisphere and the upper hemisphere may be measured by a response of at least one of an optical sensor or spectrometer such as a pyrometer and by a PV converter. The coil can be lowered after the pool is started. The bottom plate 5b3b can have a recessed outer casing for the coil 5f and at least one of the corresponding capacitor banks mounted on the actuator. The coil may comprise a water cooled radio frequency (RF) antenna. The coil can further serve as a heat exchanger to provide cooling water cooling. The coil can be used to water-cool the electromagnetic pump when the operating temperature of the electromagnetic pump is due to the low energy hydrogen reaction heating in the reaction cell chamber 5b31, wherein heat is conducted along the reservoir 5c to the EM pump. A battery assembly, such as an EM pump and a reservoir, can be insulated to maintain the desired temperature of the assembly by reducing or terminating the heating power, wherein the antenna can also provide cooling to the non-insulated assembly. An exemplary desired temperature is above the melting point of the molten metal sprayed by the EM pump. In an embodiment, if necessary, such as during startup, the inductively coupled heater may extend to the EM pump region to heat the EM pump tube to maintain molten metal. The magnet may include electromagnetic radiation shielding to reflect a major portion of the heating power from the inductively coupled heater. The shield may comprise a highly conductive covering such as one comprising aluminum or copper. The EM pump magnet can be shielded by an RF reflector to allow the coil 5f to be on the horizontal plane of the magnet. Avoiding heating the EM pump magnet can be achieved, at least in part, by using a notched coil design where the gap is at the magnet location. Inductively coupled heater power can increase as EM pump power decreases, and vice versa, to maintain a stable temperature to avoid rapid changes in EM pump and reservoir connector thread failure. The EM magnet 5k4 may contain a conduit for internal cooling. The internal cooling system can contain two concentric water lines. The water line may include an inner tube and an outer return water line that deliver water to the EM pump tube end of the magnet. The water line may include a bend or elbow to permit the vertical outlet of the outer pressure vessel 5b3a to pass through the base 5b3b. The two concentric internal water lines of each magnet can be on the central longitudinal axis of the magnet. The water line can be pressed into the passage in the magnet. The internal cooling system can further include a heat transfer paste to increase thermal contact between the cooling line and the magnet. The internal water-cooled line can reduce the size of the magnet cooling system to allow the heater coil 5f to move vertically in the region of the EM pump. The magnet may include a non-linear geometry to provide an axial magnetic field across the pump tube while further providing a tight design. The design allows the coil 5f to pass over the magnet. The magnet may comprise an L shape with an L orientation such that the cooling line can be guided in a desired direction to provide a tight design. The water line can be directed downward towards the base of the outer pressure vessel 5b3b or horizontally towards the center between the two reservoirs. Consider a clockwise circular path following the condition of the axes of the four EM pump magnets of the two reservoirs. The poles can be oriented as S-N-S-N//S-N-S-N, where // indicates that the current orientation of the two sets of EM pump magnets and one EM pump relative to the other EM pump can be reversed. Other compact magnet cooling designs are within the scope of the coolant jackets and coils of such assembled magnets of the present invention. The EM pump may include an RF shield at the EM pump magnet 5k4 to prevent the magnet from being heated by the inductively coupled heater coil 5f. When the RF coil 5f contacts the shield in a cooling mode in which the RF coupling of the inductively coupled heater is turned off, the shield can later function as a heat transfer plate. In another embodiment, a coolant line can penetrate the side of the magnet in the coolant circuit through each magnet. Other coolant geometries may be used that facilitate the removal of heat from the magnet while permitting the heater coils to pass through the other coolant geometries as they move vertically. In one embodiment, the heater indirectly heats the pump tube 5k6 by heating the reservoir 5c and the molten metal contained in the reservoir. The heat is transferred to the pump tube, such as a section having a applied magnetic field that passes through at least one of a molten metal such as silver, a reservoir wall, and a heat transfer block 5k7. The EM pump may further comprise a temperature sensor such as a thermocouple or a thermistor. Temperature readings can be input to a control system such as a programmable logic controller and a heater power controller that reads the pump tube temperature and controls the heater to maintain the temperature at a level such as above metal in the case of molten silver The melting point (such as within 100 ° C of the melting point of the molten metal) and the desired range below the melting point of the pump tube (such as in the range of 1000 ° C to 1050 ° C). A battery assembly such as at least one of the lower hemisphere 5b41, the upper hemisphere 5b42, the reservoir 5c, the heat transfer block 5k7, and the EM pump tube 5k6 may be insulated. The insulator can be removable after startup. The insulation can be reusable. The insulating member may comprise at least one of particles, beads, granules, and sheets, such as one comprising at least one of MgO, CaO, cerium oxide, aluminum oxide, ceric acid such as mica, and aluminum silicate such as zeolite. By. The insulating member may comprise grit. The insulation can be dried to remove water. The insulating member can be held in the container 5e1 (Fig. 2I102 and Fig. 2I103) which can be transparent to the radiation from the inductively coupled heater. The container can be configured to permit the heater coil 5f to move along a vertical axis. In an exemplary embodiment, the insulating member containing the grit is contained in the glass fiber or ceramic container 5e1, wherein the heater coil is vertically movable along the container inside the coil 5f. The particulate insulating container 5e1 may include an inlet 5e2 and an outlet 5e3. The insulating member can be discharged or added back to change the insulating member. The insulating member can be discharged from the container by gravity. Removal may cause the insulation to be removed in order from the top of the reservoir to the bottom of the EM pump tube. The insulators can be removed in the most recent to farthest order from the power that produces a low energy hydrogen reaction. The removed insulation can be stored in an insulator reservoir. The insulation can be recovered by returning it to the container. The insulator can be returned by at least one of a mechanical member and a pneumatic member. The insulating member can be mechanically moved by an auger or a conveyor belt. The insulating member can be pneumatically moved by a fan or a suction pump. The insulator can be moved by other components known to those skilled in the art. In an embodiment, the particulate insulation such as grit may be replaced by a heat transfer medium such as copper pellets that may be added from the storage vessel after the generator is started to move from at least one of the reservoir and the EM pump In addition to heat. The heat transfer can reach the water-cooled antenna of the inductively coupled heater. The reaction itself can be maintained under reaction conditions such as at least one of elevated battery temperature and plasma temperature. The reaction conditions can support pyrolysis at a sufficient rate to maintain temperature and low energy hydrogen reaction rates. In an embodiment wherein the low energy hydrogen reaction becomes self-sustaining, at least one of the startup power sources, such as at least one of heater power, ignition power, and molten metal pumping power, may be terminated. In one embodiment, the electromagnetic pump can be terminated when the battery temperature is sufficiently raised to maintain a sufficiently high vapor pressure of the molten metal such that metal pumping is not required to maintain the desired low energy hydrogen reaction rate. The elevated temperature can be higher than the boiling point of the molten metal. In an exemplary embodiment, the temperature of the wall of the reaction cell chamber including the black body radiator 5b4 is in the range of about 2900 K to 3600 K, and the molten silver vapor pressure is in the range of about 5 atm to 50 atm, wherein the reaction The cell chamber 5b31 acts as a boiler for reflowing molten silver so that the EM pump power can be eliminated. In one embodiment, the molten metal vapor pressure is sufficiently high that the metal vapor acts as a conductive matrix to eliminate the need for arc plasma and thereby the need for ignition current. In one embodiment, the low energy hydrogen reaction provides heat to maintain the battery components, such as reservoir 5c, lower hemisphere 5b41, and upper hemisphere 5b42, at the desired elevated temperature such that the heater power is removable. The desired temperature can be higher than the melting point of the molten metal. In an embodiment, battery activation may be achieved by at least one decimated power source such as at least one of a scrubber heater, an ignition, and an EM pump power source. Once started, the battery can operate in continuous operation. In an embodiment, activation may be achieved by an energy storage device such as at least one of a battery pack and a capacitor (such as a supercapacitor device). The device can be powered by the power output of the generator or by an independent power source. In an embodiment, the generator may be started at a plant that uses a stand-alone power supply and shipped in a continuous operation that lacks a starting power supply, such as at least one of a heater, an ignition, and a pumping power supply. . In an exemplary embodiment, the SunCell® comprises molten aluminum (MP = 660 ° C, BP = 2470 ° C) or molten silver (MP = injected into the reaction cell chamber 5b31 by a dual EM pump in a carbon reservoir). 962 ° C, BP = 2162 ° C), the reaction cell chamber comprises a carbon lower hemisphere 5b41 and a carbon upper hemisphere 5b42, the double EM pump comprising stainless steel, Ti, Nb, W, V and Zr fasteners such as Hayes 230 (such as At least one of the joint sleeves 5k9), and at least one of stainless steel, Ti, Nb, W, V and Zr EM pump tubes, carbon or iron heat transfer blocks 5k7 such as Haynes 230 or SS 316, nozzle pump tubes At least one of the stainless steel, Ti, Nb, W, V, and Zr initial sections of the W-end nozzle section 5k61 having the pump tube and the W nozzle positioned and welded. Each EM pump tube may further comprise an ignition source busbar for connection to a terminal of a power source 2 comprising the same metal as the EM pump tube. In an embodiment, the ignition system can further include circuitry including a switch that shorts the ignition source EM pump tube busbar to heat the pump tube when closed during startup. A switch in an open position during battery operation causes current to flow through the intersecting flow of molten metal. The carbon heat transfer block may comprise heat transfer carbon powder to divide the dents of the EM pump tube by wires. The reservoir can be made longer to reduce the temperature at the EM pump assembly such as fastener 5k9 and EM pump tube 5k6. With added hydrogen source (such as argon-H2 (3%)) The oxide source of the HOH catalyst may comprise CO, CO2 LiVO3 Al2 O3 And NaAlO2 At least one of them. HOH can be formed in the ignition plasma. In an embodiment, the battery component in contact with the molten aluminum may comprise a ceramic such as SiC or carbon. The reservoir and EM pump tubing and nozzles can contain carbon. The assembly may comprise a metal coated with a protective coating such as ceramic, such as stainless steel. Exemplary ceramic coatings are of the present invention, such as graphite, aluminosilicate refractories, AlN, Al2 O3 , Si3 N4 And aluminum oxynitride ceramics. In an embodiment, the battery component in contact with the molten aluminum may comprise at least one corrosion resistant material such as Nb-30Ti-20W alloy, Ti, Nb, W, V, Zr; and ceramics such as graphite, aluminum silicate refractory Material, AlN, Al2 O3 , Si3 N4 And SiAlON. In an embodiment, the separator includes an EM pump that can be located at the junction region of the two reservoirs. The EM pump can include at least one of an electromagnet and a permanent magnet. The polarity of at least one of the current on the EM pump bus and the electromagnet current may be periodically reversed to direct return silver to one reservoir and then to another reservoir to avoid between the reservoirs Electrical short circuit. In one embodiment, the ignition circuit includes an electrical diode that forces current through the dual EM pump injector liquid electrode in one direction. In one embodiment, a battery assembly comprised of carbon is coated with a coating such as a carbon coating capable of maintaining a vapor pressure of about zero at the operating temperature of the battery assembly. An exemplary operating temperature for a blackbody radiator is 3000 K. In an embodiment, the coating for suppressing sublimation applied to a surface of an outer surface such as a carbon battery assembly such as blackbody radiator 5b4 or reservoir 5c comprises pyrolytic graphite, Pyrograph coating ( Toyo Tanso), graphitized coating (Poco/Entegris), tantalum carbide, TaC, or another coating known in the art or known in the art to inhibit sublimation. The coating can be stabilized at high temperatures by applying and maintaining a high gas pressure on the coating. In an embodiment, the EM pump tube 5k6, the current bus bar 5k2, the heat transfer block 5k7, the nozzle 5q, and the fitting 5k9 may include at least one of Mo and W. In an embodiment, the joint bushing type and VCR type fitting 5k9 may comprise carbon, wherein the reservoir may comprise carbon. The carbon fitting may comprise a gasket such as a refractory metal mesh or a foil such as W. In one embodiment, the electrode penetrates at least one of the pressure vessel wall and the lower hemisphere 5b41 and the reservoir 5c of the black body radiator 5b4 at the feedthrough 10a. The electrode 8 can be locked in place by the electrode O-ring lock nut 8a1. The electrode bus bars 9 and 10 can be connected to the power source via the bus bar collector 9a. The electrode penetrating member may be coated with an electrical insulator such as ZrO. Since C has low conductivity, the electrodes can be directly sealed by a sealant such as a graphite paste at a penetrating member such as a penetrating member at the wall of the reservoir. Alternatively, the electrode can be sealed at the penetration by a VCR or a joint casing feedthrough. Mechanical engagement of components having different coefficients of thermal expansion, such as the EM pump tube and the base of the reservoir 5c and at least one of the VCR or swaged fitting between the electrode and the reservoir wall, may comprise a compressible seal , such as carbon gaskets or gaskets, such as Perma-Foil or Graphoil gaskets or gaskets or hexagonal boron nitride gaskets. The gasket can contain pressed MoS2 WS2 , CelmetTM (such as one containing Co, Ni or Ti, such as porous Ni C6NC (Sumitomo Electric)), cloth or chain cloth (such as cloth or chain cloth containing ceramic fibers, which contains high alumina and refractory oxide, Such as Cotronics Corporation Ultra Temp 391) or another material of the invention. In an exemplary embodiment, the reaction cell chamber power is 400 kW, the 6 吋 diameter carbon black body radiator operates at 3000 K, and the EM pump pump rate is about 10 cc/s for melting. The inductively coupled heater power of silver is about 3 kW, the ignition power is about 3 kW, the EM pump power is about 500 W, and the reaction cell gas contains Ag vapor and argon/H.2 (3%), the external chamber gas contains argon/H2 (3%), and the pressure of the reaction cell and the external chamber were each about 10 atm. The external pressure vessel may be pressurized to balance the pressure of the reaction cell chamber 5b31, wherein the latter pressure is attributed to the increase in temperature of the matrix metal such as silver. The pressure vessel can be initially pressurized, or the pressure can increase as the temperature of the reaction cell chamber increases. Hydrogen can be added to the pressure vessel to penetrate into the reaction cell chamber. In an embodiment wherein the blackbody radiation is isotropic carbon, the dome is at least partially permeable to the gas at equilibrium pressure and supplies hydrogen to the reaction, such as hydrogen and an inert gas such as argon. At least one. In one embodiment, the electrical power may be controlled by hydrogen controlled to the low energy hydrogen reaction in the flow reaction cell chamber 5b31. The low energy hydrogen reaction can be stopped by purging or evacuating hydrogen. Purging can be achieved by flowing an inert gas such as argon. SunCell® may comprise a high pressure water electrolyzer having water at high pressure to provide high pressure hydrogen, such as one comprising a proton exchange membrane (PEM) electrolyte. H2 And O2 Each of the chambers may be included to eliminate contaminants separately2 And H2 The composite. The PEM can act as at least one of a separator of the anode and cathode compartments and a salt bridge to allow hydrogen to be produced at the cathode and oxygen to be generated as a separation gas at the anode. The cathode can comprise a dichalcogenide hydrogen evolution catalyst, such as one that can further comprise sulfur, including at least one of rhodium and ruthenium. The cathode can comprise one known in the art, such as Pt or Ni. Hydrogen can be produced under high pressure and can be supplied to the reaction cell chamber 5b31 either directly or by infiltration, such as a permeated black body radiator. SunCell® can include a hydrogen line from the cathode chamber to the point where hydrogen is delivered to the battery. SunCell® can include an oxygen line from the anode chamber to the point where oxygen is delivered to the storage vessel or vent. In one embodiment, the SunCell® includes a sensor, a processor, and an electrolysis current controller. The sensor can sense at least one of: (i) hydrogen pressure in at least one chamber such as an electrolytic cathode chamber, a hydrogen line, an external chamber 5b3a1, and a reaction cell chamber 5b31, (ii) SunCell® The power output, and (iii) the electrolysis current. In one embodiment, the supply of hydrogen to the battery is controlled by controlling the electrolysis current. The hydrogen supply can increase with increasing electrolysis current and vice versa. Hydrogen can be at least one of the high pressure and low inventory, such that the hydrogen supply to the battery can be controlled in a fast time response by controlling the electrolysis current. In another embodiment, hydrogen can be produced by using the supplied water and thermal pyrolysis produced by SunCell®. The pyrolysis cycle can comprise one of the invention or one of those known in the art, such as based on one of a metal and an oxide thereof, such as at least one of SnO/Sn and ZnO/Zn. In an embodiment where the inductively coupled heater, EM pump, and ignition system consume power only during startup, hydrogen can be generated by pyrolysis such that parasitic power requirements are extremely low. The SunCell® may include a battery pack, such as a lithium ion battery, to provide power to operate a system such as a gas sensor and control system, such as those used to react plasma gases. The pressure of the reaction chamber 5b31 can be measured by measuring the extension or displacement of at least one of the battery components due to internal pressure. The extension or displacement due to internal pressure can be at least at least given by measuring the internal pressure caused by the non-condensing gas at a given reaction chamber temperature at a given reaction chamber 5b31 temperature. One is calibrated. In an embodiment, the coating of the graphite battery component, such as the surface of the blackbody radiator, the reservoir, and the VCR-type fitting, may comprise pyrolytic graphite, tantalum carbide, or the present invention or non-hydrogen known in the art. Another coating that reacts. The coating can be stabilized at high temperatures by applying and maintaining a high gas pressure on the coating. In an embodiment, the negative (reduction) potential is applied to withstand H2 A battery assembly of an oxidation reaction of at least one of O and oxygen, such as at least one of a black body radiator 5b4, a reservoir 5c, and a pump tube. The generator can include a voltage source to apply a negative voltage to the battery component, at least two electrical leads, a conductive substrate, a positive electrode, and an opposite electrode. In an embodiment, at least one of the black body radiator 5b4, a reservoir 5c, and an EM pump 5ka may be biased by a negative voltage or a reduction voltage. The negative electrode of the pair of electrodes 8 may comprise at least one component of a group of EM pumps 5ka, black body radiators 5b4 and a reservoir 5c such that the components are biased by a negative voltage or a reduction voltage. Electrode 8 can comprise a molten metal injector electrode. The electrically conductive substrate can comprise at least one of a plasma and a metal vapor. The positive melting electrode may include a first EM pump 5ka and a first reservoir 5c, the first reservoir and the black body radiator 5b4, the other or second reservoir 5c, and the other or second EM pump 5ka At least one of them is electrically isolated. The first reservoir 5c can at least partially comprise an electrical insulator. At least one of the ignition power and the positive bias of the first EM pump 5ka may be supplied by the power source 2. The first injector nozzle 5q of the first positive bias EM pump 5ka can be immersed. Immersion reduces or prevents damage to the nozzle by at least one of the plasma and water reactions. At least one of the black body radiator 5b4, the second reservoir 5c, and the second EM pump 5ka may be biased by a negative voltage or a reduction voltage. At least one of the ignition power and the negative bias voltage for at least one of the black body radiator 5b4, the second reservoir 5c, and the second EM pump 5ka may be supplied by the power source 2. The second reservoir can comprise an electrical conductor such as graphite. Alternatively, the second reservoir may comprise an electrical insulator, and the battery further comprises an electrical short from a source of negative bias (such as the ignition solenoid bus 5k2a) to the blackbody radiator 5b4. The short circuit may comprise an electrical conductor between the conductive portion of the EM pump assembly 5kk and the black body radiator 5b4. An exemplary short circuit comprises a graphite shell lid applied to a boron nitride tube, wherein the shell lid contacts the EM pump assembly 5kk and the black body radiator 5b4. The shell lid can also help absorb RF radiation from the inductively coupled heater. The black body radiator 5b4, the second reservoir 5c, and the second EM pump 5ka can be electrically connected under a negative bias. The negative bias may be sufficient to prevent at least one of the black body radiator 5b4, the second reservoir 5c, and the second EM pump 5ka from being H2 At least one of O and oxygen reacts. At least one of the molten metal vapor (such as silver vapor) in the reaction cell chamber 5b31 and the plasma supported by the ignition and low energy hydrogen reaction may serve as a battery assembly for completing the positive electrode and the unfavorable bias (such as the black body radiator 5b4). Means of an electrolytic circuit between at least one of the second reservoir 5c and the second EM pump 5ka. H2 O, H2 , CO and CO2 At least one of the permeable body can penetrate through at least one of the black body radiator 5b4 and the at least one reservoir 5c. H2 O, H2 , CO and CO2 At least one of them may be supplied by a passage to the reaction cell chamber 5b31 such as a reaction cell chamber containing the EM pump tube 5k6. H2 O can serve as a source of at least one of the H and HOH catalysts. Hydrogen can be at least one of: acting as a source of H to form low energy hydrogen and reacting with oxygen to form water, wherein the oxygen can be from H as a source of H to form a low energy hydrogen.2 The product of O. The carbon oxidation reaction can be further suppressed by maintaining an atmosphere of at least one of hydrogen, carbon dioxide, and carbon monoxide. In an embodiment, the generator may include only the first reservoir 5c and the first EM pump 5ka including the molten metal injector electrodes. The counter electrode may include a black body radiator 5b4. The electrodes can be powered by the power source 2. The molten metal injector electrode can be positive and the black body radiator electrode is negative. Black body radiator that can at least partially protect against unfavorable biases from H2 O and O2 At least one of them reacts. Such as CO, CO2 , H2 And H2 The gas of at least one of O can be supplied by the system and method of the present invention. H2 O, H2 , CO and CO2 At least one of the permeable body can penetrate through at least one of the black body radiator 5b4 and the reservoir 5c. H2 O, H2 , CO and CO2 At least one of them may be supplied by a passage to the reaction cell chamber 5b31 such as a reaction cell chamber containing the EM pump tube 5k6. In one embodiment, the SunCell® comprises a molten metal additive that chemically prevents oxidation or chemically reduces at least one oxidized battery component, such as at least one of an EM pump tube, a black body radiator, a water riser, and a nozzle. . A reducing agent/protecting agent can be added to the silver to prevent the EM pump tube from being H2 O and O2 At least one of them is oxidized. The additive may comprise a reducing agent known in the art, such as thiosulfate, Sn, Fe, Cr, Ni, Cu or Bi. The additive reduces the reaction of the carbon reaction cell chamber with at least one of water, oxygen, carbon dioxide, and carbon monoxide. When a carbon component is positively biased, such as reaction cell chamber 5b31, the additive protects the carbon from oxidation reactions. The additive may comprise at least one of carbon, a hydrocarbon, and hydrogen. In another embodiment, at least one of the molten metal and the additive can coat or wet the wall of the battery component to protect against oxidation. At least one of the interior of the EM pump tube 5k6 and the reaction cell chamber 5b31 (such as a carbon reaction cell chamber) may be protected. Supplying low energy hydrogen reactants (such as H2 O) may be supplied via the EM pump tube 5k6 in the case where the corresponding gas is impermeable to the battery assembly (such as the black body radiator 5b4) or the reaction electrolytic cell chamber 5b31 (such as a carbon reaction electrolytic cell chamber) due to coating or wetting. . The EM pump tube can also be protected by applying a negative potential. A negative potential can be applied using the ignition power source 2. The potential can be reversibly applied to each of the two EM pump tubes of the dual molten metal injector. The ignition power source 2 can include a switch that cyclically reverses the polarity at each of the ignition bus bars 5k2a. The SunCell® may include a blackbody radiator 5b4, such as a carbon black body radiator, which further includes a busbar to the negative terminal of the voltage source. The voltage source can include an ignition power source 2. The negative bus bar can be connected to a top sliding nut that connects the reservoir to the base of the black body radiator 5b4. The connector to the hot carbon component such as the top slide nut may contain carbon to avoid metal carbide formation of the metal connector. Any metal carbon connection can be made via expansion of the connections in the placement area, where the connection temperature is below the temperature that would result in metal carbide formation. The negative potential can comprise a constant negative potential. The bus bar may comprise a refractory electrical conductor such as Mo or W. In an embodiment, the connection providing the negative bias to the blackbody radiator may comprise a mechanical jumper to reversibly form an electrical connection directly or indirectly with the ignition busbar and the base of the blackbody radiator. The connection may comprise at least one reversible mechanical switch and a conductor covering one portion of the reservoir 5c, such as a carbon shell cover on the exterior of the reservoir (such as on the exterior of the BN tube). Chemical incompatibility should be avoided. For example, since iron and carbon can react to form iron carbide, parts containing iron should be prevented from coming into contact with components containing iron. The oxidizing additive can be regenerated after reduction of the oxidized battery component by electrolytic reduction or by chemical reduction. Electrolytic reduction can be provided by a negative potential applied to at least one of the battery components. The reaction cell chamber atmosphere 5b31 may contain water vapor. The reaction cell chamber 5b31 can comprise an electrolytic cell cathode, wherein the plasma completes the circuit between the cathode and the anode. The anode can comprise a positively biased molten metal electrode. Hydrogen formed at the negative (cathode) discharge electrode of the battery (such as at the wall of the reaction cell chamber 5b31) protects the electrode (wall) from H2 O oxidation. The water reduction/oxidation reaction can be cathode: 2H2 O + 2e- To H2 + 2OH- (41) Anode: 4OH- To O2 + 2H2 O + 4e- (42) In an embodiment, the inside of the EM pump tube 5k6 may be coated with a molten metal coating to protect it from at least one of the reaction cell chamber 5b31, the reservoir 5c, and the EM pump tube 5k6. Species corrosion, such species as water, CO2 , Co and O2 At least one of them. A silver wetting coating protects at least one component of the SunCell®. In an embodiment, at least one metal surface, such as a metal surface inside the EM pump tube 5k6, may be treated to remove the oxide coating to permit the molten metal, such as silver, to wet the surface. The oxide coating can be removed to improve the electrical conductivity across the busbar of molten metal, such as silver. The oxide coating can be removed by at least one method, such as one or more of mechanical and chemical removal. The oxide coating can be removed by using an abrasive tool such as a wire brush or by sand blasting. Can be etched by an etchant such as an acid such as HCl or HNO3 Or a reducing agent (such as hydrogen) removes the oxide coating. A molten metal such as silver may be supplied from the coating to protect the inside of the reaction cell chamber 5b31, the reservoir 5c, and the EM pump tube 5k6. At least one of the electrodes can be immersed to protect it from corrosion or erosion by the plasma. In one embodiment, the wall of the reaction cell chamber may comprise at least one of silver coated carbon, hot carbon, and silver coated hot carbon, such as isotropic carbon. The silver plated layer may be formed during battery operation or may be applied by a coating process such as plasma spraying, electroplating, vapor deposition, and other methods known to those skilled in the art. The assembly of batteries can include at least one of materials and coatings to prevent or reduce oxidation reactions, such as oxidation reactions with at least one of oxygen and water vapor. In an embodiment, the EM pump tube 5k4 may comprise boiler grade stainless steel or nickel, or the tube may be internally coated with nickel. In an embodiment, the refractory EM pump tube 5k61 may comprise a water resistant material, such as a Mo superalloy, such as TZM. The nozzle or spray portion of the EM pump tube 5k61 may contain carbon, such as hot carbon. The inside of the EM pump tube can be coated with silver to prevent reaction with water. In an embodiment, at least one of the inlet riser 5qa, the nozzle portion of the EM pump tube 5k61, and the nozzle 5q may comprise a refractory material that is stable to oxidation, such as a refractory oxide, such as MgO (MP 2825 ° C), ZrO2 (M.P. 2715 ° C), magnesium oxide, H2 O-stabilized zirconia, yttrium zirconate (SrZrO3 M.P. 2700 ° C), HfO2 (M.P. 2758 ° C), cerium oxide (M.P. 3300 ° C) or another oxide of the invention. The reaction cell chamber 5b31 may comprise carbon that may be coated with protective silver, such as hot carbon. The reaction cell chamber 5b31 can be unfavorably biased to protect it from the oxidation reaction. The reservoir may comprise boron nitride, which may contain additives or surface coatings to protect it from oxidation reactions, such as CaO, B2 O3 SiO2 AUO3 , SiC, ZrO2 And at least one of AlN, wherein at least one of water and oxygen may comprise an oxidant. Boron nitride may comprise a crystalline structure that is resistant to water reactions, such as alpha BN. The reaction mixture may contain additives such as Hx By Oz ), which may contain a gas to inhibit the oxidation reaction of BN. In an embodiment, the cellular component such as reservoir 5c may comprise a refractory oxide such as MgO (M.P. 2825 ° C), ZrO2 (M.P. 2715 ° C), magnesium oxide, H2 O-stabilized zirconia, yttrium zirconate (SrZrO3 M.P. 2700 ° C), HfO2 (M.P. 2758 ° C) or cerium oxide (M.P. 3300 ° C) which is stable to oxidation at the working temperature. In one embodiment, a gaseous source of oxygen (such as water vapor, CO)2 , CO and O2 ) can be floated to the top of the reaction cell chamber 5b31. In addition to metal vapors (such as silver vapor), the reaction cell chamber gas contains a shift of water vapor to the top dense gas (such as helium) of the reaction cell chamber due to the higher buoyancy of the water. In one embodiment, the silver vapor is maintained at a pressure sufficient to cause the water vapor to rise to the top of the reaction cell chamber. The upward shift of the water vapor prevents it from being corroded by the battery pack (such as the EM pump tube 5b6). At least one reactant gas (such as H2 O and H2 ) can be supplied via EM pump tubing. The chemical reduction can be provided by a reducing gas such as hydrogen. An exemplary reducing atmosphere containing Ar/H2 (3%) gas. Hydrogen gas can permeate through at least one of the battery components, such as at least one of the black body radiator 5b4 and the EM pump tube 5k6. The EM pump tube may comprise a hydrogen permeable metal such as stainless steel (SS) such as 430 SS, vanadium, niobium, or tantalum, or nickel. Hydrogen is permeable to the medium injection into the positive EM pump tube. In this case, oxidation of oxygen can be avoided, wherein the oxidation reaction can comprise: Anode: 2OH- + H2 To 2H2 O + 2e- (43) In an embodiment, the SunCell® further includes a positive electrode, a bias voltage source for applying a potential between the positive electrode and the at least one battery component, and a controller for biasing the power source. The positive electrode can comprise a molten metal electrode. The positive electrode may comprise at least a portion of a molten metal such as silver, such as molten metal in at least one of the lower hemisphere of the reservoir 5c or the black body radiator 5b41. The positive electrode may comprise a conductor that is stable to the oxidation reaction, such as a noble metal, which may also be a refractory metal such as Pt, Re, Ru, Rh or Ir. A positive bias can be applied external to the EM pump tube such that the interior of the tube is not positively biased. The inside of the pump tube can contain a Faraday cage. The EM pump tube can include a positive electrode that is at least one of immersion silver and silver coated on the surface. The flowing silver may form a hole in at least one of the nozzle and the EM pump tube. The apertures are selectively on the EM pump tube portion that is exposed to the plasma. At least one of the battery components, such as at least one of the black body radiator 54b, the reservoir 5c, and the EM pump 5ka, may be protected from battery reactants or products by applying a negative bias between the battery assembly and the positive electrode (such as Oxygen source, CO, CO2 , H2 O and O2 Oxidation reaction of at least one of them. The bias potential can be a potential that causes at least one of reducing the oxide of the battery component and preventing oxidation of the battery component. The bias voltage can be in a range of at least one of about 0.1 V to 25 V, 0.5 V to 10 V, and 0.5 V to 5 V. The positive electrode can be at least one of consumable and replaceable. The positive electrode can comprise carbon. A carbon positive electrode can be attached to the positive EM pump tube and nozzle 5q, wherein the positive electrode can be closer to the reaction cell chamber than the tip of the nozzle. The positive electrode can be in electrical contact with the positive EM pump tube and the nozzle. Source of at least one of hydrogen and oxygen may comprise H2 O. The low energy hydrogen reaction product may comprise H2 (1/p), such as H2 (1/4) and oxygen. The positive electrode can react with the oxygen product. Carbon electrode reacts with excess oxygen and forms CO2 . CO can be removed from the reaction cell chamber 5b312 . The CO may be removed by at least one of pumping and diffusing via at least one battery component, such as blackbody radiator 5b42 . In one embodiment shown in FIGS. 2I80 to 2I173, at least one of an inert gas, water or steam, hydrogen, and oxygen may be supplied to the reaction cell chamber 5b31 by at least one of: spraying To the pump tube 5k6 (such as at the end of the nozzle 5q); and to the reaction cell chamber 5b31. The generator may comprise at least one inert gas, water or steam, hydrogen and a source of oxygen, such as a sump and a transfer line. A valve such as a flow valve or a pressure valve, such as a solenoid valve, can control the injection. In one embodiment, the SunCell® may include a water ejector including a nozzle, a water line, a flow and pressure controller, a water source (such as a water reservoir), and vaporized water to form a gaseous H.2 At least one of the components of O. Vaporize water to form a gaseous H2 The component of O can include a steam generator. Water flowing into the interior of the battery prevents the molten metal from flowing back into the nozzle. The size of the nozzle opening or orifice can be set such that the minimum desired flow rate to maintain a low energy hydrogen reaction can be provided by the water pressure in the line, which is at least the line that reacts the pressure of the electrolytic cell chamber 5b31. Increasing the water pressure in the line provides a higher water supply rate. At least one of the nozzle and the nozzle orifice may comprise a material that is resistant to corrosion and erosion due to high pressure water jetting. Materials such as ceramics can be extremely hard and resistant to oxidation reactions, such as oxide ceramics, such as Al.2 O3 , zirconia or yttria. In one embodiment, the source of the HOH catalyst and the source of H comprise water that is sprayed into the electrode. A high current is applied to cause the ignition to be a bright luminescent plasma. The source of water can include bound water. The solid fuel injected into the electrode may comprise water and a highly conductive matrix, such as a molten metal, such as at least one of silver, copper, and a silver-copper alloy. The solid fuel can comprise a compound comprising bound water. The water-binding compound that can be supplied to the ignition may contain a hydrate such as BaI having a decomposition temperature of 740 ° C.2 2H2 O. Cocoa, which may contain water-binding compounds, is miscible with molten metal such as silver. The miscible compound may comprise a flux, such as hydrated Na2 CO3 , KCl, carbon, borax (such as Na2 B4 O7 ·10H2 O), at least one of calcium oxide and PbS. The bound water compound is stable to water loss up to the melting point of the molten metal. For example, the combined water can be stable above 1000 ° C and lose water at the ignition event. The compound comprising bound water may comprise oxygen. In the case of releasing oxygen, the molten metal may contain silver because the silver does not form a stable oxide at its melting point. The compound comprising bound water may comprise: hydroxides such as alkalis, alkaline earths, transition metals, internal transition metals, rare earths, 13, 14 groups, 15 groups and 16 groups of hydroxides; minerals such as talc, having the chemical formula H2 Mg3 (SiO3 )4 Or Mg3 Si4 O10 (OH)2 a mineral composed of hydrated magnesium citrate, and muscovite or mica, having the formula KAl2 (AlSi3 O10 )(F,OH)2 Or (KF)2 (Al2 O3 )3 (SiO2 )6(H2 O) Alumina and potassium citrate minerals. In one embodiment, the dehydrated compound acts as a desiccant to maintain low reaction cell chamber pressure. For example, barium hydroxide decomposes into barium oxide and H when heated to 800 ° C.2 O, and the resulting BaO has a boiling point of 2000 ° C such that it is still substantially vaporized for a plasma temperature above 2300 K. In one embodiment, the source of water comprises an oxide and hydrogen that can also serve as a source of H. The hydrogen source can comprise hydrogen. The oxide may be capable of being reduced by hydrogen to form H2 O. The oxide may comprise at least one of the following: Cu, Ni, Pb, Sb, Bi, Co, Cd, Ge, Au, Ir, Fe, Hg, Mo, Os, Pd, Re, Rh, Ru, Se, Ag , Tc, Te, Tl, Sn, W and Zn. Controllable H2 Source of O compound, H2 At least one of a concentration of the source of the O compound, a water vapor pressure in the reaction cell chamber, an operating temperature, and an EM pumping rate to control the amount of water supplied to the ignition. H2 The concentration of the source of the O compound may range from at least about 0.001 mol% to 50 mol%, 0.01 mol% to 20 mol%, and 0.1 mol% to 10 mol%. In one embodiment, water is dissolved in the fuel melt, such as a fuel melt comprising at least one of silver, copper, and a silver-copper alloy. The solubility of water increases with the partial pressure of water in contact with the melt, such as the partial pressure of water vapor in the chamber of the reaction cell. The water pressure in the chamber of the reaction cell can be balanced by the water vapor pressure in the chamber. The balance can be achieved by the means of the invention, such as for other gases such as argon. The water vapor pressure in the reaction cell chamber may be in the range of at least about 0.01 Torr to 100 atm, 0.1 Torr to 10 atm, and 0.5 Torr to 1 atm. The EM pumping rate can range from about 0.01 ml/s to 10,000 ml/s, 0.1 ml/s to 1000 ml/s, and at least one of 0.1 ml/s to 100 ml/s. The SunCell® may include at least one of a radiant heat exchanger and a radiant boiler (Fig. 2I153 to Fig. 2I160). The SunCell® may comprise a radiant energy absorber, such as a primary heat exchanger 87 surrounding the black body radiator 5b4. The radiant energy absorber may comprise a black body absorber (such as a carbon absorber) and may further comprise a boiler tube to receive heat from a black body absorber where steam may form in the tube and exit via hot water or steam outlet 111. The tube can be embedded in a black body absorber. The steam can be delivered to a load such as a city steam heating system. The SunCell® may include a secondary heat exchanger 87a that may transfer heat absorbed by the black body radiator 5b4 or the reaction cell chamber 5b31 by the primary heat exchanger 87 and transfer the heat to the secondary medium, such as a solid, liquid Or gaseous medium. In one embodiment, the secondary heat exchanger can transfer heat to the air that can be purged or blown through the heat exchanger 87a by the fan 31j1. Air can exit the hot air duct 112 to flow to the thermal load. In the thermal generator embodiment shown in Figures 2I156 through 2I160, cold coolant (such as cold water) is supplied to the thermal generator via water inlet 113 and output via at least one of steam and hot water outlet 111 At least one of hot water and steam. The heat generated in the reaction cell chamber 5b31 can be radiated to the boiler tube of the upper heater exchanger 114 to generate steam in the boiler chamber 116. The steam boiler further includes a high pressure upper heat exchanger and a boiler chamber casing 5b3a and a bottom plate 5b3b. Heat from the reservoir 5c and the lower battery assembly can be radiated to the lower heat exchanger 115 to form at least one of hot water and steam exiting the outlet 111. In an embodiment, the boiler tube can carry hot water instead of steam. SunCell® power can be used as thermal power in the form of direct radiation, hot air, hot water and steam. In another embodiment, the boiler or heat exchanger can comprise a liquid droplet radiator comprising a particulate absorbent (such as an aerosol or metal vapor) entrained in a gas stream or fluid stream, wherein the particles absorb heat flux and deliver It moves the gas or fluid coolant. The droplet cooling system can include a droplet spray and collection system, such as a system including an inkjet printer. The heat transfer from the black body radiator to the particle absorber can be predominantly radiation in nature. An exemplary embodiment comprising refractory particles and a gas having a higher heat transfer capacity comprises tungsten microparticles suspended in a stream of hydrogen or helium. In another embodiment, the boiler or heat exchanger may comprise a heat transfer medium (such as a solid that transfers heat from at least one of the reaction cell chamber 5b31 or the black body radiator 5b4 to the coolant of the boiler or heat exchanger. , liquid or gaseous medium). The heat transfer mechanism can include at least one of radiation, convection, and conduction. An exemplary liquid heat transfer medium comprises at least one of water, molten metal, and molten salt. The exemplary gaseous heat transfer medium can include at least one of an inert gas, hydrogen, helium, a rare gas, and nitrogen. The boiler or heat exchanger may comprise a gaseous heat transfer medium and means for regulating its pressure, such as a supply source such as a sump, regulator, pressure gauge, pump and controller to achieve a desired constant or a desired variable pressure to control the heat transfer rate. . The SunCell® may comprise a heat exchanger 87, such as a tab on the outer surface 5b4 of the reaction cell chamber 5b31, to heat a flowing working medium, such as a coolant (such as a molten salt), such as a eutectic mixture, molten metal, water Or a gas (such as air). The heat exchanger may also include a heat transfer fin on the heat sink and the heat sink, wherein the heat transfer absorbs heat from the black body radiator 5b4. The tabs exchange heat with the gas or fluid coolant/working medium. The absorber can comprise a higher emissivity material such as carbon. The Braden cycle system can include a closed pressurized gas circuit and a turbine and ambient heat exchanger where the gas is heated by SunCell®, flows to the gas turbine at the highest pressure, and can be passed to the environment via a heat exchanger The heat is lost while the pressure is lowered at the rear end of the turbine. The chemical system can include components, such as thermal decomposition systems, to convert water to H using heat from low energy hydrogen reactions.2 . Hydrogen can be used in known converters, such as combustion turbines or fuel cells, such as PEM fuel cells, to generate electricity. Alternatively, the electrochemical cycle can comprise a fuel cell having a hydride ion electrolyte, a hydrogen cathode, and a metal hydride anode. The metal hydride can be thermally decomposed to maintain a reversible metal hydride/metal hydrogenation cycle that uses electricity from the low energy hydrogen process to generate electricity. A hydride ion fuel cell is described in my prior application, such as a U.S. patent application, such as the Electrochemical Hydrogen Catalyst Power System, PCT/US11/28889, filed March 17, 2011;2 O-Based Electrochemical Hydrogen-Catalyst Power System, PCT/US12/31369 filed on March 30, 2012; CIHT Power System, PCT/US13/041938 filed on May 21, 2013; and Power Generation Systems and Methods Regarding Same PCT/IB2014/058177, filed on Jan. 10, 2014, which is incorporated by reference in its entirety. In an embodiment, a plurality of generators may be coupled to provide a desired power output. A plurality of generators may be interconnected in at least one of series and parallel to achieve a desired power output. The system of coupled generators can include a controller to control at least one of a series connection and a parallel connection between the control generators that control the superimposed output power of the plurality of coupled shaft generators At least one of power, voltage, and current. A plurality of generators may each include a power controller to control the power output. The power controller can control the low energy hydrogen reaction parameters to control the generator power output. Each generator may include a switch between at least one of a PV cell or a PV cell of PV converter 26a and further comprising a controller to control at least one of a series connection and a parallel connection between the PV cells or groups thereof One. The controller can switch the interconnect to achieve at least one of a desired voltage, current, and electrical power output from the PV converter. The central controller of the plurality of generators can control at least one of the series interconnection and the parallel interconnection between the coupled shaft generators, at least the low energy hydrogen reaction parameters on the generator, and the plurality of coupled shafts A connection between a PV cell or a PV cell of at least one PV converter of at least one generator of the generator. The central controller can control at least one of the generator and the PV connection and the low energy hydrogen reaction parameters either directly or via an individual generator controller. The power output can include DC or AC power. Each generator may include a DC to AC inverter, such as an inverter. Alternatively, the DC power of a plurality of generators may be combined via a connection between the generators and converted to AC power using a DC to AC converter, such as an inverter capable of converting superimposed DC power. An exemplary output voltage for at least one of the PV converter and the coupled-shaft generator system is about 380V DC or 780V DC. Approximately 380 V output can be converted to a two-phase AC. The approximately 760 V output can be converted to a three-phase AC. The AC power can be converted to another desired voltage, such as about 120 V, 240 V, or 480 V. A transformer can be used to convert the AC voltage. In an embodiment, the IGBT can be used to change the DC voltage to another DC voltage. In an embodiment, at least one IGBT of the inverter can also be used as an IGBT of the inductively coupled heater 5m. In an embodiment, the converter includes a plurality of converters that are coupled to include a combined cycle. The combined cycle converter can be selected from the group consisting of a photovoltaic converter, a photoelectric converter, a plasma power converter, a heat exchanger, a thermoelectric converter, a Stirling engine, a Breiden cycle engine, a Rankine cycle engine. And heat engine and heater. In one embodiment, the SF-CIHT battery primarily produces ultraviolet light and extreme ultraviolet light. The converter may comprise a combined cycle comprising an optoelectronic converter followed by a photoelectric converter, wherein the photoelectric converter is transparent to ultraviolet light and may primarily respond to extreme ultraviolet light. The converter may further include additional combined loop converter components, such as at least one of a thermoelectric converter, a Stirling engine, a Breiden cycle engine, a Rankine cycle engine, and a magnetohydrodynamic converter.Magnetic fluid power ( MHD ) converter Charge separation based on the formation of mass flow of ions or conductive media in a crossed magnetic field is a well-known technique for magnetic fluid dynamic (MHD) power conversion. The cations and anions flow in the opposite direction through the Lorentz direction and are received at the respective MHD electrodes to affect the voltage between them. Mass flow rate of forming ions A typical MHD method is to expand a high pressure gas seeded with ions via a nozzle to create a high velocity flow through a crossed magnetic field, wherein a set of MHD electrodes intersect with respect to the deflection field to receive the deflected ions. In one embodiment, the pressure is typically greater than atmospheric pressure, and the directional mass flow can be achieved by reaction to form a plasma and highly conductive, high pressure and high temperature molten metal vapor that is amplified to produce a pass through the MHD converter. High-speed flow of the transverse magnetic field portion. The flow that can pass through the MHD converter can be axial or radial. Other directional flows may be achieved by constraining magnets, such as Helmholtz coils or magnetic cylinders. In particular, the MHD electric power system shown in Figures 2I161 to 2I195 may comprise a low energy hydrogen reactive plasma source of the invention (such as a plasma source comprising an EM pump 5ka), at least one reservoir 5c, at least two Electrodes (such as electrodes comprising dual molten metal injectors 5k61), sources of low energy hydrogen reactants (such as sources of HOH catalysts and H), ignition systems (including applying voltage and current to the electrodes to form electricity from low energy hydrogen reactants) Pulp power supply 2) and MHD electric power converter. The assembly of the MHD power system comprising the low energy hydrogen reactive plasma source and the MHD converter may be comprised of at least one of an antioxidant material such as an antioxidant metal, a metal comprising an antioxidant coating, and a ceramic such that the system It can be operated in the air. In a dual molten metal injector embodiment, a high electric field is achieved by maintaining a pulsed injection comprising intermittent current. Disconnect and reconnect the pulsed plasma by a silver stream. A voltage can be applied until a double molten metal stream is connected. The pulses may comprise high frequencies corresponding to high frequencies by causing the metal flow to be disconnected-reconnected. The connection-reconnection can occur spontaneously and can be controlled by the low energy hydrogen reaction power of the components (such as the invention) and by the molten metal injection rate of the invention (such as by controlling the EM pump current) At least one of them is controlled. In an embodiment, the ignition system can include a source of voltage and current, such as a DC power supply and a set of capacitors to deliver pulsed ignition with the ability to pulse high currents. The magnetohydrodynamic power converter shown in Figures 2I161 through 2I195 can include a source of magnetic flux transverse to the z-axis of the MHD converter 300 that passes through the direction of axial molten metal vapor and plasma flow. The conductive flow may have a preferred velocity along the z-axis due to the gas expanding along the z-axis. Other directional flows may be achieved by constraining magnets, such as Helmholtz coils or magnetic cylinders. Therefore, metal electrons and ions propagate into the region of the transverse magnetic flux. The Lorentz force on the propagating electrons and ions is given byF =e v × B (44) The force is transverse to the charge velocity and magnetic field and in the opposite direction of the cation and anion. Therefore, a lateral current is formed. The source of the transverse magnetic field may comprise a component that provides a transverse magnetic field of different strengths depending on the position along the z-axis to optimize the cross-deflection (equation (44)) of the flow charge with parallel velocity dispersion. The reservoir 5c molten metal may be in at least one of a liquid state and a gaseous state. The reservoir 5c molten metal may be defined as an MHD working medium and may also be referred to as an MHD working medium or as a molten metal, wherein it implies that the molten metal may be further in at least one of a liquid and a gaseous state. It is also possible to use a specific state such as molten metal, liquid metal, metal vapor or gaseous metal, in which another physical state may exist. An exemplary molten metal is silver that can be in at least one of a liquid and a gaseous state. The MHD working medium can further comprise an additive comprising at least one of: an added metal that can be at least one of a liquid and a gaseous state at an operating temperature range; a compound, such as one of the present invention, that is at work The temperature range may be at least one of a liquid and a gaseous state; and a gas such as a rare gas (such as helium or argon), water, H2 And at least one of the other plasma gases of the present invention. The MHD working medium additive can be in any desired ratio to the MHD working medium. In one embodiment, the ratio of medium to additive medium is selected to provide the power conversion performance of the MHD converter as appropriate. Working media such as silver or silver-copper alloys can be operated under supersaturated conditions. In an embodiment, the MHD generator 300 can include at least one of a Faraday, a channel Hall, and a disk Hall type. In a channel Hall MHD embodiment, the expansion or generator channel 308 can be oriented vertically along the z-axis, with molten metal plasma (such as silver vapor and plasma) flowing through the accelerator portion (such as the restriction or nozzle introduction port 307). Then, the portion 308 is expanded. The channel may comprise a solenoid magnet 306, such as a superconducting or permanent magnet, such as a Halbach array transverse to the flow direction along the x-axis. The magnet can be fixed by the MHD magnet mounting bracket 306a. The magnet may comprise a liquid cryogen or may comprise a cryogenic refrigerator with or without a liquid cryogen. The cryogenic refrigerator can include a dry dilution refrigerator. The magnet may comprise a return path for the magnetic field, such as a yoke, such as a C-shaped or rectangular anti-yoke. An exemplary permanent magnet material is SmCo, and an exemplary yoke material is magnetic CRS, cold rolled steel or iron. The generator may include at least one set of electrodes, such as a segmented electrode 304 along the y-axis that is transverse to the magnetic field (B ) to receive lateral Lorentz deflected ions that generate a voltage across the MHD electrode 304. In another embodiment, at least one channel, such as generator channel 308, may comprise a geometry other than a geometry having a planar wall, such as a cylindrical wall channel. Magnetohydrodynamic generation is described by [EM Walsh, Energy Conversion Electromechanical, Direct, Nuclear, Ronald Press Company, NY, NY, (1967), pp. 221-248, the entire disclosure of which is incorporated herein by reference. in. The MHD magnet 306 can include at least one of a permanent magnet and an electromagnet. The electromagnet 306 can be at least one of an uncooled magnet, a water cooled magnet, and a superconducting magnet having corresponding low temperature management. An exemplary magnet is a solenoid or saddle coil that magnetizes the MHD channel 308 and the racetrack coil, which magnetizes the disk channel. The superconducting magnet may comprise at least one of a cryogenic refrigerator and a cryogen dewar system. The superconducting magnet system 306 can comprise: (i) a superconducting coil that can comprise a superconductor wire spiral of NbTi or NbSn, wherein the superconductor can be coated with a transient localized quenching that protects against superconductor states induced by means such as vibration On a normal conductor (such as a copper wire) or a high temperature superconductor (HTS), the high temperature superconductor such as YBa2 Cu3 O7 , commonly referred to as YBCO-123 or YBCO only; (ii) liquid helium dewar, which provides liquid helium on both sides of the coil; (iii) liquid nitrogen dewar, inside the solenoid magnet and The outer radius has liquid nitrogen, wherein both the liquid helium and the liquid nitrogen dewar may comprise a radiation baffle and a radiation shield (which may comprise at least one of copper, stainless steel and aluminum) and a high vacuum insulated at the wall; And (iv) an inlet for each magnet that can be attached to a cryopump and a compressor that can be powered by the power output of the SunCell® generator via its output power terminals. In one embodiment, the magnetohydrodynamic power converter is a segmented Faraday generator. In another embodiment, the lateral current formed by the Lorentz deflection of the ion current undergoes further Lorentz deflection in a direction parallel to the input stream of the ions (z-axis) to at least relatively shift along the z-axis. A Hall voltage is generated between the first MHD electrode and the second MHD electrode. This device is referred to in the art as a Hall generator embodiment of a magnetohydrodynamic power converter. A similar device in which the MHD electrode is angled with respect to the z-axis in the xy plane includes another embodiment of the present invention and is referred to as a diagonal generator having a "window frame" configuration. In each case, the voltage can drive current through the electrical load. Examples of segmented Faraday generators, Hall generators and diagonal generators in Petrick [JF Louis, VI Kovbasyuk, Open-cycle Magnetohydrodynamic Electrical Power Generation, M Petrick and B. Ya Shumyatsky, Argonne National Laboratory, Argonne , Illinois, (1978), pp. 157-163, the entire disclosure of which is hereby incorporated by reference. In another embodiment of a magnetohydrodynamic power converter,The ion current along the z-axis can then enter a compressed portion containing an increased axial magnetic field gradient, parallel to the z-axisThe direction of the electronic motion component is at least partially converted to vertical motionThis is due to the adiabatic invariant= constant. due toTherefore, an azimuthal current is formed around the z-axis. The current is radially deflected by the axial magnetic field in the plane of motion, and a Hall voltage is generated between the inner ring and the outer ring MHD electrode of the disc generator magnetic fluid power converter. The voltage drives the current through the electrical load. The plasma power can also be used with the power device of the present invention or known in the art.Direct converters or other plasmas are converted to electricity. The MHD generator can include a condenser passage portion 309 that receives the expansion flow and the generator further includes a return passage or tube 310 in which the MHD working medium (such as silver vapor) is cooled because it loses temperature, pressure, and At least one of the energy flows back to the reservoir via the channel or tube 310. The generator may include at least one return pump 312 and a return pump tube 313 to pump the reflux to the reservoir 5c and the EM pump injector 5ka. The return pump and the pump tube can pump at least one of a liquid, a vapor, and a gas. The return pump 312 and the return pump tube 313 may include an electromagnetic (EM) pump and an EM pump tube. The inlet to the EM pump can have a larger diameter than the outlet pump tube diameter to increase the pump outlet pressure. In an embodiment, the return pump may comprise an injector of the EM pump injector electrode 5ka. In a dual molten metal injector embodiment, the generator includes a return reservoir 311 each via a corresponding reflux pump, such as a return EM pump 312. The reflux reservoir 311 can perform at least one of: balancing reflux molten metal (such as molten silver) flowing and condensing or separating silver vapor mixed with liquid silver. The reservoir 311 can include a heat exchanger that condenses silver vapor. The reservoir 311 can include a first stage electromagnetic pump to preferably pump liquid silver to separate the liquid from the gaseous silver. In an embodiment, liquid metal can be selectively injected into the return EM pump 312 by centrifugal force. The return conduit or reflux reservoir can comprise a centrifugal portion. The centrifugal reservoir can be wedged from the inlet to the outlet such that the centrifugal force is greater at the top than at the bottom to force the molten metal to the bottom and separate it from gases such as metal vapor and any working medium gas. Alternatively, the SunCell® can be mounted on a centrifuge table that rotates about an axis perpendicular to the direction of flow of the reflowed molten metal to create a centrifugal force that separates the liquid and gaseous species. In one embodiment, the condensed metal vapor flows into two separate reflux reservoirs 311, and each reflux EM pump 312 pumps molten metal into the corresponding reservoir 5c. In an embodiment, at least one of the two return reservoirs 311 and the EM pump reservoirs 5c comprises a content control system, such as one of the present inventions, such as a water riser 5qa. In one embodiment, the reflowed molten metal may be pumped into the reflux reservoir 311 due to the higher or lower rate depending on the amount in the reflux reservoir, wherein the suction rate is controlled by the corresponding content control system ( Such as the inlet pipe) control. In an embodiment, the MHD converter 300 can further include at least one heater, such as an inductively coupled heater. The heater can preheat the components in contact with the MHD working medium, such as the reaction cell chamber 5b31, the MHD nozzle portion 307, the MHD generator portion 308, the MHD condensing portion 309, the return conduit 310, the reflux reservoir 311, the return EM pump At least one of 312 and return EM pump tube 313. The heater can include at least one actuator that engages and retracts the heater. The heater can include at least one of a plurality of coils and a coil portion. The coils may comprise coils known in the art. The coil portion may comprise at least one separate coil, such as one of the present invention. In an embodiment, the MHD converter can include at least one cooling system, such as heat exchanger 316. The MHD converter can include a cooler for at least one battery and MHD assembly, such as at least one of the following groups: chamber 5b31, MHD nozzle portion 307, MHD magnet 306, MHD electrode 304, MHD generator portion 308, MHD The condensing portion 309, the return conduit 310, the reflux accumulator 311, the reflux EM pump 312, and the return EM pump tube 313. The cooler may remove heat loss from the MHD flow channel, such as heat loss from at least one of: chamber 5b31, MHD nozzle portion 307, MHD generator portion 308, and MHD condensation portion 309. The cooler may remove heat from the MHD working medium return system, such as at least one of a return conduit 310, a return reservoir 311, a return EM pump 312, and a return EM pump tube 313. The cooler can include a radiant heat exchanger that can vent heat to the ambient atmosphere. In an embodiment, the cooler may include a recirculator or reheater that transfers energy from the condensing portion 309 to at least one of the reservoir 5c, the reaction cell chamber 5b31, the nozzle 307, and the MHD channel 308. The transferred energy, such as heat, may comprise heat from at least one of residual thermal energy, pressure energy, and vaporization heat of the working medium, such as at least one of a gasification metal, a kinetic aerosol, and a gas (such as a rare gas). The working medium of one. The heat pipe is a passive two-phase device that is capable of transferring a large amount of heat flux (such as up to 20 MW/m) over a distance of a few meters with a temperature drop of a few tenths of a degree.2 Therefore, the thermal stress on the material is significantly reduced, so that only a small amount of working fluid is used. The sodium and lithium heat pipes deliver a large amount of heat flux and remain nearly isothermal in the axial direction. Lithium heat pipes can deliver up to 200 MW/m2 . In an embodiment, a heat pipe such as a molten metal such as a liquid alkali metal such as sodium or lithium coated in a refractory metal such as W can transfer heat from the condenser 309 and recycle it to the reaction electrolysis The groove chamber 5b31 or the nozzle 307. In one embodiment, at least one heat pipe recovers and recirculates the heat of vaporization of the silver such that the recovered heat power is a portion of the power input to the MHD channel 308. In one embodiment, at least one of the components of the SunCell®, such as a component including an MHD converter, can include a heat pipe for at least one of: transferring heat from one portion of the SunCell® generator to another Portioning and transferring heat from a heater (such as an inductively coupled heater) to a SunCell® component, such as an EM pump tube 5k6, a reservoir 5c, a reaction cell chamber 5b31, and a MHD molten metal reflux system, such as an MHD return conduit 310, MHD return reservoir 311, MHD return EM pump 312 and MHD return EM tube. Alternatively, the SunCell® or at least one component can be heated in an oven, such as an oven known in the art. In an embodiment, at least one SunCell® component can be heated for at least a startup operation. The heater can be a resistive heater or an inductively coupled heater. In one embodiment, the heat of the low energy hydrogen reaction can be heated at a SunCell® component. In an exemplary embodiment, a heater such as an inductively coupled heater heats the EM pump tube 5k6, the reservoir 5c, and at least the bottom of the reaction cell chamber 5b31. At least one other component may be heated by heat release from a low energy hydrogen reaction, such as the top of reaction cell chamber 5b31, MHD nozzle 307, MHD channel 308, MHD condensing portion 309, and MHD molten metal reflux system. At least one of the MHD molten metal reflux systems such as the MHD return conduit 310, the MHD reflux reservoir 311, the MHD return EM pump 312, and the MHD return EM tube. In an embodiment, the MHD molten metal reflow system such as the MHD return conduit 310, the MHD reflux reservoir 311, the MHD return EM pump 312, and the MHD return EM tube may be heated with a high temperature molten metal or metal vapor such as molten silver or steam. The high temperature molten metal or metal vapor has a temperature of from about 1000 ° C to 7000 ° C, from 1100 ° C to 6000 ° C, from 1100 ° C to 5000 ° C, from 1100 ° C to 4000 ° C, from 1100 ° C to 3000 ° C, from 1100 ° C to 2300 ° C, from 1100 ° C to Temperatures in at least one of 2000 ° C, 1100 ° C to 1800 ° C, and 1100 ° C to 1500 ° C. High temperature molten metal or metal vapor can cause flow through the MHD assembly in the event of bypass or deactivation of MHD conversion to electricity. Disabling can be accomplished by removing the electric field or by electrically shorting the electrodes. In an embodiment, at least one component of the battery and the MHD converter can be insulated to prevent heat loss. At least one of the groups of the following may be insulated: a chamber 5b31, an MHD nozzle portion 307, an MHD generator portion 308, an MHD condensation portion 309, a return conduit 310, a return reservoir 311, a return EM pump 312, and The EM pump tube 313 is returned. Heat loss from the insulation can be dissipated in the corresponding cooler or heat exchanger. In an embodiment, a working fluid such as silver can act as a coolant. The EM pump injection rate can be increased to provide silver absorbing heat to cool at least one battery or MHD assembly, such as MHD nozzle 307. The gasification of silver cools the nozzle MHD 307. The circulator or reheater can contain a working medium for cooling. In an exemplary embodiment, silver is pumped through the component to be cooled, which is injected into the reaction cell chamber and the MHD converter to recover heat while providing cooling. At least the high pressure components such as the reservoir 5c, the reaction cell chamber 5b31, and the high pressure portion of the MHD converters 307 and 308 can be held in the pressure chamber 5b3a1 including the housings 5b3a and 5b3b. The pressure chamber 5b3a1 can be maintained under pressure to at least counterbalance at least a portion of the high internal reaction chamber 5b31 and the MHD nozzle 307 and the MHD generator passage 308. Pressure equalization can reduce the tension on the joints of the generator assembly, such as between the reservoir 5c and the EM pump assembly 5kk. The high pressure vessel 5b3a can selectively house a high pressure component, such as at least one of the reaction cell chamber 5b31, the reservoir 5c, and the MHD expansion channel 308. Other battery components can be housed in a low pressure vessel or housing. Such as H2 O, H2 CO2 The source of the low energy hydrogen reactant of at least one of the CO and the CO is permeable through at least one of the permeable battery assembly, such as the tank chamber 5b31, the reservoir 5c, the MHD expansion passage 308, and the MHD condensation portion 309. The low energy hydrogen reactive gas may be introduced to at least one of the low energy hydrogen reaction gas, such as via the EM pump tube 5k6, the MHD expansion channel 308, the MHD condensation portion 309, the MHD return conduit 310, the reflux reservoir 311, the MHD return pump 312, the MHD return EM pump tube 313 In the molten metal stream in the position. A gas injector, such as a mass flow controller, can be capable of being injected at a high pressure on the high pressure side of the MHD converter, such as via at least one of an EM pump tube 5k6, an MHD return pump 312, and an MHD return EM pump tube 313. The gas injector may be capable of injecting a low energy hydrogen reactant at a lower pressure, such as via the MHD condensation portion 309, the MHD return conduit 310, and the reflux reservoir 311, on a low pressure side of an MHD converter, such as at least one location. In an embodiment, at least one of water and water vapor may be injected by the fluid controller via the EM pump tube 5k4, the flow controller may further comprise a pressure trap and prevent molten metal from flowing back to the water supply (such as The reverse flow check valve in the mass flow controller can spray water via a selectively permeable membrane such as a ceramic or carbon membrane. In an embodiment, the converter can include a PV converter, wherein the low energy hydrogen reactant injector can supply reactants by at least one of means such as by infiltration or injection at a transfer position operating pressure. In another embodiment, the SunCell® can further comprise a source of hydrogen and a source of oxygen, wherein the two gases are combined to provide water vapor in the reaction cell chamber 5b31. The hydrogen source and the oxygen source may each comprise at least one of a corresponding tank, a gas flowing directly or indirectly to the reaction cell chamber 5b31, a flow regulator, a flow controller, a computer, a flow sensor, and at least one valve. . In the latter case, the gas can flow continuously into the chamber by the reaction cell chamber 5b31, such as the EM pump 5ka, the reservoir 5c, the nozzle 307, the MHD channel 308, and other MHD. At least one of a converter assembly, such as any return line 310a, conduit 313a, and pump 312a. In an embodiment, H can be2 And O2 At least one of the injectors is injected into the injection portion of the EM pump tube 5k61. Injection of O through a separate EM pump tube of a dual EM pump injector2 And H2 . Alternatively, a gas such as at least one of oxygen and hydrogen may be added to the interior of the battery via an ejector in an area having a lower silver vapor pressure, such as MHD channel 308 or MHD condensing portion 309. At least one of hydrogen and oxygen may be injected via a selective membrane such as a ceramic membrane, such as a nanoporous ceramic membrane. Oxygen can be supplied via an oxygen permeable membrane such as Bi26 Mo10 O69 BaCo coated to increase oxygen permeability0 . 7 Fe0 . 2 Nb0 . 1 O3 - δ (BCFN) One of the present inventions for oxygen permeable membranes. Hydrogen gas may be supplied via a hydrogen permeable membrane such as a palladium-silver alloy membrane. SunCell® can include electrolyzers such as high pressure electrolyzers. The electrolyser can comprise a proton exchange membrane wherein pure hydrogen can be supplied by the cathode compartment. Pure oxygen can be supplied through the anode compartment. In an embodiment, the EM pump component is coated with a non-oxidized coating or an oxidative protective coating and two mass flow controllers are used (where the flow can be controlled based on the battery concentration sensed by the corresponding gas sensor) Hydrogen and oxygen are separately injected under controlled conditions. In one embodiment, at least one component of the SunCell® and the MHD converter including the internal compartment (such as the reservoir 5c, the reaction cell chamber 5b31, the nozzle 307, the MHD channel 308, the MHD condensation portion 309, and other MHD conversions) The components (such as any return line 310a, conduit 313a, and pump 312a) are housed in a gas-tight housing or chamber with internal diffusion through a membrane that is permeable to gases and impermeable to silver vapor. The gas in the cell balance chamber. The gas selective membrane may comprise a semipermeable ceramic, such as one of the present inventions. The cell gas may comprise at least one of hydrogen, oxygen, and a noble gas such as argon or helium. The outer housing can include a pressure sensor for each gas. SunCell® can include sources and controllers for each gas. Sources of rare gases such as argon may comprise a sump. A source of at least one of hydrogen and oxygen may comprise an electrolyzer, such as a high pressure electrolyzer. The gas controller can include at least one of a flow controller, a gas regulator, and a computer. The gas pressure in the housing can be controlled to control the gas pressure of each gas in the interior of the battery, such as in the reservoir, the reaction cell chamber, and the MHD converter assembly. The pressure of each gas may range from about 0.1 Torr to 20 atm. In one exemplary embodiment shown in FIGS. 2I179 through 2I195, the linear MHD channel 308 and the MHD condensing portion 309 include a gas housing 309b, a pressure gauge 309c, and a gas supply and evacuation assembly 309e that incorporates The gas line, the air outlet line and the flange, wherein the gas permeable membrane 309d can be installed in the wall of the MHD condensation portion 309. The mount may comprise sintered joints, metallized ceramic joints, brazed joints or others of the present invention. The gas housing 309b can further include an access port. Gas housing 309b may comprise a metal such as an oxidation resistant metal (such as SS 625) or an anti-oxidation coating on a metal (such as a tantalum coating on a metal suitable for CTE (such as molybdenum)). Alternatively, the gas housing 309b may comprise a ceramic such as a metal oxide ceramic such as zirconia, alumina, magnesia, yttria, quartz or the other of the present invention. Ceramics that penetrate through the metal gas housing 309b (such as the MHD return conduit 310) can be cooled. The penetration may comprise a carbon seal wherein the sealing temperature is below the carbonization temperature of the metal and the carbon reduction temperature of the ceramic. The seal can be removed for hot molten metal to cool it. The seal may include cooling, such as passive or pressurized air or water cooling. In an exemplary embodiment, the inductively coupled heater antenna 5f may include a coil, three separate coils as shown in FIGS. 2I178 through 2I179, three consecutive coils as shown in FIGS. 2I182 through 2I183, Two separated coils or two consecutive coils as shown in Figures 2I180 through 2I181. An exemplary inductively coupled heater antenna 5f includes an upper elliptical coil and a lower EM pump tube pie coil, and the lower EM pump tube pie coil may include a spiral coil, which may include a concentric box having a continuous circumferential current direction (Fig. 2I180 to Figure 2I181). The reaction cell chamber 5b31 and the MHD nozzle 307 can comprise planar, polygonal, rectangular, cylindrical, spherical or other desired geometries, as shown in Figures 2I162 through 2I195. The inductively coupled heater antenna 5f can comprise a continuous set of three turns including two spirals surrounding each reservoir 5c and a pie coil parallel to the EM pump tube, as shown in Figures 2I182 through 2I183. The turns of the opposing spirals around the reservoir can be wound such that the currents are in the same direction to strengthen the magnetic fields of the two coils or in opposite directions to eliminate the magnetic field in the space between the spirals. The inductively coupled heater antenna 5f can be further used to cool at least one component, such as at least one of the EM pump 5kk, the reservoir 5c, the wall of the reaction cell chamber 5b31, and the yoke of the induction ignition system. The at least one cooling component may comprise a ceramic, such as one of the present invention, such as tantalum nitride, quartz, alumina, zirconia, magnesia or yttria. The SunCell® may comprise an MHD working medium return conduit from the end of the MHD expansion channel to the reservoir 5c, wherein the reservoir 5c may comprise a sealed cap that will lower the pressure and higher in the reservoir The reaction cell chamber 5b31 is pressure-separated. The EM pump injector portion 5k61 and the nozzle 5q can penetrate the cover to spray molten metal, such as silver in the reaction cell chamber 5b31. Penetration may include the seal of the present invention, such as a compression seal, a sliding nut, a gasket braze, or a fill box seal. The accumulator may include a water riser 5qa to control the molten metal content of the accumulator 5c. The covered reservoir and the EM pump assembly 5kk receiving the flow of reflowed molten metal may comprise a first injector of a dual molten metal injector system. The second injector comprising the second reservoir and the EM pump assembly can include an open reservoir that indirectly receives backflow from the first injector. The second injector can include a positive electrode. The second injector maintains the molten metal content immersed in the reservoir. The submerged riser 5qa can control the immersion. The SunCell® can include at least one gaseous metal return conduit 310 from the end of the MHD generator channel 308 to at least one reservoir 5c of the molten metal injector system. The SunCell® can include two return conduits 310 from the end of the MHD generator channel 308 to the two corresponding reservoirs 5c of the dual molten metal injector system. Each reservoir 5c can include a sealed top cover that pressure separates the lower pressure in the reservoir 5c from the higher reaction cell chamber 5b31. The EM pump injector portions 5ka and 5k61 and the nozzle 5q can penetrate the reservoir top cover to spray molten metal, such as silver in the reaction cell chamber 5b31. Penetration may include the seal of the present invention, such as a compression seal, a sliding nut, a gasket, a braze or a fill box seal. Each of the accumulators 5c may include a water inlet pipe 5qa to control the molten metal content in the accumulator 5c. The temperature of the reaction cell chamber 5b31 may be higher than the boiling point of the molten metal such that the liquid metal injected into the reaction cell chamber is vaporized and refluxed via the return conduit 310. The SunCell® can include at least one MHD working medium return conduit 310 from the end of the MHD condenser channel 309 to at least one reservoir 5c of the molten metal injector system. The SunCell® can include two MHD working medium return conduits 310 from the end of the MHD condenser channel 309 to the two corresponding reservoirs 5c of the dual molten metal injector system. Each reservoir 5c can include a sealed top cover that pressure separates the lower pressure in the reservoir 5c from the higher reaction cell chamber 5b31. The EM pump injector portions 5ka and 5k61 and the nozzle 5q can penetrate the reservoir top cover to spray molten metal, such as silver in the reaction cell chamber 5b31. Penetration may include the seal of the present invention, such as a compression seal, a sliding nut, a gasket, a braze or a fill box seal. Each of the accumulators 5c may include a water inlet pipe 5qa to control the molten metal content in the accumulator 5c. The temperature of the reaction cell chamber 5b31 may be higher than the boiling point of the molten metal, so that the liquid metal injected into the reaction cell chamber is vaporized, the vapor is accelerated by the MHD nozzle portion 307, and the kinetic energy of the vapor is converted into the generator channel 308. The electricity, vapor is condensed in the MHD condenser portion 309, and the molten metal is refluxed via the return conduit 310. The SunCell® can include at least one MHD working medium return conduit 310, a return reservoir 311, and a corresponding pump 312. Pump 312 can include an electromagnetic (EM) pump. The SunCell® can include a dual molten metal tube 310, a reflux reservoir 311, and a corresponding EM pump 312. The molten metal content in each of the reflux accumulators 311 can be controlled corresponding to the inlet riser 5qa. The return EM pump 312 can pump the MHD working medium from the end of the MHD condenser channel 309 to the return reservoir 311 and then to the corresponding injector reservoir 5c. In another embodiment, the molten metal is recirculated directly via the return conduit 310 to the corresponding reflux EM pump 312 and then to the corresponding injector reservoir 5c. In one embodiment, an MHD working medium, such as silver, is pumped for a pressure gradient (such as about 10 atm) to complete the molten metal flow circuit, including injection, ignition, expansion, and reflow. To achieve high pressure, the EM pump can contain a range of levels. The SunCell® may comprise a dual molten metal injector system comprising a pair of reservoirs 5c each comprising an EM pump injector 5ka and 5k61 and an inlet riser 5qa for controlling the corresponding reservoir 5c Molten metal content. The return can enter the base 5kk1 of the corresponding EM pump assembly 5kk. In one embodiment, the velocity of the working medium in at least one location (including the location in the MHD assembly, such as the inlet of the nozzle, the nozzle, the outlet of the nozzle, and the desired portion of the MHD channel) may be sufficiently high that even if the metal is satisfied In the case of vapor saturation conditions, condensation (such as impingement condensation) does not occur. Condensation may not occur due to the shorter transition time compared to the condensation time. The condensing kinetics can be altered or selected by controlling plasma pressure, plasma temperature, jet velocity, working medium composition, and magnetic field strength. Metal vapor, such as silver vapor, can condense on condenser 309, which can have a relatively high surface area, and the collected liquid silver can be recirculated via a return conduit and an EM pump system. In one embodiment, a shorter transition time in the nozzle that avoids impact condensation is utilized to allow for the creation of favorable MHD transition conditions in the MHD channel 307 that would otherwise cause impact condensation. In an embodiment, it is also known that the MHD expansion or generator channel as the MHD channel includes a flared MHD channel to continuously derive a capability transition in which the thermal gradient is converted to a pressure gradient that drives the kinetic energy flow. The heat from the condensation of the silver can contribute to the pressure gradient or mass flow in the MHD channel. The heat of vaporization released by the condensed silver acts as a post-combustor in the jet engine to produce a higher velocity flow. In an exemplary embodiment, the heat of silver vaporization acts as a combustion function in a jet afterburner to increase or contribute to the speed of the silver jet stream. In one embodiment, the heat of vaporization released by the condensed silver vapor is increased by a pressure that is higher than the pressure in the absence of condensation. The MHD channel may contain geometry (such as a flash flame or nozzle geometry) to convert the pressure into steered energy that is directed or converted to electricity by the MHD converter. The magnetic field provided by the MHD magnet 306 can be adjusted to prevent the plasma from stagnating if the silver vapor changes condensation by a corresponding conductivity. In one embodiment, the walls of the MHD channel 308 are maintained at a high temperature to prevent metal vapor from condensing onto the wall by corresponding mass and kinetic energy losses. Higher electrode temperatures also prevent plasma arcing, which can occur in contrast to cooling electrodes that have less conductive or more insulating boundary layers relative to the hotter plasma. The MHD channel 308 can be maintained at the desired elevated temperature by transferring heat from the reaction cell chamber 5b31 to the wall of the MHD channel. The MHD converter can include a heat exchanger that transfers heat from the reaction cell chamber to the wall of the MHD channel. The heat exchanger can comprise a conductive or convection heat exchanger, such as a heat exchanger comprising a heat transfer block that transfers heat from the reaction cell chamber to the wall of the MHD channel. The heat exchanger can include a radiant heat exchanger, wherein at least a portion of the outer wall of the reaction cell chamber includes a black body radiator to emit power and at least a portion of the wall of the MHD channel can include a black body radiator to absorb black body radiation. The heat exchanger can include a coolant that can be pumped. The pump may comprise an EM pump wherein the coolant is molten metal. In another embodiment, the low energy hydrogen reaction is further propagated and held in the MHD channel 308 to maintain the MHD channel wall temperature above the condensation temperature of the metal vapor flowing in the channel. The low energy hydrogen reaction can be maintained by supplying reactants such as H and HOH catalysts or sources thereof. The reaction can be selectively held at the electrode due to its support and promotion of conductivity at low energy hydrogen reaction rates. The MHD converter can include at least one temperature sensor that records the temperature of the MHD channel wall and a controller that controls at least one of the heat transfer members (such as a heat exchanger) and a low energy hydrogen reaction rate that maintains the desired MHD channel wall temperature . The low energy hydrogen reaction rate can be controlled by means of the present invention, such as a member that controls the flow of low energy hydrogen reactants to the MHD channel. In another embodiment, at least one of the plasma, metal vapor, and condensed metal vapor is confined in the channel and is prevented by a channel limiting member, such as a member comprising a source of at least one of electrical and magnetic fields. Collected on the MHD wall. The restraining member may comprise a magnetic limiting member, such as a magnetic bottle. The restriction member can include a field that is coupled inductively, such as an RF field. The MHD converter can include at least one of an RF power source, at least one antenna, an electrostatic electrode and a power source, and at least one source of magnetostatic magnetic fields to achieve a limit. In one embodiment, the working medium comprises a vaporized metal in the MHD channel 308, wherein the pressure and temperature of the working medium are increased by the heat released by condensing the metal vapor along the MHD channel because it is lost due to the conversion of the MHD to electricity. kinetic energy. The energy from the condensation of silver can increase at least one of the pressure, temperature, velocity, and kinetic energy of the working medium in the MHD channel. The flow rate can be increased by utilizing the channel geometry of the Venturi effect or the Bernoulli principle. In an embodiment, the flowing liquid silver can act as an aspirator medium for the vapor such that it flows in the MHD channel. In one embodiment, at least one of the diameter and volume of the MHD channel 308 is reduced according to the distance along the flow or z-axis of the MHD channel from the outlet of the nozzle 307 to the outlet of the MHD channel 308. The MHD channel 308 can include channels that only aggregate the z-axis. In another embodiment, the channel size along the z-axis remains the same and diverges less than the channel size of a conventional seeded gas MHD working medium converter. When the silver condenses and releases heat to maintain high energy plasma, the channel volume can be reduced to maintain pressure and velocity along the z-axis. The vaporization heat released from the condensed silver vapor (254 kJ/mole) by the plasma flow along the z-axis increases the temperature and pressure of the working medium to increase non-condensed silver at any given position along the z-axis of the channel. flow. The increase in flow rate can be caused by the Venturi effect or the Bernoulli principle. The magnetic flux can be permanently or dynamically varied along the flow axis (z-axis) of the MHD channel to extract the MHD power as a function of the z-axis position to maintain the desired pressure, temperature, velocity, power, and energy inventory along the channel, with The channel size as a function of the distance of the shaft can match the z-axis flux variation to at least partially achieve the energy of the vaporized metal self-extracting heat of vaporization as electrical power. The plasma gas stream can also act as a carrier gas for the condensed silver vapor. The condensed silver may contain mist or mist. The fog state can be advantageous due to the tendency of the silver to form an aerosol at temperatures well below its boiling point at the given pressure. The working medium can comprise oxygen and silver, wherein the molten silver has a tendency to form an aerosol in the presence of oxygen at a temperature well below its boiling point at a given pressure, wherein the silver can absorb a significant amount of oxygen. The working medium may comprise an aerosolizing gas such as nitrogen, oxygen, water vapor or a rare gas such as argon, other than a metal vapor such as a silver vapor that forms an aerosol of condensed silver. In one embodiment, the pressure of the aerosolized gas throughout the reaction cell chamber and the MHD channel can be maintained at its steady state distribution under operating conditions. The MHD converter may further comprise a supply of aerosolized gas, such as a reservoir of aerosolized gas, a pump, and at least one gauge that selectively measures the pressure of the aerosolized gas at one or more locations. The pump and aerosolized gas supply can be used to maintain the aerosolized gas inventory at the desired level by adding or removing an aerosolized gas. In an exemplary embodiment, the liquid silver forms a mist or aerosol at a temperature only above the melting point such that a constant ambient pressure aerosolized gas (such as argon) in the MHD channel 308 causes the silver vapor to liquid to gas The form of the sol occurs, which can carry a plasma flow and collect on the MHD condenser 309. In one embodiment, the rate of condensed vapor is stored in the condensate. The velocity of the condensate can be increased by the release of heat of vaporization. The MHD channel can include a geometry that converts vaporization heat into condensate kinetic energy. In an embodiment, the passage may be narrow to convert vaporization heat to condensate kinetic energy. In another embodiment, the heat of vaporization increases the channel pressure and the pressure is converted to kinetic energy by the nozzle. In an embodiment, the copper or silver-copper alloy can replace silver. In one embodiment, the molten metal that serves as a source of metal aerosol comprises at least one of silver, copper, and a silver-copper alloy. The aerosol can be formed in the presence of a gas such as at least one of oxygen, water vapor, and a noble gas such as argon. In one embodiment, the SunCell® comprises means for maintaining the flow of the cell gas in contact with the molten silver to form a molten metal aerosol, such as a silver aerosol. The gas stream can comprise at least one of a pressurized gas stream and a convective gas stream. In an embodiment, at least one of the reaction cell chamber 5b31 and the reservoir 5c may include at least one baffle to circulate the cell gas to increase gas flow. The flow may be driven by at least one of convection and pressure gradients, such as caused by at least one of a heat gradient and a pressure from the plasma reaction. Gases can contain rare gases, oxygen, water vapor, H2 And O2 At least one of them. The means for maintaining the gas flow may comprise at least one of a gas pump or a compressor, such as an MHD air pump or compressor 312a, an MHD converter, and a disturbance caused by at least one of an EM pump molten metal injector and a low energy hydrogen plasma reaction. flow. At least one of the gas flow rate and the composition can be controlled to control the rate of aerosol production. In one embodiment, wherein the water vapor is recycled, SunCell® further comprises heating to H2 And O2 Any H2 O reorganized into H2 a recombinator of O, a condenser that condenses water vapor to liquid water, and a liquid water pump that injects pressurized water into a line supplying at least one internal battery component, such as a reservoir 5c or a reaction cell chamber 5b31, wherein the pressurized water can be converted to steam in the path to be sprayed inside the battery. The recombiner can be a recombiner known in the art, such as a recombiner comprising at least one of Raney nickel, Pd, and Pt. The water vapor may be recirculated in a circuit comprising a high pressure compartment, such as between the reaction cell chamber 5b31 and the reservoir 5c. In one embodiment, at least one of the reservoir 5c and the reaction cell chamber 5b31 comprises a source of gas having a sufficiently low temperature to perform at least one of: condensing the silver vapor into a silver aerosol and cooling the silver Aerosol. Silver vapor is formed by the heat released by the high energy and low energy hydrogen reaction. Gasification can occur in low energy hydrogen reactive plasma. The ambient gas in contact with the low energy hydrogen contains the cell gas. Part of at least one of the cell gas and the aerosol may be heat exchanged within the region of at least one of the reservoir containing at least one of the gas aerosol and the plasma and the chamber of the reaction cell Cooler and chiller. At least one of the cell gas and the aerosol may be sufficiently cooled to perform at least one of: condensing the silver vapor into an aerosol and cooling the aerosol. At least one of the vapor condensation rate and the temperature and pressure of the cooled cell gas-aerosol-vapor mixture can be controlled by controlling the heat transfer during cooling and cooling the temperature and pressure of the cell gas and aerosol. In one embodiment, to avoid mass loss along the channel, the silver vapor causes fog to form upon condensation of the vapor. The mole fraction of kinetic energy that loses its power along the channel can result in the formation of a mist in which the corresponding vaporization heat imparts kinetic energy to the corresponding aerosol particles to maintain a constant initial velocity of otherwise lost mass. Since a portion of the atoms are polymerized into aerosol particles that flow with the remaining gas atoms, the channels can be in a straight line to maintain a rate that is accompanied by a reduced number of particles. In an embodiment, the walls of the MHD channel 308 can be maintained at a temperature such as greater than the melting point of silver to avoid condensation formation by the condensed liquid by supporting the mist. In one embodiment, the silver plasma spray contact MHD channel assembly and surface may comprise a material that is resistant to wetting by a silver liquid. At least one of the MHD channel wall 308 and the MHD electrode 304 can comprise a surface that is resistant to wetting. Aerosol particles can be charged and collected. Collection can occur at the end of the MHD channel. The aerosol particles can be removed by electrostatic precipitation or electrospray precipitation. In an embodiment, the MHD converter may comprise an aerosol particle charging member (such as at least one particle charging electrode), an electrical energy supply source (such as a high voltage source), and an electrical bias to collect charged particle charged particle collectors (such as at least One electrode). Charged particles can be collected at the end of the MHD channel by applying an electric field. In one embodiment, the metal vapor droplets are carried out by a plasma flow. The droplets may form a film on the surface of at least one of the MHD electrode and the MHD channel wall. The surplus condensed liquid can be mechanically ablated and carried by the plasma and mass flow. In one embodiment, the Faraday current passes through a condensed metal vapor (such as condensed silver vapor) and produces a Hall current that causes a trajectory of the condensed silver particles along the plasma jet from the MHD nozzle 307. The Hall current allows the condensed silver to flow out of the MHD channel to reflux to the reservoir 5c. Due to the higher conductivity than the metal vapor, current can preferably flow through the condensed silver. In another embodiment, the delivery may be assisted by at least one of divergence and convergence of the MHD channel. In an embodiment, an MHD converter such as a disk generator may include an electrode that contacts the plasma at the inlet and outlet of the MHD channel to improve the effect of shorting of the molten metal in the channel. In one embodiment, the working medium comprises a metal (such as silver) that can sublime at a temperature below its boiling point to prevent metal from condensing on the walls of the MHD channel such that it flows to the recirculation system. In one embodiment, the pressure at the outlet of the MHD channel is maintained at a low pressure (such as a pressure below atmospheric pressure). The vacuum can be maintained at the exit of the MHD channel such that the working medium metal vapor does not condense in the MHD channel 308. The vacuum can be maintained by an MHD air pump or compressor 312a (Fig. 2I67 to Fig. 2I73). In an embodiment, the MHD channel may include a generator in the inlet portion and a compressor in the outlet portion. The compressor can cause the condensed vapor to be pumped out of the MHD channel. The MHD converter can include a current source and a current controller to controllably apply a current to the working medium of the MHD channel in a vertical direction of the applied magnetic field such that the condensed working medium vapor flows from the channel, wherein the channel condition can be Control is such that the vapor condenses to effect the release of vaporization heat of the vapor. In another embodiment, the vaporization heat of the metal vapor, such as silver metal vapor, may be condensed by condensing the vapor at a heat exchanger such as MHD condenser 309. Condensation can occur at temperatures above the boiling point of the metal such as silver. Heat can be transferred to a portion of the reservoir 5c by means known in the art, such as by convection, conduction, radiation, or by a coolant. The heat transfer system can include a refractory heat transfer block that transfers heat by conduction, such as Mo, W or carbon blocks. Heat can vaporize the silver in the reservoir. Heat can be stored in the heat of vaporization. The low energy hydrogen reaction can further increase the pressure and temperature of the vaporized metal. In one embodiment comprising a working medium additive, such as a rare gas, such as argon or helium, the MHD converter further includes a gas pump or compressor 312a (Fig. 2I67 through Fig. 2I73) to recycle gas from low pressure to MHD conversion The high voltage part of the device. The air pump or compressor 312a can include a drive motor 312b and a scraper or vane 312c. The MHD converter can include a pump inlet and a pump outlet, the pump inlet can include a gas passage 310a from the MHD condensing portion 309 to the pump inlet, the pump outlet can include a gas passage from the pump or compressor 312a to the reaction cell chamber 5b31 313a. The pump can pump gas from a low pressure, such as about 1 to 2 atm, to a high pressure (such as about 4 to 15 atm). The inlet pipe 310a from the MHD condensing portion 309 to the pump 312a may include a filter, such as a selective membrane or metal condenser at the inlet, to separate a gas, such as a rare gas, from a metal vapor, such as silver vapor. The baffle 309a in the MHD condenser portion 309 can direct molten metal, such as molten metal condensed in the MHD condensing portion 309, into the MHD return conduit 310. At least one of the height of the baffle in the center and the molten metal return inlet of the MHD return conduit 310 may be at a position where the rising gas pressure exceeds the force of gravity on the condensed or liquid molten metal particles to facilitate its flow into the MHD Return to the conduit 310. The SunCell® can include a metal vapor condenser (such as a constant pressure condenser) that can be located in the MHD condensation section 309 and can include a heat exchanger 316. The working medium may comprise a carrier of a metal vapor seed or a working gas, such as a rare gas of silver vapor seed, such as helium or argon. The condenser can condense the metal vapor so that the liquid metal and the rare gas can be pumped separately. Separation can be accomplished by at least one of the following methods: gravity deposition, centrifugation, cyclonic separation, filtration, electrostatic precipitation, and other methods known to those skilled in the art. In an exemplary embodiment, the separated rare gas is removed from the top of the condenser and the separated liquid metal is removed from the bottom of the condenser. The liquid and gas may be separated by at least one of: a baffle 309a, a filter, a selectively permeable membrane, and a liquid barrier through which the gas may pass. The compressor 312a can pump gas or recirculate the gas to the reaction cell chamber 5b31. The EM pump 312 can pump liquid silver to return it to the reservoir 5c for reinjection into the reaction cell chamber 5b31. The compressor 312a and the EM pump 312 are respectively pressurized with a working medium gas such as argon or helium and a liquid metal such as liquid silver. The working medium gas can be returned to the reaction cell chamber via conduit 313a, which can connect at least one of the EM pump tube 5k6, the reservoir 5c, the base 5kk1 of the EM pump assembly 5kk, and the reaction cell chamber 5b31. Alternatively, the gas may be returned to the reaction cell chamber 5b31 via the tube 313a, which is connected to the transfer tube 313b, such as a transfer tube provided to the reservoir 5c or the guide passage in the reaction cell chamber 5b31. Gas can be used to inject molten metal into the reaction cell chamber. The molten metal can become entrained in the gas jet to replace or supplement the EM pump molten metal injector. Controlled sprayed molten metal and vapor by controlling gas flow rate, gas pressure, gas temperature, reservoir temperature, reaction cell temperature, nozzle inlet pressure, MHD nozzle flow rate, MHD nozzle outlet pressure, and low energy hydrogen reaction rate Flow rate (such as liquid and gaseous silver vapor). A return conduit 313b for at least one of a working medium gas and a molten metal, such as a working medium gas and molten metal extending through the molten metal of the reservoir 5c, may comprise a refractory material such as Mo, W, 铼, Bi-coated Mo or W, ceramic (such as metal oxides, such as ZrO2 HfO2 , MgO, Al2 O3 At least one of the above and others of the present invention. The tube may comprise a refractory tube threaded into a collar or base in the EM pump tube assembly base 5kk1. The height of the return conduit 313b may be such that the desired performance of the other components (such as metal propellant) is allowed while the gas is being delivered, and the content is controlled by the injection portions of the EM pump tube 5k61 and the inlet riser 5qa, respectively. The height may be about the reservoir molten metal content. In one embodiment shown in Figures 2I71 through 2I73, the air pump or compressor 312a can pump a mixture of gaseous working medium species such as rare gases, molten metal seeds, and molten metal vapors (such as silver). At least two of the vapors. In an embodiment, the air pump or compressor 312a can pump both gaseous and liquid working media, such as at least one of a noble gas, a metal vapor, and a liquid molten metal, such as liquid silver. The liquid and gas may be returned to the reaction cell chamber via tube 313a, which may connect at least one of the EM pump tube 5k6, the reservoir 5c, the base 5kk1 of the EM pump assembly 5kk, and the reaction cell chamber 5b31. Alternatively, the gas may be returned to the reaction cell chamber 5b31 via the tube 313a, which is connected to the transfer tube 313b, such as a transfer tube provided to the reservoir 5c or the guide passage in the reaction cell chamber 5b31. In an embodiment, the gas and liquid may flow through the EM pump tube 5k6. Gas can be used to inject molten metal into the reaction cell chamber. The molten metal may become entrained in the gas injection to perform at least one of: energizing and replacing the EM pump to pump the molten metal via the injector tube 5k61 and the nozzle 5q. The rate of injection can be controlled by controlling at least one of the flow rate and pressure of the air pump or compressor 312a and by other means of the present invention. The molten metal content of the reservoir 5c can be controlled by the horizontal sensor and controller of the present invention that controls at least one of the pressure and flow rate of an air pump or compressor 312a relative to the other pair. In an embodiment of a gas pump or compressor comprising pumping all working medium (such as a rare gas of silver seeds) and an embodiment comprising a gas pump or compressor pumping only rare gases, the compression can be operated isothermally. The MHD converter can include at least one of a heat exchange or a chiller: cooling the gaseous working medium before and during compression. The air pump or compressor may include an intercooler. The air pump or compressor may comprise a plurality of levels, such as a multi-stage intercooler compressor. Cooling increases the efficiency of the compressed gas to match the operating pressure of the reaction cell chamber 5b31. After the pumping phase in the reflux cycle, the refluxing gaseous working medium can be heated to increase its pressure. Heating may be accomplished by a heat exchanger that receives heat from the MHD converter or a regenerator that may receive heat from the MHD condensing portion 309 or other thermal components, such as at least one of the following groups: reaction cell chamber The chamber 5b31, the MHD nozzle portion 307, the MHD generator portion 308, and the MHD condensing portion 309. In one embodiment, the pump power can be substantially reduced by using inlet and outlet valves for the gas flowing into the reaction cell chamber 5b31 and out of the MHD nozzle, respectively, wherein the low pressure gas is pumped to the reaction cell chamber. The pressure in the chamber is increased by the plasma reaction power to the desired pressure, such as 10 atm. The resulting pulsed MHD power can be adjusted to stabilize DC or AC power. The reflux MHD gas tube 313a may include a valve that opens to permit a gas flow at a lower pressure than the peak reaction cell chamber operating pressure, and the MHD nozzle portion 307 may include an opening to allow the high pressure gas to pass through the reaction cell chamber 5b31 The plasma flows out of the nozzle valve after heating the gas. The valve may assist in injecting low pressure gas into the reaction cell chamber by means of a gas pump or compressor, wherein the gas is heated to a high pressure by a low energy hydrogen reaction plasma. The valves can be synchronized to permit the accumulated reaction chamber pressure by plasma heating. The valve can be 180° out of phase. The valve can include a rotary stop type. The MHD nozzle can be cooled to permit operation of the MHD nozzle valve. The return gas line 313a valve may be at or near the base of the EM pump assembly 5kk1 to avoid condensation of silver in the corresponding gas delivery tube 313b. The MHD converter may include a pulsed power system including a power system that processes an inlet valve and an outlet valve of the working medium gas of the electrolytic cell chamber 5b31. The pulsed MHD power can be leveled to output a constant power by a power conditioning device, such as a device containing power storage, such as a battery pack or capacitor. In one embodiment, the recycled molten metal (such as silver) is still in a gaseous state, including the temperature of the MHD converter of any return line 310a, tube 313a, and pump 312a at the operating pressure or silver partial pressure in the MHD system. Maintain a temperature above the boiling point of silver. Pump 312a may comprise a mechanical pump, such as a gear pump (such as a ceramic gear pump), or other pump known in the art, such as a pump containing an impeller. Pump 312a can be operated at elevated temperatures, such as in a temperature range of about 962 °C to 2000 °C. The pump may comprise a turbine type, such as a turbine for a gas turbine or a turbine of the type used as a turbocharger for an internal combustion engine. The air pump or compressor 312a can include at least one of a screw pump, an axial compressor, and a turbine compressor. The pump can contain a positive displacement type. The air pump or compressor can convert a higher gas velocity that is converted to pressure in the fixed reaction cell chamber volume according to Bernoulli's law. The return gas line 313a can include a valve, such as a back pressure containment valve, to force fluid from the compressor to flow into the reaction cell chamber and then the MHD converter. Mechanical components that are susceptible to wear by the working medium, such as the pump 312a bucket or turbine blade, may be coated with molten metal, such as molten silver, to prevent wear or wear. In one embodiment, at least one component of a gas and molten metal reflux system comprising a gas pump or compressor (such as MHD return conduit 310a, reflux reservoir 311a, MHD return gas pump or compressor 312a in contact with return gas and molten metal) Components (such as vanes) and MHD pump tubing 313a (Fig. 2I67 through Fig. 2I73) include at least one function of performing thermal protection and preventing wetting by molten metal to facilitate the flow of reflux metal to the reservoir 5c. In an embodiment, during SunCell® startup, compressor 312a may recirculate a working medium, such as helium or argon, to preheat at least one of reaction cell chamber 5b31 and the MHD assembly, such as the MHD nozzle portion. 307, MHD channel 308, MHD condensing portion 309, and at least one component of an EM return pump system including MHD return conduit 310, reflux reservoir 311, MHD return EM pump 312, and MHD return EM pump tube 313. The working medium can be split to at least one component of the EM return pump system. An inductively coupled heater, such as corresponding to antenna 5f, can heat a working medium that can be recirculated to preheat the reactive electrolysis cell chamber 5b31 and at least one of the at least one MHD assembly. In an exemplary embodiment, the MHD system includes a working medium comprising argon or helium inoculated with silver or inoculated with a silver-copper alloy, most of which may be attributable to argon or helium. The silver or silver-copper alloy mole fraction decreases as the partial pressure of a rare gas (such as argon) controlled by an argon supply, sensing, and control system is increased. The SunCell® can include a cooling system for reacting at least one of the electrolytic cell chamber 5b31 and the MHD assembly, such as the MHD nozzle portion 307, the MHD channel 308, and the MHD condensing portion 309. At least one parameter can be controlled, such as the wall temperature of the reaction cell chamber 5b31 and the MHD channel and the reaction and gas mixing conditions to determine the optimum silver or silver-copper alloy inventory or vapor pressure. In one embodiment, the optimum silver vapor pressure is the silver vapor pressure that optimizes the conductivity and energy inventory of the metal vapor to achieve optimum power conversion density and efficiency. In one embodiment, some metal vapor condenses in the MHD channel to release heat that is converted to additional kinetic energy in the MHD channel and converted to electricity. The pump or compressor 312a may comprise a mechanical pump such as for both silver and argon, or the MHD converter may comprise two pump types, gas 312a and molten metal 312. In an embodiment, the MHD converter can include a plurality of nozzles to produce a high velocity conductive stream of a plurality of levels of molten metal. The first nozzle may include a nozzle 307 coupled to the reaction cell chamber 5b31. Other nozzles may be located at the condensing portion 309 where heat released from the condensed silver may create a high pressure at the inlet of the nozzle. The MHD converter can include an MHD channel with crossed magnets and electrodes downstream of each nozzle to convert the high speed conduction stream to electrical power. In an embodiment, the MHD converter can include a plurality of reaction cell chambers 5b31, such as in a position in close proximity to the aforementioned nozzles. In an embodiment that does not include the reflux reservoir 311, where the end of the MHD channel 309 behaves like the lower hemisphere of the blackbody radiator 5b41, and the backflow EM pump 312 is faster (without limiting the reflow rate), the silver will It is distributed back to the jet reservoir 5c in the same manner as in the black body radiator design of the present invention. The relative injection rate can then be controlled by the inlet riser 5qa of each reservoir 5c, as in the case of the black body radiator design of the present invention. In one embodiment, the SunCell® includes an EM pump at a location downstream of the accelerating nozzle 307 to pump the condensed molten metal back to at least one reservoir of the molten metal injector system, such as an open double molten metal The ejector system 5ka and the reservoir 5c of 6k61. In one embodiment, the SunCell® includes return conduits 310 and 310a, reflux reservoirs 311 and 311a, return EM pump 312 and compressor 312a, open injector reservoir 5c, which are selected by those skilled in the art. Other combinations and configurations of closed ejector reservoir 5c, open EM pump injector section 5k61 and nozzle 5q, and closed EM pump injector section 5k61 and nozzle 5q to achieve MHD working medium via reaction cell chamber The desired flow circuit of the chamber 5b31 and the MHD converter 300. In an embodiment, the molten metal content controller 5qa of any of the reservoirs, such as at least one of the reflux reservoir 311 and the jet reservoir 5c, may include the inlet riser 5qa, others of the invention, and familiarity with At least one of those known to the skilled artisan. In an embodiment, the working medium may comprise a mixture of a gaseous phase and a liquid phase, such as at least one of a liquid metal and at least one gas, such as at least one of a metal vapor and a gas such as a noble gas. Exemplary working media include liquid silver and gaseous silver or liquid silver, gaseous silver, and at least one other gas, such as a rare gas or other metal vapor. In an embodiment, the MHD converter can include a liquid metal MHD (LMMHD) converter, such as a converter known in the art. The LMMHD converter may include a heat exchanger to cause heat to flow from the reaction cell chamber 5b31 to the LMMHD converter. The MHD converter can include a system that utilizes at least one of the Rankine, Brayton, Ericsson, and Allam cycles. In one embodiment, the working medium comprises a high density and maintains a high density relative to the noble gas such that at least one of the recovery of the working fluid and the recirculating pumping is maintained by less expansion of the working fluid and more heat retention. At least one of them is implemented. The working medium can comprise molten metal and its vapors, such as silver and silver vapor. The working medium may further comprise additional metals in at least one of a liquid and a vapor state and other known in the art such as rare gas, steam, nitrogen, Freon, nitrogen, and liquid metal MHD (LMMHD) converters. At least one of the gases of the person. In an embodiment, the MHD converter can include at least one of an EM pump, an MHD compressor, and a mechanical compressor or pump to recirculate the working medium. The MHD converter may further comprise a mixer to mix the liquid with the gas, wherein at least one phase may be heated prior to mixing. Alternatively, the mixed phase can be heated. The hot working medium containing the mixture of phases flows into the MHD channel to generate electricity due to the pressure generated by heating in the working medium. In another embodiment, the liquid may comprise a plurality of liquids, such as a liquid that acts as a conductive substrate (such as silver) and another liquid that has a lower boiling point to act as a gaseous working medium due to its gasification in the reaction cell chamber. . Gasification of metals permits thermodynamic MHD cycling. The electrical energy generated by the two-phase conduction flows in the MHD channel. The working medium can be heated by a heat exchanger to create pressure to provide flow in the passage. The reaction cell chamber can provide heat to the inlet of the heat exchanger to the heat exchanger outlet and then to the working medium. In one embodiment, the low energy hydrogen plasma vapor is mixed with liquid silver in a mixer to form a two phase working medium. Heating produces a high pressure flow of the main molten silver through the MHD channel and the cooler in which thermal kinetic energy is converted to electricity, and the low pressure working medium at the outlet of the MHD channel is recirculated by the MHD EM pump. In one embodiment comprising a mixing cycle (open gas cycle and closed metal cycle), the working medium can comprise at least one of oxygen, nitrogen, and air inoculated with a metal vapor, such as a silver metal vapor. The liquid metal (such as silver) vaporized in the reaction cell chamber 5b31 to contain the gas seed can be condensed after leaving the MHD channel 308 and recycled to the reservoir 5c. The gas leaving the MHD channel, such as air, can be separated from the seed crystal and can be vented to the atmosphere. Heat can be recovered from the exhaust gas. The ambient gas such as air can be drawn in by the gas pump or compressor 312a. In an embodiment, the MHD converter can include a homogeneous MHD generator that includes a metal or metal mixture that is heated to vaporize the metal at the inlet to the MHD channel. The converter may further include a channel inlet heat exchanger to transfer heat from the reaction cell chamber to the working medium such that it vaporizes prior to entering the MHD channel. The homogeneous MHD generator may further include a channel heat exchanger at the outlet of the MHD channel to act as a regenerator to transfer heat to the working medium before it flows to the inlet heat exchanger. The inlet heat exchanger can include a working medium tube that passes through the reaction cell chamber. The metal working medium can be condensed at a condensing heat exchanger downstream of the outlet heat exchanger, wherein the molten metal is then pumped by a recirculating EM pump. In one embodiment, the working medium comprises a metal and a gas that is soluble in the molten metal at low temperatures and insoluble or less soluble in the molten metal at elevated temperatures. In an exemplary embodiment, the working medium can include at least one of silver and oxygen. In one embodiment, the oxygen pressure in the reaction cell chamber is maintained at a pressure that substantially prevents the molten metal, such as silver, from undergoing gasification. The low energy hydrogen reaction plasma heats the oxygen and liquid silver to the desired temperature, such as 3500K. The mixture containing the working medium can flow through the wedge-shaped MHD channel at a pressure such as 25 atm, where the pressure and temperature drop as the thermal energy is converted to electricity. A molten metal such as silver can absorb a gas such as oxygen due to a drop in temperature. The liquid can then be pumped back to the reservoir for recirculation in the reaction cell chamber, wherein the plasma heat releases oxygen to increase the pressure and temperature conditions of the desired cell chamber to drive the MHD transition. In one embodiment, the temperature of the silver at the exit of the MHD channel is about the melting point of the molten metal, wherein the solubility of oxygen is at one atmosphere O.2 Below is about 20 cm of oxygen3 (STP) to 1 cm of silver3 . The recirculating pumping power of the liquid containing the dissolved gas can be much less than the power of the free gas. In addition, the gas cooling requirements and MHD converter volume that reduce the pressure and temperature of the free gas during the thermodynamic power cycle can be substantially reduced. In one embodiment, the MHD channel can be vertical and the pressure gradient of the working medium in the channel can be greater than the pressure equivalent due to the force of gravity, such that the working medium flow of the molten metal remains in the self-reactive cell chamber 5b31 to the MHD channel. In the circulation of the outlet, the molten metal is pumped back to the reservoir 5c. In an embodiment, the minimum pressure P isP = pgh (45) Where p is the density (for silver, 1.05×104 Kg/m3 ), g is the gravity constant, and h is the height of the metal column. For illustrative purposes, h = 0.2 m, P = 0.2 atm. The expansion in nozzle 307 can be isentropic. In one embodiment, the low energy hydrogen reaction conditions in the reaction cell chamber 5b31 provide and maintain a temperature and pressure suitable for the MHD nozzle 307 such that the nozzle can produce a high velocity jet while avoiding condensation shock. At least one of about constant velocity conditions and continuity conditions may be maintained during expansion in the MHD channel 308 (and thus the product of density, velocity, and area is about constant). In an embodiment, ultrasonic silver vapor is ejected at an inlet from MHD nozzle 307 to MHD channel 308. Some silver can condense in the channel, but due to isentropic expansion, condensation can be limited. The residual energy in the jet comprising vapor and any condensed liquid and the heat of vaporization of the silver can be at least partially recovered by condensation at condenser 309 and recycled by a recycler or regenerator such as a heat pipe. In one embodiment, regeneration is achieved using a heat pipe that recovers at least the heat of vaporization of the silver and recycles it such that the recovered heat power is part of the power input to the MHD channel; then the component of the power balance only reduces the heat pipe Efficiency. The percentage of condensed metal vapor can be insignificant, such as in the range of about 1% to 15%. In an embodiment, the condensed vapor can result in the formation of an aerosol. The reaction cell chamber, nozzle, and MHD channel may contain a gas, such as argon, that causes condensation vapor to come from the aerosol. The vapor can condense at the end of the MHD channel 308 at a condenser, such as condenser 309. The liquid metal can be recycled, and the heat of vaporization can be at least partially recovered by a regenerator, such as a regenerator containing a heat pipe. In another embodiment, the vapor may be pressurized to condense in a desired region, such as a portion of nozzle 307. The nozzle expansion can be isentropic, with condensation of pure gas (such as silver vapor) limited to 50% liquid mole fraction starting at the critical temperature and an important pressure of 506.6 MPa and 7480 K for silver, respectively. In an embodiment, this condensation limitation from the expansion of the pressurized vapor can be overcome by means such as removing heat such that the entropy value can be reduced and the at least one of the condensation zones is pressurized with at least one other gas. . The gas pressure may be equal in all portions of the region where gas continuity exists, such as in the regions of reaction cell chamber 5b31, nozzle 307, and MHD channel 308. The MHD converter can further include a reservoir of other gases, a barometer, an air pump, and a gas pressure controller. At least one other gas pressure can be controlled by a pressure controller. The gas pressure can be controlled to condense the metal vapor to a greater extent than the isentropic expansion of the pure metal vapor. In an embodiment, the gas comprises a gas that is soluble in the vapor metal. In an exemplary embodiment the metal comprises silver and the gas comprises O2 And H2 At least one of O. In one embodiment, the pressure in at least one of the nozzle 307 and the MHD channel 308 is achieved by a condensation shock generated when the metal gas phase rapidly condenses onto the liquid metal stream, resulting in a two-phase to single-phase flow. Rapid conversion to release heat of vaporization. The energy release is the kinetic energy that appears as a liquid flow. The kinetic energy of the liquid stream is converted to electricity in the MHD channel 308. In one embodiment, the vapor condenses into a mist or aerosol. The aerosol can be formed in a gaseous ambient atmosphere, such as a gaseous ambient atmosphere comprising an aerosol forming gas such as oxygen and, optionally, a rare gas such as argon. The MHD channel 308 can be linear to maintain a constant velocity and pressure of the MHD channel flow. An aerosol forming gas (such as oxygen) and, optionally, a rare gas (such as argon) may flow through the reservoir 5c, the reaction cell chamber 5b31, the MHD nozzle 307, the MHD channel 308, and other MHD converter components (such as At least one of any return line 310a, tube 313a, and pump 312a). The gas can be recycled by the MHD return air pump or compressor 312a. In one embodiment, the nozzle 307 includes a condensing jet ejector that includes a two-phase injection device in which a molten metal in a liquid phase is mixed with its gas phase to produce a liquid stream having a pressure that is higher than two The pressure of any of the water streams. Pressure may be generated in at least one of the reaction cell chamber 5b31 and the nozzle 307. The nozzle pressure can be converted to a flow velocity at the outlet of the nozzle 307. In one embodiment, the reaction cell chamber plasma comprises one phase of the injection device. The molten metal from the at least one EM pump injector may comprise other phases of the injection device. In an embodiment, the other phases, such as the liquid phase, may be injected by a separate EM pump injector, which may include an EM pump 5ka, a reservoir (such as 5c), a nozzle portion of the EM pump tube 5k61, and a nozzle. 5q. In one embodiment, the MHD nozzle 307 includes an aerosol jet injector that converts the high pressure plasma of the reaction cell chamber 5b31 into a high velocity aerosol stream or jet stream in the MHD channel 308. The kinetic energy of the jet may be derived from at least one source of the pressure group of the plasma in the reaction cell chamber 5b31 and the heat of vaporization of the metal vapor condensed to form the aerosol jet. In one embodiment, the molar volume of the condensed vapor is less than about 50 to 500 times the corresponding vapor under standard conditions. Condensation of the vapor in the nozzle 307 can cause the pressure at the outlet portion of the nozzle to decrease. The reduced pressure can result in an increase in the velocity of the condensed fluid that can include at least one of the liquid and aerosol jets. The nozzles can be extended and can be pooled to convert local pressure into kinetic energy. The passage may contain a larger cross-sectional area than the area of the nozzle outlet and may be straight to allow the aerosol flow to propagate. Other nozzles 307 and MHD channel 308 geometries, such as geometries having collection, divergence, and linear cross-sections, may be selected to achieve the desired condensation of metal vapor, wherein at least a portion of the energy is converted to a conductive flow in MHD channel 308. In an embodiment, some of the residual gas may remain non-condensing in the MHD channel 308. Uncondensed gases support the plasma in the MHD channel to provide conductive MHD channel flow. The plasma can be maintained by a low energy hydrogen reaction that can propagate in the MHD channel 308. The low energy hydrogen reactant may be provided to at least one of the reaction cell chamber 5b31 and the MHD channel 308. In one embodiment, the pressure in at least one of the nozzle 307 and the MHD channel 308 is achieved by condensation of metal vapor (such as silver metal vapor) and release of heat of vaporization. The energy release appears as the kinetic energy of the condensate. The kinetic energy of the flow can be converted to electricity in the MHD channel 308. The MHD channel 308 can be linear to maintain a constant velocity and pressure of the MHD channel flow. In one embodiment, the vapor condenses into a mist or aerosol. The aerosol can be formed in an ambient atmosphere comprising an inert gas such as an inert gas comprising argon. Aerosols can be formed in an ambient atmosphere containing oxygen. The MHD converter can comprise a source of a metal aerosol, such as a silver aerosol. The source can include at least one of a dual molten metal injector. The aerosol source may comprise a separate EM pump injector, which may comprise an EM pump 5ka, a reservoir (such as 5c), a nozzle portion of the EM pump tube 5k61, and a nozzle 5q, wherein the molten metal propellant is at least partially converted For metal aerosols. The aerosol can flow or be sprayed into the area where it is desired to condense the metal vapor, such as in the MHD nozzle 307. The aerosol can condense the metal vapor to a greater extent than is possible for metal vapors subjected to isentropic expansion, such as isentropic nozzle expansion. Metal vapor condensation can release the vaporization heat of the metal vapor, which vaporization heat can increase at least one of the temperature and pressure of the aerosol. The corresponding energy and power can contribute to the kinetic energy and power of the aerosol and plasma flow at the exit of the nozzle. Due to the contribution of the power from the vaporization heat of the metal vapor, the power of the flow can be converted to electricity as efficiency increases. The MHD converter can include a source of metal aerosol source to control at least one of aerosol flow rate and aerosol mass density. The controller controls the rate of EM pumping from the EM pump source of the aerosol. The aerosol injection rate can be controlled to optimize the vapor condensation and MHD power conversion efficiency of the recovered vapor vaporization heat. In one embodiment, the heat of vaporization released by condensation of vapor in the nozzle is at least partially transferred directly or indirectly to the reactor cell plasma. The nozzle can include a heat exchanger to transfer heat to the reaction cell chamber. Heat can be transferred by at least one of radiation, conduction, and convection. The nozzle can be heated by the release of vaporization heat and heat can be transferred to the reaction cell chamber by conduction. The nozzle may comprise a highly thermally conductive material such as a refractory thermal conductor that may comprise an oxidation resistant coating. In an exemplary embodiment, the nozzle may comprise an available oxidation resistant refractory coating (such as ZrO)2 Coating) coated boron nitride or carbon. Materials may include other refractory materials and coatings of the present invention. In one embodiment, the pressure in at least one of the nozzle 307 and the MHD channel 308 is achieved by condensation of metal vapor (such as silver metal vapor) and release of heat of vaporization. The energy release appears as the kinetic energy of the condensate. The kinetic energy of the flow can be converted to electricity in the MHD channel 308. The MHD channel 308 can be linear to maintain a constant velocity and pressure of the MHD channel flow. In one embodiment, the vapor condenses into a mist or aerosol. The aerosol can be formed in an ambient atmosphere, such as an ambient atmosphere comprising at least one of argon and oxygen. The aerosol can be formed by spraying, passively flowing or forcibly flowing through the liquid silver by at least one of oxygen and a rare gas. Compressor 312a can be used to recycle the gas. The gas may be recirculated in a high pressure gas flow loop, such as a loop that receives gas at reaction cell chamber 531 and recycles it to reservoir 5c, where the gas flows through the molten silver to increase aerosol formation. In an embodiment, the silver may comprise an additive to increase the rate and extent of aerosol formation. In an alternate embodiment, high velocity aerosol generation can be formed by circulating liquid metal at high speed. The metal can be sprayed at a high speed by at least one molten metal injector such as a dual molten metal injector including an EM pump 5kk. Pumping rates from about 1 g/s to 10 g/s, 10 g/s to 100 g/s, 1 kg/s to 10 kg/s, 10 kg/s to 100 kg/s and 100 kg/s Up to a range of 1000 kg/s. In one embodiment, the energy efficiency of forming a silver aerosol by pumping molten metal in a maintained battery atmosphere, such as an atmosphere containing a desired concentration of oxygen, may be higher than pumping gas through the molten silver. The MHD converter can comprise a source of a metal aerosol, such as a silver aerosol. The source may comprise at least one of a dual molten metal ejector and one or more of the aerosol formers from the at least one reservoir, wherein the temperature of the metal contained in the reservoir is higher than the melting point of the metal . The aerosol source may comprise a separate EM pump injector, which may comprise an EM pump 5ka, a reservoir (such as 5c), a nozzle portion of the EM pump tube 5k61, and a nozzle 5q, wherein the molten metal propellant is at least partially converted For metal aerosols. The aerosol can flow or be sprayed into the area where it is desired to condense the metal vapor, such as in the MHD nozzle 307. The aerosol can condense the metal vapor to a greater extent than is possible for metal vapors subjected to isentropic expansion, such as isentropic nozzle expansion. Metal vapor condensation can release the vaporization heat of the metal vapor, which vaporization heat can increase at least one of the temperature and pressure of the aerosol. The corresponding energy and power can contribute to the kinetic energy and power of the aerosol and plasma flow at the exit of the nozzle. Due to the contribution of the power from the vaporization heat of the metal vapor, the power of the flow can be converted to electricity as efficiency increases. The MHD converter can include a source of metal aerosol source to control at least one of aerosol flow rate and aerosol mass density. The controller controls the rate of EM pumping from the EM pump source of the aerosol. The aerosol injection rate can be controlled to optimize the vapor condensation and MHD power conversion efficiency of the recovered vapor vaporization heat. The entropy value of the silver vapor condensation caused during another isentropic expansion can be obtained by the entropy value of the gasification of silver given belowTo evaluate:among themIs the boiling point of silverIt is the silver carp for gasification. In the case of silver vapor contact with a silver mist or aerosol having an exemplary temperature of a 1500 K reservoir, the entropy value to reach the boiling point becomesamong themFor the difference smog,For fog temperature, C p Is the specific heat capacity of silver under constant pressure, andIt is the reservoir and the starting fog temperature. Thus, where the mass flow rate of the mist is about 8 times the mass flow rate of the metal vapor, the metal vapor will condense in the nozzle to release its heat of vaporization, where the corresponding energy can be significantly converted to kinetic energy. Assuming that the exemplary molar volume of the condensed vapor as a mist or aerosol is less than about 50 times the corresponding vapor, the mist flow needs to be only about 15% of the total gas/plasma volume flow to effect vapor condensation to produce About pure mist or aerosol plasma flow. The mist flow rate can be controlled by controlling the reservoir temperature, the mist source injection rate (such as the EM pumping rate), and the aerosol-forming gas pressure (such as oxygen and optionally argon). In one embodiment, the MHD thermodynamic cycle includes a process of maintaining a low energy hydrogen reactive plasma (maintaining superheated silver vapor) and condensing into a high droplet kinetic energy aerosol jet by the addition of a cold silver aerosol or liquid silver metal propellant. The aerosol jet power inventory can include primary kinetic energy. The electrical power conversion can be primarily derived from kinetic energy changes in the MHD channel 308. The mode of operation of the MHD converter may include an operational mode that is opposite to the mode of operation of the track gun or an operational mode that is the opposite of the DC-conducting electromagnetic pump. Vapor condensation of the high kinetic energy jets that form liquid silver droplets can substantially avoid loss of heat of vaporization in energy and power balance. The cold silver aerosol may be formed in the reservoir and delivered to at least one of the reaction cell chamber 5b31 and the MHD nozzle 307. The battery may further comprise a mixing chamber at a downstream side of the plasma stream passing through the reaction cell chamber to the MHD converter. The mixing of the cold aerosol and the superheated vapor may occur in at least one of the reaction cell chamber 5b31, the mixing chamber, and the MHD nozzle 307. In one embodiment, the SunCell® contains a source of oxygen to form fumed molten silver to promote silver aerosol formation. Oxygen may be supplied to at least one of: a reservoir 5c, a reaction cell chamber 5b31, an MHD nozzle 307, an MHD channel 308, an MHD condensing portion 309, and other internal chambers of the SunCell®-MHD converter generator . Oxygen can be absorbed from the molten silver to form an aerosol. The aerosol can be enhanced by the presence of a rare gas such as an argon atmosphere inside the generator. The argon atmosphere can be added and maintained at a desired pressure by the system of the present invention, such as argon storage tanks, lines, valves, controllers, and injectors. The ejector can be in the condensing section 309 or other suitable area to avoid silver backflow. In an embodiment, the super-hot silver vapor may be condensed to form an aerosol jet by spraying silver directly or indirectly into the nozzle. In an embodiment, the reaction cell chamber 5b31 can be operated at at least one of a lower temperature and a lower pressure to permit a greater fraction of the vapor to be liquefied under expansion, such as an isentropic expansion. Exemplary lower temperatures and pressures are about 2500 K and about 1 atm, respectively, compared to 3500 K and 10 atm. In the case of a reduced flow rate, the density of the mist can be raised to maintain a constant flow in the channel. The density can be increased by polymerizing silver mist droplets. Channels can contain straight channels. In other embodiments, the channels may be pooled or diverged or have other geometries suitable for optimizing MHD power conversion. In an embodiment, the nozzle may include at least one passage for a relatively cool metal vapor aerosol and at least one passage for silver vapor or super-hot silver vapor. The channel can deliver a corresponding aerosol to be mixed in the nozzle 307. Mixing reduces the entropy value to cause the silver vapor to condense. Condensation and nozzle flow create a rapid aerosol jet at the nozzle outlet. The flow rate of the relatively cold aerosol can be controlled by controlling the temperature of the source, such as the reservoir temperature, where the reservoir can act as a source. The flow rate of the superheated vapor can be controlled by controlling at least one of a low energy hydrogen reaction rate and a molten metal injection rate. In one embodiment, the nozzle outlet pressure and temperature are about the same at the outlet of the MHD channel 308, and the input power at the inlet of the MHD channel 308For about by speedv Mass flow rateThe associated kinetic energy gives the input power.Power conversion power in MHD channelGiven byWhere V is the MHD channel voltage, I is the channel current, E is the channel electric field, J is the channel current density, L is the channel length,σ For flow conductivity, v is flow rate, B is magnetic field strength, A is current cross-sectional area (nozzle exit area), d is electrode spacing, and W is the load factor (the ratio of the electric field across the load to the open circuit electric field). effectivenessη Given by the ratio of power conversion power and input power (Equation (48)) in the MHD channel (Equation (49)):Mass flow1 kg/s, conductivityσ 50,000 S/m, speed 1200 m/s, magnetic fluxB 0.25 T, load factorW 0.5, the channel width and electrode spacing of an exemplary linear square rectangular channeld 0.05 m and channel lengthL For a case of 0.2 m, the power and efficiency are:andEquation (53) is the total enthalpy efficiency when the total energy inventory is substantially kinetic energy, wherein the heat of vaporization is also converted to kinetic energy in nozzle 307. In an embodiment, the differential Lorentz forcedF L Differential distance from silver plasma flow rate and along MHD channel 308Dx Proportional:The differential Lorentz force (equation (54)) can be reconfigured to:orWhere (i) conductivityσ And the magnetic flux B can be constant along the channel, (ii) ideally there is no mass loss along the channel to make the massThe distance is constant and the mass flow rate in channel m is constant due to the constant rate of injection into the channel inlet and the continuity of flow under steady state conditions, and (iii) speed and distanceThe difference is independent of time under steady flow conditions. The constant mass flow rate as the velocity decreases along the channel may correspond to increasing the polymerization of the aerosol particles to limit complete disintegration at the exit of the MHD channel. Then, the rate of change of the speed with respect to the channel distance is proportional to the speed:among themk It is a constant determined by boundary conditions. Integration of equation (57) providesBy comparing equation (57) with equation (56), constantk forBy combining equation (58) and equation (59), the velocity as a function of channel distance isAccording to equation (49), the corresponding power of the channel is given byMass flow0.5 kg/s, conductivityσ 50,000 S/m, speed 1200 m/s, magnetic fluxB 0.1 T, load factorW 0.7, the channel width and electrode spacing of an exemplary linear square rectangular channeld 0.1 m and channel lengthL At 0.25 m, the power and efficiency are:andEquation (64) corresponds to 54% of the initial channel kinetic energy converted to power to the external load and 46% of the power dissipated in the internal impedance, where the electrical power density is 80 kW/liter. Electrical power is concentrated to the input to the MHD channelThe kinetic energy multiplied by the load factor of the MHD channelW . The power density can be increased by increasing the input kinetic energy and by reducing the channel size. The latter can be achieved by increasing at least one of mass flow rate, magnetic flux density, and flow conductivity. Mass flow2 kg/s, conductivityσ 500,000 S/m, speed 1500 m/s, magnetic fluxB 1 T, load factorW 0.7, the channel width and electrode spacing of an exemplary linear square rectangular channeld 0.05 m and channel lengthL For a case of 0.1 m, the power and efficiency are:andEquation (67) corresponds to 70% of the initial channel kinetic energy converted to power to the external load and 30% of the power dissipated in the internal impedance, where the electrical power density is 6.3 MW/liter. The power given by equation (61) can be expressed asamong themK 0 For the starting channel kinetic energy. By acquiringP onW The derivative is set to equal 0 to determine the maximum power output.among themthen,In an exemplary case where equation (65-67) of s = 125, using an iterative method, power is optimal at W = 0.96. In this case, the efficiency for the condition of equation (65-66) is 96%. In one embodiment, at least one of the reaction cell chamber 5b31 and the nozzle 307 can include a magnetic bottle that selectively forms a plasma jet along the longitudinal axis of the MHD channel 308. The power converter can include a magnetic mirror that is a source of magnetic field gradient in a desired direction of ion flow, wherein the plasma electronv || The initial parallel velocity increases because of the adiabatic invariant= constant, orbital speedAs the energy conservation decreases, linear energy is extracted from the orbital motion. As the magnetic flux B decreases, the ion cyclotron radius will increase, causing the flow rate πa2 B remains constant. The invariance of the flow of the connected track is the basis of the mechanism of the "magnetic mirror". The principle of the magnetic mirror is that the charged particles are reflected by the region of the strong magnetic field and otherwise projected from the mirror at the initial velocity for the mirror. The adiabatic invariance of the flow through the ion orbit is a means of forming an ion current along the z-axis, whereConvert toMake. Two magnetic mirrors or more magnetic mirrors may form a magnetic bottle to limit the plasma, such as the plasma formed in the reaction cell chamber 5b31. The ions that are produced in the bottle contained in the central region will spiral along the axis but will be reflected by the magnetic mirror at each end. Higher energy ions having a high component parallel to the desired axis will escape at the end of the bottle. The bottle can leak more at the end of the MHD channel. Thus, the bottle can produce a substantially linear flow of ions from the end of the magnetic bottle to the channel inlet of the magnetohydrodynamic converter. In particular, the plasma can be magnetized by a magnetic mirror that is perpendicular to the MHD channel or the z-axis.The component of the ion motion in the direction due to the adiabatic invariant= constant and at least partially converted to parallel motion. The ions have a preferred velocity along the z-axis and propagate into the magnetohydrodynamic power converter, wherein the Lorentz deflected ions form a voltage at the electrode that intersects the corresponding lateral deflection field. The voltage drives the current through the electrical load. In an embodiment, the magnetic mirror comprises an electromagnet or permanent magnet that produces a field equivalent to a Helmholtz coil or an electromagnetic coil. In the case of an electromagnetic mirror, the magnetic field strength can be adjusted by controlling the electromagnetic current to control the rate at which ions flow out of the reaction cell chamber to control power conversion. inandIn the case of the entrance to the MHD channel 308, byThe speed given can be about 95% parallel to the z-axis. In an embodiment, the low energy hydrogen reaction mixture can comprise at least one of oxygen, water vapor, and hydrogen. The MHD component may comprise a material such as ceramic, such as a metal oxide, such as at least one of zirconia and yttria, or vermiculite or quartz that is stable under an oxidizing atmosphere. In an embodiment, the MHD electrode 304 can comprise a material that can be less susceptible to corrosion or degradation during operation. In an embodiment, the MHD electrode 304 can comprise a conductive ceramic such as a conductive solid oxide. In another embodiment, the MHD electrode 304 can comprise a liquid electrode. The liquid electrode can comprise a metal that is liquid at the operating temperature of the electrode. The liquid metal may comprise a working medium metal such as molten silver. The molten electrode metal may comprise a matrix impregnated with molten metal. The substrate may comprise a refractory material such as a metal such as an electrically conductive W, carbon, ceramic or other refractory material of the invention. The negative electrode may comprise a solid refractory metal. Negative polarity protects the negative electrode from oxidation. The positive electrode can comprise a liquid electrode. The liquid electrode may comprise a member that applies an electromagnetic limit (Lorentz force) to hold the free surface liquid metal. The liquid metal electrode can include a magnetic field source and a current source to maintain electromagnetic confinement. The magnetic field source can include at least one of the MHD magnet 306 and another set of magnets, such as permanent magnets, electromagnets, and superconducting magnets. The current source can include at least one of an MHD current and an applied current from an external current source. In an embodiment, the conductive ceramic electrode may comprise one of the inventions, such as a carbide (such as ZrC, HfC or WC) or a boride (such as ZrB).2 Or a composition having a 20% SiC composition that can be processed to 1800 ° C (such as ZrC-ZrB)2 , ZrC-ZrB2 -SiC and ZrB2 ). The electrode can comprise carbon. In an embodiment, the plurality of liquid electrodes can supply liquid metal via the manifold. Liquid metal can be pumped by the EM pump. The liquid electrode can comprise a molten metal impregnated in a non-reactive matrix, such as a ceramic matrix, such as a metal oxide matrix. Alternatively, the liquid metal can be pumped through the substrate to continuously supply the molten metal. In an embodiment, the electrode may comprise a continuously ejected molten metal, such as an ignition electrode. The ejector may comprise a non-reactive refractory material such as a metal oxide such as ZrO2 . In an embodiment, each of the liquid electrodes may comprise a flow stream of molten metal exposed to the MHD channel plasma. In an embodiment, the electrodes can be configured in a Hall generator design. The negative electrode is accessible to the entrance of the MHD channel and the positive electrode is accessible to the exit of the MHD channel. The electrode accessible to the entrance of the MHD channel can comprise a liquid electrode, such as a submerged electrode. The electrode proximate the exit of the MHD channel can include a conductor that is resistant to oxidation at the electrode operating temperature, wherein the operating temperature at the outlet can be significantly lower than at the inlet of the MHD channel. An exemplary antioxidant electrode at the MHD exit may comprise a carbide such as ZrC or such as ZrB2 Boride. In an embodiment, the electrode may comprise a series of electrode portions separated by an insulator portion, the insulator portion comprising protrusions of an MHD channel wall that may comprise an electrical insulator. The raised portion can be maintained at a temperature that prevents condensation of the metal vapor. The insulating portion can include a wall strip, at least one of which is heated and insulated to maintain the strip temperature above the boiling point of the metal at the operating pressure of the MHD channel. The electrode at the exit of the channel may comprise an antioxidant electrode such as a carbide or boride that is stable to oxidize at the exit temperature. In one embodiment, the MHD channel can be maintained at a temperature below at least one of metal vapor condensation and electrode corrosion that results in an insulator portion of the wall, such as a carbide or boride electrode (such as comprising ZrC) Or ZrB2 a carbide or boride) or a composition that can be processed to 1800 ° C (such as ZrC-ZrB2 And ZrC-ZrB2 - SiC composition). In one embodiment, the working medium comprises a metal (such as silver) that can sublime at a temperature below its boiling point to prevent metal from condensing on the walls of the MHD channel such that it flows to the recirculation system. In an embodiment, the MHD magnet 306 can include an alternating field magnet (such as an electromagnet) that can apply a sinusoidal or alternating magnetic field to the MHD channel 308. The field applied by sinusoidal or alternating can cause the MHD power output to be alternating (AC) power. The alternating current and voltage frequency can be standard current and voltage frequencies, such as 50 Hz or 60 Hz. In one embodiment, the MHD power is transmitted from the channel by induction. The induction generator eliminates the electrodes that contact the plasma. The union and seal between the reaction cell chamber 5b31 and the MHD acceleration channel or nozzle 307 connected to the MHD expansion or generator channel 308 (such as the seal 314) may comprise a gasket flange seal or the present invention Other. Other seals, such as the return conduit 310, the return reservoir 311, the return EM pump 312, the jet reservoir 5c, and the seal of the jet EM pump assembly 5kk, may comprise one of the present inventions. An exemplary gasket comprises carbon (such as graphite or Graphi), wherein the bonded metal oxide portion (such as a metal oxide portion comprising at least one of alumina, yttria, zirconia, and magnesia) remains below carbon reduction Temperature (less than about 1300 ° C to 1900 ° C). The components may comprise different materials of the invention, such as refractory materials, and stainless steel based on their operating parameters and requirements. In an exemplary embodiment, at least one of the i.) EM pump assembly 5kk, the return conduit 310, the return reservoir 311, and the return EM pump tube 312 comprises stainless steel, wherein an internal oxidative protective coating (such as nickel) is available , Pt, bismuth or other precious metal) coating; ii.) at least one of the reservoir 5c, the reaction cell chamber 5b31, the nozzle 307 and the MHD expansion portion 308 comprises an electrically insulating refractory material (such as boron nitride) or Refractory oxides (such as MgO (MP 2825 ° C)), ZrO2 (M.P. 2715 ° C), magnesium oxide, H2 O-stabilized zirconia, yttrium zirconate (SrZrO3 M.P. 2700 ° C), HfO2 (MP 2758 ° C), or cerium oxide (MP 3300 ° C) which is stable to oxidation at the working temperature; iii.) The reaction cell chamber 5b31 contains graphite (such as at least one of isotropic and hot graphite) And iv.) at least one of the inlet pipe 5qa, the nozzle portion of the electromagnetic pump tube 5k61, the nozzle 5q, and the MHD electrode 304 may comprise carbon, Mo, W, ruthenium, ruthenium coated Mo, ruthenium coating At least one of the W's. In an exemplary embodiment, at least one of the EM pump assembly 5kk, the return conduit 310a, the return reservoir 311a, and the return air pump or compressor 312a comprises stainless steel, wherein the interior may be coated with an oxidation reaction protective coating, The oxidation reaction protects the coating such as nickel, Pt, ruthenium or other precious metals. The electrodes may comprise conductors coated with precious metals, such as Pt on copper, nickel, nickel alloys and cobalt alloys, or such uncoated metals, which may be cooled by backing heat exchangers or cold plate applications. The electrode may comprise a spinel type electrode such as 0.75 MgAl2 O4 -0.25 Fe3 O4 , 0.75 FeAl2 O4 -0.25 Fe3 O4 And lanthanum lanthanum La(Mg)CrO3 . In an embodiment, the MHD electrode 304 can comprise a liquid electrode, such as a liquid silver coated refractory metal electrode or a cooled metal electrode. At least one of Ni and tantalum coatings prevents coated components from being coated with H2 O reaction. The MHD atmosphere may contain hydrogen to maintain metal reduction conditions, such as EM pump tube 5k6, inlet riser 5qa, nozzle portion of electromagnetic pump tube 5k61, nozzle 5q, and MHD electrode 304. The MHD atmosphere may contain water vapor to maintain oxide ceramics such as ZrO, yttria, and ceramic components.2 Or MgO, such as at least one of the reaction cell chamber 5b31, the nozzle 307, and the MHD expansion portion 308. Ceramic glue (such as zirconia phosphate cement, ZrO)2 The cement or calcium oxide-zirconia phosphate partially bonds or bonds the metal oxide together. Exemplary Al2 O3 Adhesives were Rescor 960 alumina (Cotronics) and Ceramabond 671. Additional exemplary ceramic adhesives are Resbond 989 (Cotronics) and Ceramabond 50 (Aremco). In an embodiment, the wall assembly may comprise an insulating ceramic that is stable with MgO (such as ZrO)2 Or HfO2 And the electrode insulator of the segmented electrode may comprise a thermally conductive ceramic such as MgO. To prevent loss of gasification from the outer surface, the ceramic may be sufficiently thick to be sufficiently cooled externally, actively or passively cooled, or coated in at least one of the insulation. Several oxides can be added to ZrO2 (zirconia) or HfO2 (yttria) to stabilize the material, such as yttria (Y2 O3 ), magnesium oxide (MgO), calcium oxide (CaO), strontium oxide (SrO), strontium oxide (Ta2 O5 ), boron trioxide (B2 O3 ), TiO2 , yttrium oxide (Ce2 O3 ), SiC, niobium and tantalum. The crystal structure may be a cubic phase, which is referred to as cubic stabilized zirconia (yttria) or stabilized zirconia (yttria). In one embodiment, at least one battery component, such as reaction cell chamber 5b31, is permeable to at least one of oxygen and oxide ions. An exemplary oxide permeable material is ZrO2 . By controlling the transport of materials through oxides or oxides (such as ZrO)2 The oxide diffusivity is used to control the oxygen content of the reaction cell chamber 5b31. The battery can include a voltage and current source on the oxide permeable material and a current control system wherein the flow of oxide ions on the material is controlled by voltage and current. Other suitable refractory components include SiC (M. P. = 2830 ° C), BN (M. P. = 2970 ° C), HfB2 (M. P. = 3250 ° C) and ZrB2 At least one of (M. P. = 3250 ° C). To avoid electrical shorting of the MHD electrodes by molten metal vapor, the electrodes 304 (Fig. 2I161) may comprise conductors, each mounted on a conductive pillar covered by an electrical insulator or as a lead 305 that acts as an insulated lead, the lead further acting as an electrode and generator channel 308 a spacer on the wall. Electrode 304 can be segmented and can include cathode 302 and anode 303. In addition to the insulated leads 305, the electrodes are free to float in the generator channel 308. The electrodes spaced along the vertical axis may be sufficient to prevent shorting of the molten metal. The electrode may comprise a refractory conductor such as W or Mo. Leads 305 can be connected to wires that can be insulated by a refractory insulator such as BN. The wire can be engaged in a wire bundle that penetrates a passage at the MHD busway feedthrough flange 301 that can include metal. Outside the MHD converter, the harness can be connected to a power combiner and an inverter. In an exemplary embodiment, the MHD is converted to black and white plasma initial and final temperatures of 3000K and 1300K during power. In an embodiment, the MHD generator is cooled on the low pressure side to maintain plasma flow. The Hall or generator channel 308 can be cooled. The cooling means can be one of the inventions. The MHD generator 300 can include a heat exchanger 316 (such as a radiant heat exchanger), wherein the heat exchanger can be designed to radiate power depending on its temperature to maintain a desired minimum channel temperature range, such as in the range of about 1000 °C to 1500 °C. The radiant heat exchanger can include a higher surface to minimize at least one of its size and weight. Radiation heat exchanger 316 can include a plurality of surfaces that can be configured to have a square or square face to increase the surface area of radiation. The radiant heat exchanger can be operated in air. The surface of the radiant heat exchanger may be coated with a material having at least one of the following characteristics: (i) capable of high temperature operation, such as refractory material, (ii) having a higher emissivity, (iii) being stable to the oxidation reaction, and providing a higher Surface area, such as an engraved surface with unobstructed or unobstructed discharge. Exemplary materials are ceramics, such as oxides, such as MgO, ZrO2 HfO2 Al2 O3 And other oxidatively stable ceramics such as ZrC-ZrB2 And ZrC-ZrB2 - SiC composition. The generator may further comprise a regenerator or a regenerative heat exchanger. In one embodiment, the fluid is returned to the injection system after passing in a countercurrent manner to receive heat in the expanded portion 308 or other heat loss region to preheat the metal injected into the battery reaction chamber 5b31 to maintain the reaction cell cavity. Room temperature. In one embodiment, a working medium (such as at least one of silver and a rare gas), a cell component (such as a reservoir 5c, a reaction cell chamber 5b31, and an MHD converter assembly (such as an MHD condensing portion 309 or other heat) At least one of at least one of a component (such as at least one of a group of the reservoir 5c, the reaction cell chamber 5b31, the MHD nozzle portion 307, the MHD generator portion 308, and the MHD condensing portion 309)) The heat exchanger may be heated by a heat exchanger from at least one other battery or MHD assembly (such as reservoir 5c, reaction cell chamber 5b31, MHD nozzle portion 307, MHD generator portion 308, and MHD condensing portion 309). At least one of the groups) receives heat. Regenerators or regenerative heat exchangers transfer heat from one component to another. In an embodiment, at least one of the emissivity, area, and temperature of the radiant heater exchanger 316 can be controlled to control the rate of heat transfer. The area can be controlled by controlling the extent of coverage of the thermal shield on the radiator. The temperature can be controlled by controlling the amount of heat flowing to the radiator. In another embodiment, the heat exchanger 316 can include a coolant loop, wherein the MHD heat exchanger 316 receives coolant via the MHD coolant inlet 317 and removes heat via the MHD coolant outlet 318. Heat can be used in regenerative heat exchangers to preheat the return silver flow, battery assembly or MHD assembly. Alternatively, heat can be used for heating and thermoelectric symbiosis applications. The nozzle introduction port 307 may comprise a refractory material resistant to wear, such as a metal oxide such as ZrO.2 HfO2 Al2 O3 Or MgO), refractory nitrides, refractory carbides (such as tantalum carbide, tungsten carbide or tantalum carbide), hot graphite (such as tungsten) which may comprise a refractory coating or only other refractory materials or coated refractory materials of the invention Material on (such as carbon). Electrode 304 can comprise a fire resistant conductor such as W or Mo. Generator channels 308 or electrically insulating carriers such as electrodes 305 may be refractory insulators, such as one of the present invention, such as ceramic oxides, such as ZrO.2 , boron nitride or tantalum carbide. In another embodiment in which the MHD assembly is cooled, the MHD assembly, such as at least one of the nozzle 307 and the passage 308, may comprise a refractory material (such as Al)2 O3 ZrO2 , mullite or other) coated transition metal (such as Cu or Ni). The electrode may comprise a transition metal that may be cooled, wherein the surface may be coated with a refractory conductor such as W or Mo. Components that can be cooled by water, molten salts or other coolants are known to those skilled in the art, such as hot oils (such as ruthenium based polymers), molten metals (such as Sn, Pb, Zn, alloys), molten salts ( Such as alkaline salts) and eutectic salt mixtures (such as alkaline halide-alkali metal hydroxide mixtures (MX-MOH M = Li, Na, K, Rb, Cs; X = F, Cl, Br, I)) At least one of them. The hot coolant may be recycled to preheat the molten metal sprayed into the reaction cell chamber 5b31. The corresponding heat recovery system can include a reheater. In an embodiment, the MHD assembly (such as MHD nozzle 307, MHD channel 308, and MHD condensation portion 309) may comprise a refractory material, such as one of the present invention, such as at least one of carbide, carbon, and boride. And metal. The refractory material can be readily oxidized to at least one of oxygen and water. To inhibit the oxidation reaction, the oxygen source of the HOH catalyst can comprise a compound comprising oxygen, such as at least one of CO, an alkali metal or alkaline earth metal oxide, or other oxide or compound comprising oxygen of the present invention. The boride may comprise ZrB which may be doped with SiC2 . Carbides may contain ZrC, WC, SiC, TaC, HfC and Ta4 HfC5 At least one of them. Conductive materials such as carbides may be electrically isolated by insulating spacers or bushings as indicated, such as in the case of electrical isolation of at least one of the ignition and MHD electrodes. An exemplary MHD volume conversion density of about 70 MW/m3 (70 kW / liter). Most of the problems in MHD in history have been attributed to the low conductivity characteristics of low conductivity and slagging environments in gas and coal-fired counterparts. The conductivity of silver SunCell® plasma is estimated to be approximately 1 mΩ based on 10,000 A at 12 V. According to the arc size, the corresponding conductivity is estimated to be 1×10 compared to about 20 S/m of the alkali-inoculated inert MHD working gas (where the power density is proportional to the conductivity).5 S/m. In an embodiment, the working medium may comprise at least one of silver vapor and a rare gas inoculated with silver vapor, such as He, Ne or Ar. In one embodiment, the conductivity of the working medium can be controlled by controlling at least one of molten metal vapor pressure (such as silver vapor pressure) and ionization of the working medium. By controlling the power of low-energy hydrogen, the intensity of EUV and UV light emitted by low-energy hydrogen reaction, ignition voltage, ignition current, EM pumping rate of molten metal flow, and operating temperature (such as gas, electron, ion and At least one of the blackbody temperatures) controls the ionization of the working medium. The at least one temperature can be controlled by controlling at least one of ignition and low energy hydrogen reaction conditions. Exemplary low energy hydrogen reaction conditions are gas pressure and gas composition, such as H2 O, H2 And inert gas components. The low energy hydrogen reaction conditions and corresponding controls may be one of the inventions or other suitable conditions. In one embodiment, the SunCell® may further comprise a molten metal overflow system, such as a system comprising an overflow sump, at least one pump, a battery molten metal inventory sensor, a molten metal inventory controller, a heater, a temperature control system, and a molten metal inventory, The molten metal is stored as needed and supplied to the SunCell®, which can be determined by at least one sensor and controller. The molten metal inventory controller of the overflow system may comprise a molten metal content controller of the present invention, such as a water riser and an EM pump. The overflow system can include at least one of an MHD return conduit 310, a return reservoir 311, a return EM pump 312, and a return EM pump tube 313. In one embodiment, the expansion of the working medium is maintained under conditions that ensure isentropic flow. In one embodiment, the inlet working medium conditions are selected for expansion of the ultrasonic nozzle that will ensure reversible expansion of the nozzle and a strong drive pressure gradient of the MHD channel. Due to saturation (if it occurs in the nozzle), the rapid cooling rate (such as about 15 K/us) will result in a strong column imbalance. Cooling and this can further trigger the condensation shock in the diverging portion of the nozzle, nozzle inlet The conditions can be highly superheated so that the vapor does not become saturated during expansion. In an embodiment, condensation shock will be avoided because it results in an irreversibility that deviates from the desired isentropic flow condition and drastically reduces the nozzle exit velocity, the resulting height entrained in the vapor stream in the ultrasonic/divergent portion of the nozzle. Dense liquid Ag droplets can cause accelerated erosion of the nozzle surface. In one embodiment where the Lorentz force adversely affects the direction of flow such that the weak drive pressure gradient in the MHD channel can produce a reduced volumetric flow through the system, the nozzle inlet temperature is as high as possible to allow proper overheating, and pressure It is also suitably high to ensure a strong driving pressure gradient in the MHD portion downstream of the nozzle. In an exemplary embodiment, the pressure of the reaction cell chamber 5b31 at the nozzle inlet is about 6 atm, and the plasma temperature is about 4000 K to cause isentropic expansion and dry steam at a rate of about 722 m/s and more. The pressure at 2 atm leaves the nozzle at approximately 1.84 Mach. Lower inlet temperatures are also possible, but these can each result in smaller outlet speeds and pressures. In one embodiment in which the Lorentz force can arrest the plasma jet prior to reaching the exit temperature of the desired MHD channel 308, plasma conductivity, magnetic field strength, gas temperature, electron temperature, ion temperature, channel inlet pressure, jet velocity, and At least one of the working medium flow parameters is optimized to achieve the desired MHD conversion efficiency and power density. In an embodiment comprising a molten metal inoculated rare gas plasma, such as a silver vapor inoculated argon or helium plasma, controlling the relative flow of metal vapor to a rare gas to achieve a desired conductivity, a plasma gas temperature, The reaction chamber 5b31 pressure and at least one of the MHD passage 308 inlet injection speed, pressure, and temperature. In one embodiment, the rare gas and metal vapor flow can be controlled by controlling a corresponding reflux pump to achieve the desired relative ratio. In one embodiment, the conductivity can be controlled by controlling the amount of relatively rare gas and metal injection rate by controlling the amount of inoculation into the reaction cell chamber 5b31. In one embodiment, the conductivity can be controlled by controlling the rate of low energy hydrogen reaction. The low energy hydrogen reaction rate can be controlled by means of the present invention, such as by controlling the source of the catalyst, the source of oxygen, the source of hydrogen, water vapor, hydrogen, the flow of a conductive substrate (such as injection of molten silver), and ignition parameters (such as ignition voltage and The injection rate of at least one of at least one of the currents. In an embodiment, the MHD converter includes a sensor and control system for low energy hydrogen reaction and MHD operating parameters, such as (i) reaction conditions such as reactant pressure, temperature, and relative concentration, such as HOH and H or The flow of reactants from which they originate and the flow and pumping rates of conductive matrices such as liquids and silver sulfide, and ignition conditions such as ignition current and voltage; (ii) plasma and gas parameters, such as by MHD converters Stage pressure, velocity, flow rate, conductivity and temperature; (iii) reflux and recycle material parameters such as pumping rates and physical parameters of rare gases and molten metals such as flow rate, temperature and pressure; and (iv) A plasma conductivity sensor in at least one of the electrolytic cell chamber 5b31, the MHD nozzle portion 307, the MHD channel 308, and the MHD condensing portion 309. In an embodiment, such as hydrogen (such as H)2 Gas and H2 A gas source of at least one of O is supplied to the reaction cell chamber 5b31. The SunCell® can include at least one mass flow controller to supply a source of hydrogen, such as H, in at least one of a liquid and a gaseous form.2 Gas and H2 At least one of O. The supply may be via at least one of: a base of the EM pump assembly 5kk1, a wall of the reservoir 5c, a wall of the reaction cell chamber 5b31, a jet EM pump tube 5k6, an MHD return conduit 310, an MHD return reservoir 311 The pump tube of the MHD return EM pump 312 and the MHD return EM pump tube 313. Gas added to the interior of the battery or MHD can be injected into the MHD condenser section 309 or at any convenient battery or MHD converter assembly that is connected to the interior. In an embodiment, hydrogen may be supplied via a selective membrane, such as a hydrogen permeable membrane. Hydrogen supply membrane can be packed with Pd or Pd-Ag H2 The membrane is permeable or similar to those known to those skilled in the art. The penetration of the gas into the wall of the EM pump tube may include a flange that is welded or screwed into. Hydrogen can be supplied from a hydrogen storage tank. Hydrogen may be supplied from the hydride release, wherein the release may be controlled by means known to those skilled in the art, such as by controlling at least one of the pressure and temperature of the hydride. Hydrogen can be supplied by electrolyzing water. The water electrolyser can comprise a high pressure electrolyzer. At least one of the electrolyzer and the hydrogen mass flow controller can be controlled by a controller, such as a controller including a computer and a corresponding sensor. The hydrogen flow can be controlled based on the power output of the SunCell® that can be recorded by a converter such as a thermal meter, PV converter or MHD converter. In an embodiment, H can be2 O is supplied to the reaction electrolytic cell chamber 5b31. The supply source may comprise a line such as a line through the EM pump tube 5k6 or the EM pump assembly 5kk. H2 O can provide at least one of H and HOH catalysts. Low energy hydrogen reaction can produce O2 And H2 (1/p) and product. Such as H2 (1/4) of H2 (1/p) may diffuse from at least one of the reaction cell chamber and the MHD converter to an external region such as an ambient atmosphere or H2 (1/p) Collection system. H2 (1/p) may diffuse through the wall of at least one of the reaction cell chamber and the MHD converter due to its small volume. O2 The product may diffuse from at least one of the reaction cell chamber and the MHD converter to an external region such as an ambient atmosphere or O2 Collection system. O2 It can be diffused via selective membranes, materials or values. The selective material or film may comprise a material or film capable of conducting a conductive oxide such as yttria, nickel/yttria stabilized zirconia (YSZ)/citrate layering or other oxygen or oxidation known to those skilled in the art. Selective membrane. O2 It can be diffused via a permeable wall, such as a wall capable of conducting an oxide, such as a yttrium oxide wall. The oxygen permeable membrane may comprise a porous ceramic of a reaction cell and a low pressure component of the MHD converter, such as a ceramic wall of the MHD channel 308. The oxygen selective membrane can contain available Bi26 Mo10 O69 BaCo coated to increase oxygen permeability0.7 Fe0.2 Nb0.1 O3- δ (BCFN) oxygen permeable membrane. The oxygen selective membrane can comprise Gd1 - x Cax CoO3 - d And Ce1 - x Gdx O2 - d At least one of them. The oxygen selective membrane may comprise a ceramic oxide film such as SrFeCo0 . 5 Ox , SrFe0 . 2 Co0 . 5 Ox Ba0 . 5 Sr0 . 5 Co0 . 8 Fe0 . 2 Ox BaCo0 . 4 Fe0 . 4 Zr0 . 2 Ox La0 . 6 Sr0 . 4 CoOx And Sr0 . 5 La0 . 5 Fe0 . 8 Ga0 . 2 Ox At least one of them. An EM pump or assembly such as at least one of an EM pump assembly 5kk, an EM pump 5ka, an EM pump tube 5k6, an inlet riser 5qa, and a spray EM pump tube 5k61 may comprise an oxygen stabilized material or coating, such as ceramic, Such as Al2 O3 , ZrC, ZrC-ZrB2 , ZrC-ZrB2 -SiC and ZrB with 20% SiC composition2 At least one of, or at least one precious metal, such as at least one of platinum (Pt), palladium (Pd), ruthenium (Ru), rhenium (Rh), and iridium (Ir). In one embodiment shown in FIGS. 2I174 to 2I181, at least one of the EM pump assembly 5kk, the EM pump 5ka, the pump tube 5k6, the inlet riser 5qa, and the spray EM pump tube 5k61 may contain an oxidation reaction. Resistant ceramics. Ceramic can not be with O2 reaction. The ceramic may comprise an electrical conductor that is stable to the reaction with oxygen at elevated temperatures. Exemplary ceramics are ZrC, ZrB2 , ZrC-ZrB2 , ZrC-ZrB2 -SiC and ZrB with 20% SiC composition2 . The conductive ceramic can be doped with SiC to provide protection from oxidation reactions.铱 (M.P. = 2446 ° C) does not form an alloy or solid solution with silver; therefore, ruthenium can act as a suitable oxidation resistant coating for at least one of the EM pump assembly 5kk and the EM pump tube 5k6 to avoid oxidation reactions. The tantalum coating can be applied to a metal that matches a coefficient of thermal expansion (CTE). In an exemplary embodiment, the interior of the EM pump assembly 5kk and the EM pump tube 5k6 are plated with helium, wherein the plated assembly comprises stainless steel (SS) having a CTE similar to helium, such as Haynes 230, 310 SS or 625 SS. . Alternatively the molybdenum EM pump assembly 5kk can be coated with ruthenium with a CTE match (eg, about 7 ppm/K). In one embodiment, a tube is used as the cathode to plate the interior of the EM pump tube, and the counter electrode may include a line having an insulating spacer that periodically moves on the counter electrode to a plated area covered by the spacer. In one embodiment, a ruthenium coating can be applied by vapor deposition, such as a method comprising chemically depositing an organic molecule comprising ruthenium, such as thermal decomposition of tetradecyl carbonyl to cause ruthenium to be deposited at elevated temperatures. On the surface. The crucible may be deposited by one or more methods known in the art, such as at least one of the following: magnetron sputtering (DC electromagnetic sputtering (DCMS) and radio frequency magnetron sputtering (RFMS)) , chemical vapor deposition (CVD), metal organic CVD (MOCVD), atomic layer deposition (ALD), physical vapor deposition (PVD), laser induced chemical vapor deposition (LCVD), electrodeposition, pulsed laser deposition (PLD) and double glow photovoltaic (DGP). In an embodiment, the interior of the EM pump 5k6 tube may be covered by a crucible. The ends of the coating may be coated with tantalum by means of the means of the invention, such as CVD or electroplating. In another embodiment, an EM pump assembly, such as a stainless steel EM pump assembly, may be coated with a refractory antioxidant coating, such as at least one of an oxide and a carbide. The coating may comprise carbides (such as tantalum carbide / niobium carbide (HfC / SiC)) and oxides (such as HfO)2 ZrO2 , Y2 O3 AUO3 SiO2 Ta2 O5 And TiO2 At least one of at least one of them. In another embodiment, the EM pump tube 5k6 comprises an oxidation resistant stainless steel (SS), such as stainless steel for coal fireboxes and boiler tube coal water walls, such as austenitic stainless steel. Exemplary materials are Haynes 230, SS 310, and SS 625, which are a rare combination of austenitic nickel-chromium-molybdenum-bismuth alloys with excellent corrosion resistance and high strength combinations down to 1800 °F (982 °C). In an embodiment, a material such as Haynes 230, SS 310, or SS 625 can be pre-oxidized to form a protective oxide coating. The protective oxide coating can be formed by heating in an atmosphere containing oxygen. The SS such as Haynes 230 can be pre-oxidized in air or a controlled atmosphere such as an atmosphere containing oxygen and a rare gas such as argon. In an exemplary embodiment, Haynes 230, such as a Ni-Cr alloy with W and a Mo alloy, is pre-oxidized in air at 1000 ° C or in argon 80% / oxygen 20% for 24 hours. An oxide coating can be formed at the desired operating temperature and oxygen concentration. In an embodiment, metal components such as those containing SS 625 (such as EM pump assembly 5kk) may be 3D printed. In an embodiment, the exterior of the EM pump assembly can be protected from oxidation reactions. The protection may comprise a coating by an antioxidant coating, such as one of the present invention. Alternatively, at least a portion of the EM pump assembly 5kk can be embedded in an antioxidant material such as ceramic, quartz, glass, and cement. The protected portion can be operated in air by oxidation. In an embodiment, the molten metal such as silver may contain an additive that prevents or reduces the oxidation reaction inside the EM pump tube. The additive may comprise a reducing agent such as a thiosulfate or an oxidation product of the EM pump tube such that the additional oxidation reaction is inhibited by stabilizing the protective oxide of the tube wall. Alternatively, the molten metal additive may comprise a base that stabilizes the protective metal oxide on the wall of the pump tube. In an embodiment, the EM pump assembly can comprise a plurality of ceramics, such as conductive and non-conductive ceramics. In an exemplary embodiment, in addition to the EM pump busbar 5k2, the EM assembly 5kk may comprise a non-conductive ceramic such as an oxide such as Al.2 O3 , zirconia or yttria), and the EM pump busbar 5k2 may comprise conductive ceramics such as ZrC, ZrB2 Or a composition such as ZrC-ZrB2-SiC. The reservoir 5c can comprise the same non-conductive ceramic as the EM pump assembly 5kk. In an embodiment, the ceramic EM pump can include at least one brazed or metallized ceramic portion to form a joint between the components. The electromagnetic pumps may each comprise one of two main types of electromagnetic pumps for liquid metal: an AC or DC conducted pump in which an AC or DC magnetic field is established on a tube containing liquid metal and the AC or DC current is fed separately a liquid through electrode connected to the wall of the tube; and an induction pump in which the mobile field senses the current required, such as an induction motor in which the current can intersect the applied AC electromagnetic field. Induction pumps can be in three main forms: toroidal linear, planar linear, and spiral. The pump may include other pumps known in the art, such as mechanical and thermoelectric pumps. The mechanical pump can include a centrifugal pump having a motor driven impeller. The molten metal pump may comprise a moving magnet pump (MMP), such as described in MG Hvasta, WK Nollet, MH Anderson "Designing moving magnet pumps for high-temperature, liquid-metal systems", Nuclear Engineering and Design, Vol. 327, (2018) , Pumps on pages 228-237, the entire contents of which are incorporated by reference. The MMP can generate a moving magnetic field by at least one of a spin array of permanent magnets and a multi-phase field coil. In an embodiment, the MMP can include a multi-stage pump, such as a secondary pump for MHD recirculation and ignition injection. The secondary MMP pump can include an electric motor, such as an electric motor that rotates the shaft. The secondary MMP may further comprise two rotating drums each comprising a set of circumferentially mounted magnets alternating in polarity fixed on the surface of each drum and a ceramic container having a U-shaped portion for receiving the drum, wherein each The drum can be rotated by the shaft to cause the molten metal to flow in the ceramic vessel. In another embodiment of the MMP, the drum of the alternating magnet is replaced by two discs of alternating polar magnets on the surface of each disc at opposite locations of the sandwiched ceramic container, the container containing the rotating disc The molten metal pumped by the sheet. In another embodiment, the container may comprise a magnetic field permeable material, such as a non-divalent iron metal (such as stainless steel) or ceramic (such as one of the present invention). The magnet can be cooled by means such as air cooling or water cooling to permit operation at high temperatures. An exemplary commercial AC EM pump is CMI Novacast CA15, where the heating and cooling system can be modified to support pumping molten silver. The EM pump tube containing the inlet and outlet portions and the heater containing the silver container can be heated by the heater of the present invention, such as a resistor or an inductively coupled heater. A heater such as a resistive or inductively coupled heater may be external to the EM pump tube and further include a heat transfer member to transfer heat from the heater to the EM pump tube (such as a heat pipe). The heat pipe can be operated at high temperatures, such as by a lithium working fluid. The electromagnet of the EM pump can be cooled by the system of the invention, such as by a water cooling circuit and a chiller. In an embodiment (Fig. 2I184 to Fig. 2I185), the EM pump 400 may comprise an AC induction type in which the Lorentz force on the silver is generated by a time varying current passing through the silver and a cross-synchronous time varying magnetic field. The time varying current through silver can be induced by the Faraday of the first time varying magnetic field generated by the EM pump transformer winding circuit 401a. The source of the first time varying magnetic field may comprise a primary transformer winding 401 and the silver may act as a secondary transformer winding, such as a single turn short winding comprising an EM pump bushing section 405 of the current loop and an EM pump current loop return section 406 . The primary winding 401 can include an AC electromagnet in which a first time varying magnetic field is conducted through the silver circumferential circuits 405 and 406, the inductive current loop is conducted by a magnetic circuit or an EM pump transformer yoke 402. Silver may be contained in a container such as ceramic containers 405 and 406, such as a container comprising the ceramic of the present invention, such as tantalum nitride (MP 1900 ° C), quartz, alumina, zirconia, magnesia or yttria. Protective SiO2 The layer can be formed by controlled passivation oxidation on yttrium nitrite. The container may include channels 405 and 406 that enclose the magnetic circuit or EM pump transformer yoke 402. The container may include a flattened section 405 such that the induced current has components that flow in a vertical direction to a synchronous time varying magnetic field and a desired direction of flow of the pump according to the corresponding Lorentz force. The cross-synchronous time-varying magnetic field can be generated by an EM pump electromagnetic circuit 403c including an AC electromagnet 403 and an EM pump electromagnetic yoke 404. The magnetic yoke 404 may have a gap at the flat section of the container 405 containing silver. The electromagnet 401 of the EM pump transformer winding circuit 401a and the electromagnet 403 of the EM pump electromagnetic circuit 403c may be powered by a single phase AC power source or other suitable power source known in the art. The magnets can be positioned close to the loop bends such that there is a desired current vector component. The phase of the AC current of the power transformer winding 401 and the electromagnet winding 403 can be synchronized to maintain the desired direction of the Lorentz pumping force. In an embodiment (Fig. 2I184-2I185), the induced current loop may comprise an inlet EM pump sleeve 5k6, an EM pump sleeve section 405 of the current loop, an outlet EM pump sleeve 5k6, and a path through the silver in the reservoir 5c. The reservoir may comprise walls comprising a water riser 5qa and an ejector 5k61 in an embodiment of such components. The EM pump can include monitoring and control systems such as current and voltage for the primary winding and monitoring and control systems that use the pumping parameter feedback to control SunCell power generation. An exemplary measurement feedback parameter can be the temperature at the reaction cell chamber 5b31 and the power at the MHD converter. The monitoring and control system can include corresponding sensors, controllers, and computers. In an MHD converter embodiment having only a pair of electromagnetic pumps 400, each MHD return conduit 310 extends to the inlet of the corresponding electromagnetic pump 5kk and is connected to the inlet. The connection may include a boss 308 such as a base having a reservoir of an input of the MHD return conduit 310 (such as a Y-joint) and a reservoir of a boss such as a reservoir floor assembly 409. In an embodiment comprising a pressurized SunCell® with an MHD converter, the injection side of the EM pump, the reservoir and the reaction cell chamber 5b31 operate at a high pressure relative to the MHD return conduit 310. The inlet of each EM pump may only include the MHD return conduit 310. The connection may include a splicing such as a splicing with an input of the MHD return conduit 310 (such as a Y-joint and reservoir pedestal), wherein pump power is prevented from returning from the inlet flow from the reservoir to the MHD return conduit 310. In an MHD power generator embodiment, the injection EM pump and the MHD return EM pump may comprise any of the present invention, such as a DC or AC conductive pump and an AC induction pump. In an exemplary MHD power generator embodiment (Fig. 2I184) In the injection EM pump may comprise an inductive EM pump 400, and the MHD return EM pump 312 may comprise an inductive EM pump or a DC conductive EM pump. In another embodiment, the jet pump may further act as an MHD return EM pump. The return conduit 310 can be input to the EM pump at a lower pressure location than the inlet from the reservoir. The inlet from the MHD return conduit 310 can be at a location suitable for the low pressure in the MHD condensation section 309 and the MHD return conduit 310. Entering the EM pump. The inlet from the reservoir 5c can be accessed at the location of the higher pressure EM pump casing, such as at a location where the pressure is the operating pressure of the desired reaction cell chamber 5b31. At the injector section 5k61 The EM pump pressure can be at least the required reaction cell chamber pressure The pressure may be attached to the EM pump at the casing and current loop section 5k6, 405 or 406. The EM pump may comprise a multi-stage pump (Fig. 2I186-2I195). The multistage EM pumps may each correspond to substantially only An input metal stream is received at a different pump stage that allows the forward molten metal stream to exit the EM pump outlet and the pressure of the injector 5k61, such as an input metal stream from the MHD return conduit 310 and an input metal stream from the susceptor of the reservoir 5c. In an embodiment, the multi-stage EM pump assembly 400a (FIG. 2I188) includes at least one EM pump transformer winding circuit 401a and further includes at least one AC EM pump electromagnetic circuit 403c that includes an inductive current loop 405 And a transformer winding 401 and a transformer yoke 402. The AC EM pump electromagnetic circuit includes an AC electromagnet 403 and an EM pump electromagnetic yoke 404. The inductive current loop may include an EM pump bushing section 405 and an EM pump current loop return section. 406. The electromagnetic yoke 404 may have a gap at a flat section of the vessel or EM pump casing section containing a current circuit 405 such as silver pumped molten metal. In an embodiment, the multi-stage EM pump may comprise a supply perpendicular to the current. a plurality of AC EM pump electromagnetic circuits 403c of magnetic flux of the metal flow. The multi-stage EM pump can receive the inlet along the EM pump casing section of the current circuit 405 at a position where the inlet pressure is suitable for local pumping to achieve forward pumping Flow, wherein the pressure is increased in the next AC EM pump electromagnetic circuit 403c. In an exemplary embodiment, the MHD return conduit 310 is in front of the first AC electromagnet circuit 403c including the AC electromagnet 403a and the EM pump electromagnetic yoke 404a The current loop is entered, such as the EM pump casing section of current loop 405. The inlet stream from the reservoir 5c can enter before the first AC electromagnet circuit 403c and after the second AC electromagnet circuit 403c, the AC electromagnet circuit comprising an AC electromagnet 403b and an EM pump electromagnetic yoke 404b, wherein the pump The molten metal pressure in current loop 405 is maintained, which maintains the desired flow from each inlet to the next pump stage or to the pump outlet and injector 5k61. The pressure of each pump stage can be controlled by controlling the current of the corresponding AC electromagnet of the AC electromagnet circuit. In an embodiment, the EM pump current loop return section 406, such as a ceramic channel, may comprise a molten metal flow restrictor or may be filled with a solid electrical conductor to complete the current flow of the current loop while preventing the molten metal from flowing back to the EM from a higher pressure. Lower pressure section of the pump casing. The solid may comprise a metal such as the stainless steel of the present invention, such as Haynes 230, Pyromet® Alloy 625, Carpenter L-605 alloy, BioDur® Carpenter CCM® alloy, Haynes 230, 310 SS or 625 SS. The solid may comprise a refractory metal. The solid may comprise a metal of an antioxidant. The solid may comprise a metal such as tantalum or a conductive cap layer or coating to avoid oxidation of the solid conductor. In an embodiment, the magnetic winding of at least one of the converter and the electromagnet is at a distance from the EM pump sleeve section 405 of the current loop, comprising at least one of the transformer yoke 402 and the electromagnetic circuit yoke 404 It extends to flow the metal. The extension allows for more efficient cooling of the more efficient heating of the inductively coupled heating of the EM pump sleeve 405 and at least one of the transformer winding 401, the transformer yoke 402, and the electromagnetic circuit 403c comprising the AC electromagnet 403 and the EM pump electromagnetic yoke 404 At least one of them. In the case of a secondary EM pump, the magnetic circuit can include AC electromagnets 403a and 403b and EM pump electromagnetic yokes 404a and 404b. At least one of the transformer yoke 402 and the electromagnetic yoke 404 may comprise a ferromagnetic material having a high Curie temperature, such as iron or cobalt. At least one of the EM pump transformer winding circuit 401a and the EM pump electromagnetic circuit 403c may comprise a water cooling system such as one of the present inventions, such as one of the magnets 5k4 of the DC conductive EM pump (Fig. 2I115-2I116). At least one of the inductive EM pumps 400b can include an air cooling system 400b (Figs. 2I190-2I191). At least one of the inductive EM pumps 400c can include a water cooling system (Fig. 2I192). An exemplary transformer includes a silicon steel laminated transformer core. The ignition transformer may comprise (i) a number of windings in at least one of about 10 to 10,000 angstroms, 100 to 5,000 angstroms, and 500 to 25,000 angstroms; at about 10 watts to 1 MW, 100 watts to 500 kW, 1 kW to 100 kW and power in at least one of 1 kW to 20 kW, and (iii) in at least one of about 0.1 A to 10,000 A, 1 A to 5 kA, 1 A to 1 kA, and 1 A to 500 A Primary winding current. In an exemplary embodiment, the ignition current is in the range of about 6 V to 10 V and the current is about 1000 A; thus the winding with 50 turns operates at about 500 V and 20 A to provide 10 at 1000 A. The ignition current of V. The EM pump electromagnet may comprise flux in at least one of about 0.01 T to 10 T, 0.1 T to 5 T, and 0.1 T to 2 T. In an exemplary embodiment, the approximately 0.5 mm diameter magnetic wire is maintained at about 200 °C. The EM pump cannula can be heated using an inductively coupled heater antenna such as a pie coil antenna. The antenna can be cooled by water. In an embodiment, the reservoir 5c can be heated using an inductively coupled heater. The heater antenna 5f may comprise two cylindrical helices around the reservoir 5c that may be further connected to a coil such as a pie coil to heat the EM pump casing. The turns of the opposite spirals around the reservoir can be wound such that the currents are in the same direction to strengthen the magnetic fields of the two coils or in opposite directions to eliminate the magnetic field in the space between the spirals. In an exemplary embodiment, the inductively coupled heater antenna 5f may comprise a continuous set of three turns, as shown in Figures 2I182-2I183, 2I186, and 2I190-2I192, including two spirals of the circumference of each reservoir 5c. a wire and a pie coil parallel to the EM pump tube, wherein the two spirals are wound clockwise, and current flows from the top of one spiral to the bottom thereof, flows into the pie coil, and then from the second spiral The bottom flows to the top. The EM pump sleeve section 405 of the current loop may be an additive of EM pump sleeve 405 material by a flux concentrator, an additive such as quartz or tantalum nitride, and an absorbing carbon sleeve such as RF from an inductively coupled heater. At least one of the claddings of the pump casing 405 is selectively heated. In an embodiment, the EM pump cannula section 405 of the current loop can be selectively heated by an inductively coupled heater antenna that includes a helix around the pump cannula 405. At least one of the at least one of the MHD return conduit 310, the EM pump reservoir line 416, and the EM pump injection line 417 (FIGS. 2I192-2I195) may be heated by an inductively coupled heater, which may include An antenna 415 is wound around the pipeline of the water-coolable antenna. An assembly wound with an inductively coupled heater antenna such as 5f and 415 may include an inner insulating layer. The inductively coupled heater antenna provides dual function or heating and water cooling to maintain the desired temperature of the corresponding component. The SunCell can further include: a structural support 418 that secures components such as the MHD magnet housing 306a, the MHD nozzle 307, and the MHD channel 308, electrical outputs, sensors, and mountable to the structural support 418 and such as the EM pump reservoir line 416. And a control line 419 on the heat shield of 420 around the EM pump injection line 417. The EM pump casing section 405 of the current loop may include molten metal inlet and outlet passages connected to the corresponding EM pump casing 5k6 section (Fig. 2I185). Each inlet and outlet of the EM pump casing 5k6 can be fastened to the corresponding reservoir 5c, the inlet riser 5qa, and the injector 5k61. The fastener may comprise a joint, fastener or seal of the invention. Seal 407a can comprise a ceramic glue. The joints may each comprise a flange sealed with a gasket such as a graphite gasket. Each of the reservoirs 5c may comprise a ceramic such as a metal oxide connected to a reservoir bottom plate which may be ceramic. The backplane connection can include a flange and a gasket seal, wherein the gasket can comprise carbon. The bottom plate may include a reservoir floor assembly 409 (Fig. 2I 187) that includes a bottom plate 409a having an attached inlet riser 5qa and an ejector sleeve 5k61 having a nozzle 5q. The sleeve can penetrate the base of the reservoir bottom plate 409a as a boss 408. The boss 408 from the reservoir 5c can be coupled to the ceramic inlet and outlet of the EM pump sleeve of the inductive EM pump 400 by at least one of a flange joint 407 having a fastener and a gasket. Such as bolts, such as carbon, molybdenum or ceramic bolts, such as carbon gaskets, wherein the abutment comprising at least one ceramic component operates at a temperature below the carbon reduction temperature. In other embodiments, the union may include other abutments known in the art, such as Swagelok, sliding nut or compression fittings. In an embodiment, the ignition current is supplied by a power source having a positive terminal and a negative terminal connected to a conductive component of one of the pump casing, the reservoir, the boss, and the union. In another embodiment, the ignition system includes an inductive system (Fig. 2I186, 2I189-2I195) in which a power source is applied to the electrically conductive molten metal such that ignition of the low energy hydrogen reaction provides induced current, voltage, and power. The ignition system can include an electrodeless system in which the ignition current is applied by induction by the induction ignition transformer assembly 410. The induced current can flow through the intersecting molten metal stream from a plurality of injectors held by a pump such as EM pump 400. In an embodiment, the reservoir 5c may further comprise a ceramic interface 414, such as a channel between the bases of the reservoir 5c. The inductive ignition transformer assembly 410 can include an inductive ignition transformer winding 411 and an inductive ignition transformer yoke 412 that can extend through the intersecting molten metal stream from the plurality of molten metal injectors by the reservoir 5c and An induced current loop formed by the junction channel 414. The inductive ignition transformer assembly 410 can be similar to the inductive ignition transformer assembly of the EM pump transformer winding circuit 401a. In an embodiment, the ignition current source may comprise an AC induction type in which a current in a molten metal such as silver is induced by Faraday induction through a time varying magnetic field of silver. The source of the time varying magnetic field can include a primary transformer winding, an inductive ignition transformer winding 411, and the silver can at least partially function as a secondary transformer winding, such as a single turn shorted winding. The primary winding 411 can include an AC electromagnet, wherein the inductive ignition transformer yoke 412 conducts a time varying magnetic field through a circumferential conductive loop comprising molten silver. The transformer electromagnet can be powered by a single phase AC power source or other suitable power source known in the art. The transformer frequency can be increased to reduce the size of the transformer yoke 412. The transformer frequency can be in the range of approximately 1 Hz to 1 MHz, 1 Hz to 100 kHz, 10 Hz to 10 kHz, and 10 Hz to 1 kHz. The reservoir 5c may comprise a molten metal channel such as a junction channel 414 connecting the two reservoirs 5c. The current loop enclosing the transformer yoke 412 may include the reservoir 5c, the molten silver contained in the transfer passage 414, the silver in the ejector sleeve 5k61, and the jetted intersection to complete the molten current flow of the induced current loop. The inductive current loop may further comprise, at least in part, molten silver contained in at least one of an EM pump assembly such as a feed riser 5qa, an EM pump sleeve 5k6, a boss, and an injector 5k61. The transfer channel 414 can be at a desired level of molten metal such as silver in the reservoir. Alternatively, the transfer channel 414 can be at a location below the desired reservoir molten metal level such that the channel is continuously filled with molten metal during operation. The transfer channel 414 can be positioned towards the base of the reservoir 5c. The channel may form part of an induced current loop or circuit and further facilitates flow of molten metal from one reservoir having a higher silver level to another reservoir having a lower level to hold two reservoirs 5c The required level. The difference in the molten metal discharge pressure allows the metal to flow between the reservoirs to maintain the desired level in each reservoir. The current loop may comprise an intersecting molten metal stream, an ejector sleeve 5k61, a molten metal column in the reservoir 5c, and a reservoir 5c connected to the desired molten silver level or a reservoir below a desired level. Handover channel 414. The current loop encloses a transformer yoke 412 that induces current by the Faraday. In another embodiment, the at least one EM pump transformer yoke 402 can further include an induction ignition transformer yoke 412 to generate an induced ignition current by additionally supplying a time varying magnetic field through the ignition molten metal circuit, such as by An ignited molten metal circuit formed by the intersecting molten metal stream and the molten metal contained in the reservoir and the transfer passage 414. Reservoir 5c and channel 414 may comprise an electrical insulator such as ceramic. The inductive ignition transformer yoke 412 can include a cover plate 413 that can include at least one of an electrical insulator such as a ceramic cover plate and a thermal insulator. Sections of the inductive ignition transformer yoke 412 extending between the reservoirs may be thermally or electrically shielded by a cover plate 413, which may include circumferentially wound inductively coupled heater antennas such as spiral coils. The ceramic of at least one of the reservoir 5c, the channel 414 and the cover plate 413 may be a ceramic of the invention, such as tantalum nitride (MP 1900 ° C), quartz such as fused silica, alumina, zirconia, magnesia or Yttrium oxide. Protective SiO2 The layer can be formed by controlled passivation oxidation on yttrium nitrite. Ceramic components such as quartz components can be cast using molding such as graphite or other refractory inert molding. In an exemplary embodiment, the quartz is poured into a hot or cryogenic liquid by methods known in the art, such as the method of Hellma analysis (http://www.hellmaanalytics.com/assets/adb/32/32e6a909951dc0e2.pdf). The molding comprises four components comprising two inner and outer surfaces facing the battery assembly such as the reservoir 5c and the reaction cell chamber 5b31. In an embodiment, the transfer channel 414 maintains the reservoir silver level near constant. The SunCell® may further include an immersion nozzle 5q of the ejector 5k61. Due to the approximately constant molten metal level of each reservoir 5c, the depth of each submerged nozzle and thus the discharge pressure through which the injector is injected may remain substantially constant. In embodiments including the transfer passage 414, the inlet riser 5qa can be removed and replaced with a bore into the reservoir boss 408 or EM pump reservoir line 416. At least one of the transformer windings 401 and 411, the electromagnet 403, the yokes 402, 404, and 412 and the magnetic circuits 401a, 403a, and 410 of at least one of the EM pump and the ignition system may shield the RF magnetic field of the inductively coupled heater To reduce the heating effect. The shield can contain a Faraday cage. The cage wall thickness can be greater than the skin depth of the RF field of the inductively coupled heater. In an embodiment comprising an inductive ignition system 410, the transformer yoke 412 can be at least partially cooled by the proximity of the water cooled antenna 5f, which can be further used to cool the SunCell® and the reservoir 5c during operation. At least one. The ignition current can be time-varying, such as about 60 Hz AC, but can have other characteristics and waveforms, such as having at least 1 Hz to 1 MHz, 10 Hz to 10 kHz, 10 Hz to 1 kHz, and 10 Hz to 100 Hz. a waveform of a frequency within a range of peak currents in at least one of about 1 A to 100 MA, 10 A to 10 MA, 100 A to 1 MA, 100 A to 100 kA, and 1 kA to 100 kA, and Peak voltage in the range of approximately 1 V to 1 MV, 2 V to 100 kV, 3 V to 10 kV, 3 V to 1 kV, 2 V to 100 V, and 3 V to 30 V, where the waveform can include sinusoidal Wave, square wave, triangle or other desired waveform, which may include a duty cycle such as a duty cycle in at least one of 1% to 99%, 5% to 75%, and 10% to 50%. In an embodiment, the firing frequency is adjusted to produce a low energy hydrogen power generation corresponding frequency in at least one of the reaction cell chamber 5b31 and the MHD channel 308. The frequency of the power output, such as about 60 Hz AC, can be controlled by controlling the firing frequency. The firing frequency can be adjusted by varying the frequency of the time varying magnetic field of the induction ignition transformer assembly 410. The frequency of the inductive ignition transformer assembly 410 can be adjusted by varying the frequency of the current that induces the ignition transformer winding 411, wherein the frequency of the power of the winding 411 can be varied. The time varying power in the MHD channel 308 prevents seismic wave formation from the aerosol jet stream. In another embodiment, time varying ignition can drive time varying low energy hydrogen power generation that results in a time varying electrical power output. The MHD converter can output AC power, and the converter can also include a DC component. The AC component can be used to power at least one winding of at least one of one or more of a transformer and an electromagnet winding, such as the winding of the EM pump transformer winding circuit 401a and the EM pump electromagnetic circuit 403c At least one of the windings of the electromagnet. The pressurized SunCell® with MHD converter can operate without gravity. An EM pump, such as 400, such as a two stage air cooled EM pump 400b, can be positioned in a position that optimizes at least one of the filler and minimization of the molten metal inlet and outlet conduits or lines. An exemplary package is a package in which the EM pump is positioned intermediate the end of the MHD condensation section 309 and the base of the reservoir 5c (Fig. 2I193-2I195). In an embodiment, the silver vapor-silver aerosol mixture exiting MHD nozzle 307 and entering MHD channel 308 contains a majority of the liquid fraction. To achieve a majority of the liquid fraction at the inlet of the MHD channel 308, the mixture can contain most of the liquid at the inlet of the MHD nozzle 307. The thermal power of the reaction cell chamber 5b31 resulting from the low energy hydrogen reaction can be converted to kinetic energy by the MHD nozzle 307. In embodiments in which most of the energy inventory at the exit of the MHD nozzle 307 is kinetic energy, the mixture must be a majority of the liquid fraction, and the temperature and pressure of the mixture should be close to the temperature and pressure at which the molten metal is at its melting point. In order to convert the thermal energy inventory of a larger fraction of the mixture into kinetic energy, the nozzle area of the branching section of the polymerization-splitting MHD nozzle 307 such as the de Laval nozzle must be increased. Since the thermal energy of the mixture is converted to kinetic energy in the MHD nozzle 307, the temperature of the mixture decreases with the accompanying pressure drop. Low pressure conditions correspond to lower vapor densities. The lower vapor density reduces the cross section to transfer the forward momentum and kinetic energy to the liquid fraction of the mixture. In an embodiment, the nozzle length can be increased to produce a longer liquid acceleration time before the nozzle outlet. In an embodiment, the cross-sectional area of the aerosol spray column at the exit of the MHD nozzle can be reduced. The area reduction can be achieved by one or more of at least one focusing magnet, spacer, and other components known in the art. A focused aerosol jet with a reduced area may permit a smaller cross-sectional area of the MHD channel 308. The MHD channel power density can be higher. The MHD magnet 306 can be smaller due to the smaller volume of the magnetization channel 308. In an embodiment, the temperature of the mixture at the inlet of the MHD channel 308 is close to the melting point of the molten metal. In the case of silver, the temperature of the mixture may be in the range of at least about 965 ° C to 2265 ° C, 1000 ° C to 2000 ° C, 1000 ° C to 1900 ° C, and 1000 ° C to 1800 ° C. In an embodiment, the silver liquid may be recycled to the reservoir 5c by the EM pump 400, 400a, 400b or 400c to recover at least a portion of the thermal energy in the liquid. In embodiments including live joints, the joints comprise ceramic components and carbon gaskets, and the temperature of the recycled silver can be lower than the carbon reduction temperature of the graphite and ceramics and the failure temperature of the material of the SunCell® component such as the ceramic component. At least one of them. Included in the EM pump casing section 405, such as the return conduit 310, the current loop, the reservoir 5c, the reaction cell chamber 5b31, the MHD nozzle 307, and at least one carbon gasket flange joint 407 between the ceramic components. In an exemplary embodiment of the yttria-stabilized zirconia of the MHD channel 308 and the MHD condensation section 309, the silver temperature is less than about 1800 °C to 2000 °C. The power of an aerosol containing kinetic energy and thermal energy can be converted into electricity in the MHD channel. Aerosol kinetic energy can be converted to electricity by a liquid MHD mechanism. Some of the residual thermal power of the thermal power of any vapor, such as the mixture in the MHD channel 308, can be converted to electricity by the Lorentz force acting on the corresponding vapor. The thermal energy conversion rate causes the temperature of the mixture to drop. The silver vapor pressure can be lower corresponding to the lower mixture temperature. The MHD channel 308 can be maintained at a lower background pressure, such as at a pressure in the range of at least about 0.001 Torr to 760 Torr, 0.01 Torr to 100 Torr, and 0.1 Torr to 10 Torr to prevent aerosol spray from the nozzle 307. The column is subjected to seismic waves, such as condensed shock waves or turbulence, such that the aerosol creates a pressurization, such as back pressure in the MHD channel 308. In an embodiment, the vapor fraction of the mixture is minimized at the nozzle inlet to reduce it at the nozzle outlet. The vapor fraction may range from at least one of about 0.01 to 0.3, 0.05 to 0.25, 0.05 to 0.20, 0.05 to 0.15, and 0.05 to 0.1. 20 atmospheres, 0 m/s speed, 3253 K temperature, 0.9 liquid mass fraction of the mixture, acoustic wave velocity 137 m/s, Mach number 0 and 0 kJ/kg kinetic energy given nozzles, inlet parameters, nozzle outlet The exemplary parameters of the mixture are approximately the parameters given in Table 3. Table 3. Nozzle outlet parameters for initial pressure parameters of 20 atmosphere pressure, 0.9 liquid fraction, and 1 kg/s mass flow. In an embodiment, the vapor may be at least partially condensed at the end of the MHD channel, such as in the MHD condensation section 309. Heat exchanger 316 can remove heat to cause condensation. Alternatively, the vapor pressure may be low enough such that the MHD efficiency is increased by non-condensing vapor, wherein the vapor maintains a static equilibrium pressure in the MHD channel 308. In an embodiment, the Lorentz force is greater than the collision friction of any uncondensed vapor in the MHD channel 308. The Lorentz force can be increased to the Lorentz force required to increase the strength of the magnetic field. The magnetic flux of the MHD magnet 306 can be increased. In an embodiment, the magnetic flux may be in a range of at least one of about 0.01 T to 15 T, 0.05 T to 10 T, 0.1 T to 5 T, 0.1 T to 2 T, and 0.1 T to 1 T. In an embodiment, the silver vapor is condensed such that the heat of vaporization is recirculated to the reservoir or to the silver of the EM pump casing of the secondary EM pump that is the injector 5k61. The vapor can be compressed using compressor 312a. The compressor can be connected to a secondary EM pump such as 400c. In an embodiment, the silver vapor/aerosol mixture is oxygenated at the outlet of the MHD nozzle 307 with almost pure liquid. The solubility of oxygen in silver increases as the temperature approaches the melting point, with solubility being up to about 40 to 50 oxygen volumes for the silver volume (Figure 3). Silver absorbs oxygen at the MHD channel 308, such as at the exit, and both liquid silver and oxygen are recycled. Oxygen can be recycled to the gas absorbed in the molten silver. In the embodiment, oxygen is released into the reaction chamber 5b31 to regenerate the cycle. Temperatures above the melting point of silver also serve as a means for thermal power recycle or regeneration. The oxygen concentration is optimized to achieve a thermodynamic cycle in which the temperature of the recycled silver is less than the maximum operating temperature of a SunCell® component such as 1800 °C. In an exemplary embodiment, (i) the oxygen pressure in at least one of the reaction cell chamber 5b31 and the MHD nozzle 307 is 1 atmosphere, and (ii) the silver at the outlet of the MHD channel 308 is almost entirely such as gas. a sol liquid, (iii) an oxygen mass flow rate of about 0.3% by weight, and (iv) a temperature at the outlet of the MHD channel of about 1000 ° C, wherein O2 The aerosol was accelerated and subsequently absorbed by 1000 ° C silver. The liquid silver-oxygen mixture is recycled to the reaction cell chamber 5b31 where oxygen is released to form a thermodynamic cycle. The need for a gas compressor such as 312a and corresponding parasitic power loads can be reduced or eliminated. In an embodiment, the oxygen pressure may range from about 0.0001 atmospheres to 1000 atmospheres, from 0.01 atmospheres to 100 atmospheres, from 0.1 atmospheres to 10 atmospheres, and from 0.1 atmospheres to 1 atmosphere. Oxygen may have a higher partial pressure in a battery region, such as at least one of reaction cell chamber 5b31 and nozzle 307 with respect to MHD channel outlet 308. The SunCell® can have a background oxygen partial pressure that can be raised in a battery region such as at least one of the reaction cell chamber 5b31 and the nozzle 307 with respect to the MHD channel outlet 308. Due to the much higher oxygen heat capacity and non-condensing forces at the operating temperature, the MHD nozzle can be reduced in size relative to the size of the MHD converter using only silver vapor to achieve aerosol spray column acceleration. The thermodynamic cycle can be optimized to maximize electrical conversion efficiency. In an embodiment, the kinetic energy of the mixture is maximized while minimizing the vapor fraction. In an embodiment, thermal power recycle or regeneration is achieved as a function of the temperature of the recycled silver from the outlet of the MHD channel 308 to the reaction cell chamber 5b31. The temperature of the recycled silver can be less than the maximum operating temperature of the SunCell® component, such as 1800 °C. In another embodiment, the Lorentz force can cool the mixture to at least partially concentrate the liquid phase, wherein the corresponding released heat of vaporization is at least partially transferred to the liquid phase. At least one of the MHD nozzle extension, the MHD channel 308 extension, and the Lorentz force cooling in the MHD channel 308 may reduce the temperature of the mixture at one or more of the MHD nozzle 307 outlet and the MHD channel 308 below the melting point of the silver. . The heat released by the condensed vapor can be absorbed into the heat of fusion of the thermal capacity of silver and silver as the temperature increases. The silver heated by the condensation vaporization heat can be recycled to regenerate the corresponding thermal power. In another embodiment of increasing efficiency, the relatively low temperature aerosol may be injected into a power conversion assembly such as MHD nozzle 307 or MHD channel 308 by means such as a conduit from the reservoir 5c. Ceramic components of SunCell® can be joined by means of the present invention, such as ceramic glues of two or more ceramic components, brazing of ceramic to metal components, sliding nut seals, gasket seals, and wet seals. The gasket seal can include two flanges that are sealed with a gasket. The flange can be withdrawn along with a fastener such as a bolt. The sliding nut joint or gasket seal can include a carbon gasket. At least one of the nut, EM pump assembly 5kk, reservoir bottom plate 5b8, and lower hemisphere 5b41 may comprise materials resistant to carbonization and carbide formation, such as nickel, carbon, and carbonization resistant stainless steel such as SS 625 or Haynes 230 SS. (SS). The sliding nut engagement between the EM pump assembly and the ceramic reservoir can include an EM pump assembly 5kk and a graphite gasket, the EM pump assembly including a threaded collar and a nut that includes carbonization resistant such as SS 625 or Haynes 230 SS stainless steel (SS) with a nut threaded onto the collar to secure the gasket. The flange sealing engagement between the EM pump assembly 5kk and the reservoir 5c can include a reservoir bottom plate 5b8 having a bolt hole, a ceramic reservoir having a flange and a bolt hole, and a carbon gasket. The EM pump assembly with the reservoir bottom plate may comprise a carbonized stainless steel (SS) such as SS 625 or Haines 230 SS. The flange of the reservoir can be fastened to the bottom plate 5b8 by fastening bolts of carbon or graphite spacers. In an embodiment, a carbon reduction reaction between a carbon such as a carbon gasket and a component comprising an oxide such as oxide reservoir 5c is avoided by maintaining contact between the bond comprising oxidation and carbon at a non-reactive temperature. Oxide reservoirs such as MgO, Al2 O3 Or ZrO2 The reservoir, the non-reactive temperature is lower than the carbon reduction reaction temperature. In an embodiment, the MgO carbon reduction reaction temperature is in the range of from about 2000 °C to 2300 °C. In an exemplary embodiment, a ceramic such as an oxide ceramic may be metallized with an alloy such as Mo-Mn, such as zirconia or alumina. The two metallized ceramic parts can be joined by brazing. The metallized ceramic component and the metal component such as the EM pump busbar 5k2 can be joined by brazing. Metallization can be applied to protect it from oxidation. Exemplary coatings comprise nickel and precious metals in the case of water oxidants and noble metals in the case of oxygen. In an exemplary embodiment, the alumina or zirconia EM pump sleeve 5k6 is metallized at the penetration of the EM pump busbar 5k2, and the EM pump busbar 5k2 is connected by brazing to the metallized EM pump casing. . In another exemplary embodiment, from the EM pump assembly 5kk, the EM pump 5ka, the EM pump casing 5k6, the inlet riser 5qa, the injection EM pump casing 5k61, the reservoir, the MHD nozzle 307, and the MHD passage 308 The parts of the list of at least two of them can be glued together with ceramic glue. The ceramic component can be constructed using the present invention or methods known in the art. The ceramic components can be powder molded, poured or sintered, or glued together, or screwed together. In an embodiment, the components can be constructed and sintered in a ceramic green body. In an exemplary embodiment, the alumina components can be sintered together. In another embodiment, the plurality of components can be constructed as a green component, assembled and sintered together. The dimensions of the components and materials can be selected to compensate for component shrinkage. In an embodiment, a ceramic SunCell® component, such as a ceramic component comprising at least one of ZrC-ZrB2-SiC, may be formed by a stoichiometric mixture of ball milled component powders, formed into a desired shape during molding, and borrowed Sintering is performed by means such as heat equalization (HIP) or spark plasma sintering (SPS). Ceramics can have a relatively high density. In an embodiment, a hollow member such as an EM pump sleeve 5k6 may be cast using a bladder for a hollow member. The bladder can be deflated after casting and the parts sintered. Alternatively, the components can be constructed by 3D printing. Components such as at least one of the lower hemisphere 5b41 and the upper hemisphere 5b42 may be slidably cast, and components such as the reservoir 5c may be formed by at least one of extrusion and pressing. Other construction methods include at least one of spray drying, injection molding, processing, metallization, and coating. In an embodiment, the carbide ceramic component can be configured to produce a ZrC or SiC component from graphite that reacts with a corresponding metal such as zirconium or hafnium, respectively. Components comprising different ceramics can be joined together by methods of the invention or methods known in the art, such as tightening, gluing, wet sealing, brazing, and gasket sealing. In an embodiment, the EM pump sleeve can include a sleeve section and a bend and a bus bar tab 5k2 glued together. In an exemplary embodiment, the glued EM pump sleeve component comprises ZrC or graphite that reacts with the Zr metal to form ZrC. Alternatively, the component can include ZrB2 Or similar non-oxidized conductive ceramics. In an embodiment, the MHD electrode 304 comprises a liquid electrode such as a liquid silver electrode. At least one of the MHD electrical lead 305 and the feed aperture 301 is similar to a wet seal that can comprise a solidified molten metal such as solidified silver, wherein at least one of the lead or feedthrough can be cooled to maintain a solid metal state. The MHD converter can include a patterned structure including an MHD electrode 304, an electrically insulated wire such as 305, an insulated electrode separator, and a feedthrough such as a feedthrough that penetrates a flange of a MHD bus feedthrough hole such as 310 At least one component of the group. A patterned structural component and an insulating separator comprising a liquid electrode such as a silver electrode may comprise a wetting material to maintain a desired shape of the liquid metal and a spacing between the liquid electrode such as a silver electrode and the insulated electrode separator. At least one of the patterned structure of the wetting material and the insulating separator may comprise ceramic. The wetted material of the liquid electrode may comprise a porous ceramic. The electrically insulating separator can comprise a dense ceramic that is non-wettable for silver. The wire may comprise electrically insulating channels and sleeves that may be cooled, such as by water cooling, to maintain the hardness of the wire. The exemplary embodiment includes an electrically insulating MHD electrode lead 305 that is cooled to hold the solidified silver internally to act as a conductive lead. In another embodiment, at least one of the MHD electrical lead 305 and the feed aperture 301 can comprise a coating such as a coating such as tantalum coated Mo or an antioxidant stainless steel such as 625 SS. An exemplary material for a SunCell® having an MHD converter includes (i) a reservoir 5c, a reaction cell chamber 5b31, and a nozzle 307: a solid oxide such as stabilized zirconia or yttria; (ii) a MHD channel 308: MgO or Al2 O3 ; (iii) Electrode 304: ZrC or ZrC-ZrB2 , ZrC-ZrB2 -SiC and ZrB with 20% SiC composite working up to 1800 °C2 Or metal coated with a precious metal; (iv) EM pump 5ka: such as stainless steel coated with a precious metal or a metal coated with a material having a similar coefficient of thermal expansion such as Paloro-3V palladium gold vanadium alloy (Morgan high-grade material) The noble metal such as at least one of platinum (Pt), palladium (Pd), ruthenium (Ru), rhodium (Rh), and iridium (Ir); (v) reservoir 5c-EM pump assembly 5kk activating: ZrO such as brazing to the bottom of a 410 stainless steel EM assembly 5kk2 HfO2 Or Al2 O3 Oxide reservoir, wherein the braze comprises a Paloro-3V palladium gold vanadium alloy (Morgan high grade material); (vi) an ejector 5k61 and an inlet riser 5qa: a solid oxide such as stabilized zirconia or yttria; And (vii) oxygen selective membrane: can be coated with Bi26 Mo10 O69 BaCo to increase oxygen permeability0 . 7 Fe0 . 2 Nb0 . 1 O3 - δ (BCFN) oxygen permeable membrane. In an embodiment, the SunCell® further includes an oxygen sensor and an oxygen control system such as a means for diluting oxygen with an inert gas and pumping the inert gas away. The former may include at least one of an inert gas storage tank, a valve, a regulator, and a pump. The latter can include at least one of a valve and a pump. The low energy hydrogen reaction mixture of the reaction cell chamber 5b31 may further comprise such as H2 A source of oxygen for at least one of O and a compound comprising oxygen. The source of oxygen, such as a compound comprising oxygen, can be in an excess form to maintain a near constant source of oxygen source, wherein during battery operation, a smaller portion is reversibly associated with, such as H2 The supply of gas H is sourced to form a HOH catalyst. Exemplary compounds containing oxygen are MgO, CaO, SrO, BaO, ZrO2 HfO2 Al2 O3 Li2 O, LiVO3 Bi2 O3 Al2 O3 , WO3 And other compounds of the invention. The oxygen source compound may be an oxygen source compound for stabilizing an oxide ceramic such as cerium oxide or cerium oxide, such as cerium oxide (Y)2 O3 ), magnesium oxide (MgO), calcium oxide (CaO), strontium oxide (SrO), strontium oxide (Ta2 O5 ), boron trioxide (B2 O3 ), TiO2 , Cerium oxide (Ce2 O3 ), strontium zirconate (SrZrO)3 ), magnesium zirconate (MgZrO3 ), calcium zirconate (CaZrO)3 ) and barium zirconate (BaZrO)3 ) . In an exemplary embodiment having an electrical conductivity greater than about 20 kS/m and a plasma gas temperature of about 4000 K, the reaction chamber pressure is maintained in the range of about 15 MPa to 25 MPa to maintain the MHD channel 308 against Lorentz forces. The flow in the middle. In an exemplary embodiment, the conductivity is maintained at about 700 S/m, the plasma gas temperature is about 4000 K, the reaction cell chamber 5b31 pressure is about 0.6 MPa, and the nozzle 307 exit velocity is about Mach 1.24, nozzle exit region. Is about 3.3 cm2 The nozzle outlet diameter is about 2.04 cm, the nozzle outlet pressure is about 213 kPa, the nozzle outlet temperature is about 2640 K, the mass flow through the nozzle is about 250 g/s, and the magnetic field strength in the MHD channel 308 is about 2 T. The MHD channel 308 has a length of about 0.2 m, the MHD channel outlet pressure is about 11 kPa, the MHD channel outlet temperature is about 1175 K, and the output electrical power is about 180 kW. In a preferred embodiment, the efficiency is determined by the Carnot equation, where the inevitable power loss from plasma temperature to ambient temperature is the loss of gas and liquid metal pumps. In an embodiment, an MHD converter for any power source, such as a core or a combustion, capable of heating silver to form at least one of silver vapor and silver aerosol comprises the MHD converter of the present invention, the MHD converter further comprising at least A heat exchanger generates at least one of silver vapor and silver aerosol by transferring heat from the power source to heat at least one of the reservoir 5c and the reaction cell chamber 5b31. The MHD converter may further comprise an ionization source such as at least one of a seed crystal such as an alkali metal such as a thermal ionization crucible and an ionizer, such as a laser, an RF discharge generator, a microwave A discharge generator and a glow discharge generator. In an embodiment of a SunCell® power system including a heater power converter, the EM pumps of the dual molten metal injectors each may include an inductive electromagnetic pump to eject a stream of molten metal intersecting another stream of molten metal into the container. Internal. The power supply to the ignition system includes an inductive ignition system 410 that can include an alternating magnetic field source that passes through a short circuit of molten metal that produces an alternating current containing ignition current in the metal. The alternating magnetic field source can include a primary transformer winding 411 that includes a transformer electromagnet and a transformer yoke 412, and the silver can at least partially function as a secondary transformer winding, such as a single turn short winding that encloses the primary transformer winding and includes an inductive loop . The reservoir 5c can include a molten metal interface 414 that connects the two reservoirs such that the current loop encloses the transformer yoke 412, wherein the induced current loop includes the molten silver contained in the reservoir 5c, the interface 414 The silver in the ejector sleeve 5k61 and the injected intersection intersect to induce a current flowing in the molten silver stream. A reaction gas such as hydrogen and oxygen may be supplied to the battery through the intake port and the evacuation assembly 309e of the gas housing 309b. The gas housing 309e can be external to the spherical heat exchanger along the axis of the top pole of the sphere. The gas housing may comprise a thin gas pipe connection to the top of the spherical reaction cell chamber 5b31 at the flange connection. The trachea connection may pass through the interior of the concentric coolant flow conduit that supplies coolant flow to the spherical heat exchanger. On the reaction cell side, the flange connection to the gas pipe can be connected to a semi-permeable gas 309d membrane, such as a porous ceramic membrane. The SunCell® heater or thermal power generator embodiment (Fig. 2I196) comprises a spherical reactor cell 5b31 and a spatially separated circumferential hemispherical heat exchanger comprising a panel or section 114a that receives radiation from the spherical reactor 5b4. 114. Each panel may comprise a section of a spherical surface defined by two larger rings passing through the poles of the sphere. The heat exchanger 114 can further include a manifold 114b having a toroidal manifold from the coolant line 114c of each of the heat exchanger panels 114a and a manifold coolant outlet 114f. Each coolant line 114c can include a coolant inlet aperture 114d and a coolant outlet aperture 114e. The thermal power generator may further include a gas cylinder 421 having an inlet and an outlet 309e and a gas supply sleeve 422 extending through the top of the heat exchanger 114 to the gas permeable membrane 309d on the top of the spherical battery 5b31. Gas supply sleeve 422 can pass through coolant collection manifold 114b at the top of heat exchanger 114. In another SunCell® heater embodiment (Figs. 2I156-2I160 and 2I196), the reaction cell chamber 5b31 can be cylindrical with a cylindrical heat exchanger 114. The gas cylinder 421 may be external to the heat exchanger 114, wherein the gas supply sleeve 422 is connected to the semi-permeable gas membrane 309d on the top of the reaction cell chamber 5b31 by passing through the heat exchanger 114. Cold water may be fed into the inlet 113 and heated in the heat exchanger 114 to form steam collected in the boiler 116 and present in the steam outlet 111. The thermal power generator may further comprise a dual molten metal injector comprising an inductive EM pump 400, a reservoir 5c and a reaction cell chamber 5b31. At least one SunCell® heater assembly, such as reservoir 5c, may be heated by an inductively coupled heater antenna 5f. The SunCell® heater can include an induction ignition system such as an induction ignition system including an induction ignition transformer winding 411 and an induction ignition transformer yoke 412.Illustrative embodiment In an exemplary embodiment of the SunCell® generator of the present invention comprising a PV converter: (i) the EM pump assembly 5kk may comprise stainless steel, wherein an internal surface such as EM pump sleeve 5k6 that is exposed to oxidation may be used, such as nickel Coating of an antioxidant coating of a coating, wherein stainless steel such as Inco high nickel is selected to have a coefficient of thermal expansion similar to that of nickel; (ii) the reservoir 5c may comprise boron nitride such as BN-Ca, which may Antioxidant stabilization; (iii) the abutment between the reservoir and the EM pump assembly 5kk may comprise a wet seal; (iv) the molten metal may comprise silver; (v) the inlet riser 5qa and the injection casing 5k61 may Contains ZrO screwed into the collar of the EM pump assembly base plate 5kk12 (vi) the lower hemisphere 5b41 may comprise carbon such as heat carbon reactive with hydrogen; (vii) the upper hemisphere 5b42 may comprise carbon such as heat carbon reactive with hydrogen; (viii) the oxygen source may comprise CO, wherein CO Can be added as a gas, such as a metal carbonyl (eg W(CO))6 Ni(CO)4 ,Fe(CO)5 ,Cr(CO)6 , Re2 (CO)10 And Mn2 (CO)10 a controlled heat or other decomposition supply of the carbonyl group, and as a CO2 Source or CO2 Gas supply, where CO2 Can be decomposed in a low-energy hydrogen plasma to release CO or can react with carbon such as a supply of sacrificial carbon powder to supply CO, or O2 The oxygen permeable membrane of the present invention, such as one of the present invention, may be added, such as available Bi26 Mo10 O69 BaCo coated to increase oxygen permeability0.7 Fe0.2 Nb0.1 O3 - δ (BCFN) oxygen permeable membrane, wherein the addition can react with the sacrificial carbon powder to maintain the desired CO concentration as monitored by the detector and controlled by the controller2 (ix) The hydrogen source may comprise a hydrogen permeable membrane that can be supplied by a mass flow controller such as a Pd or Pd-Ag membrane in the wall of the EM pump casing 5k4 to control the hydrogen flow from the high pressure water electrolyzer.2 The gas; (x) the union between the reservoir and the lower hemisphere 5b41 may comprise a sliding nut, which may comprise a carbon gasket and a carbon nut; and (xi) the PV converter may comprise a dense receiver array, the dense The receiver array contains a multi-junction III-V PV cell cooled by a cold plate. The reaction cell chamber 5b31 may contain a source of sacrificial carbon such as carbon powder to remove O which will otherwise react with the walls of the carbon reaction cell chamber.2 And H2 O. The rate of reaction of water with carbon depends on the surface area of the order of magnitude greater than the surface area of the wall of the reaction cell chamber 5b31 in terms of sacrificial carbon. In an embodiment, the inner wall of the carbon reaction cell chamber contains a carbon passivation layer. In an embodiment, the inner wall of the reaction cell chamber is coated with a ruthenium coating to protect the wall from H2 O oxidation. In an embodiment, the oxygen inventory of SunCell® remains approximately constant. In an embodiment, the addition of oxygen inventory can be added as CO2 , CO, O2 And H2 At least one of O. In an embodiment, add H2 May react with the sacrificial powdered carbon to form methane such that the low energy hydrogen reactant comprises at least one hydrocarbon such as CO or CO formed from elements of O, C and H such as methane2 At least one oxygen compound formed of O, C and H elements. Oxygen compounds and hydrocarbons can serve as a source of oxygen and a source of H, respectively, to form a HOH catalyst and H. The SunCell® may further comprise a carbon monoxide safety system such as at least one of a CO sensor, a CO vent, a CO diluent gas, and a CO absorber. The CO may be limited by at least one of concentration and total inventory to provide safety. In an embodiment, CO may be limited to reaction chamber 5b31 and optionally to outer container chamber 5b3a1. In an embodiment, the SunCell® can include a secondary chamber to limit and dilute any CO leaking from the reaction cell chamber 5b31. The secondary chamber may include at least one of a battery chamber 5b3, an outer container chamber 5b3a1, a lower chamber 5b5, and another chamber, the other chamber may receive CO for at least one of: containing And dilute the leaking CO to a safe level. The CO sensor detects any leaking CO. The SunCell® can further include at least one of a diluent gas sump, a diluent gas sump valve, an exhaust valve, and a CO controller to receive input from the CO sensor and control opening and flow in the valve to dilute at a rate and Release or take CO at a concentration no greater than the required or safe level. The CO absorber in the chamber containing the leaking CO can also absorb the leaked CO. Exemplary CO adsorbents are cuprous ammonium salts, cuprous chloride dissolved in HCl solution, ammonia solution or o-methoxyaniline, and other adsorbents known to those skilled in the art. Any vented CO can be present at a concentration of less than about 25 ppm. In an exemplary embodiment in which the CO concentration in the reaction cell chamber is maintained at about 1000 ppm CO and the reaction cell chamber CO contains total CO inventory, the external containment or secondary chamber volume is greater than the volume of the reaction cell chamber. 40 times to make SunCell® inherently safe for CO leaks. In an embodiment, the SunCell® further comprises a CO reactor, such as a oxidizer, such as a burner or a decomposer, such as a plasma reactor, to react CO to a CO such as CO2 Or C and O2 It Safety product. An exemplary catalytic oxidizer product is comprised of Moleculite (Molecular,Http :// Wwww . Molecularproducts . Com / Products / Marcisorb - Co - Discharge ) Marcisorb CO absorber. In an embodiment, hydrogen can act as a catalyst. Supplying nH (n is an integer) as a catalyst and H atoms to form a low energy hydrogen source may include a hydrogen permeable membrane such as Pd or Pd-Ag in the wall of the EM pump casing 5k4 using a mass flow controller to control H supplied from the hydrogen stream of the high pressure water electrolysis agent2 The gas, the hydrogen permeable membrane such as a 23% Ag/77% Pd alloy separator. The use of hydrogen as an alternative to the HOH catalyst avoids oxidation reactions of at least one battery component such as the carbon reaction cell chamber 5b31. The plasma held in the reaction cell chamber can decompose H2 To provide H atoms. Carbon can contain hot carbon to contain the reaction between carbon and hydrogen. In an exemplary embodiment of the SunCell® heater of the present invention: (i) the EM pump assembly 5kk may comprise stainless steel, wherein an interior such as the EM pump sleeve 5k6 that is exposed to the oxidized surface may be coated with an antioxidant such as a nickel coating Coating coating; (ii) the reservoir 5c may comprise a cubic type by MgO or Y2 O3 Stabilized ZrO2 (iii) the abutment between the reservoir and the EM pump assembly 5kk may comprise a wet seal; (iv) the molten metal may comprise silver; (v) the inlet riser 5qa and the injection casing 5k61 may comprise screwed to the EM ZrO in the collar of the pump assembly bottom plate 5kk12 ; (vi) The lower hemisphere 5b41 may comprise a cubic shape by MgO or Y2 O3 Stabilized ZrO2 ; (vii) The upper hemisphere 5b42 may comprise a cubic shape by MgO or Y2 O3 Stabilized ZrO2 (viii) the source of oxygen may comprise a metal oxide such as an alkali metal oxide or an alkaline earth metal oxide or a mixture thereof; (ix) the hydrogen source may comprise a mass flow control through a hydrogen permeable membrane in the wall of the EM pump casing 5k4 Supply to control the flow of hydrogen from high pressure water electrolyzers2 a gas; (x) the joint between the reservoir and the lower hemisphere 5b41 may comprise a ceramic glue; (xi) the joint between the lower hemisphere 5b41 and the upper hemisphere 5b42 may comprise a ceramic glue; and (xii) the heat exchanger may Contains a radiant boiler. In an embodiment, at least one of the lower hemisphere 5b41 and the upper hemisphere 5b42 may comprise a material having thermal conductivity, such as a conductive ceramic, such as one of the present invention, such as ZrC, ZrB, which is stable to oxidation at 1800 °C.2 And ZrC-ZrB2 And ZrC-ZrB2 At least one of the SiC composites to improve heat transfer from the inside to the outside of the battery. In an exemplary embodiment of the SunCell® generator of the present invention comprising a magnetic fluid power (MHD) converter: (i) the EM pump assembly 5kk may comprise stainless steel, wherein the interior of the EM pump casing 5k6 is exposed to oxidation The surface may be coated with an antioxidant coating such as a nickel coating; (ii) the reservoir 5c may comprise a cubic shape by MgO or Y2 O3 Stabilized ZrO2 (iii) the abutment between the reservoir and the EM pump assembly 5kk may comprise a wet seal; (iv) the molten metal may comprise silver; (v) the inlet riser 5qa and the injection casing 5k61 may comprise screwed to the EM ZrO in the collar of the pump assembly bottom plate 5kk12 ; (vi) The lower hemisphere 5b41 may comprise a cubic shape by MgO or Y2 O3 Stabilized ZrO2 ; (vii) The upper hemisphere 5b42 may comprise a cubic shape by MgO or Y2 O3 Stabilized ZrO2 (viii) the source of oxygen may comprise a metal oxide such as an alkali metal oxide or an alkaline earth metal oxide or a mixture thereof; (ix) the hydrogen source may comprise a mass flow control through a hydrogen permeable membrane in the wall of the EM pump casing 5k4 Supplyed to control the flow of hydrogen from the high pressure water electrolyzer2 a gas; (x) the joint between the reservoir and the lower hemisphere 5b41 may comprise a ceramic glue; (xi) the joint between the lower hemisphere 5b41 and the upper hemisphere 5b42 may comprise a ceramic glue; (xii) MHD nozzle 307, channel Section 308 and condensation 309 may comprise cubic form by MgO or Y2 O3 Stabilized ZrO2 (xiii) The MHD electrode 304 may comprise a Pt-coated refractory metal such as Pt coated Mo or W, a carbon that is stable to water at 700 ° C, and an oxidation-stabilized ZrC-ZrB at 1800 ° C.2 And ZrC-ZrB2 - SiC composite, or silver liquid electrode; and (xiv) MHD return conduit 310, return EM pump 312, return EM pump sleeve 313 may comprise stainless steel, wherein the interior of the casing and the pipe is exposed to the oxidized surface It can be coated with an antioxidant coating such as a nickel coating. The MHD magnet 306 can comprise a permanent magnet such as a cobalt neodymium magnet having a 1 T magnetic flux density. In an exemplary embodiment of a SunCell® generator of the present invention comprising a magnetic fluid power (MHD) converter: (i) the EM pump can include a secondary induction type, wherein the first stage acts as a MHD return pump cut stage 2 Acting as a jet pump; (ii) current loop EM pump bushing section 405, EM pump current loop 406, joint flange 407, reservoir bottom plate assembly 409, and MHD return conduit 310 may comprise quartz, nitrogen such as fused silica矽, alumina, zirconia, magnesia or yttria; (iii) transformer winding 401, transformer yokes 404a and 404b, and electromagnets 403a and 403b may be water-cooled; (iv) reservoir 5c, reaction cell The chamber 5b31, the MHD nozzle 307, the MHD channel 308, the MHD condensation section 309, and the gas housing 309b may comprise quartz such as fused silica, tantalum nitride, alumina, zirconia, magnesia or yttria, wherein ZrO2 Cube type by MgO or Y2 O3 Stabilizing; (v) at least one of the gas housing 309b and the MHD condensation section 309 may comprise stainless steel such as 625 SS or ruthenium coated Mo; (vi) (a) the joint between the components may comprise Flange seals, gluing seals or wet seals for gaskets such as carbon gaskets, wherein the wet seal can engage dissimilar ceramics or ceramic and metal parts such as stainless steel parts, (b) flange seals with graphite gaskets can engage metal a component or a ceramic to metal component operating at a carbonization temperature below the metal, and (c) a flange seal having a gasket to engage the metal component or the ceramic to metal component, wherein the graphite gasket contact comprises a nickel-free metal such as nickel The metal portion of the metal or coating is sealed, or another high temperature gasket is used at a suitable operating temperature; (vii) the molten metal may comprise silver; (viii) the inlet riser 5qa and the injection sleeve 5k61 may be screwed to ZrO in the collar in the reservoir floor assembly 4092 (ix) The source of oxygen and the source of hydrogen may each comprise an O through a gas flow membrane 309d in the wall of the MHD condensation section 309 using a mass flow controller to control each gas stream from the high pressure water electrolyte.2 Gas and H2 The gas (x) MHD electrode 304 may comprise a Pt-coated refractory metal such as Pt coated Mo or W, a carbon that is stable to water at 700 ° C, and an oxidation stabilized ZrC-ZrB at 1800 ° C.2 And ZrC-ZrB2 - SiC composite, or silver liquid electrode; and (xi) MHD magnet 306 may comprise a permanent magnet such as a cobalt-rhenium magnet having a magnetic flux density in the range of about 0.1 to 1 T. In an embodiment, the SunCell® power supply can include an electrode such as a cathode of a refractory metal such as tungsten that can penetrate the wall of the black body radiator 5b4 and a counter electrode of the molten metal injector. The counter electrode such as the EM pump sleeve injector 5k61 and the nozzle 5q can be immersed. Alternatively, the counter electrode may include, for example, cubic ZrO2 Or an electrically insulating refractory material of cerium oxide. The tungsten electrode can be sealed at the penetration of the black body radiator 5b4. The electrodes may be electrically insulated by an electrical insulator bushing or spacer between the reservoir 5c and the blackbody radiator 5b4. Electrical insulator bushings or spacers may contain BN or such as ZrO2 HfO2 , MgO or Al2 O3 Metal oxides. In another embodiment, the black body radiator 5b4 may comprise an electrical insulator such as a refractory ceramic such as BN or such as ZrO.2 HfO2 , MgO or Al2 O3 Metal oxides.Other embodiments In an embodiment, the SunCell® may comprise a water absorber that reversibly bonds water from the atmosphere, a component that transfers heat from a SunCell® heat exchanger such as heat exchanger 26a to a water load absorber, and condensed water released. The condenser and the collection container that receives the condensate to be used in SunCell®. In an embodiment, the HOH catalyst and the H reactant are provided to form a low energy hydrogen source of HOH catalyst and at least one of the H sources is at ambient water. Water can be collected using a water absorbing material and subsequently dehydrated to release absorbed water. Water can be dehydrated or desorbed by using the heat supplied by SunCell®. The water absorbing material may comprise, for example, zirconium metal and adipic acid or M combined with water vapor and released to the condenser upon heating.2 Cl2 (BTDD) (M = Mn (1), CO (2), Ni (3); BTDD = bis (1H-1,2,3-triazolo[4,5-b], [4', 5' -l] a metal organic framework of a combination of dibenzo[1,4]dioxine. In an embodiment, SunCell® comprises a reaction mixture that forms low energy hydrogen as a reaction product. The reaction mixture may further comprise a carbon source such as at least one of graphite and a hydrocarbon. The energy plasma may bombard solid carbon or carbon deposited on the substrate from a carbon source. In an embodiment, bombardment converts graphitic carbon into Diamond Form Carbon. In the Mills Publication RL Mills, J. Sankar, A. Voigt, J. He, B. Dhandapani, "Synthesis of HDLC Films from Solid Carbon", J. Materials Science, J Mater. Sci. 39 (2004) 3309-3318 and RL Mills, J. Sankar, A. Voigt, J. He, B. Dhandapani, "Spectroscopic Characterization of the Atomic Hydrogen Energies and Densities and Carbon Species During Helium-Hydrogen- Methane Plasma CVD Synthesis of Diamond Films", Chemistry of Materials, Vol. 15, (2003), pp. 1313-1321 Exemplary embodiment, SunCell® so that the plasma source comprises an energy from non-diamond forms of carbon such as diamond. Diamonds can be produced by 1333 cm- 1 The presence of the Raman peak is measured. Molecular low energy hydrogen gas can be purified and separated by ionizing ordinary hydrogen. The ionized hydrogen can be removed by at least one of electrical and magnetic fields. Alternatively, ordinary hydrogen can be removed by reaction with a reactant that forms a condensable reaction product, wherein the reaction is advantageously carried out by plasma conditions. An exemplary reactant is a nitrogen that forms a condensable ammonia that is removed in a cryotrap to produce a purified molecular low energy hydrogen gas. Alternatively, the molecular low energy hydrogen gas can be purified and separated using a molecular sieve that separates ordinary hydrogen from molecular low energy hydrogen gas based on higher diffusion of molecular low energy hydrogen gas. An exemplary separation molecular sieve is Na8 (Al6 Si6 Otwenty four )Cl2 . In an embodiment, thermal energy from a black body radiator can be used to heat and CO2 And H2 a mixture of O reactions such as CeO2 Catalyst to form syngas (CO + H2 ). Syngas can be used to form hydrocarbon fuels. The fuel reactor can comprise a Fischer Topsig reactor. In an embodiment, the low energy hydrogen reaction slurry comprising water vapor may further comprise argon. Argon can act at least one of the following: by increasing H2 Molecular recombination time increases H atom concentration, increases the concentration of new HOH by interfering with water hydrogen bonding, and provides such as Ar+ Additional catalyst source for the catalyst. The low energy hydrogen reaction can propagate in a solid fuel comprising water in a tissue or repeating structure such as a crystal lattice. The solid fuel may comprise a hydrate which may be crystalline. The solid fuel may comprise water in the form of crystals such as ice, such as Type I ice. The ice solid fuel can have energy, wherein the energy release can include pulses. The pulses may be implemented in a sequential manner to provide power for extended durations to infinity, such as for ignition of air fuel in an internal combustion engine. The ice fuel system contains components that generate shock waves in ice water. The ice fuel system can include a shock wave limiting member. The restraining member may comprise an ice cover. The sleeve may comprise an outer casing such as a metal outer casing. At least one of the shock wave and the limit may generate a shock wave to destroy at least one of some of the hydrogen bonds between the ice water molecules and at least one oxygen hydrogen bond of some of the water molecules. The ice fuel system may contain explosives to include H in, for example, ice.2 A shock wave is generated in the crystal structure of O. The explosive may comprise an explosive of the C-N-O-H type, another explosive such as a oxyhydrogen explosive or another explosive known to those skilled in the art. The explosives can be very close to a crystalline structure such as ice to effectively couple shock waves into the crystalline structure. The explosive may be embedded in at least one of the channels such as the crystal structure of ice. Alternatively, the ice fuel system may comprise an electrical component that generates a shock wave in the ice water, such as at least one blast line. The blast line can include a high power source such as a power source of at least one of high voltage and current. The higher electrical power source can include at least one capacitor. Capacitors can have high voltages and currents. At least one of the capacitors can be exploded by discharging through at least one of the wires. Wire explosive systems can include thin conductive wires and capacitors. An exemplary wire is a wire comprising gold, aluminum, iron or platinum. In an exemplary embodiment, the wire may have a diameter of less than 0.5 mm and the capacitor may have an energy consumption of about 25 kWh/kg and release 104 - 106 A/mm2 a pulse of charge density that results in a temperature of up to 100,000 K, where the mark can be around 10- 5 - 10- 8 Appears in the second period. Specifically, 100μ F-filled capacitors can be charged to 3 kV using a DC power supply, and capacitors can be used with a knife switch or gas arc switch through a 12 inch long gauge stainless steel wire, where the wires are embedded in a steel housing. In the ice. The ice fuel system can further include a power source at at least one of a battery, a fuel cell, and a generator such as SunCell® to charge the capacitor. An exemplary energy material includes Ti + Al + H ignited by an explosive wire that can include at least one of Ti, Al, and another metal2 O (ice). In an embodiment, the energy reaction mixture and system may comprise a low energy hydrogen fuel mixture such as one of the low energy hydrogen fuel mixtures of the present invention and the prior application, which are incorporated by reference. The reaction mixture can comprise water in at least one physical state such as a frozen solid, liquid, and gaseous state. The energy response can be initiated by the application of a high current such as a current in the range of about 20 A to 50,000 A. The voltage can be lower, such as in the range of about 1 V to 100 V. The current can be carried by a conductive substrate such as a metal matrix such as Al, Cu or Ag metal powder. Alternatively, the electrically conductive substrate can comprise a container such as a metal container, wherein the container can enclose or coat the reaction mixture. An exemplary metal container comprises an Al, Cu or Ag DSC disk. An exemplary energy reaction mixture comprising chilled water (ice) or liquid water comprising at least one of: Al坩埚Ti + H2 O; Al坩埚Al + H2 O; Cu坩埚Ti + H2 O; Cu坩埚Cu + H2 O;Ag坩埚Ti + H2 O;Ag坩埚Al + H2 O;Ag坩埚Ag + H2 O;Ag坩埚Cu + H2 O;Ag坩埚Ag + H2 O O + NH4 NO3 (Mor 50:25:25); Al坩埚Al + H2 O + NH4 NO3 (Mor 50:25:25). In addition to being in a frozen state such as ice, the water may also contain a solid such as in the form of a bond in the form of a hydrate. The reaction mixture may comprise: (i) a source of oxygen such as a peroxide, (ii) a source of hydrogen such as a metal hydride, water and a water reactant such as a reducing agent, and at least one of a hydrocarbon such as a fuel oil, the reducing agent Such as a metal, such a metal as a metal powder, and (iii) a conductive substrate such as a metal powder. An exemplary reaction mixture comprising Al坩埚Ti or TiH + Na2 O2 Or such as Na2 O2 ·2H2 O2 ·4H2 O, Na2 O2 ·2H2 O, Na2 O2 ·2H2 O2 And Na2 O2 ·8H2 Hydrated Na of at least one of O2 O2 . The reaction mixture can be ignited using low voltage, high current, such as about 15 V and 27,000 A, respectively. In embodiments, the low energy hydrogen reaction mixture may comprise a water reactive metal such as a particulate metal such as an alkali or alkaline earth metal that may have a relatively high surface area. The metal particles may comprise a protective coating such as an oxide coating. An exemplary low energy hydrogen reactant comprises a particle Li metal having an oxide coating. The reaction mixture may further comprise water or ice. In an embodiment, the particulate metal is added to cold water such as 1 ° C water and snap frozen. Rapid freezing can be achieved using liquid nitrogen to avoid metal reactions. The reaction mixture can comprise a conductive matrix such as the conductive matrix of the present invention. The explosive wire can approach a crystal structure such as ice to cause the shock wave to propagate in the ice. The wires can be embedded in the ice to effectively couple the shock waves to the ice. In an embodiment, a plurality of wires embedded in the ice are knocked to cause shock waves and compression to propagate through the ice, causing the crystal ice structure to fragment to form H and HOH catalysts to form low energy hydrogen. Explosive wires can produce conductive plasma paths that support higher kinetics due to conductive arc currents that are at least one of recombining ions and reducing spatial variations due to ionization of the catalyst during catalysis Increase the reaction rate. A crystalline structure such as ice may further comprise a conductor such as an embedded metal to increase kinetics due to its electrical conductivity, such as a metal wire, metal power or metal grid. The metal can be highly conductive and chemically stable to water, such as silver or copper. In an embodiment, the ice is embedded in a conductive matrix such as a metal mesh, such as a copper, nickel, silver or aluminum mesh, such as a Celmet (Sumitomo Electric Industries, Ltd.) type mesh. In an embodiment, the ice fuel system can include a reactant that releases heat and produces hydrogen that is knocked with oxygen to create a shock wave in the ice water, wherein the reactants can be embedded and confined to the ice. The reactants may comprise, for example, Fe that is at least partially embedded and coated in ice water2 O3 /Al metal powder mixture of thermite. The sleeve can contain a metal receptacle. The thermite may contain a molar excess of aluminum to react with water to form H2 The gas uses atmospheric oxygen to act as an explosive. Excess metal can also act as a conductor to increase the rate of reaction. In an embodiment, an energy material such as an energy material comprising water in a suitable form such as ice and an additive such as an additive comprising at least one of a hydrogen source and a conductivity such as a metal, such as an additive, such as Higher surface area metals such as Al powder or alkali metal powders such as lithium powder. The energy material can be confined such that the shock wave generated by the ignition of the energy material is limited. Shock wave limits can help break H2 Bonding of O to supply H and HOH. The energy material can be encapsulated in a sealed container such as a metal container to provide a limit. In an embodiment, ignition can be performed by passing a high current through at least one electrical wire that passes through or is in close proximity to the energy material, wherein high current can cause one or more electrical wires to explode. Wire explosions can create shock waves in energy materials. The wires can be arranged to enhance shock waves in the energy material. In an exemplary embodiment, the wires may extend parallel to each other to compress the energy material from a plurality of directions. In another embodiment, an implosion can be generated in the energy material, wherein the shock wave in the energy material is directed inward. The inward shock wave may be spherically inward. The implosion can be generated by at least one of one or more electrical knocks and a knock of a conventional explosive such as TNT. Explosives can be shaped to create implosions. The explosive may comprise a spherically shaped charge. Implosion and shock waves in ice water can cause ice to knock. An exemplary energy material device can include ice having a source surrounding a spherical shock wave, such as a conventional explosive ignited with an explosive wire. At least one of the limitations and implosions involving the energy material can produce a knock supplement for the additional energy material. In an embodiment, the detonation wire may comprise a containment structure such as a solenoid or torus surrounding a source of HOH and H such as water such that it implosion to more efficiently form HOH and H to react to form a low energy hydrogen The water is like ice. In another embodiment, the crystalline solid fuel is replaced with a corresponding liquid such as liquid water. In an embodiment, the energy reaction system comprises a source of HOH catalyst and at least one of H, such as water in any physical state, such as a gas, a liquid, or a solid such as Type I ice, to generate a shock wave. In an embodiment, the energy reaction system includes a plurality of shockwave sources. The source of the shock wave may comprise at least one of one or more explosive wires such as the explosive wire of the present invention and one or more charges such as TNT or another conventional energy material of the present invention. The energy reaction system can include at least one detonator of a conventional energy material. The energy reaction system can further include a sequential trigger member, such as a delay line, or at least one timing switch such that a plurality of shock waves having a time delay between at least the first and the other shockwaves are formed. The sequential trigger can generate a delay in the explosion to create a delay between the first and at least one other knock, wherein each knock forms a shock wave. The trigger can delay the power applied to at least one of the explosive wire and the detonator of the conventional energy material. The delay time may be in the range of at least one of about 1 femtosecond to 1 second, 1 nanosecond to 1 second, 1 microsecond to 1 second, and 10 microsecond to 10 millisecond. In an embodiment, the SunCell® can comprise a chemical reactor in which, in addition to the low energy hydrogen reactant, the reaction can be supplied to the reactor to form the desired chemical product, or in addition to the low energy hydrogen reactant, the reaction can also be supplied to The reactor is formed to form the desired chemical product. The reactants can be supplied through an EM pump casing. The product can be extracted through an EM pump casing. The reactants can be added to the feed before the reactor is closed and the reaction is initiated. The product in the material can be removed by opening the reactor after the reactor operation. The reaction product can be extracted by permeation through a reactor wall such as a reaction cell chamber wall. The reactor provides continuous plasma at a blackbody temperature in the range of 1250 K to 10,000 K. The reactor pressure can range from 1 atmosphere to 25 atmospheres. The wall temperature can range from 1250 K to 4000 K. The molten metal may comprise at least one of a molten metal that supports a desired chemical reaction, such as silver, copper, and a silver-copper alloy. In an embodiment, the explosive wire encapsulated in ice water may comprise a transition metal such as at least one of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn. The wire may further comprise aluminum. The knock voltage can be a high voltage such as a voltage in at least one of 1000 V to 100,000 V and 3000 V to 10,000 V. Films comprising transition metals and low energy hydrogen hydride can form, for example, low energy hydrogen hydride, chromium or manganese, molecular low energy hydrogen complexes or atomic low energy hydrogen complexes. H Fe containing low energy hydrogen is formed by using 4000 V and kiloamperes to knock wires containing Fe, Cr and Al alloys. FeH is identified by ToF-SIM. Other compounds comprising low energy hydrogen and another element such as another metal may be formed by using an explosive wire comprising a corresponding element such as another metal. In an embodiment, the member forming a large aggregate or polymer comprising a lower energy hydrogen species such as a molecular low energy hydrogen comprises a source of HOH and water in any physical state such as in at least one of a gas, a liquid, and ice. The H source, and may further include a high current source such as a knock wire. The means for forming a large aggregate or polymer comprising a lower energy hydrogen species such as molecular low energy hydrogen further comprises a reaction chamber to limit the low energy hydrogen reaction product. An exemplary low energy hydrogen reactant is water vapor in air or another gas such as an inert gas. The water vapor pressure can range from 1 mTorr to 1000 Torr. The low energy hydrogen reaction can be initiated by the electric wire using the knock of electric power. In an exemplary embodiment, the wire of the present invention is knocked in a cavity containing ambient water vapor in the air by using the detonation member of the present invention. The ambient water vapor pressure can range from about 1 to 50 Torr. An exemplary product is such as FeH2 (1/4) of iron low energy hydrogen polymer and such as MoH (1/4)16 Molybdenum low energy hydrogen polymer. The product can be identified by unique physical properties such as novel compositions, such as novel compositions comprising metals such as iron, hydrogen, zinc hydrogen, chromium hydrogen or molybdenum hydrogen, and hydrogen. If a unique composition is present, the unique composition can be magnetic in the absence of the magnetic properties of the corresponding compositions known to contain ordinary hydrogen. In an exemplary embodiment, the unique composition polymerizes ferric hydrogen, chromium hydrogen, titanium hydrogen, zinc hydrogen, molybdenum hydrogen, and tungsten hydrogen to be magnetic. Large aggregates or polymers containing lower energy hydrogen species such as molecular low energy hydrogen can be identified by: (i) based on metal and hydride ions and such as H16 And Htwenty four Higher quality resolution of higher quality fragments of higher quality fragments and clearly recorded such as FeH and MoH16 Time-of-flight secondary ion mass spectrometry (ToF-SIMS) of unique metal and hydrogen compositions; (ii) recordable approximately 1940 cm- 1 H2 (1/4) Fourier transform infrared spectroscopy (FTIR) of at least one of the rotational energy and the absorption band in the fingerprint region, wherein there may be no other higher energy signature of the known functional group; (iii) may record such as Proton Magic Angle Rotating Nuclear Magnetic Resonance Spectra of High Field Matrix Peaks of High Field Matrix Peaks in the -4 ppm to -6 ppm Region1 H MAS NMR); (iv) X-ray diffraction (XRD) at a novel peak attributed to a unique composition that may comprise a polymeric structure; (v) recordable hydrogen polymer in an area such as 200 ° C to 900 ° C Decomposes at very low temperatures and provides a unique hydrogen stoichiometry or such as FeH or MoH16 Thermogravimetric analysis (TGA) of the composition; (vi) recordable H in the 260 nm region containing peaks spaced apart by 0.25 eV2 (1/4) Electron beam excitation emission spectroscopy analysis of the vibrating zone; (vii) H in the 260 nm region containing peaks spaced apart by 0.25 eV can be recorded2 (1/4) photoluminescence Raman spectroscopy of the second stage of the vibrating belt; (viii) recordable about 1940 cm- 1 H2 (1/4) Raman spectroscopy of the peak of rotation; and (ix) recordable H at approximately 500 eV2 X-ray photoelectron spectroscopy (XPS) of the total energy of (1/4). In an embodiment, the apparatus for collecting molecular low-energy hydrogen in a gaseous state, physically absorbed, liquefied, or otherwise comprises: a source of a large aggregate or polymer comprising a lower energy hydrogen species, comprising a species comprising a lower energy hydrogen species a large aggregate or polymer chamber, a large aggregate or polymer component containing a lower energy hydrogen species in a thermal decomposition chamber, and a large aggregate or polymer collected from a lower energy hydrogen species The component of the gas. The decomposition member may include a heater. The heater can heat the first chamber to a temperature greater than a decomposition temperature of a large aggregate or polymer comprising a lower energy hydrogen species, such as at about 10 ° C to 3000 ° C, 100 ° C to 2000 ° C, and 100 ° C to A temperature in at least one of 1000 °C. The means for collecting gas from the decomposition of large aggregates or polymers comprising lower energy hydrogen species may comprise a second chamber. The second chamber can include at least one of an air pump, a gas valve, a pressure gauge, and a mass flow controller to perform at least one of: storing and transferring the collected molecular low energy hydrogen gas. The second chamber may further comprise a getter to absorb molecular low energy hydrogen gas or a cooler such as a cryogenic system to liquefy the molecular low energy hydrogen. The cooler may comprise a cryopump or a dewar containing a cryogenic liquid such as liquid helium or liquid nitrogen. The member forming a large aggregate or polymer comprising a lower energy hydrogen species may further comprise a source of a field source, such as at least one of an electric field or a magnetic field. The source of the electric field can include at least two electrodes and a voltage source to apply an electric field to the reaction chamber where the aggregate or polymer is formed. Alternatively, the source of the electric field may comprise an electrostatic charging material. The electrostatic charging material can comprise a reaction cell chamber such as a chamber containing carbon, such as a plastic glass chamber. The knocking of the present invention electrostatically charges the chamber of the reaction cell. The source of the magnetic field may comprise at least one magnet, such as a permanent electromagnet or a superconducting magnet, to apply a magnetic field to the reaction chamber where aggregates or polymers are formed. Such as H2 (1/4) of molecular low energy hydrogen can have non-zeroAnd corresponding to the orbital angular momentum with the corresponding magnetic momentQuantum number. The magnetic characteristics of molecular low-energy hydrogen are rotated by the proton magic angle to rotate the nuclear magnetic resonance spectrum (1 H MAS NMR) proved. The presence of low molecular energy hydrogen in a solid matrix, such as an alkali metal hydroxide-alkali metal halide matrix, which may further comprise some water of hydration, is due to the paramagnetic matrix effect of the low energy hydrogen of the molecule to produce a high field1 H MAS NMR peak, usually between -4 and -5 ppm. A convenient method for generating low-energy hydrogen in a non-zero angular momentum state is in H2 In the presence of O, the wire is knocked to act as a source of low energy hydrogen and H. Wire knocking in the atmosphere containing water vapor contains, for example, having a non-zeroAnd having metal atoms or ions that can aggregate to form a webQuantum state molecular low-energy hydrogen low-energy hydrogen magnetic linear chain. Self-assembly can include magnetic order or self-assembly mechanisms. It is well known that the application of an external magnetic field produces a magnet such as a magnet (Fe) suspended in a solvent such as toluene.2 O3 Colloidal magnetic nanoparticles are assembled into a linear structure. Due to the lower mass and higher magnetic moment, the molecular low energy hydrogen is magnetically self-assembled even in the absence of a magnetic field. In embodiments that enhance self-assembly and control alternative structures that form low energy hydrogen products, external magnetic fields are applied to low energy hydrogen reactions, such as wire knock. The magnetic field can be applied by placing at least one permanent magnet in the reaction chamber. Alternatively, the detonation wire can comprise a metal that acts as a source of magnetic particles, such as a magnet, to drive the magnetic self-assembly of the molecule's low energy hydrogen, where the source can be a wire knock in water vapor or another source. In an embodiment, the molecular low energy hydrogen may comprise a non-zero angular momentum quantum number. Molecular low energy hydrogen can be magnetic, where magnetism can be attributed to non-zero angular momentum quantum numbers. Due to the intrinsic magnetic moment of the molecular low energy hydrogen, it can self-assemble into large aggregates. In an embodiment, such as H2 (1/4) of the molecular low-energy hydrogen can be assembled into a linear chain bound by a magnetic dipole force. In another embodiment, the molecular low energy hydrogen can be assembled to have, for example, H at each of the eight vertices.2 (1/4) of H2 (1/p) in the three-dimensional structure of the cube. In an embodiment, eight such as H2 (1/4) M of the molecule2 The (1/p) molecule is magnetically bonded into the cube with the center of each molecule at one of the eight vertices of the cube, and each core axis is parallel to the edge of the centered cube on the apex. The magnetic alignment is such that each north and south pole of each molecular dipole is oriented opposite each of its three closest neighbors of the cube. H16 It can act as a unit or part of a more complex macrostructure formed by self-assembly. In another embodiment, each of the four vertices of the square contains such as H2 (1/4) of H2 (1/p) of H8 Unit can be added to the cuboid H16 To includeH 16 + 8n , where n is an integer. An exemplary extra large aggregate is H16 , Htwenty four And H32 . Hydrogen macroaggregates Neutrals and ions can be combined with other species such as O, OH, C, and N as neutrals or ions. In an embodiment, the resulting structure produces H in time-of-flight secondary ion mass spectrometry (ToF-SIMS)16 Peak, where the segment can correspond to from H16 The observed mass of the integer H loss, such as H16 , H14 , H13 And H12 . Due to the mass of H of 1.00794 u, the corresponding +1 or -1 ion peak has the following qualities: 16.125, 15.119, 14.111, 13.103, 12.095...H - 16 orH The +16 hydrogen large aggregate ion may comprise a metastable substance. Hydrogen large aggregates with wide peak dielectric stability characteristicsH - 16 andH +16 was observed by ToF-SIMS at 16.125 in the positive and negative spectra.H - 15 observed in the negative ToF-SIMS spectrum at 15.119. Htwenty four Stable speciesH+ 23 andH- 25 Observed in the positive and negative ToF-SIMS spectra, respectively. In an embodiment, such as H16 Molecular low-energy hydrogen large aggregate or such as H2 (1/4) such as H2 The decomposition product of (1/p) may comprise a magnetic resonance imaging (MRI) contrast agent, such as rotationally polarized Xeon. Molecular low energy hydrogen may be inhaled and used for MRI imaging attributable to at least one of its NMR active protons or its effects on ordinary protons, such as the subject of an imaged human, animal or object. a proton of a water molecule in which the paramagnetic effect of a low-energy hydrogen molecule corresponds to an NMR shift or such as T1 andT2 At least one of the relaxation times of at least one of the ones. In an embodiment, the pair of molecular low energy hydrogens can be converted to the NMR active neighbor form by rotational exchange. Rotational exchange can be achieved using a rotary exchange reagent such as a magnetic species, such as a magnet (Fe2 O3 )particle. Gas can be incubated with rotary exchange reagents to achieve H2 (1/p) conversion of the adjacent form. The lifetime of the in vivo ortholog can be used as the basis for MRI contrast agents. In an embodiment, low energy hydrogen species such as atomic low energy hydrogen, molecular low energy hydrogen or low energy hydrogen hydride ions are H and OH and H2 At least one of the O catalysts is reacted to synthesize. In embodiments, a product such as at least one of a SunCell® reaction and an energy reaction comprising a pellet or wire of the invention ignited to form a low energy hydrogen is comprised of a component such as H that is mismatched by at least one of2 (1/p) low-energy hydrogen compounds or species of low-energy hydrogen species: (i) elements other than hydrogen; (ii) such as H+ Ordinary H2 Ordinary H- And ordinaryH+ 3 Ordinary hydrogen species of at least one of them, such as organic molecular species of organic ions or organic molecules; and (iv) inorganic species such as inorganic ions or inorganic compounds. The low energy hydrogen compound may comprise an oxyanion compound such as an alkali or alkaline earth carbonate or hydroxide or other such compounds of the invention. In an embodiment, the product comprisesM 2 CO 3H 2 (l / 4) andMOHH 2 (/4) (M = base or other cation of the invention) at least one of the complexes. Products can be identified by ToF-SIMS as containing M(M2 CO3 • H2 (l/ 4)) + n andM ( MOH H 2 (l/4)) A series of ions in the positive spectrum of + n, where n is an integer and the integer P > 1 can be replaced by 4. In an embodiment, such as SiO2 Or a compound of quartz and oxygen can act as H2 (1/4) of the getter. H2 The getter of (1/4) may comprise a transition metal, an alkali metal, an alkaline earth metal, an internal transition metal, a rare earth gold metal combination, an alloy such as Mo alloy such as MoCu, and a hydrogen storage material such as the material of the present invention. A compound comprising a low energy hydrogen species synthesized by the method of the invention may have the formula MH, MH2 Or M2 H2 Wherein M is an alkali cation and H is a low energy hydrogen species. Compounds can have the formula MHn Wherein n is 1 or 2, M is an alkaline earth cation, and H is a low energy hydrogen species. The compound may have the formula MHX wherein M is an alkali cation and X is one of a neutral atom such as a halogen atom, a molecule or a single-band negatively charged anion such as a halogen anion, and H is a low energy hydrogen species. The compound can have the formula MHX wherein M is an alkaline earth cation, X is a single band negatively charged anion, and H is a low energy hydrogen species. The compound can have the formula MHX wherein M is an alkaline earth cation, X is a double band negative anion, and H is a low energy hydrogen species. The compound can have the formula M2 HX, wherein M is an alkali cation, X is a single-band negatively charged anion, and H is a low energy hydrogen species. Compounds can have the formula MHn Wherein n is an integer, M is a basic cation, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula M2 Hn Wherein n is an integer, M is an alkaline earth cation, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula M2 XHn Wherein n is an integer, M is an alkaline earth cation, X is a single-band negatively charged anion, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula M2 X2 Hn Wherein n is 1 or 2, M is an alkaline earth cation, X is a single-band negatively charged anion, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula M2 X3 H, wherein M is an alkaline earth cation, X is a single-band negatively charged anion, and H is a low energy hydrogen species. The compound can have the formula M2 XHn Wherein n is 1 or 2, M is an alkaline earth cation, X is a double-band negatively charged anion, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula M2 XX'H, wherein M is an alkaline earth cation, X is a single-band negatively charged anion, X' is a double-band negatively charged anion, and H is a low-energy hydrogen species. The compound can have the formula MM'Hn Wherein n is an integer from 1 to 3, M is an alkaline earth cation, M' is an alkali metal cation, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound can have the formula MM'XHn Wherein n is 1 or 2, M is an alkaline earth cation, M' is an alkali metal cation, X is a single-band negatively charged anion, and the hydrogen content of the compound is Hn Containing at least one low energy hydrogen species. The compound may have the formula MM'XH, wherein M is an alkaline earth cation, M' is an alkali metal cation, X is a double band negative anion, and H is a low energy hydrogen species. The compound may have the formula MM'XX'H, wherein M is an alkaline earth cation, M' is an alkali metal cation, X and X' are single-band negatively charged anions, and H is a low energy hydrogen species. The compound can have the formula MXX'Hn Wherein n is an integer from 1 to 5, M is an alkali or alkaline earth cation, X is a single or double negatively charged anion, X' is a metal or a metalloid, a transition element, an internal transition element or a rare earth element, and the hydrogen content of the compound Hn Containing at least one low energy hydrogen species. Compounds can have the formula MHn Wherein n is an integer and M is a cation such as a transition element, an internal transition element or a rare earth element, and the hydrogen content of the compound Hn Containing at least one low energy hydrogen species. Compounds can have the formula MXHn Wherein n is an integer, M is a cation such as an alkali cation or an alkaline earth cation, and X is another cation such as a transition element, an internal transition element or a rare earth element cation, and the hydrogen content H of the compoundn Containing at least one low energy hydrogen species. Compounds can have the formula (MHm MCO3 )n Wherein M is an alkali cation or other +1 cation, m and n are integers, and the hydrogen content of the compound Hm Containing at least one low energy hydrogen species. Compounds can have formula (MH m MNO 3 ) + nnX - Wherein M is an alkali cation or other +1 cation, m and n are integers, X is a single-band negatively charged anion, and the hydrogen content of the compound is Hm Containing at least one low energy hydrogen species. Compounds can have formula (MHMNO 3 )n Wherein M is an alkali cation or other +1 cation, n is an integer, and the hydrogen content H of the compound comprises at least one low energy hydrogen species. Compounds can have formula (MHMOH )n Wherein M is an alkali cation or other +1 cation, n is an integer, and the hydrogen content H of the compound comprises at least one low energy hydrogen species. Compounds including anions or cations may have( MH m M 'X )n Wherein m and n are integers, M and M' are both alkali or alkaline earth cations, X is a single or double negatively charged anion, and the hydrogen content of the compound Hm Containing at least one low energy hydrogen species. A compound including an anion or a cation may have a formula (MH m M ' X') + nnX - Wherein m and n are integers, M and M' are both alkali or alkaline earth cations, X and X' are single or double negatively charged anions, and the hydrogen content of the compound Hm Containing at least one low energy hydrogen species. The anion may comprise one of the anions of the invention. Suitable exemplary single-band negative anions are halides, hydroxide ions, hydrogencarbonate ions or nitrate ions. Suitable exemplary dual-band negative anions are carbonate ions, oxides or sulfate ions. In an embodiment, the low energy hydrogen compound or mixture comprises at least one low energy hydrogen species such as a low energy hydrogen atom, a low energy hydrogen hydride ion, and is embedded in a crystal lattice such as a crystal lattice such as a metal or ion lattice. Two low energy hydrogen molecules. In an embodiment, the crystal lattice does not react with low energy hydrogen species. The matrix may be aprotic, such as by embedding low energy hydrogen hydride ions. The compound or mixture may comprise H(1/p), H embedded in the salt crystal lattice.2 (1/p) and H- At least one of (1/p), a salt crystal lattice such as an alkali or alkaline earth salt such as a halide. Exemplary alkali halides are KCl and KI. Salt is embedded in H- (1/p), there may be no H2 O. Other suitable salt crystal lattices comprise the salt crystal lattice of the present invention. The low energy hydrogen compound of the present invention is preferably more than 0.1 atom% pure. More preferably, the compound is more than 1 atom% pure. Even more preferably, the compound is more than 10 atomic percent pure. Most preferably, the compound is more than 50 atomic percent pure. In another embodiment, the compound is more than 90 atomic percent pure. In another embodiment, the compound is more than 95 atomic percent pure.experiment The SF-CIHT battery power generation system includes a photovoltaic power converter configured to collect plasma photons generated by a fuel ignition reaction and convert it into usable energy. In some embodiments, high conversion efficiency may be desirable. The reactor can discharge the plasma in a plurality of directions, for example, at least two directions, and the radius of the reaction can be on the order of from about several millimeters to several meters, for example, from about 1 mm to about 25 cm. Moreover, the plasma spectrum produced by fuel ignition can be similar to the plasma spectrum produced by the sun and/or can include additional short wavelength radiation. Figure 4 shows the inclusion of absorbed H2 And H2 An exemplary embodiment of an absolute spectrum of a region of 5 nm to 450 nm ignited by an 80 mg pellet of O, the absorbed H2 O is from water added to the molten silver as the silver cools into pellets, which exhibits an average optical power of substantially 1.3 MW in the ultraviolet and far ultraviolet spectral regions. The ignition was achieved with a low voltage and high current using a Taylor-Winfield model ND-24-75 spot welder. The voltage drop within the pellet is less than 1 V and the current is about 25 kA. The duration of higher intensity UV emissions is approximately 1 ms. The control spectrum is flat in the UV region. The radiation of the solid fuel, such as at least one of a spectral line and a blackbody emission, may have an intensity in at least one of about 2 to 200,000 suns, 10 to 100,000 suns, and 100 to 75,000 suns. In an embodiment, the inductance of the welder ignition circuit can be increased to increase the current decay time after ignition. Longer decay times maintain a low energy hydrogen plasma reaction to increase energy production. UV and EUV spectra can be converted to blackbody radiation. The conversion can be achieved by making the battery atmosphere optically opaque for the propagation of at least one of the UV and EUV photons. The optical thickness can be increased by vaporizing a metal such as a fuel metal in a battery. The optical thick plasma can comprise a black body. The black body temperature can be attributed to the high power density capacity of the low energy hydrogen reaction and the high energy of the photons emitted by the low energy hydrogen reaction. In an environment with about 1 Torr H2 The spectrum of the ignited molten silver pumped into the W electrodes in atmospheric vapor of O vapor pressure (due to the sapphire spectrometer window, having a cutoff of 100 nm to 500 nm at 180 nm) is shown in FIG. The power supply 2 comprises two sets of two capacitors in series (Maxwell Technologies K2 Ultracapacitor 2.85V/3400F), which are connected in parallel to provide a constant current of about 5 to 6 V and 300 A, wherein At a frequency of approximately 1 kHz to 2 kHz, the superimposed current pulse is 5 kA. The average input power of the W electrodes (1 cm × 4 cm) is about 75 W. When the atmosphere becomes optically opaque to UV radiation as the silver vaporizes, the initial UV line emission is converted to 5000K black body radiation by low energy hydrogen reaction power. A 5000K blackbody radiator with a luminescence rate of 0.15 has a power density of 5.3 MW/m2 . The area of the observed plasma is about 1 m2 . The blackbody radiation can heat the components of the battery 26, such as the cap 5b4, which can act as a blackbody radiator for the PV converter 26a in the thermal photovoltaic embodiment of the present invention. An exemplary test comprising a melt of oxygen source comprises argon/5 mole % H with optical power determined by absolute spectral analysis2 80 mg silver/1 wt% borax dehydrated pellets were ignited in the atmosphere. The welder (Acme 75 KVA spot welder) was used to apply a high current of approximately 12 kA for approximately 1 ms at a voltage drop of approximately 1 V at 250 kW. In another exemplary test comprising a source of oxygen source, argon/5 mole % H is included in the optical power determined by absolute spectral analysis2 Atmospheric ignition 80 mg silver / 2 mol% Na2 O dehydrated pellets. The welder (Acme 75 KVA spot welder) was used to apply a high current of approximately 12 kA for approximately 1 ms at a voltage drop of 370 kW at approximately 1 V. In another exemplary test comprising a source of oxygen source, argon/5 mole % H is included in the optical power determined by absolute spectral analysis2 Atmospheric ignition 80 mg silver / 2 mol% Li2 O dehydrated pellets. The welder (Acme 75 KVA spot welder) was used to apply a high current of approximately 12 kA for approximately 1 ms at a voltage drop of approximately 1 V at 500 kW. Based on the size of the plasma recorded using the Edgertronics high speed video camera, the low energy hydrogen reaction and power are dependent on the reaction volume. The volume may need to be at a minimum for optimizing reaction power and energy, such as about 0.5 to 10 liters, for igniting pellets such as silver pellets and about 30 to 100 mg of hydrated H and HOH catalyst sources. Since the pellets are ignited, the low energy hydrogen reaction rate is higher at very high silver pressures. In an embodiment, the low energy hydrogen reaction may have higher kinetics at higher plasma pressures. Based on high-speed spectra and Edgertronics data, the low-energy hydrogen reaction rate is highest at the lowest plasma volume and the highest initial vapor pressure. The 1 mm diameter Ag pellets ignite when molten (T = 1235 K). 80 mg (7.4 × 10)- 4 The initial volume of the pellets is 5.2 × 10- 7 liter. Corresponding maximum pressure is about 1.4 × 105 Atmospheric pressure. In an exemplary embodiment, the reaction was observed to expand at about sound speed (343 m/s) for about 0.5 ms. The final radius is approximately 17 cm. The final volume is about 20 liters without any back pressure. The final Ag partial pressure is about 3.7E-3 atmospheres. Since the reaction can have higher kinetics at higher pressures, the rate of reaction can be increased by applying electrode pressure and electrode limits that allow the plasma to expand perpendicular to the axis of the inter-electrode. The power released by the low energy hydrogen reaction in the presence of a 97% argon/3% hydrogen atmosphere is measured by adding one mol% or 0.5 mol% cerium oxide to the spray at 2.5 ml/s to Caused by molten silver in the ignition electrode of SunCell®. The relative change in the slope of the transient reaction cell water coolant temperature before and after the addition of the low energy hydrogen reaction power specific gravity corresponding to the oxide addition is multiplied by the constant initial input power acting as an internal standard. For repeated extensions, the total battery output power with a low energy hydrogen power specific gravity after the oxygen source is added is corresponding to the total input power of 7540 W, 8300 W, 8400 W, 9700 W, 8660 W, 8020 W, and 10,450 W. The product of the ratio of the slopes of the transient coolant temperature responses of 97, 119, 15, 538, 181, 54 and 27 is determined. Thermal peak powers were 731,000 W, 987,700 W, 126,000 W, 5,220,000 W, 1,567,000 W, 433,100 W, and 282,150 W, respectively. The power released by the low-energy hydrogen reaction in the presence of a 97% argon/3% hydrogen atmosphere is measured by reacting one mol% of yttrium oxide (Bi2 O3 ), one mol% lithium vanadate (LiVO3 ) or 0.5 mol% lithium vanadate added to the molten silver sprayed into the ignition electrode of SunCell® at 2.5 ml/s. The relative change in the slope of the transient reaction cell water coolant temperature before and after the addition of the low energy hydrogen reaction power specific gravity corresponding to the oxide addition is multiplied by the constant initial input power acting as an internal standard. For repeated extensions, the total battery output with a low energy hydrogen power specific gravity after oxygen source addition is responsive to transient coolant temperatures of 497, 200, and 26 corresponding to a total input power of 6420 W, 9000 W, and 8790 W. The product of the ratio of the slope is determined. The thermal peak powers are 3.2 MW, 1.8 MW and 230,000 W, respectively. In an exemplary embodiment, the ignition current corresponds to a voltage increase from about 0 V to 1 V in about 0.5 and a gradual rise from about 0 A to 2000 A at which the plasma is ignited. The voltage is then increased in one step to about 16 V and held for about 0.25 s, with about 1 kA flowing through the melt and 1.5 kA flowing through most of the plasma through another ground loop other than electrode 8. At an input power of approximately 25 kW at a flow rate of 9 liters/s to include Ag (0.5 mole % LiVO3 And argon-H2 In the case of (3%) SunCell®, the power output is higher than 1 MW. The firing sequence is repeated at approximately 1.3 Hz. In an exemplary embodiment, the ignition current is a constant current of about 500 A and the voltage is about 20 V. At an input power of approximately 15 kW at a flow rate of 9 liters/s to include Ag (0.5 mole % LiVO3 And argon-H2 In the case of (3%) SunCell®, the power output is above 1 MW. In the embodiment shown in Figure 6, a system 500 that forms a large aggregate or polymer comprising a lower energy hydrogen species comprises a chamber 507, such as a plastic glass chamber, a metal wire 506, having a high voltage DC The high voltage capacitor 505 of the ground connection 504 charged by the power supply 503 and a switch such as the 12 V electric switch 502 and the trigger electric flower gap switch 501, the switch closes the circuit from the capacitor to the metal wire 506 inside the chamber 507, so that the wire Knock. The chamber may contain water vapor and a gas such as atmospheric air or an inert gas. An exemplary system for forming large aggregates or polymers comprising lower energy hydrogen species comprises: a closed rectangular cuboid plastic glass chamber having a length of 46 cm and a width and height of 12.7 cm; a 10.2 cm long, 0.22 to 0.5 mm diameter Metal wire, which is mounted between two stainless steel poles using a stainless steel nut at a distance of 9 cm from the bottom of the chamber; 15 kV capacitor (Westinghouse model 5PH349001AAA, 55 uF), which corresponds to 557 J charge to approximately 4.5 kV; The 35 kV DC power supply; and the 12 V switch and trigger electric flower gap switch (Information Unlimited, model Trigatron 10, 3 kJ), which closes the circuit from the capacitor to the metal wire inside the chamber to cause the wire to knock. The wire may contain Mo (molybdenum metal mesh, 20 mesh from a 0.305 mm diameter wire, 99.95%, Alpha Aesar), Zn (0.25 mm diameter, 99.993%, Alpha Aesar), Fe-Cr-Al alloy (73%-22%) -4.8%, 31 standard size, 0.226 mm diameter, KD Cr-Al-Fe alloy wire component #1231201848, Hyndman Industrial Products Inc.) or Ti (0.25 mm diameter, 99.99%, Alpha Aesar) wire. In an exemplary extension, the chamber contains air and the air contains about 20 torr of water vapor. The high voltage DC power supply is turned off before the trigger switch is closed. A peak voltage of approximately 4.5 kV is discharged with a damped harmonic oscillator above approximately 300 us at a peak current of 5 kA. Large aggregates or polymers containing lower energy hydrogen species are formed within about 3-10 minutes after the wire is knocked. Analytical samples were collected from the bottom and walls of the chamber and on the Si wafer placed in the chamber. The results of the analysis match the low energy hydrogen labeling of the present invention. In an embodiment, the low energy hydrogen vibrational spectroscopy is observed by electron beam excitation of a reaction mixture gas comprising an inert gas such as argon and water vapor serving as a source of HOH catalyst and atomic hydrogen. Argon may be in the range of from about 100 Torr to 10 atmospheres. The water vapor pressure can range from about 1 microtorr to 10 Torr. The electron beam energy can range from about 1 keV to 100 keV. The rotating line was observed in a 145-300 nm region from an atmospheric pressure argon plasma containing about 100 mTorr of water vapor excited by a 12 keV to 16 keV electron beam through a gas in the incident chamber of the tantalum nitride window. Observing MgF through the reaction gas chamber2 The launch of another window. Hydrogen energy spacing 42 The energy spacing of the multiple determines the inter-core distance as H2 1/4 of the distance between the cores and identify H2 (1/4) (Equation (29-31)). This series matches for H2 (1/4) Vibration transition v = 1 → v = 0H2 (1/4) P branch, which includes P(1), P(2), P(3), P(4) observed at 154.94, 159.74, 165.54, 171.24, 178.14, and 183.14 nm, respectively. P(5) and P(6). In another embodiment, a composition of matter comprising low energy hydrogen such as low energy hydrogen in the present invention is thermally decomposed and comprises such as H2 (1/4) of the decomposition gas of low-energy hydrogen is introduced into the reaction gas chamber, wherein the low-energy hydrogen gas is excited using an electron beam, and the vibrational emission spectrum is recorded. In another embodiment, such as H2 The (1/4) low energy hydrogen gas is absorbed in a getter such as an alkali halide or an alkali halide alkali metal hydroxide matrix. The rotational vibrational spectroscopy can be observed by exciting the getter with an electron beam in a vacuum. The electron beam energy can range from about 1 keV to 100 keV. The rotational energy spacing between the peaks can be given by equation (30). The vibration energy given by equation (29) can be shifted to lower energy due to the higher effective mass caused by the crystallographic matrix. In an illustrative experimental example, the getter is captured in the crystal latticeH 2 (1/4) vibrating transmission by 5 × 10- 6 The pressure range of the support has 10-20μA The incident beam current was excited by a 6 KeV electron gun and recorded by windowless UV spectroscopy. Acting as Mills et al. (R. Mills, X Yu, Y. Lu, G Chu, J. He, J. Lotoski, "Catalyst induced hydrino transition (CIHT) electrochemical cell", (2012), Int. J. Energy Res. , (2013), DOI: 10.1002/er.3142, which is incorporated by reference) in the UV transparent matrix KCl of the getter in the 5 W CIHT cell stack2 The resolved vibrational spectrum of (1/4) (so-called 260 nm band) contains the peak maximum at 258 nm, where the representative positions of the peaks are at 222.7, 233.9, 245.4, 258.0, 272.2 and 287.6 nm with 0.2491 eV Equal spacing. In general, the curve of energy versus peak number is generated and used for transitions.And H of Q(0), R(0), R(1), R(2), P(1), P(2), P(3), and P(4)2 (1/4) The predicted values are extremely consistent R2 = 0.999 or better by the line given by y = -0.249 eV + 5.8 eV, where Q(0) is recognized as the strongest peak of the series. Further, a positive ion ToF-SIMS spectrum having a getter that absorbs a low-energy hydrogen reaction product gas exhibits a multimeric group of matrix compounds in which dihydrogen is part of the structure, M:H2 (M = KOH or K2 CO3 ). Specifically, it contains KOH and K.2 CO3 [26-27] or a positive ion spectrum of a previously low-energy hydrogen reaction product having a getter of such a compound as a low-energy hydrogen reaction product gas and H as a complex in the structure2 (1/p) consistentand. In another embodiment, the low energy hydrogen vibrational spectrum is excited by an electron beam comprising, for example, such as H16 Molecular low-energy hydrogen compounds or large aggregates or such as H2 The composition of the low energy hydrogen of the decomposition product of (1/p) was observed. A composition of matter comprising low energy hydrogen may comprise the low energy hydrogen compound of the present invention. The electron beam energy can range from about 1 keV to 100 keV. The emission spectrum can be recorded in a vacuum by EUV spectroscopy. In the earliest exemplary experimental examples, H2 (1/4) The oscillating line was excited from a low energy hydrogen zinc hydride in the 145-300 nm region by a 12 keV to 16 keV electron beam excitation. The beam is incident on the compound in a vacuum. The low energy zinc hydride is formed by the knocking of a zinc wire in accordance with the method of the present invention in the presence of water vapor in the air. Hydrogen energy spacing 42 The energy spacing of the multiple determines the inter-core distance as H2 1/4 of the distance between the cores and identify H2 (1/4) (Equation (29-31)). This series matches for H2 (1/4) Vibration transition v = 1 → v = 0H2 (1/4) P branch, which includes P(1), P(2), P(3), P(4), P(5), P(6), and P(7), respectively.

2‧‧‧電源2‧‧‧Power supply

13b‧‧‧泵管線13b‧‧‧ pump line

5b3‧‧‧殼體5b3‧‧‧shell

5b31‧‧‧反應電解槽腔室5b31‧‧‧Reaction cell chamber

5b3a‧‧‧外部壓力容器5b3a‧‧‧External pressure vessel

5b3a1‧‧‧電池腔室5b3a1‧‧‧ battery chamber

5b3b‧‧‧底板5b3b‧‧‧floor

5b4‧‧‧圓頂/金屬黑體輻射器5b4‧‧‧Dome/Metal Blackbody Radiator

5b41‧‧‧下部半球5b41‧‧‧ Lower hemisphere

5b4a‧‧‧黑體輻射器外表面5b4a‧‧‧Black body radiator outer surface

5b4a1‧‧‧第二空腔5b4a1‧‧‧ second cavity

5b42‧‧‧上部半球5b42‧‧‧ upper hemisphere

5b5‧‧‧下部腔室5b5‧‧‧lower chamber

5b6a‧‧‧冷卻管線5b6a‧‧‧Cooling pipeline

5b71‧‧‧墊片5b71‧‧‧shims

5b8‧‧‧儲集器支撐板5b8‧‧‧Reservoir support plate

5b81‧‧‧頂部/PV轉換器支撐板5b81‧‧‧Top/PV Converter Support Plate

5c‧‧‧導電儲集器5c‧‧‧conductive reservoir

5ca‧‧‧滴水邊緣5ca‧‧‧ dripping edge

5e1‧‧‧容器5e1‧‧‧ container

5e2‧‧‧入口5e2‧‧‧ entrance

5e3‧‧‧出口5e3‧‧‧Export

5f‧‧‧電感耦合加熱器天線5f‧‧‧Inductively coupled heater antenna

5h1‧‧‧穿透件5h1‧‧‧ penetrating parts

5h3‧‧‧穿透件5h3‧‧‧ penetrating parts

5k1‧‧‧EM泵熱交換器5k1‧‧‧EM pump heat exchanger

5k2‧‧‧EM泵匯流排5k2‧‧‧EM pump bus

5k4‧‧‧磁體5k4‧‧‧ magnet

5k6‧‧‧EM泵管5k6‧‧‧EM pump tube

5k7‧‧‧熱傳遞塊5k7‧‧‧heat transfer block

5k9‧‧‧接頭套管5k9‧‧‧ joint casing

5k10‧‧‧接頭套管型接合O形環5k10‧‧‧Connector sleeve type joint O-ring

5k11‧‧‧冷卻劑管線5k11‧‧‧ coolant pipeline

5k12‧‧‧冷板5k12‧‧‧ cold plate

5k13‧‧‧EM電力供應器5k13‧‧‧EM power supply

5k14‧‧‧滑動螺母接頭5k14‧‧‧Sliding nut joint

5k14a‧‧‧墊片5k14a‧‧‧shims

5k15‧‧‧套環5k15‧‧‧ collar

5k16‧‧‧壓縮保持套筒5k16‧‧‧Compression retaining sleeve

5k17‧‧‧蓄水器凸緣5k17‧‧‧Water reservoir flange

5k18‧‧‧冷卻劑迴路5k18‧‧‧ coolant circuit

5k19‧‧‧EM泵組合件套環凸緣5k19‧‧‧EM pump assembly collar flange

5k21‧‧‧螺母5k21‧‧‧ nut

5k31‧‧‧EM泵饋通件5k31‧‧‧EM pump feedthrough

5k33‧‧‧EM泵匯流排連接器5k33‧‧‧EM pump busbar connector

5k61‧‧‧EM泵管注射器5k61‧‧‧EM pump syringe

5kk‧‧‧EM泵組合件5kk‧‧‧EM pump assembly

5kk1‧‧‧EM泵組合件5kk1‧‧‧EM pump assembly

5m‧‧‧電感耦合加熱器5m‧‧‧Inductively coupled heater

5mc‧‧‧電感耦合加熱器天線饋通組合件5mc‧‧‧Inductively Coupled Heater Antenna Feedthrough Assembly

5p‧‧‧引線5p‧‧‧Lead

5q‧‧‧噴嘴5q‧‧‧ nozzle

5qa‧‧‧碳進水升管5qa‧‧‧carbon inlet pipe

5s1‧‧‧放射源5s1‧‧‧ Radioactive source

5s2‧‧‧輻射偵測器5s2‧‧‧radiation detector

5u‧‧‧氫貯槽5u‧‧‧ hydrogen storage tank

5u1‧‧‧氬貯槽5u1‧‧‧ argon storage tank

5ua‧‧‧氫進料管線5ua‧‧‧Hydrogen feed line

5ua1‧‧‧氬氣管線5ua1‧‧‧argon pipeline

5z1‧‧‧氣體噴射器5z1‧‧ gas injector

6k61‧‧‧雙熔融金屬噴射器系統6k61‧‧‧Double molten metal injector system

8‧‧‧電極8‧‧‧Electrode

8a1‧‧‧O形環鎖定螺母8a1‧‧‧O-ring lock nut

9‧‧‧點火匯流排9‧‧‧Ignition busbar

9a‧‧‧匯流排集電器9a‧‧‧ Bus Collector

10‧‧‧點火匯流排10‧‧‧Ignition bus

10a‧‧‧饋通件10a‧‧‧Feed parts

10a2‧‧‧點火匯流排連接器10a2‧‧‧Ignition busbar connector

13a‧‧‧泵13a‧‧‧ pump

15‧‧‧聚光型光伏打電池15‧‧‧Concentrating photovoltaic battery

23‧‧‧透明反射鏡23‧‧‧Transparent mirror

26‧‧‧電池26‧‧‧Battery

26a‧‧‧PV轉換器26a‧‧‧PV Converter

26b‧‧‧PV熱交換器/模組式平板熱交換器元件26b‧‧‧PV heat exchanger / modular plate heat exchanger components

26c‧‧‧包層26c‧‧‧ cladding

31‧‧‧輻射器/燃料回收及熱管理系統31‧‧‧radiator/fuel recovery and thermal management system

31a‧‧‧急冷器31a‧‧‧Quencher

31b‧‧‧入口/熱冷卻劑入口管線31b‧‧‧Inlet/Hot Coolant Inlet Line

31c‧‧‧出口31c‧‧‧Export

31d‧‧‧冷卻劑入口管線31d‧‧‧ coolant inlet line

31e‧‧‧冷卻劑出口管線31e‧‧‧ coolant outlet line

31k‧‧‧冷卻劑泵31k‧‧‧ coolant pump

31m‧‧‧閥門31m‧‧‧ valve

31j1‧‧‧風扇31j1‧‧‧fan

31t‧‧‧輻射器入口管線31t‧‧‧radiator inlet line

31u‧‧‧水泵出口31u‧‧‧Water pump outlet

87‧‧‧熱交換器87‧‧‧ heat exchanger

87a‧‧‧熱交換器87a‧‧‧ heat exchanger

90‧‧‧點火電容器殼體90‧‧‧Ignition capacitor housing

90a‧‧‧線圈電容器箱90a‧‧‧Coil capacitor box

92‧‧‧齒輪箱92‧‧‧ Gearbox

93‧‧‧馬達93‧‧‧Motor

94‧‧‧滾珠螺桿94‧‧‧Ball screw

94a‧‧‧軸承94a‧‧‧ Bearing

100‧‧‧電腦100‧‧‧ computer

110‧‧‧功率調節器或反相器110‧‧‧Power conditioner or inverter

111‧‧‧蒸汽出口111‧‧‧Steam exit

113‧‧‧入口113‧‧‧ entrance

114‧‧‧空間分離圓周半球狀熱交換器114‧‧‧Space separation circumferential hemispherical heat exchanger

114a‧‧‧面板或區段114a‧‧‧ panels or sections

114b‧‧‧歧管114b‧‧‧Management

114c‧‧‧冷卻劑管線114c‧‧‧ coolant pipeline

114d‧‧‧冷卻劑入口孔114d‧‧‧ coolant inlet hole

114e‧‧‧冷卻劑出口孔114e‧‧‧ coolant outlet hole

114f‧‧‧歧管冷卻劑出口114f‧‧‧Management coolant outlet

115‧‧‧下部熱交換器115‧‧‧ Lower heat exchanger

116‧‧‧鍋爐116‧‧‧Boiler

200‧‧‧熱交換器元件200‧‧‧ heat exchanger components

202‧‧‧熱冷卻劑出口202‧‧‧Hot coolant outlet

203‧‧‧罩蓋主體203‧‧‧ Cover body

204‧‧‧冷卻劑入口/冷埠204‧‧‧ coolant inlet/cold

301‧‧‧饋入孔301‧‧‧Feed hole

304‧‧‧MHD電極304‧‧‧MHD electrode

305‧‧‧MHD電導線305‧‧‧MHD electric wire

306‧‧‧MHD磁體306‧‧‧MHD magnet

306a‧‧‧MHD磁體殼體306a‧‧‧MHD magnet housing

307‧‧‧MHD噴嘴307‧‧‧MHD nozzle

308‧‧‧凸台308‧‧‧Boss

309‧‧‧MHD冷凝區段309‧‧‧MHD condensation section

309b‧‧‧氣體殼體309b‧‧‧ gas housing

309d‧‧‧半滲透氣體309d‧‧‧ semi-permeable gas

309e‧‧‧排空組合件309e‧‧‧ emptying assembly

310‧‧‧MHD回流管310‧‧‧MHD return tube

31l‧‧‧貯槽/蓄水器31l‧‧‧storage tank/water reservoir

312‧‧‧MHD傳回EM泵312‧‧‧MHD returns EM pump

312a‧‧‧壓縮機/氣泵312a‧‧‧Compressor/Air Pump

312b‧‧‧馬達312b‧‧‧Motor

312c‧‧‧刮刀或輪葉312c‧‧ s scraper or vane

313‧‧‧MHD回流EM泵管313‧‧‧MHD return EM pump tube

313a‧‧‧管氣體通路313a‧‧‧pipe gas path

316‧‧‧熱交換器316‧‧‧ heat exchanger

400‧‧‧EM泵400‧‧‧EM pump

400a‧‧‧多級EM泵組合件400a‧‧‧Multi-level EM pump assembly

400b‧‧‧感應EM泵/空氣冷卻系統400b‧‧‧Induction EM pump/air cooling system

400c‧‧‧感應EM泵400c‧‧‧Induction EM pump

401‧‧‧初級變壓器繞組401‧‧‧Primary transformer winding

401a‧‧‧EM泵變壓器繞組電路401a‧‧‧EM pump transformer winding circuit

402‧‧‧磁性電路或EM泵變壓器磁軛402‧‧‧Magnetic circuit or EM pump transformer yoke

403‧‧‧AC電磁體403‧‧‧AC electromagnet

403a‧‧‧電磁體403a‧‧Electron

403b‧‧‧電磁體403b‧‧Electron

403c‧‧‧EM泵電磁電路403c‧‧‧EM pump electromagnetic circuit

404‧‧‧EM泵電磁磁軛404‧‧‧EM pump electromagnetic yoke

404a‧‧‧變壓器磁軛404a‧‧‧ Transformer yoke

404b‧‧‧變壓器磁軛404b‧‧‧Transformer yoke

405‧‧‧EM泵套管區段405‧‧‧EM pump casing section

406‧‧‧EM泵電流迴路傳回區段406‧‧‧EM pump current loop return section

407‧‧‧凸緣接頭407‧‧‧Flange joint

407a‧‧‧密封件407a‧‧‧Seal

408‧‧‧凸台408‧‧‧Boss

409‧‧‧儲集器底板組合件409‧‧‧Reservoir bottom plate assembly

409a‧‧‧底板409a‧‧‧floor

410‧‧‧感應點火變壓器組合件410‧‧‧Induction ignition transformer assembly

411‧‧‧感應點火變壓器繞組411‧‧‧Induction ignition transformer winding

412‧‧‧感應點火變壓器磁軛412‧‧‧Induction ignition transformer yoke

413‧‧‧蓋板413‧‧‧ Cover

414‧‧‧陶瓷交接通道414‧‧‧Ceramic transfer channel

415‧‧‧天線415‧‧‧Antenna

416‧‧‧EM泵儲集器管線416‧‧‧EM pump reservoir pipeline

417‧‧‧EM泵噴射管線417‧‧‧EM pump injection line

418‧‧‧結構支架418‧‧‧Structural bracket

419‧‧‧控制管線419‧‧‧Control pipeline

420‧‧‧熱屏蔽420‧‧‧Heat shielding

421‧‧‧貯氣瓶421‧‧‧ gas cylinder

422‧‧‧氣體供應套管422‧‧‧ gas supply casing

500‧‧‧系統500‧‧‧ system

501‧‧‧觸發電花隙開關501‧‧‧Trigger electric flower gap switch

502‧‧‧12 V電開關502‧‧‧12 V electric switch

503‧‧‧高電壓DC電源503‧‧‧High voltage DC power supply

504‧‧‧接地連接504‧‧‧ Ground connection

505‧‧‧高電壓電容器505‧‧‧High voltage capacitor

506‧‧‧金屬導線506‧‧‧Metal wire

507‧‧‧腔室507‧‧ ‧ chamber

併入此說明書中且構成此說明書之一部分之隨附圖式說明本發明之若干實施例,且連同描述一起用以闡明本發明之原則。在圖式中: 圖2I28為根據本發明之實施例的SF-CIHT電池或SunCell®發電機之具有及不具有磁體之電磁泵的磁軛組合件之示意圖。 圖2I69為根據本發明之實施例之熱光伏打SunCell®發電機之示意圖,其展示電磁泵與儲集器之組合件的分解橫截面視圖。 圖2I80為根據本發明之實施例之熱光伏打SunCell®發電機之示意圖,其展示橫截面視圖,該熱光伏打SunCell®發電機包含其組件容納於單一外部壓力容器中之雙EM泵噴射器作為液體電極。 圖2I81為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示儲集器與黑體輻射器之組合件。 圖2I82為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示儲集器與黑體輻射器之組合件的透明視圖。 圖2I83為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示黑體輻射器及雙噴嘴的下部半球。 圖2I84為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示具有外部壓力容器之發電機,展示對外部壓力容器之底座的穿透。 圖2I85為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示頂部移除了外部壓力容器之發電機,展示對外部壓力容器之底座的穿透。 圖2I86為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意性冠狀xz剖面圖。 圖2I87為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意性yz截面圖。 圖2I88為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示發電機支架組件。 圖2I89為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示發電機支架組件。 圖2I90為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示發電機支架組件。 圖2I91為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示發電機支架組件。 圖2I92為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示發電機支架組件。 圖2I93為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示垂直伸縮式天線處於向上或儲集器加熱位置。 圖2I94為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示垂直伸縮式天線處於向下或冷卻位置。 圖2I95為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示用以改變加熱器線圈之垂直位置的致動器。 圖2I96為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示用以改變加熱器線圈之垂直位置的致動器之驅動機構。 圖2I97為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之橫截面示意圖,其展示用以改變加熱器線圈之垂直位置的致動器。 圖2I98為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示電磁泵組合件。 圖2I99為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示滑動螺母儲集器連接器。 圖2I100為展示根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之外部及橫截面視圖的示意圖,該熱光伏打SunCell®發電機包含滑動螺母儲集器連接器。 圖2I101為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之俯視橫截面示意圖。 圖2I102為展示根據本發明之實施例之粒子絕緣密閉容器之橫截面示意圖。 圖2I103為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之橫截面示意圖,其展示粒子絕緣密閉容器。 圖2I104至圖2I114為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機的示意圖,該熱光伏打SunCell®發電機具有X射線水平感測器、滑動螺母連接器及容納功率調節器及電力供應器之下部腔室。 圖2I115為根據本發明之實施例之容納兩個EM磁體及冷卻迴路之電磁泵(EM)法拉弟籠的示意圖。 圖2I116為根據本發明之實施例之容納一個EM磁體及冷卻迴路之電磁泵(EM)法拉弟籠的示意圖。 圖2I117至圖2I126為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機的示意圖,該熱光伏打SunCell®發電機具有X射線水平感測器、滑動螺母連接器及容納功率調節器及電力供應器之下部腔室。 圖2I127至圖2I130為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器及滑動螺母連接器之原型熱光伏打SunCell®發電機之示意圖。 圖2I131為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器及滑動螺母連接器之原型熱光伏打SunCell®發電機之部件的示意圖。 圖2I132為根據本發明之實施例之SunCell®發電機之示意圖,其展示光分佈及光伏打轉換器系統的細節。 圖2I133為根據本發明之實施例的光伏打轉換器或熱交換器之測地密集型接收器陣列的三角形元件的示意圖。 圖2I134為根據本發明之實施例之SunCell®發電機之示意圖,其展示立方體形次級輻射器及其電感耦合加熱器處於作用中位置之光伏打轉換器系統的細節。 圖2I135為根據本發明之實施例之SunCell®發電機之示意圖,其展示立方體形次級輻射器及其電感耦合加熱器處於儲存位置之光伏打轉換器系統的細節。 圖2I136為根據本發明之實施例之包含立方體形次級輻射器的立方體形光伏打轉換器系統的示意圖。 圖2I137為根據本發明之實施例之SunCell®發電機之示意圖,其展示立方體形次級輻射器及其中移除了加熱天線之光伏打轉換器系統的細節。 圖2I138為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機的示意圖,其展示具有進水升管之電磁泵組合件。 圖2I139為根據本發明之實施例之儲集器與EM泵組合件之濕封的示意圖。 圖2I140為根據本發明之實施例之儲集器與EM泵組合件之濕封的示意圖。 圖2I141為根據本發明之實施例之儲集器與EM泵組合件之內部或反向滑動螺母密封的示意圖。 圖2I142為根據本發明實施例之儲集器與EM泵組合件之壓縮密封的示意圖。 圖2I143為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示具有進水升管之傾斜電磁泵組合件及半徑增加而減小黑體光強度的PV轉換器。 圖2I144至圖2I145各為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示具有進水升管之傾斜電磁泵組合件。 圖2I146至圖2I147各為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器之熱光伏打SunCell®發電機之示意圖,其展示具有進水升管之傾斜電磁泵組合件及透明反應電解槽腔室。 圖2I148為根據本發明之實施例的電感耦合加熱器之RF天線之俯視示意圖,該電感耦合加熱器包含:兩個單獨天線線圈,其各包含上部餅狀托架及與EM泵管平面平行的下部Ω形餅狀線圈;每個天線線圈電容器箱;及用於水平移動之雙向致動器。 圖2I149為根據本發明之實施例的電感耦合加熱器之RF天線之俯視示意圖,該電感耦合加熱器包含:兩個單獨天線線圈,其各包含上部餅狀托架及與EM泵管平面平行的下部Ω形餅狀線圈;具有柔性天線連接之共同天線線圈電容器箱;及用於水平移動之雙向致動器。 圖2I150為根據本發明之實施例的電感耦合加熱器之RF天線之示意圖的兩個視圖,該電感耦合加熱器包含:為兩個儲集器圓周之上部分段橢圓,其中每一迴路包含柔性天線區段;及與EM泵管平面平行的下部Ω形餅狀線圈,其具有帶柔性天線連接之共同天線線圈電容器箱;及用於水平移動之雙向致動器。 圖2I151為根據本發明之實施例的電感耦合加熱器之RF天線之示意圖的兩個視圖,該電感耦合加熱器包含分裂的上部圓周橢圓線圈及連接至該橢圓線圈之一半的下部餅狀線圈,其中當該橢圓之兩個半部處於如圖所示之閉合位置時,該等半部由迴路電流連接器接合。 圖2I152為根據本發明之實施例的電感耦合加熱器之RF天線之示意圖的四個視圖,該電感耦合加熱器包含分裂的上部圓周橢圓線圈及連接至該橢圓線圈之一半的下部餅狀線圈,其中當所示處於斷開位置之該橢圓之兩個半部移至閉合位置時,該等半部由迴路電流連接器接合。 圖2I153至圖2I155各為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的SunCell®熱力發電機的示意圖,其展示用以接收來自黑體輻射器之熱力並將熱量傳遞至冷卻劑的壁中嵌入有冷卻劑管之空腔吸熱器,然後係用以輸出熱空氣之次級熱交換器。 圖2I156為根據本發明之實施例的包含用以輸出蒸汽之上部及下部熱交換器的SunCell®熱力發電機的示意圖。 圖2I157至圖2I158各為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的SunCell®熱力發電機的示意圖,其展示用以輸出蒸汽之上部及下部鍋爐管。 圖2I159為根據本發明之實施例的SunCell®熱力發電機之用以輸出蒸汽的鍋爐管及鍋爐腔室的示意圖。 圖2I160為根據本發明之實施例的SunCell®熱力發電機之用以輸出蒸汽的反應腔室、鍋爐管及鍋爐腔室的示意圖。 圖2I161為根據本發明之實施例的磁流體動力(MHD)轉換器組件(陰極、陽極、絕緣體及匯流排饋通凸緣)的示意圖。 圖2I162至圖2I166為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的SunCell®發電機的示意圖,其展示傾斜儲集器及包含一對MHD傳回EM泵的磁流體動力(MHD)轉換器。 圖2I167至圖2I173為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的SunCell®發電機的示意圖,其展示傾斜儲集器及包含一對MHD傳回EM泵及一對MHD回氣泵或壓縮機的磁流體動力(MHD)轉換器。 圖2I174至圖2I176為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的SunCell®發電機的示意圖,其展示傾斜儲集器、陶瓷EM泵管組合件及包含一對MHD傳回EM泵的磁流體動力(MHD)轉換器。 圖2I177為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、陶瓷EM泵管組合件及筆直MHD通道。 圖2I178為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器及筆直MHD通道。 圖2I179至圖2I183為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直MHD通道及氣體添加殼體。 圖2I184為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直磁流體動力(MHD)通道、氣體添加殼體及用於噴射之單級感應EM泵及單級感應抑或DC傳導MHD傳回EM泵。 圖2I185為根據本發明之實施例的單級感應噴射EM泵的示意圖。 圖2I186為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直磁流體動力(MHD)通道、氣體添加殼體、用於噴射及MHD傳回兩者之兩級感應EM泵及感應點火系統。 圖2I187為根據本發明之實施例的儲集器底板組合件及連接組件(進水升管、噴射器管及噴嘴)的示意圖。 圖2I188為根據本發明之實施例的兩級感應EM泵之示意圖,其中第一級充當MHD傳回EM泵且第二級充當噴射EM泵。 圖2I189為根據本發明之實施例的感應點火系統之示意圖。 圖2I190至圖2I191為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直磁流體動力(MHD)通道、氣體添加殼體、用於噴射及MHD傳回兩者之兩級感應EM泵(其各自具有強制風冷系統)及感應點火系統。 圖2I192為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直磁流體動力(MHD)通道、氣體添加殼體、用於噴射及MHD傳回兩者之兩級感應EM泵(其各自具有強制風冷系統)、感應點火系統及在EM泵管、儲集器、反應電解槽腔室及MHD回流管上的電感耦合式加熱天線。 圖2I193至圖2I195為根據本發明之實施例的包含作為液體電極之雙EM泵噴射器的磁流體動力(MHD) SunCell®發電機的示意圖,其展示傾斜儲集器、球面反應電解槽腔室、筆直磁流體動力(MHD)通道、氣體添加殼體、用於噴射及MHD傳回兩者之兩級感應EM泵(其各自具有強制風冷系統)及感應點火系統。 圖2I196為根據本發明之實施例的兩個SunCell®熱力發電機之示意圖,一者包含壁中嵌入有冷卻劑管之半球面殼形輻射熱吸收器,其用以接收來自包含黑體輻射器之反應電解槽的熱力並將熱量傳遞至冷卻劑,且另一者包含圓周圓柱形熱交換器及鍋爐。 圖3為根據本發明之實施例的來自Smithells Metals Reference Book第8版11-20的銀-氧相圖的示意圖。 圖4為根據本發明之實施例的對包含經吸收之H2 及H2 O的80 mg丸粒點火的處於5 nm至450 nm區域的絕對光譜,該經吸收之H2 及H2 O來自在滴入蓄水器中之前熔化的銀的氣體處理,其展示基本上全部處於紫外及遠紫外光譜區中的1.3 MW之平均NIST經校準光功率。 圖5為根據本發明之實施例的在具有約1 Torr之環境H2 O蒸氣壓的大氣氬中對泵抽至W個電極中之熔融銀點火的光譜(歸因於藍寶石光譜儀窗,在180 nm處具有截止之100 nm至500 nm區域),其展示在大氣隨著銀之汽化而變得對於UV輻射為光厚時轉變為5000K黑體輻射的UV線發射。 圖6為根據本發明之實施例的低能量氫反應電解槽腔室的示意圖,該低能量氫反應電解槽腔室包含使導線爆震以充當反應物來源中之至少一者的構件及用以傳播低能量氫反應以形成大型聚集體或聚合物的構件,該等大型聚集體或聚合物包含低能氫物質,諸如分子低能量氫。The accompanying drawings, which are incorporated in the claims of the claims In the drawings: FIG. 2I28 is a schematic illustration of a yoke assembly of an SF-CIHT battery or a SunCell® generator with and without a magnet in accordance with an embodiment of the present invention. 2I69 is a schematic illustration of a thermal photovoltaic SunCell® generator in accordance with an embodiment of the present invention showing an exploded cross-sectional view of an assembly of an electromagnetic pump and a reservoir. 2I80 is a schematic illustration of a thermophotovoltaic SunCell® generator showing a cross-sectional view of a dual-EM pump injector with its components housed in a single external pressure vessel, in accordance with an embodiment of the present invention. As a liquid electrode. 2I81 is a schematic illustration of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a combination of a reservoir and a blackbody radiator, in accordance with an embodiment of the present invention. 2I82 is a schematic illustration of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a transparent view of the assembly of the reservoir and the blackbody radiator, in accordance with an embodiment of the present invention. 2I83 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a black body radiator and a lower hemisphere of a dual nozzle, in accordance with an embodiment of the present invention. 2I84 is a schematic diagram of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator with an external pressure vessel showing the wear of the base of the external pressure vessel, in accordance with an embodiment of the present invention. through. 2I85 is a schematic diagram of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator with an external pressure vessel removed from the top, showing the external pressure vessel, in accordance with an embodiment of the present invention. Penetration of the base. 2I86 is a schematic coronal xz cross-sectional view of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, in accordance with an embodiment of the present invention. 2I87 is a schematic yz cross-sectional view of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, in accordance with an embodiment of the present invention. 2I88 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator bracket assembly, in accordance with an embodiment of the present invention. 2I89 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator bracket assembly, in accordance with an embodiment of the present invention. 2I90 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator bracket assembly, in accordance with an embodiment of the present invention. 2I91 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator bracket assembly, in accordance with an embodiment of the present invention. 2I92 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a generator bracket assembly, in accordance with an embodiment of the present invention. 2I93 is a schematic illustration of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing the vertical telescoping antenna in an up or reservoir heated position, in accordance with an embodiment of the present invention. 2I94 is a schematic illustration of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing the vertical telescoping antenna in a down or cooled position, in accordance with an embodiment of the present invention. 2I95 is a schematic illustration of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing an actuator for changing the vertical position of the heater coil, in accordance with an embodiment of the present invention. 2I96 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a drive mechanism for an actuator to change the vertical position of the heater coil, in accordance with an embodiment of the present invention. 2I97 is a schematic cross-sectional view of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing an actuator for changing the vertical position of the heater coil, in accordance with an embodiment of the present invention. 2I98 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing an electromagnetic pump assembly, in accordance with an embodiment of the present invention. 2I99 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a sliding nut reservoir connector, in accordance with an embodiment of the present invention. 2I100 is a schematic diagram showing an external and cross-sectional view of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, the thermal photovoltaic SunCell® generator including a sliding nut storage, in accordance with an embodiment of the present invention. Collector connector. 2I101 is a top cross-sectional view of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, in accordance with an embodiment of the present invention. 2I102 is a schematic cross-sectional view showing a particle insulated hermetic container in accordance with an embodiment of the present invention. 2I103 is a cross-sectional schematic view of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a particle insulated closed container, in accordance with an embodiment of the present invention. 2I104 through 2I114 are schematic diagrams of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode having an X-ray level sensor, in accordance with an embodiment of the present invention, Slide the nut connector and house the power regulator and the lower chamber of the power supply. 2I115 is a schematic illustration of an electromagnetic pump (EM) Faraday cage housing two EM magnets and a cooling circuit in accordance with an embodiment of the present invention. 2I116 is a schematic illustration of an electromagnetic pump (EM) Faraday cage housing an EM magnet and a cooling circuit in accordance with an embodiment of the present invention. 2I117 through 2I126 are schematic diagrams of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode having an X-ray level sensor, in accordance with an embodiment of the present invention, Slide the nut connector and house the power regulator and the lower chamber of the power supply. 2I127 through 2I130 are schematic illustrations of a prototype thermal photovoltaic SunCell® generator including a dual EM pump injector and a slip nut connector as a liquid electrode, in accordance with an embodiment of the present invention. 2I131 is a schematic illustration of a component of a prototype thermal photovoltaic SunCell® generator incorporating a dual EM pump injector and a sliding nut connector as a liquid electrode, in accordance with an embodiment of the present invention. 2I132 is a schematic illustration of a SunCell® generator showing details of a light distribution and photovoltaic converter system in accordance with an embodiment of the present invention. 2I133 is a schematic illustration of a triangular element of a geodetic intensive receiver array of a photovoltaic converter or heat exchanger in accordance with an embodiment of the present invention. 2I134 is a schematic illustration of a SunCell® generator showing details of a photovoltaic converter system with a cubic secondary radiator and its inductively coupled heater in an active position, in accordance with an embodiment of the present invention. 2I135 is a schematic illustration of a SunCell® generator in accordance with an embodiment of the present invention showing details of a cube-shaped secondary radiator and its inductively coupled heater in a storage location. 2I136 is a schematic illustration of a cubic photovoltaic converter system including a cubic secondary radiator in accordance with an embodiment of the present invention. 2I137 is a schematic illustration of a SunCell® generator in accordance with an embodiment of the present invention showing details of a cube-shaped secondary radiator and a photovoltaic converter system with a heated antenna removed. 2I138 is a schematic illustration of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing an electromagnetic pump assembly having a water riser, in accordance with an embodiment of the present invention. 2I139 is a schematic illustration of a wet seal of a reservoir and an EM pump assembly in accordance with an embodiment of the present invention. 2I140 is a schematic illustration of a wet seal of a reservoir and an EM pump assembly in accordance with an embodiment of the present invention. 2I 141 is a schematic illustration of an internal or reverse sliding nut seal of a reservoir and an EM pump assembly in accordance with an embodiment of the present invention. 2I142 is a schematic illustration of a compression seal of a reservoir and an EM pump assembly in accordance with an embodiment of the present invention. 2I143 is a schematic diagram of a thermal photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilted electromagnetic pump assembly with a riser riser and a reduced radius, in accordance with an embodiment of the present invention. Black body light intensity PV converter. 2I144 through 2I145 are each a schematic diagram of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilted electromagnetic pump assembly having a water riser, in accordance with an embodiment of the present invention. 2I146 through 2I147 are each a schematic diagram of a thermally photovoltaic SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilted electromagnetic pump assembly with a riser riser and transparent, in accordance with an embodiment of the present invention. Reaction cell chamber. 2I148 is a top plan view of an RF antenna of an inductively coupled heater including two separate antenna coils each including an upper pie-shaped carrier and a plane parallel to the plane of the EM pump tube, in accordance with an embodiment of the present invention. Lower Ω-shaped pie-shaped coils; each antenna coil capacitor box; and two-way actuators for horizontal movement. 2I149 is a top plan view of an RF antenna of an inductively coupled heater including two separate antenna coils each including an upper pie-shaped bracket and a plane parallel to the plane of the EM pump tube, in accordance with an embodiment of the present invention. Lower omega-shaped pie coil; common antenna coil capacitor box with flexible antenna connection; and bidirectional actuator for horizontal movement. 2I150 are two views of a schematic diagram of an RF antenna of an inductively coupled heater including: a partial segment ellipse above the circumference of two reservoirs, wherein each loop includes flexibility, in accordance with an embodiment of the present invention An antenna section; and a lower Ω-shaped pie coil parallel to the plane of the EM pump tube, having a common antenna coil capacitor box with a flexible antenna connection; and a bidirectional actuator for horizontal movement. 2I151 is two views of a schematic diagram of an RF antenna of an inductively coupled heater including a split upper circumferential elliptical coil and a lower pie coil connected to one half of the elliptical coil, in accordance with an embodiment of the present invention, Where the two halves of the ellipse are in the closed position as shown, the halves are engaged by the loop current connectors. 2I152 is four views of a schematic diagram of an RF antenna of an inductively coupled heater including a split upper circumferential elliptical coil and a lower pie coil connected to one half of the elliptical coil, in accordance with an embodiment of the present invention, Where the two halves of the ellipse shown in the open position are moved to the closed position, the halves are engaged by the loop current connectors. 2I153 through 2I155 are each a schematic diagram of a SunCell® thermoelectric generator including a dual EM pump injector as a liquid electrode, shown to receive heat from a blackbody radiator and transfer heat to cooling, in accordance with an embodiment of the present invention. A cavity heat sink in which a coolant tube is embedded in the wall of the agent, and then a secondary heat exchanger for outputting hot air. 2I156 is a schematic diagram of a SunCell® thermoelectric generator including upper and lower heat exchangers for outputting steam in accordance with an embodiment of the present invention. 2I157 through 2I158 are each a schematic diagram of a SunCell® thermoelectric generator including a dual EM pump injector as a liquid electrode, shown for outputting steam upper and lower boiler tubes, in accordance with an embodiment of the present invention. 2I159 is a schematic illustration of a boiler tube and a boiler chamber of a SunCell® thermoelectric generator for outputting steam in accordance with an embodiment of the present invention. 2I160 is a schematic illustration of a reaction chamber, boiler tube, and boiler chamber of a SunCell® thermogenerator for outputting steam in accordance with an embodiment of the present invention. 2I161 is a schematic illustration of a magnetic fluid power (MHD) converter assembly (cathode, anode, insulator, and bus feedthrough flange) in accordance with an embodiment of the present invention. 2I162 through 2I166 are schematic diagrams of a SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir and a magnetohydrodynamic force including a pair of MHD return EM pumps, in accordance with an embodiment of the present invention. (MHD) converter. 2I167 through 2I173 are schematic illustrations of a SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilted reservoir and including a pair of MHD return EM pumps and a pair of MHDs, in accordance with an embodiment of the present invention. A magnetohydrodynamic (MHD) converter for a return air pump or compressor. 2I174 through 2I176 are schematic illustrations of a SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilted reservoir, a ceramic EM pump tube assembly, and a pair of MHD transmissions, in accordance with an embodiment of the present invention. Back to the EM pump's magnetohydrodynamic (MHD) converter. 2I177 is a schematic diagram of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir, a ceramic EM pump tube assembly, and a straight MHD, in accordance with an embodiment of the present invention. aisle. 2I178 is a schematic illustration of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir and a straight MHD channel, in accordance with an embodiment of the present invention. 2I179 to 2I183 are schematic diagrams of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, in accordance with an embodiment of the present invention. Straight MHD channel and gas addition housing. 2I184 is a schematic diagram of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, a straight magnetic, in accordance with an embodiment of the present invention. Fluid power (MHD) channel, gas addition housing and single stage induction EM pump for injection and single stage induction or DC conduction MHD return EM pump. 2I185 is a schematic illustration of a single stage induction injection EM pump in accordance with an embodiment of the present invention. 2I186 is a schematic diagram of a magnetohydrodynamic (MHD) SunCell® generator including a dualEM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, a straight magnetic, in accordance with an embodiment of the present invention. Fluid power (MHD) channel, gas addition housing, two-stage induction EM pump for injection and MHD return, and induction ignition system. 2I187 is a schematic illustration of a reservoir floor assembly and connection assembly (inlet riser, injector tube, and nozzle) in accordance with an embodiment of the present invention. 2I188 is a schematic illustration of a two-stage inductive EM pump in which a first stage acts as an MHD passback EM pump and a second stage acts as a jet EM pump, in accordance with an embodiment of the present invention. 2I189 is a schematic illustration of an inductive ignition system in accordance with an embodiment of the present invention. 2I190 through 2I191 are schematic diagrams of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, in accordance with an embodiment of the present invention. , a straight magnetic fluid power (MHD) channel, a gas addition housing, a two-stage induction EM pump for injection and MHD return (each with a forced air cooling system) and an induction ignition system. 2I192 is a schematic diagram of a magnetohydrodynamic (MHD) SunCell® generator including a dualEM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, a straight magnetic, in accordance with an embodiment of the present invention. Fluid power (MHD) channels, gas addition housings, two-stage induction EM pumps for injection and MHD return (each with forced air cooling system), induction ignition system and EM pump tubes, reservoirs, An inductively coupled heating antenna on the reaction cell chamber and the MHD return tube. 2I193 through 2I195 are schematic diagrams of a magnetohydrodynamic (MHD) SunCell® generator including a dual EM pump injector as a liquid electrode, showing a tilt reservoir, a spherical reaction cell chamber, in accordance with an embodiment of the present invention. , a straight magnetic fluid power (MHD) channel, a gas addition housing, a two-stage induction EM pump for injection and MHD return (each with a forced air cooling system) and an induction ignition system. 2I196 is a schematic illustration of two SunCell® thermoelectric generators, including a hemispherical shell-shaped radiant heat absorber with a coolant tube embedded in the wall for receiving a reaction from a blackbody-containing radiator, in accordance with an embodiment of the present invention. The heat of the cell transfers heat to the coolant, and the other contains a cylindrical heat exchanger and a boiler. 3 is a schematic illustration of a silver-oxygen phase diagram from the Smithells Metals Reference Book, 8th Edition, 11-20, in accordance with an embodiment of the present invention. 4 is an absolute spectrum of a region from 5 nm to 450 nm ignited for 80 mg pellets containing absorbed H 2 and H 2 O according to an embodiment of the invention, the absorbed H 2 and H 2 O are derived from Gas treatment of molten mercury prior to dropping into the reservoir exhibits an average NIST calibrated optical power of substantially 1.3 MW in the ultraviolet and far ultraviolet spectral regions. 5 is a spectrum of molten silver ignited into W electrodes in atmospheric argon having an ambient H 2 O vapor pressure of about 1 Torr according to an embodiment of the invention (due to the sapphire spectrometer window, at 180) The region of nm has a cutoff of 100 nm to 500 nm), which exhibits UV line emission that is converted to 5000 K of black body radiation as the atmosphere becomes vaporized with UV radiation. 6 is a schematic illustration of a low energy hydrogen reaction cell chamber including a member for knocking a wire to act as at least one of a source of reactants, and for use in accordance with an embodiment of the present invention. A low energy hydrogen reaction is propagated to form a building of large aggregates or polymers comprising low energy hydrogen species, such as molecular low energy hydrogen.

Claims (36)

一種產生電能及熱能中之至少一者的電力系統,其包含: 至少一個容器,其能夠保持一壓力低於、處於或高於大氣壓; 反應物,該等反應物包含: a.至少一種包含初生H2 O之催化劑來源或一催化劑; b.至少一種H2 O來源或H2 O; c.至少一種原子氫來源或原子氫;以及 d.一熔融金屬; 一熔融金屬噴射系統,其包含至少兩個各自包含一泵及一噴射器管之熔融金屬儲集器; 至少一個反應物供應系統,其用以補充在反應物之一反應以產生該電能及熱能中之至少一者的過程中消耗之該等反應物; 至少一個點火系統,其包含一電源,該電源用以向該至少兩個各自包含一電磁泵之熔融金屬儲集器供應相反電壓,及 光及熱輸出中之至少一者至電功率及/或熱功率之至少一個功率轉換器或輸出系統。A power system for generating at least one of electrical energy and thermal energy, comprising: at least one container capable of maintaining a pressure below, at or above atmospheric pressure; reactants, the reactants comprising: a. at least one comprising a newborn a catalyst source of H 2 O or a catalyst; b. at least one H 2 O source or H 2 O; c. at least one atomic hydrogen source or atomic hydrogen; and d. a molten metal; a molten metal injection system comprising at least Two molten metal reservoirs each comprising a pump and an ejector tube; at least one reactant supply system for replenishing during consumption of at least one of the reactants to produce the electrical energy and thermal energy The reactants; at least one ignition system comprising a power source for supplying an opposite voltage to the at least two molten metal reservoirs each including an electromagnetic pump, and at least one of light and heat output At least one power converter or output system to electrical power and/or thermal power. 如請求項1之電力系統,其中該熔融金屬噴射系統包含該至少兩個熔融金屬儲集器,其各自包含用以噴射在該容器內部相交之該熔融金屬之流的一電磁泵。The power system of claim 1 wherein the molten metal injection system comprises the at least two molten metal reservoirs each comprising an electromagnetic pump for injecting a stream of the molten metal intersecting within the vessel. 如請求項1之電力系統,其中每一儲集器包含一熔融金屬位準控制器,其包含一進水升管。The power system of claim 1, wherein each of the reservoirs comprises a molten metal level controller comprising a water riser. 如請求項1之電力系統,其中該點火系統包含一電源,其用以向該至少兩個各自包含一電磁泵之熔融金屬儲集器供應相反電壓,該電磁泵供應流動穿過該等相交之熔融金屬流之電流及功率,以引起該等反應物之包含點火的反應,以在該容器內部形成一電漿。The power system of claim 1, wherein the ignition system includes a power source for supplying an opposite voltage to the at least two molten metal reservoirs each including an electromagnetic pump, the electromagnetic pump supply flowing through the intersecting The current and power of the molten metal stream are caused to cause an ignition-containing reaction of the reactants to form a plasma inside the vessel. 如請求項1之電力系統,其中該點火系統包含:a)該電源,其用以向該至少兩個各自包含一電磁泵之熔融金屬儲集器供應相反電壓; b)至少兩個相交的熔融金屬流,其自該至少兩個各自包含一電磁泵之熔融金屬儲集器噴出,其中該電源能夠遞送足以引起該等反應物反應以形成電漿之一短脈衝高電流電能。The power system of claim 1, wherein the ignition system comprises: a) the power source for supplying an opposite voltage to the at least two molten metal reservoirs each comprising an electromagnetic pump; b) at least two intersecting melting A metal stream is ejected from the at least two molten metal reservoirs each comprising an electromagnetic pump, wherein the power source is capable of delivering a short pulse of high current electrical energy sufficient to cause the reactants to react to form a plasma. 如請求項5之電力系統,其中用以遞送足以引起該等反應物反應以形成電漿之一短脈衝高電流電能的該電源包含至少一個超級電容器。The power system of claim 5, wherein the power source for delivering a short pulse high current electrical energy sufficient to cause the reactants to react to form one of the plasmas comprises at least one supercapacitor. 如請求項1之電力系統,其中每一電磁泵包含以下中之一者: a.DC或AC導電型,其包含經由電極供應至該熔融金屬之一DC或AC電流源及一恆定或同相交變向量交叉磁場來源,或 b.感應型,其包含穿過熔融金屬之一短路迴路之一交變磁場來源,其在該金屬中誘導一交流電;及一同相交變向量交叉磁場來源。The power system of claim 1, wherein each of the electromagnetic pumps comprises one of: a. DC or AC conductivity type comprising a DC or AC current source supplied to the molten metal via the electrode and a constant or identical intersection A variable vector cross magnetic field source, or b. an inductive type, comprising an alternating magnetic field source through one of the short circuits of the molten metal, which induces an alternating current in the metal; and an in-phase alternating vector cross magnetic field source. 如請求項1之電力系統,其中該泵與相對應的儲集器之至少一個活接或在包含該容器、噴射系統及轉換器之部件之間的另一活接可包含一濕封、一凸緣及墊片密封、一黏著密封及一滑動螺母密封中之至少一者。The power system of claim 1, wherein the pump is in contact with at least one of the corresponding reservoirs or another joint between the components including the container, the injection system, and the converter, and the wet joint, At least one of a flange and a gasket seal, an adhesive seal, and a sliding nut seal. 如請求項8之電力系統,其中該墊片包含碳。The power system of claim 8 wherein the gasket comprises carbon. 如請求項4之電力系統,其中該熔融金屬點火系統電流在10 A至50,000 A之範圍內。The power system of claim 4, wherein the molten metal ignition system current is in the range of 10 A to 50,000 A. 如請求項10之電力系統,其中該熔融金屬點火系統之該電路藉由該等熔融金屬流之相交而閉合以引起點火,從而進一步引起在0 Hz至10,000 Hz之範圍內的一點火頻率。The power system of claim 10, wherein the circuit of the molten metal ignition system is closed by the intersection of the molten metal streams to cause ignition, thereby further causing an ignition frequency in the range of 0 Hz to 10,000 Hz. 如請求項7之電力系統,其中該感應型電磁泵包含形成熔融金屬之該短路迴路之陶瓷通道。The power system of claim 7, wherein the inductive electromagnetic pump comprises a ceramic passage that forms the short circuit of molten metal. 如請求項1之電力系統,其進一步包含用以由相對應的固體金屬形成該熔融金屬之一電感耦合加熱器。The power system of claim 1, further comprising an inductively coupled heater for forming the molten metal from the corresponding solid metal. 如請求項1之電力系統,其中該熔融金屬包含銀、銀銅合金及銅中之至少一者。The power system of claim 1, wherein the molten metal comprises at least one of silver, silver copper alloy, and copper. 如請求項1之電力系統,其進一步包含一真空泵及至少一個急冷器。The power system of claim 1, further comprising a vacuum pump and at least one chiller. 如請求項1之電力系統,其中反應功率輸出之該至少一個功率轉換器或輸出系統包含諸如以下各者之群組中之至少一者:一熱光伏打轉換器、一光伏打轉換器、一光電轉換器、一磁流體動力轉換器、一電漿動力轉換器、一熱離子轉換器、一熱電轉換器、一斯特林引擎、一布累登循環引擎、一朗肯循環引擎及一熱機、一加熱器及一鍋爐。The power system of claim 1, wherein the at least one power converter or output system of the reactive power output comprises at least one of the group consisting of: a thermal photovoltaic converter, a photovoltaic converter, and a a photoelectric converter, a magnetic fluid power converter, a plasma power converter, a thermionic converter, a thermoelectric converter, a Stirling engine, a Braden cycle engine, a Rankine cycle engine, and a heat engine, A heater and a boiler. 如請求項16之電力系統,其中該鍋爐包含一輻射鍋爐。The power system of claim 16, wherein the boiler comprises a radiant boiler. 如請求項16之電力系統,其中該容器之一部分包含一黑體輻射器,其經保持在1000 K至3700 K之範圍內之一溫度下。The power system of claim 16, wherein one of the containers comprises a black body radiator that is maintained at a temperature in the range of 1000 K to 3700 K. 如請求項18之電力系統,其中該等儲集器包含氮化硼,該容器之包含該黑體輻射器之該部分包含碳,且與該熔融金屬接觸之該等電磁泵部件包含一抗氧化金屬或陶瓷。The power system of claim 18, wherein the reservoir comprises boron nitride, the portion of the container comprising the blackbody radiator comprises carbon, and the electromagnetic pump components in contact with the molten metal comprise an antioxidant metal Or ceramic. 如請求項19之電力系統,其中該等反應物包含甲烷、一氧化碳、二氧化碳、氫、氧及水中之至少一者。The power system of claim 19, wherein the reactants comprise at least one of methane, carbon monoxide, carbon dioxide, hydrogen, oxygen, and water. 如請求項20之電力系統,其中反應物供應器將該甲烷、一氧化碳、二氧化碳、氫、氧及水中之每一者保持在0.01 Torr至1 Torr之範圍內的一壓力下。The power system of claim 20, wherein the reactant supply maintains each of methane, carbon monoxide, carbon dioxide, hydrogen, oxygen, and water at a pressure in the range of 0.01 Torr to 1 Torr. 如請求項21之電力系統,其包含一熱光伏打轉換器或一光伏打轉換器,其中由該黑體輻射器發射之光主要為黑體輻射,其包含可見光及近紅外光,且該等光伏打電池為聚光電池,其包含至少一種選自以下之化合物:結晶矽、鍺、砷化鎵(GaAs)、銻化鎵(GaSb)、砷化銦鎵(InGaAs)、銻化砷鎵銦(InGaAsSb)、銻化砷磷銦(InPAsSb)、InGaP/InGaAs/Ge、InAlGaP/AlGaAs/GaInNAsSb/Ge、GaInP/GaAsP/SiGe、GaInP/GaAsP/Si、GaInP/GaAsP/Ge、GaInP/GaAsP/Si/SiGe、GaInP/GaAs/InGaAs、GaInP/GaAs/GaInNAs、GaInP/GaAs/InGaAs/InGaAs、GaInP/Ga(In)As/InGaAs、GaInP-GaAs-晶圓-InGaAs、GaInP-Ga(In)As-Ge及GaInP-GaInAs-Ge。The power system of claim 21, comprising a thermal photovoltaic converter or a photovoltaic converter, wherein the light emitted by the blackbody radiator is mainly black body radiation, which includes visible light and near-infrared light, and the photovoltaic The battery is a concentrating battery comprising at least one compound selected from the group consisting of crystalline germanium, germanium, gallium arsenide (GaAs), gallium antimonide (GaSb), indium gallium arsenide (InGaAs), and indium gallium arsenide (InGaAsSb). Indium arsenate indium (InPAsSb), InGaP/InGaAs/Ge, InAlGaP/AlGaAs/GaInNAsSb/Ge, GaInP/GaAsP/SiGe, GaInP/GaAsP/Si, GaInP/GaAsP/Ge, GaInP/GaAsP/Si/SiGe, GaInP/GaAs/InGaAs, GaInP/GaAs/GaInNAs, GaInP/GaAs/InGaAs/InGaAs, GaInP/Ga(In)As/InGaAs, GaInP-GaAs-Wafer-InGaAs, GaInP-Ga(In)As-Ge, and GaInP -GaInAs-Ge. 如請求項21之電力系統,其包含一熱光伏打轉換器或一光伏打轉換器,其中由反應電漿發射之光主要為紫外光,且該等光伏打電池為聚光電池,其包含至少一種選自以下之化合物:一III族氮化物、GaN、AlN、GaAlN及InGaN。The power system of claim 21, comprising a thermal photovoltaic converter or a photovoltaic converter, wherein the light emitted by the reactive plasma is mainly ultraviolet light, and the photovoltaic cells are concentrating batteries, which comprise at least one A compound selected from the group consisting of a Group III nitride, GaN, AlN, GaAlN, and InGaN. 如請求項16之電力系統,其中該磁流體動力功率轉換器包含連接至反應容器之一噴嘴、一磁流體動力通道、電極、磁體、一金屬採集系統、一金屬再循環系統、一熱交換器及視情況選用之一氣體再循環系統。The power system of claim 16, wherein the magnetic fluid power converter comprises a nozzle connected to the reaction vessel, a magnetic fluid power channel, an electrode, a magnet, a metal collection system, a metal recirculation system, a heat exchanger And one of the gas recycling systems is selected as appropriate. 如請求項24之電力系統,其中該等反應物包含H2 O蒸氣、氧氣及氫氣中之至少一者。The power system of claim 24, wherein the reactants comprise at least one of H 2 O vapor, oxygen, and hydrogen. 如請求項25之電力系統,其中反應物供應器將該O2 、該H2 及一反應產物H2 O中之每一者保持在0.01 Torr至1 Torr之範圍內的一壓力下。The power system of claim 25, wherein the reactant supply maintains each of O 2 , the H 2 and a reaction product H 2 O at a pressure in the range of 0.01 Torr to 1 Torr. 如請求項26之電力系統,其中用以補充在該等反應物之一反應以產生該電能及熱能中之至少一者的過程中消耗之該等反應物的該反應物供應系統包含: a.O2 及H2 氣體供應中之至少一者; b.一氣體殼體; c.一選擇性透氣膜,其在以下中之至少一者的壁中:該反應容器、該磁流體動力通道、該金屬採集系統及該金屬再循環系統; d. O2 、H2 及H2 O分壓感測器; e.流量控制器; f.至少一個閥門,及 g.一電腦,其用以保持O2 及H2 壓力中之至少一者。The power system of claim 26, wherein the reactant supply system for replenishing the reactants in the process of reacting at least one of the reactants to produce the electrical energy and thermal energy comprises: aO 2 And at least one of a supply of H 2 gas; b. a gas shell; c. a selectively permeable membrane in the wall of at least one of: the reaction vessel, the magnetohydrodynamic channel, the metal Acquisition system and the metal recirculation system; d. O 2 , H 2 and H 2 O partial pressure sensors; e. flow controller; f. at least one valve, and g. a computer for maintaining O 2 And at least one of the H 2 pressures. 如請求項1或27之電力系統,其中該電力系統之至少一個組件包含陶瓷。A power system as claimed in claim 1 or 27, wherein at least one component of the power system comprises ceramic. 如請求項28之電力系統,其中該陶瓷包含以下中之至少一者:一金屬氧化物、氧化鋁、氧化鋯、氧化鎂、氧化鉿、碳化矽、碳化鋯、二硼化鋯及氮化矽。The power system of claim 28, wherein the ceramic comprises at least one of: a metal oxide, aluminum oxide, zirconium oxide, magnesium oxide, cerium oxide, lanthanum carbide, zirconium carbide, zirconium diboride, and tantalum nitride. . 如請求項24之電力系統,其中該熔融金屬包含銀且該磁流體動力轉換器進一步包含一氧源以形成供應至該等儲集器、反應容器、磁流體動力噴嘴及磁流體動力通道中之至少一者的銀粒子之一氣溶膠。The power system of claim 24, wherein the molten metal comprises silver and the magnetic fluid power converter further comprises an oxygen source to form a supply to the reservoir, the reaction vessel, the magnetohydrodynamic nozzle, and the magnetohydrodynamic channel An aerosol of at least one of the silver particles. 如請求項30之電力系統,其中該反應物供應系統另外供應並控制該氧源以形成該銀氣溶膠。The power system of claim 30, wherein the reactant supply system additionally supplies and controls the oxygen source to form the silver aerosol. 如請求項12之電力系統,其中該感應型電磁泵包含一雙級泵,其包含一第一級,該第一級包含該金屬再循環系統之一泵,及一第二級,該第二級包含該金屬噴射系統之泵,其用以噴射將與該容器內部之另一熔融金屬流相交之該熔融金屬流。The power system of claim 12, wherein the inductive electromagnetic pump comprises a two-stage pump comprising a first stage, the first stage comprising a pump of the metal recirculation system, and a second stage, the second The stage comprises a pump of the metal injection system for injecting the molten metal stream that will intersect another molten metal stream inside the vessel. 如請求項32之電力系統,其中包含一電源之點火系統包括一感應點火系統。The power system of claim 32, wherein the ignition system including a power source includes an induction ignition system. 如請求項之33電力系統,其中感應點火系統包含穿過熔融金屬之一短路迴路之一交變磁場來源,其在該金屬中產生包含該點火電流之一交流電。The power system of claim 33, wherein the inductive ignition system comprises an alternating magnetic field source through one of the short circuits of the molten metal, wherein an alternating current comprising the ignition current is generated in the metal. 如請求項34之電力系統,其中該交變磁場來源可包含一初級變壓器繞組,其包含一變壓器電磁體及一變壓器磁軛,且該熔融金屬至少部分地充當諸如一單匝短路繞組之一次級變壓器繞組,其圍封該初級變壓器繞組且包含一感應電流迴路。The power system of claim 34, wherein the alternating magnetic field source comprises a primary transformer winding comprising a transformer electromagnet and a transformer yoke, and the molten metal at least partially acts as a secondary such as a single turn shorted winding A transformer winding enclosing the primary transformer winding and including an inductive current loop. 如請求項35之電力系統,其中該等儲集器包含一熔融金屬交接通道,其連接該兩個儲集器以使得該電流迴路圍封該變壓器磁軛,其中該感應電流迴路包含在該等儲集器、該交接通道中所含之熔融金屬、噴射管中之銀及相交以接通該感應電流迴路之該等經噴射熔融金屬流中產生的電流。The power system of claim 35, wherein the reservoirs comprise a molten metal interface that connects the two reservoirs such that the current loop encloses the transformer yoke, wherein the induced current loop is included The reservoir, the molten metal contained in the transfer passage, the silver in the injection tube, and the currents generated in the flow of the injected molten metal that intersect the induction current loop.
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