TW200947725A - Improved HIT solar cell structure - Google Patents
Improved HIT solar cell structure Download PDFInfo
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- TW200947725A TW200947725A TW98102895A TW98102895A TW200947725A TW 200947725 A TW200947725 A TW 200947725A TW 98102895 A TW98102895 A TW 98102895A TW 98102895 A TW98102895 A TW 98102895A TW 200947725 A TW200947725 A TW 200947725A
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- 239000000758 substrate Substances 0.000 claims description 24
- 229910052732 germanium Inorganic materials 0.000 claims description 20
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 17
- 239000004065 semiconductor Substances 0.000 claims description 17
- 230000005641 tunneling Effects 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- 239000004020 conductor Substances 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 claims 2
- 229910003437 indium oxide Inorganic materials 0.000 claims 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 210000004027 cell Anatomy 0.000 abstract description 26
- 229910021417 amorphous silicon Inorganic materials 0.000 abstract description 9
- 230000000873 masking effect Effects 0.000 abstract description 4
- 229910021420 polycrystalline silicon Inorganic materials 0.000 abstract description 4
- 229920005591 polysilicon Polymers 0.000 abstract description 4
- 230000008021 deposition Effects 0.000 abstract description 3
- 238000003780 insertion Methods 0.000 abstract description 2
- 230000037431 insertion Effects 0.000 abstract description 2
- 210000004692 intercellular junction Anatomy 0.000 abstract description 2
- 238000000059 patterning Methods 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 58
- 238000000576 coating method Methods 0.000 description 5
- 229910052715 tantalum Inorganic materials 0.000 description 5
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 238000005121 nitriding Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910004613 CdTe Inorganic materials 0.000 description 1
- 229910052691 Erbium Inorganic materials 0.000 description 1
- 229920006771 PE-C Polymers 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical group CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- KRWFMQBZMQBPNH-UHFFFAOYSA-N oxotin yttrium Chemical compound [Sn]=O.[Y] KRWFMQBZMQBPNH-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/072—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type
- H01L31/0745—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type comprising a AIVBIV heterojunction, e.g. Si/Ge, SiGe/Si or Si/SiC solar cells
- H01L31/0747—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type comprising a AIVBIV heterojunction, e.g. Si/Ge, SiGe/Si or Si/SiC solar cells comprising a heterojunction of crystalline and amorphous materials, e.g. heterojunction with intrinsic thin layer
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- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/072—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type
- H01L31/0745—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type comprising a AIVBIV heterojunction, e.g. Si/Ge, SiGe/Si or Si/SiC solar cells
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- H—ELECTRICITY
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022466—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers
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Abstract
Description
200947725 六、發明說明: 【發明所屬之技術領域】 本發明與光伏裝置有關,且特別是與用於提供式 或多晶碎射極太陽能電池之改良結構的方法與設備有 關。 【先前技術】 HIT式太陽能電池是結構相對簡單的高效率裝置。曰 本三洋公司已經提出其實驗室效率為215〇/〇,且製造效 率為中等19。/。範圍内。有許多其他團隊也已研究此裝 置,然仍未見其有高效率。 第1A與1B圖中繪示了典型的HIT太陽能電池結構。 該裝置是對稱的,其η型基板106前部與背部都塗佈有 各別的塗層102、110以及各別的金屬格線1〇4、1〇8。 ❹ 如第1Β圖中分解圖部分所示,前部上的塗層1〇2是由兩 層非晶質矽層所組成(一 ρ型層124與其下方之本質層 126) ’其皆約50Α厚。在背部上,非晶質矽層是由一 η 型層與其下方之一本質層(i)所組成。如第1Β圖所示, - 塗層102還包括一層透明傳導氧化物(transparent conductive oxide, TCO) 122。 薄α-Si層用於保護表面並提供與一寬能帶隙窗層之異 質接面以增進開啟電路電壓,如第1C圖所示。更特別 地’第ic圖說明了這種裝置的能帶結構。如第ic圖所 200947725 示’在前表面處具有大位能階,產生了一種與p型和” 型摻質間階部處之接面十分相似的接面'然而,因為此 -接面是由沉積-非晶質_層所形成,因此其非常不連 貫且近乎空想。 儘管具有其優勢,這些非晶質矽層在HIT電池之製造 中也會產生可觀的複雜度。舉例而言,這些層必須形成 於一個悉心製備的表面上,其製備細節並未公開說明。 〇 &外’ ^必須不結晶化,然這將發生在結晶石夕基板對非 晶質矽進行種晶時,而這會消除有利之保護與異質接面 效應。 因此,需要一種可受良好控制與理解、並易於製造的 改良界面’且不會種晶成長。 【發明内容】 本發明係關於改良式HIT型或多晶矽射極太陽能電 © 池。根據特定態樣’本發明包括在電池的前部與背部上 形成一掩蔽氧化物層,並接著在該掩蔽氧化物中囷案化 孔洞,然後在該經圖案化氧化物上形成一 Hit電池結構 或多晶矽射極太陽能電池結構,僅於孔洞已被切割的區 域中產生電池接面。本發明的優勢包括其藉由薄穿随氧 化物的插置而提供了一種HIT電池之受控制界面。此 外’穿隧氧化物避免非晶矽的磊晶成長,使其保持非晶 質以供最佳能帶結構之用。更甚者,其提供了一層以於 5 200947725 非晶質矽層(α-Si)沉積期間保護該表面不受電漿破壞。 此外,也可結合點狀接觸結構的使用來進—步提昇效率。 進一步就這些與其他態樣而言,根據本發明實施例之 - 太陽能電池包括了一非晶質半導體層,其形成於一基板 上;以及一介電層’其插置在該基板與該非晶質半導體 層之間’其中該介電層係足夠薄以支撐通過其間之一穿 隧電流。 Ο 更進一步就這些與其他態樣而言,根據本發明實施例 之用於製造一太陽能電池的方法包括於一基板上形成一 介電層,其中該介電層係足夠薄以支撐通過其間之一穿 隧電流;以及於該介電層上形成一非晶質半導體層。 【實施方式】 以下將參照圖式詳細說明本發明,其係用以描述本發 〇 明之示例,以使該領域技術人士能夠實施本發明。可理 解的是,以下圖式與示例並不表示其將本發明之範脅限 制於單一實施例,而是藉由替換部分或所有的描述元件 亦使其他實施例變為可行。此外,本發明之特定元件可 部分或完全以習知組件予以實施,在此僅描述這些習知 組件中需用於瞭解本發明的部分,至於這些習知組件的 詳細描述與其他部分則予以省略,以避免混淆本發明。 在說明書中’說明單一組件之實施例不應被認為是限 6 200947725 制’相反的’本發明意欲涵蓋包括複數個相同組件的其 他實施例(且反之亦然)’除非另行指明。同時,申請人 於說明書或申請專利範圍中所使用之任何用語並不具非 常見或特疋含意’除非另行指明。此外,本發明涵蓋了 與用於說明之習知組件相當的現有及未來可見的等效方 式。 一般而言,本發明認同可於太陽能電池中使用薄穿隧 ❹ 氧化物層;舉例而言,可以利用穿隧氧化物上之鋁來製 造某些MIS電池。本發明也認同可於重摻雜或多晶矽絕 緣層與結晶矽基板之間使用穿隧氧化物,而形成一種多 晶矽射極太陽能電池。這種太陽能電池具有與ΗΙΤ電池 (其本質上係以多晶矽取代TC〇與a_Si層)相似的能帶 結構。然而,因a_Si的能帶隙較高,這種電池並不提供 異質接面與其高電池電壓之優勢。 根據本發明實施例之一示例太陽能電池結構與其相關 © 能帶結構係分別繪示於第2A與2B圖中。 如第2A圖所示,其係與第1圓所示者相似之HIT型 太陽能電池前表面的一部分’一薄介電& 228 (例如穿 隨氧化物)係提供於HIT電池中的心層224 226和η 里基板206之間。介電層較佳為薄至8_ΐ5Α之等級,以 支撐基板與a-Si層之間的穿隧電流。如以下將更詳細說 月者,可使料統方法(例如快速熱氧化、爐管氧化或 mox處理(於臭氧化H2〇2浴中形成))來形成層 在某二清況中,該層可經氮化或利用其他材料(如氮化 7 200947725 石夕或氮氧化石夕)來加以形成。 如第2B圖所示,在界面處之附加介電層提供了一個 、導體能帶隙更大的能帶隙,載子無法跨越此能量阻 障’但當該層足夠薄時(<15A),載子將穿隧於其間。 :意氧化物與氮化物具有*肖的阻障高度,因此所示之 該層並不特定代表任何-種材料。氮化物的阻障高度約 且呈對稱,氧化物的阻障高度則非對稱(對電子而 ^ 言較低)〇 〇 介電層228提供之優勢有數種面向。舉例而言,其係 利用傳統表面清潔與製備方式而形成,用於產生積體 電路之MOS閘極者;因此’這種表面製備方式已廣為所 知及理解,並可以高量產製造方式慣f地施行。同時, 由於其係一非晶質層,其使後續的α-Si層與基板分隔開 來,因而避免α-Si層中晶體成長之磊晶種晶。此外,其 提供一干預層以於α-Si層沉積期間保護結晶矽表面不受 ❿ 電漿破壞。 應注意’雖然本發明之優勢係藉由形成於結晶矽基板 上之《-Si層而獲得,但其並非限制,且本發明也可應用 至其他類型基板與薄半導體層。進一步應知許多太陽能 電池都使用異質接面,因此,舉例而言,本發明也可與 在微晶矽上具有非晶矽之薄臈太陽能電池一起使用。本 發明也可用於CdTe、CIGS或A1/GaAs/GaAs電池,其皆 使用異質接面。 亦即,進一步應注意,已知在矽上方之非晶矽可提供 8 200947725 絕佳的保護特性,其幾乎消除了表面再結合。這是因為 在表面處的高能帶彎曲排斥載子之故。因此,這是使用 矽上非晶矽的一項優點。 Ο200947725 VI. INSTRUCTIONS OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to photovoltaic devices, and more particularly to methods and apparatus for providing improved structures for providing or employing polycrystalline solar cells. [Prior Art] The HIT type solar cell is a highly efficient device having a relatively simple structure.曰 Ben Sanyo has proposed a laboratory efficiency of 215 〇 / 〇, and a manufacturing efficiency of medium 19 . /. Within the scope. There are many other teams that have also studied this device, but still have not seen it to be efficient. A typical HIT solar cell structure is illustrated in Figures 1A and 1B. The apparatus is symmetrical, and the front and back of the n-type substrate 106 are coated with respective coatings 102, 110 and respective metal grid lines 1〇4, 1〇8. ❹ As shown in the exploded view in Figure 1, the coating 1〇2 on the front is composed of two layers of amorphous germanium (a p-type layer 124 and the underlying layer 126). thick. On the back, the amorphous tantalum layer consists of an n-type layer and one of the underlying layers (i) below it. As shown in Figure 1, the coating 102 also includes a layer of transparent conductive oxide (TCO) 122. A thin alpha-Si layer is used to protect the surface and provide a heterojunction to a wide bandgap window layer to enhance the turn-on circuit voltage, as shown in Figure 1C. More specifically, the ic diagram illustrates the energy band structure of such a device. As shown in Figure ic, 200947725, 'has a large energy level at the front surface, resulting in a junction that is very similar to the junction between the p-type and the type of dopant. However, because this junction is It is formed by a deposited-amorphous layer, so it is very incoherent and almost imaginary. Despite its advantages, these amorphous germanium layers can also produce considerable complexity in the manufacture of HIT cells. For example, these The layer must be formed on a carefully prepared surface, the details of which are not disclosed. 〇 & external ' ^ must not be crystallized, but this will occur when the crystalline enamel substrate is seeded with amorphous germanium, and This eliminates the advantageous protection and heterojunction effects. Therefore, there is a need for an improved interface that can be well controlled and understood, and that is easy to manufacture, and that does not grow crystallize. [Invention] The present invention relates to an improved HIT type or polysilicon. Emitter solar power © cell. According to a particular aspect, the invention includes forming a masking oxide layer on the front and back of the cell, and then patterning the hole in the masking oxide, and then Forming a Hit cell structure or a polysilicon emitter solar cell structure on the cased oxide, creating a cell junction only in the region where the hole has been cut. Advantages of the invention include that it is provided by thin insertion of oxides A controlled interface of the HIT battery. In addition, the tunneling oxide prevents the epitaxial growth of the amorphous germanium, keeping it amorphous for the best energy band structure. Moreover, it provides a layer for 5 200947725 Amorphous tantalum layer (α-Si) protects the surface from plasma damage during deposition. In addition, the use of point contact structures can be combined to further improve efficiency. Further, in these and other aspects, According to an embodiment of the present invention, a solar cell includes an amorphous semiconductor layer formed on a substrate, and a dielectric layer 'interposed between the substrate and the amorphous semiconductor layer> wherein the dielectric The layer is sufficiently thin to support tunneling current through one of the layers. Further, in these and other aspects, a method for fabricating a solar cell according to an embodiment of the present invention includes a substrate Forming a dielectric layer on the plate, wherein the dielectric layer is sufficiently thin to support a tunneling current through one of the dielectric layers; and forming an amorphous semiconductor layer on the dielectric layer. [Embodiment] Reference will be made to the following drawings. The present invention is described in detail to illustrate the embodiments of the invention, and the embodiments of the invention are The embodiments, but by the replacement of some or all of the description elements, also make other embodiments possible. Furthermore, the specific elements of the invention may be implemented partially or completely with conventional components, only those of which are described herein. The detailed description and other parts of the conventional components are omitted to avoid obscuring the present invention. In the specification, the description of a single component embodiment should not be considered as a limitation. Conversely, the invention is intended to cover other embodiments (including vice versa) including a plurality of identical components, unless otherwise indicated. In the meantime, any terms used by the applicant in the specification or the scope of the patent application are not uncommon or special meanings unless otherwise indicated. Furthermore, the present invention encompasses both existing and future equivalents equivalent to the conventional components described. In general, the present invention recognizes that a thin tunneling oxide layer can be used in solar cells; for example, some of the MIS cells can be fabricated by tunneling the aluminum on the oxide. The present invention also recognizes that a tunneling oxide can be used between a heavily doped or polycrystalline tantalum insulating layer and a crystalline germanium substrate to form a polycrystalline germanium emitter solar cell. This solar cell has an energy band structure similar to that of a tantalum battery which is essentially a polycrystalline germanium substituted for the TC〇 and a_Si layers. However, due to the high band gap of a_Si, this battery does not provide the advantage of a heterojunction and its high battery voltage. An example solar cell structure and its associated © energy band structure are shown in Figures 2A and 2B, respectively, in accordance with an embodiment of the present invention. As shown in Fig. 2A, a portion of the front surface of a HIT-type solar cell similar to that shown in the first circle, 'a thin dielectric & 228 (e.g., an oxide with an oxide) is provided in the core layer of the HIT cell. Between the 224 226 and the η substrate 206. The dielectric layer is preferably as thin as 8 ΐ 5 , to support the tunneling current between the substrate and the a-Si layer. As will be described in more detail below, the method can be used to form a layer in a certain two conditions, such as rapid thermal oxidation, furnace tube oxidation or mox treatment (formed in ozonated H2〇2 bath). It can be formed by nitriding or by using other materials such as nitriding 7 200947725 or nitrous oxide. As shown in Figure 2B, the additional dielectric layer at the interface provides a band gap with a larger band gap of the conductor, and the carrier cannot cross the energy barrier 'but when the layer is thin enough (<15A) ), the carrier will tunnel through it. The oxides and nitrides have a barrier height of *Sha, so the layer shown is not specifically representative of any material. The barrier height of the nitride is approximately symmetrical, and the barrier height of the oxide is asymmetrical (lower for electrons). 介 The advantages provided by the dielectric layer 228 are several. For example, it is formed by a conventional surface cleaning and preparation method for generating a MOS gate of an integrated circuit; therefore, this surface preparation method is widely known and understood, and can be manufactured in a high-volume manner. Habitually implemented. At the same time, since it is an amorphous layer, it separates the subsequent α-Si layer from the substrate, thereby avoiding epitaxial seed crystal growth in the α-Si layer. In addition, it provides an intervening layer to protect the surface of the crystalline crucible from ruthenium plasma during the deposition of the alpha-Si layer. It should be noted that although the advantages of the present invention are obtained by the "-Si layer formed on the crystalline germanium substrate, it is not limited, and the present invention is also applicable to other types of substrates and thin semiconductor layers. It is further understood that many solar cells use heterojunctions, so that, for example, the invention can also be used with thin tantalum solar cells having amorphous germanium on the microcrystalline germanium. The invention is also applicable to CdTe, CIGS or A1/GaAs/GaAs batteries, all using a heterojunction. That is, it should be further noted that the amorphous germanium above the crucible is known to provide excellent protection properties of 8 200947725, which virtually eliminates surface recombination. This is because the high energy band at the surface bends to repel the carrier. Therefore, this is an advantage of using an amorphous germanium on the crucible. Ο
第3圖係用於形成第2Α圖之結構的一示例流程圖。 首先,在步驟S302中’粗化(texture)n型基板的前表面。 其可利用傳統蝕刻而行,例如異丙基醇與KOH。接著在 步驟S304中,對該表面施以標準m〇S潔淨以移除天然 氧化物、離子污染物與有機物。 在一實施例中’接著於步驟S306中使用快速熱氧化處 理以於前表面上形成一薄穿隧氧化物,其一般為12人 厚。在本發明之另一實施例中,係同時於前部與背部形 成氧化物》接著,在前表面上沉積a_Si層。在一實施例 中’ a-Si層係形成為前表面上的兩層堆疊,其中一層為 在步驟S308中首先形成之20-50A厚的本質a-Si層,其 係藉由例如電漿增強化學氣相沉積(PE-C VD )且通常在 氣的存在下形成,電漿增強化學氣相沉積乃矽烷在電襞 中分解。這些程序都可從文獻中充分獲知。可添加硼以 提供P型摻雜,且可添加磷以提供n型摻雜。其次,在 步驟S312中,藉由例如相同的pE_CVD程序,於本質a_si 層的頂部形成20-50A厚之p型α-Si。在另一實施例中, 僅在步驟S3 10中,於前表面上形成一摻雜p型層,而不 形成1型層。在步驟S304中沉積TCO,其可為氧化錮錫 成的四力波厚層(quarter wave thick layer)。 接著將晶圓反轉’如步驟S316所示,並以相同方式、 9 200947725 以η型a-Si層取代p型a_Si層而在背側上沉積結構。如 圖所示,根據氧化物層是否已經形成,程序係返回步驟 S306或步驟S308。應可進一步理解,當氧化物層已經形 成時’該程序也可返回步驟S31〇。最後,在步驟S3l8 中’藉由例如網印或濺鍍程序而形成接點。 除上述程序以外’也可實施在共同申請案(N0.) _ II» ^ 中所說明之一種形成HIT或多晶矽射極太陽能電池之點 狀接觸的方法’其藉由引用形式而併入本文。 雖然本發明係參照其較佳實施例而加以描述,然該領 域技術人士應可顯然得知可在不背離本發明之精神與範 鳴下改變與修飾其形式和細節。如附申請專利範圍意欲 涵蓋這些變化與修飾。 【圖式簡單說明】 本領域技術人士在結合伴隨圖式而參閱本發明特定實 施例說明後,將可清楚瞭解本發明之上述與其他態樣和 特徵_,其中: 第1A至1C圖繪示了 一傳統HIT電池與其能帶結構; 第2A與2B圖分別繪示了本發明之一示例太陽能電池 結構與其能帶結構;以及 第3圖係根據本發明態樣用於形成第2圖結構之一示 例流程圖。 【主要元件符號說明】 200947725 102塗層 104金屬格線 106 η型基板 108金屬格線 11 0塗層 122透明傳導氧化物(TCO) 124 ρ型層 126本質層 224 α-Si 層 226 a-Si 層 228介電層 S302-S318 步驟 206 η型基板 ❹ ❿ 11Figure 3 is an exemplary flow chart for forming the structure of the second figure. First, the front surface of the n-type substrate is 'textured' in step S302. It can be done using conventional etching, such as isopropyl alcohol and KOH. Next, in step S304, the surface is subjected to standard m〇S clean to remove natural oxides, ionic contaminants and organic matter. In an embodiment, a rapid thermal oxidation treatment is then employed in step S306 to form a thin tunneling oxide on the front surface, which is typically 12 people thick. In another embodiment of the invention, the oxide is formed simultaneously on the front and back. Next, an a-Si layer is deposited on the front surface. In one embodiment, the 'a-Si layer is formed as a two-layer stack on the front surface, one of which is a 20-50 A thick intrinsic a-Si layer first formed in step S308, which is enhanced by, for example, plasma Chemical vapor deposition (PE-C VD ) is usually formed in the presence of gas, and plasma enhanced chemical vapor deposition is the decomposition of decane in electricity. These procedures are fully known from the literature. Boron may be added to provide P-type doping, and phosphorus may be added to provide n-type doping. Next, in step S312, 20-50 A thick p-type ?-Si is formed on top of the essential a_si layer by, for example, the same pE_CVD procedure. In another embodiment, only in step S310, a doped p-type layer is formed on the front surface without forming a type 1 layer. A TCO is deposited in step S304, which may be a quarter wave thick layer of yttrium tin oxide. The wafer is then inverted' as shown in step S316, and in the same manner, 9 200947725 replaces the p-type a-Si layer with an n-type a-Si layer to deposit a structure on the back side. As shown in the figure, depending on whether or not the oxide layer has been formed, the program returns to step S306 or step S308. It should be further understood that the process may also return to step S31 when the oxide layer has been formed. Finally, a contact is formed in step S3108 by, for example, a screen printing or sputtering process. In addition to the above-described procedures, a method of forming a point contact for forming a HIT or a polycrystalline erbium emitter solar cell as described in the co-pending application (N0.) _ II» ^ may also be incorporated herein by reference. Although the present invention has been described with reference to the preferred embodiments thereof, it will be apparent to those skilled in the art that the form and details may be modified and modified without departing from the spirit and scope of the invention. The scope of the patent application is intended to cover such variations and modifications. BRIEF DESCRIPTION OF THE DRAWINGS The above and other aspects and features of the present invention will become apparent to those skilled in the <RTIgt; A conventional HIT battery and its energy band structure; FIGS. 2A and 2B respectively illustrate an exemplary solar cell structure and its energy band structure of the present invention; and FIG. 3 is used to form the structure of FIG. 2 according to the aspect of the present invention. An example flow chart. [Main component symbol description] 200947725 102 coating 104 metal grid 106 n-type substrate 108 metal grid 11 0 coating 122 transparent conductive oxide (TCO) 124 p-type layer 126 essential layer 224 α-Si layer 226 a-Si Layer 228 Dielectric Layer S302-S318 Step 206 η-type Substrate ❹ ❿ 11
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