TW200923976A - Metal substrate for a superconducting thin-film strip conductor - Google Patents
Metal substrate for a superconducting thin-film strip conductor Download PDFInfo
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- TW200923976A TW200923976A TW097117605A TW97117605A TW200923976A TW 200923976 A TW200923976 A TW 200923976A TW 097117605 A TW097117605 A TW 097117605A TW 97117605 A TW97117605 A TW 97117605A TW 200923976 A TW200923976 A TW 200923976A
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- metal substrate
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- 239000000758 substrate Substances 0.000 title claims abstract description 70
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 50
- 239000002184 metal Substances 0.000 title claims abstract description 50
- 239000004020 conductor Substances 0.000 title claims abstract description 12
- 239000010409 thin film Substances 0.000 title abstract 2
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 11
- 230000003746 surface roughness Effects 0.000 claims abstract description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- 229910052759 nickel Inorganic materials 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 239000007858 starting material Substances 0.000 claims description 3
- 150000004770 chalcogenides Chemical class 0.000 claims description 2
- 239000010410 layer Substances 0.000 claims 13
- 239000011247 coating layer Substances 0.000 claims 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims 1
- 239000004519 grease Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 20
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 10
- 229910052717 sulfur Inorganic materials 0.000 description 10
- 239000011593 sulfur Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- 238000000137 annealing Methods 0.000 description 6
- 229910002113 barium titanate Inorganic materials 0.000 description 5
- 229960000583 acetic acid Drugs 0.000 description 4
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- UONKPUCNKMOKDK-UHFFFAOYSA-N 1-decoxyethanol Chemical compound CCCCCCCCCCOC(C)O UONKPUCNKMOKDK-UHFFFAOYSA-N 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- KKMOSYLWYLMHAL-UHFFFAOYSA-N 2-bromo-6-nitroaniline Chemical compound NC1=C(Br)C=CC=C1[N+]([O-])=O KKMOSYLWYLMHAL-UHFFFAOYSA-N 0.000 description 2
- MJXUFBUYCLOLBZ-UHFFFAOYSA-N C(C)(=N)N.CC(=O)C Chemical compound C(C)(=N)N.CC(=O)C MJXUFBUYCLOLBZ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical group [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001786 chalcogen compounds Chemical class 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- FFQALBCXGPYQGT-UHFFFAOYSA-N 2,4-difluoro-5-(trifluoromethyl)aniline Chemical compound NC1=CC(C(F)(F)F)=C(F)C=C1F FFQALBCXGPYQGT-UHFFFAOYSA-N 0.000 description 1
- NCOYDQIWSSMOEW-UHFFFAOYSA-K 2-hydroxypropane-1,2,3-tricarboxylate;lanthanum(3+) Chemical compound [La+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NCOYDQIWSSMOEW-UHFFFAOYSA-K 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- YFHNDHXQDJQEEE-UHFFFAOYSA-N acetic acid;hydrazine Chemical compound NN.CC(O)=O YFHNDHXQDJQEEE-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- AOWKSNWVBZGMTJ-UHFFFAOYSA-N calcium titanate Chemical compound [Ca+2].[O-][Ti]([O-])=O AOWKSNWVBZGMTJ-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- VGBWDOLBWVJTRZ-UHFFFAOYSA-K cerium(3+);triacetate Chemical compound [Ce+3].CC([O-])=O.CC([O-])=O.CC([O-])=O VGBWDOLBWVJTRZ-UHFFFAOYSA-K 0.000 description 1
- 238000000224 chemical solution deposition Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- NFSAPTWLWWYADB-UHFFFAOYSA-N n,n-dimethyl-1-phenylethane-1,2-diamine Chemical compound CN(C)C(CN)C1=CC=CC=C1 NFSAPTWLWWYADB-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005289 physical deposition Methods 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical class O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229910021521 yttrium barium copper oxide Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/02—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B12/00—Superconductive or hyperconductive conductors, cables, or transmission lines
- H01B12/02—Superconductive or hyperconductive conductors, cables, or transmission lines characterised by their form
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N60/00—Superconducting devices
- H10N60/01—Manufacture or treatment
- H10N60/0268—Manufacture or treatment of devices comprising copper oxide
- H10N60/0296—Processes for depositing or forming copper oxide superconductor layers
- H10N60/0576—Processes for depositing or forming copper oxide superconductor layers characterised by the substrate
- H10N60/0632—Intermediate layers, e.g. for growth control
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
Description
200923976 九、發明說明: 【發明所屬之技術領域】 本發明係關於高溫超導薄膜條狀導體且具體而言其金屬 基材。 【先前技術】 尚起導溥膜條狀導體,或簡言之經塗敷導體(在下文 中稱為HTSL-CC)係起始於織構化金屬條根據先前技術所 製成。該條(在下文中稱為金屬基材)包含較佳面心立方結 晶金屬(例如,鎳、銅、金)。以鎳尤為適用,具體而言具 有較小原子。/。鶴之鎳,參考德國專利第1〇1 43 68〇 C1號。 將該織構化金屬基材使用緩衝層塗敷,其係用於達到以習 知方式將金屬基材之織構轉移至隨後產生之超導層的目 的。對金屬基材以及欲結晶之高溫超導薄膜二者皆具有低 晶格失配之材料尤其適用於緩衝層。在金屬基材上旋轉 45°生長之材料(例如,鍅酸鑭或其他具有氟化物或焦氣化 物結構之材料)以及彼等未旋轉生長且通常具有鈣鈦礦型 結構(例如’鈦酸锶及鈦酸鈣)或尖晶石型結構(例如,釕酸 魏及錄酸鈥)之材料二者皆可使用。 自 Effect of sulfur on cube texture formation in micro-alloyed nickel substrate tapes” (J. Eickemeyer 等人), Physica C 418 (2005) 9-15 ' "Growths of oxide seed layers on nickel and other technologically interesting metal substrates: issues related to formation in control of sulfur superstructures for texture optimization”(C_ Cantoni 等人), I3094I.doc 200923976 IEEE—Transactions 〇n Applied 8ιιρ^〇η^αν办第 i3 卷第2期,2〇〇3及其他出版物得知,通常早已自金屬基 材之3染物形成之硫屬化合物上層結構、具體而言硫上層 、、=構可促進緩衝層之磊晶生長,該等緩衝層係使用物理方 法、尤其藉由金屬基材在高真空中之氣相沈積來沈積。因 此,根據先前技術目標係可再現地產生具有高覆蓋度之最 均勻可旎上層結構。然而,緩衝層之物理沈積係一種高成 本方法,因此其並不適用於HTSL_CC或甚至僅其載體基材 之生產。 使用化學塗敷方法(CSD/MOD)生產HTSL-CC亦已習知且 明顯更具成本效益,參考”Chemical soluti〇n deposition of <100>oriented SrTi03 buffer layers on nickel substrates"; J.T. Dawley 等人;J· Mater. Res.,第 17 卷,第 7 期, 2002。在具有硫上層結構之鎳基材(其上已生長锆酸鑭)上 已經獲付良好結果,參考"Detailed investigations on La2Zr207 buffer layers for YBCO coated conductors prepared by chemical solution deposition" (K· Knoth 等人), Acta Materialica 55,2007, 517-529。 然而’使用未旋轉45。(如鍅酸鑭)且更明確地說未旋轉 (例如,鈦酸勰等)生長之材料並不能獲得可比較的結果, 即使如原本所習知使用具有較低表面粗糙度之金屬基材亦 不能獲得可比較的結果。所施加之欽酸魏層係未織構化或 僅略微織構化。 【發明内容】 130941.doc 200923976 本發明係基於提供具有以化學方式所產生高度織構化緩 衝層之HTSL-CC且具體而言作為其起始材料之金屬基材的 目的。 【實施方式】 此係根據本發明藉由ΐ軎Ψ、τ5,+ 楮宙β求項1中所指定之方法達成,其 中施:緩衝層之前,自金屬基材之表面去除上層結構。 特疋而5 ’已令人驚訝地展示,在使用未旋轉生長之材 料(例如彼等具㈣鈦礦型或尖晶石型結構者)之化學處理 之ί月’兄下使用物理方法所產生之緩衝層及使用化學方法 所產生具有氟化物或焦氣化物結構之緩衝層所需的上層結 構、具體而言硫屬化合物上層結構且尤其硫上層結構相反 地會阻止良好織構之實現。 此結果與去除上層結構之類型(機械研磨、電拋光、用 噴砂物體(例如,乾冰顆粒)進行喷砂處理、或使用稍濃的 硝酸選擇性蝕刻)以及化學塗敷技術類型(即,旋塗、浸塗 或印刷(狹縫模具式澆注、喷墨印刷))二者無關,且亦與以 下製程參數(例如退火溫度、氣氛及保留時間)無關。 §在去除上層結構期間將基材研磨至表面粗梭度小於⑺ 奈米時獲得最好的結果。 晶格常數與金屬基材之晶格常數相差小於5%、較佳 小於士 10%之材料有利地用於該緩衝層。 此外本發明係關於具有凊求項8中所給定特徵之雙轴 織構化金屬基材的用途。 該緩衝層可特定包含晶格常數與金屬基材之晶格常數相 130941.doc 200923976 差小於±15%、較佳小於土10%之材料。然而,具體而言, 晶格常數與金屬基材之晶格常數相差在_5%至+1 5%範圍内 之材料皆可考慮。 因此,本發明提供具有請求項1 〇之特徵的高溫超導薄膜 條狀導體。 鎳或包含85原子%、較佳90原子%鎳之鎳合金尤其適宜 用作金屬基材。在此情況下,尤其鈦酸鹽、釕酸鹽、錳酸 鹽、鎳酸鹽及銅酸鹽係適宜用作緩衝層材料,例如,
CaTi〇3、La2Ni04、Sr2RU〇4、NdBa2Cu3〇x、Gd2Cu〇4、 SrTi03、Nd2Cu04、BaTi03、(CaxSrl_x) Ti〇3、及 (SrxBal-x) Ti03。 實例: 使用來自evico之兩種不同鎳(5原子%鎢)金屬基材(條寬 度為1〇毫米,條厚度為80微米)。該兩種金屬基材皆具有 立方織構(00 1),其中半峰全幅值(FWHM)為5.5。。 兩種基材皆經受相同的滾壓成型且隨後在間歇式退火製 程中再結晶。纟間歇式退火製程中藉助緩慢冷卻在兩個基 板上形成硫上層結構。 使用AFM顯微鏡量測該兩種金屬基材之粗糙度,如下: 基材1 : RMS=40奈米 基材2 : RMS = 5奈米。 在具有0.1微米金剛石懸浮 。該基材之粗糙度可藉由 藉由研磨去除所有黏著表面 將基材1之一部分機械研磨。 液之研磨台(Struers)上實施研磨 研磨而降低至RMS = 5奈米。|| 130941.doc 200923976 層,即,同樣去除硫上層結構。由於直至塗敷前仍未實施 退火處理,故亦無法再產生此結構。 基材1(經研磨):RMS = 5奈米 將所有基材在超音波浴中先用丙酮且隨後用異丙醇清洗 各5分鐘。 由此,以下基材係適用於隨後試驗: 基材1 : RMS=40奈米;硫上層結構 基材2 : RMS = 5奈米;硫上層結構 基材3 : RMS = 5奈米;無硫上層結構,即,基材1但經研磨 製備3種塗敷溶液: 溶液1 :純鈦酸锶(STO) 溶液2 :摻雜鈮的STO,導電 溶液3 :摻雜鈣的STO,與鎳基材具有較好的晶格匹配 對於溶液1,將0.15莫耳Ti(OCH2CH2CH2CH3)4以莫耳 比1:2溶於乙醯丙酮中。隨後,將0· 1 5莫耳乙酸锶以莫耳比 1:5溶於冰乙酸中。將兩個溶液合倂並用由冰乙酸及曱氧 基乙醇構成之混合物以使冰乙酸與曱氧基乙醇之總比例為 1:2之方式稀釋至500毫升。隨後將溶液過濾以去除任何可 能沈澱物。ICP-OES分析(SPECTRO Genesis)展示為一化學 計量〇. 3克分子之溶液。 對於溶液2,將0.1425莫耳Ti(OCH2CH2CH2CH3)4以莫 耳比1:2溶於乙醯丙酮中並與0.0075莫耳溶於丁醇中之 Nb(OCH2CH3)5混合。如用於溶液1般實施所有其他步驟, 以便獲得0.3克分子具有5%鈮摻雜之鈦酸锶的塗敷溶液。 130941.doc 200923976 如溶液1般製備溶液3,只是不使用〇.〖5莫耳乙酸鳃,而 是使用由0.135莫耳乙酸勰與0.015莫耳乙酸鈣構成之混合 物獲得〇.3莫耳經釣取代的鈦酸銘之塗敷溶液。 用所有溶液如下塗敷所有經清洗之基材: f V, 先在旋轉塗敷機上以500 rpm使用經稀釋6倍之塗敷溶液 塗敷5 A刀長的經清洗基材。使用由冰乙酸與曱氧基乙醇 構成之2:1混合物進行稀釋。隨後,在ι〇%κΝ2中之^之下 在800 C之溫度下實施溫度處理5分鐘。在第一塗敷步驟中 2於溶液之稀釋而產生所謂的種晶層,即,未黏著層(覆 蓋率)丨於20-80 /〇之間),其島係用作隨後層之晶種。 在相同條件τ實施兩次進—步塗敷及溫度處理,只是利 未稀釋办液。在各種情況下3次塗敷後所得總層厚度為 2 5 0不米。使用輪廓儀在層邊緣上量測層厚度。 針對退火溫度在75〇與_。範圍内改變且退火氣氛在% 15%於Ν2中之Η2範圍内改變進行試驗並未對試驗結果展示 :何顯著影響。當使用浸塗設備時,所有溶液必須稀釋2 倍以10米/小時之塗敷球声 Α咖 迷度以獲侍相同結果。較高浸潰速 度需要較低稀釋。 對於溶液1(ST_於該3個基材觀㈣以下結果: 使用 200(32。)與 11 〇(47。)反私 )反射之比率1作為量度。約5的值 可呈現良好織構。
結果 ΐ(2〇〇)/κη^> 130941.doc 200923976 在與基材2相同之表面粗糙度下,去除基材3中之硫上層 結構可使緩衝層之織構改良3倍。 130941.doc -11 -
Claims (1)
- 200923976 十、申請專利範圍: 1 ’ 一種處理雙軸織構化金屬基材之方法,該金屬基材係作 為高溫超導薄膜條狀導體(HTSL-CC)之起始材料,該導 體包含該金屬基材、以化學方式產生於該金屬基材上且 相對於該金屬基材以結晶學上未旋轉方式生長之緩衝 層、及該緩衝層上以化學方式產生的超導塗層,該方法 之特徵在於在產生該緩衝層之前去除該金屬基材之上層 結構。 f , ' 2.如請求項1之方法,其特徵在於去除硫屬化合物上層結 構。 3·如請求項1或2之方法,其特徵在於該金屬基材係經處理 至一表面粗糙度且RMS<50奈米、較佳RMS<2〇奈米、尤 佳RMS<i〇奈米。 4·如請求項1或2之方法,其特徵在於該上層結構係藉由研 磨去除。如請求項1或2之方法,其特徵在於將晶格常數與該金屬 基材之晶格常數相差小於:t15%、較佳小於土1〇%之材料 用於該緩衝層。 =μ求項1或2之方法,其特徵在於去除該上層結構之後 清洗該金屬基材。 :印求項6之方法’其特徵在於該金屬基材係在超音波 洛中清洗。 8.如請求項ό之方法,其特徵在於且體 ”遐而&使用丙酮及異 丙醇去除該金屬基材之油脂。 130941.doc 200923976 9· 一種雙軸織構化金屬基材之用途,該基材無上層結構且 具有RMS<50奈米、較佳RMS<2〇奈米、尤佳RMS<l〇| 米之表面粗糙度,該基材係作為高溫超導薄膜條狀導體 (HTSL-CC)之起始材料,該導體包含金屬基材、以化學 方式產生於该金屬基材上且相對於該金屬基材以結晶學 上未旋轉方式生長之緩衝層、及該緩衝層上以化學方式 產生的超導塗層。 10·如請求項9之雙軸織構化金屬基材的用途,其中該緩衝 層包含晶格常數與該金屬基材之晶格常數相差小於 土15〇/〇、較佳小於士 10〇/〇之材料。 11. 一種高溫超導薄膜條狀導體(HTSL_CC),其包含金屬基 材、以化學方式產生於該金屬基材上且相對於該金屬^ 材以結晶學上未旋轉方式生長之緩衝層、及該緩衝層上 以化學方式產生的超導塗層,其特徵在於該金屬基材具 有RMS 50奈米、較佳議8<2〇奈米、尤佳R奈米 之表面粗糙度’且料衝層係彳目對於該金屬基材之晶體 、。構以“曰曰學上未旋轉之方式直接生長於該金屬基材表 面上而無中間層。 12. 一種如請求項1至11中任-項所定義之金屬基材,其特 徵在於其包含至少8 5原子%、較佳9 0原子%鎳。 130941.doc 200923976 七、指定代表圖: (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 八、本案若有化學式時,請揭示最能顯示發明特徵的化學式: (無) 130941.doc
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US7879763B2 (en) * | 2006-11-10 | 2011-02-01 | Superpower, Inc. | Superconducting article and method of making |
KR100766052B1 (ko) * | 2006-11-10 | 2007-10-12 | 학교법인 한국산업기술대학 | 필라멘트 타입용 고온초전도 선재의 제조방법 |
DE102008058768B4 (de) | 2008-11-24 | 2011-12-15 | Zenergy Power Gmbh | Verfahren zur Herstellung von Metallsubstraten für HTS-Schichtanordnungen |
-
2007
- 2007-05-24 DE DE102007024166A patent/DE102007024166B4/de active Active
-
2008
- 2008-04-24 EP EP08007957A patent/EP1995798A3/de not_active Withdrawn
- 2008-05-08 CA CA002630946A patent/CA2630946A1/en not_active Abandoned
- 2008-05-13 TW TW097117605A patent/TW200923976A/zh unknown
- 2008-05-19 NZ NZ568360A patent/NZ568360A/en not_active IP Right Cessation
- 2008-05-22 AU AU2008202268A patent/AU2008202268B2/en not_active Ceased
- 2008-05-23 CN CNA200810109064XA patent/CN101312084A/zh active Pending
- 2008-05-23 KR KR1020080048035A patent/KR20080103460A/ko not_active Application Discontinuation
- 2008-05-23 US US12/126,242 patent/US8513163B2/en active Active
- 2008-05-23 JP JP2008135080A patent/JP2008293976A/ja active Pending
Also Published As
Publication number | Publication date |
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AU2008202268A1 (en) | 2008-12-11 |
AU2008202268B2 (en) | 2010-03-25 |
CN101312084A (zh) | 2008-11-26 |
KR20080103460A (ko) | 2008-11-27 |
CA2630946A1 (en) | 2008-11-24 |
US20080293576A1 (en) | 2008-11-27 |
NZ568360A (en) | 2009-09-25 |
EP1995798A2 (de) | 2008-11-26 |
EP1995798A3 (de) | 2010-11-10 |
DE102007024166B4 (de) | 2011-01-05 |
DE102007024166A1 (de) | 2008-12-04 |
JP2008293976A (ja) | 2008-12-04 |
US8513163B2 (en) | 2013-08-20 |
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