WO2005029512A1 - 超電導体およびその製造方法 - Google Patents
超電導体およびその製造方法 Download PDFInfo
- Publication number
- WO2005029512A1 WO2005029512A1 PCT/JP2004/011679 JP2004011679W WO2005029512A1 WO 2005029512 A1 WO2005029512 A1 WO 2005029512A1 JP 2004011679 W JP2004011679 W JP 2004011679W WO 2005029512 A1 WO2005029512 A1 WO 2005029512A1
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- WIPO (PCT)
- Prior art keywords
- thickness
- superconducting layer
- layer
- superconductor
- superconducting
- Prior art date
Links
- 239000002887 superconductor Substances 0.000 title claims abstract description 58
- 238000000034 method Methods 0.000 title claims abstract description 23
- 230000015572 biosynthetic process Effects 0.000 claims description 31
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 230000008021 deposition Effects 0.000 abstract description 35
- 230000007423 decrease Effects 0.000 abstract description 8
- 238000000151 deposition Methods 0.000 description 33
- 230000000052 comparative effect Effects 0.000 description 29
- 238000005755 formation reaction Methods 0.000 description 29
- 239000000758 substrate Substances 0.000 description 18
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 10
- 239000013078 crystal Substances 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000000407 epitaxy Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 238000004943 liquid phase epitaxy Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
Definitions
- the present invention relates to a superconductor and a method for manufacturing the same, and more particularly, to a superconductor having a superconducting layer having a large layer thickness and a large critical current (hereinafter referred to as Ic), and a method for manufacturing the same.
- Ic critical current
- the superconducting layer is to be formed thick by a single film formation, oxygen cannot be sufficiently taken into the superconducting layer during film formation, and the critical current density (hereinafter referred to as J c) decreases. As a result, I c cannot be increased. Also, if the superconducting layer is to be formed thickly by one film formation, the time for one film formation becomes long, and elements such as Ni contained in the underlayer diffuse into the superconducting layer, and the superconducting layer and the There were problems such as reaction.
- the present invention is to provide a superconductor in which the decrease in Jc is small and the Ic is increased even when the thickness of the superconducting layer is increased, and a method for producing the same, in a multilayer film forming method. Aim.
- a method of manufacturing a superconductor according to the present invention is a method of manufacturing a superconductor in which a superconducting layer is formed by forming a superconducting layer on an underlayer two or more times.
- the film thickness is set to 0.3 ⁇ or less.
- the layer thickness is 0.75 ⁇ !
- a superconducting layer of ⁇ 3 / _im may be formed.
- the supply area speed of the underlayer in each film formation may be 0.04 m 2 / h or more.
- the superconductor according to the present invention has a layer thickness of 0.75 ⁇ !
- 1 (a) to 1 (d) are diagrams illustrating a method for manufacturing one superconductor according to the present invention.
- one method for manufacturing a superconductor according to the present invention is a method for manufacturing a superconductor 100 in which a superconducting layer 2 is formed by forming a superconducting layer 2 on an underlayer 1 two or more times.
- the thickness of the superconducting film in the film formation is set to 0.3 / m or less.
- the first deposition as shown in FIG. 1 (b) is performed on the underlayer 1 as shown in FIG. 1 (a).
- the first deposition 21 is performed to form the superconducting layer 2 so that the film thickness 1 of the superconducting film in Step 1 is 0.3 ⁇ m or less.
- the thickness T 2 of the superconducting film in the second film formation is adjusted to be 0.3 ⁇ or less.
- the second film formation 22 is performed to increase the layer thickness ⁇ of the superconducting layer 2.
- the layer thickness ⁇ of the superconducting layer 2 is TT ⁇ + Ts.
- a third deposition 23 is performed on the superconducting layer 2 formed as described above so that the thickness T 3 of the superconducting film in the third deposition is 0.3 ⁇ or less.
- the thickness ⁇ of the superconducting layer 2 is further increased.
- the film thickness is sequentially increased to increase the thickness of the superconducting layer.
- ⁇ is an integer of 2 or more.
- the thickness of the superconductor film in each film formation is 0.3 ⁇ or less. If the film thickness exceeds 0.3 ⁇ , it becomes difficult to sufficiently incorporate oxygen into the superconducting layer during film formation, so that Jc of the superconducting layer decreases and even if the layer thickness of the superconducting layer is increased. It is difficult to increase Ic of the superconducting layer.
- R EiB a 2 C u 3 0 7 _ 6 (RE shows a rare earth element, hereinafter the same) of oxide superconducting material such as Preferred are mentioned.
- the method for forming the superconducting layer 2, that is, the method for forming the superconducting film is not particularly limited as long as it can be formed in an oxygen atmosphere.
- Examples of the vapor phase method include laser vapor deposition, electron beam vapor deposition, and sputtering.
- Examples of the liquid phase method include MOD (Metal Organic Deposition), TFA—MOD (Trif luoroacetic acid Metal Organic Deposition), and LPE (Liquid Phase). Epitaxy; liquid phase epitaxy).
- the underlayer 1 means a layer on which a superconducting layer is formed, and may be a substrate or an intermediate layer formed on the substrate and the substrate.
- the superconductor 100 is constituted by the substrate as the underlayer 1 and the superconducting layer 2
- the superconductor 100 is constituted by the substrate and the intermediate layer as the underlayer 1 and the superconducting layer 2.
- the adjacent underlayer 11 at least the underlayer adjacent to the superconducting layer in the underlayer 1 (hereinafter, referred to as the adjacent underlayer 11) needs to have biaxial orientation. Therefore, when the substrate is to be the adjacent underlayer 11, the substrate needs to have biaxial orientation.
- having biaxial orientation includes not only perfect biaxial orientation but also one having a crystal axis shift angle of 25 ° or less in an adjacent underlayer.
- the biaxial orientation biaxial refers to a crystal axis in a direction perpendicular to the adjacent underlayer surface and one crystal axis in a direction parallel to the underlayer surface, and the shift angle of the crystal axis in the adjacent underlayer is The deviation angle of one crystal axis in a direction parallel to the surface of the adjacent underlayer in a plane parallel to the surface of the underlayer, and is indicated by an average value of the deviation angles in the adjacent underlayer.
- the substrate is not particularly limited, but may have a biaxial orientation, such as Ni, Cr, Mn, Co, Fe, Pd, Cu, Ag, Au, or two of these. Alloys composed of the above metals are preferably used. In addition, not only the above-mentioned metal or alloy alone but also the above-mentioned metal or alloy can be laminated with another metal or alloy.
- the intermediate layer is not particularly limited, but may have one or more metal elements having a pyrochlore type, a fluorite type, a rock salt type or a perovskite type crystal structure that can take a biaxial orientation. Metal oxides are preferably used.
- the rare earth element oxides such as C e 0 2, YS Z (yttria stabilized zirconate Nia), B ZO (B a Z R_ ⁇ 3), S TO (S r T I_ ⁇ 3), A 1 2 0 3, YA 10 3, Mg O, Ln- M- O compound (Ln is one or more lanthanoid de element, M is S r, 1 or more selected from among Z r and G a Element, ⁇ is oxygen) and the like.
- Such an oxide plays a role in alleviating the difference between the oriented metal substrate and the superconducting layer from the viewpoint of the crystal constant and the crystal orientation, and preventing the outflow of metal atoms from the oriented metal substrate to the superconducting layer.
- two or more intermediate layers can be formed as the intermediate layer.
- the superconducting layer is formed directly on the biaxially oriented Ag substrate without providing the intermediate layer. You can also.
- a superconducting layer having a thickness of 0.75 ⁇ 111 to 3 zm can be formed by forming the underlayer three or more times.
- the thickness of the superconducting layer is less than 0.75 / m, Jc is large but the thickness is small, so that Ic does not increase, and when it exceeds 3.0 ⁇ m, Jc increases with the number of depositions. Since c is small, I c does not increase even if the layer thickness increases.
- the thickness of the superconducting layer is 0.9 tn! It is preferably set to ⁇ 3.0 ⁇ m.
- the supply area per hour of the underlayer (hereinafter, referred to as the underlayer supply area speed) in each film formation can be 0.04 m 2 / h or more. . If the supply area speed of the underlayer is less than 0.04 m 2 / h, when the substrate becomes an adjacent underlayer, the reaction between the substrate and the superconducting layer formed on the substrate increases, and the Ic and the Ic of the superconducting layer increase. Properties such as Jc may be reduced.
- One superconductor according to the present invention has a superconducting layer having a layer thickness of 0.75 ⁇ to 3.0 ⁇ m by three or more depositions on the underlayer 1.
- the superconductor 100 on which the layer 2 is formed wherein the thickness of the superconducting film in each film formation is not more than 0.
- J c is large, but I c does not increase due to the small thickness, and exceeds 3. ⁇ ⁇ .
- the thickness of the superconducting layer is 0.9 ⁇ ! ⁇ 3 O / zm.
- a biaxially oriented Ni alloy substrate having a width of 1 Omm and a thickness of 0.1 mm and a biaxially oriented YSZ intermediate having a thickness of 0.1 mm are used as the underlayer 1 in FIG. 1 (a).
- Gas pressure of 26.6 Pa (20 OmT orr) was obtained by laser evaporation using a Ni-based alloy tape (here, the biaxially oriented YSZ intermediate layer becomes the adjacent underlayer 11) on which the layer was formed. )
- a biaxially oriented YS Z intermediate layer is an adjacent underlying layer 1 1 of the underlying layer 1, thickness 0. 25 [mu] m of Ho 1 B a 2 C u 3 0 7 - ⁇ films formed
- the film was formed into a superconducting layer 2. Further, under the same film forming conditions as above, as shown in FIG. 1 (c) and thereafter, the layer thickness of the superconducting layer 2 was increased by performing the second and subsequent film formation.
- Example 2 a superconductor having a 0.5 ⁇ superconducting layer formed twice and a superconductor having a 0.75 ⁇ superconducting layer formed three times (Example 1) Example 2), a superconductor having a superconducting layer with a thickness of 1.0 ⁇ formed by four depositions (Example 3), and a superconductor having a superconducting layer with a thickness of 1.25 ⁇ formed by five depositions (Example 4), a superconductor having a superconducting layer with a thickness of 1.5 m formed six times (Example 5), a superconductor having a superconducting layer with a thickness of 1.7 ⁇ formed by seven times (Example 6) ), A superconductor having a superconducting layer with a thickness of 2.0 ⁇ formed by eight depositions (Example 7), and a superconductor having a superconducting layer with a thickness of 2.5 ⁇ formed by ten depositions (
- a superconductor having a superconducting layer having a large thickness by a single film formation under the same film forming conditions as in Example 1 except for using the same underlayer as in Example 1 and using the same film forming conditions as in Example 1 except for the supply area speed of the underlayer. was prepared.
- the layer thickness of the superconducting layer can be increased by decreasing the supply area speed of the underlayer.
- a superconductor having a 0.25 m superconducting layer (Comparative Example 1), a superconductor having a 0.5 Aim superconducting layer (Comparative Example 2), and a layer thickness of 0.75 Superconductor with superconducting layer of ⁇ (Comparative Example 3), superconductor with superconducting layer of 1.0 im thickness (Comparative Example 4), superconductor with superconducting layer of 1.25 ⁇ m thickness (Comparative Example) 5), a superconductor having a superconducting layer having a layer thickness of 1.5 / m (Comparative Example 6) and a superconductor having a superconducting layer having a layer thickness of 1.75 ⁇ m (Comparative Example 7) were produced. These Jc and Ic were measured, and the results are summarized in Table 1.
- the superconducting layer is formed two or more times, and the film thickness of the superconducting film in each film formation is set to 0.25 ⁇ . Since the decrease in Jc is small, Ic can be increased by increasing the thickness of the superconducting layer.
- a superconductor having a superconducting layer with a thickness of 1.5 ⁇ by six depositions In the five examples (Examples 5 to 9) from Example 5) to the superconductor having a superconducting layer with a thickness of ⁇ (Example 9) I c could be increased to about 30 cm 2 width.
- the Jc of the superconducting layer was extremely reduced as the layer thickness of the superconducting layer was increased, and the layer thickness of the superconducting layer was 0.5 ⁇ to 1. ⁇ ⁇ In Examples 2 to 4), I c increased only to about 10 O AZ cm width. Even if the thickness of the superconducting layer was further increased, I c decreased.
- the Ic of the superconductor having a 0.5 ⁇ m-thick superconducting layer formed by two depositions is 120 A / c ni
- the Ic of the superconductor having a 0.75 Atm superconducting layer formed by three depositions has a width of 180 AZcm
- the width of the superconductor having the 0.75 ⁇ m superconducting layer was 75 A / cm larger than the Ic105 AZ cm width. Therefore, by performing film formation three times or more and setting the superconducting film thickness in one film formation to 0.3 m or less and forming a superconducting layer having a layer thickness of 0.75 ⁇ m or more, I c is remarkably increased. Can be increased.
- the film thickness of the superconducting film in each film formation is adjusted to 0.1 ⁇ by adjusting the supply area rate of the underlayer (Example 11).
- 0.2 ⁇ (Example 12), 0.25 ⁇ m (Example 13), 0.3 ⁇ m (Example 14), 0.35 ⁇ m (Comparative example 8), 0.4 ⁇ m (Comparative Example 9) or 0.5 ⁇ (Comparative Example 10), and a superconductor was produced in the same manner as in Example 1 except that film formation was performed three times.
- Thickness of one deposition (; Um) 0.1 0.2 0.25 0.3 0.35 0.4 0.5 Layer thickness (three depositions) (jUm) 0.3 0.6 0.75 0.9 1.05 1.2 1.5
- the present invention performs the film formation two or more times, and forms the superconducting layer with a film thickness of 0.3 m or less in each film formation, thereby increasing the layer thickness of the superconducting layer.
- the decrease in Jc is small, and the increase in Ic is possible, and it can be widely used to increase Ic of a superconductor.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
- Physical Vapour Deposition (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2004275128A AU2004275128B8 (en) | 2003-09-17 | 2004-08-06 | Superconductor and process for producing the same |
EP04771646.9A EP1667174B1 (en) | 2003-09-17 | 2004-08-06 | Superconductor and process for producing the same |
CA002510635A CA2510635A1 (en) | 2003-09-17 | 2004-08-06 | Superconductor and method of producing the same |
US10/536,694 US7371586B2 (en) | 2003-09-17 | 2004-08-06 | Superconductor and process for producing the same |
NZ540721A NZ540721A (en) | 2003-09-17 | 2004-08-06 | Superconductor and method of producing the same |
KR1020057012535A KR101056227B1 (ko) | 2003-09-17 | 2004-08-06 | 초전도체 및 그 제조방법 |
HK06105357.0A HK1085304A1 (en) | 2003-09-17 | 2006-05-08 | Superconductor and method of producing the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003-324167 | 2003-09-17 | ||
JP2003324167A JP4626134B2 (ja) | 2003-09-17 | 2003-09-17 | 超電導体およびその製造方法 |
Publications (1)
Publication Number | Publication Date |
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WO2005029512A1 true WO2005029512A1 (ja) | 2005-03-31 |
Family
ID=34372740
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2004/011679 WO2005029512A1 (ja) | 2003-09-17 | 2004-08-06 | 超電導体およびその製造方法 |
Country Status (11)
Country | Link |
---|---|
US (1) | US7371586B2 (ja) |
EP (1) | EP1667174B1 (ja) |
JP (1) | JP4626134B2 (ja) |
KR (1) | KR101056227B1 (ja) |
CN (1) | CN100472670C (ja) |
AU (1) | AU2004275128B8 (ja) |
CA (1) | CA2510635A1 (ja) |
HK (1) | HK1085304A1 (ja) |
NZ (1) | NZ540721A (ja) |
RU (1) | RU2332738C2 (ja) |
WO (1) | WO2005029512A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8216979B2 (en) * | 2006-02-16 | 2012-07-10 | Sumitomo Electric Industries, Ltd. | Method of manufacturing superconducting thin film material, superconducting device and superconducting thin film material |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007094147A1 (ja) * | 2006-02-16 | 2007-08-23 | Sumitomo Electric Industries, Ltd. | 超電導薄膜材料の製造方法、超電導機器、および超電導薄膜材料 |
JP2007311194A (ja) * | 2006-05-18 | 2007-11-29 | Sumitomo Electric Ind Ltd | 超電導薄膜材料および超電導薄膜材料の製造方法 |
JP4690246B2 (ja) | 2006-05-19 | 2011-06-01 | 住友電気工業株式会社 | 超電導薄膜材料およびその製造方法 |
EP2800106A4 (en) * | 2012-02-01 | 2015-03-11 | Furukawa Electric Co Ltd | METHOD FOR PRODUCING A SUPER-LEADING WIRE MATERIAL AND SUPER-LEADING WIRE MATERIAL |
EP2960954A1 (de) | 2014-06-24 | 2015-12-30 | Basf Se | Verfahren zur Herstellung eines Komposits umfassend eine Hochtemperatursupraleiter(HTS)-Schicht |
JP6374365B2 (ja) * | 2015-09-16 | 2018-08-15 | 株式会社東芝 | 酸化物超電導体、およびその製造方法 |
RU2757450C1 (ru) * | 2020-09-09 | 2021-10-15 | Автономная некоммерческая образовательная организация высшего образования "Сколковский институт науки и технологий" | Высокотемпературный сверхпроводящий гидрид и способ его получения |
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-
2003
- 2003-09-17 JP JP2003324167A patent/JP4626134B2/ja not_active Expired - Fee Related
-
2004
- 2004-08-06 KR KR1020057012535A patent/KR101056227B1/ko active IP Right Grant
- 2004-08-06 AU AU2004275128A patent/AU2004275128B8/en not_active Ceased
- 2004-08-06 WO PCT/JP2004/011679 patent/WO2005029512A1/ja active Application Filing
- 2004-08-06 RU RU2005119004/09A patent/RU2332738C2/ru not_active IP Right Cessation
- 2004-08-06 EP EP04771646.9A patent/EP1667174B1/en not_active Revoked
- 2004-08-06 CA CA002510635A patent/CA2510635A1/en not_active Abandoned
- 2004-08-06 CN CNB2004800023614A patent/CN100472670C/zh not_active Expired - Fee Related
- 2004-08-06 US US10/536,694 patent/US7371586B2/en not_active Expired - Fee Related
- 2004-08-06 NZ NZ540721A patent/NZ540721A/en not_active IP Right Cessation
-
2006
- 2006-05-08 HK HK06105357.0A patent/HK1085304A1/xx not_active IP Right Cessation
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JPH0353413A (ja) * | 1989-07-21 | 1991-03-07 | Nippon Telegr & Teleph Corp <Ntt> | 超伝導配線 |
JPH0375300A (ja) * | 1989-08-11 | 1991-03-29 | Hitachi Ltd | 酸化物超格子材料 |
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US8216979B2 (en) * | 2006-02-16 | 2012-07-10 | Sumitomo Electric Industries, Ltd. | Method of manufacturing superconducting thin film material, superconducting device and superconducting thin film material |
Also Published As
Publication number | Publication date |
---|---|
RU2005119004A (ru) | 2006-01-27 |
AU2004275128A1 (en) | 2005-03-31 |
NZ540721A (en) | 2008-04-30 |
EP1667174A4 (en) | 2010-11-24 |
AU2004275128B8 (en) | 2009-12-03 |
CA2510635A1 (en) | 2005-03-31 |
CN100472670C (zh) | 2009-03-25 |
EP1667174B1 (en) | 2013-10-09 |
JP2005093205A (ja) | 2005-04-07 |
HK1085304A1 (en) | 2006-08-18 |
KR101056227B1 (ko) | 2011-08-11 |
US20060014304A1 (en) | 2006-01-19 |
CN1739171A (zh) | 2006-02-22 |
US7371586B2 (en) | 2008-05-13 |
EP1667174A1 (en) | 2006-06-07 |
AU2004275128B2 (en) | 2009-05-28 |
KR20060115956A (ko) | 2006-11-13 |
JP4626134B2 (ja) | 2011-02-02 |
RU2332738C2 (ru) | 2008-08-27 |
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