WO2013183132A1 - 固体型二次電池の電極構造 - Google Patents
固体型二次電池の電極構造 Download PDFInfo
- Publication number
- WO2013183132A1 WO2013183132A1 PCT/JP2012/064593 JP2012064593W WO2013183132A1 WO 2013183132 A1 WO2013183132 A1 WO 2013183132A1 JP 2012064593 W JP2012064593 W JP 2012064593W WO 2013183132 A1 WO2013183132 A1 WO 2013183132A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- electrode
- slit
- semiconductor circuit
- main
- semiconductor
- Prior art date
Links
- 239000007787 solid Substances 0.000 title description 3
- 239000004065 semiconductor Substances 0.000 claims abstract description 84
- 239000000758 substrate Substances 0.000 claims abstract description 38
- 229910052751 metal Inorganic materials 0.000 claims abstract description 26
- 239000002184 metal Substances 0.000 claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 claims abstract description 20
- 229920005989 resin Polymers 0.000 claims abstract description 13
- 239000011347 resin Substances 0.000 claims abstract description 13
- 239000010410 layer Substances 0.000 claims description 87
- 229910044991 metal oxide Inorganic materials 0.000 claims description 22
- 150000004706 metal oxides Chemical class 0.000 claims description 22
- 230000008859 change Effects 0.000 claims description 17
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 16
- 239000002346 layers by function Substances 0.000 claims description 16
- 229910052804 chromium Inorganic materials 0.000 claims description 15
- 239000011651 chromium Substances 0.000 claims description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- 239000007769 metal material Substances 0.000 claims description 11
- 230000001443 photoexcitation Effects 0.000 claims description 11
- 230000003647 oxidation Effects 0.000 claims description 9
- 238000007254 oxidation reaction Methods 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
- 238000010030 laminating Methods 0.000 claims description 6
- 229910052750 molybdenum Inorganic materials 0.000 claims description 6
- 239000011733 molybdenum Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910045601 alloy Inorganic materials 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 2
- 239000011810 insulating material Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 abstract description 16
- 239000011800 void material Substances 0.000 abstract description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 40
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 36
- 229910052802 copper Inorganic materials 0.000 description 36
- 239000010949 copper Substances 0.000 description 36
- 230000035882 stress Effects 0.000 description 36
- 239000004408 titanium dioxide Substances 0.000 description 20
- 229920001721 polyimide Polymers 0.000 description 17
- 229920001296 polysiloxane Polymers 0.000 description 17
- 238000010586 diagram Methods 0.000 description 15
- 239000004642 Polyimide Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 238000006073 displacement reaction Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000011521 glass Substances 0.000 description 10
- 239000010408 film Substances 0.000 description 8
- 229910000679 solder Inorganic materials 0.000 description 8
- 239000000919 ceramic Substances 0.000 description 7
- 238000010304 firing Methods 0.000 description 5
- 230000003014 reinforcing effect Effects 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910000480 nickel oxide Inorganic materials 0.000 description 4
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 239000003574 free electron Substances 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 230000005641 tunneling Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- PLLZRTNVEXYBNA-UHFFFAOYSA-L cadmium hydroxide Chemical compound [OH-].[OH-].[Cd+2] PLLZRTNVEXYBNA-UHFFFAOYSA-L 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229940116318 copper carbonate Drugs 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000005300 metallic glass Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical compound [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 229910052815 sulfur oxide Inorganic materials 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M14/00—Electrochemical current or voltage generators not provided for in groups H01M6/00 - H01M12/00; Manufacture thereof
- H01M14/005—Photoelectrochemical storage cells
-
- 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
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/425—Structural combination with electronic components, e.g. electronic circuits integrated to the outside of the casing
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/46—Accumulators structurally combined with charging apparatus
- H01M10/465—Accumulators structurally combined with charging apparatus with solar battery as charging system
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02J—CIRCUIT ARRANGEMENTS OR SYSTEMS FOR SUPPLYING OR DISTRIBUTING ELECTRIC POWER; SYSTEMS FOR STORING ELECTRIC ENERGY
- H02J7/00—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
- H02J7/32—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries for charging batteries from a charging set comprising a non-electric prime mover rotating at constant speed
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N99/00—Subject matter not provided for in other groups of this subclass
- H10N99/05—Devices based on quantum mechanical effects, e.g. quantum interference devices or metal single-electron transistors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to an electrode structure of a solid-state secondary battery in which a charging functional layer having a function of charging electric energy is sandwiched between electrodes and stacked on a substrate.
- Secondary batteries are widely used from mobile terminals such as mobile phones and laptop computers to electric vehicles, and are used repeatedly after charging and discharging.
- Conventional secondary batteries include nickel-cadmium batteries and lithium ion batteries, and the basic structure is that a layer having a charging function is sandwiched between electrodes.
- the nickel-cadmium battery is a battery using nickel hydroxide for the positive electrode and cadmium hydroxide for the negative electrode
- the lithium ion battery is a battery using an oxide containing lithium for the positive electrode and graphite for the negative electrode (patent) Reference 1 etc.).
- a quantum battery an all-solid-state semiconductor battery (hereinafter referred to as a quantum battery) that can be reduced in cost and stably operated with a simple configuration (PCT / JP2010-067643).
- This quantum cell uses a photoexcitation structure change of metal oxide by ultraviolet irradiation to form a new energy level in the band gap and charge by trapping electrons in this intermediate energy level based on.
- a metal oxide coated with an insulator is used as a charge layer.
- this charge layer is manufactured, there is a baking process by heating, and the thermal expansion coefficient of the base material and the electrode is different. Cracks may occur.
- a photoelectric conversion element and a thin-film solar cell in which a stress relaxation layer is provided on the insulating layer and peeling of the layers constituting the photoelectric conversion element is suppressed are proposed.
- a formed stress relaxation layer, a lower electrode formed on the stress relaxation layer, a photoelectric conversion layer formed on the lower electrode and composed of a compound semiconductor layer, and an upper electrode formed on the photoelectric conversion layer (Refer to Patent Document 2).
- a stress relaxation connection medium As an example of using a stress relaxation connection medium, further.
- a printed wiring board having a thermal expansion coefficient different from that of a land grid array type package is bonded with high reliability.
- a first connection pad for connecting a land grid array type semiconductor package having arrayed terminal electrodes and a printed wiring board having electrodes arranged in the same manner as the arrayed terminal electrodes to array type electrodes of the land grid array type package And a second connection pad connected to an electrode on the printed wiring board, and electrically connected via a flexible stress relaxation connection medium.
- the stress relaxation connection medium is a flexible sheet, has a through hole for electrode connection, and is cut out in a predetermined portion of the flexible sheet (see Patent Document 3).
- a stress relaxation slit As an example using the stress relaxation slit, there is an example applied to a surface mount ceramic substrate. Due to the difference in thermal expansion coefficient between the ceramic substrate body and the wiring substrate, it is possible to prevent the occurrence of cracks in the joint portion interposed between the external connection electrode and the wiring substrate conductor pattern, and A crack is prevented from occurring in the ceramic substrate body due to the tensile stress generated in the ceramic substrate body.
- a stress relaxation slit is formed between a portion of the ceramic substrate body where the external connection electrode is provided and a portion where the heat dissipating conductor is provided. The portion of the ceramic substrate body where the tensile stress is concentrated has a thickness dimension larger than that of the portion where the external connection electrode is provided (see Patent Document 4).
- the solder after melting the solder bumps and the conductive adhesive include a circuit board and a glass substrate. Due to the difference in coefficient of thermal expansion of the semiconductor chip, thermal stress concentrates on the solder and the conductive adhesive after melting the solder bumps, causing separation between the circuit board and the solder, and the glass substrate and the conductive adhesive. For this reason, in Japanese Patent Laid-Open No.
- a reinforcing plate provided with a slit is used to relieve and disperse the stress generated by the difference in thermal expansion between the TAB tape reinforcing plate and the mounting substrate. Proposed. After a signal wiring is formed on a heat-resistant insulating resin film such as polyimide and the tip of the signal wiring is electrically connected to the electrode of the semiconductor element, a reinforcing plate having a semiconductor element mounting opening is formed.
- the present invention changes the photogap structure of a conductive first electrode and an n-type metal oxide semiconductor covered with an insulating material to change the band gap. It is intended for a quantum battery that is a secondary battery formed by stacking a charge layer that forms an energy level therein and captures electrons, a p-type semiconductor layer, and a conductive second electrode.
- This quantum battery uses a substrate in which a polyimide film, which is an insulating resin, is laminated on a glass plate, and has a laminated structure in which a charging layer and a p-type semiconductor layer are sandwiched from both sides by electrodes. Metal materials are used.
- a laminated structure there is a problem in that cracks occur in the electrodes because the thermal expansion coefficients of the polyimide film and the electrodes differ due to heating in the firing step during the manufacture of the quantum battery.
- the present invention provides an electrode structure for preventing cracks generated in a metal electrode due to heating in a manufacturing process when an insulating resin and a metal electrode having different thermal expansion coefficients are laminated. It aims at providing the semiconductor functional element which prevented generation
- the present invention relates to an electrode laminated on a substrate made of an insulating resin for a semiconductor circuit, and the electrode structure is provided in order to prevent the occurrence of cracks in the manufacturing process due to a difference in thermal expansion coefficient with the substrate.
- An electrode for a semiconductor circuit comprising a main electrode having a slit formed by cutting out a portion and an auxiliary electrode covering the slit of the main electrode.
- the insulating resin expands due to heating, and the displacement increases as the distance from the center portion increases. For this reason, a greater stress is applied to the stacked electrodes as the distance from the center portion increases. For this reason, it is preferable that a plurality of slits are provided in the main electrode, and the slit interval is narrowed as the distance from the center of the main electrode surface increases.
- the plurality of slits of the main electrode are formed concentrically from the center of the main electrode, or are formed in a rectangular shape so as to surround the center of the main electrode.
- the electrode section divided by the plurality of slits provided in the main electrode and the auxiliary electrode is further provided with a re-dividing slit for re-dividing into a plurality of electrodes, and the stress is distributed by making the electrode pattern a small surface. May be.
- the subdivision slit arranged in the main electrode and the subdivision slit arranged in the auxiliary electrode are arranged at positions where they do not overlap.
- the portion where the re-dividing slit overlaps with the slit provided in the main electrode and the auxiliary electrode should not be provided with the dividing slit so that there is no gap due to the slit and the re-dividing slit. it can.
- the slit of the auxiliary electrode can be arranged by shifting the same pattern as the slit of the main electrode, or may be arranged by rotating the same pattern as the slit of the main electrode.
- the slit of the main electrode in this case is a mesh shape that divides the electrode into rectangles, and may be a slit that divides the electrode into circles.
- the rectangular or circular divided electrode divided by the slit can cope with a larger stress by making the divided electrode at a position away from the center of the electrode smaller than the divided electrode at the center.
- the portion where the slit of the main electrode and the slit of the auxiliary electrode overlap is not provided with a slit, and the presence of a gap due to the slit can be eliminated.
- the present invention provides an electrode structure for preventing the generation of cracks in the electrode in the manufacturing process resulting from the difference in thermal expansion coefficient between the substrate and the electrode.
- the used electrode is oxidized and deteriorated by heating.
- the main electrode and the auxiliary electrode are made of metal materials having a passive characteristic for preventing oxidation.
- a metal layer having a passive characteristic may be laminated so that oxygen in the air does not come into contact.
- the metal material that can be used as the passive layer is at least one of chromium, nickel, titanium, and molybdenum, or an alloy that includes any one of chromium, nickel, titanium, and molybdenum.
- a semiconductor circuit electrode according to the present invention By using a semiconductor circuit electrode according to the present invention and laminating a functional layer functioning by electrical energy supplied from this electrode on a substrate, it can be applied to a semiconductor functional element that requires a heating step.
- a semiconductor functional element as a secondary battery in which a functional layer charges electrical energy must cover the entire functional layer with an electrode, and it is necessary to prevent the occurrence of cracks in the electrode over a wide area. The application of the slit electrode is effective.
- the functional layer is composed of a charging layer made of an n-type metal oxide semiconductor that has an insulating coating and is irradiated with ultraviolet rays to cause a photoexcitation structure change, and a p-type metal oxide semiconductor layer.
- a charging layer made of an n-type metal oxide semiconductor that has an insulating coating and is irradiated with ultraviolet rays to cause a photoexcitation structure change
- a p-type metal oxide semiconductor layer there is a step of firing the n-type metal oxide semiconductor in the manufacturing process, and the use of the slit electrode can prevent cracks generated in the electrode due to heating in the firing step. it can.
- the electrode structure with slits when manufacturing a semiconductor functional element using materials having different coefficients of thermal expansion between the electrode and the substrate, the difference in expansion coefficient between the electrode and the substrate due to heating in the manufacturing process. Can be absorbed by the slit of the electrode, so that the generation of cracks on the electrode surface can be prevented.
- a secondary battery having a charging function in the functional layer requires an electrode having a large area because the electrode is laminated on the entire surface of the charging layer, and cracks are likely to occur in the electrode. Even in this case, the electrode for a semiconductor circuit according to the present invention is highly effective, and the occurrence of cracks can be prevented by absorbing the displacement by the slit.
- the electrode material a metal material having passive characteristics, the problem of electrode peeling due to oxidation of the metal electrode caused by heating in the manufacturing process is prevented, and oxidation of the electrode due to secular change is suppressed.
- it is possible to provide a stable quantum battery that can be prevented from being deteriorated and peeled off and repeatedly charged and discharged over a long period of time.
- segmented by the slit further by the subdivision slit.
- the figure which shows the main electrode which provided the rectangular slit The figure which shows the main electrode which provided the rectangular slit which made the corner circular
- An electrode laminated on a substrate made of an insulating resin for a semiconductor circuit generally uses a metal material, and has a large difference in thermal expansion coefficient from a substrate using an insulating resin or the like. For this reason, when using the lamination technique heated to high temperature at the time of manufacture of the functional layer formed by laminating on the electrode, a crack may occur in the electrode due to a difference in thermal expansion coefficient.
- a slit is formed in the electrode to absorb the displacement due to the difference in thermal expansion coefficient.
- electrodes must be formed in a solid pattern on the entire surface of the charging layer, and the effect is remarkable when the area of such a functional layer is wide.
- FIG. 1 is a cross-sectional view of a quantum battery which is an all solid state secondary battery as a semiconductor functional element and has an intermediate band in an energy gap.
- the quantum battery 10 has a substrate 11 and a first electrode 12 laminated thereon.
- the first electrode 12 has a double laminated structure of a main electrode 13 provided with a slit 20 and an auxiliary electrode 15 composed of an electrode covering the slit 20 of the main electrode.
- an electrode having a double laminated structure of the main electrode 13 provided with the slit 20 and the auxiliary electrode 15 composed of an electrode covering the slit 20 of the main electrode will be referred to as a slit electrode.
- the slit is referred to as a slit in a broad sense as a shape that forms not only a narrow groove-like gap but also a gap that leaves an electrode.
- the slit electrode is intended to prevent the generation of cracks in the manufacturing process of heating at a high temperature when the functional layer 17 is formed.
- a metal material is used for the electrode when heated at a high temperature, for example, copper or copper alloy
- nickel, aluminum, zinc, tin or the like is used, the electrode material is also deteriorated by oxidation.
- a passive layer 19 is provided with a slit electrode in between.
- Passivity refers to the state of a metal that corrodes at an extremely slow rate despite the fact that the electrochemical column of the metal is in a base (active) position, and is a property that underlies the corrosion resistance of metal materials. Metals that are highly polarized by a small anode current passivate by approaching the behavior of electrochemically noble (inactive) metals.
- the oxide film as a corrosion product has a protective property and is given corrosion resistance.
- the metal material having passive characteristics include chromium, nickel, titanium, molybdenum, or an alloy containing at least one kind of chromium, nickel, titanium, molybdenum, and the like.
- the functional layer 17 is laminated on the first electrode 12.
- the charge layer 14 and the p-type metal oxide semiconductor layer 16 are stacked as the functional layer 17.
- the 2nd electrode 18 and the passive layer 19 are laminated
- the second electrode 18 is made of the same metal material as that of the first electrode 12, but is not oxidized by heating because it is formed after the manufacturing process of the functional layer 17 heated at a high temperature. However, if left in an atmospheric environment, it will deteriorate by reacting with oxygen in the atmosphere and oxidizing for a long time.
- the second electrode when copper is used as the second electrode, a cuprous oxide film is formed. If the humidity is high, basic copper carbonate is formed. Furthermore, it may be oxidized by sulfur oxides in the air to form copper sulfide or copper sulfate. When the deterioration is significant, peeling occurs, which deteriorates long-term reliability and becomes a major factor in shortening the product life. For this reason, the passivation layer 19 for preventing oxidation is also provided on the second electrode 18.
- FIG. 2 is a diagram illustrating the charge layer 14 of the quantum battery 10.
- the charging layer 14 uses silicone as the insulating coating 22 and titanium dioxide as the n-type metal oxide semiconductor 21, and covers the atomized titanium dioxide with silicone so that the charging layer 14 is filled. It has become. It has the function of storing energy by irradiating titanium dioxide with ultraviolet rays to cause a photoexcitation structural change.
- the material of the n-type metal oxide semiconductor 21 used for the charging layer 14 includes titanium dioxide, stannic oxide, and zinc oxide, which are manufactured by decomposing a metal aliphatic acid salt. For this reason, a metal aliphatic acid salt that can be converted into a metal oxide by combustion in an oxidizing atmosphere is used. By using a material having passive characteristics as the metal electrode, oxidation due to combustion can be prevented.
- the insulating coating 22 may be used for the insulating coating 22 as an inorganic insulator.
- the insulating resin include thermoplastic resins such as polyethylene and polypropylene, Thermosetting resins such as phenol resins and amino resins may be used.
- the material irradiated with ultraviolet rays forms a new energy level due to the change of the photoexcitation structure.
- the photoexcited structure change is a phenomenon in which the interstitial distance of a substance excited by light irradiation changes, and the n-type metal oxide semiconductor 21 which is an amorphous metal oxide has a property of causing a photoexcited structure change. is doing.
- the n-type metal oxide semiconductor 21 which is an amorphous metal oxide has a property of causing a photoexcited structure change. is doing.
- the formation state of a new energy level due to the photoexcitation structure change will be described below with reference to band diagrams. To do.
- 3A and 3B show a case where a silicone 34 as an insulating coating 22 is present between a metal copper 30 as the first electrode 12 and a titanium dioxide 32 as the n-type metal oxide semiconductor 21. It is a band figure explaining the formation state of the new energy level 44 by photoexcitation structure change. Due to the photoexcited structure change phenomenon, a new energy level 44 is formed in the band gap of the n-type metal oxide semiconductor 21.
- the conduction band 36 has a barrier due to an insulating layer made of silicone 34.
- FIG. 3 (A) shows a state in which an ultraviolet ray 38 is irradiated when an insulating layer made of silicone 34 is provided between titanium dioxide 32 and copper 30.
- the electrons 42 in the valence band 40 of the titanium dioxide 32 are excited to the conduction band 36.
- the electrons 42 pass through the insulating layer of the silicone 34 with a certain probability and temporarily move to the copper 30.
- the photoexcited structural change of the titanium dioxide 32 occurs in the absence of the electrons 42, and the interatomic distance of the site from which the electrons 42 of the valence band 40 are removed changes.
- the energy level 44 has moved to the band gap in the Fermi level 46.
- FIG. 3B shows a state in which the above-described phenomenon occurs repeatedly while the ultraviolet ray 38 is irradiated, and a large number of energy levels 44 are formed in the band gap. However, the electrons 42 to be trapped in these energy levels 44 are excited by the ultraviolet rays 38 and moved to the copper 30. The energy level 44 in the band gap in the absence of electrons thus generated remains even after the ultraviolet irradiation is finished.
- the role of the silicone 34 as an insulating layer is to create a barrier between the copper 30 and the titanium dioxide 32 and allow the excited electrons 42 to pass through the tunnel effect to form an energy level 44 in the band gap in the absence of electrons. It is. The electrons 42 that have moved to the copper 30 remain on the copper 30 due to the charging potential around the silicone 34.
- FIG. 4 is a diagram schematically showing a state in which the titanium dioxide 32 covered with the silicone 34 has undergone a photoexcitation structural change due to ultraviolet irradiation, and the electrons 42 have moved to the copper 30.
- the electrons 42 pass through the barrier due to the silicone 34 by the tunneling effect, move to the copper 30, and remain with a weak trapping force generated by the potential of the silicone 34.
- a p-type metal oxide semiconductor layer 16 is further stacked on the charging layer 14 to form a blocking layer, and a second electrode 18 is provided thereon.
- the principle of the secondary battery having such a structure will be described with reference to the band diagram of FIG.
- FIG. 5A shows that the copper 30 and the second electrode 18 constituting the first electrode 12 are sandwiched between the copper 48 and the silicone 34 and the titanium dioxide 32 in the charging layer 14, and the p-type metal oxide semiconductor.
- the quantum battery 10 composed of the nickel oxide 50 functioning as the layer 16
- a negative voltage is applied to the copper 48 constituting the second electrode 18, and the copper 30 constituting the first electrode 12 is grounded to 0V.
- the electrons 42 of the copper 30 pass through the barrier due to the silicone 34 (tunneling) and move to the titanium dioxide 32. Since the transferred electrons 42 are blocked from further movement to the copper 48 by the nickel oxide 50, they are trapped in the energy level 44 existing between the band gaps of the titanium dioxide 32, thereby storing energy. It is done. That is, it is in a charged state, and the charge layer 14 is filled with electrons 42. Since this state is maintained even after the application of the bias electric field is canceled, it has a function as a secondary battery.
- FIG. 5B is a band diagram in the case of discharging by connecting a load (not shown) to the copper 30 and the copper 48.
- the electrons 42 trapped in the band gap become free electrons in the conduction band 36.
- the free electrons move to the copper 30 and flow to the load. This phenomenon is an energy output state and a discharge state.
- the energy level 44 in the band gap is in a state where no electrons 42 exist, and all the energy is used.
- the energy level formed in the band gap of titanium dioxide that is, the intermediate band is filled with electrons by applying an external voltage to connect the load to the electrode.
- electrons are emitted to extract energy and function as a battery. By repeating this phenomenon, it can be used as a secondary battery.
- the manufacture of the quantum battery 10 uses a substrate 11 in which a polyimide film having a thickness of about 4 ⁇ m is laminated on a glass plate.
- the normal flat plate-shaped first electrode 12 is formed by laminating 50 nm of chromium having passive characteristics, 300 nm of copper, and 50 nm of chromium on the substrate 11. Examples of the method for forming each layer include vapor phase film forming methods such as sputtering, ion plating, electron beam vapor deposition, vacuum vapor deposition, and chemical vapor deposition.
- the metal electrode can be formed by an electrolytic plating method, an electroless plating method, or the like.
- the charging layer 14 is obtained by mixing atomized titanium dioxide 32 with a silicone liquid and spin-coating the first electrode 12 to form a thin layer of 1000 nm or more, and then baking at about 300 ° C. At this stage, the charging layer 14 is irradiated with ultraviolet rays to change the photoexcitation structure of the titanium dioxide 32 to form a new intermediate band.
- the quantum battery 10 is manufactured by further laminating 150 nm of nickel oxide as the p-type metal oxide semiconductor layer 16, laminating 300 nm of copper as the second electrode 18 and 50 nm of chromium as the passive layer 19.
- the heating in the firing process causes cracks in the first electrode.
- the linear expansion coefficient due to heat is 9.9 ppm / ° C for glass, 46 ppm / ° C for polyimide, 6.2 ppm / ° C for chromium, and 16.6 ppm / ° C for copper. Compared to chromium and copper, the linear expansion coefficient of polyimide is extremely large.
- FIG. 6 is a schematic diagram for explaining a state in which cracks are generated by heating during the firing process of the charge layer 14.
- a polyimide layer 56 is formed on a glass plate 54, a chromium layer 58 is laminated as a passive layer with a copper layer 60 interposed therebetween, and the charging layer 14 is spin-coated.
- the polyimide layer 56 and the metal electrodes thermally expand in the direction of the arrow shown in FIG. Since the linear expansion coefficient of polyimide is extremely large with respect to chromium and copper, a large tensile force is applied to the metal electrode, and cracks occur when the limit is exceeded. As a result, cracks also occur in the charge layer 14.
- FIG. 7 shows a metal electrode composed of a 300 nm thick copper layer sandwiched from both sides of a 4 ⁇ m thick polyimide layer 56 and a 50 nm thick chromium layer in order to observe the occurrence of cracks.
- This is a sample in which 62 is laminated. The sample was heated to 300 ° C. in a heating furnace, and then cooled to room temperature and taken out.
- FIG. 8 shows the surface state 64 of the metal electrode 62 in the sample. As is clear from FIG. 8, many cracks are generated. Cracks occurred on the entire electrode surface.
- This crack is due to the fact that a tensile force is generated due to a difference in thermal expansion that is greatly different between the two superimposed materials, and the metal electrode that cannot withstand the stress is torn.
- FIG. 9 shows an analysis model.
- the analysis model is a rectangular laminated plate composed of a polyimide layer 56 and a copper layer 60 and having a length in the XY axis direction of 15 mm.
- This analytical model is a linear viscoelastic model, and the thermal deformation and Mises stress are calculated by considering the thermal expansion coefficient by applying the Maxwell model.
- the laminate is isotropic and uniform in the in-plane direction, no stress is generated in the direction perpendicular to the plane, the laminate is not constrained, and a uniform temperature distribution is given. It shall be warped.
- the strain of each layer is considered independently, and the entire warpage is obtained assuming that each interface is continuous.
- FIG. 12 shows the analysis results when the temperature is 300 ° C. What is important in the analysis is the distribution state of the displacement and the Mises stress.
- the displacement in the Z-axis direction is normalized by the maximum displacement ⁇ ⁇ ⁇ with the center point set to 0, and the Mises stress is also normalized by the maximum value. Further, the length in the XY axis direction is also standardized.
- the displacement is a concentric distribution from the center point of the rectangular laminated plate, and the displacement is abruptly larger as the distance from the center point increases. Accordingly, the Mises stress also rapidly increases as the distance from the center point of the rectangular laminate plate increases.
- FIG. 13 shows an effective slit position for dispersing the stress of the electrode based on the analysis result shown in FIG. Since the stress rapidly increases as the distance from the center of the laminated plate increases, if the positions of the slits from the center are d1, d2, d3, and d4, d1> d2> It can be seen that it is effective to satisfy d3> d4.
- the electrodes divided by the slits are divided so that the tensile strength is equal to or less than the yield strength that the electrodes can withstand.
- the electrode divided by the slit is called the main electrode. Since the charge layer does not function as a charge layer in the gap formed by the slit of the main electrode, an auxiliary electrode that covers the slit in the main electrode is provided so that no gap is generated on the entire surface of the electrode.
- a slit electrode is a combination of the main electrode and the auxiliary electrode. In the slit electrode, the slit may be formed so that the tensile strength is equal to or less than the proof stress, and various patterns can be considered and will be described below.
- FIG. 14 shows an example in which a circular slit pattern is provided on the main electrode.
- the slit width of the circular slit pattern provided with the main electrode 70 may be about 10 to 100 ⁇ m, or may be a wider slit width. There is no limitation on the width of the slit, as long as the electrodes are separated by the slit.
- the circular slits 72 are formed concentrically from the center point of the rectangular electrode, and the distance between the circular slits 72 is reduced as the distance from the center point increases.
- FIG. 15 is a circular slit pattern in the auxiliary electrode for covering the slit portion of the circular slit pattern shown in FIG.
- FIG. 14A shows an auxiliary electrode 74 provided with a circular slit 76 having a wide slit width and leaving only an electrode portion sufficient to cover the slit portion of the main electrode 70.
- FIG. 14B shows an example in which a circular slit 76 similar to the main electrode is provided at a position not overlapping the slit of the main electrode 70.
- FIG. 16 shows a slit electrode in which the auxiliary electrode 74 shown in FIG. 15 is laminated on the main electrode 70 provided with the circular slit 72 shown in FIG. 16A shows a slit electrode 78 in which the auxiliary electrode 74 in FIG. 15A is stacked, and FIG. 16B shows a slit electrode 80 in which the auxiliary electrode 74 in FIG. 15B is stacked.
- the auxiliary electrode 74 has a pattern in which the slit portion of the main electrode 70 only needs to be covered with the auxiliary electrode 74.
- the auxiliary electrode 74 is also subjected to stress due to thermal expansion of polyimide, and therefore a slit is always required. .
- FIG. 17 shows a slit pattern of the main electrode 70.
- the re-dividing slits 82 are longitudinal and lateral slits passing through the central portion of the main electrode, and the portion overlapping the circular slit 76 of the auxiliary electrode is provided with a bridge 84 without the slit.
- FIG. 17B shows a slit pattern of the auxiliary electrode 74.
- the subdivision slit 86 is a slit in the diagonal direction of the auxiliary electrode 74, and a portion overlapping the circular slit 72 of the main electrode is provided with a bridge 88 without the slit.
- FIG. 18 shows a slit electrode 90 produced by superposing a main electrode 70 provided with a subdivision slit 82 and an auxiliary electrode 74 provided with a subdivision slit 86. Even if the electrodes divided by the re-dividing slits 82 and 86 are provided with bridges 84 and 88, the electrodes cover the entire charging layer even if they are overlapped with each other, so that a portion that becomes a void can be eliminated.
- the division pattern by the slits of the main electrode is not limited to a circle, and various shapes are conceivable.
- a rectangular slit 92 is shown in FIG. 19, and a corner of the rectangular slit 92 shown in FIG.
- a rectangular slit 94 is shown. This is because stress is concentrated in the same electrode pattern by rounding the corners.
- polygonal and elliptical slit patterns are conceivable, and the shape is not limited.
- the auxiliary electrode is based on the concept of covering the gap generated by the formation of the slit of the main electrode.
- a slit shape was provided.
- the cost can be reduced by using the same mask pattern.
- the electrodes are formed by the same film formation technique, for example, sputtering, vapor deposition, screen printing, etc., a further effect can be obtained in terms of cost.
- FIG. 21 shows a rectangular mesh slit electrode pattern A96 for forming the same slit for the main electrode and the auxiliary electrode.
- the electrode is divided into a rectangular shape by a mesh-like rectangular mesh slit 98, and the divided electrode 100 is arranged. In any region of this divided electrode 100, if the tensile strength is less than the yield strength, the generation of cracks in the electrode can be suppressed.
- FIG. 22 is an explanatory diagram for producing slit electrodes by forming slits of the main electrode and the auxiliary electrode by the rectangular mesh slit electrode pattern A96 shown in FIG.
- FIG. 22A shows a state where the slit positions of the main electrode and the auxiliary electrode are shifted and overlapped by the same rectangular mesh slit electrode patterns A96-1 and 96-2.
- FIG. 22B shows a rectangular mesh slit in which the same rectangular mesh slit electrode patterns A96-1 and 96-2 described in FIG. 22A are shifted to a position where the slits do not overlap to produce a main electrode and an auxiliary electrode. Electrode 102.
- FIG. 23 is an explanatory diagram in which the slit of the auxiliary electrode is formed by rotating the mask when the auxiliary electrode slit is formed by the same mask as the rectangular mesh slit electrode pattern A96 of the main electrode.
- the rectangular mesh slit electrode pattern A96-2 is rotated by 45 degrees.
- FIG. 23B shows a rectangular mesh slit electrode 104 produced by rotating the same rectangular mesh slit electrode pattern A described in FIG. 23A at the center of the electrode.
- FIG. 24 shows a rectangular mesh slit electrode pattern B106 in which the electrode divided in the vicinity of the center is enlarged and the electrode divided in the periphery is made smaller in the mesh slit pattern.
- the electrode division at the rectangular mesh slit 108 does not have to be the same electrode shape, and can be made smaller as the periphery of the electrode where strong stress occurs.
- FIG. 25 is a diagram in which slits of the main electrode and the auxiliary electrode are formed by the rectangular mesh slit electrode pattern B106 shown in FIG. 24 to produce a slit electrode.
- FIG. 25A shows a diagram in which the slit positions of the main electrode and the auxiliary electrode are shifted and overlapped by the same rectangular mesh slit electrode pattern B106-1, 106-2.
- FIG. 25 (B) shows a rectangular mesh slit in which the same rectangular mesh slit electrode patterns A106-1 and 106-2 described in FIG. 25 (A) are shifted to a position where the slits do not overlap to produce a main electrode and an auxiliary electrode. This is the electrode 112.
- FIG. 26 shows a circular mesh slit electrode pattern 114 in which the electrodes are divided into circular shapes and the stress is dispersed.
- the circular mesh slit 116 makes the electrode a circular segmented electrode 118 and eliminates corners where the stress is strong. For this reason, generation
- FIG. 27 is an explanatory diagram for producing a main electrode and an auxiliary electrode by shifting the circular mesh slit electrode pattern 114 shown in FIG.
- FIG. 27A is a diagram in which circular mesh slit electrode patterns 114-1 and 114-2 having the same shape are shifted from the main electrode and the auxiliary electrode.
- the circular electrode slit pattern 106 has a large area of the slit portion, and is shifted by the radius of the circular electrode in order to minimize the gap when overlapped.
- FIG. 27B shows a circular mesh slit electrode 120 in which a main electrode and an auxiliary electrode are produced by shifting the circular mesh slit electrode patterns 114-1 and 114-2 as described in FIG. 27A.
- the slit patterns for dividing the electrodes have been described with reference to FIGS. 21, 24, and 26. However, since the divided electrodes are separated from each other, and the same pattern is used for forming the divided electrodes of the main electrode and the auxiliary electrode, In the position where the slits of the main electrode and the auxiliary electrode overlap, a gap where no electrode is formed is generated. In order to eliminate the gap portion of the electrode, a position where the pattern is shifted is determined in advance, and a bridge for connecting the divided electrodes is provided in a portion where the slits overlap.
- FIG. 28 shows a rectangular mesh slit electrode pattern with a bridge. It was formed by a rectangular mesh slit 124 with a bridge.
- the rectangular mesh slit electrode pattern 122 with a bridge is provided with a connecting bridge 126 that connects the divided electrodes in the horizontal direction with respect to the rectangular mesh slit electrode pattern A96 shown in FIG. For this reason, the divided electrode 128 does not become an independent electrode, but the width of the connection bridge 126 is narrow and has little influence on the occurrence of cracks.
- FIG. 29 is an explanatory diagram in the case where the main mesh and auxiliary electrode patterns are shifted using the rectangular mesh slit electrode pattern 122 with bridge.
- FIG. 29A shows a positional relationship of superposition in which a main electrode is produced by a rectangular mesh slit electrode pattern 122-1 with a bridge, and an auxiliary electrode is produced by shifting the rectangular mesh slit electrode pattern 122-2 with a bridge having the same shape. Is shown.
- a rectangular mesh slit electrode pattern 122-2 with a bridge is superimposed on a rectangular mesh slit electrode pattern 122-1 with a bridge for the main electrode at a position where no gap is generated in the electrode by using a connecting bridge 126. Yes.
- FIG. 29B shows a rectangular mesh slit electrode 130 with a bridge in which a main electrode and an auxiliary electrode are produced by a rectangular mesh slit electrode pattern 122 with a bridge. There is no gap in the electrode, and charging using the entire charging layer is possible.
- FIG. 30 shows a circular mesh slit electrode pattern with a bridge.
- the circular mesh slit electrode pattern 132 with bridges formed by the circular mesh slits 134 with bridges is a connecting bridge 136 that connects the divided circular electrodes laterally with respect to the circular mesh slit electrode pattern 114 shown in FIG. Is provided.
- the position where the circular mesh slit electrode pattern 114 is shifted is determined by the shape of the radius, so the position where the connection bridge 136 is provided is also a position that naturally connects the centers of the circular electrodes. In this case as well, the width of the connecting bridge 136 is narrow and has little influence on the occurrence of cracks.
- FIG. 31 is an explanatory diagram in the case where the main mesh and auxiliary electrode patterns are shifted using the circular mesh slit electrode pattern 132 with bridge.
- FIG. 30A shows a positional relationship of superposition in which a main electrode is produced by a circular mesh slit electrode pattern 132-1 with bridge, and an auxiliary electrode is produced by shifting the rectangular mesh slit electrode pattern 132-2 with bridge of the same shape. Is shown.
- a rectangular mesh slit electrode pattern 132-2 with a bridge for an auxiliary electrode is used for a circular mesh slit electrode pattern 132-1 with a bridge for a main electrode, and a connecting bridge 126 is used at a position where no gap is generated in the electrode. Are superimposed.
- FIG. 31B shows a circular mesh slit electrode 140 with a bridge in which a main electrode and an auxiliary electrode are produced by a circular mesh slit electrode pattern 122 with a bridge. There is no gap in the electrode, and charging using the entire charging layer is possible.
- this invention includes the appropriate deformation
Landscapes
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Sustainable Energy (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Sustainable Development (AREA)
- Power Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Photovoltaic Devices (AREA)
- Secondary Cells (AREA)
- Connection Of Batteries Or Terminals (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
Description
11 基板
12 第1電極
13 主電極
14 充電層
15 補助電極
17 機能層
16 p型金属酸化物半導体層
18 第2電極
19 不動態層
20 スリット
21 n型金属酸化物半導体
22 絶縁被膜
30,48 銅
32 二酸化チタン
34 シリコーン
36 伝導帯
38 紫外線
40 価電子帯
42 電子
44 エネルギー準位
46 フェルミレベル
48 銅
50 酸化ニッケル
54 ガラス板
56 ポリイミド層
58 クロム層
60 銅層
62 金属電極
64 金属電極の表面状態
66 解析モデル
70 主電極
72,76 円形スリット
74 補助電極
78,80,90 スリット電極
82,86 再分割スリット
84,88 ブリッジ
92,94 矩形スリット
96,96-1,96-2 矩形メッシュスリット電極パターンA
98 矩形メッシュスリット
100,110,118,128,138 分割電極
102,104,112 矩形メッシュスリット電極
106,106-1,106-2 矩形メッシュスリット電極パターンB
108 矩形メッシュスリット
114,114-1,114-2 円形メッシュスリット電極パターン
116 円形メッシュスリット
120 円形メッシュスリット電極
122 ブリッジ付矩形メッシュスリット電極パターン
124 ブリッジ付矩形メッシュスリット
126,136 連結ブリッジ
130 ブリッジ付矩形メッシュスリット電極
132 ブリッジ付円形メッシュスリット電極パターン
134 ブリッジ付円形メッシュスリット
140 ブリッジ付円形メッシュスリット電極
Claims (19)
- 半導体回路用の絶縁性樹脂からなる基板に積層される電極であって、
前記電極は、前記基板との熱膨張係数の違いから生ずる製造工程でのクラック発生を防止するため、一部を切り欠いて形成したスリットを備えた主電極と、前記主電極のスリットを覆う補助電極とから構成されていること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記主電極には複数のスリットが配設され、前記主電極面の中心から遠ざかるに従いスリット間隔が狭くなっていること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記主電極のスリットは、前記主電極の中心部から同心円状に複数形成されていること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記主電極のスリットは、前記主電極の中心部を囲うように矩形状に複数形成されていること、
を特徴とする半導体回路用電極。
- 請求項3乃至4に記載の半導体回路用電極において、
前記主電極及び前記助電極に複数配設されたスリットにより分割された電極部は、さらに複数の電極に再分割する再分割スリットが配設されていること、
を特徴とする半導体回路用電極。
- 請求項5に記載の半導体回路用電極において、
前記主電極に配設される再分割スリットと、前記補助電極配設される再分割スリットとは、互いに重ならない位置に配設されていること、
を特徴とする半導体回路用電極。
- 請求項6に記載の半導体回路用電極において、
前記再分割スリットは、前記主電極及び前記補助電極に配設されている前記スリットと重なる部分には配設しないこと
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記補助電極のスリットは、前記主電極のスリットと同一のパターンをずらして配設されていること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記補助電極のスリットは、前記主電極のスリットと同一のパターンを回転して配設されていること、
を特徴とする半導体回路用電極。
- 請求項8乃至9に記載の半導体回路用電極において、
前記主電極のスリットは、電極を矩形に分割するメッシュ状であること、
を特徴とする半導体回路用電極。
- 請求項8に記載の半導体回路用電極において、
前記主電極のスリットは、電極を円形に分割すること、
を特徴とする半導体回路用電極。
- 請求項10乃至11に記載の半導体回路用電極において、
前記スリットにより分割された矩形又は円形の分割電極は、電極の中心部から離れた位置にある分割電極が中心部にある分割電極よりも小さいこと、
を特徴とする半導体回路用電極。
- 請求項8乃至9に記載の半導体回路用電極において、
前記主電極のスリットと前記補助電極のスリットが重なる部分には、スリットを設けないこと、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記主電極と前記補助電極は、酸化を防止するための不動態特性を有する金属材料であること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極において、
前記半導体回路用電極は、酸化を防止するための不動態特性を有する金属層を積層したものであること、
を特徴とする半導体回路用電極。
- 請求項13乃至14のいずれかに記載の半導体回路用電極において、
前記不動態層の金属材料は、少なくともクロム、ニッケル、チタン、モリブデンのいずれか1種、又は、クロム、ニッケル、チタン、モリブデンのいずれか1種が含まれる合金であること、
を特徴とする半導体回路用電極。
- 請求項1に記載の半導体回路用電極と、
前記半導体回路用電極から供給される電気的エネルギーにより機能する機能層と、
基板と、
を備えたことを特徴とする半導体機能素子。
- 請求項17に記載の半導体機能素子において、
前記機能層は、電気的エネルギーを充電する機能を有すること、
を特徴とする半導体機能素子。
- 請求項17に記載の半導体機能素子において、
前記機能層は、絶縁性材料で被膜された後、紫外線照射されて光励起構造変化を生じさせたn型金属酸化物半導体からなる充電層と、p型金属酸化物半導体層とであること、
を特徴とする半導体機能素子。
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/406,425 US9865908B2 (en) | 2012-06-06 | 2012-06-06 | Electrode structure of solid type secondary battery |
CN201280073767.6A CN104428899B (zh) | 2012-06-06 | 2012-06-06 | 固态型二次电池的电极结构 |
EP12878597.9A EP2860759B1 (en) | 2012-06-06 | 2012-06-06 | Electrode structure of solid type rechargeable battery |
KR20147034242A KR20150029635A (ko) | 2012-06-06 | 2012-06-06 | 고체형 2차 전지의 전극 구조 |
JP2014519753A JP5988401B2 (ja) | 2012-06-06 | 2012-06-06 | 固体型二次電池の電極構造 |
CA2872684A CA2872684C (en) | 2012-06-06 | 2012-06-06 | Electrode structure of solid type secondary battery |
PCT/JP2012/064593 WO2013183132A1 (ja) | 2012-06-06 | 2012-06-06 | 固体型二次電池の電極構造 |
TW102110733A TWI481099B (zh) | 2012-06-06 | 2013-03-26 | 固體型二次電池之電極構造 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2012/064593 WO2013183132A1 (ja) | 2012-06-06 | 2012-06-06 | 固体型二次電池の電極構造 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013183132A1 true WO2013183132A1 (ja) | 2013-12-12 |
Family
ID=49711549
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2012/064593 WO2013183132A1 (ja) | 2012-06-06 | 2012-06-06 | 固体型二次電池の電極構造 |
Country Status (8)
Country | Link |
---|---|
US (1) | US9865908B2 (ja) |
EP (1) | EP2860759B1 (ja) |
JP (1) | JP5988401B2 (ja) |
KR (1) | KR20150029635A (ja) |
CN (1) | CN104428899B (ja) |
CA (1) | CA2872684C (ja) |
TW (1) | TWI481099B (ja) |
WO (1) | WO2013183132A1 (ja) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015129051A1 (ja) * | 2014-02-25 | 2015-09-03 | 株式会社日本マイクロニクス | 二次電池搭載回路チップ及びその製造方法 |
JP2017034082A (ja) * | 2015-07-31 | 2017-02-09 | 株式会社日本マイクロニクス | 二次電池搭載チップの製造方法 |
WO2017212578A1 (ja) * | 2016-06-08 | 2017-12-14 | 三菱電機株式会社 | 半導体装置 |
WO2018025654A1 (ja) * | 2016-08-01 | 2018-02-08 | 株式会社日本マイクロニクス | 二次電池 |
US20180175293A1 (en) * | 2015-07-02 | 2018-06-21 | Kabushiki Kaisha Nihon Micronics | Battery and method of charging and discharging the same |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016028408A (ja) * | 2014-03-24 | 2016-02-25 | パナソニックIpマネジメント株式会社 | 蓄電素子及び蓄電素子の製造方法 |
CN105609570A (zh) * | 2016-02-03 | 2016-05-25 | 泰州优宾晶圆科技有限公司 | 一种肖特基二极管 |
JP6872388B2 (ja) * | 2016-05-19 | 2021-05-19 | 株式会社日本マイクロニクス | 二次電池の製造方法 |
JP6854100B2 (ja) * | 2016-08-31 | 2021-04-07 | 株式会社日本マイクロニクス | 二次電池 |
TWI618260B (zh) * | 2016-10-28 | 2018-03-11 | 行政院原子能委員會核能研究所 | 具核殼結構之量子電池的製法及其製品 |
JP7010843B2 (ja) * | 2016-12-21 | 2022-01-26 | 株式会社東芝 | 半導体固体電池 |
US10230212B1 (en) * | 2017-12-22 | 2019-03-12 | Cisco Technology, Inc. | Method and apparatus to prevent laser kink failures |
CN110010908A (zh) * | 2019-04-09 | 2019-07-12 | 深圳市致远动力科技有限公司 | 一种燃料电池及电池堆 |
CN110010910A (zh) * | 2019-04-09 | 2019-07-12 | 深圳市致远动力科技有限公司 | 一种基于阳极的固体燃料电池及其制备方法 |
CN109980257A (zh) * | 2019-04-09 | 2019-07-05 | 深圳市致远动力科技有限公司 | 一种以阴电极为支持体的电池及其制备工艺 |
CN109888308A (zh) * | 2019-04-09 | 2019-06-14 | 深圳市致远动力科技有限公司 | 一种以电解质层为基体的燃料电池及其制备方法 |
CN111129125B (zh) * | 2019-12-18 | 2022-07-12 | 武汉华星光电半导体显示技术有限公司 | Tft阵列基板 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04342172A (ja) * | 1991-05-17 | 1992-11-27 | Mitsubishi Electric Corp | 半導体装置 |
JPH08236898A (ja) | 1995-02-27 | 1996-09-13 | Matsushita Electric Ind Co Ltd | 応力緩和用接続媒体、応力緩和型実装体及び応力緩和型部品 |
JPH10223698A (ja) | 1997-02-13 | 1998-08-21 | Nec Corp | Tape−BGAタイプの半導体装置 |
JP2000114556A (ja) * | 1998-09-30 | 2000-04-21 | Sharp Corp | 太陽電池およびその製造方法 |
JP2000260811A (ja) | 1999-03-08 | 2000-09-22 | Citizen Watch Co Ltd | 半導体装置 |
JP3531866B2 (ja) | 2000-07-28 | 2004-05-31 | 独立行政法人 科学技術振興機構 | 薄膜固体リチウムイオン二次電池 |
JP2007179893A (ja) * | 2005-12-28 | 2007-07-12 | Dainippon Printing Co Ltd | 触媒層−電解質膜積層体及びその製造方法 |
JP2008071537A (ja) * | 2006-09-12 | 2008-03-27 | Nissan Motor Co Ltd | 固体酸化物形燃料電池用電極及び固体酸化物形燃料電池 |
JP2008288536A (ja) | 2007-05-21 | 2008-11-27 | Panasonic Electric Works Co Ltd | 表面実装型セラミック基板 |
JP2011178288A (ja) | 2010-03-02 | 2011-09-15 | Toyota Auto Body Co Ltd | シートベルト装置 |
WO2012046326A1 (ja) * | 2010-10-07 | 2012-04-12 | グエラテクノロジー株式会社 | 太陽電池 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0622141B2 (ja) * | 1986-08-14 | 1994-03-23 | 呉羽化学工業株式会社 | リブ高さの異なる複合電極基板及びその製造方法 |
JPH0692949B2 (ja) * | 1990-12-11 | 1994-11-16 | トステム株式会社 | 建物用雨センサー |
JP3906653B2 (ja) * | 2000-07-18 | 2007-04-18 | ソニー株式会社 | 画像表示装置及びその製造方法 |
JP4148501B2 (ja) * | 2002-04-02 | 2008-09-10 | 三井金属鉱業株式会社 | プリント配線板の内蔵キャパシタ層形成用の誘電体フィラー含有樹脂及びその誘電体フィラー含有樹脂を用いて誘電体層を形成した両面銅張積層板並びにその両面銅張積層板の製造方法 |
US20090133741A1 (en) * | 2005-09-02 | 2009-05-28 | Kyocera Corporation | Photoelectric Conversion Device and Method of Manufacturing the Same, and Photoelectric Power Generation Device |
EP1887632B1 (en) * | 2005-11-28 | 2011-01-19 | Mitsubishi Electric Corporation | Solar battery cell and method for manufacturing same |
US8034724B2 (en) * | 2006-07-21 | 2011-10-11 | Semiconductor Energy Laboratory Co., Ltd. | Method for manufacturing semiconductor device |
US20080085439A1 (en) * | 2006-09-28 | 2008-04-10 | Hilliard Donald B | Solid oxide electrolytic device |
EP2264779B1 (en) * | 2008-03-31 | 2018-09-05 | Sharp Kabushiki Kaisha | Solar cell, solar cell string and solar cell module |
KR101094635B1 (ko) * | 2009-06-24 | 2011-12-20 | 서울대학교산학협력단 | 양호한 도전성 및 투명성을 갖는 플렉시블 투명 전극 및 그의 제조 방법 |
JP5285571B2 (ja) * | 2009-10-23 | 2013-09-11 | シャープ株式会社 | 太陽電池および太陽電池の製造方法 |
JP2011176288A (ja) | 2010-02-01 | 2011-09-08 | Fujifilm Corp | 光電変換素子、薄膜太陽電池および光電変換素子の製造方法 |
CN201859886U (zh) * | 2010-05-13 | 2011-06-08 | 无锡尚德太阳能电力有限公司 | 太阳电池、网版及其太阳电池组件 |
KR101117704B1 (ko) * | 2010-06-24 | 2012-02-29 | 삼성에스디아이 주식회사 | 광전 변환 모듈과, 이의 제조 방법 |
JP2012064933A (ja) * | 2010-08-19 | 2012-03-29 | Semiconductor Energy Lab Co Ltd | 光電変換モジュール及びその作製方法 |
JP5508542B2 (ja) | 2010-10-07 | 2014-06-04 | グエラテクノロジー株式会社 | 二次電池 |
JP5594069B2 (ja) * | 2010-11-05 | 2014-09-24 | セイコーエプソン株式会社 | 電気泳動表示装置及び電子機器 |
-
2012
- 2012-06-06 WO PCT/JP2012/064593 patent/WO2013183132A1/ja active Application Filing
- 2012-06-06 KR KR20147034242A patent/KR20150029635A/ko not_active Application Discontinuation
- 2012-06-06 JP JP2014519753A patent/JP5988401B2/ja not_active Expired - Fee Related
- 2012-06-06 CN CN201280073767.6A patent/CN104428899B/zh not_active Expired - Fee Related
- 2012-06-06 EP EP12878597.9A patent/EP2860759B1/en not_active Not-in-force
- 2012-06-06 US US14/406,425 patent/US9865908B2/en not_active Expired - Fee Related
- 2012-06-06 CA CA2872684A patent/CA2872684C/en not_active Expired - Fee Related
-
2013
- 2013-03-26 TW TW102110733A patent/TWI481099B/zh not_active IP Right Cessation
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04342172A (ja) * | 1991-05-17 | 1992-11-27 | Mitsubishi Electric Corp | 半導体装置 |
JPH08236898A (ja) | 1995-02-27 | 1996-09-13 | Matsushita Electric Ind Co Ltd | 応力緩和用接続媒体、応力緩和型実装体及び応力緩和型部品 |
JPH10223698A (ja) | 1997-02-13 | 1998-08-21 | Nec Corp | Tape−BGAタイプの半導体装置 |
JP2000114556A (ja) * | 1998-09-30 | 2000-04-21 | Sharp Corp | 太陽電池およびその製造方法 |
JP2000260811A (ja) | 1999-03-08 | 2000-09-22 | Citizen Watch Co Ltd | 半導体装置 |
JP3531866B2 (ja) | 2000-07-28 | 2004-05-31 | 独立行政法人 科学技術振興機構 | 薄膜固体リチウムイオン二次電池 |
JP2007179893A (ja) * | 2005-12-28 | 2007-07-12 | Dainippon Printing Co Ltd | 触媒層−電解質膜積層体及びその製造方法 |
JP2008071537A (ja) * | 2006-09-12 | 2008-03-27 | Nissan Motor Co Ltd | 固体酸化物形燃料電池用電極及び固体酸化物形燃料電池 |
JP2008288536A (ja) | 2007-05-21 | 2008-11-27 | Panasonic Electric Works Co Ltd | 表面実装型セラミック基板 |
JP2011178288A (ja) | 2010-03-02 | 2011-09-15 | Toyota Auto Body Co Ltd | シートベルト装置 |
WO2012046326A1 (ja) * | 2010-10-07 | 2012-04-12 | グエラテクノロジー株式会社 | 太陽電池 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2860759A4 |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015159222A (ja) * | 2014-02-25 | 2015-09-03 | 株式会社日本マイクロニクス | 二次電池搭載回路チップ及びその製造方法 |
CN105264656A (zh) * | 2014-02-25 | 2016-01-20 | 日本麦可罗尼克斯股份有限公司 | 搭载二次电池的电路芯片及其制造方法 |
WO2015129051A1 (ja) * | 2014-02-25 | 2015-09-03 | 株式会社日本マイクロニクス | 二次電池搭載回路チップ及びその製造方法 |
US20180175293A1 (en) * | 2015-07-02 | 2018-06-21 | Kabushiki Kaisha Nihon Micronics | Battery and method of charging and discharging the same |
US10686210B2 (en) | 2015-07-31 | 2020-06-16 | Kabushiki Kaisha Nihon Micronics | Secondary battery mounted chip manufacturing method |
JP2017034082A (ja) * | 2015-07-31 | 2017-02-09 | 株式会社日本マイクロニクス | 二次電池搭載チップの製造方法 |
WO2017022347A1 (ja) * | 2015-07-31 | 2017-02-09 | 株式会社日本マイクロニクス | 二次電池搭載チップの製造方法 |
WO2017212578A1 (ja) * | 2016-06-08 | 2017-12-14 | 三菱電機株式会社 | 半導体装置 |
JPWO2017212578A1 (ja) * | 2016-06-08 | 2018-11-01 | 三菱電機株式会社 | 半導体装置 |
US10685932B2 (en) | 2016-06-08 | 2020-06-16 | Mitsubishi Electric Corporation | Semiconductor device |
WO2018025654A1 (ja) * | 2016-08-01 | 2018-02-08 | 株式会社日本マイクロニクス | 二次電池 |
TWI650890B (zh) * | 2016-08-01 | 2019-02-11 | Kabushiki Kaisha Nihon Micronics | 二次電池 |
US10991933B2 (en) | 2016-08-01 | 2021-04-27 | Kabushiki Kaisha Nihon Micronics | Secondary battery |
Also Published As
Publication number | Publication date |
---|---|
US9865908B2 (en) | 2018-01-09 |
TW201414055A (zh) | 2014-04-01 |
EP2860759B1 (en) | 2019-03-06 |
CN104428899B (zh) | 2017-10-03 |
TWI481099B (zh) | 2015-04-11 |
CA2872684C (en) | 2018-10-09 |
JPWO2013183132A1 (ja) | 2016-01-21 |
KR20150029635A (ko) | 2015-03-18 |
US20150155608A1 (en) | 2015-06-04 |
JP5988401B2 (ja) | 2016-09-07 |
CN104428899A (zh) | 2015-03-18 |
EP2860759A1 (en) | 2015-04-15 |
CA2872684A1 (en) | 2013-12-12 |
EP2860759A4 (en) | 2016-01-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5988401B2 (ja) | 固体型二次電池の電極構造 | |
JP5963765B2 (ja) | 繰り返し充放電できる量子電池 | |
US20190334206A1 (en) | Multiple active and inter layers in a solid-state device | |
JP2007103129A (ja) | 薄膜固体二次電池および薄膜固体二次電池の製造方法 | |
WO2020158884A1 (ja) | 固体電池およびその製造方法 | |
EP2975671B1 (en) | Thin film battery structure and manufacturing method thereof | |
KR101493569B1 (ko) | 전기 공급 시스템 및 이의 전기 공급 소자 | |
JP7474977B2 (ja) | 電池 | |
JP7437786B2 (ja) | 電池 | |
JP6688631B2 (ja) | 全固体型電極体及び電気化学セル | |
WO2020100682A1 (ja) | 固体電池 | |
KR102050439B1 (ko) | 다중 접합 박막 전지 및 그 제조 방법 | |
WO2021210287A1 (ja) | 電池 | |
US20220037713A1 (en) | Battery | |
WO2022239449A1 (ja) | 電池および積層電池 | |
WO2022153642A1 (ja) | 電池及び積層電池 | |
US20230290996A1 (en) | Battery and laminated battery | |
WO2023079792A1 (ja) | 積層電池 | |
WO2022149336A1 (ja) | 電池及び電池の製造方法 | |
KR101210372B1 (ko) | 박막전지 | |
US20240213436A1 (en) | Battery and method for manufacturing battery |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12878597 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2014519753 Country of ref document: JP Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 2872684 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012878597 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20147034242 Country of ref document: KR Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14406425 Country of ref document: US |