WO2011093126A1 - 電力貯蔵デバイスセルとその製造方法、保管方法および蓄電デバイス - Google Patents
電力貯蔵デバイスセルとその製造方法、保管方法および蓄電デバイス Download PDFInfo
- Publication number
- WO2011093126A1 WO2011093126A1 PCT/JP2011/050313 JP2011050313W WO2011093126A1 WO 2011093126 A1 WO2011093126 A1 WO 2011093126A1 JP 2011050313 W JP2011050313 W JP 2011050313W WO 2011093126 A1 WO2011093126 A1 WO 2011093126A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- electrode
- electrode layer
- current collector
- collector foil
- storage device
- Prior art date
Links
- 238000003860 storage Methods 0.000 title claims abstract description 108
- 238000000034 method Methods 0.000 title claims description 16
- 230000005611 electricity Effects 0.000 title claims description 8
- 230000008569 process Effects 0.000 title description 5
- 239000011888 foil Substances 0.000 claims abstract description 179
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 151
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 151
- 239000003990 capacitor Substances 0.000 claims abstract description 113
- 239000002245 particle Substances 0.000 claims abstract description 47
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 42
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 41
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 40
- 239000010450 olivine Substances 0.000 claims abstract description 25
- 229910052609 olivine Inorganic materials 0.000 claims abstract description 25
- 229910001416 lithium ion Inorganic materials 0.000 claims abstract description 21
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims abstract description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 53
- 230000005540 biological transmission Effects 0.000 claims description 31
- 238000004519 manufacturing process Methods 0.000 claims description 31
- 239000011230 binding agent Substances 0.000 claims description 24
- GELKBWJHTRAYNV-UHFFFAOYSA-K lithium iron phosphate Chemical compound [Li+].[Fe+2].[O-]P([O-])([O-])=O GELKBWJHTRAYNV-UHFFFAOYSA-K 0.000 claims description 23
- 239000006258 conductive agent Substances 0.000 claims description 17
- 239000010419 fine particle Substances 0.000 claims description 14
- 230000000149 penetrating effect Effects 0.000 claims description 10
- -1 lithium phosphate compound Chemical class 0.000 claims description 9
- 238000003825 pressing Methods 0.000 claims description 9
- 238000010030 laminating Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- OQPHEVHDBFEJRQ-UHFFFAOYSA-N [Li].P(O)(O)(O)=O Chemical compound [Li].P(O)(O)(O)=O OQPHEVHDBFEJRQ-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 238000003475 lamination Methods 0.000 claims 1
- 229910001386 lithium phosphate Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 230000005923 long-lasting effect Effects 0.000 abstract 1
- 230000002459 sustained effect Effects 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 84
- 230000006866 deterioration Effects 0.000 description 21
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- 239000003792 electrolyte Substances 0.000 description 15
- 239000013078 crystal Substances 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 13
- 239000002033 PVDF binder Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 13
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 13
- 238000012360 testing method Methods 0.000 description 13
- 229910052799 carbon Inorganic materials 0.000 description 11
- 239000011889 copper foil Substances 0.000 description 11
- 238000010586 diagram Methods 0.000 description 11
- 239000008151 electrolyte solution Substances 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 229910017052 cobalt Inorganic materials 0.000 description 9
- 239000010941 cobalt Substances 0.000 description 9
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 9
- 229910044991 metal oxide Inorganic materials 0.000 description 9
- 150000004706 metal oxides Chemical class 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 238000010828 elution Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000006230 acetylene black Substances 0.000 description 7
- 230000002427 irreversible effect Effects 0.000 description 7
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 6
- 239000010439 graphite Substances 0.000 description 6
- 229910002804 graphite Inorganic materials 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 238000007599 discharging Methods 0.000 description 5
- 238000005553 drilling Methods 0.000 description 5
- 239000002003 electrode paste Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000012423 maintenance Methods 0.000 description 5
- 238000011056 performance test Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 238000012544 monitoring process Methods 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910013870 LiPF 6 Inorganic materials 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- LRJNNJLCNGFADW-UHFFFAOYSA-N diethyl carbonate;1,3-dioxolan-2-one Chemical compound O=C1OCCO1.CCOC(=O)OCC LRJNNJLCNGFADW-UHFFFAOYSA-N 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000005001 laminate film Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 239000011882 ultra-fine particle Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 210000001787 dendrite Anatomy 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 229910021385 hard carbon Inorganic materials 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910000625 lithium cobalt oxide Inorganic materials 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- BFZPBUKRYWOWDV-UHFFFAOYSA-N lithium;oxido(oxo)cobalt Chemical compound [Li+].[O-][Co]=O BFZPBUKRYWOWDV-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- 239000011301 petroleum pitch Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 238000004804 winding Methods 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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/04—Hybrid capacitors
- H01G11/06—Hybrid capacitors with one of the electrodes allowing ions to be reversibly doped thereinto, e.g. lithium ion capacitors [LIC]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/32—Carbon-based
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/32—Carbon-based
- H01G11/36—Nanostructures, e.g. nanofibres, nanotubes or fullerenes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/50—Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
-
- 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
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- 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
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/058—Construction or manufacture
- H01M10/0585—Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
-
- 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
- H01M10/4264—Structural combination with electronic components, e.g. electronic circuits integrated to the outside of the casing with capacitors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1393—Processes of manufacture of electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
- H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
- H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/661—Metal or alloys, e.g. alloy coatings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/50—Methods or arrangements for servicing or maintenance, e.g. for maintaining operating temperature
- H01M6/5072—Preserving or storing cells
-
- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
-
- 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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/60—Other road transportation technologies with climate change mitigation effect
- Y02T10/70—Energy storage systems for electromobility, e.g. batteries
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
- Y10T29/49115—Electric battery cell making including coating or impregnating
Definitions
- the present invention relates to a configuration of a power storage device cell incorporating a configuration of a lithium ion capacitor and a lithium ion battery, a manufacturing method thereof, a storage method, and a power storage device.
- Power storage device cells include a capacitor that physically stores electric charge and a secondary battery that stores energy through an electrochemical reaction. Although the capacitor has a low energy density, it has a high output density and can respond to rapid charge / discharge, and the secondary battery has a feature that it has a high energy density and excellent sustainability although it is inferior in instantaneous power compared to the capacitor. Therefore, if a power storage device cell having both the instantaneous power of the capacitor and the sustainability of the secondary battery can be realized, it can be used for various applications such as a hybrid vehicle and various types of brake regeneration.
- Capacitors and secondary batteries have different mechanisms for storing power as described above.
- capacitors that use electrolyte also called electric double layer capacitors, supercapacitors, electrochemical capacitors, etc.
- Lithium ion capacitor is a member of the same), which has polarizable electrodes (positive and negative electrodes) facing each other across the separator, and the electrostatic property of the electric double layer formed on the surface of the polarizable electrode in the electrolyte. Charges are stored using capacity, and are made of a material similar to that of a secondary battery.
- the inventor of the present invention pays attention to a lithium ion battery having a particularly high energy density among secondary batteries, and uses a common negative electrode for a lithium ion capacitor and a lithium ion battery that operate with a common electrolyte solution.
- a new power storage device cell having a single structure has been proposed (see, for example, Patent Document 1). As a result, an electric power storage device cell having both the instantaneous power of the electric double layer capacitor and the sustainability of the lithium ion battery could be realized.
- JP 2009-141181 A (paragraphs 0015 and 0068, FIGS. 1 and 12) JP 2007-273241 A (paragraphs 0027 to 0032, FIGS. 1 and 4)
- the copper foil used for the negative electrode of the lithium ion capacitor is used for the current collector foil of the common negative electrode, it cannot be discharged to 0 V unlike the electric double layer capacitor, and the terminal voltage is at least. If a voltage of 1 V or higher is not maintained, copper will be eluted and cause irreversible degradation. Therefore, at the time of charging / discharging, it is necessary to always monitor not only the upper limit value of the terminal voltage but also the lower limit value of the terminal voltage (see, for example, Patent Document 2). In addition, even when stored, if the terminal voltage is not maintained at 1V or more, it deteriorates, so that the positive electrode and the negative electrode cannot be short-circuited and retained as in the case of an electric double layer capacitor. It was necessary to keep it in, and management was difficult.
- the present invention has been made to solve the above-described problems.
- the lower limit voltage is drastically lowered to enable a low terminal voltage with a terminal voltage of 0.1 V or less, and deterioration due to overdischarge is eliminated.
- the present invention provides a power storage device cell that does not require monitoring of the lower limit value of the terminal voltage.
- the power storage device cell includes a first electrode in which a first electrode layer containing activated carbon fine particles is formed on one surface of a first current collector foil made of aluminum, and a second electrode made of aluminum.
- a power storage device cell in which a lithium ion battery is formed as a common negative electrode with the capacitor, and the first electrode and the second electrode are short-circuited, and the second electrode layer has an olivine structure.
- the third electrode layer is composed of lithium titanate particles as a main component, and includes phosphoric acid lithium compound particles.
- FIG. 1 It is a partial cross section schematic diagram of the electric power storage device cell concerning Embodiment 1 of this invention. It is a figure for demonstrating the effect of this invention, Comprising: The figure which shows the relationship between the electric potential at the time of using a cobalt-type metal oxide lithium for a positive electrode, and using graphite-type carbon for a negative electrode in the conventional cell structure. It is. It is a figure for demonstrating the effect of this invention, Comprising: The figure which shows the relationship between the electric potential at the time of using the olivine type lithium iron phosphate for a positive electrode, and using graphite-type carbon for a negative electrode in the conventional cell structure. It is.
- the capacitor positive electrode which has the particle
- a diagram for explaining the effects of the present invention, the lithium titanate of the power storage device cell according to the first embodiment of the present invention, the general formula Li X Ti 5 O 12 when charging rate 0% (4.
- FIG. 1 is a cross-sectional view showing a partial configuration of the power storage device cell according to the first embodiment of the present invention.
- an electric power storage device cell includes a capacitor positive electrode 11a in which a capacitor positive electrode layer 8 containing activated carbon fine particles is formed on the lower surface of an aluminum current collector foil 10a, and an aluminum current collector foil 10b.
- An aluminum current collector foil having a lithium positive electrode 11b in which a lithium positive electrode layer 9 including particles of an olivine-type lithium iron phosphate, which is a kind of a phosphate-type lithium compound having an olivine-type structure, is formed on the upper surface and a transmission hole 4 3, a common negative electrode 7 in which a capacitor negative electrode layer 5 and a lithium negative electrode layer 6 are formed on the upper surface and the lower surface, respectively, a first separator 12 made of a porous insulating film, and a second made of a porous insulating film.
- the separator 13 is provided with a first separator between the capacitor positive electrode layer 8 and the surface of the common negative electrode 7 on which the capacitor negative electrode layer 5 is formed.
- the capacitor portion is formed by sandwiching the data 12, and the lithium battery portion is formed by sandwiching the second separator 13 between the lithium positive electrode layer 9 and the surface of the common negative electrode 7 on which the lithium negative electrode layer 6 is formed.
- the capacitor positive electrode 11a and the lithium battery positive electrode 11b are short-circuited.
- the negative electrode of the capacitor unit and the lithium battery unit are shared by the common negative electrode 7, and the capacitor positive electrode 11a and the lithium positive electrode 11b are short-circuited. Therefore, when charging / discharging, Li ions between the capacitor part and the lithium battery part can move quickly through the transmission hole 4 provided in the common negative electrode 7, so that the capacitor part can also participate in charging / discharging and rapidly. It becomes possible to handle charging and discharging.
- a common negative electrode 7 includes a capacitor negative electrode layer 5 mainly composed of lithium titanate particles and lithium on the front and back sides of an aluminum negative electrode current collector foil 3 in which a plurality of transmission holes are dispersed in a plane. It is configured by forming the battery negative electrode layer 6.
- the positive electrode is configured as a hybrid positive electrode 11 in which a capacitor positive electrode layer 8 containing activated carbon particles and a lithium battery positive electrode layer 9 containing olivine type lithium iron phosphate particles are formed on the front and back of the positive electrode current collector foil 10. Yes.
- the capacitor positive electrode layer 8 and the capacitor negative electrode layer 5 are opposed to each other via the first separator 12 to form a capacitor portion.
- the lithium ion battery positive electrode layer 9 and the lithium battery negative electrode layer 6 are connected to the second separator 13.
- the hybrid cathode 11 of the same specification in which the capacitor positive electrode layer 8 is formed on one surface of the current collector foil 10 and the lithium battery positive electrode layer 9 is formed on the other surface is shown in FIG. Therefore, the role of 11a is changed to the positive electrode of the capacitor and the role of 11b is changed to the positive electrode of the lithium battery.
- the capacitor positive electrode provided with the capacitor positive electrode layer 8 on one side (lower side) of the strip-shaped positive electrode current collector foil 10a, the first separator 12, the common negative electrode 7, the second separator 13, and the positive electrode
- the capacitor positive electrode provided with the capacitor positive electrode layer 8 on one side (lower side) of the strip-shaped positive electrode current collector foil 10a, the first separator 12, the common negative electrode 7, the second separator 13, and the positive electrode
- a so-called stacked power storage device is configured.
- the parallel laminated type it is desirable to arrange the common negative electrode 7 at both ends on the outermost layer. If the hybrid positive electrode 11 is disposed in the outermost layer, the capacitor positive electrode layer 8 or the lithium battery positive electrode layer 9 may be at a high potential and may be deteriorated.
- the outermost layers at both ends are the capacitor negative electrode provided with the capacitor negative electrode layer 5 on one side of the strip-shaped negative electrode current collector foil, and the lithium battery negative electrode layer 6 on one side of the negative electrode current collector foil.
- a lithium battery negative electrode provided with can also be used.
- a negative electrode current collector foil having no transmission hole may be used.
- the outermost layers at both ends are a capacitor positive electrode provided with a capacitor positive electrode layer 8 on one side of a strip-like positive electrode current collector foil, and a lithium battery positive electrode provided with a lithium battery positive electrode layer 9 on one side of the positive electrode current collector foil. It can also be used.
- the outermost layer is preferably the first separator 12 in contact with the common negative electrode 7. If the outermost layer is the second separator 13 in contact with the hybrid positive electrode 11, the capacitor positive electrode layer 8 or the lithium battery positive electrode layer 9 has a high potential and may be deteriorated.
- the capacitor negative electrode layer 5 and the lithium battery negative electrode layer 6 are mainly composed of lithium titanate particles, and a binder such as PVDF and a conductive agent such as acetylene black are mixed.
- the lithium titanate particles are desirably fine particles of less than 1 ⁇ m, and carbon fibers may be mixed in order to improve conductivity.
- ultrafine particles of lithium titanate having a level of several nanometers may be supported on carbon fibers such as carbon nanotubes and carbon nanohorns.
- Capacitor positive electrode layer 8 is made of phenol resin, petroleum pitch, petroleum coke, coconut husk, etc. as raw materials, water vapor activated or alkali activated particles having an average particle size of about 1 to 10 ⁇ m, and styrene butylene rubber. It is configured by mixing a conductive agent such as a polyethylene binder, a polytetrafluoroethylene binder, or acetylene black. Carbon particles called nanogate carbon or nanostorage carbon may be used instead of activated carbon.
- particles of lithium iron phosphate compound having an olivine type structure are mainly composed of particles having carbon ultrafine particles attached thereto, and a binder such as PVDF and acetylene. It is configured by mixing with a conductive agent such as black.
- a part of iron of lithium iron phosphate may be substituted with at least one transition metal element such as manganese or cobalt.
- the negative electrode current collector foil 3 includes a punching metal aluminum foil or an expanded metal aluminum foil having a thickness of about 10 ⁇ m to 20 ⁇ m, in which the transmission holes 4 are formed in the surface in advance. An etching foil in which holes are formed by chemical etching may be used.
- the capacitor negative electrode layer 5 and the lithium battery negative electrode layer 6 can be formed and used on the front and back.
- As the positive electrode current collector foil 10 an aluminum foil having a thickness of 7 ⁇ m or more and 50 ⁇ m or less can be used.
- an electrolytic solution containing LiPF 6 as an electrolyte in an organic solvent can be used, which is shared by the capacitor unit and the lithium battery unit.
- organic solvent for example, propylene carbonate (PC), ethylene carbonate (EC) and diethyl carbonate (DEC) can be used.
- the first separator 12 and the second separator 13 are, for example, porous having a thickness of about 10 to 50 ⁇ m, a porosity (porosity) of about 60 to 80% by volume, and an average pore diameter of about several to several tens of ⁇ m.
- An insulating film such as cellulose, polyethylene, or polypropylene can be used.
- FIG. 2 shows the relationship between the potential and the charge rate when cobalt-based metal oxide lithium is used for the positive electrode and graphite-based carbon is used for the negative electrode.
- the charge rate is generally called SOC (State of Charge), and is an index that defines 0 to 100% with the chargeable / dischargeable amount of electricity as 100%.
- the minimum required voltage is about 2.5V, and when it is much lower than this, for example, when it drops to 1V or less due to an external short circuit or the like, the copper foil is eluted and is extremely large. Since the deterioration has occurred, the battery itself must be replaced.
- FIG. 3 shows the relationship between the potential and the charging rate when olivine type lithium iron phosphate is used for the positive electrode and graphite-based carbon is used for the negative electrode, and the positive electrode material is changed with respect to the system of FIG. It is a relationship in the case of. Also in FIG. 3, when the charge rate becomes close to 0% due to overdischarge, the negative electrode potential also rises and the positive electrode potential falls. When the negative electrode potential rises, the copper foil starts to be slightly eluted, resulting in irreversible and rapid deterioration. If the positive electrode potential is too low, the crystal structure of the olivine-type lithium iron phosphate changes, leading to irreversible degradation.
- olivine type lithium iron phosphate is used for the positive electrode and graphite-based carbon is used for the negative electrode, an alarm is issued when the minimum voltage exists and falls below that. It is necessary to constantly monitor the lower limit voltage.
- the minimum required voltage at that time is about 1V, which is smaller than the case where a cobalt-based material is used.
- the voltage drops to 0.5V or less due to an external short circuit or the like. Since the copper foil has undergone extremely large deterioration such as elution, the battery itself must be replaced.
- FIG. 4 shows the relationship between the potential and the charge rate when cobalt-based metal oxide lithium is used for the positive electrode and lithium titanate is used for the negative electrode.
- the negative electrode material is changed with respect to the system of FIG. It is a relationship in the case of. Also in FIG. 4, when the charge rate becomes close to 0% due to overdischarge, the negative electrode potential also rises and the positive electrode potential falls. When lithium titanate is used, the negative electrode potential becomes higher than 1 V, so that an aluminum foil instead of a copper foil can be used as the negative electrode current collector foil.
- FIG. 5 shows the relationship between the potential and the charging rate when olivine type lithium iron phosphate is used for the positive electrode and lithium titanate is used for the negative electrode. This is the relationship when both are changed. Also in FIG. 5, when the charge rate becomes close to 0% due to overdischarge, the negative electrode potential also increases and the positive electrode potential decreases.
- lithium titanate aluminum foil instead of copper foil can be used for the negative electrode current collector foil, and even if the negative electrode potential rises, elution of the copper foil does not occur. However, if lithium is excessively extracted from lithium titanate, the potential rises and the crystal system changes, and if the potential rises too much, it leads to deterioration.
- olivine type lithium iron phosphate is used for the positive electrode and lithium titanate is used for the negative electrode, for example, when it drops to near 0 V due to an external short circuit or the like, olivine type lithium iron phosphate or titanium is used. Deterioration due to a change in the crystal system of lithium acid becomes remarkable.
- the charging rate is 0%, and the lower limit of the terminal voltage can be reduced to 0.1 V or less.
- FIG. 6 and FIG. 7 show the potential diagrams of the lithium battery unit in the power storage device cell according to the first exemplary embodiment of the present invention.
- FIG. 6 shows a hybrid positive electrode composed of a capacitor positive electrode mainly composed of activated carbon particles and a lithium battery positive electrode mainly composed of olivine type lithium iron phosphate as a positive electrode, and lithium titanate particles as a main negative electrode. This shows the relationship between the potential and the charging rate when used as.
- olivine type lithium iron phosphate is used for the positive electrode and lithium titanate is used for the negative electrode.
- the positive electrode of the capacitor part and the lithium battery part are short-circuited, It has a different curve due to the influence of.
- a significant difference in the charging rate range from 90% to 100% is the potential of the hybrid positive electrode (one-dot chain line), and there is a portion that decreases at a constant slope from 4.3 V to 3.5 V due to the influence of the capacitor positive electrode. This part is based on the discharge from the capacitor. Similarly, even in the region of 10% to 0%, there is a portion based on the discharge from the capacitor, and an inclination occurs. For this reason, it is significantly lower than the case of olivine-type lithium iron phosphate alone (solid line). On the other hand, the potential of the common negative electrode (two-dot chain line) is also affected by the capacitor portion, and increases more than in the case of only lithium titanate (dashed line).
- the terminal voltage is lower than 0.1 V when the charging rate is 0%.
- the terminal voltage is less than 0.1 V, there is an internal resistance, so that it is substantially difficult to extract current, and deterioration due to overdischarge does not occur. Therefore, it is possible to eliminate the need for constant monitoring of the minimum voltage.
- FIG. 7 uses a hybrid positive electrode of a capacitor positive electrode mainly composed of activated carbon particles and a lithium battery positive electrode mainly composed of olivine type lithium iron phosphate as a positive electrode, and titanic acid as a common negative electrode.
- the relationship between the potential and the charging rate when lithium particles are used as the main component is shown.
- the difference from FIG. 6 is that when the composition of lithium titanate, which is the electrode material of the common negative electrode 7, is 0%, the crystal of the general formula Li X Ti 5 O 12 (4.0 ⁇ x ⁇ 4.1) It was adjusted to include the system.
- the liquid still has room for accepting lithium ions, and further lithium ions are released from the lithium titanate, resulting in a crystal system having the general formula Li X Ti 5 O 12 (4.0 ⁇ x ⁇ 4.1).
- the terminal voltage can be reduced to 0V when the charging rate is 0%.
- the positive electrode and the negative electrode can be safely short-circuited using a metal wire or the like, and can be safely carried, transported, installed and removed.
- the effect of increasing durability at high temperatures can be obtained. That is, the power storage device cell and the electricity storage device according to the embodiment of the present invention can be safely stored by short-circuiting the positive electrode terminal and the common negative electrode that are short-circuited between the lithium battery positive electrode and the capacitor positive electrode.
- the terminal voltage may become a negative voltage in some power storage device cells at the end of discharge.
- the charging rate is 0%
- the terminal voltage becomes negative if the general formula Li X Ti 5 O 12 (4.0 ⁇ x ⁇ 4.1) is adjusted. Therefore, the deterioration during overdischarge can be drastically improved.
- the positive electrode was not a hybrid positive electrode, but a positive electrode dedicated to a lithium battery positive electrode and a positive electrode dedicated to a capacitor positive electrode were used.
- PVDF polyvinylidene fluoride
- This negative electrode was cut into a 32 mm ⁇ 52 mm strip, a 20 mm ⁇ 20 mm portion was cut from the corner, and a 7 mm ⁇ 20 mm tab portion was provided as a current terminal tab portion.
- capacitor positive electrode As a capacitor positive electrode layer, an electrode paste made of activated carbon having an average particle diameter of 5 ⁇ m, an acrylic polymer as a binder, and water as a solvent was mixed and prepared. Next, this paste was applied to one surface of a current collector foil 10C made of pure aluminum having a width of 300 mm and a thickness of 50 ⁇ m to form a capacitor positive electrode layer 8 having a thickness of 100 ⁇ m to obtain a capacitor positive electrode 11C.
- This positive electrode 11C is cut into a 30 mm ⁇ 50 mm strip, a 23 mm ⁇ 20 mm portion is cut from the corner, a 7 mm ⁇ 20 mm tab portion is provided, the capacitor positive electrode layer 8 in that portion is peeled off, and the foil portion is exposed.
- Current terminal tab is cut into a 30 mm ⁇ 50 mm strip, a 23 mm ⁇ 20 mm portion is cut from the corner, a 7 mm ⁇ 20 mm tab portion is provided, the capacitor positive electrode layer 8 in that portion is peeled off, and the foil portion is exposed.
- Current terminal tab is cut into a 30 mm ⁇ 50 mm strip, a 23 mm ⁇ 20 mm portion is cut from the corner, a 7 mm ⁇ 20 mm tab portion is provided, the capacitor positive electrode layer 8 in that portion is peeled off, and the foil portion is exposed.
- Current terminal tab is cut into a 30 mm ⁇ 50 mm strip, a 23 mm ⁇ 20 mm portion is
- olivine type lithium iron phosphate having an average particle size of 5 ⁇ m
- acetylene black and polyvinylidene fluoride (PVDF) as a binder are n-methylpyrrolidone ( NMP) and dried at 100 ° C. to form a lithium battery positive electrode layer 9 having a thickness of 100 ⁇ m and hot roll pressed at 150 ° C. to obtain a lithium battery positive electrode 11L.
- NMP n-methylpyrrolidone
- This positive electrode 11L is cut into a 30 mm ⁇ 50 mm strip, a 23 mm ⁇ 20 mm portion is cut from the corner, a 7 mm ⁇ 20 mm tab portion is provided, the lithium battery positive electrode layer 9 is peeled off, and the foil portion is exposed. It was set as the current terminal tab part.
- Capacitor positive electrode 11C (only one side of electrode layer 8 is formed), common negative electrode 7, and lithium battery positive electrode 11L (only one side of electrode layer 9 is formed) are laminated in such a manner that the respective electrode layers face each other, with a thickness between them.
- a 35 ⁇ m cellulosic paper separator was sandwiched one by one.
- the current collector tabs of the two positive electrodes 11C and 11L were overlapped, and an aluminum foil was connected to the current collector tab by ultrasonic welding (short circuit) to obtain a positive electrode current collector terminal TP. As shown in FIG.
- FIG. 8 is a semi-transparent view of a test cell with an aluminum laminate sheath.
- an aluminum laminate film exterior 19 is folded in two and three sides are heat-sealed 20 with a thermoplastic resin.
- the current terminal portions TP and TN are heat-sealed to the exterior after mounting the thermoplastic resin 17 with improved adhesion to metal.
- the exterior 19 is longer than the size of the electrode part because the gas accompanying deterioration from the electrode when performing a charge / discharge test by applying a surface pressure to the electrode part of 3 cm ⁇ 3 cm. This is because the gas generated in the extended exterior portion can be accumulated even if the gas is generated so that the test can be continued.
- the negative electrode 7 has an outer shape that is 1 mm larger than the positive electrodes 11C and 11L on all four sides, thereby preventing measurement errors due to misalignment between the positive electrode and the negative electrode.
- Example 2 The electrolytic solution was the same as Example 1 except that a mixed solvent of ethylene carbonate-diethyl carbonate 3: 7 containing 1.2 mol / l LiPF 6 was used.
- Capacitor negative electrode layer 5 and lithium negative electrode layer 6 were prepared using, as common negative electrode current collector foil 3, a copper foil containing graphite-based carbon particles as a main component and punched and provided with a through-hole instead of an aluminum foil. Except for this, it was the same as Example 1.
- Example 1 was the same as Example 1 except that the lithium negative electrode layer 6 was prepared using fine particles of lithium cobalt oxide.
- Table 1 summarizes the evaluation results of Examples 1 and 2 and Comparative Examples 1 and 2.
- Example 2 has a higher capacitance maintenance ratio than Example 1, and is more stable than Example 1. Is clear.
- the positive electrode and the negative electrode were further electrically short-circuited using a clip and held at room temperature for one month, and charged and discharged three times to examine the capacitance.
- the capacitance retention rate was maintained at a high value of 96%, and the internal resistance was not increased, so that it was clarified that it could be retained by an electrical short circuit.
- the first electrode layer including the activated carbon fine particles on one surface of the first current collector foil 10a made of aluminum.
- the first electrode (capacitor positive electrode) 11a in which the capacitor positive electrode layer 8 is formed, and the lithium battery positive electrode layer 9 as the second electrode layer is formed on one surface of the second current collector foil 10b made of aluminum.
- a transmission hole 4 is formed in the third current collector foil 3, and the first electrode layer 8 and the second separator 13 are formed. 3 between the first electrode 12 and the surface on the electrode 5 side.
- a capacitor having the third electrode 7 as a negative electrode is formed by sandwiching the second separator 13 between the second electrode layer 9 and the surface of the third electrode 7 on the electrode layer 6 side.
- the third electrode layers 5 and 6 are mainly composed of lithium titanate particles and the third current collector foil 3 is formed of an aluminum foil, the third electrode layers 5 and 6 are composed of aluminum foil.
- a low terminal voltage of 0.1V or less can be achieved, the deterioration due to overdischarge can be eliminated, and a power storage device cell that does not require monitoring of the lower limit value of the terminal voltage can be obtained.
- the composition of lithium titanate is such that the general formula Li x Ti 5 O 12 (4.0 ⁇ x ⁇ 4.1) Even if the terminal voltage is completely 0V, no deterioration occurs.
- FIG. FIG. 9 is a schematic cross-sectional view of a power storage device cell according to the second embodiment of the present invention.
- a transmission hole of the current collector foil is formed by a through hole penetrating the common negative electrode.
- the common negative electrode 207 is made of an aluminum foil having a thickness of about 10 ⁇ m to 20 ⁇ m with no through holes formed as the material of the negative electrode current collector foil 203, and a paste in which hard carbon particles and graphite particles are mixed is applied to the front and back sides.
- Kenzan a tool for fixing the roots of flowers and branches
- a plurality of needles are arranged upward on a metal stand.
- a through-hole 14 that physically penetrates the common negative electrode 207 is formed by using a needle-like object having a sharp tip like that in the plane. That is, after the electrode layer is applied to the aluminum foil before drilling, the protrusions are pressed to form the through holes 14, and the current collector foil 203 portion of the through term 14 is made of the current collector foil of the first embodiment.
- a permeation hole was formed.
- the large number of through-holes 14 penetrating the entire thickness direction of the common negative electrode 207 keeps the electrochemical potential of the common negative electrode 207 constant, and there is a risk of corrosion due to local high potential or low potential of the capacitor positive electrode 11a or the lithium battery positive electrode 11b.
- the effect which can reduce a property significantly is acquired.
- the electrolyte and ions can be quickly moved between the front and back separators 12 and 13 through the through-holes 14, they quickly respond to the expansion and contraction of the electrodes and prevent deterioration due to rapid charge and discharge. Effect is obtained.
- an electrode layer can be apply
- FIG. 9 shows the case where the electrode layers 205 and 206 are formed on both sides of the negative electrode current collector foil 203
- the present invention is not limited to this.
- the through-hole 14 can be formed after the electrode layer is formed, and the electrolyte and ions can be quickly moved between the separators 12 and 13 on the front and back sides.
- the common negative electrode 207 that is the third electrode is provided with the through hole 14 that penetrates the thickness direction of the common negative electrode 207. Therefore, the electrolyte moves smoothly between the capacitor side and the lithium battery side, and the response to rapid charge / discharge is improved.
- the third electrode layer 205 is formed before the transmission hole is formed in the negative electrode current collector foil 203 which is the third current collector foil. , 206 is applied, and the protrusions are pressed to form the through holes 14 after application, so that the current collector foil can be provided with transmission holes and the electrode layer can be applied satisfactorily. And quality is stable.
- FIG. FIG. 10 is a schematic sectional view of a power storage device cell according to the third embodiment of the present invention.
- the through hole penetrating the entire common negative electrode is provided.
- the shape of the through hole penetrating the entire common negative electrode is conical, and the capacitor negative electrode Two types (two directions) of through holes 314A narrowing toward the layer side and through holes 314B narrowing toward the lithium battery negative electrode layer side are provided. Therefore, the protrusions are pressed from both the capacitor negative electrode layer 305 side and the lithium battery negative electrode layer 306 side.
- a drilling method for the common negative electrode 307 for example, a metal mold in which quadrangular pyramid protrusions having a base of 0.4 mm and a height of 0.7 mm are formed at intervals of 0.8 mm, and the surface is formed. It can be formed by installing a common negative electrode 307 having electrode layers 305 and 306 coated on both sides between smooth metal plates, and performing an operation of pressing at a pressure of about 0.3 MPa on the front side and the back side. In addition, a large number of holes can be made in the same manner by turning it upside down on a roller with a needle and passing it twice.
- the through-hole 30 having a quadrangular pyramid configured from the front and back surfaces of the common negative electrode 307 facilitates the selective flow of the electrolyte in the narrowing direction.
- the electrolyte from the first separator 12 to the second separator 13 is transmitted through the through-hole 314B.
- the electrolyte solution is easily moved from the second separator 13 to the first separator 12 to make the lithium ion concentration uniform, and the generation of lithium dendrite near the through hole in the current collector foil 303 is prevented. The effect of suppressing is acquired.
- the opening area of the portion corresponding to the transmission hole of the current collector foil 303 is preferably 1 to 50 area%, more preferably 5 to 20 area%, with respect to the total area of the negative electrode current collector foil 303. If it is in the range of 1 to 50 area%, both ionic conductivity and electrical conductivity can be ensured, and if it is in the range of 5 to 20 area%, the balance between ionic conductivity and electrical conductivity is good. At the same time, the strength of the current collector foil can be sufficiently maintained.
- the opening area By changing the opening area, the ion conduction resistance when passing through the through-holes 314A and 314B changes, so that the difference in electrochemical potential between the capacitor part and the lithium battery part can be controlled, and the opening area can be reduced. As a result, the difference in electrochemical potential increases, and the electrochemical potential of the lithium battery section changes slowly.
- the third electrode layers 305 and 306 are provided on both surfaces of the third current collector foil 303, and as the through holes, The first through hole 314B and the first through hole 314B that become narrower from the one surface side where the electrode layer 305 of the third electrode 307 is provided toward the other surface side where the electrode layer 306 is provided.
- the method for manufacturing the power storage device cell according to the third exemplary embodiment of the present invention after applying the paste for forming the electrode layers 305 and 306 on the both sides of the metal foil on the through holes 314A and 314B, respectively. Since the projection is pressed from the surface, the electrode layer can be applied satisfactorily and the quality is stabilized.
- the hole formed in the current collector foil when the through hole is opened is the electrolyte transmission hole.
- the transmission hole is formed separately from the through hole, the through hole Needless to say, the effect of smoothing the movement of the electrolyte can be obtained.
- Embodiment 4 FIG. FIG. 11 is a cross-sectional schematic diagram of the electric power storage device cell concerning Embodiment 4 of this invention.
- the common negative electrode 407 has a capacitor negative electrode layer 405 formed on one surface of the current collector foil 403, and the other surface of the current collector foil 403 has a lithium battery part side. That is, an electrical insulating layer 18 is formed.
- the electrical insulating layer 18 is preferably a film such as polyethylene or polypropylene, or a layer coated with PVDF.
- the capacitor negative electrode layer 5 also functions as the lithium battery negative electrode layer 6.
- the conical through hole 414 that penetrates the entire common negative electrode 407 including the electric insulating layer 18 is formed from the electric insulating layer 18 side, and becomes narrower from the electric insulating layer 18 side toward the capacitor negative electrode layer 405. It is supposed to be.
- a large number of through holes 414 can be opened by passing the common negative electrode 407 through a roller having a needle so that the electric insulating layer 18 side faces the needle.
- the porosity is preferably 30% or more and 70% or less. When the porosity is less than 30%, the function of the capacitor negative electrode layer 5 as the lithium battery negative electrode layer 6 is lowered. On the other hand, if the open area ratio exceeds 70%, the performance of the negative electrode layer may be reduced due to a decrease in area.
- the lithium battery positive electrode layer 9 includes particles of olivine type lithium iron phosphate, and the electrode layer of the common negative electrode 7 is titanic acid. It is important that the current collector foil 3 made of lithium particles as a main component and the common negative electrode current collector foil 3 be an aluminum foil, and the terminal voltage when the filling rate is 0% can be lowered to prevent deterioration. Furthermore, since the electrical insulating layer 18 is provided on the surface of the negative electrode current collector foil 403 where the electrode layer is not provided, a portion of the current collector foil that does not contribute to the reaction does not come into contact with the electrolyte. Elution (corrosion) of current collector foil can be suppressed.
- the common negative electrode 407 serves as a surface facing the capacitor positive electrode layer 8 through the separator 12 of the current collector foil 403.
- An electrode layer 405 is formed on the surface, and the insulating film 18 is provided on the other surface that faces the electrode layer 9 with the separator 13 of the current collector foil 403 interposed therebetween. Since the through-hole 414 passing through the thickness direction of the common negative electrode 407 to be narrowed is provided, the portion of the current collector foil that does not contribute to the reaction does not come into contact with the electrolytic solution, and the collector does not contact the electrolyte solution. Elution (corrosion) of the foil can be suppressed.
- FIG. FIG. 12 is a schematic cross-sectional view of a power storage device cell according to Embodiment 5 of the present invention.
- the common negative electrode 507 has a lithium battery negative electrode layer 507 formed on one surface of the current collector foil 503, and the capacitor surface, which is the other surface of the current collector foil 503, has an electric An insulating layer 518 is formed.
- the common negative electrode 507 has a configuration opposite to that of the common negative electrode 407 in the fourth embodiment in the thickness direction.
- the lithium battery negative electrode layer 506 also functions as the capacitor negative electrode layer 505.
- the conical through hole 514 penetrating the entire common negative electrode 507 is formed from the electric insulating layer 518 side, and becomes narrower from the electric insulating layer 518 side toward the lithium negative electrode layer 506.
- a large number of through holes 514 can be opened by passing the common negative electrode 507 through a roller having a needle so that the electrical insulating layer 518 side faces the needle.
- the porosity is preferably 30% or more and 70% or less. When the porosity is less than 30%, the function of the capacitor negative electrode layer 5 as the lithium battery negative electrode layer 6 is lowered. On the other hand, if the open area ratio exceeds 70%, the performance of the negative electrode layer may be reduced due to a decrease in area.
- the lithium battery positive electrode layer 9 includes particles of olivine type lithium iron phosphate, and the electrode layer of the common negative electrode 7 is titanic acid. It is important that the current collector foil 3 made of lithium particles as a main component and the common negative electrode current collector foil 3 be an aluminum foil, and the terminal voltage when the filling rate is 0% can be lowered to prevent deterioration. Also in this embodiment, since the electrical insulating layer 518 is provided on the surface of the negative electrode current collector foil 503 where the electrode layer is not provided, the portion of the metal portion of the aluminum current collector foil that does not contribute to the reaction is the electrolyte solution. The elution (corrosion) of the current collector foil can be suppressed.
- the common negative electrode 507 is provided on one surface that is the surface facing the electrode layer 9 through the separator 13 of the current collector foil 503.
- An electrode layer 506 is formed, and an insulating film 518 is provided on the other surface of the current collector foil 503 that faces the capacitor positive electrode layer 8 via the separator 12, and the electrode layer 506 moves from the insulating film 518 side toward the electrode layer 506. Since the through-hole 514 penetrating in the thickness direction of the common negative electrode 507 is formed, the portion of the aluminum metal portion of the current collector foil that does not contribute to the reaction does not come into contact with the electrolyte, and the current collector is not collected. Elution (corrosion) of the foil can be suppressed.
- FIG. 13 is a schematic cross-sectional view of a power storage device cell according to the sixth embodiment
- FIG. 14 is a flowchart for explaining a method of manufacturing the power storage device cell.
- the electrode layer 606 bites into the electrode layer 605 from the through hole 624 serving as a transmission hole in the current collector foil 603.
- a plurality of biting portions 21 are provided.
- Other configurations are the same as those of the power storage device described in the first embodiment.
- grains which comprise an electrode layer was apply
- the inside of the electrode layer 605 is reached by drilling from the side of the current collector foil 603 that is the other surface, and a reaching hole 624 that functions as a transmission hole is drilled (step S20).
- the electrode layer 606 bites into the electrode layer 605 into the plurality of biting portions 21. It becomes an electrode layer which has.
- the biting portion 21 functions as the electrode layer 605 functionally.
- the electrode density is adjusted by pressing the electrode layer after step S30 (step S40). Thereafter, the electrodes are stacked (step S50) to produce a power storage device cell.
- the inside of the reaching hole 624 drilled during the manufacturing process is filled with a plurality of biting portions 21 formed integrally with the electrode layer 606 main body, and the current collector foil 603 and the electrode layers 605 and 606 are in close contact with each other.
- the reaching hole 624 formed by the perforation may penetrate to the surface of the electrode (electrode layer 605), but may stop halfway through the electrode layer. In short, it is sufficient that lithium passes through the current collector foil 603 and a hole reaching the inside of the electrode layer 605 is formed.
- FIG. 13 when the arrival hole 624 is formed through the electrode surface, unevenness due to the penetration is formed on the electrode surface, and it is desirable to flatten this by pressing. In FIG.
- a power storage device cell can be manufactured by sequentially laminating a separator, a capacitor positive electrode, and a lithium positive electrode (or hybrid positive electrode) in the same manner as in the above embodiments.
- step S20 if step S20 is omitted, it corresponds to the manufacturing method of the first embodiment, and if step S20 is brought behind step S30, the flow corresponds to the manufacturing method of the second and third embodiments. Become.
- Embodiment 7 the current collector foil of the common negative electrode is formed with burrs extending from the periphery of the transmission hole to the electrode layer provided on at least one surface of the common negative electrode. Details will be described below.
- FIG. 15 is a schematic sectional view of a power storage device cell according to the seventh embodiment
- FIG. 16 is a flowchart for explaining a method for manufacturing the power storage device cell.
- the current collector foil 703 constituting the common negative electrode 707 is formed with burrs 22 extending from the peripheral edge of the through hole 714 to the electrode layer 706.
- Other configurations are the same as those of the power storage device described in the first embodiment or the second embodiment.
- grains which comprise an electrode layer was apply
- the burr 22 extending from the peripheral edge of the through hole 714 to the electrode layer 706 is formed on the current collector foil 703, and the electrode layer 706 is formed so as to wrap around the burr 22. Thereafter, the negative electrode 707 is pressed to adjust the electrode density (step S740), and then stacked (step S750) to manufacture a power storage device cell.
- a soft base material such as rubber is laid under the current collector foil 603 at the time of perforation, so that when the protrusions push through the current collector foil 703, the burr 22 is applied to the electrode layer 706.
- the electrode layer 706 protrudes toward the electrode layer 706 so as to open from the center of the hole.
- the electrode layer 706 is formed so as to wrap the burr 22, and thus the adhesion strength between the negative electrode layer 706 and the negative electrode current collector foil 703 is improved.
- a power storage device cell can be manufactured by sequentially laminating a separator, a capacitor positive electrode, and a lithium positive electrode (or hybrid positive electrode) in the same manner as in the above embodiments.
- the structure in the case of having an electrode layer on both surfaces of current collection foil and the manufacturing method were demonstrated, it does not necessarily need to form in both surfaces.
- the electrode layer may be applied to the surface side where the burr appears. Therefore, the perforation direction may be changed so that burrs appear on both sides of the current collector foil.
- the positive electrode is not a hybrid positive electrode, but a positive electrode dedicated to a lithium battery positive electrode and a positive electrode dedicated to a capacitor positive electrode are used. .
- PVDF polyvinylidene fluoride
- This electrode is placed between a flat metal mold in which quadrangular pyramid projections with a base of 0.4 mm and a height of 0.7 mm are formed at intervals of 0.8 mm, and a metal plate with a smooth surface, and further thereon The operation of placing an acrylic plate and pressing at a pressure of 0.5 MPa was repeated twice to obtain a common negative electrode.
- This negative electrode was cut into a 32 mm ⁇ 52 mm strip, a 20 mm ⁇ 20 mm portion was cut from the corner, and a 7 mm ⁇ 20 mm tab portion was provided as a current terminal tab portion.
- PVDF polyvinylidene fluoride
- this paste was used as a negative electrode current collector foil, coated on one side of a plain aluminum foil having a width of 300 mm and a thickness of 20 ⁇ m and dried, and then this electrode was formed into a square pyramid having a base of 0.4 mm and a height of 0.7 mm. Is installed between a flat metal mold with projections of 0.8 mm apart and a metal plate with a smooth surface, and an acrylic plate is placed on it and pressed at a pressure of 0.5 MPa to collect current The operation of drilling a reaching hole reaching the inside of the electrode layer from the foil side was repeated twice.
- PVDF polyvinylidene fluoride
- An electrode layer is placed between a flat metal mold having projections of 0.8 mm apart and a metal plate having a smooth surface, and an acrylic plate placed thereon and pressed at a pressure of 0.5 MPa.
- the operation of drilling from the side was repeated twice.
- the current collector foil was pierced by perforation, and a burr of about 90 ⁇ m was generated around the hole. Thereafter, the paste described above was applied onto the current collector foil, and an electrode layer was formed so as to wrap the burr, thereby forming a negative electrode having electrode layers on both sides. This electrode was hot roll pressed at 110 ° C. to obtain a common negative electrode.
- each example has a common negative electrode in which electrode layers are formed on both sides of the current collector foil.
- the resistivity of the electrode of Example 1 and the electrode of Example 3 in which each of the electrode layers on both sides is separated from the current collector foil is 12 ⁇ cm or more, whereas one electrode layer 606 is the other.
- the resistivity is as low as 8.5 ⁇ cm. This is because the electrode layer 606 formed later in the common negative electrode is formed so as to fill the arrival hole 724 reaching the electrode layer 605 formed earlier, so that the current collector foil 603 is suppressed by both the electrode layers 605 and 606. It is considered that the adhesion between the current collector foil 603 and the electrode layers 605 and 606 is improved.
- the electrode of Example 4 When comparing the resistivity of the electrode of Example 1 and the electrode of Example 3 with the electrode of Example 4 where the burr of the current collector foil 703 is applied to the electrode layer 706, the electrode of Example 4 is also 9.2 ⁇ cm.
- the resistivity is lower than that of the first and third electrodes. This is because the electrode layer 706 is formed so as to wrap the burr 22 generated when the through-hole 714 penetrating the current collector foil 703 is formed in the manufacturing process of the common negative electrode, so that the current collector foil 703 and the electrode layer 606 are in close contact with each other. This is thought to be due to the improvement in performance.
- the positive electrode and the negative electrode were further electrically short-circuited using a saw clip, held at room temperature for 1 month, and charged and discharged three times to obtain the capacitance. Examined. As a result, the capacitance maintenance ratio was maintained at a high value of 92%, and the internal resistance was not high, so that it was clarified that it could be held by an electrical short circuit.
- the common negative electrode 607 is provided with the electrode layers 605 and 606 on both sides of the current collector foil 603 and provided on both sides of the current collector foil 603.
- the electrode layers 605 and 606 thus obtained, at least one electrode layer 606 is configured to be provided with a plurality of biting portions 21 that bite into the other electrode layer 605 from the transmission hole 624 of the current collector foil 603. Therefore, the adhesion between the current collector foil 603 and the electrode layers 605 and 606 is improved, and a highly reliable power storage device cell is obtained.
- a conductive agent and a binder are added to the lithium titanate particles on one surface of the current collector foil 603.
- a protrusion is pressed from the other surface side of the current collector foil 603 to reach the inside of at least one of the electrode layers 605 and function as a transmission hole 614 is perforated (step S20), and a paste obtained by adding a conductive agent and a binder to lithium titanate particles is applied from the side of the surface of the current collector foil 603 pressed against the projection to fill the arrival hole 614 (step S30).
- step S the other electrode layer 606 is formed, and then the electrode 11a, the separator 12, the common negative electrode 607, the separator 13, and the electrode 11b are stacked (step S). 0) to, since it is configured to produce a power storage device cell, it is possible to easily manufacture the power storage devices described above.
- the current collector foil 703 of the common negative electrode 707 is formed with the burr 22 extending from the periphery of the transmission hole 714 to the electrode layer 703 on at least one surface.
- the adhesion between the current collector foil 703 and the electrode layer 706 is improved, and a highly reliable power storage device cell is obtained.
- the step of forming the common negative electrode 707 in the step of forming the common negative electrode 707, the surface on the opposite side of the surface of the current collector foil 703 where the electrode layer is not formed. A protrusion is pressed from the side to penetrate at least the current collector foil 703 to form a through hole 714 functioning as a transmission hole, and the burr 22 of the current collector foil 703 is formed on the surface where the through hole 714 is formed.
- the paste is applied to form the electrode layer 706, and then the electrode 11a, the separator 12, the common negative electrode 607, the separator 13, and the electrode 11b are stacked (step S40) to manufacture a power storage device cell. Therefore, the power storage device described above can be easily manufactured.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Power Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Nanotechnology (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Secondary Cells (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Hybrid Cells (AREA)
Abstract
Description
図1は、本発明の実施の形態1にかかる電力貯蔵デバイスセルの部分的な構成を示す断面図である。図において、電力貯蔵デバイスセルは、アルミニウム製の集電箔10aの図中下面に活性炭の微粒子を含むキャパシタ正極電極層8が形成されたキャパシタ正極11aと、アルミニウム製の集電箔10bの図中上面にオリビン型構造を有するリン酸型リチウム化合物の1種であるオリビン型リン酸鉄リチウムの粒子を含んだリチウム正極層9が形成されたリチウム正極11bと、透過孔4を有するアルミニウム集電箔3の上面と下面にそれぞれキャパシタ負極電極層5とリチウム負極電極層6が形成された共通負極7と、多孔質の絶縁フィルムからなる第1のセパレータ12と、多孔質の絶縁フィルムからなる第2のセパレータ13を備え、キャパシタ正極電極層8と共通負極7のキャパシタ負極電極層5が形成された面との間に第1のセパレータ12を挟持してキャパシタ部を形成し、リチウム正極層9と共通負極7のリチウム負極電極層6が形成された面との間に第2のセパレータ13を挟持してリチウム電池部を形成しキャパシタ正極11aとリチウム電池正極11bを短絡接続したものである。
図1において、共通負極7は、複数の透過孔を面内に分散して設けたアルミニウム製の負極集電箔3の表裏に、チタン酸リチウム粒子を主成分とするキャパシタ負極電極層5とリチウム電池負極電極層6を形成することにより構成される。正極としては、正極集電箔10の表裏に、活性炭粒子を含むキャパシタ正極電極層8と、オリビン型リン酸鉄リチウムの粒子を含むリチウム電池正極電極層9を形成したハイブリッド正極11として構成している。キャパシタ正極電極層8とキャパシタ負極電極層5を第1のセパレータ12を介して対峙させ、キャパシタ部を構成し、リチウムイオンの電池正極電極層9とリチウム電池負極電極層6を第2のセパレータ13を介して対峙させている。つまり、集電箔10の一方の面に、キャパシタ正極電極層8、他方の面にリチウム電池正極電極層9が形成された同仕様のハイブリッド正極11を、図1では配置の違い(使用する面の違い)により、11aをキャパシタ正極、11bをリチウム電池正極と、それぞれ役割を変えるようにしている。
キャパシタ負極電極層5とリチウム電池負極電極層6としては、チタン酸リチウムの粒子を主成分とし、PVDFなどのバインダーとアセチレンブラックなどの導電剤とを混合して構成される。チタン酸リチウムの粒子は、1μm未満の微粒子であることが望ましく、導電性を改善するために、カーボン繊維が混合されていてよい。あるいは、カーボンナノチューブやカーボンナノホーンなどのカーボン繊維に数nmレベルのチタン酸リチウム超微粒子が担持されていてもよい。
従来のリチウム電池において、下限電圧が存在する理由について、図2~図5を用いて説明する。図2は、正極にコバルト系金属酸化物リチウムを用い、負極に黒鉛系カーボンを用いた場合の電位と充電率との関係を示したものである。充電率は、一般にSOC(State of Charge)と呼ばれ、充放電可能な電気量を100%として、0から100%まで
を定義した指標である。
[共通負極の作製]
一般式LiXTi5O12(x=4.0)のチタン酸リチウム微粒子と導電剤としてのアセチレンブラックとバインダーとしてのポリフッ化ビニリデン(PVDF)を重量比87:5:8で混合し、溶媒としてのn-メチルピロリドンからなる電極ペーストを混合調製した。次にこのペーストを負極集電箔3として、幅300mm、厚さ20μmで、直径1mmの孔(透過孔4)が5mmピッチでパンチングされたアルミニウム箔の両面に塗工形成して乾燥し150℃でホットプレスし共通負極とした。この負極を32mm×52mmの短冊に切断し、角から20mm×20mmの部分を切除して、7mm×20mmのタブ部を設け電流端子タブ部とした。
キャパシタ正極電極層として、平均粒径5μmの活性炭とバインダーとしてのアクリル系ポリマー、溶媒としての水からなる電極ペーストを混合調製した。次にこのペーストを幅300mm、厚さ50μmの純アルミニウム製の集電箔10Cの片面に塗工し厚さ100μmのキャパシタ正極電極層8を形成して、キャパシタ正極11Cを得た。この正極11Cを30mm×50mmの短冊に切断し、角から23mm×20mmの部分を切除して、7mm×20mmのタブ部を設け、その部分のキャパシタ正極電極層8を剥がし、箔部を露出させて電流端子タブ部とした。
厚さ50μmの純アルミ集電箔10Lの裏面にリチウム電池正極電極層として、平均粒径5μmのオリビン型リン酸鉄リチウム、アセチレンブラック、バインダーとしてのポリフッ化ビニリデン(PVDF)をn-メチルピロリドン(NMP)に分散させ100℃で乾燥させて厚さ100μmのリチウム電池正極電極層9を形成し、150℃でホットロールプレスして、リチウム電池正極11Lを得た。この正極11Lを30mm×50mmの短冊に切断し、角から23mm×20mmの部分を切除して、7mm×20mmのタブ部を設け、そのリチウム電池正極電極層9を剥がし、箔部を露出させて電流端子タブ部とした。
キャパシタ正極11C(電極層8のみ片面形成)、共通負極7、リチウム電池正極11L(電極層9のみ片面形成)の順に互いの電極層が対向するように中心を揃えて積層し、間にそれぞれ厚さ35μmのセルロース系紙セパレータを1枚ずつはさんだ。2枚の正極11C、11Lの集電タブを重ねてこの集電タブにアルミニウム箔を超音波溶接により接続(短絡)して正極集電端子TPとした。この電極積層体を図8のようにアルミラミネートフィルムの外装に収納し、電解液として、1.5mol/lのLiPF6を含む、エチレンカーボネート-ジエチルカーボネート3:7混合溶媒を注液し、最後にアルミラミネート外装19を封口し試験用セルとした。図8は、アルミラミネート外装を施した試験用セルの半透過図である。図において、アルミラミネートフィルムの外装19は2つ折りして、3辺を熱可塑性樹脂で熱融着20する。電流端子部TP、TNには、金属との密着性を改善した熱可塑性樹脂17を装着した後、外装に熱融着している。図5の底辺については、真空引きを行って電解液を含浸した後、最終的に熱融着して封止した。なお、図5において、外装19が電極部分の大きさと較べて長くなっているのは、3cm×3cmの電極部に面圧をかけて充放電試験を実施する際に、電極から劣化に伴うガスが発生しても、長くなった外装部に発生したガスを溜めて、試験を継続できるようにするためである。なお、正極11C、11Lよりも負極7を外形で4辺とも1mm大きくして、正極と負極のずれによる測定誤差を防いでいる。
このセルについて3cm×3cmの電極部にステンレス製の押さえ板で5kg/cm2の面圧をかけて、5℃環境下で下限電圧0V、上限電圧4.0Vで20分間充電、20分間放電(3C)を48時間繰り返す充放電試験を行った。試験前と試験後に、充放電を3回繰り返し、3回目の放電曲線から、静電容量を求めた。初期の静電容量を100%として、試験後の静電容量維持率を求めた。
電解液として、1.2mol/lのLiPF6を含む、エチレンカーボネート-ジエチルカーボネート3:7混合溶媒を用いたこと以外は、実施例1と同じとした。
キャパシタ負極電極層5およびリチウム負極電極層6を、黒鉛系カーボン粒子を主成分とし、アルミ箔ではなく、パンチングして貫通孔を設けた銅箔を共通負極集電箔3として用いて作製したこと以外は、実施例1と同じとした。
リチウム負極電極層6をコバルト酸リチウムの微粒子を用いて作製したこと以外は、実施例1と同じとした。
図9は、この発明の実施の形態2にかかる電力貯蔵デバイスセルの断面模式図である。実施の形態1との違いは、共通負極を貫通する貫通孔によって集電箔の透過孔を形成していることである。図において、共通負極207には、負極集電箔203材料として透過孔が形成されていない厚さ約10μm以上20μm以下のアルミニウム箔を用い、表裏にハードカーボン粒子と黒鉛粒子を混合したペーストを塗布してキャパシタ負極電極層205とリチウム電池負極電極層206を形成した後に、剣山(生け花で、花や枝の根元と固定するための道具で、金属の台に、複数の針を上向きに並べたもの)のような先端の尖った針状物が面内に並んだものを用いて物理的に共通負極207を貫く貫通孔14を開口して形成した。つまり、孔開け前のアルミ箔に電極層を塗布した後、突起物を押し当てて貫通孔14を形成し、貫通項14のうちの集電箔203部分を実施の形態1における集電箔の透過孔とした。
図10は、この発明の実施の形態3にかかる電力貯蔵デバイスセルの断面模式図である。実施の形態2と同様に、共通負極全体を貫通する貫通孔を有しているが、実施の形態2との違いとして、共通負極全体を貫通する貫通孔の形状を錐状とし、キャパシタ負極電極層側に向かって狭まる貫通孔314Aとリチウム電池負極電極層側に向かって狭まる貫通孔314Bとの2種類(2方向)の貫通孔を設けたことである。そのため突起物は、キャパシタ負極電極層305側からとリチウム電池負極電極層306側からの両方から押し当てることになる。具体的には、共通負極307の穴開け加工方法としては、例えば、底辺0.4mm、高さ0.7mmの四角錐の突起が0.8mm間隔で形成されている金属金型と、表面が平滑な金属板の間に両面に電極層305、306を塗布した共通負極307を設置し、0.3MPa程度の圧力でプレスする操作を表側、裏側それぞれでおこなうことで形成できる。また、針をもったローラーに表裏ひっくり返して2回通して同様に多数の孔を開けることができる。
図11は、この発明の実施の形態4にかかる電力貯蔵デバイスセルの断面模式図である。実施の形態1との違いは、共通負極407には、集電箔403の一方の面にキャパシタ負極電極層405が形成され、集電箔403の他方の面であるリチウム電池部側には、電気絶縁層18が形成されていることである。電気絶縁層18としては、ポリエチレン、ポリプロピレンなどのフィルムやPVDFを塗布した層などが望ましい。キャパシタ負極電極層5は、リチウム電池負極電極層6としても機能する。そして、電気絶縁層18も含めて共通負極407全体を貫通する錐状の貫通孔414は、電気絶縁層18側から形成しており、電気絶縁層18側からキャパシタ負極電極層405に向かうにつれて狭くなるようになっている。針をもったローラーに、電気絶縁層18側が針に向かうように共通負極407を通すことにより、多数の貫通孔414を開けることができる。開孔率としては、30%以上70%以下が望ましく、開孔率が30%を下回ると、キャパシタ負極電極層5の、リチウム電池負極電極層6としての機能が低下する。また、開孔率が70%を上回ると、負極電極層の面積低下による性能低下をもたらす恐れがある。
図12は、この発明の実施の形態5にかかる電力貯蔵デバイスセルの断面模式図である。実施の形態1との違いは、共通負極507には、集電箔503の一方の面にリチウム電池負極電極層507が形成され、集電箔503の他方の面であるキャパシタ側には、電気絶縁層518が形成されていることである。共通負極507については、実施の形態4の共通負極407と厚み方向でちょうど逆の構成になる。リチウム電池負極電極層506は、キャパシタ負極電極層505としても機能する。
本実施の形態6では、共通負極の両面に電極層を設けた電力貯蔵デバイスセルで、両面に設けられた電極層のうち、少なくとも一方の電極層に、透過孔から他方の電極層内に食い込む複数の食い込み部を設けるようにしたものである。以下、詳細を説明する。図13は本実施の形態6にかかる電力貯蔵デバイスセルの断面模式図、図14は電力貯蔵デバイスセルの製造方法を説明するためのフローチャートである。図13において、共通負極607を構成する集電箔603、電極層605、606のうち、電極層606には、集電箔603内の透過孔となる貫通孔624から電極層605内部にまで食い込む複数の食い込み部21が設けられている。その他の構成については、実施の形態1で説明した電力貯蔵デバイスと同様である。
本実施の形態7では、共通負極の集電箔には、透過孔の周縁から共通負極の少なくとも一方の面に設けられた電極層に掛かるバリが形成されているようにしたものである。以下、詳細を説明する。図15は本実施の形態7にかかる電力貯蔵デバイスセルの断面模式図、図16は電力貯蔵デバイスセルの製造方法を説明するためのフローチャートである。図15において、共通負極707を構成する集電箔703には、貫通孔714の周縁から電極層706に掛かるバリ22が形成されている。その他の構成については、実施の形態1あるいは実施の形態2で説明した電力貯蔵デバイスと同様である。
[共通負極の作製]
一般式LixTi5O12(x=4.0)のチタン酸リチウム微粒子と導電剤としてのアセチレンブラックとバインダーとしてのポリフッ化ビニリデン(PVDF)を重量比87:5:8で混合し、溶媒としてのn-メチルピロリドンからなる電極ペーストを混合調製した。次にこのペーストを負極集電箔として、幅300mm、厚さ20μmのプレーンなアルミニウム箔の両面に塗工形成して乾燥し110℃でホットロールプレスをした。この電極を底辺0.4mm、高さ0.7mmの四角錐の突起が0.8mm間隔で形成されている平板型の金属金型と、表面が平滑な金属板の間に設置し、さらにその上にアクリル板を乗せて0.5MPaの圧力でプレスする操作を2回繰り返し共通負極とした。この負極を32mm×52mmの短冊に切断し、角から20mm×20mmの部分を切除して、7mm×20mmのタブ部を設け電流端子タブ部とした。
実施の形態1で説明した実施例1と同様に作製した。
実施の形態1で説明した実施例1と同様に作製した。
実施の形態1で説明した実施例1と同様に作製した。
[共通負極の作製]
一般式LixTi5O12(x=4.0)のチタン酸リチウム微粒子と導電剤としてのアセチレンブラックとバインダーとしてのポリフッ化ビニリデン(PVDF)を重量比87:5:8で混合し、溶媒としてのn-メチルピロリドンからなる電極ペーストを混合調製した。次にこのペーストを負極集電箔として、幅300mm、厚さ20μmのプレーンなアルミニウム箔の片面に塗工形成して乾燥した後、この電極を底辺0.4mm、高さ0.7mmの四角錐の突起が0.8mm間隔で形成されている平板型の金属金型と、表面が平滑な金属板の間に設置し、さらにその上にアクリル板を乗せて0.5MPaの圧力でプレスして集電箔側から電極層内部に達する到達孔を穿孔する操作を2回繰り返した。この後前述したペーストを集電箔上に塗布し、到達孔を埋めるようにもう一方の電極層を形成することにより、両面に電極層を有する負極を形成した。この電極を110℃でホットロールプレスして共通負極とした。
一般式LiXTi5O12(x=4.0)のチタン酸リチウム微粒子と導電剤としてのアセチレンブラックとバインダーとしてのポリフッ化ビニリデン(PVDF)を重量比87:5:8で混合し、溶媒としてのn-メチルピロリドンからなる電極ペーストを混合調製した。次にこのペーストを負極集電箔として、幅300mm、厚さ20μmのプレーンなアルミニウム箔の片面に塗工形成して乾燥した後、この電極を底辺0.4mm、高さ0.7mmの四角錐の突起が0.8mm間隔で形成されている平板型の金属金型と、表面が平滑な金属板の間に設置し、さらにその上にアクリル板を乗せて0.5MPaの圧力でプレスして電極層側から穿孔する操作を2回繰り返した。穿孔により集電箔は突き破られ孔の周辺に約90μmのバリが生じていた。この後前述したペーストを集電箔上に塗布し、バリを包み込むように電極層を形成することにより、両面に電極層を有する負極を形成した。この電極を110℃でホットロールプレスして共通負極とした。
実施例3~5の共通負極について、14mm×14mmのサイズに切り出し、上下面に10mm×10mmのアルミニウム箔を挟み、上から10kg/cm2の圧力で加圧した状態で電極の抵抗を測定した。表2に各電極の抵抗率を示す。
実施例3~5のセルについて、3cm×3cmの電極部にステンレス製の押さえ板で5kg/cm2の面圧をかけて、5℃環境下で下限電圧0V、上限電圧4.0Vで20分間充電、20分間放電(3C)を48時間繰り返す充放電試験を行った。試験前と試験後に、充放電を3回繰り返し、3回目の放電曲線から、静電容量を求めた。初期の静電容量を100%として、試験後の静電容量維持率を求めた。この評価結果および、実施の形態1における実施例1の結果(表1)を表3に示す。
11 正極(11a:ハイブリッド正極(キャパシタ正極扱い)、11b:ハイブリッド正極(リチウム電池正極扱い)、11C:キャパシタ正極、
11L:リチウム電池正極、 12 第1のセパレータ、 13 第2のセパレータ、 14 共通負極の貫通孔、 18 電気絶縁層、 19 外装、 20 熱融着部、 21 食い込み部、 22 バリ
100位の数字は実施の形態ごとの変形例を示す。
Claims (17)
- アルミニウム製の第1の集電箔の一方の面に活性炭の微粒子を含む第1の電極層が形成された第1の電極と、
アルミニウム製の第2の集電箔の一方の面に第2の電極層が形成された第2の電極と、
アルミニウム製の第3の集電箔の少なくとも一方の面に第3の電極層が形成された第3の電極と、
多孔質の絶縁フィルムからなる第1のセパレータと、
多孔質の絶縁フィルムからなる第2のセパレータと、を備え、
前記第3の集電箔には透過孔が形成され、前記第1の電極層と前記第3の電極の一方の面との間に前記第1のセパレータを挟持して前記第3の電極を負極とするキャパシタを形成し、前記第2の電極層と前記第3の電極の他方の面との間に前記第2のセパレータを挟持して前記第3の電極を前記キャパシタとの共通負極とするリチウムイオン電池を形成し、前記第1の電極と前記第2の電極を短絡接続した電力貯蔵デバイスセルであって、
前記第2の電極層がオリビン型構造を有するリン酸型リチウム化合物の粒子を含んで構成され、前記第3の電極層がチタン酸リチウムの粒子を主成分として構成されていることを特徴とする電力貯蔵デバイスセル。 - 当該電力貯蔵デバイスセルでの充電率が0%のときに、前記チタン酸リチウムの組成が、一般式LixTi5O12(4.0≦x≦4.1)となることを特徴とする請求項1記載の電力貯蔵デバイスセル。
- 前記第3の電極に前記第3の電極の厚み方向を貫通する貫通孔が設けられていることを特徴とする請求項1または2に記載の電力貯蔵デバイスセル。
- 前記第3の電極層は、前記第3の集電箔の両面に設けられており、
前記貫通孔は、当該第3の電極の一方の面側から他方の面側に向かうにつれて狭くなる第1の貫通孔と、当該第3の電極の他方の面側から一方の面側に向かうにつれて狭くなる第2の貫通孔との2種類の貫通孔であることを特徴とする請求項3に記載の電力貯蔵デバイスセル。 - 前記第3の電極は、前記第3の集電箔の両面に前記第3の電極層が設けられており、
前記第3の集電箔の両面に設けられた第3の電極層のうち、少なくとも一方の電極層には、前記透過孔から他方の電極層内に食い込む複数の食い込み部が設けられていることを特徴とする請求項1または2に記載の電力貯蔵デバイスセル。 - 前記第3の集電箔には、前記透過孔の周縁から前記第3の電極層に掛かるバリが形成されていることを特徴とする請求項1または2に記載の電力貯蔵デバイスセル。
- 前記第3の電極は、前記第3の集電箔の一方の面に前記第3の電極層が形成され、前記第3の集電箔の他方の面に絶縁皮膜が設けられ、前記絶縁被膜側から前記第3の電極層に向かうにつれて狭くなる前記第3の電極の厚み方向を貫通する貫通孔が設けられていることを特徴とする請求項1または2に記載の電力貯蔵デバイスセル。
- 前記第3の電極層を前記第1のセパレータを介して前記第1の電極層に対峙させ、前記絶縁皮膜を前記第2のセパレータを介して前記第2の電極層に対峙させたことを特徴とする請求項7に記載の電力貯蔵デバイスセル。
- 前記第3の電極層を前記第2のセパレータを介して前記第2の電極層に対峙させ、前記絶縁皮膜を前記第1のセパレータを介して前記第1の電極層に対峙させたことを特徴とする請求項7に記載の電力貯蔵デバイスセル。
- 活性炭の微粒子にバインダーを加えたペーストを前記第1の集電箔に塗布して前記第1の電極層を有する前記第1の電極を形成し、
オリビン型構造を有するリン酸型リチウム化合物の粒子に導電剤とバインダーを加えたペーストを前記第2の集電箔に塗布して前記第2の電極層を有する前記第2の電極を形成し、
チタン酸リチウムの粒子に導電剤とバインダーを加えたペーストを前記第3の集電箔に塗布して前記第3の電極層を有する前記第3の電極を形成し、
前記第1の電極、前記第1のセパレータ、前記第3の電極、前記第2のセパレータ、前記第2の電極を積層して、前記電力貯蔵デバイスセルを製造する方法であって、
前記第3の電極は、前記第3の集電箔に前記透過孔が形成される前にペーストを塗布し、塗布後に突起物を押し当てて前記貫通孔を形成することを特徴とする請求項3または4に記載の電力貯蔵デバイスセルの製造方法。 - 活性炭の微粒子にバインダーを加えたペーストを前記第1の集電箔に塗布して前記第1の電極層を有する前記第1の電極を形成し、
オリビン型構造を有するリン酸型リチウム化合物の粒子に導電剤とバインダーを加えたペーストを前記第2の集電箔に塗布して前記第2の電極層を有する前記第2の電極を形成し、
チタン酸リチウムの粒子に導電剤とバインダーを加えたペーストを前記第3の集電箔の両面に塗布して前記第3の電極層を両面に有する前記第3の電極を形成し、
前記第1の電極、前記第1のセパレータ、前記第3の電極、前記第2のセパレータ、前記第2の電極を積層して、前記電力貯蔵デバイスセルを製造する方法であって、
前記第3の電極を形成する工程において、
前記第3の集電箔の一方の面にペーストを塗布して、前記両面の電極層のうちの一方の電極層を形成し、
前記一方の電極層を形成した後に、前記第3の集電箔の他方の面側から突起物を押し当てて、少なくとも前記一方の電極層内部に達し、前記透過孔として機能する到達孔を穿孔し、
前記第3の集電箔の前記突起物を押し当てた面側から前記到達孔を埋めるようにペーストを塗布して、他方の電極層を形成することを特徴とする請求項5に記載の電力貯蔵デバイスセルの製造方法。 - 活性炭の微粒子にバインダーを加えたペーストを前記第1の集電箔に塗布して前記第1の電極層を有する前記第1の電極を形成し、
オリビン型構造を有するリン酸型リチウム化合物の粒子に導電剤とバインダーを加えたペーストを前記第2の集電箔に塗布して前記第2の電極層を有する前記第2の電極を形成し、
チタン酸リチウムの粒子に導電剤とバインダーを加えたペーストを前記第3の集電箔に塗布して前記第3の電極層を有する第3の電極を形成し、
前記第1の電極、前記第1のセパレータ、前記第3の電極、前記第2のセパレータ、前記第2の電極を積層して、前記電力貯蔵デバイスセルを製造する方法であって、
前記第3の電極を形成する工程において、
前記第3の集電箔の面のうち、電極層が形成されていない面の反対側の面側から突起物を押し当てて、少なくとも前記第3の集電箔を貫通し、前記透過孔として機能する貫通孔を形成し、
前記貫通孔の形成に伴い、前記第3の集電箔のバリが生じた面にペーストを塗布して、前記第3の電極層を形成することを特徴とする請求項6に記載の電力貯蔵デバイスセルの製造方法。 - 活性炭の微粒子にバインダーを加えたペーストを前記第1の集電箔に塗布して前記第1の電極層を有する前記第1の電極を形成し、
オリビン型リン酸鉄リチウムに導電剤とバインダーを加えたペーストを前記第2の集電箔に塗布して前記第2の電極層を有する前記第2の電極を形成し、
チタン酸リチウムの粒子に導電剤とバインダーを加えたペーストを前記第3の集電箔に塗布して前記第3の電極層を有する前記第3の電極を形成し、
前記第1の電極、前記第1のセパレータ、前記第3の電極、前記第2のセパレータ、前記第2の電極を積層して、前記電力貯蔵デバイスセルを製造する方法であって、
前記第3の電極は、前記第3の集電箔に前記透過孔が形成される前にペーストを塗布し、塗布後に前記絶縁被膜側から突起物を押し当てて前記貫通孔を形成することを特徴とする請求項7ないし9のいずれか1項に記載の電力貯蔵デバイスセルの製造方法。 - 前記第1の電極および前記第2の電極は、集電箔の一方の面に前記第1の電極層を形成し、他方の面に前記第2の電極層を形成したハイブリッド電極であり、
前記第3の電極、前記第1のセパレータ、前記ハイブリッド電極、前記第2のセパレータの順で積層を繰り返して請求項1ないし9のいずれかに記載の電力貯蔵デバイスセルの複数を積層した主積層部を有する積層体で構成したことを特徴とする蓄電デバイス。 - 前記積層体の両端部が前記第3の電極となるように積層したことを特徴とする請求項14に記載の蓄電デバイス。
- 前記第1の電極および前記第2の電極は、集電箔の一方の面に前記第1の電極層を形成し、他方の面に前記第2の電極層を形成したハイブリッド電極であり、
前記第3の電極、前記第1のセパレータ、前記ハイブリッド電極、前記第2のセパレータの順で積層し、積層したものを巻回して請求項1ないし9のいずれかに記載の電力貯蔵デバイスセルを構成したことを特徴とする蓄電デバイス。 - 前記短絡した第1の電極と第2の電極との端子と、前記第3の電極とを電気的に短絡して保管することを特徴とする請求項1ないし9のいずれか1項に記載の電力貯蔵デバイスセルの保管方法。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201180007321.9A CN102771007B (zh) | 2010-01-28 | 2011-01-12 | 电力储存器件单元及其制造方法、保管方法以及蓄电器件 |
JP2011551792A JP5357276B2 (ja) | 2010-01-28 | 2011-01-12 | 電力貯蔵デバイスセル、およびその製造方法と保管方法 |
US13/520,296 US9461347B2 (en) | 2010-01-28 | 2011-01-12 | Power storage device cell, manufacturing method and storing method therefor, and electric storage device |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010016587 | 2010-01-28 | ||
JP2010-016587 | 2010-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011093126A1 true WO2011093126A1 (ja) | 2011-08-04 |
Family
ID=44319117
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/050313 WO2011093126A1 (ja) | 2010-01-28 | 2011-01-12 | 電力貯蔵デバイスセルとその製造方法、保管方法および蓄電デバイス |
Country Status (4)
Country | Link |
---|---|
US (1) | US9461347B2 (ja) |
JP (1) | JP5357276B2 (ja) |
CN (1) | CN102771007B (ja) |
WO (1) | WO2011093126A1 (ja) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2011092990A1 (ja) * | 2010-01-28 | 2013-05-30 | 三菱電機株式会社 | 電力貯蔵デバイスセルとその製造方法および蓄電デバイス |
JP2014026931A (ja) * | 2012-07-30 | 2014-02-06 | Nissan Motor Co Ltd | 電極及び電極の製造方法 |
WO2014037156A1 (de) * | 2012-09-07 | 2014-03-13 | Robert Bosch Gmbh | Energiespeicher |
KR20140083904A (ko) * | 2012-12-26 | 2014-07-04 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 축전 장치 및 그 충전 방법 |
JP2014158415A (ja) * | 2013-01-21 | 2014-08-28 | Semiconductor Energy Lab Co Ltd | 二次電池、二次電池モジュール、二次電池および二次電池モジュールの充電方法、二次電池および二次電池モジュールの放電方法、二次電池および二次電池モジュールの駆動方法、蓄電システム、及び蓄電システムの駆動方法 |
CN105762332A (zh) * | 2014-12-17 | 2016-07-13 | 绍兴文理学院 | 一种锂离子电池的制作方法 |
US10020532B2 (en) * | 2014-05-27 | 2018-07-10 | Apple Inc. | Thin film battery structures having sloped cell sidewalls |
JP2019021390A (ja) * | 2017-07-11 | 2019-02-07 | 株式会社豊田自動織機 | リチウムイオン二次電池 |
WO2023170960A1 (ja) * | 2022-03-11 | 2023-09-14 | 武蔵精密工業株式会社 | 蓄電セル、蓄電モジュール、および、蓄電セルの製造方法 |
WO2023175698A1 (ja) * | 2022-03-15 | 2023-09-21 | 武蔵精密工業株式会社 | 蓄電池、および、蓄電装置 |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10319536B1 (en) * | 2012-11-19 | 2019-06-11 | Prakash Achrekar | High-capacity electrical energy storage device |
JP6262686B2 (ja) * | 2015-04-27 | 2018-01-17 | ファナック株式会社 | 平滑コンデンサの寿命予測手段を有するモータ制御装置 |
WO2017037213A1 (fr) * | 2015-09-02 | 2017-03-09 | Sweetch Energy | Dispositif de production d'energie par gradient de salinite a travers des membranes nano-fluidiques a base d'oxyde de titane |
JP2017139844A (ja) * | 2016-02-01 | 2017-08-10 | 川崎重工業株式会社 | 電力貯蔵装置 |
US10637040B2 (en) * | 2016-07-28 | 2020-04-28 | GM Global Technology Operations LLC | Blended or multi-coated electrodes for lithium ion battery and capacitor hybrid system |
US10693176B2 (en) | 2016-07-28 | 2020-06-23 | GM Global Technology Operations LLC | Hybrid cell design of alternatively stacked or wound lithium ion battery and capacitor electrodes |
CN111976505A (zh) * | 2019-05-21 | 2020-11-24 | 重庆九环新越新能源科技发展有限公司 | Iems控制电池与电容复合储能设备的动力输出方法及*** |
WO2020233407A1 (zh) * | 2019-05-22 | 2020-11-26 | 青岛九环新越新能源科技股份有限公司 | 复合动力储能电芯、单体、模组和设备及控制方法 |
WO2021220294A1 (en) * | 2020-04-28 | 2021-11-04 | Savari Rathinam Sahaya Prabaharan | A single cell hybrid capattery energy storage system |
CN112448069A (zh) * | 2020-11-17 | 2021-03-05 | 河北工业大学 | 一种金属空气电池与超级电容器一体化器件及其制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004355823A (ja) * | 2003-05-27 | 2004-12-16 | Nec Tokin Corp | ハイブリッド型蓄電部品 |
JP2006190528A (ja) * | 2005-01-05 | 2006-07-20 | Gs Yuasa Corporation:Kk | 非水電解質電池用正極及び非水電解質電池 |
JP2008282838A (ja) * | 2007-05-08 | 2008-11-20 | Nec Tokin Corp | ハイブリット電気二重層キャパシタ |
JP2009026480A (ja) * | 2007-07-17 | 2009-02-05 | Fuji Heavy Ind Ltd | 蓄電デバイス |
JP2009141181A (ja) * | 2007-12-07 | 2009-06-25 | Mitsubishi Electric Corp | 電力貯蔵デバイスセルおよびその制御方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA94750B (en) * | 1993-09-02 | 1994-09-29 | Technology Finance Corp | Electrochemical cell |
EP1117145B1 (en) * | 1998-08-27 | 2011-10-05 | NEC Corporation | Nonaqueous electrolyte secondary cell |
JP4825344B2 (ja) | 2000-06-07 | 2011-11-30 | Fdk株式会社 | 電池・キャパシタ複合素子 |
US6908711B2 (en) * | 2002-04-10 | 2005-06-21 | Pacific Lithium New Zealand Limited | Rechargeable high power electrochemical device |
JP4693372B2 (ja) * | 2004-07-16 | 2011-06-01 | 三洋電機株式会社 | 非水電解質二次電池 |
JP2006040748A (ja) | 2004-07-28 | 2006-02-09 | Yuasa Corp | 電気化学デバイス |
JP4956019B2 (ja) | 2005-03-02 | 2012-06-20 | パナソニック株式会社 | 点灯ユニット及びランプ |
JP5083588B2 (ja) | 2006-03-31 | 2012-11-28 | 日立工機株式会社 | リチウム電池パック |
JP2009123385A (ja) * | 2007-11-12 | 2009-06-04 | Fuji Heavy Ind Ltd | 蓄電デバイス |
CN101162789A (zh) * | 2007-11-16 | 2008-04-16 | 山东神工海特电子科技有限公司 | 1.5v的充电电容电池 |
CN102696144B (zh) | 2010-01-28 | 2015-01-14 | 三菱电机株式会社 | 电力储存设备单元及其制造方法以及蓄电设备 |
-
2011
- 2011-01-12 WO PCT/JP2011/050313 patent/WO2011093126A1/ja active Application Filing
- 2011-01-12 JP JP2011551792A patent/JP5357276B2/ja not_active Expired - Fee Related
- 2011-01-12 CN CN201180007321.9A patent/CN102771007B/zh not_active Expired - Fee Related
- 2011-01-12 US US13/520,296 patent/US9461347B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004355823A (ja) * | 2003-05-27 | 2004-12-16 | Nec Tokin Corp | ハイブリッド型蓄電部品 |
JP2006190528A (ja) * | 2005-01-05 | 2006-07-20 | Gs Yuasa Corporation:Kk | 非水電解質電池用正極及び非水電解質電池 |
JP2008282838A (ja) * | 2007-05-08 | 2008-11-20 | Nec Tokin Corp | ハイブリット電気二重層キャパシタ |
JP2009026480A (ja) * | 2007-07-17 | 2009-02-05 | Fuji Heavy Ind Ltd | 蓄電デバイス |
JP2009141181A (ja) * | 2007-12-07 | 2009-06-25 | Mitsubishi Electric Corp | 電力貯蔵デバイスセルおよびその制御方法 |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2011092990A1 (ja) * | 2010-01-28 | 2013-05-30 | 三菱電機株式会社 | 電力貯蔵デバイスセルとその製造方法および蓄電デバイス |
JP5368589B2 (ja) * | 2010-01-28 | 2013-12-18 | 三菱電機株式会社 | 電力貯蔵デバイスセルとその製造方法および蓄電デバイス |
US9040182B2 (en) | 2010-01-28 | 2015-05-26 | Mitsubishi Electric Corporation | Power storage device cell, manufacturing method therefor, and electric storage device |
JP2014026931A (ja) * | 2012-07-30 | 2014-02-06 | Nissan Motor Co Ltd | 電極及び電極の製造方法 |
WO2014037156A1 (de) * | 2012-09-07 | 2014-03-13 | Robert Bosch Gmbh | Energiespeicher |
KR20140083904A (ko) * | 2012-12-26 | 2014-07-04 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 축전 장치 및 그 충전 방법 |
JP2014143184A (ja) * | 2012-12-26 | 2014-08-07 | Semiconductor Energy Lab Co Ltd | 蓄電装置及びその充電方法 |
US11777108B2 (en) | 2012-12-26 | 2023-10-03 | Semiconductor Energy Laboratory Co., Ltd. | Power storage device and method for charging the same |
US10944281B2 (en) | 2012-12-26 | 2021-03-09 | Semiconductor Energy Laboratory Co., Ltd. | Power storage device and method for charging the same |
KR102165593B1 (ko) | 2012-12-26 | 2020-10-14 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 축전 장치 및 그 충전 방법 |
JP2014158415A (ja) * | 2013-01-21 | 2014-08-28 | Semiconductor Energy Lab Co Ltd | 二次電池、二次電池モジュール、二次電池および二次電池モジュールの充電方法、二次電池および二次電池モジュールの放電方法、二次電池および二次電池モジュールの駆動方法、蓄電システム、及び蓄電システムの駆動方法 |
US10044182B2 (en) | 2013-01-21 | 2018-08-07 | Semiconductor Energy Laboratory Co., Ltd. | Secondary battery, secondary battery module, power storage system, and method for operating thereof |
US10637093B2 (en) | 2014-05-27 | 2020-04-28 | Apple Inc. | Thin film battery structures having sloped cell sidewalls |
US10020532B2 (en) * | 2014-05-27 | 2018-07-10 | Apple Inc. | Thin film battery structures having sloped cell sidewalls |
CN105762332A (zh) * | 2014-12-17 | 2016-07-13 | 绍兴文理学院 | 一种锂离子电池的制作方法 |
JP2019021390A (ja) * | 2017-07-11 | 2019-02-07 | 株式会社豊田自動織機 | リチウムイオン二次電池 |
JP7021466B2 (ja) | 2017-07-11 | 2022-02-17 | 株式会社豊田自動織機 | リチウムイオン二次電池 |
WO2023170960A1 (ja) * | 2022-03-11 | 2023-09-14 | 武蔵精密工業株式会社 | 蓄電セル、蓄電モジュール、および、蓄電セルの製造方法 |
WO2023175698A1 (ja) * | 2022-03-15 | 2023-09-21 | 武蔵精密工業株式会社 | 蓄電池、および、蓄電装置 |
Also Published As
Publication number | Publication date |
---|---|
CN102771007A (zh) | 2012-11-07 |
US20120282495A1 (en) | 2012-11-08 |
CN102771007B (zh) | 2014-12-10 |
JPWO2011093126A1 (ja) | 2013-05-30 |
JP5357276B2 (ja) | 2013-12-04 |
US9461347B2 (en) | 2016-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5357276B2 (ja) | 電力貯蔵デバイスセル、およびその製造方法と保管方法 | |
JP5368589B2 (ja) | 電力貯蔵デバイスセルとその製造方法および蓄電デバイス | |
JP4857073B2 (ja) | リチウムイオンキャパシタ | |
US8288032B2 (en) | Energy storage device cell and control method thereof | |
JP4854112B2 (ja) | リチウムイオン電池及びその制御方法 | |
US8906525B2 (en) | Energy storage device cell | |
JP2012169576A (ja) | 電気化学デバイス | |
WO2006112068A1 (ja) | リチウムイオンキャパシタ | |
JP2006286919A (ja) | リチウムイオンキャパシタ | |
JP2009200302A (ja) | 蓄電デバイスの製造方法および蓄電デバイス | |
KR20080081297A (ko) | 리튬이온 커패시터 | |
JP2012138408A (ja) | 電気化学デバイスおよびその製造方法 | |
US20120129047A1 (en) | Non-aqueous electrolyte secondary battery | |
JP5308646B2 (ja) | リチウムイオンキャパシタ | |
JPWO2012127991A1 (ja) | 蓄電デバイス | |
JP2012248556A (ja) | 電気化学デバイスおよびその製造方法 | |
KR101979040B1 (ko) | 리튬 축전지 | |
JP2011159642A (ja) | 電気化学デバイス | |
JP5921897B2 (ja) | リチウムイオンキャパシタ | |
JP6254360B2 (ja) | 蓄電デバイス | |
JP2011258798A (ja) | 電気化学デバイス | |
JP2011165930A (ja) | 電力貯蔵デバイス及び電力貯蔵デバイスの共通負極の製造方法 | |
JP5650029B2 (ja) | リチウムイオンキャパシタ | |
WO2015005294A1 (ja) | 蓄電デバイス | |
JP5355429B2 (ja) | 電力貯蔵デバイス用正極とその製造方法および電力貯蔵デバイスセル |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201180007321.9 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11736841 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011551792 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13520296 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 11736841 Country of ref document: EP Kind code of ref document: A1 |