WO2011155164A1 - Condensateur - Google Patents

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Publication number
WO2011155164A1
WO2011155164A1 PCT/JP2011/003133 JP2011003133W WO2011155164A1 WO 2011155164 A1 WO2011155164 A1 WO 2011155164A1 JP 2011003133 W JP2011003133 W JP 2011003133W WO 2011155164 A1 WO2011155164 A1 WO 2011155164A1
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WO
WIPO (PCT)
Prior art keywords
active material
material layer
positive electrode
compound
capacitor
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Application number
PCT/JP2011/003133
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English (en)
Japanese (ja)
Inventor
鈴木　隆
Original Assignee
イノベーションエネルギー株式会社
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Publication of WO2011155164A1 publication Critical patent/WO2011155164A1/fr

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    • 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
    • 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

Definitions

  • the present invention relates to a capacitor. More specifically, the present invention relates to a capacitor including a positive electrode active material layer containing a V 3+ compound and a negative electrode active material layer containing a V 4+ compound.
  • the electric double layer capacitor uses electric energy accumulated in the electric double layer formed at the interface between the polarizable electrode and the electrolyte. Since electric double layer capacitors do not involve chemical reactions during charge and discharge, they have the advantages of superior input / output characteristics, life characteristics, and safety compared to lithium ion secondary batteries and nickel metal hydride secondary batteries. . Such an electric double layer capacitor is widely used as a capacitor that can be reduced in size and charged with a large capacity, for backup applications such as microcomputers, memories, and timers, and for assisting various power sources. In addition, in recent years, development of larger-capacity products has been promoted taking advantage of the characteristics.
  • an electric double layer capacitor Compared to a secondary battery that generates electricity by a chemical reaction, an electric double layer capacitor has a problem that the energy density is small although it has a higher output density.
  • a redox capacitor or pseudocapacitor using charge transfer at the electrode interface, a hybrid capacitor combining them, and an ionic liquid capacitor using an ionic liquid as an electrolyte Development is progressing.
  • an electric double layer capacitor using a negative electrode sheet sprayed with lithium on its surface has been proposed (see Patent Document 1).
  • the present invention provides a capacitor having a novel structure for storing electric energy by using charge transfer between a polarizable electrode and a metal compound in addition to an electric double layer formed at the interface between the polarizable electrode and the electrolyte. It is.
  • the capacitor of the present invention comprises: a positive electrode current collector; a carbon material, polylactic acid, and a V 3+ compound selected from the group consisting of V 2 O 3 , VF 3 , VCl 3 , V (acac) 3 , VSO 4 OH
  • a capacitor according to another embodiment of the present invention includes a plurality of first electrode stacks, one or more second electrode stacks, a plurality of separators, and an electrolyte solution, wherein the first electrode stack is , A first current collector and a first active material layer containing one of a carbon material, polylactic acid, and a V 3+ compound or a V 4+ compound, and the second electrode stack includes a second current collector, A carbon material, polylactic acid, and a second active material layer containing the other of the V 3+ compound or the V 4+ compound, and each of the plurality of separators is interposed between the first electrode laminate and the second electrode laminate.
  • the electrolyte solution is impregnated in the first active material layer, the second active material layer, and the separator.
  • the first active material layer includes a V 3+ compound
  • the first electrode stack is a positive current collector
  • the second active material layer includes a V 4+ compound
  • the second electrode stack is It may be a negative electrode current collector.
  • the first active material layer includes a V 4+ compound
  • the first electrode stack is a negative electrode current collector
  • the second active material layer includes a V 3+ compound
  • the second electrode stack is It may be a positive electrode current collector.
  • the plurality of first electrode stacks may be electrically connected, and the one or more second electrode stacks may be electrically connected.
  • the carbon material in the first active material layer and the second active material layer may be a mixture of activated carbon and carbon nanotubes or fullerenes.
  • the V 3+ compound may be selected from the group consisting of V 2 O 3 , VF 3 , VCl 3 , V (acac) 3 , VSO 4 OH.
  • the V 4+ compound may be selected from the group consisting of V 2 O 4 , VOSO 4 , VF 4 , VCl 4 , VO (acac) 2 , V (SO 4 ) 2 .
  • the capacitor according to the present invention has an advantage that it can cope with rapid charging and can be manufactured at low cost.
  • the capacitor of the present invention does not generate any ignitable components or toxic gases which are problematic in lithium secondary batteries even in an overcharged state, and does not cause any problems.
  • the capacitor of the present invention has no problem even when it is overdischarged.
  • the material used for the capacitor of the present invention is inexpensive and does not use rare metal or the like, it can be supplied stably.
  • the capacitor of the present invention includes a positive electrode current collector 110, a positive electrode active material layer 120, a separator 130, a negative electrode active material layer 140, a negative electrode current collector 150, and a positive electrode active material layer 120. And the electrolyte solution impregnated in the separator 130 and the negative electrode active material layer 140.
  • the positive electrode current collector 110 in the present invention is formed using a metal, preferably copper. In order to facilitate the formation of the capacitor and the like, it is preferable to use a copper foil having a film thickness of 40 to 50 ⁇ m as the positive electrode current collector 110.
  • the negative electrode current collector 150 in the present invention is formed using a metal, preferably aluminum.
  • a metal preferably aluminum.
  • an aluminum foil having a thickness of 40 to 50 ⁇ m is preferably used as the negative electrode current collector 150 in order to facilitate the formation of a capacitor.
  • the unevenness on the surface of the negative electrode current collector 150 provides an anchor effect for fixing nanocarbon in the negative electrode active material layer 140 that may be dissociated from the negative electrode current collector 150 during the formation of the capacitor.
  • the separator 130 maintains the positive electrode active material layer 120 and the negative electrode active material layer 140 in a non-contact state to prevent a short circuit of the capacitor, and ions in the electrolyte solution cause the positive electrode active material layer 120 and the negative electrode active material to be in contact with each other. It is a component for facilitating ion transfer between the layer 140.
  • insulating paper formed using wood pulp, glass fiber, polyolefin fiber, fluorine fiber, polyimide fiber, aramid fiber, or the like can be used.
  • insulating paper formed using polylactic acid fibers may be used as the separator 130.
  • the separator 130 is an insulating paper formed using glass fiber or polylactic acid fiber.
  • the separator 130 preferably has a film thickness of 8 to 100 ⁇ m and a porosity of 30 to 95%.
  • the positive electrode active material layer 120 in the present invention is a porous layer that contains a carbon material, polylactic acid, and a V 3+ compound and can be impregnated with an electrolytic solution.
  • the carbon material in the present invention is a mixture of nanocarbon having dimensions on the order of nanometers and carbonaceous or graphite materials having dimensions on the order of microns.
  • the nanocarbon commercially available carbon nanotubes, fullerenes and the like can be used.
  • the carbonaceous or graphitic material having a micron-order dimension is desirably a material having an average particle diameter of 2 to 6 ⁇ m and pores having a nanometer-order dimension.
  • Preferred carbonaceous or graphitic materials include activated carbon.
  • the polylactic acid in the positive electrode active material layer 120 functions as a binder that binds the carbonaceous or graphitic material and the nanocarbon.
  • Polylactic acid also functions as a binder for bonding the carbon material bonded with polylactic acid and the positive electrode current collector as described above.
  • the polylactic acid desirably has a number average molecular weight of 30,000 to 100,000.
  • the V 3+ compound in the positive electrode active material layer 120 is a trivalent vanadium salt.
  • the V 3+ compound is selected from the group consisting of V 2 O 3 , VF 3 , VCl 3 , V (acac) 3 (wherein acac represents acetylacetonate), and VSO 4 OH.
  • the central metal V 3+ emits one electron and becomes V 4+ during charging, and V 4+ accepts one electron and becomes V 3+ during discharging, thereby realizing a charge storage function. Contributes to increased capacity.
  • the positive electrode active material layer 120 includes 20 to 65 parts by mass of polylactic acid and 1 to 3 parts by mass of a V 3+ compound per 100 parts by mass of the carbon material.
  • the carbon material includes 1 to 50% by mass of nanocarbon and 50 to 99% by mass of carbonaceous or graphitic material based on the total mass of the carbon material.
  • the carbon material includes 1 to 5% by mass of nanocarbon and 95 to 99% by mass of carbonaceous or graphitic material based on the total mass of the carbon material.
  • the positive electrode active material layer 120 can be formed by applying the positive electrode composition to one side or both sides of the positive electrode current collector 110. Application on the positive electrode current collector 110 may be performed by any means known in the art such as a gravure coating method, a doctor blade method, and a roll coating method.
  • the positive electrode active material layer 120 of the present invention desirably has a thickness of 100 to 200 ⁇ m.
  • the self-supporting positive electrode active material layer 120 may be formed by applying the positive electrode composition to a temporary support and subsequently peeling the obtained coating film from the temporary support.
  • the negative electrode active material layer 140 in the present invention is a porous layer that contains nanocarbon, polylactic acid, and a V 3+ compound, and can be impregnated with an electrolytic solution.
  • the nanocarbon and polylactic acid in the negative electrode active material layer 140 may be the same as the nanocarbon and polylactic acid in the positive electrode active material layer.
  • the V 4+ compound in the negative electrode active material layer 140 is a tetravalent vanadium salt.
  • the V 4+ compound is selected from the group consisting of V 2 O 4 , VOSO 4 , VF 4 , VCl 4 , VO (acac) 2 , V (SO 4 ) 2 .
  • the central metal V 4+ accepts one electron and becomes V 3+ during charging, and V 3+ emits one electron and becomes V 4+ during discharging, thereby realizing a charge storage function. Contributes to increased capacity.
  • the negative electrode active material layer 140 includes 20 to 65 parts by mass of polylactic acid and 1 to 3 parts by mass of a V 4+ compound per 100 parts by mass of the carbon material.
  • the ratio of nanocarbon in the carbon material to the carbonaceous or graphite material is the same as that of the positive electrode active material layer 120.
  • the negative electrode active material layer 140 can be formed using a procedure similar to that of the positive electrode active material layer 120.
  • the negative electrode active material layer of the present invention has a thickness of 100 to 200 ⁇ m.
  • the electrolytic solution of the present invention is an organic electrolytic solution containing an electrolyte and an organic solvent.
  • the electrolyte includes a quaternary ammonium salt, an imidazolium salt, a pyridinium salt, and the like as a cation component, and BF 4 ⁇ , PF 6 ⁇ , CF 3 SO 3 ⁇ , (CF 3 SO 2 ) 2 as an anion component. N- and the like are included.
  • the electrolyte of the present invention is preferably BF 4 quaternary ammonium - a salt, more preferably a (C 2 H 5) 3 ( CH 3) NBF 4.
  • the electrolyte of the present invention is present in the electrolyte solution in the range of 1 to 1.5 mol%.
  • the organic solvent used in the electrolytic solution of the present invention includes aprotic polar solvents such as propylene carbonate, sulfolane, ethylene carbonate, ⁇ -butyrolactone, N, N-dimethylformamide, dimethyl sulfoxide. Mixtures of the aforementioned solvents may be used as the organic solvent of the present invention.
  • the organic solvent is a mixture of propylene carbonate and sulfolane.
  • a capacitor according to another embodiment of the present invention includes a plurality of first electrode stacks, one or more second electrode stacks, a plurality of separators, and an electrolyte solution, wherein the first electrode stack is , A first current collector and a first active material layer containing one of a carbon material, polylactic acid, and a V 3+ compound or a V 4+ compound, and the second electrode stack includes a second current collector, A carbon material, polylactic acid, and a second active material layer containing the other of the V 3+ compound or the V 4+ compound, and each of the plurality of separators is interposed between the first electrode laminate and the second electrode laminate.
  • the electrolyte solution is impregnated in the first active material layer, the second active material layer, and the separator.
  • FIGS. 2A to 2E show examples of configurations in which the first electrode stack is a positive electrode current collector and the second electrode current collector is a negative electrode current collector.
  • the positive electrode current collector is shown.
  • the negative electrode active material layer 140 was formed on both sides of the separator 130 and the negative electrode current collector 150 between the top single-side positive electrode laminate 210T and the bottom single-side positive electrode laminate 210B in which the positive electrode active material layer 120 was formed on one side of the body 110.
  • the double-sided negative electrode laminate 220 and the separator 130 are included, and the positive electrode active material layer 120, the negative electrode active material layer 140, and the separator 130 are impregnated with an electrolytic solution.
  • the double-sided positive electrode laminate 210M having the positive electrode active material layer 120 formed on both sides of the positive electrode current collector 110, the separator 130, the double-sided negative electrode laminate 220, and the additional structure 240 including the separator 130 are further laminated.
  • a larger number of internal capacitors may be formed. If necessary, a plurality of stacked structures 240 may be stacked.
  • FIG. 2A illustrates a configuration in which a plurality of internal capacitors are connected in series.
  • the top single-sided positive electrode laminate 210T, the one or more double-sided positive electrode laminates 210M, and the bottom single-sided positive electrode laminate 210B are electrically connected and the one or more double-sided negative electrode laminates 220 are electrically connected.
  • a multilayer capacitor in which a plurality of internal capacitors are connected in parallel may be formed.
  • FIG. 2A the example which has arrange
  • the negative electrode laminate and the separator 130 are laminated and pressed in this order, and these layers are integrated and wound into a roll shape.
  • the roll-shaped intermediate body is compressed and formed into a desired shape (for example, a substantially rectangular parallelepiped shape).
  • the electrolytic solution is impregnated in the positive electrode active material layer, the negative electrode active material layer, and the separator in the intermediate.
  • the capacitor of the present invention can be obtained by attaching terminals for external connection, packaging with an insulating sealing material, and the like.
  • an insulating sealing material any material known in the art can be used as long as leakage of the electrolytic solution can be prevented and electrical connection inside and outside the capacitor can be prevented.
  • a capacitor manufacturing method includes a component 130 shown in FIGS. 2A to 2E (a separator 130 and a double-sided negative electrode laminate 220 between the top single-sided positive electrode laminate 210T and the bottom single-sided positive electrode laminate 210B). And a step of laminating the separator 130, and a step of impregnating the positive electrode active material layer 120, the negative electrode active material layer 140, and the separator 130 with an electrolytic solution.
  • the additional structure 240 may be further laminated.
  • the capacitor of the present invention may be formed using 120 and the negative electrode active material layer 140.
  • the positive electrode active material layer 120, the positive electrode current collector 110, the positive electrode active material layer 120, the separator 130, the negative electrode active material layer 140, the negative electrode current collector 150, the negative electrode active material layer 150, and the separator 130 are laminated in this order.
  • the capacitor of the present invention can be formed in the same manner as described above.
  • the capacitor obtained as described above can be subjected to processing such as cutting, cutting, bending, drilling and molding.
  • Example 1 3.572 g of polylactic acid having a number average molecular weight of 32,000 was heated to 200 ° C. under a reduced pressure to melt. To the melted polylactic acid, 0.64 g of carbon nanotubes and 5 g of activated carbon having an average particle diameter of 1 ⁇ m were added and kneaded. Subsequently, 0.188 g of VSO 4 OH was added and kneaded to obtain a positive electrode composition. A positive electrode laminate in which a positive electrode composition is applied to both sides of a copper foil having a thickness of 40 ⁇ m using a roll coating method, and a positive electrode active material layer having a thickness of 150 ⁇ m is formed on both sides of the copper foil (positive electrode current collector). Got the body.
  • Triethylmethylammonium tetrafluoroborate was dissolved in a 1: 2.8 mass ratio mixture of sulfolane and propylene carbonate to form an electrolytic solution.
  • the concentration of triethylmethylammonium tetrafluoroborate was 1.5 mol%.
  • a positive electrode laminate, a separator (pulp separator made by NKK), a negative electrode laminate, and a separator are passed between a pair of pressure rolls so as to be laminated in this order, the constituent layers are integrated, and wound into a roll. It was.
  • the roll-shaped intermediate body was placed in a rectangular parallelepiped mold and pressed to form a substantially rectangular parallelepiped shape.
  • the electrolytic solution was impregnated in the positive electrode active material layer, the negative electrode active material layer, and the separator in the intermediate. Thereafter, connection of external connection terminals and packaging with an insulating sealing material were performed to obtain a capacitor.
  • the obtained capacitor had a mass of 22.9 g, an equivalent series resistance (ESR) of 400 m ⁇ , a residual voltage of 10 mV, and a capacitance of 640F.
  • ESR equivalent series resistance
  • a current of 3.7 V and 1 A could be extracted from the obtained capacitor.
  • Example 2 3.572 g of polylactic acid having a number average molecular weight of 32,000 was heated to 200 ° C. under a reduced pressure to melt. To the melted polylactic acid, 0.64 g of carbon nanotubes and 5 g of activated carbon having an average particle diameter of 1 ⁇ m were added and kneaded. Subsequently, 0.188 g of VSO 4 OH was added and kneaded to obtain a positive electrode composition.
  • the positive electrode current collector 110 was formed using a copper foil having a thickness of 30 ⁇ m.
  • the positive electrode current collector 110 is composed of an electrode portion having a long side of 5.9 cm ⁇ short side of 3.9 cm and an external connection tab disposed on the short side of the electrode portion and having a dimension of 1.5 cm ⁇ 0.5 cm. It was done.
  • a positive electrode composition is applied onto the electrode portion on one side of the positive electrode current collector 110 using a roll coating method to form top and bottom single-sided positive electrode laminates 210T and 210B on which a positive electrode active material layer 120 having a thickness of 80 ⁇ m is formed. did.
  • the positive electrode composition was applied onto the electrode portions on both sides of the positive electrode current collector 110 by using a roll coating method to form a double-sided positive electrode laminate 210M in which the positive electrode active material layer 120 having a single-sided film thickness of 80 ⁇ m was formed.
  • the negative electrode current collector 150 was formed using an aluminum foil having a thickness of 30 ⁇ m and subjected to “A20” processing.
  • the negative electrode current collector 150 is disposed on the long side 5.9 cm ⁇ the short side 3.9 cm and the short side of the electrode part, and has a size of 1.5 cm ⁇ 0.5 cm. And an external connection tab.
  • the negative electrode composition was applied onto the electrode portions on both sides of the negative electrode current collector 150 by using a roll coating method to form a double-sided negative electrode laminate 220 in which the negative electrode active material layer 140 having a film thickness of 60 ⁇ m was formed.
  • Triethylmethylammonium tetrafluoroborate was dissolved in a 1: 2.8 mass ratio mixture of sulfolane and propylene carbonate to form an electrolytic solution.
  • the concentration of triethylmethylammonium tetrafluoroborate was 1.5 mol%.
  • Separator 130 (pulver separator made by NKK, long side 6 cm ⁇ short side 4 cm ⁇ thickness 20 ⁇ m), double-sided negative electrode laminate 220, separator 130, and double-sided positive electrode laminate on the positive electrode active material layer 120 side of bottom single-sided positive electrode laminate 210 ⁇ / b> B.
  • the body 210M was laminated in this order. This lamination was repeated 16 times.
  • the separator 130, the double-sided negative electrode laminate 220, the separator 130, and the top single-sided positive electrode laminate 210T were laminated on the uppermost double-sided positive electrode laminate 210M.
  • the positive electrode active material layer 120 of the top single-sided positive electrode laminate 210 ⁇ / b> T was brought into contact with the separator 130.
  • the external connection tabs of the positive electrode laminate (210B, 210M, 210T) are arranged on one straight line extending in the lamination direction, and the external connection tab of the negative electrode laminate (220) is arranged in another direction extending in the lamination direction.
  • the external connection tab of the positive electrode laminate (210B, 210M, 210T) and the external connection tab of the negative electrode laminate (220) did not overlap in the stacking direction.
  • the obtained laminate has 18 positive electrode laminates (210B, 210M, 210T) and 17 negative electrode laminates (220), and adjacent positive electrode laminates (210B, 210M, 210T) and negative electrode laminates. (220) had a structure separated by a separator.
  • the obtained laminate was passed between a pair of pressure rolls to integrate the constituent layers. Further, the separator 130, the positive electrode active material layer 120, and the negative electrode active material layer 140 were impregnated with an electrolytic solution. After that, the external connection tabs of all the positive electrode laminates (210B, 210M, 210T) are connected to the positive terminal for external connection, and the external connection tabs of all the negative electrode laminates (220) are the negative electrodes for external connection.
  • An internal capacitor composed of a pair of a positive electrode laminate (210B, 210M, 210T) and a negative electrode laminate (220) was connected in parallel to the terminal.
  • a substantially rectangular capacitor having a long side of 6.2 cm, a short side of 4.0 cm, and a height of 7.0 mm (excluding connection terminals).
  • the obtained capacitor had a mass of 42.0 g, an equivalent series resistance (ESR) of 25 m ⁇ , and a capacity of 2000 mAh.
  • ESR equivalent series resistance
  • a current of 3.7 V and 2 A could be extracted from the obtained capacitor.
  • the following procedure was used to conduct a charge / discharge durability test of the obtained capacitor.
  • One cycle of discharge was composed of 1A 2A constant current (1C) charge, 10 seconds idle, and 1 minute 2A constant current (1C) discharge.
  • Charging and discharging were performed using a charge / discharge cycle checker manufactured by Electronic Representation Co., Ltd. prepared for this test, and the interval between cycles was set to 10 seconds.
  • the capacitor was fully charged under conditions of a constant voltage of 4.1 V and a constant current of 2 A using a LiPo8 expert charger (manufactured by ABCHObby).
  • the capacitor of the present invention has a discharge capacity of about 92% of the initial discharge capacity even after repeating 1800 discharge / charge cycles. From this, it was found that the capacitor of the present invention has a high discharge and charge resistance. Moreover, although this test was performed under adverse conditions at a low temperature of 10 to 17 ° C., the above results were obtained. Due to the characteristics of this capacitor, it is estimated that even better results can be obtained under higher temperature conditions.

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  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Nanotechnology (AREA)
  • Electric Double-Layer Capacitors Or The Like (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

La présente invention concerne un condensateur présentant une nouvelle configuration dans laquelle, en plus d'une double couche électrique formée au niveau de l'interface entre une électrode polarisable et un électrolyte, de l'énergie électrique est stockée en utilisant le transfert de charge entre l'électrode polarisable et un composé métallique. Le condensateur comprend : un collecteur d'électrode positive ; une couche de matériau actif d'électrode positive contenant un matériau de carbone ; un acide polylactique et un composé V3+ ; un séparateur ; un matériau de carbone ; une couche de matériau actif d'électrode négative contenant un acide polylactique et un composé V4+ ; un collecteur d'électrode négative ; et un électrolyte qui s'infiltre dans la couche de matériau actif d'électrode positive, le séparateur, et la couche de matériau actif d'électrode négative.
PCT/JP2011/003133 2010-06-10 2011-06-02 Condensateur WO2011155164A1 (fr)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013076762A1 (fr) * 2011-11-22 2013-05-30 イノベーションエネルギー株式会社 Condensateur

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110892574A (zh) * 2017-07-04 2020-03-17 优化公司 二次电池和二次电池的制造方法

Citations (4)

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Publication number Priority date Publication date Assignee Title
JP2005032633A (ja) * 2003-07-08 2005-02-03 Tdk Corp 電極及び電気化学素子
JP2005166459A (ja) * 2003-12-03 2005-06-23 Yuasa Corp 電気化学デバイス、電気化学デバイス用電極、電気化学デバイス用電極材料及びその製造方法
JP2009519565A (ja) * 2005-12-14 2009-05-14 アヴェスター リミティッド パートナーシップ 電気化学バッテリー及びその製造方法
JP2010034300A (ja) * 2008-07-29 2010-02-12 Jfe Chemical Corp 電気二重層キャパシタの分極性電極用炭素材料、その製造方法および電気二重層キャパシタ

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005032633A (ja) * 2003-07-08 2005-02-03 Tdk Corp 電極及び電気化学素子
JP2005166459A (ja) * 2003-12-03 2005-06-23 Yuasa Corp 電気化学デバイス、電気化学デバイス用電極、電気化学デバイス用電極材料及びその製造方法
JP2009519565A (ja) * 2005-12-14 2009-05-14 アヴェスター リミティッド パートナーシップ 電気化学バッテリー及びその製造方法
JP2010034300A (ja) * 2008-07-29 2010-02-12 Jfe Chemical Corp 電気二重層キャパシタの分極性電極用炭素材料、その製造方法および電気二重層キャパシタ

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013076762A1 (fr) * 2011-11-22 2013-05-30 イノベーションエネルギー株式会社 Condensateur

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