WO2010067509A1 - 電気二重層キャパシタ及びその製造方法 - Google Patents
電気二重層キャパシタ及びその製造方法 Download PDFInfo
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- WO2010067509A1 WO2010067509A1 PCT/JP2009/005898 JP2009005898W WO2010067509A1 WO 2010067509 A1 WO2010067509 A1 WO 2010067509A1 JP 2009005898 W JP2009005898 W JP 2009005898W WO 2010067509 A1 WO2010067509 A1 WO 2010067509A1
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- separator
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- pressure
- double layer
- electric double
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Images
Classifications
-
- 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
- H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
-
- 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
- H01G11/10—Multiple hybrid or EDL capacitors, e.g. arrays or modules
- H01G11/12—Stacked hybrid or EDL capacitors
-
- 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
- H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
- H01G11/28—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features arranged or disposed on a current collector; Layers or phases between electrodes and current collectors, e.g. adhesives
-
- 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
-
- 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
- Y02E60/13—Energy storage using capacitors
Definitions
- the present invention relates to an electric double layer capacitor using conductive fine fibers such as carbon nanotubes and a method for manufacturing the same.
- nanowires such as nanowires, nanotubes, and nanohorns
- materials constituting the nanowires silver, silicon, gold, copper, zinc oxide, titanium oxide, gallium nitride, and the like have been studied.
- Carbon nanotubes are known as nanotubes
- carbon nanohorns are known as nanohorns.
- the most promising carbon nanotube as a conductive material has a structure in which a graphite sheet is rolled into a cylindrical shape.
- the material has a hollow structure having a diameter of about 0.7 to 100 nm and a length of several ⁇ m to several mm.
- the electrical properties of carbon nanotubes show semiconducting properties from metals depending on the diameter and chirality. Furthermore, since it does not have dangling bonds, it is chemically stable. It is also attracting attention as a material with low environmental impact because it consists of carbon atoms only.
- carbon nanotubes have the properties described above, they are expected to be applied as electron emission sources for flat panel displays, electrode materials for lithium batteries, electrode materials for electric double layer capacitors, and probe probes. .
- Carbon nanotubes can be synthesized by an arc discharge method using a carbon electrode, a thermal decomposition method of benzene, a laser deposition method, or the like. However, in these methods, graphite is synthesized together with carbon nanotubes. Therefore, when the carbon nanotube is applied to the electron source, battery electrode, probe probe, etc., it is necessary to remove impurities such as graphite and carbon nanoparticles in advance. In addition, since carbon nanotubes of various lengths are synthesized in random directions, the characteristics as an electron emission source are limited.
- the electric double layer capacitor is a capacitor that uses an electric double layer generated between an active material and an electrolyte, and has been used as a backup power source. Growth is expected.
- an active material of an electric double layer capacitor one using activated carbon is widely known (see, for example, Patent Document 1).
- carbon nanotubes have an external surface area of 2600 to 3000 m 2 / g, which is higher than that of activated carbon. Electric double layer capacitors using carbon nanotubes as an active material have attracted attention because of their much larger and extremely tough mechanical properties and excellent electronic properties.
- An electric double layer capacitor has a different operating principle from a battery using an oxidation-reduction reaction, and is an electricity storage device that performs charging and discharging by adsorbing and desorbing cations and anions in the electrolyte on the surface of the active material. is there.
- An electric double layer capacitor has a long life because it does not involve a chemical reaction, has many advantages over batteries, such as easy measurement of residual charge and low environmental load.
- FIG. 11 shows an example of a structure for illustrating the electrical operation principle of a general electric double layer capacitor.
- the electric double layer capacitor 1100 includes a positive electrode 1111 and a negative electrode 1112.
- the positive electrode 1111 includes a current collector 1107 and an active material layer 1108 provided on the current collector.
- the negative electrode 1112 includes a current collector 1104 and an active material layer 1105 provided on the current collector.
- the positive electrode 1111 and the negative electrode 1112 are in the electrolytic solution 1106.
- An electric field is generated between the positive electrode 1111 and the negative electrode 1112 by applying a voltage from the power source 1101 to the positive electrode 1111 and the negative electrode 1112.
- FIG. 12 shows an electrical equivalent circuit corresponding to FIG. As shown in FIG. 12, the electric double layer capacitor has a structure in which two capacitors 1202 and 1203 are connected in series.
- Non-Patent Document 1 as a technique for increasing the density of carbon nanotubes, a simple high-pressure press (1 to 10 t / cm 2 (98 to 980 MPa)) is used to reduce the surface area and electric capacity to a maximum of about 0.00 at most. It has been reported that densification exceeding 6 g / cm 3 has been achieved.
- Non-Patent Document 1 the carbon nanotube layer 1302 formed on the current collector 1301 is compressed using pressing plates 1303 and 1304.
- the carbon nanotube layer is transferred to the pressing plate 1303 that is in contact with the carbon nanotube layer 1302, and there is a problem that a part of the carbon nanotube layer 1306 is peeled off from the current collector 1301.
- the remaining carbon nanotube layer 1305 can achieve high density, a region not covered with the carbon nanotube layer is generated on the surface of the current collector. Therefore, the energy density cannot be sufficiently increased for the electric double layer capacitor as a whole.
- the present invention is an electric double layer capacitor using conductive fine fibers such as carbon nanotubes as an active material, the electric double layer capacitor having an increased energy density by compressing the active material at a high density, and It aims at providing the manufacturing method.
- the electric double layer capacitor of the present invention includes a positive electrode, a separator, and a negative electrode laminated in this order in a container, and a space between the positive electrode and the negative electrode is filled with an electrolyte.
- the electric double layer capacitor one or both of the positive electrode and the negative electrode are erected such that one end thereof is electrically connected to the current collector and the surface of the current collector.
- the electrode plate is covered with the separator, and the electrode plate and the separator are pressed and integrated with each other.
- the method for producing an electric double layer capacitor of the present invention includes a positive electrode, a separator, and a negative electrode laminated in this order in a container, and an electric double layer in which a space between the positive electrode and the negative electrode is filled with an electrolyte.
- a method of manufacturing a capacitor comprising: a current collector; and an electrode plate comprising a plurality of conductive fine fibers erected so that one end is electrically connected to the surface of the current collector, and a separator.
- a pressure bonding step of forming a pressure-bonded laminate by pressing and integrating the plate and the separator, and an impregnation step of impregnating the pressure-bonded laminate with an electrolytic solution are included.
- the active material layer is compressed by pressing and integrating the electrode plate and the separator, the active material layer made of conductive fine fibers is transferred to the pressure member. Without increasing the density of the active material layer, the energy density is increased.
- an electric double layer capacitor of the present invention can be easily manufactured.
- FIG.2 The figure showing the process flow of the manufacturing method of this invention, and the manufacturing method of a comparative example.
- Schematic which shows the coating
- Schematic which shows the coating process and compression process in the case of manufacturing the electrical double layer capacitor which has the structure of FIG.2 (b).
- Schematic shows the pre-pressurization process in the case of manufacturing the electrical double layer capacitor which has the structure of Fig.2 (a), a coating process, and a compression process.
- Schematic which shows the pre-pressurization process, coating
- FIG. 2 is an electron micrograph of a cross section of a pressure-bonded laminate in Example 1.
- FIG. The cyclic voltammogram of the electric double layer capacitor measured in Example 2.
- FIG. 2 (a) is a conceptual diagram of an electric double layer capacitor according to an embodiment of the present invention.
- the electric double layer capacitor 200 includes a separator 205, and a positive electrode 206 and a negative electrode 207 arranged to face each other with the separator 205 interposed therebetween.
- the positive electrode 206 includes a current collector 201 and a plurality of fine fibers 202 erected on the current collector 201.
- the negative electrode 207 includes a current collector 203 and a plurality of fine fibers 204 provided upright on the current collector 203.
- the separator 205 is in contact with the fine fiber 202 on one side and in contact with the fine fiber 204 on the other side.
- the separator 205, the positive electrode 206, and the negative electrode 207 are pressure-bonded and integrated. According to this embodiment, since there is only one separator, the resistance of the electric double layer capacitor can be reduced.
- FIG. 2 (b) showing another embodiment is different from FIG. 2 (a) in that two separators 205a and 205b exist.
- the positive electrode separator 205a facing the positive electrode 206 is disposed so as to be laminated with the positive electrode 206 so as to be in contact with the fine fibers 202, and these are integrated by pressure bonding.
- the negative electrode separator 205b facing the negative electrode 207 is disposed so as to be laminated with the negative electrode 207 so as to be in contact with the fine fibers 204, and these are integrated by pressure bonding.
- the two sets of pressure-bonded laminates are superposed so that the two separators 205a and 205b are in contact with each other. According to this embodiment, when only one separator is viewed, only one surface is pressure-bonded to the fine fiber, so that the risk of occurrence of a short circuit can be reduced.
- the current collectors 201 and 203 are plate-shaped formed of a conductive material.
- the conductive material include, but are not limited to, silicon, stainless steel, iron, aluminum, nickel, titanium, copper, and the like.
- aluminum is used as a current collector of an electric double layer capacitor using activated carbon as an active material, and can be particularly preferably used in the present invention. This is because aluminum forms a thin passive film on the surface, so that aluminum does not melt even when a high voltage is applied.
- Separator 205 or 205a, 205b is a material that separates both electrodes by being disposed between the positive electrode and the negative electrode, and retains the electrolytic solution to ensure ionic conductivity between the positive electrode and the negative electrode.
- the material constituting the separator include organic materials such as cellulose, polypropylene, polytetrafluoroethylene, polyolefin, fluorine-containing resin, acrylic resin, polyamide resin, nylon, polyester, polycarbonate, sulfonic acid group-containing resin, and phenol resin; Although inorganic materials, such as glass fiber, are mentioned, it is not specifically limited.
- the electric double layer capacitor of the present invention can be manufactured by separately preparing an electrode plate including a current collector and fine fibers and a separator, and then laminating and crimping the separator, the separator is a thermosetting resin. Even if it is made of a material other than the above, it is easy to manufacture. In this invention, what is generally marketed can be used as a separator for electric double layer capacitors.
- the diameters of the fine fiber 202 and the fine fiber 204 are preferably 0.1 to 100 nm.
- the fine fiber 202 and the fine fiber 204 can be erected at a high density on the current collector 201 and the current collector 203, and the energy density A high electric double layer capacitor can be constructed.
- the fine fiber 202 and the fine fiber 204 include, but are not limited to, nanowires made of silver, gold, or copper, carbon nanotubes, carbon nanohorns, activated carbon fibers, and the like. Of these, carbon nanotubes are preferred because of the ease of orientation synthesis.
- Carbon nanotubes are extremely fine tube (tube) -like substances having a hole diameter of nanometers and formed by bonding carbon atoms in a network.
- the carbon nanotube When the carbon nanotube is used, it may be a single layer, that is, a single tube, or may be a multilayer, that is, a concentric plurality of different diameter tubes.
- the diameter of the carbon nanotube is not limited, but considering that it is used for an electrode of an electric double layer capacitor, lithium ions having an ionic radius of 0.074 nm and electrolyte ions having an ionic radius of about 0.5 nm are present in the inside thereof. Since it is assumed to enter, the range of 0.1 nm to 10 nm is preferable, and the range of 0.1 nm to 3 nm is more preferable.
- the space between the positive electrode and the negative electrode is filled with an electrolytic solution, and the electrolytic solution is held by a separator.
- the electrolytic solution one composed of a solvent and an electrolytic solution can be used.
- the solvent of the electrolytic solution is not particularly limited.
- the electrolyte of the electrolytic solution is not particularly limited, but for example, selected from tetraethylammonium tetrafluoroborate, triethylmethylammonium tetrafluoroborate, triethylmethylammonium bis, tetraethylammonium hexafluorophosphate, and tetraethylammonium bis One or more combinations can be used.
- an ionic liquid imidazolium-based, pyridinium-based, aliphatic-based, pyrrolidinium-based, ammonium-based, phosphonium-based, or sulfonium-based compound or a combination of a plurality of compounds is used. Also good.
- the capacity per unit volume (F / cm 3 ) is proportional to the density of the active material. Therefore, in the case where the active material is an electrode composed of fine fibers, it is considered that the density and the capacity are proportional to each other as long as the surface area of the active material does not change. Therefore, it is considered that the energy per unit volume (energy density) increases if the density of the active material layer is increased.
- the maximum density of the fine fiber layer achieved by the synthesis is not necessarily the ideal maximum density as the active material layer (per unit volume for adsorption / desorption of ions). It is not always the density that maximizes the surface area of In order to approach the ideal maximum density, in the present invention, compression is performed in a state in which the separator is laminated on the fine fiber layer, thereby increasing the density of the fine fiber layer and pressing the electrode plate and the separator together. Turn into. Thereby, since the density of a fine fiber layer can be raised without producing problems, such as peeling of a fine fiber layer, the energy density of an electric double layer capacitor can be improved. Moreover, since the electrode plate and the separator are integrated, handling is easy when they are stored in a container.
- the separator and the current collector are integrated by being pressure-bonded with an active material layer made of fine fibers interposed therebetween.
- the pressure bonding means that the separator and the electrode plate are fixed without using an adhesive, and specifically, 2.5 ⁇ 10 4 Pa or more for separating the separator and the electrode plate. This refers to the state where stress is required.
- the separator and the electrode plate are not pressure-bonded and integrated, the separator and the electrode plate are easily separated when a stress of less than 2.5 ⁇ 10 4 Pa is applied.
- FIG. 1 the process flow in the manufacturing method of this invention and the process flow in the manufacturing method of a comparative example were contrasted and shown.
- two electrode plates (a positive electrode and a negative electrode) and a separator are prepared.
- Either one or both of the two electrode plates are a current collector and a plurality of conductive fine particles erected so that one end is electrically connected to one or both surfaces of the current collector.
- fine fibers can be used as described above, and a method for standing a plurality of carbon nanotubes on the surface of the current collector will be described below when the fine fibers are carbon nanotubes.
- Carbon nanotubes can be formed by a transfer method. However, a method of directly synthesizing on the current collector is preferable from the viewpoint of obtaining a carbon nanotube with good orientation. In this case, the carbon nanotubes are synthesized through catalytic metal particles attached to the surface of the current collector.
- the catalyst examples include nickel, iron, cobalt, zinc, molybdenum, gold, silver and copper metals; alloys of these combinations; oxides and carbides of these metals; And the synthesis method thereof.
- ⁇ Catalyst metal particles are enlarged by performing heating at the time of carbon nanotube synthesis or preheating before synthesis. It is said that there is a correlation between the catalyst metal particle diameter and the synthesized carbon nanotube diameter. Therefore, when a carbon nanotube diameter of 1 to 100 nm is desired, the catalyst metal particle diameter is desirably adjusted to 1 to 100 nm.
- Methods for directly synthesizing carbon nanotubes standing on a current collector include vapor phase chemical vapor deposition (CVD), laser ablation, arc discharge, and electrolytic synthesis in solution.
- CVD vapor phase chemical vapor deposition
- the CVD method is used. preferable.
- CVD methods There are two main types of CVD methods: a thermal CVD method that thermally decomposes a source gas and a plasma CVD method that decomposes a source gas with plasma.
- Carbon nanotubes can be synthesized by a CVD method at a temperature of 550 ° C. to 750 ° C. and a pressure of 200 Pa.
- Carbon nanotubes are decomposed directly by flowing a hydrocarbon gas such as methane, ethylene or acetylene, or an alcohol such as methanol into the chamber, and directly decomposing the carbon source on a current collector equipped with catalytic metal particles. Synthesize. Furthermore, a gas such as argon, nitrogen, or hydrogen may be used as a carrier gas for the carbon source.
- the growth time of the carbon nanotube is controlled according to the length of the target carbon nanotube. Although the growth time varies depending on the growth temperature, gas pressure, and the type of carbon source used, the growth time cannot be generally stated. Can be about 10 minutes to 4 hours.
- the coating process is performed.
- the surface of the electrode plate (the surface on the side where the fine fibers are erected) is covered with a separator to form a laminate composed of the electrode plate and the separator.
- a crimping process is performed.
- pressure is applied from above and below to the laminate obtained in the coating step.
- the method of pressurization is not specifically limited, For example, the method of pressing a laminated body between plates, the method of pressing by pressing between rollers, etc. can be used.
- compression-bonding process is not specifically limited, Since the density of an active material layer will be 0.5 g / cm ⁇ 2 > or less, for example, if a pressure is too small, the effect of an energy density improvement cannot fully be achieved. On the other hand, if the pressure is too high, the separator is broken during the pressure-bonding process, and a short circuit problem is likely to occur. In consideration of these circumstances, the pressure during the compression step can be appropriately determined, but specifically, it is preferably about 30 MPa to 70 MPa.
- a cushioning material such as rubber is stacked on both sides of the laminate so that pressure is uniformly applied to the entire surface of the electrode plate.
- the electrode plate and the separator are crimped and integrated.
- the active material layer is composed of fine fibers standing upright
- the separator is composed of a fibrous material such as cellulose
- the fibrous material enters into the separator by pressurization and the fibrous material. It is considered that the electrode plate and the separator can be physically fixed.
- the separator is composed of a sheet made of an organic material or the like, it is considered that physical adhesion between the electrode plate and the separator becomes possible by pressing fine fibers into the sheet by pressurization.
- activated carbon is not composed of fine fibers, even if the separator is stacked on an electrode plate using activated carbon as an active material and compressed with a very high pressure (for example, 100 MPa or more), the activated carbon and the separator are not pressure-bonded.
- the distance between the positive electrode and the negative electrode is closer than in the case where the compression process is not performed.
- FIG. 3 schematically shows a coating process and a compression process in the case of manufacturing the electric double layer capacitor having the configuration of FIG.
- the positive electrode 306 and the negative electrode 307 are compressed with the separator 305 interposed therebetween.
- FIG. 14 is a modification of FIG. 3, in which a plurality of positive electrodes and a plurality of negative electrodes are produced by forming fine fibers on both sides of a current collector, and these positive electrodes and negative electrodes are alternately arranged with a separator in between.
- stacks and compresses is shown.
- FIG. 4 schematically shows a coating process and a compression process in the case of manufacturing the electric double layer capacitor having the configuration of FIG.
- compression is performed in a state where the positive electrode 406 and the positive electrode separator 405a are laminated, and compression is performed separately in a state where the negative electrode 407 and the negative electrode separator 405b are laminated, and two sets of the pressure-bonded laminates thus obtained are obtained.
- FIG. 15 is a modification of FIG. 4. After forming fine fibers on both sides of the current collector, a plurality of sets of compressed laminates are manufactured by covering both sides of the electrode plate with a separator and compressing them. The example which superimposes alternately is shown.
- An electric double layer capacitor can be manufactured by impregnating an electrolyte solution into the pressure-bonded laminate obtained as described above and finally storing it in a container.
- a pre-pressurizing step for inclining fine fibers before carrying out the coating step.
- a weak pressure is applied to the fine fibers on the current collector that is smaller than the pressure in the crimping process and does not peel off the fine fibers.
- by tilting the fine fibers in a direction that is not perpendicular to the current collector in the pre-pressurization step it is possible to prevent the occurrence of a short circuit between the two electrodes due to the fine fibers breaking through the separator during the crimping step. .
- the material of the pressing plate in contact with the fine fibers when the pre-pressing is performed is not particularly limited, but it is preferable to use a material having a smooth surface in order to prevent the transfer of the fine fibers.
- a material having a smooth surface in order to prevent the transfer of the fine fibers.
- glass, alumina, silicon wafer or the like can be used.
- the pressure during the pre-pressurization step may be appropriately determined in consideration of the above-mentioned purpose, but is preferably about 2.5 MPa to 5 MPa.
- FIG. 5 schematically shows a pre-pressurization step, a covering step, and a compression step when manufacturing the electric double layer capacitor having the configuration of FIG.
- the pre-pressing plate 510 is placed on the fine fiber 502, and pressure is applied to the pre-pressing plate 511 to compress the fine fiber 502 weakly.
- the pre-pressurization plate 512 is placed on the fine fiber 504, and pressure is applied between the pre-pressurization plate 513 to weakly compress the fine fiber 504.
- the positive electrode 506 and the negative electrode 507 are stacked with the separator 505 interposed therebetween, and then a pressure bonding step is performed.
- FIG. 6 schematically shows a pre-pressurization step, a covering step, and a compression step when manufacturing the electric double layer capacitor having the configuration of FIG.
- each electrode is covered with the separators 605a and 605b, and then a crimping process is performed.
- a double layer capacitor is formed.
- Comparative Example 1 Comparative Example 1
- a method of directly compressing fine fibers erected on the surface of the current collector without being laminated with a separator was performed. Carbon nanotubes were used as the fine fibers.
- an aluminum plate for an electric double layer capacitor having a size of 7 mm ⁇ 14 mm and a thickness of 300 ⁇ m was prepared and cleaned.
- a cleaning solution in which DK Beakrya (Daiichi Kogyo Seiyaku Co., Ltd.) was dissolved in pure water at a concentration of 3 wt% was kept at 40 ° C. and washed by immersing the current collector in it.
- the current collector was immersed in the cleaning solution for 5 minutes, and then rinsed with pure water for 5 minutes with an ultrasonic cleaner. The rinse was repeated 3 times. After rinsing, N 2 blow was performed to dry the current collector.
- the current collector was set in an EB vapor deposition machine, and Al was deposited as a catalyst material at a layer thickness of 3 nm, and further Fe was deposited at a layer thickness of 1 nm.
- the degree of vacuum before vapor deposition was set to 1.2 ⁇ 10 ⁇ 5 Pa.
- the deposition rate of Al and Fe was 1 nm / s.
- the current collector was heat-treated at 300 ° C. for 30 minutes in a vacuum to form catalytic metal particles. At this stage, when the diameter of the catalytic metal particles was measured by AFM, an average value of 2.9 nm was obtained.
- carbon nanotubes with an average length of 638 ⁇ m that were vertically aligned from the current collector could be synthesized.
- information such as the diameter of the carbon nanotube can be obtained. It was confirmed that the mixture was a single-walled carbon nanotube having a diameter of 3 nm and a double-walled carbon nanotube.
- the above-mentioned aluminum plate with carbon nanotubes grown thereon was prepared, a Si wafer was placed on the carbon nanotubes, and the carbon nanotubes were compressed with a pressure that did not transfer to the Si wafer. Next, when a Si wafer was placed on the carbon nanotubes and compressed with a press at a pressure of 20 MPa, a part of the carbon nanotubes was transferred to the Si wafer.
- the above-mentioned aluminum plate with carbon nanotubes grown thereon was prepared, a Si wafer was placed on the carbon nanotubes, and the carbon nanotubes were compressed with a pressure that did not transfer to the Si wafer.
- a sapphire substrate was placed on the carbon nanotubes and compressed with a press at a pressure of 20 MPa, a part of the carbon nanotubes was transferred to the sapphire substrate.
- photographed this state is shown in FIG.
- the above-mentioned aluminum plate with carbon nanotubes grown thereon was prepared, a Si wafer was placed on the carbon nanotubes, and the carbon nanotubes were compressed with a pressure that did not transfer to the Si wafer.
- a glass rod having a diameter of 4 mm was prepared and the glass rod was rolled while applying pressure on the carbon nanotube, a part of the carbon nanotube was transferred to the glass rod.
- photographed this state is shown in FIG.
- Example 1 an electrode for an electric double layer capacitor was manufactured by placing a separator on fine fibers standing on the surface of a current collector, and applying pressure to a laminate composed of an electrode plate and a separator. Carbon nanotubes were used as the fine fibers.
- the Si wafer was placed on the carbon nanotube, and the carbon nanotube was compressed with a pressure (4 MPa) that does not transfer to the Si wafer.
- the carbon nanotubes on the two current collectors were placed facing each other with a 25 ⁇ m-thick polypropylene separator in between, and pressurized with a press at a pressure of 50 MPa.
- a rubber sheet was placed between both the current collectors side, that is, the aluminum side, and the press plate of the press machine in order to disperse the pressure evenly.
- the positive electrode, the separator, and the negative electrode were pressure-bonded and integrated, and could not be easily separated. When the stress required for pulling off the five samples was measured, it was 2.5 ⁇ 10 4 to 5 ⁇ 10 4 MPa.
- the stress was measured by applying a stress with a spring scale to a positive electrode and a negative electrode fixed to a stainless steel plate, and obtaining the stress when peeling. In addition, after separating the positive electrode and the negative electrode, carbon nanotubes were partially transferred to the separator.
- the bonded structure was cut and cross-sectional observation was performed with an electron microscope.
- the electron micrograph is shown in FIG.
- the thickness of the 638 ⁇ m carbon nanotubes was compressed to 17 ⁇ m.
- the density of the carbon nanotubes that prior to compression was 0.027 g / cm 3 becomes compressed after 1.0 g / cm 3.
- the separator thickness was compressed from 25 ⁇ m to 20 ⁇ m.
- Example 2 an electric double layer capacitor was produced using the electrode for electric double layer capacitor produced by integrating the positive electrode, separator and negative electrode produced in Example 1.
- the electric double layer capacitor electrode was immersed in an electrolytic solution.
- an electrolytic solution a solution obtained by dissolving tetraethylammonium tetrafluoroborate in propylene carbonate was used.
- the concentration of tetraethylammonium tetrafluoroborate was 0.7 mol / l.
- the pressure was reduced to such an extent that the electrolyte did not boil, and the electrolyte was infiltrated into the details of the active material.
- Cyclic voltammogram measurement was performed on the electrode impregnated with the electrolytic solution as described above at a voltage sweep rate of 40 mV / sec and a voltage range of 0 V and 3.5 V. A graph obtained by the measurement is shown in FIG. As shown in FIG. 10, the electric double layer capacitor of this example exhibited good capacitor characteristics.
- the energy density per liter of the active material was 5.1 Wh / L.
- the energy density per liter of the active material was 0.26 Wh / L. Therefore, the energy density could be improved by about 20 times by performing the crimping process.
- Example 3 In this example, the positive electrode and the positive electrode separator manufactured in Example 1 were bonded together by pressure bonding, and the negative electrode and the negative electrode separator were bonded and integrated, and then the separators were stacked to form an electric double layer. An example of manufacturing a capacitor will be described.
- the method of impregnation is the same as the method described in Example 2 and will be omitted.
- the capacitor characteristics were measured in the same manner as in Example 2. Since the measurement method and the method for obtaining the capacity are the same as those described in the second embodiment, a description thereof will be omitted. As a result, the capacitor capacity was 9 F / g. The energy density per liter of the active material was 1.0 Wh / L.
- the energy density could be improved about 4 times by the configuration of this example.
- Example 4 the advantages of carrying out a process of compressing the fine fibers with a weak pressure before the fine fibers and the separator standing on the current collector were pressure-bonded were examined. Carbon nanotubes were used as the fine fibers.
- the prepared capacitor was charged and discharged from 0 to 2.5 V, and when (charge required for charge) / (discharged charge) was 1.3 or more, it was judged as a short circuit.
- the results are shown in Table 1.
- the electric double layer capacitor according to the present invention has a high density of fine fibers constituting the active material layer and can improve the energy density
- the portable terminal device such as a mobile phone and a portable computer, an automobile, a bicycle, and a train It is useful as an energy source for mobile devices.
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Abstract
Description
本比較例では、図1の比較例に従い、セパレータと積層せずに、集電体の表面に立設した微細繊維を直接圧縮する方法を行った。微細繊維としてカーボンナノチューブを用いた。
本実施例では、集電体の表面に立設した微細繊維の上にセパレータを置き、極板とセパレータとからなる積層体に圧力をかけることにより、電気二重層キャパシタ用電極を製造した。微細繊維としてカーボンナノチューブを用いた。
本実施例では、実施例1で製造した、正極とセパレータと負極とが圧着されて一体化した電気二重層キャパシタ用電極を用いて、電気二重層キャパシタを製造した。
本実施例では、実施例1で製造した、正極と正極用のセパレータとを圧着して一体化し、負極と負極用のセパレータとを圧着して一体化した後、セパレータ同士を重ねて電気二重層キャパシタを製造した例について説明する。
本実施例では、高圧で集電体上に立設した微細繊維とセパレータとを圧着する前に、微細繊維を弱い圧力で圧縮する行程を実施することによる利点を検討した。微細繊維としてカーボンナノチューブを用いた。
201、203 集電体
202、204 微細繊維
205、205a、205b セパレータ
206 正極
207 負極
301、303 集電体
302、304 微細繊維
305 セパレータ
306 正極
307 負極
401、403 集電体
402、404 微細繊維
405a、405b セパレータ
406 正極
407 負極
501、503 集電体
502、504 微細繊維
505 セパレータ
506 正極
507 負極
510、511、512、513 予備加圧用板
601、603 集電体
602、604 微細繊維
605a、605b セパレータ
606 正極
607 負極
610、611、612、613 予備加圧用板
1100 電気二重層キャパシタ
1101 電源
1102 陽イオン
1103 負電荷
1104 集電体
1105 活物質
1106 電解液
1107 集電体
1108 活物質
1109 正電荷
1110 陰イオン
1111 正極
1112 負極
1201 電源
1202 正極に発生したコンデンサ
1203 負極に発生したコンデンサ
1301 集電体
1302 微細繊維
1303、1304 圧縮用板
1305 集電体に残った微細繊維
1306 転写された微細繊維
Claims (14)
- 容器内に、正極、セパレータ及び負極をこの順で積層して含み、前記正極と前記負極との間が電解液で満たされている電気二重層キャパシタであって、
前記正極及び前記負極のうちいずれか一方又は双方の極板が、集電体と、前記集電体の表面に一端が電気的に接続するように立設された複数本の導電性微細繊維とからなり、
前記極板の前記表面側が前記セパレータで被覆され、
前記極板とセパレータとが圧着され一体化していることを特徴とする電気二重層キャパシタ。 - 前記正極と1枚のセパレータと前記負極がこの順序で、圧着され一体化している、請求項1記載の電気二重層キャパシタ。
- 前記セパレータは、正極用のセパレータと負極用のセパレータを含み、
前記正極と前記正極用のセパレータとが圧着され一体化しており、前記負極と前記負極用のセパレータとが圧着され一体化している、請求項1記載の電気二重層キャパシタ。 - 前記微細繊維は、直径が0.1nm~100nmである、請求項1~3のいずれかに記載の電気二重層キャパシタ。
- 前記微細繊維は、カーボンナノチューブである、請求項1~4のいずれかに記載の電気二重層キャパシタ。
- 前記セパレータは、熱硬化性樹脂以外の材料からなる、請求項1~5のいずれかに記載の電気二重層キャパシタ。
- 容器内に、正極、セパレータ及び負極をこの順で積層して含み、前記正極と前記負極との間が電解液で満たされている電気二重層キャパシタの製造方法であって、
集電体と、前記集電体の表面に一端が電気的に接続するように立設された複数本の導電性微細繊維とからなる極板、及び、セパレータを準備する準備工程、
前記極板の前記表面側を前記セパレータで被覆して、前記極板と前記セパレータからなる積層体を形成する被覆工程、
前記積層体に上下から圧力をかけることで、前記極板とセパレータとを圧着し、一体化することで、圧着積層体を形成する圧着工程、
前記圧着積層体に電解液を含浸させる含浸工程、を含む、電気二重層キャパシタの製造方法。 - 前記準備工程において、2枚の極板及び1枚のセパレータを準備し、
前記被覆工程において、前記2枚の極板それぞれの前記表面が前記1枚のセパレータを間に挟んで対向するように、前記2枚の極板と前記1枚のセパレータとを積層し、
前記圧着工程において、前記2枚の極板と前記1枚のセパレータとが圧着してなる圧着積層体を形成する、請求項7に記載の製造方法。 - 前記準備工程において、2枚の極板及び2枚のセパレータを準備し、
前記被覆工程において、前記2枚の極板における前記表面を各々1枚のセパレータで被覆して二組の積層体を形成し、
前記圧着工程において、1枚の極板と1枚のセパレータとが圧着してなる圧着積層体を二組形成し、
前記含浸工程の前後に、前記二組の圧着積層体を、前記セパレータ同士が接触するように重ね合わせる工程をさらに含む、請求項7に記載の製造方法。 - 前記圧着工程における前記圧力は、30MPa以上70MPa以下である、請求項7~9のいずれかに記載の製造方法。
- 前記準備工程の後で前記被覆工程の前に、前記集電体上の前記導電性微細繊維に対して、前記圧着工程における前記圧力よりも小さい圧力をかけることで、前記微細繊維を傾斜させる予備加圧工程をさらに含む、請求項7~10のいずれかに記載の製造方法。
- 前記微細繊維は、直径が0.1nm~100nmである、請求項7~11のいずれかに記載の製造方法。
- 前記微細繊維は、カーボンナノチューブである、請求項7~12のいずれかに記載の製造方法。
- 前記カーボンナノチューブは、触媒を介して前記集電体の前記表面上に立設されている、請求項13に記載の製造方法。
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