WO2014050653A1 - 集電体、電極構造体、非水電解質電池、導電性フィラーおよび蓄電部品 - Google Patents
集電体、電極構造体、非水電解質電池、導電性フィラーおよび蓄電部品 Download PDFInfo
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- WO2014050653A1 WO2014050653A1 PCT/JP2013/075119 JP2013075119W WO2014050653A1 WO 2014050653 A1 WO2014050653 A1 WO 2014050653A1 JP 2013075119 W JP2013075119 W JP 2013075119W WO 2014050653 A1 WO2014050653 A1 WO 2014050653A1
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- current collector
- conductive
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- layer
- particles
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Images
Classifications
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- H—ELECTRICITY
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- H01M4/00—Electrodes
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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
- H01G11/66—Current collectors
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- 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
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- H—ELECTRICITY
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- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/4235—Safety or regulating additives or arrangements in electrodes, separators or electrolyte
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- H—ELECTRICITY
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- 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
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- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- H01M4/623—Binders being polymers fluorinated polymers
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- H—ELECTRICITY
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- H01M2220/00—Batteries for particular applications
- H01M2220/30—Batteries in portable systems, e.g. mobile phone, laptop
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- 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
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- 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
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- Y02E60/13—Energy storage using capacitors
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- 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
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- 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
Definitions
- the present invention relates to a current collector, an electrode structure, a nonaqueous electrolyte battery, a conductive filler, and a power storage component.
- lithium ion secondary batteries are increasingly used as power sources for small or portable electronic devices such as mobile phones and notebook computers. Furthermore, in recent years, it has been expected to be used as a power source for electric vehicles that are becoming popular due to consideration for the environment, and its importance is also increasing as a power source for vehicles.
- the lithium ion secondary battery has the advantage of high energy density, it uses a non-aqueous electrolyte and has a problem with respect to safety. For example, if the battery becomes hot due to unintentional external heating and internal heat generation, the non-aqueous electrolyte component may decompose, causing problems such as internal pressure rising and battery swelling. There is also a risk of ignition. Heat generation inside the battery may be caused when an internal short circuit occurs due to unauthorized use, overcharge, or impact.
- a built-in PTC (Positive Temperature Coefficient) element whose resistance increases as the temperature rises is prevented and a current is generated during heat generation. It is also possible to provide a mechanism for blocking. For example, a method of attaching a PTC element to a positive electrode cap portion of a cylindrical battery is also known.
- the method of attaching the PTC element to the positive electrode cap portion does not respond to the temperature rise inside the battery, and therefore there is a problem that the short-circuit current cannot be suppressed when an internal short circuit occurs and the temperature inside the battery rises. there were.
- a method using a separator that exhibits a shutdown function by melting the resin during abnormal heat generation is widely known.
- the separator does not always melt at a location away from the heat generating portion, and may not exhibit a shutdown function.
- there is still room for improvement in improving the safety against internal heat generation For example, when the heat generation proceeds, the separator may be deformed and contracted, and the internal short circuit may proceed.
- Patent Document 1 As one means for improving safety against such internal short circuit / internal heat generation, a conductive layer having a PTC function on the surface of the current collector (hereinafter, a conductive layer having a PTC function may be simply referred to as a PTC layer).
- Patent Document 2 In Patent Document 1, in a lithium secondary battery, an element (PTC element) having a positive resistance temperature coefficient is superimposed on the electrode surface of at least one of a positive electrode current collector and a negative electrode current collector. are listed. Further, Patent Document 2 describes that an active material of secondary particles in which an electron conductive particle having a PTC characteristic is entangled on the surface of an active material particle to form an active part and an inactive part having a PTC characteristic is described. ing.
- Patent Document 3 proposes to coat a current collector with a PTC layer composed of a crystalline thermoplastic resin, a conductive agent, and a binder.
- a paste in which a crystalline thermoplastic resin and a conductive agent are dispersed in a solution in which a binder is dissolved is prepared, applied to a current collector, and the solvent is removed by drying to obtain a conductive layer. ing.
- Patent Document 4 for a coin-type lithium ion secondary battery, a conductive layer comprising a resin as a core and a conductive agent with a conductive material coated on the surface is formed between the battery case and the positive electrode agent. Therefore, a technique for providing safety performance has been proposed.
- JP-A-7-220755 Japanese Patent Laid-Open No. 10-241665 JP 2001-357854 A JP 2010-61941 A
- a sheet made of a mixture of polyethylene and conductive carbon is bonded to a current collector as a PTC layer.
- polyethylene has weak adhesion to metal and does not have high adhesion to the active material layer. For this reason, the current collector and the active material layer are easily peeled off, which may increase the internal resistance of the battery, and may cause deterioration in characteristics such as shortening the life of the battery during charge and discharge cycles.
- the crystalline thermoplastic resin and the conductive agent are different in wettability, so that both are separated during the drying of the solvent, and a conductive layer in which both are uniformly dispersed is obtained. It is very difficult. In the conductive layer that has not been uniformly dispersed, there may be a problem that the desired PTC performance is not exhibited, and a problem that the initial resistance is increased.
- the present invention has been made in view of the above circumstances, and has excellent adhesion and stability when used in electrode structures such as capacitors and nonaqueous electrolyte batteries, and power storage components such as capacitors and nonaqueous electrolyte batteries.
- An object of the present invention is to provide a current collector having a conductive layer that exhibits PTC performance that contributes to safety.
- a current collector comprising a metal foil and a conductive layer formed on at least a part or the entire surface of at least one side of the metal foil.
- the conductive layer includes core-shell particles including core particles mainly composed of an insulating crystalline polymer and conductive shell layers formed on the surfaces of the core particles.
- a current collector including a conductive layer that exhibits an excellent PTC function by the action of the core-shell particles can be obtained. That is, according to this configuration, when used in a power storage component or an electrode structure, a current collector having a conductive layer that exhibits excellent PTC performance and exhibits excellent PTC performance that contributes to safety can be obtained.
- an electrode structure comprising the above-described current collector and an active material layer provided on the conductive layer of the current collector.
- the current collector provided with a conductive layer that exhibits an excellent PTC function due to the action of the core-shell particles is used, the PTC that stably contributes to safety when used in a power storage component or an electrode structure. An electrode structure that exhibits performance is obtained.
- a power storage component such as a nonaqueous electrolyte battery including the above-described current collector and an active material layer provided on a conductive layer of the current collector.
- the current collector including a conductive layer that exhibits an excellent PTC function due to the action of the core-shell particles is used, a non-aqueous electrolyte battery or a power storage component that stably exhibits PTC performance that contributes to safety is provided. can get.
- a conductive filler having core-shell particles including a core particle mainly composed of an insulating crystalline polymer and a conductive shell layer formed on the surface of the core particle.
- this conductive filler is applied to an active material layer in addition to the current collector, it can be used for an electrode structure or a power storage component to exhibit a PCT function according to various needs.
- a current collector having a conductive layer that has excellent adhesion and stably exhibits PTC performance that contributes to safety when used in a power storage component or an electrode structure, a current collector having a conductive layer that has excellent adhesion and stably exhibits PTC performance that contributes to safety can be obtained.
- FIG. 1 is a cross-sectional view showing the structure of an electrode structure using a current collector according to this embodiment.
- the electrode structure 100 using the current collector 108 of the present embodiment has a safety function against overcharge and unexpected overheating when used in a power storage component such as a nonaqueous electrolyte battery.
- the current collector 108 includes a metal foil 102 and a conductive layer 104 formed on at least a part or the entire surface of at least one side of the metal foil 102.
- the electrode structure 100 includes a current collector 108 and an active material layer 106 provided on the conductive layer 104 of the current collector 108.
- FIG. 2 is a cross-sectional view illustrating the structure of the conductive layer of the current collector according to the present embodiment.
- the conductive layer 104 of the current collector 108 according to this embodiment includes a conductive filler (hereinafter also referred to as core-shell particles) 110 and an insulating organic binder 112.
- FIG. 3 is a cross-sectional view illustrating the structure of the conductive filler 110 contained in the conductive layer of the current collector according to the present embodiment.
- the conductive filler 110 includes a core-shell particle including a core particle 114 mainly composed of an insulating crystalline polymer and a conductive shell layer 116 formed on the surface of the core particle 114. 110.
- the conductive filler 110 can exert an excellent PTC function in the conductive layer.
- a synergistic effect of the conductive filler 110 and the insulating organic binder 112 provides a conductive layer 104 that has excellent adhesion to the metal foil 102 and adhesion to the active material layer 106 and exhibits an excellent PTC function.
- the electric body 108 is obtained. That is, according to this configuration, when used in the electrode structure 100 of a non-aqueous electrolyte battery or a power storage component, it has excellent adhesion and has a capacity for a power storage component such as a non-aqueous electrolyte battery typified by a lithium ion battery.
- the current collector 108 that satisfies the requirements and exhibits the PTC performance that stably contributes to safety in case of emergency can be obtained.
- metal foil 102 used in this embodiment various metal foils for secondary batteries or capacitors can be used.
- various metal foils 102 for the positive electrode and the negative electrode can be used.
- aluminum, copper, stainless steel, nickel, and the like can be used.
- aluminum and copper are preferable from the balance between high conductivity and cost.
- “aluminum” includes aluminum and an aluminum alloy
- “copper” includes pure copper and a copper alloy.
- the aluminum foil can be suitably used as the secondary battery positive electrode side, the secondary battery negative electrode side, or the capacitor electrode, and the copper foil can be used on the secondary battery negative electrode side.
- Aluminum foil Various things, such as 1000 series generally known as a battery use, 3000 series, can be used. Moreover, it is the same also as copper foil, although it does not specifically limit, Rolled copper foil and electrolytic copper foil are used preferably.
- the thickness of the metal foil 102 is selected according to the purpose of use and is not particularly limited, but in the case of a secondary battery, it is preferably 5 ⁇ m or more and 50 ⁇ m or less. If the thickness is less than 5 ⁇ m, the strength of the foil may be insufficient and it may be difficult to form a conductive layer or the like. On the other hand, if the thickness exceeds 50 ⁇ m, other components, particularly the active material layer 106 or the electrode material layer (not shown) must be thinned. In some cases, the thickness of the material layer 106 must be reduced, and a necessary and sufficient capacity cannot be obtained.
- the conductive layer 104 of the present embodiment is formed on the surface of the metal foil 102, and has a core-shell structure in which a shell layer 116 having conductivity is formed on the surface of the particles composed of the core particles 114. 110 and an insulating organic binder 112 are contained.
- the resistance value of the conductive layer 104 is sufficiently low in normal times, but the temperature rises and shows a PTC function in which the resistance value suddenly increases from the vicinity of the melting point of the core particle 114 toward the melting point. It is possible to provide a function to suppress.
- the thickness of the conductive layer 104 can be arbitrarily determined. However, if the thickness is too large, the capacity of the battery may be reduced by changing the configuration of the active material layer by the thickness, which is not preferable. On the other hand, if the PTC function is manifested when the thickness is too thin, there may be a case where the resistance value cannot be increased enough to sufficiently reduce the discharge current of the battery. Therefore, the thickness of the conductive layer 104 is preferably 0.1 to 100 ⁇ m, more preferably 0.5 to 10 ⁇ m, and further preferably 1 to 5 ⁇ m.
- Examples of a method for forming such a conductive layer 104 include a method in which a paste obtained by mixing and dispersing an insulating organic binder 112 and a conductive filler 110 in a solvent is applied onto the metal foil 102 and dried. .
- the insulating organic binder 112 may be dissolved in the solvent used here, or may be dispersed in the form of fine particles.
- the solvent may be an organic solvent or water.
- the coating method is not particularly limited, and a known method such as a cast method, a bar coater method, a dip method, or a gravure coating method can be used. The same applies to the drying method, and drying by heat treatment in a hot air circulation path can be used.
- the surface state of the conductive layer 104 according to the present embodiment can be appropriately made. For example, when the surface becomes rough, the contact area with the active material layer 106 can be increased, the adhesion with the active material layer 106 can be further increased, and the contact resistance can be reduced.
- the PTC function of this embodiment is given by the conductive filler 110. Since the conductive filler 110 of the present embodiment can be used in the same manner as a known conductive filler and can exhibit a PTC function, it may be blended in the active material layer in addition to the conductive layer described above. Moreover, it can be used also about the well-known material for which use of a conductive filler is scheduled.
- the core particle 114 has an insulating crystalline polymer as a main component, and the shell layer 116 contains a conductive material.
- the conductive fillers 110 included in the conductive layer 104 are in contact with each other or at a sufficiently close distance. Since the conductive filler 110 has conductivity on the surface, a conductive path is formed. As a result, the conductive layer exhibits a sufficiently low resistance value at room temperature.
- the conductive filler 110 reaches a high temperature and reaches the melting point of the insulating crystalline polymer contained in the core particle 114, it melts and expands its volume. As a result, the conductive path of the shell layer 116 that cannot follow the expansion is broken.
- the conductive path is interrupted by dispersing the conductive material contained in the shell layer 116 into the molten insulating crystalline polymer.
- the insulating crystalline polymer forms a film on the surface of the conductive layer 104 due to the phase separation of the conductive filler 110. A combination of any one or more of these mechanisms causes a significant increase in the resistance value of the conductive layer 104.
- the conductive filler according to the present embodiment has a core-shell structure, the amount of the conductive material used can be considerably lower than that of the conventional crystalline crystalline polymer. That is, by adopting the core-shell structure, the ratio of the insulating crystalline polymer is relatively high with respect to the conductive material, which is effective in that high insulation can be exhibited when the PTC function is exhibited.
- a method for imparting a PTC function to the conductive layer 104 in general a method of mixing the conductive material and the core particles 114 can also be mentioned.
- the conductive material and the core particle 114 have different compatibility and tend to separate, so it is difficult to form a film in which both are dispersed in a uniform state.
- the compounding quantity of an electrically-conductive material is inadequate, the resistance value in normal temperature will become high.
- the ratio of the conductive filler 110 contained in the conductive layer 104 can be arbitrarily determined within a range not departing from the gist of the present invention. However, if the proportion of the conductive filler 110 in the conductive layer 104 is too high, the proportion of the insulating organic binder 112 decreases, leading to a decrease in adhesion and unstable PTC performance. Absent. On the other hand, if the ratio is too low, the increase in the resistance value when the PTC function is exhibited is insufficient, and a sufficient effect for suppressing the current value is not exhibited.
- the preferred proportion of the conductive filler 110 contained in the conductive layer 104 depends on the shape and particle size of the conductive filler 110, the ratio of the thickness of the shell layer and the 116 core particles 114 in the core-shell structure, and the type of the insulating organic binder 112. However, when the total volume of the conductive filler 110 and the insulating organic binder 112 is 1, it is generally 0.01 to 0.9, more preferably 0.05 to 0.5, most preferably Is 0.1 to 0.3. In addition, the ratio here is a volume ratio.
- the conductive filler content is 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1. , 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, and 0.9.
- the conductive filler 110 included in the conductive layer 104 may be one type or a mixture of a plurality of types.
- the conductive fillers 110 including core particles 114 made of core particles 114 having different melting points it is possible to develop a two-stage PTC function, and a PTC function over a wide temperature range. Can be expressed.
- the conductive filler 110 has a core-shell structure, the core particles 114 are mainly composed of an insulating crystalline polymer, and the shell layer 116 contains a conductive material.
- the conductive filler 110 can be of any shape, for example, a spherical shape, a flat shape, or a fiber shape. However, since it is possible to achieve a low resistance value at a blending ratio as compared to a true sphere, it is preferable that the particles have an aspect ratio larger than 1, such as a flat shape or a fiber shape, particularly preferably larger than 2, more preferably. Is greater than 3.
- the aspect ratio is the maximum diameter / minimum diameter of the particles, and can be obtained from a particle image obtained by an optical microscope or an electron microscope, for example.
- this aspect ratio is based on one of the values 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100. It may be large, and may be within a range of any two of these values (excluding values at both ends).
- the particle size of the conductive filler 110 having the core-shell structure according to the present embodiment can be arbitrarily determined by the practitioner in consideration of the desired thickness of the conductive layer 104.
- the particle diameter here is an average particle diameter measured from a particle image obtained by observing the conductive filler 110 with an optical microscope or an electron microscope, and specifically, 100 particles observed. It can be obtained as an arithmetic average value of the diameter (the minimum diameter in the case of particles having a high aspect ratio).
- the conductive filler 110 having a core-shell structure if the thickness of the conductive shell layer 116 is too thick, a sufficient PTC function may not be exhibited. If the shell layer 116 is thick, the amount of the insulating crystalline polymer is reduced, so that even when it melts, the conductive path is not sufficiently cut off and the PTC function may not be exhibited. Even when the insulating crystalline polymer is phase-separated to form an insulating film, if the shell layer 116 is thick, it takes a long time for the insulating crystalline polymer to move from the inside to the surface. When the temperature becomes high, the PTC function cannot be expressed quickly.
- the effect of the present invention is not impaired by the thin shell layer of the conductive filler 110 itself.
- a shell layer that is too thin makes it difficult to form itself on the core particles 114 as intended.
- the thickness of the shell layer 116 has a preferable ratio to the particle diameter of the core particles 114. That is, the thickness of the shell layer 116 t S, the particle size of the core particle 114 is taken as D C, the value of a as defined in the formula 1, preferably from 1.003 to 8, more preferably 1 .003-2.
- the value a represents the volume ratio of the core-shell particles to the core particles.
- An increase in this ratio means an increase in the thickness of the shell layer
- a value of 8 means that when the radius of the core particle and the thickness of the shell layer are equal
- a value of 2 means the volume of the shell layer and the core. It means when the volume of particles becomes equal.
- a smaller value of a indicates that the thickness of the shell layer is smaller
- 1.003 means that the shell thickness is 0.1% of the core particles.
- the values of a are 1.003, 1.005, 1.01, 1.02, 1.03, 1.04, 1.05, 1.1, 1.5, 2.0, 2. Any two of 5, 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0 It may be within the range of values.
- a represented by Formula 1 is expressed as follows, where V C is the volume of the core particle 114 included in the entire core-shell particle 110 included in the conductive layer 104, and V S is the volume of the conductive material that is the shell layer 116. ) Represented by a). That is, a ′ is preferably in the range of 1.003 to 8, and more preferably 1.003 to 2, with respect to the entire conductive filler 110 contained in the conductive layer 104.
- a ′ is also 1.003, 1.005, 1.01, 1.02, 1.03, 1.04, 1.05, 1.1, 1.5, 2.0, 2 .5, 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, any 2 It may be within a range of two values.
- the shell layer 116 having conductivity can form a conductive path on the surface of the core particle 114, the shell layer 116 needs to completely cover the core particle 114.
- the core particles may be partially exposed.
- the conductive shell layer 116 of the conductive filler 110 having the core-shell structure according to the present embodiment is made of a conductive material, and the conductive material is conductive to the core particles 114 made of an insulating crystalline polymer.
- the highly reliable shell layer 116 can be formed, and a metal, a carbonaceous material, a conductive polymer material, or the like can be used.
- the shell layer 116 may be a homogeneous film or an aggregate of particles.
- conductive materials include gold, silver, copper, platinum, nickel, cobalt, iron, titanium, aluminum, and alloys thereof as metal materials, and acetylene black, ketjen as carbonaceous materials. Examples include black, carbon nanotubes, carbon nanofibers, and flake graphite.
- Polymer materials that have conductivity include polyolefins that contain conductive particles in addition to polymers that have conductivity. Can be mentioned.
- Examples of a method for forming such a shell layer 116 having conductivity on the surface of the core particle 114 made of an insulating crystalline polymer include the following methods.
- Method of forming a metal film on the surface of core particle 114 by electroless plating or vapor deposition of metal, core particle 114 made of insulating crystalline polymer, and conductive particle made of metal particle, conductive carbon or conductive polymer A mechanochemical method in which a shell layer 116 made of conductive particles 118 is formed on the surface of the core particle 114 by subjecting the powder of 118 to a ball mill, a conductive polymer and an insulating crystalline polymer as a core.
- the fiber obtained by melting and extruding the two layers may be cut and pulverized.
- the shell layer 116 is preferably made of an aggregate of conductive particles 118 or a conductive polymer. This is because it is usually not preferable to form a metal film on the core particle 114 in view of the complexity of the manufacturing process and cost.
- the shell layer 116 is formed of an aggregate of conductive particles 118, since there is no binder between the conductive particles 118, the shell layer 116 is generally brittle and core particles made of an insulating crystalline polymer. When 114 melts and exhibits the PTC function, the conduction path is likely to be broken. That is, it can be advantageous for the expression of the PTC function.
- the shell layer 116 is formed of an aggregate of conductive particles 118, the conductive particles 118 are likely to be peeled off.
- a dropped conductive particle 118 is not a problem if it is in a small amount, but if it is in a large amount, an unintended conductive path is formed in the conductive layer 104 and there is a risk of deteriorating the PTC function.
- Such a situation is likely to occur particularly when the particle diameter D C of the core particle 114 is less than the particle diameter D S of the conductive particles 118 to form the shell layer 116.
- the particle size D S of the conductive particles 118 is smaller than the particle diameter D C of the core particle 114
- the value b represented by the following formula 3 is preferably 1 or less, more preferably 0.1 or less, and most preferably 0.01 or less.
- the value of b is 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0,. It may be less than or equal to any value of 2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or within a range of any two values. .
- the shell layer 116 is formed by an aggregate of the conductive particles 118
- the conductive particles 118 made of a carbonaceous material is preferable to use as the conductive particles 118. This is because the specific gravity is lower than that of the conductive particles 118 made of metal, the side reaction is less likely to occur particularly when incorporated in a lithium ion secondary battery, and the particles having a small particle size are easily available. It is preferable because it is possible.
- the method of producing the shell layer 116 made of a conductive polymer by two-layer extrusion or the like is excellent in that the conductive filler 110 having a core-shell structure can be continuously produced, and the above-described drop-off is also possible.
- the core particles 114 of the conductive filler 110 having a core-shell structure according to the present embodiment are mainly composed of an insulating crystalline polymer.
- the insulating crystalline polymer include polyethylene, polypropylene, and ethylene copolymers such as ethylene-glycidyl methacrylate and ethylene-vinyl acetate copolymers, polyvinylidene fluoride, polyester, and acid-modified products thereof.
- ethylene-glycidyl methacrylate and ethylene-vinyl acetate copolymers polyvinylidene fluoride, polyester, and acid-modified products thereof.
- a polymer having high crystallinity is preferably used from the viewpoint of PTC performance, and it is preferable to use polyethylene, polypropylene, and an ethylene copo
- the embodiment in which the metal particles, the conductive carbon, or the conductive polymer is included alone as the conductive particles 118 in the shell layer 116 having conductivity is described in detail, but the mode of mixing at the same time is excluded. Not the purpose. That is, conductive particles 118 (conductive carbon) and a conductive polymer may be mixed and used in the shell layer 116 having conductivity. Also in this case, a suitable PTC effect can be obtained as shown in Examples described later.
- the shell layer 116 when the shell layer 116 is formed of an aggregate of conductive carbon, since there is no binder between the conductive carbons, the shell layer 116 is generally fragile and is insulated. When the core particle 114 made of a crystalline polymer melts and develops the PTC function, the conductive path is likely to break. On the other hand, in the case of a conductive polymer, the shell layer 116 made of a conductive polymer can be produced by two-layer extrusion or the like, which is excellent in that a conductive filler having a core-shell structure can be continuously produced.
- the conductivity at the temperature during normal operation is excellent. That is, it can be advantageous for the expression of the PTC function.
- metal particles it is usually not preferable to form a metal film on the core particles 114 from the viewpoint of the complexity of the manufacturing process and the cost. It is less preferable than the case.
- conductive carbon or conductive polymer it is most preferable to use conductive carbon from the viewpoint of manufacturing cost and availability.
- the PTC performance is manifested by melting the insulating crystalline polymer that is the main component of the core particle 114. Therefore, the melting point is important for safety performance. It is natural that melting and resistance increase at a low temperature close to the actual use temperature of the battery is not preferable for use of the battery, and the PTC function is manifested at a temperature higher than the ignition point of the electrolyte. Even if the resistance value increases, it does not contribute to the intended safety and is meaningless.
- the expression temperature of the PTC function should be selected in consideration of the components other than the current collector, such as an electrolytic solution, an active material, and a separator, but is generally appropriate to be 80 to 180 ° C. It can be appropriately adjusted according to the power storage component.
- the melting point of the insulating crystalline polymer is preferably in the range of 80 to 180 ° C., particularly preferably 100 to 160 ° C. If the melting point is too high, the PTC function is not exhibited even when the battery is abnormally heated, which is not preferable because it does not contribute to safety. On the other hand, if the melting point is too low, it melts at a temperature close to the actual use temperature of the battery and the resistance value increases, which is not preferable for use of the battery. This melting point may be within the range of any two values of 80, 90 ° C, 100 ° C, 110 ° C, 120 ° C, 130 ° C, 140 ° C, 150 ° C, 160 ° C, 170 ° C, 180 ° C.
- the insulating organic binder 112 included in the conductive layer 104 according to the present embodiment is not particularly limited as long as it has good adhesion to the metal foil 102 that is the current collector 108 and the active material layer 106, but the crystalline It is preferable to have a melting point higher than that of the insulating crystalline polymer.
- this insulating organic binder 112 has crystallinity and its melting point is lower than the melting point of the insulating crystalline polymer forming the core particles 114 of the conductive filler 110, when the temperature rises, Before the PTC function is manifested, the insulating organic binder 112 is melted and the conductive layer 104 itself flows, causing the active material layer 106 to peel off, resulting in problems such as an increase in resistance.
- the temperature at which the PTC function develops that is, the melting point of the insulating crystalline polymer that forms the core particles of the conductive filler 110 increases in resistance at temperatures higher than that temperature, and the resistance value at temperatures lower than that. It is selected with the intention that no increase will occur, and if the melting point of the insulating organic binder 112 is lower than this, that is, an unintended increase in resistance value will be caused.
- the insulating organic binder 112 included in the conductive layer 104 according to the present embodiment has a crystallinity and a melting point higher than the melting point of the insulating crystalline polymer.
- Group-introduced polyolefin, ethylene-glycidyl methacrylate, ethylene-based copolymers such as ethylene-vinyl acetate copolymer, polyvinylidene fluoride, polysaccharide polymers, etc. be able to.
- polyvinylidene fluoride which is stable and excellent in adhesion in the battery and this acid-modified product can be preferably used.
- the insulating organic binder 112 may be amorphous. Since the amorphous organic binder 112 does not have a melting point, a phenomenon in which the resistance value and adhesion of the conductive layer 104 change suddenly from a certain temperature does not occur, and the electrical characteristics can be controlled only by the conductive filler. Therefore, it is preferable because it can appropriately meet various needs of the PTC function. Further, since there are many softer materials than the insulating binder having crystallinity, that is, many of them have excellent adhesion, and there is an advantage that it is easy to improve the adhesion with the metal foil and the active material layer. Examples of the amorphous material include (meth) acrylic copolymers, ethylene-propylene rubber, silicone rubber, polystyrene, and the like.
- a desirable ratio of the insulating organic binder 112 included in the conductive layer 104 according to the present embodiment includes the shape and particle size of the conductive filler 110, the ratio of the thickness of the shell layer and the 116 core particles 114 in the core-shell structure, and the insulating property.
- the ratio is a volume ratio.
- the content of the insulating organic binder 112 is 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 0 It may be within a range of any two numerical values of .91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, and 0.99.
- the electrode structure 100 of this embodiment includes an active material layer 106 containing an active material on a conductive layer 104 formed on a metal foil 102.
- the active material layer 106 generally includes an active material, a binder, and a conductive additive as main components. Since the electrode structure 100 includes the active material layer 106 on the conductive layer 104 formed on the metal foil 102, the current collector 108 and the active material layer 106 have good adhesion and low internal resistance is realized. Long life expectancy is expected.
- the active material particles contained in the active material layer 106 of the electrode structure 100 of the present embodiment may be either a positive electrode active material or a negative electrode active material. If it is the electrode structure 100 for lithium ion secondary batteries, it will not specifically limit as a positive electrode active material, The substance which can occlude / release lithium ion can be used.
- lithium cobalt oxide LiCoO 2
- lithium manganate LiMn 2 O 4
- lithium nickelate LiNiO 2
- ternary lithium compounds of Co, Mn, and Ni Li (Co x Mn y Ni 1-xy ) O 2
- a sulfur compound TiS 2
- an olivine compound LiFePO 4 , LiMnPO 4
- a well-known thing can be used also as a negative electrode active material.
- graphite such as graphite, amorphous graphite, and oxide.
- the electrode structure 100 is used for an electric double layer capacitor
- a known material can be used as the active material.
- graphite such as graphite, amorphous graphite, and oxide.
- a fluorine resin typified by polyvinylidene fluoride, a polysaccharide polymer, a styrene butadiene rubber, or the like can be used. However, it is not limited to these.
- a paste in which an active material is dispersed together with a conductive additive in a solvent in which a binder is dissolved or dispersed is applied on a conductive layer 104 formed on a metal foil 102 and dried.
- the active material layer 106 is formed.
- nonaqueous electrolyte battery or power storage component of this embodiment can be produced by a known method using the electrode structure, separator, and nonaqueous electrolyte solvent according to this embodiment.
- conductive filler having core-shell structure was produced by a ball mill.
- Polyethylene particles (melting point 135 ° C.) having an average particle diameter of 70 ⁇ m were used as core particles made of an insulating crystalline polymer, and acetylene black having an average particle diameter of primary particles of 35 nm was used as conductive particles.
- Polyethylene particles (50 g) and acetylene black (15 g) were encapsulated in a stainless steel pot having an internal volume of 930 ml together with a ball medium made of 19 mm stainless steel. This was processed for 24 hours at 120 rpm. The surface of the obtained composite particles was observed with a scanning electron microscope (SEM), and it was confirmed that the polyethylene particles were coated with acetylene black (FIG. 4).
- SEM scanning electron microscope
- Formation of conductive layer 0.75 g of the prepared conductive filler was mixed with 30 g of N-methyl-pyrrolidone (NMP) solution of 10 wt% polyvinylidene fluoride (PVDF) (melting point: 170 ° C.) and dispersed uniformly with a disper. Stir. The obtained paste was applied to an Al foil with an applicator, and then NMP was dried to obtain a current collector having a conductive layer.
- NMP N-methyl-pyrrolidone
- PVDF polyvinylidene fluoride
- Example 2 A collection having a conductive layer in the same manner as in Example 1 except that polyethylene particles having a particle size of 3 ⁇ m (melting point: 121 ° C.) are used as core particles made of an insulating crystalline polymer, and the amount of acetylene black is 30 g. I got an electric body.
- Example 3 A collection having a conductive layer in the same manner as in Example 1 except that polypropylene particles having a particle size of 5 ⁇ m (melting point: 145 ° C.) are used as core particles made of an insulating crystalline polymer and the amount of acetylene black is 20 g. I got an electric body.
- a conductive polymer was obtained by melt-kneading polyethylene (melting point: 121 ° C.) so that acetylene black was 20 vol% by a roll mixer.
- the obtained conductive polymer and polyethylene (melting point 121 ° C.) were extruded into two layers to obtain a strand in which a polyethylene core was coated with the conductive polymer.
- the fibrous conductive filler which has the core which consists of polyethylene, and the shell layer which consists of a conductive polymer was obtained by extending
- a current collector having a conductive layer was obtained in the same manner as in Example 1 except that this fiber was used.
- Example 5 A conductive current collector was obtained in the same manner as in Example 1 except that 10 g of a 30 wt% polypropylene emulsion (melting point: 160 ° C.) was used as the insulating organic binder solution.
- Example 6 A current collector having a conductive layer in the same manner as in Example 1 except that core-shell particles obtained by coating gold with 100 nm of polyethylene particles (melting point: 128 ° C.) having an average particle diameter of 30 ⁇ m were used as conductive fillers having a core-shell structure Got the body
- Example 7 0.25 g of the flat conductive filler prepared in Example 1 and 0.5 g of the fibrous conductive filler prepared in Example 4 were added to N—10 wt% polyvinylidene fluoride (PVDF) (melting point: 170 ° C.). The mixture was mixed with 30 g of a methyl-pyrrolidone (NMP) solution and stirred so as to be uniformly dispersed with a disper. The obtained paste was applied to an Al foil with an applicator, and then NMP was dried to obtain a current collector having a conductive layer.
- PVDF polyvinylidene fluoride
- NMP methyl-pyrrolidone
- Example 8 A current collector having a conductive layer was obtained in the same manner as in Example 1 except that 30 g of a 10 wt% amorphous polystyrene toluene solution was used as the insulating organic binder solution.
- Example 9 Example except that ethylene-vinyl acetate copolymer particles (VA ratio: 14%, melting point: 90 ° C.) having a particle size of 50 ⁇ m were used as core particles made of an insulating crystalline polymer, and the amount of acetylene black was 20 g. In the same manner as in Example 1, a current collector having a conductive layer was obtained.
- VA ratio 14%, melting point: 90 ° C.
- Example 1 A current collector having a conductive layer was obtained in the same manner as in Example 1 except that polyethylene particles and acetylene black were directly blended into an NMP solution of PVDF except for the step of producing a conductive filler having a core-shell structure.
- Example 2 A current collector having a conductive layer in the same manner as in Example 1 except that particles having a particle size of 5 ⁇ m made of PMMA having no crystallinity are used as core particles instead of polyethylene particles and the amount of acetylene black is 30 g. Got the body.
- a current collector having a conductive layer was obtained by directly heat-sealing the conductive filler having a core-shell structure obtained in Example 1 to a current collector made of metal foil without using a binder.
- ⁇ PTC function evaluation> The obtained current collector having a conductive layer was punched into a 1 cm ⁇ circle to make a measurement sample. The resistance value when the upper and lower surfaces were sandwiched between brass electrodes and contacted with a load of 5 N was measured. It was measured with (Hioki Electric 3451). The measured value at 30 ° C. was used as the initial resistance value, and then the resistance value was measured while heating up to 150 ° C. at 10 ° C./min. As representative examples of these measurement results, the measurement results of Example 1, Comparative Example 1, and Comparative Example 3 are shown in FIGS.
- the ratio between the maximum resistance value and the initial resistance value obtained was recorded as the PTC magnification.
- the resistance value measured at 30 ° C. or higher is equal to or lower than the initial resistance value, it is expressed as “ ⁇ ”.
- the stability of the expression of the PTC performance when the number of measurements was increased was expressed as (number of times the PTC function was expressed / number of measurements). The results are shown in Tables 1 and 2.
- the item “core shell formation” indicates that ⁇ : the conductive filler is core-shelled ⁇ : the conductive filler is not core-shelled.
- the presence or absence of core-shell formation was confirmed by observation with a scanning electron microscope (SEM).
- the value a is obtained from a particle image obtained by observation with a scanning electron microscope (SEM).
- the value a represents the volume ratio of the core-shell particles to the core particles.
- An increase in this ratio means an increase in the thickness of the shell layer
- a value of 8 means that when the radius of the core particle and the thickness of the shell layer are equal
- a value of 2 means the volume of the shell layer and the core. It means when the volume of particles becomes equal.
- Electrode structure 102
- Metal foil 104
- Conductive layer 106
- Active material layer 108
- Current collector 110
- Conductive filler core shell particle
- Insulating organic binder 114
- Core particles insulating crystalline polymer
- Shell layer conductive material
- Conductive particle t S shell layer thickness D C core particle size D S conductive particle size
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Abstract
Description
図1は、本実施形態に係る集電体を用いた電極構造体の構造を示した断面図である。本実施形態の集電体108を用いた電極構造体100は、非水電解質電池等の蓄電部品に用いられた場合に、過充電ならびに予期せぬ過熱に対する安全機能を有するものである。
本実施形態に用いる金属箔102としては、二次電池またはキャパシタ用の各種金属箔が使用可能である。具体的には、正極用、負極用の種々の金属箔102を使用することができ、例えば、アルミニウム、銅、ステンレス、ニッケルなどが使用可能である。その中でも導電性の高さとコストのバランスからアルミニウム、銅が好ましい。なお、本明細書において、「アルミニウム」は、アルミニウム及びアルミニウム合金を含み、「銅」は、純銅および銅合金を含むものとする。本実施形態において、アルミニウム箔は、二次電池正極側、二次電池負極側、またはキャパシタ電極等として好適に用いることができ、銅箔は二次電池負極側に用いることができる。アルミニウム箔としては、特に限定されないが、電池用途として一般に知られる1000系や、3000系など種々のものが使用できる。また、銅箔としても同様であり、特に限定されないが、圧延銅箔や、電解銅箔が好んで用いられる。
本実施形態の導電層104は、金属箔102の表面に形成されたものであって、コア粒子114からなる粒子の表面に導電性を有するシェル層116が形成されたコアシェル構造を有する導電性フィラー110および、絶縁性有機バインダ112を含有している。導電層104の抵抗値は、通常時は十分低いが、温度が上昇し、コア粒子114の融点近傍から融点に向かって急激に抵抗値が上昇するPTC機能を示し、これにより以降の放電電流を抑制する機能を備えることが可能である。
本実施形態の電極構造体100は、金属箔102上に形成された導電層104の上に活物質を含む活物質層106を備える。この活物質層106は、一般的には、活物質ならびに結着剤、導電助剤を主たる成分として含んでなる。この電極構造体100は上記の金属箔102上に形成された導電層104上に活物質層106を備えるため、集電体108と活物質層106との密着性が良く、低い内部抵抗を実現できると共に長い寿命が期待される。
コアシェル構造を有する導電性フィラーの作製
コアシェル構造を有する導電性フィラーはボールミルにより作製した。絶縁性結晶性高分子からなるコア粒子として、平均粒径が70μmであるポリエチレン粒子(融点135℃)を用い、導電性粒子として1次粒子の平均粒径が35nmであるアセチレンブラックを用いた。ポリエチレン粒子50gとアセチレンブラック15gを19mmのステンレスからなるボールメディアと共に、内容量930mlのステンレス製のポットに封入した。これを回転数120rpmで24時間処理した。得られた複合化粒子の表面を走査電子顕微鏡(SEM)により観察し、ポリエチレン粒子がアセチレンブラックにより被覆されていることを確認した(図4)。
作成した導電性フィラー0.75gを、10wt%のポリフッ化ビニリデン(PVDF)(融点170℃)のN-メチル-ピロリドン(NMP)溶液30gに配合し、ディスパーで均一分散するように攪拌した。得られたペーストをアプリケーターによりAl箔に塗工後、NMPを乾燥させ、導電層を有する集電体を得た。
絶縁性結晶性高分子からなるコア粒子として粒径が3μmのポリエチレン粒子(融点121℃)を用い、アセチレンブラックの配合量を30gとしたこと以外は実施例1と同様にして導電層を有する集電体を得た。
絶縁性結晶性高分子からなるコア粒子として粒径が5μmのポリプロピレン粒子(融点145℃)を用い、アセチレンブラックの配合量を20gとしたこと以外は実施例1と同様にして導電層を有する集電体を得た。
まず、ロールミキサーにより、ポリエチレン(融点121℃)にアセチレンブラックが20vol%となるように溶融混練し導電性高分子を得た。得られた導電性高分子とポリエチレン(融点121℃)を二層押し出しにより、ポリエチレンの芯線に導電性高分子が被覆されたストランドを得た。さらにこれを引き伸ばして細線化した後に切断することで、ポリエチレンからなるコアと、導電性高分子からなるシェル層とを有する繊維状の導電性フィラーを得た。この繊維を用いること以外は実施例1と同様にして導電層を有する集電体を得た。
<実施例5>
絶縁性有機バインダの溶液として30wt%のポリプロピレンエマルション(融点160℃)10gを用いたこと以外は実施例1と同様にして導電性を有する集電体を得た。
コアシェル構造を有する導電性フィラーとして、平均粒径30μmのポリエチレン粒子(融点128℃)に金を蒸着により100nm被覆したコアシェル粒子を用いたこと以外は実施例1と同様にして導電層を有する集電体を得た
実施例1で作製した扁平状の導電性フィラー0.25gおよび実施例4で作製した繊維状の導電性フィラー0.5gを、10wt%のポリフッ化ビニリデン(PVDF)(融点170℃)のN-メチル-ピロリドン(NMP)溶液30gに配合し、ディスパーで均一分散するように攪拌した。得られたペーストをアプリケーターによりAl箔に塗工後、NMPを乾燥させ、導電層を有する集電体を得た。
絶縁性有機バインダの溶液として、10wt%の非晶性のポリスチレンのトルエン溶液30gを用いたこと以外は実施例1と同様にして導電層を有する集電体を得た。
絶縁性結晶性高分子からなるコア粒子として粒径が50μmのエチレン-酢酸ビニル共重合体粒子(VA率14% 融点90℃)を用い、アセチレンブラックの配合量を20gとしたこと以外は実施例1と同様にして導電層を有する集電体を得た。
コアシェル構造を有する導電性フィラーを作製する工程を除き、ポリエチレン粒子とアセチレンブラックを直接PVDFのNMP溶液に配合したこと以外は実施例1と同様にして導電層を有する集電体を得た。
ポリエチレン粒子の代わりに、結晶性を持たないPMMAからなる粒径5μmの粒子をコア粒子として用い、アセチレンブラックの配合量を30gとしたこと以外は実施例1と同様にして導電層を有する集電体を得た。
実施例1により得られたコアシェル構造を有する導電性フィラーを、バインダを用いずに、金属箔からなる集電体に直接熱融着させることで導電層を有する集電体を得た。
得られた導電層を有する集電体を1cmφの円形に打ち抜いて測定用試料とし、その上下面を真鍮製の電極で挟み、5Nの荷重をかけて接触させたときの抵抗値を、抵抗計(日置電機 3451)で測定した。30℃での測定値を初期抵抗値とし、その後、10℃/minで150℃まで昇温しながら抵抗値を測定した。これらの測定結果の代表例として、実施例1、比較例1、比較例3の測定結果を図5~7として示す。
○:導電性フィラーがコアシェル化されている
×:導電性フィラーがコアシェル化されていない
ことを示すものとする。なお、コアシェル化の有無については走査電子顕微鏡(SEM)により観察して確認した。
◎:<1(単位Ωcm2)
○:1~10(単位Ωcm2)
△:10~100(単位Ωcm2)
×:>100(単位Ωcm2)
実施例1では図5のように温度に対して抵抗値の増大が見られた。実施例2~9でも同様の抵抗値の増大が見られた。また、n数を増やしたとき(n=3)も同様の抵抗値の増大が安定して確認された。これに対して比較例1では抵抗値は温度に対して図6のように変化し、温度に対して抵抗値の増大は確認されなかった。比較例2でも同様に抵抗値の増大は確認されなかった。比較例3でも図7に示すような抵抗値の変化を示し、抵抗値の増大が確認されなかった。
102 金属箔
104 導電層
106 活物質層
108 集電体
110 導電性フィラー(コアシェル粒子)
112 絶縁性有機バインダ
114 コア粒子(絶縁性結晶性高分子)
116 シェル層(導電材)
118 導電性粒子
tS シェル層の厚さ
DC コア粒子の粒径
DS 導電性粒子の粒径
Claims (16)
- 金属箔と、
該金属箔の少なくとも片面の一部または全面に形成されている導電層と、
を備える集電体であって、
前記導電層が、
絶縁性結晶性高分子を主成分とするコア粒子と、
該コア粒子の表面に形成されている導電性を有するシェル層と、
を含むコアシェル粒子を含有する
ことを特徴とする集電体。 - 請求項1に記載の集電体において、
前記絶縁性結晶性高分子の融点が80~180℃の範囲にある
ことを特徴とする集電体。 - 請求項1または2に記載の集電体において、
前記シェル層が、導電性粒子を含有する
ことを特徴とする集電体。 - 請求項3に記載の集電体において、
前記導電性粒子が導電性カーボンである
ことを特徴とする集電体。 - 請求項1乃至4に記載の集電体において、
前記シェル層が、導電性高分子を含有する
ことを特徴とする集電体。 - 請求項1乃至5のいずれかに記載の集電体において、
前記コアシェル粒子が、扁平状もしくは繊維状である
ことを特徴とする集電体。 - 請求項1乃至6のいずれかに記載の集電体において、
前記導電層が、絶縁性有機バインダをさらに含み、
前記絶縁性有機バインダが、
結晶性を有しかつ前記絶縁性結晶性高分子の融点よりも高い融点を有する、または
非晶性である
ことを特徴とする集電体。 - 請求項7記載の集電体において、
前記絶縁性有機バインダがポリフッ化ビニリデン(PVDF)を含有する
ことを特徴とする集電体。 - 請求項1乃至8のいずれかに記載の集電体において、
前記絶縁性結晶性高分子が、ポリエチレンもしくはポリプロピレンを含有する
ことを特徴とする集電体。 - 請求項1乃至9のいずれかに記載の集電体において、
前記金属箔が、Al箔もしくはCu箔を含む、
ことを特徴とする集電体。 - 請求項1乃至10のいずれかに記載の集電体と、
前記集電体の導電層上に設けられている活物質層と、
を備える
ことを特徴とする電極構造体。 - 請求項1乃至10のいずれかに記載の集電体と、
前記集電体の導電層上に設けられている活物質層と、
を備える
ことを特徴とする非水電解質電池。 - 請求項1乃至10のいずれかに記載の集電体と、
前記集電体の導電層上に設けられている活物質層と、
を備える
ことを特徴とする蓄電部品。 - 絶縁性結晶性高分子を主成分とするコア粒子と、
該コア粒子の表面に形成されている導電性を有するシェル層と、
を含むコアシェル粒子である
ことを特徴とする導電性フィラー。 - 金属箔と、
活物質層と
を備える電極構造体であって、
前記活物質層が請求項14記載の導電性フィラーを含有する
ことを特徴とする電極構造体。 - 金属箔と、
活物質層と
を備える蓄電部品であって、
前記活物質層が請求項14記載の導電性フィラーを含有する
ことを特徴とする蓄電部品。
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- 2013-09-18 US US14/427,298 patent/US20150280241A1/en not_active Abandoned
- 2013-09-18 CN CN201380050630.3A patent/CN104685681A/zh active Pending
- 2013-09-18 EP EP13840765.5A patent/EP2903063A4/en not_active Withdrawn
- 2013-09-18 KR KR1020157007501A patent/KR20150063050A/ko not_active Application Discontinuation
- 2013-09-18 WO PCT/JP2013/075119 patent/WO2014050653A1/ja active Application Filing
- 2013-09-23 TW TW102134033A patent/TWI591889B/zh not_active IP Right Cessation
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CN105449263A (zh) * | 2014-08-22 | 2016-03-30 | 宁德时代新能源科技股份有限公司 | 锂离子二次电池 |
WO2016093095A1 (ja) * | 2014-12-08 | 2016-06-16 | 日立化成株式会社 | リチウムイオン二次電池用正極及びそれを用いたリチウムイオン二次電池 |
JPWO2016093095A1 (ja) * | 2014-12-08 | 2017-07-27 | 日立化成株式会社 | リチウムイオン二次電池用正極及びそれを用いたリチウムイオン二次電池 |
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US11978907B2 (en) | 2016-02-19 | 2024-05-07 | Samsung Sdi Co., Ltd. | Positive electrode for lithium secondary battery, winding element for lithium secondary battery, and lithium secondary battery |
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JPWO2018124042A1 (ja) * | 2016-12-28 | 2019-10-31 | パナソニックIpマネジメント株式会社 | 電気化学デバイス |
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WO2018124042A1 (ja) * | 2016-12-28 | 2018-07-05 | パナソニックIpマネジメント株式会社 | 電気化学デバイス |
JP2019053912A (ja) * | 2017-09-15 | 2019-04-04 | トヨタ自動車株式会社 | 非水電解質二次電池およびその製造方法 |
JP2019200947A (ja) * | 2018-05-18 | 2019-11-21 | トヨタ自動車株式会社 | 全固体電池 |
JP2020095867A (ja) * | 2018-12-13 | 2020-06-18 | トヨタ自動車株式会社 | 非水電解質二次電池 |
US11641017B2 (en) | 2018-12-13 | 2023-05-02 | Toyota Jidosha Kabushiki Kaisha | Non-aqueous electrolyte secondary battery having an intermediate layer comprising metal-covered microcapsules |
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Also Published As
Publication number | Publication date |
---|---|
CN104685681A (zh) | 2015-06-03 |
KR20150063050A (ko) | 2015-06-08 |
TW201424106A (zh) | 2014-06-16 |
EP2903063A1 (en) | 2015-08-05 |
TWI591889B (zh) | 2017-07-11 |
JPWO2014050653A1 (ja) | 2016-08-22 |
US20150280241A1 (en) | 2015-10-01 |
EP2903063A4 (en) | 2016-04-27 |
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