WO2023162414A1 - 非水電解質二次電池用正極活物質及び非水電解質二次電池 - Google Patents

非水電解質二次電池用正極活物質及び非水電解質二次電池 Download PDF

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WO2023162414A1
WO2023162414A1 PCT/JP2022/045844 JP2022045844W WO2023162414A1 WO 2023162414 A1 WO2023162414 A1 WO 2023162414A1 JP 2022045844 W JP2022045844 W JP 2022045844W WO 2023162414 A1 WO2023162414 A1 WO 2023162414A1
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positive electrode
electrolyte secondary
aqueous electrolyte
secondary battery
active material
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English (en)
French (fr)
Japanese (ja)
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晶子 村田
浩史 川田
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Panasonic Intellectual Property Management Co Ltd
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Panasonic Intellectual Property Management Co Ltd
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Priority to US18/839,615 priority Critical patent/US20250167226A1/en
Priority to EP22928931.9A priority patent/EP4489124A4/en
Priority to JP2024502852A priority patent/JPWO2023162414A1/ja
Priority to CN202280091373.7A priority patent/CN118679601A/zh
Publication of WO2023162414A1 publication Critical patent/WO2023162414A1/ja
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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
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00—Compounds of nickel
    • C01G53/40—Complex oxides containing nickel and at least one other metal element
    • C01G53/42—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2
    • C01G53/44—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2 containing manganese
    • C01G53/50—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2 containing manganese of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2
    • C01G53/502—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2 containing manganese of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 containing lithium and cobalt
    • C01G53/504—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2 containing manganese of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 containing lithium and cobalt with the molar ratio of nickel with respect to all the metals other than alkali metals higher than or equal to 0.5, e.g. Li(MzNixCoyMn1-x-y-z)O2 with x ≥ 0.5
    • C01G53/506—Complex oxides containing nickel and at least one other metal element containing alkali metals, e.g. LiNiO2 containing manganese of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 containing lithium and cobalt with the molar ratio of nickel with respect to all the metals other than alkali metals higher than or equal to 0.5, e.g. Li(MzNixCoyMn1-x-y-z)O2 with x ≥ 0.5 with the molar ratio of nickel with respect to all the metals other than alkali metals higher than or equal to 0.8, e.g. Li(MzNixCoyMn1-x-y-z)O2 with x ≥ 0.8
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/362—Composites
    • H01M4/366—Composites as layered products
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/50—Solid solutions
    • C01P2002/52—Solid solutions containing elements as dopants
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/40—Electric properties
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/021—Physical characteristics, e.g. porosity, surface area
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/028—Positive electrodes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present disclosure relates to a positive electrode active material for non-aqueous electrolyte secondary batteries and technology of non-aqueous electrolyte secondary batteries.
  • a non-aqueous electrolyte secondary battery that includes a positive electrode, a negative electrode, and a non-aqueous electrolyte, and charges and discharges by moving lithium ions or the like between the positive electrode and the negative electrode. Widely used.
  • Patent Documents 1 to 11 propose non-aqueous electrolyte secondary batteries using a lithium-containing composite oxide containing W as a positive electrode active material for non-aqueous electrolyte secondary batteries.
  • An object of the present disclosure is to provide a positive electrode active material for a non-aqueous electrolyte secondary battery capable of suppressing the amount of gas generated during the initial charge and discharge of the battery and reducing the direct current resistance (DCIR) of the battery, and the non-aqueous electrolyte secondary battery.
  • An object of the present invention is to provide a non-aqueous electrolyte secondary battery comprising a positive electrode active material for
  • a positive electrode active material for a nonaqueous electrolyte secondary battery which is one aspect of the present disclosure, includes a composite oxide containing at least one element selected from Ni, Mn, Co, and Al, W, and Li. , an intermediate layer formed on the composite oxide, wherein the intermediate layer does not contain W and contains at least one element of Ca, P and B; and and a coating layer containing W.
  • a non-aqueous electrolyte secondary battery includes a positive electrode having the positive electrode active material for a non-aqueous electrolyte secondary battery.
  • a positive electrode active material for a non-aqueous electrolyte secondary battery capable of suppressing the amount of gas generated and reducing the DC resistance of the battery during the initial charge and discharge of the battery, and the non-aqueous electrolyte secondary battery It is possible to provide a non-aqueous electrolyte secondary battery comprising a positive electrode active material for
  • FIG. 1 is a cross-sectional view of a non-aqueous electrolyte secondary battery that is an example of an embodiment
  • FIG. 1 is a schematic cross-sectional view showing an example of a non-aqueous electrolyte secondary battery according to an embodiment.
  • the non-aqueous electrolyte secondary battery 10 shown in FIG. It has insulating plates 18 and 19 arranged and a battery case 15 that accommodates the above members.
  • the battery case 15 is composed of a bottomed cylindrical case body 16 and a sealing member 17 that closes the opening of the case body 16 .
  • the wound electrode body 14 another form of electrode body such as a stacked electrode body in which positive and negative electrodes are alternately stacked via a separator may be applied.
  • Examples of the battery case 15 include cylindrical, rectangular, coin-shaped, button-shaped, and other metal cases, and resin cases formed by laminating resin sheets (so-called laminate type).
  • a non-aqueous electrolyte includes, for example, a non-aqueous solvent and an electrolyte salt dissolved in the non-aqueous solvent.
  • non-aqueous solvents include esters, ethers, nitriles, amides, and mixed solvents of two or more thereof.
  • the non-aqueous solvent may contain a halogen-substituted product obtained by substituting at least part of the hydrogen atoms of these solvents with halogen atoms such as fluorine.
  • a lithium salt such as LiPF 6 is used as the electrolyte salt.
  • the non-aqueous electrolyte is not limited to a liquid electrolyte, and may be a solid electrolyte using a gel polymer or the like.
  • the case body 16 is, for example, a bottomed cylindrical metal container.
  • a gasket 28 is provided between the case body 16 and the sealing member 17 to ensure hermeticity inside the battery.
  • the case main body 16 has an overhanging portion 22 that supports the sealing member 17, for example, a portion of the side surface overhanging inward.
  • the protruding portion 22 is preferably annularly formed along the circumferential direction of the case body 16 and supports the sealing member 17 on the upper surface thereof.
  • the sealing body 17 has a structure in which a filter 23, a lower valve body 24, an insulating member 25, an upper valve body 26, and a cap 27 are layered in order from the electrode body 14 side.
  • Each member constituting the sealing member 17 has, for example, a disk shape or a ring shape, and each member except for the insulating member 25 is electrically connected to each other.
  • the lower valve body 24 and the upper valve body 26 are connected to each other at their central portions, and an insulating member 25 is interposed between their peripheral edge portions.
  • the lower valve body 24 deforms and breaks so as to push the upper valve body 26 upward toward the cap 27, thereby breaking the lower valve body 24 and the upper valve.
  • the current path between bodies 26 is interrupted.
  • the upper valve body 26 is broken and the gas is discharged from the opening of the cap 27 .
  • the positive electrode lead 20 attached to the positive electrode 11 extends through the through hole of the insulating plate 18 toward the sealing member 17, and the negative electrode lead 21 attached to the negative electrode 12 is insulated. It extends to the bottom side of the case body 16 through the outside of the plate 19 .
  • the positive electrode lead 20 is connected to the lower surface of the filter 23, which is the bottom plate of the sealing member 17, by welding or the like, and the cap 27, which is the top plate of the sealing member 17 electrically connected to the filter 23, serves as a positive electrode terminal.
  • the negative lead 21 is connected to the inner surface of the bottom of the case body 16 by welding or the like, and the case body 16 serves as a negative terminal.
  • the positive electrode 11, the negative electrode 12, and the separator 13 are described in detail below.
  • the positive electrode 11 is composed of, for example, a positive electrode current collector such as a metal foil, and a positive electrode mixture layer formed on the positive electrode current collector.
  • a positive electrode current collector such as a metal foil
  • a positive electrode mixture layer formed on the positive electrode current collector.
  • a foil of a metal such as aluminum that is stable in the positive electrode potential range, a film having the metal on the surface layer, or the like can be used.
  • the positive electrode mixture layer contains, for example, a positive electrode active material, a binder, a conductive material, and the like.
  • a positive electrode mixture slurry containing a positive electrode active material, a binder, a conductive material, etc. is applied onto the positive electrode current collector and dried to form a positive electrode mixture layer on the positive electrode current collector. , obtained by rolling the positive electrode mixture layer.
  • the positive electrode active material includes composite particles having a composite oxide, an intermediate layer formed on the composite oxide, and a coating layer formed on the intermediate layer.
  • the composite oxide contains at least one element selected from Ni, Mn, Co, and Al, W, and Li.
  • the ratio of Ni, Mn, Co, and Al in the composite oxide is, for example, in terms of increasing the capacity of the battery and suppressing deterioration of charge-discharge cycle characteristics, with respect to the total molar amount of metal elements excluding Li, It is preferably 75 mol % or more, more preferably 85 mol % or more.
  • the ratio of W in the composite oxide is, for example, the point that the amount of gas generated during the initial charge and discharge of the battery can be further suppressed, or the DC resistance of the battery can be further reduced. On the other hand, it is preferably 0.01 mol % or more, more preferably 0.05 mol % or more.
  • suitable composite oxides include general formula: Li 1+x Ma (1-z) Mb z W y O 2 (wherein Ma is at least one of Ni, Mn, Co, and Al and Mb is at least one of Ti, Zr, Nb, Ta, Mo, Sb, Bi, Ca, Sr, Mg, Y, Sc and V, and x, y and z are 0 .02 ⁇ x ⁇ 0.07, 0.0005 ⁇ y ⁇ 0.01, 0 ⁇ z ⁇ 0.1).
  • Examples of more suitable composite oxides include general formula: Li 1+x Ni q Mc (1-qz) Mb z W y O 2 (wherein Ma is at least one of Mn, Co, and Al and Mb is at least one of Ti, Zr, Nb, Ta, Mo, Sb, Bi, Ca, Sr, Mg, Y, Sc, V, and x, y, z includes composite oxides represented by 0.02 ⁇ x ⁇ 0.07, 0.7 ⁇ q ⁇ 0.95, 0.0005 ⁇ y ⁇ 0.01, 0 ⁇ z ⁇ 0.1) .
  • the intermediate layer formed on the composite oxide is an intermediate layer that does not contain W and contains at least one element of Ca, P and B.
  • W is contained in the intermediate layer
  • the ratio of the molar amount of Ca, P and B contained in the intermediate layer to the total molar amount of the composite oxide is, for example, a point that further suppresses the amount of gas generated during the initial charge and discharge of the battery or further reduces the direct current resistance of the battery. 0.01 mol % to 1 mol %, and more preferably 0.05 mol % to 0.5 mol %.
  • the thickness of the intermediate layer is preferably in the range of 5 nm to 200 nm.
  • the thickness of the intermediate layer is less than 5 nm, side reactions of the composite oxide under the intermediate layer are likely to occur during charging and discharging. The amount of gas generated or the DC resistance of the battery may increase during the initial charge and discharge. Further, when the thickness of the intermediate layer exceeds 200 nm, the intermediate layer becomes a resistance component, which hinders the charge-discharge reaction of the composite oxide, which may lead to a decrease in battery capacity.
  • the thickness of the intermediate layer can be measured as follows.
  • the positive electrode 11 or the composite particles are embedded in a resin, and cross-sections of the composite particles are exposed by cross-section polisher (CP) processing or the like, and the cross-sections are photographed with a scanning electron microscope (SEM). Then, 30 composite particles are randomly selected from this cross-sectional SEM image. The thickness of the intermediate layer of each of the selected 30 composite particles is measured and the average value is calculated. Then, this average value is used as the thickness of the intermediate layer.
  • CP cross-section polisher
  • SEM scanning electron microscope
  • the coverage of the intermediate layer covering the composite oxide is, for example, preferably 75% or more, more preferably 85% or more.
  • the coverage of the intermediate layer is less than 75%, side reactions of the composite oxide under the intermediate layer are more likely to occur during charging and discharging. As a result, the amount of gas generated or the direct current resistance of the battery may increase during the initial charging and discharging of the battery.
  • the coverage of the intermediate layer formed on the composite oxide is measured by X-ray photoelectron spectroscopy (XPS).
  • the coating layer formed on the intermediate layer is a coating layer containing W.
  • the ratio of the molar amount of W in the coating layer to the total molar amount of the composite oxide is 0.00 in terms of further suppressing the amount of gas generated during the initial charge and discharge of the battery, or in terms of further reducing the direct current resistance of the battery. It is preferably in the range of 05 mol % to 1 mol %, more preferably in the range of 0.05 mol % to 0.5 mol %.
  • the coverage of the coating layer formed on the intermediate layer is, for example, preferably in the range of 10% to 40%, more preferably in the range of 10% to 25%. If the coverage of the coating layer is too high, the coating layer may inhibit the charge-discharge reaction of the composite oxide, leading to a decrease in battery capacity.
  • the coverage of the coating layer is measured by X-ray photoelectron spectroscopy. Specifically, it is calculated from the molar fraction of the element (W) of the coating layer with respect to the total molar amount of the metal elements of the composite oxide and the elements (Ca, P and B) of the intermediate layer.
  • the composition of the composite oxide can be confirmed by Rietveld analysis of the parameters obtained by inductively coupled plasma emission spectroscopy, X-ray photoelectron spectroscopy, and powder X-ray diffraction.
  • Qualitative and quantitative analysis of the intermediate layer and coating layer can be performed by X-ray photoelectron spectroscopy, inductively coupled plasma emission spectroscopy, electron probe macroanalyzer (EPMA), or the like.
  • the analysis by EPMA is, for example, a method of exposing a cross section of the sample to be analyzed and analyzing the cross section by EPMA mapping (cross-section EPMA mapping analysis).
  • a hydroxide or oxide containing at least one element selected from Ni, Mn, Co and Al, a Li compound, and a W compound are mixed, and the mixture is fired to produce Ni, Mn , Co and Al, W, and Li.
  • Hydroxides containing at least one element selected from Ni, Mn, Co and Al are prepared by adding an alkaline solution such as sodium hydroxide while stirring an aqueous solution of Ni salt, Co salt and Al salt. By adding dropwise and adjusting the pH to the alkaline side (eg, 8.5 to 11.5), composite hydroxides containing Ni, Co, Al, etc. are precipitated (coprecipitated).
  • Li compounds are, for example, lithium hydroxide, lithium carbonate, and the like.
  • the W compound is tungsten oxide such as WO3 .
  • the firing temperature of the mixture is, for example, in the range of 500°C to 900°C, and the firing time is in the range of, for example, 1 hour to 20 hours.
  • a compound containing at least one of Ca, P and B is deposited on the surface of the composite oxide obtained above.
  • the coating method may be either a wet method or a dry method, but the wet method is preferable in that the coverage of the intermediate layer can be increased.
  • a solution containing a compound containing at least one element of Ca, P and B is dropped or sprayed onto the composite oxide obtained above.
  • particles are obtained in which an intermediate layer containing at least one of Ca, P and B is formed on the surface of the composite oxide.
  • the composite oxide obtained above is put into a solution containing a compound containing at least one element selected from Ca, P and B, and stirred. After stirring, the solution is filtered to obtain particles in which an intermediate layer containing at least one of Ca, P and B is formed on the surface of the composite oxide.
  • the solution containing the compound containing at least one element of Ca, P and B is preferably an alkaline solution so that the compound can be easily dissolved.
  • Compounds containing Ca are, for example, calcium hydroxide, calcium phosphate, calcium dihydrogen phosphate, hydroxyapatite, calcium carbonate, calcium acetate, and calcium oxide
  • compounds containing P are, for example, phosphoric acid, lithium phosphate, and phosphonic acid.
  • Acids, calcium phosphate, calcium dihydrogen phosphate, hydroxyapatite, and compounds containing B are, for example, boric acid, lithium metaborate, lithium tetraborate.
  • the particles obtained above may be dried by heating under reduced pressure.
  • the heat-drying temperature is, for example, in the range of 100° C. to 300° C.
  • the heat-drying time is, for example, in the range of 1 hour to 5 hours.
  • a W-containing compound is deposited on the intermediate layer of the obtained particles.
  • the deposition method may be a wet method or a dry method. However, if the coverage of the coating layer is high, the battery capacity or the like is affected, so the dry method is preferable in terms of suppressing the coverage of the coating layer.
  • the particles obtained above and a W compound are mixed and dried by heating under reduced pressure.
  • the W compound is tungsten oxide such as WO3 .
  • the heat-drying temperature is, for example, in the range of 100° C. to 300° C.
  • the heat-drying time is, for example, in the range of 1 hour to 5 hours.
  • the composite particles of the present embodiment are obtained in which a coating layer containing W is formed on the surface of the intermediate layer formed on the composite oxide.
  • Examples of the conductive material contained in the positive electrode mixture layer include carbon black, acetylene black, ketjen black, graphene, fibrous carbon such as carbon nanotubes, and carbon materials such as graphite.
  • the binder contained in the positive electrode mixture layer includes fluororesins such as polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVdF), polyacrylonitrile (PAN), polyimide resins, acrylic resins, polyolefin resins, styrene-butadiene rubber (SBR), carboxymethyl cellulose (CMC) or salts thereof, polyacrylic acid (PAA) or salts thereof (PAA-Na, PAA-K, etc., may also be partially neutralized salts), polyethylene oxide (PEO), polyvinyl alcohol (PVA) and the like.
  • fluororesins such as polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVdF), polyacrylon
  • the negative electrode 12 includes, for example, a negative electrode current collector such as metal foil, and a negative electrode mixture layer formed on the negative electrode current collector.
  • a negative electrode current collector such as metal foil
  • a negative electrode mixture layer formed on the negative electrode current collector.
  • a foil of a metal such as copper that is stable in the potential range of the negative electrode, a film having the metal on the surface layer, or the like can be used.
  • the negative electrode mixture layer includes, for example, a negative electrode active material, a binder, and the like.
  • a negative electrode mixture slurry containing a negative electrode active material, a binder, etc. is applied onto the negative electrode current collector and dried to form a negative electrode mixture layer on the negative electrode current collector. It is obtained by rolling the composite layer.
  • the negative electrode mixture layer may be provided on one side of the negative electrode current collector, or may be provided on both sides of the negative electrode current collector.
  • the negative electrode active material is, for example, a material capable of intercalating and deintercalating lithium ions, and specifically, a carbon material, a metal capable of forming an alloy with lithium, an alloy compound containing such a metal, or the like. is mentioned.
  • a carbon material natural graphite, non-graphitizable carbon, graphites such as artificial graphite, cokes, and the like can be used. Alloy compounds include those containing at least one metal capable of forming an alloy with lithium. Silicon and tin are preferable as elements capable of forming an alloy with lithium, and silicon oxide, tin oxide, etc., in which these are combined with oxygen, can also be used. A mixture of the above carbon material and a compound of silicon or tin can also be used. In addition to the above, lithium titanate and the like can also be used.
  • the same binding material as that of the positive electrode 11 may be used.
  • the negative electrode mixture layer may contain a conductive material.
  • a conductive material similar to that used for the positive electrode 11 may be used.
  • a porous sheet or the like having ion permeability and insulation is used.
  • porous sheets include microporous thin films, woven fabrics, and non-woven fabrics.
  • Suitable materials for the separator 13 include olefin resins such as polyethylene and polypropylene, and cellulose.
  • the separator 13 may be a laminate having a cellulose fiber layer and a thermoplastic resin fiber layer such as an olefin resin.
  • a multilayer separator including a polyethylene layer and a polypropylene layer may be used, and a separator whose surface is coated with a material such as aramid resin or ceramic may be used.
  • Example 1 [Production of composite particles] A composite oxide containing Ni, Mn, Nb, W and Li (general formula: LiNi 0.82 Mn 0.18 Nb 0.0025 W 0.005 O 2 ) is added to water, stirred, and then this solution was suction filtered. After that, a solution (concentration: 0.02 mol/L) in which calcium dihydrogen phosphate was dissolved was added, and filtered again. The obtained filtrate and tungsten oxide were mixed at a molar ratio of 1:0.001, and the mixture was dried under reduced pressure at 180° C. for 2 hours to obtain composite particles.
  • Ethylene carbonate (EC), dimethyl carbonate (DMC) and ethylmethyl carbonate (EMC) were mixed in a volume ratio of 20:75:5.
  • a non-aqueous electrolyte was prepared by dissolving LiPF 6 in the mixed solvent so as to have a concentration of 1.3 mol/L.
  • the positive electrode and the negative electrode were each cut into a predetermined size, an electrode lead was attached thereto, and a wound electrode body was produced by winding the cut piece with a separator interposed therebetween.
  • the electrode assembly was housed in an aluminum laminate film, the above non-aqueous electrolyte was injected, and the assembly was sealed. This was used as the non-aqueous electrolyte secondary battery of Example 1.
  • Example 2 Example 1 except that a solution of borate (B concentration: 0.6 mol/L, pH: 10) was used instead of the solution of calcium dihydrogen phosphate in the preparation of the composite particles.
  • Composite particles were obtained by the same method. As a result of analyzing the obtained composite particles in the same manner as in Example 1, an intermediate layer containing B but not containing W was formed on the composite oxide containing Ni, Mn, Nb, W and Li. It was confirmed that a coating layer containing W was formed thereon.
  • a non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as the positive electrode active material.
  • Example 1 A non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite oxide containing Ni, Mn, Nb, W and Li used in Example 1 was used as the positive electrode active material.
  • Example 2 The composite oxide containing Ni, Mn, Nb, W and Li used in Example 1 and tungsten oxide were mixed at a molar ratio of 1:0.001, and the mixture was Composite particles were obtained by drying at 180° C. for 2 hours.
  • a non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as a positive electrode active material.
  • a non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as a positive electrode active material.
  • Example 4 The filtrate obtained in Example 1 and boric acid were mixed at a molar ratio of 1:0.01, and the mixture was dried under reduced pressure at 180°C for 2 hours to obtain composite particles. got
  • Example 2 As a result of analyzing the obtained composite particles in the same manner as in Example 1, an intermediate layer containing Ca and P but not W was formed on the composite oxide containing Ni, Mn, Nb, W and Li, It was confirmed that a coating layer containing B but not W was formed on the intermediate layer.
  • a non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as a positive electrode active material.
  • Example 2 As a result of analyzing the obtained composite particles in the same manner as in Example 1, a coating layer containing B and not containing W was formed on the composite oxide containing Ni, Mn, Nb, Ca, W and Li. I confirmed that there is A non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as a positive electrode active material.
  • Comparative Example 6 The composite oxide used in Comparative Example 5 was added to water, and after stirring, this solution was subjected to suction filtration. After that, a solution in which tungsten oxide was dissolved (W concentration: 0.06 mol/L, pH: 11) was added, and suction filtration was performed again. The obtained filtrate and tungsten oxide were mixed at a molar ratio of 1:0.001, and the mixture was dried under reduced pressure at 180° C. for 2 hours to obtain composite particles.
  • W concentration 0.06 mol/L, pH: 11
  • Example 2 As a result of analyzing the obtained composite particles in the same manner as in Example 1, an intermediate layer containing W was formed on the composite oxide containing Ni, Mn, Nb, Ca, W and Li, and on the intermediate layer , W was formed.
  • a non-aqueous electrolyte secondary battery was produced in the same manner as in Example 1, except that the composite particles were used as a positive electrode active material.
  • the volume of the non-aqueous electrolyte secondary battery of each example and each comparative example was measured by the Archimedes method. Then, under an ambient temperature of 25° C., the non-aqueous electrolyte secondary batteries of each example and each comparative example were charged at a constant current of 0.5 C until the voltage reached 4.2 V, and then charged at 0.05 C. Constant voltage charging was carried out until reaching After that, the battery was discharged at a constant current of 0.5C until the battery voltage reached 2.5V. After charging and discharging, the volume of the non-aqueous electrolyte secondary battery of each example and each comparative example was measured by the Archimedes method.
  • the amount of gas generated during the initial charging/discharging was calculated.
  • the object to be measured in this example, a non-aqueous electrolyte secondary battery
  • a liquid medium eg, distilled water, alcohol, etc.
  • Table 1 shows the amount of gas generated and the DC resistance of the battery during the initial charge and discharge in each example and each comparative example.
  • non-aqueous electrolyte secondary battery 11 positive electrode, 12 negative electrode, 13 separator, 14 electrode body, 15 battery case, 16 case body, 17 sealing body, 18, 19 insulating plate, 20 positive electrode lead, 21 negative electrode lead, 22 overhang , 23 filter, 24 lower valve body, 25 insulating member, 26 upper valve body, 27 cap, 28 gasket.

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US20250167226A1 (en) 2025-05-22

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