WO2023042567A1 - 組成物、電池、および組成物の製造方法 - Google Patents

組成物、電池、および組成物の製造方法 Download PDF

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WO2023042567A1
WO2023042567A1 PCT/JP2022/029802 JP2022029802W WO2023042567A1 WO 2023042567 A1 WO2023042567 A1 WO 2023042567A1 JP 2022029802 W JP2022029802 W JP 2022029802W WO 2023042567 A1 WO2023042567 A1 WO 2023042567A1
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solid electrolyte
composition
electrolyte material
composition according
negative electrode
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English (en)
French (fr)
Japanese (ja)
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真志 境田
和史 宮武
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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 EP22869715.7A priority Critical patent/EP4404217A4/en
Priority to JP2023548158A priority patent/JPWO2023042567A1/ja
Priority to CN202280060329.XA priority patent/CN117916825A/zh
Publication of WO2023042567A1 publication Critical patent/WO2023042567A1/ja
Priority to US18/593,798 priority patent/US20250006983A1/en
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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
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • 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
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562—Solid materials
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00—Compounds of titanium
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G25/00—Compounds of zirconium
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • 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
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H01M10/0585—Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • 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
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0068—Solid electrolytes inorganic
    • H01M2300/008—Halides
    • 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 compositions, batteries, and methods of manufacturing compositions.
  • Patent Document 1 discloses an all-solid battery using a sulfide solid electrolyte.
  • Patent Document 2 discloses LiBF 4 as a fluoride solid electrolyte material.
  • An object of the present disclosure is to provide a composition suitable for improving the ionic conductivity of solid electrolyte materials.
  • compositions of the present disclosure are LiF and at least one compound selected from the group consisting of TiF 4 , AlF 3 , Li 2 TiF 6 and Li 3 AlF 6 ; and a solvent.
  • compositions suitable for improving the ionic conductivity of solid electrolyte materials are provided.
  • FIG. 1 shows a cross-sectional view of a battery 1000 according to a second embodiment.
  • 2A shows a Scanning Electron Microscope (SEM) image obtained to evaluate the particle size of the particles contained in the composition according to Example 1.
  • FIG. 2B shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 2.
  • FIG. 2C shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 3.
  • FIG. 2D shows an SEM image taken to assess the particle size of the particles contained in the composition according to Example 4.
  • FIG. 2E shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 5.
  • FIG. 2F shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 6.
  • SEM Scanning Electron Microscope
  • FIG. 2G shows an SEM image taken to assess the particle size of the particles contained in the composition according to Example 7.
  • FIG. 2H shows an SEM image obtained to evaluate the particle size of the particles contained in the composition according to Example 8.
  • FIG. 2I shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 9.
  • FIG. 2J shows an SEM image taken to assess the particle size of the particles contained in the composition according to Example 10.
  • FIG. 2K shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 11.
  • FIG. 2L shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 12.
  • FIG. 2M shows an SEM image taken to assess the particle size of the particles contained in the composition according to Example 13.
  • FIG. 2N shows an SEM image taken to assess the particle size of the particles contained in the composition according to Example 14.
  • FIG. 3 shows a schematic diagram of a pressure forming die 300 used to evaluate the ionic conductivity of solid electrolyte materials.
  • 4 is a graph showing a Cole-Cole plot obtained by impedance measurement of the solid electrolyte material according to Example 1.
  • FIG. 5 is a graph showing the initial discharge characteristics of the batteries according to Example 1 and Comparative Example 1;
  • the composition according to the first embodiment includes LiF, at least one compound selected from the group consisting of TiF 4 , AlF 3 , Li 2 TiF 6 and Li 3 AlF 6 , and a solvent.
  • the compound is, for example, particulate.
  • the average particle size of the particulate compound is determined by morphological observation using an SEM image. Specifically, first, the composition according to the first embodiment is dried (for example, vacuum dried) to extract particles of the compound, and an SEM image of the particles is obtained. Randomly select 40 primary particles of the compound in the resulting SEM image, measure the unidirectional diameter (Ferrey diameter) of the selected primary particles, the particle diameter of the bottom 10 of the 40 particle diameters The average particle size is calculated by simply averaging the particle sizes of the remaining 30 particles after rounding them off.
  • composition according to the first embodiment is suitable for improving the ionic conductivity of solid electrolyte materials.
  • a solidified product (that is, a solid electrolyte material) obtained by removing the solvent from the composition according to the first embodiment is a solid electrolyte material having improved lithium ion conductivity.
  • the composition according to the first embodiment is heated to produce a solid electrolyte material.
  • the particles dispersed in the composition have a small particle size. Specifically, if the average particle size is less than 500 nm, for example, the formation reaction proceeds efficiently, and a solid electrolyte material with improved ionic conductivity can be obtained.
  • the raw materials react with each other in the process of micronizing or dispersing the raw materials to form a precursor of the solid electrolyte material, it is expected that the production reaction of the solid electrolyte material proceeds more efficiently.
  • the average particle size of the compound contained in the composition according to the first embodiment may be less than 160 nm.
  • the lower limit of the average particle size of the compound is not particularly limited, but the average particle size may be, for example, 10 nm or more, or 50 nm or more.
  • a solid electrolyte material obtained from the composition of the first embodiment (hereinafter referred to as "solid electrolyte material according to the first embodiment") can be used to obtain a battery with excellent charge/discharge characteristics.
  • An example of such a battery is an all solid state battery.
  • the all-solid-state battery may be a primary battery or a secondary battery.
  • the solvent contained in the composition according to the first embodiment may contain a compound having an ester group.
  • the dispersion particles in the composition according to the first embodiment that is, the particle size reduction of the compound can be efficiently progressed.
  • the solvent contained in the composition according to the first embodiment may contain at least one selected from the group consisting of ⁇ -butyrolactone, propylene carbonate, butyl acetate, dimethylsulfoxide, and tetralin.
  • the solvent may contain at least one selected from the group consisting of ⁇ -butyrolactone, propylene carbonate, butyl acetate, and tetralin.
  • the compound for example, using a planetary ball mill, the compound is pulverized in a state where LiF, a compound such as TiF 4 or AlF 3 , and a solvent are mixed, and the compound is pulverized and dispersed. simultaneously.
  • synthesis, pulverization, and slurrying of the solid electrolyte material can be performed simultaneously, and it is expected that the number of steps can be reduced.
  • the compound contained in the composition according to the first embodiment may be the raw material of the solid electrolyte material.
  • a compound contained in the composition according to the first embodiment may be a raw material of a solid electrolyte containing Li, Ti, Al, and F, for example.
  • composition according to the first embodiment may contain at least one selected from the group consisting of Li 2 TiF 6 and Li 3 AlF 6 as the compound.
  • the solid electrolyte material according to the first embodiment desirably does not contain sulfur.
  • a sulfur-free solid electrolyte material does not generate hydrogen sulfide even when exposed to the atmosphere, and is therefore excellent in safety.
  • the sulfide solid electrolyte disclosed in Patent Document 1 can generate hydrogen sulfide when exposed to the air.
  • the solid electrolyte material according to the first embodiment contains F and thus can have high oxidation resistance. This is because F has a high redox potential. On the other hand, since F has high electronegativity, it has a relatively strong bond with Li. As a result, solid electrolyte materials containing Li and F typically have low lithium ion conductivity. For example, LiBF 4 disclosed in Patent Document 2 has a low ionic conductivity of 6.67 ⁇ 10 ⁇ 9 S/cm. On the other hand, when the solid electrolyte material obtained from the composition of Embodiment 1 further contains Ti and Al in addition to Li and F, for example, high ionic conductivity of 7 ⁇ 10 ⁇ 9 S/cm or more degree.
  • the solid electrolyte material according to the first embodiment may contain anions other than F in order to increase the ion conductivity of the solid electrolyte material.
  • anions are Cl, Br, I, O or Se.
  • the ratio of the amount of F to the total amount of anions constituting the solid electrolyte material according to the first embodiment is 0.50 or more and 1.0 or less. good too.
  • the solid electrolyte material according to the first embodiment may consist essentially of Li, Ti, Al, and F.
  • the solid electrolyte material according to the first embodiment consists essentially of Li, Ti, Al, and F
  • the total amount of all elements constituting the solid electrolyte material according to the first embodiment It means that the total molar ratio (that is, molar fraction) of the amount of Li, Ti, Al, and F to the total amount of substances is 90% or more. As an example, the molar ratio (ie, mole fraction) may be 95% or greater.
  • the solid electrolyte material according to the first embodiment may consist of Li, Ti, Al, and F only.
  • the solid electrolyte material according to the first embodiment may further contain Zr.
  • the solid electrolyte material according to the first embodiment may consist essentially of Li, Ti, Zr, Al and F.
  • the solid electrolyte material according to the first embodiment consists essentially of Li, Ti, Zr, Al, and F
  • the substance amount of all elements constituting the solid electrolyte material according to the first embodiment means that the ratio of the total amount of substances of Li, Ti, Zr, Al, and F (that is, the molar fraction) to the total of is 90% or more.
  • the ratio (ie, mole fraction) may be 95% or greater.
  • the solid electrolyte material according to the first embodiment may consist of Li, Ti, Zr, Al, and F only.
  • the solid electrolyte material according to the first embodiment may contain elements that are unavoidably mixed. Examples of such elements are hydrogen, oxygen or nitrogen. Such elements can be present in the raw powder of the solid electrolyte material or in the atmosphere for manufacturing or storing the solid electrolyte material.
  • the ratio of the amount of Li substance to the total amount of Zr and Al is 1.12 or more and 5.07 or less. There may be.
  • the solid electrolyte material according to the first embodiment may be a material represented by the following compositional formula (1).
  • equation (1) the equations: 0 ⁇ x ⁇ 1 and 0 ⁇ b ⁇ 1.5 are satisfied.
  • a solid electrolyte material having such a composition has high ionic conductivity.
  • the composition according to the first embodiment comprises Li, Ti, Al, and F
  • x and y satisfy 0 ⁇ x ⁇ 1 and 0 ⁇ b ⁇ 1.5.
  • the formula: 0.01 ⁇ x ⁇ 0.99 may be satisfied in formula (1).
  • the formula: 0.2 ⁇ x ⁇ 0.95 may be satisfied.
  • the upper and lower limits of the range of x in formula (1) are 0.01, 0.2, 0.4, 0.5, 0.5, 0.7, 0.8, 0.95, and 0 It can be defined by any combination of numbers selected from 0.99.
  • the formula: 0.7 ⁇ b ⁇ 1.3 may be satisfied in formula (1).
  • the formula: 0.9 ⁇ b ⁇ 1.04 may be satisfied.
  • the upper and lower limits of the range of b in formula (1) are 0.7, 0.8, 0.9, 0.96, 1, 1.04, 1.1, 1.2, and 1.3. can be defined by any combination selected from the numerical values of
  • the solid electrolyte material according to the first embodiment may be Li2.7Ti0.3Al0.7F6 .
  • the solid electrolyte material according to the first embodiment may be a material represented by the following compositional formula (2).
  • a solid electrolyte material having such a composition has high ionic conductivity.
  • the composition according to the first embodiment contains Li, Ti, Zr, Al, and F
  • 0 ⁇ x ⁇ 1, 0 ⁇ y ⁇ 1, 0 ⁇ x+y ⁇ 1 and 0 ⁇ b ⁇ 1.5 are satisfied.
  • the upper and lower limits of the range of x in equation (2) are 0.01, 0.2, 0.4, 0.5, 0.5, 0.7, 0.8, 0.95, and 0 It can be defined by any combination of numbers selected from 0.99.
  • the upper and lower limits of the range of y in formula (2) are 0.01, 0.1, 0.15, 0.2, 0.4, 0.5, 0.5, 0.7, 0.01, 0.1, 0.15, 0.2, 0.4, 0.5, 0.5, 0.7, 0.00. It can be defined by any combination selected from the numbers 8, 0.95, and 0.99.
  • the upper and lower limits of the range of b in formula (2) are 0.7, 0.8, 0.9, 0.96, 1, 1.04, 1.1, 1.2, and 1.3. can be defined by any combination selected from the numerical values of
  • the solid electrolyte material according to the first embodiment is Li2.7Ti0.1Zr0.2Al0.7F6 , Li2.7Ti0.2Zr0.1Al0.7F6 , or Li 2.8Ti0.05Zr0.15Al0.8F6 .
  • the solid electrolyte material according to the first embodiment may be crystalline or amorphous.
  • the solid electrolyte material according to the first embodiment may contain a crystal phase represented by formula (1) or formula (2).
  • the shape of the solid electrolyte material according to the first embodiment is not limited. Examples of such shapes are acicular, spherical, or ellipsoidal.
  • the solid electrolyte material obtained from the composition of the first embodiment may be particles.
  • the solid electrolyte material obtained from the composition of the first embodiment may have the shape of pellets or plates.
  • a composition according to the first embodiment is produced, for example, by the following method.
  • a raw material composition containing a compound containing Li and at least one selected from the group consisting of Ti, Al, and F, and a solvent (for example, an organic solvent) are mixed while pulverizing in a mixing device.
  • the raw material composition may further contain, in addition to the above compounds, another compound that serves as a raw material for the solid electrolyte material.
  • the composition of the intended solid electrolyte material is Li2.7Ti0.3Al0.7F6
  • LiF, TiF4 , and AlF3 are 2.7:0.3:0
  • the raw material powders may be mixed in pre-adjusted molar ratios to compensate for possible compositional changes in the synthesis process.
  • Raw material powder (raw material composition) and an organic solvent are put into a mixing device such as a planetary ball mill, and mixed while pulverizing. That is, a wet ball mill is performed.
  • the raw material powder may be mixed before being charged into the mixing device.
  • the composition according to the first embodiment is obtained.
  • pulverization of the charged raw material composition is also performed at the same time, and in the composition according to the first embodiment, the particle size of the particles of the raw material composition dispersed in the solvent is larger than the charged raw material. expected to be smaller.
  • the particle size of the dispersed raw material composition particles can be obtained, for example, by the same method as the method for obtaining the average particle size of the particulate compound in the composition according to the first embodiment described above.
  • a solid electrolyte material according to the first embodiment is obtained from the composition according to the first embodiment. For example, it is manufactured by the following method.
  • a solidified product is obtained by drying the composition according to the first embodiment at a temperature corresponding to the boiling point of the solvent used.
  • the reactant that is, the solid electrolyte material according to the first embodiment is obtained.
  • the resulting reactant may be calcined in vacuum or in an inert atmosphere. Firing is performed at, for example, 100° C. or higher and 300° C. or lower for 1 hour or longer. In order to suppress composition change during firing, firing may be performed in a sealed container such as a quartz tube.
  • a battery according to the second embodiment includes a positive electrode, an electrolyte layer, and a negative electrode.
  • the electrolyte layer is provided between the positive electrode and the negative electrode.
  • At least one selected from the group consisting of the positive electrode, the electrolyte layer, and the negative electrode contains the solidified material of the composition according to the first embodiment (that is, the solid electrolyte material according to the first embodiment).
  • the battery according to the second embodiment contains the solid electrolyte material according to the first embodiment, it has excellent charge/discharge characteristics.
  • FIG. 1 shows a cross-sectional view of a battery 1000 according to the second embodiment.
  • a battery 1000 according to the second embodiment includes a positive electrode 201 , an electrolyte layer 202 and a negative electrode 203 .
  • Electrolyte layer 202 is provided between positive electrode 201 and negative electrode 203 .
  • a positive electrode 201 contains a positive electrode active material 204 and a solid electrolyte 100 .
  • the electrolyte layer 202 contains an electrolyte material.
  • the negative electrode 203 contains a negative electrode active material 205 and a solid electrolyte 100 .
  • the solid electrolyte 100 includes, for example, the solid electrolyte material according to the first embodiment.
  • the solid electrolyte 100 may be particles containing the solid electrolyte material according to the first embodiment as a main component.
  • a particle containing the solid electrolyte material according to the first embodiment as a main component means a particle in which the component contained in the largest molar ratio is the solid electrolyte material according to the first embodiment.
  • the solid electrolyte 100 may be particles made of the solid electrolyte material according to the first embodiment.
  • the positive electrode 201 contains a material that can occlude and release metal ions (eg, lithium ions).
  • the material is, for example, the positive electrode active material 204 .
  • cathode active material 204 examples include lithium-containing transition metal oxides, transition metal fluorides, polyanions, fluorinated polyanion materials, transition metal sulfides, transition metal oxyfluorides, transition metal oxysulfides, or transition metal oxynitrides. be.
  • lithium-containing transition metal oxides are Li(Ni,Co,Mn) O2 , Li(Ni,Co,Al) O2 or LiCoO2 .
  • (A, B, C) means "at least one selected from the group consisting of A, B, and C.”
  • the shape of the positive electrode active material 204 is not limited to a specific shape.
  • the cathode active material 204 may be particles.
  • the positive electrode active material 204 may have a median diameter of 0.1 ⁇ m or more and 100 ⁇ m or less.
  • positive electrode active material 204 and solid electrolyte 100 can be well dispersed in positive electrode 201 . Thereby, the charge/discharge characteristics of the battery 1000 are improved.
  • the positive electrode active material 204 has a median diameter of 100 ⁇ m or less, the diffusion rate of lithium in the positive electrode active material 204 is improved. This allows battery 1000 to operate at high output.
  • the positive electrode active material 204 may have a larger median diameter than the solid electrolyte 100 . Thereby, the positive electrode active material 204 and the solid electrolyte 100 can be well dispersed in the positive electrode 201 .
  • the ratio of the volume of the positive electrode active material 204 to the total volume of the positive electrode active material 204 and the volume of the solid electrolyte 100 is 0.30 or more and 0.95. It may be below.
  • a coating layer may be formed on at least part of the surface of the positive electrode active material 204 .
  • a coating layer can be formed on the surface of the positive electrode active material 204, for example, before mixing with the conductive aid and the binder.
  • coating materials contained in the coating layer are sulfide solid electrolytes, oxide solid electrolytes or halide solid electrolytes.
  • the coating material may contain the solid electrolyte material according to the first embodiment in order to suppress oxidative decomposition of the sulfide solid electrolyte.
  • the coating material may contain an oxide solid electrolyte in order to suppress oxidative decomposition of the solid electrolyte material.
  • Lithium niobate which has excellent stability at high potentials, may be used as the oxide solid electrolyte. By suppressing oxidative decomposition, an overvoltage rise of the battery 1000 can be suppressed.
  • the positive electrode 201 may have a thickness of 10 ⁇ m or more and 500 ⁇ m or less.
  • the electrolyte layer 202 contains an electrolyte material.
  • the electrolyte material is, for example, a solid electrolyte material.
  • the solid electrolyte material may include the solid electrolyte material according to the first embodiment.
  • the electrolyte layer 202 may be a solid electrolyte layer.
  • the electrolyte layer 202 may contain 50% by mass or more of the solid electrolyte material according to the first embodiment.
  • the electrolyte layer 202 may contain 70% by mass or more of the solid electrolyte material according to the first embodiment.
  • the electrolyte layer 202 may contain 90% by mass or more of the solid electrolyte material according to the first embodiment.
  • the electrolyte layer 202 may consist only of the solid electrolyte material according to the first embodiment.
  • the solid electrolyte material according to the first embodiment will be referred to as the first solid electrolyte material.
  • a solid electrolyte material different from the first solid electrolyte material is referred to as a second solid electrolyte material.
  • the electrolyte layer 202 may contain not only the first solid electrolyte material but also the second solid electrolyte material. In the electrolyte layer 202, the first solid electrolyte material and the second solid electrolyte material may be uniformly dispersed. A layer made of the first solid electrolyte material and a layer made of the second solid electrolyte material may be stacked along the stacking direction of battery 1000 .
  • the battery according to the second embodiment may include the positive electrode 201, the second electrolyte layer, the first electrolyte layer, and the negative electrode 203 in this order.
  • the solid electrolyte material contained in the first electrolyte layer may have a lower reduction potential than the solid electrolyte material contained in the second electrolyte layer.
  • the solid electrolyte material contained in the second electrolyte layer can be used without being reduced.
  • the charge/discharge efficiency of the battery 1000 can be improved.
  • the first electrolyte layer may contain a sulfide solid electrolyte in order to suppress reductive decomposition of the solid electrolyte material.
  • the second electrolyte layer may contain the first solid electrolyte material. Since the first solid electrolyte material has high oxidation resistance, it is possible to realize a battery with excellent charge/discharge characteristics.
  • the electrolyte layer 202 may consist only of the second solid electrolyte material.
  • the electrolyte layer 202 may have a thickness of 1 ⁇ m or more and 1000 ⁇ m or less. When the electrolyte layer 202 has a thickness of 1 ⁇ m or more, the short circuit between the positive electrode 201 and the negative electrode 203 is less likely to occur. If the electrolyte layer 202 has a thickness of 1000 ⁇ m or less, the battery 1000 can operate at high power.
  • Examples of the second solid electrolyte material are Li2MgX4 , Li2FeX4 , Li(Al,Ga,In) X4 , Li3 ( Al ,Ga,In) X6 , or LiI.
  • X is at least one selected from the group consisting of F, Cl, Br and I.
  • the electrolyte layer 202 may have a thickness of 1 ⁇ m or more and 1000 ⁇ m or less.
  • the negative electrode 203 contains a material capable of intercalating and deintercalating metal ions (eg, lithium ions).
  • the material is, for example, the negative electrode active material 205 .
  • Examples of the negative electrode active material 205 are metal materials, carbon materials, oxides, nitrides, tin compounds, or silicon compounds.
  • the metallic material may be a single metal or an alloy.
  • Examples of metallic materials are lithium metal or lithium alloys.
  • Examples of carbon materials are natural graphite, coke, ungraphitized carbon, carbon fibers, spherical carbon, artificial graphite, or amorphous carbon. From the viewpoint of capacity density, suitable examples of negative electrode active materials are silicon (ie, Si), tin (ie, Sn), silicon compounds, or tin compounds.
  • the negative electrode active material 205 may be selected in consideration of the reduction resistance of the solid electrolyte material contained in the negative electrode 203 .
  • the negative electrode active material 205 may be a material capable of intercalating and deintercalating lithium ions at 0.27 V or higher with respect to lithium.
  • examples of such negative electrode active materials are titanium oxide, indium metal, or lithium alloys.
  • examples of titanium oxides are Li4Ti5O12 , LiTi2O4 , or TiO2 .
  • the shape of the negative electrode active material 205 is not limited to a specific shape.
  • the negative electrode active material 205 may be particles.
  • the negative electrode active material 205 may have a median diameter of 0.1 ⁇ m or more and 100 ⁇ m or less.
  • negative electrode active material 205 and solid electrolyte 100 can be well dispersed in negative electrode 203 . Thereby, the charge/discharge characteristics of the battery 1000 are improved.
  • the negative electrode active material 205 has a median diameter of 100 ⁇ m or less, the diffusion rate of lithium in the negative electrode active material 205 is improved. This allows battery 1000 to operate at high output.
  • the negative electrode active material 205 may have a larger median diameter than the solid electrolyte 100 . Thereby, the negative electrode active material 205 and the solid electrolyte 100 can be well dispersed in the negative electrode 203 .
  • the ratio of the volume of the negative electrode active material 205 to the total volume of the negative electrode active material 205 and the volume of the solid electrolyte 100 is 0.30 or more and 0.95. It may be below.
  • the negative electrode 203 may have a thickness of 10 ⁇ m or more and 500 ⁇ m or less.
  • At least one selected from the group consisting of positive electrode 201, electrolyte layer 202, and negative electrode 203 contains a second solid electrolyte material for the purpose of enhancing ion conductivity, chemical stability, and electrochemical stability. may be
  • the second solid electrolyte material may be a sulfide solid electrolyte.
  • Examples of sulfide solid electrolytes are Li 2 S—P 2 S 5 , Li 2 S—SiS 2 , Li 2 S—B 2 S 3 , Li 2 S—GeS 2 , Li 3.25 Ge 0.25 P 0 .75 S 4 , or Li 10 GeP 2 S 12 .
  • the negative electrode 203 may contain a sulfide solid electrolyte in order to suppress reductive decomposition of the solid electrolyte material.
  • the contact of the first solid electrolyte material with the negative electrode active material can be suppressed. As a result, the internal resistance of battery 1000 can be reduced.
  • the second solid electrolyte material may be an oxide solid electrolyte.
  • oxide solid electrolytes are (i) a NASICON-type solid electrolyte such as LiTi2 ( PO4 ) 3 or elemental substitutions thereof; (ii) perovskite-type solid electrolytes such as (LaLi) TiO3 , (iii) LISICON -type solid electrolytes such as Li14ZnGe4O16 , Li4SiO4 , LiGeO4 or elemental substitutions thereof ; (iv) a garnet- type solid electrolyte such as Li7La3Zr2O12 or its elemental substitutions , or (v) Li3PO4 or its N substitutions, is.
  • NASICON-type solid electrolyte such as LiTi2 ( PO4 ) 3 or elemental substitutions thereof
  • perovskite-type solid electrolytes such as (LaLi) TiO3
  • LISICON -type solid electrolytes such as Li14ZnGe4O16 , Li4SiO4 ,
  • the second solid electrolyte material may be a halide solid electrolyte.
  • halide solid electrolytes are Li2MgX4 , Li2FeX4 , Li(Al,Ga,In) X4 , Li3 ( Al ,Ga,In) X6 , or LiI.
  • X is at least one selected from the group consisting of F, Cl, Br and I.
  • halide solid electrolyte is the compound represented by LiaMebYcZ6 .
  • Me is at least one selected from the group consisting of metal elements other than Li and Y and metalloid elements.
  • Z is at least one selected from the group consisting of F, Cl, Br and I;
  • m represents the valence of Me.
  • Simetallic elements are B, Si, Ge, As, Sb, and Te.
  • Metallic element means all elements contained in Groups 1 to 12 of the periodic table (excluding hydrogen), and all elements contained in Groups 13 to 16 of the periodic table (however, , B, Si, Ge, As, Sb, Te, C, N, P, O, S, and Se).
  • Me is the group consisting of Mg, Ca, Sr, Ba, Zn, Sc, Al, Ga, Bi, Zr, Hf, Ti, Sn, Ta, and Nb to improve the ionic conductivity of the halide solid electrolyte. It may be at least one selected from.
  • the halide solid electrolyte may be Li3YCl6 or Li3YBr6 .
  • the second solid electrolyte material may be an organic polymer solid electrolyte.
  • organic polymer solid electrolytes examples include polymeric compounds and lithium salt compounds.
  • the polymer compound may have an ethylene oxide structure. Since a polymer compound having an ethylene oxide structure can contain a large amount of lithium salt, the ionic conductivity can be further increased.
  • lithium salts are LiPF6 , LiBF4 , LiSbF6, LiAsF6 , LiSO3CF3 , LiN ( SO2CF3 ) 2 , LiN( SO2C2F5 ) 2 , LiN( SO2CF3 ) . ( SO2C4F9 ) , or LiC ( SO2CF3 )3 .
  • One lithium salt selected from these may be used alone. Alternatively, a mixture of two or more lithium salts selected from these may be used.
  • At least one selected from the group consisting of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 is composed of a non-aqueous electrolyte liquid, a gel electrolyte, or an ion in order to facilitate the transfer of lithium ions and improve the output characteristics of the battery. It may contain liquids.
  • the non-aqueous electrolyte contains a non-aqueous solvent and a lithium salt dissolved in the non-aqueous solvent.
  • non-aqueous solvents examples include cyclic carbonate solvents, chain carbonate solvents, cyclic ether solvents, chain ether solvents, cyclic ester solvents, chain ester solvents, or fluorine solvents.
  • cyclic carbonate solvents are ethylene carbonate, propylene carbonate, or butylene carbonate.
  • linear carbonate solvents are dimethyl carbonate, ethyl methyl carbonate, or diethyl carbonate.
  • examples of cyclic ether solvents are tetrahydrofuran, 1,4-dioxane, or 1,3-dioxolane.
  • Chain ether solvents are 1,2-dimethoxyethane or 1,2-diethoxyethane.
  • An example of a cyclic ester solvent is ⁇ -butyrolactone.
  • An example of a linear ester solvent is methyl acetate.
  • fluorosolvents are fluoroethylene carbonate, methyl fluoropropionate, fluorobenzene, fluoroethyl methyl carbonate, or fluorodimethylene carbonate.
  • One non-aqueous solvent selected from these may be used alone. Alternatively, a combination of two or more non-aqueous solvents selected from these may be used.
  • lithium salts are LiPF6 , LiBF4 , LiSbF6, LiAsF6 , LiSO3CF3 , LiN ( SO2CF3 ) 2 , LiN( SO2C2F5 ) 2 , LiN( SO2CF3 ) . ( SO2C4F9 ) , or LiC ( SO2CF3 )3 .
  • One lithium salt selected from these may be used alone. Alternatively, a mixture of two or more lithium salts selected from these may be used.
  • the lithium salt concentration is, for example, in the range of 0.5 mol/L or more and 2 mol/L or less.
  • a polymer material impregnated with a non-aqueous electrolyte can be used as the gel electrolyte.
  • examples of polymeric materials are polyethylene oxide, polyacrylonitrile, polyvinylidene fluoride, polymethyl methacrylate, or polymers with ethylene oxide linkages.
  • ionic liquids examples include (i) aliphatic chain quaternary salts such as tetraalkylammonium or tetraalkylphosphonium; (ii) aliphatic cyclic ammoniums such as pyrrolidiniums, morpholiniums, imidazoliniums, tetrahydropyrimidiniums, piperaziniums, or piperidiniums; or (iii) nitrogen-containing heteroatoms such as pyridiniums or imidazoliums ring aromatic cation.
  • aliphatic chain quaternary salts such as tetraalkylammonium or tetraalkylphosphonium
  • aliphatic cyclic ammoniums such as pyrrolidiniums, morpholiniums, imidazoliniums, tetrahydropyrimidiniums, piperaziniums, or piperidiniums
  • nitrogen-containing heteroatoms such as pyridiniums
  • Examples of anions contained in ionic liquids are PF 6 ⁇ , BF 4 ⁇ , SbF 6 ⁇ , AsF 6 ⁇ , SO 3 CF 3 ⁇ , N(SO 2 CF 3 ) 2 ⁇ , N(SO 2 C 2 F 5 ) 2 ⁇ , N(SO 2 CF 3 )(SO 2 C 4 F 9 ) ⁇ , or C(SO 2 CF 3 ) 3 ⁇ .
  • the ionic liquid may contain a lithium salt.
  • At least one selected from the group consisting of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may contain a binder in order to improve adhesion between particles.
  • binders include polyvinylidene fluoride, polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, polyacrylic acid methyl ester, polyacrylic acid ethyl ester, Polyacrylic acid hexyl ester, polymethacrylic acid, polymethacrylic acid methyl ester, polymethacrylic acid ethyl ester, polymethacrylic acid hexyl ester, polyvinyl acetate, polyvinylpyrrolidone, polyether, polyether sulfone, hexafluoropolypropylene, styrene-butadiene rubber , or carboxymethyl cellulose.
  • Copolymers can also be used as binders.
  • binders are tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkyl vinyl ethers, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid , and hexadiene.
  • a mixture of two or more materials selected from these may be used as the binder.
  • At least one selected from the positive electrode 201 and the negative electrode 203 may contain a conductive aid in order to improve electronic conductivity.
  • Examples of conductive aids are (i) graphites such as natural or artificial graphite; (ii) carbon blacks such as acetylene black or ketjen black; (iii) conductive fibers such as carbon or metal fibers; (iv) carbon fluoride, (v) metal powders such as aluminum; (vi) conductive whiskers such as zinc oxide or potassium titanate; (vii) a conductive metal oxide such as titanium oxide, or (viii) a conductive polymeric compound such as polyaniline, polypyrrole, or polythiophene; is.
  • the conductive aid (i) or (ii) may be used.
  • Examples of the shape of the battery according to the second embodiment are coin-shaped, cylindrical, rectangular, sheet-shaped, button-shaped, flat-shaped, and laminated.
  • a material for forming a positive electrode, a material for forming an electrolyte layer, and a material for forming a negative electrode are prepared, and the positive electrode, the electrolyte layer, and the negative electrode are arranged in this order by a known method. It may also be manufactured by making laminated laminates.
  • Example 1 (Production of composition)
  • These raw material powders were put into a 45 cc planetary ball mill pod together with balls (25 g) of 0.5 mm ⁇ .
  • ⁇ -Butyrolactone (GBL) as an organic solvent was added dropwise to the pod so that the solid content ratio was 30%.
  • the solid content ratio is calculated by ⁇ (mass of input raw material)/(mass of input raw material+mass of input solvent) ⁇ 100.
  • a planetary ball mill was used for milling at 500 rpm for 12 hours.
  • the composition according to Example 1 was obtained by separating the balls after milling.
  • the particles were leveled with a mortar as necessary.
  • a SEM (Regulus 8230, Hitachi High-Tech Innovations) was used for morphological observation. Randomly select 40 primary particles of the compound in the resulting SEM image, measure the unidirectional diameter (Ferrey diameter) of the selected primary particles, the particle diameter of the bottom 10 of the 40 particle diameters The average particle size was calculated by simply averaging the particle sizes of the remaining 30 particles after rounding them off. The observation magnification was 50,000 times.
  • 2A shows an SEM image taken to evaluate the particle size of the particles contained in the composition according to Example 1.
  • FIG. The average particle size of the dispersed particles of Example 1 was 68.47 nm.
  • Example 1 (Preparation of solid electrolyte material) The composition according to Example 1 was dried at 200° C. for 1 hour under nitrogen flow using a heating mantle. A powder of the solid electrolyte material according to Example 1 was obtained by pulverizing the resulting solidified material with a mortar. The solid electrolyte material according to Example 1 had a composition represented by Li2.7Ti0.3Al0.7F6 .
  • FIG. 3 shows a schematic diagram of a pressure forming die 300 used to evaluate the ionic conductivity of solid electrolyte materials.
  • the pressure forming die 300 had a punch upper part 301 , a frame mold 302 and a punch lower part 303 .
  • the frame mold 302 was made of insulating polycarbonate.
  • Punch top 301 and punch bottom 303 were made of electronically conductive stainless steel.
  • the ionic conductivity of the solid electrolyte material according to Example 1 was evaluated by the following method.
  • the inside of the pressure molding die 300 was filled with the powder of the solid electrolyte material according to Example 1. Inside the pressing die 300, a pressure of 400 MPa was applied to the solid electrolyte material according to Example 1 using the upper punch 301 and the lower punch 303. As shown in FIG.
  • the upper punch 301 and lower punch 303 were connected to a potentiostat (BioLogic, VSP300) equipped with a frequency response analyzer.
  • the punch upper part 301 was connected to the working electrode and the terminal for potential measurement.
  • the punch bottom 303 was connected to the counter and reference electrodes.
  • the impedance of the solid electrolyte material was measured by electrochemical impedance measurement at room temperature.
  • FIG. 4 is a graph showing a Cole-Cole plot obtained by impedance measurement of the solid electrolyte material according to Example 1.
  • the real value of the impedance at the measurement point where the absolute value of the phase of the complex impedance was the smallest was regarded as the resistance to ion conduction of the solid electrolyte material. See arrow R SE shown in FIG. 4 for the real value.
  • the ionic conductivity was calculated based on the following formula (3) using the resistance value.
  • ⁇ (R SE ⁇ S/t) ⁇ 1 (3)
  • ⁇ represents ionic conductivity.
  • S represents the contact area of the solid electrolyte material with the punch upper part 301 . That is, S is equal to the cross-sectional area of the hollow portion of the frame mold 302 in FIG.
  • R SE represents the resistance value of the solid electrolyte material in impedance measurements.
  • t represents the thickness of the solid electrolyte material. That is, t represents the thickness of the layer formed from the solid electrolyte material powder 101 in FIG.
  • Li 3 PS 4 (57.41 mg), the solid electrolyte material according to Example 1 (26 mg), and the positive electrode mixture (9.1 mg) were laminated in this order. was done.
  • a pressure of 300 MPa was applied to the obtained laminate to form a first electrolyte layer, a second electrolyte layer, and a positive electrode. That is, the second electrolyte layer formed from the solid electrolyte material according to Example 1 was sandwiched between the first electrolyte layer and the positive electrode.
  • the thicknesses of the first electrolyte layer and the second electrolyte layer were 450 ⁇ m and 150 ⁇ m, respectively.
  • metal Li (thickness: 200 ⁇ m) was laminated on the first electrolyte layer.
  • current collectors made of stainless steel were attached to the positive and negative electrodes, and current collecting leads were attached to the current collectors.
  • Example 1 a battery according to Example 1 was obtained.
  • (Charging and discharging test) 5 is a graph showing the initial discharge characteristics of the battery according to Example 1.
  • FIG. Initial charge/discharge characteristics were measured by the following method.
  • the battery according to Example 1 was placed in a constant temperature bath at 85°C.
  • Example 1 The cell according to Example 1 was then discharged at a current density of 67.6 ⁇ A/cm 2 until a voltage of 2.5 V was reached.
  • the battery according to Example 1 had an initial discharge capacity of 891 ⁇ Ah.
  • Example 2 to 14> (Preparation of composition and solid electrolyte material)
  • Table 1 shows the type of solvent, solid content ratio, ball diameter, amount of balls, and processing time in the milling treatment of the composition.
  • compositions according to Examples 2 to 14 were obtained in the same manner as in Example 1 except for the conditions shown in Table 1.
  • Example 2 A charge/discharge test was performed in the same manner as in Example 1 using the batteries according to Examples 2 to 14. As a result, the batteries according to Examples 2 to 14 were charged and discharged as well as the battery according to Example 1.
  • a battery according to Comparative Example 1 was obtained in the same manner as in Example 1, except that the solid electrolyte material according to Comparative Example 2 was used as the positive electrode mixture and the solid electrolyte used for the electrolyte layer.
  • Example 1 A charge/discharge test was performed in the same manner as in Example 1 using the battery according to Comparative Example 1. As a result, the initial discharge capacity of the battery according to Comparative Example 1 was 0.01 ⁇ Ah or less. That is, the battery according to Comparative Example 1 was neither charged nor discharged.
  • the composition according to the present disclosure can provide a solid electrolyte material having high lithium ion conductivity, and is suitable for providing batteries that can be charged and discharged well.
  • composition of the present disclosure is used, for example, in all-solid lithium ion secondary batteries.

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2025004750A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 ハロゲン化物固体電解質の製造方法、ハロゲン化物固体電解質、正極材料、および電池
WO2025004620A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 固体電解質材料の製造方法
WO2025004753A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 ハロゲン化物固体電解質の製造方法、ハロゲン化物固体電解質、正極材料、および電池
WO2025022870A1 (ja) * 2023-07-21 2025-01-30 パナソニックＩｐマネジメント株式会社 電池
WO2025022869A1 (ja) * 2023-07-21 2025-01-30 パナソニックＩｐマネジメント株式会社 電池
WO2025070256A1 (ja) * 2023-09-29 2025-04-03 日本碍子株式会社 固体電解質、固体電解質の製造方法、および、電池

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023042560A1 (ja) * 2021-09-15 2023-03-23 パナソニックＩｐマネジメント株式会社 固体電解質材料およびそれを用いた電池

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001068154A (ja) * 1999-06-25 2001-03-16 Sanyo Electric Co Ltd リチウム二次電池
JP2008277170A (ja) 2007-04-27 2008-11-13 Ohara Inc リチウム二次電池およびリチウム二次電池用の電極
JP2011509232A (ja) * 2008-01-11 2011-03-24 ツィンファ ユニバーシティ 低温同時焼成セラミック粉末及び特別な原料、並びにその使用
JP2011129312A (ja) 2009-12-16 2011-06-30 Toyota Motor Corp 硫化物固体電解質材料の製造方法、硫化物固体電解質材料およびリチウム電池
JP2013107134A (ja) * 2011-10-26 2013-06-06 Kobe Steel Ltd フラックス組成物及びブレージングシート
CN111606362A (zh) * 2020-05-27 2020-09-01 惠州亿纬锂能股份有限公司 一种助熔剂辅助制备高镍三元材料的方法、得到的产品和用途

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5101068B2 (ja) * 2006-09-19 2012-12-19 三星エスディアイ株式会社 非水二次電池用負極材料及びそれを用いた非水二次電池
CN115244750B (zh) * 2020-03-18 2025-06-10 松下知识产权经营株式会社 固体电解质材料及使用了该固体电解质材料的电池
CN117321789A (zh) * 2021-05-27 2023-12-29 松下知识产权经营株式会社 电极及电池

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001068154A (ja) * 1999-06-25 2001-03-16 Sanyo Electric Co Ltd リチウム二次電池
JP2008277170A (ja) 2007-04-27 2008-11-13 Ohara Inc リチウム二次電池およびリチウム二次電池用の電極
JP2011509232A (ja) * 2008-01-11 2011-03-24 ツィンファ ユニバーシティ 低温同時焼成セラミック粉末及び特別な原料、並びにその使用
JP2011129312A (ja) 2009-12-16 2011-06-30 Toyota Motor Corp 硫化物固体電解質材料の製造方法、硫化物固体電解質材料およびリチウム電池
JP2013107134A (ja) * 2011-10-26 2013-06-06 Kobe Steel Ltd フラックス組成物及びブレージングシート
CN111606362A (zh) * 2020-05-27 2020-09-01 惠州亿纬锂能股份有限公司 一种助熔剂辅助制备高镍三元材料的方法、得到的产品和用途

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP4404217A4

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2025004750A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 ハロゲン化物固体電解質の製造方法、ハロゲン化物固体電解質、正極材料、および電池
WO2025004620A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 固体電解質材料の製造方法
WO2025004753A1 (ja) * 2023-06-29 2025-01-02 パナソニックＩｐマネジメント株式会社 ハロゲン化物固体電解質の製造方法、ハロゲン化物固体電解質、正極材料、および電池
WO2025022870A1 (ja) * 2023-07-21 2025-01-30 パナソニックＩｐマネジメント株式会社 電池
WO2025022869A1 (ja) * 2023-07-21 2025-01-30 パナソニックＩｐマネジメント株式会社 電池
WO2025070256A1 (ja) * 2023-09-29 2025-04-03 日本碍子株式会社 固体電解質、固体電解質の製造方法、および、電池

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