WO2021199549A1 - 固体電解質材料およびこれを用いた電池 - Google Patents

固体電解質材料およびこれを用いた電池 Download PDF

Info

Publication number
WO2021199549A1
WO2021199549A1 PCT/JP2020/049233 JP2020049233W WO2021199549A1 WO 2021199549 A1 WO2021199549 A1 WO 2021199549A1 JP 2020049233 W JP2020049233 W JP 2020049233W WO 2021199549 A1 WO2021199549 A1 WO 2021199549A1
Authority
WO
WIPO (PCT)
Prior art keywords
solid electrolyte
electrolyte material
material according
less
battery
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2020/049233
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
和史 宮武
勇祐 西尾
敬 久保
哲也 浅野
章裕 酒井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Intellectual Property Management Co Ltd
Original Assignee
Panasonic Intellectual Property Management Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Panasonic Intellectual Property Management Co Ltd filed Critical Panasonic Intellectual Property Management Co Ltd
Priority to CN202080098573.6A priority Critical patent/CN115315755B/zh
Priority to EP20928245.8A priority patent/EP4131286A4/en
Priority to JP2022511543A priority patent/JP7555031B2/ja
Publication of WO2021199549A1 publication Critical patent/WO2021199549A1/ja
Priority to US17/931,561 priority patent/US20230008629A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00—Compounds of rare earth metals
    • C01F17/30—Compounds containing rare earth metals and at least one element other than a rare earth metal, oxygen or hydrogen, e.g. La4S3Br6
    • 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
    • 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
    • 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
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • 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
    • 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 a solid electrolyte material and a battery using the same.
  • Patent Document 1 discloses an all-solid-state battery using a sulfide solid electrolyte.
  • Patent Document 2 discloses a solid electrolyte material represented by Li 6-3z Y z X 6 (where 0 ⁇ z ⁇ 2 is satisfied and X is Cl or Br).
  • An object of the present disclosure is to provide a solid electrolyte material having high lithium ion conductivity.
  • the solid electrolyte materials of the present disclosure include Li, Ca, Y, Sm, X, O, and H, wherein X is at least one selected from the group consisting of F, Cl, Br, and I. Yes, the molar ratio of O to the sum of Y and Sm is greater than 0 and less than 0.32.
  • the present disclosure provides a solid electrolyte material having high lithium ion conductivity.
  • FIG. 1 shows a cross-sectional view of the battery 1000 according to the second embodiment.
  • FIG. 2 is a graph showing the X-ray diffraction pattern of the solid electrolyte material according to Examples 1 to 3 and Comparative Example 1.
  • FIG. 3 shows a schematic view of a pressure forming die 300 used for evaluating the ionic conductivity of a solid electrolyte material.
  • FIG. 4 is a graph showing a Core-Cole plot obtained by measuring the impedance of the solid electrolyte material according to Example 1.
  • FIG. 5 is a graph showing infrared absorption spectra of the solid electrolyte material according to Examples 1 to 3, Comparative Example 1, and Reference Example 1.
  • FIG. 6 is a graph showing the initial discharge characteristics of the batteries according to Example 1 and Comparative Example 1.
  • the solid electrolyte material according to the first embodiment includes Li, Ca, Y, Sm, X, O, and H.
  • X is at least one selected from the group consisting of F, Cl, Br, and I.
  • the molar ratio of O to the sum of Y and Sm is greater than 0 and less than 0.32.
  • the solid electrolyte material according to the first embodiment has high lithium ion conductivity.
  • the high lithium ion conductivity is, for example, 1 ⁇ 10 -5 S / cm or more. That is, the solid electrolyte material according to the first embodiment can have, for example, an ionic conductivity of 1 ⁇ 10 -5 S / cm or more.
  • the solid electrolyte material according to the first embodiment can be used to obtain an all-solid-state battery having excellent charge / discharge characteristics.
  • the all-solid-state battery may be a primary battery or a secondary battery.
  • the solid electrolyte material according to the first embodiment does not contain sulfur.
  • the sulfur-free solid electrolyte material is excellent in safety because hydrogen sulfide is not generated even when exposed to the atmosphere.
  • the sulfide solid electrolyte disclosed in Patent Document 1 can generate hydrogen sulfide when exposed to the atmosphere.
  • the solid electrolyte material according to the first embodiment may substantially consist of Li, Ca, Y, Sm, X, O and H.
  • the solid electrolyte material according to the first embodiment is substantially composed of Li, Ca, Y, Sm, X, O and H
  • the solid electrolyte material according to the first embodiment constitutes the solid electrolyte material. It means that the molar ratio (that is, mole fraction) of the total amount of substances of Li, Ca, Y, Sm, X, O and H to the total amount of substances of all elements is 90% or more. As an example, the molar ratio may be 95% or more.
  • the solid electrolyte material according to the first embodiment may consist only of Li, Ca, Y, Sm, X, O and H.
  • X may be Cl and Br in order to increase the ionic conductivity of the solid electrolyte material.
  • the solid electrolyte material according to the first embodiment is composed of the group consisting of Gd, Sr, Ba, Al, Sc, Ga, Bi, La, Zr, Hf, Ta, and Nb. It may further include at least one selected.
  • the transition metal contained in the solid electrolyte material according to the present embodiment may be only Y and Sm, excluding the element contained as an unavoidable impurity.
  • O bonded to H may be present in the surface region of the solid electrolyte material according to the first embodiment.
  • the surface region of the solid electrolyte material according to the first embodiment means a region from the surface of the solid electrolyte material to a depth of about 1 ⁇ m in the internal direction.
  • the X-ray diffraction pattern of the solid electrolyte material according to the first embodiment can be obtained by using Cu—K ⁇ rays.
  • the obtained X-ray diffraction pattern 14.9 ° or more and 16.0 ° or less, 16.3 ° or more and 17.3 ° or less, 22.3 ° or more and 23.4 ° or less, 28.1 ° or more and 29.2 ° ° or less, 30.0 ° or more and 31.1 ° or less, 32.2 ° or more and 33.3 ° or less, 39.2 ° or more and 40.3 ° or less, 46.9 ° or more and 48.1 ° or less, and 51.
  • the peak may exist in the range of the diffraction angle 2 ⁇ of 5 ° or more and 52.6 ° or less.
  • Such a solid electrolyte material has high ionic conductivity.
  • x represents the molar ratio of Li to the sum of Y and Sm.
  • y represents the molar ratio of Ca to the sum of Y and Sm.
  • z represents the molar ratio of Br to the sum of Y and Sm.
  • w represents the molar ratio of Cl to the sum of Y and Sm.
  • the molar ratio of O to the total of Y and Sm may be greater than 0 and less than or equal to 0.23.
  • the molar ratio of O to the total of Y and Sm may be greater than 0 and less than or equal to 0.05.
  • the molar ratio of O to the sum of Y and Sm may be greater than 0 and less than or equal to 0.01.
  • the shape of the solid electrolyte material according to the first embodiment is not limited. Examples of such shapes are needle-shaped, spherical, or elliptical spherical.
  • the solid electrolyte material according to the first embodiment may be particles.
  • the solid electrolyte material according to the first embodiment may be formed to have the shape of a pellet or a plate.
  • the solid electrolyte material according to the first embodiment may have a median diameter of 0.1 ⁇ m or more and 100 ⁇ m or less.
  • the median diameter means a particle size at which the cumulative deposition in the volume-based particle size distribution is 50%.
  • the volume-based particle size distribution is measured, for example, by a laser diffraction measuring device or an image analyzer.
  • the median diameter is 0.5 ⁇ m or more and 10 ⁇ m or less in order to increase the ionic conductivity of the solid electrolyte material according to the first embodiment and to disperse the solid electrolyte material and the active material according to the first embodiment satisfactorily. good.
  • the solid electrolyte material according to the first embodiment can be produced by the following method.
  • the raw material powder is prepared and mixed so as to have the desired composition.
  • LiCl raw material powder, LiBr raw material powder, YCl 3 raw material powder, SmCl 3 raw material powder, and CaBr 2 are mixed.
  • the obtained mixed powder is fired in an inert gas atmosphere in which the oxygen concentration and the water concentration are adjusted (for example, an argon atmosphere having a dew point of ⁇ 60 ° C. or lower).
  • the firing temperature may be, for example, 200 ° C. or higher and 650 ° C. or lower.
  • the obtained fired product is allowed to stand in an atmosphere having a relatively high dew point (for example, a dry atmosphere having a dew point of ⁇ 30 ° C.).
  • the raw material flour may be mixed in a pre-adjusted molar ratio so as to offset the compositional changes that may occur in the synthetic process.
  • the amount of oxygen in the solid electrolyte material is determined by the selection of the raw material powder, the oxygen concentration in the atmosphere, the water concentration in the atmosphere, and the reaction time. In this way, the solid electrolyte material according to the first embodiment is obtained.
  • the raw material powder to be mixed may be an oxide and a halide.
  • Y 2 O 3 , Sm 2 O 3 , NH 4 Cl, NH 4 Br, LiCl, LiBr, CaCl 2 , and CaBr 2 may be used as the raw material powder.
  • the oxygen constituting the solid electrolyte material according to the first embodiment is taken in from the above-mentioned atmosphere having a relatively high dew point.
  • the battery according to the second embodiment includes a positive electrode, a negative electrode, and an electrolyte layer.
  • the electrolyte layer is arranged between the positive electrode and the negative electrode.
  • At least one selected from the group consisting of a positive electrode, an electrolyte layer, and a negative electrode contains 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 the battery 1000 according to the second embodiment.
  • the battery 1000 includes a positive electrode 201, an electrolyte layer 202, and a negative electrode 203.
  • the electrolyte layer 202 is arranged between the positive electrode 201 and the negative electrode 203.
  • the positive electrode 201 contains the positive electrode active material particles 204 and the solid electrolyte particles 100.
  • the electrolyte layer 202 contains an electrolyte material (for example, a solid electrolyte material).
  • the negative electrode 203 contains negative electrode active material particles 205 and solid electrolyte particles 100.
  • the solid electrolyte particle 100 is a particle containing the solid electrolyte material according to the first embodiment as a main component.
  • the particles containing the solid electrolyte material according to the first embodiment as the main component mean the particles in which the component contained most in the mass ratio is the solid electrolyte material according to the first embodiment.
  • the solid electrolyte particles 100 may be particles made of the solid electrolyte material according to the first embodiment.
  • the positive electrode 201 contains a material capable of occluding and releasing metal ions (for example, lithium ions).
  • the material is, for example, a positive electrode active material (for example, positive electrode active material particles 204).
  • positive electrode active materials are lithium-containing transition metal oxides, transition metal fluorides, polyanionic materials, fluorinated polyanionic materials, transition metal sulfides, transition metal oxyfluorides, transition metal oxysulfides, or transition metal oxynitrides.
  • lithium-containing transition metal oxide LiNi 1-df Co d Al f O 2 (where, 0 ⁇ d, 0 ⁇ f , and 0 ⁇ (d + f) ⁇ 1) or LiCoO 2.
  • the positive electrode active material particles 204 may have a median diameter of 0.1 ⁇ m or more. The good dispersion improves the charge / discharge characteristics of the battery 1000. In order to rapidly diffuse lithium in the positive electrode active material particles 204, the positive electrode active material particles 204 may have a median diameter of 100 ⁇ m or less. Due to the rapid diffusion of lithium, the battery 1000 can operate at high output. As described above, the positive electrode active material particles 204 may have a median diameter of 0.1 ⁇ m or more and 100 ⁇ m or less.
  • the positive electrode active material particles 204 may have a median diameter larger than that of the solid electrolyte particles 100.
  • the ratio of the volume of the positive electrode active material particles 204 to the total volume of the positive electrode active material particles 204 and the solid electrolyte particles 100 is 0.30 or more and 0.95. The following may be present.
  • 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 may be the solid electrolyte material according to the first embodiment.
  • the electrolyte layer 202 may be a solid electrolyte layer.
  • the electrolyte layer 202 may be composed of only the solid electrolyte material according to the first embodiment. Alternatively, the electrolyte layer 202 may be composed only of a solid electrolyte material different from the solid electrolyte material according to the first embodiment.
  • X' is at least one selected from the group consisting of F, Cl, Br, and I.
  • (A, B, C) means "at least one selected from the group consisting of A, B, and C”.
  • the solid electrolyte material according to the first embodiment is referred to as the first solid electrolyte material.
  • a solid electrolyte material different from the solid electrolyte material according to the first embodiment is called 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.
  • the first solid electrolyte material and the second solid electrolyte material may be uniformly dispersed.
  • the layer made of the first solid electrolyte material and the layer made of the second solid electrolyte material may be laminated along the stacking direction of the battery 1000.
  • the electrolyte layer 202 may have a thickness of 1 ⁇ m or more and 100 ⁇ m or less in order to suppress a short circuit between the positive electrode 201 and the negative electrode 203 and increase the output of the battery.
  • the negative electrode 203 contains a material capable of occluding and releasing metal ions (for example, lithium ions).
  • the material is, for example, a negative electrode active material (for example, negative electrode active material particles 205).
  • Examples of negative electrode active materials are metal materials, carbon materials, oxides, nitrides, tin compounds, or silicon compounds.
  • the metal material may be a simple substance metal or an alloy.
  • Examples of metallic materials are lithium metals or lithium alloys.
  • Examples of carbon materials are natural graphite, coke, developing carbon, carbon fibers, spheroidal carbon, artificial graphite, or amorphous carbon. From the point of view of capacitance density, suitable examples of the negative electrode active material are silicon (ie, Si), tin (ie, Sn), a silicon compound, or a tin compound.
  • the negative electrode active material particles 205 may have a median diameter of 0.1 ⁇ m or more. The good dispersion improves the charge / discharge characteristics of the battery. In order to rapidly diffuse lithium in the negative electrode active material particles 205, the negative electrode active material particles 205 may have a median diameter of 100 ⁇ m or less. Due to the rapid diffusion of lithium, the battery can operate at high power. As described above, the negative electrode active material particles 205 may have a median diameter of 0.1 ⁇ m or more and 100 ⁇ m or less.
  • the negative electrode active material particles 205 may have a median diameter larger than that of the solid electrolyte particles 100.
  • the ratio of the volume of the negative electrode active material particles 205 to the total volume of the negative electrode active material particles 205 and the solid electrolyte particles 100 is 0.30 or more and 0.95. It may be as follows.
  • 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 a positive electrode 201, an electrolyte layer 202, and a negative electrode 203 contains a second solid electrolyte material to enhance ionic conductivity, chemical stability, and electrochemical stability. May be.
  • the second solid electrolyte material may be a halide solid electrolyte.
  • halide solid electrolyte Li 2 MgX '4, Li 2 FeX' 4, Li (Al, Ga, In) X '4, Li 3 (Al, Ga, In) X' 6, or LiI.
  • X' is at least one selected from the group consisting of F, Cl, Br, and I.
  • the second solid electrolyte material may be a sulfide solid electrolyte.
  • Examples of sulfide solid electrolytes are Li 2 SP 2 S 5 , Li 2 S-SiS 2 , Li 2 SB 2 S 3 , Li 2 S-GeS 2 , Li 3.25 Ge 0.25 P 0.75 S 4 , or It is Li 10 GeP 2 S 12 .
  • the second solid electrolyte material may be an oxide solid electrolyte.
  • a solid oxide electrolyte is (I) NASICON type solid electrolytes such as LiTi 2 (PO 4 ) 3 or elemental substituents thereof, (Ii) Perovskite-type solid electrolytes such as (LaLi) TiO 3, (Iii) Lithium-type solid electrolytes such as Li 14 ZnGe 4 O 16 , Li 4 SiO 4 , LiGeO 4, or elemental substituents thereof, (Iv) A garnet-type solid electrolyte, such as Li 7 La 3 Zr 2 O 12 or an elemental substituent thereof. Or (v) Li 3 PO 4 or its N-substituted product.
  • NASICON type solid electrolytes such as LiTi 2 (PO 4 ) 3 or elemental substituents thereof
  • Perovskite-type solid electrolytes such as (LaLi) TiO 3
  • Lithium-type solid electrolytes such as Li 14 ZnGe 4 O 16 , Li 4 SiO 4 , LiGeO
  • the second solid electrolyte material may be an organic polymer solid electrolyte.
  • organic polymer solid electrolytes examples include polymer compounds and lithium salt compounds.
  • the polymer compound may have an ethylene oxide structure. Since the polymer compound having an ethylene oxide structure can contain a large amount of lithium salts, the ionic conductivity can be further increased.
  • lithium salt LiPF 6, LiBF 4, LiSbF 6, LiAsF 6, LiSO 3 CF 3, LiN (SO 2 CF 3) 2, LiN (SO 2 C 2 F 5) 2, LiN (SO 2 CF 3) (SO 2 C 4 F 9 ) or LiC (SO 2 CF 3 ) 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 a non-aqueous electrolyte solution, a gel electrolyte, or a gel electrolyte for the purpose of facilitating the transfer of lithium ions and improving the output characteristics of the battery 1000. It may contain an ionic liquid.
  • the non-aqueous electrolyte solution 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.
  • chain 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 chain ester solvent is methyl acetate.
  • fluorine solvents 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 mixture of two or more non-aqueous solvents selected from these may be used.
  • lithium salt LiPF 6, LiBF 4, LiSbF 6, LiAsF 6, LiSO 3 CF 3, LiN (SO 2 CF 3) 2, LiN (SO 2 C 2 F 5) 2, LiN (SO 2 CF 3) (SO 2 C 4 F 9 ) or LiC (SO 2 CF 3 ) 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 concentration of the lithium salt is, for example, in the range of 0.5 mol / liter or more and 2 mol / liter or less.
  • a polymer material impregnated with a non-aqueous electrolyte solution can be used.
  • polymer materials are polyethylene oxide, polyacrylonitrile, polyvinylidene fluoride, polymethylmethacrylate, or polymers with ethylene oxide bonds.
  • cations contained in ionic liquids are (I) Aliphatic chain quaternary salts such as tetraalkylammonium or tetraalkylphosphonium, (Ii) Aliphatic cyclic ammonium such as pyrrolidiniums, morpholiniums, imidazoliniums, tetrahydropyrimidiniums, piperaziniums, or piperidiniums, or (iii) nitrogen-containing heteros such as pyridiniums or imidazoliums. It is a ring aromatic cation.
  • anion contained in the ionic liquid 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 - a.
  • 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 for the purpose of improving the adhesion between the particles.
  • binders are polyvinylidene fluoride, polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylic nitrile, 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, polyvinylidene 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 ether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid.
  • a copolymer of two or more materials selected from the group consisting of hexadiene A mixture of two or more selected from these may be used as a binder.
  • At least one selected from the positive electrode 201 and the negative electrode 203 may contain a conductive auxiliary agent in order to enhance electron conductivity.
  • a conductive aid is (I) Graphites such as natural graphite or artificial graphite, (Ii) Carbon blacks such as acetylene black or ketjen black, (Iii) Conductive fibers such as carbon fibers or metal fibers, (Iv) Carbon fluoride, (V) Metal powders such as aluminum, (Vi) Conductive whiskers, such as zinc oxide or potassium titanate, It is a conductive metal oxide such as (vii) titanium oxide, or a conductive polymer compound such as (vii) polyaniline, polypyrrole, or polythiophene. In order to reduce the cost, the conductive auxiliary agent (i) or (ii) described above may be used.
  • Examples of the shape of the battery according to the second embodiment are coin type, cylindrical type, square type, sheet type, button type, flat type, or laminated type.
  • 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 be manufactured by producing the laminated body.
  • Example 1 [Preparation of solid electrolyte material] LiCl, LiBr, YCl 3 , SmCl 3 , and CaBr as raw material powders in an argon atmosphere having a dew point of -60 ° C. or lower and an oxygen concentration of 0.0001% by volume or less (hereinafter referred to as “dry argon atmosphere”).
  • These ingredients were ground and mixed in a mortar. The resulting mixture was calcined in an alumina crucible at 500 ° C.
  • composition analysis of solid electrolyte material The contents of Li, Ca, Sm, and Y per unit weight of the solid electrolyte material according to Example 1 were determined by high frequency inductively coupled plasma emission spectroscopy (iCAP7400, manufactured by Thermo Fisher Scientific). It was measured by spectroscopic analysis. The Br and Cl contents of the solid electrolyte material according to Example 1 were measured by an ion chromatography method using an ion chromatograph device (manufactured by Dionex, ICS-2000). The Li: Ca: Y: Sm: Br: Cl molar ratio was calculated based on the contents of Li, Ca, Y, Sm, Br, and Cl obtained from these measurement results. As a result, the solid electrolyte material according to Example 1 had a Li: Ca: Y: Sm: Br: Cl molar ratio of 3.07: 0.10: 0.80: 0.20: 1.85: 3.87. Had had.
  • the mass of O with respect to the total mass of the solid electrolyte material according to Example 1 was measured by a non-dispersive infrared absorption method using an oxygen / nitrogen / hydrogen analyzer (manufactured by HORIBA, Ltd., EMGA-930). As a result, the mass ratio of O was 0.05%. Based on this, the (Y + Sm): O molar ratio was calculated. As a result, the solid electrolyte material according to Example 1 had a (Y + Sm): O molar ratio of 1.00: 0.01.
  • the solid electrolyte material according to Example 1 was analyzed by a total internal reflection measurement method using an infrared spectroscope (manufactured by BRUKER, ALPHA). The prism was made of diamond. The results indicate the presence of a binding oxygen and protons (H +), the peak from 3100 cm -1 to the area of 3640cm -1 was detected.
  • the surface region in the present disclosure means a region measured in this way.
  • the surface region of the solid electrolyte material according to the first embodiment was about 1 ⁇ m inward from the surface of the solid electrolyte material.
  • FIG. 5 is a graph showing an infrared absorption spectrum of the solid electrolyte material according to Example 1.
  • the X-ray diffraction pattern of the solid electrolyte material according to Example 1 was measured using an X-ray diffractometer (manufactured by RIGAKU, MiniFlex 600) in a dry environment having a dew point of ⁇ 45 ° C. or lower.
  • Cu-K ⁇ rays (wavelengths 1.5405 ⁇ and 1.5444 ⁇ ) were used as the X-ray source.
  • FIG. 2 is a graph showing an X-ray diffraction pattern of the solid electrolyte material according to Example 1.
  • FIG. 3 shows a schematic view of the pressure forming die 300 used to evaluate the ionic conductivity of the solid electrolyte material.
  • the pressure forming die 300 included a punch upper portion 301, a frame mold 302, and a punch lower portion 303.
  • the frame 302 was made of insulating polycarbonate.
  • Both the upper punch 301 and the lower punch 303 were made of electron-conducting stainless steel.
  • the ionic conductivity of the solid electrolyte material according to Example 1 was measured by the following method.
  • the powder of the solid electrolyte material according to Example 1 was filled inside the pressure forming die 300. Inside the pressure forming die 300, a pressure of 400 MPa was applied to the solid electrolyte material according to Example 1 (that is, the powder 101 of the solid electrolyte material in FIG. 3) using the punch upper part 301 and the punch lower part 303.
  • the upper punch 301 and the lower punch 303 were connected to a potentiostat (Princeton Applied Research, VersaSTAT4).
  • the upper part 301 of the punch was connected to the working electrode and the terminal for measuring the potential.
  • the lower part of the punch 303 was connected to the counter electrode and the reference electrode.
  • the impedance of the solid electrolyte material according to Example 1 was measured at room temperature by an electrochemical impedance measurement method.
  • FIG. 4 is a graph showing a Core-Cole plot obtained by measuring the impedance 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 is the smallest was regarded as the resistance value to the ion conduction of the solid electrolyte material according to Example 1. See the arrow R SE shown in FIG. 4 for the real value.
  • ⁇ is the ionic conductivity.
  • S is the contact area of the solid electrolyte material with the punch upper portion 301 (in FIG. 3, it is equal to the cross-sectional area of the hollow portion of the frame mold 302).
  • R SE is the resistance value of the solid electrolyte material in impedance measurement.
  • t is the thickness of the solid electrolyte material to which the pressure is applied (in FIG. 3, equal to the thickness of the layer formed from the powder 101 of the solid electrolyte material).
  • the ionic conductivity of the solid electrolyte material according to Example 1 measured at 25 ° C. was 7.9 ⁇ 10 -4 S / cm.
  • the solid electrolyte material (100 mg) according to Example 1, the above-mentioned mixture (12.0 mg), and aluminum powder (14.7 mg) were laminated in this order in an insulating cylinder having an inner diameter of 9.5 mm. A pressure of 300 MPa was applied to this laminate to form the first electrode and the solid electrolyte layer.
  • the solid electrolyte layer had a thickness of about 500 ⁇ m.
  • a metal In foil was laminated on the solid electrolyte layer.
  • the solid electrolyte layer was sandwiched between the metal In foil and the first electrode.
  • the metal In foil had a thickness of 200 ⁇ m.
  • a pressure of 80 MPa was applied to the metal In foil to form a second electrode.
  • a current collector made of stainless steel was attached to the first and second electrodes, and then a current collector lead was attached to the current collector. Finally, using an insulating ferrule, the inside of the insulating cylinder was shielded from the outside air atmosphere and the inside of the cylinder was sealed. In this way, the battery according to Example 1 was obtained.
  • FIG. 6 is a graph showing the initial discharge characteristics of the battery according to the first embodiment. The charge / discharge test was performed as follows.
  • the battery according to Example 1 was placed in a constant temperature bath at 25 ° C.
  • the batteries according to Example 1 were charged until a voltage of 3.7 V was reached at a current density of 91 ⁇ A / cm 2.
  • the current density corresponds to a 0.05 C rate.
  • the batteries according to Example 1 were discharged at a current density of 91 ⁇ A / cm 2 until a voltage of 1.9 V was reached.
  • the battery according to Example 1 had an initial discharge capacity of 463 ⁇ Ah.
  • Example 2 (Examples 2 and 3)
  • the calcined product was allowed to stand in a dry atmosphere having a dew point of ⁇ 30 ° C. and an oxygen concentration of 20.9% by volume or less for about 30 minutes instead of about 5 minutes. Except for this, the solid electrolyte material according to Example 2 was obtained in the same manner as in Example 1.
  • Example 3 the time during which the fired product was allowed to stand in a dry atmosphere having a dew point of ⁇ 30 ° C. and an oxygen concentration of 20.9% by volume or less was set to about 2 hours instead of about 5 minutes. Except for this, the solid electrolyte material according to Example 3 was obtained in the same manner as in Example 1.
  • Example 2 In the same manner as in Example 1, the element ratio (molar ratio), infrared absorption spectrum, X-ray diffraction, and ionic conductivity of the solid electrolyte material according to Examples 2 and 3 were measured. The measurement results are shown in Tables 1 and 2.
  • FIG. 2 is a graph showing the X-ray diffraction pattern of the solid electrolyte material according to Examples 2 and 3.
  • FIG. 5 is a graph showing an infrared absorption spectrum of the solid electrolyte material according to Examples 2 and 3.
  • the mass ratios of O to the total solid electrolyte material according to Examples 2 and 3 were 0.19% and 0.82%, respectively.
  • Example 2 Using the solid electrolyte material according to Examples 2 and 3, the batteries according to Examples 2 and 3 were obtained in the same manner as in Example 1.
  • a charge / discharge test was carried out in the same manner as in Example 1 using the batteries according to Examples 2 and 3.
  • the batteries according to Examples 2 and 3 were well charged and discharged, as were the batteries according to Example 1.
  • Comparative Example 1 In Comparative Example 1, the time during which the fired product was allowed to stand in an atmosphere having a dew point of ⁇ 30 ° C. and an oxygen concentration of 20.9% by volume or less was set to about 10 hours instead of about 5 minutes. Except for this, the solid electrolyte material according to Comparative Example 1 was obtained in the same manner as in Example 1.
  • Example 2 the element ratio (molar ratio), infrared absorption spectrum, X-ray diffraction, and ionic conductivity of the solid electrolyte material according to Comparative Example 1 were measured. The measurement results are shown in Tables 1 and 2.
  • FIG. 2 is a graph showing an X-ray diffraction pattern of the solid electrolyte material according to Comparative Example 1.
  • FIG. 5 is a graph showing an infrared absorption spectrum of the solid electrolyte material according to Comparative Example 1.
  • the mass ratio of O to the whole solid electrolyte material according to Comparative Example 1 was 1.15%.
  • Example 1 Using the solid electrolyte material according to Comparative Example 1, the battery according to Comparative Example 1 was obtained in the same manner as in Example 1.
  • FIG. 6 is a graph showing the initial discharge characteristics of the battery according to Comparative Example 1.
  • Reference Example 1 In Reference Example 1, the fired product was not allowed to stand in an atmosphere having a dew point of ⁇ 30 ° C. and an oxygen concentration of 20.9% by volume or less. Except for this, the solid electrolyte material according to Comparative Example 1 was obtained in the same manner as in Example 1.
  • FIG. 5 is a graph showing an infrared absorption spectrum of the solid electrolyte material according to Reference Example 1.
  • the solid electrolyte materials according to Examples 1 to 3 have a high ionic conductivity of 1 ⁇ 10 -5 S / cm or more in the vicinity of room temperature.
  • the solid electrolyte material is 1 ⁇ 10 -5 S / cm or more. Has high ionic conductivity.
  • the solid electrolyte material is more than 1 ⁇ 10 -4 S / cm. Has high ionic conductivity.
  • the batteries according to Examples 1 to 3 were charged and discharged at 25 ° C.
  • the solid electrolyte material according to the present disclosure is suitable for providing a battery having high lithium ion conductivity and being able to be charged and discharged well.
  • the solid electrolyte material of the present disclosure is used, for example, in an all-solid-state lithium ion secondary battery.
  • Solid electrolyte particles 101 Solid electrolyte material powder 201 Positive electrode 202 Electrode layer 203 Negative electrode 204 Positive electrode active material particles 205 Negative electrode active material particles 300 Pressurized die 301 Punch upper 302 Frame type 303 Punch lower 1000 Battery

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Conductive Materials (AREA)
  • Secondary Cells (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
  • Battery Electrode And Active Subsutance (AREA)
PCT/JP2020/049233 2020-03-31 2020-12-28 固体電解質材料およびこれを用いた電池 Ceased WO2021199549A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CN202080098573.6A CN115315755B (zh) 2020-03-31 2020-12-28 固体电解质材料及使用该固体电解质材料的电池
EP20928245.8A EP4131286A4 (en) 2020-03-31 2020-12-28 SOLID ELECTROLYTE MATERIAL AND BATTERY USING SAME
JP2022511543A JP7555031B2 (ja) 2020-03-31 2020-12-28 固体電解質材料およびこれを用いた電池
US17/931,561 US20230008629A1 (en) 2020-03-31 2022-09-13 Solid electrolyte material and battery using same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020064826 2020-03-31
JP2020-064826 2020-03-31

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/931,561 Continuation US20230008629A1 (en) 2020-03-31 2022-09-13 Solid electrolyte material and battery using same

Publications (1)

Publication Number Publication Date
WO2021199549A1 true WO2021199549A1 (ja) 2021-10-07

Family

ID=77928459

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2020/049233 Ceased WO2021199549A1 (ja) 2020-03-31 2020-12-28 固体電解質材料およびこれを用いた電池

Country Status (5)

Country Link
US (1) US20230008629A1 (https=)
EP (1) EP4131286A4 (https=)
JP (1) JP7555031B2 (https=)
CN (1) CN115315755B (https=)
WO (1) WO2021199549A1 (https=)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4131506A4 (en) * 2020-03-31 2023-09-27 Panasonic Intellectual Property Management Co., Ltd. Solid electrolyte material and battery using same
EP4131500A4 (en) * 2020-03-31 2023-09-27 Panasonic Intellectual Property Management Co., Ltd. Solid electrolyte material and battery using same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011119158A (ja) * 2009-12-04 2011-06-16 Toyota Motor Corp 固体イオン伝導体、固体電解質膜、全固体リチウム二次電池
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
JP2017091955A (ja) * 2015-11-16 2017-05-25 旭化成株式会社 リチウムイオン伝導体及びこれを用いたリチウムイオン電池
WO2018025582A1 (ja) 2016-08-04 2018-02-08 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、電池
WO2019135343A1 (ja) * 2018-01-05 2019-07-11 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、電池
JP2019530963A (ja) * 2016-10-07 2019-10-24 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 固体電池用安定化コーティング

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8795902B2 (en) * 2010-04-13 2014-08-05 Toyota Jidosha Kabushiki Kaisha Solid electrolyte material, lithium battery, and method of producing solid electrolyte material
WO2017047015A1 (ja) * 2015-09-16 2017-03-23 パナソニックＩｐマネジメント株式会社 電池
JP2017224474A (ja) * 2016-06-15 2017-12-21 出光興産株式会社 正極合材
JP7228773B2 (ja) * 2018-01-17 2023-02-27 パナソニックＩｐマネジメント株式会社 正極活物質、および、電池

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011119158A (ja) * 2009-12-04 2011-06-16 Toyota Motor Corp 固体イオン伝導体、固体電解質膜、全固体リチウム二次電池
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
JP2017091955A (ja) * 2015-11-16 2017-05-25 旭化成株式会社 リチウムイオン伝導体及びこれを用いたリチウムイオン電池
WO2018025582A1 (ja) 2016-08-04 2018-02-08 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、電池
JP2019530963A (ja) * 2016-10-07 2019-10-24 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 固体電池用安定化コーティング
WO2019135343A1 (ja) * 2018-01-05 2019-07-11 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、電池

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP4131286A4

Also Published As

Publication number Publication date
EP4131286A1 (en) 2023-02-08
EP4131286A4 (en) 2023-10-04
CN115315755B (zh) 2024-09-13
JPWO2021199549A1 (https=) 2021-10-07
US20230008629A1 (en) 2023-01-12
JP7555031B2 (ja) 2024-09-24
CN115315755A (zh) 2022-11-08

Similar Documents

Publication Publication Date Title
JP7418014B2 (ja) 固体電解質材料およびそれを用いた電池
JP7535700B2 (ja) 固体電解質材料およびそれを用いた電池
JPWO2020070958A1 (ja) ハロゲン化物固体電解質材料およびこれを用いた電池
WO2021070595A1 (ja) 固体電解質材料およびそれを用いた電池
WO2021186809A1 (ja) 固体電解質材料およびそれを用いた電池
JP7478989B2 (ja) 固体電解質材料およびこれを用いた電池
WO2021161604A1 (ja) 固体電解質材料およびそれを用いた電池
WO2020188914A1 (ja) 固体電解質材料およびこれを用いた電池
WO2021186833A1 (ja) 固体電解質材料およびそれを用いた電池
WO2021250985A1 (ja) 固体電解質材料およびそれを用いた電池
WO2022018946A1 (ja) 固体電解質材料およびそれを用いた電池
WO2021199676A1 (ja) 固体電解質材料およびそれを用いた電池
JP7478988B2 (ja) 固体電解質材料およびこれを用いた電池
WO2021186845A1 (ja) 固体電解質材料およびそれを用いた電池
US20230023022A1 (en) Solid electrolyte material and battery using same
WO2020188915A1 (ja) 固体電解質材料およびこれを用いた電池
JP7555031B2 (ja) 固体電解質材料およびこれを用いた電池
JP7584107B2 (ja) 固体電解質材料およびこれを用いた電池
JP7724436B2 (ja) 固体電解質材料およびこれを用いた電池
CN115280425B (zh) 固体电解质材料及使用该固体电解质材料的电池
WO2022018990A1 (ja) 固体電解質材料およびそれを用いた電池
WO2021152979A1 (ja) 固体電解質材料およびこれを用いた電池
JP7724435B2 (ja) 固体電解質材料およびこれを用いた電池
EP4303949A1 (en) Solid electrolyte material and battery using same
EP4303950A1 (en) Solid electrolyte material and battery using same

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20928245

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2022511543

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2020928245

Country of ref document: EP

Effective date: 20221031