WO2021033424A1 - 蓄電デバイス用電極および蓄電デバイス - Google Patents

蓄電デバイス用電極および蓄電デバイス Download PDF

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WO2021033424A1
WO2021033424A1 PCT/JP2020/024711 JP2020024711W WO2021033424A1 WO 2021033424 A1 WO2021033424 A1 WO 2021033424A1 JP 2020024711 W JP2020024711 W JP 2020024711W WO 2021033424 A1 WO2021033424 A1 WO 2021033424A1
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Prior art keywords
lithium ion
electrode
solid electrolyte
ion conductive
oxide
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PCT/JP2020/024711
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English (en)
French (fr)
Japanese (ja)
Inventor
眞人 打田
大介 獅子原
英昭 彦坂
山本　洋
彩子 近藤
卓 宮本
水谷　秀俊
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Niterra Co Ltd
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NGK Spark Plug Co Ltd
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Priority to JP2021540649A priority Critical patent/JP7593928B2/ja
Priority to US17/636,704 priority patent/US12300780B2/en
Priority to KR1020227005744A priority patent/KR102900090B1/ko
Priority to CN202080059071.2A priority patent/CN114270559B/zh
Priority to EP20855406.3A priority patent/EP4020618A4/en
Publication of WO2021033424A1 publication Critical patent/WO2021033424A1/ja
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—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
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/54—Electrolytes
    • H01G11/56—Solid electrolytes, e.g. gels; Additives therein
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/30—Electrodes characterised by their material
    • H01G11/32—Carbon-based
    • H01G11/38—Carbon pastes or blends; Binders or additives therein
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/30—Electrodes characterised by their material
    • H01G11/46—Metal oxides
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/30—Electrodes characterised by their material
    • H01G11/50—Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
    • 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
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
    • 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
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/04—Hybrid capacitors
    • H01G11/06—Hybrid capacitors with one of the electrodes allowing ions to be reversibly doped thereinto, e.g. lithium ion capacitors [LIC]
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/021—Physical characteristics, e.g. porosity, surface area
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0068—Solid electrolytes inorganic
    • H01M2300/0071—Oxides
    • 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
    • H01M2300/0071—Oxides
    • H01M2300/0074—Ion conductive at high temperature
    • H01M2300/0077—Ion conductive at high temperature based on zirconium oxide
    • 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 technology disclosed herein relates to electrodes for power storage devices.
  • all-solid-state battery an all-solid-state lithium-ion secondary battery (hereinafter referred to as an "all-solid-state battery") in which all battery elements are solid is expected.
  • the all-solid-state battery is safer than the conventional lithium-ion secondary battery that uses an organic electrolytic solution in which a lithium salt is dissolved in an organic solvent, because there is no risk of leakage or ignition of the organic electrolytic solution. Since the exterior can be simplified, the energy density per unit mass or unit volume can be improved.
  • an oxide-based lithium ion conductive solid electrolyte or a sulfide-based lithium ion conductive solid electrolyte is used as the solid electrolyte layer of the all-solid-state battery. Since the oxide-based lithium ion conductive solid electrolyte is relatively hard in the powder state, it is in the state of a molded body (compact powder) obtained by pressure-molding the powder or in the state of a molded body formed into a sheet using a binder. Has low adhesion between particles and low lithium ion conductivity.
  • Lithium ion conductivity can be increased by sintering or vapor deposition using oxide-based lithium ion conductive solid electrolyte powder, but it becomes difficult to increase the size of the battery due to warpage or deformation due to heat treatment. ..
  • the sulfide-based lithium ion conductive solid electrolyte is relatively soft in the powder state, the particles adhere to each other in the state of the molded body obtained by pressure-molding the powder or the molded body formed into a sheet using a binder. High property and high lithium ion conductivity.
  • the sulfide-based lithium ion conductive solid electrolyte may be unfavorable in terms of safety because it reacts with moisture in the atmosphere to generate hydrogen sulfide gas.
  • an all-solid-state battery for example, in order to improve the lithium ion conductivity of an electrode (positive electrode and / or negative electrode, the same applies hereinafter), it is conceivable to add a lithium ion conductive solid electrolyte to the electrode in addition to the active material. ..
  • a lithium ion conductive solid electrolyte to be added to the electrode, it was molded into a sheet shape using a pressure-molded molded body or a binder, as in the case of the solid electrolyte layer described above. In the state of the molded body, the adhesion between the particles is low, and the lithium ion conductivity is low.
  • a sulfide-based lithium ion conductive solid electrolyte is used as the solid electrolyte added to the electrode, it may not be preferable in terms of safety. Further, when a mixture of the oxide-based lithium ion conductive solid electrolyte and the sulfide-based lithium ion conductive solid electrolyte as described above is used as the solid electrolyte to be added to the electrode, the sulfide-based lithium ion conductive solid electrolyte can be used. Although the content ratio is reduced, there is room for improvement in terms of safety because it also contains a sulfide-based lithium ion conductive solid electrolyte.
  • This specification discloses a technique capable of solving the above-mentioned problems.
  • the electrode for a power storage device disclosed in the present specification contains an oxide-based lithium ion conductive solid electrolyte, an active material, and an ionic liquid.
  • the electrode for this power storage device is toxic because it contains an oxide-based lithium ion conductive solid electrolyte that does not generate toxic gas, not a sulfide-based lithium ion conductive solid electrolyte that may generate toxic gas. It is possible to avoid the generation of gas. Further, since the oxide-based lithium ionic conductive solid electrolyte is a material that is not easily plastically deformed, the contact between particles becomes insufficient unless it is fired, and high lithium ionic conductivity cannot be exhibited.
  • the electrode contains an ionic liquid that is non-volatile, flame-retardant, and functions as a fluid lithium-ion conductive component, lithium in the electrode and at the interface between the electrode and other members due to the presence of the ionic liquid. Ion conductivity can be improved. Therefore, if the power storage device is configured by using this electrode, the performance of the power storage device can be improved.
  • the volume content of the active material is 40 vol% or more and 85 vol% or less, and the volume content of the oxide-based lithium ion conductive solid electrolyte is 5 vol% or more and 40 vol. % Or less, and the volume content of the ionic liquid may be 3 vol% or more and 35 vol% or less.
  • the oxide-based lithium ion conductive solid electrolyte may have a garnet-type crystal structure containing at least Li, La, Zr, and O. Since such an oxide-based lithium ion conductive solid electrolyte has a wider potential window than other oxide-based lithium ion conductive solid electrolytes, if this configuration is adopted, the material selection range of the active material of the electrode can be selected. Can be widened, and an electrode containing the optimum active material can be constructed.
  • the power storage device disclosed in the present specification includes a solid electrolyte layer, a positive electrode, a negative electrode, and a current collector, and at least one of the positive electrode and the negative electrode is the electrode for the power storage device. It may have a certain configuration. According to this power storage device, the performance of the power storage device can be improved by improving the lithium ion conductivity in the electrode and at the interface between the electrode and other members.
  • the technology disclosed in the present specification can be realized in various forms, for example, in the form of an electrode for a power storage device, a power storage device including an electrode for a power storage device, a method for manufacturing the same, and the like. It is possible.
  • Explanatory drawing schematically showing the cross-sectional structure of the all-solid-state lithium ion secondary battery 102 in this embodiment.
  • Explanatory drawing schematically showing the structure of a part of a positive electrode 114 Explanatory drawing schematically showing the structure of a part of the negative electrode 116
  • Explanatory drawing schematically showing a garnet-type crystal structure Explanatory drawing which shows result of performance evaluation about positive electrode 114
  • Explanatory drawing which shows result of performance evaluation about negative electrode 116 Explanatory drawing which shows result of performance evaluation about negative electrode 116
  • Explanatory drawing schematically showing the configuration of the pressurizing jig 300 and the sample S used for the performance evaluation of the positive electrode 114 Explanatory drawing schematically showing the configuration of the pressurizing jig 300 and the sample S used for the performance evaluation of the negative electrode 116.
  • FIG. 1 is an explanatory diagram schematically showing a cross-sectional configuration of an all-solid-state lithium-ion secondary battery (hereinafter, referred to as “all-solid-state battery”) 102 in the present embodiment.
  • FIG. 1 shows XYZ axes that are orthogonal to each other to specify the direction.
  • the Z-axis positive direction is referred to as an upward direction
  • the Z-axis negative direction is referred to as a downward direction.
  • the all-solid-state battery 102 includes a battery body 110, a positive electrode side current collector 154 arranged on one side (upper side) of the battery body 110, and a negative electrode side current collector arranged on the other side (lower side) of the battery body 110. It has a body 156.
  • the positive electrode side current collector 154 and the negative electrode side current collector 156 are substantially flat plate-shaped members having conductivity, for example, stainless steel, Ni (nickel), Ti (titanium), Fe (iron), Cu (copper). , Al (aluminum), a conductive metal material selected from these alloys, a carbon material, and the like.
  • the positive electrode side current collector 154 and the negative electrode side current collector 156 are also collectively referred to as a current collector.
  • the battery body 110 is a lithium ion secondary battery body in which all battery elements are solid.
  • the fact that the battery elements are all made of solid means that the skeletons of all the battery elements are made of solid, for example, a form in which the skeleton is impregnated with a liquid or the like. It does not exclude it.
  • the battery body 110 includes a positive electrode 114, a negative electrode 116, and a solid electrolyte layer 112 arranged between the positive electrode 114 and the negative electrode 116.
  • the positive electrode 114 and the negative electrode 116 are also collectively referred to as electrodes.
  • the all-solid-state battery 102 or the battery body 110 corresponds to a power storage device within the scope of the claims.
  • the solid electrolyte layer 112 is a member having a substantially flat plate shape, and contains a lithium ion conductive solid electrolyte (for example, an LLZ-based lithium ion conductive solid electrolyte described later).
  • the solid electrolyte layer 112 may further contain an ionic liquid having lithium ion conductivity.
  • the solid electrolyte layer 112 may be a molded product (compact powder) obtained by pressure-molding a powder of a lithium ion conductive solid electrolyte, or may be formed into a sheet by adding a binder to the powder of the lithium ion conductive solid electrolyte. It may be a molded product.
  • the positive electrode 114 is a member having a substantially flat plate shape.
  • FIG. 2 is an explanatory diagram schematically showing the configuration of a part of the positive electrode 114 (X1 part in FIG. 1).
  • the positive electrode 114 contains the positive electrode active material 214.
  • the positive electrode active material 214 is added, for example, to increase the amount of lithium ions that can be inserted / removed from the positive electrode 114 and to improve the energy density.
  • Examples of the positive electrode active material 214 include S (sulfur), TiS 2 , LiCoO 2 (hereinafter referred to as “LCO”), LiMn 2 O 4 , LiFePO 4 , and Li (Co 1/3 Ni 1/3 Mn 1 /).
  • the positive electrode 114 may further contain a conductive auxiliary agent (for example, conductive carbon, Ni (nickel), Pt (platinum), Ag (silver)).
  • a conductive auxiliary agent for example, conductive carbon, Ni (nickel), Pt (platinum), Ag (silver)
  • the positive electrode 114 contains an ionic liquid 224 having lithium ion conductivity.
  • the ionic liquid 224 is added, for example, to reduce the internal resistance of the positive electrode 114.
  • the ionic liquid 224 having lithium ion conductivity is, for example, an ionic liquid in which a lithium salt is dissolved.
  • the ionic liquid is composed of only cations and anions, is a liquid at room temperature, and is a non-volatile, flame-retardant substance. The specific material of the ionic liquid 224 contained in the positive electrode 114 will be described later.
  • the positive electrode 114 contains an oxide-based lithium ion conductive solid electrolyte 204.
  • the oxide-based lithium ion conductive solid electrolyte 204 is used, for example, in order to suppress a decrease in the lithium ion conductivity of the positive electrode 114, and the ionic liquid 224 comes into contact with the positive electrode side current collector 154 provided adjacent to the positive electrode 114. It is added to suppress corrosion of the positive electrode side current collector 154 by reducing the area.
  • the specific material of the oxide-based lithium ion conductive solid electrolyte 204 contained in the positive electrode 114 will be described later.
  • the negative electrode 116 is a member having a substantially flat plate shape.
  • FIG. 3 is an explanatory diagram schematically showing the configuration of a part of the negative electrode 116 (X2 portion in FIG. 1).
  • the negative electrode 116 contains the negative electrode active material 216.
  • the negative electrode active material 216 is added, for example, to increase the amount of lithium ions that can be inserted / removed from the negative electrode 116 and to improve the energy density.
  • Examples of the negative electrode active material 216 include Li metal, Li—Al alloy, Li 4 Ti 5 O 12 (hereinafter referred to as “LTO”), carbon (graphite, natural graphite, artificial graphite, and low crystalline carbon on the surface). (Coated core-shell type graphite), Si (silicon), SiO and the like are used.
  • the negative electrode 116 may further contain a conductive auxiliary agent (for example, conductive carbon, Ni, Pt, Ag).
  • the negative electrode 116 contains an ionic liquid 226 having lithium ion conductivity.
  • the ionic liquid 226 is added, for example, to reduce the internal resistance of the negative electrode 116.
  • the ionic liquid 226 having lithium ion conductivity is, for example, an ionic liquid in which a lithium salt is dissolved. The specific material of the ionic liquid 226 contained in the negative electrode 116 will be described later.
  • the negative electrode 116 contains an oxide-based lithium ion conductive solid electrolyte 206.
  • the oxide-based lithium ion conductive solid electrolyte 206 is used, for example, in order to suppress a decrease in the lithium ion conductivity of the negative electrode 116, and the ionic liquid 226 comes into contact with the negative electrode side current collector 156 provided adjacent to the negative electrode 116. It is added to suppress corrosion of the negative electrode side current collector 156 by reducing the area.
  • the specific material of the oxide-based lithium ion conductive solid electrolyte 204 contained in the negative electrode 116 will be described later.
  • the positive electrode 114 contains the oxide-based lithium ion conductive solid electrolyte 204 in addition to the positive electrode active material 214
  • the negative electrode 116 contains the oxide-based lithium ion conductive in addition to the negative electrode active material 216. It contains the sex solid electrolyte 206.
  • the oxide-based lithium ion conductive solid electrolytes 204 and 206 include solid electrolytes having a garnet-type crystal structure containing at least Li (lithium), La (lantern), Zr (zirconium), and O (oxygen).
  • LLZ Li 7 La 3 Zr 2 O 12
  • Mg manganesium
  • A Ca (calcium), Sr (strontium).
  • Ba barium
  • at least one element selected from the group at least one element substituted (for example, LLZ subjected to element substitution of Mg and Sr (hereinafter). , "LLZ-MgSr"))
  • LLZ-MgSr lithium ion conductive solid electrolytes
  • these lithium ion conductive solid electrolytes are referred to as "LLZ-based lithium ion conductive solid electrolytes (or LLZ-based lithium ion conductive powder)".
  • the "garnet-type crystal structure” is a crystal structure represented by the general formula C 3 A 2 B 3 O 12.
  • FIG. 4 is an explanatory diagram schematically showing a garnet-type crystal structure. As shown in FIG. 4, in the garnet-type crystal structure, C-site Sc is dodecahedron-coordinated with oxygen atom Oa, A-site Sa is octahedrally coordinated with oxygen atom Oa, and B-site Sb is oxygen atom Oa and 4 It is face-to-face.
  • the lithium ion conductive powder (lithium ion conductive solid electrolyte) having a garnet type crystal structure
  • the normal garnet type crystal structure it is a place where the oxygen atom Oa is octahedrally coordinated and becomes a void V.
  • Lithium can be present.
  • the gap V is, for example, a portion sandwiched between the B site Sb1 and the B site Sb2 in FIG.
  • Lithium present in the void V is octahedrally coordinated with oxygen atoms Oa constituting an octahedron including a tetrahedral surface Fb1 forming B site Sb1 and a tetrahedral surface Fb2 forming B site Sb2. doing.
  • a lithium ion conductive powder lithium ion conductive solid electrolyte
  • C-site Sc is occupied by lantern and
  • A-site Sa is occupied by zirconium.
  • B site Sb and void V can be occupied by lithium.
  • the lithium ion conductive solid electrolyte (lithium ion conductive powder) has a garnet-type crystal structure containing at least Li, La, Zr and O. It can be confirmed by.
  • an X-ray diffraction pattern is obtained by analyzing the lithium ion conductive solid electrolyte with an X-ray diffractometer. The obtained X-ray diffraction pattern was compared with the ICDD (International Center for Diffraction Data) card (01-080-4497) (Li 7 La 3 Zr 2 O 12 ) corresponding to LLZ, and the diffraction of the diffraction peak in both was compared.
  • ICDD International Center for Diffraction Data
  • the lithium ion conductive solid electrolyte has a garnet-type crystal structure containing at least Li, La, Zr, and O.
  • Preferred aspects of LLZ-based lithium ion conductive powder" described later corresponds to the X-ray diffraction pattern and LLZ obtained from the lithium ion conductive powder. Since the diffraction angles and diffraction intensity ratios of the diffraction peaks in both of the ICDD cards are substantially the same, it is determined that the product has a garnet-type crystal structure containing at least Li, La, Zr, and O.
  • solid electrolytes other than the LLZ-based lithium ion conductive solid electrolyte may be used.
  • a solid electrolyte having a perovskite-type crystal structure containing at least Li, Ti, La, and O for example, (La, Li) TiO 3
  • a solid electrolyte having an antiperovskite crystal structure containing at least Li, Cl and O for example, Li 2 (OH) Cl.
  • the average particle size of the oxide-based lithium ion conductive solid electrolytes 204 and 206 contained in the electrodes is preferably 0.1 ⁇ m or more and 10 ⁇ m or less.
  • the positive electrode 114 contains the ionic liquid 224 in which the lithium salt is dissolved
  • the negative electrode 116 contains the ionic liquid 226 in which the lithium salt is dissolved.
  • the lithium salt include lithium tetrafluoride (LiBF 4 ), lithium hexafluorophosphate (LiPF 6 ), lithium perchlorate (LiClO 4 ), and lithium trifluoromethanesulfonate (CF 3 SO 3 Li).
  • Li-TFSI Lithium bis (trifluoromethanesulfonyl) imide
  • LiN (SO 2 F) 2 Lithium bis (fluorosulfonyl) imide
  • Li-FSI Lithium bis (pentafluoroethanesulfonyl) imide
  • LiN (SO 2 C 2 F 5 ) 2 Lithium bis (trifluoromethanesulfonyl) imide
  • Ammonium-based products such as butyltrimethylammonium and trimethylpropylammonium, Imidazoles such as 1-ethyl-3 methylimidazolium and 1-butyl-3-methylimidazolium, Piperidinium-based products such as 1-butyl-1-methylpiperidinium and 1-methyl-1-propylpiperidinium, Pyridinium-based products such as 1-butyl-4-methylpyridinium and 1-ethylpyridinium, Pyrrolidiniums such as 1-butyl-1-methylpyrrolidinium and 1-methyl-1-propylpyrrolidinium, Sulfonium-based products such as trimethylsulfonium and triethylsulfonium, Phosphonium type, Morphorinium-based, Etc. are used.
  • Ammonium-based products such as butyltrimethylammonium and trimethylpropylammonium
  • Imidazoles such as 1-ethyl-3 methylimidazolium
  • ionic liquid as an anion, Cl -, Br -, etc. halide-based, BF 4 - such as boron hydride system, (NC) 2 N -, (CF 3 SO 2) 2 N -, (FSO 2) 2 N - , etc. amines, CH 3 SO 4 -, CF 3 SO 3 - etc. Sulfate, sulphonate system, PF 6 - such as phosphoric acid-based, Etc. are used.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment are not sintered bodies formed by high-temperature firing. Therefore, the electrode of this embodiment contains a hydrocarbon. More specifically, the ionic liquid constituting the electrode of the present embodiment contains a hydrocarbon.
  • the fact that the electrode (ionic liquid) contains hydrocarbons means that NMR (nuclear magnetic resonance), Raman spectroscopy, LC-MS (liquid chromatography-mass spectrometry), GC-MS (gas chromatography-mass spectrometry) ), FT-IR (Fourier transform infrared spectroscopy), etc., can be specified by one or a combination of two or more.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment include lithium ions in addition to the oxide-based lithium ion conductive solid electrolytes 204 and 206 and the active materials (positive electrode active material 214 and negative electrode active material 216). It contains 224,226 conductive ionic liquids and has high lithium ion conductivity in the state of a pressure-molded molded body (compact powder). Therefore, the performance of the battery body 110 can be improved by using the electrodes of the present embodiment.
  • the reason why the electrode of the present embodiment has such high lithium ion conductivity is not necessarily clear, but it is presumed as follows.
  • oxide-based lithium ion conductive solid electrolytes are harder than oxide-based lithium ion conductive solid electrolytes (for example, sulfide-based lithium ion conductive solid electrolytes), and thus oxide-based lithium ion conduction.
  • oxide-based lithium ion conductive solid electrolytes for example, sulfide-based lithium ion conductive solid electrolytes
  • oxide-based lithium ion conduction In the state of a molded body (compact powder) obtained by pressure-molding the powder of the sexual solid electrolyte, the contact between the particles becomes point contact, the resistance between the particles increases, and the lithium ion conductivity becomes relatively low. Further, although the lithium ion conductivity can be increased by firing the powder of the oxide-based lithium ion conductive solid electrolyte at a high temperature, it is difficult to increase the size of the battery due to warpage and deformation caused by the high temperature firing.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment contain ionic liquids 224,226 having lithium ion conductivity in addition to the oxide-based lithium ion conductive solid electrolytes 204 and 206.
  • the ionic liquids 224 and 226 are distributed around the particles of the oxide-based lithium ion conductive solid electrolytes 204 and 206, as shown in FIGS. 2 and 3.
  • ionic liquids 224 and 226 functioning as lithium ion conductive paths are interposed at the grain boundaries of the oxide-based lithium ion conductive solid electrolytes 204 and 206 throughout the molded body. It is considered that the lithium ion conductivity at the grain boundary is improved, and as a result, the lithium ion conductivity is improved in the electrode and at the interface between the electrode and another member (for example, the solid electrolyte layer 112).
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment are added to the oxide-based lithium ion conductive solid electrolytes 204 and 206, the active materials (positive electrode active material 214, negative electrode active material 216) and the ionic liquids 224 and 226.
  • the structure may be formed in the form of a sheet containing a binder.
  • the binder include polyvinylidene fluoride (PVDF), a copolymer of polyvinylidene fluoride (PVDF) and hexafluoropropylene (HFP) (hereinafter referred to as “PVDF-HFP”), polytetrafluoroethylene (PTFE), and the like.
  • Polyethylene polyamide, silicone (polysiloxane), styrene-butadiene rubber (SBR), acrylic resin (PMMA), polyethylene oxide (PEO) and the like are used. With such a configuration, it is possible to improve the moldability and handling of the electrode while improving the lithium ion conductivity of the electrode.
  • the volume content of the active materials is preferably 40 vol% or more and 85 vol% or less. If the volume content of the active material in the electrode is excessively low, the capacity of the battery is not sufficiently secured, while if the volume content of the active material in the electrode is excessively high, the internal resistance of the electrode is effectively reduced. Can't.
  • the volume content of the active material in the electrode is more preferably 40 vol% or more and 70 vol% or less.
  • the volume content of the oxide-based lithium ion conductive solid electrolytes 204 and 206 is preferably 5 vol% or more and 40 vol% or less. If the volume content of the oxide-based lithium ion conductive solid electrolytes 204 and 206 in the electrode is excessively low, the decrease in the lithium ion conductivity of the electrode cannot be suppressed and the corrosion of the current collector is effective. On the other hand, if the volume content of the oxide-based lithium ion conductive solid electrolytes 204 and 206 in the electrode is excessively high, the internal resistance of the electrode cannot be effectively reduced.
  • the volume content of the oxide-based lithium ion conductive solid electrolytes 204 and 206 in the electrode is more preferably 10 vol% or more and 40 vol% or less, and further preferably 20 vol% or more and 40 vol% or less.
  • the volume content of the ionic liquids 224 and 226 is preferably 3 vol% or more and 35 vol% or less. If the volume content of the ionic liquids 224,226 in the electrode is excessively low, the internal resistance of the electrode cannot be effectively reduced, while the volume content of the ionic liquids 224,226 in the electrode is excessively high. , The ionic liquid may seep out.
  • the volume content of the ionic liquid 224,226 in the electrode is more preferably 10 vol% or more and 25 vol% or less.
  • the volume content of the active materials (positive electrode active material 214, negative electrode active material 216) is set to 40 vol% or more and 85 vol% or less, and the oxide-based lithium ionic conductive solid electrolyte 204,206 If the volume content of the ionic liquid is 5 vol% or more and 40 vol% or less, and the volume content of the ionic liquids 224 and 226 is 3 vol% or more and 35 vol% or less, corrosion of the current collector and exudation of the ionic liquid are performed.
  • the lithium ionic conductivity can be effectively improved in the electrode and at the interface between the electrode and another member (for example, the solid electrolyte layer 112), and the battery body 110 using the electrode can be effectively improved. Performance can be effectively improved.
  • the solid electrolyte layer 112 is prepared. For example, by mixing powder of an oxide-based lithium ion conductive solid electrolyte and an ionic liquid and press-molding this mixture at a predetermined pressure, or by adding a binder to form a sheet. The solid electrolyte layer 112 is prepared.
  • the positive electrode 114 and the negative electrode 116 are separately manufactured. Specifically, the powder of the oxide-based lithium ion conductive solid electrolyte 204 and the ionic liquid 224 are mixed, and the powder of the positive electrode active material 214 (when a conductive auxiliary agent is used, the positive electrode active material) is added to the mixture. A mixture of the powder of 214 and the conductive additive) is added and further mixed. A positive electrode 114 is produced by pressure molding this mixture at a predetermined pressure or by adding a binder to form a sheet.
  • the powder of the oxide-based lithium ion conductive solid electrolyte 206 and the ionic liquid 226 are mixed, and the powder of the negative electrode active material 216 (in the case of using a conductive auxiliary agent, the negative electrode active material 216) is added to the mixture.
  • a mixture of the powder and the conductive additive is added and further mixed.
  • the negative electrode 116 is produced by pressure molding this mixture at a predetermined pressure or by adding a binder to form a sheet.
  • the positive electrode side current collector 154, the positive electrode 114, the solid electrolyte layer 112, the negative electrode 116, and the negative electrode side current collector 156 are laminated in this order and pressurized to integrate them.
  • the all-solid-state battery 102 having the above-described configuration is manufactured.
  • the electrodes (positive electrode 114 and negative electrode 116) for the battery body 110 of the present embodiment are the oxide-based lithium ionic conductive solid electrolytes 204 and 206 and the active materials (positive electrode active material 214 and negative electrode active material). 216) and ionic liquids 224 and 226.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment are not sulfide-based lithium ion conductive solid electrolytes that may generate toxic gas, but oxide-based lithium that does not generate toxic gas. Since it contains ionic conductive solid electrolytes 204 and 206, it is possible to avoid the generation of toxic gas.
  • the oxide-based lithium ionic conductive solid electrolytes 204 and 206 are materials that are not easily plastically deformed, the contact between the particles becomes insufficient unless they are fired, and high lithium ionic conductivity cannot be exhibited.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment contain ionic liquids 224 and 226 that are non-volatile, flame-retardant, and function as fluid lithium ion conductive components, they are ionic liquids.
  • the presence of 224,226 can improve lithium ionic conductivity within the electrode and at the interface between the electrode and other members (eg, the solid electrolyte layer 112). Therefore, if the battery body 110 is configured by using the electrodes of the present embodiment, the performance of the battery body 110 can be improved.
  • the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment contain the oxide-based lithium ionic conductive solid electrolytes 204 and 206, the electrodes (positive electrode 114 and the negative electrode 116) do not contain the oxide-based lithium ionic conductive solid electrolytes 204 and 206.
  • the area where the ionic liquids 224 and 226 come into contact with the current collectors (positive electrode side current collector 154 and negative electrode side current collector 156) provided adjacent to the electrodes can be reduced, and the current collectors are corroded. Can be suppressed.
  • the concentration of the lithium salt contained in the ionic liquids 224 and 226 is high (specifically, if it is 0.4 mol / L or more), corrosion of the current collector is likely to occur, so that the oxide system is used.
  • the effect of suppressing corrosion of the current collector by containing the lithium ion conductive solid electrolytes 204 and 206 becomes more useful.
  • the volume content of the active materials is preferably 40 vol% or more and 85 vol% or less, and the oxide.
  • the volume content of the system lithium ion conductive solid electrolytes 204 and 206 is preferably 5 vol% or more and 40 vol% or less, and the volume content of the ionic liquids 224 and 226 is 3 vol% or more and 35 vol% or less. Is preferable. With such a configuration, lithium ion conductivity can be effectively improved in the electrode and at the interface between the electrode and another member (for example, the solid electrolyte layer 112). Therefore, if the battery body 110 is configured by using the electrodes having such a structure, the performance of the battery body 110 can be effectively improved.
  • the oxide-based lithium ion conductive solid electrolytes 204 and 206 contained in the electrodes (positive electrode 114 and negative electrode 116) of the present embodiment are solids having a garnet-type crystal structure containing at least Li, La, Zr and O. It is preferably an electrolyte (LLZ-based lithium ion conductive solid electrolyte). Since the LLZ-based lithium ion conductive solid electrolyte has a wider potential window than other oxide-based lithium ion conductive solid electrolytes, the material selection range of the electrode active material (positive electrode active material 214, negative electrode active material 216) Can be widened, and an electrode containing the optimum active material can be constructed.
  • positive electrode materials include LCO, LiMn 2 O 4 , LiFePO 4 , NCM, NCA, and the like
  • negative electrode materials include Li metal, Li—Al alloy, LTO, carbon (graphite, natural graphite, artificial graphite, etc.). Core-shell type graphite whose surface is coated with low crystalline carbon), Si (silicon), SiO, and the like.
  • A-5 Method for specifying the electrode composition (volume content of each component): The composition of the electrodes (positive electrode 114, negative electrode 116) constituting the battery body 110, that is, the active material (positive electrode active material 214, negative electrode active material 216), oxide-based lithium ion conductive solid electrolytes 204, 206, and ionic liquid.
  • the method for specifying the volume content (vol%) of each of 224 and 226 is as follows.
  • the target electrode mixture is dissolved in a solvent (for example, chloroform) to form a soluble substance (binder, ionic liquid) and a precipitate (active material, oxide-based lithium ion conductive solid electrolyte, conductive auxiliary agent).
  • a solvent for example, chloroform
  • the components of the binder and the components of the ionic liquid are specified by performing a qualitative analysis of the material components (ionic liquid, binder) by LC-MS measurement (liquid chromatography-mass spectrometry).
  • LC-MS measurement liquid chromatography-mass spectrometry
  • the precipitate For the precipitate, measure the weight of the entire precipitate. In addition, by performing XRD measurement (X-ray analysis) on the precipitate, the chemical composition is analyzed and the material components of the active material and the oxide-based lithium ion conductive solid electrolyte are specified. In addition, the ratio of material components is measured by performing XRF measurement (fluorescent X-ray analysis) on the precipitate. Thereby, the ratio of the active material, the oxide-based lithium ion conductive solid electrolyte, and the conductive auxiliary agent is specified.
  • XRD measurement X-ray analysis
  • the chemical composition is analyzed and the material components of the active material and the oxide-based lithium ion conductive solid electrolyte are specified.
  • the ratio of material components is measured by performing XRF measurement (fluorescent X-ray analysis) on the precipitate.
  • the content of the active material and the oxide-based lithium ion conductive solid electrolyte is determined from the weight of the entire precipitate and the ratio of the active material, the oxide-based lithium ion conductive solid electrolyte, and the conductive auxiliary agent.
  • the volume content of each component is specified from the content of each component (binder, ionic liquid, active material, oxide-based lithium ion conductive solid electrolyte) calculated above.
  • the ratio of the active material and the oxide-based lithium ion conductive solid electrolyte can also be determined by the following method.
  • the target electrode is frozen in liquid nitrogen or the like in order to obtain a fixed state of each substance, a cross section is obtained by the CP method (cross-section polisher method), and this cross section is targeted for EDS (energy dispersive X-ray).
  • EDS energy dispersive X-ray
  • FIG. 9 is an explanatory diagram schematically showing the configuration of the pressurizing jig 300 and the sample S used for the performance evaluation of the positive electrode 114
  • FIG. 10 is an explanatory diagram showing the configuration of the negative electrode 116. It is explanatory drawing which shows typically the structure of the pressurizing jig 300 and sample S.
  • each sample has a different composition (material and volume content of each component).
  • the samples S1 to S10 include a positive electrode active material 214, an oxide-based lithium ion conductive solid electrolyte 204, an ionic liquid 224, a conductive auxiliary agent, and a binder. It is a sheet-like molded body containing. Further, the sample S11 is a green compact containing a positive electrode active material 214, an oxide-based lithium ion conductive solid electrolyte 204, an ionic liquid 224, and a conductive auxiliary agent, and does not contain a binder.
  • the sample S12 is a sheet-like molded body containing the positive electrode active material 214, the oxide-based lithium ion conductive solid electrolyte 204, the conductive auxiliary agent, and the binder, but unlike other samples, the sample S12 contains ions. Does not contain liquid 224.
  • the positive electrode active material 214 As the positive electrode active material 214, the above-mentioned NCA (LiNi 0.8 Co 0.15 Al 0.05 O 2 ) was used in the samples S1 to S9 and S12, and the above-mentioned LCO (LiCoO 2 ) was used in the sample S10. ) was used, and in sample S11, the above-mentioned NCM (Li (Co 1/3 Ni 1/3 Mn 1/3 ) O 2 ) was used. Further, as the oxide-based lithium ion conductive solid electrolyte 204, the above-mentioned LLZ-Mg and Sr were used in all the samples.
  • the oxide-based lithium ion conductive solid electrolyte 204 As the oxide-based lithium ion conductive solid electrolyte 204, the above-mentioned LLZ-Mg and Sr were used in all the samples.
  • Li-FSI lithium salt
  • Li-FSI lithium salt
  • acetylene black (AB) was used in the samples S1 to S6, S11 and S12, and vapor phase grown carbon fiber (VGCF) was used in the samples S7 to S10. Further, as the binder, the above-mentioned PVDF-HFP was used in all the samples (S1 to S10, S12) containing the binder.
  • the samples S21 to S30 and S32 contain the negative electrode active material 216, the oxide-based lithium ion conductive solid electrolyte 206, the ionic liquid 226, and the binder. It is a sheet-like molded body containing.
  • the samples S29, S30, and S32 further contain a conductive auxiliary agent (VGCF).
  • the sample S31 is a green compact containing the negative electrode active material 216, the oxide-based lithium ion conductive solid electrolyte 206, and the ionic liquid 226, and does not contain a binder.
  • sample S33 is a sheet-shaped molded body containing a negative electrode active material 216, an oxide-based lithium ion conductive solid electrolyte 206, and a binder, but unlike other samples, it contains an ionic liquid 226. Not.
  • the negative electrode active material 216 artificial graphite (MCMB) was used in samples S21 to S27 and S31 to S33, and natural graphite was used in samples S28 to S30. Further, as the oxide-based lithium ion conductive solid electrolyte 206, the above-mentioned LLZ-Mg and Sr were used in all the samples. As the ionic liquid 226, 1.0 M Li-FSI (EMI-FSI) was used for all the samples (S21 to S32) containing the ionic liquid 226. As the binder, the above-mentioned PVDF-HFP was used in all the samples (S21 to S30, S32, S33) containing the binder.
  • EMI-FSI 1.0 M Li-FSI
  • LLZ-MgSr powder as an oxide-based lithium ion conductive solid electrolyte was prepared as follows. That is, Li 2 CO 3 , MgO, La (OH) 3 , SrCO so that the composition is Li 6.95 Mg 0.15 La 2.75 Sr 0.25 Zr 2.0 O 12 (LLZ-MgSr). 3 , ZrO 2 was weighed. At that time, in consideration of the volatilization of Li during firing, Li 2 CO 3 was further added so as to be excessive by about 15 mol% in terms of elements.
  • This raw material was put into a nylon pot together with zirconia balls, and pulverized and mixed in an organic solvent for 15 hours with a ball mill. After pulverization and mixing, the slurry was dried and calcined on an MgO plate at 1100 ° C. for 10 hours. A binder was added to the powder after calcination, and the powder was pulverized and mixed in an organic solvent for 15 hours with a ball mill. After pulverizing and mixing, the slurry is dried, placed in a mold having a diameter of 12 mm, press-molded to a thickness of about 1.5 mm, and then pressed using a cold hydrostatic isotropic press (CIP). A molded product was obtained by applying a hydrostatic pressure of 5 t / cm 2.
  • CIP cold hydrostatic isotropic press
  • This molded product was covered with a calcined powder having the same composition as the molded product and fired at 1100 ° C. for 4 hours in a reducing atmosphere to obtain a sintered body.
  • This sintered body was pulverized in a glove box having an argon atmosphere to obtain a powder of LLZ-MgSr.
  • the particle size of the obtained LLZ-MgSr was about 0.3 to 0.8 ⁇ m.
  • the ionic liquid specified for each sample is added and mixed in a dairy pot to form a mixture of the solid electrolyte and the ionic liquid. Obtained.
  • the positive electrode 114 the positive electrode active material 214 and the conductive auxiliary agent determined for each sample are added and mixed in a dairy pot, and this mixed material is mixed with the above-mentioned solid electrolyte and ionic liquid (however, sample S12). Was added to the solid electrolyte) and mixed to obtain an electrode composite powder.
  • the negative electrode active material 216 determined for each sample is added to the above-mentioned mixture of the solid electrolyte and the ionic liquid (however, the solid electrolyte for the sample S33) and mixed to form an electrode composite. Obtained powder.
  • a 10 wt% PVDF-DMC (dimethyl carbonate) solution was added dropwise to the above-mentioned electrode composite powder and mixed in an agate mortar, and a DMC solvent was added little by little to increase the viscosity.
  • a DMC solvent was added little by little to increase the viscosity.
  • An electrode composite slurry was applied to a metal foil uniformly adhered on glass using a DMC and a roller using an applicator, and dried under reduced pressure at 80 ° C. for 10 hours to obtain an electrode composite sheet.
  • a Macol tube was set on the minor axis of the pressurizing jig 300, and an oxide-based lithium ion conductive solid electrolyte (LLZ-MgSr) and an ionic liquid (1) were separately prepared.
  • a mixture material of the solid electrolyte layer
  • EMI-FSI Li-FSI
  • the short shaft is pulled out, the material of the electrode (positive electrode 114 or negative electrode 116), that is, the electrode composite sheet (or electrode composite powder) punched to a diameter of 10 mm is put in, and the short shaft is set in the Macol tube.
  • the pressure was increased at 500 MPa.
  • the pressurizing jig is inverted to remove the long axis, the counter electrode material, that is, the In-Li foil punched to a diameter of 10 mm is charged, and the Cu foil punched to a diameter of 10 mm is charged, and then the long axis is inserted. It was set in a Macol tube and pressurized at 80 MPa. After that, a fixing jig (collar) was attached and fastened and fixed with bolts at 8N.
  • the positive electrode 114 when the discharge capacity is less than 50 ⁇ Ah, it is judged as “x” (failed), and when the discharge capacity is 50 ⁇ Ah or more and less than 400 ⁇ Ah, it is judged as “ ⁇ ” (pass) and discharged. When the capacitance was 400 ⁇ Ah or more, it was judged as “ ⁇ ” (excellent).
  • the negative electrode 116 if the discharge capacity is less than 100 ⁇ Ah, it is judged as “x” (failed), and if the discharge capacity is 100 ⁇ Ah or more and less than 400 ⁇ Ah, it is judged as “ ⁇ ” (pass) and discharged. When the capacitance was 400 ⁇ Ah or more, it was judged as “ ⁇ ” (excellent).
  • the positive electrode 114 was judged to be rejected (x) because the discharge capacity of the sample S12 containing no ionic liquid 224 was less than 50 ⁇ Ah. Since the sample S12 does not contain the ionic liquid 224, the contact between the particles of the oxide-based lithium ion conductive solid electrolyte 204 becomes a point contact and the resistance between the particles increases, and as a result, the inside of the electrode and the electrode and others It is probable that the lithium ion conductivity at the interface with the member of the battery was lowered, and the capacity of the battery was lowered.
  • the discharge capacity was 50 ⁇ Ah or more, so it was judged to be acceptable ( ⁇ ) or excellent ( ⁇ ). Since these samples contain an ionic liquid 224, the ionic liquid 224 that functions as a lithium ion conduction path is interposed between the particles of the oxide-based lithium ion conductive solid electrolyte 204, and the lithium ion conductivity at the grain boundary is increased. It is considered that this was improved, and as a result, the lithium ion conductivity in the electrode and at the interface between the electrode and other members was improved, and the capacity of the battery was increased.
  • the positive electrode 114 contains the ionic liquid 224 in addition to the oxide-based lithium ion conductive solid electrolyte 204 and the positive electrode active material 214, lithium in the electrode and at the interface between the electrode and other members It can be said that the ionic conductivity can be improved.
  • the discharge capacity was 400 ⁇ Ah or more, so it was judged to be excellent ( ⁇ ).
  • the volume content of the positive electrode active material 214 is 40 vol% or more and 85 vol% or less
  • the volume content of the oxide-based lithium ion conductive solid electrolyte 204 is 5 vol% or more and 40 vol% or less.
  • the volume content of the liquid 224 is 3 vol% or more and 35 vol% or less.
  • the sample S6 was determined to be unmeasurable ( ⁇ ) because the ionic liquid exuded during molding.
  • the electrode satisfies the above-mentioned volume content condition, the lithium ion conductivity in the electrode and at the interface between the electrode and other members can be effectively improved while suppressing the occurrence of ionic liquid exudation. It can be said that it can be improved.
  • the negative electrode 116 was judged to be rejected (x) because the discharge capacity of the sample S33 containing no ionic liquid 226 was less than 100 ⁇ Ah. Since the sample S33 does not contain the ionic liquid 226, the contact between the particles of the oxide-based lithium ion conductive solid electrolyte 206 becomes a point contact, and the resistance between the particles increases, and as a result, the inside of the electrode and the electrode and others It is probable that the lithium ion conductivity at the interface with the member of the battery was lowered, and the capacity of the battery was lowered.
  • the discharge capacity was 100 ⁇ Ah or more, so that the samples were judged to be acceptable ( ⁇ ) or excellent ( ⁇ ). Since these samples contain an ionic liquid 226, the ionic liquid 226 that functions as a lithium ion conduction path is interposed between the particles of the oxide-based lithium ion conductive solid electrolyte 206, and the lithium ion conductivity at the grain boundary is increased. It is considered that this was improved, and as a result, the lithium ion conductivity in the electrode and at the interface between the electrode and other members was improved, and the capacity of the battery was increased.
  • the negative electrode 116 contains the ionic liquid 226 in addition to the oxide-based lithium ion conductive solid electrolyte 206 and the negative electrode active material 216, lithium is contained in the electrode and at the interface between the electrode and other members. It can be said that the ionic conductivity can be improved.
  • the discharge capacity was 400 ⁇ Ah or more, so it was judged to be excellent ( ⁇ ).
  • the volume content of the negative electrode active material 216 is 40 vol% or more and 85 vol% or less, and the volume content of the oxide-based lithium ion conductive solid electrolyte 206 is 5 vol% or more and 40 vol% or less.
  • the volume content of the liquid 226 is 3 vol% or more and 35 vol% or less.
  • the sample S26 was determined to be unmeasurable ( ⁇ ) because the ionic liquid exuded during molding.
  • the electrode satisfies the above-mentioned volume content condition, the lithium ion conductivity in the electrode and at the interface between the electrode and other members can be effectively improved while suppressing the occurrence of ionic liquid exudation. It can be said that it can be improved.
  • the lithium ion conductor in the present embodiment contains an LLZ-based ion conductive powder (an ion conductive solid electrolyte powder having a garnet-type crystal structure containing at least Li, La, Zr, and O).
  • LLZ-based ion conductive powder an ion conductive solid electrolyte powder having a garnet-type crystal structure containing at least Li, La, Zr, and O.
  • the LLZ-based ion conductive powder include Mg, Al, Si, Ca (calcium), Ti, V (vanadium), Ga (gallium), Sr, Y (yttrium), Nb (niobium), Sn (tin), and Sb.
  • the LLZ-based ion conductive powder contains at least one of Mg and an element A (A is at least one element selected from the group consisting of Ca, Sr and Ba), and each element contained is a molar. It is preferable to use a ratio that satisfies the following formulas (1) to (3). Since Mg and element A have relatively large reserves and are inexpensive, if Mg and / or element A is used as a substitution element for the LLZ-based ion conductive powder, the LLZ-based ion conductive powder can be stably supplied. Can be expected and the cost can be reduced. (1) 1.33 ⁇ Li / (La + A) ⁇ 3 (2) 0 ⁇ Mg / (La + A) ⁇ 0.5 (3) 0 ⁇ A / (La + A) ⁇ 0.67
  • the LLZ-based ionic conductive powder it is possible to adopt a powder containing both Mg and element A, in which each contained element satisfies the following formulas (1') to (3') in terms of molar ratio. More preferred. (1') 2.0 ⁇ Li / (La + A) ⁇ 2.5 (2') 0.01 ⁇ Mg / (La + A) ⁇ 0.14 (3') 0.04 ⁇ A / (La + A) ⁇ 0.17
  • the LLZ-based ion conductive powder preferably satisfies any of the following (a) to (c), more preferably (c) among these, and (d). It can be said that it is more preferable to satisfy.
  • (A) It contains Mg, and the content of each element satisfies 1.33 ⁇ Li / La ⁇ 3 and 0 ⁇ Mg / La ⁇ 0.5 in terms of molar ratio.
  • (C) Contains Mg and element A, and the content of each element is 1.33 ⁇ Li / (La + A) ⁇ 3, 0 ⁇ Mg / (La + A) ⁇ 0.5, and 0 ⁇ A / ( La + A) ⁇ 0.67 is satisfied.
  • (D) Contains Mg and element A, and the content of each element is 2.0 ⁇ Li / (La + A) ⁇ 2.5, 0.01 ⁇ Mg / (La + A) ⁇ 0.14, and 0 in molar ratio. .04 ⁇ A / (La + A) ⁇ 0.17 is satisfied.
  • the LLZ-based ion conductive powder has good lithium ions when the above (a) is satisfied, that is, when Li, La, Zr and Mg are contained so as to satisfy the above formulas (1) and (2) in molar ratio. Shows conductivity.
  • the mechanism is not clear, but for example, when the LLZ-based ionic conductive powder contains Mg, the ionic radius of Li and the ionic radius of Mg are close, so that Mg is arranged at the Li site where Li is arranged in the LLZ crystal phase.
  • Li is replaced with Mg, which causes vacancies in the Li sites in the crystal structure due to the difference in charge between Li and Mg, which makes it easier for Li ions to move, and as a result, the lithium ionic radius. Is expected to improve.
  • the molar ratio of Li to the sum of La and element A is less than 1.33 or more than 3, not only the ionic conductive powder having a garnet-type crystal structure but also another metal oxide Is more likely to be formed.
  • the content of another metal oxide increases, the content of the ionic conductive powder having a garnet-type crystal structure becomes relatively small, and the lithium ion conductivity of another metal oxide is low, so that the lithium ion conductivity Decreases.
  • Mg in the LLZ-based ion conductive powder increases, Mg is arranged at the Li site, pores are formed at the Li site, and the lithium ion conductivity is improved.
  • the ratio exceeds 0.5, another metal oxide containing Mg is likely to be formed.
  • the larger the content of the other metal oxide containing Mg the smaller the content of the ionic conductive powder having a garnet-type crystal structure. Since the lithium ion conductivity of another metal oxide containing Mg is low, if the molar ratio of Mg to the sum of La and the element A exceeds 0.5, the lithium ion conductivity decreases.
  • the LLZ-based ionic conductive powder is good lithium when the above (b) is satisfied, that is, when Li, La, Zr and the element A are contained so as to satisfy the above formulas (1) and (3) in molar ratio. Shows ionic conductivity.
  • the mechanism is not clear, but for example, when the LLZ-based ionic conductive powder contains the element A, the ionic radius of La and the ionic radius of the element A are close to each other, so that the La site where La is arranged in the LLZ crystal phase.
  • the element A is easily arranged in the element A and La is replaced with the element A, lattice strain occurs, and free Li ions increase due to the difference in charge between La and the element A, and the lithium ionic conductivity is improved.
  • the LLZ-based ionic conductive powder when the molar ratio of Li to the sum of La and element A is less than 1.33 or more than 3, not only the ionic conductive powder having a garnet-type crystal structure but also another metal oxide Is more likely to be formed. As the content of another metal oxide increases, the content of the ionic conductive powder having a garnet-type crystal structure becomes relatively small, and the lithium ion conductivity of another metal oxide is low, so that the lithium ion conductivity Decreases.
  • element A in the LLZ-based ion conductive powder increases, element A is arranged at the La site, the lattice strain increases, and free Li ions increase due to the difference in charge between La and element A, and lithium.
  • the ionic conductivity is improved, when the molar ratio of element A to the sum of La and element A exceeds 0.67, another metal oxide containing element A is likely to be formed.
  • the larger the content of another metal oxide containing the element A the smaller the content of the ionic conductive powder having a garnet-type crystal structure, and the lithium of another metal oxide containing the element A. Since the ion conductivity is low, the lithium ion conductivity is lowered.
  • the element A is at least one element selected from the group consisting of Ca, Sr and Ba.
  • Ca, Sr and Ba are Group 2 elements in the periodic table and tend to be divalent cations, and all have a common property that the ionic radii are close to each other. Since Ca, Sr and Ba all have an ionic radius close to that of La, they are easily replaced with La arranged at the La site in the LLZ-based ion conductive powder. It is preferable that the LLZ-based ion conductive powder contains Sr among these elements A because it can be easily formed by sintering and a high lithium ion conductivity can be obtained.
  • the LLZ-based ion conductive powder is baked when the above (c) is satisfied, that is, when Li, La, Zr, Mg and the element A are contained so as to satisfy the above formulas (1) to (3) in a molar ratio. It can be easily formed by bundling, and the lithium ion conductivity is further improved. Further, when the LLZ-based ionic conductive powder satisfies the above (d), that is, Li, La, Zr, Mg and the element A are satisfied with the above formulas (1') to (3') in molar ratio. When included, the lithium ion conductivity is further improved.
  • the mechanism is not clear, but for example, Li at the Li site in the LLZ-based ionic conductive powder is replaced with Mg, and La at the La site is replaced with the element A, so that holes are formed in the Li site. It is also considered that the number of free Li ions increases and the lithium ion conductivity becomes even better. Further, the LLZ-based ionic conductive powder so that Li, La, Zr, Mg and Sr satisfy the above formulas (1) to (3), and particularly satisfy the above formulas (1') to (3'). It is preferable to include it from the viewpoint that high lithium ion conductivity can be obtained and a lithium ion conductor having a high relative density can be obtained.
  • the LLZ-based ion conductive powder preferably contains Zr in a molar ratio so as to satisfy the following formula (4).
  • Zr in this range, an ionic conductive powder having a garnet-type crystal structure can be easily obtained.
  • the configuration of the all-solid-state battery 102 in the above embodiment is merely an example and can be changed in various ways.
  • the positive electrode 114 and the negative electrode 116 contain an oxide-based lithium ion conductive solid electrolyte, an active material, and an ionic liquid, but the positive electrode 114 and the negative electrode 116 are other than these. May contain the components of.
  • both the positive electrode 114 and the negative electrode 116 are configured to contain an oxide-based lithium ion conductive solid electrolyte, an active material, and an ionic liquid, but the positive electrode 114 and the negative electrode 116 are used.
  • the configuration may be adopted for only one of them.
  • the positive electrode 114 may contain an ionic liquid, but the negative electrode 116 may not contain an ionic liquid.
  • each element constituting the all-solid-state battery 102 is merely an example, and each element may be formed of another material. Further, in the above embodiment, the manufacturing method of the all-solid-state battery 102 is merely an example, and other manufacturing methods may be adopted.
  • the technique disclosed in the present specification is not limited to the electrodes for the all-solid-state battery 102, and can be applied to electrodes for other power storage devices (for example, lithium air batteries, lithium flow batteries, solid capacitors, etc.). is there.

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