WO2024014261A1 - パッケージ化された固体電池 - Google Patents

パッケージ化された固体電池 Download PDF

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Publication number
WO2024014261A1
WO2024014261A1 PCT/JP2023/023290 JP2023023290W WO2024014261A1 WO 2024014261 A1 WO2024014261 A1 WO 2024014261A1 JP 2023023290 W JP2023023290 W JP 2023023290W WO 2024014261 A1 WO2024014261 A1 WO 2024014261A1
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Prior art keywords
state battery
solid
electrode
substrate
end electrode
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PCT/JP2023/023290
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English (en)
French (fr)
Japanese (ja)
Inventor
高之 長野
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Murata Manufacturing Co Ltd
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Murata Manufacturing Co Ltd
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Priority to EP23839435.7A priority Critical patent/EP4557438A1/en
Priority to CN202380053275.9A priority patent/CN119452498A/zh
Priority to JP2024533612A priority patent/JP7838652B2/ja
Publication of WO2024014261A1 publication Critical patent/WO2024014261A1/ja
Priority to US19/002,145 priority patent/US20250149689A1/en
Anticipated expiration legal-status Critical
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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
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/102—Primary casings; Jackets or wrappings characterised by their shape or physical structure
    • H01M50/11—Primary casings; Jackets or wrappings characterised by their shape or physical structure having a chip structure, e.g. micro-sized batteries integrated on chips
    • 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
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/04—Construction or manufacture in general
    • H01M10/0413—Large-sized flat cells or batteries for motive or stationary systems with plate-like electrodes
    • 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
    • H01M10/04—Construction or manufacture in general
    • H01M10/0436—Small-sized flat cells or batteries for portable equipment
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/054—Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H01M10/0585—Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/102—Primary casings; Jackets or wrappings characterised by their shape or physical structure
    • H01M50/103—Primary casings; Jackets or wrappings characterised by their shape or physical structure prismatic or rectangular
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/116—Primary casings; Jackets or wrappings characterised by the material
    • H01M50/117—Inorganic material
    • H01M50/119—Metals
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/116—Primary casings; Jackets or wrappings characterised by the material
    • H01M50/121—Organic material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/116—Primary casings; Jackets or wrappings characterised by the material
    • H01M50/124—Primary casings; Jackets or wrappings characterised by the material having a layered structure
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/131—Primary casings; Jackets or wrappings characterised by physical properties, e.g. gas permeability, size or heat resistance
    • 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
    • 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
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present disclosure relates to packaged solid state batteries. More specifically, the present disclosure relates to solid state batteries packaged to facilitate board mounting.
  • Secondary batteries that can be repeatedly charged and discharged have been used for a variety of purposes.
  • secondary batteries are used as power sources for electronic devices such as smartphones and notebook computers.
  • a liquid electrolyte is generally used as a medium for ion movement that contributes to charging and discharging.
  • electrolytes are used in secondary batteries.
  • such secondary batteries are generally required to be safe in terms of preventing electrolyte leakage.
  • the organic solvent used in the electrolyte is a flammable substance, safety is also required in this respect.
  • a solid-state battery may be mounted on a substrate such as a printed wiring board together with other electronic components.
  • a solid state battery placed on a substrate may be covered with a covering member to prevent water vapor from passing through (Patent Document 1).
  • the covering member is provided so as to also cover the end face electrode provided on the solid state battery.
  • the end electrode is in physical contact with the solid-state battery and can deform as the solid-state battery expands and contracts during charging and discharging.
  • the covering member is placed on the solid battery via the end electrode in a region covering the end electrode. Therefore, the covering member is inferior to the end electrode in its ability to follow the expansion and contraction of the solid battery, and may act to prevent deformation of the end electrode. As a result, distortion may occur inside the end electrode, and the end electrode may be damaged.
  • the present invention has been made in view of such problems. That is, the main objective of the present disclosure is to provide a packaged solid-state battery in which the risk of damage to the end electrodes due to expansion and contraction of the solid-state battery is reduced.
  • the exterior portion includes resin
  • a packaged solid state battery is provided that includes a void between the end electrode and the exterior.
  • the packaged solid-state battery according to an embodiment of the present disclosure can reduce the risk of damage to the end electrodes due to expansion and contraction of the solid-state battery.
  • FIG. 1 is a cross-sectional view schematically showing the internal structure of a solid-state battery.
  • FIG. 2 is a cross-sectional view schematically showing the configuration of a packaged solid-state battery according to an embodiment of the present disclosure.
  • FIG. 3 is an enlarged cross-sectional view schematically showing part A of the packaged solid state battery shown in FIG.
  • FIG. 4 is an enlarged cross-sectional view schematically showing part A of a packaged solid-state battery according to another embodiment of the present disclosure.
  • FIG. 5 is a cross-sectional view schematically showing the configuration of a packaged solid state battery according to an embodiment of the present disclosure.
  • FIG. 6 is an enlarged sectional view schematically showing part B of the packaged solid state battery shown in FIG. FIG.
  • FIG. 7A is a process cross-sectional view schematically showing a manufacturing process of a packaged solid-state battery according to an embodiment of the present disclosure.
  • FIG. 7B is a process cross-sectional view schematically showing a manufacturing process of a packaged solid-state battery according to an embodiment of the present disclosure.
  • FIG. 7C is a process cross-sectional view schematically showing a manufacturing process of a packaged solid-state battery according to an embodiment of the present disclosure.
  • FIG. 7D is a process cross-sectional view schematically showing a manufacturing process of a packaged solid-state battery according to an embodiment of the present disclosure.
  • FIG. 7E is a process cross-sectional view schematically showing a manufacturing process of a packaged solid-state battery according to an embodiment of the present disclosure.
  • packaged solid-state battery refers in a broad sense to a solid-state battery device configured to protect the solid-state battery from the external environment, and in a narrow sense, it refers to a solid-state battery device that is configured to protect the solid-state battery from the external environment. It refers to a solid state battery device that includes a substrate and protects the solid state battery from the external environment.
  • cross-sectional view refers to the shape viewed from a direction substantially perpendicular to the stacking direction in the stacked structure of a solid-state battery (simply put, the cross-sectional view when cut along a plane parallel to the thickness direction of the layers) form).
  • planar view or “planar view shape” as used in this specification is based on a sketch when the object is viewed from above or below along the thickness direction of such layers (i.e., the above-mentioned lamination direction). ing.
  • the vertically downward direction corresponds to the "downward direction"/"bottom side
  • the opposite direction corresponds to the "upward direction"/"top side”. I can do it.
  • a member such as a substrate, a solid battery, or a layer includes not only the case where the member contacts the upper surface of the member, but also the case where the member does not contact the upper surface of the member.
  • “on top” of a member such as a substrate, solid-state battery, or layer means that a new member is formed above the member, and/or that another member is interposed between the member and the member. Including cases etc.
  • “above” does not necessarily mean the upper side in the vertical direction. "Above” merely indicates the relative positional relationship of a plurality of members.
  • Secondary battery refers to a battery that can be repeatedly charged and discharged. Therefore, the secondary battery according to the present disclosure is not excessively limited by its name, and may also include, for example, power storage devices.
  • a “solid-state battery” refers to a battery whose constituent elements are made of solid matter, and in a narrow sense it refers to an all-solid-state battery whose constituent elements (especially preferably all constituent elements) are made of solid matter.
  • the solid-state battery of the present disclosure is a stacked solid-state battery configured such that layers constituting battery structural units are stacked on each other, and preferably each layer is made of a fired body.
  • a “solid battery” includes not only a so-called “secondary battery” that can be repeatedly charged and discharged, but also a "primary battery” that can only be discharged.
  • the "solid-state battery” is a secondary battery.
  • the term “secondary battery” is not excessively limited by its name, and may include, for example, power storage devices. Note that in the present disclosure, the solid state battery included in the package can also be referred to as a "solid state battery element.”
  • a solid-state battery has at least positive and negative electrode layers and a solid electrolyte.
  • the solid-state battery 100 includes a solid-state battery laminate including battery constituent units consisting of a positive electrode layer 110, a negative electrode layer 120, and at least a solid electrolyte 130 interposed between them. .
  • each layer constituting it may be formed by firing, and the positive electrode layer, negative electrode layer, solid electrolyte, etc. may form the fired layers.
  • the positive electrode layer, the negative electrode layer, and the solid electrolyte are each integrally fired, and therefore, it is preferable that the solid battery stack forms an integrally fired body.
  • the positive electrode layer is an electrode layer containing at least a positive electrode active material.
  • the positive electrode layer may further contain a solid electrolyte.
  • the positive electrode layer is composed of a fired body containing at least positive electrode active material particles and solid electrolyte particles.
  • the negative electrode layer is an electrode layer containing at least a negative electrode active material.
  • the negative electrode layer may further contain a solid electrolyte.
  • the negative electrode layer is composed of a sintered body containing at least negative electrode active material particles and solid electrolyte particles.
  • a positive electrode active material and a negative electrode active material are substances that participate in the transfer of electrons in a solid battery. Ions move (conduct) between the positive electrode layer and the negative electrode layer via the solid electrolyte, and electrons are exchanged to perform charging and discharging. It is preferable that each electrode layer of the positive electrode layer and the negative electrode layer is a layer capable of intercalating and deintercalating lithium ions or sodium ions. That is, the solid battery is preferably an all-solid-state secondary battery in which lithium ions or sodium ions move between a positive electrode layer and a negative electrode layer via a solid electrolyte to charge and discharge the battery.
  • Examples of the positive electrode active material contained in the positive electrode layer include a lithium-containing phosphoric acid compound having a Nasicon-type structure, a lithium-containing phosphoric acid compound having an olivine-type structure, a lithium-containing layered oxide, and a lithium-containing phosphoric acid compound having a spinel-type structure. At least one selected from the group consisting of oxides and the like can be mentioned.
  • An example of a lithium-containing phosphoric acid compound having a Nasicon type structure includes Li 3 V 2 (PO 4 ) 3 and the like.
  • Examples of lithium-containing phosphate compounds having an olivine structure include Li 3 Fe 2 (PO 4 ) 3 , LiFePO 4 , and/or LiMnPO 4 .
  • lithium-containing layered oxides examples include LiCoO 2 and/or LiCo 1/3 Ni 1/3 Mn 1/3 O 2 .
  • Examples of lithium-containing oxides having a spinel structure include LiMn 2 O 4 and/or LiNi 0.5 Mn 1.5 O 4 .
  • the type of lithium compound is not particularly limited, but may be, for example, a lithium transition metal composite oxide or a lithium transition metal phosphate compound.
  • Lithium transition metal composite oxide is a general term for oxides containing lithium and one or more types of transition metal elements as constituent elements
  • lithium transition metal phosphate compounds are oxides containing lithium and one or more types of transition metal elements as constituent elements. It is a general term for phosphoric acid compounds containing transition metal elements as constituent elements.
  • the type of transition metal element is not particularly limited, and examples thereof include cobalt (Co), nickel (Ni), manganese (Mn), and iron (Fe).
  • sodium-containing phosphoric acid compounds having a Nasicon-type structure sodium-containing phosphoric acid compounds having an olivine-type structure, sodium-containing layered oxides, and spinel-type structures are used. At least one selected from the group consisting of sodium-containing oxides and the like can be mentioned.
  • the sodium-containing layered oxide may include at least one selected from the group consisting of 2FeP2O7 , Na4Fe3 ( PO4 ) 2 ( P2O7 ) , and NaFeO2 as the sodium - containing layered oxide.
  • the positive electrode active material may be, for example, an oxide, a disulfide, a chalcogenide, or a conductive polymer.
  • the oxide may be, for example, titanium oxide, vanadium oxide or manganese dioxide.
  • the disulfide is, for example, titanium disulfide or molybdenum sulfide.
  • the chalcogenide may be, for example, niobium selenide.
  • the conductive polymer may be, for example, disulfide, polypyrrole, polyaniline, polythiophene, polyparastyrene, polyacetylene or polyacene.
  • Examples of the negative electrode active material contained in the negative electrode layer include a group consisting of titanium (Ti), silicon (Si), tin (Sn), chromium (Cr), iron (Fe), niobium (Nb), and molybdenum (Mo).
  • lithium alloy is Li-Al.
  • lithium-containing phosphoric acid compounds having a Nasicon type structure include Li 3 V 2 (PO 4 ) 3 and/or LiTi 2 (PO 4 ) 3 .
  • examples of the lithium-containing phosphoric acid compound having an olivine structure include Li 3 Fe 2 (PO 4 ) 3 and/or LiCuPO 4 .
  • An example of a lithium-containing oxide having a spinel structure is Li 4 Ti 5 O 12 and the like.
  • negative electrode active materials capable of intercalating and releasing sodium ions include sodium-containing phosphoric acid compounds having a Nasicon-type structure, sodium-containing phosphoric acid compounds having an olivine-type structure, and sodium-containing oxides having a spinel-type structure. At least one selected from the group consisting of:
  • the positive electrode layer and the negative electrode layer may be made of the same material.
  • the positive electrode layer and/or the negative electrode layer may contain a conductive material.
  • the conductive material contained in the positive electrode layer and the negative electrode layer include at least one metal material such as silver, palladium, gold, platinum, aluminum, copper, and nickel, and carbon.
  • the positive electrode layer and/or the negative electrode layer may contain a sintering aid.
  • the sintering aid include at least one selected from the group consisting of lithium oxide, sodium oxide, potassium oxide, boron oxide, silicon oxide, bismuth oxide, and phosphorus oxide.
  • the thickness of the positive electrode layer and the negative electrode layer is not particularly limited, but may be, for example, independently 2 ⁇ m or more and 50 ⁇ m or less, particularly 5 ⁇ m or more and 30 ⁇ m or less.
  • the positive electrode layer and the negative electrode layer may each include a positive electrode current collecting layer and a negative electrode current collecting layer.
  • the positive electrode current collecting layer and the negative electrode current collecting layer may each have a foil form. However, if more emphasis is placed on improving electronic conductivity through integral firing, reducing manufacturing costs of solid-state batteries, and/or reducing internal resistance of solid-state batteries, then the positive electrode current collecting layer and the negative electrode current collecting layer should each form a fired body. It may have.
  • the positive electrode current collector constituting the positive electrode current collector layer and the negative electrode current collector constituting the negative electrode current collector it is preferable to use a material with high electrical conductivity, such as silver, palladium, gold, platinum, aluminum, copper, etc. , and/or nickel may be used.
  • the positive electrode current collector and the negative electrode current collector may each have an electrical connection part for electrically connecting with the outside, and may be configured to be electrically connectable to the end surface electrode. Note that when the positive electrode current collecting layer and the negative electrode current collecting layer have the form of fired bodies, they may be constituted by fired bodies containing a conductive material and a sintering aid.
  • the conductive material contained in the positive electrode current collection layer and the negative electrode current collection layer may be selected from the same materials as the conductive materials that may be contained in the positive electrode layer and the negative electrode layer, for example.
  • the sintering aid contained in the positive electrode current collecting layer and the negative electrode current collecting layer may be selected from the same materials as the sintering aid that may be contained in the positive electrode layer and the negative electrode layer, for example.
  • a positive electrode current collecting layer and a negative electrode current collecting layer are not necessarily required in a solid state battery, and a solid state battery that is not provided with such a positive electrode current collecting layer and a negative electrode current collecting layer is also conceivable. That is, the solid state battery included in the package of the present disclosure may be a solid state battery without a current collecting layer.
  • a solid electrolyte is a material that can conduct lithium ions or sodium ions.
  • the solid electrolyte that forms a battery constituent unit in a solid-state battery may form a layer between the positive electrode layer 110 and the negative electrode layer 120 that can conduct lithium ions (see FIG. 1).
  • the solid electrolyte only needs to be provided at least between the positive electrode layer and the negative electrode layer. That is, the solid electrolyte may be present around the positive electrode layer and/or the negative electrode layer so as to protrude from between the positive electrode layer and the negative electrode layer.
  • Specific solid electrolytes include, for example, one or more of a crystalline solid electrolyte, a glass-based solid electrolyte, a glass-ceramic solid electrolyte, and the like.
  • Examples of the crystalline solid electrolyte include oxide-based crystal materials and sulfide-based crystal materials.
  • oxide-based crystal materials include lithium-containing phosphate compounds having a Nasicon structure, oxides having a perovskite structure, oxides having a garnet type or garnet-like structure, oxide glass ceramics-based lithium ion conductors, etc. It will be done.
  • Lithium-containing phosphoric acid compounds having a Nasicon structure include Li x My (PO 4 ) 3 (1 ⁇ x ⁇ 2, 1 ⁇ y ⁇ 2, M is titanium (Ti), germanium (Ge), aluminum (Al ), gallium (Ga), and zirconium (Zr).
  • An example of a lithium-containing phosphoric acid compound having a Nasicon structure includes Li 1.2 Al 0.2 Ti 1.8 (PO 4 ) 3 and the like.
  • oxides having a perovskite structure include La 0.55 Li 0.35 TiO 3 and the like.
  • An example of an oxide having a garnet type or garnet type similar structure includes Li 7 La 3 Zr 2 O 12 and the like.
  • the sulfide-based crystal material examples include thio-LISICON, such as Li 3.25 Ge 0.25 P 0.75 S 4 and Li 10 GeP 2 S 12 .
  • the crystalline solid electrolyte may include a polymeric material (eg, polyethylene oxide (PEO), etc.).
  • Examples of the glass-based solid electrolyte include oxide-based glass materials and sulfide-based glass materials.
  • oxide glass material include 50Li 4 SiO 4 .50Li 3 BO 3 .
  • Sulfide glass materials include , for example, 30Li 2 S.26B 2 S 3.44LiI, 63Li 2 S.36SiS 2.1Li 3 PO 4 , 57Li 2 S.38SiS 2.5Li 4 SiO 4 and 70Li 2 S. Examples include 30P 2 S 5 and 50Li 2 S.50GeS 2 .
  • the glass-ceramic solid electrolyte examples include oxide-based glass-ceramic materials and sulfide-based glass-ceramic materials.
  • oxide-based glass-ceramic material for example, a phosphoric acid compound (LATP) containing lithium, aluminum, and titanium as constituent elements, and a phosphoric acid compound (LAGP) containing lithium, aluminum, and germanium as constituent elements can be used.
  • LATP is, for example, Li 1.07 Al 0.69 Ti 1.46 (PO 4 ) 3 .
  • LAGP is, for example, Li 1.5 Al 0.5 Ge 1.5 (PO 4 ).
  • examples of the sulfide-based glass ceramic materials include Li 7 P 3 S 11 and Li 3.25 P 0.95 S 4 .
  • Examples of the solid electrolyte that can conduct sodium ions include sodium-containing phosphoric acid compounds having a Nasicon structure, oxides having a perovskite structure, and oxides having a garnet type or garnet type similar structure.
  • sodium-containing phosphate compound having a Nasicon structure Na x My (PO 4 ) 3 (1 ⁇ x ⁇ 2, 1 ⁇ y ⁇ 2, M is from the group consisting of Ti, Ge, Al, Ga and Zr) at least one selected type).
  • the solid electrolyte may contain a sintering aid.
  • the sintering aid contained in the solid electrolyte may be selected from, for example, the same materials as the sintering aid that may be contained in the positive electrode layer and the negative electrode layer.
  • the thickness of the solid electrolyte is not particularly limited.
  • the thickness of the solid electrolyte layer located between the positive electrode layer and the negative electrode layer may be, for example, 1 ⁇ m or more and 15 ⁇ m or less, particularly 1 ⁇ m or more and 5 ⁇ m or less.
  • the solid battery 100 is generally provided with an end electrode 140.
  • an end surface electrode 140 is provided on the side surface 100C of the solid battery 100.
  • a positive end surface electrode 140A connected to the positive electrode layer 110 and a negative end surface electrode 140B connected to the negative electrode layer 120 are provided (see FIG. 1).
  • such end electrodes include a material with high electrical conductivity.
  • Specific materials for the end electrodes are not particularly limited, but may include at least one selected from the group consisting of silver, gold, platinum, aluminum, copper, tin, and nickel.
  • the present disclosure is a packaged solid state battery.
  • it is a packaged solid-state battery that includes a mountable substrate and has a configuration in which the solid-state battery is protected from the external environment.
  • FIG. 2 is a cross-sectional view schematically showing the configuration of a packaged solid-state battery according to an embodiment of the present disclosure.
  • a packaged solid state battery 1000 according to an embodiment of the present disclosure includes a substrate 200 on which the solid state battery 100 is supported.
  • packaged solid state battery 1000 includes a mountable substrate 200 and solid state battery 100 provided on substrate 200 and protected from the external environment.
  • the substrate 200 has a main surface larger than, for example, a solid state battery.
  • the substrate 200 may be a resin substrate or a ceramic substrate.
  • the board 200 may fall into the categories of a printed wiring board, a flexible board, an LTCC board, or an HTCC board.
  • the substrate 200 may be a substrate configured to include resin as a base material, for example, a layered structure of the substrate may include a resin layer.
  • the resin material of such a resin layer may be any thermoplastic resin and/or any thermosetting resin.
  • the resin layer may be formed by, for example, impregnating glass fiber cloth with a resin material such as epoxy resin.
  • the substrate is preferably a member for external terminals of the packaged solid state battery.
  • the substrate serves as a terminal substrate for the external terminals of the solid-state battery.
  • a packaged solid state battery equipped with such a substrate can be mounted on another secondary substrate such as a printed wiring board with the substrate interposed therebetween.
  • a solid state battery can be surface mounted via a substrate through solder reflow or the like.
  • the packaged solid state battery of the present disclosure is preferably an SMD (Surface Mount Device) type battery package.
  • Such a substrate can also be understood as a support substrate, as it can be provided to support a solid-state battery.
  • the substrate is a terminal board, it is preferable that the substrate has wiring or an electrode layer, and particularly preferably an electrode layer that electrically connects the upper and lower surfaces or the upper and lower surfaces.
  • a substrate in a preferred embodiment includes wiring or electrode layers that electrically connect the upper and lower surfaces of the substrate, and serves as a terminal substrate for external terminals of a packaged solid-state battery.
  • the wiring on the board can be used to take out the solid state battery to the external terminal, so there is no need to pack it in the exterior part and take it out to the outside of the exterior part, which will be described later, and the degree of freedom in designing the external terminal is increased. There is.
  • a substrate 200 includes electrode layers (an upper main surface electrode layer 210, a lower main surface electrode layer 220) that electrically connects the upper and lower main surfaces of the substrate, and is a packaged solid state. It is a member for the external terminal of the battery (see Figure 2).
  • the electrode layer of the substrate and the terminal portion of the solid-state battery are connected to each other.
  • the electrode layer of the substrate and the end face electrode of the solid state battery are electrically connected to each other.
  • the end face electrode 140A on the positive electrode side of the solid state battery is electrically connected to the electrode layer (210A, 220A) on the positive electrode side of the substrate.
  • the end face electrode 140B on the negative electrode side of the solid battery is electrically connected to the electrode layer (210B, 220B) on the negative electrode side of the substrate.
  • the electrode layers on the positive and negative sides of the substrate are respectively connected to the positive electrode terminal of the packaged solid-state battery. and will be used as a negative terminal.
  • a bonding member 600 is used to connect the end electrode 140 of the solid battery 100 and the substrate electrode layer 210 of the substrate 200. Can be connected via.
  • This joining member 600 is responsible for at least the electrical connection between the end face electrode 140 of the solid battery 100 and the substrate 200, and may contain, for example, a conductive adhesive.
  • the bonding member 600 may be made of an epoxy conductive adhesive containing a metal filler such as Ag.
  • the solid state battery package 1000 may be covered with the exterior part 150 so that the solid state battery 100 provided on the substrate 200 is completely surrounded.
  • the "exterior part” in this specification refers to a covering member that surrounds the solid state battery 100 on the substrate 200, and the "exterior part” can also be referred to as a "covering part” or a "package part.”
  • the solid battery 100 on the substrate 200 may be packaged so that the main surface 100A and the side surface 100C are surrounded by the exterior part 150. According to this configuration, all the surfaces forming the solid-state battery 100 are not exposed to the outside, so that it is possible to suitably prevent water vapor from permeating (that is, water vapor from entering the solid-state battery).
  • water vapor as used herein is not particularly limited to water in a gaseous state, but also includes water in a liquid state.
  • water vapor is used to broadly encompass water in a gaseous state, water in a liquid state, etc., regardless of its physical state. Therefore, “water vapor” can also be referred to as moisture, and in particular, water in a liquid state may also include condensed water, which is water in a gaseous state condensed. Since the infiltration of water vapor into a solid-state battery causes deterioration of battery characteristics, the form of the solid-state battery packaged as described above contributes to extending the life of the battery characteristics of the solid-state battery.
  • the exterior portion 150 may be comprised of a covering insulating layer 160 and a covering inorganic layer 170.
  • the solid state battery 100 may have a configuration in which the exterior portion 150 is covered with a covering insulating layer 160 and a covering inorganic layer 170.
  • the covering inorganic layer 170 is provided to cover the covering insulating layer 160. Since the covering inorganic layer 170 is positioned on the covering insulating layer 160, the covering inorganic layer 170 has a shape that largely envelops the solid battery 100 on the substrate 200 together with the covering insulating layer 160. Furthermore, the covering inorganic layer 170 can also cover the side surface 250 of the substrate 200.
  • the insulating cover layer 160 is formed so as to form a suitable water vapor barrier in combination with the inorganic cover layer 170, and the inorganic cover layer 170 also forms a suitable water vapor barrier in combination with the insulating cover layer 160.
  • the covering insulating layer 160 may extend onto the side surface 250 of the substrate.
  • the covering insulating layer 160 covering the top surface region 100B and the side surface region 100C of the solid-state battery may also cover the side surface 250 of the substrate, and the covering inorganic layer 170 may be provided on the covering insulating layer 160.
  • the material of the covering insulating layer may be any type as long as it exhibits insulation properties.
  • the covering insulating layer may contain a resin, and the resin may be either a thermosetting resin or a thermoplastic resin.
  • the insulating coating layer may contain an inorganic filler.
  • the covering insulating layer may be made of an epoxy resin containing an inorganic filler such as SiC.
  • the material of the covering inorganic layer is not particularly limited, and may be metal, glass, oxide ceramics, or a mixture thereof.
  • the covering inorganic layer may correspond to an inorganic layer in the form of a thin film, for example a metal film.
  • the coating inorganic layer contains Cu (copper), Sn (tin), Zn (zinc), Bi (bismuth), Au (gold), Ag (silver), Ni (nickel), Cr (chromium),
  • the plating film may include at least one member selected from the group consisting of Pd (palladium) and Pt (platinum).
  • the coating inorganic layer is made of a Cu-based and/or Ni-based material formed by plating and having a size of 2 ⁇ m or more and 50 ⁇ m or less.
  • the present disclosure has a technical concept of "a structure including a gap between the end electrode and the exterior part". More specifically, the present disclosure has a technical idea of ⁇ a structure including a gap between the end electrode and the exterior part, and the end electrode and the exterior part being separated by the gap.''
  • the solid state battery 100 disposed on the substrate 200 includes an end face electrode 140 provided on the side surface 100C of the solid state battery 100.
  • the exterior part 150 is provided so as to surround the solid battery 100 on the substrate 200 along with the end electrode 140.
  • FIG. 3 is an enlarged cross-sectional view schematically showing part A, which is a part of the boundary area between the end electrode 140 and the exterior part 150, in the packaged solid-state battery 1000 shown in FIG.
  • a gap 180 is included between the end electrode 140 and the exterior portion 150. That is, the end electrode 140 and the exterior part 150 may face each other with the gap 180 interposed therebetween.
  • the exterior part 150 may be provided so as to cover the solid battery 100 with a gap formed between the exterior part 150 and the end electrode 140 via the void part 180 .
  • the end electrode 140 and the exterior part 150 may be separated from each other with a gap 180 interposed therebetween. That is, the packaged solid-state battery of the present disclosure includes a portion where the solid-state battery 100 and the exterior portion 150 are spaced apart from each other and a portion where the solid-state battery 100 and the exterior portion 150 are in contact. In such a configuration, the spaced apart opposing portions may be located between the end electrode 140 and the exterior portion 150. In short, the packaged solid state battery of the present disclosure includes a portion where the end electrode 140 and the exterior portion 150 face each other and are separated from each other. This means that the exterior part 150 can be provided so as to cover the solid state battery with end electrodes, at least partially separated from the end electrodes 140.
  • the solid battery 100 covered by the exterior part 150 includes a first main surface 100A facing the substrate 200 and a second main surface 100B located opposite the first main surface 100A. That is, assuming a typical solid state battery that has two opposing main surfaces, the second main surface 100B located opposite to the substrate 200 is the main surface on the mounting surface side in the SMD type. It may also be referred to as a "bottom surface” or “lower surface.” Further, the second main surface 100B refers to a main surface located on the opposite side of the first main surface 100A, and can also be referred to as a "top surface", “top surface”, or "upper surface”.
  • the "side surface of the solid-state battery” means the surface connecting the first main surface 100A and the second main surface 100B.
  • the end surface electrode 140 may be provided on each of two mutually opposing side surfaces 100C of the solid state battery 100. Specifically, as shown in FIG. 1, a positive end surface electrode 140A connected to the positive electrode layer 110 and a negative end surface electrode 140B connected to the negative electrode layer 120 are arranged on two side surfaces 100C facing each other. It's okay to stay.
  • the cavity 180 may be provided in at least one of the positive end surface electrode 140A and the negative end surface electrode 140B. That is, the exterior part 150 may cover the solid battery, including a portion that faces and is spaced apart from at least one of the positive end surface electrode 140A and the negative end surface electrode 140B.
  • the exterior portion 150 may include the covering insulating layer 160.
  • an insulating cover layer 160 is provided to cover the solid battery 100, and an inorganic cover layer 170 is provided on the insulating cover layer 160.
  • the end electrode 140 may include a gap 180 between the end electrode 140 and the covering insulating layer 160.
  • the end electrode 140 and the covering insulating layer 160 may face each other and be separated from each other with the gap 180 interposed therebetween.
  • a force that pulls the solid battery 100 in the direction of expansion and contraction may act on the end electrode 140.
  • the direction of expansion and contraction is the same direction as the direction in which the end electrodes 140 extend (see FIG. 1). That is, the direction of expansion and contraction can also be understood to be the same direction as the extending direction of the side surface 100C of the solid battery.
  • the end face electrode 140 is joined to the solid state battery 100.
  • the exterior part 150 is disposed on the solid battery 100 via the end electrode 140 in a region covering the end electrode 140.
  • the force acting in the extending direction of the end electrode 140 due to expansion and contraction of the solid battery is difficult to propagate to the exterior part 150. Therefore, the exterior portion 150 may have poor ability to follow the expansion and contraction of the solid state battery 100.
  • the exterior part 150 may be inferior in ability to follow the expansion and contraction of the solid battery 100 compared to the end electrode 140. Therefore, when the end electrode 140 and the exterior part 150 are bonded to each other, the exterior part 150 restrains the end electrode 140 at the joint surface with the end electrode 140 (i.e., the outer surface 145 of the end electrode). , deformation of the end electrode 140 that follows the expansion and contraction of the solid battery 100 can be suppressed. As a result, when the solid battery 100 expands and contracts, the outer surface 145 of the end electrode 140 is not easily deformed due to the restraint by the exterior part 150, while the inner surface of the end electrode 140 that is physically connected to the solid battery 100 is hard to deform. The side surface easily deforms following the expansion and contraction. As a result, the ease of deformation is different between the inner surface of the end electrode 140 and the outer surface 145 of the end electrode joined to the exterior part 150, which may cause distortion inside the end electrode 140. There is a possibility that the end electrode 140 may be damaged.
  • the outer surface 145 of the end electrode located on the exterior part 150 side includes a portion separated from the exterior part 150 by the cavity 180, so that the outer surface of the end electrode is not restricted by the exterior part 150. That is, by providing the gap 180 between the end electrode 140 and the exterior part 150, the restriction of the outer side of the end electrode 140 by the exterior part 150 can be relaxed as a whole. Therefore, when the end electrode 140 deforms due to a volume change such as expansion and contraction of the solid battery 100, the influence of restraint by the exterior part 150 can be reduced. As a result, distortion within the end electrode 140 caused by expansion and contraction of the solid battery 100 can be suppressed, and the risk of damage to the end electrode 140 can be reduced.
  • the exterior part 150 is in physical contact with the second main surface 100B of the solid battery. Therefore, when the solid battery 100 expands and contracts in the stacking direction of the electrode layers, the exterior part 150 located on the second main surface 100B of the solid battery can suitably follow the expansion and contraction direction of the solid battery 100. . Furthermore, the exterior portion 150 is also bonded to a substrate 200 on which the solid battery 100 is placed. Such bonding can play a role in helping suitably hold the exterior part 150 on the solid state battery 100. Therefore, even in the embodiment in which the gap 180 is formed between the end electrode 140 and the exterior part 150 as described above, the exterior part 150 is easily damaged and/or peeled off due to deformation due to expansion and contraction of the solid battery. It can be suitably held on the solid state battery 100 without having to do so.
  • the end electrode 140 and the exterior part 150 do not necessarily have to be completely separated. In other words, the end electrode 140 may be partially in contact with the exterior part 150.
  • the end electrode 140 includes a non-contact portion 145A and a contact portion 145B with the exterior portion 150 (see FIG. 4). According to this configuration, the contact portion 145B can contribute to supporting the exterior portion 150 on the end surface electrode 140. For example, even when stress is applied near the cavity 180, the stress is suitably dispersed to the end electrode 140 and/or the exterior portion 150 by the contact portion 145B, and damage to the end electrode 140 and the exterior portion 150 can be prevented. .
  • the strength of the exterior portion 150 as a whole can be improved. Further, in the contact portion 145B, the end electrode 140 can be held on the solid battery 100 by the exterior portion 150.
  • the contact portion 145B between the end electrode 140 and the exterior part 150 can suitably hold the end electrode 140 on the solid-state battery, and can help prevent the end electrode 140 from peeling off from the solid-state battery.
  • the contact portion between the end surface electrode 140 and the exterior portion 150 may be at least the end portion 141 of the end surface electrode 140.
  • the end electrode 140 has at least one of a substrate side end 141a located on the first main surface 100A side of the solid battery and a top surface side end 141b located on the second main surface 100B side. It may be in contact with the exterior part 150.
  • the "top side end” and the “bottom side end” respectively refer to the end 141 located on the distal side with respect to the substrate 200 and the end portion 141 located on the proximal side with respect to the substrate 200 in the end electrode 140. This corresponds to the end portion 141. That is, the contact portion between the end electrode 140 and the exterior part 150 may be positioned at the end 141 of the end electrode located on the second main surface 100B side and/or the substrate 200 side of the solid battery.
  • the exterior portion 150 includes a contact portion with the end portion 141 of the end electrode, the joint portion between the end portion 141 of the end electrode and the solid battery 100 is covered by the exterior portion 150.
  • the end portion 141 of the end electrode can be suitably held between the solid battery by the exterior portion 150. Therefore, it may be possible to suitably prevent the end face electrode from peeling off from the solid state battery due to expansion and contraction of the solid state battery 100.
  • the infiltration of water vapor from the joint between the end electrode 140 and the solid battery 100 into the solid battery 100 is suitably suppressed. obtain. That is, according to the present disclosure, it is possible to provide a packaged solid-state battery that both reduces the risk of damage to the end electrodes due to expansion and contraction and prevents water vapor from entering the solid-state battery.
  • FIG. 5 is a cross-sectional view schematically showing a packaged solid-state battery according to another embodiment.
  • the end surface electrode 140 may extend to at least one of the first main surface 100A and the second main surface 100B of the solid state battery. That is, the end portion 141 of the end electrode may extend to at least one of the first main surface 100A and the second main surface 100B of the solid battery.
  • the end surface electrode extends to the first main surface 100A, so that the bonding area between the end surface electrode 140 and the bonding member 600 can be made larger. Therefore, the above-described structure can contribute to improving the connection reliability between the end face electrode 140 and the joining member 600.
  • the exterior part 150 may be in contact with the end electrode 140 at the end 141 of the end electrode positioned on the first main surface 100A and/or the second main surface 100B.
  • the contact portion between the exterior portion 150 and the end electrode 140 may be positioned at the end 141 of the end electrode extending on the first main surface 100A and/or the second main surface 100B.
  • the end electrode 140 can extend along the side surface 100C, and the first main surface 100A and/or the second main surface 100B of the solid state battery. That is, since the bonding area between the end electrode 140 and the solid battery 100 becomes larger, it may be possible to suitably prevent separation of the end electrode due to a change in the volume of the solid battery. Furthermore, the exterior part 150 and the end electrode 140 are joined to each other at the end 141 of the end electrode extending on the first main surface 100A and/or the second main surface 100B, so that the end electrode 140 is It can be suitably held on the solid battery 100 by the portion 150. Thereby, peeling of the end face electrode from the solid battery due to expansion and contraction of the solid battery can be more preferably prevented.
  • FIG. 4 is an enlarged cross-sectional view schematically showing the boundary region between the end electrode 140 and the exterior part 150 in another embodiment of the present disclosure.
  • the packaged solid state battery may include a plurality of voids 180.
  • the plurality of voids 180 may be formed intermittently along the end electrode 140. That is, in the end electrode 140, a plurality of contact portions 145B and a plurality of non-contact portions 145A with the exterior portion 150 may be provided, so that a plurality of void portions 180 may be formed intermittently.
  • interruptedly formed voids does not necessarily mean that the plurality of voids 180 are each formed independently.
  • the plurality of voids 180 may be in a state where adjacent voids 180 are partially connected to each other.
  • the inner surface 155 of the exterior portion facing the end electrode 140 may be a surface including irregularities in cross-sectional view.
  • the contact portions 145B and non-contact portions 145A between the end electrode 140 and the exterior portion 150 may be alternately and repeatedly provided.
  • the plurality of voids 180 may be provided irregularly or substantially regularly along the end electrode.
  • non-contact portions 145A where the end electrode 140 is not restrained by the exterior portion 150 are provided at multiple locations on the end electrode 140. This makes it possible to avoid localization of the unrestricted portion and the restricted portion of the end electrode. Therefore, the strain that occurs in the end electrodes due to expansion and contraction of the solid-state battery is more effectively alleviated as a whole, and the risk of damage to the end electrodes can be suitably reduced.
  • the non-contact portion 145A suppresses the occurrence of distortion in the end electrode 145, and the contact portion 145B connects the end electrode 145 to the solid state battery. It can be suitably maintained at 100.
  • the cavity 180 has an elongated shape extending along the end electrode 140 in cross-sectional view.
  • the cross-sectional shape of the cavity 180 may be an elongated shape or a flat shape along the direction in which the end electrode 140 extends.
  • the cross-sectional shapes of the voids 180 do not necessarily have to be the same, and may have mutually different cross-sectional shapes.
  • the cross-sectional shapes of the plurality of voids 180 may be elongated shapes with different dimensions.
  • the cavity 180 having an elongated cross-sectional shape may extend along the main surface region 143 of the end electrode.
  • the cavity 180 has an elongated cross-sectional shape extending along the outer surface 145 of the main surface region 143 of the end electrode.
  • the "principal surface area of the end electrode” means the area of the end electrode 140 located on the side surface 100C of the solid battery. That is, the cavity 180 may be located on the end electrode 140 located on the side surface 100C of the solid battery.
  • the end electrode 140 is separated from the exterior part 150 over a wider area, and the restriction of the end electrode 140 by the exterior part 150 can be more effectively relaxed. Therefore, the end surface electrode can more suitably follow the volume change of the solid battery, and distortion that may occur in the end surface electrode is suppressed, thereby reducing the risk of breakage of the end surface electrode.
  • the cross-sectional shape of the cavity 180 may correspond to the cross-sectional shape of the outer surface 145 of the end electrode.
  • the cavity 180 may have a shape corresponding to the cross-sectional shape of the outer contour forming surface of the end electrode 140.
  • the cavity 180 may have an elongated cross-sectional shape curved along the curved portion.
  • the cavity 180 can extend along the outer surface 145 of the end electrode so as to have a constant width when viewed in cross section.
  • the end surface electrode 140 and the exterior part 150 may include portions that face each other with a certain distance between them.
  • the restraining force of the end electrode 140 by the exterior part 150 is more appropriately reduced, so even if the end electrode 140 is deformed due to expansion and contraction of the solid battery 100, excessive strain is caused inside the end electrode 140. Therefore, the risk of damage to the end electrode 140 can be reduced.
  • the void portion 180 may be continuous over the entire main surface region 143 of the end electrode.
  • the end electrode 140 may face the exterior portion 150 at a distance over the entire main surface region 143.
  • the cavity 180 may have an elongated cross-sectional shape extending across the main surface region 143 of the end electrode, as shown in FIGS. 2 and 5.
  • the void portion 180 may communicate not only in the plan view direction but also in the cross-sectional direction. That is, the void portion 180 may be two-dimensionally continuous across the main surface region 143 of the end electrode.
  • the width W of the cavity 180 may be 1 ⁇ m or more and 50 ⁇ m or less, 1 ⁇ m or more and 30 ⁇ m or less, or 1 ⁇ m or more and 25 ⁇ m or less, for example, 2 ⁇ m or more and 10 ⁇ m or less (see FIG. 3).
  • the width W of the gap can also be understood as the distance by which the end electrode 140 and the exterior part 150 are separated from each other by the gap 180 and face each other. It should be noted that the above-mentioned width W of the gap can be changed as appropriate depending on the size of the solid-state battery, the thickness of the end electrode, the thickness of the exterior part, and the like. For example, as shown in FIG. 4, the plurality of voids 180 may have different widths.
  • the non-contact portion 145A between the exterior portion 150 and the end electrode 140 may be larger than the contact portion 145B (see FIG. 4).
  • the contact ratio between the exterior portion 150 and the end electrode 140 may be smaller than 50%.
  • the non-contact portion 145A may occupy 50% or more of the outer surface 145 of the end electrode.
  • the ratio of the non-contact portion 145A to the length of the outer surface of the end electrode is 50% or more and 100% or less, 60% or more and 99% or less, or 65% or more and 99% or less. For example, it may be 70% or more and 95% or less.
  • the end electrode can suitably follow the expansion and contraction of the solid-state battery, and the change due to the volume change of the solid-state battery can be avoided. The risk of breakage of the end face electrode can be reduced.
  • the end electrode 140 may be provided to cover the corner of the solid state battery.
  • corner of a solid-state battery means a corner between the main surface 100A or 100B and the side surface 100C of the solid-state battery, and the corner where the main surface 100A or 100B and the two side surfaces 100C intersect. It includes both the corner and the ridge between the main surface 100A or 100B and the side surface 100C.
  • the solid-state battery 100 includes a first corner 102a located on the proximal side with respect to the substrate 200, and a second corner 102b located on the distal side with respect to the substrate 200, and includes an end electrode 140.
  • the end electrode 140 covering the first corner 102a can be referred to as a first corner covering region 142a
  • the end electrode 140 covering the second corner 102b can be referred to as a second corner covering region 142b.
  • FIG. 6 is an enlarged cross-sectional view schematically showing a portion B, which is a connecting portion between the end electrode 140 and the joining member, in the packaged solid-state battery 1000 shown in FIG. 5.
  • the thickness Ta of the first corner covering region 142a may be larger than the thickness of other regions other than the first corner covering region 142a.
  • the thickness of the corner covering region means the thickness of the end surface electrode 140 in the extending direction of the main surface of the solid battery. Specifically, from the contact point between the corner of the solid battery covered by the corner covering region and the inner surface of the end electrode 140, to the extension line in the extending direction of the main surface of the solid battery and the outside of the end electrode. It means the distance to the intersection with the side surface 145.
  • the end electrode 140 covering the first corner 102a may have a larger thickness than other regions.
  • the end face electrode 140 may be provided so as to be relatively thick in the first corner covering region 142a when viewed in cross section.
  • the stress that acts from the solid battery 100 side to the substrate 200 side can increase as it goes from the solid battery 100 to the end electrode 140 side. That is, among the stresses that act from the solid battery 100 side to the substrate 200 side, the stress along the end electrode 140 can be relatively the largest. In particular, a larger stress can act on the first corner covering region 142a that covers the first corner 102a located on the substrate 200 side, so there is a possibility that the first corner covering region 142a is damaged by such stress.
  • a packaged solid-state battery is provided in which the connection reliability of the end electrodes is improved by including the end electrodes having a relatively large thickness in the first corner covering region 142a. obtain.
  • the thickness Ta of the first corner covering region 142a of the end electrode is equal to the thickness Tb of the second corner covering region 142b located on the distal side with respect to the substrate 200 (FIG. Reference) Bigger is better.
  • the stress caused by the expansion and contraction of the solid-state battery is applied to the second corner 102b located on the second main surface 100B side of the solid-state battery, which is located closer to the connection point with the substrate 200. It may become larger on the first corner 102a side. Therefore, in cross-sectional view, the first corner covering region 142a may have a greater thickness than the second corner covering region 142b. According to such a structure, a packaged solid-state battery can be provided in which the risk of damage to the end face electrode in the corner covering region is reduced.
  • the ratio of the thickness Ta of the first corner covering region 142a to the thickness Tb of the second corner covering region 142b of the end electrode is 101% or more and 500% or less, 200% or more and 400% or less, or 280%. It may be greater than or equal to 370%, and may be, for example, greater than or equal to 300% and less than or equal to 350%.
  • a packaged solid state battery with improved connection reliability of the end electrode can be provided.
  • the thickness Ta of the end surface electrode 140 in the first corner covering region 142a may be larger than the thickness Tc of the end surface electrode 140 in the main surface region 143 located on the side surface 100C of the solid battery.
  • the thickness of the end electrode 140 gradually increases from the region on the substrate 200 side in the main surface region to the first corner covering region 142a. It's okay to do so. According to such a structure, a packaged solid-state battery can be provided in which the risk of damage to the end face electrode in the corner covering region is reduced.
  • the structure of the packaged solid-state battery in this specification is obtained by cutting out a cross section in the cross-sectional view direction using an ion milling device (manufactured by Hitachi High-Tech Corporation, model number SU-8040), and using a scanning electron microscope (SEM) (manufactured by Hitachi High-Tech Corporation, model number SU-8040). ) may be used for observation from images obtained using Furthermore, the dimensions of the void portion and the end electrodes as used herein may refer to values calculated from dimensions measured from images acquired by the method described above.
  • the object of the present disclosure is obtained by preparing a solid battery including a battery constituent unit having a positive electrode layer, a negative electrode layer, and a solid electrolyte between these electrodes, and then packaging the solid battery. (See Figures 7A-7E).
  • the production of the solid-state battery of the present disclosure can be broadly divided into production of the solid-state battery itself (hereinafter also referred to as "pre-packaged battery"), which corresponds to the stage before packaging, preparation of the substrate, and packaging. .
  • the pre-packaged battery can be manufactured by a printing method such as a screen printing method, a green sheet method using a green sheet, or a combination thereof.
  • the pre-packaged battery itself may be manufactured according to the conventional manufacturing method of solid-state batteries (therefore, the solid electrolyte, organic binder, solvent, optional additives, positive electrode active material, negative electrode active material, etc. described below)
  • the raw materials used in the production of known solid-state batteries may be used).
  • (Laminated block formation) Prepare a slurry by mixing the solid electrolyte, organic binder, solvent, and optional additives. Next, a sheet containing a solid electrolyte is formed from the prepared slurry by firing. -Create a positive electrode paste by mixing the positive electrode active material, solid electrolyte, conductive material, organic binder, solvent, and optional additives. Similarly, a negative electrode paste is prepared by mixing the negative electrode active material, solid electrolyte, conductive material, organic binder, solvent, and optional additives. - Print a positive electrode paste on the sheet, and also print a current collecting layer and/or a negative layer as necessary.
  • a negative electrode paste is printed on the sheet, and if necessary, a current collecting layer and/or a negative layer are printed.
  • a laminate by alternately stacking sheets printed with positive electrode paste and sheets printed with negative electrode paste.
  • the outermost layer (the uppermost layer and/or the lowermost layer) of the laminate may be an electrolyte layer, an insulating layer, or an electrode layer.
  • the laminate is crimped and integrated, it is cut into a predetermined size.
  • the obtained cut laminate is subjected to degreasing and firing. Thereby, a fired laminate is obtained.
  • the laminate may be degreased and fired before cutting, and then the laminate may be cut.
  • the end electrode 140A on the positive electrode side can be formed by applying a conductive paste to the exposed side surface of the positive electrode in the fired laminate.
  • the negative end electrode 140B can be formed by applying a conductive paste to the exposed side surface of the negative electrode in the fired laminate.
  • the end face electrodes 140 on the positive electrode side and the negative electrode side may be provided so as to extend to the main surface of the fired laminate.
  • the component of the end electrode may be selected from at least one selected from silver, gold, platinum, aluminum, copper, tin, and nickel.
  • end face electrodes 140 on the positive electrode side and the negative electrode side are not limited to being formed after firing the laminate, but may be formed before firing and subjected to simultaneous firing.
  • a desired pre-packaged battery (corresponding to the solid state battery 100 shown in FIG. 7A) can finally be obtained.
  • the outer surface 145 of the end electrode may be treated to form a gap between the end electrode 140 and the exterior part.
  • the gap between the end electrode 140 and the exterior part may be formed by applying a gap forming agent 190 before forming the exterior part (see FIG. 7B).
  • a gap forming agent 190 for forming a void portion may be applied to the end electrode 140.
  • the void forming agent 190 only needs to be applied to the portions of the end electrode 140 where voids are to be provided.
  • the void-forming agent 190 may be applied over the entirety of the end electrode 140, or only in some areas of the end electrode, such as the main surface area 143 of the end electrode located on the side of the solid state battery (see FIG. 5). ) may be applied only to
  • Examples of the void forming agent that can be used include known materials that vaporize near the heating temperature during mold processing for forming the covering insulating layer 160 (see FIG. 7C), which will be described later. Any material may be selected as the void-forming agent depending on the conditions for forming the insulating coating layer (for example, heating temperature, etc.).
  • examples of such void-forming agents include wax-based materials such as paraffin wax and microcrystalline wax.
  • the void-forming agent vaporizes when heated during the molding process for forming the insulating covering layer, disappears by permeating the insulating covering layer, and as a result, the end electrode 140 A void is formed between the insulating layer and the insulating covering layer.
  • the void forming agent may be a material that reduces the adhesion between the end electrode 140 and the exterior part.
  • the void forming agent may be a known material that improves the releasability of the exterior part provided on the end electrode 140 from the end electrode.
  • examples of such void-forming agents include fluorine-based materials, silicone-based materials, and wax-based materials.
  • the void forming agent may be a foamable material such as a foamed resin.
  • the foamed resin may be a resin that is foamed to form a foam during molding of the exterior part.
  • the foamed resin is not particularly limited, and any known foamed resin used for foam molding of resin can be used.
  • the foamable material may be a thermoplastic resin blended with at least one of a chemical foaming agent and foam beads.
  • the packaged solid state battery may contain a void forming agent.
  • the substrate is prepared.
  • a resin substrate when used as the substrate, it may be prepared by laminating a plurality of layers and subjecting them to heating and pressure treatment.
  • a substrate precursor is formed using a resin sheet made by impregnating a fiber cloth serving as a base material with a resin raw material. After forming the substrate precursor, the substrate precursor is heated and pressurized using a press.
  • a ceramic substrate when used as a substrate, its preparation is, for example, by thermocompression bonding a plurality of green sheets to form a green sheet laminate, and by subjecting the green sheet laminate to firing to obtain a ceramic substrate. I can do it.
  • the ceramic substrate can be prepared, for example, in accordance with the preparation of an LTCC substrate.
  • a semirac substrate may have vias and/or lands.
  • holes may be formed in the green sheet using a punch press or carbon dioxide laser, and the holes may be filled with conductive paste material, or vias, lands, etc. may be formed by printing or the like. may form a precursor of the electrically conductive portion. Note that the lands and the like can also be formed after the green sheet laminate is fired.
  • the desired substrate 200 can finally be obtained.
  • the pre-packaged battery 100 is placed on the substrate 200. That is, an "unpackaged solid-state battery” is placed on the substrate (hereinafter, the battery used for packaging is also simply referred to as a “solid-state battery”).
  • the solid-state battery 100 is placed on the substrate so that the conductive portion of the substrate and the end electrode 140 of the solid-state battery 100 are electrically connected to each other.
  • a conductive paste may be provided on the substrate, thereby electrically connecting the conductive portion of the substrate and the end electrode 140 of the solid state battery 100 to each other.
  • the conductive parts on the positive and negative sides of the main surface of the substrate are aligned with the positive and negative end surface electrodes 140 of the solid battery 100, respectively. Alignment is performed, and connections are made using conductive paste (for example, Ag conductive paste). That is, a precursor of a bonding member responsible for electrical connection between the solid state battery 100 and the substrate may be provided on the substrate in advance.
  • the precursor of such a joining member can be provided by printing a conductive paste that does not require cleaning with flux or the like after formation, such as nanopaste, alloy paste, brazing material, etc. .
  • the solid state battery 100 is placed on the substrate so that the end electrode 140 and the precursor of the bonding member are in contact with each other, and heat treatment is performed to form an electrical connection between the solid state battery 100 and the board from the precursor.
  • a joining member that contributes to this process is formed.
  • the exterior portion 150 is formed.
  • a covering insulating layer 160 and a covering inorganic layer 170 may be provided.
  • the covering insulating layer 160 is formed so as to cover the solid battery 100 on the substrate 200 (see FIG. 7C). Therefore, the raw material for the covering insulating layer is provided so that the solid state battery 100 on the substrate is completely covered.
  • the insulating cover layer is made of a resin material
  • the insulating cover layer is formed by providing a resin precursor on the substrate and subjecting it to curing.
  • the covering insulating layer may be formed by applying pressure with a mold.
  • the overlying insulating layer encapsulating the solid state battery 100 on the substrate may be molded through compression molding.
  • the raw material for the insulating coating layer may be in the form of granules, and may be thermoplastic. Note that such molding is not limited to mold molding, and may be performed through polishing, laser processing, and/or chemical treatment.
  • a gap 180 is formed between the end electrode 140 and the insulating cover layer 160 by the gap forming agent 190 applied onto the end electrode 140 as described above (see FIG. 7D).
  • the void portion 180 may be formed by vaporizing and disappearing the void forming agent by heating during the molding process of the covering insulating layer 160.
  • the covering inorganic layer 170 is formed (see FIG. 7E).
  • the coating inorganic layer 170 may be formed by plating a coating precursor.
  • the coating inorganic layer is formed on the coating precursor by forming a plating film on an exposed surface other than the bottom surface of the coating precursor (ie, other than the bottom surface of the supporting substrate).
  • the covering inorganic layer may extend to the main surface of the substrate on the bottom side, which is located on the opposite side to the main surface of the substrate facing the solid-state battery.
  • the insulating coating layer and/or the inorganic coating layer as the exterior part extends to the side surface of the substrate, and extends beyond the side surface to the bottom main surface of the substrate (particularly its peripheral portion). It's okay.
  • a packaged solid-state battery can be provided in which moisture infiltration from the outside into the solid-state battery is more preferably prevented.
  • the covering inorganic layer can also be provided as a multilayer structure consisting of at least two layers.
  • a multi-layer structure is not limited to materials of different types, but may be formed between materials of the same type.
  • the covering inorganic layer may have a multilayer structure in which two or more dry plating films formed by dry plating and two or more wet plating films formed by wet plating are laminated in any order.
  • a coating inorganic layer having such a multilayer structure it is easier to configure a water vapor barrier for a solid-state battery more suitably.
  • a water vapor barrier layer may be formed on the substrate.
  • a water vapor barrier may be formed on the substrate before packaging the substrate and the solid-state battery.
  • the water vapor barrier layer is not particularly limited as long as it can form a desired barrier layer.
  • a water vapor barrier layer having Si--O bonds and Si--N bonds it is preferably formed by applying a liquid raw material and irradiating with ultraviolet rays. That is, the water vapor barrier layer is formed under relatively low temperature conditions (for example, at a temperature of about 100° C.) without using a vapor phase deposition method such as CVD or PVD.
  • a raw material containing silazane for example, is prepared as a liquid raw material, and the liquid raw material is applied to a substrate by spin coating or spray coating, and dried to form a barrier precursor.
  • a "water vapor barrier layer with Si--O and Si--N bonds" can then be obtained by subjecting the barrier precursor to UV irradiation in an ambient atmosphere containing nitrogen.
  • a mask may be utilized to prevent the formation of a water vapor barrier layer at the joint. That is, a water vapor barrier layer may be formed entirely by applying a mask to the region to be the joint, and then the mask may be removed.
  • First aspect comprising a substrate, a solid-state battery with an end electrode provided on the substrate, and an exterior part that covers the solid-state battery, the exterior portion includes resin, A packaged solid state battery including a gap between the end electrode and the exterior part.
  • Second aspect In the first aspect, the solid-state battery and the exterior part include a part where the solid-state battery and the exterior part face each other at a distance, and a part where the solid-state battery and the exterior part come into contact with each other, A packaged solid state battery, wherein the spaced apart opposing portions are located between the end face electrode and the exterior part.
  • Third aspect The packaged solid-state battery according to the first aspect or the second aspect, wherein the void portion is between the exterior portion and at least one of the end surface electrode on the positive electrode side and the end surface electrode on the negative electrode side.
  • Fourth aspect The packaged solid-state battery according to any one of the first to third aspects, wherein the plurality of voids are formed intermittently along the end electrode.
  • Fifth aspect The packaged solid battery according to any one of the first to fourth aspects, wherein the end electrode includes a contact portion and a non-contact portion with the exterior portion.
  • the contact portion is positioned at at least one of a top surface side end of the end electrode located distally to the substrate and a substrate side end located proximal to the substrate.
  • the solid-state battery includes a first main surface facing the substrate, and a second main surface located opposite the first main surface, An end of the end electrode extends over at least one of the first main surface and the second main surface, A packaged solid state battery, wherein the contact portion is located at the end.
  • Eighth aspect The packaged solid state battery according to any one of the first to seventh aspects, wherein the void portion has an elongated shape extending along the main surface region of the end electrode when viewed in cross section.
  • Ninth aspect The packaged solid-state battery according to any one of the first to eighth aspects, wherein the void portion is continuous over the entire main surface region of the end electrode.
  • the exterior portion includes an insulating covering layer covering the solid state battery, A packaged solid state battery, wherein the end face electrode and the covering insulating layer face each other and are spaced apart from each other with the gap interposed therebetween.
  • Eleventh aspect The packaged solid-state battery according to any one of the first to tenth aspects, wherein the cross-sectional shape of the void corresponds to the cross-sectional shape of the outer surface of the end electrode.
  • Twelfth aspect The packaged solid-state battery according to any one of the first to eleventh aspects, wherein the non-contact portion occupies 50% or more and 100% or less of the outer surface of the end electrode when viewed in cross section.
  • the solid state battery includes a first corner located on the proximal side with respect to the substrate, The end electrode includes a first corner covering region that covers the first corner, In the packaged solid state battery, the thickness of the first corner covering region is larger than the thickness of other regions other than the first corner covering region in a cross-sectional view.
  • the solid state battery includes a second corner located on a distal side with respect to the substrate, the end electrode includes a second corner covering region that covers the second corner; A packaged solid state battery, wherein the other region is the second corner covering region.
  • the packaged solid-state battery of the present disclosure can be used in various fields where battery use or power storage is expected. Although this is just an example, the packaged solid-state battery of the present disclosure can be used in the electrical, information, and communication fields where mobile devices are used (e.g., mobile phones, smartphones, notebook computers, digital cameras, activity monitors, armrests, etc.).
  • mobile devices e.g., mobile phones, smartphones, notebook computers, digital cameras, activity monitors, armrests, etc.
  • electric/electronic equipment field or mobile equipment field including computers, e-paper, RFID tags, card-type electronic money, small electronic devices such as smart watches, etc.), household and small industrial applications (e.g., power tools, golf carts, etc.) household/nursing care/industrial robots), large industrial applications (e.g., forklifts, elevators, harbor cranes), transportation systems (e.g., hybrid vehicles, electric vehicles, buses, trains, electrically assisted bicycles, electric motorcycles, etc.), power system applications (e.g., various power generation, road conditioners, smart grids, home-installed power storage systems, etc.), medical applications (medical equipment such as earphones and hearing aids), and pharmaceutical applications (medicine applications). It can be used in fields such as management systems), IoT fields, and space/deep sea applications (for example, fields such as space probes and underwater research vessels).

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PCT/JP2023/023290 2022-07-11 2023-06-23 パッケージ化された固体電池 Ceased WO2024014261A1 (ja)

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EP23839435.7A EP4557438A1 (en) 2022-07-11 2023-06-23 Packaged solid-state battery
CN202380053275.9A CN119452498A (zh) 2022-07-11 2023-06-23 经封装的固体电池
JP2024533612A JP7838652B2 (ja) 2022-07-11 2023-06-23 パッケージ化された固体電池
US19/002,145 US20250149689A1 (en) 2022-07-11 2024-12-26 Packaged solid-state battery

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JP2022-111323 2022-07-11
JP2022111323 2022-07-11

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004095200A (ja) * 2002-08-29 2004-03-25 Kyocera Corp 積層型電池
JP2021099996A (ja) * 2019-03-12 2021-07-01 大日本印刷株式会社 全固体電池用外装材、全固体電池及びその製造方法
WO2021256403A1 (ja) * 2020-06-15 2021-12-23 株式会社村田製作所 固体電池および固体電池の製造方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004095200A (ja) * 2002-08-29 2004-03-25 Kyocera Corp 積層型電池
JP2021099996A (ja) * 2019-03-12 2021-07-01 大日本印刷株式会社 全固体電池用外装材、全固体電池及びその製造方法
WO2021256403A1 (ja) * 2020-06-15 2021-12-23 株式会社村田製作所 固体電池および固体電池の製造方法

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JPWO2024014261A1 (https=) 2024-01-18
JP7838652B2 (ja) 2026-04-01

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