Positive electrode active material layer, electrode, and solid-state battery

Abstract

To provide: a positive electrode active material layer capable of forming a positive electrode exhibiting excellent adhesion between the positive electrode active material layer and a current collector; an electrode provided with the positive electrode active material layer; and a semi-solid-state battery or an all-solid-state battery provided with the electrode.SOLUTION: There is provided a positive electrode active material layer which contains a positive electrode active material, a solid electrolyte, and a binder. The binder is a vinylidene fluoride copolymer containing a constituent unit derived from vinylidene fluoride and a constituent unit derived from a monomer other than vinylidene fluoride. The constituent unit derived from a monomer other than vinylidene fluoride contains a constituent unit derived from at least one selected from unsaturated dibasic acids, unsaturated dibasic acid monoesters, and compounds represented by carboxylic acids with a specific structure. The constituent unit derived from vinylidene fluoride is contained in an amount of 90 mass% or more with respect to 100 mass% of total constituent units contained in the vinylidene fluoride copolymer.SELECTED DRAWING: None

Description

[Technical Field]

[0001] This invention relates to a positive electrode active material layer, an electrode, and a solid-state battery. [Background technology]

[0002] In conventional rechargeable batteries containing electrolytes, there was a very high risk of fire if an abnormality occurred in the cell, such as an internal short circuit, causing the cell temperature to rise. Therefore, from the perspective of improving cell safety, studies are being conducted on semi-solid-state batteries or all-solid-state batteries (hereinafter referred to as "(semi)solid-state batteries") in which most or all of the electrolyte is replaced with a solid electrolyte. (Semi)solid-state batteries contain only a very small amount or no electrolyte containing flammable organic solvents, so safety devices can be simplified, and they are considered to have advantages in terms of manufacturing costs and productivity.

[0003] The active material layer of the electrodes of a (semi-)solid-state battery is expected to contain a solid electrolyte in addition to the active material, conductive additive, and binder that make up the electrode active material layer of a conventional secondary battery.

[0004] For example, Patent Document 1 discloses that by including a positive electrode active material, a solid electrolyte, and an ionic liquid in the positive electrode active material layer, and using PVDF as a binder, it is possible to suppress the decrease in output in an all-solid-state battery and to suppress the decrease in charging capacity associated with an increase in positive electrode potential. Furthermore, for example, Patent Document 2 discloses that by including a positive electrode active material layer containing a positive electrode active material, a solid electrolyte, LiFSI and LiPF6 as the in-liquid, and PVDF as the binder, corrosion of the current collector foil can be suppressed and high charge / discharge efficiency can be achieved. [Prior art documents] [Patent Documents]

[0005] [Patent Document 1] Japanese Patent Publication No. 2020-113444 [Patent Document 2] Japanese Patent Publication No. 2020-126807 [Overview of the Initiative] [Problems that the invention aims to solve]

[0006] Incidentally, according to the inventors' studies, when a positive electrode binder used in conventional secondary batteries containing an electrolyte is used in a positive electrode having a positive electrode active material layer containing a solid electrolyte, the adhesion between the positive electrode active material layer and the current collector is sometimes insufficient. This is thought to be due to insufficient adhesion of the positive electrode binder used in conventional secondary batteries to the solid electrolyte. Poor adhesion between the positive electrode active material layer and the current collector makes it difficult to stably achieve various required characteristics such as high charge-discharge efficiency. For this reason, even in positive electrodes having a positive electrode active material layer containing a solid electrolyte, there is a need for technology to improve the adhesion between the positive electrode active material layer and the current collector.

[0007] The present invention has been made in view of the above problems, and aims to provide a positive electrode active material layer capable of forming a positive electrode with excellent adhesion between the positive electrode active material layer and the current collector, an electrode equipped with the positive electrode active material layer, and a semi-solid-state battery or a fully solid-state battery equipped with the electrode. [Means for solving the problem]

[0008] As a result of diligent research to solve the above problems, the present inventors have found that the above problems can be solved by including a specific vinylidene fluoride copolymer as a binder in the positive electrode active material layer containing the positive electrode active material and solid electrolyte, and have completed the present invention.

[0009] Aspects of the present invention relate to the following positive electrode active material layer, electrode, and semi-solid battery or all-solid battery, each containing a positive electrode active material (A), a solid electrolyte (B), and a binder (C).

[0010] [1] A positive electrode active material layer comprising a positive electrode active material (A), a solid electrolyte (B), and a binder (C), The binder (C) is a vinylidene fluoride copolymer containing a constituent unit (Ca) derived from vinylidene fluoride and a constituent unit (Cb) derived from a monomer other than vinylidene fluoride, The constituent unit (Cb) derived from monomers other than vinylidene fluoride contains a constituent unit derived from at least one selected from unsaturated dibasic acids, unsaturated dibasic acid monoesters, and compounds represented by the following formula (C-1), A positive electrode active material layer in which, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, the constituent units (Ca) derived from vinylidene fluoride account for 90% by mass or more. [ka] (In equation (C-1), R 1 , R 2 and R 3 Each of these is independently a hydrogen atom, a chlorine atom, or an alkyl group having 1 to 5 carbon atoms, and X 1 This refers to an atomic group whose main chain consists of 1 to 19 atoms and has a molecular weight of 472 or less, and which contains at least one heteroatom selected from oxygen and nitrogen atoms.

[0011] [2] The positive electrode active material layer according to [1], wherein the intrinsic viscosity of the vinylidene fluoride copolymer is 2.3 dL / g or more. [3] The vinylidene fluoride copolymer contains a constituent unit derived from hexafluoropropylene as a constituent unit different from the constituent unit (Cb), The positive electrode active material layer according to [2], wherein, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, the constituent units derived from hexafluoropropylene are 2% by mass or more and 8% by mass or less. [4] The constituent unit (Cb) derived from monomers other than vinylidene fluoride contains the constituent unit derived from an unsaturated dibasic acid monoester, The positive electrode active material layer according to any one of [1] to [3], wherein the unsaturated dibasic acid monoester is monomethyl maleate. [5] The positive electrode active material layer according to any one of [1] to [4], wherein the solid electrolyte (B) is an oxide-based solid electrolyte. [6] The solid electrolyte (B) is represented by the following formula (B-1): Li 1+x+y Al x Ti 2x Si y P 3y O 12 ···(B-1) (In the formula (B-1), x and y satisfy 0 ≦ x ≦ 1 and 0 ≦ y ≦ 1.) The positive electrode active material layer according to [5], containing a material represented by the above formula. [7] The positive electrode active material (A) contains lithium metal phosphate, The positive electrode active material layer according to any one of [1] to [6], wherein the lithium metal phosphate is selected from the group consisting of LiFePO4, LiMnPO4, LiCoPO4, and LiNiPO4. [8] An electrode comprising a current collector and the positive electrode active material layer according to any one of [1] to [7]. [9] A semi-solid battery or an all-solid battery comprising the electrode according to [8].

Advantages of the Invention

[0012] According to the present invention, there can be provided a positive electrode active material layer capable of forming a positive electrode excellent in adhesion between the positive electrode active material layer and the current collector, an electrode comprising the positive electrode active material layer, and a semi-solid battery or an all-solid battery comprising the electrode.

Embodiments for Carrying Out the Invention

[0013] ≪Positive Electrode Active Material Layer≫ The positive electrode active material layer contains a positive electrode active material (A), a solid electrolyte (B), and a binder (C). The binder (C) contained in the positive electrode active material layer is a vinylidene fluoride copolymer containing a structural unit (C-a) derived from vinylidene fluoride and a structural unit (C-b) derived from a monomer other than vinylidene fluoride. The constituent units (Cb) derived from monomers other than vinylidene fluoride include at least one selected from unsaturated dibasic acids, unsaturated dibasic acid monoesters, and compounds represented by the following formula (C-1), as described later.

[0014] In a vinylidene fluoride copolymer, when the total number of constituent units contained in the vinylidene fluoride copolymer is taken as 100% by mass, the constituent units (Ca) derived from vinylidene fluoride account for 90% or more by mass. By including a specific binder (C) in the positive electrode active material layer, it is possible to form an electrode with excellent adhesion between the positive electrode active material layer and the current collector.

[0015] The following describes the essential and optional components included in the positive electrode active material layer.

[0016] <Cathode active material (A)> The positive electrode active material (A) is not particularly limited, and for example, conventionally known positive electrode active materials can be used. A lithium-based positive electrode active material containing at least lithium is preferred. Examples of lithium-based positive electrode active materials include those with the general formula Li x M y O z Positive electrode active materials can be given by the formula (where M is a transition metal element, x = 0.02 to 2.2, y = 1 to 2, z = 1.4 to 4). In the above general formula, M can be at least one selected from the group consisting of Co, Mn, Ni, V, Fe, and Si, and may be at least one selected from the group consisting of Co, Ni, and Mn. Specifically, such positive electrode active materials include LiCoO2, LiMnO2, LiNiO2, LiVO2, and LiNi 1 / 3 Co 1 / 3 Mn 1 / 3 O2, LiMn2O4, Li(Ni 0.5 Mn 1.5 Examples include O4, Li2FeSiO4, and Li2MnSiO4.

[0017] Furthermore, the above general formula Li x M yO z Other positive electrode active materials (A) include lithium titanate (e.g., Li4Ti5O 12 Examples include lithium metal phosphate (LiFePO4, LiMnPO4, LiCoPO4, LiNiPO4), transition metal oxides (V2O5, MoO3), TiS2, LiCoN, Si, SiO2, Li2SiO3, Li4SiO4, and lithium storage intermetallic compounds (e.g., Mg2Sn, Mg2Ge, Mg2Sb, Cu3Sb). Among these, lithium metal phosphate is preferred, and among lithium metal phosphates, LiFePO4 is preferred.

[0018] The shape of the positive electrode active material (A) is not particularly limited, but it can be particulate or thin film, for example, and particulate is preferable from the viewpoint of ease of handling. When the positive electrode active material is in the form of particles, the average particle size (D50) of these particles is preferably, for example, 1 nm to 100 μm, and more preferably 10 nm to 30 μm.

[0019] A coating layer containing a Li-ion conductive oxide may be formed on the surface of the positive electrode active material (A) from the viewpoint of suppressing the reaction between the positive electrode active material and the solid electrolyte. Examples of lithium-ion conductive oxides include LiNbO3 and Li4Ti5O 12 Examples include Li3PO4, etc. The lower limit of the coating layer thickness is preferably 0.1 nm or more, and more preferably 1 nm or more. The upper limit of the coating layer thickness is preferably 100 nm or less, and more preferably 20 nm or less.

[0020] The content of the positive electrode active material (A) is not particularly limited, but is preferably 50% to 98% by mass, more preferably 60% to 95% by mass, and even more preferably 70% to 90% by mass, based on 100% by mass of the positive electrode active material layer.

[0021] <Solid electrolyte (B)> As the solid electrolyte (B), sulfide-based solid electrolytes and oxide-based solid electrolytes can be used. Among these, oxide-based solid electrolytes are preferred from the viewpoint of electrolyte safety and stability.

[0022] Examples of sulfide-based solid electrolytes include Li2S-SiS2, LiI-Li2S-SiS2, LiI-Li2S-P2S5, LiI-Li2O-Li2S-P2S5, LiI-Li2S-P2O5, LiI-Li3PO4-P2S5, Li2S-P2S5, and Li3PS4.

[0023] Examples of oxide-based solid electrolytes include LLTO compounds ((La,Li)TiO3) and Li6La2CaTa2O 12 Li6La2ANb2O 12 (A: Alkaline earth metal), Li2Nd3TeSbO 12 Li3BO 2.5 N 0.5 , Li9SiAlO8, LAGP-based compounds (Li 1+x Al x Ge 2-x (PO4)3 (0≦x≦1)), LATP-based compounds such as Li2O-Al2O3-TiO2-P2O5 (Li 1+x Al x Ti 2-x (PO4)3(0≦x≦1)), Li 1+x Ti 2-x Al x Si y (PO4) 3-y (0≦x≦1, 0≦y≦1), Li 1+y Al x M 2-x (PO4)3(M is one or more elements selected from the group consisting of Ti, Ge, Sr, Sn, Zr, and Ca, where 0≦x≦1, 0≦y≦1), LiTi x Zr 2-x (PO4)3(0≦x≦1), LISICON(Li 4-2x Zn x GeO4 (0≦x≦1)), LIPON-based compounds (Li 3+y PO 4-x N x(0≦x≦1, 0≦y≦1), NASICON compounds (LiTi2(PO4)3, etc.), garnet compounds (Li7La3Zr2O 12 Li 7-x La3Zr 1-x Nb x O 12 Examples include (0≦x≦1, etc.)

[0024] Among oxide-based solid electrolytes, LATP compounds are preferred from the viewpoint of having high lithium ion conductivity. Examples of LATP compounds are given by formula (1): Li 1+x+y Al x Ti 2-x Si y P 3-y O 12 ...(1) (In equation (1), x and y satisfy 0 ≤ x ≤ 1 and 0 ≤ y ≤ 1.) It is preferable that the material includes the material represented by .

[0025] Furthermore, other preferred oxide-based solid electrolytes besides the LATP-based compounds mentioned above include, for example, Li7La3Zr2O 12 (LLZO), Li 6.75 La3Zr 1.75 Ta 0.25 O 12 (LLZTO), Li 0.33 La 0.56 TiO3 (LLTO), Li 1.6 Al 0.6 Ge 1.4 Examples include (PO4)3(LAGP).

[0026] The content of the solid electrolyte (B) is not particularly limited, but is preferably 1% by mass or more and 40% by mass or less, more preferably 2% by mass or more and 30% by mass or less, and even more preferably 3% by mass or more and 20% by mass or less, based on 100% by mass of the positive electrode active material layer.

[0027] <Binder (C)> The binder (C) is a vinylidene fluoride copolymer containing constituent units (Ca) derived from vinylidene fluoride and constituent units (Cb) derived from monomers other than vinylidene fluoride. The above-mentioned constituent units (Cb) derived from monomers other than vinylidene fluoride include constituent units derived from at least one selected from unsaturated dibasic acids, unsaturated dibasic acid monoesters, and compounds represented by formula (C-1) described later. When the total constituent units contained in the vinylidene fluoride copolymer are considered to be 100% by mass, the above constituent units (Ca) derived from vinylidene fluoride account for 90% by mass or more. The binder (C) is used to improve the adhesion between the solid electrolyte and other components (current collector, active material, conductive additive, etc.).

[0028] Examples of the unsaturated dibasic acids that provide the constituent unit (Cb) include fumaric acid, maleic acid, citraconic acid, and phthalic acid.

[0029] Examples of the unsaturated dibasic acid monoesters that provide the constituent unit (Cb) include monomethyl fumarate, monoethyl fumarate, monomethyl maleate, monoethyl maleate, monomethyl citraconate, monoethyl citraconate, monomethyl phthalate, and monoethyl phthalate.

[0030] The compounds represented by formula (C-1) that give the constituent unit (Cb) are as follows: [ka]

[0031] In equation (C-1), R 1 , R 2 and R 3 Each of these is independently a hydrogen atom, a chlorine atom, or an alkyl group having 1 to 5 carbon atoms, and X 1 This refers to an atomic group whose main chain consists of 1 to 19 atoms and has a molecular weight of 472 or less, and which contains at least one heteroatom selected from oxygen atoms and nitrogen atoms.

[0032] As the compound represented by the above formula (C-1), the compound represented by the following formula (C-2) is preferred. [ka]

[0033] In formula (C-2), R 1 , R 2 , R 3 This is the same as equation (C-1) above, and X 2 This refers to an atomic group whose main chain consists of 1 to 18 atoms and has a molecular weight of 456 or less.

[0034] In formulas (C-1) and (C-2), from the viewpoint of polymerization reactivity, particularly R 1 , R 2 The substituent is preferably one with low steric hindrance, and is preferably a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and more preferably a hydrogen atom or a methyl group.

[0035] In equation (C-1), X 1 The molecular weight of the atomic group represented by is 472 or less, but preferably 172 or less. Also, X 1 There is no particular lower limit to the molecular weight of the atomic group represented by , but usually X is in the form of -CH2-, i.e., the molecular weight is 14. Also, in formula (C-2), X 2 The molecular weight of the atomic group represented by is 456 or less, but preferably 156 or less. Also, X 2 There is no particular limit to the lower limit of the molecular weight of the atomic group represented by this, but it is usually X 2 In terms of the -CH2- configuration, i.e., the molecular weight, it is 14.

[0036] X 1 or X 2 From the viewpoint of polymerizability, it is preferable that the molecular weight of the atomic group represented by is within the aforementioned range.

[0037] Examples of compounds represented by formula (C-2) include 2-carboxyethyl acrylate, 2-carboxyethyl methacrylate, acryloyloxyethyl succinic acid, methacryloyloxyethyl succinic acid, acryloyloxypropyl succinic acid, methacryloyloxypropyl succinic acid, acryloyloxyethyl phthalic acid, and methacryloyloxyethyl phthalic acid.

[0038] In a vinylidene fluoride copolymer used as a binder (C), the content of constituent units (Ca) derived from vinylidene fluoride is preferably 90.0% by mass or more, more preferably 95.0% by mass or more, and more preferably 98.0% by mass or more, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, from the viewpoint of improving the adhesion between the solid electrolyte and other components (current collector, active material, conductive additive, etc.).

[0039] In the vinylidene fluoride copolymer as a binder (C), the content of constituent units (Cb) derived from monomers other than vinylidene fluoride is not particularly limited, but for example, it is preferably 0.01% by mass or more and 10.0% by mass or less, more preferably 0.1% by mass or more and 5.0% by mass or less, and even more preferably 0.2% by mass or more and 2.0% by mass or less, relative to the total constituent units in the vinylidene fluoride copolymer.

[0040] As a vinylidene fluoride copolymer, from the viewpoint of improving the adhesion between the solid electrolyte and other components (current collector, active material, conductive additive, etc.), it may contain a constituent unit (Cc) derived from a monomer other than the monomer that gives the aforementioned constituent units (Ca) and (Cb). Other monomers include, for example, constituent units derived from fluorine-containing monomers other than vinylidene fluoride; and constituent units derived from hydrocarbon monomers such as ethylene and propylene. Examples of fluorine-containing monomers include vinyl fluoride, trifluoroethylene, tetrafluoroethylene, chlorotrifluoroethylene, hexafluoropropylene, hexafluoroethylene, fluoroalkyl vinyl ethers, and perfluoroalkyl vinyl ethers, such as perfluoromethyl vinyl ether. Among these, chlorotrifluoroethylene or hexafluoropropylene are preferred, and hexafluoropropylene is more preferred.

[0041] In a vinylidene fluoride copolymer as binder (C), the content of constituent units derived from the above-mentioned other monomers is preferably 0.1% by mass or more and less than 10% by mass, and more preferably 2.0% by mass or more and 8% by mass or less, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass. When the vinylidene fluoride copolymer as binder (C) contains constituent units derived from the above-mentioned other monomers, the content of constituent units (Ca) derived from vinylidene fluoride is preferably 90% by mass or more, preferably 91% by mass or more, and more preferably 92% by mass or more, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, from the viewpoint of improving the adhesion between the solid electrolyte and other components (current collector, active material, conductive additive, etc.). Furthermore, the content of constituent units (Cb) derived from monomers other than vinylidene fluoride is preferably 0.01% by mass or more and 2% by mass or less, more preferably 0.1% by mass or more and 1.5% by mass or less, and even more preferably 0.2% by mass or more and 0.8% by mass or less.

[0042] The intrinsic viscosity of the vinylidene fluoride copolymer as binder (C) is preferably 2.3 dL / g or higher, and more preferably 2.5 dL / g or higher, from the viewpoint of improving the adhesion between the solid electrolyte and other components (current collector, active material, conductive additive, etc.).

[0043] The content of binder (C) is not particularly limited, but is preferably 1% to 40% by mass, more preferably 2% to 30% by mass, and even more preferably 3% to 20% by mass, based on 100% by mass of the positive electrode active material layer.

[0044] (Method of manufacturing binder (C)) The method for producing the binder (C) is not particularly limited and is usually carried out by methods such as suspension polymerization, emulsion polymerization, or solution polymerization. From the viewpoint of ease of post-processing, aqueous suspension polymerization and emulsion polymerization are preferred, and aqueous suspension polymerization is more preferred.

[0045] The aqueous suspension polymerization method is not particularly limited and includes, for example, a method in which monomers used for polymerization are polymerized in an aqueous medium in the presence of a suspension agent, polymerization initiator, chain transfer agent, etc.

[0046] The suspending agent is not particularly limited and examples include methylcellulose, methoxylated methylcellulose, propoxylated methylcellulose, hydroxyethyl methylcellulose, hydroxypropyl methylcellulose, polyvinyl alcohol, polyethylene oxide, gelatin, etc. The amount of suspending agent used is not particularly limited, but for example, it is preferably 0.005 parts by mass or more and 1.0 part by mass or less, and more preferably 0.01 parts by mass or more and 0.4 parts by mass or less, per 100 parts by mass of the total monomer used for polymerization.

[0047] The polymerization initiator is not particularly limited, and examples include diisopropyl peroxydicarbonate, di-n-propyl peroxydicarbonate, di-n-heptafluoropropyl peroxydicarbonate, isobutyryl peroxide, di(chlorofluoroacyl)peroxide, di(perfluoroacyl)peroxide, t-butyl peroxypivalate, etc. The amount of polymerization initiator used is not particularly limited, but for example, it is preferably 0.05 parts by mass or more and 5 parts by mass or less, and more preferably 0.15 parts by mass or more and 2 parts by mass or less, per 100 parts by mass of the total monomer used for polymerization.

[0048] The chain transfer agent is not particularly limited and includes, for example, ethyl acetate, propyl acetate, acetone, and diethyl carbonate.

[0049] Furthermore, the amount of monomer used for polymerization is typically 1:1 to 1:10 in mass ratio of total monomer to water, and preferably 1:2 to 1:5. The polymerization conditions, such as polymerization temperature and polymerization time, when performing suspension polymerization are not particularly limited, and known polymerization conditions may be used, for example. The polymerization temperature T is appropriately selected according to the 10-hour half-life temperature T10 of the polymerization initiator, and is usually selected within the range of T10-25℃≦T≦T10+25℃. For example, the T10 of t-butyl peroxypivalate and diisopropyl peroxydicarbonate are 54.6℃ and 40.5℃, respectively (see NOF Corporation product catalog). Therefore, in polymerization using t-butyl peroxypivalate and diisopropyl peroxydicarbonate as polymerization initiators, the polymerization temperature T is appropriately selected within the range of 29.6℃≦T≦79.6℃ and 15.5℃≦T≦65.5℃, respectively. The polymerization time is not particularly limited, but considering productivity and other factors, it is preferably 1 to 24 hours.

[0050] <Other ingredients> The positive electrode active material layer may contain components other than the positive electrode active material (A), solid electrolyte (B), and binder (C) described above (hereinafter also referred to as "other components"), as long as the effects of the present invention are not impaired. Any known additives can be used as other components, and examples include conductive additives, insulating inorganic fillers such as alumina, magnesia, and silica, insulating organic fillers such as polytetrafluoroethylene, polyimide, and polyacrylonitrile, plasticizers such as ethylene carbonate, propylene carbonate, and ethyl methyl carbonate, Li salts such as LiPF6, LiFSI, and LiTFSI, dispersants, flame retardants, and defoamers.

[0051] Examples of conductive additives (D) include carbon black and carbon nanotubes. These may be used individually or in combination of two or more.

[0052] The content of the conductive additive (D) is not particularly limited, but is preferably 0.05% to 15% by mass, more preferably 0.1% to 10% by mass, and even more preferably 0.5% to 8% by mass, based on 100% by mass of the positive electrode active material layer.

[0053] ≪Electrode≫ The term "electrode" refers to the positive electrode. The electrode comprises a current collector and the positive electrode active material layer mentioned above. By incorporating the above-mentioned positive electrode active material layer, the electrode exhibits the effect of suppressing the interfacial resistance between the current collector and the positive electrode active material layer.

[0054] (Current collector) A current collector is a terminal for extracting electricity. The material of the current collector is not particularly limited, and metal foils or metal meshes made of aluminum, copper, iron, stainless steel, steel, nickel, titanium, etc., can be used. Alternatively, the metal foils or metal meshes may be applied to the surface of other media.

[0055] The bulk density of the electrode is not particularly limited, but is preferably, for example, 1.5 g / cm³ or more and 5 g / cm³ or less. The basis weight of the electrode is not particularly limited; for example, 20 gm 2 More than 1000g / m 2 The following is preferable:

[0056] ≪Electrode Manufacturing Method≫ Examples of electrode manufacturing methods include the steps of: preparing a positive electrode slurry by mixing the aforementioned positive electrode active material (A), solid electrolyte (B), binder (C), other components as needed, and a non-aqueous solvent (S); and applying the obtained positive electrode slurry to a current collector and then drying it. In other words, in the above embodiment, the positive electrode active material layer is prepared and the electrode is prepared through the step of drying the positive electrode slurry.

[0057] Examples of non-aqueous solvents (S) include N-methyl-2-pyrrolidone (hereinafter also referred to as "NMP"), dimethylformamide, N-dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, N,N-dimethyl sulfoxide, hexamethylphosphoamide, dioxane, tetrahydrofuran, tetramethylurea, triethyl phosphate, trimethyl phosphate, acetone, cyclohexanone, methyl ethyl ketone, and tetrahydrofuran. These may be used individually or in combination of two or more.

[0058] The application method is not particularly limited, and for example, the doctor blade method, reverse roll method, comma bar method, gravure method, air knife method, die coat method, and dip coat method can be applied.

[0059] The drying temperature is preferably 80°C to 300°C, more preferably 90°C to 200°C, and even more preferably 100°C to 180°C. The drying time is preferably, for example, 10 seconds to 300 minutes, and more preferably 1 minute to 200 minutes. Drying may be carried out multiple times at different temperatures. Pressure may be applied during drying.

[0060] ≪All-solid-state battery≫ The all-solid-state battery comprises the electrodes of the embodiment described above. For the all-solid-state battery, components other than the positive electrode, such as the negative electrode and separator, can be those that are conventionally known.

[0061] ≪Semi-solid battery≫ The semi-solid battery comprises the electrodes of the embodiment described above. For the semi-solid battery, components other than the positive electrode, such as the negative electrode and separator, can be those that are conventionally known. The amount of electrolyte contained in the semi-solid battery is preferably 1 to 95%, more preferably 1 to 90%, and even more preferably 1 to 80%, when the volume of electrolyte contained in a conventional secondary battery is taken as 100%. [Examples]

[0062] Hereinafter, the present invention will be described more specifically based on Examples and Comparative Examples, but the present invention is not limited to the following Examples.

[0063] [Examples 1 to 5 and Comparative Examples 1 to 3] [Materials Used] In the Examples and Comparative Examples, the following A1 was used as the positive electrode active material (A). A1: LiFePO4

[0064] In the Examples and Comparative Examples, the following B1 was used as the solid electrolyte (B). B1: Li 1+x+y Al x Ti 2x Si y P 3y O 12 (LATP) (manufactured by Ohara, "LICGC TM PW-01 (particle size 1 μm)")

[0065] In the Examples and Comparative Examples, the following C1 to C8 were prepared and used as the binder (C). Also, the intrinsic viscosity of each prepared binder was measured according to the following method. The monomers used are as follows. (1) Monomer that gives a structural unit (C-a) derived from vinylidene fluoride: Vinylidene fluoride (VDF) (2) Monomer that gives a structural unit (C-b) derived from a monomer other than vinylidene fluoride: [[ID=4i]] Monomethyl maleate (MMM) (unsaturated dibasic acid monoester) Acryloyloxypropyl succinic acid (APS) (compound represented by the above formula (C-2)) (3) Monomer that gives a structural unit (C-c): Hexafluoropropylene (HFP)

[0066] (Measurement of Intrinsic Viscosity) 80 mg of each binder was dissolved in 20 ml of N,N-dimethylformamide to prepare a binder-containing solution. The viscosity η1 of this binder-containing solution was measured using an Ubbelohde viscometer in a 30°C constant temperature bath. Similarly, the viscosity η0 of N,N-dimethylformamide was measured using an Ubbelohde viscometer in a 30°C constant temperature bath. The intrinsic viscosity η was then determined based on the following formula. Intrinsic viscosity η=(1 / C)·ln(η1 / η0)

[0067] (Example of Binder C1 (VDF / HFP / MMM) fabrication) In a 2 L autoclave, 240.2 parts by mass of deionized water, 0.2 parts by mass of methylcellulose, 97 parts by mass of vinylidene fluoride (VDF), 3 parts by mass of hexafluoropropylene (HFP), 0.3 parts by mass of monomethyl maleate (MMM), and 0.47 parts by mass of diisopropyl peroxydicarbonate (IPP) were added and polymerized at 26°C. The resulting copolymer was heat-treated at 95°C for 60 minutes, then dehydrated, washed with water, and further dried at 80°C for 20 hours to obtain binder C1. Binder C1 contained 97.4% by mass of VDF, 2.3% by mass of HFP, and 0.3% by mass of MMM relative to the total constituent units. The intrinsic viscosity (η) of binder C1 was 3.1 dL / g. The amounts of each monomer in binder C1 were determined by first calculating the VDF / HFP ratio using 19F-NMR, then calculating the VDF / MMM ratio using the method described below, and finally calculating so that the sum of VDF, HFP, and MMM equals 100 mol%. The VDF / MMM ratio in the polymer (the molar ratio of the amount of constituent units derived from vinylidene fluoride to the amount of constituent units derived from monomethyl maleate) was calculated based on the calculation method using IR spectra and calibration curves disclosed in WO International Publication No. 2009 / 084483.

[0068] (Example of binder C2 (VDF / HFP / MMM) fabrication) Binder C2 was obtained by polymerizing VDF, HFP, and MMM in the same manner as in the preparation example of Binder C1, except that the amounts of ion-exchanged water (259 parts by mass), methylcellulose (0.15 parts by mass), VDF (90 parts by mass), HFP (10 parts by mass), MMM (0.5 parts by mass), and IPP (0.5 parts by mass). Binder C2 contained 92.5% by mass of VDF, 7.0% by mass of HFP, and 0.5% by mass of MMM relative to the total constituent units. The intrinsic viscosity (η) of Binder C2 was 2.6 dL / g.

[0069] (Example of binder C3 (VDF / APS) fabrication) Binder C3 was obtained by polymerizing VDF and APS in the same manner as in the preparation example of Binder C1, except that 231.3 parts by mass of deionized water, 0.05 parts by mass of methylcellulose, 99 parts by mass of VDF, 1.0 part by mass of acryloyloxypropyl succinic acid (APS), and 0.5 parts by mass of IPP were used. Binder C3 contained 99.0% by mass of VDF and 1.0% by mass of APS relative to the total constituent units. The intrinsic viscosity (η) of Binder C3 was 2.5 dL / g.

[0070] (Example of binder C4 (VDF / HFP / APS) fabrication) Binder C4 was obtained by polymerizing VDF, HFP, and APS in the same manner as in the preparation example of Binder C1, except that 273 parts by mass of deionized water, 0.05 parts by mass of methylcellulose, 92 parts by mass of VDF, 2 parts by mass of HFP, 0.5 parts by mass of APS, and 0.4 parts by mass of IPP were used. Binder C4 contained 94.1% by mass of VDF, 5.4% by mass of HFP, and 0.5% by mass of APS relative to the total constituent units. The intrinsic viscosity (η) of Binder C4 was 2.1 dL / g.

[0071] (Example of binder C5 (VDF / HFP / APS) fabrication) Binder C5 was obtained by polymerizing VDF, HFP, and APS in the same manner as in the preparation example of Binder C1, except that 256 parts by mass of deionized water, 0.05 parts by mass of methylcellulose, 90 parts by mass of VDF, 10 parts by mass of HFP, 0.5 parts by mass of APS, 1.0 part by mass of IPP, and 0.22 parts by mass of ethyl acetate were used. Binder C5 contained 91.8% by mass of VDF, 7.7% by mass of HFP, and 0.5% by mass of APS relative to the total constituent units. The intrinsic viscosity (η) of Binder C5 was 2.6 dL / g.

[0072] (Example of Binder C6 (PVDF) fabrication) Binder C6 was obtained by polymerizing VDF in the same manner as in the preparation example of Binder C1, except that 231.8 parts by mass of deionized water, 0.05 parts by mass of methylcellulose, 100 parts by mass of VDF, 0.7 parts by mass of IPP, and 0.7 parts by mass of ethyl acetate were used. Binder C6 contained 100.0% by mass of VDF relative to the total constituent units. The intrinsic viscosity (η) of Binder C6 was 2.1 dL / g.

[0073] (Example of Binder C7 (VDF / HFP / MMM) fabrication) Binder C7 was obtained by polymerizing VDF, HFP, and MMM in the same manner as in the preparation example of Binder C1, except that 290 parts by mass of deionized water, 0.1 parts by mass of methylcellulose, 85 parts by mass of VDF, 15 parts by mass of HFP, 0.5 parts by mass of MMM, 0.9 parts by mass of IPP, and 0.3 parts by mass of ethyl acetate were used. Binder C7 contained 87.6% by mass of VDF, 11.9% by mass of HFP, and 0.5% by mass of MMM relative to the total constituent units. The intrinsic viscosity (η) of Binder C7 was 1.3 dL / g.

[0074] (Example of binder C8 (VDF / HFP) fabrication) Binder C8 was obtained by polymerizing VDF and HFP in the same manner as in the preparation example of Binder C1, except that 253 parts by mass of deionized water, 0.05 parts by mass of methylcellulose, 90 parts by mass of VDF, 10 parts by mass of HFP, 0.4 parts by mass of IPP, and 1.0 part by mass of ethyl acetate were used. Binder C8 contained 93.0% by mass of VDF and 7.0% by mass of HFP relative to the total constituent units. The intrinsic viscosity (η) of Binder C8 was 1.9 dL / g.

[0075] Detailed information on the obtained binders C1 to C8 is shown in Table 1.

[0076] [Table 1]

[0077] In the examples and comparative examples, the following D1 was used as the conductive additive (D). D1: Carbon nanotube (CNT) dispersion

[0078] In the examples and comparative examples, the following S1 was used as the non-aqueous solvent (S). S1: N-methyl-2-pyrrolidone (NMP)

[0079] (Preparation of positive electrode slurry) Each binder (C) was dispersed in N-methyl-2-pyrrolidone (NMP) at room temperature to achieve a desired concentration, and then the solution temperature was raised to 50°C to dissolve each binder (C) (hereinafter referred to as "binder solution"). Using the positive electrode active material (A), solid electrolyte (B), conductive additive (D), and each of the above binder solutions, the components were mixed so that the ratio of positive electrode active material (A) / solid electrolyte (B) / conductive additive (D) / binder (C) = 90 / 10 / 2 / 10 (mass%) to obtain each positive electrode slurry. The solid content of the positive electrode slurry was adjusted using NMP.

[0080] (Fabrication of positive electrode) Each obtained positive electrode slurry was applied to an Al foil (thickness: 15 μm) and then dried at 120°C. Each obtained preliminary positive electrode was pressed and further heat-treated at 120°C for 3 hours. As a result, positive electrodes with an electrode bulk density of 2.3 g / cm 3 and a basis weight of 200 g / m 2 were obtained.

[0081] <Evaluation> The peel strength of each obtained positive electrode was measured according to the following method.

[0082] (Peel strength) Each obtained positive electrode was cut into a size of 2.0 cm × 5.0 cm, double-sided tape was attached to the positive electrode active material layer side of each positive electrode, and the positive electrode active material layer and an acrylic plate were bonded together and pressed at 4 MPa for 20 seconds. Half of the Al foil of the positive electrode fixed on the acrylic plate was peeled off and clamped in a chuck, and the measurement was carried out in accordance with JIS K6854-1. The measurement conditions were a head speed of 10 mm / min and a chuck distance of 10 mm, and the measurement was carried out at 90°C peel. The results are shown in Table 2.

[0083]

Table 2

[0084] From Table 2, in the positive electrodes of Comparative Examples 1 to 3 having a positive electrode active material layer containing binder C6 (PVDF), which is a homopolymer of vinylidene fluoride, binder C7 (VDF / HFP / MMM) in which the constituent unit (C-a) derived from vinylidene fluoride is less than 90% by mass, and binder C8 (VDF / HFP) not containing a constituent unit (C-b) derived from a monomer other than vinylidene fluoride, the peel strength was at most 67.4 gf / mm. On the other hand, in the positive electrode active material layer containing binder C1 to C5 containing a constituent unit (C-a) derived from vinylidene fluoride and a specific constituent unit (C-b) derived from a monomer other than vinylidene fluoride and having a content of the constituent unit (C-a) of 90% by mass or more, as shown in Examples 1 to 5, the peel strength was at least 107.5 gf / mm, indicating that the adhesiveness was greatly improved.

Claims

1. A positive electrode active material layer containing a positive electrode active material (A), a solid electrolyte (B), and a binder (C), The binder (C) is a vinylidene fluoride copolymer containing a constituent unit (C-a) derived from vinylidene fluoride and a constituent unit (C-b) derived from a monomer other than vinylidene fluoride, The constituent unit (C-b) derived from monomers other than vinylidene fluoride contains a constituent unit derived from at least one selected from unsaturated dibasic acids, unsaturated dibasic acid monoesters, and compounds represented by the following formula (C-1), The acid group of the unsaturated dibasic acid and the unsaturated dibasic acid monoester is a carboxyl group. A positive electrode active material layer in which, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, the constituent unit (C-a) derived from vinylidene fluoride accounts for 90% by mass or more. 【Chemistry 1】 (In equation (C-1), R １ , R ２ and R ３ Each is independently a hydrogen atom, a chlorine atom, or an alkyl group having 1 to 5 carbon atoms, and X １ This refers to an atomic group whose main chain consists of 1 to 19 atoms and has a molecular weight of 472 or less, and which contains at least one heteroatom selected from oxygen and nitrogen atoms.

2. The positive electrode active material layer according to claim 1, wherein the intrinsic viscosity of the vinylidene fluoride copolymer is 2.3 dL / g or more.

3. The vinylidene fluoride copolymer contains a constituent unit derived from hexafluoropropylene as a constituent unit different from the constituent unit (C-b), The positive electrode active material layer according to claim 2, wherein, when the total constituent units contained in the vinylidene fluoride copolymer are taken as 100% by mass, the constituent units derived from hexafluoropropylene are 2% by mass or more and 8% by mass or less.

4. The constituent unit (C-b) derived from monomers other than vinylidene fluoride contains the constituent unit derived from an unsaturated dibasic acid monoester, The positive electrode active material layer according to any one of claims 1 to 3, wherein the unsaturated dibasic acid monoester is monomethyl maleate.

5. The positive electrode active material layer according to claim 1 or 2, wherein the solid electrolyte (B) is an oxide-based solid electrolyte.

6. The solid electrolyte (B) is given by the following formula (B-1): Li １＋ｘ＋ｙ Al ｘ Ti ２ｘ Si ｙ P ３ｙ O １２ ・・・(B-1) (In equation (B-1), x and y satisfy 0 ≤ x ≤ 1 and 0 ≤ y ≤ 1.) The positive electrode active material layer according to claim 5, comprising the material represented by .

7. The positive electrode active material (A) contains metallic lithium phosphate, The aforementioned lithium metal phosphate is LiFePO ４ LiMnPO ４ LiCoPO ４ , and LiNiPO ４ A positive electrode active material layer according to any one of claims 1 to 3, selected from the group consisting of the following.

8. An electrode comprising a current collector and a positive electrode active material layer according to any one of claims 1 to 3.

9. A semi-solid-state battery or a fully solid-state battery comprising the electrodes described in claim 8.

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