Secondary battery binder, slurry, electrode, method for producing secondary battery, and secondary battery

Abstract

To provide a new secondary battery binder capable of suitably contributing to production of a battery and / or battery characteristics, or a slurry containing the secondary battery binder.SOLUTION: A secondary battery binder comprising an aqueous polymer, wherein a neutralization titration amount of 70g of an aqueous solution obtained by dissolving the aqueous polymer in water at a concentration of 2 mass% in an aqueous 0.1 mol / L sodium hydroxide solution is 0.1 mL or more and less than 0.6 mL.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present disclosure relates to a secondary battery binder, a slurry, an electrode, a method for manufacturing a secondary battery, and a secondary battery. [Background technology]

[0002] Slurries containing binders are used in the manufacturing process of secondary batteries, particularly in the manufacturing process of electrodes. In recent years, due to concerns about the impact on the environment, interest has been shifting from slurries using organic solvents to aqueous slurries using water as the solvent. Patent Document 1 discloses the use of an aqueous slurry containing a latex-based binder. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Japanese Patent Application Laid-Open No. 2012-49061 Summary of the Invention [Problem to be solved by the invention]

[0004] The types and properties of binders are not sufficiently considered in Patent Document 1. An object of the present disclosure is to provide a novel secondary battery binder that can favorably contribute to battery production and / or battery properties, or a slurry containing the secondary battery binder. [Means for solving the problem]

[0005] The present disclosure includes the following aspects: [Section 1] Contains water-based polymers, A secondary battery binder, wherein the neutralization titer of 70 g of an aqueous solution obtained by dissolving the water-based polymer in water at a concentration of 2% by mass with a 0.1 mol / L sodium hydroxide aqueous solution is 0.1 mL or more but less than 0.6 mL. [Section 2] Item 2. The secondary battery binder according to Item 1, wherein the aqueous polymer is a vinyl polymer having an acidic functional group-containing repeating unit. [Section 3] The water-based polymer is formula: -[CH2-C(R 1 )(C(=O)R 2 )]- [In the formula, R 1 is a hydrogen atom or CH3, R 2 NH2, OM (M is a hydrogen atom or a counter cation), O(CH2) n OH, NH(CH2) n OH (wherein each n is independently 1 or more and 6 or less). A repeating unit (1) represented by the formula: formula: -[CH2-CH(OH)]- Repeating unit (2) Item 3. The secondary battery binder according to item 1 or 2, comprising a repeating unit selected from [Section 4] In the water-based polymer, the amount of the repeating unit selected from the repeating unit (1) and the repeating unit (2) is 40 mol % or more, The amount of repeating units containing an acidic functional group is 0.8 mol% or more, 4. The secondary battery binder according to any one of items 1 to 3, wherein the amount of nonionic repeating units is 40 mol % or more. [Section 5] Item 5. The secondary battery binder according to any one of items 1 to 4, which contains SBR. [Section 6] Item 6. A slurry comprising the secondary battery binder according to any one of items 1 to 5 and water. [Section 7] Item 7. The slurry according to item 6, further comprising an electrode active material. [Section 8] Item 8. A method for producing a secondary battery, comprising applying the slurry according to Item 6 or 7. [Section 9] Item 6. An electrode comprising the secondary battery binder according to any one of Items 1 to 5 or a component derived from the secondary battery binder. [Section 10] Item 6. An electrode comprising a heated and dried slurry according to Item 6 or 7. [Section 11] Item 11. A secondary battery comprising the electrode according to item 9 or 10. [Effects of the Invention]

[0006] The binder or a slurry containing the binder according to the present disclosure has one or more properties suitable for batteries or the manufacture of batteries. In particular, the use of the binder or a slurry containing the binder according to the present disclosure results in favorable battery properties (particularly, capacity retention rate) after charge-discharge cycles. DETAILED DESCRIPTION OF THE INVENTION

[0007] <Definitions of terms, etc.> In this specification, when a term (symbol) that may appear multiple times in a chemical structure is defined, that definition applies independently to each occurrence, unless otherwise stated, regardless of whether "each independently" or a similar expression is explicitly stated.

[0008] In this specification, "(meth)acrylic" means "acrylic or methacrylic", and "(meth)allyl" means "allyl or methallyl".

[0009] In this specification, when multiple lower limit values ​​and multiple upper limit values ​​are separately described, any lower limit value and any upper limit value can be selected, and a numerical range that is a combination of the lower limit value and the upper limit value can be selected.

[0010] <Secondary battery binder> The secondary battery binder of the present disclosure is used for secondary batteries to enhance the binding strength between particles inside an electrode and the binding strength between an active material layer and a current collector.

[0011] [Water-based polymer] The secondary battery binder in the present disclosure includes a water-based polymer. The water-based polymer in the present disclosure is a polymer that can be dispersed in water by itself, and in particular, is water-soluble.

[0012] [Characteristics of water-based polymers] The properties of water-based polymers are shown below.

[0013] (water soluble) When 2.0 g of the aqueous polymer is dissolved in 100 g of water at 25°C, the insoluble content may be 20% by mass or less, or 15% by mass or less, preferably 5% by mass or less, and more preferably 1% by mass or less, relative to the aqueous polymer.

[0014] (molecular weight, etc.) The Mw / Mn (breadth of molecular weight distribution) of the aqueous polymer as determined by GPC-triple detector may be 1.2 or more, 1.5 or more, 2.0 or more, or 3.0 or more, preferably 2.0 or more, more preferably 2.5 or more, and may be 5.0 or less, 4.0 or less, 3.5 or less, or 3.0 or less, preferably 4.0 or less, more preferably 3.5 or less. This value is determined by the method described in the Examples.

[0015] The Mw (weight average molecular weight) of the aqueous polymer measured by GPC-RI may be 50,000 or more, 100,000 or more, 300,000 or more, 500,000 or more, 750,000 or more, or 1,500,000 or more, preferably 100,000 or more, more preferably 150,000 or more, and may be 2,000,000 or less, 1,000,000 or less, 500,000 or less, or 250,000 or less, preferably 2,000,000 or less, more preferably 1,800,000 or less. This value is determined by the method described in the examples.

[0016] (pH) When the aqueous solution obtained by dissolving the aqueous polymer in water at a concentration of 2% by mass, the pH (25 °C) may be 5.0 or more, 5.5 or more, 6.0 or more, 6.5 or more, 7.0 or more, 7.5 or more, 8.0 or more, 8.5 or more, or 9.0 or more, preferably 7.0 or more, more preferably 8.0 or more. Also, it may be 10 or less, 9.5 or less, 9.0 or less, 8.5 or less, 8.0 or less, 7.5 or less, or 7.0 or less, preferably 10.0 or less, more preferably 9.5 or less. This value is determined by the method described in the examples. Usually, ion-exchanged water is used as the water. When the pH is not less than the above lower limit value (especially 7.0 or more (neutral to alkaline)), the flexibility of the polymer component containing the aqueous polymer becomes high, and it can show high followability to the expansion and contraction of the active material. When the pH is within the above range (especially 7.0 or more and 10.0 or less), the dispersibility of the slurry can be good.

[0017] (0.1 mol / L NaOH neutralization titration amount) The neutralization titration amount of 70 g of the aqueous solution obtained by dissolving the aqueous polymer in water at a concentration of 2% by mass with 0.1 mol / L sodium hydroxide aqueous solution is 0.1 mL or more and less than 0.6 mL. The neutralization titration amount may be, for example, 0.2 mL or more, 0.3 mL or more, 0.4 mL or more, or 0.5 mL or more, preferably 0.2 mL or more. Also, for example, it may be 0.5 mL or less, 0.4 mL or less, or 0.3 mL or less, preferably 0.5 mL or less. This value is determined by the method described in the examples. Usually, ion-exchanged water is used as the water. When the neutralization titration amount is within the above range (especially 0.1 mL or more and less than 0.6 mL), the capacity retention rate after cycling becomes good. When the neutralization titration amount is relatively small, the proportion of free acid decreases, which preferably contributes to the binding property between the active material and the current collector (for example, copper foil) due to conductivity and ion-ion interaction, and the capacity retention rate is considered to increase.

[0018] (Weight loss at 170 - 290 °C) The weight loss of the aqueous polymer at 170 to 290°C may be 5.0% by mass or more, 7.5% by mass or more, 10% by mass or more, 12.5% ​​by mass or more, or 15.0% by mass or more, preferably 7.5% by mass or more, more preferably 13.0% by mass or more, and may be 40% by mass or less, 35% by mass or less, 30% by mass or less, 25% by mass or less, 20% by mass or less, or 15% by mass or less, preferably 30% by mass or less, more preferably 20% by mass or less. This value is determined by the method described in the Examples.

[0019] [Water-based polymer structure, etc.] The aqueous polymer can be obtained by polymerizing one or more types of monomers. The aqueous polymer can be a vinyl polymer. The vinyl polymer is a polymer obtained by polymerizing a vinyl monomer. The vinyl monomer can be any compound having a polymerizable carbon-carbon double bond (ethylenically unsaturated double bond) (>C=C<), and can be a monomer containing a vinyl group, a vinylene group, a vinylidene group, an acryloyl group, a methacryloyl group, or a derivative group thereof. The aqueous polymer can be a (meth)acrylic polymer containing a repeating unit derived from a monomer having an acryloyl group or a methacryloyl group.

[0020] The water-based polymer may be a random polymer or a block polymer, for example a random polymer.

[0021] (hydrophilic repeating unit) The aqueous polymer has a hydrophilic repeating unit. The hydrophilic repeating unit contains a hydrophilic group. Examples of the hydrophilic group include anionic groups such as a carboxyl group, a sulfonic acid group, a phosphate group, and a nitrate group; cationic groups such as an amino group; a hydroxyl group; a polyoxyethylene group (e.g., having a repeating number of 2 or more, 5 or more, or 10 or more); and nonionic hydrophilic groups such as an amide group. The anionic group and the cationic group may be in a free acid / base state, or may be partially or completely in the form of a salt.

[0022] In this specification, when an anionic group or a cationic group or a structure containing such a group (for example, a repeating unit containing an acidic functional group) is mentioned, it is intended to encompass not only the anionic group and the cationic group but also salts thereof, unless explicitly stated otherwise.

[0023] Examples of counter cations of anionic groups include metal ions, preferably light metal ions, more preferably lithium ions, sodium ions, or potassium ions, and particularly lithium ions or sodium ions. The counter cations may be monovalent to trivalent, monovalent to divalent, or monovalent, preferably monovalent. Examples of counter anions of cationic groups include inorganic acid ions such as phosphate ions, nitrate ions, and sulfate ions, and halide ions. The aqueous polymer may be anionic, or may not have a cationic group.

[0024] The aqueous polymer of the present disclosure preferably has a repeating unit having an acidic functional group as a hydrophilic repeating unit. The acidic functional group may be an anionic group such as a carboxy group, a sulfonic acid group, a phosphate group, or a nitrate group, and is preferably a carboxy group or a sulfonic acid group. These groups may exist in the form of a salt, and in this case, the above-mentioned metal ions are suitable as counter cations. Examples of repeating units having an acidic functional group include repeating units derived from (meth)acrylic acid, maleic acid, vinylsulfonic acid, or (meth)allylsulfonic acid.

[0025] The aqueous polymer of the present disclosure may have a nonionic hydrophilic repeating unit, examples of which include (meth)acrylamide, hydroxyalkyl (meth)acrylate, hydroxyalkyl (meth)acrylamide, polyoxyalkylene (meth)acrylate, polyoxyalkylene (meth)acrylamide, and vinyl alcohol.

[0026] Examples of suitable hydrophilic repeating units include: formula: -[CH2-C(R1 )(C(=O)R 2 )]- [In the formula, R 1 is a hydrogen atom or CH3, R 2 NH2, OM (M is a hydrogen atom or a counter cation), O(CH2) n OH, NH(CH2) n OH (wherein each n is independently 1 or more and 6 or less). A repeating unit (1) represented by the formula: formula: -[CH2-CH(OH)]- Repeating unit (2) Examples of repeating units include those selected from the following:

[0027] In the repeating unit (1), R 1 is preferably a hydrogen atom.

[0028] In the repeating unit (1), R 2 In the formula (I), M may be a metal cation, preferably a light metal cation, more preferably a lithium ion, a sodium ion, or a potassium ion, and particularly preferably a lithium ion or a sodium ion. M may be monovalent to trivalent, monovalent to divalent, or monovalent, and is preferably monovalent.

[0029] In the repeating unit (1), R 2 In the formula, n may be 6 or less, 5 or less, 4 or less, 3 or less, or 2 or less, preferably 3 or less, and especially 2 or less.

[0030] The repeating unit (1) is R 2 It is preferable that the repeating unit (1) contains at least one of an NH group, an OH group, an ONa group, and an OLi group. 2 is only NH2 group, R 2 is only OH group, R 2 is only ONa group, or R 2 The repeating unit (1) may be only an OLi group. 2may contain ONa groups and OH groups, and R 2 may contain OLi groups and OH groups, may contain NH2 groups and OH groups, may contain NH2 groups, OH groups and ONa groups, may contain NH2 groups, OH groups, ONa groups and OLi groups, or R 2 may include those with OH groups, OLi groups, and NH2 groups.

[0031] The repeating unit (2) can be introduced, for example, by polymerizing a vinyl ester (vinyl acetate, vinyl propionate, etc., particularly vinyl acetate) and then saponifying it, or by reacting it with a polymer having a vinyl alcohol-based repeating unit (for example, polyvinyl alcohol).

[0032] The aqueous polymer preferably contains a repeating unit derived from (meth)acrylic acid (particularly a sodium salt or lithium salt).

[0033] (non-hydrophilic repeating unit) The aqueous polymer may have a non-hydrophilic repeating unit. The non-hydrophilic repeating unit does not have a hydrophilic group (e.g., an ionic group). Examples of the non-hydrophilic repeating unit include repeating units derived from (meth)acrylonitrile, (meth)acrylic acid alkyl ester, vinyl chloride, etc.

[0034] [Composition of water-based polymers] The amount of hydrophilic repeating units in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 20 mol% or more, more preferably 40 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less.

[0035] The amount of the acidic functional group-containing repeating unit in the aqueous polymer may be 0.8 mol% or more, 3 mol% or more, 5 mol% or more, 10 mol% or more, or 20 mol% or more, preferably 0.8 mol% or more, more preferably 10 mol% or more, and may be 70 mol% or less, 60 mol% or less, or 50 mol% or less, preferably 60 mol% or less, more preferably 50 mol% or less.

[0036] The amount of nonionic hydrophilic repeating units in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 20 mol% or more, more preferably 40 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, preferably 99 mol% or less, more preferably 70 mol% or less.

[0037] The amount of non-hydrophilic repeating units in the aqueous polymer may be 0 mol% or more, 1 mol% or more, 3 mol% or more, 5 mol% or more, 20 mol% or more, 40 mol% or more, or 50 mol% or more, or may be 70 mol% or less, 50 mol% or less, 40 mol% or less, 30 mol% or less, 20 mol% or less, 10 mol% or less, 5 mol% or less, or 3 mol% or less, and the aqueous polymer may not contain non-hydrophilic repeating units.

[0038] The amount of nonionic repeating units in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 20 mol% or more, more preferably 40 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, preferably 99 mol% or less, more preferably 70 mol% or less.

[0039] The total amount of repeating units (1) and repeating units (2) in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 40 mol% or more, more preferably 60 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less.

[0040] The amount of repeating unit (1) in the aqueous polymer may be 10 mol% or more, 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 10 mol% or more, more preferably 20 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, preferably 99 mol% or less, more preferably 70 mol% or less.

[0041] The amount of repeating unit (2) in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 20 mol% or more, more preferably 40 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, preferably 90 mol% or less, more preferably 85 mol% or less. The aqueous polymer may not contain repeating unit (2).

[0042] A repeating unit derived from (meth)acrylamide (R 2 The amount of NH2) in the aqueous polymer may be 20 mol% or more, 40 mol% or more, 60 mol% or more, 80 mol% or more, or 90 mol% or more, preferably 20 mol% or more, more preferably 40 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, preferably 99 mol% or less, more preferably 70 mol% or less.

[0043] A repeating unit derived from (meth)acrylic acid or a salt thereof (R2 The amount of OM) in the aqueous polymer may be 10 mol% or more, 20 mol% or more, 40 mol% or more, 60 mol% or more, or 80 mol% or more, preferably 10 mol% or more, more preferably 20 mol% or more, and may be 90 mol% or less, 80 mol% or less, 70 mol% or less, or 60 mol% or less, preferably 70 mol% or less, more preferably 60 mol% or less.

[0044] [Method of manufacturing water-based polymers] The aqueous polymer can be produced by any known method for producing copolymers. Preferably, it can be synthesized by aqueous radical polymerization. Specifically, a radical polymerization initiator and, if necessary, a chain transfer agent are added to a monomer mixture, and the resulting mixture is stirred while undergoing a polymerization reaction at a reaction temperature of approximately 50 to 100°C (e.g., 60 to 70°C). The reaction time is not particularly limited and may be approximately 1 to 10 hours. After the reaction time has elapsed, the mixture may be further aged for 15 minutes to 2 hours (e.g., 30 minutes to 1.5 hours) at a temperature 3°C to 10°C above the reaction temperature (e.g., 4°C to 8°C). Aging can reduce the amount of unreacted monomer. When the aqueous polymer contains vinyl alcohol units, the saponification conditions may be set with reference to, for example, the method for producing a copolymer of vinyl alcohol and an alkali metal neutralized product of an ethylenically unsaturated carboxylic acid, as described in WO2017 / 168947.

[0045] The monomer concentration at the start of polymerization may be 5% by mass or more, 10% by mass or more, 15% by mass or more, 20% by mass or more, or 25% by mass or more, and may be 30% by mass or less, 25% by mass or less, 20% by mass or less, 15% by mass or less, or 10% by mass or less, and in one aspect, is 10% by mass or more and 11% by mass or less, 15% by mass or more and 17% by mass or less, or 11% by mass or more and 13% by mass or less.

[0046] Various known initiators can be used without particular limitation. Examples of radical polymerization initiators include persulfates such as potassium persulfate and ammonium persulfate; redox polymerization initiators that combine such persulfates with reducing agents such as sodium hydrogen sulfite; and azo initiators such as 2,2'-azobis-2-amidinopropane dihydrochloride (NC-32) (V-50) and 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (VA-044). The amount of radical polymerization initiator used is preferably about 0.05 to 2% by mass, more preferably about 0.1 to 1.5% by mass, based on 100% by mass of the monomers that serve as raw materials for the aqueous polymer of the present disclosure.

[0047] The polymerization conditions can be appropriately set in accordance with the structure of the target compound.

[0048] [Amount of water-based polymer] The amount of the aqueous polymer in the secondary battery binder may be 25% by mass or more, 50% by mass or more, 75% by mass or more, 95% by mass or more, or 99% by mass or more, preferably 50% by mass or more, more preferably 75% by mass or more, and may be 99% by mass or less, 90% by mass or less, 80% by mass or less, or 70% by mass or less. The secondary battery binder may be the aqueous polymer alone.

[0049] [Other binder components] The secondary battery binder of the present disclosure may contain other binder components in addition to the aqueous polymer. Examples of other components include known binder resins, such as styrene-butadiene rubber (SBR), styrene-ethylene-butylene-styrene copolymer (SEBS), polyimide (PI), polyamide, and ethylene-vinyl acetate copolymer (EVA).

[0050] The amount of other binder components in the binder may be 0% by mass or more, 0.5% by mass or more, 5% by mass or more, 10% by mass or more, or 25% by mass or more, and may be 50% by mass or less, 40% by mass or less, 30% by mass or less, 20% by mass or less, 10% by mass or less, or 5% by mass or less, for example, 3% by mass or less.

[0051] <Slurry> The slurry of the present disclosure contains the secondary battery binder and water, and may further contain an electrode active material. The slurry may also contain battery particles such as a conductive additive and other liquid media, and is typically an electrode slurry containing an electrode active material. The slurry may be a positive electrode slurry containing a positive electrode active material or a negative electrode slurry containing a negative electrode active material.

[0052] [Liquid medium] The slurry contains a liquid medium (aqueous medium) containing water. The liquid medium is preferably water alone from the viewpoint of environmental concerns, but may also contain an organic solvent, such as alcohol (ethanol, methanol, isopropyl alcohol, etc.). The amount of the organic solvent in the liquid medium may be 30% by mass or less, 20% by mass or less, 10% by mass or less, 5% by mass or less, or 3% by mass or less, and is preferably 10% by mass or less.

[0053] [Amount of liquid medium] The amount of the liquid medium is adjusted according to the desired slurry solids concentration. The amount of the liquid medium may be 20% by mass or more, 40% by mass or more, 60% by mass or more, 80% by mass or more, or 100% by mass or more, preferably 30% by mass or more, and may be 200% by mass or less, 100% by mass or less, 80% by mass or less, 60% by mass or less, 50% by mass or less, or 40% by mass or less, preferably 160% by mass or less, more preferably 150% by mass or less, based on 100% by mass of the slurry solids (total amount of binder, active material, and conductive additive).

[0054] [Secondary battery binder] The slurry contains a binder, the types of which are as described above.

[0055] [Amount of secondary battery binder] The amount of secondary battery binder in the slurry solids (total amount of binder, active material, and conductive additive) may be 0.1% by mass or more, 0.3% by mass or more, 0.5% by mass or more, 1.0% by mass or more, 1.5% by mass or more, 3.0% by mass or more, or 5.0% by mass or more, preferably 0.3% by mass or more, and may be 10% by mass or less, 7.5% by mass or less, 5.0% by mass or less, 3.0% by mass or less, 1.0% by mass or less, 0.5% by mass or less, preferably 3.0% by mass or less, more preferably 1.0% by mass or less. A content equal to or greater than the above lower limit is preferred from the viewpoint of achieving a good binder effect. A content equal to or less than the above upper limit is preferred from the viewpoint of achieving a high capacity battery.

[0056] [Active material] The active material is an electrode active material, and may be a negative electrode active material or a positive electrode active material. When the active material is a negative electrode active material, it may contain, for example, a carbon material, and may also contain, for example, at least one of silicon and silicon oxide. Specific examples of the negative electrode active material and the positive electrode active material are shown below.

[0057] (Negative electrode active material) The negative electrode active material is not particularly limited, and any negative electrode active material commonly used in the art may be used.

[0058] Carbon materials such as crystalline carbon and amorphous carbon may be used as the negative electrode active material. Examples of crystalline carbon include graphite, such as natural graphite or artificial graphite, which may be amorphous, plate-like, flake-like, spherical, or fibrous. Examples of amorphous carbon include soft carbon (easily graphitizable carbon) or hard carbon (non-graphitizable carbon), mesophase pitch carbide, and calcined coke.

[0059] As the negative electrode active material, materials capable of storing and releasing a large amount of lithium ions such as silicon (Si), tin (Sn), titanium (Ti), etc. may be used. These materials can be used in the form of simple substances, alloys, compounds, solid solutions, or composite active materials containing silicon-containing materials, tin-containing materials, titanium-containing materials. Examples of silicon-containing materials include Si, Si / C, SiOx (0.05 < x < 1.95), or alloys, compounds, or solid solutions in which at least one element selected from the group consisting of B, Mg, Ni, Ti, Mo, Co, Ca, Cr, Cu, Fe, Mn, Nb, Ta, V, W, Zn, C, N, and Sn substitutes for a part of Si. The silicon-containing material may be a silicon oxide. Examples of tin-containing materials include Ni2Sn4, Mg2Sn, SnOx (0 < x < 2), SnO2, SnSiO3, LiSnO, etc. Examples of titanium-containing materials include lithium titanates such as Li2TiO3, Li4Ti5O 12 and niobium titanium composite compounds, etc. These materials can be used alone or in combination of two or more. Among these, silicon or silicon oxide is preferable, and for example, it may be a simple substance of Si or silicon oxide.

[0060] As the negative electrode active material, it is more preferable to use a composite obtained by mixing a silicon or silicon oxide as the first negative electrode active material and a carbon material as the second negative electrode active material as the negative electrode active material. As the carbon material, any carbon material generally used in secondary batteries, particularly non-aqueous electrolyte secondary batteries, can be used, and crystalline carbon, amorphous carbon, or both of them may be used. Examples of crystalline carbon include those described above.

[0061] The manufacturing method of the negative electrode active material is not particularly limited. When manufacturing an active material composite in which the first negative electrode active material and the second negative electrode active material are mixed, a method in which both are uniformly dispersed may be adopted. For example, a method of mixing the first negative electrode active material and the second negative electrode active material with a ball mill can be mentioned.

[0062] (Positive electrode active material) The cathode active material is not particularly limited, and a cathode active material used in this technical field may be used.

[0063] The cathode active material may be a lithium-containing composite oxide. Examples of the lithium-containing composite oxide include, for example, LiMnO2, LiFeO2, LiCoO2, LiMn2O4, Li2FeSiO4, LiNi 1 / 3 Co 1 / 3 Mn 1 / 3 O2, LiNi 0.5 Co 0.2 Mn 0.3 O2, LiNi 0.6 Co 0.2 Mn 0.2 O2, LiNi 0.8 Co 0.1 Mn 0.1 O2, LiNi x Co y M z O2 (where 0 ≤ x < 1, 0 ≤ y < 1, 0 ≤ z < 1, and x + y + z = 1, and M is at least one element selected from the group consisting of Mn, V, Mg, Mo, Nb, Fe, Cu, and Al), LiMn (1-w) Fe w PO4 (where 0 < w < 1), LiFePO4, and the like.

[0064] [Amount of active material] The amount of the active material may be 35% by mass or more, 45% by mass or more, 55% by mass or more, 65% by mass or more, 75% by mass or more, 95% by mass or more in the slurry solid content (total amount of the binder, the active material, and the conductive assistant), preferably 55% by mass or more, more preferably 75% by mass or more, and also 99% by mass or less, 95% by mass or less, 90% by mass or less, or 85% by mass or less.

[0065] [Conductive assistant] As the conductive aid, conductive aids used in the present technical field can be used. The conductive aid is not particularly limited as long as it has conductivity, but carbon powder is preferred. Examples of carbon powder include commonly used carbon materials such as acetylene black (AB), ketjen black (KB), graphite, carbon fiber, carbon tube, graphene, amorphous carbon, hard carbon, soft carbon, glassy carbon, carbon nanofiber, and carbon nanotube. These may be used alone or in combination of two or more.

[0066] [Amount of conductive additive] The amount of the conductive additive may be 0.1 mass% or more, 0.5 mass% or more, 1.0 mass% or more, 3.0 mass% or more, or 5.0 mass% or more, and preferably 0.3 mass% or more, based on the slurry solids content (total amount of binder, active material, and conductive additive), and may be 10 mass% or less, 5.0 mass% or less, 3.0 mass% or less, or 1.0 mass% or less, and preferably 3.0 mass% or less, and more preferably 1.0 mass% or less.

[0067] [Dispersion aid] The slurry of the present disclosure may further contain a dispersing aid. Examples of the dispersing aid include an organic acid containing at least one substituent selected from the group consisting of a hydroxy group, an amino group, and an imino group, and a carboxy group, or humic acid. Examples of organic acids containing a hydroxy group and a carboxy group include lactic acid, tartaric acid, citric acid, malic acid, glycolic acid, tartronic acid, glucuronic acid, and humic acid. Examples of organic acids containing an amino group and a carboxy group include glycine, alanine, phenylalanine, 4-aminobutyric acid, leucine, isoleucine, lysine, glutamic acid, aspartic acid, glutamine, asparagine, histidine, tryptophan, cysteine, and polymers thereof. Examples of organic acids containing an imino group and a carboxy group include proline, 3-hydroxyproline, 4-hydroxyproline, and pipecolic acid. Among these, glucuronic acid, humic acid, glycine, polyglycine, aspartic acid, and glutamic acid are preferred from the viewpoint of availability.

[0068] [Amount of dispersing agent] The amount of the dispersion aid may be 0.1 mass% or more, 0.5 mass% or more, 1.0 mass% or more, 1.5 mass% or more, or 3.0 mass% or more, and is preferably 0.3 mass% or more, and may be 5.0 mass% or less, 3.0 mass% or less, or 1.0 mass% or less, and is preferably 3.0 mass% or less, and more preferably 1.0 mass% or less, based on the slurry solids content (total amount of binder, active material, and conductive aid).

[0069] [Other ingredients] The slurries of the present disclosure may also contain other ingredients, such as conventional additives.

[0070] [Amount of other ingredients] The amount of other components (individual amount or total amount) of the slurry solids (total amount of binder, active material, and conductive aid) may be 0.1 mass% or more, 0.5 mass% or more, 1.0 mass% or more, 3.0 mass% or more, or 5.0 mass% or more, and is preferably 0.3 mass% or more, and may be 10 mass% or less, 5.0 mass% or less, 3.0 mass% or less, 1.0 mass% or less, or 0.5 mass% or less, and is preferably 3.0 mass% or less, and more preferably 1.0 mass% or less.

[0071] [Method for producing slurry] The method for producing the slurry of the present disclosure is not particularly limited, and the slurry is produced by mixing the components. For example, a binder, a liquid medium, an active material, and optionally, a conductive additive, a dispersing aid, etc. are mixed to form a slurry. The timing of adding the liquid medium is not particularly limited. The secondary battery binder of the present disclosure may be dispersed or dissolved in the liquid medium in advance, and then the active material and other components may be mixed to form a slurry. Alternatively, the active material, the secondary battery binder of the present disclosure, and optionally, a conductive additive, a dispersing aid, etc. may be mixed in a solid state, and then the liquid medium may be added to form a paste-like slurry.

[0072] <Electrode> The electrode of the present disclosure is an electrode for a secondary battery, and includes the secondary battery binder (or a component derived from the secondary battery binder) and an active material. That is, the electrode of the present disclosure can be produced, for example, by applying the slurry of the present disclosure to a current collector and drying it. Therefore, the electrode may include a heat-dried product of the slurry. The binder may be decomposed or reacted by heat drying and converted into a component derived from the binder.

[0073] The temperature during heat drying may be 50°C or higher, 70°C or higher, 90°C or higher, 110°C or higher, or 130°C or higher, preferably 70°C or higher, and 300°C or lower, 250°C or lower, 200°C or lower, 175°C or lower, 150°C or lower, or 125°C or lower, preferably 150°C or lower. Heat drying may be carried out under reduced pressure (e.g., 0.05 MPa or lower, 0.03 MPa or lower, 0.01 MPa or lower). The heat drying time may be 1 hour or longer, 3 hours or longer, 6 hours or longer, 10 hours or longer, or 15 hours or longer, preferably 6 hours or longer, and may be 72 hours or shorter, 48 hours or shorter, 36 hours or shorter, 24 hours or shorter, or 18 hours or shorter, preferably 24 hours or shorter.

[0074] When the electrode of the present disclosure is a negative electrode, the material constituting the current collector may be, for example, a conductive substance such as C, Cu, Ni, Fe, V, Nb, Ti, Cr, Mo, Ru, Rh, Ta, W, Os, Ir, Pt, Au, or Al, or an alloy containing two or more of these conductive substances (e.g., stainless steel). The current collector may also be made of Fe plated with Cu. From the viewpoints of high electrical conductivity, stability in the electrolyte, and oxidation resistance, Cu, Ni, stainless steel, etc. are preferred as materials for the negative electrode current collector, and Cu or Ni is more preferred from the viewpoint of material cost.

[0075] When the electrode of the present disclosure is a positive electrode, the material constituting the current collector may be, for example, a conductive substance such as C, Ti, Cr, Mo, Ru, Rh, Ta, W, Os, Ir, Pt, Au, or Al, or an alloy containing two or more of these conductive substances (for example, stainless steel). From the viewpoints of high electrical conductivity, stability in the electrolyte, and oxidation resistance, C, Al, stainless steel, etc. are preferred as the material for the positive electrode current collector, and Al is more preferred from the viewpoint of material cost.

[0076] The shape of the current collector is not particularly limited, and for example, a foil-like substrate, a three-dimensional substrate, etc. Use of a three-dimensional substrate (foam metal, mesh, woven fabric, nonwoven fabric, expanded fabric, etc.) tends to improve high-rate charge / discharge characteristics.

[0077] <Battery> The secondary battery of the present disclosure includes the aforementioned secondary battery electrode of the present disclosure. The secondary battery of the present disclosure may be any battery that includes the secondary battery electrode of the present disclosure as either one or both of a positive electrode and a negative electrode. The secondary battery of the present disclosure is fabricated using the secondary battery electrode of the present disclosure (i.e., using the secondary battery binder of the present disclosure) by a method used in the technical field.

[0078] The secondary battery of the present disclosure is preferably a nonaqueous electrolyte secondary battery, and particularly preferably a lithium ion secondary battery. Because lithium ion secondary batteries must contain lithium ions, a lithium salt is preferred as the electrolyte. Examples of the lithium salt include lithium hexafluorophosphate, lithium perchlorate, lithium tetrafluoroborate, lithium trifluoromethanesulfonate, and lithium trifluoromethanesulfonyl imide. The electrolyte may be used alone or in combination of two or more.

[0079] Examples of the electrolyte solution that can be used include propylene carbonate, ethylene carbonate, dimethyl carbonate, diethyl carbonate, and γ-butyrolactone. The electrolyte solution can be used alone or in combination of two or more. Propylene carbonate alone, a mixture of ethylene carbonate and diethyl carbonate, or γ-butyrolactone alone are particularly preferred. The mixing ratio of the above-mentioned mixture of ethylene carbonate and diethyl carbonate can be adjusted as long as one of the components accounts for 10 to 90% by volume.

[0080] Other configurations of the secondary battery may also be the same as those of known secondary batteries.

[0081] Although the embodiments have been described above, it will be understood that various changes in form and details can be made without departing from the spirit and scope of the claims. [Example]

[0082] The present disclosure will be described in detail below with reference to examples, but the present disclosure is not limited to these examples.

[0083] The abbreviations have the following meanings: AA: acrylic acid AAm: acrylamide MAS: methallylsulfonic acid VA: vinyl alcohol CMC: Carboxymethyl cellulose SBR: Styrene butadiene rubber

[0084] <Preparation of polymer> The polymer was prepared according to the procedure described below.

[0085] Example 1 A sealable vial with an internal volume of 500 ml was charged with 126.6 g (1.78 mol) of acrylamide, 2.9 g (0.02 mol) of sodium methallylsulfonate, 1.45 g of 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (Fujifilm Wako Pure Chemical Industries, Ltd. product name "VA-044"), and 250.0 g of ion-exchanged water, and the resulting mixture was mixed to prepare an aqueous monomer solution, which was then deoxygenated. Separately, a 2 L reactor equipped with a stirrer, thermometer, N2 gas inlet, reflux condenser, and dropping funnel was charged with 831.0 g of ion-exchanged water. N2 gas was blown into the reactor to deoxygenate the system, and the internal temperature was then raised to 68 °C. Subsequently, the prepared monomer aqueous solution was added dropwise to the reactor over 3 hours using the dropping funnel while maintaining the internal temperature at 68 °C. After the addition, the mixture was stirred at the same temperature for 1.5 hours. Subsequently, 1.45 g of VA-044 and 20 g of ion-exchanged water were added, and the mixture was stirred at the same temperature for 1 hour. The mixture was further stirred at 73 °C for 1 hour, yielding an aqueous solution containing a water-based polymer. The repeating unit composition of the water-based polymer was AAm / MAS (H / Na) = 99 / 1 (molar ratio).

[0086] Example 2 46.5 g (0.54 mol) of methyl acrylate and 211.8 g (2.46 mol) of vinyl acetate were added to a sealable vial having an internal volume of 500 ml and mixed to prepare an aqueous monomer solution. Separately, a 2 L reactor equipped with a stirrer, thermometer, N2 gas inlet, reflux condenser, and dropping funnel was charged with 768 g of ion-exchanged water and 12 g of anhydrous sodium sulfate, and N2 gas was blown in to deoxygenate the system. Subsequently, 1 g of partially saponified polyvinyl alcohol (saponification degree 88%) and 1.2 g of lauryl peroxide were added, and the internal temperature was raised to 60°C. Subsequently, the prepared aqueous monomer solution was added dropwise to the reactor over 4 hours using the dropping funnel while stirring. After the addition, the internal temperature was raised to 65°C and stirring was continued for 2 hours, and the precipitated solid was filtered. The obtained solid, 450 g of methanol, 420 g of ion-exchanged water, 140 g of sodium hydroxide, and 0.52 g of hydrazine were charged to the same reactor as above, and the mixture was stirred at 35°C for 3 hours. Subsequently, the internal temperature was cooled to 30°C, acetic acid was added to adjust the pH to 7.5, and the solid content was filtered off. The solid content was washed with methanol and dried under reduced pressure at 60°C for 8 hours to obtain an aqueous polymer. The composition of the repeating units of the aqueous polymer was VA / AA (H / Na) = 82 / 18 (molar ratio).

[0087] Example 3 103.6 g (1.20 mol) of methyl acrylate and 156.0 g (1.81 mol) of vinyl acetate were mixed in a beaker having an internal volume of 500 ml to prepare an aqueous monomer solution. Separately, a 2 L reactor equipped with a stirrer, thermometer, N2 gas inlet, reflux condenser, and dropping funnel was charged with 768 g of ion-exchanged water and 12 g of anhydrous sodium sulfate, and N2 gas was blown in to deoxygenate the system. Subsequently, 1 g of partially saponified polyvinyl alcohol (saponification degree 88%) and 1.2 g of lauryl peroxide were added, and the internal temperature was raised to 60°C. Subsequently, the prepared aqueous monomer solution was added dropwise to the reactor over 4 hours using the dropping funnel while stirring. After the addition, the internal temperature was raised to 65°C and stirring was continued for 2 hours, and the precipitated solid was filtered. The obtained solid, 450 g of methanol, 420 g of ion-exchanged water, 140 g of sodium hydroxide, and 0.52 g of hydrazine were charged to the same reactor as above, and the mixture was stirred at 35°C for 3 hours. Subsequently, the internal temperature was cooled to 30°C, acetic acid was added to adjust the pH to 7.5, and the solid content was filtered off. The solid content was washed with methanol and dried under reduced pressure at 60°C for 8 hours to obtain an aqueous polymer. The composition of the repeating units of the aqueous polymer was VA / AA (H / Na) = 60 / 40 (molar ratio).

[0088] Comparative Example 1 A 1 L reactor equipped with a stirrer, thermometer, N2 gas inlet tube, reflux condenser, and dropping funnel was charged with 485.3 g of ion-exchanged water and 100.0 g of terminally thiol-modified polyvinyl alcohol (degree of polymerization: 375, degree of saponification: 98.7 mol%). N2 gas was blown in to deoxygenate the system, and the internal temperature was raised to 95°C and then cooled to room temperature. The pH was then adjusted to 3.0 with 0.5 N sulfuric acid. The internal temperature was then raised to 62°C, and 9.9 g (0.14 mol) of acrylic acid, 1.70 g of ammonium persulfate, and 75.2 g of ion-exchanged water were added dropwise via the dropping funnel over 1.5 hours with stirring. After the dropwise addition, the mixture was stirred at an internal temperature of 62°C for 0.5 hours, followed by stirring at 67°C for 1 hour. The internal temperature was then cooled to 30°C, and 5.72 g (0.69 mol) of 48% by mass aqueous sodium hydroxide solution was added to obtain an aqueous solution containing a water-based polymer. The composition of the repeating units of the water-based polymer was VA / AA (H / Na) = 94 / 6 (molar ratio).

[0089] Comparative Example 2 A mixture of carboxymethyl cellulose and styrene-butadiene rubber (CMC / SBR=1 / 2 (solid weight ratio)) was used.

[0090] <Measurement of polymer properties> The properties of the polymers obtained in the above Examples and Comparative Examples were measured. The test methods are as follows. In each test, an aqueous polymer solution was used in which an aqueous polymer was dissolved in ion-exchanged water.

[0091] [Molecular weight, etc.] The polymers obtained in the above Examples and Comparative Examples were measured for Mw / Mn (breadth of molecular weight distribution) in terms of standard polyethylene glycol / polyethylene oxide using a GPC triple detector. Mw (weight average molecular weight) was measured using GPC-RI. Detailed conditions are as follows: [GPC-Triple Detector] GPC light scattering device: CHR6000 (Malvern OMNISEC REVERAL) Column: COL9002 (Malvern OMNISEC REVERAL) Carrier: 0.1M sodium nitrate Column temperature: 35℃ Flow rate: 1.0mL / min Injection volume: 150μL Concentration: 2.0mg / mL [GPC-RI] GPC equipment: HLC-8320GPC (Tosoh Corporation) Column: TSK GMPW XL (Tosoh Corporation) Carrier: 0.1M sodium nitrate Column temperature: 40℃ Flow rate: 1.0mL / min Injection volume: 200μL Concentration: 0.5mg / mL

[0092] [pH] A polymer aqueous solution was prepared by dissolving a water-based polymer in water to a solids concentration of 2% by mass. After keeping the solution at 25°C, the pH was measured using a pH meter (manufactured by Horiba, Ltd., model "D-71" and glass pH electrode: model "9681S-10D"). The pH was calculated by rounding the measured value to one decimal place.

[0093] [0.1mol / LNaOH neutralization titer] A polymer aqueous solution was prepared by dissolving a water-based polymer in water to a solids concentration of 2% by mass. 70 g of the solution was added to a 100 mL beaker, and neutralization titration was performed with 0.1 mol / L NaOH using an automatic titrator (manufactured by Hiranuma Corporation, model "COM-1700A"), and the titer was calculated using the pH inflection point detection method.

[0094] [Weight loss between 170 and 290°C] A polymer aqueous solution was prepared by dissolving a water-based polymer in water to a solids concentration of 2% by mass, and 20 g of the solution was placed in a polypropylene tray (manufactured by AS ONE, model "DT-1") and dried at 60°C for 8 hours in a constant temperature incubator (manufactured by Yamato Scientific, model "DKM300") to produce a film. The dried film was used for measurements under the following conditions using a differential scanning calorimeter (manufactured by Hitachi High-Tech Science, model "STA200RV"). Measurement conditions: Temperature was increased from 30°C to 500°C at a rate of 10°C / min, and weight change was observed. Sample pan: Aluminum pan Measurement sample mass: 4 mg Calculation of weight loss: The measured sample mass was Wa, and the weight change detected between 170°C and 290°C was Wb, and the weight loss rate was calculated using the following formula. Weight loss rate = Wb / Wa x 100 [mass %]

[0095] <Characteristics of batteries / slurries / polymer aqueous solutions, etc.> Using the polymers obtained in the above Examples and Comparative Examples, a battery / slurry / aqueous polymer solution was prepared, and its properties were measured. The test methods were as follows.

[0096] [Capacity retention rate after 100 cycles] The capacity retention rate after 100 cycles was determined according to the following procedure. [Electrode preparation] As electrode active materials, 23.3 parts by mass of artificial graphite (G-49, manufactured by Jiangxi Zichen Technology), 5.8 parts by mass of silicon monoxide (KSC-1265, manufactured by Shin-Etsu Chemical Co., Ltd.), and 0.9 parts by mass of a polymer aqueous solution (solid content equivalent) were kneaded together. Water was then added to the mixture to achieve a solid content of 58% by mass, followed by kneading to prepare a negative electrode slurry. The resulting negative electrode slurry was applied to a rolled copper foil with a thickness of 18 μm and dried. The rolled copper foil and the coating were then intimately bonded together using a roll press (manufactured by Ohno Roll Co., Ltd.). A heat treatment (reduced pressure, 100°C, 12 hours or more) was then performed to prepare a negative electrode. The thickness of the active material layer in the resulting negative electrode was 36 μm, and the capacity density of the negative electrode was 3.5 mAh / cm. 2 It was.

[0097] [Coin cell assembly] A coin cell (CR2032) was prepared comprising the negative electrode prepared above and the following positive electrode, separator, and electrolyte. ·Positive electrode: LiNi 0.5 Co 0.2 Mn 0.3 O2 (manufactured by Hachisansha Co., Ltd.) Separator: Glass filter (Advantech Co., Ltd., product name GA-100) Electrolyte: A solution in which LiPF6 is dissolved at a concentration of 1 mol / L in a solvent made by mixing ethylene carbonate (EC) and diethyl carbonate (DEC) in a volume ratio of 1:1, and 1 mass% of vinylene carbonate (VC) and 1 mass% of fluoroethylene carbonate (FEC), which are electrolyte additives, are added.

[0098] [Capacity retention rate measurement] Each coin cell prepared as described above was charged to 4.2 V at 30°C with a current equivalent to 0.1 C, discharged to 2.5 V at a current equivalent to 0.1 C, charged to 4.2 V at a current equivalent to 0.5 C, and discharged to 2.5 V at a current equivalent to 0.5 C for three cycles to age the battery. Subsequently, the battery was charged to 4.2 V at a current equivalent to 0.5 C, then discharged to SOC50 at a current equivalent to 0.5 C, discharged at a constant current for 12 seconds at a current equivalent to 0.2 C, then charged at a current equivalent to 0.1 C for 24 seconds, discharged at a constant current for 12 seconds at a current equivalent to 0.5 C, then charged at a current equivalent to 0.1 C for 1 minute, discharged at a constant current for 12 seconds at a current equivalent to 1 C, then charged at a current equivalent to 0.1 C for 2 minutes, discharged at a constant current for 12 seconds at a current equivalent to 2 C, and then discharged to 2.5 V at a current equivalent to 0.2 C, and the initial discharge capacity was measured. Subsequently, the battery was charged to 4.2 V at a current equivalent to 1 C and discharged to 2.5 V at a current equivalent to 1 C, and this cycle was repeated for 97 cycles (4th to 100th cycles). Thereafter, the same operation as that used to measure the initial discharge capacity was carried out to measure the discharge capacity after 100 cycles. Capacity retention rate after 100 cycles = [Discharge capacity after 100 cycles (mAh / g)] / [Initial discharge capacity after aging (mAh / g)] × 100 [%]

[0099] [Discharge capacity after 100 cycles] In the above test for [Capacity retention rate after 100 cycles], the discharge capacity after 100 cycles was measured.

[0100] The test results are summarized in the table below. TIFF2026035053000001.tif78164 [Industrial Applicability]

[0101] The present disclosure is suitable for use as a power source for mobile communication devices, portable electronic devices, electric bicycles, electric motorcycles, electric vehicles, and the like.

Claims

1. Contains water-based polymers, A secondary battery binder, wherein the neutralization titer of 70 g of an aqueous solution obtained by dissolving the aqueous polymer in water at a concentration of 2% by mass with a 0.1 mol / L aqueous sodium hydroxide solution is 0.1 mL or more but less than 0.6 mL.

2. 2. The secondary battery binder according to claim 1, wherein the aqueous polymer is a vinyl polymer having an acidic functional group-containing repeating unit.

3. The water-based polymer is formula: -[CH ２ -C(R １ )(C(=O)R ２ )]- [In the formula, R 1 is a hydrogen atom or CH ３ and R 2 is NH ２ , OM (M is a hydrogen atom or a counter cation), O(CH ２ ) ｎ OH, NH(CH ２ ) ｎ OH (wherein each n is independently 1 or more and 6 or less). A repeating unit (1) represented by the formula: formula: -[CH ２ -CH(OH)]- Repeating unit (2) represented by 3. The secondary battery binder according to claim 1, comprising a repeating unit selected from:

4. In the water-based polymer, the amount of the repeating unit selected from the repeating unit (1) and the repeating unit (2) is 40 mol % or more, the amount of repeating units containing an acidic functional group is 0.8 mol% or more; 4. The secondary battery binder of claim 3, wherein the amount of nonionic repeating units is 40 mol % or more.

5. 3. The secondary battery binder of claim 1 or 2, comprising SBR.

6. A slurry comprising the secondary battery binder according to claim 1 or 2 and water.

7. The slurry of claim 6 further comprising an electrode active material.

8. A method for producing a secondary battery, comprising the step of applying the slurry according to claim 6 .

9. 3. An electrode comprising the secondary battery binder according to claim 1 or 2 or a component derived from said secondary battery binder.

10. An electrode comprising the heat-dried slurry according to claim 7.

11. A secondary battery comprising the electrode according to claim 9.

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