WO2013002322A1 - Composition de liant pour électrode négative d'accumulateur, composition de suspension pour électrode négative d'accumulateur, électrode négative pour accumulateur et accumulateur - Google Patents

Composition de liant pour électrode négative d'accumulateur, composition de suspension pour électrode négative d'accumulateur, électrode négative pour accumulateur et accumulateur Download PDF

Info

Publication number
WO2013002322A1
WO2013002322A1 PCT/JP2012/066524 JP2012066524W WO2013002322A1 WO 2013002322 A1 WO2013002322 A1 WO 2013002322A1 JP 2012066524 W JP2012066524 W JP 2012066524W WO 2013002322 A1 WO2013002322 A1 WO 2013002322A1
Authority
WO
WIPO (PCT)
Prior art keywords
negative electrode
secondary battery
active material
binder
electrode active
Prior art date
Application number
PCT/JP2012/066524
Other languages
English (en)
Japanese (ja)
Inventor
智一 佐々木
Original Assignee
日本ゼオン株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 日本ゼオン株式会社 filed Critical 日本ゼオン株式会社
Priority to KR1020137033337A priority Critical patent/KR101910988B1/ko
Priority to JP2013522935A priority patent/JP6115468B2/ja
Publication of WO2013002322A1 publication Critical patent/WO2013002322A1/fr

Links

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present invention relates to a binder composition for a negative electrode of a secondary battery, and particularly relates to a binder composition for a negative electrode of a lithium ion secondary battery.
  • the present invention also relates to a slurry composition, a negative electrode and a secondary battery using such a secondary battery negative electrode binder.
  • portable terminals such as notebook personal computers, mobile phones, and PDAs (Personal Digital Assistants) have been widely used.
  • a nickel hydrogen secondary battery, a lithium ion secondary battery, and the like are frequently used.
  • Mobile terminals are required to have more comfortable portability, and are rapidly becoming smaller, thinner, lighter, and higher in performance.
  • mobile terminals are used in various places.
  • the battery is required to be smaller, thinner, lighter, and higher in performance as in the case of the portable terminal.
  • a conductive carbonaceous material is used as a negative electrode active material because of its light weight and high energy density, and the binder is used for shape retention of the electrode active material layer and adhesion to the current collector.
  • a polymer hereinafter sometimes referred to as “polymer binder”.
  • This polymer binder is required to have adhesion with an electrode active material, resistance to a polar solvent used as an electrolyte, and stability in an electrochemical environment. From such required characteristics, fluorine-based polymers such as polyvinylidene fluoride are used. However, the fluorine-based polymer has problems such as impeding conductivity when the electrode active material layer is formed and insufficient adhesive strength between the current collector and the electrode active material layer. Furthermore, when a fluorine-based polymer is used for the negative electrode which is a reduction condition, there are problems such as insufficient stability and deterioration of the cycle characteristics of the secondary battery.
  • Patent Document 1 Japanese Patent Laid-Open No. 11-25899
  • Patent Document 2 Japanese Patent Laid-Open No. 2010-140684
  • an ethylenically unsaturated acid monomer such as (meth) acrylic acid and a conjugated material such as butadiene
  • a polymer binder obtained by copolymerizing a diene and an aromatic vinyl such as styrene is disclosed. According to such a polymer binder, a battery having high adhesion between the current collector and the electrode active material layer and high cycle characteristics can be obtained.
  • various studies have been made to improve the characteristics by blending various additives with the polymer binder.
  • Patent Documents 3 to 5 teach that an alkenyl group-containing compound is added to the electrolytic solution for the purpose of preventing deterioration of the electrolytic solution.
  • the present invention is excellent in adhesion between a current collector after charging and discharging and an electrode active material layer, and can be used for secondary battery negative electrodes that can contribute to improvement of cycle characteristics and low-temperature output characteristics of secondary batteries at high temperatures.
  • An object is to provide a binder composition.
  • the inventors of the present invention have continually studied to solve the above-mentioned problems.
  • the polymer binder used for the negative electrode active material layer and the specific compound are used in combination, whereby the current collector and the electrode active material layer after charging and discharging are used.
  • the present inventors have found that a secondary battery having improved cycle characteristics at low temperatures and improved low-temperature output characteristics can be obtained.
  • a binder composition for a secondary battery negative electrode comprising a binder and a propargyl group-containing compound, wherein the content of the propargyl group-containing compound is 0.1 to 20 parts by mass with respect to 100 parts by mass of the binder.
  • binder composition for secondary battery negative electrodes as described in (1) or (2) in which the binder contains an ethylenically unsaturated carboxylic acid monomer unit.
  • a secondary battery negative electrode slurry composition comprising the secondary battery negative electrode binder composition according to any one of (1) to (4) above and a negative electrode active material.
  • a negative electrode for a secondary battery comprising a negative electrode active material layer comprising the negative electrode binder composition for a secondary battery and the negative electrode active material according to any one of (1) to (4) above on a current collector.
  • a secondary battery comprising a positive electrode, a negative electrode, an electrolytic solution, and a separator, wherein the negative electrode is a negative electrode for a secondary battery according to any one of (7) to (9).
  • the adhesion between the current collector and the electrode active material layer is improved, and in particular, the high temperature cycle characteristics and the low temperature output characteristics are improved.
  • a secondary battery is obtained.
  • Such an action mechanism of the present invention is not necessarily clear.
  • the present inventors presume the mechanism by which the above effect is achieved as follows. That is, by adding a propargyl group-containing compound to the negative electrode active material layer, the propargyl group-containing compound is adsorbed on the negative electrode active material surface, and a thin layer called SEI (Solid Electrolyte Interface) coating is formed on the negative electrode active material surface. Will be promoted.
  • SEI Solid Electrolyte Interface
  • Secondary battery negative electrode binder composition contains a binder and a propargyl group-containing compound.
  • the binder used in the present invention is not particularly limited, and various polymer compounds that have been conventionally used as binders for negative electrode active material layers such as fluoropolymers, diene polymers, and nitrile polymers can be used. Used. Among these, a polymer compound that can be easily synthesized in an aqueous system and easily obtained in the form of an aqueous latex is preferable. Examples of such a polymer compound include a polymer compound containing an ethylenically unsaturated acid monomer unit, preferably an ethylenically unsaturated carboxylic acid monomer unit.
  • the polymer compound containing an ethylenically unsaturated carboxylic acid monomer unit preferably contains an aliphatic conjugated diene monomer unit as a comonomer, and, if necessary, other monomers that can be copolymerized with these monomers. Units derived from the mer may be included. Furthermore, it is particularly preferable to contain these monomer units in a specific ratio from the viewpoint of the durability, flexibility, adhesiveness, and the like of the binder.
  • the binder particularly preferably used in the present invention comprises an ethylenically unsaturated carboxylic acid monomer unit, an aliphatic conjugated diene monomer unit, and other monomer units copolymerizable therewith, Those containing monomer units in a specific ratio are preferred.
  • the ethylenically unsaturated carboxylic acid monomer unit is a polymer repeating unit obtained by polymerizing an ethylenically unsaturated carboxylic acid monomer
  • the aliphatic conjugated diene monomer unit is an aliphatic conjugated diene type. It is a polymer repeating unit obtained by polymerizing monomers, and other monomer units copolymerizable with these are polymer repeating units obtained by polymerizing other copolymerizable monomers. is there.
  • Examples of the ethylenically unsaturated carboxylic acid monomer include mono- or dicarboxylic acids (anhydrides) such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, and itaconic acid. Can be used. Among these, acrylic acid, methacrylic acid, and itaconic acid are preferable, and itaconic acid is particularly preferable in terms of excellent adhesion to the current collector.
  • a polymer binder is used in combination with a propargyl group-containing compound described later, the dispersibility of the binder composition in water increases as the amount of the propargyl group-containing compound increases (hereinafter, sometimes abbreviated as water dispersibility). May decrease. However, water dispersibility is improved by introducing a unit containing a carboxylic acid into the polymer binder. In particular, when itaconic acid, which is a dicarboxylic acid, is introduced, the affinity between the binder and water increases.
  • Aliphatic conjugated diene monomers include 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 2-chloro-1,3-butadiene, substituted Examples thereof include linear conjugated pentadienes, substituted and side chain conjugated hexadienes, and one or more kinds can be used. In particular, 1,3-butadiene is preferred.
  • Other monomers copolymerizable with these include aromatic vinyl monomers, vinyl cyanide monomers, unsaturated carboxylic acid alkyl ester monomers, and unsaturated monomers containing hydroxyalkyl groups. Body, unsaturated carboxylic acid amide monomer, etc., and these can be used alone or in combination.
  • an aromatic vinyl monomer is preferable from the viewpoint that swelling with respect to the electrolytic solution can be suppressed.
  • aromatic vinyl monomer examples include styrene, ⁇ -methylstyrene, vinyltoluene, divinylbenzene and the like, and one or more kinds can be used.
  • styrene is particularly preferable in that swelling with respect to the electrolytic solution can be suppressed.
  • vinyl cyanide monomer examples include acrylonitrile, methacrylonitrile, ⁇ -chloroacrylonitrile, ⁇ -ethylacrylonitrile and the like, and one or more can be used. In particular, acrylonitrile and methacrylonitrile are preferable.
  • unsaturated carboxylic acid alkyl ester monomers include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, glycidyl methacrylate, dimethyl fumarate, diethyl fumarate, dimethyl maleate, diethyl maleate, dimethyl itaconate, Examples thereof include monomethyl fumarate, monoethyl fumarate, 2-ethylhexyl acrylate and the like, and one or more can be used. Particularly preferred is methyl methacrylate.
  • Examples of unsaturated monomers containing a hydroxyalkyl group include ⁇ -hydroxyethyl acrylate, ⁇ -hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, 3-chloro-2-hydroxypropyl Examples include methacrylate, di- (ethylene glycol) maleate, di- (ethylene glycol) itaconate, 2-hydroxyethyl maleate, bis (2-hydroxyethyl) maleate, 2-hydroxyethyl methyl fumarate, etc. More than one species can be used. In particular, ⁇ -hydroxyethyl acrylate is preferred.
  • Examples of the unsaturated carboxylic acid amide monomer include acrylamide, methacrylamide, N-methylolacrylamide, N-methylolmethacrylamide, N, N-dimethylacrylamide, and the like, and one or more can be used. Particularly preferred are acrylamide and methacrylamide.
  • any of the monomers used in ordinary emulsion polymerization such as ethylene, propylene, vinyl acetate, vinyl propionate, vinyl chloride, vinylidene chloride, can be used.
  • the ratio of each monomer unit of the binder in the present invention is preferably 0.1 to 20% by mass, more preferably 0.5 to 15% by mass, and more preferably 1 to ethylenically unsaturated carboxylic acid monomer units.
  • the aliphatic conjugated diene monomer unit is preferably 20 to 80% by mass, more preferably 25 to 70% by mass, and even more preferably 30 to 60% by mass.
  • the other polymerizable monomer units are preferably 5 to 79.9% by mass, more preferably 10 to 70% by mass, and more preferably 20 to 60% by mass.
  • the stability of the binder composition and the slurry composition is improved, and sufficient adhesion between the negative electrode active material and the current collector in the negative electrode for a secondary battery is obtained. Sex can be obtained. As a result, durability of the obtained secondary battery, in particular, high temperature cycle characteristics is improved, which is preferable.
  • the flexibility of the negative electrode for secondary battery and the adhesion between the negative electrode active material and the current collector are highly balanced, which is preferable.
  • the durability of the obtained secondary battery, in particular, the high temperature cycle characteristics is improved, which is preferable.
  • the flexibility of the negative electrode for a secondary battery and the adhesion between the negative electrode active material and the current collector are highly balanced, which is preferable.
  • the durability of the obtained secondary battery, in particular, the high temperature cycle characteristics is improved, which is preferable.
  • the glass transition temperature (Tg) of the binder is preferably ⁇ 60 to 40 ° C., more preferably ⁇ 50 to 30 ° C., and particularly preferably ⁇ 40 to 20 ° C.
  • Tg of the binder is within the above range, characteristics such as flexibility, binding and winding properties of the negative electrode, and adhesion between the negative electrode active material and the current collector are highly balanced, which is preferable.
  • hydrogenation may be performed on the diene unit after polymerization.
  • the method for hydrogenation is not particularly limited, and a normal method can be used.
  • the binder composition for a secondary battery negative electrode of the present invention contains a specific amount of a propargyl group-containing compound with respect to 100 parts by mass (in terms of solid content) of the binder.
  • a specific amount of a propargyl group-containing compound when containing a specific amount of a propargyl group-containing compound, propargyl is brought into contact with the negative electrode active material. It is considered that the group-containing compound forms an SEI film in the vicinity of the active point of the negative electrode active material.
  • the SEI coating prevents the components of the electrolytic solution from coming into contact with the active points, so that the decomposition of the electrolytic solution in the battery is suppressed.
  • the increase in the electrolyte viscosity due to the decomposition of the electrolyte and the increase in the internal resistance of the secondary battery are suppressed, so that the high-temperature storage characteristics, the high-temperature cycle characteristics, and the low-temperature output characteristics of the secondary battery are improved.
  • swelling of the negative electrode active material layer due to the decomposition product of the electrolyte component is prevented, the peel strength is maintained, and the high temperature cycle characteristics and the low temperature output characteristics can be further improved.
  • the content of the propargyl group-containing compound in the binder composition is 0.1 to 20 parts by weight, preferably 0.5 to 10 parts by weight, more preferably 1 to 5 parts by weight with respect to 100 parts by weight of the binder (in terms of solid content). Part.
  • the content of the propargyl group-containing compound is too small, the formation of the SEI coating becomes insufficient, the electrolytic solution component is easily decomposed, and the battery cycle characteristics and output characteristics may be deteriorated.
  • the content of the propargyl group-containing compound is too large, the stability of the slurry prepared using the binder composition is impaired, and the viscosity of the slurry tends to increase. As a result, it becomes difficult to apply the slurry, the uniformity of the obtained negative electrode is lowered, and the output characteristics may be lowered.
  • the propargyl group-containing compound used in the present invention has one or more propargyl groups (HC—C—CH 2 —) in the molecule.
  • the number of propargyl groups is not particularly limited. However, when the number of propargyl groups is increased, the dispersibility in water may be reduced, and a uniform aqueous slurry may not be obtained. Therefore, the number of propargyl groups per molecule of the propargyl group-containing compound is preferably 2 or less, particularly preferably 1. Accordingly, monopropargyl group-containing compounds are particularly preferably used in the present invention.
  • propargyl group-containing compound examples include monopropargyl group-containing compounds such as propargyl benzenesulfonate, propargyl acrylate, propargyl methacrylate, and propargyl acetate; Examples include dipropargyl group-containing compounds such as dipropargyl carbonate.
  • the binder composition for secondary battery negative electrode of the present invention may contain a dispersion medium for dispersing these components in addition to the binder and the propargyl group-containing compound.
  • the dispersion medium may be either water or an organic solvent.
  • a hydrophilic solvent may be mixed with water as the dispersion medium. Examples of the hydrophilic solvent include methanol, ethanol, N-methylpyrrolidone and the like, and it is preferably 5% by mass or less based on water.
  • a reaction solvent at the time of preparing the binder described later may be used as a dispersion medium as it is, or the solvent may be replaced after preparing the binder.
  • the total solid concentration of the binder and the propargyl group-containing compound is not particularly limited, but about 20 to 60% by mass is appropriate.
  • the binder composition may contain various dispersants used at the time of preparing the binder.
  • the binder composition may further contain an antiaging agent, an antiseptic, and the like as long as the dispersibility of the composition is not impaired.
  • antioxidant examples include amine-based antioxidants, phenol-based antioxidants, quinone-based antioxidants, organic phosphorus-based antioxidants, sulfur-based antioxidants, and phenothiazine-based antioxidants.
  • preservative examples include isothiazoline compounds and pyrithione compounds.
  • a monomer composition containing the above monomer is polymerized in an aqueous solvent to prepare an aqueous dispersion containing a binder (a binder having a binding force).
  • a solution or dispersion in which a binder as a coalesced particle is dissolved or dispersed in an aqueous solvent), and a specific amount of a propargyl group-containing compound and other optional components are added to and mixed with an aqueous dispersion containing the binder.
  • the method for producing the binder composition is not limited to this.
  • a propargyl group-containing compound, an anti-aging agent, or an antiseptic may be blended in advance in the monomer composition, and then polymerization may be performed. Good. Moreover, you may mix
  • the ratio of each monomer in the monomer composition in the step of obtaining an aqueous dispersion containing a binder is preferably 0.1 to 20% by mass, more preferably 0. 5 to 15% by mass, more preferably 1.0 to 10% by mass, and aliphatic conjugated diene monomer is preferably 20 to 80% by mass, more preferably 25 to 70% by mass, and more preferably 30 to 30% by mass.
  • the amount of the other monomer copolymerizable with these is preferably 5 to 79.9% by mass, more preferably 10 to 70% by mass, and still more preferably 20 to 60% by mass.
  • the aqueous solvent is not particularly limited as long as it can disperse the binder, and is usually selected from dispersion media having a boiling point of 80 to 350 ° C., preferably 100 to 300 ° C. at normal pressure.
  • the number in parentheses after the name of the following exemplified dispersion medium is a boiling point (unit: ° C) at normal pressure, and a value after the decimal point is rounded off or rounded down.
  • glycol ethers include propylene glycol monomethyl ether (120), methyl cellosolve (124), ethyl cellosolve (136), ethylene glycol tertiary butyl ether (152) Butyl cellosolve (171), 3-methoxy-3-methyl-1-butanol (174), ethylene glycol monopropyl ether (150), diethylene glycol monobutyl pyrute (230), triethylene glycol monobutyl ether (271), dipropylene glycol monomethyl ether (188); ethers include 1,3-dioxolane (75), 1,4-dioxolane (101), and tetrahydrofuran (
  • water is most preferable from the viewpoint that it is not flammable and a binder dispersion is easily obtained.
  • water may be used as the main solvent, and an aqueous solvent other than the above-described water may be mixed and used within a range in which the dispersion state of the binder can be ensured.
  • the polymerization method is not particularly limited, and any method such as a solution polymerization method, a suspension polymerization method, a bulk polymerization method, and an emulsion polymerization method can be used.
  • Examples of the polymerization reaction include ionic polymerization, radical polymerization, and living radical polymerization. Manufacturing efficiency, such as easy to obtain high molecular weight, obtained in a state where the polymer is dispersed in water as it is, no redispersion treatment is required, and can be used as it is for slurry composition preparation for secondary battery negative electrode From the viewpoint of the above, the emulsion polymerization method is most preferable.
  • the emulsion polymerization method is a conventional method, for example, the method described in “Experimental Chemistry Course” Vol. 28, (Publisher: Maruzen Co., Ltd., edited by The Chemical Society of Japan), that is, water in a sealed container with a stirrer and a heating device.
  • Add additives such as dispersants, emulsifiers and crosslinkers, initiators and monomers to the prescribed composition, stir to emulsify the monomers in water, start the polymerization by increasing the temperature while stirring Is the method. Or after emulsifying the said composition, it is the method of starting reaction similarly in an airtight container.
  • Emulsifiers, dispersants, polymerization initiators and the like are those generally used in these polymerization methods, and the amount used thereof may be generally used.
  • seed particles can be employed (seed polymerization).
  • the polymerization temperature and polymerization time can be arbitrarily selected depending on the polymerization method and the type of polymerization initiator used, but the polymerization temperature is usually about 30 ° C. or higher and the polymerization time is about 0.5 to 30 hours.
  • Additives such as amines can also be used as polymerization aids.
  • an aqueous dispersion of polymer particles obtained by these methods is mixed with an alkali metal (Li, Na, K, Rb, Cs) hydroxide, ammonia, an inorganic ammonium compound (NH 4 Cl, etc.), an organic amine compound (ethanol).
  • a basic aqueous solution in which amine, diethylamine, etc.) are dissolved can be added to adjust the pH to 5 to 10, preferably 5 to 9.
  • the pH adjustment with the alkali metal hydroxide is preferable because the binding property (peel strength) between the binder composition, the current collector and the active material is improved.
  • the above-mentioned binder may be composite polymer particles composed of two or more kinds of polymers.
  • the composite polymer particles can also be obtained by a method (two-stage polymerization method) in which at least one monomer component is polymerized by a conventional method, and then at least one other monomer component is added and polymerized by a conventional method. Can do.
  • polymerization initiator used for the polymerization examples include lauroyl peroxide, diisopropyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, t-butyl peroxypivalate, 3,3,5-trimethylhexanoyl peroxide, and the like.
  • a chain transfer agent may be added.
  • the chain transfer agent is preferably an alkyl mercaptan, specifically, n-butyl mercaptan, t-butyl mercaptan, n-hexyl mercaptan, n-octyl mercaptan, t-octyl mercaptan, n-dodecyl mercaptan, t-dodecyl mercaptan.
  • N-stearyl mercaptan N-stearyl mercaptan.
  • n-octyl mercaptan and t-dodecyl mercaptan are preferable from the viewpoint of good polymerization stability.
  • chain transfer agents may be used in combination with the alkyl mercaptan.
  • chain transfer agents that may be used in combination include terpinolene, allyl alcohol, allylamine, sodium allyl sulfonate (potassium), and sodium methallyl sulfonate (potassium).
  • the amount of the serial transfer agent used is not particularly limited as long as the effect of the present invention is not hindered.
  • the number average particle size of the binder in the aqueous dispersion is preferably 50 to 500 nm, and more preferably 70 to 400 nm. When the number average particle diameter of the binder is in the above range, the strength and flexibility of the obtained negative electrode are improved.
  • the presence of the polymer particles can be easily measured by a transmission electron microscope method, a Coulter counter, a laser diffraction scattering method, or the like.
  • the binder may be a binder composed of polymer particles having a core-shell structure obtained by polymerizing the above monomers stepwise.
  • the method of adding and mixing the propargyl group-containing compound and other optional components to the aqueous dispersion containing the binder is not particularly limited.
  • the mixing method include a method using a mixing apparatus such as a stirring type, a shaking type, and a rotary type.
  • a method using a dispersion kneader such as a homogenizer, a ball mill, a sand mill, a roll mill, a planetary mixer, and a planetary kneader can be used.
  • an additive may be added to the obtained binder composition for a negative electrode of the secondary battery of the present invention in order to improve applicability and charge / discharge characteristics.
  • additives include cellulose polymers such as carboxymethyl cellulose, methyl cellulose, hydroxypropyl cellulose, polyacrylates such as sodium polyacrylate, polyvinyl alcohol, polyethylene oxide, polyvinyl pyrrolidone, acrylic acid-vinyl alcohol copolymer, Examples thereof include methacrylic acid-vinyl alcohol copolymer, maleic acid-vinyl alcohol copolymer, modified polyvinyl alcohol, polyethylene glycol, ethylene-vinyl alcohol copolymer, and partially saponified polyvinyl acetate.
  • these additives can also be added to the slurry composition for a secondary battery negative electrode of the present invention described later.
  • the secondary battery negative electrode slurry composition of the present invention comprises the above secondary battery negative electrode binder composition and a negative electrode active material. Below, the aspect which uses the slurry composition for secondary battery negative electrodes of this invention as a slurry composition for lithium ion secondary battery negative electrodes is demonstrated.
  • the negative electrode active material used in the present invention is a material that transfers electrons in the negative electrode for a secondary battery.
  • Examples of the negative electrode active material for a lithium ion secondary battery include a carbon material-based active material and an alloy-based active material.
  • the carbon material-based active material refers to an active material having carbon as a main skeleton into which lithium can be inserted, and specifically includes a carbonaceous material and a graphite material.
  • the carbonaceous material generally indicates a carbon material having a low graphitization (low crystallinity) obtained by heat-treating (carbonizing) a carbon precursor at 2000 ° C. or less, and the graphitic material is a graphitizable carbon at 2000 ° C.
  • a graphitic material having high crystallinity close to that of the graphite obtained by heat treatment as described above will be shown.
  • Examples of the carbonaceous material include graphitizable carbon that easily changes the carbon structure depending on the heat treatment temperature, and non-graphitic carbon having a structure close to an amorphous structure typified by glassy carbon.
  • graphitizable carbon examples include carbon materials made from tar pitch obtained from petroleum and coal, such as coke, mesocarbon microbeads (MCMB), mesophase pitch-based carbon fibers, pyrolytic vapor-grown carbon fibers, etc. Is mentioned.
  • MCMB is a carbon fine particle obtained by separating and extracting mesophase spherules produced in the process of heating pitches at around 400 ° C.
  • mesophase pitch-based carbon fiber is a mesophase pitch obtained by growing and coalescing the mesophase spherules. Is a carbon fiber made from a raw material.
  • non-graphitizable carbon examples include phenol resin fired bodies, polyacrylonitrile-based carbon fibers, pseudo-isotropic carbon, and furfuryl alcohol resin fired bodies (PFA).
  • Examples of the graphite material include natural graphite and artificial graphite.
  • Examples of artificial graphite include artificial graphite heat-treated at 2800 ° C or higher, graphitized MCMB heat-treated MCMB at 2000 ° C or higher, and graphitized mesophase pitch carbon fiber heat-treated at 2000 ° C or higher. It is done.
  • a graphite material is preferable.
  • the alloy-based active material used in the present invention refers to an active material containing an element capable of inserting lithium in the structure and having a theoretical electric capacity per mass of 500 mAh / g or more when lithium is inserted.
  • Lithium metal, a single metal forming a lithium alloy and an alloy thereof, and oxides, sulfides, nitrides, silicides, carbides, phosphides, and the like thereof are used.
  • Examples of single metals and alloys forming lithium alloys include compounds containing metals such as Ag, Al, Ba, Bi, Cu, Ga, Ge, In, Ni, P, Pb, Sb, Si, Sn, Sr, and Zn. Is mentioned. Among these, silicon (Si), tin (Sn) or lead (Pb) simple metals, alloys containing these atoms, or compounds of these metals are used.
  • the alloy-based active material used in the present invention may further contain one or more nonmetallic elements.
  • SiC, SiO x C y (hereinafter referred to as “Si—O—C”) (0 ⁇ x ⁇ 3, 0 ⁇ y ⁇ 5), Si 3 N 4 , Si 2 N 2 O, Examples thereof include SiO x (0 ⁇ x ⁇ 2), SnO x (0 ⁇ x ⁇ 2), LiSiO, LiSnO, etc.
  • SiO x C y capable of inserting and releasing lithium at a low potential is preferable.
  • SiO x C y can be obtained by firing a polymer material containing silicon.
  • the range of 0.8 ⁇ x ⁇ 3 and 2 ⁇ y ⁇ 4 is preferably used in view of the balance between capacity and cycle characteristics.
  • oxides, sulfides, nitrides, silicides, carbides, and phosphides examples include oxides, sulfides, nitrides, silicides, carbides, and phosphides of elements into which lithium can be inserted.
  • Oxides are particularly preferred. Specifically, an oxide such as tin oxide, manganese oxide, titanium oxide, niobium oxide, vanadium oxide, or a lithium-containing metal composite oxide material containing a metal element selected from the group consisting of Si, Sn, Pb, and Ti atoms is used. It has been.
  • the silicon oxide include materials such as silicon carbide (Si—O—C).
  • a lithium titanium composite oxide represented by Li x Ti y M z O 4 (0.7 ⁇ x ⁇ 1.5, 1.5 ⁇ y ⁇ 2.3, 0 ⁇ z ⁇ 1.6, M includes Na, K, Co, Al, Fe, Ti, Mg, Cr, Ga, Cu, Zn, and Nb), among which Li 4/3 Ti 5/3 O 4 , Li1Ti 2 O 4 and Li 4/5 Ti 11/5 O 4 are used.
  • silicon-containing materials materials containing silicon
  • Si—O—C materials containing carbon
  • insertion / extraction of Li to / from Si (silicon) occurs at a high potential and C (carbon) at a low potential, and expansion / contraction is suppressed as compared with other alloy-based active materials.
  • the negative electrode active material a graphite material and a silicon-containing material are preferable, and natural graphite and Si—O—C are particularly preferable.
  • an SEI film is formed by contact with a propargyl group-containing compound, the active sites at the edge portion are easily deactivated, and decomposition of the electrolyte component can be effectively prevented.
  • the present invention is effective for an electrode containing a carbon material-based active material.
  • a negative electrode active material may be used individually by 1 type, and may use 2 or more types together.
  • a combination of a graphite material and a silicon-containing material is preferred.
  • the blending ratio (graphitic material / silicon-containing material) is preferably 99/1 to 40/60, more preferably 95/5 to 45/55, by weight.
  • the shape of the negative electrode active material is preferably a granulated particle. When the shape of the particles is spherical, a higher density electrode can be formed during electrode molding.
  • the volume average particle diameter of the negative electrode active material is appropriately selected in consideration of other constituent elements of the battery, but is usually 0.1 to 100 ⁇ m, preferably 1 to 50 ⁇ m, more preferably 5 to 20 ⁇ m. Further, the 50% volume cumulative diameter of the negative electrode active material is usually 1 to 50 ⁇ m, preferably 15 to 30 ⁇ m, from the viewpoint of improving battery characteristics such as initial efficiency, load characteristics, and cycle characteristics.
  • the volume average particle diameter is determined by measuring the particle size distribution by laser diffraction.
  • the 50% volume cumulative diameter is a 50% volume average particle diameter calculated by measuring with a laser diffraction particle size distribution analyzer (SALD-3100; manufactured by Shimadzu Corporation).
  • the tap density of the negative electrode active material is not particularly limited, but 0.6 g / cm 3 or more is preferably used.
  • the BET specific surface area of the negative electrode active material is preferably 3 to 20 m 2 / g, more preferably 3 to 15 m 2 / g, and particularly preferably 3 to 10 m 2 / g.
  • the BET specific surface area of the negative electrode active material is in the above range, the active points on the surface of the negative electrode active material are increased, so that the low-temperature output characteristics of the secondary battery are excellent.
  • the total content of the negative electrode active material and the binder composition in the secondary battery negative electrode slurry composition of the present invention is preferably 10 to 90 parts by mass, more preferably 30 parts, relative to 100 parts by mass of the slurry composition. ⁇ 80 parts by mass.
  • the content of the binder composition relative to the total amount of the negative electrode active material is preferably 0.1 to 5 parts by mass, more preferably 0.005 parts by mass with respect to 100 parts by mass of the total amount of the negative electrode active material. 5 to 2 parts by mass.
  • the viscosity of the obtained slurry composition for secondary battery negative electrode is optimized, and the coating is smoothly performed.
  • sufficient adhesion strength can be obtained without increasing the resistance of the obtained negative electrode.
  • peeling of the negative electrode active material layer from the current collector in the electrode plate pressing step can be suppressed.
  • water is preferably used as a dispersion medium for the slurry.
  • a mixture of water and a hydrophilic solvent may be used as a dispersion medium.
  • the hydrophilic solvent include methanol, ethanol, N-methylpyrrolidone and the like, and it is preferably 5% by mass or less based on water.
  • the slurry composition for secondary battery negative electrodes of this invention it is preferable to contain a electrically conductive agent.
  • a electrically conductive agent conductive carbon such as acetylene black, ketjen black, carbon black, graphite, vapor-grown carbon fiber, and carbon nanotube can be used.
  • the content of the conductive agent in the slurry composition is preferably 1 to 20 parts by mass, more preferably 1 to 10 parts by mass with respect to 100 parts by mass of the negative electrode active material.
  • thickener In the slurry composition for secondary battery negative electrodes of this invention, it is preferable to contain a thickener.
  • thickeners include cellulose polymers such as carboxymethylcellulose, methylcellulose, hydroxypropylcellulose, and ammonium salts and alkali metal salts thereof; (Modified) poly (meth) acrylic acid and ammonium salts and alkali metal salts thereof; (Modified) Polyvinyl alcohols such as polyvinyl alcohol, a copolymer of acrylic acid or acrylate and vinyl alcohol, maleic anhydride or a copolymer of maleic acid or fumaric acid and vinyl alcohol; Examples include polyethylene glycol, polyethylene oxide, polyvinyl pyrrolidone, modified polyacrylic acid, oxidized starch, phosphate starch, casein, and various modified starches.
  • the blending amount of the thickener is preferably 0.5 to 1.5 parts by mass with respect to 100 parts by mass of the negative electrode active material. When the blending amount of the thickener is within the above range, the coating property and the adhesion with the current collector are good.
  • (modified) poly means “unmodified poly” or “modified poly”
  • (meth) acryl means “acryl” or “methacryl”.
  • the slurry composition for secondary battery negative electrode may further contain other components such as a reinforcing material, a leveling agent, and an electrolyte additive having a function of inhibiting electrolyte decomposition, It may be contained in a negative electrode for a secondary battery described later. These are not particularly limited as long as they do not affect the battery reaction.
  • the reinforcing material various inorganic and organic spherical, plate-like, rod-like or fibrous fillers can be used.
  • a reinforcing material By using a reinforcing material, a tough and flexible negative electrode can be obtained, and excellent long-term cycle characteristics can be exhibited.
  • the content of the reinforcing material in the slurry composition is usually 0.01 to 20 parts by mass, preferably 1 to 10 parts by mass with respect to 100 parts by mass of the negative electrode active material. By being included in the above range, high capacity and high load characteristics are exhibited.
  • the leveling agent examples include surfactants such as alkyl surfactants, silicone surfactants, fluorine surfactants, and metal surfactants.
  • the content of the leveling agent in the slurry composition is preferably 0.01 to 10 parts by mass with respect to 100 parts by mass of the negative electrode active material.
  • the productivity, smoothness, and battery characteristics during the production of the negative electrode are excellent.
  • the surfactant By containing the surfactant, the dispersibility of the negative electrode active material and the like in the slurry composition can be improved, and the smoothness of the negative electrode can be improved.
  • the electrolytic solution additive used in the slurry composition and the electrolytic solution vinylene carbonate or the like can be used.
  • the content of the electrolytic solution additive in the slurry composition is preferably 0.01 to 10 parts by mass with respect to 100 parts by mass of the negative electrode active material.
  • the cycle characteristics and the high temperature characteristics are excellent.
  • Other examples include nanoparticles such as fumed silica and fumed alumina. By mixing the nanoparticles, the thixotropy of the slurry composition can be controlled, and the leveling property of the negative electrode can be improved.
  • the content of the nanoparticles in the slurry composition is preferably 0.01 to 10 parts by mass with respect to 100 parts by mass of the negative electrode active material. When the nanoparticles are in the above range, the slurry stability and productivity are excellent, and high battery characteristics are exhibited.
  • the slurry composition for a secondary battery negative electrode of the present invention can contain a water-soluble polymer in addition to the binder composition.
  • the water-soluble polymer include ethylenically unsaturated carboxylic acid monomer units of 20 to 60% by mass, (meth) acrylic acid ester monomer units of 20 to 80% by mass and other monomer units copolymerizable therewith.
  • a water-soluble polymer consisting of 0 to 20% by mass is preferred.
  • the water-soluble polymer in the present invention refers to a polymer having a 1% aqueous solution viscosity of 0.1 to 100,000 mPa ⁇ s at pH 12.
  • Examples of the ethylenically unsaturated carboxylic acid monomer include mono- or dicarboxylic acids (anhydrides) such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, and itaconic acid. Can be used.
  • the ratio of these ethylenically unsaturated carboxylic acid monomer units is more preferably 25 to 55% by mass, particularly preferably 30 to 50% by mass.
  • (Meth) acrylic acid ester monomers include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, t-butyl acrylate, pentyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate, 2- Acrylic acid alkyl esters such as ethylhexyl acrylate, nonyl acrylate, decyl acrylate, lauryl acrylate, n-tetradecyl acrylate, stearyl acrylate; methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, t-butyl methacrylate , Pentyl methacrylate, hexyl methacrylate, heptyl meth
  • Other monomers that can be copolymerized include carboxylic acid ester monomers having two or more carbon-carbon double bonds such as ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, trimethylolpropane triacrylate; styrene, chlorostyrene, Styrene monomers such as vinyl toluene, t-butyl styrene, vinyl benzoic acid, methyl vinyl benzoate, vinyl naphthalene, chloromethyl styrene, hydroxymethyl styrene, ⁇ -methyl styrene, divinylbenzene; acrylamide, N-methylol aqua amide, Amide monomers such as acrylamide-2-methylpropanesulfonic acid; ⁇ , ⁇ -unsaturated nitrile compounds such as acrylonitrile and methacrylonitrile; Olefins such as ethylene and propylene; Halogen atom-containing monomers such as vinyl chloride and vinyl
  • ⁇ , ⁇ -unsaturated nitrile compounds and styrene monomers are preferable, and ⁇ , ⁇ -unsaturated nitrile compounds are particularly preferable.
  • the ratio of these copolymerizable monomer units is more preferably 0 to 10% by mass, particularly preferably 0 to 5% by mass.
  • Examples of the method for producing a water-soluble polymer include a method in which a monomer composition containing the above monomer is polymerized in an aqueous solvent to obtain a water-dispersible polymer and alkalized to pH 7-13. About an aqueous solvent and the polymerization method, it is the same as that of the above-mentioned binder composition for secondary battery negative electrodes.
  • the method for alkalinizing to pH 7 to 13 is not particularly limited, but alkaline earth solutions such as an aqueous alkali metal solution such as an aqueous lithium hydroxide solution, an aqueous sodium hydroxide solution, and an aqueous potassium hydroxide solution, an aqueous calcium hydroxide solution, and an aqueous magnesium hydroxide solution.
  • alkaline earth solutions such as an aqueous alkali metal solution such as an aqueous lithium hydroxide solution, an aqueous sodium hydroxide solution, and an aqueous potassium hydroxide solution, an aqueous calcium hydroxide solution, and an aqueous magnesium hydroxide solution.
  • alkaline earth solutions such as an aqueous alkali metal solution such as an aqueous lithium hydroxide solution, an aqueous sodium hydroxide solution, and an aqueous potassium hydroxide solution, an aqueous calcium hydroxide solution, and an aqueous magnesium hydroxide solution.
  • examples include
  • the slurry composition for a secondary battery negative electrode is obtained by mixing the binder composition, the negative electrode active material, and a conductive agent used as necessary.
  • the mixing method is not particularly limited, and examples thereof include a method using a mixing apparatus such as a stirring type, a shaking type, and a rotary type.
  • a method using a dispersion kneader such as a homogenizer, a ball mill, a sand mill, a roll mill, a planetary mixer, and a planetary kneader can be used.
  • Negative electrode for secondary battery comprises the binder composition and the negative electrode active material, and specifically, the slurry composition for secondary battery negative electrode of the present invention is collected. It is obtained by applying and drying on an electric body.
  • the method for producing the negative electrode for secondary battery of the present invention is not particularly limited.
  • a method of forming the negative electrode active material layer by applying and drying the slurry composition on at least one surface, preferably both surfaces of the current collector. can be mentioned.
  • the method for applying the slurry composition onto the current collector is not particularly limited.
  • Examples of the method include a doctor blade method, a dip method, a reverse roll method, a direct roll method, a gravure method, an extrusion method, and a brush coating method.
  • drying method examples include drying with warm air, hot air, low-humidity air, vacuum drying, and drying by irradiation with (far) infrared rays or electron beams.
  • the drying time is usually 5 to 30 minutes, and the drying temperature is usually 40 to 180 ° C.
  • the porosity of the negative electrode active material layer is lowered by pressure treatment using a die press or a roll press after applying and drying the slurry composition on the current collector. It is preferable to have the process to do.
  • a preferable range of the porosity is 5 to 30%, more preferably 7 to 20%. If the porosity is too high, charging efficiency and discharging efficiency are deteriorated. When the porosity is too low, it is difficult to obtain a high volume capacity, and the negative electrode active material layer is liable to be peeled off from the current collector, resulting in a defect.
  • the thickness of the negative electrode active material layer in the negative electrode for secondary battery of the present invention is usually 5 to 300 ⁇ m, preferably 30 to 250 ⁇ m. When the thickness of the negative electrode active material layer is in the above range, both load characteristics and cycle characteristics are high.
  • the content ratio of the negative electrode active material in the negative electrode active material layer is preferably 85 to 99% by mass, more preferably 88 to 97% by mass.
  • the density of the negative electrode active material layer of the negative electrode for a secondary cell preferably 1.6 ⁇ 1.9g / cm 3, more preferably 1.65 ⁇ 1.85g / cm 3.
  • the density of the negative electrode active material layer is in the above range, a high-capacity battery can be obtained.
  • the current collector used in the present invention is not particularly limited as long as it is an electrically conductive and electrochemically durable material.
  • a metal material is preferable because it has heat resistance.
  • iron, copper, aluminum Nickel, stainless steel, titanium, tantalum, gold, platinum and the like are particularly preferable as the current collector used for the negative electrode for the secondary battery.
  • the shape of the current collector is not particularly limited, but a sheet shape having a thickness of about 0.001 to 0.5 mm is preferable.
  • the current collector is preferably used after roughening in advance. Examples of the roughening method include a mechanical polishing method, an electrolytic polishing method, and a chemical polishing method.
  • an abrasive cloth paper with a fixed abrasive particle, a grindstone, an emery buff, a wire brush provided with a steel wire or the like is used. Further, an intermediate layer may be formed on the current collector surface in order to increase the adhesive strength and conductivity with the negative electrode active material layer.
  • the secondary battery of the present invention is a secondary battery comprising a positive electrode, a negative electrode, a separator and an electrolytic solution, and the negative electrode is the negative electrode for a secondary battery.
  • the positive electrode is formed by laminating a positive electrode active material layer containing a positive electrode active material and a secondary battery positive electrode binder composition on a current collector.
  • Positive electrode active material an active material that can be doped and dedoped with lithium ions is used, and the positive electrode active material is roughly classified into an inorganic compound and an organic compound.
  • Examples of the positive electrode active material made of an inorganic compound include transition metal oxides, transition metal sulfides, lithium-containing composite metal oxides of lithium and transition metals, and the like.
  • Examples of the transition metal include Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Mo.
  • Transition metal oxides include MnO, MnO 2 , V 2 O 5 , V 6 O 13 , TiO 2 , Cu 2 V 2 O 3 , amorphous V 2 O—P 2 O 5 , MoO 3 , V 2 O. 5 , V 6 O 13 and the like. Among them, MnO, V 2 O 5 , V 6 O 13 and TiO 2 are preferable from the viewpoint of cycle stability and capacity.
  • the lithium-containing composite metal oxide include a lithium-containing composite metal oxide having a layered structure, a lithium-containing composite metal oxide having a spinel structure, and a lithium-containing composite metal oxide having an olivine structure.
  • lithium-containing composite metal oxide having a layered structure lithium-containing cobalt oxide (LiCoO 2 ), lithium-containing nickel oxide (LiNiO 2 ), Co—Ni—Mn lithium composite oxide, Ni—Mn—Al lithium
  • lithium-containing cobalt oxide (LiCoO 2 ) lithium-containing nickel oxide (LiNiO 2 ), Co—Ni—Mn lithium composite oxide, Ni—Mn—Al lithium
  • examples thereof include composite oxides and lithium composite oxides of Ni—Co—Al.
  • the lithium-containing composite metal oxide having a spinel structure include lithium manganate (LiMn 2 O 4 ) and Li [Mn 3/2 M 1/2 ] O 4 in which a part of Mn is substituted with another transition metal (wherein M may be Cr, Fe, Co, Ni, Cu or the like.
  • Li X MPO 4 (wherein, M is Mn, Fe, Co, Ni, Cu, Mg, Zn, V, Ca, Sr, Ba, Ti, Al, Li X MPO 4 as the lithium-containing composite metal oxide having an olivine structure)
  • An olivine type lithium phosphate compound represented by at least one selected from Si, B, and Mo, 0 ⁇ X ⁇ 2) may be mentioned.
  • a conductive polymer such as polyacetylene or poly-p-phenylene can be used.
  • An iron-based oxide having poor electrical conductivity may be used as an electrode active material covered with a carbon material by allowing a carbon source material to be present during reduction firing. These compounds may be partially element-substituted.
  • the positive electrode active material for the secondary battery may be a mixture of the above inorganic compound and organic compound.
  • the volume average particle diameter of the positive electrode active material is usually 0.01 to 50 ⁇ m, preferably 0.05 to 30 ⁇ m.
  • the volume average particle diameter is in the above range, the amount of the binder composition for the positive electrode when preparing the slurry composition for the positive electrode described later can be reduced, the decrease in the capacity of the battery can be suppressed, and for the positive electrode It becomes easy to prepare the slurry composition to have a viscosity suitable for application, and a uniform electrode can be obtained.
  • the content ratio of the positive electrode active material in the positive electrode active material layer is preferably 90 to 99.9% by mass, more preferably 95 to 99% by mass.
  • the binder composition for the secondary battery positive electrode is not particularly limited and a known one can be used.
  • resins such as polyethylene, polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), tetrafluoroethylene-hexafluoropropylene copolymer (FEP), polyacrylic acid derivatives, polyacrylonitrile derivatives, acrylic soft heavy
  • PTFE polytetrafluoroethylene
  • PVDF polyvinylidene fluoride
  • FEP tetrafluoroethylene-hexafluoropropylene copolymer
  • polyacrylic acid derivatives polyacrylonitrile derivatives
  • acrylic soft heavy A soft polymer such as a polymer, a diene soft polymer, an olefin soft polymer, or a vinyl soft polymer can be used. These may be used alone or in combination of two or more.
  • the positive electrode may further contain other components such as an electrolyte additive having a function of suppressing the above-described electrolyte decomposition. These are not particularly limited as long as they do not affect the battery reaction.
  • the current collector used in the above-described negative electrode for a secondary battery can be used, and there is no particular limitation as long as the material has electrical conductivity and is electrochemically durable.
  • Aluminum is particularly preferred for the secondary battery positive electrode.
  • the thickness of the positive electrode active material layer is usually 5 to 300 ⁇ m, preferably 10 to 250 ⁇ m. When the thickness of the positive electrode active material layer is in the above range, both load characteristics and energy density are high.
  • the positive electrode can be produced in the same manner as the above-described negative electrode for secondary battery.
  • the separator is a porous substrate having pores
  • usable separators include (a) a porous separator having pores, and (b) a porous separator in which a polymer coat layer is formed on one or both sides. Or (c) a porous separator in which a porous resin coat layer containing an inorganic ceramic powder is formed.
  • Non-limiting examples of these include high-grade polypropylene, polyethylene, polyolefin, or aramid porous separators, polyvinylidene fluoride, polyethylene oxide, polyacrylonitrile, or polyvinylidene fluoride hexafluoropropylene copolymers.
  • Examples include a separator having a molecular film and a coat layer, or a separator coated with a porous film layer made of an inorganic filler or a dispersant for inorganic filler.
  • the electrolytic solution used in the present invention is not particularly limited.
  • a solution obtained by dissolving a lithium salt as a supporting electrolyte in a non-aqueous solvent can be used.
  • the lithium salt include LiPF 6 , LiAsF 6 , LiBF 4 , LiSbF 6 , LiAlCl 4 , LiClO 4 , CF 3 SO 3 Li, C 4 F 9 SO 3 Li, CF 3 COOLi, (CF 3 CO) 2 NLi , (CF 3 SO 2 ) 2 NLi, (C 2 F 5 SO 2 ) NLi, and other lithium salts.
  • LiPF 6 , LiClO 4 , and CF 3 SO 3 Li that are easily soluble in a solvent and exhibit a high degree of dissociation are preferably used. These can be used alone or in admixture of two or more.
  • the amount of the supporting electrolyte is usually 1% by mass or more, preferably 5% by mass or more, and usually 30% by mass or less, preferably 20% by mass or less, with respect to the electrolytic solution. If the amount of the supporting electrolyte is too small or too large, the ionic conductivity is lowered and the battery charging and discharging characteristics are lowered.
  • the solvent used in the electrolytic solution is not particularly limited as long as it can dissolve the supporting electrolyte.
  • Alkyl carbonates such as carbonate (BC) and methyl ethyl carbonate (MEC); esters such as ⁇ -butyrolactone and methyl formate; ethers such as 1,2-dimethoxyethane; tetrahydrofuran; sulfolane and dimethyl sulfoxide Sulfur-containing compounds are used.
  • dimethyl carbonate, ethylene carbonate, propylene carbonate, diethyl carbonate, and methyl ethyl carbonate are preferable because high ion conductivity is easily obtained and the use temperature range is wide. These can be used alone or in admixture of two or more. Moreover, it is also possible to use an electrolyte containing an additive. Moreover, as an additive, carbonate type compounds, such as vinylene carbonate (VC), are preferable, and vinylene carbonate is more preferable especially. By including vinylene carbonate in the electrolytic solution, the propargyl-containing compound and vinylene carbonate can promote decomposition on the negative electrode active material and suppress decomposition of the electrolytic solution itself. The content of vinylene carbonate in the electrolytic solution is preferably 0.01 to 8% by volume.
  • Examples of the electrolytic solution other than the above include a gel polymer electrolyte obtained by impregnating a polymer electrolyte such as polyethylene oxide and polyacrylonitrile with an electrolytic solution, and an inorganic solid electrolyte such as lithium sulfide, LiI, and Li 3 N.
  • the manufacturing method of the secondary battery of the present invention is not particularly limited.
  • the above-described negative electrode and positive electrode are overlapped via a separator, and this is wound or folded according to the shape of the battery and placed in the battery container, and the electrolytic solution is injected into the battery container and sealed.
  • an expanded metal, an overcurrent prevention element such as a fuse or a PTC element, a lead plate and the like can be inserted to prevent an increase in pressure inside the battery and overcharge / discharge.
  • the shape of the battery may be any of a laminated cell type, a coin type, a button type, a sheet type, a cylindrical type, a square type, a flat type, and the like.
  • ⁇ Adhesion strength peel strength of negative electrode active material layer>
  • the negative electrode for a secondary battery manufactured in Examples and Comparative Examples was cut into a rectangle having a length of 100 mm and a width of 10 mm to obtain a test piece, and a cellophane tape (in JIS Z1522 2009) was formed on the surface of the negative electrode active material layer with the negative electrode active material layer side down. Then, stress was measured when one end of the current collector was pulled in a vertical direction at a pulling speed of 50 mm / min and peeled off (the cellophane tape was fixed to a test stand). The measurement was performed three times, and the average value was obtained and used as the peel strength. The higher the peel strength, the greater the binding force of the negative electrode active material layer to the current collector, that is, the higher the adhesion strength.
  • ⁇ Durability: High-temperature cycle characteristics> Using a negative electrode for a lithium ion secondary battery produced in the examples and comparative examples, a lithium ion secondary battery of a laminate type cell was prepared and left to stand in an environment of 25 ° C. for 24 hours. After that, under an environment of 25 ° C., charge / discharge operation of charging to 4.2 V and discharging to 3.0 V was performed by a constant current method of 0.1 C, and an initial capacity C0 was measured. Furthermore, in a 60 ° C. environment, charging / discharging of charging to 4.2 V and discharging to 3.0 V was repeated by a constant current method of 0.1 C, and the capacity C2 after 100 cycles was measured. The high-temperature cycle characteristics were evaluated by a capacity change rate represented by ⁇ C C2 / C0 ⁇ 100 (%). Higher values indicate better high temperature cycle characteristics.
  • a lithium ion secondary battery of a laminate type cell was prepared and left at 25 ° C. for 24 hours.
  • the charging / discharging operation of charging to 4.2V and discharging to 3.0V was performed by the constant current method.
  • the battery was charged to a 50% charged state (SOC 50%) by a constant current method of 0.1 C under an environment of 25 ° C., and a voltage V 0 (V) was measured.
  • the battery was discharged from the voltage V 0 (V) at a discharge rate of 0.1 C in an environment of ⁇ 25 ° C., and the voltage V 10 after 10 seconds of discharge was measured.
  • Example 1 Manufacture of binder composition
  • a 5 MPa pressure vessel equipped with a stirrer 33 parts of 1,3-butadiene, 4 parts of itaconic acid, 63 parts of styrene, 4 parts of sodium dodecylbenzenesulfonate as an emulsifier, 150 parts of ion-exchanged water, and potassium persulfate 0.5 as a polymerization initiator
  • a portion was added and stirred sufficiently, and then heated to 50 ° C. to initiate polymerization.
  • the reaction was stopped by cooling to obtain an aqueous dispersion containing a binder.
  • the glass transition temperature of the binder was 10 ° C.
  • aqueous sodium hydroxide solution After adding 5% aqueous sodium hydroxide solution to the aqueous dispersion containing the binder and adjusting the pH to 8, the unreacted monomer is removed by heating under reduced pressure, and then cooled to 30 ° C. or lower to obtain a binder solid.
  • a propargyl group-containing compound 3 parts of propargyl benzenesulfonate was added to 100 parts per minute to obtain a binder composition.
  • the above mixture was mixed with 1 part of the binder (based on solid content) and ion-exchanged water, adjusted to a final solid content concentration of 42%, and further mixed for 10 minutes. This was defoamed under reduced pressure to obtain a slurry composition for a secondary battery negative electrode having good fluidity.
  • the dispersion stability of the slurry was evaluated as described above.
  • the secondary battery negative electrode slurry composition was applied on a copper foil having a thickness of 20 ⁇ m with a comma coater so that the film thickness after drying was about 150 ⁇ m, heat-treated at 60 ° C. for 1 minute, and then 120 An electrode raw material was obtained by heat treatment at 0 ° C. for 1 minute.
  • the raw electrode was rolled with a roll press to obtain a negative electrode for a secondary battery having a negative electrode active material layer thickness of 80 ⁇ m.
  • a positive electrode active material 100 parts of LiFePO 4 having a volume average particle diameter of 0.5 ⁇ m and an olivine crystal structure is used, and a 1% aqueous solution of carboxymethyl cellulose (CMC, “BSH-12” manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) is used as a dispersant.
  • CMC carboxymethyl cellulose
  • a planetar such that a 40% aqueous dispersion of a copolymer obtained by emulsion polymerization of a monomer mixture containing% by mass is 5 parts in terms of solids and the total solids concentration is 40% with ion-exchanged water.
  • a slurry for a positive electrode composition layer was prepared by mixing with a Lee mixer.
  • the secondary battery positive electrode slurry composition was applied onto a 20 ⁇ m thick copper foil with a comma coater so that the film thickness after drying was about 200 ⁇ m, and heat-treated at 60 ° C. for 1 minute, and then 120 A positive electrode for a secondary battery was obtained by heat treatment at 0 ° C. for 1 minute.
  • a single-layer polypropylene separator (width 65 mm, length 500 mm, thickness 25 ⁇ m, manufactured by a dry method, porosity 55%) was cut into a circle having a diameter of 18 mm.
  • the obtained positive electrode for a lithium ion secondary battery was disposed such that the current collector surface was in contact with the aluminum packaging exterior.
  • a separator was disposed on the surface of the positive electrode on the positive electrode active material layer side.
  • the negative electrode for a lithium ion secondary battery obtained above was placed on the separator so that the surface on the negative electrode active material layer side faces the separator.
  • the electrolyte was poured into the packaging material so that no air remained. Furthermore, in order to seal the opening of the aluminum packaging material, heat sealing at 150 ° C. was performed to close the aluminum exterior, and a lithium ion secondary battery was manufactured.
  • the obtained negative electrode and secondary battery were evaluated for adhesion strength, durability, and low-temperature output characteristics as described above.
  • Example 2 The same procedure as in Example 1 was performed except that the amount of propargyl benzenesulfonate was 7 parts with respect to 100 parts of binder solid content. The results are shown in Table 1.
  • Example 3 The amount of propargyl benzenesulfonate added was the same as in Example 1 except that the amount was 15 parts with respect to 100 parts of binder solid content. The results are shown in Table 1.
  • Example 4 The same procedure as in Example 1 was conducted except that propargyl acrylate was used instead of propargyl benzenesulfonate as the propargyl group-containing compound. The results are shown in Table 1.
  • Example 5 The same procedure as in Example 1 was conducted except that propargyl methacrylate was used instead of propargyl benzenesulfonate as the propargyl group-containing compound. The results are shown in Table 1.
  • Example 6 The same procedure as in Example 1 was performed except that methacrylic acid was used in place of itaconic acid as a comonomer at the time of preparing the binder. The results are shown in Table 1.
  • Example 7 As the negative electrode active material, natural graphite having a BET specific surface area of 8 m 2 / g (average particle diameter: 22 ⁇ m) was used instead of natural graphite having a BET specific surface area of 5 m 2 / g (average particle diameter: 24.5 ⁇ m). Same as Example 1. The results are shown in Table 1.
  • Example 8 As the negative electrode active material, natural graphite having a BET specific surface area of 15 m 2 / g (average particle diameter: 15 ⁇ m) was used instead of natural graphite having a BET specific surface area of 5 m 2 / g (average particle diameter: 24.5 ⁇ m). Same as Example 1. The results are shown in Table 1.
  • Example 9 As the negative electrode active material, natural graphite (average particle size: 24.5 ⁇ m) of a BET specific surface area of 5 m 2 / g natural graphite (average particle size: 24.5 ⁇ m) of a BET specific surface area of 5 m 2 / g instead of 80 parts and The procedure was the same as Example 1 except that 20 parts of SiOC (average particle size: 10 ⁇ m) having a BET specific surface area of 6.5 m 2 / g was used. The BET specific surface area of the negative electrode active material was 5.2 m 2 / g. The results are shown in Table 1.
  • Example 10 As the negative electrode active material, natural graphite (average particle size: 24.5 ⁇ m) of a BET specific surface area of 5 m 2 / g BET specific instead of surface area 5.0 m 2 / g natural graphite (average particle size: 24.5 ⁇ m) 50 Parts and a BET specific surface area of 6.5 m 2 / g of SiOC (average particle size: 10 ⁇ m) were used in the same manner as in Example 1 except that 50 parts were used. The BET specific surface area of the negative electrode active material was 5.8 m 2 / g. The results are shown in Table 1.
  • Example 11 The same procedure as in Example 1 was performed except that dipropargyl carbonate was used as the propargyl group-containing compound instead of propargyl benzenesulfonate. The results are shown in Table 1.
  • Example 12 The same procedure as in Example 1 was conducted except that itaconic acid was not used as a comonomer for preparing the binder.
  • the glass transition temperature of the binder was 7 ° C. The results are shown in Table 1.
  • Example 1 The procedure was the same as Example 1 except that the propargyl group-containing compound was not blended in the binder composition. The results are shown in Table 1.
  • Example 1 (Comparative Example 4) Example 1 was repeated except that methyl 2-octanoate was used in place of propargyl benzenesulfonate. The results are shown in Table 1.
  • the adhesion between the current collector and the electrode active material layer was improved, and in particular, a secondary battery with improved cycle characteristics and low-temperature output characteristics was obtained. .

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Secondary Cells (AREA)

Abstract

L'objectif est de fournir une composition de liant grâce à laquelle l'adhésion entre un collecteur et une couche de matériau actif d'électrode reste élevée après le chargement et le déchargement et il est possible d'améliorer les propriétés du cycle dans des conditions d'exploitation de l'accumulateur à haute température et à basse température, en particulier. La composition de liant selon la présente invention est caractérisée en ce qu'elle comprend un liant et un composé contenant un groupement propargyle et en ce que la proportion du composé contenant un groupement propargyle est comprise entre 0,1 et 20 parties en masse pour 100 parties en masse du liant.
PCT/JP2012/066524 2011-06-29 2012-06-28 Composition de liant pour électrode négative d'accumulateur, composition de suspension pour électrode négative d'accumulateur, électrode négative pour accumulateur et accumulateur WO2013002322A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1020137033337A KR101910988B1 (ko) 2011-06-29 2012-06-28 이차 전지 부극용 바인더 조성물, 이차 전지 부극용 슬러리 조성물, 이차 전지용 부극 및 이차 전지
JP2013522935A JP6115468B2 (ja) 2011-06-29 2012-06-28 二次電池負極用バインダー組成物、二次電池負極用スラリー組成物、二次電池用負極および二次電池

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2011-144590 2011-06-29
JP2011144590 2011-06-29

Publications (1)

Publication Number Publication Date
WO2013002322A1 true WO2013002322A1 (fr) 2013-01-03

Family

ID=47424208

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2012/066524 WO2013002322A1 (fr) 2011-06-29 2012-06-28 Composition de liant pour électrode négative d'accumulateur, composition de suspension pour électrode négative d'accumulateur, électrode négative pour accumulateur et accumulateur

Country Status (3)

Country Link
JP (1) JP6115468B2 (fr)
KR (1) KR101910988B1 (fr)
WO (1) WO2013002322A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013131368A (ja) * 2011-12-21 2013-07-04 Toyo Kagaku Kk 電極用バインダー
CN109461884A (zh) * 2018-12-08 2019-03-12 广东维都利新能源有限公司 一种能够在高温下工作并保存的锂电池
CN113614975A (zh) * 2018-12-13 2021-11-05 株式会社Lg新能源 锂二次电池用电解质和包含该电解质的锂二次电池
US12125980B2 (en) 2018-12-13 2024-10-22 Lg Energy Solution, Ltd. Electrolyte for lithium secondary battery and lithium secondary battery including the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009093839A (ja) * 2007-10-04 2009-04-30 Ube Ind Ltd ベンゼンスルホン酸エステル、それを用いたリチウム二次電池用電解液、及びそれを用いたリチウム二次電池
JP2011077029A (ja) * 2009-09-07 2011-04-14 Adeka Corp 非水電解液及び該電解液を用いた非水電解液二次電池
JP2011124039A (ja) * 2009-12-09 2011-06-23 Denso Corp 電池用非水電解液及び該電解液を用いた非水電解液二次電池

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002203558A (ja) * 2000-12-28 2002-07-19 Sony Corp 非水電解質二次電池
US6537698B2 (en) * 2001-03-21 2003-03-25 Wilson Greatbatch Ltd. Electrochemical cell having an electrode with a phosphonate additive in the electrode active mixture
KR100893227B1 (ko) * 2006-07-28 2009-04-16 주식회사 엘지화학 고온 저장 성능을 개선하는 음극 및 이를 포함하는 리튬이차 전지
JP5222538B2 (ja) * 2007-05-22 2013-06-26 株式会社デンソー 非水電解液及び該電解液を用いた非水電解液二次電池
JP2009099530A (ja) * 2007-09-27 2009-05-07 Sanyo Electric Co Ltd 非水電解質電池用正極及び非水電解質電池
JP2010199043A (ja) * 2009-02-27 2010-09-09 Mitsubishi Heavy Ind Ltd 二次電池用負極電極の製造方法及び非水電解質二次電池
JP5754098B2 (ja) 2009-09-15 2015-07-22 三菱化学株式会社 リチウムイオン二次電池用炭素材料

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009093839A (ja) * 2007-10-04 2009-04-30 Ube Ind Ltd ベンゼンスルホン酸エステル、それを用いたリチウム二次電池用電解液、及びそれを用いたリチウム二次電池
JP2011077029A (ja) * 2009-09-07 2011-04-14 Adeka Corp 非水電解液及び該電解液を用いた非水電解液二次電池
JP2011124039A (ja) * 2009-12-09 2011-06-23 Denso Corp 電池用非水電解液及び該電解液を用いた非水電解液二次電池

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ABE KOJI ET AL.: "Functional Electrolytes: Triple-Bonded compound as an additive for Negative Electrode", J. ELECTROCHEM. SOC., vol. 154, no. 8, 2007, pages A810 - A815 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013131368A (ja) * 2011-12-21 2013-07-04 Toyo Kagaku Kk 電極用バインダー
CN109461884A (zh) * 2018-12-08 2019-03-12 广东维都利新能源有限公司 一种能够在高温下工作并保存的锂电池
CN113614975A (zh) * 2018-12-13 2021-11-05 株式会社Lg新能源 锂二次电池用电解质和包含该电解质的锂二次电池
CN113614975B (zh) * 2018-12-13 2024-03-29 株式会社Lg新能源 锂二次电池用电解质和包含该电解质的锂二次电池
US12125980B2 (en) 2018-12-13 2024-10-22 Lg Energy Solution, Ltd. Electrolyte for lithium secondary battery and lithium secondary battery including the same

Also Published As

Publication number Publication date
JP6115468B2 (ja) 2017-04-19
JPWO2013002322A1 (ja) 2015-02-23
KR101910988B1 (ko) 2018-10-23
KR20140039226A (ko) 2014-04-01

Similar Documents

Publication Publication Date Title
JP5761197B2 (ja) 二次電池負極用バインダー組成物、二次電池負極用スラリー組成物、二次電池負極、二次電池及び二次電池負極用バインダー組成物の製造方法
KR101807543B1 (ko) 이차 전지 부극용 슬러리, 이차 전지용 부극 및 그 제조 방법, 그리고 이차 전지
JP6627763B2 (ja) 二次電池電極用バインダー組成物、二次電池電極用スラリー組成物、二次電池用電極および二次電池
JP5708301B2 (ja) 二次電池用負極、二次電池、負極用スラリー組成物及び二次電池用負極の製造方法
JP6245173B2 (ja) 二次電池用負極及び二次電池
JP5987471B2 (ja) 二次電池用負極、二次電池、負極用スラリー組成物及び二次電池用負極の製造方法
WO2012115096A1 (fr) Électrode négative de cellule secondaire, cellule secondaire, composition de pâte pour une électrode négative et procédé de production d'une électrode négative de cellule secondaire
KR20150027059A (ko) 부극 슬러리 조성물, 리튬 이온 이차 전지 부극 및 리튬 이온 이차 전지
US10529989B2 (en) Binder composition for secondary battery electrode, slurry composition for secondary battery electrode, electrode for secondary battery, and secondary battery
JP6111895B2 (ja) リチウムイオン二次電池負極用スラリー組成物、二次電池用負極および二次電池
JP6168059B2 (ja) リチウムイオン二次電池負極用スラリー組成物
US10249879B2 (en) Binder composition for secondary battery electrode-use, slurry composition for secondary battery electrode-use, electrode for secondary battery-use and production method therefor, and secondary battery
JPWO2013176232A1 (ja) リチウムイオン二次電池
JP7276326B2 (ja) 蓄電デバイス用バインダー組成物、蓄電デバイス電極用スラリー組成物、蓄電デバイス用電極、および蓄電デバイス
JP7327398B2 (ja) 電気化学素子電極用バインダー組成物、電気化学素子電極用スラリー組成物、電気化学素子用電極、および電気化学素子
JP6115468B2 (ja) 二次電池負極用バインダー組成物、二次電池負極用スラリー組成物、二次電池用負極および二次電池
JP6455015B2 (ja) 二次電池用バインダー組成物、二次電池電極用スラリー組成物、二次電池用電極および二次電池
JP6579250B2 (ja) 二次電池用バインダー組成物、二次電池電極用スラリー組成物、二次電池用電極および二次電池

Legal Events

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

Ref document number: 12803761

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2013522935

Country of ref document: JP

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 20137033337

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 12803761

Country of ref document: EP

Kind code of ref document: A1