JP2009037868A - Nonaqueous electrolytic liquid secondary battery using nitroxy radical group containing high-molecular weight polymer - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a nonaqueous electrolytic liquid secondary battery using a nitroxy radical compound as an electrode active material in which the nitroxy radical compound can function efficiently as the electrode active material, without having to make the thickness of the electrode small or the concentration of the electrolyte in the nonaqueous electrolytic liquid high. <P>SOLUTION: The nonaqueous electrolytic liquid secondary battery with an electrode active material a nitroxy radical group-contained high molecular weight polymer which has lithium base of organic acid inside the molecule. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a non-aqueous electrolyte secondary battery using a nitroxy radical group-containing high molecular weight polymer having a specific structure as an electrode active material, and more specifically, a nitroxy having an organic acid lithium base in the molecule. The present invention relates to a non-aqueous electrolyte secondary battery using a radical group-containing high molecular weight polymer as an electrode active material. The nonaqueous electrolyte secondary battery of the present invention can be used as a power source for portable electronic devices such as portable personal computers and handy video cameras, battery cars, and hybrid cars.

  With the spread of portable electronic devices such as portable personal computers and handy video cameras in recent years, non-aqueous electrolyte secondary batteries having high voltage and high energy density have been widely used as power sources. Also, from the viewpoint of environmental problems, battery cars and hybrid cars using electric power as a part of power have been put into practical use.

  As the non-aqueous electrolyte secondary battery, a lithium ion secondary battery is most popular due to its superior performance balance. However, although the lithium ion secondary battery has an advantage of high capacity, it cannot always be said that the required level of backup power sources for electric vehicles, hybrid vehicles, and electronic devices is satisfied in terms of output characteristics.

Japanese Patent No. 3687736 proposes a non-aqueous electrolyte secondary battery using a radical compound such as a nitroxy radical compound as an electrode active material. Although a non-aqueous electrolyte secondary battery using a nitroxy radical compound has excellent characteristics in terms of output characteristics, it is difficult to design a battery to make use of the characteristics.
That is, in order for a nitroxy radical compound to function as an electrode active material inside a battery, a counter anion equivalent to the nitroxy radical group in the compound is required, and the counter anion is supplied only by a non-aqueous electrolyte. When trying to do so, the general design criteria lack the counter anion. As a method for compensating for the shortage of the counter anion, a method of reducing the thickness of the electrode using the nitroxy radical compound as an electrode active material or increasing the concentration of the electrolyte in the nonaqueous electrolytic solution can be mentioned.
However, when the thickness of the electrode is reduced, the capacity density of the battery is reduced, and when the concentration of the electrolyte in the non-aqueous electrolyte is increased, the capacity deterioration of the battery due to a side reaction at the negative electrode is increased.

Japanese Patent No. 3687736

  Accordingly, an object of the present invention is to reduce the thickness of the electrode or increase the concentration of the electrolyte in the non-aqueous electrolyte in the non-aqueous electrolyte secondary battery using the nitroxy radical compound as the electrode active material. And providing a non-aqueous electrolyte secondary battery in which a nitroxy radical compound can efficiently function as an electrode active material.

  As a result of intensive studies, the present inventors have found that in a non-aqueous electrolytic solution in which an electrolyte salt is dissolved in an organic solvent, a nitroxy radical group-containing high molecular weight polymer having an organic acid lithium base such as a lithium carboxylate in the molecule. It has been found that the above object can be achieved by using a coalescence as an electrode active material.

  That is, the present invention has been made based on the above knowledge, and provides a non-aqueous electrolyte secondary battery using a nitroxy radical group-containing high molecular weight polymer having a lithium base of an organic acid in the molecule as an electrode active material. Thus, the above object is achieved.

  In the nonaqueous electrolyte secondary battery of the present invention, the nitroxy radical group-containing high molecular weight polymer having a specific structure used as an electrode active material contains a lithium base of an organic acid. Since the lithium base of the organic acid is present in the molecule, a counter anion is secured at the time of charging, so that the nitroxy radical group can function effectively as an electrode active material.

  The nonaqueous electrolyte secondary battery using the nitroxy radical group-containing high molecular weight polymer of the present invention will be described in detail below.

  The nonaqueous electrolyte secondary battery of the present invention uses a nitroxy radical group-containing high molecular weight polymer having an organic acid lithium base in the molecule as an electrode active material, preferably a positive electrode active material.

  As the nitroxy radical group-containing high molecular weight polymer, a nitroxy radical group-containing high molecular weight polymer composed of a structural unit represented by the following general formula (1) and / or (2) is preferably used.

（式中において、Ｒ₁およびＲ₂は、それぞれ独立して、水素原子または炭素数１〜４のアルキル基を示す。ｎ／（ｎ＋ｍ＋ｐ）は、０．２から０．９９であり、好ましくは０．４〜０．９５であり、より好ましくは０．６〜０．９ある。ｍ／(ｎ＋ｍ＋ｐ)は、０から０．８であり、好ましくは０〜０．４であり、より好ましくは０〜０．３である。ｐ／(ｎ＋ｍ＋ｐ)は、０．０１から０．８であり、好ましくは０．０５〜０．６であり、より好ましくは０．１〜０．４である。）

(In the formula, R ₁ and R ₂ each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. N / (n + m + p) is 0.2 to 0.99, preferably 0.4 to 0.95, more preferably 0.6 to 0.9, m / (n + m + p) is 0 to 0.8, preferably 0 to 0.4, more preferably P / (n + m + p) is from 0.01 to 0.8, preferably from 0.05 to 0.6, more preferably from 0.1 to 0.4. )

In the general formulas (1) and (2), the alkyl group having 1 to 4 carbon atoms represented by R ₁ and R ₂ includes methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. Can be mentioned.

  The nitroxy radical group-containing high molecular weight polymer has a constitution represented by the general formula (1) and / or (2) within a range not to impair the effects of the present invention (preferably 0.01 to 20% by mass) Structures other than units may be included. Such structures include linear alkyl imide, linear alkyl amide, sodium carboxylate, potassium carboxylate, magnesium carboxylate bromide, magnesium carboxylate, magnesium iodide carboxylate, carboxylate ester, carbonate ester, urethane, fluoro Examples include alkyl, polyacetylene, polypyrrole, and polythiophene.

  The non-aqueous electrolyte secondary battery of the present invention is configured in the same manner as a known non-aqueous electrolyte secondary battery except that the nitroxy radical group-containing high molecular weight polymer is used as an electrode active material.

The electrode material used in the non-aqueous electrolyte secondary battery of the present invention includes a positive electrode and a negative electrode, and the positive electrode is obtained by slurrying a positive electrode active material, a binder and a conductive material with an organic solvent or water. Is applied to a current collector and dried to form a sheet.
In the non-aqueous electrolyte secondary battery of the present invention, the nitroxy radical group-containing high molecular weight polymer may be used alone as the positive electrode active material, and the range in which the effects of the present invention are not impaired (preferably 0). 0.01 to 90% by mass), and a positive electrode active material used in a normal lithium ion secondary battery may be mixed and used. Examples of the positive electrode active material used in the lithium ion secondary battery that may be mixed include TiS ₂ , TiS ₃ , MoS ₃ , FeS ₂ , Li _(1-x) MnO ₂ , Li _(1-x) Mn ₂ O ₄ , Li _(1-x) CoO ₂ , Li _(1-x) NiO ₂ , LiV ₂ O ₃ , V ₂ O _{5 and the} like. In addition, X in these positive electrode active materials shows the number of 0-1. A material obtained by adding or substituting a transition metal such as Li, Mg, Al, or Co, Ti, Nb, or Cr may be used. Not only these -metal composite oxides are mixed alone, but also a plurality of these can be mixed and used. Examples of the binder for the positive electrode active material include, but are not limited to, polyvinylidene fluoride (PVDF), polytetrafluoroethylene, EPDM, SBR, NBR, and fluororubber.
Moreover, as the usage-amount of a binder, it is 0.1-20 mass parts with respect to 100 mass parts of positive electrode active materials, More preferably, it is 0.2-10 mass parts.

Examples of the conductive material for the positive electrode include fine particles of graphite, carbon black such as acetylene black and ketjen black, fine particles of amorphous carbon such as needle coke, and the like, but are not limited thereto. Moreover, as the usage-amount of a electrically conductive material, it becomes like this. Preferably it is 10-90 mass parts with respect to 100 mass parts of positive electrode active materials, More preferably, it is 20-60 mass parts.
As the solvent for forming a slurry, an organic solvent or water that dissolves the binder is used. Examples of the organic solvent include N-methylpyrrolidone (NMP), dimethylformamide, dimethylacetamide, methyl ethyl ketone, cyclohexanone, methyl acetate, methyl acrylate, diethyltriamine, N, N-dimethylaminopropylamine, ethylene oxide, tetrahydrofuran and the like. Although it is mentioned, it is not limited to this. The amount of the organic solvent or water used is preferably 20 to 100 parts by mass of the positive electrode active material.
300 parts by mass, more preferably 50 to 200 parts by mass.

As the negative electrode, a negative electrode active material and a binder slurryed with an organic solvent or water is applied to a current collector and dried to form a sheet, but a metal foil is used. It is also possible to do. Examples of the negative electrode active material include lithium, lithium alloys, inorganic compounds such as tin / silicon compounds, titanium oxides, carbonaceous materials, and conductive polymers. In particular, a carbonaceous material that can occlude and release highly safe lithium ions is preferable. The carbonaceous material is not particularly limited, but graphite, petroleum-based coke, coal-based coke, petroleum-based pitch carbide, coal-based pitch carbide, phenolic resin / crystalline cellulose resin carbide, etc., and partially carbonized thereof. Carbon materials, furnace black, acetylene black, pitch-based carbon fibers, PAN-based carbon fibers, and the like.
Examples of the binder for the negative electrode active material include the same binders for the positive electrode active material. Moreover, as the usage-amount of a binder, it is 0.1-20 mass parts with respect to 100 mass parts of negative electrode active materials, More preferably, it is 1-10 mass parts. As the solvent for forming a slurry, an organic solvent or water that dissolves the binder is used. Examples of the organic solvent include the same organic solvents as those used for the positive electrode. The amount of the organic solvent or water used is preferably 40 to 300 parts by mass, more preferably 80 to 200 parts by mass with respect to 100 parts by mass of the negative electrode active material.

  Usually, aluminum, stainless steel, nickel-plated steel or the like is used for the current collector of the positive electrode, and copper, nickel, stainless steel, nickel-plated steel or the like is usually used for the current collector of the negative electrode.

In the non-aqueous electrolyte secondary battery of the present invention, an organic solvent is used for the non-aqueous electrolyte. As this organic solvent, what is normally used for the non-aqueous electrolyte can be used 1 type or in combination of 2 or more types.
Specifically, it contains one or more selected from the group consisting of cyclic carbonate compounds, cyclic ester compounds, sulfone or sulfoxide compounds, amide compounds, chain carbonate compounds, chain or cyclic ether compounds, and chain ester compounds. It is preferable. In particular, it is preferable to contain at least one cyclic carbonate compound and a chain carbonate compound, and by using this combination, not only the cycle characteristics are excellent, but also the viscosity of the electrolyte, the electric capacity / output of the obtained battery, etc. A non-aqueous electrolyte with a good balance can be provided.

  More specifically, organic solvents used in the non-aqueous electrolyte are listed below. However, the organic solvent used in the present invention is not limited by the following examples.

  Since the cyclic carbonate compound, the cyclic ester compound, the sulfone or sulfoxide compound, and the amide compound have a high relative dielectric constant, they serve to increase the dielectric constant of the electrolytic solution. Specifically, examples of the cyclic carbonate compound include ethylene carbonate (EC), propylene carbonate (PC), 1,2-butylene carbonate, and isobutylene carbonate. Examples of the cyclic ester compound include γ-butyrolactone and γ-valerolactone. Examples of the sulfone or sulfoxide compound include sulfolane, sulfolene, tetramethylsulfolane, diphenyl sulfone, dimethyl sulfone, dimethyl sulfoxide, propane sultone, butylene sultone, and among these, sulfolanes are preferable. Examples of the amide compound include N-methylpyrrolidone, dimethylformamide, dimethylacetamide and the like.

  The chain carbonate compound, the chain or cyclic ether compound, and the chain ester compound can lower the viscosity of the non-aqueous electrolyte. Therefore, battery characteristics such as power density can be improved, such as the mobility of electrolyte ions can be increased. Moreover, since it is low-viscosity, the performance of the non-aqueous electrolyte at low temperatures can be increased. Specifically, as the chain carbonate compound, dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), ethyl-n-butyl carbonate, methyl-t-butyl carbonate, di-i-propyl Examples thereof include carbonate and t-butyl-i-propyl carbonate. Examples of the chain or cyclic ether compound include dimethoxyethane (DME), ethoxymethoxyethane, diethoxyethane, tetrahydrofuran, dioxolane, dioxane, 1,2-bis (methoxycarbonyloxy) ethane, 1,2-bis (ethoxycarbonyloxy). ) Ethane, 1,2-bis (ethoxycarbonyloxy) propane, ethylene glycol bis (trifluoroethyl) ether, i-propylene glycol (trifluoroethyl) ether, ethylene glycol bis (trifluoromethyl) ether, diethylene glycol bis (tri Fluoroethyl) ether and the like. Among these, dioxolanes are preferable. Examples of the chain ester compound include a carboxylic acid ester compound represented by the following general formula (3).

（式中、Ｒは、炭素原子数１〜４のアルキル基を示し、ｎは０、１又は２を示す。）

(In the formula, R represents an alkyl group having 1 to 4 carbon atoms, and n represents 0, 1 or 2.)

  In the general formula (3), examples of the alkyl group having 1 to 4 carbon atoms represented by R include methyl, ethyl, propyl, isopropyl, butyl, sec-butyl and tert-butyl. Specific examples of the carboxylic acid ester compound represented by the general formula (3) include methyl formate, ethyl formate, methyl acetate, ethyl acetate, propyl acetate, sec-butyl acetate, butyl acetate, methyl propionate, and propionic acid. And ethyl. The carboxylic acid ester compound represented by the general formula (3) has a low freezing point, and when further added to an organic solvent, particularly an organic solvent containing at least one cyclic carbonate compound and at least one chain carbonate compound, even at a low temperature. It is preferable because battery characteristics can be improved. The addition amount of the carboxylic acid ester compound represented by the general formula (3) is preferably 1 to 50% by volume in the organic solvent.

  As the organic solvent used for the non-aqueous electrolyte, acetonitrile, propionitrile, nitromethane, and derivatives thereof can also be used.

  In order to impart flame retardancy, halogen-based, phosphorus-based, and other flame retardants can be appropriately added to the non-aqueous electrolyte. Examples of the phosphorus flame retardant include phosphate esters such as trimethyl phosphate and triethyl phosphate.

  5-100 mass% is preferable with respect to the organic solvent which comprises the non-aqueous electrolyte used for this invention, and, as for the addition amount of the said flame retardant, 10-50 mass% is especially preferable. If it is less than 5% by mass, sufficient flame retarding effect cannot be obtained.

As the electrolyte salt used in the non-aqueous electrolyte, a conventionally known electrolyte salt is used. For example, LiPF ₆ , LiBF ₄ , LiAsF ₆ , LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiC (CF _{3 SO 2) 3, LiSbF 6} , LiSiF 5, LiAlF 4, LiSCN, LiClO 4, LiCl, LiF, LiBr, LiI, LiAlF 4, LiAlCl 4, NaClO 4, NaBF 4, NaI, these derivatives, and the like, among _{them, LiPF 6, LiBF 4, LiClO} 4, LiAsF 6, LiCF 3 SO 3, LiN (CF 3 SO 2) 2 and LiC (CF ₃ SO _{2) 3} and derivatives _{LiCF 3 SO 3, LiN (CF} 3 One or more selected from the group consisting of a derivative of SO ₂ ) _{2 and} a derivative of LiC (CF ₃ SO ₂ ) ₃ Is preferable because of its excellent electrical characteristics.

  The electrolyte salt is added to the organic solvent so that the concentration in the non-aqueous electrolyte used in the present invention is 0.1 to 3.0 mol / liter, particularly 0.5 to 2.0 mol / liter. It is preferable to dissolve. If the concentration of the electrolyte salt is less than 0.1 mol / liter, a sufficient current density may not be obtained. If the concentration is more than 3.0 mol / liter, the stability of the nonaqueous electrolyte may be impaired. .

  In addition, various additives can be appropriately added to the nonaqueous electrolytic solution used in the present invention for the purpose of reducing the irreversible capacity at the negative electrode and suppressing the decomposition reaction of the electrolytic solution at the negative electrode. They are mainly added to form a coating (SEI) on the negative electrode surface. Unsaturated carbonates such as vinylene carbonate, vinyl ethylene carbonate, diallyl carbonate, allyl ethyl carbonate, allyl methyl carbonate, propane sultone , Sulfur compounds such as butane sultone, sulfolene, dimethyl maleate, diethyl maleate, dimethyl fumarate, diethyl fumarate, dimethyl acetylenedicarboxylate, diethyl acetylenedicarboxylate, tetravinylsilane, methyltrivinylsilane, dimethyldi Vinyl silane, diethyl divinyl silane, trimethyl vinyl silane, tetraallyl silane, triallyl methyl silane, diallyl dimethyl silane, diallyl diethyl silane, allyl trimethyl Unsaturated silane compound such as silane, hexamethyl disilane, disilanes, such as 1,2-divinyl tetramethyl disilane, and the like.

In the non-aqueous electrolyte secondary battery of the present invention, a separator is used between the positive electrode and the negative electrode. As the separator, a commonly used polymer microporous film can be used without any particular limitation. Examples of the film include polyethylene, polypropylene, polyvinylidene fluoride, polyvinylidene chloride, polyacrylonitrile, polyacrylamide, polytetrafluoroethylene, polysulfone, polyethersulfone, polycarbonate, polyamide, polyimide, polyethylene oxide and polypropylene oxide. Films composed of ethers, various celluloses such as carboxymethylcellulose and hydroxypropylcellulose, polymer compounds mainly composed of poly (meth) acrylic acid and various esters thereof, derivatives thereof, copolymers and mixtures thereof. Etc. These films may be used alone, or may be used as a multilayer film by superimposing these films. Furthermore, various additives may be used for these films, and the type and content thereof are not particularly limited. Among these films, a film made of polyethylene, polypropylene, polyvinylidene fluoride, or polysulfone is preferably used for the nonaqueous electrolyte secondary battery of the present invention.
These films are microporous so that the electrolyte can penetrate and ions can easily pass therethrough. The microporosity method includes a phase separation method in which a polymer compound and a solvent solution are formed into a film while microphase separation is performed, and the solvent is extracted and removed to make it porous. The film is extruded and then heat-treated, the crystals are aligned in one direction, and a gap is formed between the crystals by stretching to make it porous, and so on.

  In the non-aqueous electrolyte secondary battery of the present invention, the electrode material, the non-aqueous electrolyte, and the separator include a phenol-based antioxidant, a phosphorus-based antioxidant, and a thioether-based antioxidant for the purpose of improving safety. A hindered amine compound or the like may be added.

  Examples of the phenol-based antioxidant include 1,6-hexamethylene bis [(3-tert-butyl-5-methyl-4-hydroxyphenyl) propionic acid amide], 4,4′-thiobis (6-tert. Tributyl-m-cresol), 4,4′-butylidenebis (6-tert-butyl-m-cresol), 1,1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane 1,3,5-tris (2,6-dimethyl-3-hydroxy-4-tert-butylbenzyl) isocyanurate, 1,3,5-tris (3,5-ditert-butyl-4-hydroxybenzyl) ) Isocyanurate, 1,3,5-tris (3,5-ditert-butyl-4-hydroxybenzyl) -2,4,6-trimethylbenzene, tetrakis [3- (3,5-ditert-butyl- 4-hi Roxyphenyl) methyl propionate] methane, thiodiethylene glycol bis [(3,5-ditert-butyl-4-hydroxyphenyl) propionate], 1,6-hexamethylenebis [(3,5-ditert-butyl-4 -Hydroxyphenyl) propionate], bis [3,3-bis (4-hydroxy-3-tert-butylphenyl) butyric acid] glycol ester, bis [2-tert-butyl-4-methyl-6- (2- Hydroxy-3-tert-butyl-5-methylbenzyl) phenyl] terephthalate, 1,3,5-tris [(3,5-ditert-butyl-4-hydroxyphenyl) propionyloxyethyl] isocyanurate, 3,9 -Bis [1,1-dimethyl-2-{(3-tert-butyl-4-hydroxy-5-methylphenyl) propioni Ruoxy} ethyl] -2,4,8,10-tetraoxaspiro [5,5] undecane, triethylene glycol bis [(3-tert-butyl-4-hydroxy-5-methylphenyl) propionate] and the like. When adding to an electrode material, it is preferable to use 0.01-10 mass parts with respect to 100 mass parts of electrode materials, especially 0.05-5 mass parts.

  Examples of the phosphorus antioxidant include trisnonylphenyl phosphite, tris [2-tert-butyl-4- (3-tert-butyl-4-hydroxy-5-methylphenylthio) -5-methylphenyl]. Phosphite, tridecyl phosphite, octyl diphenyl phosphite, di (decyl) monophenyl phosphite, di (tridecyl) pentaerythritol diphosphite, di (nonylphenyl) pentaerythritol diphosphite, bis (2,4-di Tert-butylphenyl) pentaerythritol diphosphite, bis (2,6-ditert-butyl-4-methylphenyl) pentaerythritol diphosphite, bis (2,4,6-tritert-butylphenyl) pentaerythritol diphosphite Phosphite, bis (2,4-dicumylphenyl) pen Erythritol diphosphite, tetra (tridecyl) isopropylidene diphenol diphosphite, tetra (tridecyl) -4,4′-n-butylidenebis (2-tert-butyl-5-methylphenol) diphosphite, hexa (tridecyl) -1 , 1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane triphosphite, tetrakis (2,4-ditert-butylphenyl) biphenylene diphosphonite, 9,10-dihydro-9 -Oxa-10-phosphaphenanthrene-10-oxide, 2,2'-methylenebis (4,6-tert-butylphenyl) -2-ethylhexyl phosphite, 2,2'-methylenebis (4,6- Tributylphenyl) -octadecyl phosphite, 2,2′-ethylidenebis (4,6- Tert-butylphenyl) fluorophosphite, tris (2-[(2,4,8,10-tetrakis tert-butyldibenzo [d, f] [1,3,2] dioxaphosphin-6-yl) Oxy] ethyl) amine, phosphite of 2-ethyl-2-butylpropylene glycol and 2,4,6-tritert-butylphenol, and the like.

  Examples of the thioether-based antioxidant include dialkylthiodipropionates such as dilauryl thiodipropionate, dimyristyl thiodipropionate, and distearyl thiodipropionate, and pentaerythritol tetra (β-alkylmercaptopropionate esters). Is mentioned.

  Examples of the hindered amine compound include 2,2,6,6-tetramethyl-4-piperidyl stearate, 1,2,2,6,6-pentamethyl-4-piperidyl stearate, 2,2,6,6. -Tetramethyl-4-piperidylbenzoate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, tetrakis (2,2,6,6-tetramethyl-4-piperidyl) -1,2, 3,4-butanetetracarboxylate, tetrakis (1,2,2,6,6-pentamethyl-4-piperidyl) -1,2,3,4-butanetetracarboxylate, bis (2,2,6,6) -Tetramethyl-4-piperidyl) -di (tridecyl) -1,2,3,4-butanetetracarboxylate, bis (1,2,2,6,6-pentamethyl-4-pi Lysyl) .di (tridecyl) -1,2,3,4-butanetetracarboxylate, bis (1,2,2,4,4-pentamethyl-4-piperidyl) -2-butyl-2- (3,5 -Di-tert-butyl-4-hydroxybenzyl) malonate, 1- (2-hydroxyethyl) -2,2,6,6-tetramethyl-4-piperidinol / diethyl succinate polycondensate, 1,6- Bis (2,2,6,6-tetramethyl-4-piperidylamino) hexane / 2,4-dichloro-6-morpholino-s-triazine polycondensate, 1,6-bis (2,2,6,6 -Tetramethyl-4-piperidylamino) hexane / 2,4-dichloro-6-tert-octylamino-s-triazine polycondensate, 1,5,8,12-tetrakis [2,4-bis (N-butyl) -N- (2,2,6, -Tetramethyl-4-piperidyl) amino) -s-triazin-6-yl] -1,5,8,12-tetraazadodecane, 1,5,8,12-tetrakis [2,4-bis (N- Butyl-N- (1,2,2,6,6-pentamethyl-4-piperidyl) amino) -s-triazin-6-yl] -1,5,8-12-tetraazadodecane, 1,6,11 -Tris [2,4-bis (N-butyl-N- (2,2,6,6-tetramethyl-4-piperidyl) amino) -s-triazin-6-yl] aminoundecane, 1,6,11 Hindered amine compounds such as tris [2,4-bis (N-butyl-N- (1,2,2,6,6-pentamethyl-4-piperidyl) amino) -s-triazin-6-yl] aminoundecane Can be mentioned.

  The shape of the non-aqueous electrolyte secondary battery of the present invention having the above configuration is not particularly limited, and can be various shapes such as a coin shape, a cylindrical shape, and a square shape. FIG. 1 shows an example of a coin-type battery of the nonaqueous electrolyte secondary battery of the present invention, and FIGS. 2 and 3 show examples of a cylindrical battery, respectively.

  In the coin-type nonaqueous electrolyte secondary battery 10 shown in FIG. 1, 1 is a positive electrode using a nitroxy radical group-containing high molecular weight polymer having a lithium base of an organic acid in the molecule as a positive electrode active material. A positive electrode current collector, 2 is a negative electrode made of a carbonaceous material capable of absorbing and releasing lithium ions released from the positive electrode, 2a is a negative electrode current collector, 3 is a non-aqueous electrolyte, 4 is a stainless steel positive electrode case, 5 is A stainless steel negative electrode case, 6 is a polypropylene gasket, and 7 is a polyethylene separator.

  Further, in the cylindrical nonaqueous electrolyte secondary battery 10 ′ shown in FIGS. 2 and 3, 11 is a negative electrode, 12 is a negative electrode assembly, and 13 is a nitroxy radical group containing a lithium base of an organic acid in the molecule. Positive electrode using high molecular weight polymer as positive electrode active material, 14 positive electrode aggregate, 15 non-aqueous electrolyte, 16 separator, 17 positive electrode terminal, 18 negative electrode terminal, 19 negative electrode plate, 20 negative electrode lead, 21 is a positive electrode plate, 22 is a positive electrode lead, 23 is a case, 24 is an insulating plate, 25 is a gasket, 26 is a safety valve, and 27 is a PTC element.

  Hereinafter, the present invention will be described in detail by way of examples and comparative examples. However, the present invention is not limited by the following examples.

[Examples 1 to 4 and Comparative Example 1]
In the examples and comparative examples, nonaqueous electrolyte secondary batteries (lithium secondary batteries) were produced according to the following production procedure.

<Production procedure>
(Preparation of positive electrode)
60 parts by mass of a nitroxy radical group-containing high molecular weight polymer (sample compound A) obtained in the following production example as a positive electrode active material, 30 parts by mass of Ketjen black as a conductive material, and 10 PVDF as a binder. Part by mass was dispersed in 100 parts by mass of NMP to obtain a slurry. This slurry was applied to one side of a positive electrode current collector made of aluminum so that the thickness of the dried electrode material was 100 microns, dried, and then molded into a disk shape to obtain a positive electrode plate.

(Preparation of negative electrode)
As the negative electrode active material, a lithium metal foil having a thickness of 0.15 mm was formed into a disk shape to obtain a negative electrode plate.

(Preparation of non-aqueous electrolyte)
LiPF ₆ as an electrolyte salt was dissolved at a concentration of 1 mol / liter in a mixed solvent composed of 30% by volume of ethylene carbonate and 70% by volume of diethyl carbonate to obtain a nonaqueous electrolytic solution.

(Battery assembly)
By overlaying the above positive electrode and negative electrode with a polyethylene microporous film having a thickness of 25 μm sandwiched between them, setting it in a coin cell, dropping a predetermined amount of non-aqueous electrolyte, and sealing with a caulking machine A coin-type secondary battery was manufactured.

(Production of high molecular weight polymer containing nitroxy radical group)
[Production Example 1] Compound No. 1 Synthesis of 1 Maleic anhydride-isobutylene copolymer (manufactured by Kuraray Co., Ltd .; Isoban 10; weight average molecular weight 165,000) was added to a four-neck 1000 ml flask equipped with a stirrer, thermometer, nitrogen inlet tube and Dimroth condenser tube. ) 46.3 g (0.3 mol as carboxylic anhydride) and 463 g of N, N-dimethylacetamide were added and stirred and dissolved. Next, 35.2 g (0.23 mol) of 2,2,6,6-tetramethyl-4-piperidylamine was slowly added dropwise to this solution at 110 to 120 ° C. After completion of the dropwise addition, the temperature was gradually raised and reacted at 150 to 155 ° C. for 10 hours to complete imidization. After the reaction, the reaction system was diluted with 300 ml of methanol and dropped into 4200 ml of acetone for reprecipitation purification. The precipitate was filtered, washed and then dried under reduced pressure to obtain 71.2 g (yield 92%, weight average molecular weight 310,000) of a pale yellow solid. The obtained pale yellow solid was confirmed by IR analysis to be an imide that was the target intermediate. The IR analysis results are shown below.
<IR analysis results>
3410 cm ⁻¹ (N—H), 1777 cm ⁻¹ (anhydride), 1697 cm ⁻¹ (imide), 1625 cm ⁻¹ (N—H)
The obtained light yellow solid (51.6 g), water (150 ml) and ethanol (350 ml) were charged and dissolved by heating. To this solution, 4.2 g (0.1 mol) of lithium hydroxide monohydrate was added at 40 ° C. to obtain a lithium salt. The mixture was further heated, and 68.0 g (0.6 mol) of 30% hydrogen peroxide was gradually added dropwise at 55-60 ° C. The reaction was carried out at 70 to 75 ° C. for 10 hours, and it was confirmed that hydrogen peroxide was completely consumed, and the oxidation reaction was completed. The reaction solution was concentrated with an evaporator to obtain a concentrate, and the precipitate in the concentrate was thoroughly washed with acetone and filtered. Then dry well and orange solid 40. 7 g (74% yield) was obtained. The obtained orange solid was confirmed to be the target product (Compound No. 1) by IR analysis. The IR analysis results are shown below. In addition, the obtained compound No. The NO conversion ratio contained in each unit structure of 1 was calculated to be 60%.
<IR analysis results>
1698 cm ^-1 (imide)

[Production Example 2] Compound No. Synthesis of 2 The amount of maleic anhydride-isobutylene copolymer (manufactured by Kuraray Co., Ltd .; Isoban 10; weight average molecular weight 165,000) was 46.3 g (0.3 mol as carboxylic anhydride), The amount of 2,6,6-tetramethyl-4-piperidylamine used was 40.0 g (0.26 mol), the amount of lithium hydroxide monohydrate used was 2.5 g (0.06 mol), N: m: p in the above [Chemical Formula 4] is 70:15:15 except that the amount of 30% hydrogen peroxide water used was 68.0 g (0.6 mol). A certain compound No. 55.8g of 2 was obtained (yield 65%).

[Production Example 3] Compound No. Synthesis of 3 A four-necked 3000 ml flask equipped with a stirrer, thermometer, nitrogen inlet tube and Dimroth condenser tube was mixed with maleic anhydride-isobutylene copolymer (manufactured by Kuraray Co., Ltd .; Isoban 06; weight average molecular weight 85,000). 77.1 g (0.50 mol as carboxylic anhydride), 150 ml of methanol and 600 ml of water were added and stirred, and then 58.6 g (0,0) of 2,2,6,6-tetramethyl-4-piperidylamine at room temperature. .38 mol) was added dropwise. After dropping, the mixture was heated to 80 to 85 ° C. and reacted for 1 hour. After cooling to 60 ° C. or lower, 26.2 g (0.62 mol) of lithium hydroxide monohydrate was added and stirred for 1 hour. Thereto, 480.0 g (4.5 mol) of 30% aqueous hydrogen peroxide was added dropwise in about 3 hours while maintaining the temperature at 55 to 60 ° C., followed by stirring for 5 hours. After the reaction, the reaction system was dropped into 3000 ml of acetone solvent, and the precipitated solid was separated by filtration. Thereafter, it was washed with acetone and dried to obtain an orange solid (yield 111.1 g, yield 76%). The obtained solid was confirmed to be the target product (the following compound No. 3) by IR analysis. The IR analysis results are shown below. In addition, the obtained compound No. The NO conversion ratio contained in each unit structure of 3 was calculated to be 60%.
<IR analysis results>
3465 cm ⁻¹ (N—H), 1637 cm ⁻¹ , 1559 cm ⁻¹ (amide + carboxylate)

[Production Example 4] Compound No. Synthesis of 4 Maleic anhydride-isobutylene copolymer (manufactured by Kuraray Co., Ltd .; Isoban 06; weight average molecular weight 85,000) was used in an amount of 77.1 g (0.5 mol as carboxylic anhydride), The amount of 2,6,6-tetramethyl-4-piperidylamine used was 70.0 g (0.45 mol), the amount of lithium hydroxide monohydrate used was 10.5 g (0.25 mol), Compound in which n: m: p in the above [Chemical Formula 5] is 75:15:10 in the same manner as in Production Example 3 except that the amount of 30% hydrogen peroxide water used is 480 g (4.5 mol) No. 129 g of 4 was obtained (yield 82%).

<Battery evaluation test method>
The coin-type secondary battery is placed in a thermostatic chamber at an ambient temperature of 25 ° C., and is charged with a constant current up to 4.1 V at a current value equivalent to 1C (1C is a current value that discharges the battery capacity in one hour). A cycle of performing constant current discharge up to 3.0 V at a current value was repeated 100 times.
The theoretical capacity per positive electrode active material (nitroxy radical group-containing high molecular weight polymer) used was calculated, and the capacity expression rate (%) was calculated from the numerical value and the measured discharge capacity according to the following formula.
Capacity expression rate (%) = [discharge capacity / theoretical capacity] × 100

As is clear from the results in Table 1, the non-aqueous electrolyte secondary battery of the present invention using the nitroxy radical group-containing high molecular weight polymer represented by the general formulas (1) and (2) as an electrode active material It was confirmed that the capacity expression rate was excellent. In contrast, in a non-aqueous electrolyte secondary battery using a conventional nitroxy radical group-containing high molecular weight polymer different from the present invention as an electrode active material, the capacity expression rate is the non-aqueous electrolyte secondary battery of the present invention. It was inferior to. In addition, since the capacity of the electrode used in Example 3 is expressed even when a solvent not containing LiPF ₆ is used instead of the electrolyte, lithium carboxylate present in the molecule is used as a counter anion for nitro. It was confirmed that it functions effectively on the xyl radical group.

  The non-aqueous electrolyte secondary battery of the present invention provides a non-aqueous electrolyte secondary battery having an excellent capacity expression rate by using a nitroxy radical group-containing high molecular weight polymer having a specific structure as an electrode active material. it can.

FIG. 1 is a longitudinal sectional view schematically showing an example of the structure of a coin-type battery of the nonaqueous electrolyte secondary battery of the present invention. FIG. 2 is a schematic diagram showing a basic configuration of a cylindrical battery of the nonaqueous electrolyte secondary battery of the present invention. FIG. 3 is a perspective view showing the internal structure of the cylindrical battery of the nonaqueous electrolyte secondary battery of the present invention as a cross section.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Positive electrode 1a Positive electrode collector 2 Negative electrode 2a Negative electrode collector 3 Electrolyte 4 Positive electrode case 5 Negative electrode case 6 Gasket 7 Separator 10 Coin type nonaqueous electrolyte secondary battery 10 'Cylindrical type nonaqueous electrolyte secondary battery 11 Negative electrode 12 Negative electrode assembly 13 Positive electrode 14 Positive electrode assembly 15 Electrolyte 16 Separator 17 Positive electrode terminal 18 Negative electrode terminal 19 Negative electrode plate 20 Negative electrode lead 21 Positive electrode 22 Positive electrode lead 23 Case 24 Insulating plate 25 Gasket 26 Safety valve 27 PTC element

Claims (2)

  A non-aqueous electrolyte secondary battery using a nitroxy radical group-containing high molecular weight polymer having an organic acid lithium base in the molecule as an electrode active material. The non-aqueous electrolyte secondary battery according to claim 1, wherein the nitroxy radical group-containing high molecular weight polymer is composed of a structural unit represented by the following general formula (1) and / or (2).

(In the formula, R ₁ and R ₂ each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. N / (n + m + p) is 0.2 to 0.99, m / (n + m + p) is from 0 to 0.8, and p / (n + m + p) is from 0.01 to 0.8.)

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