JP6019663B2 - Non-aqueous electrolyte and non-aqueous electrolyte battery using the same - Google Patents

Description

  The present invention relates to a non-aqueous electrolyte and a non-aqueous electrolyte battery using the same.

With the rapid progress of portable electronic devices such as mobile phones and notebook personal computers, there is an increasing demand for higher capacities for batteries used for main power supplies and backup power supplies. Non-aqueous electrolyte batteries such as lithium ion secondary batteries having higher energy density than hydrogen batteries have attracted attention.
As an electrolytic solution of the lithium ion secondary battery, an electrolyte such as LiPF ₆ , LiBF ₄ , LiN (CF ₃ SO ₂ ) ₂ , LiCF ₃ (CF ₂ ) ₃ SO ₃ is used as a high dielectric constant such as ethylene carbonate or propylene carbonate. A typical example is a non-aqueous electrolyte solution dissolved in a mixed solvent of a solvent and a low-viscosity solvent such as dimethyl carbonate, diethyl carbonate, or ethyl methyl carbonate.

  In addition, as a negative electrode active material of a lithium ion secondary battery, a carbonaceous material capable of occluding and releasing lithium ions is mainly used, and natural graphite, artificial graphite, amorphous carbon, etc. are listed as representative examples. It is done. Furthermore, metal or alloy negative electrodes using silicon, tin or the like for increasing the capacity are also known. As the positive electrode active material, a transition metal composite oxide capable of mainly inserting and extracting lithium ions is used, and representative examples of the transition metal include cobalt, nickel, manganese, iron and the like.

Such a lithium ion secondary battery uses a highly active positive electrode and negative electrode, and it is known that the charge / discharge capacity decreases due to a side reaction between the electrode and the electrolyte, improving battery characteristics. Therefore, various studies have been made on non-aqueous solvents and electrolytes.
In Patent Document 1, by using a nonaqueous electrolytic solution containing an alkyne derivative, the alkyne derivative is decomposed on the surface of the carbon negative electrode to form a passive film. Further, the decomposition product is oxidatively decomposed on the positive electrode, thereby suppressing the oxidative decomposition of the electrolytic solution. It has been proposed to improve the charge / discharge cycle life.

In addition, Patent Document 2 discloses that after adding an alkynyl compound having a specific structure in which an alkynyl group is bonded via a specific group to a non-aqueous electrolyte, low-temperature and high-temperature cycle characteristics, and after high-temperature charge storage It has been proposed that the load characteristics of can be improved.
Patent Document 3 proposes that cycle characteristics, storage characteristics, and load characteristics can be obtained by using a specific compound in combination with an oxalate ester or sulfonate ester having a carbon-carbon unsaturated bond. Has been.

  Further, in Patent Document 4, a protective film is formed on the electrode surface by using a non-aqueous electrolytic solution containing a compound in which a halogen atom is bonded to a carbon atom adjacent to a carbon-carbon multiple bond, and thus a high temperature storage is performed. It has been proposed to suppress time expansion and further improve the charge / discharge cycle life.

JP 2000-195545 A WO2011 / 096450 gazette JP 2011-238373 A JP 2009-181846 A

  However, the demand for improving the characteristics of lithium non-aqueous electrolyte secondary batteries in recent years has been increasing, and all the performances such as high-temperature storage characteristics, energy density, output performance, life, high-speed charge / discharge characteristics, and low-temperature characteristics have been achieved. Although it is required to have a high level, it has not yet been achieved. The durability performance including high temperature storage characteristics and the performance such as capacity, resistance, and output characteristics are in a trade-off relationship.

  The present invention has been made in view of the above-described problems. That is, with respect to a lithium non-aqueous electrolyte secondary battery, an object is to provide a battery having a good balance of overall performance with respect to performance such as durability and capacity, resistance, and output characteristics.

  As a result of various studies to achieve the above object, the present inventors have determined that a compound having at least one triple bond in a molecule and a compound having a certain amount of at least one halogen atom are non-aqueous electrolysis. The above-mentioned problems are solved by including in a non-aqueous electrolyte a compound having at least one triple bond in a molecule containing a specific amount of a compound having at least one kind of halogen atom. As a result, the inventors have found that this can be done, and have completed the present invention described later.

The gist of the present invention is as follows.
(I) A non-aqueous electrolyte solution for a non-aqueous electrolyte battery comprising a positive electrode and a negative electrode capable of occluding and releasing metal ions, the non-aqueous electrolyte solution together with an electrolyte and a non- aqueous solvent,
(A) A compound having an alkynyloxy group in the structure represented by the following formula (1) is represented by the following formula (2) in a non-aqueous electrolyte solution in an amount of 0.01% by mass to 5% by mass. is a compound having a molecular weight 55 to 200 in which a chlorine atom, a non-aqueous electrolytic solution to less than 0.2 ppm by weight 500 ppm by weight,
Nonaqueous electrolyte characterized in that it comprises free.

(In formula (1), R ¹ and R ² are each independently a hydrogen atom, a halogen atom, or an alkyl group, alkenyl group, alkynyl group, aryl group, alkoxy group, cyano group optionally substituted with a halogen atom. An organic group which may have an isocyanato group, an ether group, a carbonate group, a carbonyl group, a carboxyl group, a sulfonyl group and a phosphoryl group, which may be the same or different, but R ¹ or Either one or both of R ² is an organic group containing one or more S═O groups.)

(In Formula (2), R ³ is a hydrogen atom, and R ⁴ is an organic group that may have a substituent .)
(Ii) The compound having a chlorine atom represented by the formula (2) is contained in an amount of 20 mass ppm to 5 mass% with respect to the compound represented by the formula (1), (i) The non-aqueous electrolyte solution described in 1.
( Iii ) The nonaqueous electrolytic solution according to (i) or ( ii ), wherein in formula (2), R ⁴ is a methylene group which may have a substituent.
( Iv ) At least one selected from the group consisting of a cyclic carbonate having a fluorine atom, a cyclic carbonate having a carbon-carbon unsaturated bond, a monofluorophosphate, a difluorophosphate, an isocyanate compound, a cyclic sulfonate ester, and a nitrile compound. The nonaqueous electrolytic solution according to any one of (i) to ( iii ), further comprising a seed compound.
( V ) The cyclic carbonate having a fluorine atom is at least one compound selected from the group consisting of monofluoroethylene carbonate, 4,4-difluoroethylene carbonate, and 4,5-difluoroethylene carbonate, and is carbon-carbon unsaturated. The cyclic carbonate having a bond is vinylene carbonate, vinyl ethylene carbonate, ethynyl ethylene carbonate, the isocyanate compound is a compound having at least two isocyanate groups, and the nitrile compound is a compound having at least two nitrile groups. The non-aqueous electrolyte solution described in ( iv ).
(Vi) A non-aqueous electrolyte secondary battery including a negative electrode and a positive electrode capable of inserting and extracting lithium ions, and a non-aqueous electrolyte, wherein the non-aqueous electrolyte is any one of (i) to ( v ) A non-aqueous electrolyte secondary battery, which is the non-aqueous electrolyte solution described in 1.

  ADVANTAGE OF THE INVENTION According to this invention, regarding a lithium non-aqueous electrolyte secondary battery, a battery with a good balance of overall performance can be provided with respect to performance such as durability performance, capacity, resistance, and output characteristics. The non-aqueous electrolyte secondary battery produced using the non-aqueous electrolyte solution of the present invention and the non-aqueous electrolyte secondary battery of the present invention are not clear in terms of the action and principle of improving battery characteristics, but the following I think so. However, the present invention is not limited to the operations and principles described below.

  Normally, when only the alkyne compound described in Patent Documents 1 to 3 is contained in the non-aqueous electrolyte, a decomposition product generated on the negative electrode acts on the positive electrode, but at that time, side reactions also proceed simultaneously on the positive electrode. To do. As a result, a deposit having low lithium conductivity is generated on the electrode, and the efficiency of high-speed charge / discharge characteristics is reduced. Therefore, in order to suppress the side reaction on the positive electrode as much as possible, it is a problem to prevent the decomposition product from flowing around the positive electrode.

In addition, when a compound in which a halogen atom is bonded to the carbon atom adjacent to the carbon-carbon multiple bond described in Patent Document 4 is contained alone in the non-aqueous electrolyte, lithium halide is generated on the surface of the electrode. Interfacial resistance tends to increase. Furthermore, when it is used in combination with the additive described in Patent Document 2 and contained in a non-aqueous electrolyte, the degree of polymerization of the protective film on the electrode surface is increased, and the overvoltage is increased during charge and discharge, thereby deteriorating battery characteristics. . Therefore, it is a problem to solve these problems.

  In order to solve such a problem, in the present invention, the compound represented by the formula (1) (hereinafter, sometimes referred to as a compound having at least one triple bond in the molecule) and a specific amount of at least one kind. Or a compound having at least one triple bond in a molecule containing a certain amount of a compound having at least one halogen atom is contained in the non-aqueous electrolyte. It has been found that the above-mentioned problems can be solved by adding to the composition.

  A compound having at least one halogen atom is reduced on the negative electrode to generate a radical by a dehalogenation anion reaction. This radical reacts with a compound having at least one triple bond, thereby forming a polymer film having an appropriate molecular weight with high lithium conductivity. Furthermore, since this film formation reaction proceeds efficiently, it becomes difficult to generate a decomposition product of a compound having at least one triple bond. Therefore, the contribution of the decomposition product to the positive electrode is reduced, and the above-described problems of Patent Documents 1 to 3 are solved.

On the other hand, when a compound having a double bond mainly described in Patent Document 4 is used instead of the compound having at least one triple bond, the polymerization reaction proceeds intermittently, and the degree of polymerization is greatly increased. End up.
Furthermore, in the present invention, there is an optimum addition amount because it is sufficient that a compound having at least one halogen atom serves as a base point for polymerization. If added within the range described in Patent Document 4, a large amount of lithium halide is generated on the electrode surface, which increases the resistance at the electrode interface, which is not suitable. In this invention, the above-mentioned subject is solved by limiting the addition amount of the compound which has at least 1 type of halogen atom to the specified range.

Addition amount of 3-chloro-1-propyne and initial 1C rate characteristics Addition amount of 3-chloro-1-propyne and voltage after storage

Hereinafter, embodiments of the present invention will be described, but the present invention is not limited to the following embodiments, and can be arbitrarily modified and implemented without departing from the gist of the present invention.
In addition, “wt%”, “wt ppm”, “part by weight”, “mass%”, “mass ppm”, and “mass part” are synonymous with each other. In addition, when simply described as ppm, it means “mass ppm”.

1. Non-aqueous electrolyte 1-1. Compound represented by formula (1)

In formula (1), R ¹ and R ² are each independently a hydrogen atom, a halogen atom, or an organic group that may have a substituent, and may be the same or different.
Here, the organic group represents a functional group composed of atoms selected from the group consisting of carbon atoms, hydrogen atoms, nitrogen atoms, oxygen atoms and halogen atoms. Specific examples include alkyl groups, alkenyl groups, alkynyl groups, aryl groups, alkoxy groups, cyano groups, isocyanato groups, ether groups, carbonate groups, carbonyl groups, sulfonyl groups, phosphoryl groups, and the like.

Specific examples of the substituent include alkyl groups, alkenyl groups, alkynyl groups, aryl groups, alkoxy groups, cyano groups, isocyanato groups, ether groups, carbonate groups, carbonyl groups, carboxyl groups which may be substituted with halogen atoms. Group, sulfonyl group, phosphoryl group and the like.
In the formula (1), it is preferable that either one or both of R ^{1 and} R ² is an organic group containing one or more S═O groups. By having an S═O group, it becomes easy to act on the positive electrode, and side reactions on the positive electrode caused by a decomposition product of a compound having at least one triple bond in the molecule are suppressed.

  The molecular weight of the compound represented by the formula (1) is not particularly limited, and is arbitrary as long as the effects of the present invention are not significantly impaired. The molecular weight is preferably 100 or more, more preferably 130 or more, still more preferably 145 or more, and is 500 or less, preferably 300 or less, and more preferably 270 or less. If it is this range, it will be easy to ensure the solubility of the compound shown by (1) with respect to a non-aqueous electrolyte solution, and the effect of this invention will be easy to be expressed.

Specific examples of the compound represented by the formula (1) include the following compounds.
1-pentyne, 2-pentyne, 1-hexyne, 2-hexyne, 3-hexyne, 1-heptin, 2-heptin, 3-heptin, 1-octyne, 2-octyne, 3-octyne, 4-octyne, 1- Nonin, 2-nonine, 3-nonine, 4-nonine, 1-dodecin, 2-dodecin, 3-dodecin, 4-dodecin, 5-dodecin, phenylacetylene, 1-phenyl-1-propyne, 1-phenyl-2 -Propyne, 1-phenyl-1-butyne, 4-phenyl-1-butyne, 4-phenyl-1-butyne, 1-phenyl-1-pentyne, 5-phenyl-1-pentyne, 1-phenyl-1-hexyne , Hydrocarbon compounds such as 6-phenyl-1-hexyne, diphenylacetylene, 4-ethynyltoluene, dicyclohexylacetylene; 2-propynylmethylcar 2-propynylethyl carbonate, 2-propynylpropyl carbonate, 2-propynylbutyl carbonate, 2-propynylphenyl carbonate, 2-propynylcyclohexyl carbonate, di-2-propynyl carbonate, 1-methyl-2-propynylmethyl carbonate, 1 1-dimethyl-2-propynylmethyl carbonate, 2-butynylmethyl carbonate, 3-butynylmethyl carbonate, 2-pentynylmethyl carbonate, 3-pentynylmethyl carbonate, 4-pentynylmethyl carbonate, etc. 2-butyne-1,4-diol dimethyl dicarbonate, 2-butyne-1,4-diol diethyl dicarbonate, 2-butyne-1,4-diol dipropyl dicarbonate , 2-butyne-1,4-diol dibutyl carbonate, 2-butyne-1,4-diol diphenyl carbonate, dicarbonate such as 2-butyne-1,4-diol and dicyclohexyl carbonate;

2-propynyl acetate, 2-propynyl propionate, 2-propynyl butyrate, 2-propynyl benzoate, -2-propynyl cyclohexylcarboxylate, acetic acid-1, 1-dimethyl-2-propynyl, propionic acid-1 1-dimethyl-2-propynyl, butyric acid-1, 1-dimethyl-2-propynyl, benzoic acid-1, 1-dimethyl-2-propynyl, cyclohexylcarboxylic acid-1, 1-dimethyl-2-propynyl, acetic acid 2-butynyl, acetic acid-3-butynyl, acetic acid-2-pentynyl, acetic acid-3-pentynyl, acetic acid-4-pentynyl, 2-propanoic acid methyl, 2-propanoic acid ethyl, 2-propionic acid propyl, 2-propionic acid Vinyl, 2-propionic acid-2-propenyl, 2-propionic acid-2-butenyl, 2-propionic acid-3-butenyl, 2- Methyl butyrate, ethyl 2-butyrate, 2-propyl butyrate, vinyl 2-butyrate, 2-butynoic acid-2-propenyl, 2-butynoic acid-2-butenyl, 2-butynoic acid-3-butenyl, 3 Methyl butyrate, ethyl 3-butyrate, propyl 3-butyrate, vinyl 3-butyrate, 3-butynoic acid-2-propenyl, 3-butynoic acid-2-butenyl, 3-butynoic acid-3-butenyl, 2-pentynoic acid methyl, 2-pentynoic acid ethyl, 2-pentynoic acid propyl, 2-pentynoic acid vinyl, 2-pentynoic acid-2-propenyl, 2-pentynoic acid-2-butenyl, 2-pentynoic acid-3-butenyl Methyl 3-pentynoate, ethyl 3-pentynoate, propyl 3-pentynoate, vinyl 3-pentynoate, 3-pentynoic acid-2-propenyl, 3-pentynoic acid-2-butenyl, -Pentynoic acid-3-butenyl, 4-pentynoic acid methyl, 4-pentynoic acid ethyl, 4-pentynoic acid propyl, 4-pentynoic acid vinyl, 4-pentynoic acid-2-propenyl, 4-pentynoic acid-2-butenyl, 4-pentynoic acid-3-butenyl, 2- (methanesulfonyloxy) propionic acid-2-propynyl, 2- (methanesulfonyloxy) propionic acid-3-butynyl, methanesulfonyloxyacetic acid-2-propynyl, methanesulfonyloxyacetic acid Monobutyric acid esters such as -3-butynyl; 2-butyne-1,4-diol diacetate, 2-butyne-1,4-diol dipropionate, 2-butyne-1,4-diol dibutyrate, 2-butyne- 1,4-diol dibenzoate, 2-butyne-1,4-diol dicyclohexane Dicarboxylic acid esters such as Kishireto;

  Methyl-2-propynyl oxalate, ethyl-2-propynyl oxalate, propyl-2-propynyl oxalate, 2-propynyl oxalate (vinyl), allyl-2-propynyl oxalate, di-2-propynyl oxalate, 2-butynyl oxalate methyl, 2-butynyl oxalate (ethyl), 2-butynyl oxalate (propyl), -2-butynyl oxalate (vinyl), allyl-2-butynyl oxalate, di-oxalate 2-butynyl, oxalate-3-butynyl (methyl), oxalate-3-butynyl (ethyl), oxalate-3-butynyl (propyl), oxalate-3-butynyl (vinyl), allyl oxalate-3- Oxalic acid diesters such as butynyl and di-3-butynyl oxalate; methyl-2-propynylsulfone, ethyl-2-propynylsulfone, Lopyl-2-propynylsulfone, 2-propynylvinylsulfone, 2-propenyl-2-propynylsulfone, di-2-propynylsulfone, 3-butenyl-2-propynylsulfone, 3-butenyl-2-propynylsulfone, 1,1 -Sulfone compounds such as dimethyl-2-propynyl vinyl sulfone and 1,1-dimethyl-2-propynyl-2-propenyl sulfone;

Methanesulfonic acid-2-propynyl, ethanesulfonic acid-2-propynyl, propanesulfonic acid-2-propynyl, p-toluenesulfonic acid-2-propynyl, cyclohexylsulfonic acid-2-propynyl, vinylsulfonic acid-2-propynyl, 2-propynylsulfonic acid-2-propynyl, 2-propynylsulfonic acid methyl, 2-propynylsulfonic acid ethyl, 2-propynylsulfonic acid butyl, 2-propynylsulfonic acid-2-propenyl, 2-propynylsulfonic acid-2-propynyl Methanesulfonic acid-1, 1-dimethyl-2-propynyl, ethanesulfonic acid-1, 1-dimethyl-2-propynyl, propanesulfonic acid-1, 1-dimethyl-2-propynyl, p-toluenesulfonic acid-1 1-dimethyl-2-propynyl, cyclohe Silsulfonic acid-1, 1-dimethyl-2-propynyl, vinylsulfonic acid-1, 1-dimethyl-2-propynyl, 2-propenylsulfonic acid-1, 1-dimethyl-2-propynyl, methanesulfonic acid-2-pentynyl Methanesulfonic acid-3-pentynyl, methanesulfonic acid-4-pentynyl, vinylsulfonic acid-2-butynyl, vinylsulfonic acid-3-butynyl, vinylsulfonic acid-2-pentynyl, vinylsulfonic acid-3-pentynyl, vinyl Sulfonic acid-4-pentynyl, 2-propenylsulfonic acid-2-butynyl, 2-propenylsulfonic acid-3-butynyl, 2-propenylsulfonic acid-2-pentynyl, 2-propenylsulfonic acid-3-pentynyl, 2-propenyl Sulfonic acid-4-pentynyl, 2-propynylsulfonic acid-2 Butynyl, 2-propynylsulfonic acid-3-butynyl, 2-propynylsulfonic acid-2-pentynyl, 2-propynylsulfonic acid-3-pentynyl, 2-propynylsulfonic acid-4-pentynyl, 2-oxoethanesulfonic acid-2 -Propynyl, 3-oxopropanesulfonic acid-2-propynyl, 4-oxobutanesulfonic acid-2-propynyl, 5-oxopentanesulfonic acid-2-propynyl, 6-oxohexanesulfonic acid-2-propynyl, 7-oxo Heptanesulfonic acid-2-propynyl, 3-oxopropoxymethanesulfonic acid-2-propynyl, 2-oxopropanesulfonic acid-2-propynyl, 3-oxobutanesulfonic acid-2-propynyl, 4-oxopentanesulfonic acid-2 -Propynyl, 5-oxohexanesulfonic acid 2-propynyl, 2-propynyl 6-oxoheptanesulfonate, 2-propynyl 7-oxooctanesulfonate, 2-propynyl 2-oxobutanesulfonate, 2-propynyl 3-oxopentanesulfonate, 4 -Oxohexanesulfonic acid-2-propynyl, 5-oxoheptanesulfonic acid-2-propynyl, 6-oxooctanesulfonic acid-2-propynyl, 7-oxononanesulfonic acid-2-propynyl, 2- (3-oxobutoxy ) -2-propynyl ethanesulfonate, 2-propynyl methanesulfonylmethanesulfonate, 2-propynyl 2- (methanesulfonyl) ethanesulfonate, 2-propynyl 3- (methanesulfonyl) propanesulfonate, 4- ( Methanesulfonyl) butanesulfonic acid-2-propynyl 5- (Methanesulfonyl) pentanesulfonic acid-2-propynyl, 6- (methanesulfonyl) hexanesulfonic acid-2-propynyl, ethanesulfonylmethanesulfonic acid-2-propynyl, 2- (ethanesulfonyl) ethanesulfonic acid-2- Propinyl, 3- (ethanesulfonyl) propanesulfonic acid-2-propynyl, 4- (ethanesulfonyl) butanesulfonic acid-2-propynyl, 5- (ethanesulfonyl) pentanesulfonic acid-2-propynyl, 6- (ethanesulfonyl) Hexanesulfonic acid-2-propynyl, trifluoromethanesulfonylmethanesulfonic acid-2-propynyl, 2- (trifluoromethanesulfonyl) ethanesulfonic acid-2-propynyl, 3- (trifluoromethanesulfonyl) propanesulfonic acid-2-propynyl 4- (trifluoromethanesulfonyl) butanesulfonic acid-2-propynyl, 5- (trifluoromethanesulfonyl) pentanesulfonic acid-2-propynyl, 6- (trifluoromethanesulfonyl) hexanesulfonic acid-2-propynyl, 2- ( 2- (Methanesulfonyl) ethoxy) ethanesulfonic acid-2-propynyl, benzenesulfonylmethanesulfonic acid-2-propynyl, 2- (benzenesulfonyl) ethanesulfonic acid-2-propynyl, 3- (benzenesulfonyl) propanesulfonic acid- 2-propynyl, 4- (benzenesulfonyl) butanesulfonic acid-2-propynyl, 5- (benzenesulfonyl) pentanesulfonic acid-2-propynyl, 6- (benzenesulfonyl) hexanesulfonic acid-2-propynyl, 4-methylbenze 2-propynyl sulfonylmethanesulfonate-2-propynyl 2- (4-methylbenzenesulfonyl) ethanesulfonate-2-propynyl 3- (4-methylbenzenesulfonyl) propanesulfonate, 4- (4-methyl) Benzenesulfonyl) butanesulfonic acid-2-propynyl, 5- (4-methylbenzenesulfonyl) pentanesulfonic acid-2-propynyl, 6- (4-methylbenzenesulfonyl) hexanesulfonic acid-2-propynyl, 4-fluorobenzenesulfonyl 2-propynyl methanesulfonate, 2-propynyl 2- (4-fluorobenzenesulfonyl) ethanesulfonate, 2-propynyl 3- (4-fluorobenzenesulfonyl) propanesulfonate, 4- (4-fluorobenzenesulfonyl) ) Butanesulfonic acid 2-propynyl, 5- (4-fluorobenzenesulfonyl) pentanesulfonic acid-2-propynyl, 6- (4-fluorobenzenesulfonyl) hexanesulfonic acid-2-propynyl, 2- (2-benzenesulfonylethoxy) ethanesulfonic acid 2-propynyl, methoxysulfonylmethanesulfonic acid-2-propynyl, 2- (methoxysulfonyl) ethanesulfonic acid-2-propynyl, 3- (methoxysulfonyl) propanesulfonic acid-2-propynyl, 4- (methoxysulfonyl) butane 2-propynyl sulfonate, 2-propynyl 5- (methoxysulfonyl) pentanesulfonate, 2-propynyl 6- (methoxysulfonyl) hexanesulfonate, 2-propynyl ethoxysulfonylmethanesulfonate, 2- (ethoxysulfone) ) Ethane sulfonic acid-2-propynyl, 3- (ethoxy-benzenesulfonyl) propanesulfonic acid 2-propynyl, 4
-(Ethoxysulfonyl) butanesulfonic acid-2-propynyl, 5- (ethoxysulfonyl) pentanesulfonic acid-2-propynyl, 6- (ethoxysulfonyl) hexanesulfonic acid-2-propynyl, 2- (2- (methoxysulfonyl) Ethoxy) ethanesulfonic acid-2-propynyl, 2-propenyloxysulfonylmethanesulfonic acid-2-propynyl, 2- (2-propenyloxysulfonyl) ethanesulfonic acid-2-propynyl, 3- (2-propenyloxysulfonyl) propane 2-propynyl sulfonic acid, 4- (2-propenyloxysulfonyl) butanesulfonic acid-2′-propynyl, 2- (2-propenyloxysulfonyl) pentanesulfonic acid-2-propynyl, 6- (2-propenyloxysulfonyl) ) Hexanesulfo 2-propynyl acid, 2- (2- (2-propenyloxysulfonyl) ethoxy) ethanesulfonic acid-2-propynyl, dimethoxyphosphorylmethanesulfonic acid-2-propynyl, 2- (dimethoxyphosphoryl) ethanesulfonic acid-2 -Propynyl, 3- (dimethoxyphosphorylpropane) sulfonic acid-2-propynyl, 4- (dimethoxyphosphoryl) butanesulfonic acid-2-propynyl, 5- (dimethoxyphosphoryl) pentanesulfonic acid-2-propynyl, 6- (dimethoxyphosphoryl) ) -2-propynyl hexanesulfonate, 2-propynyl diethoxyphosphoryl methanesulfonate, 2-propynyl 2- (diethoxyphosphoryl) ethanesulfonate, 2-propynyl 3- (diethoxyphosphoryl) propanesulfonate, 4- ( Ethoxyphosphoryl) butanesulfonic acid-2-propynyl, 5- (diethoxyphosphoryl) pentanesulfonic acid-2-propynyl, 6- (diethoxyphosphoryl) hexanesulfonic acid-2-propynyl, 2- (2- (dimethoxyphosphoryl) Ethoxy) ethanesulfonic acid-2-propynyl, methoxy (methyl) phosphorylmethanesulfonic acid-2-propynyl, 2- (methoxy (methyl) phosphoryl) ethanesulfonic acid-2-propynyl, 3- (methoxy (methyl) phosphoryl) propane 2-propynyl sulfonic acid, 4- (methoxy (methyl) phosphoryl) butanesulfonic acid-2-propynyl, 5- (methoxy (methyl) phosphoryl) pentanesulfonic acid-2-propynyl, 6- (methoxy (methyl) phosphoryl) Hexanesulfonic acid-2 Propynyl, 2- (2- (methoxy (methyl) phosphoryl) ethoxy) ethanesulfonic acid-2-propynyl, ethoxy (methyl) phosphorylmethanesulfonic acid-2-propynyl, 2- (ethoxy (methyl) phosphoryl) ethanesulfonic acid- 2-propynyl, 3- (ethoxy (methyl) phosphoryl) propanesulfonic acid-2-propynyl, ethyl (methoxy) phosphorylmethanesulfonic acid-2-propynyl, 2- (ethyl (methoxy) phosphoryl) ethanesulfonic acid-2-propynyl 3- (ethyl (methoxy) phosphoryl) propanesulfonic acid-2-propynyl, dimethylphosphorylmethanesulfonic acid-2-propynyl, 2- (dimethylphosphoryl) ethanesulfonic acid-2-propynyl, 3- (dimethylphosphoryl) propanesulfone Acid-2 -Propynyl, 4- (dimethylphosphoryl) butanesulfonic acid-2-propynyl, 5- (dimethylphosphoryl) pentanesulfonic acid-2-propynyl, 6- (dimethylphosphoryl) hexanesulfonic acid-2-propynyl, 2- (2- (Dimethylphosphoryl) ethoxy) ethanesulfonic acid-2-propynyl, methoxymethanesulfonic acid-2-propynyl, 2-methoxyethanesulfonic acid-2-propynyl, 3-methoxypropanesulfonic acid-2-propynyl, 4-methoxybutanesulfone 2-propynyl acid, 2-propynyl 5-methoxypentanesulfonate, 2-propynyl 6-methoxyhexanesulfonate, 2-propynyl ethoxymethanesulfonate, 2-propynyl 2-ethoxyethanesulfonate, 3- Ethoxypropane sulfo Acid-2-propynyl, 4-ethoxybutanesulfonic acid-2-propynyl, 5-ethoxypentanesulfonic acid-2-propynyl, 6-ethoxyhexanesulfonic acid-2-propynyl, 2- (2-methoxyethoxy) ethanesulfonic acid 2-propynyl, 2-propynyl formyloxymethanesulfonate, 2-propynyl 2- (formyloxy) ethanesulfonate, 2-propynyl 3- (formyloxy) propanesulfonate, 4- (formyloxy) butane 2-propynyl sulfonic acid, 2-propynyl 5- (formyloxy) pentanesulfonic acid, 2-propynyl 6- (formyloxy) hexanesulfonic acid, 2- (2- (formyloxy) ethoxy) ethanesulfonic acid 2-propynyl, acetyloxymethanesulfonic acid-2
-Propynyl, 2- (acetyloxy) ethanesulfonic acid-2-propynyl, 3- (acetyloxy) propanesulfonic acid-2-propynyl, 4- (acetyloxy) butanesulfonic acid-2-propynyl, 5- (acetyloxy) ) Pentanesulfonic acid-2-propynyl, 6- (acetyloxy) hexanesulfonic acid-2-propynyl, propionyloxymethanesulfonic acid-2-propynyl, 2- (propionyloxy) ethanesulfonic acid-2-propynyl, 3- ( Propionyloxy) propanesulfonic acid-2-propynyl, 4- (propionyloxy) butanesulfonic acid-2-propynyl, 5- (propionyloxy) pentanesulfonic acid-2-propynyl, 6- (propionyloxy) hexanesulfonic acid-2 -Propynyl, 2- (2 (Acetyloxy) ethoxy) ethanesulfonic acid-2-propynyl, methanesulfonyloxymethanesulfonic acid-2-propynyl, 2- (methanesulfonyloxy) ethanesulfonic acid-2-propynyl, 3- (methanesulfonyloxy) propanesulfonic acid 2-propynyl, 4- (methanesulfonyloxy) butanesulfonic acid-2-propynyl, 5- (methanesulfonyloxy) pentanesulfonic acid-2-propynyl, 6- (methanesulfonyloxy) hexanesulfonic acid-2-propynyl, Ethanesulfonyloxymethanesulfonic acid-2-propynyl, 2- (ethanesulfonyloxy) ethanesulfonic acid-2-propynyl, 3- (ethanesulfonyloxy) propanesulfonic acid-2-propynyl, 4- (ethanesulfonyloxy) butane 2-propynyl sulfonic acid, 2-propynyl 5- (ethanesulfonyloxy) pentanesulfonic acid, 2-propynyl 5- (ethanesulfonyloxy) hexanesulfonic acid, 2-propynyl trifluoromethanesulfonyloxymethanesulfonic acid, 2 -(Trifluoromethanesulfonyloxy) ethanesulfonic acid-2-propynyl, 3- (trifluoromethanesulfonyloxy) propanesulfonic acid-2-propynyl, 4- (trifluoromethanesulfonyloxy) butanesulfonic acid-2-propynyl, 5- ( Trifluoromethanesulfonyloxy) pentanesulfonic acid-2-propynyl, 6- (trifluoromethanesulfonyloxy) hexanesulfonic acid-2-propynyl, 2- (2- (methanesulfonyloxy) ethoxy) ethane 2-propynyl sulfonate, 2-propynyl dimethoxyphosphoryloxymethanesulfonate, 2-propynyl 2- (dimethoxyphosphoryloxy) ethanesulfonate, 2-propynyl propanesulfonate, 3- (dimethoxyphosphoryloxy) propane, 4- (Dimethoxyphosphoryloxy) butanesulfonic acid-2-propynyl, 5- (dimethoxyphosphoryloxy) pentanesulfonic acid-2-propynyl, 6- (dimethoxyphosphoryloxy) hexanesulfonic acid-2-propynyl, diethoxyphosphoryloxymethanesulfonic acid 2-propynyl, 2- (diethoxyphosphoryloxy) ethanesulfonic acid-2-propynyl, 3- (diethoxyphosphoryloxy) propanesulfonic acid-2-propynyl, 4- (diethoxyphosphoryloxy) 2-propynyl tansulfonic acid, 2-propynyl 5- (diethoxyphosphoryloxy) pentanesulfonic acid, 2-propynyl hexanesulfonic acid, 2- (2- (dimethoxyphosphoryloxy) Ethoxy) ethanesulfonic acid-2-propynyl, methoxy (methyl) phosphoryloxymethanesulfonic acid-2-propynyl, 2- (methoxy (methyl) phosphoryloxy) ethanesulfonic acid-2-propynyl, 3- (methoxy (methyl) phosphoryl Oxy) propanesulfonic acid-2-propynyl, 4- (methoxy (methyl) phosphoryloxy) butanesulfonic acid-2-propynyl, 5- (methoxy (methyl) phosphoryloxy) pentanesulfonic acid-2-propynyl, 6- (methoxy) (Methyl) phosphori Oxy) hexanesulfonic acid-2-propynyl, 2- (2- (methoxy (methyl) phosphoryloxy) ethoxy) ethanesulfonic acid-2-propynyl, ethoxy (methyl) phosphoryloxymethanesulfonic acid-2-propynyl, 2- ( Ethoxy (methyl) phosphoryloxy) ethanesulfonic acid-2-propynyl, 3- (ethoxy (methyl) phosphoryloxy) propanesulfonic acid-2-propynyl, ethyl (methoxy) phosphoryloxymethanesulfonic acid-2-propynyl, 2- ( Ethyl (methoxy) phosphoryloxy) ethanesulfonic acid-2-propynyl, 3- (ethyl (methoxy) phosphoryloxy) propanesulfonic acid-2-propynyl, dimethylphosphoryloxymethanesulfonic acid-2-propynyl, 2- (dimethylphosphoryloxy) Ii) Ethanesulfonic acid-2-propynyl, 3- (dimethylphosphoryloxy) propanesulfonic acid-2-propynyl, 4- (dimethylphosphoryloxy) butanesulfonic acid-2-propynyl, 5- (dimethylphosphoryloxy) pentanesulfonic acid Monosulfonic acid esters such as 2-propynyl, 6- (dimethylphosphoryloxy) hexanesulfonic acid-2-propynyl, 2- (2- (dimethylphosphoryloxy) ethoxy) ethanesulfonic acid-2-propynyl;

2-butyne-1,4-diol dimethanesulfonate, 2-butyne-1,4-diol dipropanesulfonate, 2-butyne-1,4-diol di-p-toluenesulfonate, 2-butyne-1,4- Diol Dicyclohexanesulfonate, 2-butyne
1,4-diol divinyl sulfonate, 2-butyne-1,4-diol diallyl sulfonate, 2-butyne-1,4-diol dipropynyl sulfonate, methane-1,1
-Di (2-propynyl) disulfonate, di (2-propynyl) ethane-1,2-disulfonate, di (2-propynyl) propane-1,3-disulfonate, di (butane-1,4-disulfonate) 2-propynyl), pentane-1,5-disulfonic acid di (2-propynyl), hexane-1,6-disulfonic acid di (2-propynyl), 2,2′-oxydiethanesulfonic acid di (2-propynyl) A disulfonic acid ester such as methyl-2-propynyl sulfate, ethyl-2-propynyl sulfate, propyl-2-propynyl sulfate, vinyl-2-propynyl sulfate, 2-propenyl 2-propynyl sulfate, di-2-propynyl sulfate, 2-propenyl 1,1-dimethyl-2-propynyl sulfate, 3-butenyl 2-propynyl sulfate and 3-butenyl 1,1-dimethyl-2-pro Sulfate esters such as pinyl sulfate; methyl (2-propynyl) (vinyl) phosphine oxide, divinyl (2-propynyl) phosphine oxide, di (2-propynyl) (vinyl) phosphine oxide, di (2-propenyl) 2 (-propynyl) Phosphine oxides such as) phosphine oxide, di (2-propynyl) (2-propenyl) phosphine oxide, di (3-butenyl) (2-propynyl) phosphine oxide, and di (2-propynyl) (3-butenyl) phosphine oxide ;

Methyl (2-propenyl) phosphinic acid-2-propynyl, 2-butenyl (methyl) phosphinic acid-2-propynyl, di (2-propenyl) phosphinic acid-2-propynyl, di (3-butenyl) phosphinic acid-2- Propinyl, methyl (2-propenyl) phosphinic acid-1,1-dimethyl-2-propynyl, 2-butenyl (methyl) phosphinic acid-1,1-dimethyl-2-propynyl, di (2-propenyl) phosphinic acid-1 , 1-dimethyl-2-propynyl, and di (3-butenyl) phosphinic acid-1,1-dimethyl-2-propynyl, methyl (2-propynyl) phosphinic acid-2-propenyl, methyl (2-propynyl) phosphinic acid -3-butenyl, di (2-propynyl) phosphinic acid-2-propenyl, di (2-propynyl) phosphine Phosphonic acid esters such as 3-butenyl acid, 2-propynyl (2-propenyl) phosphinic acid-2-propenyl, and 2-propynyl (2-propenyl) phosphinic acid-3-butenyl; methyl 2-propenylphosphonate 2-propynyl, 2-butenylphosphonic acid methyl-2-propynyl, 2-propenylphosphonic acid-2-propynyl (-2-propenyl), 3-butenylphosphonic acid-3-butenyl (-2-propynyl), 2-propenylphosphonic acid -1,1-dimethyl-2-propynyl (methyl), 2-butenylphosphonic acid-1,1-dimethyl-2-propynyl (methyl), 2-propenylphosphonic acid-1,1-dimethyl-2-propynyl (-2) -Propenyl), and 3-butenylphosphonic acid-3-butenyl (-1,1-dimethyl-) -Propynyl), methylphosphonic acid-2-propynyl (-2-propenyl), methylphosphonic acid-3-butenyl (-2-propynyl), methylphosphonic acid-1,1-dimethyl-2-propynyl (-2-propenyl), methylphosphone Acid-3-butenyl (-1,1-dimethyl-2-propynyl), ethylphosphonic acid-2-propynyl (-2-propenyl), ethylphosphonic acid-3-butenyl (-2-propynyl), ethylphosphonic acid- 1,1-dimethyl-2-propynyl (-
2-propenyl), and phosphonic acid esters such as ethylphosphonic acid-3-butenyl (-1,1-dimethyl-2-propynyl); methyl phosphate (-2-propenyl) (-2-propynyl), ethyl phosphate (-2-propenyl) (-2-propynyl), 2-butenyl (methyl) phosphate (-2-propynyl), 2-butenyl (ethyl) phosphate (-2-propynyl), phosphate-1, 1-dimethyl-2-propynyl (methyl) (-2-propenyl), 1,1-dimethyl-2-propynyl (ethyl) phosphate (-2-propenyl) phosphate, 2-butenyl phosphate (-1,1) -Phosphate esters such as dimethyl-2-propynyl) (methyl) and 2-butenyl (ethyl) phosphate (-1,1-dimethyl-2-propynyl).

Among these, a compound having an alkynyloxy group is preferable because it reacts with a compound having at least one halogen atom to form a negative electrode film more stably.
Furthermore, 2-propynylmethyl carbonate, di-2-propynyl carbonate, 2-butyne-1,4-diol dimethyl dicarbonate, 2-propynyl acetate, 2- (methanesulfonyloxy) propionate-2-propynyl, 2- Butyne-1,4-diol diacetate, methyl-2-propynyl oxalate, di-2-propynyl oxalate, -2-propynyl methanesulfonate, 2-propynyl vinylsulfonate, 2-propenylsulfonate-2- More preferred are compounds such as propynyl, 2-butyne-1,4-methanedisulfonate, 2-butyne-1,4-vinyldisulfonate, 2-butyne-1,4-allyldisulfonate, and methanesulfonic acid. -2-propynyl, 2-propynyl vinyl sulfonate, 2-propenylsulfur Compounds such as phosphate-2-propynyl is particularly preferred from the viewpoint of storage property improvement.

  The compound represented by the formula (1) may be included singly or in combination of two or more in the nonaqueous electrolytic solution of the present invention. The content of the compound represented by the formula (1) in the nonaqueous electrolytic solution (in the case of two or more types) is 0.01% by mass or more, preferably 0.05% by mass or more, more preferably 0. .1% by mass or more, and usually 5% by mass or less, preferably 4% by mass or less, more preferably 3% by mass or less. If this concentration is too low, the chemical and physical stability of the film may be insufficient. If the concentration is too high, the insulating properties of the film may increase, and the discharge capacity may decrease due to increased resistance. When the content of the compound represented by the formula (1) is within the above range, a synergistic effect with the compound having at least one halogen atom is easily obtained, and the reductive decomposition reaction of the nonaqueous solvent that occurs at the time of charging is further suppressed. It is possible to improve battery life such as high-temperature storage characteristics and cycle characteristics, improve charge / discharge efficiency of the battery, and improve low-temperature characteristics.

1-2. Compound having chlorine atom The compound having a chlorine atom used in the present invention is not particularly limited as long as it is a compound having a chlorine atom. For example, alkyl chloride, alkenyl chloride, alkynyl chloride, aryl chloride, carboxyl Acid chloride, alkyl carbonate chloride, alkenyl carbonate chloride, alkynyl carbonate chloride, aryl carbonate chloride, alkyl sulfate chloride, alkenyl sulfate chloride, alkynyl sulfate chloride, aryl sulfate chloride, alkyl sulfonate chloride, alkenyl sulfonate chloride, alkynyl sulfonate chloride, Aryl sulfonic acid chloride, alkyl sulfite chloride, alkenyl sulfite chloride, alkynyl sulfite chloride, aryl sulfite chloride , Alkylsulfinic acid chloride, alkenylsulfinic acid chloride, alkynylsulfinic acid chloride, arylsulfinic acid chloride, phosphoryl chloride and the like. The reason for this is that the chlorine atom has an appropriate desorption ability and can maximize the effect of improving the battery characteristics by reacting with the compound represented by the formula (1) to form a composite film. is there.
Among them, the compound represented by the following formula (2) is preferable.

In Formula (2), R ³ and R ⁴ are each independently a hydrogen atom, a halogen atom, or an organic group that may have a substituent, and may be the same or different.
Here, the organic group represents a functional group composed of atoms selected from the group consisting of carbon atoms, hydrogen atoms, nitrogen atoms, oxygen atoms and halogen atoms. Specific examples include alkyl groups, alkenyl groups, alkynyl groups, aryl groups, alkoxy groups, cyano groups, isocyanato groups, ether groups, carbonate groups, carbonyl groups, sulfonyl groups, phosphoryl groups, and the like.

Specific examples of the substituent include alkyl groups, alkenyl groups, alkynyl groups, aryl groups, alkoxy groups, cyano groups, isocyanato groups, ether groups, carbonate groups, carbonyl groups, carboxyl groups which may be substituted with halogen atoms. Group, sulfonyl group, phosphoryl group and the like.
In the formula (2), R ⁴ is preferably a methylene group which may have a substituent. By having a methylene group, the radical at the methylene site generated after the elimination of the chlorine atom is subjected to a resonance stabilizing effect by the adjacent triple bond, so that the lifetime of the radical is improved. Therefore, it reacts more with the compound represented by the formula (1), and it becomes easier to efficiently form a composite film on the electrode.

  The molecular weight of the compound represented by the formula (2) is not particularly limited, and is arbitrary as long as the effects of the present invention are not significantly impaired. The molecular weight is preferably 55 or more, more preferably 60 or more, still more preferably 70 or more, and 350 or less, preferably 200 or less, and more preferably 150 or less. If it is this range, it will be easy to ensure the solubility of the compound shown by (2) with respect to a non-aqueous electrolyte solution, and the effect of this invention will be easy to be expressed.

Specific examples of the compound represented by the formula (2) include the following compounds.
3-chloro-1-propyne, 3-chloro-1-butyne, 3-chloro-3-methyl-1-butyne, 1-chloro-2-butyne, 1-chloro-1-methyl-2-butyne, 1- Chloro-1,1-dimethyl-2-butyne, 1,4-dichloro-2-butyne, 1,4-dichloro-1,4-dimethyl-2-butyne, 1,4-dichloro-1,1,4 4-tetramethyl-2-butyne, 4-chloro-2-butyn-1-ol, 1,6-dichloro-2,4-hexadiyne, 1,6-dichloro-1,6-dimethyl-2,4-hexadiyne 1,6-dichloro-1,1,6,6-tetramethyl-2,4-hexadiyne, 1-chloro-6-hydroxy-2,4-hexadiyne.

Among them, 3-chloro-1-propyne, 3-chloro-1-butyne, 3-chloro-3-methyl-1-butyne,
A compound having a proton at the triple bond end such as the like is more preferable because it can form a denser film by interacting with the compound represented by the formula (1).
The compound having at least one halogen atom may be contained singly or in combination of two or more in the nonaqueous electrolytic solution of the present invention. The content of the compound having at least one halogen atom in the non-aqueous electrolyte (the total amount in the case of two or more) is 0.2 mass ppm or more, preferably 0.5 mass ppm or more, more preferably 0.7 mass ppm or more, usually less than 500 mass ppm, preferably 250 mass ppm or less, more preferably 100 mass ppm or less, further preferably 50 mass ppm or less, still more preferably 10 pp mass ppm or less, particularly preferably 5 mass ppm or less, most preferably 2 mass ppm
The range is as follows.

  The content of the compound having at least one halogen atom in the compound represented by the formula (1) (the total amount in the case of two or more types) is 20 mass ppm or more, preferably 50 mass ppm or more. Preferably it is 100 mass ppm or more, and is 5 mass% or less normally, Preferably it is 1 mass% or less, More preferably, it is 0.5 mass% or less, More preferably, it is the range of 0.1 mass% or less. If this concentration is too low, the reaction with the compound represented by formula (1) may be small and the effect may be insufficient. If the concentration is too high, the electrode interface resistance increases due to an increase in the generated lithium chloride. However, the discharge capacity may decrease due to the increase in resistance.

When the compound having at least one halogen atom is in the above range, a synergistic effect with the compound represented by the formula (1) can be easily obtained, and the reductive decomposition reaction of the nonaqueous solvent that occurs during charging can be further suppressed. It is possible to improve battery life such as high-temperature storage characteristics and cycle characteristics, improve battery charge / discharge efficiency, and improve low-temperature characteristics.
1-3. A cyclic carbonate having a fluorine atom, a cyclic carbonate having a carbon-carbon unsaturated bond, a monofluorophosphate, a difluorophosphate, an isocyanate compound, a cyclic sulfonic acid ester, and a nitrile compound. , A cyclic carbonate having a fluorine atom, a cyclic carbonate having a carbon-carbon unsaturated bond, a monofluorophosphate, a difluorophosphate, an isocyanate compound, a cyclic sulfonic acid ester, and a nitrile compound. The thing containing is preferable. It is because the side reaction caused by each additive can be efficiently suppressed by using these together.

Furthermore, the cyclic carbonate having a fluorine atom and the cyclic carbonate having a carbon-carbon unsaturated bond form a stable protective film on the surface of the compound represented by the formula (1) and the negative electrode, This is more preferable because the reaction can be suppressed and high-temperature storage characteristics and cycle characteristics can be improved.
1-3-1. The cyclic carbonate having a fluorine atom The cyclic carbonate having a fluorine atom (hereinafter sometimes referred to as “fluorinated cyclic carbonate”) is not particularly limited as long as it is a cyclic carbonate having a fluorine atom.

  Examples of the fluorinated cyclic carbonate include a fluorinated product of a cyclic carbonate having an alkylene group having 2 to 6 carbon atoms, and derivatives thereof, and examples thereof include a fluorinated product of ethylene carbonate and derivatives thereof. Examples of the derivatives of fluorinated ethylene carbonate include fluorinated ethylene carbonate substituted with an alkyl group (for example, an alkyl group having 1 to 4 carbon atoms). Of these, ethylene carbonate having 1 to 8 fluorine atoms and derivatives thereof are preferred.

In particular,
Monofluoroethylene carbonate, 4,4-difluoroethylene carbonate, 4,5-difluoroethylene carbonate, 4-fluoro-4-methylethylene carbonate, 4,5-difluoro-4-methylethylene carbonate, 4-fluoro-5-methyl Ethylene carbonate, 4,4-difluoro-5-methylethylene carbonate, 4- (fluoromethyl) -ethylene carbonate, 4- (difluoromethyl) -ethylene carbonate, 4- (trifluoromethyl) -ethylene carbonate, 4- (fluoro Methyl) -4-fluoroethylene carbonate, 4- (fluoromethyl) -5-fluoroethylene carbonate, 4-fluoro-4,5-dimethylethylene carbonate, 4,5-difluoro-4,5-dimethylethylene Boneto, 4,4-difluoro-5,5-dimethylethylene carbonate.

Among them, at least one selected from the group consisting of monofluoroethylene carbonate, 4,4-difluoroethylene carbonate and 4,5-difluoroethylene carbonate gives high ionic conductivity and suitably forms an interface protective film. And more preferable.
A fluorinated cyclic carbonate may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.

  The content of the fluorinated cyclic carbonate is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, still more preferably 1% by mass or more, and preferably 1% by mass or more with respect to the non-aqueous electrolyte solution. It is 10 mass% or less, More preferably, it is 5 mass% or less, More preferably, it is 3 mass% or less. The blending amount when fluorinated cyclic carbonate is used as the non-aqueous solvent is preferably 100% by volume in the non-aqueous solvent, preferably 1% by volume or more, more preferably 5% by volume or more, and still more preferably 10% by volume or more. Moreover, it is preferably 50% by volume or less, more preferably 35% by volume or less, and further preferably 25% by volume or less.

If it is within the above range, the non-aqueous electrolyte secondary battery is likely to exhibit a sufficient cycle characteristic improvement effect, and avoids a decrease in discharge capacity maintenance rate due to a decrease in high-temperature storage characteristics or an increase in gas generation amount. It's easy to do.
In the nonaqueous electrolytic solution of the present invention, the compound represented by the above formula (1) and the cyclic carbonate having a fluorine atom form a composite film on the negative electrode. From the viewpoint of satisfactorily forming such a film, the blending mass ratio of the compound represented by the above formula (1) and the fluorinated cyclic carbonate is preferably 0.4: 100 to 100: 100, and 1: 100 More preferably, it is -50: 100, and it is further more preferable that it is 1.4: 100-35: 100. When it mix | blends in this range, the side reaction in the positive / negative electrode of each additive can be suppressed efficiently, and a battery characteristic improves.

1-3-2. Cyclic carbonate having carbon-carbon unsaturated bond Cyclic carbonate having carbon-carbon unsaturated bond (hereinafter sometimes referred to as “unsaturated cyclic carbonate”) includes a carbon-carbon double bond or a carbon-carbon triple bond. Any cyclic carbonate having a bond is not particularly limited, and any unsaturated carbonate can be used. The cyclic carbonate having an aromatic ring is also included in the unsaturated cyclic carbonate.

As unsaturated cyclic carbonate,
Examples include vinylene carbonates, ethylene carbonates substituted with an aromatic ring or a substituent having a carbon-carbon double bond or carbon-carbon triple bond, phenyl carbonates, vinyl carbonates, allyl carbonates, catechol carbonates, and the like. .

As vinylene carbonates,
Vinylene carbonate, methyl vinylene carbonate, 4,5-dimethyl vinylene carbonate, phenyl vinylene carbonate, 4,5-diphenyl vinylene carbonate, vinyl vinylene carbonate, 4,5-divinyl vinylene carbonate, allyl vinylene carbonate, 4,5-diallyl vinylene carbonate 4-fluoro vinylene carbonate, 4-fluoro-5-methyl vinylene carbonate, 4-fluoro-5-phenyl vinylene carbonate, 4-fluoro-5-vinyl vinylene carbonate, 4-allyl-5-fluoro vinylene carbonate and the like. .

Specific examples of ethylene carbonates substituted with a substituent having an aromatic ring or a carbon-carbon double bond or a carbon-carbon triple bond include:
Vinylethylene carbonate, 4,5-divinylethylene carbonate, 4-methyl-5-vinylethylene carbonate, 4-allyl-5-vinylethylene carbonate, ethynylethylene carbonate, 4,5-diethynylethylene carbonate, 4-methyl-5 -Ethynylethylene carbonate, 4-vinyl-5-ethynylethylene carbonate, 4-allyl-5-ethynylethylene carbonate, phenylethylene carbonate, 4,5-diphenylethylene carbonate, 4-phenyl-5-vinylethylene carbonate, 4-allyl Examples include -5-phenylethylene carbonate, allylethylene carbonate, 4,5-diallylethylene carbonate, 4-methyl-5-allylethylene carbonate, and the like.

Among these, as an unsaturated cyclic carbonate particularly preferable for use in combination with the compound represented by the formula (1),
Vinylene carbonate, methyl vinylene carbonate, 4,5-dimethyl vinylene carbonate, vinyl vinylene carbonate, 4,5-vinyl vinylene carbonate, allyl vinylene carbonate, 4,5-diallyl vinylene carbonate, vinyl ethylene carbonate, 4,5-divinyl ethylene carbonate 4-methyl-5-vinylethylene carbonate, allylethylene carbonate, 4,5-diallylethylene carbonate, 4-methyl-5-allylethylene carbonate, 4-allyl-5-vinylethylene carbonate, ethynylethylene carbonate, 4,5 -Diethynyl ethylene carbonate, 4-methyl-5-ethynyl ethylene carbonate, 4-vinyl-5-ethynyl ethylene carbonate. Vinylene carbonate, vinyl ethylene carbonate, and ethynyl ethylene carbonate are particularly preferable because they form a more stable interface protective film.

  The molecular weight of the unsaturated cyclic carbonate is not particularly limited and is arbitrary as long as the effects of the present invention are not significantly impaired. The molecular weight is preferably 80 or more and 250 or less. If it is this range, it will be easy to ensure the solubility of the unsaturated cyclic carbonate with respect to a non-aqueous electrolyte solution, and the effect of this invention will fully be expressed easily. The molecular weight of the unsaturated cyclic carbonate is more preferably 85 or more, and more preferably 150 or less.

The production method of the unsaturated cyclic carbonate is not particularly limited, and can be produced by arbitrarily selecting a known method.
An unsaturated cyclic carbonate may be used individually by 1 type, or may use 2 or more types together by arbitrary combinations and a ratio. Moreover, the compounding quantity of unsaturated cyclic carbonate is not restrict | limited in particular, As long as the effect of this invention is not impaired remarkably, it is arbitrary. The blending amount of the unsaturated cyclic carbonate is preferably 0.001% by mass or more, more preferably 0.01% by mass or more, and further preferably 0.1% by mass or more, in 100% by mass of the non-aqueous electrolyte solution. Moreover, Preferably it is 5 mass% or less, More preferably, it is 4 mass% or less, More preferably, it is 3 mass% or less. Within this range, the non-aqueous electrolyte battery tends to exhibit a sufficient cycle characteristics improvement effect, and the high temperature storage characteristics deteriorate, the amount of gas generated increases, and the discharge capacity maintenance ratio decreases. Easy to avoid.

1-3-3. Monofluorophosphate and difluorophosphate There are no particular limitations on the countercation of monofluorophosphate and difluorophosphate, but lithium, sodium, potassium, magnesium, calcium, and NR ¹¹ R ¹² R ¹³ R ¹⁴ (wherein, R ^{11 to} R ¹⁴ each independently represents a hydrogen atom or an organic group having 1 to 12 carbon atoms), and the like.

Although it does not specifically limit as a C1-C12 organic group represented by R < ¹¹ > -R < ¹⁴ > of the said ammonium, For example, it is substituted by the alkyl group, the halogen atom, or the alkyl group which may be substituted by the halogen atom. Examples thereof include an cycloalkyl group which may be substituted, an aryl group which may be substituted with a halogen atom or an alkyl group, and a nitrogen atom-containing heterocyclic group which may have a substituent. Among these, as R ^{11 to} R ¹⁴ , a hydrogen atom, an alkyl group, a cycloalkyl group, or a nitrogen atom-containing heterocyclic group is preferable.

Specific examples of monofluorophosphate and difluorophosphate include
Lithium monofluorophosphate, sodium monofluorophosphate, potassium monofluorophosphate, lithium difluorophosphate, sodium difluorophosphate, potassium difluorophosphate and the like, lithium monofluorophosphate and lithium difluorophosphate are preferred, More preferred is lithium difluorophosphate.

Monofluorophosphate and difluorophosphate may be used singly or in combination of two or more in any combination and ratio. Moreover, the compounding quantity of a monofluoro phosphate and a difluoro phosphate is not restrict | limited in particular, As long as the effect of this invention is not impaired remarkably, it is arbitrary.
The blending amount of monofluorophosphate and difluorophosphate is preferably 0.001% by mass or more, more preferably 0.01% by mass or more, and still more preferably 0.1% in 100% by mass of the non-aqueous electrolyte. It is at least 5% by mass, preferably at most 5% by mass, more preferably at most 4% by mass, even more preferably at most 3% by mass.

Within this range, the non-aqueous electrolyte battery tends to exhibit a sufficient cycle characteristics improvement effect, and the high temperature storage characteristics deteriorate, the amount of gas generated increases, and the discharge capacity maintenance ratio decreases. Easy to avoid.
1-3-4. Isocyanate compound The type of the isocyanate compound is not particularly limited as long as it is a compound having an isocyanate group in the molecule.

Specific examples of the isocyanate compound include, for example,
Monoisocyanates such as methyl isocyanate, ethyl isocyanate, propyl isocyanate, isopropyl isocyanate, butyl isocyanate, tertiary butyl isocyanate, pentyl isocyanate hexyl isocyanate, cyclohexyl isocyanate, vinyl isocyanate, allyl isocyanate, ethynyl isocyanate, propynyl isocyanate, phenyl isocyanate, fluorophenyl isocyanate Compound;

Monomethylene diisocyanate, dimethylene diisocyanate, trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, heptamethylene diisocyanate, octamethylene diisocyanate, nonamethylene diisocyanate, decamethylene diisocyanate, dodecamethylene diisocyanate, 1,3-diisocyanate Natopropane, 1,4-diisocyanato-2-butene, 1,4-diisocyanato-2-fluorobutane, 1,4-diisocyanato-2,3-difluorobutane, 1,5-diisocyanato-2-pentene, 1,5 -Diisocyanato-2-methylpentane, 1,6-diisocyanato-2-hexene, 1,6-diisocyanato-3-hexene, 1,6 Diisocyanato-3-fluorohexane, 1,6-diisocyanato-3,4-difluorohexane, toluene diisocyanate, xylene diisocyanate, tolylene diisocyanate, 1,2-bis (isocyanatomethyl) cyclohexane, 1,3-bis (isocyanato) Methyl) cyclohexane, 1,4-bis (isocyanatomethyl) cyclohexane, 1,2-diisocyanatocyclohexane, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, dicyclohexylmethane-1,1 ′ -Diisocyanate, dicyclohexylmethane-2,2'-diisocyanate, dicyclohexylmethane-3,3'-diisocyanate, dicyclohexylmethane-
4,4′-diisocyanate, bicyclo [2.2.1] heptane-2,5-diylbis (
Methyl isocyanate), bicyclo [2.2.1] heptane-2,6-diylbis (methyl isocyanate), isophorone diisocyanate, carbonyl diisocyanate, 1,4-diisocyanatobutane-1,4-dione, 1,5- Diisocyanate compounds such as diisocyanatopentane-1,5-dione, 2,2,4-trimethylhexamethylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate;
Etc.

Among these, monomethylene diisocyanate, dimethylene diisocyanate, trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, heptamethylene diisocyanate, octamethylene diisocyanate, nonamethylene diisocyanate, decamethylene diisocyanate, dodecamethylene diisocyanate, 1, 3-bis (isocyanatomethyl) cyclohexane, dicyclohexylmethane-4,4′-diisocyanate, bicyclo [2.2.1]
Heptane-2,5-diylbis (methylisocyanate), bicyclo [2.2.1] heptane-2,6-diylbis (methylisocyanate), isophorone diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 2 Diisocyanate compounds such as 4,4-trimethylhexamethylene diisocyanate are preferred from the standpoint of improving storage characteristics.

  The isocyanate compound used in the present invention may be a trimer compound derived from a compound having at least two isocyanate groups in the molecule, or an aliphatic polyisocyanate obtained by adding a polyhydric alcohol thereto. Examples thereof include biuret, isocyanurate, adduct, and bifunctional type modified polyisocyanate represented by the basic structures of the following general formulas (3-1) to (3-4) (the following general formula (3-1) ) To (3-4), R and R ′ are each independently an arbitrary hydrocarbon group).

  The compound having at least two isocyanate groups in the molecule used in the present invention also includes so-called blocked isocyanate which is blocked with a blocking agent to enhance storage stability. Examples of the blocking agent include alcohols, phenols, organic amines, oximes, and lactams. Specific examples include n-butanol, phenol, tributylamine, diethylethanolamine, methyl ethyl ketoxime, and ε-caprolactam. Etc.

In order to promote a reaction based on a compound having at least two isocyanate groups in the molecule and obtain a higher effect, a metal catalyst such as dibutyltin dilaurate or the like, 1,8-diazabicyclo [5.4.0] undecene- It is also preferable to use an amine catalyst such as 7 in combination.
Furthermore, the compound which has an isocyanate group may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.

  There is no restriction | limiting in the compounding quantity of the compound which has an isocyanate group with respect to the whole nonaqueous electrolyte solution of this invention, Although it is arbitrary unless the effect of this invention is impaired remarkably, Usually, it is 0.8 with respect to the nonaqueous electrolyte solution of this invention. 001% by mass or more, preferably 0.1% by mass or more, more preferably 0.3% by mass or more, and usually 10% by mass or less, preferably 5% by mass or less, more preferably 3% by mass or less. Let

When the above range is satisfied, effects such as output characteristics, load characteristics, low temperature characteristics, cycle characteristics, and high temperature storage characteristics are further improved.
1-3-5. Cyclic sulfonic acid ester The cyclic sulfonic acid ester is not particularly limited as long as it is a sulfonic acid ester having a cyclic structure.

Specific examples of the cyclic sulfonate ester include, for example,
1,3-propane sultone, 1-fluoro-1,3-propane sultone, 2-fluoro-1,3-propane sultone, 3-fluoro-1,3-propane sultone, 1-methyl-1,3-propane sultone 2-methyl-1,3-propane sultone, 3-methyl-1,3-propane sultone 1-propene-1,3-sultone, 2-propene-1,3-sultone, 1-fluoro-1-propene- 1,3-sultone, 2-fluoro-1-propene-1,3-sultone, 3-fluoro-1-propene-1,3-sultone, 1-fluoro-2-propene-1,3-sultone, 2- Fluoro-2-propene-1,3-sultone, 3-fluoro-2-propene-1,3-sultone, 1-methyl-1-propene-1,3-sultone, 2-methyl-1-propene 1,3-sultone, 3-methyl-1-propene-1,3-sultone, 1-methyl-2-propene-1,3-sultone, 2-methyl-2-propene-1,3-sultone, 3- Methyl-2-propene-1,3-sultone, 1,4-butane sultone, 1-fluoro-1,4-butane sultone, 2-fluoro-1,4-butane sultone, 3-fluoro-1,4-butane sultone, 4- Fluoro-1,4-butane sultone, 1-methyl-1,4-butane sultone, 2-methyl-1,4-butane sultone, 3-methyl-1,4-butane sultone, 4-methyl-1,4-butane sultone, 1- Butene-1,4-sultone, 2-butene-1,4-sultone, 3-butene-1,4-sultone, 1-fluoro-1-butene-1,4-sultone, 2-fluoro-1 Butene-1,4-sultone, 3-fluoro-1-butene-1,4-sultone, 4-fluoro-1-butene-1,4-sultone, 1-fluoro-2-butene-1,4-sultone, 2-fluoro-2-butene-1,4-sultone, 3-fluoro-2-butene-1,4-sultone, 4-fluoro-2-butene-1,4-sultone, 1-fluoro-3-butene- 1,4-sultone, 2-fluoro-3-butene-1,4-sultone, 3-fluoro-3-butene-1,4-sultone, 4-fluoro-3-butene-1,4-sultone, 1- Methyl-1-butene-1,4-sultone, 2-methyl-1-butene-1,4-sultone, 3-methyl-1-butene-1,4-sultone, 4-methyl-1-butene-1, 4-sultone, 1-methyl-2-butene-1,4- Sultone, 2-methyl-2-butene-1,4-sultone, 3-methyl-2-butene-1,4-sultone, 4-methyl-2-butene-1,4-sultone, 1-methyl-3- Butene-1,4-sultone, 2-methyl-3-butene-1,4-sultone, 3-methyl-3-butene-1,4-sultone, 4-methyl-3-butene-1,4-sultone, 1,5-pentane sultone, 1-fluoro-1,5-pentane sultone, 2-fluoro-1,5-pentane sultone, 3-fluoro-1,5-pentane sultone, 4-fluoro-1,5-pentanthruton 5-fluoro-1,5-pentane sultone, 1-methyl-1,5-pentane sultone, 2-methyl-1,5-pentane sultone, 3-methyl-1,5-pentane sultone, 4-methyl-1 , 5-pe Tan sultone, 5-methyl-1,5-pentanthrutone, 1-pentene-1,5-sultone, 2-pentene-1,5-sultone, 3-pentene-1,5-sultone, 4-pentene-1,5 -Sultone, 1-fluoro-1-pentene-1,5-sultone, 2-fluoro-1-pentene-1,5-sultone, 3-fluoro-1-
Pentene-1,5-sultone, 4-fluoro-1-pentene-1,5-sultone, 5-fluoro-1-pentene-1,5-sultone, 1-fluoro-2-pentene-1,5-sultone, 2-fluoro-2-pentene-1,5-sultone, 3-fluoro-2-pentene-1,5-sultone, 4-fluoro-2-pentene-1,5-sultone, 5-fluoro-2-pentene- 1,5-sultone, 1-fluoro-3-pentene-1,5-sultone, 2-fluoro-3-pentene-1,5-sultone, 3-fluoro-3-pentene-1,5-sultone, 4- Fluoro-3-pentene-1,5-sultone, 5-fluoro-3-pentene-1,5-sultone, 1-fluoro-4-pentene-1,5-sultone, 2-fluoro-4-pentene-1, 5-sul 3-fluoro-4-pentene-1,5-sultone, 4-fluoro-4-pentene-1,5-sultone, 5-fluoro-4-pentene-1,5-sultone, 1-methyl-1- Pentene-1,5-sultone, 2-methyl-1-pentene-1,5-sultone, 3-methyl-1-pentene-1,5-sultone, 4-methyl-1-pentene-1,5-sultone, 5-methyl-1-pentene-1,5-sultone, 1-methyl-2-pentene-1,5-sultone, 2-methyl-2-pentene-1,5-sultone, 3-methyl-2-pentene- 1,5-sultone, 4-methyl-2-pentene-1,5-sultone, 5-methyl-2-pentene-1,5-sultone, 1-methyl-3-pentene-1,5-sultone, 2- Methyl-3-pentene-1,5-sul 3-methyl-3-pentene-1,5-sultone, 4-methyl-3-pentene-1,5-sultone, 5-methyl-3-pentene-1,5-sultone, 1-methyl-4- Pentene-1,5-sultone, 2-methyl-4-pentene-1,5-sultone, 3-methyl-4-pentene-1,5-sultone, 4-methyl-4-pentene-1,5-sultone, Sultone compounds such as 5-methyl-4-pentene-1,5-sultone;

Sulfate compounds such as methylene sulfate, ethylene sulfate, propylene sulfate;
Disulfonate compounds such as methylene methane disulfonate and ethylene methane disulfonate;
1,2,3-oxathiazolidine-2,2-dioxide, 3-methyl-1,2,3-oxathiazolidine-2,2-dioxide, 3H-1,2,3-oxathiazol-2,2-dioxide 5H-1,2,3-oxathiazol-2,2-dioxide, 1,2,4-oxathiazolidine-2,2-dioxide, 4-methyl-1,2,4-oxathiazolidine-2,2- Dioxide, 3H-1,2,4-oxathiazole-2,2-dioxide, 5H-1,2,4-oxathiazole-2,2-dioxide, 1,2,5-oxathiazolidine-2,2-dioxide 5-methyl-1,2,5-oxathiazolidine-2,2-dioxide, 3H-1,2,5-oxathiazole-2,2-dioxide, 5H-1,2,5-oxathiazole-2 2-dioxide, 1,2,3-oxathiazinane-2,2-dioxide, 3-methyl-1,2,3-oxathiazinane-2,2-dioxide, 5,6-dihydro-1,2,3-oxathiazine- 2,2-dioxide, 1,2,4-oxathiazinane-2,2-dioxide, 4-methyl-1,2,4-oxathiazinane-2,2-dioxide, 5,6-dihydro-1,2,4- Oxathiazine-2,2-dioxide, 3,6-dihydro-1,2,4-oxathiazine-2,2-dioxide, 3,4-dihydro-1,2,4-oxathiazine-2,2-dioxide, 1, 2,5-oxathiazinane-2,2-dioxide, 5-methyl-1,2,5-oxathiazinane-2,2-dioxide, 5,6-dihydro-1,2,5-oxathiazine-2 2-dioxide, 3,6-dihydro-1,2,5-oxathiazine-2,2-dioxide, 3,4-dihydro-1,2,5-oxathiazine-2,2-dioxide, 1,2,6- Oxathiazinane-2,2-dioxide, 6-methyl-1,2,6-oxathiazinane-2,2-dioxide, 5,6-dihydro-1,2,6-oxathiazine-2,2-dioxide, 3,4- Nitrogen-containing compounds such as dihydro-1,2,6-oxathiazine-2,2-dioxide, 5,6-dihydro-1,2,6-oxathiazine-2,2-dioxide;
Etc.

Of these,
1,3-propane sultone, 1-fluoro-1,3-propane sultone, 2-fluoro-1,3-propane sultone, 3-fluoro-1,3-propane sultone, 1-propene-1,3-sultone, 1-fluoro-1-propene-1,3-sultone, 2-fluoro-1-propene-1,3-sultone, 3-fluoro-1-propene-1,3-sultone, 1,4-butane sultone, methylenemethane Disulfonate, ethylene methane disulfonate is preferred from the viewpoint of improving storage characteristics,
1,3-propane sultone, 1-fluoro-1,3-propane sultone, 2-fluoro-1,3-propane sultone, 3-fluoro-1,3-propane sultone, 1-propene-1,3-sultone More preferred.

  A cyclic sulfonic acid ester may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio. There is no limitation on the amount of the cyclic sulfonate ester added to the entire non-aqueous electrolyte of the present invention, and it is optional as long as the effects of the present invention are not significantly impaired. It is contained at a concentration of not less than mass%, preferably not less than 0.1 mass%, more preferably not less than 0.3 mass%, and usually not more than 10 mass%, preferably not more than 5 mass%, more preferably not more than 3 mass%. . When the above range is satisfied, effects such as output characteristics, load characteristics, low temperature characteristics, cycle characteristics, and high temperature storage characteristics are further improved.

<Nitrile compound>
The type of nitrile compound is not particularly limited as long as it is a compound having a nitrile group in the molecule.
Specific examples of nitrile compounds include, for example,
Acetonitrile, propionitrile, butyronitrile, isobutyronitrile, valeronitrile, isovaleronitrile, lauronitrile, 2-methylbutyronitrile, trimethylacetonitrile, hexanenitrile, cyclopentanecarbonitrile, cyclohexanecarbonitrile, acrylonitrile, methacrylonitrile , Crotononitrile, 3-methylcrotononitrile, 2-methyl-2-butenenitryl, 2-pentenenitrile, 2-methyl-2-pentenenitrile, 3-methyl-2-pentenenitrile, 2-hexenenitrile, Fluoroacetonitrile, difluoroacetonitrile, trifluoroacetonitrile, 2-fluoropropionitrile, 3-fluoropropionitrile, 2,2-difluoropropionitrile, 2,3-diph Oropropionitrile, 3,3-difluoropropionitrile, 2,2,3-trifluoropropionitrile, 3,3,3-trifluoropropionitrile, 3,3′-oxydipropionitrile, 3,3 ′ A compound having one nitrile group such as thiodipropionitrile, 1,2,3-propanetricarbonitrile, 1,3,5-pentanetricarbonitrile, pentafluoropropionitrile;

Malononitrile, succinonitrile, glutaronitrile, adiponitrile, pimonitrile, suberonitrile, azeronitrile, sebacononitrile, undecandinitrile, dodecandinitrile, methylmalononitrile, ethylmalononitrile, isopropylmalononitrile, tert-butylmalononitrile, methylsuccinonitrile 2,2-dimethylsuccinonitrile, 2,3-dimethylsuccinonitrile, 2,3,3-trimethylsuccinonitrile, 2,2,3,3-tetramethylsuccinonitrile, 2,3-diethyl- 2,3-dimethylsuccinonitrile, 2,2-diethyl-3,3-dimethylsuccinonitrile, bicyclohexyl-1,1-dicarbonitrile, bicyclohexyl-2,2-dicarbonitrile, bicyclohexyl- , 3-dicarbonitrile, 2,5-dimethyl-2,5-hexanedicarbonitrile, 2,3-diisobutyl-2,3-dimethylsuccinonitrile, 2,2-diisobutyl-3,3-dimethylsuccino Nitrile, 2-methylglutaronitrile, 2,3-dimethylglutaronitrile, 2,4-dimethylglutaronitrile, 2,2,3,3-tetramethylglutaronitrile, 2,2,4,4-tetra Methylglutaronitrile, 2,2,3,4-tetramethylglutaronitrile, 2,3,3,4-tetramethylglutaronitrile, maleonitrile, fumaronitrile, 1,4-dicyanopentane, 2,6-dicyanoheptane 2,7-dicyanooctane, 2,8-dicyanononane, 1,6-dicyanodecane, 1,2-didiananobenzene, 1,3-disi Nobenzene, 1,4-dicyanobenzene, 3,3 ′-(ethylenedioxy) dipropionitrile, 3,3 ′-(ethylenedithio) dipropionitrile, 3,9-bis (2-cyanoethyl) -2,4 , 8,10-tetraoxaspiro [5,5] undecane and other compounds having two nitrile groups;
Compounds having three cyano groups such as cyclohexanetricarbonitrile, triscyanoethylamine, triscyanoethoxypropane, tricyanoethylene, pentanetricarbonitrile, propanetricarbonitrile, heptanetricarbonitrile;
Etc.

  Among these, lauronitrile, crotononitrile, succinonitrile, glutaronitrile, adiponitrile, pimeonitrile, suberonitrile, azeronitrile, sebacononitrile, undecandinitrile, dodecandinitrile, fumaronitrile, 3,9-bis (2-cyanoethyl)- 2,4,8,10-Tetraoxaspiro [5,5] undecane is preferred from the viewpoint of improving storage characteristics. Also, succinonitrile, glutaronitrile, adiponitrile, pimeonitrile, suberonitrile, azeronitrile, sebacononitrile, undecandinitrile, dodecandinitrile, fumaronitrile, 3,9-bis (2-cyanoethyl) -2,4,8,10-tetra Particularly preferred are dinitrile compounds such as oxaspiro [5,5] undecane.

  A nitrile compound may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio. There is no limitation on the amount of the nitrile compound added to the whole non-aqueous electrolyte solution of the present invention, and it is optional as long as the effect of the present invention is not significantly impaired, but usually 0.001% by mass with respect to the non-aqueous electrolyte solution of the present invention. Above, preferably 0.1% by mass or more, more preferably 0.3% by mass or more, and usually 10% by mass or less, preferably 5% by mass or less, more preferably 3% by mass or less. When the above range is satisfied, effects such as output characteristics, load characteristics, low temperature characteristics, cycle characteristics, and high temperature storage characteristics are further improved.

1-3. Electrolyte <Lithium salt>
As the electrolyte, a lithium salt is usually used. The lithium salt is not particularly limited as long as it is known to be used for this purpose, and any lithium salt can be used. Specific examples include the following.

For _{example, LiPF 6, LiBF 4, LiClO} 4, LiAlF 4, LiSbF 6, inorganic lithium salts LiTaF 6, LiWF ₇ and the like;
Lithium tungstates such as LiWOF ₅ ;
HCO ₂ Li, CH ₃ CO ₂ Li, CH ₂ FCO ₂ Li, CHF ₂ CO ₂ Li, CF ₃ CO ₂ Li, CF ₃ CH ₂ CO ₂ Li, CF ₃ CF ₂ CO ₂ Li, CF ₃ CF ₂ CF ₂ Carboxylic acid lithium salts such as CO ₂ Li, CF ₃ CF ₂ CF ₂ CF ₂ CO ₂ Li;
FSO ₃ Li, CH ₃ SO ₃ Li, CH ₂ FSO ₃ Li, CHF ₂ SO ₃ Li, CF ₃ SO ₃ Li, CF ₃ CF ₂ SO ₃ Li, CF ₃ CF ₂ CF ₂ SO ₃ Li, CF ₃ CF ₂ Sulfonic acid lithium salts such as CF ₂ CF ₂ SO ₃ Li;
LiN (FCO) ₂ , LiN (FCO) (FSO ₂ ), LiN (FSO ₂ ) ₂ , LiN (FSO ₂ ) (CF ₃ SO ₂ ), LiN (CF ₃ SO ₂ ) ₂ , LiN (C ₂ F ₅ SO ₂ )
₂ , lithium imide salts such as lithium cyclic 1,2-perfluoroethanedisulfonylimide, lithium cyclic 1,3-perfluoropropane disulfonylimide, LiN (CF ₃ SO ₂ ) (C ₄ F ₉ SO ₂ );
Lithium metide salts such as LiC (FSO ₂ ) ₃ , LiC (CF ₃ SO ₂ ) ₃ , LiC (C ₂ F ₅ SO ₂ ) ₃ ;
Lithium oxalatoborate salts such as lithium difluorooxalatoborate and lithium bis (oxalato) borate;
Lithium oxalate phosphate salts such as lithium tetrafluorooxalatophosphate, lithium difluorobis (oxalato) phosphate, lithium tris (oxalato) phosphate;
In addition, LiPF ₄ (CF ₃ ) ₂ , LiPF ₄ (C ₂ F ₅ ) ₂ , LiPF ₄ (CF ₃ SO ₂ ) ₂ , LiPF ₄ (C ₂ F ₅ SO ₂ ) ₂ , LiBF ₃ CF ₃ , LiBF ₃ C _{2 F 5, LiBF 3 C 3} F 7, LiBF 2 (CF 3) 2, LiBF 2 (C 2 F 5) 2, LiBF 2 (CF 3 SO 2) 2, LiBF 2 (C 2 F 5 SO 2) 2 Fluorine-containing organic lithium salts such as;

Among them, LiPF ₆ , LiBF ₄ , LiSbF ₆ , LiTaF ₆ , FSO ₃ Li, CF ₃ SO ₃ Li, LiN (FSO ₂ ) ₂ , LiN (FSO ₂ ) (CF ₃ SO ₂ ), LiN (CF ₃ SO ₂ ) ₂ , LiN (C ₂ F ₅ SO ₂ ) ₂ , lithium cyclic 1,2-perfluoroethanedisulfonylimide, lithium cyclic 1,3-perfluoropropane disulfonylimide, LiC (FSO ₂ ) ₃ , LiC (CF _{3 SO 2) 3, LiC (C} 2 F 5 SO 2) 3, lithium Bisuo Kisara oxalatoborate, lithium difluoro oxalatoborate, lithium tetrafluoro-oxa Lato phosphate, lithium difluoro bis oxa Lato _phosphate, LiBF ₃ CF _3, LiBF ₃ C ₂ F ₅ , LiPF ₃ (CF ₃ ) ₃ , LiPF ₃ (C ₂ F ₅ ) _{3 and the} like are particularly preferable because they have an effect of improving output characteristics, high-rate charge / discharge characteristics, high-temperature storage characteristics, cycle characteristics, and the like.

These lithium salts may be used alone or in combination of two or more. A preferable example in the case of using two or more types in combination is a combination of LiPF ₆ and LiBF ₄ or LiPF ₆ and FSO ₃ Li, which has an effect of improving load characteristics and cycle characteristics.
In this case, the concentration of LiBF ₄ or FSO ₃ Li with respect to 100% by mass of the entire non-aqueous electrolyte solution is not limited as long as it does not significantly impair the effects of the present invention. On the other hand, it is usually 0.01% by mass or more, preferably 0.1% by mass or more, and usually 30% by mass or less, preferably 20% by mass or less.

Another example is the combined use of an inorganic lithium salt and an organic lithium salt, and the combined use of both has the effect of suppressing deterioration due to high-temperature storage. As the organic lithium salt, CF ₃ SO ₃ Li, LiN (FSO ₂ ) ₂ , LiN (FSO ₂ ) (CF ₃ SO ₂ ), LiN (CF ₃ SO ₂ ) ₂ , LiN (C ₂ F ₅ SO ₂ ) ₂ , Lithium cyclic 1,2-perfluoroethanedisulfonylimide, lithium cyclic 1,3-perfluoropropane disulfonylimide, LiC (FSO ₂ ) ₃ , LiC (CF ₃ SO ₂ ) ₃ , LiC (C ₂ F ₅ SO ₂ ) ₃ , lithium bisoxalatoborate, lithium difluorooxalatoborate, lithium tetrafluorooxalate phosphate, lithium difluorobisoxalatophosphate, LiBF ₃ CF ₃ , LiBF ₃ C ₂ F ₅ , LiPF ₃ (CF ₃ ) ₃ LiPF ₃ (C ₂ F ₅ ) ₃ or the like is preferable. In this case, the ratio of the organic lithium salt to 100% by mass of the entire non-aqueous electrolyte is preferably 0.1% by mass or more, particularly preferably 0.5% by mass or more, and preferably 30% by mass or less. Especially preferably, it is 20 mass% or less.

The concentration of these lithium salts in the non-aqueous electrolyte solution is not particularly limited as long as the effects of the present invention are not impaired. Therefore, the total molar concentration of lithium in the non-aqueous electrolyte is preferably 0.3 mol / L or more, more preferably 0.4 mol / L or more, and further preferably 0.5 mol / L or more. Preferably it is 3 mol / L or less, More preferably, it is 2.5 mol / L or less, More preferably, it is 2.0 mol / L or less.
If the total molar concentration of lithium is too low, the electrical conductivity of the electrolyte may be insufficient. On the other hand, if the concentration is too high, the electrical conductivity may decrease due to an increase in viscosity, resulting in decreased battery performance. There is a case.

1-4. Nonaqueous solvent There is no restriction | limiting in particular about the nonaqueous solvent in this invention, It is possible to use a well-known organic solvent. Examples thereof include cyclic carbonates having no fluorine atom, chain carbonates, cyclic and chain carboxylic acid esters, ether compounds, sulfone compounds, and the like.

<Cyclic carbonate not having fluorine atoms>
Examples of the cyclic carbonate having no fluorine atom include cyclic carbonates having an alkylene group having 2 to 4 carbon atoms.
Specific examples of the cyclic carbonate having an alkylene group having 2 to 4 carbon atoms and having no fluorine atom include ethylene carbonate, propylene carbonate, and butylene carbonate. Among these, ethylene carbonate and propylene carbonate are particularly preferable from the viewpoint of improving battery characteristics resulting from an improvement in the degree of lithium ion dissociation.

The cyclic carbonate which does not have a fluorine atom may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and ratios.
The blending amount of the cyclic carbonate not having a fluorine atom is not particularly limited, and is arbitrary as long as the effects of the present invention are not significantly impaired. However, the blending amount when one kind is used alone is 100 volumes of a non-aqueous solvent. %, 5% by volume or more, more preferably 10% by volume or more. By setting this range, the decrease in electrical conductivity due to the decrease in the dielectric constant of the non-aqueous electrolyte is avoided, and the high current discharge characteristics, stability against the negative electrode, and cycle characteristics of the non-aqueous electrolyte battery are in a good range. And it will be easier. Moreover, it is 95 volume% or less, More preferably, it is 90 volume% or less, More preferably, it is 85 volume% or less. By setting it as this range, the viscosity of the non-aqueous electrolyte solution is set to an appropriate range, the decrease in ionic conductivity is suppressed, and the load characteristics of the non-aqueous electrolyte battery are easily set in a favorable range.

<Chain carbonate>
As the chain carbonate, a chain carbonate having 3 to 7 carbon atoms is preferable, and a dialkyl carbonate having 3 to 7 carbon atoms is more preferable.
Specific examples of the chain carbonate include dimethyl carbonate, diethyl carbonate, di-n-propyl carbonate, diisopropyl carbonate, n-propyl isopropyl carbonate, ethyl methyl carbonate, methyl-n-propyl carbonate, n-butyl methyl carbonate, isobutyl methyl. Examples include carbonate, t-butyl methyl carbonate, ethyl-n-propyl carbonate, n-butyl ethyl carbonate, isobutyl ethyl carbonate, t-butyl ethyl carbonate, and the like.

Among them, dimethyl carbonate, diethyl carbonate, di-n-propyl carbonate, diisopropyl carbonate, n-propyl isopropyl carbonate, ethyl methyl carbonate, and methyl n-propyl carbonate are preferable, and dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate are particularly preferable. is there.
Further, chain carbonates having a fluorine atom (hereinafter sometimes referred to as “fluorinated chain carbonate”) can also be suitably used.

The number of fluorine atoms contained in the fluorinated chain carbonate is not particularly limited as long as it is 1 or more, but is usually 6 or less, preferably 4 or less. When the fluorinated chain carbonate has a plurality of fluorine atoms, they may be bonded to the same carbon or may be bonded to different carbons.
Examples of the fluorinated chain carbonate include fluorinated dimethyl carbonate and derivatives thereof, fluorinated ethyl methyl carbonate and derivatives thereof, and fluorinated diethyl carbonate and derivatives thereof.

Fluorinated dimethyl carbonate and derivatives thereof include fluoromethyl methyl carbonate, difluoromethyl methyl carbonate, trifluoromethyl methyl carbonate, bis (fluoromethyl) carbonate, bis (difluoro) methyl carbonate, bis (trifluoromethyl) carbonate, and the like. It is done.
Fluorinated ethyl methyl carbonate and derivatives thereof include 2-fluoroethyl methyl carbonate, ethyl fluoromethyl carbonate, 2,2-difluoroethyl methyl carbonate, 2-fluoroethyl fluoromethyl carbonate, ethyl difluoromethyl carbonate, 2,2,2 -Trifluoroethyl methyl carbonate, 2,2-difluoroethyl fluoromethyl carbonate, 2-fluoroethyl difluoromethyl carbonate, ethyl trifluoromethyl carbonate, etc. are mentioned.

  Fluorinated diethyl carbonate and its derivatives include ethyl- (2-fluoroethyl) carbonate, ethyl- (2,2-difluoroethyl) carbonate, bis (2-fluoroethyl) carbonate, ethyl- (2,2,2- Trifluoroethyl) carbonate, 2,2-difluoroethyl-2′-fluoroethyl carbonate, bis (2,2-difluoroethyl) carbonate, 2,2,2-trifluoroethyl-2′-fluoroethyl carbonate, 2, Examples include 2,2-trifluoroethyl-2 ′, 2′-difluoroethyl carbonate, bis (2,2,2-trifluoroethyl) carbonate, and the like.

A chain carbonate may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.
The amount of the chain carbonate is preferably 5% by volume or more, more preferably 10% by volume or more, and further preferably 15% by volume or more in 100% by volume of the non-aqueous solvent. By setting the lower limit in this way, the viscosity of the non-aqueous electrolyte solution is set in an appropriate range, the decrease in ionic conductivity is suppressed, and the large current discharge characteristics of the non-aqueous electrolyte battery are easily set in a favorable range. Further, the chain carbonate is preferably 90% by volume or less, more preferably 85% by volume or less, in 100% by volume of the nonaqueous solvent. By setting the upper limit in this way, it is easy to avoid a decrease in electrical conductivity resulting from a decrease in dielectric constant of the nonaqueous electrolyte solution, and to make the large current discharge characteristics of the nonaqueous electrolyte solution battery in a favorable range.

<Cyclic carboxylic acid ester>
The cyclic carboxylic acid ester is preferably one having 3 to 12 carbon atoms.
Specific examples include gamma butyrolactone, gamma valerolactone, gamma caprolactone, epsilon caprolactone, and the like. Among these, gamma butyrolactone is particularly preferable from the viewpoint of improving battery characteristics resulting from an improvement in the degree of lithium ion dissociation.

A cyclic carboxylic acid ester may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.
The amount of the cyclic carboxylic acid ester is usually 5% by volume or more, more preferably 10% by volume or more, in 100% by volume of the non-aqueous solvent. If it is this range, it will become easy to improve the electrical conductivity of a non-aqueous electrolyte solution, and to improve the large current discharge characteristic of a non-aqueous electrolyte battery. Moreover, the compounding quantity of cyclic carboxylic acid ester becomes like this. Preferably it is 50 volume% or less, More preferably, it is 40 volume% or less. By setting the upper limit in this way, the viscosity of the non-aqueous electrolyte solution is set to an appropriate range, a decrease in electrical conductivity is avoided, an increase in negative electrode resistance is suppressed, and a large current discharge of the non-aqueous electrolyte secondary battery is performed. It becomes easy to make a characteristic into a favorable range.

<Chain carboxylic acid ester>
The chain carboxylic acid ester is preferably one having 3 to 7 carbon atoms. In particular,
Methyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, n-butyl acetate, isobutyl acetate, t-butyl acetate, methyl propionate, ethyl propionate, n-propyl propionate, isopropyl propionate, propion Acid-n-butyl, isobutyl propionate, t-butyl propionate, methyl butyrate, ethyl butyrate, butyric acid n-propyl, isopropyl butyrate, methyl isobutyrate, ethyl isobutyrate, isobutyric acid n-propyl, isopropyl isobutyrate Etc.

Among them, methyl acetate, ethyl acetate, acetate-n-propyl acetate-n-butyl acetate, methyl propionate, ethyl propionate, propionate-n-propyl, isopropyl propionate, methyl butyrate, ethyl butyrate, etc. It is preferable from the viewpoint of improvement of ionic conductivity.
A chain carboxylic acid ester may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.

  The compounding amount of the chain carboxylic acid ester is usually 10% by volume or more, more preferably 15% by volume or more, in 100% by volume of the non-aqueous solvent. By setting the lower limit in this way, the electrical conductivity of the non-aqueous electrolyte solution is improved, and the large current discharge characteristics of the non-aqueous electrolyte battery are easily improved. Moreover, the compounding quantity of chain | strand-shaped carboxylic acid ester is 60 volume% or less preferably in 100 volume% of nonaqueous solvents, More preferably, it is 50 volume% or less. By setting the upper limit in this way, an increase in negative electrode resistance is suppressed, and the large current discharge characteristics and cycle characteristics of the non-aqueous electrolyte battery are easily set in a favorable range.

<Ether compound>
As the ether compound, a chain ether having 3 to 10 carbon atoms and a cyclic ether having 3 to 6 carbon atoms in which part of hydrogen may be substituted with fluorine is preferable.
As the chain ether having 3 to 10 carbon atoms,
Diethyl ether, di (2-fluoroethyl) ether, di (2,2-difluoroethyl) ether, di (2,2,2-trifluoroethyl) ether, ethyl (2-fluoroethyl) ether, ethyl (2, 2,2-trifluoroethyl) ether, ethyl (1,1,2,2-tetrafluoroethyl) ether, (2-fluoroethyl) (2,2,2-trifluoroethyl) ether, (2-fluoroethyl) ) (1,1,2,2-tetrafluoroethyl) ether, (2,2,2-trifluoroethyl) (1,1,2,2-tetrafluoroethyl) ether, ethyl-n-propyl ether, ethyl (3-Fluoro-n-propyl) ether, ethyl (3,3,3-trifluoro-n-propyl) ether, ethyl (2,2,3,3-teto Fluoro-n-propyl) ether, ethyl (2,2,3,3,3-pentafluoro-n-propyl) ether, 2-fluoroethyl-n-propylether, (2-fluoroethyl) (3-fluoro- n-propyl) ether, (2-fluoroethyl) (3,3,3-trifluoro-n-propyl) ether, (2-fluoroethyl) (2,2,3,3-tetrafluoro-n-propyl) Ether, (2-fluoroethyl) (2,2,3,3,3-pentafluoro-n-propyl) ether, 2,2,2-trifluoroethyl-n-propyl ether, (2,2,2- Trifluoroethyl) (3-fluoro-n-propyl) ether, (2,2,2-trifluoroethyl) (3
, 3,3-trifluoro-n-propyl) ether, (2,2,2-trifluoroethyl) (2,2,3,3-tetrafluoro-n-propyl) ether, (2,2,2- Trifluoroethyl) (2,2,3,3,3-pentafluoro-n-propyl) ether, 1,1,2,2-tetrafluoroethyl-n-propyl ether, (1,1,2,2- Tetrafluoroethyl) (3-fluoro-n-propyl) ether, (1,1,2,2-tetrafluoroethyl) (3,3,3-trifluoro-n-propyl) ether, (1,1,2 , 2-tetrafluoroethyl) (2,2,3,3-tetrafluoro-n-propyl) ether, (1,1,2,2-tetrafluoroethyl) (2,2,3,3,3-penta Fluoro-n-propyl) ether Di-n-propyl ether, (n-propyl) (3-fluoro-n-propyl) ether, (n-propyl) (3,3,3-trifluoro-n-propyl) ether, (n-propyl) ( 2,2,3,3-tetrafluoro-n-propyl) ether, (n-propyl) (2,2,3,3,3-pentafluoro-n-propyl) ether, di (3-fluoro-n- Propyl) ether, (3-fluoro-n-propyl) (3,3,3-trifluoro-n-propyl) ether, (3-fluoro-n-propyl) (2,2,3,3-tetrafluoro- n-propyl) ether, (3-fluoro-n-propyl) (2,2,3,3,3-pentafluoro-n-propyl) ether, di (3,3,3-trifluoro-n-propyl) ether Ether, (3 3,3-trifluoro-n-propyl) (2,2,3,3-tetrafluoro-n-propyl) ether, (3,3,3-trifluoro-n-propyl) (2,2,3 3,3-pentafluoro-n-propyl) ether, di (2,2,3,3-tetrafluoro-n-propyl) ether, (2,2,3,3-tetrafluoro-n-propyl) (2 , 2,3,3,3-pentafluoro-n-propyl) ether, di (2,2,3,3,3-pentafluoro-n-propyl) ether, di-n-butyl ether, dimethoxymethane, methoxyethoxy Methane, methoxy (2-fluoroethoxy) methane, methoxy (2,2,2-trifluoroethoxy) methanemethoxy (1,1,2,2-tetrafluoroethoxy) methane, diethoxymethane, Toxi (2-fluoroethoxy) methane, ethoxy (2,2,2-trifluoroethoxy) methane, ethoxy (1,1,2,2-tetrafluoroethoxy) methane, di (2-fluoroethoxy) methane, (2 -Fluoroethoxy) (2,2,2-trifluoroethoxy) methane, (2-fluoroethoxy) (1,1,2,2-tetrafluoroethoxy) methanedi (2,2,2-trifluoroethoxy) methane, (2,2,2-trifluoroethoxy) (1,1,2,2-tetrafluoroethoxy) methane, di (1,1,2,2-tetrafluoroethoxy) methane, dimethoxyethane, methoxyethoxyethane, methoxy (2-fluoroethoxy) ethane, methoxy (2,2,2-trifluoroethoxy) ethane, methoxy (1,1,2,2- Trifluoroethoxy) ethane, diethoxyethane, ethoxy (2-fluoroethoxy) ethane, ethoxy (2,2,2-trifluoroethoxy) ethane, ethoxy (1,1,2,2-tetrafluoroethoxy) ethane, di (2-fluoroethoxy) ethane, (2-fluoroethoxy) (2,2,2-trifluoroethoxy) ethane, (2-fluoroethoxy) (1,1,2,2-tetrafluoroethoxy) ethane, di ( 2,2,2-trifluoroethoxy) ethane, (2,2,2-trifluoroethoxy) (1,1,2,2-tetrafluoroethoxy) ethane, di (1,1,2,2-tetrafluoro) Ethoxy) ethane, ethylene glycol di-n-propyl ether, ethylene glycol di-n-butyl ether, diethylene glycol Methyl ether, and the like.

Examples of the cyclic ether having 3 to 6 carbon atoms include tetrahydrofuran, 2-methyltetrahydrofuran, 3-methyltetrahydrofuran, 1,3-dioxane, 2-methyl-1,3-dioxane, 4-methyl-1,3-dioxane, 1 , 4-dioxane and the like, and fluorinated compounds thereof.
Among them, dimethoxymethane, diethoxymethane, ethoxymethoxymethane, ethylene glycol di-n-propyl ether, ethylene glycol di-n-butyl ether, and diethylene glycol dimethyl ether have high solvating ability to lithium ions and improve ion dissociation. Of these, dimethoxymethane, diethoxymethane, and ethoxymethoxymethane are preferable because they have low viscosity and give high ionic conductivity.

An ether type compound may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.
The compounding amount of the ether compound is usually in 100% by volume of the non-aqueous solvent, preferably 5% by volume or more, more preferably 10% by volume or more, further preferably 15% by volume or more, and preferably 70% by volume or less. More preferably, it is 60 volume% or less, More preferably, it is 50 volume% or less.
If it is this range, it is easy to ensure the improvement effect of the lithium ion dissociation degree of chain ether, and the improvement of the ionic conductivity derived from a viscosity fall, and when a negative electrode active material is a carbonaceous material, a chain ether with lithium ion It is easy to avoid a situation where the capacity is reduced due to co-insertion.

<Sulfone compound>
As the sulfone compound, a cyclic sulfone having 3 to 6 carbon atoms and a chain sulfone having 2 to 6 carbon atoms are preferable. The number of sulfonyl groups in one molecule is preferably 1 or 2.
As cyclic sulfone having 3 to 6 carbon atoms,
Monosulfone compounds trimethylene sulfones, tetramethylene sulfones, hexamethylene sulfones;
Examples include disulfone compounds such as trimethylene disulfones, tetramethylene disulfones, and hexamethylene disulfones.

Among these, from the viewpoint of dielectric constant and viscosity, tetramethylene sulfones, tetramethylene disulfones, hexamethylene sulfones, and hexamethylene disulfones are more preferable, and tetramethylene sulfones (sulfolanes) are particularly preferable.
As the sulfolanes, sulfolane and / or sulfolane derivatives (hereinafter sometimes referred to as “sulfolanes” including sulfolane) are preferable. The sulfolane derivative is preferably one in which one or more hydrogen atoms bonded to the carbon atoms constituting the sulfolane ring are substituted with a fluorine atom or an alkyl group.

  Among them, 2-methylsulfolane, 3-methylsulfolane, 2-fluorosulfolane, 3-fluorosulfolane, 2,2-difluorosulfolane, 2,3-difluorosulfolane, 2,4-difluorosulfolane, 2,5-difluorosulfolane, 3,4-difluorosulfolane, 2-fluoro-3-methylsulfolane, 2-fluoro-2-methylsulfolane, 3-fluoro-3-methylsulfolane, 3-fluoro-2-methylsulfolane, 4-fluoro-3-methyl Sulfolane, 4-fluoro-2-methylsulfolane, 5-fluoro-3-methylsulfolane, 5-fluoro-2-methylsulfolane, 2-fluoromethylsulfolane, 3-fluoromethylsulfolane, 2-difluoromethylsulfolane, 3-difluoro Methyl sulfolane, 2- Trifluoromethylsulfolane, 3-trifluoromethylsulfolane, 2-fluoro-3- (trifluoromethyl) sulfolane, 3-fluoro-3- (trifluoromethyl) sulfolane, 4-fluoro-3- (trifluoromethyl) sulfolane , 5-fluoro-3- (trifluoromethyl) sulfolane and the like are preferable in terms of high ionic conductivity and high input / output characteristics.

In addition, as the chain sulfone having 2 to 6 carbon atoms,
Dimethylsulfone, ethylmethylsulfone, diethylsulfone, n-propylmethylsulfone, n-propylethylsulfone, di-n-propylsulfone, isopropylmethylsulfone, isopropylethylsulfone, diisopropylsulfone, n-butylmethylsulfone, n-butylethyl Sulfone, t-butylmethylsulfone, t-butylethylsulfone, monofluoromethylmethylsulfone, difluoromethylmethylsulfone, trifluoromethylmethylsulfone, monofluoroethylmethylsulfone, difluoroethylmethylsulfone, trifluoroethylmethylsulfone, pentafluoro Ethyl methyl sulfone, ethyl monofluoromethyl sulfone, ethyl difluoromethyl sulfone, ethyl trifluoromethyl sulfone, perf Oroethyl methyl sulfone, ethyl trifluoroethyl sulfone, ethyl pentafluoroethyl sulfone, di (trifluoroethyl) sulfone, perfluorodiethyl sulfone, fluoromethyl-n-propyl sulfone, difluoromethyl-n-propyl sulfone, trifluoromethyl- n-propylsulfone, fluoromethylisopropylsulfone, difluoromethylisopropylsulfone, trifluoromethylisopropylsulfone, trifluoroethyl-n-propylsulfone, trifluoroethylisopropylsulfone, pentafluoroethyl-n-propylsulfone, pentafluoroethylisopropylsulfone , Trifluoroethyl-n-butylsulfone, trifluoroethyl-t-butylsulfone, pentafluoroethyl- - butyl sulfone, pentafluoroethyl -t- butyl sulfone, and the like.

  Among them, dimethyl sulfone, ethyl methyl sulfone, diethyl sulfone, n-propyl methyl sulfone, isopropyl methyl sulfone, n-butyl methyl sulfone, t-butyl methyl sulfone, monofluoromethyl methyl sulfone, difluoromethyl methyl sulfone, trifluoromethyl methyl sulfone , Monofluoroethyl methyl sulfone, difluoroethyl methyl sulfone, trifluoroethyl methyl sulfone, pentafluoroethyl methyl sulfone, ethyl monofluoromethyl sulfone, ethyl difluoromethyl sulfone, ethyl trifluoromethyl sulfone, ethyl trifluoroethyl sulfone, ethyl pentafluoro Ethyl sulfone, trifluoromethyl-n-propyl sulfone, trifluoromethyl isopropyl sulfone, tri Ruoroechiru -n- butyl sulfone, trifluoroethyl -t- butyl sulfone, trifluoromethyl -n- butyl sulfone, trifluoromethyl -t- butyl sulfone is high ion conductivity, preferable because the input-output characteristic is high.

A sulfone compound may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.
The compounding amount of the sulfone compound is usually 0.3% by volume or more, more preferably 1% by volume or more, further preferably 5% by volume or more in 100% by volume of the nonaqueous solvent, and preferably 40%. Volume% or less, More preferably, it is 35 volume% or less, More preferably, it is 30 volume% or less.

  Within this range, durability improvement effects such as cycle characteristics and storage characteristics can be easily obtained, and the viscosity of the non-aqueous electrolyte can be set to an appropriate range to avoid a decrease in electrical conductivity. When charging / discharging an aqueous electrolyte battery at a high current density, it is easy to avoid a situation in which the charge / discharge capacity retention rate decreases.

<When using a cyclic carbonate having a fluorine atom as a non-aqueous solvent>
In the present invention, when a cyclic carbonate having a fluorine atom is used as a non-aqueous solvent, one of the non-aqueous solvents exemplified above is combined with a cyclic carbonate having a fluorine atom as a non-aqueous solvent other than the cyclic carbonate having a fluorine atom. Two or more kinds may be used in combination with a cyclic carbonate having a fluorine atom.

For example, one preferred combination of non-aqueous solvents is a combination mainly composed of a cyclic carbonate having a fluorine atom and a chain carbonate. Among them, the total of the cyclic carbonate having a fluorine atom and the chain carbonate in the non-aqueous solvent is preferably 60% by volume or more, more preferably 80% by volume or more, and further preferably 90% by volume or more, and the fluorine atom. The ratio of the cyclic carbonate having a fluorine atom to the total of the cyclic carbonate having a chain and the chain carbonate is 3% by volume or more, preferably 5% by volume or more, more preferably 10% by volume or more, and further preferably 15% by volume or more. Further, it is preferably 60% by volume or less, more preferably 50% by volume or less, still more preferably 40% by volume or less, and particularly preferably 35% by volume or less.

When a combination of these non-aqueous solvents is used, the balance between the cycle characteristics and high-temperature storage characteristics (particularly, the remaining capacity and high-load discharge capacity after high-temperature storage) of a battery produced using the non-aqueous solvent may be improved.
For example, as a specific example of a preferable combination of a cyclic carbonate having a fluorine atom and a chain carbonate,
Monofluoroethylene carbonate and dimethyl carbonate, monofluoroethylene carbonate and diethyl carbonate, monofluoroethylene carbonate and ethyl methyl carbonate, monofluoroethylene carbonate and dimethyl carbonate and diethyl carbonate, monofluoroethylene carbonate and dimethyl carbonate and ethyl methyl carbonate, monofluoro Examples thereof include ethylene carbonate, diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, dimethyl carbonate, diethyl carbonate and ethyl methyl carbonate.

  Among the combinations of cyclic carbonates having a fluorine atom and chain carbonates, those containing symmetric chain alkyl carbonates as chain carbonates are more preferable, and in particular, monofluoroethylene carbonate, dimethyl carbonate, ethyl methyl carbonate, Cycle characteristics include monofluoroethylene carbonate, symmetric chain carbonates and asymmetric chain carbonates such as fluoroethylene carbonate, diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, dimethyl carbonate, diethyl carbonate and ethyl methyl carbonate. And a large current discharge characteristic are preferable. Among these, the symmetric chain carbonate is preferably dimethyl carbonate, and the alkyl group of the chain carbonate preferably has 1 to 2 carbon atoms.

  A combination in which a cyclic carbonate not having a fluorine atom is further added to the combination of the cyclic carbonate having a fluorine atom and the chain carbonate is also a preferable combination. Among them, the total of the cyclic carbonate having a fluorine atom and the cyclic carbonate having no fluorine atom in the non-aqueous solvent is preferably 10% by volume or more, more preferably 15% by volume or more, and further preferably 20% by volume or more. The ratio of the cyclic carbonate having a fluorine atom to the total of the cyclic carbonate having a fluorine atom and the cyclic carbonate having no fluorine atom is 5% by volume or more, preferably 10% by volume or more, more preferably 15% by volume. % Or more, more preferably 25% by volume or more, preferably 95% by volume or less, more preferably 85% by volume or less, still more preferably 75% by volume or less, and particularly preferably 60% by volume or less.

When the cyclic carbonate which does not have a fluorine atom is contained in this concentration range, the electrical conductivity of the electrolytic solution can be maintained while forming a stable protective film on the negative electrode.
As a specific example of a preferable combination of a cyclic carbonate having a fluorine atom and a cyclic carbonate having no fluorine atom and a chain carbonate,
Monofluoroethylene carbonate and ethylene carbonate and dimethyl carbonate, monofluoroethylene carbonate and ethylene carbonate and diethyl carbonate, monofluoroethylene carbonate and ethylene carbonate and ethyl methyl carbonate, monofluoroethylene carbonate and ethylene carbonate, dimethyl carbonate and diethyl carbonate, monofluoro Ethylene carbonate, ethylene carbonate, dimethyl carbonate, and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, diethyl carbonate, and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate Monofluoroethylene carbonate and propylene carbonate and dimethyl carbonate, monofluoroethylene carbonate and propylene carbonate and diethyl carbonate, monofluoroethylene carbonate and propylene carbonate and ethyl methyl carbonate, monofluoroethylene carbonate and propylene carbonate, dimethyl carbonate and diethyl carbonate, Monofluoroethylene carbonate, propylene carbonate, dimethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, propylene carbonate, diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, propylene carbonate, dimethyl carbonate and diethyl carbonate Tylmethyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, dimethyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, diethyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, ethyl methyl carbonate, monofluoroethylene Carbonate, ethylene carbonate, propylene carbonate, dimethyl carbonate and diethyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, dimethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate and propylene carbonate Examples include diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate.

Among the combinations of a cyclic carbonate having a fluorine atom and a cyclic carbonate having no fluorine atom and a chain carbonate, those containing a symmetric chain alkyl carbonate as the chain carbonate are more preferred,
Monofluoroethylene carbonate, ethylene carbonate, dimethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, propylene carbonate, dimethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, dimethyl carbonate and ethyl methyl carbonate, monofluoro Ethylene carbonate, ethylene carbonate, diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, propylene carbonate, diethyl carbonate and ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, diethyl carbonate and ethyl methyl carbonate Nate, monofluoroethylene carbonate, ethylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, monofluoroethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, monofluoroethylene carbonate, ethylene carbonate, propylene carbonate, and dimethyl carbonate It is preferable to use monofluoroethylene carbonate, symmetric chain carbonates, and asymmetric chain carbonates such as sodium carbonate, diethyl carbonate, and ethyl methyl carbonate because the balance between cycle characteristics and large current discharge characteristics is good. Among these, the symmetric chain carbonate is preferably dimethyl carbonate, and the alkyl group of the chain carbonate preferably has 1 to 2 carbon atoms.

When dimethyl carbonate is contained in the non-aqueous solvent, the proportion of dimethyl carbonate in the total non-aqueous solvent is preferably 10% by volume or more, more preferably 20% by volume or more, and even more preferably 25% by volume or more. Preferably, the content is 30% by volume or more, preferably 90% by volume or less, more preferably 80% by volume or less, still more preferably 75% by volume or less, and particularly preferably 70% by volume or less. The load characteristics may be improved.

Above all, it contains dimethyl carbonate and ethyl methyl carbonate, and by increasing the content ratio of dimethyl carbonate over the content ratio of ethyl methyl carbonate, the electric conductivity of the electrolyte can be maintained, but the battery characteristics after high temperature storage are improved. Therefore, it is preferable.
The volume ratio of dimethyl carbonate to ethyl methyl carbonate in all non-aqueous solvents (dimethyl carbonate / ethyl methyl carbonate) is 1.1 or more in terms of improving the electric conductivity of the electrolyte and improving the battery characteristics after storage. Is preferable, 1.5 or more is more preferable, and 2.5 or more is more preferable.

The volume ratio (dimethyl carbonate / ethyl methyl carbonate) is preferably 40 or less, more preferably 20 or less, still more preferably 10 or less, and particularly preferably 8 or less, from the viewpoint of improving battery characteristics at low temperatures.
In the combination mainly composed of the cyclic carbonate having a fluorine atom and the chain carbonate, in addition to the cyclic carbonate having no fluorine atom, a cyclic carboxylic acid ester, a chain carboxylic acid ester, a cyclic ether, Other solvents such as chain ethers, sulfur-containing organic solvents, phosphorus-containing organic solvents, and fluorine-containing aromatic solvents may be mixed.

<When using a cyclic carbonate having a fluorine atom as an auxiliary agent>
In the present invention, when a cyclic carbonate having a fluorine atom is used as an auxiliary agent, as the non-aqueous solvent other than the cyclic carbonate having a fluorine atom, the above-exemplified non-aqueous solvent may be used alone, or two or more thereof. May be used in any combination and ratio.
For example, one preferred combination of non-aqueous solvents is a combination mainly composed of a cyclic carbonate having no fluorine atom and a chain carbonate.

  Among them, the total of cyclic carbonate and chain carbonate having no fluorine atom in the non-aqueous solvent is preferably 70% by volume or more, more preferably 80% by volume or more, and still more preferably 90% by volume or more, The ratio of the cyclic carbonate having no fluorine atom to the total of the cyclic carbonate and the chain carbonate is preferably 5% by volume or more, more preferably 10% by volume or more, and further preferably 15% by volume or more. Preferably it is 50 volume% or less, More preferably, it is 35 volume% or less, More preferably, it is 30 volume% or less, Most preferably, it is 25 volume% or less.

When a combination of these non-aqueous solvents is used, the balance between the cycle characteristics and high-temperature storage characteristics (particularly, the remaining capacity and high-load discharge capacity after high-temperature storage) of a battery produced using the non-aqueous solvent may be improved.
For example, as a specific example of a preferable combination of a cyclic carbonate having no fluorine atom and a chain carbonate,
Ethylene carbonate and dimethyl carbonate, ethylene carbonate and diethyl carbonate, ethylene carbonate and ethyl methyl carbonate, ethylene carbonate and dimethyl carbonate and diethyl carbonate, ethylene carbonate and dimethyl carbonate and ethyl methyl carbonate, ethylene carbonate and diethyl carbonate and ethyl methyl carbonate, ethylene carbonate And dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate.

Among the combinations of cyclic carbonates and chain carbonates not having a fluorine atom, those containing asymmetric chain alkyl carbonates as chain carbonates are more preferable, in particular, ethylene carbonate, dimethyl carbonate and ethyl methyl carbonate, Those containing ethylene carbonate, symmetric chain carbonates and asymmetric chain carbonates such as ethylene carbonate, diethyl carbonate and ethyl methyl carbonate, ethylene carbonate, dimethyl carbonate, diethyl carbonate and ethyl methyl carbonate have cycle characteristics and large current discharge characteristics. This is preferable because of a good balance.

Among them, the asymmetric chain carbonate is preferably ethyl methyl carbonate, and the alkyl group of the chain carbonate preferably has 1 to 2 carbon atoms.
A combination in which propylene carbonate is further added to the combination of these ethylene carbonates and chain carbonates is also a preferable combination.
In the case of containing propylene carbonate, the volume ratio of ethylene carbonate to propylene carbonate is preferably 99: 1 to 40:60, particularly preferably 95: 5 to 50:50. Further, the proportion of propylene carbonate in the whole non-aqueous solvent is preferably 0.1% by volume or more, more preferably 1% by volume or more, still more preferably 2% by volume or more, and preferably 20% by volume or less. Preferably it is 8 volume% or less, More preferably, it is 5 volume% or less.

It is preferable to contain propylene carbonate in this concentration range because the low temperature characteristics may be further improved while maintaining the combination characteristics of ethylene carbonate and chain carbonate.
When dimethyl carbonate is contained in the non-aqueous solvent, the proportion of dimethyl carbonate in the total non-aqueous solvent is preferably 10% by volume or more, more preferably 20% by volume or more, and even more preferably 25% by volume or more. Preferably it is 30% by volume or more, preferably 90% by volume or less, more preferably 80% by volume or less, further preferably 75% by volume or less, and particularly preferably 70% by volume or less. The load characteristics of the battery may be improved.

Above all, it contains dimethyl carbonate and ethyl methyl carbonate, and by increasing the content ratio of dimethyl carbonate over the content ratio of ethyl methyl carbonate, the electric conductivity of the electrolyte can be maintained, but the battery characteristics after high temperature storage are improved. This is preferable.
The volume ratio of dimethyl carbonate to ethyl methyl carbonate in all non-aqueous solvents (dimethyl carbonate / ethyl methyl carbonate) is 1.1 or more in terms of improving the electric conductivity of the electrolyte and improving the battery characteristics after storage. Is preferable, 1.5 or more is more preferable, and 2.5 or more is more preferable. The volume ratio (dimethyl carbonate / ethyl methyl carbonate) is preferably 40 or less, more preferably 20 or less, still more preferably 10 or less, and particularly preferably 8 or less, from the viewpoint of improving battery characteristics at low temperatures.

In the combination mainly composed of a cyclic carbonate having no fluorine atom and a chain carbonate, a cyclic carboxylic acid ester, a chain carboxylic acid ester, a cyclic ether, a chain ether, a sulfur-containing organic solvent, You may mix other solvents, such as a phosphorus organic solvent and an aromatic fluorine-containing solvent.
In this specification, the volume of the non-aqueous solvent is a measured value at 25 ° C., but the measured value at the melting point is used for a solid at 25 ° C. such as ethylene carbonate.

1-5. Auxiliary Agent In the non-aqueous electrolyte battery of the present invention, an auxiliary agent may be appropriately used according to the purpose other than the carboxylic dianhydride represented by the formula (1). Examples of auxiliary agents include unsaturated cyclic carbonates having fluorine atoms, overcharge inhibitors, and other auxiliary agents shown below.

<Fluorinated unsaturated cyclic carbonate>
As the fluorinated cyclic carbonate, it is also preferable to use a cyclic carbonate having an unsaturated bond and a fluorine atom (hereinafter sometimes referred to as “fluorinated unsaturated cyclic carbonate”). The number of fluorine atoms contained in the fluorinated unsaturated cyclic carbonate is not particularly limited as long as it is 1 or more. Among them, the fluorine atom is usually 6 or less, preferably 4 or less, and most preferably 1 or 2.

Examples of the fluorinated unsaturated cyclic carbonate include fluorinated vinylene carbonate derivatives, fluorinated ethylene carbonate derivatives substituted with an aromatic ring or a substituent having a carbon-carbon double bond.
Fluorinated vinylene carbonate derivatives include 4-fluoro vinylene carbonate, 4-fluoro-5-methyl vinylene carbonate, 4-fluoro-5-phenyl vinylene carbonate, 4-allyl-5-fluoro vinylene carbonate, 4-fluoro-5- And vinyl vinylene carbonate.

As the fluorinated ethylene carbonate derivative substituted with a substituent having an aromatic ring or a carbon-carbon double bond,
4-fluoro-4-vinylethylene carbonate, 4-fluoro-4-allylethylene carbonate, 4-fluoro-5-vinylethylene carbonate, 4-fluoro-5-allylethylene carbonate, 4,4-difluoro-4-vinylethylene Carbonate, 4,4-difluoro-4-allylethylene carbonate, 4,5-difluoro-4-vinylethylene carbonate, 4,5-difluoro-4-allylethylene carbonate, 4-fluoro-4,5-divinylethylene carbonate, 4-fluoro-4,5-diallylethylene carbonate, 4,5-difluoro-4,5-divinylethylene carbonate, 4,5-difluoro-4,5-diallylethylene carbonate, 4-fluoro-4-phenylethylene carbonate, 4-fu Oro-5-phenylethylene carbonate, 4,4-difluoro-5-phenylethylene carbonate, 4,5-difluoro-4-phenylethylene carbonate.

Among them, as a fluorinated unsaturated cyclic carbonate particularly preferable for use in combination with the carboxylic dianhydride represented by the formula (1),
4-fluoro vinylene carbonate, 4-fluoro-5-methyl vinylene carbonate, 4-fluoro-5-vinyl vinylene carbonate, 4-allyl-5-fluoro vinylene carbonate, 4-fluoro-4-vinyl ethylene carbonate, 4-fluoro- 4-allylethylene carbonate, 4-fluoro-5-vinylethylene carbonate, 4-fluoro-5-allylethylene carbonate, 4,4-difluoro-4-vinylethylene carbonate, 4,4-difluoro-4-allylethylene carbonate, 4,5-difluoro-4-vinylethylene carbonate, 4,5-difluoro-4-allylethylene carbonate, 4-fluoro-4,5-divinylethylene carbonate, 4-fluoro-4,5-diallylethylene carbonate 4,5-difluoro-4,5-divinyl ethylene carbonate, 4,5-difluoro-4,5-diallyl ethylene carbonate, because it forms a stable interface protective coating, more preferably used.

The molecular weight of the fluorinated unsaturated cyclic carbonate is not particularly limited and is arbitrary as long as the effects of the present invention are not significantly impaired. The molecular weight is preferably 50 or more and 250 or less. If it is this range, it will be easy to ensure the solubility of the fluorinated cyclic carbonate with respect to a non-aqueous electrolyte solution, and the effect of this invention will be easy to be expressed.
The production method of the fluorinated unsaturated cyclic carbonate is not particularly limited, and can be produced by arbitrarily selecting a known method. The molecular weight is more preferably 100 or more, and more preferably 200 or less.

A fluorinated unsaturated cyclic carbonate may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio. Further, the blending amount of the fluorinated unsaturated cyclic carbonate is not particularly limited and is arbitrary as long as the effects of the present invention are not significantly impaired.
The compounding amount of the fluorinated unsaturated cyclic carbonate is usually 0.01% by mass or more, more preferably 0.1% by mass or more, further preferably 0.2% by mass or more, in 100% by mass of the nonaqueous electrolytic solution. Moreover, it is preferably 5% by mass or less, more preferably 4% by mass or less, and further preferably 3% by mass or less.
Within this range, the non-aqueous electrolyte battery tends to exhibit a sufficient cycle characteristics improvement effect, and the high temperature storage characteristics deteriorate, the amount of gas generated increases, and the discharge capacity maintenance ratio decreases. Easy to avoid.

<Overcharge prevention agent>
In the non-aqueous electrolyte solution of the present invention, an overcharge inhibitor can be used in order to effectively prevent the battery from bursting or igniting when the non-aqueous electrolyte battery is overcharged.
As an overcharge prevention agent,
Aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, partially hydrogenated terphenyl, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, dibenzofuran; 2-fluorobiphenyl, o-cyclohexylfluorobenzene, p -Partially fluorinated product of the above aromatic compound such as cyclohexylfluorobenzene;
Examples thereof include fluorine-containing anisole compounds such as 2,4-difluoroanisole, 2,5-difluoroanisole, 2,6-difluoroanisole, and 3,5-difluoroanisole. Above all,
Aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, partially hydrogenated terphenyl, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, and dibenzofuran are preferred.

  These may be used alone or in combination of two or more. When two or more kinds are used in combination, in particular, a combination of cyclohexylbenzene and t-butylbenzene or t-amylbenzene, biphenyl, alkylbiphenyl, terphenyl, partially hydrogenated terphenyl, cyclohexylbenzene, t-butylbenzene, Using at least one selected from aromatic compounds not containing oxygen, such as t-amylbenzene, and at least one selected from oxygen-containing aromatic compounds such as diphenyl ether, dibenzofuran, and the like is an overcharge preventing property and a high temperature storage property. From the standpoint of balance.

The amount of the overcharge inhibitor is not particularly limited, and is arbitrary as long as the effects of the present invention are not significantly impaired. The overcharge inhibitor is preferably 0.1% by mass or more and 5% by mass or less in 100% by mass of the non-aqueous electrolyte solution. If it is this range, it will be easy to fully express the effect of an overcharge inhibiting agent, and it will be easy to avoid the situation where the characteristics of batteries, such as a high temperature storage characteristic, fall.
The overcharge inhibitor is more preferably 0.2% by mass or more, further preferably 0.3% by mass or more, particularly preferably 0.5% by mass or more, and more preferably 3% by mass or less, still more preferably. Is 2% by mass or less.

<Other auxiliaries>
Other known auxiliary agents can be used in the non-aqueous electrolyte solution of the present invention. As other auxiliaries,
Carbonate compounds such as erythritan carbonate, spiro-bis-dimethylene carbonate, methoxyethyl-methyl carbonate;
Succinic anhydride, glutaric anhydride, maleic anhydride, citraconic anhydride, glutaconic anhydride, itaconic anhydride, diglycolic anhydride, cyclohexanedicarboxylic anhydride, cyclopentanetetracarboxylic dianhydride, phenylsuccinic anhydride, etc. A carboxylic anhydride other than the carboxylic dianhydride represented by the formula (1):
Spiro compounds such as 2,4,8,10-tetraoxaspiro [5.5] undecane and 3,9-divinyl-2,4,8,10-tetraoxaspiro [5.5] undecane;
Ethylene sulfite, methyl fluorosulfonate, ethyl fluorosulfonate, methyl methanesulfonate, ethyl methanesulfonate, busulfan, sulfolene, diphenylsulfone, N, N-dimethylmethanesulfonamide, N, N-diethylmethanesulfonamide, vinyl Methyl sulfonate, ethyl vinyl sulfonate, allyl vinyl sulfonate, propargyl vinyl sulfonate, methyl allyl sulfonate, ethyl allyl sulfonate, allyl sulfonate, propargyl allyl sulfonate, 1,2-bis (vinylsulfonoxy) Sulfur-containing compounds such as ethane;

Nitrogen-containing compounds such as 1-methyl-2-pyrrolidinone, 1-methyl-2-piperidone, 3-methyl-2-oxazolidinone, 1,3-dimethyl-2-imidazolidinone and N-methylsuccinimide;
Trimethyl phosphite, triethyl phosphite, triphenyl phosphite, trimethyl phosphate, triethyl phosphate, triphenyl phosphate, dimethyl methylphosphonate, diethyl ethylphosphonate, dimethyl vinylphosphonate, diethyl vinylphosphonate, diethylphospho Phosphorus-containing compounds such as ethyl noacetate, methyl dimethylphosphinate, ethyl diethylphosphinate, trimethylphosphine oxide, triethylphosphine oxide;
Hydrocarbon compounds such as heptane, octane, nonane, decane, cycloheptane;
Fluorine-containing aromatic compounds such as fluorobenzene, difluorobenzene, hexafluorobenzene and benzotrifluoride;
Etc. These may be used alone or in combination of two or more. By adding these auxiliaries, capacity maintenance characteristics and cycle characteristics after high temperature storage can be improved.

The blending amount of other auxiliary agents is not particularly limited, and is arbitrary as long as the effects of the present invention are not significantly impaired. The other auxiliary agent is preferably 0.01% by mass or more and 5% by mass or less in 100% by mass of the non-aqueous electrolyte solution. Within this range, the effects of other auxiliaries can be sufficiently exhibited, and it is easy to avoid a situation in which battery characteristics such as high-load discharge characteristics deteriorate.
The blending amount of other auxiliaries is more preferably 0.1% by mass or more, further preferably 0.2% by mass or more, more preferably 3% by mass or less, and further preferably 1% by mass or less. .
As mentioned above, what exists in the inside of the non-aqueous electrolyte battery as described in this invention is also contained in the above-mentioned non-aqueous electrolyte.

  Specifically, the components of the non-aqueous electrolyte solution such as lithium salt, solvent, and auxiliary agent are separately synthesized, and the non-aqueous electrolyte solution is prepared from what is substantially isolated by the method described below. In the case of a nonaqueous electrolyte solution in a nonaqueous electrolyte battery obtained by pouring into a separately assembled battery, the components of the nonaqueous electrolyte solution of the present invention are individually placed in the battery, In order to obtain the same composition as the non-aqueous electrolyte solution of the present invention by mixing in a non-aqueous electrolyte battery, the compound constituting the non-aqueous electrolyte solution of the present invention is further generated in the non-aqueous electrolyte battery. The case where the same composition as the aqueous electrolyte is obtained is also included.

2. Battery Configuration The non-aqueous electrolyte battery of the present invention is suitable for use as an electrolyte for a secondary battery, for example, a lithium secondary battery, among non-aqueous electrolyte batteries. Hereinafter, a non-aqueous electrolyte battery using the non-aqueous electrolyte of the present invention will be described.
The non-aqueous electrolyte battery of the present invention can adopt a known structure. Typically, the negative electrode and the positive electrode capable of occluding and releasing ions (for example, lithium ions), and the non-aqueous electrolysis of the present invention described above. Liquid.

2-1. Negative electrode The negative electrode active material used for the negative electrode is described below. The negative electrode active material is not particularly limited as long as it can electrochemically occlude and release lithium ions. Specific examples include carbonaceous materials, alloy materials, lithium-containing metal composite oxide materials, and the like. These may be used individually by 1 type, and may be used together combining 2 or more types arbitrarily.

<Negative electrode active material>
Examples of the negative electrode active material include carbonaceous materials, alloy materials, lithium-containing metal composite oxide materials, and the like.
Examples of the carbonaceous material include (1) natural graphite, (2) artificial graphite, (3) amorphous carbon, (4) carbon-coated graphite, (5) graphite-coated graphite, and (6) resin-coated graphite. .

(1) Examples of natural graphite include scaly graphite, scaly graphite, soil graphite, and / or graphite particles obtained by subjecting these graphites to spheroidization or densification. Among these, spherical or ellipsoidal graphite subjected to spheroidizing treatment is particularly preferable from the viewpoints of particle filling properties and charge / discharge rate characteristics.
As an apparatus used for the spheroidization treatment, for example, an apparatus that repeatedly gives mechanical action such as compression, friction, shearing force, etc. including the interaction of particles mainly with impact force to the particles can be used. Specifically, it has a rotor with a large number of blades installed inside the casing, and mechanical action such as impact compression, friction, shearing force, etc. on the carbon material introduced inside the rotor by rotating at high speed. And a device for performing the spheroidizing treatment is preferable. Moreover, it is preferable to have a mechanism that repeatedly gives mechanical action by circulating the carbon material.

  For example, when the spheroidizing treatment is performed using the above-described apparatus, the peripheral speed of the rotating rotor is preferably 30 to 100 m / second, more preferably 40 to 100 m / second, and 50 to 100 m / second. More preferably. The treatment can be performed by simply passing a carbonaceous material, but it is preferable to circulate or stay in the apparatus for 30 seconds or longer, and it is preferable to circulate or stay in the apparatus for 1 minute or longer. More preferred.

  (2) Artificial graphite includes coal tar pitch, coal heavy oil, atmospheric residue, petroleum heavy oil, aromatic hydrocarbon, nitrogen-containing cyclic compound, sulfur-containing cyclic compound, polyphenylene, polyvinyl chloride, Organic compounds such as polyvinyl alcohol, polyacrylonitrile, polyvinyl butyral, natural polymer, polyphenylene sulfide, polyphenylene oxide, furfuryl alcohol resin, phenol-formaldehyde resin, imide resin are usually in the range of 2500 ° C. or higher and usually 3200 ° C. or lower. Examples thereof include those produced by graphitization at a temperature and, if necessary, pulverized and / or classified. At this time, a silicon-containing compound or a boron-containing compound can also be used as a graphitization catalyst. In addition, artificial graphite obtained by graphitizing mesocarbon microbeads separated in the heat treatment process of pitch can be mentioned. Furthermore, the artificial graphite of the granulated particle which consists of primary particles is also mentioned. For example, by mixing mesocarbon microbeads and graphitizable carbonaceous material powders such as coke, graphitizable binders such as tar and pitch, and graphitization catalyst, graphitizing, and pulverizing as necessary Examples of the resulting graphite particles include a plurality of flat particles and aggregated or bonded so that the orientation planes are non-parallel.

(3) As amorphous carbon, amorphous carbon that has been heat-treated at least once in a temperature range (400 to 2200 ° C.) in which no graphitizable carbon precursor such as tar or pitch is used as a raw material. Examples thereof include amorphous carbon particles that are heat-treated using particles or a non-graphitizable carbon precursor such as a resin as a raw material.
(4) Carbon-coated graphite can be obtained by mixing natural graphite and / or artificial graphite with a carbon precursor that is an organic compound such as tar, pitch, or resin, and heat-treating it at least once in the range of 400 to 2300 ° C. Examples thereof include a carbon graphite composite in which natural graphite and / or artificial graphite is used as nuclear graphite, and amorphous carbon coats the nuclear graphite. The composite form may cover the entire surface or a part thereof, or may be a composite of a plurality of primary particles using carbon originating from the carbon precursor as a binder. Carbon can also be deposited (CVD) by reacting natural graphite and / or artificial graphite with hydrocarbon gases such as benzene, toluene, methane, propane, and aromatic volatiles at a high temperature to deposit carbon on the graphite surface. A graphite composite can also be obtained.

(5) As graphite-coated graphite, natural graphite and / or artificial graphite and a carbon precursor of an easily graphitizable organic compound such as tar, pitch or resin are mixed and once in a range of about 2400 to 3200 ° C. Examples thereof include graphite-coated graphite in which natural graphite and / or artificial graphite obtained by heat treatment is used as nuclear graphite, and graphitized material covers the whole or part of the surface of nuclear graphite.
(6) As the resin-coated graphite, natural graphite and / or artificial graphite obtained by mixing natural graphite and / or artificial graphite with a resin and drying at a temperature of less than 400 ° C. is used as nuclear graphite, and the resin is nuclear graphite. And resin-coated graphite covering the surface.
Moreover, the carbonaceous material of (1)-(6) may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and ratios.

  Examples of organic compounds such as tar, pitch and resin used in the above (2) to (5) include coal-based heavy oil, direct-current heavy oil, cracked heavy petroleum oil, aromatic hydrocarbon, N-ring compound. , S ring compound, polyphenylene, organic synthetic polymer, natural polymer, thermoplastic resin and carbonizable organic compound selected from the group consisting of thermosetting resins. The raw material organic compound may be used after being dissolved in a low molecular organic solvent in order to adjust the viscosity at the time of mixing.

Moreover, as natural graphite and / or artificial graphite used as a raw material of nuclear graphite, natural graphite subjected to spheroidization treatment is preferable.
As an alloy material used as the negative electrode active material, as long as lithium can be occluded / released, lithium alone, simple metals and alloys forming lithium alloys, or oxides, carbides, nitrides, silicides, sulfides thereof Any of compounds such as products or phosphides may be used and is not particularly limited. The single metal and alloy forming the lithium alloy are preferably materials containing group 13 and group 14 metal / metalloid elements (that is, excluding carbon), more preferably aluminum, silicon and tin single metals and An alloy or compound containing these atoms. These may be used individually by 1 type and may use 2 or more types together by arbitrary combinations and a ratio.

<Physical properties of carbonaceous materials>
When using a carbonaceous material as a negative electrode active material, it is desirable to have the following physical properties.
(X-ray parameters)
The d-value (interlayer distance) of the lattice plane (002 plane) obtained by X-ray diffraction by the Gakushin method of carbonaceous materials is usually 0.335 nm or more, usually 0.360 nm or less, and 0.350 nm. The following is preferable, and 0.345 nm or less is more preferable. Further, the crystallite size (Lc) of the carbonaceous material obtained by X-ray diffraction by the Gakushin method is preferably 1.0 nm or more, and more preferably 1.5 nm or more.

(Volume-based average particle size)
The volume-based average particle diameter of the carbonaceous material is a volume-based average particle diameter (median diameter) obtained by a laser diffraction / scattering method, and is usually 1 μm or more, preferably 3 μm or more, more preferably 5 μm or more, and 7 μm. The above is particularly preferable, and is usually 100 μm or less, preferably 50 μm or less, more preferably 40 μm or less, further preferably 30 μm or less, and particularly preferably 25 μm or less.

If the volume-based average particle size is below the above range, the irreversible capacity may increase, leading to loss of initial battery capacity. On the other hand, when the above range is exceeded, when an electrode is produced by coating, an uneven coating surface tends to be formed, which may be undesirable in the battery production process.
The volume-based average particle size is measured by dispersing carbon powder in a 0.2% by weight aqueous solution (about 10 mL) of polyoxyethylene (20) sorbitan monolaurate, which is a surfactant, and laser diffraction / scattering particle size distribution. This is performed using a meter (for example, LA-700 manufactured by Horiba, Ltd.). The median diameter determined by the measurement is defined as the volume-based average particle diameter of the carbonaceous material of the present invention.

(Raman R value)
The Raman R value of the carbonaceous material is a value measured using a laser Raman spectrum method, and is usually 0.01 or more, preferably 0.03 or more, more preferably 0.1 or more, and usually 1. 5 or less, preferably 1.2 or less, more preferably 1 or less, and particularly preferably 0.5 or less.

When the Raman R value is below the above range, the crystallinity of the particle surface becomes too high, and there are cases where the number of sites where Li enters between layers decreases with charge / discharge. That is, charge acceptance may be reduced. In addition, when the negative electrode is densified by applying it to the current collector and then pressing it, the crystals are likely to be oriented in a direction parallel to the electrode plate, which may lead to a decrease in load characteristics.
On the other hand, if it exceeds the above range, the crystallinity of the particle surface is lowered, the reactivity with the non-aqueous electrolyte is increased, and the efficiency may be lowered and the gas generation may be increased.

The Raman spectrum is measured using a Raman spectrometer (for example, a Raman spectrometer manufactured by JASCO Corporation), and the sample is naturally dropped into the measurement cell and filled, and an argon ion laser beam (or semiconductor) is applied to the sample surface in the cell. While irradiating a laser beam, the cell is rotated in a plane perpendicular to the laser beam. The resulting Raman spectrum, the intensity _{I A} of the peak _{P A} in the vicinity of 1580 cm ^-1, and measuring the intensity _{I B} of a peak _{P B} in the vicinity of 1360 cm ^-1, the intensity ratio _{R (R = I B / I} A) Is calculated. The Raman R value calculated by the measurement is defined as the Raman R value of the carbonaceous material of the present invention.

Moreover, said Raman measurement conditions are as follows.
・ Laser wavelength: Ar ion laser 514.5 nm (semiconductor laser 532 nm)
Measurement range: 1100 cm ^{−1 to} 1730 cm ⁻¹
-Raman R value: background processing,
-Smoothing processing: Simple average, 5 points of convolution

(BET specific surface area)
BET specific surface area of the carbonaceous material is a value of the measured specific surface area using the BET method is usually 0.1 m ² · ^{g -1} or more, 0.7 m ² · ^{g -1} or more, 1. 0 m ² · ^{g -1} or more, and particularly preferably 1.5 m ² · ^{g -1} or more, generally not more than 100 m ² · ^{g -1,} preferably ^{25 m} 2 · ^{g -1} or less, 15 m ² · g ^-1 more preferably less, ^{10 m} 2 · ^{g -1} or less are especially preferred.

When the value of the BET specific surface area is less than this range, the acceptability of lithium tends to deteriorate during charging when it is used as a negative electrode material, lithium tends to precipitate on the electrode surface, and stability may be lowered. On the other hand, if it exceeds this range, when used as a negative electrode material, the reactivity with the non-aqueous electrolyte increases, gas generation tends to increase, and a preferable battery may be difficult to obtain.

  The specific surface area is measured by the BET method using a surface area meter (for example, a fully automated surface area measuring device manufactured by Okura Riken), preliminarily drying the sample at 350 ° C. for 15 minutes under nitrogen flow, Using a nitrogen helium mixed gas that is accurately adjusted so that the relative pressure value of nitrogen is 0.3, the nitrogen adsorption BET one-point method is performed by a gas flow method.

(Roundness)
When the circularity is measured as the degree of the sphere of the carbonaceous material, it is preferably within the following range. The circularity is defined as “circularity = (peripheral length of an equivalent circle having the same area as the particle projection shape) / (actual perimeter of the particle projection shape)”, and is theoretical when the circularity is 1. Become a true sphere.
The circularity of the particles having a particle size of 3 to 40 μm in the range of the carbonaceous material is desirably closer to 1, and is preferably 0.1 or more, more preferably 0.5 or more, and more preferably 0.8 or more, 0.85 or more is more preferable, and 0.9 or more is particularly preferable. High current density charge / discharge characteristics improve as the degree of circularity increases. Therefore, when the circularity is less than the above range, the filling property of the negative electrode active material is lowered, the resistance between particles is increased, and the high current density charge / discharge characteristics may be lowered for a short time.

  The circularity is measured using a flow type particle image analyzer (for example, FPIA manufactured by Sysmex Corporation). About 0.2 g of a sample was dispersed in a 0.2% by mass aqueous solution (about 50 mL) of polyoxyethylene (20) sorbitan monolaurate as a surfactant, and irradiated with 28 kHz ultrasonic waves at an output of 60 W for 1 minute. The detection range is specified as 0.6 to 400 μm, and the particle size is measured in the range of 3 to 40 μm.

  The method for improving the circularity is not particularly limited, but a sphere-shaped sphere is preferable because the shape of the interparticle void when the electrode body is formed is preferable. Examples of spheroidizing treatment include a method of mechanically approaching a sphere by applying a shearing force and a compressive force, a mechanical / physical processing method of granulating a plurality of fine particles by the binder or the adhesive force of the particles themselves, etc. Is mentioned.

(Tap density)
The tap density of the carbonaceous material is usually 0.1 g · cm ⁻³ or more, preferably 0.5 g · cm ⁻³ or more, more preferably 0.7 g · cm ⁻³ or more, and 1 g · cm ⁻³ or more. Particularly preferable, 2 g · cm ⁻³ or less is preferable, 1.8 g · cm ⁻³ or less is more preferable, and 1.6 g · cm ⁻³ or less is particularly preferable. When the tap density is below the above range, the packing density is difficult to increase when used as a negative electrode, and a high-capacity battery may not be obtained. On the other hand, when the above range is exceeded, there are too few voids between particles in the electrode, it is difficult to ensure conductivity between the particles, and it may be difficult to obtain preferable battery characteristics.
The tap density is measured by passing through a sieve having an opening of 300 μm, dropping the sample onto a 20 cm ³ tapping cell and filling the sample to the upper end surface of the cell, and then measuring a powder density measuring device (for example, manufactured by Seishin Enterprise Co., Ltd.). Using a tap denser, tapping with a stroke length of 10 mm is performed 1000 times, and the tap density is calculated from the volume at that time and the mass of the sample.

(Orientation ratio)
The orientation ratio of the carbonaceous material is usually 0.005 or more, preferably 0.01 or more, more preferably 0.015 or more, and usually 0.67 or less. When the orientation ratio is below the above range, the high-density charge / discharge characteristics may deteriorate. The upper limit of the above range is the theoretical upper limit value of the orientation ratio of the carbonaceous material.
The orientation ratio is measured by X-ray diffraction after pressure-molding the sample. 0.47 g of sample diameter 1
X-ray diffraction is measured by setting a molded body obtained by filling a molding machine of 7 mm and compressing at 58.8 MN · m ^{-2 so} that it is flush with the surface of the measurement sample holder. . From the (110) diffraction and (004) diffraction peak intensities of the obtained carbon, a ratio represented by (110) diffraction peak intensity / (004) diffraction peak intensity is calculated.

The X-ray diffraction measurement conditions are as follows. “2θ” indicates a diffraction angle.
・ Target: Cu (Kα ray) graphite monochromator ・ Slit:
Divergence slit = 0.5 degree Light receiving slit = 0.15 mm
Scattering slit = 0.5 degree / measurement range and step angle / measurement time:
(110) plane: 75 degrees ≦ 2θ ≦ 80 degrees 1 degree / 60 seconds (004) plane: 52 degrees ≦ 2θ ≦ 57 degrees 1 degree / 60 seconds

(Aspect ratio (powder))
The aspect ratio of the carbonaceous material is usually 1 or more and usually 10 or less, preferably 8 or less, and more preferably 5 or less. If the aspect ratio exceeds the above range, streaking or a uniform coated surface cannot be obtained when forming an electrode plate, and the high current density charge / discharge characteristics may deteriorate. The lower limit of the above range is the theoretical lower limit value of the aspect ratio of the carbonaceous material.

  The aspect ratio is measured by magnifying and observing the carbonaceous material particles with a scanning electron microscope. Carbonaceous material particles when three-dimensional observation is performed by selecting arbitrary 50 graphite particles fixed to the end face of a metal having a thickness of 50 μm or less and rotating and tilting the stage on which the sample is fixed. The longest diameter A and the shortest diameter B orthogonal thereto are measured, and the average value of A / B is obtained.

<Configuration and production method of negative electrode>
Any known method can be used for producing the electrode as long as the effects of the present invention are not significantly impaired. For example, it is formed by adding a binder, a solvent, and, if necessary, a thickener, a conductive material, a filler, etc. to a negative electrode active material to form a slurry, which is applied to a current collector, dried and then pressed. Can do.
In the case of using an alloy-based material, a method of forming a thin film layer (negative electrode active material layer) containing the above-described negative electrode active material by a technique such as vapor deposition, sputtering, or plating is also used.

(Electrode density)
The electrode structure when the negative electrode active material is made into an electrode is not particularly limited, but the density of the negative electrode active material present on the current collector is preferably 1 g · cm ⁻³ or more, and 1.2 g · cm ⁻³ or more. but more preferably, particularly preferably 1.3 g · ^{cm -3} or more, preferably 2.2 g · ^{cm -3} or less, more preferably 2.1 g · ^{cm -3} or less, 2.0 g · ^{cm -3} or less Further preferred is 1.9 g · cm ⁻³ or less. When the density of the negative electrode active material existing on the current collector exceeds the above range, the negative electrode active material particles are destroyed, and the initial irreversible capacity increases or non-aqueous system near the current collector / negative electrode active material interface. There is a case where high current density charge / discharge characteristics are deteriorated due to a decrease in permeability of the electrolytic solution. On the other hand, if the amount is less than the above range, the conductivity between the negative electrode active materials decreases, the battery resistance increases, and the capacity per unit volume may decrease.

2-2. Positive electrode <Positive electrode active material>
The positive electrode active material (lithium transition metal compound) used for the positive electrode is described below.
<Lithium transition metal compound>
A lithium transition metal compound is a compound having a structure capable of desorbing and inserting Li ions, and examples thereof include sulfides, phosphate compounds, and lithium transition metal composite oxides. Examples of sulfides include compounds having a two-dimensional layered structure such as TiS ₂ and MoS ₂ , and strong compounds represented by the general formula Me _x Mo ₆ S ₈ (Me is various transition metals including Pb, Ag, and Cu). Examples thereof include a sugar compound having a three-dimensional skeleton structure. Examples of the phosphate compound include those belonging to the olivine structure, and are generally represented by LiMePO ₄ (Me is at least one or more transition metals), specifically LiFePO ₄ , LiCoPO ₄ , LiNiPO ₄ , Examples include LiMnPO ₄ . Examples of the lithium transition metal composite oxide include spinel structures capable of three-dimensional diffusion and those belonging to a layered structure capable of two-dimensional diffusion of lithium ions. Those having a spinel structure are generally expressed as LiMe ₂ O ₄ (Me is at least one transition metal), specifically, LiMn ₂ O ₄ , LiCoMnO ₄ , LiNi _0.5 Mn _1.5 O. ₄ , LiCoVO _{4 and the} like. Those having a layered structure are generally expressed as LiMeO ₂ (Me is at least one transition metal). LiCoO _{2 Specifically, LiNiO 2, LiNi 1-x} Co x O 2, LiNi 1-x-y Co x Mn y O 2, LiNi 0.5 Mn 0.5 O 2, Li 1.2 Cr 0. _{4 Mn 0.4 O 2, Li 1.2} Cr 0.4 Ti 0.4 O 2, such as LiMnO ₂ and the like.

<composition>
The lithium-containing transition metal compound is, for example, a lithium transition metal compound represented by the following composition formula (A) or (B).
1) In the case of a lithium transition metal compound represented by the following composition formula (A)
Li _{1 + x} MO ₂ (A)
However, x is usually 0 or more and 0.5 or less. M is an element composed of Ni and Mn or Ni, Mn and Co, and the Mn / Ni molar ratio is usually 0.1 or more and 5 or less. The Ni / M molar ratio is usually 0 or more and 0.5 or less. The Co / M molar ratio is usually 0 or more and 0.5 or less. In addition, the rich portion of Li represented by x may be replaced with the transition metal site M.

  In the composition formula (A), the atomic ratio of the oxygen amount is described as 2 for convenience, but there may be some non-stoichiometry. Moreover, x in the said compositional formula is the preparation composition in the manufacture stage of a lithium transition metal type compound. Usually, batteries on the market are aged after the batteries are assembled. For this reason, the Li amount of the positive electrode may be deficient with charge / discharge. In this case, x may be measured to be −0.65 or more and 1 or less when discharged to 3 V in composition analysis.

A lithium transition metal-based compound is excellent in battery characteristics when fired at a high temperature in an oxygen-containing gas atmosphere in order to enhance the crystallinity of the positive electrode active material. Further, the lithium transition metal-based compound represented by the composition formula (A) may be a solid solution with Li ₂ MO ₃ called a 213 layer, as shown in the general formula (A ′) below.
αLi ₂ MO ₃ · (1-α) LiM′O ₂ (A ′)
In the general formula, α is a number satisfying 0 <α <1.

M is at least one metallic element average oxidation number of 4 ^+, specifically, at least one metal element Mn, Zr, Ti, Ru, selected from the group consisting of Re and Pt.
M 'is at least one metallic element average oxidation number of 3 ^+, preferably, V, Mn, Fe, at least one metallic element selected from the group consisting of Co and Ni, more preferably , At least one metal element selected from the group consisting of Mn, Co and Ni.

2) A lithium transition metal compound represented by the following general formula (B).
_{Li [Li a M b Mn 2} -b-a] O 4 + δ ··· (B)
However, M is an element comprised from at least 1 sort (s) of the transition metals chosen from Ni, Cr, Fe, Co, Cu, Zr, Al, and Mg.
The value of b is usually 0.4 or more and 0.6 or less.

When the value of b is within this range, the energy density per unit weight in the lithium transition metal compound is high.
The value of a is usually 0 or more and 0.3 or less. Moreover, a in the above composition formula is a charged composition in the production stage of the lithium transition metal compound. Usually, batteries on the market are aged after the batteries are assembled. For this reason, the Li amount of the positive electrode may be deficient with charge / discharge. In this case, a may be measured to be −0.65 or more and 1 or less when discharged to 3 V in composition analysis. When the value of a is within this range, the energy density per unit weight in the lithium transition metal compound is not significantly impaired, and good load characteristics can be obtained.

Furthermore, the value of δ is usually in the range of ± 0.5.
If the value of δ is within this range, the stability as a crystal structure is high, and the cycle characteristics and high-temperature storage of a battery having an electrode produced using this lithium transition metal compound are good.
Here, the chemical meaning of the lithium composition in the lithium nickel manganese composite oxide, which is the composition of the lithium transition metal compound, will be described in more detail below.

In order to obtain a and b in the composition formula of the lithium transition metal compound, each transition metal and lithium are analyzed with an inductively coupled plasma emission spectrometer (ICP-AES) to obtain a ratio of Li / Ni / Mn. It is calculated by the thing.
From a structural point of view, it is considered that lithium related to a is substituted for the same transition metal site. Here, due to the lithium according to a, the average valence of M and manganese becomes larger than 3.5 due to the principle of charge neutrality.
Further, the lithium transition metal based compound may be substituted with fluorine, it is expressed as _{LiMn 2 O 4-x F 2x} .

<blend>
Specific examples of the lithium transition metal compound having the above composition include, for example, Li _{1 + x} Ni _0.5 Mn _0.5 O ₂ , Li _{1 + x} Ni _0.85 Co _0.10 Al _0.05 O ₂ , Li _{1 + x} Ni _0.33 Mn _0.33 Co _0.33 O ₂ , Li _{1 + x} Ni _0.45 Mn _0.45 Co _0.1 O ₂ , Li _{1 + x} Mn _1.8 Al _0.2 O ₄ , Li _{1 + x} Mn _1.5 Ni _0.5 O ₄ and the like. These lithium transition metal compounds may be used alone or in a blend of two or more.

<Introduction of foreign elements>
Moreover, a different element may be introduce | transduced into a lithium transition metal type compound. As the different elements, B, Na, Mg, Al, K, Ca, Ti, V, Cr, Fe, Cu, Zn, Sr, Y, Zr, Nb, Ru, Rh, Pd, Ag, In, Sb, Te , Ba, Ta, Mo, W, Re, Os, Ir, Pt, Au, Pb, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Bi , N, F, S, Cl, Br, I, As, Ge, P, Pb, Sb, Si, and Sn. These foreign elements may be incorporated into the crystal structure of the lithium transition metal compound, or may not be incorporated into the crystal structure of the lithium transition metal compound, and may be a single element or compound on the particle surface or grain boundary. May be unevenly distributed.

[Positive electrode for lithium secondary battery]
The positive electrode for a lithium secondary battery is formed by forming a positive electrode active material layer containing the above-described lithium transition metal compound powder for a lithium secondary battery positive electrode material and a binder on a current collector.
The positive electrode active material layer is usually formed by mixing a positive electrode material, a binder, and a conductive material and a thickener, which are used if necessary, in a dry form into a sheet shape, and then pressing the positive electrode current collector on the positive electrode current collector. Alternatively, these materials are dissolved or dispersed in a liquid medium to form a slurry, which is applied to the positive electrode current collector and dried.

As the material for the positive electrode current collector, metal materials such as aluminum, stainless steel, nickel plating, titanium, and tantalum, and carbon materials such as carbon cloth and carbon paper are usually used. As for the shape, in the case of a metal material, a metal foil, a metal cylinder, a metal coil, a metal plate, a metal thin film, an expanded metal, a punch metal, a foam metal, etc., and in the case of a carbon material, a carbon plate, a carbon thin film, a carbon cylinder Etc. In addition, you may form a thin film suitably in mesh shape.
When a thin film is used as the positive electrode current collector, its thickness is arbitrary, but a range of usually 1 μm or more and 100 mm or less is suitable. If it is thinner than the above range, the strength required for the current collector may be insufficient. On the other hand, if it is thicker than the above range, the handleability may be impaired.

  The binder used in the production of the positive electrode active material layer is not particularly limited, and in the case of a coating method, any material that is stable with respect to the liquid medium used during electrode production may be used. Specific examples include polyethylene, Resin polymers such as polypropylene, polyethylene terephthalate, polymethyl methacrylate, aromatic polyamide, cellulose, nitrocellulose, SBR (styrene butadiene rubber), NBR (acrylonitrile butadiene rubber), fluorine rubber, isoprene rubber, butadiene rubber, ethylene・ Rubber polymers such as propylene rubber, styrene / butadiene / styrene block copolymers and hydrogenated products thereof, EPDM (ethylene / propylene / diene terpolymers), styrene / ethylene / butadiene / ethylene copolymers, Styrene / isoprene styrene bromide Copolymer and its hydrogenated thermoplastic elastomeric polymer, syndiotactic-1,2-polybutadiene, polyvinyl acetate, ethylene / vinyl acetate copolymer, propylene / α-olefin copolymer, etc. Fluorine polymers such as soft resinous polymers, polyvinylidene fluoride, polytetrafluoroethylene, fluorinated polyvinylidene fluoride, polytetrafluoroethylene / ethylene copolymers, ion conductivity of alkali metal ions (especially lithium ions) And a polymer composition having the same. In addition, these substances may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and ratios.

The ratio of the binder in the positive electrode active material layer is usually 0.1% by weight or more and 80% by weight or less. If the proportion of the binder is too low, the positive electrode active material cannot be sufficiently retained and the positive electrode has insufficient mechanical strength, which may deteriorate battery performance such as cycle characteristics. Battery capacity and conductivity may be reduced.
The positive electrode active material layer usually contains a conductive material in order to increase conductivity. There are no particular restrictions on the type, but specific examples include metal materials such as copper and nickel, graphite such as natural graphite and artificial graphite, carbon black such as acetylene black, and amorphous carbon such as needle coke. And carbon materials. In addition, these substances may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and ratios. The proportion of the conductive material in the positive electrode active material layer is usually 0.01% by weight or more and 50% by weight or less. If the proportion of the conductive material is too low, the conductivity may be insufficient, and conversely if it is too high, the battery capacity may be reduced.

  As a liquid medium for forming a slurry, it is possible to dissolve or disperse a lithium transition metal compound powder as a positive electrode material, a binder, and a conductive material and a thickener used as necessary. If it is a solvent, there is no restriction | limiting in particular in the kind, You may use either an aqueous solvent or an organic solvent. Examples of the aqueous solvent include water and alcohol. 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 (THF), toluene, acetone, dimethyl ether, dimethylacetamide, hexamethylphosphalamide, dimethyl sulfoxide, benzene, xylene, quinoline, pyridine, methylnaphthalene, hexane, etc. be able to. In particular, when an aqueous solvent is used, a dispersant is added together with the thickener, and a slurry such as SBR is slurried. In addition, these solvents may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.

The content ratio of the lithium transition metal-based compound powder as the positive electrode material in the positive electrode active material layer is usually 10% by weight or more and 99.9% by weight or less. If the proportion of the lithium transition metal compound powder in the positive electrode active material layer is too large, the strength of the positive electrode tends to be insufficient, and if it is too small, the capacity may be insufficient.
The thickness of the positive electrode active material layer is usually about 10 to 200 μm.

The electrode density after pressing the positive electrode is usually 2.2 g / cm ³ or more and 4.2 g / cm ³ or less.
The positive electrode active material layer obtained by coating and drying is preferably consolidated by a roller press or the like in order to increase the packing density of the positive electrode active material.
Thus, a positive electrode for a lithium secondary battery can be prepared.

2-3. Separator Normally, a separator is interposed between the positive electrode and the negative electrode in order to prevent a short circuit. In this case, the nonaqueous electrolytic solution of the present invention is usually used by impregnating the separator.
The material and shape of the separator are not particularly limited, and known ones can be arbitrarily adopted as long as the effects of the present invention are not significantly impaired. Among them, a resin, glass fiber, inorganic material, etc. formed of a material that is stable with respect to the non-aqueous electrolyte solution of the present invention is used, and a porous sheet or a nonwoven fabric-like material having excellent liquid retention properties is used. Is preferred.

  As materials for the resin and glass fiber separator, for example, polyolefins such as polyethylene and polypropylene, aromatic polyamides, polytetrafluoroethylene, polyethersulfone, glass filters and the like can be used. Of these, glass filters and polyolefins are preferred, and polyolefins are more preferred. These materials may be used individually by 1 type, and may use 2 or more types together by arbitrary combinations and a ratio.

  The thickness of the separator is arbitrary, but is usually 1 μm or more, preferably 5 μm or more, more preferably 10 μm or more, and usually 50 μm or less, preferably 40 μm or less, more preferably 30 μm or less. If the separator is too thin than the above range, the insulating properties and mechanical strength may decrease. On the other hand, if it is thicker than the above range, not only the battery performance such as the rate characteristic may be lowered, but also the energy density of the whole non-aqueous electrolyte secondary battery may be lowered.

Furthermore, when using a porous material such as a porous sheet or nonwoven fabric as the separator, the porosity of the separator is arbitrary, but is usually 20% or more, preferably 35% or more, more preferably 45% or more, Further, it is usually 90% or less, preferably 85% or less, and more preferably 75% or less. If the porosity is too smaller than the above range, the membrane resistance tends to increase and the rate characteristics tend to deteriorate. Moreover, when larger than the said range, it exists in the tendency for the mechanical strength of a separator to fall and for insulation to fall.

Moreover, although the average pore diameter of a separator is also arbitrary, it is 0.5 micrometer or less normally, 0.2 micrometer or less is preferable, and it is 0.05 micrometer or more normally. If the average pore diameter exceeds the above range, a short circuit tends to occur. On the other hand, below the above range, the film resistance may increase and the rate characteristics may deteriorate.
On the other hand, as inorganic materials, for example, oxides such as alumina and silicon dioxide, nitrides such as aluminum nitride and silicon nitride, and sulfates such as barium sulfate and calcium sulfate are used. Used.

  As the form, a thin film shape such as a non-woven fabric, a woven fabric, or a microporous film is used. In the thin film shape, those having a pore diameter of 0.01 to 1 μm and a thickness of 5 to 50 μm are preferably used. In addition to the above-described independent thin film shape, a separator formed by forming a composite porous layer containing the inorganic particles on the surface layer of the positive electrode and / or the negative electrode using a resin binder can be used. For example, a porous layer may be formed by using alumina particles having a 90% particle size of less than 1 μm on both surfaces of the positive electrode and using a fluororesin as a binder.

  The characteristics of the separator in the non-electrolyte secondary battery can be grasped by the Gurley value. The Gurley value indicates the difficulty of air passage in the film thickness direction, and is expressed as the number of seconds required for 100 ml of air to pass through the film. It means that it is harder to go through. That is, a smaller value means better communication in the thickness direction of the film, and a larger value means lower communication in the thickness direction of the film. Communication is the degree of connection of holes in the film thickness direction. If the Gurley value of the separator of the present invention is low, it can be used for various purposes. For example, when used as a separator for a non-aqueous lithium secondary battery, a low Gurley value means that lithium ions can be easily transferred and is preferable because of excellent battery performance. Although the Gurley value of a separator is arbitrary, Preferably it is 10-1000 second / 100ml, More preferably, it is 15-800 second / 100ml, More preferably, it is 20-500 second / 100ml. If the Gurley value is 1000 seconds / 100 ml or less, the electrical resistance is substantially low, which is preferable as a separator.

2-4. Battery design <Electrode group>
The electrode group has a laminated structure in which the positive electrode plate and the negative electrode plate are interposed through the separator, and a structure in which the positive electrode plate and the negative electrode plate are wound in a spiral shape through the separator. Either is acceptable. The ratio of the volume of the electrode group to the internal volume of the battery (hereinafter referred to as the electrode group occupation ratio) is usually 40% or more, preferably 50% or more, and usually 90% or less, preferably 80% or less. .

  When the electrode group occupancy is below the above range, the battery capacity decreases. Also, if the above range is exceeded, the void space is small, the battery expands, and the member expands or the vapor pressure of the electrolyte liquid component increases and the internal pressure rises. In some cases, the gas release valve that lowers various characteristics such as storage at high temperature and the like, or releases the internal pressure to the outside is activated.

<Exterior case>
The material of the outer case is not particularly limited as long as it is a substance that is stable with respect to the non-aqueous electrolyte used. Specifically, a nickel-plated steel plate, stainless steel, aluminum, an aluminum alloy, a metal such as a magnesium alloy, or a laminated film (laminate film) of a resin and an aluminum foil is used. From the viewpoint of weight reduction, an aluminum or aluminum alloy metal or a laminate film is preferably used.

  In an exterior case using metals, the metal is welded together by laser welding, resistance welding, or ultrasonic welding to form a sealed sealed structure, or a caulking structure using the above metals via a resin gasket. Things. Examples of the outer case using the laminate film include a case where a resin-sealed structure is formed by heat-sealing resin layers. In order to improve sealing performance, a resin different from the resin used for the laminate film may be interposed between the resin layers. In particular, when a resin layer is heat-sealed through a current collecting terminal to form a sealed structure, a metal and a resin are joined, so that a resin having a polar group or a modified group having a polar group introduced as an intervening resin is used. Resins are preferably used.

<Protective element>
Protection elements such as PTC (Positive Temperature Coefficient), thermal fuse, thermistor, which increases resistance when abnormal heat is generated or excessive current flows, shuts off current flowing through the circuit due to sudden increase in battery internal pressure or internal temperature during abnormal heat generation A valve (current cutoff valve) or the like can be used. It is preferable to select a protective element that does not operate under normal use at a high current, and it is more preferable that the protective element is designed so as not to cause abnormal heat generation or thermal runaway even without the protective element.

<Exterior body>
The non-aqueous electrolyte secondary battery of the present invention is usually configured by housing the non-aqueous electrolyte, the negative electrode, the positive electrode, the separator, and the like in an exterior body. This exterior body is not particularly limited, and any known one can be arbitrarily adopted as long as the effects of the present invention are not significantly impaired. Specifically, the material of the exterior body is arbitrary, but usually, for example, nickel-plated iron, stainless steel, aluminum or an alloy thereof, nickel, titanium, or the like is used.

  The shape of the exterior body is also arbitrary, and may be any of a cylindrical shape, a square shape, a laminate shape, a coin shape, a large size, and the like.

EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples, but the present invention is not limited to these examples.
The compounds represented by formula (1) used in this example are shown below.

  The compounds having at least one halogen atom used in this example are shown below.

<Examples 1 and 2 and Comparative Examples 1 to 6 (battery evaluation)>
[Example 1]
[Preparation of non-aqueous electrolyte]
Under a dry argon atmosphere, 1.0 mol of LiPF ₆ was added to a mixture (volume ratio 30:70) of ethylene carbonate (hereinafter sometimes referred to as EC) and dimethyl carbonate (hereinafter sometimes referred to as DMC). A vinyl electrolyte containing 147 mass ppm of 3-chloro-1-propyne (hereinafter sometimes referred to as CP) with respect to the standard electrolyte. An electrolyte solution was prepared by adding 0.5% by mass of sulfonic acid-2-propynyl (hereinafter sometimes referred to as compound (A)).
In addition, content of CP in this non-aqueous electrolyte is 0.74 mass ppm with respect to a reference | standard electrolyte.

[Production of positive electrode]
97% by mass of lithium cobaltate (LiCoO ₂ ) as a positive electrode active material, 1.5% by mass of acetylene black as a conductive material, and 1.5% by mass of polyvinylidene fluoride (PVdF) as a binder, N-methylpyrrolidone Slurry by mixing in a solvent. This was uniformly applied, dried and pressed on one side of an aluminum foil. Thereafter, it was punched into a disk shape having a diameter of 12.5 mm to obtain a positive electrode for a non-aqueous electrolyte battery (coin type).

[Manufacture of negative electrode]
100 parts by weight of graphite powder as the negative electrode active material, 1 part by weight of aqueous dispersion of sodium carboxymethyl cellulose (concentration of 1% by weight of sodium carboxymethyl cellulose) as the thickener and binder, respectively, and aqueous dispersion of styrene-butadiene rubber 1 part by mass (concentration of styrene-butadiene rubber 50% by mass) was added and mixed with a disperser to form a slurry. This slurry was uniformly applied to one side of a 12 μm thick copper foil, dried and then pressed. Thereafter, it was punched into a disk shape having a diameter of 12.5 mm to obtain a negative electrode for a non-aqueous electrolyte battery (coin type). Hereinafter, this is referred to as a carbon negative electrode.

[Manufacture of non-aqueous electrolyte batteries (coin type)]
Using the above positive electrode and negative electrode and the non-aqueous electrolyte prepared in each Example and Comparative Example, a coin-type cell was produced by the following procedure. That is, the negative electrode was placed through a polyethylene separator impregnated with an electrolytic solution on a positive electrode accommodated in a stainless steel can body also serving as a positive electrode conductor. The can body and a sealing plate serving also as a negative electrode conductor were caulked and sealed via an insulating gasket to produce a coin-type cell.

[Rate characteristics evaluation]
A non-aqueous electrolyte battery (coin type) was CCCV charged (0.05 C cut) to 4.1 V at a current corresponding to 0.2 C at 25 ° C., and then discharged to 3 V at a constant current of 0.2 C. Next, after CCCV charge (0.05 C cut) to 4.33 V at 0.2 C, the battery was discharged to 3 V at 0.2 C. Again, after CCCV charge (0.05C cut) to 4.33V at 0.2C, the battery was discharged to 3V at 0.2C to obtain a 0.2C capacity.

Again, after CCCV charge (0.05C cut) to 4.2V at 0.2C, 3V at 1C
1C capacity was determined. Then, an initial 1C rate characteristic (%) was obtained from a calculation formula of (1C capacity) ÷ (0.2C capacity) × 100.
Here, 1C represents a current value for discharging the reference capacity of the battery in one hour, and for example, 0.2C represents a current value of 1/5 thereof.

[High temperature storage characteristics evaluation]
After the initial capacity evaluation, the non-aqueous electrolyte battery was CCCV charged (0.05 C cut) at 25 ° C. to 4.33 V at 0.2 C, and then stored at 85 ° C. for 24 hours at a high temperature. Went. After the battery was sufficiently cooled, the voltage after storage was measured to obtain the voltage (V) after storage.
Rate characteristics were evaluated using this non-aqueous electrolyte battery. The evaluation results are shown in Table 1, FIG. 1 and FIG.

[Example 2]
In the electrolyte solution of Example 1-1, instead of adding 0.5 mass% of the compound (A) containing 147 mass ppm of CP, 0.5 mass of the compound (A) containing 2.0 mass% of CP A non-aqueous electrolyte battery was produced in the same manner as in Example 1 except that% addition was performed, and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 100.0 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 1]
Example 1 except that 0.13 mass ppm of CP was added to the reference electrolyte solution instead of adding 0.5 mass% of the compound (A) containing 147 mass ppm of CP in the electrolyte solution of Example 1. In the same manner as above, a non-aqueous electrolyte battery was prepared and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 0.13 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 2]
Example 1 except that in the electrolytic solution of Example 1, 0.54 mass% of the compound (A) containing 147 mass ppm of CP was added, 0.74 mass ppm of CP was added to the reference electrolytic solution. In the same manner as above, a non-aqueous electrolyte battery was prepared and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 0.74 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 3]
Example 1 except that in the electrolytic solution of Example 1, 0.5% by mass of the compound (A) containing 147 mass ppm of CP was added, 100.0 mass ppm of CP was added to the reference electrolytic solution. In the same manner as above, a non-aqueous electrolyte battery was prepared and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 100.0 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 4]
Example 1 except that in the electrolytic solution of Example 1, 0.5 wt% of the compound (A) containing 147 mass ppm of CP was added, 500.0 mass ppm of CP was added to the reference electrolytic solution. In the same manner as above, a non-aqueous electrolyte battery was prepared and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 500.0 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 5]
In the electrolyte solution of Example 1, instead of adding 0.5 mass% of the compound (A) containing 147 mass ppm of CP, the compound (A) containing 25.0 mass ppm of CP with respect to the reference electrolyte solution A non-aqueous electrolyte battery was produced in the same manner as in Example 1 except that 0.5% by mass was added, and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 0.13 mass ppm with respect to a reference | standard electrolyte.

[Comparative Example 6]
Instead of adding 0.5% by mass of the compound (A) containing 147 mass ppm of CP in the electrolyte solution of Example 1, 0.5% of the compound (A) containing 10% CP with respect to the reference electrolyte solution was used. A non-aqueous electrolyte battery was produced in the same manner as in Example 1 except for adding mass%, and rate characteristics were evaluated. The evaluation results are shown in Table 1, FIG. 1 and FIG.
In addition, content of CP in this non-aqueous electrolyte is 500.0 mass ppm with respect to a reference | standard electrolyte.

  * The initial 1C rates of Examples 1 and 2 and Comparative Examples 1 to 6 are relative values when Comparative Example 1 is 100%. Further, the improvement rate shown in Example 1 is an increase / decrease with respect to the value of each rate characteristic of Comparative Example 2, and the improvement rate shown in Example 2 is an increase / decrease with respect to the value of the rate characteristic of Comparative Example 3. The improvement rate shown in Comparative Example 5 is an increase / decrease relative to the value of the rate characteristic of Comparative Example 1, and the improvement rate shown in Comparative Example 6 is an increase / decrease relative to the value of the rate characteristic of Comparative Example 4 Minutes.

From Table 1, when the non-aqueous electrolyte solution of Example 1 and Example 2 according to the first invention is used, the compound having at least one chlorine atom is added alone (Comparative Examples 1 to 4). In comparison, it can be seen that the 1C rate characteristics and the voltage after storage are excellent. This is clear from the improvement rate. In addition, when the compound represented by the formula (1) and the compound having at least one chlorine atom exceed the addition amount range described in the present invention (Comparative Examples 5 and 6), the voltage is improved after storage. The 0.5C and 1C rate characteristics are insufficient. This is clear from the improvement rate.

This factor is considered as follows. By adding a compound represented by the formula (1) and a compound having at least one halogen atom, a negative electrode film having high lithium conductivity is formed. Moreover, since this film formation reaction proceeds efficiently, a decomposition product of the compound represented by the formula (1) is hardly generated. These effects are comprehensively exhibited and the rate characteristics are improved. Furthermore, since the produced negative electrode film has high thermal stability, the elution during the storage test and the contribution of oxidation at the positive electrode are reduced, and as a result, the battery voltage drop during the storage test is suppressed.
On the other hand, when the amount of the compound having at least one chlorine atom is increased, a large amount of lithium chloride is generated on the electrode surface, so that the resistance at the electrode interface is increased. As a result, the rate characteristic improvement effect becomes insufficient. Therefore, from the viewpoint of improving the rate characteristics, it is preferable to limit the addition amount of the compound having at least one halogen atom to a specified range.

  According to the non-aqueous electrolyte solution of the present invention, capacity deterioration and gas generation during high-temperature storage of a non-aqueous electrolyte battery can be improved. Therefore, the non-aqueous electrolyte solution of the present invention and the non-aqueous electrolyte battery using the same can be used for various known applications. Specific examples include notebook computers, pen input computers, mobile computers, electronic book players, mobile phones, mobile faxes, mobile copy, mobile printers, headphone stereos, video movies, LCD TVs, handy cleaners, portable CDs, minidiscs, etc. , Walkie Talkie, Electronic Notebook, Calculator, Memory Card, Portable Tape Recorder, Radio, Backup Power Supply, Motor, Automobile, Motorcycle, Motorbike, Bicycle, Lighting Equipment, Toy, Game Equipment, Clock, Electric Tool, Strobe, Camera, Load Examples include leveling power sources and natural energy storage power sources.

Claims (6)

A non-aqueous electrolyte solution for a non-aqueous electrolyte battery comprising a positive electrode and a negative electrode capable of occluding and releasing metal ions, the non-aqueous electrolyte solution together with an electrolyte and a non- aqueous solvent,
(A) A compound having an alkynyloxy group in the structure represented by the following formula (1) is represented by the following formula (2) in a non-aqueous electrolyte solution in an amount of 0.01% by mass to 5% by mass. is a compound having a molecular weight 55 to 200 in which a chlorine atom, a non-aqueous electrolytic solution to less than 0.2 ppm by weight 500 ppm by weight,
Nonaqueous electrolyte characterized in that it comprises free.

(In formula (1), R ¹ and R ² are each independently a hydrogen atom, a halogen atom, or an alkyl group, alkenyl group, alkynyl group, aryl group, alkoxy group, cyano group optionally substituted with a halogen atom. An organic group which may have an isocyanato group, an ether group, a carbonate group, a carbonyl group, a carboxyl group, a sulfonyl group and a phosphoryl group, which may be the same or different, but R ¹ or Either one or both of R ² is an organic group containing one or more S═O groups.

(In Formula (2), R ³ is a hydrogen atom, and R ⁴ is an organic group that may have a substituent.)   The compound having a chlorine atom represented by the formula (2) with respect to the compound represented by the formula (1) is contained in an amount of 20 mass ppm to 5 mass%. Non-aqueous electrolyte. The non-aqueous electrolyte solution according to claim 1 or 2 , wherein in the formula (2), R ⁴ is a methylene group which may have a substituent. At least one compound selected from the group consisting of a cyclic carbonate having a fluorine atom, a cyclic carbonate having a carbon-carbon unsaturated bond, a monofluorophosphate, a difluorophosphate, an isocyanate compound, a cyclic sulfonate, and a nitrile compound. The nonaqueous electrolytic solution according to any one of claims 1 to 3 , further comprising: The cyclic carbonate having a fluorine atom is at least one compound selected from the group consisting of monofluoroethylene carbonate, 4,4-difluoroethylene carbonate, and 4,5-difluoroethylene carbonate, and has a carbon-carbon unsaturated bond. The cyclic carbonate is vinylene carbonate, vinyl ethylene carbonate, ethynyl ethylene carbonate, the isocyanate compound is a compound having at least two isocyanate groups, and the nitrile compound is a compound having at least two nitrile groups. Item 5. A nonaqueous electrolytic solution according to Item 4 . A non-aqueous electrolyte secondary battery comprising a negative electrode and a positive electrode capable of inserting and extracting lithium ions, and a non-aqueous electrolyte solution, wherein the non-aqueous electrolyte solution is a non-aqueous electrolyte according to any one of claims 1 to 5. A non-aqueous electrolyte secondary battery, characterized by being an electrolyte.

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