JPWO2013099735A1 - Non-aqueous electrolyte and power storage device using the same - Google Patents

Abstract

The present invention can improve electrochemical characteristics in a wide temperature range containing an imidyloxy group-containing compound represented by the following general formula (I) in a nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a nonaqueous solvent. A non-aqueous electrolyte and an electricity storage device using the same. (Wherein R1 represents a divalent linking group, and X represents a specific substituent containing a phosphoryl group, a sulfonyl group, etc.)

Description

  The present invention relates to a nonaqueous electrolytic solution capable of improving electrochemical characteristics in a wide temperature range, and an electricity storage device using the same.

In recent years, power storage devices, particularly lithium secondary batteries, have been widely used for small electronic devices such as mobile phones and notebook computers, electric vehicles, and power storage. Since these electronic devices and automobiles may be used in a wide temperature range such as a high temperature in midsummer or a low temperature of extremely cold, it is required to improve electrochemical characteristics in a wide range of temperatures.
In particular, in order to prevent global warming, there is an urgent need to reduce CO ₂ emissions. Among environmentally friendly vehicles equipped with power storage devices consisting of power storage devices such as lithium secondary batteries and capacitors, hybrid electric vehicles ( HEV), plug-in hybrid electric vehicles (PHEV), and battery electric vehicles (BEV) are required to spread quickly. Due to the long travel distance of automobiles, automobiles may be used in areas with a wide temperature range from extremely hot areas in the tropics to extremely cold areas. Therefore, in particular, these in-vehicle power storage devices are required not to deteriorate in electrochemical characteristics even when used in a wide temperature range from high temperature to low temperature.
Note that in this specification, the term lithium secondary battery is used as a concept including a so-called lithium ion secondary battery.

The lithium secondary battery is mainly composed of a positive electrode and a negative electrode containing a material capable of occluding and releasing lithium, a non-aqueous electrolyte composed of a lithium salt and a non-aqueous solvent, and the non-aqueous solvent includes ethylene carbonate (EC), Carbonates such as propylene carbonate (PC) are used.
In addition, as the negative electrode, metal lithium, metal compounds that can occlude and release lithium (metal simple substance, oxide, alloy with lithium, etc.) and carbon materials are known, and in particular, lithium can be occluded and released. Lithium secondary batteries using carbon materials such as coke, artificial graphite and natural graphite have been widely put into practical use.

For example, a lithium secondary battery using a highly crystallized carbon material such as natural graphite or artificial graphite as a negative electrode material is a decomposition product generated by reductive decomposition of a solvent in a non-aqueous electrolyte on the negative electrode surface during charging. It has been found that the gas interferes with the desired electrochemical reaction of the battery, resulting in poor cycle characteristics. Moreover, when the decomposition product of the nonaqueous solvent accumulates, it becomes impossible to smoothly occlude and release lithium into the negative electrode, and the electrochemical characteristics in a wide temperature range are liable to deteriorate.
Furthermore, lithium secondary batteries using lithium metal, alloys thereof, simple metals such as tin or silicon, and oxides as negative electrode materials have high initial capacities, but fine powders progress during the cycle. In comparison, it is known that reductive decomposition of a non-aqueous solvent occurs at an accelerated rate, and battery performance such as battery capacity and cycle characteristics is greatly reduced. In addition, when these anode materials are finely powdered or decomposition products of non-aqueous solvents accumulate, it becomes impossible to smoothly occlude and release lithium into the anode, and the electrochemical characteristics in a wide temperature range are likely to deteriorate. .
On the other hand, a lithium secondary battery using, for example, LiCoO ₂ , LiMn ₂ O ₄ , LiNiO ₂ , LiFePO _4, or the like as the positive electrode has a non-aqueous solvent in a non-aqueous electrolyte charged and a positive electrode material and a non-aqueous electrolyte. It has been found that degradation products and gases generated by partial oxidative decomposition locally at the interface of the battery inhibit the desired electrochemical reaction of the battery, resulting in degradation of electrochemical characteristics over a wide temperature range. Yes.

  As described above, the battery performance has been deteriorated due to the movement of lithium ions or the expansion of the battery due to the decomposition product or gas when the non-aqueous electrolyte is decomposed on the positive electrode or the negative electrode. In spite of such a situation, electronic devices equipped with lithium secondary batteries are becoming more and more multifunctional and power consumption is increasing. As a result, the capacity of lithium secondary batteries has been increasing, and the volume occupied by non-aqueous electrolyte in the battery has become smaller, such as increasing the electrode density and reducing the useless space volume in the battery. . Therefore, the electrochemical characteristics in a wide temperature range are likely to be deteriorated by a slight decomposition of the nonaqueous electrolytic solution.

  Patent Document 1 shows that when succinimidyl acrylate is added to a non-aqueous electrolyte, cycle characteristics and flame retardancy are improved.

JP 2011-228103 A

  An object of the present invention is to provide a nonaqueous electrolytic solution capable of improving electrochemical characteristics in a wide temperature range and an electricity storage device using the same.

The present inventors have examined in detail the performance of the above-described prior art non-aqueous electrolyte. As a result, the non-aqueous electrolyte of Patent Document 1 cannot be said to be sufficiently satisfactory for the problem of improving electrochemical characteristics in a wide temperature range such as low-temperature discharge characteristics after storage at high temperature. It was the actual situation.
Therefore, as a result of intensive studies to solve the above problems, the present inventors have added an imidyloxy group-containing compound having a specific electron-withdrawing group to a non-aqueous electrolyte solution, so that a wide temperature range can be obtained. The inventors have found that the electrochemical characteristics, particularly the electrochemical characteristics of lithium batteries can be improved, and have completed the present invention.

That is, the present invention provides the following (1) and (2).
(1) A nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a nonaqueous solvent, containing an imidyloxy group-containing compound represented by the following general formula (I):

（式中、Ｒ¹は、水素原子がハロゲン原子で置換されていてもよい炭素数２〜６の２価の連結基を示し、Ｘは下記一般式（II）〜（Ｖ）で表される置換基のいずれかを示す。）

(In the formula, R ¹ represents a divalent linking group having 2 to 6 carbon atoms in which a hydrogen atom may be substituted with a halogen atom, and X is represented by the following general formulas (II) to (V)). Indicates any of the substituents.)

（式中、Ｒ²は、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、炭素数６〜１２のアリール基、又は−Ｎ（Ｃ＝Ｏ）₂Ｒ¹で表される基を示す。ただし、Ｒ¹は前記と同義であり、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ² is an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or 6 to 12 carbon atoms. Or a group represented by —N (C═O) ₂ R ¹ , wherein R ¹ is as defined above, and the alkyl group, cycloalkyl group, alkenyl group, alkynyl group, or In the aryl group, the hydrogen atom may be substituted with a halogen atom.)

（式中、Ｒ³及びＲ⁴はそれぞれ独立して、水素原子、ハロゲン原子、炭素数１〜６のアルキル基を示し、Ｒ⁵及びＲ⁶はそれぞれ独立して、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、又は炭素数６〜１２のアリール基を示す。ただし、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ³ and R ⁴ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁵ and R ⁶ each independently represent an alkyl having 1 to 6 carbon atoms. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cyclo (In the alkyl group, alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)

（式中、Ｒ⁷及びＲ⁸はそれぞれ独立して、水素原子、ハロゲン原子、炭素数１〜６のアルキル基を示し、Ｒ⁹はそれぞれ独立して、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、又は炭素数６〜１２のアリール基を示す。ただし、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ⁷ and R ⁸ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁹ each independently represents an alkyl group having 1 to 6 carbon atoms or a carbon atom. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cycloalkyl group, (In the alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)

(2) In an electricity storage device provided with a nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a positive electrode, a negative electrode, and a nonaqueous solvent, the imidyloxy group-containing compound represented by the general formula (I) is contained in the nonaqueous electrolytic solution. An electricity storage device comprising at least one kind.

  According to the present invention, it is possible to provide a non-aqueous electrolyte capable of improving electrochemical characteristics in a wide temperature range, particularly low-temperature discharge characteristics after storage at high temperature, and an electricity storage device such as a lithium battery using the non-aqueous electrolyte.

[Non-aqueous electrolyte]
The nonaqueous electrolytic solution of the present invention contains at least one succinimidyloxy group-containing compound represented by the following general formula (I) in a nonaqueous electrolytic solution in which an electrolyte is dissolved in a nonaqueous solvent. It is characterized by that.

The reason why the non-aqueous electrolyte of the present invention can greatly improve the electrochemical characteristics in a wide temperature range is not clear, but is considered as follows.
The imidyloxy group-containing compound represented by the general formula (I) of the present invention has a plurality of electron-withdrawing groups. For this reason, it undergoes reductive decomposition at a higher potential than the main solvent. Therefore, reductive decomposition on the negative electrode proceeds at a higher potential than that of the main solvent during the first charge, and a film containing a decomposition product of the imidyloxy group-containing compound is formed on the negative electrode surface. It was found that the coating contains a decomposition product of both the imidyloxy group and the substituent X, and therefore has a specific effect of improving the electrochemical characteristics in a wide temperature range from a low temperature to a high temperature. Among them, as the substituent X, if it is a substituent having an ester structure such as phosphoric acid or sulfonic acid as in the general formulas (III) and (IV), electrochemical characteristics in a wide temperature range can be greatly improved. preferable.

The imidyloxy group-containing compound contained in the nonaqueous electrolytic solution of the present invention is represented by the following general formula (I).

（式中、Ｒ¹は、水素原子がハロゲン原子で置換されていてもよい炭素数２〜６の２価の連結基を示し、Ｘは下記一般式（II）〜（Ｖ）で表される置換基のいずれかを示す。）

(In the formula, R ¹ represents a divalent linking group having 2 to 6 carbon atoms in which a hydrogen atom may be substituted with a halogen atom, and X is represented by the following general formulas (II) to (V)). Indicates any of the substituents.)

（式中、Ｒ²は、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、炭素数６〜１２のアリール基、又は−Ｎ（Ｃ＝Ｏ）₂Ｒ¹で表される基を示す。ただし、Ｒ¹は前記と同義であり、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ² is an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or 6 to 12 carbon atoms. Or a group represented by —N (C═O) ₂ R ¹ , wherein R ¹ is as defined above, and the alkyl group, cycloalkyl group, alkenyl group, alkynyl group, or In the aryl group, the hydrogen atom may be substituted with a halogen atom.)

（式中、Ｒ³及びＲ⁴はそれぞれ独立して、水素原子、ハロゲン原子、炭素数１〜６のアルキル基を示し、Ｒ⁵及びＲ⁶はそれぞれ独立して、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、又は炭素数６〜１２のアリール基を示す。ただし、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ³ and R ⁴ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁵ and R ⁶ each independently represent an alkyl having 1 to 6 carbon atoms. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cyclo (In the alkyl group, alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)

（式中、Ｒ⁷及びＲ⁸はそれぞれ独立して、水素原子、ハロゲン原子、炭素数１〜６のアルキル基を示し、Ｒ⁹はそれぞれ独立して、炭素数１〜６のアルキル基、炭素数３〜６のシクロアルキル基、炭素数２〜６のアルケニル基、炭素数３〜６のアルキニル基、又は炭素数６〜１２のアリール基を示す。ただし、前記のアルキル基、シクロアルキル基、アルケニル基、アルキニル基、又はアリール基は、その水素原子がハロゲン原子で置換されていてもよい。）

(In the formula, R ⁷ and R ⁸ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁹ each independently represents an alkyl group having 1 to 6 carbon atoms or a carbon atom. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cycloalkyl group, (In the alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)

In the general formula (I), R ¹ represents a divalent linking group having 2 to 6 carbon atoms in which a hydrogen atom may be substituted with halogen, and has 2 to 4 carbon atoms in which it may be substituted with halogen. Alkanediyl groups are preferred.
Specific examples of R ¹ include ethane-1,2-diyl group, propane-1,2-diyl group, propane-1,3-diyl group, butane-1,2-diyl group, butane-2,3. -Diyl group, 2-methylpropane-1,2-diyl group, butane-1,3-diyl group, butane-1,4-diyl group, pentane-1,2-diyl group, pentane-1,5-diyl Group, alkanediyl group such as hexane-1,2-diyl group, hexane-1,6-diyl, cyclohexane-1,2-diyl group, and alkanediyl halide such as 1-fluoroethane-1,2-diyl group Preferred examples include ethane-1,2-diyl group (ethylene group), propane-1,2-diyl group, propane-1,3-diyl group (trimethylene group), butane-1,2-diyl. Group, butane-2,3-diyl Alkanediyl groups such as 2-methylpropane-1,2-diyl group, butane-1,3-diyl group, butane-1,4-diyl group (tetramethylene group), cyclohexane-1,2-diyl group, An ethane-1,2-diyl group (ethylene group) is more preferable. When R ¹ is an ethane-1,2-diyl group (ethylene group), the imidyloxy group-containing compound represented by the general formula (I) is a succinimidyloxy group-containing compound.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

In the general formula (II), preferable R ² is an alkyl group having 1 to 4 carbon atoms which may be substituted with a halogen atom, or a cycloalkyl group having 5 to 6 carbon atoms which may be substituted with a halogen atom. , An alkenyl group having 2 to 4 carbon atoms which may be substituted with a halogen atom, an alkynyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, and 6 to 6 carbon atoms which may be substituted with a halogen atom 10 aryl groups, or a succinimidyloxy group. Among these, an alkenyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, an alkynyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, or a carbon which may be substituted with a halogen atom An aryl group having 6 to 8 carbon atoms or a succinimidyloxy group is more preferable, and an alkenyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, or 3 to 3 carbon atoms which may be substituted with a halogen atom. More preferred are 4 alkynyl groups or succinimidyloxy groups.

Specific examples of R ² include
Straight chain alkyl group such as methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, iso-propyl group, sec-butyl group, tert-butyl group, tert- A branched alkyl group such as an amyl group, an alkyl group in which a part of hydrogen atoms such as a fluoromethyl group, a trifluoromethyl group, and a 2,2,2-trifluoroethyl group are substituted with a fluorine atom;
Linear chain such as vinyl group, 2-propen-1-yl group, 2-buten-1-yl group, 3-buten-1-yl group, 4-penten-1-yl group, and 5-hexen-1-yl group Alkenyl group, 3-buten-2-yl group, 2-methyl-1-propen-1-yl group, 2-methyl-2-propen-1-yl group, 3-penten-2-yl group, 2- A branched alkenyl group such as methyl-3-buten-2-yl group and 3-methyl-2-buten-1-yl group;
Linear alkynyl such as 2-propyn-1-yl group, 2-butyn-1-yl group, 3-butyn-1-yl group, 4-pentyn-1-yl group, and 5-hexyn-1-yl group Branched alkynyl groups such as a group, 3-butyn-2-yl group, 3-pentyn-2-yl group, 2-methyl-3-butyn-2-yl group;
Cycloalkyl groups such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, phenyl group, 2-methylphenyl group, 3-methylphenyl group, 4-methylphenyl group, 4-tert-butylphenyl group, 2,4 , 6-trimethylphenyl group, 2-fluorophenyl group, 3-fluorophenyl group, 4-fluorophenyl group, 2,4-difluorophenyl group, 2,6-difluorophenyl group, 3,4-difluorophenyl group, 2 , 4,6-trifluorophenyl group, pentafluorophenyl group, 2-trifluoromethylphenyl group, 4-trifluoromethylphenyl group and the like aryl groups.
Among these, methyl group, ethyl group, n-propyl group, iso-propyl group, cyclopentyl group, cyclohexyl group, 2,2,2-trifluoroethyl group, 2-propen-1-yl group, 2-propyne- 1-yl group, 2-butyn-1-yl group, 2-fluorophenyl group, 3-fluorophenyl group, 4-fluorophenyl group, 2,4-difluorophenyl group, 2,6-difluorophenyl group, pentafluoro More preferred is a phenyl group, a 2-trifluoromethylphenyl group, or a succinimidyloxy group, a 2-propen-1-yl group, a 2-propyn-1-yl group, a 2-butyn-1-yl group, or A succinimidyloxy group is more preferred.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

In the general formula (III), preferred examples of R ³ and R ⁴ include a hydrogen atom and an alkyl group having 1 to 4 carbon atoms.
Specific examples of R ³ and R ⁴ include hydrogen atom, fluorine atom, chlorine atom, bromine atom, methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, Examples include iso-propyl group, sec-butyl group, and tert-butyl group.
Among these, a hydrogen atom, a fluorine atom, a methyl group, or an ethyl group is preferable, and a hydrogen atom or a methyl group is more preferable.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

In the general formula (III), preferable examples of R ⁵ and R ⁶ include an alkyl group having 1 to 4 carbon atoms which may be substituted with a halogen atom, and 5 to 6 carbon atoms which may be substituted with a halogen atom. A cycloalkyl group, an alkenyl group having 2 to 4 carbon atoms that may be substituted with a halogen atom, an alkynyl group having 3 to 4 carbon atoms that may be substituted with a halogen atom, or a carbon that may be substituted with a halogen atom An aryl group of several 6-10 is mentioned. Among these, an alkyl group having 1 to 4 carbon atoms which may be substituted with a halogen atom, or an aryl group having 6 to 8 carbon atoms which may be substituted with a halogen atom is more preferable, and has 1 to 4 carbon atoms. More preferred is an alkyl group.

Specific examples of R ⁵ and R ⁶ include the branched alkyl group, the alkyl group in which a part of the hydrogen atoms are substituted with fluorine atoms, the straight chain alkenyl group, and the like as the specific examples of R ² . Examples include aryl groups such as branched alkenyl groups, linear alkynyl groups, branched alkynyl groups, cycloalkyl groups, various phenyl groups, and various fluorine-substituted phenyl groups.
Among these, methyl group, ethyl group, n-propyl group, iso-propyl group, cyclopentyl group, cyclohexyl group, 2,2,2-trifluoroethyl group, 2-propen-1-yl group, 2-propyne- A 1-yl group, a 2-butyn-1-yl group, a phenyl group, a 4-fluorophenyl group, or a 2-trifluoromethylphenyl group is preferable, and a methyl group, an ethyl group, or an n-propyl group is more preferable.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

In the general formula (IV), preferable examples of R ⁷ and R ⁸ include a hydrogen atom and an alkyl group having 1 to 4 carbon atoms.
Specific examples of R ⁷ and R ⁸ include hydrogen atom, fluorine atom, chlorine atom, bromine atom, methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, Examples include iso-propyl group, sec-butyl group, and tert-butyl group.
Among these, a hydrogen atom, a fluorine atom, a methyl group, or an ethyl group is preferable, and a hydrogen atom or a methyl group is more preferable.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

In the general formula (IV), preferable R ⁹ is an alkyl group having 1 to 4 carbon atoms which may be substituted with a halogen atom, or a cycloalkyl group having 5 to 6 carbon atoms which may be substituted with a halogen atom. , An alkenyl group having 2 to 4 carbon atoms which may be substituted with a halogen atom, an alkynyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, or 6 carbon atoms which may be substituted with a halogen atom Is preferably an aryl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 4 carbon atoms which may be substituted with a halogen atom, an alkynyl group having 3 to 4 carbon atoms which may be substituted with a halogen atom, or a halogen atom. An aryl group having 6 to 8 carbon atoms which may be present is more preferable, and an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 8 carbon atoms is more preferable.

Specific examples of R ⁹ include the branched alkyl group, the alkyl group in which a part of the hydrogen atoms are substituted with fluorine atoms, the straight chain alkenyl group, the branched chain, which are exemplified as the specific examples of R ^2. Aryl groups such as alkenyl groups, linear alkynyl groups, branched alkynyl groups, cycloalkyl groups, various phenyl groups, and various fluorine-substituted phenyl groups.
Among these, methyl group, ethyl group, n-propyl group, iso-propyl group, 2,2,2-trifluoroethyl group, vinyl group, 2-propen-1-yl group, 2-propyn-1-yl Group, 2-butyn-1-yl group, phenyl group or 4-methylphenyl group is preferable, and methyl group, ethyl group, n-propyl group, phenyl group or 4-methylphenyl group is more preferable.
The range of the above substituent is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

Specific examples of the compound represented by the general formula (I) include the following.
When X is general formula (II), the following compounds A1-A27 are mentioned suitably.

  As a case where X is general formula (III), the following compounds B1 to B20 are preferably exemplified.

  As a case where X is the general formula (IV), the following compounds C1 to C25 are preferably exemplified.

Among the imidyloxy group-containing compounds represented by the general formula (I), X is preferably a compound represented by the general formula (III) or (IV), and more preferably a compound represented by the general formula (III).
Specific examples thereof include one or two selected from the compounds having the structures A1, A17 to A19, B1, B10, B13, B14, C1, C10, C13, C14, C19, C20, C24, and C25. More than species.

Among these, bis (2,5-dioxopyrrolidin-1-yl) oxalate (compound A1), 2,5-dioxopyrrolidin-1-yl 2- (diethoxyphosphoryl) acetate (compound B1), 2, 5-dioxopyrrolidin-1-yl 2- (diethoxyphosphoryl) propanoate (compound B10), 2,5-dioxopyrrolidin-1-yl 2- (dimethoxyphosphoryl) acetate (compound B13), 2,5-di Oxopyrrolidin-1-yl 2- (dipropoxyphosphoryl) acetate (compound B14), 2,5-dioxopyrrolidin-1-yl (2- (methanesulfonyl) oxy) propanoate (compound C1), 2,5-di Oxopyrrolidin-1-yl (2- (ethanesulfonyl) oxy) propanoate (Compound C13), 2,5-dioxopyrrolidin-1-yl (2- (4-methylphenylsulfonyl) oxy) acetate (Compound C20) and 2,5-dioxopyrrolidin-1-yl (2- (4-methylphenylsulfonyl) One or more selected from) oxy) propanoate (compound C25) is more preferred.
In the case of the range of the above compounds, it is preferable because electrochemical characteristics in a wide temperature range can be greatly improved.

  In the nonaqueous electrolytic solution of the present invention, the content of the imidyloxy group-containing compound represented by the general formula (I) contained in the nonaqueous electrolytic solution is 0.001 to 10% by mass in the nonaqueous electrolytic solution. preferable. When the content is 10% by mass or less, there is little possibility that a coating film is excessively formed on the electrode and the low-temperature characteristics are deteriorated. The effect of improving storage characteristics is enhanced. The content is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.3% by mass or more, and the upper limit is preferably 7% by mass or less in the non-aqueous electrolyte. 5 mass% or less is more preferable, and 3 mass% or less is still more preferable.

  In the non-aqueous electrolyte solution of the present invention, the compound represented by the general formula (I) can be combined with a non-aqueous solvent, an electrolyte salt, and other additives described below, so that electrochemical characteristics in a wide temperature range can be obtained. It produces a unique effect of synergistic improvement.

[Nonaqueous solvent]
Examples of the nonaqueous solvent used in the nonaqueous electrolytic solution of the present invention include cyclic carbonates, chain esters, lactones, ethers, amides, sulfones, etc., but only cyclic carbonates, or both cyclic carbonates and chain esters. Is preferably included.
The term chain ester is used as a concept including chain carbonate and chain carboxylic acid ester.
Examples of the cyclic carbonate include ethylene carbonate (EC), propylene carbonate (PC), 1,2-butylene carbonate, 2,3-butylene carbonate, 4-fluoro-1,3-dioxolan-2-one (FEC), trans or Cis-4,5-difluoro-1,3-dioxolan-2-one (hereinafter collectively referred to as “DFEC”), vinylene carbonate (VC), vinyl ethylene carbonate (VEC), and 4-ethynyl-1 , 3-dioxolan-2-one (EEC).
Among these, in addition to ethylene carbonate, at least one of cyclic carbonates having a methyl group at the 4-position of ethylene carbonate, that is, propylene carbonate (PC), carbon-carbon double bonds, or cyclic carbonates having a fluorine atom is used. Then, since the low-temperature discharge characteristic after high temperature charge storage improves further, it is preferable, and it is more preferable that both the cyclic carbonate which has a carbon-carbon double bond, and the cyclic carbonate which has a fluorine atom are included. The cyclic carbonate having a carbon-carbon double bond is preferably one or two selected from VC and VEC, and the cyclic carbonate having a fluorine atom is preferably one or two selected from FEC and DFEC.

The content of the cyclic carbonate having a carbon-carbon double bond is preferably 0.07% by volume or more, more preferably 0.2% by volume or more, still more preferably 0.7% by volume based on the total volume of the nonaqueous solvent. The upper limit is preferably 7% by volume or less, more preferably 4% by volume or less, and still more preferably 2.5% by volume or less. Within the above range, the stability of the coating during storage at high temperature can be further increased without impairing the Li ion permeability at low temperatures, which is preferable.
The content of the cyclic carbonate having a fluorine atom is preferably 0.07% by volume or more, more preferably 4% by volume or more, and further preferably 7% by volume or more with respect to the total volume of the nonaqueous solvent. Is preferably 35% by volume or less, more preferably 25% by volume or less, and even more preferably 15% by volume or less, further increasing the stability of the coating during storage at high temperature without impairing the Li ion permeability at low temperatures. This is preferable.
Further, when the non-aqueous solvent contains EC, PC, or both EC and PC, the resistance of the film formed on the electrode is reduced, and the content of EC, PC, or both EC and PC is preferably Preferably it is 3 volume% or more with respect to the total volume of a nonaqueous solvent, More preferably, it is 5 volume% or more, More preferably, it is 7 volume% or more, As an upper limit, Preferably it is 45 volume% or less, More preferably, it is 35 volume%. Volume% or less, More preferably, it is 25 volume% or less.

These cyclic carbonates may be used singly or in combination of two or more, since electrochemical characteristics in a wide temperature range are improved, and it is more preferable to use a combination of three or more. preferable.
Preferred combinations of these cyclic carbonates include EC and VC, EC and PC, PC and VC, VC and FEC, EC and FEC, PC and FEC, FEC and DFEC, EC and DFEC, PC and DFEC, VC and DFEC , VC and EEC, EC and EEC, VEC and DFEC, EC and PC and VC, EC and PC and FEC, EC and VC and FEC, EC and VC and VEC, EC and VC and EEC, EC and VC and EEC, EC and PC and EEC, EC And EEC and FEC, PC and VC and FEC, EC and VC and DFEC, PC and VC and DFEC, EC and PC and VC and FEC, EC and PC and VC and DFEC and the like are preferable. Of the above combinations, EC and VC, EC and PC, EC and FEC, PC and FEC, EC and PC and VC, EC and PC and FEC, EC and VC and FEC, PC and VC and FEC, EC and PC A combination of VC and FEC is more preferable, EC and VC, EC and PC, EC and PC and VC, EC and VC and FEC, PC and VC and FEC, EC and VC and EEC, EC and PC and EEC, EC and A combination of EEC and FEC, EC, PC, VC and FEC is more preferable, and a combination of EC and VC, EC and PC, EC, PC and VC is particularly preferable.

Examples of chain esters include asymmetric chain carbonates such as methyl ethyl carbonate (MEC), methyl propyl carbonate (MPC), methyl isopropyl carbonate (MIPC), methyl butyl carbonate, and ethyl propyl carbonate, dimethyl carbonate (DMC), and diethyl carbonate ( DEC), symmetric chain carbonates such as dipropyl carbonate and dibutyl carbonate, pivalate esters such as methyl pivalate, ethyl pivalate, and propyl pivalate, chains such as methyl propionate, ethyl propionate, methyl acetate, and ethyl acetate One type or two or more types selected from carboxylic acid esters are preferred.
The content of the chain ester is not particularly limited, but it is preferably used in the range of 60 to 90% by volume with respect to the total volume of the nonaqueous solvent. If the content is 60% by volume or more, the effect of lowering the viscosity of the non-aqueous electrolyte is sufficiently obtained, and if it is 90% by volume or less, the electrical conductivity of the non-aqueous electrolyte is sufficiently increased, and in a wide temperature range. The above-mentioned range is preferable since the electrochemical characteristics of the above are improved.

Among the chain esters, chain esters having a methyl group selected from dimethyl carbonate, methyl ethyl carbonate, methyl propyl carbonate, methyl isopropyl carbonate, methyl butyl carbonate, methyl propionate, methyl acetate, and ethyl acetate are preferable, particularly methyl. A chain carbonate having a group is preferred.
Moreover, when using chain carbonate, it is preferable to use 2 or more types. Further, it is more preferable that both a symmetric chain carbonate and an asymmetric chain carbonate are contained, and it is further more preferable that the content of the symmetric chain carbonate is more than that of the asymmetric chain carbonate.
The volume ratio of the symmetric chain carbonate in the chain carbonate is preferably 51% by volume or more, and more preferably 55% by volume or more. As an upper limit, 95 volume% or less is more preferable, and it is still more preferable in it being 85 volume% or less. It is particularly preferred that the symmetric chain carbonate contains dimethyl carbonate. The asymmetric chain carbonate preferably has a methyl group, and methyl ethyl carbonate is particularly preferable.
The above case is preferable because electrochemical characteristics in a wider temperature range are improved.

  The ratio of the cyclic carbonate to the chain ester is preferably 10:90 to 45:55, and 15:85 to 40:55, from the viewpoint of improving the electrochemical properties in a wide temperature range. 60 is more preferable, and 20:80 to 35:65 is still more preferable.

  Examples of other non-aqueous lactones include γ-butyrolactone, γ-valerolactone, α-angelica lactone, and the like. Examples of ethers include tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane, 1,3- Examples include cyclic ethers such as dioxane and 1,4-dioxane, and chain ethers such as 1,2-dimethoxyethane, 1,2-diethoxyethane, and 1,2-dibutoxyethane. As the amide, dimethylformamide Suitable examples of the sulfone include sulfolane.

  The above non-aqueous solvents are usually used as a mixture in order to achieve appropriate physical properties. The combination includes, for example, a combination of a cyclic carbonate and a chain carbonate, a combination of a cyclic carbonate and a chain carboxylic acid ester, a combination of a cyclic carbonate, a chain carbonate and a lactone, and a combination of a cyclic carbonate, a chain carbonate and an ether. A combination, a combination of a cyclic carbonate, a chain carbonate, and a chain carboxylate, and the like are preferable.

For the purpose of improving electrochemical characteristics over a wider temperature range, it is preferable to add other additives to the non-aqueous electrolyte.
Specific examples of other additives include at least one selected from a phosphate ester compound, an isocyanate, an S═O bond-containing compound, a nitrile, an acid anhydride, an aromatic compound, and a cyclic phosphazene compound.
Examples of the phosphoric acid ester compound include trimethyl phosphate, tributyl phosphate, and trioctyl phosphate, among which trimethyl phosphate is preferable.
Preferred examples of the isocyanate include diisocyanates such as tetramethylene diisocyanate, hexamethylene diisocyanate, and octamethylene diisocyanate. Among them, hexamethylene diisocyanate is preferable.
Examples of the compound containing S═O bond include 1,3-propane sultone, 1,3-butane sultone, 2,4-butane sultone, 1,4-butane sultone, 1,3-propene sultone, and the like, ethylene sulfite, hexa Hydrobenzo [1,3,2] dioxathiolane-2-oxide (also called 1,2-cyclohexanediol cyclic sulfite), 5-vinyl-hexahydro1,3,2-benzodioxathiol-2-oxide, etc. Cyclic sulfite compounds, sulfonic acid ester compounds such as 2-propynyl methanesulfonate and methylenemethane disulfonate, vinylsulfones such as divinylsulfone, 1,2-bis (vinylsulfonyl) ethane, bis (2-vinylsulfonylethyl) ether Compounds, etc., among which 1,3 Propane sultone, ethylene sulfite, 2,4-butane sultone is preferable.
Examples of nitriles include acetonitrile, propionitrile, succinonitrile, glutaronitrile, adiponitrile, and pimelonitrile. Among them, dinitriles such as succinonitrile, glutaronitrile, adiponitrile, and pimelonitrile are preferable, and succinonitrile, adiponitrile are preferred. Pimeronitrile is more preferable, and adiponitrile and pimelonitrile are still more preferable.
Examples of the acid anhydride include chain carboxylic acid anhydrides such as acetic anhydride and propionic anhydride, cyclic acids such as succinic anhydride, maleic anhydride, glutaric anhydride, itaconic anhydride, and 3-sulfo-propionic anhydride. An anhydride is mentioned, Especially, cyclic acid anhydrides, such as a succinic anhydride, are preferable.
Aromatic compounds include cyclohexyl benzene, fluorocyclohexyl benzene compounds (1-fluoro-2-cyclohexylbenzene, 1-fluoro-3-cyclohexylbenzene, 1-fluoro-4-cyclohexylbenzene), tert-butylbenzene, tert-amyl. Aromatic compounds having a branched alkyl group such as benzene and 1-fluoro-4-tert-butylbenzene, biphenyl, terphenyl (o-, m-, p-isomer), diphenyl ether, fluorobenzene, difluorobenzene (o -, M-, p-form), anisole, 2,4-difluoroanisole, terphenyl partially hydride (1,2-dicyclohexylbenzene, 2-phenylbicyclohexyl, 1,2-diphenylcyclohexane, o-cyclohexylbifu) Yl) and the like.
Examples of the cyclic phosphazene compound include methoxypentafluorocyclotriphosphazene, ethoxypentafluorocyclotriphosphazene, phenoxypentafluorocyclotriphosphazene, ethoxyheptafluorocyclotetraphosphazene, and the like.

  Although content in particular of the said other additive is not restrict | limited, 0.001-10 mass% is preferable in a non-aqueous electrolyte. When the content is 10% by mass or less, there is little possibility that a coating film is excessively formed on the electrode and the low-temperature characteristics are deteriorated. The effect of improving storage characteristics is enhanced. The content is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.3% by mass or more, and the upper limit is preferably 9% by mass or less in the non-aqueous electrolyte. 7 mass% or less is more preferable, and 5 mass% or less is still more preferable.

[Electrolyte salt]
Preferred examples of the electrolyte salt used in the present invention include the following lithium salts and onium salts.

(Lithium salt)
Examples of lithium salts include inorganic lithium salts such as LiPF ₆ , LiPO ₂ F ₂ , Li ₂ PO ₃ F, LiBF ₄ , LiClO ₄ , FSO ₃ Li, LiN (SO ₂ F) ₂ , LiN (SO ₂ CF ₃ ) _2. LiN (SO ₂ C ₂ F ₅ ) ₂ , LiCF ₃ SO ₃ , LiC (SO ₂ CF ₃ ) ₃ , LiPF ₄ (CF ₃ ) ₂ , LiPF ₃ (C ₂ F ₅ ) ₃ , LiPF ₃ (CF ₃ ) ₃ , LiPF ₃ (iso-C ₃ F ₇ ) ₃ , lithium salts containing a chain-like fluorinated alkyl group such as LiPF ₅ (iso-C ₃ F ₇ ), and (CF ₂ ) ₂ (SO ₂ ) ₂ Lithium salt having a cyclic fluorinated alkylene chain such as NLi, (CF ₂ ) ₃ (SO ₂ ) ₂ NLi, lithium bis [oxalate-O, O ′] borate, difluoro [oxalate-O, O ′] boric acid Lithium, difluorobis [oxalate- , O ′] lithium phosphate and lithium salts having an oxalate complex such as tetrafluoro [oxalate-O, O ′] lithium phosphate as anions are preferably used, and one or two or more of these may be used in combination. can do.
Among these, LiPF ₆ , LiPO ₂ F ₂ , Li ₂ PO ₃ F, LiBF ₄ , FSO ₃ Li, LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ C ₂ F ₅ ) ₂ , LiN (SO ₂ F ) ₂ , at least one selected from difluorobis [oxalate-O, O ′] lithium phosphate and tetrafluoro [oxalate-O, O ′] lithium phosphate is preferable, and LiPF ₆ , LiPO ₂ F ₂ , LiBF _4. And LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ F) ₂ , and at least selected from difluorobis [oxalate-O, O ′] lithium phosphate and tetrafluoro [oxalate-O, O ′] lithium phosphate One is more preferred.
The concentration of the lithium salt is usually preferably 0.3 M or more, more preferably 0.7 M or more, and further preferably 1.1 M or more with respect to the non-aqueous solvent. Moreover, the upper limit is preferably 2.5M or less, more preferably 2.0M or less, and still more preferably 1.6M or less.
Further, suitable combinations of these lithium salts include LiPF ₆ , and further LiPO ₂ F ₂ , LiBF ₄ , LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ F) ₂ , difluorobis [oxalate-O , O ′] lithium phosphate and at least one lithium salt selected from tetrafluoro [oxalate-O, O ′] lithium phosphate is preferable in the non-aqueous electrolyte.
When the proportion of lithium salt other than LiPF _{6 in the} non-aqueous solvent is 0.001M or more, the effect of improving electrochemical characteristics at high temperatures is easily exhibited, and when it is 0.005M or less, electrochemical characteristics at high temperatures. This is preferable because there is little concern that the effect of improving the resistance will decrease. Preferably it is 0.01M or more, Especially preferably, it is 0.03M or more, Most preferably, it is 0.04M or more. The upper limit is preferably 0.4M or less, particularly preferably 0.2M or less.

(Onium salt)
Moreover, as an onium salt, the various salts which combined the onium cation and anion shown below are mentioned suitably.
Specific examples of the onium cation include tetramethylammonium cation, ethyltrimethylammonium cation, diethyldimethylammonium cation, triethylmethylammonium cation, tetraethylammonium cation, N, N-dimethylpyrrolidinium cation, N-ethyl-N-methylpyrrole. Dinium cation, N, N-diethylpyrrolidinium cation, spiro- (N, N ′)-bipyrrolidinium cation, N, N′-dimethylimidazolinium cation, N-ethyl-N′-methylimidazoli Preferable examples include nium cation, N, N′-diethylimidazolinium cation, N, N′-dimethylimidazolium cation, N-ethyl-N′-methylimidazolium cation, and N, N′-diethylimidazolium cation. Is The
Specific examples of anions include PF ₆ anion, BF ₄ anion, ClO ₄ anion, AsF ₆ anion, CF ₃ SO ₃ anion, N (CF ₃ SO ₂ ) ₂ anion, N (C ₂ F ₅ SO ₂ ) ₂ anion. , Etc. are mentioned suitably.
These electrolyte salts can be used singly or in combination of two or more.

[Production of non-aqueous electrolyte]
The nonaqueous electrolytic solution of the present invention is, for example, mixed with the above nonaqueous solvent, added with the above electrolyte salt, and further represented by the general formula (I) with respect to the obtained nonaqueous electrolytic solution. It can be obtained by adding a compound to be prepared.
At this time, it is preferable that the compound added to the non-aqueous solvent and the non-aqueous electrolyte to be used is one that is purified in advance and has as few impurities as possible within a range that does not significantly reduce the productivity.

  The nonaqueous electrolytic solution of the present invention can be used in the following first to fourth power storage devices, and not only a liquid but also a gelled one can be used as the nonaqueous electrolyte. Furthermore, the non-aqueous electrolyte of the present invention can be used for a solid polymer electrolyte. In particular, it is preferably used for the first electricity storage device (that is, for a lithium battery) or the fourth electricity storage device (that is, for a lithium ion capacitor) that uses a lithium salt as an electrolyte salt, and is used for a lithium battery. More preferably, it is most suitable for use as a lithium secondary battery.

[First power storage device (lithium battery)]
The lithium battery of the present invention is a generic term for a lithium primary battery and a lithium secondary battery. In this specification, the term lithium secondary battery is used as a concept including a so-called lithium ion secondary battery. The lithium battery of the present invention comprises the nonaqueous electrolyte solution in which an electrolyte salt is dissolved in a positive electrode, a negative electrode, and a nonaqueous solvent. Components other than the non-aqueous electrolyte, such as a positive electrode and a negative electrode, can be used without particular limitation.
For example, as the positive electrode active material for a lithium secondary battery, a composite metal oxide with lithium containing at least one selected from cobalt, manganese, and nickel is used. These positive electrode active materials can be used individually by 1 type or in combination of 2 or more types.
Examples of such lithium composite metal oxides include LiCoO ₂ , LiMn ₂ O ₄ , LiNiO ₂ , LiCo _1-x Ni _x O ₂ (0.01 <x <1), LiCo _1/3 Ni _1/3. Examples thereof include at least one selected from Mn _1/3 O ₂ , LiNi _1/2 Mn _3/2 O ₄ , LiCo _0.98 Mg _0.02 O _{2 and the} like. Further, LiCoO ₂ and LiMn ₂ O ₄ , LiCoO ₂ and LiNiO ₂ , LiMn ₂ O ₄ and LiNiO ₂ may be used in combination.

In addition, in order to improve safety and cycle characteristics during overcharge, or to enable use at a charging potential of 4.3 V or higher, a part of the lithium composite metal oxide may be substituted with another element. . For example, a part of cobalt, manganese, nickel is replaced with at least one element selected from Sn, Mg, Fe, Ti, Al, Zr, Cr, V, Ga, Zn, Cu, Bi, Mo, La, and the like. Or a part of O may be substituted with S or F, or a compound containing these other elements may be coated.
Among these, there are lithium composite metal oxides that can be used at a charging potential of the positive electrode in a fully charged state such as at least one selected from LiCoO ₂ , LiMn ₂ O ₄ , and LiNiO ₂ at 4.3 V or more on the basis of Li. Preferably, LiCo _1-x M _x O ₂ (where M is at least one element selected from Sn, Mg, Fe, Ti, Al, Zr, Cr, V, Ga, Zn, Cu, 0.001 ≦ x ≦ 0.05), LiCo _1/3 Ni _1/3 Mn _1/3 O ₂ , LiNi _1/2 Mn _3/2 O ₄ , Li ₂ MnO ₃ and LiMO ₂ (M is Co, Ni, Mn, More preferable is a lithium composite metal oxide that can be used at 4.4 V or higher, such as at least one selected from a solid solution with a transition metal such as Fe. When a lithium composite metal oxide that operates at a high charging voltage is used, the electrochemical characteristics in a wide temperature range are likely to be deteriorated due to a reaction with the electrolyte during charging, but in the lithium secondary battery according to the present invention, these A decrease in electrochemical characteristics can be suppressed.
In particular, in the case of a positive electrode containing Mn, the resistance of the battery tends to increase with the elution of Mn ions from the positive electrode, so that the electrochemical characteristics in a wide temperature range tend to be lowered. Lithium secondary batteries are preferred because they can suppress a decrease in these electrochemical characteristics.

Furthermore, lithium-containing olivine-type phosphate can also be used as the positive electrode active material. In particular, a lithium-containing olivine-type phosphate containing at least one selected from iron, cobalt, nickel, and manganese is preferable. Specific examples thereof include at least one selected from LiFePO ₄ , LiCoPO ₄ , LiNiPO ₄ , LiMnPO ₄ , and the like.
Some of these lithium-containing olivine-type phosphates may be substituted with other elements, and some of iron, cobalt, nickel, and manganese are replaced with Co, Mn, Ni, Mg, Al, B, Ti, V, and Nb. , Cu, Zn, Mo, Ca, Sr, W and Zr can be substituted with one or more elements selected from these, or can be coated with a compound or carbon material containing these other elements. Among these, LiFePO ₄ or LiMnPO ₄ is preferable.
Moreover, lithium containing olivine type | mold phosphate can also be mixed with the said positive electrode active material, for example, and can be used.

As the positive electrode for lithium primary _{battery, CuO, Cu 2 O, Ag} 2 O, Ag 2 CrO 4, CuS, CuSO 4, TiO 2, TiS 2, SiO 2, SnO, V 2 O 5, V 6 O 12 , VO _x , Nb ₂ O ₅ , Bi ₂ O ₃ , Bi ₂ Pb ₂ O ₅ , Sb ₂ O ₃ , CrO ₃ , Cr ₂ O ₃ , MoO ₃ , WO ₃ , SeO ₂ , MnO ₂ , Mn ₂ O ₃ , Fe ₂ O ₃ , FeO, Fe ₃ O ₄ , Ni ₂ O ₃ , NiO, CoO ₃ , CoO and the like, oxides of one or more metal elements or chalcogen compounds, sulfur such as SO ₂ and SOCl ₂ Examples thereof include compounds, and fluorocarbons (fluorinated graphite) represented by the general formula (CF _x ) _n . Among these, at least one selected from MnO ₂ , V ₂ O ₅ and fluorinated graphite is preferable.

  The conductive agent for the positive electrode is not particularly limited as long as it is an electron conductive material that does not cause a chemical change. Examples thereof include graphite such as natural graphite (flaky graphite and the like) and artificial graphite, carbon black such as acetylene black, ketjen black, channel black, furnace black, lamp black and thermal black. Further, graphite and carbon black may be appropriately mixed and used. 1-10 mass% is preferable and, as for the addition amount to the positive mix of a electrically conductive agent, 2-5 mass% is especially preferable.

The positive electrode is composed of a conductive agent such as acetylene black and carbon black, polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), a copolymer of styrene and butadiene (SBR), acrylonitrile and butadiene. Mixing with a binder such as copolymer (NBR), carboxymethyl cellulose (CMC), ethylene propylene diene terpolymer, etc., and adding a high boiling point solvent such as 1-methyl-2-pyrrolidone to knead and mix Then, this positive electrode mixture was applied to a current collector aluminum foil, a stainless steel lath plate, etc., dried and pressure-molded, and then subjected to vacuum at a temperature of about 50 ° C. to 250 ° C. for about 2 hours. It can be manufactured by heat treatment.
The density of the part except the collector of the positive electrode is usually at 1.5 g / cm ³ or more, for further increasing the capacity of the battery, it is preferably 2 g / cm ³ or more, more preferably, 3 g / cm ³ It is above, More preferably, it is 3.6 g / cm ³ or more. In addition, as an upper limit, 4 g / cm < ³ > or less is preferable.

Examples of the negative electrode active material for a lithium secondary battery include lithium metal, lithium alloy, and a carbon material capable of occluding and releasing lithium (easily graphitized carbon and a (002) plane spacing of 0.37 nm or more). Non-graphitizable carbon, graphite with (002) plane spacing of 0.34 nm or less, etc.], tin (single), tin compound, silicon (single), silicon compound, lithium titanate such as Li ₄ Ti ₅ O ₁₂ The at least 1 sort (s) chosen from a compound etc. is mentioned.
Among these, in terms of the ability to occlude and release lithium ions, it is more preferable to use a highly crystalline carbon material such as artificial graphite and natural graphite, and the lattice spacing (002) of the lattice plane ( ₀₀₂ ) is 0.00. It is particularly preferable to use a carbon material having a graphite-type crystal structure of 340 nm (nanometer) or less, particularly 0.335 to 0.337 nm.
The artificial graphite particles having a massive structure in which a plurality of flat graphite fine particles are assembled or bonded non-parallel to each other, for example, scaly natural graphite particles are repeatedly given mechanical action such as compression force, friction force, shear force, By using graphite particles that have been subjected to spheroidization treatment, the density of the portion excluding the current collector of the negative electrode can be obtained from X-ray diffraction measurement of the negative electrode sheet when pressure-molded to a density of 1.5 g / cm ³ or more. When the ratio I (110) / I (004) of the peak intensity I (110) of the (110) plane of the graphite crystal and the peak intensity I (004) of the (004) plane is 0.01 or more, the temperature becomes even wider. It is preferable because electrochemical characteristics are improved, more preferably 0.05 or more, and still more preferably 0.1 or more. Moreover, since it may process too much and crystallinity may fall and the discharge capacity of a battery may fall, an upper limit is preferable 0.5 or less, and 0.3 or less is more preferable.
In addition, it is preferable that the highly crystalline carbon material (core material) is coated with a carbon material having lower crystallinity than the core material because electrochemical characteristics in a wide temperature range are further improved. The crystallinity of the carbon material of the coating can be confirmed by TEM.
When a highly crystalline carbon material is used, it reacts with the non-aqueous electrolyte during charging and tends to lower the electrochemical characteristics at low or high temperatures due to an increase in interface resistance. However, in the lithium secondary battery according to the present invention, Excellent electrochemical characteristics over a wide temperature range.

  Examples of the metal compound capable of inserting and extracting lithium as the negative electrode active material include Si, Ge, Sn, Pb, P, Sb, Bi, Al, Ga, In, Ti, Mn, Fe, Co, Ni, and Cu. , Zn, Ag, Mg, Sr, Ba, and other compounds containing at least one metal element. These metal compounds may be used in any form such as a simple substance, an alloy, an oxide, a nitride, a sulfide, a boride, and an alloy with lithium, but any of a simple substance, an alloy, an oxide, and an alloy with lithium. Is preferable because the capacity can be increased. Among these, those containing at least one element selected from Si, Ge and Sn are preferable, and those containing at least one element selected from Si and Sn are particularly preferable because the capacity of the battery can be increased.

The negative electrode is kneaded using the same conductive agent, binder, and high-boiling solvent as in the production of the positive electrode, and then the negative electrode mixture is applied to the copper foil of the current collector. After being dried and pressure-molded, it can be produced by heat treatment under vacuum at a temperature of about 50 ° C. to 250 ° C. for about 2 hours.
The density of the portion excluding the current collector of the negative electrode is usually 1.1 g / cm ³ or more, and is preferably 1.5 g / cm ³ or more, more preferably 1.7 g / cm ^{3 in} order to further increase the battery capacity. ³ or more. In addition, as an upper limit, 2 g / cm < ³ > or less is preferable.

  Moreover, lithium metal or a lithium alloy is mentioned as a negative electrode active material for lithium primary batteries.

The structure of the lithium battery is not particularly limited, and a coin-type battery, a cylindrical battery, a square battery, a laminated battery, or the like having a single-layer or multi-layer separator can be applied.
Although it does not restrict | limit especially as a separator for batteries, The single layer or laminated | stacked microporous film, woven fabric, a nonwoven fabric, etc. of polyolefin, such as a polypropylene and polyethylene, can be used.

  The lithium secondary battery according to the present invention has excellent electrochemical characteristics in a wide temperature range even when the end-of-charge voltage is 4.2 V or more, particularly 4.3 V or more, and the characteristics are also good at 4.4 V or more. is there. The end-of-discharge voltage is usually 2.8 V or higher, and more preferably 2.5 V or higher, but the lithium secondary battery in the present invention can be 2.0 V or higher. Although it does not specifically limit about an electric current value, Usually, it uses in the range of 0.1-30C. Moreover, the lithium battery in this invention can be charged / discharged at -40-100 degreeC, Preferably it is -10-80 degreeC.

  In the present invention, as a countermeasure against an increase in the internal pressure of the lithium battery, a method of providing a safety valve on the battery lid or cutting a member such as a battery can or a gasket can be employed. Further, as a safety measure for preventing overcharge, the battery lid can be provided with a current interruption mechanism that senses the internal pressure of the battery and interrupts the current.

[Second power storage device (electric double layer capacitor)]
It is an electricity storage device that stores energy by using the electric double layer capacity at the interface between the electrolyte and the electrode. An example of the present invention is an electric double layer capacitor. The most typical electrode active material used for this electricity storage device is activated carbon. Double layer capacity increases roughly in proportion to surface area.

[Third power storage device]
It is an electrical storage device which stores energy using dope / dedope reaction of an electrode. Examples of the electrode active material used in this power storage device include metal oxides such as ruthenium oxide, iridium oxide, tungsten oxide, molybdenum oxide, and copper oxide, and π-conjugated polymers such as polyacene and polythiophene derivatives. Capacitors using these electrode active materials can store energy associated with electrode doping / dedoping reactions.

[Fourth storage device (lithium ion capacitor)]
It is an electricity storage device that stores energy by utilizing lithium ion intercalation with a carbon material such as graphite as a negative electrode. It is called a lithium ion capacitor (LIC). Examples of the positive electrode include those using an electric double layer between an activated carbon electrode and an electrolytic solution, and those using a π-conjugated polymer electrode doping / dedoping reaction. The electrolyte contains at least a lithium salt such as LiPF ₆ .

Examples 1-11, Comparative Examples 1-2
[Production of lithium ion secondary battery]
94% by mass of LiCoO _{2 and} 3% by mass of acetylene black (conductive agent) are mixed, and added to a solution in which 3% by mass of polyvinylidene fluoride (binder) is dissolved in 1-methyl-2-pyrrolidone in advance. Then, a positive electrode mixture paste was prepared. This positive electrode mixture paste was applied to one side of an aluminum foil (current collector), dried and pressurized, punched out to a predetermined size, and a positive electrode sheet was produced. The density of the portion excluding the current collector of the positive electrode was 3.6 g / cm ³ . Further, 95% by mass of artificial graphite (d ₀₀₂ = 0.335 nm, negative electrode active material) is added to a solution in which 5% by mass of polyvinylidene fluoride (binder) is dissolved in 1-methyl-2-pyrrolidone in advance. And mixed to prepare a negative electrode mixture paste. This negative electrode mixture paste was applied to one side of a copper foil (current collector), dried and pressurized, and punched into a predetermined size to produce a negative electrode sheet. The density of the portion excluding the current collector of the negative electrode was 1.5 g / cm ³ . As a result of X-ray diffraction measurement using this electrode sheet, the ratio of the peak intensity I (110) of the (110) plane of the graphite crystal to the peak intensity I (004) of the (004) plane [I (110) / I (004)] was 0.1. Then, a positive electrode sheet, a microporous polyethylene film separator, and a negative electrode sheet were laminated in this order, and the compositions shown in Table 1 (the compounds of Examples 1 to 5 and 8 to 11 are 2,5-dioxopyrrolidin-1-yl). 2- (diethoxyphosphoryl) acetate; Compound B1, the compound of Example 6 is bis (2,5-dioxopyrrolidin-1-yl) oxalate; Compound A1, the compound of Example 7 is 2,5-dioxopyrrolidine A non-aqueous electrolyte solution of -1-yl (2- (methanesulfonyl) oxy) propanoate; compound C1) was added to prepare a 2032 type coin battery.

[Evaluation of low temperature characteristics after high temperature charge storage]
(I) Initial discharge capacity Using the coin battery produced by the above method, in a constant temperature bath at 25 ° C., charge at a constant current of 1 C and a constant voltage for 3 hours to a final voltage of 4.2 V and constant temperature at 0 ° C. The temperature of the tank was lowered and discharged to a final voltage of 2.75 V under a constant current of 1 C, and the initial discharge capacity of 0 ° C. was determined.
(Ii) High temperature charge storage test Next, this coin battery was charged in a constant temperature bath at 25 ° C. with a constant current and constant voltage of 0.2 C for 7 hours to a final voltage of 4.2 V, and placed in a high temperature bath at 85 ° C. Stored for 1 day. Then, it put into the thermostat of 25 degreeC, and discharged once to the final voltage 2.75V under the constant current of 1C.
(Iii) Discharge capacity after storage at high temperature charge After that, after storage at high temperature charge (after full charge and storage at a high temperature of 85 ° C. as described in (ii)) in the same manner as the measurement of the initial discharge capacity. The discharge capacity at 0 ° C. was determined.
(Iv) Low-temperature characteristics after high-temperature charge storage The low-temperature characteristics after high-temperature charge storage were determined from the following maintenance rate of 0 ° C. discharge capacity.
0 ° C. discharge capacity retention rate after storage at high temperature (%) = (0 ° C. discharge capacity after high temperature storage / initial 0 ° C. discharge capacity) × 100
In addition, Table 1 and Table 2 show battery manufacturing conditions and battery characteristics.

Example 12 and Comparative Example 3
In place of the negative electrode active material used in Example 3 and Comparative Example 1, a negative electrode sheet was prepared using silicon (single element) (negative electrode active material). 80% by mass of silicon (single substance) and 15% by mass of acetylene black (conductive agent) are mixed and added to a solution in which 5% by mass of polyvinylidene fluoride (binder) is previously dissolved in 1-methyl-2-pyrrolidone. And mixed to prepare a negative electrode mixture paste. Example 3 and Comparative Example 1 except that this negative electrode mixture paste was applied onto a copper foil (current collector), dried and pressurized, punched to a predetermined size, and a negative electrode sheet was produced. A coin battery was prepared in the same manner as described above, and the battery was evaluated. The results are shown in Table 3.

Example 13 and Comparative Example 4
Instead of the positive electrode active material used in Example 3 and Comparative Example 1, a positive electrode sheet was prepared using LiFePO ₄ (positive electrode active material) coated with amorphous carbon. 90% by mass of LiFePO ₄ coated with amorphous carbon and 5% by mass of acetylene black (conductive agent) are mixed, and 5% by mass of polyvinylidene fluoride (binder) is dissolved in 1-methyl-2-pyrrolidone in advance. The positive electrode mixture paste was prepared by adding to and mixing with the previously-prepared solution. This positive electrode mixture paste was applied onto an aluminum foil (current collector), dried, pressurized and punched to a predetermined size to produce a positive electrode sheet, and the end-of-charge voltage during battery evaluation was 3. A coin battery was manufactured and evaluated in the same manner as in Example 3 and Comparative Example 1 except that 6 V and the discharge end voltage were set to 2.0 V. The results are shown in Table 4.

In any of the lithium secondary batteries of Examples 1 to 11 described above, nonaqueous electrolysis to which succinimidyl acrylate described in Comparative Example 1 and Patent Document 1 in which the compound is not added in the nonaqueous electrolytic solution of the present invention is added Compared with the lithium secondary battery of Comparative Example 2 which is a liquid, the electrochemical characteristics in a wide temperature range are remarkably improved. From the above, it has been found that the effect of the present invention is a characteristic effect when a specific compound of the present invention is contained in a nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a nonaqueous solvent.
Further, from the comparison between Example 12 and Comparative Example 3 and the comparison between Example 13 and Comparative Example 4, when silicon (single) Si was used for the negative electrode, or lithium-containing olivine-type iron phosphate (LiFePO ₄ ) was used for the positive electrode. The same effect can be seen when using. Therefore, it is clear that the effect of the present invention is not an effect dependent on a specific positive electrode or negative electrode.

  Furthermore, the non-aqueous electrolyte of the present invention also has an effect of improving the discharge characteristics in a wide temperature range of the lithium primary battery.

  The electricity storage device using the non-aqueous electrolyte of the present invention is useful as an electricity storage device such as a lithium secondary battery having excellent electrochemical characteristics in a wide temperature range.

Claims (15)

A nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a nonaqueous solvent, containing an imidyloxy group-containing compound represented by the following general formula (I):

(In the formula, R ¹ represents a divalent linking group having 2 to 6 carbon atoms in which a hydrogen atom may be substituted with a halogen atom, and X is represented by the following general formulas (II) to (V)). Indicates any of the substituents.)

(In the formula, R ² is an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or 6 to 12 carbon atoms. Or a group represented by —N (C═O) ₂ R ¹ , wherein R ¹ is as defined above, and the alkyl group, cycloalkyl group, alkenyl group, alkynyl group, or In the aryl group, the hydrogen atom may be substituted with a halogen atom.)

(In the formula, R ³ and R ⁴ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁵ and R ⁶ each independently represent an alkyl having 1 to 6 carbon atoms. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cyclo (In the alkyl group, alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)

(In the formula, R ⁷ and R ⁸ each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms, and R ⁹ each independently represents an alkyl group having 1 to 6 carbon atoms or a carbon atom. A cycloalkyl group having 3 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 3 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, provided that the alkyl group, cycloalkyl group, (In the alkenyl group, alkynyl group, or aryl group, the hydrogen atom may be substituted with a halogen atom.)   The nonaqueous electrolytic solution according to claim 1, wherein the content of the imidyloxy group-containing compound represented by the general formula (I) is 0.001 to 10% by mass in the nonaqueous electrolytic solution.   The imidyloxy group-containing compound represented by the general formula (I) is bis (2,5-dioxopyrrolidin-1-yl) ogizarate (Structural Formula A1), 2,5-dioxopyrrolidin-1-yl 2- ( Diethoxyphosphoryl) acetate (Structural Formula B1), 2,5-dioxopyrrolidin-1-yl 2- (diethoxyphosphoryl) propanoate (Structural Formula B10), 2,5-dioxopyrrolidin-1-yl 2- ( Dimethoxyphosphoryl) acetate (Structural Formula B13), 2,5-dioxopyrrolidin-1-yl 2- (dipropoxyphosphoryl) acetate (Structural Formula B14), 2,5-dioxopyrrolidin-1-yl (2- ( Methanesulfonyl) oxy) propanoate (Structural Formula C1), 2,5-dioxopyrrolidin-1-yl (2- (ethanesulfonyl) Oxy) propanoate (Structural Formula C13), 2,5-dioxopyrrolidin-1-yl (2- (4-methylphenylsulfonyl) oxy) acetate (Structural Formula C20), and 2,5-dioxopyrrolidine-1- The nonaqueous electrolytic solution according to claim 1 or 2, which is one or more selected from yl (2- (4-methylphenylsulfonyl) oxy) propanoate (Structural Formula C25).   The nonaqueous electrolytic solution according to claim 1, wherein the nonaqueous solvent contains at least one cyclic carbonate.   Cyclic carbonates include ethylene carbonate, propylene carbonate, vinylene carbonate, vinyl ethylene carbonate, 4-fluoro-1,3-dioxolan-2-one, and trans or cis-4,5-difluoro-1,3-dioxolane-2 -The non-aqueous electrolyte of Claim 4 which is 1 type, or 2 or more types chosen from ON.   The nonaqueous electrolytic solution according to any one of claims 1 to 5, wherein the nonaqueous solvent further contains a chain ester.   Symmetrical chain ester selected from asymmetric chain carbonate selected from methyl ethyl carbonate, methyl propyl carbonate, methyl isopropyl carbonate, methyl butyl carbonate, and ethyl propyl carbonate, dimethyl carbonate, diethyl carbonate, dipropyl carbonate, and dibutyl carbonate The nonaqueous electrolytic solution according to claim 6, which is one or more selected from a chain carbonate and a chain carboxylic acid ester.   The nonaqueous electrolytic solution further contains at least one selected from a phosphate ester compound, an isocyanate, an S═O bond-containing compound, a nitrile, an acid anhydride, an aromatic compound, and a cyclic phosphazene compound. 8. The nonaqueous electrolytic solution according to any one of 7 above. The electrolyte salt is LiPF ₆ , LiPO ₂ F ₂ , Li ₂ PO ₃ F, LiBF ₄ , FSO ₃ Li, LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ C ₂ F ₅ ) ₂ , LiN (SO ₂ F ) ₂ , and at least one lithium salt selected from difluorobis [oxalate-O, O ′] lithium phosphate and tetrafluoro [oxalate-O, O ′] lithium phosphate. A non-aqueous electrolyte according to any one of the above. The lithium salt contains LiPF ₆ , and LiPO ₂ F ₂ , LiBF ₄ , FSO ₃ Li, LiN (SO ₂ CF ₃ ) ₂ , LiN (SO ₂ F) ₂ , difluorobis [oxalate-O, O ′] phosphorus The nonaqueous electrolytic solution according to claim 9, comprising at least one selected from lithium acid lithium and tetrafluoro [oxalate-O, O ′] lithium phosphate.   The nonaqueous electrolytic solution according to claim 1, wherein the concentration of the lithium salt is 0.3 to 2.5 M with respect to the nonaqueous solvent.   A power storage device comprising a positive electrode, a negative electrode, and a non-aqueous electrolyte in which an electrolyte salt is dissolved in a non-aqueous solvent, wherein at least one of the imidyloxy group-containing compounds represented by the general formula (I) in the non-aqueous electrolyte An electricity storage device comprising a seed.   The nonaqueous electrolytic solution according to claim 12, wherein the content of the imidyloxy group-containing compound represented by the general formula (I) is 0.001 to 10% by mass in the nonaqueous electrolytic solution.   Lithium-containing olivine type in which the positive electrode active material contains a composite metal oxide with lithium containing at least one selected from cobalt, manganese, and nickel, or at least one selected from iron, cobalt, nickel, and manganese The electricity storage device according to claim 12 or 13, which is a phosphate.   The negative electrode active material includes at least one selected from lithium metal, a lithium alloy, a carbon material capable of inserting and extracting lithium, tin, a tin compound, silicon, a silicon compound, and a lithium titanate compound. The electrical storage device in any one of 12-14.