WO2016060038A1 - Non-aqueous electrolyte and non-aqueous electrolyte secondary cell - Google Patents
Non-aqueous electrolyte and non-aqueous electrolyte secondary cell Download PDFInfo
- Publication number
- WO2016060038A1 WO2016060038A1 PCT/JP2015/078463 JP2015078463W WO2016060038A1 WO 2016060038 A1 WO2016060038 A1 WO 2016060038A1 JP 2015078463 W JP2015078463 W JP 2015078463W WO 2016060038 A1 WO2016060038 A1 WO 2016060038A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- carbon atoms
- hydrocarbon group
- represented
- groups
- Prior art date
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/78—Halides of sulfonic acids
- C07C309/86—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0567—Liquid materials characterised by the additives
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/4235—Safety or regulating additives or arrangements in electrodes, separators or electrolyte
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to a non-aqueous electrolyte secondary battery, and more particularly, to a non-aqueous electrolyte secondary battery having a non-aqueous electrolyte containing a specific compound.
- non-aqueous electrolyte secondary batteries having high voltage and high energy density have been widely used as power sources. Also, from the viewpoint of environmental problems, battery cars and hybrid cars using electric power as a part of power have been put into practical use.
- additives for non-aqueous electrolyte solutions have been proposed in order to improve the stability and electrical characteristics of non-aqueous electrolyte secondary batteries.
- additives include 1,3-propane sultone (for example, see Patent Document 1), vinyl ethylene carbonate (for example, see Patent Document 2), vinylene carbonate (for example, see Patent Document 3), 1, 3-Propane sultone, butane sultone (for example, see Patent Document 4), vinylene carbonate (for example, see Patent Document 5), vinyl ethylene carbonate (for example, see Patent Document 6), and the like have been proposed. Carbonate is widely used because of its great effect.
- SEI Solid Electrolyte Interface
- a non-aqueous electrolyte secondary battery When a non-aqueous electrolyte secondary battery is supplied with an excessive current due to erroneous operation or the like, it may be charged beyond a predetermined voltage, and this phenomenon is called overcharging. Since the overcharged state may significantly reduce the safety of the nonaqueous electrolyte secondary battery, a mechanism for cutting off the charging current when a predetermined voltage is exceeded is provided. As one of mechanisms for interrupting the charging current, an overcharge inhibitor such as cyclohexylbenzene is used.
- the overcharge preventing agent is a mechanism that generates a gas when the secondary battery reaches the voltage in the overcharge region and blocks the current by sensing the pressure sensor of the battery.
- an object of the present invention is to provide a non-aqueous electrolyte that is excellent in overcharge prevention capability and can maintain a small internal resistance and high electric capacity even after charging and discharging, and a non-aqueous electrolyte secondary battery using the same. There is.
- the present inventors have found that the above object can be achieved by using a nonaqueous electrolytic solution containing a compound having a specific structure, and have completed the present invention.
- the present invention provides a non-aqueous electrolyte characterized by containing at least one compound represented by the following general formula (1) in a non-aqueous electrolyte in which a lithium salt is dissolved in an organic solvent.
- Ar represents a benzene ring or a naphthalene ring
- Z represents R 1 O—S ( ⁇ O) 2 —, R 12 —S ( ⁇ O) 2 —, R 1 O—S ( ⁇ O) — or R 12 —S ( ⁇ O) —
- R 1 represents a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms
- R 2 represents a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 , a phosphate group, or a substituted or unsubstit
- R 12 represents a halogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms
- the group that replaces the hydrocarbon group represented by R 1 , R 2 and R 12 is a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 or A phosphate group
- R 9 , R 10 and R 11 represent a hydrocarbon group having 1 to 16 carbon atoms, m and n each represent an integer of 1 or more, and when Ar represents a benzene ring, m + n is 6 or less, and when Ar represents a naphthalene ring, m + n is 10 or less, When m is 2 or more, Z may be the same or different, and when n is 2 or more, R 2 may be the same or different. However, at least one of n R 2 is a group represented by the following general formula (2) or (3).
- R 3 , R 4 , R 5 and R 6 each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms
- Groups that substitute for the hydrocarbon groups represented by R 3 , R 4 , R 5 and R 6 are halogen atoms, nitrile groups, nitro groups, amino groups, carboxyl groups, hydroxyl groups, thiol groups, formyl groups, sulfone groups, —SiR.
- R 10 R 11 or a phosphate group The alkylene group in the hydrocarbon group represented by R 3 , R 4 , R 5 and R 6 is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, -S-, -SO-, -SO 2- , -NR-CO- or -CO-NR- may be interrupted 1 to 3 times under the condition that they are not adjacent to each other, R represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms, R 7 and R 8 are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 R 10 R 11 or phosphate group Represents R 9 , R 10 and R 11 each independently represents a hydrocarbon group having 1 to 16 carbon atoms, However, in the general formulas (2)
- the present invention also provides a non-aqueous electrolyte secondary battery comprising a non-aqueous electrolyte secondary battery having an anode from which lithium can be inserted and removed, a cathode containing a transition metal and lithium, and a non-aqueous electrolyte in which a lithium salt is dissolved in an organic solvent.
- the present invention provides a non-aqueous electrolyte secondary battery, wherein the solution is the non-aqueous electrolyte described above.
- the present invention also provides a compound represented by the following general formula (1 ′).
- Ar ′ represents a benzene ring or a naphthalene ring
- R 12 '-S ( O) 2 -
- R 1 ′ represents a hydrocarbon group having 1 to 20 carbon atoms having a substituent
- R 2 ′ has a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 ′ R 10 ′ R 11 ′, a phosphate group, a phosphate group, or a substituent.
- R 12 ′ represents a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms having a substituent
- R 1 ', R 2' and R 12 'group substituting the hydrocarbon group represented by a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, -SiR 9' R 10 is a 'R 11' or phosphoric acid group
- the alkylene in the hydrocarbon group represented by R 1 ′, R 2 ′ and R 12 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR′—, -S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are
- R 9 ′, R 10 ′ and R 11 ′ represent a hydrocarbon group having 1 to 16 carbon atoms
- m ′ and n ′ each represents an integer of 1 or more
- Ar ′ represents a benzene ring
- m ′ + n ′ is 6 or less
- Ar ′ represents a naphthalene ring
- m ′ + n ′ is 10 or less.
- Z ′ may be the same or different.
- R 2 ′ may be the same or different.
- R 2 ′ may be the same or different. However, at least one of n ′ R 2 ′ is a group represented by the following general formula (2 ′) or (3 ′). ) (Wherein R 3 ′, R 4 ′, R 5 ′ and R 6 ′ each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms, The hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is a halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone.
- a group, -SiR 9 'R 10 ' R 11 'or a phosphate group The alkylene group in the hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, -NR '-, - S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are not adjacent, may also be interrupted 1-3 times, R ′ represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms, R 7 ′ and R 8 ′ are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 ′ R 10 ′ R 11 'Or represents a
- a non-aqueous electrolyte solution that is excellent in overcharge prevention capability by using a non-aqueous electrolyte solution containing a compound having a specific structure and that can maintain a small internal resistance and high electric capacity even after charging and discharging.
- a secondary battery can be provided.
- FIG. 1 is a longitudinal sectional view schematically showing an example of the structure of a coin-type battery of the nonaqueous electrolyte secondary battery of the present invention.
- FIG. 2 is a schematic diagram showing a basic configuration of a cylindrical battery of the nonaqueous electrolyte secondary battery of the present invention.
- FIG. 3 is a perspective view showing the internal structure of the cylindrical battery of the nonaqueous electrolyte secondary battery of the present invention as a cross section.
- Non-aqueous electrolyte and the non-aqueous electrolyte secondary battery of the present invention will be described in detail based on preferred embodiments.
- a nonaqueous electrolytic solution of the present invention A nonaqueous electrolytic solution in which a lithium salt used in the present invention is dissolved in an organic solvent (hereinafter also referred to as a nonaqueous electrolytic solution of the present invention) will be described.
- the nonaqueous electrolytic solution of the present invention contains a compound represented by the above general formula (1). Hereinafter, this compound will be described.
- the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 , R 2 and R 12 in the general formula (1) is a saturated or unsaturated aliphatic hydrocarbon group having 1 to 20 carbon atoms, the number of carbon atoms Examples include 6 to 20 aromatic hydrocarbon groups.
- saturated and unsaturated hydrocarbon groups having 1 to 20 carbon atoms include methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, Saturated hydrocarbon groups such as hexyl, 2-ethylhexyl, decyl, dodecyl, octadecyl, and unsaturated hydrocarbons such as vinyl, ethynyl, allyl, propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, etc.
- alkylene in the case of R 2 , including a site bonded to Ar is —O—, —CO—, —OCO.
- R is an aliphatic hydrocarbon group having 1 to 5 carbon atoms.
- the interrupting group includes a carbon atom
- the number of carbon atoms including the number of carbon atoms of the interrupting group is 1 to 20.
- Examples of the aliphatic hydrocarbon group having 1 to 5 carbon atoms that represents R include saturated and unsaturated aliphatic hydrocarbon groups having 1 to 5 carbon atoms among those described for R 1 .
- R 1 , R 2 and R 12 represent a group that substitutes for a hydrocarbon group having 1 to 20 carbon atoms, such as a halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group,- It is SiR 9 R 10 R 11 or a phosphate group, and R 9 , R 10 and R 11 are hydrocarbon groups having 1 to 16 carbon atoms.
- the group to be substituted is a group containing a carbon atom, the number of carbon atoms including the number of carbon atoms of the group to be substituted is 1 to 20.
- halogen atom examples include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. In addition, all the halogen atoms in this specification are the same as this.
- examples of the aliphatic hydrocarbon group having 1 to 16 carbon atoms represented by R 9 , R 10 and R 11 include the same groups as those having 1 to 16 carbon atoms among those described for R 1 .
- At least one of the n R 2 in the general formula (1) is a group represented by the general formula (2) or (3).
- the hydrocarbon group having 1 to 18 carbon atoms represented by R 3 , R 4 , R 5 and R 6 in the general formula (2) or (3) has 1 to 18 carbon atoms among those described for R 1. And the same groups as those mentioned above.
- the alkylene group in the hydrocarbon group having 1 to 18 carbon atoms represented by R 3 , R 4 , R 5 and R 6 is —O—, —CO—, —OCO—, —COO—, —O—CO—.
- O—, —NR—, —S—, —SO—, —SO 2 —, —NR—CO—, —CO or —NR— may be interrupted 1 to 3 times under the condition that they are not adjacent to each other, R is an aliphatic hydrocarbon group having 1 to 5 carbon atoms. However, when the interrupting group includes a carbon atom, the number of carbon atoms including the number of carbon atoms of the interrupting group is 1 to 18.
- R 3 , R 4 , R 5 and R 6 can be substituted with a hydrocarbon group having 1 to 18 carbon atoms such as halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl Group, a sulfone group, —SiR 9 R 10 R 11 or a phosphoric acid group, and R 9 , R 10 and R 11 are hydrocarbon groups having 1 to 16 carbon atoms.
- the group to be substituted is a group containing a carbon atom, the number of carbon atoms including the number of carbon atoms of the group to be substituted is 1 to 16.
- examples of the number and position of substitution of Z and R 2 with respect to Ar are as follows: # 1 to # 7. Further, in # 1 ⁇ # 7, of R 2, general formula (2) or a group represented by (3), R 2A, the other group, as R 2B, Z for Ar, R 2A and Reflecting the number of R 2B substitutions and the substitution position, the following # 8 to # 17 are given as an example.
- n R 2 is a group represented by the general formula (2), particularly isopropyl, s-butyl, s A compound that is pentyl is preferred because it is excellent as an overcharge inhibitor.
- preferred groups in the group (R 2B ) other than the general formula (2) or (3) include a halogen atom, an ester group, an amide group, and the like.
- R 1 is the number of carbon atoms substituted or unsubstituted by a halogen atom 1 to 6 saturated or unsaturated aliphatic hydrocarbon groups (methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, hexyl, vinyl Ethynyl, allyl, propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, or a group in which a part of these groups is substituted with a halogen atom, etc.
- R 12 is a halogen atom, a halogen atom-substituted or unsubstituted carbon atom having 1 to 6 carbon atoms.
- Saturated or unsaturated aliphatic hydrocarbon group (methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, hexyl, vinyl, ethynyl, allyl , Propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, or a group in which a part of these groups is substituted with a halogen atom is preferred.
- Specific examples of the compound represented by the general formula (1) include compound no. Although 1 to 23 are mentioned, the present invention is not limited to these compounds.
- the compound represented by the general formula (1) can be produced by sulfonating and esterifying an aromatic compound having a substituent.
- the compound represented by the general formula (1) may be used alone or in combination of two or more. Further, in the nonaqueous electrolytic solution of the present invention, when the content of the compound represented by the general formula (1) is too small, a sufficient effect cannot be exhibited, and when the content is too large, the compounding amount is met.
- the content of the compound represented by the general formula (1) is 0.001 in the non-aqueous electrolyte because not only the increase effect is obtained but also the characteristics of the non-aqueous electrolyte may be adversely affected. Is preferably 10 to 10% by mass, more preferably 0.01 to 8% by mass, and most preferably 0.1 to 5% by mass.
- organic solvent used in the non-aqueous electrolyte of the present invention those usually used for non-aqueous electrolytes can be used alone or in combination of two or more. Specific examples include saturated cyclic carbonate compounds, saturated cyclic ester compounds, sulfoxide compounds, sulfone compounds, amide compounds, saturated chain carbonate compounds, chain ether compounds, cyclic ether compounds, and saturated chain ester compounds.
- saturated cyclic carbonate compounds saturated cyclic ester compounds, sulfoxide compounds, sulfone compounds and amide compounds have a high relative dielectric constant, and thus serve to increase the dielectric constant of non-aqueous electrolytes.
- Compounds are preferred.
- saturated cyclic carbonate compounds include ethylene carbonate, 1-fluoroethylene carbonate, 1,2-propylene carbonate, 1,3-propylene carbonate, 1,2-butylene carbonate, 1,3-butylene carbonate, 1, Examples thereof include 1, -dimethylethylene carbonate.
- saturated cyclic ester compound examples include ⁇ -butyrolactone, ⁇ -valerolactone, ⁇ -caprolactone, ⁇ -hexanolactone, and ⁇ -octanolactone.
- sulfoxide compound examples include dimethyl sulfoxide, diethyl sulfoxide, dipropyl sulfoxide, diphenyl sulfoxide, thiophene, and the like.
- sulfone compounds include dimethylsulfone, diethylsulfone, dipropylsulfone, diphenylsulfone, sulfolane (also referred to as tetramethylenesulfone), 3-methylsulfolane, 3,4-dimethylsulfolane, 3,4-diphenimethylsulfolane, sulfolene. , 3-methylsulfolene, 3-ethylsulfolene, 3-bromomethylsulfolene and the like, and sulfolane and tetramethylsulfolane are preferable.
- amide compound examples include N-methylpyrrolidone, dimethylformamide, dimethylacetamide and the like.
- saturated chain carbonate compounds, chain ether compounds, cyclic ether compounds and saturated chain ester compounds can lower the viscosity of the non-aqueous electrolyte and increase the mobility of electrolyte ions. Battery characteristics such as output density can be made excellent. Moreover, since it is low-viscosity, the performance of the non-aqueous electrolyte at a low temperature can be enhanced, and among them, a saturated chain carbonate compound is preferable.
- saturated chain carbonate compounds include dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), ethyl butyl carbonate, methyl-t-butyl carbonate, diisopropyl carbonate, and t-butyl propyl carbonate. Etc.
- Examples of the chain ether compound or cyclic ether compound include dimethoxyethane (DME), ethoxymethoxyethane, diethoxyethane, tetrahydrofuran, dioxolane, dioxane, 1,2-bis (methoxycarbonyloxy) ethane, 1,2 -Bis (ethoxycarbonyloxy) ethane, 1,2-bis (ethoxycarbonyloxy) propane, ethylene glycol bis (trifluoroethyl) ether, propylene glycol bis (trifluoroethyl) ether, ethylene glycol bis (trifluoromethyl) ether And diethylene glycol bis (trifluoroethyl) ether.
- DME dimethoxyethane
- ethoxymethoxyethane diethoxyethane
- tetrahydrofuran dioxolane
- dioxane 1,2-bis (methoxycarbonyloxy) ethane
- dioxolane is preferred.
- monoester compounds and diester compounds having a total number of carbon atoms in the molecule of 2 to 8 are preferable.
- Specific compounds include methyl formate, ethyl formate, methyl acetate, ethyl acetate, Propyl acetate, isobutyl acetate, butyl acetate, methyl propionate, ethyl propionate, methyl butyrate, methyl isobutyrate, methyl trimethyl acetate, ethyl trimethyl acetate, methyl malonate, ethyl malonate, methyl succinate, ethyl succinate, 3- Methyl methoxypropionate, ethyl 3-methoxypropionate, ethylene glycol diacetyl, propylene glycol diacetyl, and the like, such as methyl formate, ethyl formate, methyl acetate, ethy
- acetonitrile acetonitrile, propionitrile, nitromethane and their derivatives can be used as the organic solvent.
- the lithium salt can be dissolved in the organic solvent so that the concentration in the non-aqueous electrolyte of the present invention is 0.1 to 3.0 mol / L, particularly 0.5 to 2.0 mol / L. preferable. If the concentration of the lithium salt is less than 0.1 mol / L, a sufficient current density may not be obtained, and if it is more than 3.0 mol / L, the stability of the nonaqueous electrolyte may be impaired.
- the lithium salt may be used in combination of two or more lithium salts.
- an overcharge preventing effect can be mentioned, but another overcharge preventing agent can be further added to the nonaqueous electrolytic solution of the present invention.
- aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, partially hydrogenated terphenyl, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, dibenzofuran; 2-fluorobiphenyl, Partially fluorinated products of the above aromatic compounds such as o-cyclohexylfluorobenzene and p-cyclohexylfluorobenzene; 2,4-difluoroanisole, 2,5-difluoroanisole, 2,6-difluoroanisole, 3,5-difluoroanisole and the like And a fluorine-containing anisole compound.
- aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, terphenyl partially hydrogenated compounds, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, and dibenzofuran are preferable.
- the compound represented by following General formula (4) can also be used preferably.
- R 21 , R 22 , R 23 , R 24 and R 25 are each independently a substituted or unsubstituted aliphatic hydrocarbon group having 1 to 20 carbon atoms, halogen, Represents an atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, a sulfone group, —SiR 29 R 30 R 31 or a phosphate group;
- the alkylene (including the portion bonded to the benzene ring) in the group is —O—, —CO—, —OCO—, —COO—, —O—CO.
- R a represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms
- At least one of R 21 , R 22 , R 23 , R 24 and R 25 represents an aliphatic hydrocarbon group having 1 to 20 carbon atoms substituted with at least one halogen atom
- R 28 represents a p-valent group
- R 26 , R 27 , R 29 , R 30 and R 31 each independently have a substituent or an unsubstituted aliphatic hydrocarbon group having 1 to 20 carbon atoms or a substituent.
- p represents an integer of 1 to 3.
- R 21 to R 27 and R 29 to R 31 represent an aliphatic hydrocarbon group having 1 to 20 carbon atoms, an aromatic hydrocarbon group having 6 to 20 carbon atoms, and R a Examples of the aliphatic hydrocarbon group having 1 to 5 carbon atoms include the same groups as those described in the general formula (1).
- the aliphatic hydrocarbon group having 1 to 20 carbon atoms represented by R 21 to R 26 and R 29 to R 31, and the number of carbon atoms represented by R 26 , R 27 , R 29 , R 30 and R 31 are 6 to 20 Examples of the group for substituting the aromatic hydrocarbon group include the same groups as those described in the general formula (1).
- Specific examples of the compound represented by the general formula (4) include, but are not limited to, the following 4-1 to 4-4.
- the addition amount is not particularly limited, but is preferably 1 to 500 parts by mass with respect to 100 parts by mass of the compound represented by the general formula (1).
- halogen-based, phosphorus-based, and other flame retardants can be appropriately added to the non-aqueous electrolyte of the present invention to impart flame retardancy. If the amount of flame retardant added is too small, sufficient flame retarding effect cannot be exerted.If it is too large, not only an increase effect corresponding to the blending amount can be obtained, but on the other hand, the characteristics of the non-aqueous electrolyte Since it may have an adverse effect, the content is preferably 1 to 50% by mass, more preferably 3 to 10% by mass with respect to the organic solvent constituting the nonaqueous electrolytic solution of the present invention.
- the non-aqueous electrolyte of the present invention can be used as a non-aqueous electrolyte of either a primary battery or a secondary battery.
- a non-aqueous electrolyte secondary battery such as the present invention, particularly a lithium ion secondary battery, is used. By using it as a non-aqueous electrolyte to constitute, the above effects are exhibited.
- a non-aqueous electrolyte secondary battery includes an anode from which lithium can be inserted and removed, a cathode containing a transition metal and lithium, and a non-aqueous electrolyte in which a lithium salt is dissolved in an organic solvent.
- the nonaqueous electrolytic solution of the present invention is used as the nonaqueous electrolytic solution.
- the anode from which lithium can be inserted / removed is not particularly limited as long as lithium can be inserted / removed, but is preferably as follows. That is, as the anode of the non-aqueous electrolyte secondary battery of the present invention, a slurry obtained by slurrying an anode active material and a binder with an organic solvent or water was applied to a current collector and dried to form a sheet. A thing is used and a electrically conductive material is mix
- anode active material natural graphite, artificial graphite, non-graphitizable carbon, graphitizable carbon, lithium, lithium alloy, tin alloy, silicon alloy, silicon oxide, titanium oxide, and the like are used, but not limited thereto.
- binder for the anode include, but are not limited to, polyvinylidene fluoride, polytetrafluoroethylene, EPDM, SBR, NBR, fluororubber, and polyacrylic acid.
- the amount of the anode binder used is preferably 0.001 to 5 parts by mass, more preferably 0.05 to 3 parts by mass, and most preferably 0.01 to 2 parts by mass with respect to 100 parts by mass of the anode active material. .
- Examples of the slurry for the anode slurry include N-methylpyrrolidone, dimethylformamide, dimethylacetamide, methyl ethyl ketone, cyclohexanone, methyl acetate, methyl acrylate, diethyltriamine, N, N-dimethylaminopropylamine, polyethylene oxide, tetrahydrofuran and the like.
- the amount of the solvent used is preferably 30 to 300 parts by mass, more preferably 50 to 200 parts by mass, with respect to 100 parts by mass of the anode active material.
- copper, nickel, stainless steel, nickel-plated steel or the like is used for the current collector of the anode.
- the conductive material blended as necessary graphene, fine particles of graphite, carbon black such as acetylene black and ketjen black, fine particles of amorphous carbon such as needle coke, carbon nanofiber, etc. are used. However, it is not limited to these.
- the cathode containing a transition metal and lithium used in the present invention is a current collector obtained by slurrying a cathode active material, a binder, a conductive material, etc. with an organic solvent or water, as in a normal secondary battery. It is used after being applied to and dried to form a sheet.
- the cathode active material contains a transition metal and lithium, and a material containing one kind of transition metal and lithium is preferable. Examples thereof include a lithium transition metal composite oxide and a lithium-containing transition metal phosphate compound. These may be used in combination.
- the transition metal of the lithium transition metal composite oxide vanadium, titanium, chromium, manganese, iron, cobalt, nickel, copper and the like are preferable.
- the lithium transition metal composite oxide include lithium cobalt composite oxide such as LiCoO 2 , lithium nickel composite oxide such as LiNiO 2 , and lithium manganese composite oxide such as LiMnO 2 , LiMn 2 O 4 , and Li 2 MnO 3.
- Some of the transition metal atoms that are the main components of these lithium transition metal composite oxides are aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, lithium, nickel, copper, zinc, magnesium, gallium, zirconium, etc. The thing substituted with the other metal etc. are mentioned.
- substituted ones include, for example, LiNi 0.5 Mn 0.5 O 2 , LiNi 0.80 Co 0.17 Al 0.03 O 2 , LiNi 1/3 Co 1/3 Mn 1/3 O 2 , LiMn 1.8 Al 0.2 O 4 , LiMn 1.5 Ni 0.5 O 4 or the like.
- transition metal of the lithium-containing transition metal phosphate compound vanadium, titanium, manganese, iron, cobalt, nickel and the like are preferable.
- iron phosphates such as LiFePO 4 and phosphorus such as LiCoPO 4.
- Cobalt acids some of the transition metal atoms that are the main components of these lithium transition metal phosphate compounds are aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, lithium, nickel, copper, zinc, magnesium, gallium, zirconium And those substituted with other metals such as niobium.
- the cathode binder and slurry solvent are the same as those used in the anode.
- the amount of the binder used for the cathode is preferably 0.001 to 20 parts by mass, more preferably 0.01 to 10 parts by mass, and most preferably 0.02 to 8 parts by mass with respect to 100 parts by mass of the cathode active material.
- the amount of the cathode solvent used is preferably from 30 to 300 parts by weight, more preferably from 50 to 200 parts by weight, based on 100 parts by weight of the cathode active material.
- Examples of the conductive material for the cathode include graphene, graphite fine particles, carbon black such as acetylene black and ketjen black, amorphous carbon fine particles such as needle coke, and carbon nanofibers, but are not limited thereto.
- the amount of the conductive material used for the cathode is preferably 0.01 to 20 parts by mass, more preferably 0.1 to 10 parts by mass with respect to 100 parts by mass of the cathode active material.
- As the cathode current collector aluminum, stainless steel, nickel-plated steel or the like is usually used.
- a separator between the cathode and the anode it is preferable to use a separator between the cathode and the anode, and as the separator, a commonly used polymer microporous film can be used without any particular limitation.
- the film include polyethylene, polypropylene, polyvinylidene fluoride, polyvinylidene chloride, polyacrylonitrile, polyacrylamide, polytetrafluoroethylene, polysulfone, polyethersulfone, polycarbonate, polyamide, polyimide, polyethylene oxide and polypropylene oxide.
- the microporosity method includes a phase separation method in which a polymer compound and a solvent solution are formed into a film while microphase separation is performed, and the solvent is extracted and removed to make it porous.
- the film is extruded and then heat treated, the crystals are arranged in one direction, and a “stretching method” or the like is performed by forming a gap between the crystals by stretching, and is appropriately selected depending on the film used.
- the cathode material, the non-aqueous electrolyte, and the separator include a phenol-based antioxidant, a phosphorus-based antioxidant, and a thioether-based antioxidant for the purpose of improving safety.
- a hindered amine compound or the like may be added.
- the shape of the nonaqueous electrolyte secondary battery of the present invention having the above configuration is not particularly limited, and can be various shapes such as a coin shape, a cylindrical shape, and a square shape.
- FIG. 1 shows an example of a coin-type battery of the nonaqueous electrolyte secondary battery of the present invention
- FIGS. 2 and 3 show examples of a cylindrical battery.
- 1 is a cathode capable of releasing lithium ions
- 1a is a cathode current collector
- 2 is a carbonaceous material capable of occluding and releasing lithium ions released from the cathode.
- An anode current collector, 2a is an anode current collector
- 3 is a non-aqueous electrolyte of the present invention
- 4 is a stainless steel cathode case
- 5 is a stainless steel anode case
- 6 is a polypropylene gasket
- 7 is a polyethylene separator. It is.
- 11 is an anode
- 12 is an anode current collector
- 13 is a cathode
- 14 is a cathode current collector
- 15 is the present invention.
- Nonaqueous electrolyte, 16 is a separator
- 17 is a cathode terminal
- 18 is an anode terminal
- 19 is an anode plate
- 20 is an anode lead
- 21 is a cathode plate
- 22 is a cathode lead
- 23 is a case
- 24 is an insulating plate
- 25 is A gasket
- 26 is a safety valve
- 27 is a PTC element.
- the novel compound of the present invention is represented by the general formula (1 ′), and among the compounds represented by the general formula (1) described in the above item ⁇ Non-aqueous electrolyte>, Z (Z ′) is R 1 O—S ( ⁇ O) 2 —, R 12 —S ( ⁇ O) 2 —, R 1 O—S ( ⁇ O) — or R 12 —S ( ⁇ O) —, and R 1 (R 1 ′) is a hydrocarbon group having 1 to 20 carbon atoms having a substituent, or R 12 (R 12 ′) is a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms having a substituent. To do.
- Examples of the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 ′ and R 12 ′ include the groups exemplified as the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 and R 12 .
- group substituting the hydrocarbon group represented by R 1 'and R 12' is a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, -SiR 9 'R 10' R 11 ′ or a phosphate group.
- the 'Ar in the general formula (1)' is the same as Ar in formula (1), identical to the 'R 1 in the general formula (1)', R 1 in the formula (1) ' R ′ in the general formula (1 ′) is the same as R in the general formula (1), and R 9 ′, R 10 ′ and R 11 ′ in the general formula (1 ′) are respectively R 9 , R 10 and R 11 in general formula (1) are the same, and m ′ and n ′ in general formula (1 ′) are the same as m and n in general formula (1), respectively. .
- novel compound of this invention can be used for uses, such as surfactant and its precursor other than the use as an additive of the non-aqueous electrolyte mentioned above.
- Synthesis Examples 1 to 3 below are synthesis examples of the compound represented by the general formula (1) used in the non-aqueous electrolyte of the present invention.
- Example 1 and Comparative Examples 1 and 2 below are examples of the non-aqueous electrolyte secondary battery of the present invention and comparative examples thereof.
- nonaqueous electrolyte secondary batteries lithium secondary batteries
- LiPF 6 was dissolved at a concentration of 1 mol / L in a mixed solvent consisting of 30% by volume of ethylene carbonate, 40% by volume of ethyl methyl carbonate, and 30% by volume of dimethyl carbonate to prepare an electrolyte solution.
- ⁇ Discharge capacity ratio test method The lithium secondary battery was placed in a constant temperature bath at 20 ° C., charged at a constant current and a constant voltage up to 4.2 V with a charging current of 0.3 mA / cm 2 (current value corresponding to 0.2 C), and a discharge current of 0.3 mA / The operation of discharging a constant current to 3.0 V at cm 2 (current value corresponding to 0.2 C) was performed 5 times. Thereafter, the battery was charged at a constant current and a constant voltage up to 4.2 V at a charging current of 0.3 mA / cm 2 and discharged at a constant current of 3.0 mA at a discharge current of 0.3 mA / cm 2 .
- the discharge capacity measured at the sixth time is defined as the initial discharge capacity of the battery.
- the compound represented by the general formula (1) used in the non-aqueous electrolyte of the present invention can suppress an increase in voltage during overcharging without deteriorating battery characteristics (discharge capacity). is there.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Inorganic Chemistry (AREA)
- Secondary Cells (AREA)
Abstract
Description
(式中、Arは、ベンゼン環又はナフタレン環を表し、
Zは、R1O-S(=O)2-、R12-S(=O)2-、R1O-S(=O)-又はR12-S(=O)-を表し、
R1は、置換基を有する又は無置換の炭素原子数1~20の炭化水素基を表し、
R2は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9R10R11、リン酸基、又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R12は、ハロゲン原子又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R1、R2及びR12が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9R10R11又はリン酸基であり、
R1、R2及びR12が表す炭化水素基中のアルキレンは、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-又は-CO-NR-が隣り合わない条件で、1~3回中断していてもよく、
Rは、炭素原子数1~5の脂肪族炭化水素基を表し、
R2が炭化水素基を表す場合、R2とArが結合する部位は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-NR-CO-、-CO-NR-又は-N=により中断していてもよく、
R9、R10及びR11は、炭素原子数1~16の炭化水素基を表し、
m及びnは、それぞれ1以上の整数を表し、Arがベンゼン環を表す場合、m+nは6以下であり、Arがナフタレン環を表す場合、m+nは10以下であり、
mが2以上の場合、Zは同一でも異なっていてもよく、nが2以上の場合、R2は同一でも異なっていてもよい。
但し、n個のR2のうち、少なくとも1つは、下記一般式(2)又は(3)で表される基である。)
(式中、R3、R4、R5及びR6は各々独立に置換基を有するか又は無置換の炭素原子数1~18の炭化水素基を表し、
R3、R4、R5及びR6が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9R10R11又はリン酸基であり、
R3、R4、R5及びR6が表す炭化水素基中のアルキレン基は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-又は-CO-NR-が隣り合わない条件で、1~3回中断していてもよく、
Rは、炭素原子数1~5の脂肪族炭化水素基を表し、
R7及びR8は、各々独立に水素原子、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9R10R11又はリン酸基を表し、
R9、R10及びR11は、各々独立に炭素原子数1~16の炭化水素基を表し、
但し、一般式(2)及び(3)は、基全体として炭素原子数が3~20の範囲内である。) That is, the present invention provides a non-aqueous electrolyte characterized by containing at least one compound represented by the following general formula (1) in a non-aqueous electrolyte in which a lithium salt is dissolved in an organic solvent. Is.
(In the formula, Ar represents a benzene ring or a naphthalene ring,
Z represents R 1 O—S (═O) 2 —, R 12 —S (═O) 2 —, R 1 O—S (═O) — or R 12 —S (═O) —,
R 1 represents a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms,
R 2 represents a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 , a phosphate group, or a substituted or unsubstituted carbon atom. Represents a hydrocarbon group of the number 1 to 20,
R 12 represents a halogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms,
The group that replaces the hydrocarbon group represented by R 1 , R 2 and R 12 is a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 or A phosphate group,
The alkylene in the hydrocarbon group represented by R 1 , R 2 and R 12 is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, —S—, -SO-, -SO 2- , -NR-CO- or -CO-NR- may be interrupted 1 to 3 times under the condition that they are not adjacent to each other,
R represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
When R 2 represents a hydrocarbon group, the site where R 2 and Ar are bonded is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, —S. May be interrupted by-, -NR-CO-, -CO-NR- or -N =,
R 9 , R 10 and R 11 represent a hydrocarbon group having 1 to 16 carbon atoms,
m and n each represent an integer of 1 or more, and when Ar represents a benzene ring, m + n is 6 or less, and when Ar represents a naphthalene ring, m + n is 10 or less,
When m is 2 or more, Z may be the same or different, and when n is 2 or more, R 2 may be the same or different.
However, at least one of n R 2 is a group represented by the following general formula (2) or (3). )
(Wherein R 3 , R 4 , R 5 and R 6 each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms,
Groups that substitute for the hydrocarbon groups represented by R 3 , R 4 , R 5 and R 6 are halogen atoms, nitrile groups, nitro groups, amino groups, carboxyl groups, hydroxyl groups, thiol groups, formyl groups, sulfone groups, —SiR. 9 R 10 R 11 or a phosphate group,
The alkylene group in the hydrocarbon group represented by R 3 , R 4 , R 5 and R 6 is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, -S-, -SO-, -SO 2- , -NR-CO- or -CO-NR- may be interrupted 1 to 3 times under the condition that they are not adjacent to each other,
R represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
R 7 and R 8 are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 R 10 R 11 or phosphate group Represents
R 9 , R 10 and R 11 each independently represents a hydrocarbon group having 1 to 16 carbon atoms,
However, in the general formulas (2) and (3), the number of carbon atoms as a whole is in the range of 3 to 20. )
(式中、Ar’は、ベンゼン環又はナフタレン環を表し、
Z’は、R1’O-S(=O)2-、R12’-S(=O)2-、R1’O-S(=O)-又はR12’-S(=O)-を表し、
R1’は、置換基を有する炭素原子数1~20の炭化水素基を表し、
R2’は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9’R10’R11’、リン酸基、又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R12’は、ハロゲン原子又は置換基を有する炭素原子数1~20の炭化水素基を表し、
R1’、R2’及びR12’が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9’R10’R11’又はリン酸基であり、
R1’、R2’及びR12’が表す炭化水素基中のアルキレンは、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-SO-、-SO2-、-NR’-CO-又は-CO-NR’-が隣り合わない条件で、1~3回中断していてもよく、
R’は、炭素原子数1~5の脂肪族炭化水素基を表し、
R2’が炭化水素基を表す場合、R2’とAr’が結合する部位は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-NR’-CO-、-CO-NR’-又は-N=により中断していてもよく、
R9’、R10’及びR11’は、炭素原子数1~16の炭化水素基を表し、
m’及びn’は、それぞれ1以上の整数を表し、Ar’がベンゼン環を表す場合、m’+n’は6以下であり、Ar’がナフタレン環を表す場合、m’+n’は10以下であり、
m’が2以上の場合、Z’は同一でも異なっていてもよく、n’が2以上の場合、R2’は同一でも異なっていてもよい。
が2以上の場合、R2’は同一でも異なっていてもよい。
但し、n’個のR2’のうち、少なくとも1つは、下記一般式(2’)又は(3’)で表される基である。)
(式中、R3’、R4’、R5’及びR6’は各々独立に置換基を有するか又は無置換の炭素原子数1~18の炭化水素基を表し、
R3’、R4’、R5’及びR6’が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9’R10’R11’又はリン酸基であり、
R3’、R4’、R5’及びR6’が表す炭化水素基中のアルキレン基は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-SO-、-SO2-、-NR’-CO-又は-CO-NR’-が隣り合わない条件で、1~3回中断していてもよく、
R’は、炭素原子数1~5の脂肪族炭化水素基を表し、
R7’及びR8’は、各々独立に水素原子、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9’R10’R11’又はリン酸基を表し、
R9’、R10’及びR11’は、各々独立に炭素原子数1~16の炭化水素基を表し、
但し、一般式(2’)及び(3’)は、基全体として炭素原子数が3~20の範囲内である。) The present invention also provides a compound represented by the following general formula (1 ′).
(In the formula, Ar ′ represents a benzene ring or a naphthalene ring,
Z 'is, R 1' O-S ( = O) 2 -, R 12 '-S (= O) 2 -, R 1' O-S (= O) - or R 12 '-S (= O) -Represents
R 1 ′ represents a hydrocarbon group having 1 to 20 carbon atoms having a substituent,
R 2 ′ has a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 ′ R 10 ′ R 11 ′, a phosphate group, a phosphate group, or a substituent. Represents a substituted hydrocarbon group having 1 to 20 carbon atoms,
R 12 ′ represents a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms having a substituent,
R 1 ', R 2' and R 12 'group substituting the hydrocarbon group represented by a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, -SiR 9' R 10 is a 'R 11' or phosphoric acid group,
The alkylene in the hydrocarbon group represented by R 1 ′, R 2 ′ and R 12 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR′—, -S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are not adjacent, may also be interrupted 1-3 times,
R ′ represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
When R 2 ′ represents a hydrocarbon group, the sites where R 2 ′ and Ar ′ are bonded are —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR ′. May be interrupted by-, -S-, -NR'-CO-, -CO-NR'- or -N =,
R 9 ′, R 10 ′ and R 11 ′ represent a hydrocarbon group having 1 to 16 carbon atoms,
m ′ and n ′ each represents an integer of 1 or more, and when Ar ′ represents a benzene ring, m ′ + n ′ is 6 or less, and when Ar ′ represents a naphthalene ring, m ′ + n ′ is 10 or less. And
When m ′ is 2 or more, Z ′ may be the same or different. When n ′ is 2 or more, R 2 ′ may be the same or different.
Are 2 or more, R 2 ′ may be the same or different.
However, at least one of n ′ R 2 ′ is a group represented by the following general formula (2 ′) or (3 ′). )
(Wherein R 3 ′, R 4 ′, R 5 ′ and R 6 ′ each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms,
The hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is a halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone. A group, -SiR 9 'R 10 ' R 11 'or a phosphate group,
The alkylene group in the hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, -NR '-, - S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are not adjacent, may also be interrupted 1-3 times,
R ′ represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
R 7 ′ and R 8 ′ are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 ′ R 10 ′ R 11 'Or represents a phosphate group,
R 9 ′, R 10 ′ and R 11 ′ each independently represents a hydrocarbon group having 1 to 16 carbon atoms,
However, in the general formulas (2 ′) and (3 ′), the number of carbon atoms as a whole group is in the range of 3 to 20. )
<非水電解液>
本発明で用いられるリチウム塩を有機溶媒に溶解させた非水電解液(以下、本発明の非水電解液ともいう)について説明する。本発明の非水電解液は、上記一般式(1)で表される化合物を含有する。以下、この化合物について説明する。
一般式(1)におけるR1、R2及びR12が表す炭素原子数1~20の炭化水素基としては、炭素原子数1~20の飽和及び不飽和の脂肪族炭化水素基、炭素原子数6~20の芳香族炭化水素基が挙げられる。炭素原子数1~20の飽和及び不飽和の炭化水素基としては、メチル、エチル、プロピル、イソプロピル、2-プロピニル、ブチル、イソブチル、s-ブチル、t-ブチル、ペンチル、イソペンチル、s-ペンチル、ヘキシル、2-エチルヘキシル、デシル、ドデシル、オクタデシル等の飽和炭化水素基や、ビニル、エチニル、アリル、プロパルギル、3-ブテニル、イソブテニル、3-ブチニル、4-ペンテニル、5-ヘキセニル等の不飽和炭化水素基が挙げられる。炭素原子数6~20の芳香族炭化水素基としては、フェニル、ナフチル、シクロヘキシルフェニル、ビフェニル、フルオレイル、2’-フェニル-プロピルフェニル、ベンジル、ナフチルメチル等が挙げられる。
R1、R2及びR12が表す炭素原子数1~20の炭化水素基中のアルキレン(R2の場合は、Arと結合する部位も含む)は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-、-CO、-NR-又は-N=が隣り合わない条件で、1~3回中断していてもよく、Rは、炭素原子数1~5の脂肪族炭化水素基である。
但し、中断する基が炭素原子を含む場合、中断する基の炭素原子数を含めた炭素原子数が1~20となる。
Rを表す炭素原子数1~5の脂肪族炭化水素基としては、R1で説明したもののうち、炭素原子数1~5の飽和及び不飽和の脂肪族炭化水素基等が挙げられる。
R1、R2及びR12が表す炭素原子数1~20の炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9R10R11又はリン酸基であり、R9、R10及びR11は、炭素原子数1~16の炭化水素基である。尚、置換する基が炭素原子を含む基である場合、置換する基の炭素原子数を含めた炭素原子数が1~20となる。
ハロゲン原子としては、フッ素原子、塩素原子、臭素原子、ヨウ素原子等が挙げられる。尚、本明細書中におけるハロゲン原子は、全てこれと同様である。
R9、R10及びR11が表す炭素原子数1~16の脂肪族炭化水素基としては、R1で説明したもののうち、炭素原子数が1~16のものと同様の基が挙げられる。 Hereinafter, the non-aqueous electrolyte and the non-aqueous electrolyte secondary battery of the present invention will be described in detail based on preferred embodiments.
<Non-aqueous electrolyte>
A nonaqueous electrolytic solution in which a lithium salt used in the present invention is dissolved in an organic solvent (hereinafter also referred to as a nonaqueous electrolytic solution of the present invention) will be described. The nonaqueous electrolytic solution of the present invention contains a compound represented by the above general formula (1). Hereinafter, this compound will be described.
The hydrocarbon group having 1 to 20 carbon atoms represented by R 1 , R 2 and R 12 in the general formula (1) is a saturated or unsaturated aliphatic hydrocarbon group having 1 to 20 carbon atoms, the number of carbon atoms Examples include 6 to 20 aromatic hydrocarbon groups. Examples of saturated and unsaturated hydrocarbon groups having 1 to 20 carbon atoms include methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, Saturated hydrocarbon groups such as hexyl, 2-ethylhexyl, decyl, dodecyl, octadecyl, and unsaturated hydrocarbons such as vinyl, ethynyl, allyl, propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, etc. Groups. Examples of the aromatic hydrocarbon group having 6 to 20 carbon atoms include phenyl, naphthyl, cyclohexylphenyl, biphenyl, fluoryl, 2′-phenyl-propylphenyl, benzyl, naphthylmethyl and the like.
In the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 , R 2 and R 12 , alkylene (in the case of R 2 , including a site bonded to Ar) is —O—, —CO—, —OCO. —, —COO—, —O—CO—O—, —NR—, —S—, —SO—, —SO 2 —, —NR—CO—, —CO, —NR— or —N═ are adjacent to each other. May be interrupted 1 to 3 times, and R is an aliphatic hydrocarbon group having 1 to 5 carbon atoms.
However, when the interrupting group includes a carbon atom, the number of carbon atoms including the number of carbon atoms of the interrupting group is 1 to 20.
Examples of the aliphatic hydrocarbon group having 1 to 5 carbon atoms that represents R include saturated and unsaturated aliphatic hydrocarbon groups having 1 to 5 carbon atoms among those described for R 1 .
R 1 , R 2 and R 12 represent a group that substitutes for a hydrocarbon group having 1 to 20 carbon atoms, such as a halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group,- It is SiR 9 R 10 R 11 or a phosphate group, and R 9 , R 10 and R 11 are hydrocarbon groups having 1 to 16 carbon atoms. When the group to be substituted is a group containing a carbon atom, the number of carbon atoms including the number of carbon atoms of the group to be substituted is 1 to 20.
Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. In addition, all the halogen atoms in this specification are the same as this.
Examples of the aliphatic hydrocarbon group having 1 to 16 carbon atoms represented by R 9 , R 10 and R 11 include the same groups as those having 1 to 16 carbon atoms among those described for R 1 .
一般式(2)又は(3)におけるR3、R4、R5及びR6が表す炭素原子数1~18の炭化水素基は、R1で説明したもののうち、炭素原子数が1~18のものと同様の基が挙げられる。
R3、R4、R5及びR6が表す炭素原子数1~18の炭化水素基中のアルキレン基は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-、-CO又は-NR-が隣り合わない条件で、1~3回中断していてもよく、Rは、炭素原子数1~5の脂肪族炭化水素基である。
但し、中断する基が炭素原子を含む場合、中断する基の炭素原子数を含めた炭素原子数が1~18となる。
R3、R4、R5及びR6が表す炭素原子数1~18の炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9R10R11又はリン酸基であり、R9、R10及びR11は、炭素原子数1~16の炭化水素基である。尚、置換する基が炭素原子を含む基である場合、置換する基の炭素原子数を含めた炭素原子数が1~16となる。 At least one of the n R 2 in the general formula (1) is a group represented by the general formula (2) or (3).
The hydrocarbon group having 1 to 18 carbon atoms represented by R 3 , R 4 , R 5 and R 6 in the general formula (2) or (3) has 1 to 18 carbon atoms among those described for R 1. And the same groups as those mentioned above.
The alkylene group in the hydrocarbon group having 1 to 18 carbon atoms represented by R 3 , R 4 , R 5 and R 6 is —O—, —CO—, —OCO—, —COO—, —O—CO—. O—, —NR—, —S—, —SO—, —SO 2 —, —NR—CO—, —CO or —NR— may be interrupted 1 to 3 times under the condition that they are not adjacent to each other, R is an aliphatic hydrocarbon group having 1 to 5 carbon atoms.
However, when the interrupting group includes a carbon atom, the number of carbon atoms including the number of carbon atoms of the interrupting group is 1 to 18.
R 3 , R 4 , R 5 and R 6 can be substituted with a hydrocarbon group having 1 to 18 carbon atoms such as halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl Group, a sulfone group, —SiR 9 R 10 R 11 or a phosphoric acid group, and R 9 , R 10 and R 11 are hydrocarbon groups having 1 to 16 carbon atoms. When the group to be substituted is a group containing a carbon atom, the number of carbon atoms including the number of carbon atoms of the group to be substituted is 1 to 16.
また、♯1~♯7において、R2のうち、一般式(2)又は(3)で表される基を、R2A、それ以外の基を、R2Bとして、Arに対するZ、R2A及びR2Bの置換数及び置換位置を反映させると、下記の♯8~♯17が一例として挙げられる。
Further, in # 1 ~ # 7, of R 2, general formula (2) or a group represented by (3), R 2A, the other group, as R 2B, Z for Ar, R 2A and Reflecting the number of R 2B substitutions and the substitution position, the following # 8 to # 17 are given as an example.
また、R2のうち、一般式(2)又は(3)以外の基(R2B)で好ましい基としては、ハロゲン原子、エステル基、アミド基等が挙げられる。
また、Zとしては、ZがR1O-S(=O)2-又はR1O-S(=O)-の場合、R1が、ハロゲン原子で置換された又は無置換の炭素原子数1~6の飽和又は不飽和の脂肪族炭化水素基(メチル、エチル、プロピル、イソプロピル、2-プロピニル、ブチル、イソブチル、s-ブチル、t-ブチル、ペンチル、イソペンチル、s-ペンチル、ヘキシル、ビニル、エチニル、アリル、プロパルギル、3-ブテニル、イソブテニル、3-ブチニル、4-ペンテニル、5-ヘキセニル又はこれらの基の一部がハロゲン原子で置換されたもの等)であるものが好ましく、
またZがR12-S(=O)2-又はR12-S(=O)-である場合、R12がハロゲン原子又はハロゲン原子で置換された若しくは無置換の炭素原子数1~6の飽和又は不飽和の脂肪族炭化水素基(メチル、エチル、プロピル、イソプロピル、2-プロピニル、ブチル、イソブチル、s-ブチル、t-ブチル、ペンチル、イソペンチル、s-ペンチル、ヘキシル、ビニル、エチニル、アリル、プロパルギル、3-ブテニル、イソブテニル、3-ブチニル、4-ペンテニル、5-ヘキセニル又はこれらの基の一部がハロゲン原子で置換されたもの等)であるものが好ましい。 Among the compounds represented by the general formula (1), at least one of n R 2 is a group represented by the general formula (2), particularly isopropyl, s-butyl, s A compound that is pentyl is preferred because it is excellent as an overcharge inhibitor.
In addition, among R 2 , preferred groups in the group (R 2B ) other than the general formula (2) or (3) include a halogen atom, an ester group, an amide group, and the like.
In addition, as Z, when Z is R 1 O—S (═O) 2 — or R 1 O—S (═O) —, R 1 is the number of carbon atoms substituted or unsubstituted by a halogen atom 1 to 6 saturated or unsaturated aliphatic hydrocarbon groups (methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, hexyl, vinyl Ethynyl, allyl, propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, or a group in which a part of these groups is substituted with a halogen atom, etc.
In addition, when Z is R 12 —S (═O) 2 — or R 12 —S (═O) —, R 12 is a halogen atom, a halogen atom-substituted or unsubstituted carbon atom having 1 to 6 carbon atoms. Saturated or unsaturated aliphatic hydrocarbon group (methyl, ethyl, propyl, isopropyl, 2-propynyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, s-pentyl, hexyl, vinyl, ethynyl, allyl , Propargyl, 3-butenyl, isobutenyl, 3-butynyl, 4-pentenyl, 5-hexenyl, or a group in which a part of these groups is substituted with a halogen atom is preferred.
また、本発明の非水電解液において、上記一般式(1)で表わされる化合物の含有量が、あまりに少ない場合には十分な効果を発揮できず、またあまりに多い場合には、配合量に見合う増量効果は得られないばかりか、却って非水電解液の特性に悪影響を及ぼすことがあることから、一般式(1)で表される化合物の含有量は、非水電解液中、0.001~10質量%が好ましく、0.01~8質量%が更に好ましく、0.1~5質量%が最も好ましい。 In the nonaqueous electrolytic solution of the present invention, the compound represented by the general formula (1) may be used alone or in combination of two or more.
Further, in the nonaqueous electrolytic solution of the present invention, when the content of the compound represented by the general formula (1) is too small, a sufficient effect cannot be exhibited, and when the content is too large, the compounding amount is met. The content of the compound represented by the general formula (1) is 0.001 in the non-aqueous electrolyte because not only the increase effect is obtained but also the characteristics of the non-aqueous electrolyte may be adversely affected. Is preferably 10 to 10% by mass, more preferably 0.01 to 8% by mass, and most preferably 0.1 to 5% by mass.
上記有機溶媒のうち、飽和鎖状カーボネート化合物、鎖状エーテル化合物、環状エーテル化合物及び飽和鎖状エステル化合物は、非水電解液の粘度を低くすることができ、電解質イオンの移動性を高くすることができる等、出力密度等の電池特性を優れたものにすることができる。また、低粘度であるため、低温での非水電解液の性能を高くすることができ、中でも、飽和鎖状カーボネート化合物が好ましい。斯かる飽和鎖状カーボネート化合物としては、例えば、ジメチルカーボネート(DMC)、エチルメチルカーボネート(EMC)、ジエチルカーボネート(DEC)、エチルブチルカーボネート、メチル-t-ブチルカーボネート、ジイソプロピルカーボネート、t-ブチルプロピルカーボネート等が挙げられる。上記の鎖状エーテル化合物又は環状エーテル化合物としては、例えば、ジメトキシエタン(DME)、エトキシメトキシエタン、ジエトキシエタン、テトラヒドロフラン、ジオキソラン、ジオキサン、1,2-ビス(メトキシカルボニルオキシ)エタン、1,2-ビス(エトキシカルボニルオキシ)エタン、1,2-ビス(エトキシカルボニルオキシ)プロパン、エチレングリコールビス(トリフルオロエチル)エーテル、プロピレングリコールビス(トリフルオロエチル)エーテル、エチレングリコールビス(トリフルオロメチル)エーテル、ジエチレングリコールビス(トリフルオロエチル)エーテル等が挙げられ、これらの中でも、ジオキソランが好ましい。
上記飽和鎖状エステル化合物としては、分子中の炭素数の合計が2~8であるモノエステル化合物及びジエステル化合物が好ましく、具体的な化合物としては、ギ酸メチル、ギ酸エチル、酢酸メチル、酢酸エチル、酢酸プロピル、酢酸イソブチル、酢酸ブチル、プロピオン酸メチル、プロピオン酸エチル、酪酸メチル、イソ酪酸メチル、トリメチル酢酸メチル、トリメチル酢酸エチル、マロン酸メチル、マロン酸エチル、コハク酸メチル、コハク酸エチル、3-メトキシプロピオン酸メチル、3-メトキシプロピオン酸エチル、エチレングリコールジアセチル、プロピレングリコールジアセチル等が挙げられ、ギ酸メチル、ギ酸エチル、酢酸メチル、酢酸エチル、酢酸プロピル、酢酸イソブチル、酢酸ブチル、プロピオン酸メチル、及びプロピオン酸エチルが好ましい。 Among the above organic solvents, saturated cyclic carbonate compounds, saturated cyclic ester compounds, sulfoxide compounds, sulfone compounds and amide compounds have a high relative dielectric constant, and thus serve to increase the dielectric constant of non-aqueous electrolytes. Compounds are preferred. Examples of such saturated cyclic carbonate compounds include ethylene carbonate, 1-fluoroethylene carbonate, 1,2-propylene carbonate, 1,3-propylene carbonate, 1,2-butylene carbonate, 1,3-butylene carbonate, 1, Examples thereof include 1, -dimethylethylene carbonate. Examples of the saturated cyclic ester compound include γ-butyrolactone, γ-valerolactone, γ-caprolactone, δ-hexanolactone, and δ-octanolactone. Examples of the sulfoxide compound include dimethyl sulfoxide, diethyl sulfoxide, dipropyl sulfoxide, diphenyl sulfoxide, thiophene, and the like. Examples of the sulfone compounds include dimethylsulfone, diethylsulfone, dipropylsulfone, diphenylsulfone, sulfolane (also referred to as tetramethylenesulfone), 3-methylsulfolane, 3,4-dimethylsulfolane, 3,4-diphenimethylsulfolane, sulfolene. , 3-methylsulfolene, 3-ethylsulfolene, 3-bromomethylsulfolene and the like, and sulfolane and tetramethylsulfolane are preferable. Examples of the amide compound include N-methylpyrrolidone, dimethylformamide, dimethylacetamide and the like.
Among the above organic solvents, saturated chain carbonate compounds, chain ether compounds, cyclic ether compounds and saturated chain ester compounds can lower the viscosity of the non-aqueous electrolyte and increase the mobility of electrolyte ions. Battery characteristics such as output density can be made excellent. Moreover, since it is low-viscosity, the performance of the non-aqueous electrolyte at a low temperature can be enhanced, and among them, a saturated chain carbonate compound is preferable. Examples of such saturated chain carbonate compounds include dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), ethyl butyl carbonate, methyl-t-butyl carbonate, diisopropyl carbonate, and t-butyl propyl carbonate. Etc. Examples of the chain ether compound or cyclic ether compound include dimethoxyethane (DME), ethoxymethoxyethane, diethoxyethane, tetrahydrofuran, dioxolane, dioxane, 1,2-bis (methoxycarbonyloxy) ethane, 1,2 -Bis (ethoxycarbonyloxy) ethane, 1,2-bis (ethoxycarbonyloxy) propane, ethylene glycol bis (trifluoroethyl) ether, propylene glycol bis (trifluoroethyl) ether, ethylene glycol bis (trifluoromethyl) ether And diethylene glycol bis (trifluoroethyl) ether. Among these, dioxolane is preferred.
As the saturated chain ester compound, monoester compounds and diester compounds having a total number of carbon atoms in the molecule of 2 to 8 are preferable. Specific compounds include methyl formate, ethyl formate, methyl acetate, ethyl acetate, Propyl acetate, isobutyl acetate, butyl acetate, methyl propionate, ethyl propionate, methyl butyrate, methyl isobutyrate, methyl trimethyl acetate, ethyl trimethyl acetate, methyl malonate, ethyl malonate, methyl succinate, ethyl succinate, 3- Methyl methoxypropionate, ethyl 3-methoxypropionate, ethylene glycol diacetyl, propylene glycol diacetyl, and the like, such as methyl formate, ethyl formate, methyl acetate, ethyl acetate, propyl acetate, isobutyl acetate, butyl acetate, methyl propionate, and Professional Ethyl propionic acid are preferred.
また、下記一般式(4)で表される化合物も好ましく用いることができる。 As an effect of adding the compound represented by the general formula (1), an overcharge preventing effect can be mentioned, but another overcharge preventing agent can be further added to the nonaqueous electrolytic solution of the present invention. As the overcharge inhibitor, aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, partially hydrogenated terphenyl, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, dibenzofuran; 2-fluorobiphenyl, Partially fluorinated products of the above aromatic compounds such as o-cyclohexylfluorobenzene and p-cyclohexylfluorobenzene; 2,4-difluoroanisole, 2,5-difluoroanisole, 2,6-difluoroanisole, 3,5-difluoroanisole and the like And a fluorine-containing anisole compound. Of these, aromatic compounds such as biphenyl, alkylbiphenyl, terphenyl, terphenyl partially hydrogenated compounds, cyclohexylbenzene, t-butylbenzene, t-amylbenzene, diphenyl ether, and dibenzofuran are preferable.
Moreover, the compound represented by following General formula (4) can also be used preferably.
(式中、R21、R22、R23、R24及びR25は、それぞれ独立して、置換基を有しているか若しくは無置換の炭素原子数1~20の脂肪族炭化水素基、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR29R30R31又はリン酸基を表し、
炭素原子数1~20の脂肪族炭化水素基は、基中のアルキレン(ベンゼン環と結合する部位も含む)が、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NRa-、-S-、-SO-、-SO2-、-NRa-CO-又は-CO-NRa-が隣り合わない条件で、1~3回中断していてもよく、
Raは、炭素原子数1~5の脂肪族炭化水素基を表し、
R21、R22、R23、R24及びR25の少なくとも一つはハロゲン原子により少なくとも一つ置換された炭素原子数1~20の脂肪族炭化水素基を表し、
R28は、p価の基を表し、
R26、R27、R29、R30及びR31は、それぞれ独立して、置換基を有している若しくは無置換の炭素原子数1~20の脂肪族炭化水素基又は置換基を有している若しくは無置換の炭素原子数6~20の芳香族炭化水素基を表し、
pは、1~3の整数を表す。)
(Wherein R 21 , R 22 , R 23 , R 24 and R 25 are each independently a substituted or unsubstituted aliphatic hydrocarbon group having 1 to 20 carbon atoms, halogen, Represents an atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, a sulfone group, —SiR 29 R 30 R 31 or a phosphate group;
In the aliphatic hydrocarbon group having 1 to 20 carbon atoms, the alkylene (including the portion bonded to the benzene ring) in the group is —O—, —CO—, —OCO—, —COO—, —O—CO. Interrupted 1 to 3 times under the condition that —O—, —NR a —, —S—, —SO—, —SO 2 —, —NR a —CO— or —CO—NR a — are not adjacent to each other. Well,
R a represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
At least one of R 21 , R 22 , R 23 , R 24 and R 25 represents an aliphatic hydrocarbon group having 1 to 20 carbon atoms substituted with at least one halogen atom;
R 28 represents a p-valent group,
R 26 , R 27 , R 29 , R 30 and R 31 each independently have a substituent or an unsubstituted aliphatic hydrocarbon group having 1 to 20 carbon atoms or a substituent. Represents an unsubstituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms,
p represents an integer of 1 to 3. )
また、R21~R26及びR29~R31が表す炭素原子数1~20の脂肪族炭化水素基並びにR26、R27、R29、R30及びR31が表す炭素原子数6~20の芳香族炭化水素基を置換する基としては、上記一般式(1)で説明しているものと同様の基が挙げられる。
上記一般式(4)で表される化合物の具体例としては、下記4-1~4-4等が挙げられるがこれに限定されない。 In the general formula (4), R 21 to R 27 and R 29 to R 31 represent an aliphatic hydrocarbon group having 1 to 20 carbon atoms, an aromatic hydrocarbon group having 6 to 20 carbon atoms, and R a Examples of the aliphatic hydrocarbon group having 1 to 5 carbon atoms include the same groups as those described in the general formula (1).
In addition, the aliphatic hydrocarbon group having 1 to 20 carbon atoms represented by R 21 to R 26 and R 29 to R 31, and the number of carbon atoms represented by R 26 , R 27 , R 29 , R 30 and R 31 are 6 to 20 Examples of the group for substituting the aromatic hydrocarbon group include the same groups as those described in the general formula (1).
Specific examples of the compound represented by the general formula (4) include, but are not limited to, the following 4-1 to 4-4.
本発明の非水電解液二次電池は、リチウムが脱挿入可能なアノード、遷移金属とリチウムを含有するカソード、及びリチウム塩を有機溶媒に溶解させた非水電解液を有する非水電解液二次電池において、非水電解液として、本発明の非水電解液を用いたものである。 <Nonaqueous electrolyte secondary battery>
A non-aqueous electrolyte secondary battery according to the present invention includes an anode from which lithium can be inserted and removed, a cathode containing a transition metal and lithium, and a non-aqueous electrolyte in which a lithium salt is dissolved in an organic solvent. In the secondary battery, the nonaqueous electrolytic solution of the present invention is used as the nonaqueous electrolytic solution.
本発明で用いられるリチウムが脱挿入可能なアノードは、リチウムが脱挿入可能であれば特に限定されないが、好ましくは次の通りである。すなわち、本発明の非水電解液二次電池のアノードとしては、アノード活物質と結着剤とを有機溶媒又は水でスラリー化したものを集電体に塗布し、乾燥してシート状にしたものが使用され、必要に応じて導電材が配合される。 <Anode>
The anode from which lithium can be inserted / removed is not particularly limited as long as lithium can be inserted / removed, but is preferably as follows. That is, as the anode of the non-aqueous electrolyte secondary battery of the present invention, a slurry obtained by slurrying an anode active material and a binder with an organic solvent or water was applied to a current collector and dried to form a sheet. A thing is used and a electrically conductive material is mix | blended as needed.
アノードの結着剤としては、例えば、ポリフッ化ビニリデン、ポリテトラフルオロエチレン、EPDM、SBR、NBR、フッ素ゴム、ポリアクリル酸等が挙げられるが、これらに限定されない。アノードの結着剤の使用量は、アノード活物質100質量部に対し、0.001~5質量部が好ましく、0.05~3質量部が更に好ましく、0.01~2質量部が最も好ましい。
アノードのスラリー化する溶媒としては、例えば、N-メチルピロリドン、ジメチルホルムアミド、ジメチルアセトアミド、メチルエチルケトン、シクロヘキサノン、酢酸メチル、アクリル酸メチル、ジエチルトリアミン、N,N-ジメチルアミノプロピルアミン、ポリエチレンオキシド、テトラヒドロフラン等が挙げられるが、これに限定されない。溶媒の使用量は、アノード活物質100質量部に対し、30~300質量部が好ましく、50~200質量部が更に好ましい。
アノードの集電体には、通常、銅、ニッケル、ステンレス鋼、ニッケルメッキ鋼等が使用される。
また、必要に応じて配合される導電材としては、グラフェン、グラファイトの微粒子、アセチレンブラック、ケッチェンブラック等のカーボンブラック、ニードルコークス等の無定形炭素の微粒子等、カーボンナノファイバー等が使用されるが、これらに限定されない。 As the anode active material, natural graphite, artificial graphite, non-graphitizable carbon, graphitizable carbon, lithium, lithium alloy, tin alloy, silicon alloy, silicon oxide, titanium oxide, and the like are used, but not limited thereto. .
Examples of the binder for the anode include, but are not limited to, polyvinylidene fluoride, polytetrafluoroethylene, EPDM, SBR, NBR, fluororubber, and polyacrylic acid. The amount of the anode binder used is preferably 0.001 to 5 parts by mass, more preferably 0.05 to 3 parts by mass, and most preferably 0.01 to 2 parts by mass with respect to 100 parts by mass of the anode active material. .
Examples of the slurry for the anode slurry include N-methylpyrrolidone, dimethylformamide, dimethylacetamide, methyl ethyl ketone, cyclohexanone, methyl acetate, methyl acrylate, diethyltriamine, N, N-dimethylaminopropylamine, polyethylene oxide, tetrahydrofuran and the like. However, it is not limited to this. The amount of the solvent used is preferably 30 to 300 parts by mass, more preferably 50 to 200 parts by mass, with respect to 100 parts by mass of the anode active material.
Usually, copper, nickel, stainless steel, nickel-plated steel or the like is used for the current collector of the anode.
Further, as the conductive material blended as necessary, graphene, fine particles of graphite, carbon black such as acetylene black and ketjen black, fine particles of amorphous carbon such as needle coke, carbon nanofiber, etc. are used. However, it is not limited to these.
本発明で用いられる遷移金属とリチウムを含有するカソードとしては、通常の二次電池と同様に、カソード活物質、結着剤、導電材等を有機溶媒又は水でスラリー化したものを集電体に塗布し、乾燥してシート状にしたものが使用される。カソード活物質は、遷移金属とリチウムを含有するものであり、1種の遷移金属とリチウムを含有する物質が好ましく、例えば、リチウム遷移金属複合酸化物、リチウム含有遷移金属リン酸化合物等が挙げられ、これらを混合して用いてもよい。上記リチウム遷移金属複合酸化物の遷移金属としてはバナジウム、チタン、クロム、マンガン、鉄、コバルト、ニッケル、銅等が好ましい。リチウム遷移金属複合酸化物の具体例としては、LiCoO2等のリチウムコバルト複合酸化物、LiNiO2等のリチウムニッケル複合酸化物、LiMnO2、LiMn2O4、Li2MnO3等のリチウムマンガン複合酸化物、これらのリチウム遷移金属複合酸化物の主体となる遷移金属原子の一部をアルミニウム、チタン、バナジウム、クロム、マンガン、鉄、コバルト、リチウム、ニッケル、銅、亜鉛、マグネシウム、ガリウム、ジルコニウム等の他の金属で置換したもの等が挙げられる。置換されたものの具体例としては、例えば、LiNi0.5Mn0.5O2、LiNi0.80Co0.17Al0.03O2、LiNi1/3Co1/3Mn1/3O2、LiMn1.8Al0.2O4、LiMn1.5Ni0.5O4等が挙げられる。上記リチウム含有遷移金属リン酸化合物の遷移金属としては、バナジウム、チタン、マンガン、鉄、コバルト、ニッケル等が好ましく、具体例としては、例えば、LiFePO4等のリン酸鉄類、LiCoPO4等のリン酸コバルト類、これらのリチウム遷移金属リン酸化合物の主体となる遷移金属原子の一部をアルミニウム、チタン、バナジウム、クロム、マンガン、鉄、コバルト、リチウム、ニッケル、銅、亜鉛、マグネシウム、ガリウム、ジルコニウム、ニオブ等の他の金属で置換したもの等が挙げられる。 <Cathode>
The cathode containing a transition metal and lithium used in the present invention is a current collector obtained by slurrying a cathode active material, a binder, a conductive material, etc. with an organic solvent or water, as in a normal secondary battery. It is used after being applied to and dried to form a sheet. The cathode active material contains a transition metal and lithium, and a material containing one kind of transition metal and lithium is preferable. Examples thereof include a lithium transition metal composite oxide and a lithium-containing transition metal phosphate compound. These may be used in combination. As the transition metal of the lithium transition metal composite oxide, vanadium, titanium, chromium, manganese, iron, cobalt, nickel, copper and the like are preferable. Specific examples of the lithium transition metal composite oxide include lithium cobalt composite oxide such as LiCoO 2 , lithium nickel composite oxide such as LiNiO 2 , and lithium manganese composite oxide such as LiMnO 2 , LiMn 2 O 4 , and Li 2 MnO 3. Some of the transition metal atoms that are the main components of these lithium transition metal composite oxides are aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, lithium, nickel, copper, zinc, magnesium, gallium, zirconium, etc. The thing substituted with the other metal etc. are mentioned. Specific examples of the substituted ones include, for example, LiNi 0.5 Mn 0.5 O 2 , LiNi 0.80 Co 0.17 Al 0.03 O 2 , LiNi 1/3 Co 1/3 Mn 1/3 O 2 , LiMn 1.8 Al 0.2 O 4 , LiMn 1.5 Ni 0.5 O 4 or the like. As the transition metal of the lithium-containing transition metal phosphate compound, vanadium, titanium, manganese, iron, cobalt, nickel and the like are preferable. Specific examples thereof include iron phosphates such as LiFePO 4 and phosphorus such as LiCoPO 4. Cobalt acids, some of the transition metal atoms that are the main components of these lithium transition metal phosphate compounds are aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, lithium, nickel, copper, zinc, magnesium, gallium, zirconium And those substituted with other metals such as niobium.
カソードの導電材としては、グラフェン、グラファイトの微粒子、アセチレンブラック、ケッチェンブラック等のカーボンブラック、ニードルコークス等の無定形炭素の微粒子等、カーボンナノファイバー等が使用されるが、これらに限定されない。カソードの導電材の使用量は、カソード活物質100質量部に対し、0.01~20質量部が好ましく、0.1~10質量部が更に好ましい。
カソードの集電体としては、通常、アルミニウム、ステンレス鋼、ニッケルメッキ鋼等が使用される。 The cathode binder and slurry solvent are the same as those used in the anode. The amount of the binder used for the cathode is preferably 0.001 to 20 parts by mass, more preferably 0.01 to 10 parts by mass, and most preferably 0.02 to 8 parts by mass with respect to 100 parts by mass of the cathode active material. . The amount of the cathode solvent used is preferably from 30 to 300 parts by weight, more preferably from 50 to 200 parts by weight, based on 100 parts by weight of the cathode active material.
Examples of the conductive material for the cathode include graphene, graphite fine particles, carbon black such as acetylene black and ketjen black, amorphous carbon fine particles such as needle coke, and carbon nanofibers, but are not limited thereto. The amount of the conductive material used for the cathode is preferably 0.01 to 20 parts by mass, more preferably 0.1 to 10 parts by mass with respect to 100 parts by mass of the cathode active material.
As the cathode current collector, aluminum, stainless steel, nickel-plated steel or the like is usually used.
本発明の新規化合物は、一般式(1’)で表され、上述の<非水電解液>の項目において説明した一般式(1)で表される化合物のうち、Z(Z’)が、R1O-S(=O)2-、R12-S(=O)2-、R1O-S(=O)-又はR12-S(=O)-であり、R1(R1’ )が置換基を有する炭素原子数1~20の炭化水素基であるもの、又はR12(R12’)がハロゲン原子又は置換基を有する炭素原子数1~20の炭化水素基が該当する。
R1’及びR12’が表す炭素原子数1~20の炭化水素基としては、R1及びR12が表す炭素原子数1~20の炭化水素基として例示した基が挙げられる。
尚、R1’ 及びR12’が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9’R10’R11’又はリン酸基である。
一般式(1’)中のAr’は、一般式(1)中のArと同一であり、一般式(1’)中のR1’は、一般式(1)中のR1’と同一であり、一般式(1’)中のR’は、一般式(1)中のRと同一であり、一般式(1’)中のR9’、R10’及びR11’は、それぞれ一般式(1)中のR9、R10及びR11と同一であり、一般式(1’)中のm’及びn’は、それぞれ一般式(1)中のm及びnと同一である。 <New compound>
The novel compound of the present invention is represented by the general formula (1 ′), and among the compounds represented by the general formula (1) described in the above item <Non-aqueous electrolyte>, Z (Z ′) is R 1 O—S (═O) 2 —, R 12 —S (═O) 2 —, R 1 O—S (═O) — or R 12 —S (═O) —, and R 1 (R 1 ′) is a hydrocarbon group having 1 to 20 carbon atoms having a substituent, or R 12 (R 12 ′) is a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms having a substituent. To do.
Examples of the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 ′ and R 12 ′ include the groups exemplified as the hydrocarbon group having 1 to 20 carbon atoms represented by R 1 and R 12 .
Note that group substituting the hydrocarbon group represented by R 1 'and R 12' is a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, -SiR 9 'R 10' R 11 ′ or a phosphate group.
The 'Ar in the general formula (1)' is the same as Ar in formula (1), identical to the 'R 1 in the general formula (1)', R 1 in the formula (1) ' R ′ in the general formula (1 ′) is the same as R in the general formula (1), and R 9 ′, R 10 ′ and R 11 ′ in the general formula (1 ′) are respectively R 9 , R 10 and R 11 in general formula (1) are the same, and m ′ and n ′ in general formula (1 ′) are the same as m and n in general formula (1), respectively. .
また、本発明の新規化合物は、上述した非水電解液の添加剤としての用途のほか、界面活性剤及びその前駆体等の用途に用いることができる。 It can be produced by the same method as the compound represented by the general formula (1) described above.
Moreover, the novel compound of this invention can be used for uses, such as surfactant and its precursor other than the use as an additive of the non-aqueous electrolyte mentioned above.
フラスコに水素化ナトリウム(3.20g、80.0mmоl)を加え、減圧乾燥後、アルゴン置換した。テトラヒドロフランを20.0mL加え、氷冷下で2-プロパノール(6.12mL、80.0mmоl)、テトラヒドロフラン5.00mLをゆっくり滴下した。その後、氷冷下で2,4,6-トリイソプロピルベンゼンスルホニルクロリド(9.692g、32.0mmоl)、テトラヒドロフラン20.0mLを滴下し、室温3時間撹拌した。次に、蒸留水を40.0mL、酢酸エチル40.0mLを加え、油水分離し、さらに蒸留水40.0mLで2回水洗を行った。得られた有機層に無水硫酸ナトリウムを加え、濾過した後にエバポレートした。粗生成物を中圧カラム(展開溶媒,酢酸エチル:ヘキサン=19:1)により単離し、白色固体の目的物を6.77g(収率67.7%)得た。得られた固体が、目的物であることを1H-NMR、IRを用いて確認した。データを〔表1〕に示す。 [Synthesis Example 1] Compound No. 1 Synthesis of 9 Sodium hydride (3.20 g, 80.0 mmol) was added to the flask, dried under reduced pressure, and purged with argon. Tetrahydrofuran (20.0 mL) was added, and 2-propanol (6.12 mL, 80.0 mmol) and tetrahydrofuran (5.00 mL) were slowly added dropwise under ice cooling. Thereafter, 2,4,6-triisopropylbenzenesulfonyl chloride (9.692 g, 32.0 mmol) and 20.0 mL of tetrahydrofuran were added dropwise under ice cooling, followed by stirring at room temperature for 3 hours. Next, 40.0 mL of distilled water and 40.0 mL of ethyl acetate were added to separate the oil and water, and further washed twice with 40.0 mL of distilled water. Anhydrous sodium sulfate was added to the obtained organic layer, filtered and evaporated. The crude product was isolated by a medium pressure column (developing solvent, ethyl acetate: hexane = 19: 1) to obtain 6.77 g (yield 67.7%) of the desired product as a white solid. It was confirmed by 1 H-NMR and IR that the obtained solid was the desired product. The data is shown in [Table 1].
フラスコに2,4,6-トリイソプロピルベンゼンスルホニルクロリド(4.12g、13.6mmоl)を加え、減圧乾燥後、アルゴン置換した。テトラヒドロフランを10.0mL、トリエチルアミン(4.74mL、34.0mmоl)加え、氷冷下で2,2,2-トリフルオロエタノール(2.43mL、34.0mmоl)をゆっくり滴下した。40℃で1時間30分撹拌した後に、蒸留水を20.0mL、酢酸エチル20.0mLを加え、油水分離し、さらに蒸留水20.0mLで2回水洗を行った。得られた有機層に無水硫酸ナトリウムを加え、濾過した後にエバポレートした。粗生成物を再結晶(貧溶媒,ヘキサン)して白色固体の目的物を1.47g(収率29.3%)得た。得られた固体が、目的物であることを1H-NMR、IRを用いて確認した。データを〔表1〕に示す。 [Synthesis Example 2] Compound No. 2 Synthesis of 22 2,4,6-triisopropylbenzenesulfonyl chloride (4.12 g, 13.6 mmol) was added to the flask, dried under reduced pressure, and purged with argon. Tetrahydrofuran (10.0 mL) and triethylamine (4.74 mL, 34.0 mmol) were added, and 2,2,2-trifluoroethanol (2.43 mL, 34.0 mmol) was slowly added dropwise under ice cooling. After stirring at 40 ° C. for 1 hour and 30 minutes, 20.0 mL of distilled water and 20.0 mL of ethyl acetate were added to separate the oil and water, and further washed twice with 20.0 mL of distilled water. Anhydrous sodium sulfate was added to the obtained organic layer, filtered and evaporated. The crude product was recrystallized (poor solvent, hexane) to obtain 1.47 g (yield 29.3%) of the desired product as a white solid. It was confirmed by 1 H-NMR and IR that the obtained solid was the desired product. The data is shown in [Table 1].
フラスコに2,4,6-トリイソプロピルベンゼンスルホニルクロリド(5.30g、17.5mmоl)、フッ化カリウム(1.32g、22.8mmоl)、1,4,7,10,13,16-ヘキサオキサシクロオクタデカン(0.25g、0.95mmоl)を加え、減圧乾燥後、アルゴン置換した。アセトニトリルを40.0mL加え、室温で終夜撹拌した。次に、蒸留水40mLを加え、固体を晶析させた。得られた固体を濾別し、白色固体の目的物を4.05g(収率81.0%)得た。得られた固体が、目的物であることを1H-NMR、IRを用いて確認した。データを〔表1〕に示す。 [Synthesis Example 3] Compound No. Synthesis of 23 In a flask, 2,4,6-triisopropylbenzenesulfonyl chloride (5.30 g, 17.5 mmol), potassium fluoride (1.32 g, 22.8 mmol), 1,4,7,10,13,16 -Hexaoxacyclooctadecane (0.25 g, 0.95 mmol) was added, dried under reduced pressure, and then purged with argon. 40.0 mL of acetonitrile was added and stirred overnight at room temperature. Next, 40 mL of distilled water was added to crystallize the solid. The obtained solid was separated by filtration to obtain 4.05 g (yield: 81.0%) of the desired product as a white solid. It was confirmed by 1 H-NMR and IR that the obtained solid was the desired product. The data is shown in [Table 1].
実施例及び比較例において、非水電解液二次電池(リチウム二次電池)は、以下の作製手順に従って作製された。 [Examples 1 to 5 and Comparative Examples 1 and 2] Production and Evaluation of Nonaqueous Electrolyte Secondary Batteries In Examples and Comparative Examples, nonaqueous electrolyte secondary batteries (lithium secondary batteries) were prepared as follows. It was made according to.
〔カソードの作製〕
活物質としてLiMn2O490質量部、導電材としてアセチレンブラック5質量部、及びバインダーとしてポリフッ化ビニリデン(PVDF)5質量部を混合した後、N-メチル-2-ピロリドン(NMP)140質量部に分散させてスラリー状とした。このスラリーをアルミニウム製の集電体に塗布し、乾燥後、プレス成型した。その後、このカソードを所定の大きさにカットして円盤状カソードを作製した。 <Production procedure>
[Production of cathode]
After mixing 90 parts by mass of LiMn 2 O 4 as an active material, 5 parts by mass of acetylene black as a conductive material, and 5 parts by mass of polyvinylidene fluoride (PVDF) as a binder, 140 parts by mass of N-methyl-2-pyrrolidone (NMP) To form a slurry. This slurry was applied to an aluminum current collector, dried and press-molded. Thereafter, the cathode was cut into a predetermined size to produce a disc-shaped cathode.
活物質として人造黒鉛97.0質量部、及びバインダーとしてスチレンブタジエンゴム1.5質量部、増粘剤としてカルボキシメチルセルロース 1.5質量部を混合し、水120質量部に分散させてスラリー状とした。このスラリーを銅製の負極集電体に塗布し、乾燥後、プレス成型した。その後、このアノードを所定の大きさにカットし、円盤状アノードを作製した。 [Production of anode]
97.0 parts by weight of artificial graphite as an active material, 1.5 parts by weight of styrene butadiene rubber as a binder, and 1.5 parts by weight of carboxymethyl cellulose as a thickener are mixed in 120 parts by weight of water to form a slurry. . This slurry was applied to a copper negative electrode current collector, dried and press-molded. Thereafter, this anode was cut into a predetermined size to produce a disc-shaped anode.
エチレンカーボネート30体積%、エチルメチルカーボネート40体積%、ジメチルカーボネート30体積%からなる混合溶媒に、LiPF6を1mol/Lの濃度で溶解し電解質溶液を調製した。 (Preparation of electrolyte solution)
LiPF 6 was dissolved at a concentration of 1 mol / L in a mixed solvent consisting of 30% by volume of ethylene carbonate, 40% by volume of ethyl methyl carbonate, and 30% by volume of dimethyl carbonate to prepare an electrolyte solution.
電解液添加剤として、〔表1〕に示す化合物を記載の割合で電解質溶液に溶解し、本発明の非水電解液及び比較の非水電解液を調製した。尚、比較化合物1はシクロヘキシルベンゼン、東京化成工業社製である。
化合物No.4は、J. Chem. Soc., Perkin trans. 1, 1980, (5), 1076-1079を参考に合成した。尚、〔表1〕中の( )内の数字は、非水電解液における濃度(質量%)を表す。 (Preparation of non-aqueous electrolyte)
As the electrolytic solution additive, the compounds shown in [Table 1] were dissolved in the electrolytic solution at the stated ratios to prepare the nonaqueous electrolytic solution of the present invention and the comparative nonaqueous electrolytic solution. Comparative compound 1 is cyclohexylbenzene, manufactured by Tokyo Chemical Industry Co., Ltd.
Compound No. 4 was synthesized with reference to J. Chem. Soc., Perkin trans. 1, 1980, (5), 1076-1079. In addition, the number in () in [Table 1] represents the concentration (% by mass) in the non-aqueous electrolyte.
得られた円盤状正極と円盤状負極を、厚さ25μmのポリエチレン製の微多孔フィルムをはさんでケース内に保持した。その後、それぞれの非水電解液をケース内に注入し、ケースを密閉、封止して、実施例1~5並びに比較例1及び2のリチウム二次電池(φ20mm、厚さ3.2mmのコイン型)を製作した。 [Assembling the battery]
The obtained disc-shaped positive electrode and disc-shaped negative electrode were held in a case with a microporous film made of polyethylene having a thickness of 25 μm interposed therebetween. Thereafter, each non-aqueous electrolyte was poured into the case, the case was sealed and sealed, and the lithium secondary batteries of Examples 1 to 5 and Comparative Examples 1 and 2 (a coin having a diameter of 20 mm and a thickness of 3.2 mm). Mold).
リチウム二次電池を、20℃の恒温槽内に入れ、充電電流0.3mA/cm2(0.2C相当の電流値)で4.2Vまで定電流定電圧充電し、放電電流0.3mA/cm2(0.2C相当の電流値)で3.0Vまで定電流放電する操作を5回行った。その後、充電電流0.3mA/cm2で4.2Vまで定電流定電圧充電し、放電電流0.3mA/cm2で3.0Vまで定電流放電した。この6回目に測定した放電容量を、電池の初期放電容量とし、下記式に示すように、放電容量比(%)を、比較例1(電解液添加剤無添加)の初期放電容量を100として算出した。
放電容量比(%)=[(初期放電容量)/(比較例1における初期放電容量)]×100 <Discharge capacity ratio test method>
The lithium secondary battery was placed in a constant temperature bath at 20 ° C., charged at a constant current and a constant voltage up to 4.2 V with a charging current of 0.3 mA / cm 2 (current value corresponding to 0.2 C), and a discharge current of 0.3 mA / The operation of discharging a constant current to 3.0 V at cm 2 (current value corresponding to 0.2 C) was performed 5 times. Thereafter, the battery was charged at a constant current and a constant voltage up to 4.2 V at a charging current of 0.3 mA / cm 2 and discharged at a constant current of 3.0 mA at a discharge current of 0.3 mA / cm 2 . The discharge capacity measured at the sixth time is defined as the initial discharge capacity of the battery. As shown in the following formula, the discharge capacity ratio (%) is defined as 100 as the initial discharge capacity of Comparative Example 1 (no addition of electrolyte additive). Calculated.
Discharge capacity ratio (%) = [(initial discharge capacity) / (initial discharge capacity in Comparative Example 1)] × 100
リチウム二次電池を、20℃の恒温槽内に入れ、充電電流0.3mA/cm2(0.2C相当の電流値)で過充電状態(5.5V)まで定電流定電圧充電したときの、容量(mAh/g)を測定した。比較例1(電解液添加剤無添加)の容量を100として算出した。 <Overcharge resistance test>
When a lithium secondary battery is placed in a constant temperature bath at 20 ° C. and charged at a constant current and constant voltage to an overcharged state (5.5 V) at a charging current of 0.3 mA / cm 2 (current value equivalent to 0.2 C). The capacity (mAh / g) was measured. The capacity of Comparative Example 1 (no addition of electrolytic solution additive) was calculated as 100.
1a カソード集電体
2 アノード
2a アノード集電体
3 電解液
4 カソードケース
5 アノードケース
6 ガスケット
7 セパレータ
10 コイン型の非水電解液二次電池
10’ 円筒型の非水電解液二次電池
11 アノード
12 アノード集電体
13 カソード
14 カソード集電体
15 電解液
16 セパレータ
17 カソード端子
18 アノード端子
19 アノード板
20 アノードリード
21 カソード
22 カソードリード
23 ケース
24 絶縁板
25 ガスケット
26 安全弁
27 PTC素子 DESCRIPTION OF SYMBOLS 1 Cathode 1a Cathode current collector 2 Anode 2a Anode current collector 3 Electrolyte 4 Cathode case 5
Claims (3)
- リチウム塩を有機溶媒に溶解させた非水電解液において、
下記一般式(1)で表される化合物を少なくとも1種含有することを特徴とする非水電解液。
(式中、Arは、ベンゼン環又はナフタレン環を表し、
Zは、R1O-S(=O)2-、R12-S(=O)2-、R1O-S(=O)-又はR12-S(=O)-を表し、
R1は、置換基を有する又は無置換の炭素原子数1~20の炭化水素基を表し、
R2は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9R10R11、リン酸基、又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R12は、ハロゲン原子又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R1、R2及びR12が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9R10R11又はリン酸基であり、
R1、R2及びR12が表す炭化水素基中のアルキレンは、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-又は-CO-NR-が隣り合わない条件で、1~3回中断していてもよく、
Rは、炭素原子数1~5の脂肪族炭化水素基を表し、
R2が炭化水素基を表す場合、R2とArが結合する部位は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-NR-CO-、-CO-NR-又は-N=により中断していてもよく、
R9、R10及びR11は、炭素原子数1~16の炭化水素基を表し、
m及びnは、それぞれ1以上の整数を表し、Arがベンゼン環を表す場合、m+nは6以下であり、Arがナフタレン環を表す場合、m+nは10以下であり、
mが2以上の場合、Zは同一でも異なっていてもよく、nが2以上の場合、R2は同一でも異なっていてもよい。
但し、n個のR2のうち、少なくとも1つは、下記一般式(2)又は(3)で表される基である。)
(式中、R3、R4、R5及びR6は各々独立に置換基を有するか又は無置換の炭素原子数1~18の炭化水素基を表し、
R3、R4、R5及びR6が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9R10R11又はリン酸基であり、
R3、R4、R5及びR6が表す炭化水素基中のアルキレン基は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR-、-S-、-SO-、-SO2-、-NR-CO-又は-CO-NR-が隣り合わない条件で、1~3回中断していてもよく、
Rは、炭素原子数1~5の脂肪族炭化水素基を表し、
R7及びR8は、各々独立に水素原子、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9R10R11又はリン酸基を表し、
R9、R10及びR11は、各々独立に炭素原子数1~16の炭化水素基を表し、
但し、一般式(2)及び(3)は、基全体として炭素原子数が3~20の範囲内である。) In a non-aqueous electrolyte solution in which a lithium salt is dissolved in an organic solvent,
A nonaqueous electrolytic solution comprising at least one compound represented by the following general formula (1).
(In the formula, Ar represents a benzene ring or a naphthalene ring,
Z represents R 1 O—S (═O) 2 —, R 12 —S (═O) 2 —, R 1 O—S (═O) — or R 12 —S (═O) —,
R 1 represents a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms,
R 2 represents a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 , a phosphate group, or a substituted or unsubstituted carbon atom. Represents a hydrocarbon group of the number 1 to 20,
R 12 represents a halogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms,
The group that replaces the hydrocarbon group represented by R 1 , R 2 and R 12 is a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 R 10 R 11 or A phosphate group,
The alkylene in the hydrocarbon group represented by R 1 , R 2 and R 12 is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, —S—, -SO-, -SO 2- , -NR-CO- or -CO-NR- may be interrupted 1 to 3 times under the condition that they are not adjacent to each other,
R represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
When R 2 represents a hydrocarbon group, the site where R 2 and Ar are bonded is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, —S. May be interrupted by-, -NR-CO-, -CO-NR- or -N =,
R 9 , R 10 and R 11 represent a hydrocarbon group having 1 to 16 carbon atoms,
m and n each represent an integer of 1 or more, and when Ar represents a benzene ring, m + n is 6 or less, and when Ar represents a naphthalene ring, m + n is 10 or less,
When m is 2 or more, Z may be the same or different, and when n is 2 or more, R 2 may be the same or different.
However, at least one of n R 2 is a group represented by the following general formula (2) or (3). )
(Wherein R 3 , R 4 , R 5 and R 6 each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms,
Groups that substitute for the hydrocarbon groups represented by R 3 , R 4 , R 5 and R 6 are halogen atoms, nitrile groups, nitro groups, amino groups, carboxyl groups, hydroxyl groups, thiol groups, formyl groups, sulfone groups, —SiR. 9 R 10 R 11 or a phosphate group,
The alkylene group in the hydrocarbon group represented by R 3 , R 4 , R 5 and R 6 is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR—, -S-, -SO-, -SO 2- , -NR-CO- or -CO-NR- may be interrupted 1 to 3 times under the condition that they are not adjacent to each other,
R represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
R 7 and R 8 are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 R 10 R 11 or phosphate group Represents
R 9 , R 10 and R 11 each independently represents a hydrocarbon group having 1 to 16 carbon atoms,
However, in the general formulas (2) and (3), the number of carbon atoms as a whole is in the range of 3 to 20. ) - リチウムが脱挿入可能なアノード、遷移金属とリチウムを含有するカソード、及びリチウム塩を有機溶媒に溶解させた非水電解液を有する非水電解液二次電池において、非水電解液が、請求項1に記載の非水電解液であることを特徴とする非水電解液二次電池。 A nonaqueous electrolyte secondary battery comprising an anode from which lithium can be inserted and removed, a cathode containing a transition metal and lithium, and a nonaqueous electrolyte in which a lithium salt is dissolved in an organic solvent. A nonaqueous electrolyte secondary battery, which is the nonaqueous electrolyte solution according to 1.
- 下記一般式(1’)で表される化合物。
(式中、Ar’は、ベンゼン環又はナフタレン環を表し、
Z’は、R1’O-S(=O)2-、R12’-S(=O)2-、R1’O-S(=O)-又はR12’-S(=O)-を表し、
R1’は、置換基を有する炭素原子数1~20の炭化水素基を表し、
R2’は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9’R10’R11’、リン酸基、又は置換基を有する若しくは無置換の炭素原子数1~20の炭化水素基を表し、
R12’は、ハロゲン原子又は置換基を有する炭素原子数1~20の炭化水素基を表し、
R1’、R2’及びR12’が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、-SiR9’R10’R11’又はリン酸基であり、
R1’、R2’及びR12’が表す炭化水素基中のアルキレンは、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-SO-、-SO2-、-NR’-CO-又は-CO-NR’-が隣り合わない条件で、1~3回中断していてもよく、
R’は、炭素原子数1~5の脂肪族炭化水素基を表し、
R2’が炭化水素基を表す場合、R2’とAr’が結合する部位は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-NR’-CO-、-CO-NR’-又は-N=により中断していてもよく、
R9’、R10’及びR11’は、炭素原子数1~16の炭化水素基を表し、
m’及びn’は、それぞれ1以上の整数を表し、Ar’がベンゼン環を表す場合、m’+n’は6以下であり、Ar’がナフタレン環を表す場合、m’+n’は10以下であり、
m’が2以上の場合、Z’は同一でも異なっていてもよく、n’が2以上の場合、R2’は同一でも異なっていてもよい。
が2以上の場合、R2’は同一でも異なっていてもよい。
但し、n’個のR2’のうち、少なくとも1つは、下記一般式(2’)又は(3’)で表される基である。)
(式中、R3’、R4’、R5’及びR6’は各々独立に置換基を有するか又は無置換の炭素原子数1~18の炭化水素基を表し、
R3’、R4’、R5’及びR6’が表す炭化水素基を置換する基は、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9’R10’R11’又はリン酸基であり、
R3’、R4’、R5’及びR6’が表す炭化水素基中のアルキレン基は、-O-、-CO-、-OCO-、-COO-、-O-CO-O-、-NR’-、-S-、-SO-、-SO2-、-NR’-CO-又は-CO-NR’-が隣り合わない条件で、1~3回中断していてもよく、
R’は、炭素原子数1~5の脂肪族炭化水素基を表し、
R7’及びR8’は、各々独立に水素原子、ハロゲン原子、ニトリル基、ニトロ基、アミノ基、カルボキシル基、水酸基、チオール基、ホルミル基、スルホン基、-SiR9’R10’R11’又はリン酸基を表し、
R9’、R10’及びR11’は、各々独立に炭素原子数1~16の炭化水素基を表し、
但し、一般式(2’)及び(3’)は、基全体として炭素原子数が3~20の範囲内である。)
A compound represented by the following general formula (1 ′).
(In the formula, Ar ′ represents a benzene ring or a naphthalene ring,
Z 'is, R 1' O-S ( = O) 2 -, R 12 '-S (= O) 2 -, R 1' O-S (= O) - or R 12 '-S (= O) -Represents
R 1 ′ represents a hydrocarbon group having 1 to 20 carbon atoms having a substituent,
R 2 ′ has a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, —SiR 9 ′ R 10 ′ R 11 ′, a phosphate group, a phosphate group, or a substituent. Represents a substituted hydrocarbon group having 1 to 20 carbon atoms,
R 12 ′ represents a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms having a substituent,
R 1 ', R 2' and R 12 'group substituting the hydrocarbon group represented by a halogen atom, a nitrile group, a nitro group, an amino group, a carboxyl group, a hydroxyl group, a thiol group, a formyl group, -SiR 9' R 10 is a 'R 11' or phosphoric acid group,
The alkylene in the hydrocarbon group represented by R 1 ′, R 2 ′ and R 12 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR′—, -S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are not adjacent, may also be interrupted 1-3 times,
R ′ represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
When R 2 ′ represents a hydrocarbon group, the sites where R 2 ′ and Ar ′ are bonded are —O—, —CO—, —OCO—, —COO—, —O—CO—O—, —NR ′. May be interrupted by-, -S-, -NR'-CO-, -CO-NR'- or -N =,
R 9 ′, R 10 ′ and R 11 ′ represent a hydrocarbon group having 1 to 16 carbon atoms,
m ′ and n ′ each represents an integer of 1 or more, and when Ar ′ represents a benzene ring, m ′ + n ′ is 6 or less, and when Ar ′ represents a naphthalene ring, m ′ + n ′ is 10 or less. And
When m ′ is 2 or more, Z ′ may be the same or different. When n ′ is 2 or more, R 2 ′ may be the same or different.
Are 2 or more, R 2 ′ may be the same or different.
However, at least one of n ′ R 2 ′ is a group represented by the following general formula (2 ′) or (3 ′). )
(Wherein R 3 ′, R 4 ′, R 5 ′ and R 6 ′ each independently represents a substituent or an unsubstituted hydrocarbon group having 1 to 18 carbon atoms,
The hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is a halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone. A group, -SiR 9 'R 10 ' R 11 'or a phosphate group,
The alkylene group in the hydrocarbon group represented by R 3 ′, R 4 ′, R 5 ′ and R 6 ′ is —O—, —CO—, —OCO—, —COO—, —O—CO—O—, -NR '-, - S -, - SO -, - SO 2 -, - NR'-CO- or -CO-NR'- is under conditions which are not adjacent, may also be interrupted 1-3 times,
R ′ represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms,
R 7 ′ and R 8 ′ are each independently a hydrogen atom, halogen atom, nitrile group, nitro group, amino group, carboxyl group, hydroxyl group, thiol group, formyl group, sulfone group, —SiR 9 ′ R 10 ′ R 11 'Or represents a phosphate group,
R 9 ′, R 10 ′ and R 11 ′ each independently represents a hydrocarbon group having 1 to 16 carbon atoms,
However, in the general formulas (2 ′) and (3 ′), the number of carbon atoms as a whole group is in the range of 3 to 20. )
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020167033489A KR20170069960A (en) | 2014-10-16 | 2015-10-07 | Non-aqueous electrolyte and non-aqueous electrolyte secondary cell |
JP2016554051A JP6760843B2 (en) | 2014-10-16 | 2015-10-07 | Non-aqueous electrolyte and non-aqueous electrolyte secondary batteries |
CN201580027496.4A CN106463773B (en) | 2014-10-16 | 2015-10-07 | Nonaqueous electrolytic solution and nonaqueous electrolytic solution secondary battery |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014212088 | 2014-10-16 | ||
JP2014-212088 | 2014-10-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2016060038A1 true WO2016060038A1 (en) | 2016-04-21 |
Family
ID=55746585
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2015/078463 WO2016060038A1 (en) | 2014-10-16 | 2015-10-07 | Non-aqueous electrolyte and non-aqueous electrolyte secondary cell |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP6760843B2 (en) |
KR (1) | KR20170069960A (en) |
CN (1) | CN106463773B (en) |
TW (1) | TW201620192A (en) |
WO (1) | WO2016060038A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3985774A1 (en) * | 2020-10-13 | 2022-04-20 | Hyundai Motor Company | Electrolyte for lithium secondary battery and lithium secondary battery comprising the same |
WO2023074592A1 (en) * | 2021-10-25 | 2023-05-04 | 学校法人東京理科大学 | Potassium-ion battery electrolytic solution additive, potassium-ion battery electrolytic solution, potassium-ion battery, potassium-ion capacitor electrolytic solution additive, potassium-ion capacitor electrolytic solution, potassium-ion capacitor, and negative electrode |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111313090A (en) * | 2020-02-18 | 2020-06-19 | 白银科奥夫化学科技有限公司 | Lithium ion battery electrolyte and lithium ion secondary battery containing same |
CN114552014A (en) * | 2022-02-25 | 2022-05-27 | 惠州锂威新能源科技有限公司 | Electrolyte and electrochemical device containing same |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05148219A (en) * | 1991-05-06 | 1993-06-15 | Ciba Geigy Ag | Preparation of benzenesulfonamide |
JP2000268830A (en) * | 1999-03-17 | 2000-09-29 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
JP2002008720A (en) * | 2000-04-18 | 2002-01-11 | Sony Corp | Nonaqueous electrolyte battery |
JP2003203673A (en) * | 2001-12-28 | 2003-07-18 | Mitsui Chemicals Inc | Nonaqueous electrolyte liquid and lithium secondary cell containing the same |
WO2011152534A1 (en) * | 2010-06-04 | 2011-12-08 | 宇部興産株式会社 | Nonaqueous electrolyte solution and electrochemical element using same |
JP2012121816A (en) * | 2010-12-06 | 2012-06-28 | Sumitomo Seika Chem Co Ltd | Production method of high purity 4-tert-butylbenzenesulfonyl chloride |
JP2012180349A (en) * | 2005-10-13 | 2012-09-20 | Sumitomo Chemical Co Ltd | Dihalobenzene compound |
JP2013012486A (en) * | 2012-08-20 | 2013-01-17 | Ube Ind Ltd | Benzene sulfonic ester, electrolyte solution for lithium secondary battery using the same, and lithium secondary battery using the same |
JP2014192145A (en) * | 2013-03-28 | 2014-10-06 | Fujifilm Corp | Nonaqueous secondary battery, and electrolytic solution for secondary battery use |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001307772A (en) * | 2000-04-21 | 2001-11-02 | Tonen Chem Corp | Nonaqueous electrolyte and nonaqueous electrolyte battery using the same |
JP4281895B2 (en) * | 2001-12-28 | 2009-06-17 | 三井化学株式会社 | Non-aqueous electrolyte and lithium secondary battery using the same |
JP2004087168A (en) * | 2002-08-23 | 2004-03-18 | Mitsui Chemicals Inc | Nonaqueous electrolytic solution and lithium secondary battery including it |
JP4968615B2 (en) * | 2004-12-16 | 2012-07-04 | 日本電気株式会社 | Secondary battery electrolyte and secondary battery |
JP5470675B2 (en) * | 2005-10-13 | 2014-04-16 | 住友化学株式会社 | Polyarylene and production method thereof |
JP4396675B2 (en) * | 2006-06-16 | 2010-01-13 | ソニー株式会社 | Nonaqueous electrolyte secondary battery |
JP5125379B2 (en) * | 2007-10-04 | 2013-01-23 | 宇部興産株式会社 | Electrolytic solution for lithium secondary battery containing benzenesulfonic acid ester, and lithium secondary battery using the same |
WO2009057515A1 (en) * | 2007-11-01 | 2009-05-07 | Ube Industries, Ltd. | Phenyl sulfonate compound, nonaqueous electrolyte solution using the same, and lithium battery |
JP2009140921A (en) * | 2007-11-15 | 2009-06-25 | Ube Ind Ltd | Sulfonic acid phenyl compound, non-aqueous electrolytic liquid using it, and lithium battery |
CN102449842B (en) * | 2009-06-10 | 2015-03-04 | 旭化成电子材料株式会社 | Electrolytic solution and lithium ion secondary battery utilizing same |
KR20120083290A (en) * | 2009-08-31 | 2012-07-25 | 미쓰비시 가가꾸 가부시키가이샤 | Non-aqueous electrolytic solution, and non-aqueous electrolyte battery comprising same |
JP5589796B2 (en) * | 2009-11-27 | 2014-09-17 | 宇部興産株式会社 | Non-aqueous electrolyte, electrochemical device using the same, and trialkylsilyloxy group-containing compound used therefor |
CN103460495B (en) * | 2011-04-12 | 2016-01-27 | 宇部兴产株式会社 | Nonaqueous electrolytic solution and employ the electric energy storage device of this nonaqueous electrolytic solution |
JP6295197B2 (en) * | 2012-07-26 | 2018-03-14 | 株式会社Adeka | Power storage device |
JP6225923B2 (en) * | 2013-01-23 | 2017-11-08 | 宇部興産株式会社 | Non-aqueous electrolyte and power storage device using the same |
-
2015
- 2015-10-07 CN CN201580027496.4A patent/CN106463773B/en not_active Expired - Fee Related
- 2015-10-07 JP JP2016554051A patent/JP6760843B2/en not_active Expired - Fee Related
- 2015-10-07 KR KR1020167033489A patent/KR20170069960A/en unknown
- 2015-10-07 WO PCT/JP2015/078463 patent/WO2016060038A1/en active Application Filing
- 2015-10-14 TW TW104133741A patent/TW201620192A/en unknown
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05148219A (en) * | 1991-05-06 | 1993-06-15 | Ciba Geigy Ag | Preparation of benzenesulfonamide |
JP2000268830A (en) * | 1999-03-17 | 2000-09-29 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
JP2002008720A (en) * | 2000-04-18 | 2002-01-11 | Sony Corp | Nonaqueous electrolyte battery |
JP2003203673A (en) * | 2001-12-28 | 2003-07-18 | Mitsui Chemicals Inc | Nonaqueous electrolyte liquid and lithium secondary cell containing the same |
JP2012180349A (en) * | 2005-10-13 | 2012-09-20 | Sumitomo Chemical Co Ltd | Dihalobenzene compound |
WO2011152534A1 (en) * | 2010-06-04 | 2011-12-08 | 宇部興産株式会社 | Nonaqueous electrolyte solution and electrochemical element using same |
JP2012121816A (en) * | 2010-12-06 | 2012-06-28 | Sumitomo Seika Chem Co Ltd | Production method of high purity 4-tert-butylbenzenesulfonyl chloride |
JP2013012486A (en) * | 2012-08-20 | 2013-01-17 | Ube Ind Ltd | Benzene sulfonic ester, electrolyte solution for lithium secondary battery using the same, and lithium secondary battery using the same |
JP2014192145A (en) * | 2013-03-28 | 2014-10-06 | Fujifilm Corp | Nonaqueous secondary battery, and electrolytic solution for secondary battery use |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3985774A1 (en) * | 2020-10-13 | 2022-04-20 | Hyundai Motor Company | Electrolyte for lithium secondary battery and lithium secondary battery comprising the same |
US11830979B2 (en) | 2020-10-13 | 2023-11-28 | Hyundai Motor Company | Electrolyte for lithium secondary battery and lithium secondary battery comprising same |
WO2023074592A1 (en) * | 2021-10-25 | 2023-05-04 | 学校法人東京理科大学 | Potassium-ion battery electrolytic solution additive, potassium-ion battery electrolytic solution, potassium-ion battery, potassium-ion capacitor electrolytic solution additive, potassium-ion capacitor electrolytic solution, potassium-ion capacitor, and negative electrode |
Also Published As
Publication number | Publication date |
---|---|
CN106463773B (en) | 2019-06-07 |
KR20170069960A (en) | 2017-06-21 |
JP6760843B2 (en) | 2020-09-23 |
CN106463773A (en) | 2017-02-22 |
TW201620192A (en) | 2016-06-01 |
JPWO2016060038A1 (en) | 2017-07-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5955629B2 (en) | Non-aqueous electrolyte secondary battery | |
JP6738815B2 (en) | Non-aqueous electrolyte and non-aqueous electrolyte secondary battery | |
JP6714506B2 (en) | Non-aqueous electrolyte and non-aqueous electrolyte secondary battery | |
JP6713452B2 (en) | Non-aqueous electrolyte and non-aqueous electrolyte secondary battery | |
WO2016013480A1 (en) | Nonaqueous electrolyte secondary battery, nonaqueous electrolyte solution and compound | |
JP2013145702A (en) | Nonaqueous electrolyte secondary battery, and nonaqueous electrolyte for secondary battery | |
JP5897869B2 (en) | New fluorosilane compounds | |
WO2016060038A1 (en) | Non-aqueous electrolyte and non-aqueous electrolyte secondary cell | |
JP2023130374A (en) | Non-aqueous electrolytic solution and energy device using the same | |
WO2015147003A1 (en) | Electrolyte solution, electrochemical device, lithium ion secondary battery and module | |
JP7194688B2 (en) | NON-AQUEOUS ELECTROLYTE AND ENERGY DEVICE USING THE SAME | |
JP6524084B2 (en) | Nonaqueous electrolyte secondary battery and nonaqueous electrolyte |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15851077 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2016554051 Country of ref document: JP Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 20167033489 Country of ref document: KR Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 15851077 Country of ref document: EP Kind code of ref document: A1 |