Electrolytic solution

Patent metadata

Field	Value
Publication number	US-2017324114-A1
Application number	US-201515527575-A
Country	US
Kind code	A1
Filing date	Oct 5, 2015
Priority date	Nov 18, 2014
Publication date	Nov 9, 2017
Grant date	—

Abstract

An electrolytic solution including
a heteroelement-containing organic solvent at a mole ratio of not greater than 1.5 relative to a metal salt, the heteroelement-containing organic solvent containing a linear carbonate represented by general formula (1) below, the metal salt being a metal salt whose cation is an alkali metal, an alkaline earth metal, or aluminum and whose anion has a chemical structure represented by general formula (2) below.

R 10 OCOOR 11   general formula (1)

(R 21 X 21 )(R 22 SO 2 )N  general formula (2)

First claim

1 . An electrolytic solution containing
a heteroelement-containing organic solvent at a mole ratio of not greater than 1.5 relative to a metal salt, the heteroelement-containing organic solvent containing a linear carbonate represented by general formula (1) below, the metal salt being a metal salt whose cation is an alkali metal, an alkaline earth metal, or aluminum and whose anion has a chemical structure represented by general formula (2) below:
R 10 OCOOR 11   general formula (1)

(R 10 and R 11 are each independently selected from C n H a F b Cl c Br d I e that is a linear alkyl, or C m H f F g Cl h Br i I j that includes a cyclic alkyl in a chemical structure thereof. “n” is an integer not smaller than 1, “m” is an integer not smaller than 3, and “a”, “b”, “c”, “d”, “e”, “f”, “g”, “h”, “i”, and “j” are each independently an integer not smaller than 0 and satisfy 2n+1=a+b+c+d+e and 2m=f+g+h+i+j.)
(R 21 X 21 )(R 22 SO 2 )N  general formula (2)

(R 21 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 22 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 21 and R 22 optionally bind with each other to form a ring. X 21 is selected from SO 2 , C═O, C═S, R a P═O, R b P═S, S═O, or Si═O. R a and R b are each independently selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; OH; SH; CN; SCN; or OCN. R a and R b each optionally bind with R 21 or R 22 to form a ring.)

2 . The electrolytic solution according to claim 1 , wherein
the heteroelement-containing organic solvent contains the linear carbonate by not less than 80 vol % or not less than 80 mole %.

3 . An electrolytic solution containing
a linear carbonate at a mole ratio of not greater than 1.5 relative to a metal salt, the linear carbonate being represented by general formula (1) according to claim 1 , the metal salt being a metal salt whose cation is an alkali metal, an alkaline earth metal, or aluminum and whose anion has a chemical structure represented by general formula (2) according to claim 1 .

4 . The electrolytic solution according to claim 1 , wherein
the chemical structure of the anion of the metal salt is represented by general formula (2-1) below.
(R 23 X 22 )(R 24 SO 2 )N  general formula (2-1)

(R 23 and R 24 are each independently C n H a F b Cl c Br d I e (CN) f (SCN) g (OCN) h . “n”, “a”, “b”, “c”, “d”, “e”, “f”, “g”, and “h” are each independently an integer not smaller than 0 and satisfy 2n+1=a+b+c+d+e+f+g+h. R 23 and R 24 optionally bind with each other to form a ring, and in that case, satisfy 2n=a+b+c+d+e+f+g+h. X 22 is selected from SO 2 , C═O, C═S, R c P═O, R d P═S, S═O, or Si═O. R c and R d are each independently selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; OH; SH; CN; SCN; or OCN. R c and R d each optionally bind with R 23 or R 24 to form a ring.)

5 . The electrolytic solution according to claim 1 , wherein
the chemical structure of the anion of the metal salt is represented by general formula (2-2) below.
(R 25 SO 2 )(R 26 SO 2 )N  general formula (2-2)

(R 25 and R 26 are each independently C n H a F b Cl c Br d I e . “n”, “a”, “b”, “c”, “d”, and “e” are each independently an integer not smaller than 0 and satisfy 2n+1=a+b+c+d+e. R 25 and R 26 optionally bind with each other to form a ring, and in that case, satisfy 2n=a+b+c+d+e.)

6 . The electrolytic solution according to claim 1 , wherein
the metal salt is (CF 3 SO 2 ) 2 NLi, (FSO 2 ) 2 NLi, (C 2 F 5 SO 2 ) 2 NLi, FSO 2 (CF 3 SO 2 )NLi, (SO 2 CF 2 CF 2 SO 2 )NLi, or (SO 2 CF 2 CF 2 CF 2 SO 2 )NLi.

7 . The electrolytic solution according to claim 1 , wherein
the linear carbonate is represented by general formula (1-1) below.
R 13 OCOOR 14   general formula (1-1)

(R 13 and R 14 are each independently selected from C n H a F b that is a linear alkyl or C m H f F g that includes a cyclic alkyl in a chemical structure thereof. “n” is an integer not smaller than 1, “m” is an integer not smaller than 3, and “a”, “b”, “f”, and “g” are each independently an integer not smaller than 0 and satisfy 2n+1=a+b and 2m=f+g.)

8 . The electrolytic solution according to claim 1 , wherein
the linear carbonate is selected from dimethyl carbonate, ethyl methyl carbonate, or diethyl carbonate.

9 . The electrolytic solution according to claim 1 , wherein
the mole ratio is in a range of 1 to 1.5.

10 . A secondary battery provided with the electrolytic solution according to claim 1 .

11 . The secondary battery according to claim 10 , provided with a positive electrode active material whose reaction potential is not lower than 4.5 V versus Li reference.

12 . The secondary battery according to claim 10 , provided with a lithium metal complex oxide having a spinel structure as the positive electrode active material.

13 . The secondary battery cla

Assignees

• Univ Tokyo

Inventors

• Kawai Tomoyuki
• Niwa Junichi
• Yamada Atsuo
• Yamada Yuki

Classifications

• H01M10/0525

  Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title

• H01M10/0564 Primary

  the electrolyte being constituted of organic materials only · CPC title

• H01M2300/0034

  Fluorinated solvents · CPC title

• C07C69/96

  Esters of carbonic or haloformic acids · CPC title

• H01G11/60 Primary

  characterised by the solvent · CPC title