IP Library Granted Patent US 8,455,142
Granted Patent B2
US 8,455,142 · App. 12/419,486 · Granted Jun 4, 2013

Non-aqueous electrolyte and non-aqueous electrolyte secondary battery using the same

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Quick Facts
Patent No.
US 8,455,142
App. No.
12/419,486
Granted
Jun 4, 2013
Kind
B2
Abstract

A non-aqueous electrolyte can suppress decomposition of a solvent, improve the cycle life of a secondary battery, suppress the rise of resistance of a secondary battery and improve the capacity maintenance ratio of a secondary battery. A non-aqueous electrolyte secondary battery formed by using such a non-aqueous electrolyte includes a non-aqueous electrolyte containing an aprotic solvent and a disulfonic acid ester as expressed by chemical formula 1 shown below, a positive electrode and a negative electrode:

Claims (32)

1. A non-aqueous electrolyte containing an aprotic solvent and a disulfonic acid ester compound as expressed by chemical formula 1 shown below:

where A and B respectively and independently represent alkylene groups having 1 to 5 carbon atoms and at least either A or B has an alkenyl group as substituent.

2. The non-aqueous electrolyte according to claim 1 , further containing:

one or more than one compounds having a sulfonyl group in addition to the compound expressed by the chemical formula 1.

3. The non-aqueous electrolyte according to claim 2 , wherein

the one or more than one compounds having a sulfonyl group include a compound expressed by chemical formula 2 shown below:

where Q represents an oxygen atom, a methylene group or a single bond, A represents a group selected from a substituted or unsubstituted alkylene group having 1 to 5 carbon atoms, a carbonyl group, a sulfinyl group, a polyfluoroalkylene group having 1 to 5 carbon atoms, a substituted or unsubstituted fluoroalkylene group having 1 to 5 carbon atoms, a group formed by turning at least one of the C—C bonds of a substituted or unsubstituted alkylene group having 1 to 5 carbon atoms to a C—O—C bond, a group formed by turning at least one of the C—C bonds of a polyfluoroalkylene group having 1 to 5 carbon atoms to a C—O—C bond and a group formed by turning at least one of the C—C bonds of a substituted or unsubstituted fluoroalkylene group having 1 to 5 carbon atoms to a C—O—C bond, and B represents a group selected from a substituted or unsubstituted alkylene group having 1 to 5 carbon atoms, a polyfluoroalkylene group having 1 to 5 carbon atoms and a substituted or unsubstituted fluoroalkylene group having 1 to 5 carbon atoms.

4. The non-aqueous electrolyte according to claim 2 , further containing:

a sultone compound expressed by chemical formula 3 shown below as one or more than one compounds having a sulfonyl group:

where n represents an integer not smaller than 0 and not greater than 2, and each of R1 through R6 represents a hydrogen atom or a group selected from an alkyl group having not less than 1 and not more than 12 carbon atoms, a cycloalkyl group having not less than 3 and not more than 6 carbon atoms and an aryl group having not less than 6 and not more than 12 carbon atoms.

5. The non-aqueous electrolyte according to claim 4 , further containing:

vinylene carbonate or a derivative thereof.

6. The non-aqueous electrolyte according to claim 2 , further containing:

vinylene carbonate or a derivative thereof.

7. The non-aqueous electrolyte according to claim 1 containing:

a compound expressed by the above chemical formula 1 by not less than 0.005 mass % and not more than 10 mass % of the entire electrolyte.

8. The non-aqueous electrolyte according to claim 1 , wherein

the aprotic solvent contains one or more solvents selected from a group of cyclic carbonates, linear chain carbonates, aliphatic carboxylic acid esters, γ-lactones, cyclic ethers, linear chain ethers and fluorine derivatives of any of them.

9. The non-aqueous electrolyte according to claim 1 , further containing:

as lithium salt one or more than one compounds selected from a group of LiPF 6 , LiBF 4 , LiAsF 6 , LiSbF 6 , LiClO 4 , LiAlCl 4 and LiN(C n F 2n+1 SO 2 ) (C m F 2m+1 SO 2 ) (where n and m are natural numbers).

10. A non-aqueous electrolyte secondary battery comprising a non-aqueous electrolyte containing an aprotic solvent and a disulfonic acid ester compound as expressed by chemical formula 1 shown below, a positive electrode and a negative electrode:

where A and B respectively and independently represent alkylene groups having 1 to 5 carbon atoms and at least either A or B has an alkenyl group as substituent.

11. The secondary battery according to claim 10 , wherein the positive electrode active substance of the positive electrode contains a lithium-containing complex oxide that can occlude and discharge lithium.

12. The secondary battery according to claim 11 , wherein the lithium-containing complex oxide has a lithium-manganese complex oxide having a spinel structure.

13. The secondary battery according to claim 10 , wherein

the negative electrode active substance of the negative electrode contains one or more substances selected from a group of materials that can occlude and discharge lithium and oxide materials.

14. The secondary battery according to claim 13 , wherein

the negative electrode active substance contains a carbon material.

15. The secondary battery according to claim 14 , wherein

the carbon material is graphite.

16. The secondary battery according to claim 14 , wherein

the carbon material is amorphous carbon.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Oct 28, 2024
From: SUMITOMO MITSUI BANKING CORPORATION, AS SECURITY AGENT
To: ENVISION AESC JAPAN LTD.; ENVISION AESC ENERGY DEVICES LTD.
Reel/Frame 069461/0179 →
SECURITY AGREEMENT SUPPLEMENT Recorded Jul 2, 2019
From: ENVISION AESC ENERGY DEVICES, LTD.
To: SUMITOMO MITUSI BANKING CORPORATION, AS SECURITY AGENT
Reel/Frame 049649/0924 →
CHANGE OF NAME Recorded Jun 21, 2019
From: NEC ENERGY DEVICES, LTD.
To: ENVISION AESC ENERGY DEVICES, LTD.
Reel/Frame 049556/0123 →