IP Library Granted Patent US 7,691,539
Granted Patent B2
US 7,691,539 · App. 10/383,790 · Granted Apr 6, 2010

Non-aqueous secondary battery having increased discharge capacity retention

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,691,539
App. No.
10/383,790
Granted
Apr 6, 2010
Kind
B2
Abstract

A method of increasing the discharge capacity retention of a non-aqueous lithium ion secondary battery having a positive electrode active material, a combination of a lithium element and a complex metal oxide, a negative electrode, and a non-aqueous electrolytic solution comprising an electrolyte dissolved in a non-aqueous solvent which is a combination of a cyclic carbonate and a linear carbonate by incorporating a disulfide derivative having the formula: R 1 —S—S—R 2 wherein each of R 1 and R 2 independently represents a phenyl group, a benzyl group, a tolyl group, a pyridyl group, a pyrimidyl group, an alkyl group having 1 to 12 carbon atom, or a cycloalkyl group having 3 to 6 carbon atoms, in which each group has no substituent groups or has one or more alkyl groups into the non-aqueous electrolytic solution.

Claims (13)

1. A non-aqueous secondary battery having a positive electrode comprising, as the positive electrode active material, a combination of a lithium element and a complex metal oxide, a negative electrode comprising carbonaceous material having a graphite crystalline structure, and a non-aqueous electrolytic solution comprising an electrolyte dissolved in a non-aqueous solvent comprising a combination of a cyclic carbonate and a linear carbonate wherein the ratio of cyclic carbonate to linear carbonate ranges from 1:4 to 7:3 and which contains a disulfide derivative having the following formula:

R 1 —S—S—R 2

wherein each of R 1 and R 2 independently represents a phenyl group, a benzyl group, a tolyl group, a pyridyl group, a pyrimidyl group, an alkyl group having 1 to 12 carbon atom, or a cycloalkyl group having 3 to 6 carbon atoms, provided that each group may have one or more substituent groups in an amount of 0.02 to 0.9 weight % based on the amount of the electrolytic solution, whereby the discharge capacity retention after 50 discharge cycles is maintained at least 85% of the discharge capacity measured at a first discharge procedure and is higher than a discharge capacity retention after 50 discharge cycles measured on an equivalent non-aqueous electrolytic solution not containing the disulfide derivative by at least 4%.

2. The non-aqueous secondary battery of claim 1 , wherein the disulfide derivative is contained in the non-aqueous electrolytic solution in such an amount that the discharge capacity retention after 50 discharge cycles is maintained at least 90% of the discharge capacity measured at a first discharge procedure.

3. The non-aqueous secondary battery of claim 1 , wherein the disulfide derivative is contained in the non-aqueous electrolytic solution in an amount of 0.01 to 2 weight % based on the amount of the electrolytic solution.

4. The non-aqueous secondary battery of claim 1 , wherein the disulfide derivative is contained in the non-aqueous electrolytic solution in an amount of 0.02 to 0.9 weight % based on the amount of the electrolytic solution.

5. The non-aqueous secondary battery of claim 1 , wherein the disulfide derivative is contained in the non-aqueous electrolytic solution in an amount of 0.05 to 0.5 weight % based on the amount of the electrolytic solution.

6. The non-aqueous secondary battery of claim 1 , wherein the disulfide derivative is diphenyl disulfide.

7. A non-aqueous electrolytic solution comprising an electrolyte dissolved in a non-aqueous solvent comprising a combination of a cyclic carbonate and a linear carbonate, wherein the ratio of cyclic carbonate to linear carbonate ranges from 1:4 to 7:3 and which contains a disulfide derivative having the following formula:

R 1 —S—S—R 2

wherein each of R 1 and R 2 independently represents a phenyl group, a benzyl group, a tolyl group, a pyridyl group, a pyrimidyl group, an alkyl group having 1 to 12 carbon atom, or a cycloalkyl group having 3 to 6 carbon atoms, provided that each group may have one or more substituent groups in an amount of 0.02 to 0.9 weight %.

8. The non-aqueous electrolytic solution of claim 7 , wherein the disulfide derivative is contained in an amount of 0.05 to 0.5 weight %.

9. The non-aqueous electrolytic solution of claim 7 , wherein the disulfide derivative is diphenyl disulfide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2021
From: UBE INDUSTRIES, LTD.
To: MU IONIC SOLUTIONS CORPORATION
Reel/Frame 055221/0564 →
ASSIGNMENT Recorded Feb 17, 2010
From: HAMAMOTO, TOSHIKAZU; ABE, KOJI; TAKAI, TSUTOMU; MATSUMORI, YASUO
To: UBE INDUSTRIES, LTD.
Reel/Frame 023948/0957 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2003
From: IVO, GLYNNE GUT; DORIS, LECHNER
To: CONSORTIUM NATIONAL DE RECHERCHE EN GENOMIQUE (CNRG)
Reel/Frame 014212/0766 →