IP Library › Granted Patent US 11,688,881
Granted Patent B2
US 11,688,881 · App. 16/728,477 · Granted Jun 27, 2023

Nonaqueous electrolytic solution and nonaqueous electrolytic solution secondary battery using same

Inventors: Hiroaki Yoshida (Ibaraki, JP); Yasuyuki Shigematsu (Kanagawa, JP); Minoru Kotato (Mie, JP)
Assignees: Mitsubishi Chemical Corporation; MU Ionic Solutions Corporation
H01M10/0567H01M10/052H01M10/056H01M10/0525H01M4/386H01M4/505H01M4/525H01M4/587H01M10/0568H01M10/0569H01M2300/004
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Quick Facts
Patent No.
US 11,688,881
App. No.
16/728,477
Granted
Jun 27, 2023
Kind
B2
Abstract

The present invention relates to a nonaqueous electrolytic solution for use in a nonaqueous electrolytic solution secondary battery that comprises a negative electrode and a positive electrode capable of storing and releasing metal ions, and a nonaqueous electrolytic solution, wherein the nonaqueous electrolytic solution contains the specific compounds (A) and (B).

Claims (39)

1. A nonaqueous electrolytic solution suitable for use in a nonaqueous electrolytic solution secondary battery that comprises a negative electrode and a positive electrode capable of storing and releasing metal ions, and the nonaqueous electrolytic solution, the nonaqueous electrolytic solution comprising, based on total nonaqueous electrolytic solution weight:

(A) a first compound (A) of formula (4), in a range of from 0.01 to 10 wt. %,

A 1 to A 6 being independently H, a halogen atom, a hydrocarbon group of 1 to 10 carbon atoms that may have a heteroatom, or an optionally substituted hydrogen silicide group of 1 to 10 silicon atoms, A 1 to A 6 optionally binding to one another to form a ring, wherein none of A 1 to A 6 is an aliphatic substituent having an unsaturated bond; and

(B) at least one second compound, in a range of from 0.01 to 2 wt. %, the second compound being selected from the group consisting of a difluorophosphate, a fluorosulfonate, and an imide salt,

wherein the nonaqueous electrolytic solution comprises no carbonate ester having a halogen atom.

2. The solution of claim 1 , further comprising:

a third compound, having a NCO group, of formula (3),

wherein

R 5 is an organic group of 1 to 20 carbon atoms, optionally having a branched structure or an aromatic group, and

Q is a hydrogen atom or an NCO group.

3. The solution of claim 1 , further comprising:

a monofluorophosphate.

4. The solution of claim 1 , wherein the second compound (B) comprises the difluorophosphate.

5. The solution of claim 1 , wherein the second compound (B) comprises the fluorosulfonate.

6. The solution of claim 1 , wherein the second compound (B) comprises the imide salt.

7. The solution of claim 1 , further comprising:

at least one fourth compound selected from the group consisting of ethynylethylene sulfate, propynyl vinyl sulfonate, and hexamethylene diisocyanate.

8. The solution of claim 1 , wherein the second compound (B) is at least one compound selected from the group consisting of lithium difluorophosphate, lithium fluorosulfonate, LiN(FSO 2 ) 2 , LiN(CF 3 SO 2 ) 2 , and LiN(C 2 F 5 SO 2 ) 2 .

9. The solution of claim 1 , wherein, in the first compound (A) of formula (4), A 1 to A 6 are independently H, methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl, or phenyl.

10. The solution of claim 1 , wherein the first compound (A) is at least one selected from the group consisting of hexamethyldisilane, hexaethyldisilane, 1,2-diphenyltetramethyldisilane, and 1,1,2,2-tetraphenyldisilane.

11. The solution of claim 1 , comprising the first compound (A) is present in a range of from 0.01 to 2.0 wt. %, based on the total nonaqueous electrolytic solution weight.

12. The solution of claim 1 , further comprising:

lithium monofluorophosphate.

13. The solution of claim 1 , wherein second compound (B) is

14. The solution of claim 1 , wherein second compound (B) is

15. The solution of claim 1 , wherein second compound (B) is

16. The solution of claim 1 , wherein, in the first compound (A) of formula (4), A 1 to A 6 are independently H, methyl, ethyl, or phenyl.

17. The solution of claim 1 , wherein, in the first compound (A) of formula (4), A 1 to A 6 are independently H, methyl, or a substituted hydrogen silicide group of 1 silicon atom,

wherein at least one of A 1 to A 6 is H,

wherein at least one of A 1 to A 6 is methyl, and

wherein at least one of A 1 to A 6 is a substituted hydrogen silicide group of 1 silicon atom.

18. The solution of claim 1 , wherein the first compound (A) comprises

19. The solution of claim 18 , wherein the first compound (A) has only one Si—Si bond.

20. The solution of claim 1 , wherein the second compound (B) comprises

21. The solution of claim 1 , wherein the second compound (B) is at least one selected from the group consisting of

22. A nonaqueous electrolytic solution secondary battery, comprising:

a carbon-based negative electrode;

a positive electrode capable of storing and releasing metal ions; and

the nonaqueous electrolytic solution of claim 1 .

Assignments (1)
PARTIAL ASSIGNMENT Recorded Dec 23, 2020
From: MITSUBISHI CHEMICAL CORPORATION
To: MU IONIC SOLUTIONS CORPORATION
Reel/Frame 054839/0093 →
Priority Claims (2)
JP 2011-018561 · Jan 31, 2011 · national
JP 2011-024873 · Feb 8, 2011 · national
Continuity (4)
Continuation 15719258 · Sep 28, 2017
Continuation 13955373 · Jul 31, 2013
Continuation PCTJP2012052017 · Jan 30, 2012
Related Publication 20200144670A1 · May 7, 2020