IP Library › Granted Patent US 10,128,541
Granted Patent B2
US 10,128,541 · App. 15/792,994 · Granted Nov 13, 2018

Power storage device

Inventors: Toru Itakura (Kanagawa, JP); Kyosuke Ito (Saitama, JP); Jun Ishikawa (Kanagawa, JP); Rie Yokoi (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
H01M10/0569H01G11/06H01G11/32H01G11/50H01G11/60H01G11/62H01G11/84H01M2/162H01M2/1653H01M4/133H01M4/136H01M4/587H01M4/5825H01M4/623H01M4/625H01M4/661H01M10/0525H01M10/0568H01M10/0585H01M4/043H01M4/0404H01M4/0471H01M4/1397H01M4/621H01M2004/021H01M2004/027H01M2004/028H01M2220/20H01M2220/30H01M2300/0034H01M2300/0045Y02E60/122Y02E60/13Y02T10/7011Y02T10/7022
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 10,128,541
App. No.
15/792,994
Granted
Nov 13, 2018
Kind
B2
Abstract

A power storage device with reduced initial irreversible capacity is provided. The power storage device includes a positive electrode including a positive electrode current collector and a positive electrode active material layer, a negative electrode including a negative electrode current collector and a negative electrode active material layer, and an electrolyte solution. In the negative electrode active material layer, the content percentage of a carbon material with an R value of 1.1 or more is less than 2 wt %. The R value refers to a ratio of a peak intensity I 1360 to a peak intensity I 1580 (I 1360 /I 1580 ). The peak intensity I 1360 and the peak intensity I 1580 are observed by Raman spectrometry at a Raman shift of 1360 cm −1 and a Raman shift of 1580 cm −1 , respectively. The electrolyte solution contains a lithium ion and an ionic liquid composed of an organic cation and an anion.

Claims (84)

1. A method for manufacturing a power storage device comprising the steps of:

mixing a carbon material and binder with a solvent to form a paste;

drying the paste to form a negative electrode; and

stacking a positive electrode and the negative electrode with a separator and an electrolyte solution interposed therebetween, the electrolyte solution containing a lithium ion and an ionic liquid composed of an organic cation and an anion,

wherein a melting point of the ionic liquid is −10° C. or lower,

wherein a content percentage of the carbon material with an R value of 1.1 or more is less than 2 wt % in the negative electrode,

wherein the R value is a ratio of a peak intensity I 1360 to a peak intensity I 1580 (I 1360 /I 1580 ), the peak intensity I 1360 and the peak intensity I 1580 are observed by Raman spectrometry at a Raman shift of 1360 cm −1 and a Raman shift of 1580 cm −1 , respectively.

2. The method for manufacturing a power storage device according to claim 1 , wherein the organic cation is a quaternary ammonium cation, a tertiary sulfonium cation, a quaternary phosphonium cation, an imidazolium cation, or a pyridinium cation.

3. The method for manufacturing a power storage device according to claim 1 ,

wherein the ionic liquid is represented by a General Formula (G1),

wherein R 1 to R 6 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

4. The method for manufacturing a power storage device according to claim 1 ,

wherein the ionic liquid is represented by a General Formula (G2),

wherein R 7 to R 13 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

5. The method for manufacturing a power storage device according to claim 1 ,

wherein the ionic liquid includes two aliphatic rings and is represented by a General Formula (G3),

wherein n and m are greater than or equal to 1 and less than or equal to 3,

wherein α is greater than or equal to 0 and less than or equal to 4 when n is 1, α is greater than or equal to 0 and less than or equal to 5 when n is 2, and α is greater than or equal to 0 and less than or equal to 6 when n is 3,

wherein β is greater than or equal to 0 and less than or equal to 4 when m is 1, β is greater than or equal to 0 and less than or equal to 5 when m is 2, and β is greater than or equal to 0 and less than or equal to 6 when m is 3,

wherein “α or β is 0” means that at least one of the two aliphatic rings is unsubstituted, and a case where both α and β are 0 is excluded,

wherein X or Y is a substituent which is a straight chain or lateral chain alkyl group having 1 to 4 carbon atoms, a straight chain or lateral chain alkoxy group having 1 to 4 carbon atoms, or a straight chain or lateral chain alkoxyalkyl group having 1 to 4 carbon atoms, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

6. The method for manufacturing a power storage device according to claim 1 ,

wherein the carbon material comprises an active material and a conductive additive,

wherein the active material comprises graphite, and

wherein the conductive additive does not comprise acetylene black.

7. A method for manufacturing a power storage device comprising the steps of:

mixing a carbon material comprising graphite and binder with a solvent to form a paste;

drying the paste to form a negative electrode; and

stacking a positive electrode and the negative electrode with a separator and an electrolyte solution interposed therebetween, the electrolyte solution containing a lithium ion and an ionic liquid composed of an organic cation and an anion,

wherein a content percentage of the carbon material with an R value of 1.1 or more is less than 2 wt % in the negative electrode,

wherein the R value is a ratio of a peak intensity I 1360 to a peak intensity I 1580 (I 1360 /I 1580 ), the peak intensity I 1360 and the peak intensity I 1580 are observed by Raman spectrometry at a Raman shift of 1360 cm −1 and a Raman shift of 1580 cm −1 , respectively.

8. The method for manufacturing a power storage device according to claim 7 ,

wherein the organic cation is a quaternary ammonium cation, a tertiary sulfonium cation, a quaternary phosphonium cation, an imidazolium cation, or a pyridinium cation.

9. The method for manufacturing a power storage device according to claim 7 ,

wherein the ionic liquid is represented by a General Formula (G1),

wherein R 1 to R 6 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

10. The method for manufacturing a power storage device according to claim 7 ,

wherein the ionic liquid is represented by a General Formula (G2),

wherein R 7 to R 13 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

11. The method for manufacturing a power storage device according to claim 7 ,

wherein the ionic liquid includes two aliphatic rings and is represented by a General Formula (G3),

wherein n and m are greater than or equal to 1 and less than or equal to 3,

wherein α is greater than or equal to 0 and less than or equal to 4 when n is 1, α is greater than or equal to 0 and less than or equal to 5 when n is 2, and α is greater than or equal to 0 and less than or equal to 6 when n is 3,

wherein β is greater than or equal to 0 and less than or equal to 4 when m is 1, β is greater than or equal to 0 and less than or equal to 5 when m is 2, and β is greater than or equal to 0 and less than or equal to 6 when m is 3,

wherein “α or β is 0” means that at least one of the two aliphatic rings is unsubstituted, and a case where both α and β are 0 is excluded,

wherein X or Y is a substituent which is a straight chain or lateral chain alkyl group having 1 to 4 carbon atoms, a straight chain or lateral chain alkoxy group having 1 to 4 carbon atoms, or a straight chain or lateral chain alkoxyalkyl group having 1 to 4 carbon atoms, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

12. The method for manufacturing a power storage device according to claim 7 ,

wherein the carbon material comprises an active material and a conductive additive,

wherein the active material comprises graphite, and

wherein the conductive additive does not comprise acetylene black.

13. A method for manufacturing a power storage device comprising the steps of:

mixing a carbon material comprising graphene and binder with a solvent to form a paste;

drying the paste to form a negative electrode; and

stacking a positive electrode and the negative electrode with a separator and an electrolyte solution interposed therebetween, the electrolyte solution containing a lithium ion and an ionic liquid composed of an organic cation and an anion,

wherein a content percentage of the carbon material with an R value of 1.1 or more is less than 2 wt % in the negative electrode,

wherein the R value is a ratio of a peak intensity I 1360 to a peak intensity I 1580 (I 1360 /I 1580 ), the peak intensity I 1360 and the peak intensity I 1580 are observed by Raman spectrometry at a Raman shift of 1360 cm −1 and a Raman shift of 1580 cm −1 , respectively.

14. The method for manufacturing a power storage device according to claim 13 ,

wherein the organic cation is a quaternary ammonium cation, a tertiary sulfonium cation, a quaternary phosphonium cation, an imidazolium cation, or a pyridinium cation.

15. The method for manufacturing a power storage device according to claim 13 ,

wherein the ionic liquid is represented by a General Formula (G1),

wherein R 1 to R 6 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

16. The method for manufacturing a power storage device according to claim 13 ,

wherein the ionic liquid is represented by a General Formula (G2),

wherein R 7 to R 13 separately represent an alkyl group having 1 to 20 carbon atoms, a methoxy group, a methoxymethyl group, a methoxyethyl group, or a hydrogen atom, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a fluorosulfonate anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

17. The method for manufacturing a power storage device according to claim 13 ,

wherein the ionic liquid includes two aliphatic rings and is represented by a General Formula (G3),

wherein n and m are greater than or equal to 1 and less than or equal to 3,

wherein α is greater than or equal to 0 and less than or equal to 4 when n is 1, α is greater than or equal to 0 and less than or equal to 5 when n is 2, and α is greater than or equal to 0 and less than or equal to 6 when n is 3,

wherein β is greater than or equal to 0 and less than or equal to 4 when m is 1, β is greater than or equal to 0 and less than or equal to 5 when m is 2, and β is greater than or equal to 0 and less than or equal to 6 when m is 3,

wherein “α or β is 0” means that at least one of the two aliphatic rings is unsubstituted, and a case where both α and β are 0 is excluded,

wherein X or Y is a substituent which is a straight chain or lateral chain alkyl group having 1 to 4 carbon atoms, a straight chain or lateral chain alkoxy group having 1 to 4 carbon atoms, or a straight chain or lateral chain alkoxyalkyl group having 1 to 4 carbon atoms, and

wherein A − represents a monovalent amide anion, a monovalent methide anion, a perfluoroalkylsulfonate anion, tetrafluoroborate, perfluoroalkylborate, hexafluorophosphate, or perfluoroalkylphosphate.

18. The method for manufacturing a power storage device according to claim 13 ,

wherein the carbon material comprises an active material and a conductive additive,

wherein the active material comprises graphite, and

wherein the conductive additive does not comprise acetylene black.

Priority Claims (1)
JP 2012-224603 · Oct 9, 2012 · national
Continuity (4)
Continuation 15477670 · Apr 3, 2017
Continuation 15167300 · May 27, 2016
Continuation 14046104 · Oct 4, 2013
Related Publication 20180048027A1 · Feb 15, 2018
Cited By (3)
US 12,191,496 US 12,463,220 US 12,603,290