Method for manufacturing non-aqueous secondary battery electrode
US-2024332484-A1 · Oct 3, 2024 · US
US9774057B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9774057-B2 |
| Application number | US-201213705709-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 5, 2012 |
| Priority date | Dec 8, 2011 |
| Publication date | Sep 26, 2017 |
| Grant date | Sep 26, 2017 |
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A mixture useful as an electrolyte in lithium ion batteries and use thereof are provided. Lithium ion batteries with good performance, especially good cyclability after prolonged operation are obtained. The mixture contains an aprotic organic solvent, a cyclic compound containing C 1 -C 10 -alkyl, C 1 -C 10 -alkoxy, C 3 -C 10 -cycloalkyl, benzyl or C 6 -C 14 -aryl, water, optionally an additive and a lithium salt.
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We claim: 1. A mixture, comprising: an aprotic organic solvent or an aprotic organic solvent mixture; at least one compound selected from the group consisting of formula (I) and formula (II) from 0 to 30 ppm of water; optionally an additive; and a lithium salt, wherein the aprotic organic solvent or the aprotic organic solvent mixture is liquid at room temperature; R 1 is independently a C 1 -C 10 -alkyl; R 2 is independently a C 1 -C 10 -alkyl; R 3 is hydrogen or >C(R 3 ) 2 is a >C═O group; R 4 is hydrogen; X is independently selected from the group consisting of oxygen, sulfur, N—R 5 , and C(R 6 ) 2 ; R 5 is selected from the group consisting of C 1 -C 10 -alkyl, C 3 -C 10 -cycloalkyl, benzyl, and C 6 -C 14 -aryl, optionally substituted by C 1 -C 4 -alkyl, benzyl, or phenyl; R 6 is independently selected from the group consisting of hydrogen, C 1 -C 10 -alkyl, C 3 -C 10 -cycloalkyl, benzyl, and C 6 -C 14 -aryl, optionally substituted by C 1 -C 4 -alkyl, benzyl, or phenyl; and n is an integer from 1 to 3. 2. The mixture according to claim 1 , wherein the aprotic organic solvent is selected from the group consisting of cyclic organic carbonate or noncyclic organic carbonate, di-C 1 -C 10 -alkyl ester, di-C 1 -C 4 -alkyl-C 2 -C 6 -alkylene ester, cyclic ester, cyclic acetal, acyclic acetal, cyclic ketal , or acyclic ketal orthocarboxylic ester and cyclic carboxylic ester or noncyclic carboxylic ester. 3. The mixture according to claim 1 , wherein the compound of formula (I) or (II) is (Ia), (Ib), (IIa), or (IIb): wherein R 1 is independently a C 1 -C 4 -alkyl; R 2 is independently a C 1 -C 4 -alkyl; and R 6 is selected from the group consisting of hydrogen and methyl. 4. The mixture according to claim 1 , wherein the additive is selected from the group consisting of sultone, cyclic exo-methylene carbonate, lithium bisoxalatoborate (LiBOB), and lithium (difluoroxalato)borate (LiDFOB). 5. The mixture according to claim 1 , wherein the compound of formula (I) or (II) is selected from the group consisting of (Ia.1), (Ib.1), (IIa.1), and (IIb.1): 6. The mixture according to claim 1 , wherein the lithium salt is selected from the group consisting of LiPF 6 , LiBF 4 , LiSbF 6 , LiBOB, LDFOB, and LiPF 3 (CF 2 CF 3 ) 3 (LiFAP). 7. The mixture according to claim 1 comprising: from 50 to 99.5 wt % of the aprotic organic solvent or of the aprotic organic solvent mixture; from 0.01 to 4 wt % of the compound of formula (I) or (II); from 0 to 30 ppm of the water; from 0 to 10 wt % of the additive; and more than zero to 20 wt % of the lithium salt, based on a total amount of the mixture. 8. A lithium ion battery, comprising the mixture according to claim 1 . 9. The lithium ion battery according to claim 8 , comprising a cathodic active material having manganese from 50 to 80 wt %, based on a content of transition metal. 10. The lithium ion battery according to claim 8 , comprising an anode comprising an electrically conductive carbon. 11. A process for producing the mixture according to claim 1 , comprising: providing the aprotic organic solvent; optionally mixing with an additional aprotic organic solvent; optionally mixing with the additive; drying; mixing with the compound of formula (I) or (II) with the lithium salt, and optionally with the additive. 12. The process according to claim 11 , wherein the drying is effected with a molecular sieve.
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