Method for producing ultra-pure bis(chlorosulfonyl)imide
US-2024391774-A1 · Nov 28, 2024 · US
US2016233548A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016233548-A1 |
| Application number | US-201415024418-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 25, 2014 |
| Priority date | Sep 25, 2013 |
| Publication date | Aug 11, 2016 |
| Grant date | — |
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To provide a nonaqueous electrolyte secondary battery that suppresses elution of Al from a positive electrode current collector formed of aluminum or an aluminum alloy, and is superior in thermal characteristics and input-output characteristics. Provided is a nonaqueous electrolyte secondary battery including a positive electrode, a negative electrode, and an electrolytic solution. The positive electrode has a positive electrode current collector formed of aluminum or an aluminum alloy. The electrolytic solution contains a metal salt and an organic solvent having a heteroelement. Regarding an intensity of a peak derived from the organic solvent in a vibrational spectroscopy spectrum of the electrolytic solution, Is>Io is satisfied when an intensity of an original peak of the organic solvent is represented as Io and an intensity of a peak resulting from shifting of the original peak is represented as Is.
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1 . A nonaqueous electrolyte secondary battery comprising a positive electrode, a negative electrode, and an electrolytic solution, wherein the positive electrode has a positive electrode current collector formed of aluminum or an aluminum alloy, the electrolytic solution contains a salt whose cation is an alkali metal, an alkaline earth metal, or aluminum, and an organic solvent having a heteroelement, and, regarding an intensity of a peak derived from the organic solvent in a vibrational spectroscopy spectrum of the electrolytic solution, Is>Io is satisfied when an intensity of an original peak of the organic solvent is represented as Io and an intensity of a peak resulting from shifting of the original peak is represented as Is, or d/c obtained by dividing a density d (g/cm 3 ) of the electrolytic solution by a concentration c (mol/L) of the electrolytic solution is within a range of 0.15≦d/c≦0.71. 2 . The nonaqueous electrolyte secondary battery according to claim 1 , wherein the cation of the salt is lithium. 3 . The nonaqueous electrolyte secondary battery according to claim 1 , wherein a chemical structure of an anion of the salt includes at least one element selected from a halogen, boron, nitrogen, oxygen, sulfur, or carbon. 4 . The nonaqueous electrolyte secondary battery according to claim 1 , wherein a chemical structure of an anion of the salt is represented by general formula (1), general formula (2), or general formula (3) below: (R 1 X 1 )(R 2 X 2 )N General Formula (1) (R 1 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 2 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 1 and R 2 optionally bind with each other to form a ring. X 1 is selected from SO 2 , C═O, C═S, R a P═O, R b P═S, S═O, or Si═O. X 2 is selected from SO 2 , C═O, C═S, R c P═O, R d P═S, S═O, or Si═O. R a , R b , R c , and R d are each independently selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; OH; SH; CN; SCN; or OCN. R a , R b , R c , and R d each optionally bind with R 1 or R 2 to form a ring.); R 3 X 3 Y General Formula (2) (R 3 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. X 3 is selected from SO 2 , C═O, C═S, R e P═O, R f P═S, S═O, or Si═O. R e and R f are each independently selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; OH; SH; CN; SCN; or OCN. R e and R f each optionally bind with R 3 to form a ring. Y is selected from O or S.); and (R 4 X 4 )(R 5 X 5 )(R 6 X 6 )C General Formula (3) (R 4 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 5 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optionally substituted with a substituent group; an aromatic group optionally substituted with a substituent group; a heterocyclic group optionally substituted with a substituent group; an alkoxy group optionally substituted with a substituent group; an unsaturated alkoxy group optionally substituted with a substituent group; a thioalkoxy group optionally substituted with a substituent group; an unsaturated thioalkoxy group optionally substituted with a substituent group; CN; SCN; or OCN. R 6 is selected from: hydrogen; a halogen; an alkyl group optionally substituted with a substituent group; a cycloalkyl group optionally substituted with a substituent group; an unsaturated alkyl group optionally substituted with a substituent group; an unsaturated cycloalkyl group optiona
characterised by the additives · CPC title
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
characterised by the solutes · CPC title
Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx · CPC title
Metal or alloys, e.g. alloy coatings (H01M4/669 take precedence) · CPC title
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