Method for producing ultra-pure bis(chlorosulfonyl)imide
US-2024391774-A1 · Nov 28, 2024 · US
US10305145B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10305145-B2 |
| Application number | US-201515124220-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 19, 2015 |
| Priority date | Mar 28, 2014 |
| Publication date | May 28, 2019 |
| Grant date | May 28, 2019 |
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The problem to be solved is to provide a liquid electrolyte for a fluoride ion battery which allows a larger capacity of the battery. Solving the problem by providing a liquid electrolyte for a fluoride ion battery including a fluoride salt and a solvent to dissolve the fluoride salt, characterized in that the solvent is an aromatic material having an aromatic cation and an anion, and a molar ratio of the aromatic cation to a fluoride ion is more than 1.
Opening claim text (preview).
The invention claimed is: 1. A fluoride ion battery comprising a cathode active material layer containing a cathode active material, an anode active material layer containing an anode active material, and an electrolyte layer formed between the cathode active material layer and the anode active material layer, wherein the electrolyte layer comprises a liquid electrolyte, the liquid electrolyte comprises a fluoride salt and a solvent to dissolve the fluoride salt, the solvent contains at least an aromatic material having an aromatic cation and an anion, a molar ratio of the aromatic cation to a fluoride ion is more than 1, the cathode active material is an active material which is defluoridated during discharge, and the anode active material is an active material which is fluoridated during discharge. 2. The fluoride ion battery according to claim 1 , wherein the aromatic material is an ionic liquid. 3. The fluoride ion battery according to claim 1 , wherein the aromatic cation is a cation represented by the following general formula: in the formula, R 1 to R 6 being each independently hydrogen, an alkyl group or a fluoroalkyl group. 4. The fluoride ion battery according to claim 1 , wherein the anion of the aromatic material is bisfluorosulfonylamide(FSA)anion. 5. The fluoride ion battery according to claim 1 , wherein a proportion of F(HF)x-anion to all anions existing in the liquid electrolyte is 0.5 mol % or less, including 0 mol %. 6. The fluoride ion battery according to claim 1 , wherein the fluoride salt has F − anion. 7. The fluoride ion battery according to claim 1 , wherein the fluoride salt has a complex cation. 8. The fluoride ion battery according to claim 7 , wherein the complex cation is selected from the group consisting of an alkylammonium cation, an alkylphosphonium cation and an alkylsulfonium cation. 9. The fluoride ion battery according to claim 1 , wherein the fluoride salt is present in a concentration of 0.4 mol % to 45 mol % in the liquid electrolyte. 10. The fluoride ion battery according to claim 1 , wherein the fluoride salt is present in a concentration of 0.7 mol % to 10 mol % in the liquid electrolyte. 11. The fluoride ion battery according to claim 1 , wherein the molar ratio of the aromatic cation to a fluoride ion is 5 or more and no more than 200. 12. The fluoride ion battery according to claim 1 , wherein the molar ratio of the aromatic cation to a fluoride ion is 10 or more and no more than 200.
characterised by the solvents · CPC title
Room temperature molten salts comprising at least one organic ion · CPC title
Halogenides · CPC title
Batteries in motive systems, e.g. vehicle, ship, plane · CPC title
characterised by the solutes · CPC title
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