IP Library Granted Patent US 12,548,798
Granted Patent B2
US 12,548,798 · App. 17/940,799 · Granted Feb 10, 2026

Hydrofluorocarbon (HFC)-based safe electrolyte for secondary batteries

Inventors: Jie Xiao (Richland, WA); Bingbin Wu (Richland, WA); Wei Wang (West Richland, WA); Dianying Liu (Richland, WA); Ruozhu Feng (Richland, WA)
Assignee: Battelle Memorial Institute
H01M10/0569H01M4/364H01M4/382H01M4/386H01M4/505H01M4/525H01M4/5825H01M4/587H01M8/02H01M8/188H01M10/0568H01M10/4235H01M50/105H01M2004/027H01M2004/028H01M2300/0034H01M2300/0037
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Quick Facts
Patent No.
US 12,548,798
App. No.
17/940,799
Granted
Feb 10, 2026
Kind
B2
Abstract

An electrolyte composition comprising a solution comprising an active salt; and a solvent portion that comprises a first solvent and a second solvent, wherein the first solvent is a hydrofluorocarbon compound having a structure of C x H y F z , wherein x is from 4 to 10, y is from 1 to 10, z is from 5 to 20, and the z:y ratio is from 2:1 to 10:1.

Claims (18)

1 . A nonaqueous redox flow battery system, comprising:

an anolyte;

a catholyte; and

an ion-exchange membrane or porous separator,

wherein at least one of the anolyte or the catholyte comprises a solution comprising a solvent portion that comprises a first solvent and a second solvent, wherein the first solvent is a fluorohexane or a fluorocyclohexane.

2 . The battery system of claim 1 , wherein the first solvent is 1H,6H-dodecafluorohexane, or 1,1,2,2,3,3,4,4,5,5-decafluorocyclohexane.

3 . The battery system of claim 1 , wherein the second solvent is at least one carbonate.

4 . The battery system of claim 1 , wherein the second solvent comprises ethylene carbonate (EC), dimethyl carbonate (DMC), vinylene carbonate (VC), fluoroethylene carbonate (FEC), difluoroethylene carbonate (DFEC), trifluoroethylene carbonate (TFEC), vinyl ethylene carbonate (VEC), 4-methylene ethylene carbonate (MEC), propylene carbonate (PC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), methyl 2,2,2-trifluoroethyl carbonate (MFEC), dimethoxyethane (DME), 1,3-dioxolane (DOL), tetrahydrofuran (THF), allyl ether, triethyl phosphate (TEP), trimethyl phosphate (TMP), tributyl phosphate, triphenyl phosphate, tris(2,2,2-trifluoroethyl) phosphate, bis(2,2,2-trifluoroethyl) methyl phosphate, triphenyl phosphite, tris(2,2,2-trifluoroethyl) phosphite; dimethyl methylphosphonate, diethyl ethylphosphonate, diethyl phenylphosphonate, bis(2,2,2-trifluoroethyl) methylphosphonate; hexamethylphosphoramide; hexamethoxyphosphazene, hexafluorophosphazene, dimethyl sulfoxide (DMSO), dimethyl sulfone (DMS), ethyl methyl sulfone (EMS), ethyl vinyl sulfone (EVS), tetramethylene sulfone (TMS), trifluoromethyl ethyl sulfone (FMES), trifluoromethyl isopropyl sulfone (FMIS), trifluoropropyl methyl sulfone (FPMS), diethylene glycol dimethyl ether (diglyme), triethylene glycol dimethyl ether (triglyme), tetraethylene glycol dimethyl ether (tetraglyme), methyl butyrate, ethyl propionate, gamma-butyrolactone, acetonitrile (AN), succinonitrile (SN), adiponitrile, triallyl amine, triallyl cyanurate, triallyl isocyanurate, or any combination thereof.

5 . The battery system of claim 4 , wherein the first solvent is 1H,6H-dodecafluorohexane or 1,1,2,2,3,3,4,4,5,5-decafluorocyclohexane.

6 . The battery system of claim 1 , wherein the solution has a flashpoint>93° C.

7 . The battery system of claim 1 , wherein the anolyte comprises a quinoxaline compound, a quinone compound, a ketone compound, an acylpyridine compound, a viologen compound, an anthraquinone compound, a phthalimide compound, a phenazine compound, a thiadiazole compound or metal anode.

8 . The battery system of claim 7 , wherein the catholyte comprises a metallocene, a dialkoxybenzene, a phenothiazine compound, a catechol ether compound, a catecholborane compound, a borane cluster compound, a 1,3-benzodioxole compound, a benzodioxin compound, a carbonyl compound, a 1,4-dialkoxybisphosphinyl benzene compound, a 1,4-phenylene diphosphate ester compound, an organic nitroxide radical, or a 5,10-dihydro-5,10-dialkylphenazine compound.

9 . The battery system of claim 8 , wherein the first solvent is 1H,6H-dodecafluorohexane or 1,1,2,2,3,3,4,4,5,5-decafluorocyclohexane.

10 . The battery system of claim 1 , wherein the catholyte comprises a metallocene, a dialkoxybenzene, a phenothiazine compound, a catechol ether compound, a catecholborane compound, a borane cluster compound, a 1,3-benzodioxole compound, a benzodioxin compound, a carbonyl compound, a 1,4-dialkoxybisphosphinyl benzene compound, a 1,4-phenylene diphosphate ester compound, an organic nitroxide radical, or a 5,10-dihydro-5,10-dialkylphenazine compound.

11 . The battery system of claim 1 , wherein the first solvent is from 10 vol % to 90 vol % of the solvent portion of the solution.

12 . The battery system of claim 1 , wherein the first solvent is from 20 vol % to 50 vol % of the solvent portion of the solution.

13 . The battery system of claim 1 , wherein the first solvent is from 70 vol % to 75 vol % of the solvent portion of the solution.

14 . The battery system of claim 1 , wherein the first solvent is from 75 vol % to 85 vol % of the solvent portion of the solution.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2022
From: XIAO, JIE; WU, BINGBIN; WANG, WEI; LIU, DIANYING; FENG, RUOZHU
To: BATTELLE MEMORIAL INSTITUTE
Reel/Frame 061047/0229 →
Continuity (1)
Related Publication 20240113340A1 · Apr 4, 2024
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