High performance inorganic complexes for next-generation redox flow batteries

US10840504B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10840504-B2
Application numberUS-201815903553-A
CountryUS
Kind codeB2
Filing dateFeb 23, 2018
Priority dateFeb 23, 2017
Publication dateNov 17, 2020
Grant dateNov 17, 2020

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  5. First independent claim

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Abstract

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In an aspect, a redox flow battery comprises a catholyte and an anolyte; wherein at least one of said catholyte and said anolyte is a metal-coordination complex, said metal-coordination complex comprising: (i) a metal; (ii) one or more first ligands coordinated with said metal atom, wherein each of said first ligands is independently a Lewis basic ligand; and one or more second ligands associated with said one or more first ligands, wherein each of said second ligands is independently a Lewis acid ligand; and a nonaqueous solvent, wherein said catholyte, said anolyte or both are dissolved in said nonaqueous solvent. One or more first ligands may be provided in a primary coordination sphere of said metal-coordination complex and one or more second ligands may be provided in a secondary coordination sphere of said metal-coordination complex. The one or more first ligands independently may comprise a Lewis basic functional group and each of said one or more second ligands independently may comprise a Lewis acidic functional group.

First claim

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We claim: 1. A redox flow battery comprising: a catholyte; an anolyte; wherein at least one of said catholyte and said anolyte is a metal-coordination complex, said metal-coordination complex comprising: (i) a metal; (ii) one or more first ligands coordinated with said metal atom, wherein each of said first ligands is independently a Lewis basic ligand; and (iii) one or more second ligands coordinated with said one or more first ligands, wherein each of said second ligands is independently a Lewis acidic ligand; and a nonaqueous solvent, wherein said catholyte, said anolyte or both are dissolved in said nonaqueous solvent. 2. The redox flow battery of claim 1 , wherein said one or more first ligands are provided in a primary coordination sphere of said metal-coordination complex, and wherein said one or more second ligands are provided in a secondary coordination sphere of said metal-coordination complex. 3. The redox flow battery of claim 1 , wherein each of said one or more first ligands independently comprises one or more Lewis basic functional groups and each of said one or more second ligands independently comprises one or more Lewis acidic functional groups. 4. The redox flow battery of claim 3 , wherein said one or more second ligands associate with said first ligands to result in electron density being distributed away from said Lewis basic functional groups and to said Lewis acidic functional groups. 5. The redox flow battery of claim 1 , wherein each of said catholyte and said anolyte is independently a metal-coordination complex. 6. The redox flow battery of claim 1 , wherein said metal-coordination complex is characterized by the formula (F1): [ M j ( L 1 ) x ( L 2 ) y ] z   (F1), wherein: M is said metal selected from the group consisting of Cr, Mn, Fe, Co, Ni, Mo, Tc, Ru, Re, Os, W, Rh, Ir, Pd, and Pt; each of L 1 is independently said first ligand; each of L 2 is independently said second ligand; z is 0 or an integer selected from the range of −5 to 5; each of x and y is independently an integer selected from the range of 1 to 8; and j is an integer selected from the range of 1 to 3. 7. The redox flow battery of claim 6 , wherein each of L1 is independently nitrogen or a substituted or unsubstituted functional group or molecule corresponding to a nitrile, a pyridyl, a diamine, a triamine, an imine, an amine, an azide, a diimine, a triimine, an amide, a diimide, pyridine, pyrazine, imidazole, pyrazole, pyridazine, pyrimidine, triazine, quinoline, isoquinoline, quinoxaline, acridine, quinazoline, cinnoline, phthalazine, indazole, indole, isoindole, pyrrole, benzimidazole, purine, oxazole, bipyridine, terpyridine, phenanthroline, or any combination thereof. 8. The redox flow battery of claim 6 , wherein each of L 2 is independently —G a (G b ) q ; where: G a is selected from the group consisting of C, B, Si, Ge, Al, Zn, Sn, Sb, Te, Bi, and Pb; each of G b is independently selected from the group consisting of a hydrogen, a halide, nitrogen, and a substituted or an unsubstituted C 1 -C 10 alkyl, C 3 -C 10 cycloalkyl, C 5 -C 10 aryl, C 5 -C 10 heteroaryl, acyl, C 1 -C 10 hydroxyl, C 1 -C 10 alkoxy, C 2 -C 10 alkenyl, C 2 -C 10 alkynyl, C 5 -C 10 alkylaryl, C 3 -C 10 arylene, C 3 -C 10 heteroarylene, C 2 -C 10 alkenylene, C 3 -C 10 cycloalkenylene, C 2 -C 10 alkynylene, cyanide, pyridine, pyrazine, imidazole, pyrazole, pyridazine, pyrimidine, bipyridine, terpyridine, phenanthroline, a diamine, a triamine, an imine, an amine, an azide, a diimine, a triimine, an amide, or any combination thereof; and q is an integer selected from the range of 1 to 8. 9. The redox flow battery of claim 8 , wherein G b is characterized by the formula (F2): wherein: each of R 2 is independently selected from the group consisting of a hydrogen, a halide, a C 5 -C 6 aryl, a C 1 -C 5 alkyl, and any combination thereof. 10. The redox flow battery of claim 8 , wherein G a is B and wherein G b is a quintuply fluorinated phenyl group [—(C 6 F 5 )]. 11. The redox flow battery of claim 6 , wherein L 1 is characterized by the formula (F3), (F4), (F5a), (F5b), (F5c), (F5d), or (F5e): 12. The redox flow battery of claim 6 , wherein L 2 is characterized by the formula (F6), (F7), or (F8): where: each of R 2 is independently selected from the group consisting of a hydrogen, a halide, a C 5 -C 6 aryl, a C 1 -C 5 alkyl, and any combination thereof. 13. The redox flow battery of claim 6 , wherein said metal-coordination complex is selected from the group consisting of [Fe(CN) 6 (BPh 3 ) 6 ] 3− or 4− or 5− , [Fe(CN) 6 (B(C 6 F 5 ) 3 ) 6 ] 3− or 4− or 5− , [Mn(CN) 6 (BPh 3 ) 6 ] 2− or 3− or 4− or 5− , [Mn(CN) 6 (B(C 6 F 5 ) 3 ) 6 ] 2− or 3− or 4− or 5− , [Co(CN) 6 (BPh 3 ) 6 ] 3− or 4− , [Co(CN) 6 (B(C 6 F 5 ) 3 ) 6 ] 3− or 4− , [Mo(CN) 8 (BPh 3 ) 8 ] 4− or 5− , [Mo(CN) 8 (B(C 6 F 5 ) 3 ) 8 ] 4− or 5− , [Mo(CN) 8 (BPh 3 ) 6 ] 4− or 5− , [Mo(CN) 8 (B(C 6 F 5 ) 3 ) 6 ] 4− or 5− and [Fe(CN) 6 (CH 3 ) 6 ] 3+ or 2+ or 1+ . 14. The redox flow battery of claim 1 , wherein a redox potential of said metal-coordination complex increases by ΔP milliVolts; wherein ΔP=(m)(x), m is selected from the range of 200 to 700, and x is the number of first ligands coordinated with the metal in said metal-coordination complex. 15. The redox flow battery of claim 1 , wherein a redox potential of said metal-coordination complex is selected from the range of −1.77 V to 2.30 V vs. Fc +/0 . 16. The redox flow battery of claim 1 , wherein a solubility limit of said metal-coordination complex in said nonaqueous solvent is at least 1.0 M. 17. The redox flow battery of claim 1 , wherein said catholyte and said anolyte are selected such that said redox flow battery has a theoretical open circuit voltage greater than 1.0 V. 18. The redox flow battery of claim 1 , wherein a concentration of said metal-coordination complex in said nonaqueous solvent is at least 1.0 M. 19. The redox flow battery of claim 1 , wherein said redox flow battery has an operating potential equal to or greater than 1 V. 20. The redox flow battery of claim 1 , wherein said redox flow battery has an energy density equal to or greater than 50 Wh/L. 21. The redox flow battery of claim 1 , wherein said redox flow battery has a lifetime of at least 200 cycles of discharging and charging. 22. The redox flow battery of claim 1 , further comprising a separator configured to separate said catholyte and said anolyte, wherein said separator is an ion-exchange membrane. 23. The redox flow battery of claim 22 , wherein said metal-coordination complex is positively charged and said separator is positively charged or said metal-coordination complex is negatively charged and said separator is negatively charged. 24. The redox flow battery of claim 22 , further comprising a plurality of counter ions associated with said metal-coordination complex, wherein said counter ions are configured to pass through said separator during charging and discharging of said redox flow battery. 25. The redox flow battery of claim 22 , wherein said separator

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What does patent US10840504B2 cover?
In an aspect, a redox flow battery comprises a catholyte and an anolyte; wherein at least one of said catholyte and said anolyte is a metal-coordination complex, said metal-coordination complex comprising: (i) a metal; (ii) one or more first ligands coordinated with said metal atom, wherein each of said first ligands is independently a Lewis basic ligand; and one or more second ligands associat…
Who is the assignee on this patent?
California Inst Of Techn
What technology area does this patent fall under?
Primary CPC classification H01M4/9008. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Nov 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).