Redox flow battery

Patent metadata

Field	Value
Publication number	US-9673473-B2
Application number	US-201314077452-A
Country	US
Kind code	B2
Filing date	Nov 12, 2013
Priority date	Dec 14, 2012
Publication date	Jun 6, 2017
Grant date	Jun 6, 2017

Abstract

Provided is a redox flow battery including a positive electrode cell having a positive electrode and a catholyte solution; a negative electrode cell having a negative electrode and an anolyte solution; and an ion-exchange membrane disposed between the positive electrode cell and the negative electrode cell, wherein the catholyte solution and the anolyte solution each includes a non-aqueous solvent, a supporting electrolyte, and an electrolyte, and wherein the electrolyte includes a metal-ligand coordination compound, and at least one of the metal-ligand coordination compounds includes a ligand having an electron donating group.

First claim

What is claimed is:

1. A redox flow battery comprising:
a positive electrode cell comprising
a positive electrode and
a catholyte solution;

a negative electrode cell comprising
a negative electrode and
an anolyte solution; and

an ion-exchange membrane disposed between the positive electrode cell and the negative electrode cell,
wherein the catholyte solution and the anolyte solution each comprises
a non-aqueous solvent,
a supporting electrolyte, and
an electrolyte comprising a metal-ligand coordination compound,

wherein the metal-ligand coordination compound has a metal and a ligand,
wherein the metal-ligand coordination compound comprises a nitrogen-containing heteroaromatic ligand, a nitrogen-containing heteroaliphatic ligand, or a combination thereof,
wherein the metal-ligand coordination compound in at least one of the catholyte solution and the anolyte solution further comprises at least one electron donating group,
wherein when the metal-ligand coordination compound comprises the nitrogen-containing heteroaromatic ligand, the at least one electron donating group is selected from a hydroxyl group, a thiol group, an alkyl group, an alkoxy group, an alkylthio group, an aryl group, an aryloxy group, an arylthio group, an alkenyl group, an alkynyl group, an amide group, an ester group, and an amine group (—NR 2 , wherein R is an alkyl group having 1 to 6 carbon atoms), and
wherein when the metal-ligand coordination compound comprises the nitrogen-containing heteroaliphatic ligand, the at least one electron donating group is selected from a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl group, an aryloxy group, an arylthio group, an alkenyl group, an alkynyl group, an amide group, an ester group, and an amine group (—NR 2 , wherein R is an alkyl group having 1 to 6 carbon atoms).

2. The redox flow battery of claim 1 , wherein the metal-ligand coordination compound comprises at least one metal selected from nickel, cobalt, iron, ruthenium, zinc, manganese, yttrium, zirconium, titanium, chromium, magnesium, cerium, copper, lead, and vanadium.

3. The redox flow battery of claim 1 , wherein the nitrogen-containing heteroaromatic ligand or the nitrogen-containing heteroaliphatic ligand is at least one selected from a substituted or unsubstituted dipyridyl, a substituted or unsubstituted terpyridyl, a substituted or unsubstituted phenanthroline, a substituted or unsubstituted ethylenediamine, a substituted or unsubstituted propylenediamine, and a substituted or unsubstituted N-heterocyclic carbene.

4. The redox flow battery of claim 3 , wherein the N-heterocyclic carbene is at least one selected from 2,6-bis(methylimidazole-2-ylidene)pyridine, 1,3-dimesitylimidazole, 1,3-bis(2,5-diisopropylphenyl)imidazole, 1,3-dimethylimidazole, 1,3-di-tert-butylimidazole, 1,3-dicyclohexylimidazole, and 1-ethyl-3-methylimidazole.

5. The redox flow battery of claim 1 , wherein the electron donating group is at least one selected from a methyl group, a methoxy group, a methylthio group, a phenyl group, a hydroxyl group, an alkylcarboxy group, an alkylcarbamino group, and an amino group.

6. The redox flow battery of claim 5 , wherein the metal-ligand coordination compound is at least one selected from the compounds:

wherein X is H, OH, Br, or Cl.

7. The redox flow battery of claim 1 , wherein the electrolyte further comprises a metal-ligand coordination compound comprising a ligand comprising an electron withdrawing group.

8. The redox flow battery of claim 7 , wherein the electron withdrawing group is at least one selected from a haloalkyl group, an alkenyl group, a halogen atom, —N-(alkyl) 3 + , —N-(alkyl) 2 H + , —N-(alkyl)H 2 + , —S-(alkyl) 2 + , —NH 3 + , —SO-(alkyl), —SO-(aryl), —SO 2 -(alkyl), —SO 2 -(aryl), —P(O)(OH) 2 , —P(O)(OH)(O-alkyl), —P(O)(OH)(O-aryl), —P(O)(O-alkyl) 2 , —P(O)(O-aryl) 2 , —P(O)(O-alkyl)(O-aryl), —C(O)OH, a cyclopentadienyl group, —C(O)O-(alkyl), —C(O)O-(aryl), —C(O)NH-(alkyl), —C(O)NH-(aryl), —C(O)-(alkyl), —C(O)-(aryl), —CHO, a nitrile group, a nitro group, a heterocyclic group, and an aryl group.

9. The redox flow battery of claim 1 , wherein the anolyte solution comprises the metal-ligand coordination compound.

10. The redox flow battery of claim 1 , wherein the metal-ligand coordination compound having the metal and the ligand is at least one selected from the compounds:

11. The redox flow battery of claim 1 , wherein the metal-ligand coordination compound having the metal and the ligand and further comprising the electron donating group bound to the ligand is at least one selected from the compounds:

12. The redox flow battery of claim 1 , wherein the metal-ligand coordination compound undergoes a reversible oxidation/reduction reaction.

13. The redox flow battery of claim 12 , wherein a non-aqueous solvent is at least one selected from dimethyl acetamide, diethyl carbonate, dimethyl carbonate, acetonitrile, γ-butyrolactone, propylene carbonate, ethylene carbonate, N-methyl-2-pyrrolidone, fluoroethylene carbonate, and N,N-dimethylacetamide.

14. The redox flow battery of claim 1 , wherein the metal-ligand coordination compound comprises BF 4 − , PF 6 − , CF 3 SO 3 − , or (CF 3 SO 2 ) 2 N − as a counter ion.

15. The redox flow battery of claim 1 , wherein the supporting electrolyte is at least one selected from LiBF 4 , LiPF 6 , LiClO 4 , LiCF 3 SO 3 , Li(CF 3 SO 2 ) 2 N, LiSbF 6 , LiAsF 6 , LiC 4 F 9 SO 3 , LiAlO 2 , LiAlCl 4 , LiN(C x F 2x+1 SO 2 )(C y F 2y+1 SO 2 ) (where x and y are natural numbers), LiCl, LiI, triethylamine tetrafluorborate, tributylamine tetrafluorborate, NaBF 4 , NaPF 6 , trimethylsulfonyl chloride, and (NH 4 ) 2 SO 4 .

16. The redox flow battery of claim 1 , wherein the ion-exchange membrane is an anion exchange membrane.

17. The redox flow battery of claim 16 , wherein the anion exchange membrane is a product of aminating a copolymer of styrene-divinylbenzene comprising a chloromethyl group, a product of substituting a copolymer of vinylpyridine-divinylbenzene with a quarternary pyridinium salt, or a product of aminating an aromatic polysulfone copolymer comprising a chloromethyl group.

18. The redox flow battery of claim 1 further comprising a catholyte tank and an anolyte tank, wherein the catholyte tank is fluid connected to the positive electrode cell, and the anolyte tank is fluid connected to the negative electrode cell.

Assignees

• Samsung Electronics Co Ltd

Inventors

• Park Joung-Won
• Lee Myung-Jin
• Roy Basab
• Oh Duk-Jin
• Lee Doo-Yeon

Classifications

• H01M2300/0091

  in the form of mixtures · CPC title

• H01M8/188 Primary

  by recharging of redox couples containing fluids; Redox flow type batteries · CPC title

• H01M2300/0025

  Organic electrolyte · CPC title

• H01M8/20

  Indirect fuel cells, e.g. fuel cells with redox couple being irreversible (H01M8/18 takes precedence) · CPC title

• Y02E60/50

  Fuel cells · CPC title