Flow batteries incorporating active materials containing doubly bridged aromatic groups

Patent metadata

Field	Value
Publication number	US-10930937-B2
Application number	US-201615360918-A
Country	US
Kind code	B2
Filing date	Nov 23, 2016
Priority date	Nov 23, 2016
Publication date	Feb 23, 2021
Grant date	Feb 23, 2021

Abstract

Electrolyte solutions for flow batteries and other electrochemical systems can contain an active material that is capable of transferring one or more electrons per molecule during an oxidation-reduction cycle. Doubly bridged aromatic groups or their coordination compounds can be particularly suitable active materials. Flow batteries can include a first half-cell containing a first electrolyte solution, and a second half-cell containing a second electrolyte solution, in which at least one of the first electrolyte solution and the second electrolyte solution contains an active material having at least two aromatic groups doubly bridged by a carbonyl moiety and a bridging moiety containing a bridging atom selected from carbon, nitrogen, oxygen, sulfur, selenium and tellurium. Such bridged compounds can directly function as the active material, or coordination compounds containing the bridged compounds as at least one ligand can serve as the active material.

First claim

What is claimed is the following:

1. A flow battery comprising:
a first half-cell containing a first electrolyte solution; and
a second half-cell containing a second electrolyte solution;
wherein at least one of the first electrolyte solution and the second electrolyte solution comprises:
an active material comprising a bridged compound having a structure of:

a coordination compound thereof, or a salt thereof;
wherein:
Ary 1 is a substituted aromatic ring or a substituted heteroaromatic ring, wherein the aromatic or heteroaromatic ring of Ary 1 is substituted with one or more of an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; C 2 -C 6 polyol; OR 3 ; SR 3 ; S(═O)R 3 ; S(═O) 2 R 3 ; NR 9 R 10 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; C(═O)R 4 ; and/or sulfonyl;
Ary 2 is an unsubstituted aromatic ring, an unsubstituted heteroaromatic ring, a substituted aromatic ring, or a substituted heteroaromatic ring, wherein, when substituted, the aromatic or heteroaromatic ring of Ary 2 is substituted with one or more of an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; C 2 -C 6 polyol; OR 3 ; SR 3 ; S(═O)R 3 ; S(═O) 2 R 3 ; NR 9 R 10 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; C(═O)R 4 ; and/or sulfonyl; and
Z is CR 1 R 2 , NR 8 , O, S, S(═O), or S(═O) 2 , wherein:
R 1 is H; unsubstituted or substituted Akyl; C 2 -C 6 polyol; OR 3 ; SR 3 ; S(═O)R 3 ; S(═O) 2 R 3 ; NR 9 R 10 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; or C(═O)R 4 ;
R 2 is an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; C 2 -C 6 polyol; OR 3 ; SR 3 ; S(═O)R 3 ; S(═O) 2 R 3 ; NR 9 R 10 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; or C(═O)R 4 ; and
R 3 is H; an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; (CH 2 CH 2 O) x CH 3 ; C(═O)NR 5 R 6 ; or C(═O)R 7 ; and
R 5 and R 6 are, independently, H; an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; (CH 2 CH 2 O) x CH 3 ; or CH 2 (OCH 2 CH 2 ) x OCH 3 ; and
R 7 is OH or an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; and
R 4 is R 5 , OR 5 , or NR 5 R 6 ; and
R 8 is H; an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; (CH 2 CH 2 O) x CH 3 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; C(═O)R 5 ; C(═O)OR 5 ; or C(═O)NR 5 R 6 ; and
R 9 and R 10 are, independently, H; an alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; (CH 2 CH 2 O) x CH 3 ; or CH 2 (OCH 2 CH 2 ) x OCH 3 ; and
x is an integer ranging between 0 and 100.

2. The flow battery of claim 1 , wherein Z is NR 8 .

3. The flow battery of claim 1 , wherein:
Ary 1 is a substituted benzene ring, naphthyl ring, pyridine ring, pyrazine ring, pyrimidine ring, triazine ring, quinolone ring, isoquinoline ring, phthalazine ring, quinazoline ring, quinoxaline ring, thiophene ring, benzothiophene ring, pyrrole ring, indole ring, isoindole ring, pyrazole ring, indazole ring, imidazole ring, benzimidazole ring, triazole ring, benzotriazole ring, oxazole ring, benzoxazole ring, isoxazole ring, benzisoxazole ring, thiazole ring, benzothiazole ring, isothiazole ring, benzisothiazole ring, furan ring, benzofuran ring, or isobenzofuran ring; and
Ary 2 is a substituted or unsubstituted benzene ring, naphthyl ring, pyridine ring, pyrazine ring, pyrimidine ring, triazine ring, quinolone ring, isoquinoline ring, phthalazine ring, quinazoline ring, quinoxaline ring, thiophene ring, benzothiophene ring, pyrrole ring, indole ring, isoindole ring, pyrazole ring, indazole ring, imidazole ring, benzimidazole ring, triazole ring, benzotriazole ring, oxazole ring, benzoxazole ring, isoxazole ring, benzisoxazole ring, thiazole ring, benzothiazole ring, isothiazole ring, benzisothiazole ring, furan ring, benzofuran ring, or isobenzofuran ring.

4. The flow battery of claim 1 , wherein the active material is an unbound form of the bridged compound.

5. The flow battery of claim 1 , wherein the active material is the coordination compound comprising the bridged compound as at least one ligand.

6. The flow battery of claim 5 , wherein the coordination compound has a formula of
D g M(L 1 )(L 2 )(L 3 );

wherein
M is a transition metal;
D is ammonium, tetraalkylammonium, or an alkali metal ion; g ranges between 0 and 6; and
L 1 , L 2 and L 3 are ligands, at least one of L 1 , L 2 and L 3 being the bridged compound.

7. The flow battery of claim 6 , wherein the transition metal is Ti.

8. The flow battery of claim 6 , wherein at least one of L 1 , L 2 and L 3 is a catecholate ligand or a substituted catecholate ligand.

9. The flow battery of claim 1 , wherein the bridged compound has a structure of

wherein:
R 11 and R 12 are, independently, alkyl substituted with one or more of hydroxyl, carboxyl, amine, or sulfonyl; C 2 -C 6 polyol; OR 3 ; SR 3 ; S(═O)R 3 ; S(═O) 2 R 3 ; NR 9 R 10 ; CH 2 (OCH 2 CH 2 )—OCH 3 ; or C(═O)R 4 ; and
n is 0, 1, 2, or 3 and m is 1, 2, or 3.

10. The flow battery of claim 9 , wherein the active material is an unbound form of the bridged compound.

11. The flow battery of claim 9 , wherein the active material is the coordination compound comprising the bridged compound as at least one ligand.

12. The flow battery of claim 11 , wherein the coordination compound has a formula of:
D g M(L 1 )(L 2 )(L 3 );

wherein
M is a transition metal; D is ammonium, tetraalkylammonium, or an alkali metal ion;
g ranges between 0 and 6; and
L 1 , L 2 and L 3 are ligands, at least one of L 1 , L 2 and L 3 being the bridged compound.

13. The flow battery of claim 12 , wherein the transition metal is Ti.

14. The flow battery of claim 12 , wherein at least one of L 1 , L 2 and L 3 is a catecholate ligand or a substituted catecholate ligand.

15. The flow battery of claim 1 , wherein Z is S.

16. The flow battery of claim 1 , wherein Z is S(═O).

17. The flow battery of claim 1 , wherein Z is S(═O) 2 .

18. The flow battery of claim 1 , wherein Z is CR 1 R 2 .

19. The flow battery of claim 1 , wherein Z is O.

Assignees

• Lockheed Martin Energy Llc

Inventors

• Millard Matthew
• Norman Zachariah M

Classifications

• H01M8/188 Primary

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

• Y02E60/50

  Fuel cells · CPC title

• H01M8/20

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

• H01M8/04276

  Arrangements for managing the electrolyte stream, e.g. heat exchange · CPC title

• H01M4/9008 Primary

  Organic or organo-metallic compounds · CPC title