Quinones having high capacity retention for use as electrolytes in aqueous redox flow batteries

Patent metadata

Field	Value
Publication number	US-2021009497-A1
Application number	US-201916968684-A
Country	US
Kind code	A1
Filing date	Feb 11, 2019
Priority date	Feb 9, 2018
Publication date	Jan 14, 2021
Grant date	—

Abstract

We disclose quinone compounds and related species (Formula I) that possess significant advantages when used as a redox active material in a battery, e.g., a redox flow battery. In particular, the compounds provide redox flow batteries (RFBs) with extremely high capacity retention. For example, RFBs of the invention can be cycled for 500 times with negligible loss of capacity, and such batteries could be employed for years of service. Thus, the invention provides a high efficiency, long cycle life redox flow battery with reasonable power cost, low energy cost, and all the energy scaling advantages of a flow battery.

First claim

What is claimed is:

1 . A redox flow battery comprising:
a first aqueous electrolyte comprising a first redox active material; and a second aqueous electrolyte comprising a second redox active material that is a compound of formula I:

or an ion, salt, or hydroquinone thereof,
wherein each of R 1 -R 8 is independently H; halo; optionally substituted C 1-6 alkyl; optionally substituted C 3-10 carbocyclyl; optionally substituted C 1-9 heterocyclyl having one to four heteroatoms independently selected from O, N, and S; optionally substituted C 6-20 aryl; optionally substituted C 1-9 heteroaryl having one to four heteroatoms independently selected from O, N, and S; oxo; —NO 2 ; —OR a ; —N(R a ) 2 ; —C(═O)R a ; —C(═O)OR a ; —S(═O) 2 R a ; —S(═O) 2 OR a ; —OS(═O) 2 OR a ; —P(═O)R a2 ; —P(═O)(OR a ) 2 ; and —OP(═O)(OR a ) 2 ; —X 1 -L 1 -C(O)O—Y 1 ; —X 2 -L 2 -C(O)O—Y 2 ; —X 3 -L 3 -P(═O)(OY 3 ) 2 ; or —X 4 -L 4 -P(═O)(OY 4 ) 2 ;
wherein each R a is independently H; optionally substituted C 1 -6 alkyl; optionally substituted C 3-10 carbocyclyl; optionally substituted C 1-9 heterocyclyl having one to four heteroatoms independently selected from O, N, and S; optionally substituted C 6-20 aryl; or optionally substituted C 1-9 heteroaryl having one to four heteroatoms independently selected from O, N, and S;
X 1 , X 2 , X 3 , and X 4 are independently O, S, or CH 2 ; L 1 , L 2 , L 3 , and L 4 are independently C 1 -C 6 alkylene; and Y 1 , Y 2 , Y 3 , and Y 4 are independently H or optionally substituted C 1 -C 6 alkyl, provided that one and only one of R 1 -R 8 is —X 1 -L 1 -C(O)O—Y 1 or —X 3 -L 3 -P(═O)(OY 3 ) 2 and one and only one of R 1 -R 8 is —X 2 -L 2 -C(O)O—Y 2 or —X 4 -L 4 -P(═O)(OY 4 ) 2 .

2 . The battery of claim 1 , wherein X 1 and X 2 are O.

3 . The battery of claim 1 or 2 , wherein each of R 1 -R 8 is independently H; halo; optionally substituted C 1-6 alkyl; —X 1 -L 1 -C(O)O—Y 1 ; or —X 2 -L 2 -C(O)O—Y 2 .

4 . The battery of any one of claims 1 - 3 , wherein R 2 is —X 1 -L 1 -C(O)O—Y 1 and R 6 is —X 2 -L 2 -C(O)O—Y 2 .

5 . The battery of any one of claims 1 - 4 , wherein Y 1 and Y 2 are H.

6 . The battery of claim 1 , wherein X 3 and X 4 are O.

7 . The battery of claim 6 , wherein each of R 1 -R 8 is independently H; halo; optionally substituted C 1-6 alkyl; —X 3 -L 3 -P(═O)(OY 3 ) 2 ; or —X 4 -L 4 -P(═O)(OY 4 ) 2 .

8 . The battery of claim 6 or 7 , wherein R 2 is —X 3 -L 3 -P(═O)(OY 3 ) 2 and R 6 is —X 4 -L 4 -P(═O)(OY 4 ) 2 .

9 . The battery of any one of claims 6 - 8 , wherein Y 3 and Y 4 are H.

10 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

11 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

12 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

13 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

14 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

15 . The battery of claim 1 , wherein the quinone is

or an ion, salt, or hydroquinone thereof.

16 . The battery of any one of claims 1 - 15 , wherein the second redox active material is the hydroquinone of formula I, which is oxidized to the corresponding quinone during discharge.

17 . The battery of any one of claims 1 - 16 , wherein the pH of the second aqueous electrolyte is 7.

18 . The battery of claim 17 , wherein the pH is from 8 to 13.

19 . The battery of any one of claims 1 - 18 , wherein the first redox active material comprises bromine, chlorine, iodine, oxygen, vanadium, chromium, cobalt, iron, aluminum, manganese, cobalt, nickel, copper, or lead.

20 . A compound of formula I:

or an ion, salt, or hydroquinone thereof,
wherein each of R 1 -R 8 is independently H; halo; optionally substituted C 1-6 alkyl; optionally substituted C 3-10 carbocyclyl; optionally substituted C 1-9 heterocyclyl having one to four heteroatoms independently selected from O, N, and S; optionally substituted C 6-20 aryl; optionally substituted C 1-9 heteroaryl having one to four heteroatoms independently selected from O, N, and S; oxo; —NO 2 ; —OR a ; —N(R a ) 2 ; —C(═O)R a ; —C(═O)OR a ; —S(═O) 2 R a ; —S(═O) 2 OR a ; —OS(═O) 2 OR a ; —P(═O)R a2 ; —P(═O)(OR a ) 2 ; and —OP(═O)(OR a ) 2 ; —X 1 -L 1 -C(O)O—Y 1 ; —X 2 -L 2 -C(O)O—Y 2 ; —X 3 -L 3 -P(═O)(OY 3 ) 2 ; or —X 4 -L 4 -P(═O)(OY 4 ) 2 ;
wherein each R a is independently H; optionally substituted C 1 -6 alkyl; optionally substituted C 3-10 carbocyclyl; optionally substituted C 1-9 heterocyclyl having one to four heteroatoms independently selected from O, N, and S; optionally substituted C 6-20 aryl; or optionally substituted C 1-9 heteroaryl having one to four heteroatoms independently selected from O, N, and S;
X 1 , X 2 , X 3 , and X 4 are independently O, S, or CH 2 ; L 1 , L 2 , L 3 , and L 4 are independently C 1 -C 6 alkylene; and Y 1 , Y 2 , Y 3 , and Y 4 are independently H or optionally substituted C 1 -C 6 alkyl, provided that one and only one of R 1 -R 8 is —X 1 -L 1 -C(O)O—Y 1 or —X 3 -L 3 -P(═O)(OY 3 ) 2 and one and only one of R 1 -R 8 is —X 2 -L 2 -C(O)O—Y 2 or —X 4 -L 4 -P(═O)(OY 4 ) 2 , and
provided that:
i. when R 2 -R 4 and R 6 -R 8 are H, R 1 and R 5 are not both —SCH 2 C(O)OH, —OCH 2 C(O)OH, or —OCH 2 C(O)OCH 2 CH 3 ;
ii. when R 4 and R 8 are H and R 2 , R 3 , R 6 , and R 7 are —O(CH 2 ) 3 (CH 3 ), R 1 and R 5 are not both —O(CH 2 ) 3 C(O)OH;
iii. when R 4 and R 8 are H and R 2 , R 3 , R 6 , and R 7 are —O(CH 2 ) 4 (CH 3 ), R 1 and R 5 are not both —O(CH 2 ) 4 C(O)OH;
iv. when R 1 and R 8 are OH and R 3 -R 6 are H, R 2 and R 7 are not both —(CH 2 ) 3 C(O)OH or —(CH 2 ) 3 C(O)OCH 3 ;
v. when R 1 , R 4 , R 5 , and R 8 are NH 2 and R 3 and R 6 are H, R 2 and R 7 are not both —O(CH 2 ) 3 C(O)O(CH 2 ) 4 CH 3 ;
vi. when R 1 , R 3 -R 5 , R 7 , and R 8 are H, R 2 and R 6 are not both —OCH(CH 3 )C(O)OCH 3 , —OCH(CH 3 )C(O)OH, or —OCH 2 C(O)OCH 3 ;
vii. when R 1 , R 3 , R 5 , and R 7 are H, and R 4 and R 8 are —N(R a ) 2 , R 2 and R 6 are not both —S(CH 2 ) n C(O)OCH 2 CH 3 , wherein n is 1 to 5;
viii. when R 1 and R 4 are OCH 3 , and R 5 -R 8 are H, R 2 and R 3 are not both —CH 2 CH 2 C(O)OH, —CH 2 CH 2 C(O)OCH 3 , or —CH 2 CH(C(O)CH 3 )C(O)OCH 2 CH 3 ;
ix. when R 1 and R 4 are OH, and R 5 -R 8 are H, R 2 and R 3 are not both —CH 2 CH 2 C(O)OCH 3 ;
x. when R 1 and R 4 -R 8 are H, R 2 and R 3 are not both —CH 2 C(NHC(O)CH 3 )(C(O)OCH 2 CH 3 ) 2 or —CH 2

Assignees

• Harvard College

Inventors

• Aziz Michael J
• Gordon Roy G
• Lin Kaixiang
• Kwabi David Gator
• Ji Yunlong

Classifications

• Y02E60/10

  Energy storage using batteries · CPC title

• H01M2300/0002

  Aqueous electrolytes · CPC title

• H01M4/60

  of organic compounds · CPC title

• C07C59/90 Primary

  containing singly bound oxygen-containing groups · CPC title

• C07F9/3808

  Acyclic saturated acids which can have further substituents on alkyl · CPC title