Quinones having high capacity retention for use as electrolytes in aqueous redox flow batteries
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.
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, and/or
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 , provided R 2 is —X 1 -L 1 -C(O)O—Y 1 or —X 2 -L 2 -C(O)O—Y 2 , and/or
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 , and/or
wherein Y 1 and Y 2 are H.
3. The battery of claim 1 , wherein X 3 and X 4 are O, and/or
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 , provided R 2 is —X 3 -L 3 -(═O)(OY 3 ) 2 , or —X 4 -L 4 -P(═O)(OY 4 ) 2 , and/or
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 , and/or
wherein Y 3 and Y 4 are H.
4. The battery of claim 1 , wherein the compound of formula I is
or an ion, salt, or
hydroquinone thereof; wherein R 2 is —O(CH 2 ) 3 C(O)OH.
5. The battery of claim 1 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof.
6. The battery of claim 1 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof.
7. The battery of claim 1 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof; wherein R 2 is —O(CH 2 ) 3 P(O)(OH) 2 .
8. The battery of claim 1 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof.
9. The battery of claim 1 , wherein the second redox active material is the hydroquinone of formula I, which is oxidized to the corresponding quinone during discharge, and/or
wherein the pH of the second aqueous electrolyte is ≥7, and/or
wherein the first redox active material comprises bromine, chlorine, iodine, oxygen, vanadium, chromium, cobalt, iron, aluminum, manganese, cobalt, nickel, copper, or lead.
10. The battery of claim 9 , wherein the pH is from 8 to 13.
11. 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 ; provided R 2 is —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:
ii. when R 4 -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 CH(NHC(O)CH 3 )C(O)OCH 2 CH 3 ;
xv. when R 3 -R 7 are H and R 1 is NH 2 , R 2 and R 8 are not both —SCH 2 C(O)OH;
xvi. when R 3 -R 8 are H, R 1 and R 2 are not both —OC(O)CH 2 CH 2 C(O)O CH 2 CH 3 ;
xvii. when R 1 , R 3 -R 5 , R 7 , and R 8 are H, R 2 and R 6 are not both —OC(O)CH 2 CH 2 C(O)OCH 2 CH 3 ;
xx. when R 2 , R 3 , R 6 , and R 7 are H and R 4 and R 5 are —(CH 2 ) 5 CH 3 , R 1 and R 8 are not both —(CH 2 ) 7 C(O)OH;
xxii. when R 3 and R 6 are H and R 1 , R 4 , R 5 , and R 8 are —NH 2 , R 2 and R7 5 are not both —O(CH 2 ) 3 C(O)OCH 3 .
12. The compound of claim 11 , wherein X 1 and X 2 are O, and/or
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 , provided R 2 is —X 1 -L 1 -C(O)O—Y 1 or —X 2 -L 2 -C(O)O—Y 2 , and/or
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 , and/or
wherein Y 1 and Y 2 are H.
13. The compound of claim 11 , wherein X 3 and X 4 are O, and/or
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 , provided R 2 is —X 3 -L 3 -P(═O)(OY 3 ) 2 , or —X 4 -L 4 -P(═O)(OY 4 ) 2 , and/or
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 , and/or
wherein Y 3 and Y 4 are H.
14. The compound of claim 11 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof; wherein R 2 is —O(CH 2 ) 3 C(O)OH.
15. The compound of claim 11 , wherein the compound of formula I is
or a salt, ion, or hydroquinone thereof.
16. The compound of claim 11 , wherein the compound of formula I is
or an ion, salt, or hydroquinone thereof.
17. The compound of claim 11 , wherein the compound of formula I is:
or an ion, salt, or hydroquinone thereof; wherein R 2 is —O(CH 2 ) 3 P(O)(OH) 2 .
18. The compound of claim 11 , wherein the compound of formula 1 is:
or an ion, salt, or hydroquinone thereof.