Small organic molecule based flow battery
US-2016043423-A1 · Feb 11, 2016 · US
US9614245B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9614245-B2 |
| Application number | US-201414307030-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 17, 2014 |
| Priority date | Jun 17, 2013 |
| Publication date | Apr 4, 2017 |
| Grant date | Apr 4, 2017 |
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A flow battery includes a positive electrode, a positive electrode electrolyte, a negative electrode, a negative electrode electrolyte, and a polymer electrolyte membrane interposed between the positive electrode and the negative electrode. The positive electrode electrolyte includes water and a first redox couple. The first redox couple includes a first organic compound which includes a first moiety in conjugation with a second moiety. The first organic compound is reduced during discharge while during charging the reduction product of the first organic compound is oxidized to the first organic compound. The negative electrode electrolyte includes water and a second redox couple. The second couple includes a second organic compound including a first moiety in conjugation with a second moiety. The reduction product of the second organic compound is oxidized to the second organic compound during discharge.
Opening claim text (preview).
What is claimed is: 1. A flow battery comprising: a positive electrode; a positive electrode electrolyte including water and a first redox couple, the positive electrode electrolyte flowing over and contacting the positive electrode, the first redox couple including a first organic compound, the first organic compound including a first moiety having formula 1 in conjugation with a second moiety having formula 2 and a reduction product of the first organic compound, the first organic compound being reduced during discharge: wherein: Y 1 and Y 2 are each independently O or NR; and R is H or carbon atom; a negative electrode; a negative electrode electrolyte including water and a second redox couple, the negative electrode electrolyte flowing over and contacting the negative electrode, the second redox couple including a second organic compound having formula 8 or 9: wherein R 16 -R 23 are each independently H, NH 2 , —NHR 2 , —N(R 2 ) 2 , —O − M + , —NHCOR 2 , —OR 2 , —CH 3 , —C 2 H 5 , —SO 3 H, —PO 3 H 2 , —COOH, —OH, —N(R 2 ) 3 + X − , —CF 3 , CCl 3 , —CN, —COOR 2 , F, Cl, Br, —CHO, —COR 2 —O − M + , —SO 3 − M + , —PO 3 2− M + 2 , —COO − M + , pyridinyl, imidazoyl, pyrroyl, or phenyl where R 2 is H or C 1-10 alkyl and M + is a positively charged counter ion and is X − a negatively charged counterion, at least one of R 16 -R 23 being an electron donating group or an electron withdrawing group; and a polymer electrolyte membrane interposed between the positive electrode and the negative electrode. 2. The flow battery of claim 1 further comprising: a positive electrode reservoir in fluid communication with the positive electrode, the positive electrode electrolyte being stored in the positive electrode reservoir to charge and discharge the flow battery; and a negative electrode reservoir in fluid communication with the negative electrode, the negative electrode electrolyte being stored in the negative electrode reservoir to charge and discharge the flow battery. 3. The flow battery of claim 1 wherein: the first organic compound is a first quinone and the reduction product of the first organic compound is a first hydroquinone. 4. The flow battery of claim 3 wherein the first quinone has a standard electrode potential greater than 0.6 volts relative to a standard hydrogen electrode. 5. The flow battery of claim 3 wherein the first quinone is described by formula 5 or 6 or salts thereof: wherein R 4 , R 5 , R 6 , R 7 are each independently selected from the group consisting of hydrogen and electron withdrawing groups. 6. The flow battery of claim 5 wherein R 4 , R 5 , R 6 , R 7 are each independently —NO 2 , —N(R 2 ) 3 + X −, —CF 3 , CCl 3 , —CN, —SO 3 H, —PO 3 H 2 , —COOH, —OH, —O − M + , —SO 3 − M + , PO 3 2−M + 2 , —COO − M + , —COOR 2 , F, Cl, Br, —CHO, —COR 2 where R 2 is H or C 1-10 alkyl, M + is a positively charged counter-ion, and X − is a negatively charged-ion. 7. The flow battery of claim 5 wherein R 4 , R 5 , R 6 , R 7 are each independently H, —NO 2 , —CF 3 , or —SO 3 H. 8. The flow battery of claim 3 wherein the first quinone includes a component selected from the group consisting of: and salts thereof. 9. The flow battery of claim 1 wherein the positive electrode electrolyte and/or the negative electrode electrolyte includes a component selected from the group consisting of: and salts thereof. 10. The flow battery of claim 1 wherein the second organic compound has the following formula: 11. The flow battery of claim 1 wherein the positive electrode electrolyte and/or the negative electrode electrolyte has a pH from 9 to 14. 12. The flow battery of claim 11 wherein the positive electrolyte has a pH from 9 to 14 and includes a compound selected from the group consisting of: wherein M is a Na + or K + . 13. The flow battery of claim 1 wherein the positive electrode electrolyte and/or the negative electrode electrolyte further includes an additional solvent other than water. 14. The flow battery of claim 13 wherein the additional solvent is selected from the group consisting of dimethylformamide, C 1-4 alcohols, acetone nitrile, and combinations thereof. 15. The flow battery of claim 1 wherein 1, 2, 3, 4, 5, or 6 of R 16 -R 23 are electron withdrawing groups selected from the group consisting of —NO 2 , —N(R 2 ) 3 + X − , —CF 3 , CCl 3 , —CN, —SO 3 H, —PO 3 H 2 , —COOH, —OH, —O − M + , —SO 3 − M + , —PO 3 2− M + 2 , —COO − M + , —COOR 2 , F, Cl, Br, —CHO, and —COR 2 where R 2 is H or C 1-10 alkyl and M + is a positively charged counter-ion. 16. The flow battery of claim 1 wherein 1, 2, 3, 4, 5, or 6 of R 16 -R 23 are electron donating groups selected from the group consisting of C 1-10 alkyl, NH 2 , —NHR 2 , —N(R 2 ) 2 , —O − M + , —NHCOR 2 , —OR 2 , —CH 3 , —C 2 H 5 , and phenyl where R 2 is H or C 1-10 alkyl and M + is a positively charged counter-ion. 17. The flow battery of claim 1 wherein 1, 2, 3, 4, 5, or 6 of R 16 -R 23 are a functional groups that increases water solubility selected from the group consisting of —SO 3 H, , —PO 3 H 2 , —COOH, —OH, —O − M + , —SO 3 − M + , —PO 3 2− M + 2 , —COO − M + , pyridinyl, imidazoyl, and pyrroyl, where M + is a positively charged counter-ion. 18. A flow battery comprising: a positive electrode; a positive electrode electrolyte including water and a first quinone redox couple, the first quinone redox couple including a first quinone and a first hydroquinone, the first quinone being reduced to the first hydroquinone during discharge, the first quinone selected from the group consisting of benzoquinone and benzoquinones that are substituted with an electron withdrawing group; a negative electrode; a negative electrode electrolyte flowing over and contacting the negative electrode, the negative electrode electrolyte including a second organic compound having formula 8 or 9: wherein R 16 -R 23 are each independently H, NH 2 —NHR 2 , —N(R 2 ) 2 , —O − M + , —NHCOR 2 , —OR 2 , —CH 3 , —C 2 H 5 , —SO 3 H, , —PO 3 H 2 , —COOH, —OH, —N(R 2 ) 3 − X − , —CF 3 , CCl 3 , —CN, —COOR 2 , F, Cl, Br, —CHO, —COR 2 —O − M + , —SO 3 − M + , —PO 3 2− M + 2 , —COO − M + , pyridinyl, imidazoyl, pyrroyl, or phenyl where R 2 is H or C 1-10 alkyl and M + is a positively charged counter ion and is X − a negatively charged counter ion, at least one of R 16 -R 23 being an electron withdrawing group or an electron donating group; and a polymer electrolyte membrane interposed between the positive electrode and the negative electrode. 19. The flow battery of claim 18 wherein the electron withdrawing group is —
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