200-Fold Lifetime Extension of 2,6- Dihydroxyanthraquinone Electrolyte during Flow Battery Operation.

Autor: Bahari M; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States., Jing Y; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States., Jin S; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States., Goulet MA; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States., Tsukamoto T; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States., Gordon RG; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States., Aziz MJ; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States.
Jazyk: angličtina
Zdroj: ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Oct 02; Vol. 16 (39), pp. 52144-52152. Date of Electronic Publication: 2024 Sep 23.
DOI: 10.1021/acsami.4c06073
Abstrakt: We study the capacity fade rate of a flow battery utilizing 2,6-dihydroxyanthraquinone (DHAQ) and its dependence on hydroxide concentration, state of charge, cutoff voltages for the discharge step and for the electrochemical regeneration (oxidation of decomposition compounds back to active species) step, and the period of performing the electrochemical regeneration events. Our observations confirm that the first decomposition product, 2,6-dihydroxyanthrone (DHA), is stable, but after electro-oxidative dimerization, the anthrone dimer decomposes. We identify conditions for which there is little time after dimerization until the dimer is rapidly reoxidized electrochemically to form DHAQ. Combining these approaches, we decrease the fade rate to 0.02%/day, which is 18 times lower than the lowest rate reported previously of 0.38%/day, and over 200 times lower than the value under standard cycling conditions of 4.3%/day. The findings and their mechanistic interpretation are expected to extend the lifetime and enhance the effectiveness of in situ electrochemical regeneration for other electroactive species with finite lifetimes.
Databáze: MEDLINE