| Literature DB >> 35710986 |
Yan Jing1, Evan Wenbo Zhao2,3, Marc-Antoni Goulet4,5, Meisam Bahari4, Eric M Fell4, Shijian Jin4, Ali Davoodi4,6,7, Erlendur Jónsson2, Min Wu4, Clare P Grey8, Roy G Gordon9,10, Michael J Aziz11.
Abstract
Aqueous organic redox flow batteries offer a safe and potentially inexpensive solution to the problem of storing massive amounts of electricity produced from intermittent renewables. However, molecular decomposition represents a major barrier to commercialization-and although structural modifications can improve stability, it comes at the expense of synthetic cost and molecular weight. Now, utilizing 2,6-dihydroxy-anthraquinone (DHAQ) without further structural modification, we demonstrate that the regeneration of the original molecule after decomposition represents a viable route to achieve low-cost, long-lifetime aqueous organic redox flow batteries. We used in situ (online) NMR and electron paramagnetic resonance, and complementary electrochemical analyses to show that the decomposition compound 2,6-dihydroxy-anthrone (DHA) and its tautomer, 2,6-dihydroxy-anthranol (DHAL) can be recomposed to DHAQ electrochemically through two steps: oxidation of DHA(L)2- to the dimer (DHA)24- by one-electron transfer followed by oxidation of (DHA)24- to DHAQ2- by three-electron transfer per DHAQ molecule. This electrochemical regeneration process also rejuvenates the positive electrolyte-rebalancing the states of charge of both electrolytes without introducing extra ions.Entities:
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Year: 2022 PMID: 35710986 DOI: 10.1038/s41557-022-00967-4
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274