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In situ electrochemical recomposition of decomposed redox-active species in aqueous organic flow batteries.
Jing, Yan; Zhao, Evan Wenbo; Goulet, Marc-Antoni; Bahari, Meisam; Fell, Eric M; Jin, Shijian; Davoodi, Ali; Jónsson, Erlendur; Wu, Min; Grey, Clare P; Gordon, Roy G; Aziz, Michael J.
Afiliación
  • Jing Y; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
  • Zhao EW; Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
  • Goulet MA; Magnetic Resonance Research Center, Institute for Molecules and Materials, Radboud University Nijmegen, Nijmegen, the Netherlands.
  • Bahari M; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Fell EM; Department of Chemical and Materials Engineering, Concordia University, Montreal, Quebec, Canada.
  • Jin S; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Davoodi A; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Jónsson E; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Wu M; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Grey CP; Materials and Metallurgical Engineering Department, Faculty of Engineering, Ferdowsi University of Mashhad (FUM), Mashhad, Iran.
  • Gordon RG; Sichuan University-Pittsburgh Institute, Sichuan University, Chengdu, China.
  • Aziz MJ; Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
Nat Chem ; 14(10): 1103-1109, 2022 10.
Article en En | MEDLINE | ID: mdl-35710986
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antralina / Mitoxantrona Idioma: En Revista: Nat Chem Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antralina / Mitoxantrona Idioma: En Revista: Nat Chem Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos