In Situ Electro-Synthesis and Resynthesis of Redox Actives in Aqueous Organic Redox Flow Batteries

Tuesday, 11 October 2022: 09:20
Room 215 (The Hilton Atlanta)
Y. Jing (Harvard Department of Chemistry and Chemical Biology, Harvard University), M. Wu (Harvard University), E. W. W. Zhao (University of Cambridge), M. A. Goulet, E. M. Fell, M. Jin (Harvard University), C. P. Grey (University of Cambridge), R. G. Gordon, and M. J. Aziz (Harvard University)
Aqueous anthraquinone redox flow batteries (AARFBs) offer a safe and potentially inexpensive solution to the problem of storing massive amounts of electricity produced from intermittent renewables and are especially well-suited for large-scale stationary deployment.1,2 However, production cost of anthraquinone-based electrolytes and molecular decomposition are the two major challenges preventing them from being commercialized.3,4 We report electrochemical approaches to both these problems: anthraquinone electrosynthesis from lower-cost anthracene feedstock, and the electrochemically-induced reversal of decomposition.

We demonstrate the electrochemical oxidation of an anthracene derivative to a redox-active anthraquinone at room temperature in a continuous flow cell without the use of hazardous oxidants or noble metal catalysts. The anthraquinone, generated in situ, was used as the active species in a flow battery electrolyte without further modification or purification.5,6

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 AARFBs. We used in situ (online) NMR and EPR and complementary electrochemical analyses to show that the decomposition compounds 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.7

References:

  1. Huskinson, B. T.; Marshak, M. P.; Suh, C.; Er, S.; Gerhardt, M. R.; Galvin, C. J.; Chen, X.; Aspuru-Guzik, A.; Gordon, R. G.; Aziz, M. J. A metal-free organic-inorganic aqueous flow battery. Nature 2014, 505 (7482), 195.
  2. Lin, K.; Chen, Q.; Gerhardt, M. R.; Tong, L.; Kim, S. B.; Eisenach, L.; Valle, A. W.; Hardee, D.; Gordon, R. G.; Aziz, M. J.et al. Alkaline quinone flow battery. Science 2015, 349 (6255), 1529.
  3. Kwabi, D. G.; Ji, Y.; Aziz, M. J. Electrolyte lifetime in aqueous organic redox flow batteries: A critical review. Chem. Rev. 2020, 120 (14), 6467.
  4. Brushett, F. R.; Aziz, M. J.; Rodby, K. E. On lifetime and cost of redox-active organics for aqueous flow batteries. ACS Energy Letters 2020, 5, 879.
  5. Wu, M.; Jing, Y.; Wong, A. A.; Fell, E. M.; Jin, S.; Tang, Z.; Gordon, R. G.; Aziz, M. J. Extremely stable anthraquinone negolytes synthesized from common precursors. Chem 2020, 6, 11.
  6. Jing, Y.; Wu, M.; Wong, A. A.; Fell, E. M.; Jin, S.; Pollack, D. A.; Kerr, E. F.; Gordon, R. G.; Aziz, M. J. In situ electrosynthesis of anthraquinone electrolytes in aqueous flow batteries. Green Chemistry 2020, 22 (18), 6084.
  7. Jing, Y.; Zhao, E. W.; Goulet, M.-A.; Bahari, M.; Fell, E. M.; Jin, S.; Davoodi, A.; Jónsson, E.; Wu, M.; Grey, C. P.; Gordon, R. G.; Aziz, M. J. Closing the Molecular Decomposition-Recomposition Loop in Aqueous Organic Flow Batteries. Nature Chemistry 14, in press (2022); preprint: ChemRxiv, 2021, 10.33774/chemrxiv-2021- x05x1.