4.8 Article

Extending the Lifetime of Organic Flow Batteries via Redox State Management

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 20, Pages 8014-8019

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b13295

Keywords

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Funding

  1. U.S. DOE through PNNL [DE-AC05-76RL01830, 428977]
  2. U.S. DOE ARPA-E [DE-AR-0000767]
  3. Innovation Fund Denmark via the Grand Solutions project ORBATS [7046-00018B]
  4. Massachusetts Clean Energy Technology Center
  5. Harvard School of Engineering and Applied Sciences
  6. NSF Graduate Research Fellowship Program [DGE1144152, DGE1745303]
  7. Canada 150 Research Chair Program

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Redox flow batteries based on quinone-bearing aqueous electrolytes have emerged as promising systems for energy storage from intermittent renewable sources. The lifetime of these batteries is limited by quinone stability. Here, we confirm that 2,6-dihydroxyanthrahydroquinone tends to form an anthrone intermediate that is vulnerable to subsequent irreversible dimerization. We demonstrate quantitatively that this decomposition pathway is responsible for the loss of battery capacity. Computational studies indicate that the driving force for anthrone formation is greater for anthraquinones with lower reduction potentials. We show that the decomposition can be substantially mitigated. We demonstrate that conditions minimizing anthrone formation and avoiding anthrone dimerization slow the capacity loss rate by over an order of magnitude. We anticipate that this mitigation strategy readily extends to other anthraquinone-based flow batteries and is thus an important step toward realizing renewable electricity storage through long-lived organic flow batteries.

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