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Spatially Constrained Organic Diquat Anolyte for Stable Aqueous Flow Batteries AITranslate

United States|Argonne National Laboratory; United States|Pacific Northwest National Laboratory; United States|Pacific Northwest National Laboratory;Pacific Northwest National Laboratory;Pacific Northwest National Laboratory; United States|Argonne National Laboratory; United States|Argonne National Laboratory; United States|Argonne National Laboratory; United States|Pacific Northwest National Laboratory; United States|Argonne National Laboratory
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Publisher: ACS
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Abstract AITranslate

Redox-active organic materials (ROMs) are becoming increasingly attractive for use in redox flow batteries as promising alternatives to traditional inorganic counterparts. However, the reported ROMs are often accompanied by challenges, including poor solubility and stability. Herein, we demonstrate that the commonly used diquat herbicides, with solubilities of >2 M in aqueous electrolytes, can be used as stable anolyte materials in organic flow batteries. When coupled with a ferrocene-derived catholyte, the flow cells with the diquat anolyte demonstrate long galvanic cycling with high capacity retention. Notably, the mechanistic underpinnings of this remarkable stability are attributed to the improved π-conjugation that originated from the near-planar molecular conformations of the spatially constrained 2,2′-bipyridyl rings, suggesting a viable structural engineering strategy for designing stable organic materials.

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DOI:https://doi.org/10.1021/acsenergylett.8b01550

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Citation Information:

Redox-active organic materials (ROMs) are becoming increasingly attractive for use in redox flow batteries as promising alternatives to traditional inorganic counterparts. However, the reported ROMs are often accompanied by challenges, including poor solubility and stability. Herein, we demonstrate that the commonly used diquat herbicides, with solubilities of >2 M in aqueous electrolytes, can be used as stable anolyte materials in organic flow batteries. When coupled with a ferrocene-derived catholyte, the flow cells with the diquat anolyte demonstrate long galvanic cycling with high capacity retention. Notably, the mechanistic underpinnings of this remarkable stability are attributed to the improved π-conjugation that originated from the near-planar molecular conformations of the spatially constrained 2,2′-bipyridyl rings, suggesting a viable structural engineering strategy for designing stable organic materials.

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GB/T 7714-2015 [1] Jinhua Huang, Zheng Yang, Vijayakumar Murugesan, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b01550.
MLA [1] Jinhua Huang, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b01550.
APA [1] Jinhua Huang, Zheng Yang, Vijayakumar Murugesan, Eric Walter, Aaron Hollas, Baofei Pan, Rajeev S. Assary, Ilya A. Shkrob, Xiaoliang Wei, & Zhengcheng Zhang. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b01550
IEEE [1] Jinhua Huang, Zheng Yang, Vijayakumar Murugesan, Eric Walter, Aaron Hollas, Baofei Pan, Rajeev S. Assary, Ilya A. Shkrob, Xiaoliang Wei, and Zhengcheng Zhang, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b01550.