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Bioinspired trimesic acid anchored electrocatalysts with unique static and dynamic compatibility for enhanced water oxidation

Author

Listed:
  • Xiaojing Lin

    (China University of Petroleum)

  • Zhaojie Wang

    (China University of Petroleum)

  • Shoufu Cao

    (China University of Petroleum)

  • Yuying Hu

    (China University of Petroleum)

  • Siyuan Liu

    (China University of Petroleum)

  • Xiaodong Chen

    (China University of Petroleum)

  • Hongyu Chen

    (China University of Petroleum)

  • Xingheng Zhang

    (China University of Petroleum)

  • Shuxian Wei

    (China University of Petroleum)

  • Hui Xu

    (China University of Petroleum)

  • Zhi Cheng

    (China University of Petroleum)

  • Qi Hou

    (China University of Petroleum)

  • Daofeng Sun

    (China University of Petroleum)

  • Xiaoqing Lu

    (China University of Petroleum)

Abstract

Layered double hydroxides are promising candidates for the electrocatalytic oxygen evolution reaction. Unfortunately, their catalytic kinetics and long-term stabilities are far from satisfactory compared to those of rare metals. Here, we investigate the durability of nickel-iron layered double hydroxides and show that ablation of the lamellar structure due to metal dissolution is the cause of the decreased stability. Inspired by the amino acid residues in photosystem II, we report a strategy using trimesic acid anchors to prepare the subsize nickel-iron layered double hydroxides with kinetics, activity and stability superior to those of commercial catalysts. Fundamental investigations through operando spectroscopy and theoretical calculations reveal that the superaerophobic surface facilitates prompt release of the generated O2 bubbles, and protects the structure of the catalyst. Coupling between the metals and coordinated carboxylates via C‒O‒Fe bonding prevents dissolution of the metal species, which stabilizes the electronic structure by static coordination. In addition, the uncoordinated carboxylates formed by dynamic evolution during oxygen evolution reaction serve as proton ferries to accelerate the oxygen evolution reaction kinetics. This work offers a promising way to achieve breakthroughs in oxygen evolution reaction stability and dynamic performance by introducing functional ligands with static and dynamic compatibilities.

Suggested Citation

  • Xiaojing Lin & Zhaojie Wang & Shoufu Cao & Yuying Hu & Siyuan Liu & Xiaodong Chen & Hongyu Chen & Xingheng Zhang & Shuxian Wei & Hui Xu & Zhi Cheng & Qi Hou & Daofeng Sun & Xiaoqing Lu, 2023. "Bioinspired trimesic acid anchored electrocatalysts with unique static and dynamic compatibility for enhanced water oxidation," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42292-5
    DOI: 10.1038/s41467-023-42292-5
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    References listed on IDEAS

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    1. Yasufumi Umena & Keisuke Kawakami & Jian-Ren Shen & Nobuo Kamiya, 2011. "Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å," Nature, Nature, vol. 473(7345), pages 55-60, May.
    2. Dong Young Chung & Pietro P. Lopes & Pedro Farinazzo Bergamo Dias Martins & Haiying He & Tomoya Kawaguchi & Peter Zapol & Hoydoo You & Dusan Tripkovic & Dusan Strmcnik & Yisi Zhu & Soenke Seifert & Su, 2020. "Dynamic stability of active sites in hydr(oxy)oxides for the oxygen evolution reaction," Nature Energy, Nature, vol. 5(3), pages 222-230, March.
    3. Wenlong Li & Fusheng Li & Hao Yang & Xiujuan Wu & Peili Zhang & Yu Shan & Licheng Sun, 2019. "A bio-inspired coordination polymer as outstanding water oxidation catalyst via second coordination sphere engineering," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
    4. Dong Young Chung & Pietro P. Lopes & Pedro Farinazzo Bergamo Dias Martins & Haiying He & Tomoya Kawaguchi & Peter Zapol & Hoydoo You & Dusan Tripkovic & Dusan Strmcnik & Yisi Zhu & Soenke Seifert & Su, 2020. "Author Correction: Dynamic stability of active sites in hydr(oxy)oxides for the oxygen evolution reaction," Nature Energy, Nature, vol. 5(7), pages 550-550, July.
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