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Lattice-strained metal–organic-framework arrays for bifunctional oxygen electrocatalysis

Author

Listed:
  • Weiren Cheng

    (University of Science and Technology of China)

  • Xu Zhao

    (University of Science and Technology of China)

  • Hui Su

    (University of Science and Technology of China)

  • Fumin Tang

    (University of Science and Technology of China)

  • Wei Che

    (University of Science and Technology of China)

  • Hui Zhang

    (University of Science and Technology of China)

  • Qinghua Liu

    (University of Science and Technology of China)

Abstract

Oxygen electrocatalysis is central to technologies such as fuel cells and electrolysers, but challenges remain due to the lack of effective earth-abundant electrocatalysts and insufficient understanding of catalytic mechanisms. Here we demonstrate that robust bifunctional oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity can be achieved by inducing lattice strain in noble-metal-free metal–organic frameworks (MOFs). Lattice-strained NiFe MOFs exhibit mass activities of 500 A gmetal−1 at a half-wave potential of 0.83 V for the ORR and 2,000 A gmetal−1 at an overpotential of 0.30 V for the OER, which are 50–100 times that of pristine NiFe metal–organic frameworks. The catalyst maintains ~97% of its initial activity after 200 h of continuous ORR/OER reaction at a high current density of 100–200 mA cm−2. Using operando synchrotron spectroscopies, we observed a key superoxide *OOH intermediate emerging on Ni4+ sites during both the ORR and OER processes, which suggests a four-electron mechanistic pathway.

Suggested Citation

  • Weiren Cheng & Xu Zhao & Hui Su & Fumin Tang & Wei Che & Hui Zhang & Qinghua Liu, 2019. "Lattice-strained metal–organic-framework arrays for bifunctional oxygen electrocatalysis," Nature Energy, Nature, vol. 4(2), pages 115-122, February.
  • Handle: RePEc:nat:natene:v:4:y:2019:i:2:d:10.1038_s41560-018-0308-8
    DOI: 10.1038/s41560-018-0308-8
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    Cited by:

    1. Yu Du & Fakang Xie & Mengfei Lu & Rongxian Lv & Wangxi Liu & Yuandong Yan & Shicheng Yan & Zhigang Zou, 2024. "Continuous strain tuning of oxygen evolution catalysts with anisotropic thermal expansion," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    2. Xiaoran Zhang & Xiaorong Zhu & Shuowen Bo & Chen Chen & Mengyi Qiu & Xiaoxiao Wei & Nihan He & Chao Xie & Wei Chen & Jianyun Zheng & Pinsong Chen & San Ping Jiang & Yafei Li & Qinghua Liu & Shuangyin , 2022. "Identifying and tailoring C–N coupling site for efficient urea synthesis over diatomic Fe–Ni catalyst," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    3. Xiubei Yang & Qizheng An & Xuewen Li & Yubin Fu & Shuai Yang & Minghao Liu & Qing Xu & Gaofeng Zeng, 2024. "Charging modulation of the pyridine nitrogen of covalent organic frameworks for promoting oxygen reduction reaction," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    4. Lingyou Zeng & Zhonglong Zhao & Fan Lv & Zhonghong Xia & Shi-Yu Lu & Jiong Li & Kaian Sun & Kai Wang & Yingjun Sun & Qizheng Huang & Yan Chen & Qinghua Zhang & Lin Gu & Gang Lu & Shaojun Guo, 2022. "Anti-dissolution Pt single site with Pt(OH)(O3)/Co(P) coordination for efficient alkaline water splitting electrolyzer," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    5. Shuang Wang & Wenhe Xie & Ping Wu & Geyu Lin & Yan Cui & Jiawei Tao & Gaofeng Zeng & Yonghui Deng & Huibin Qiu, 2022. "Soft nanobrush-directed multifunctional MOF nanoarrays," Nature Communications, Nature, vol. 13(1), pages 1-8, December.

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