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High-entropy alloyed single-atom Pt for methanol oxidation electrocatalysis

Author

Listed:
  • Mingda Liu

    (Tsinghua University
    Tsinghua University)

  • Zhichao Zhang

    (Tsinghua University)

  • Chenyu Li

    (Tsinghua University
    Tsinghua University)

  • Sen Jin

    (Tsinghua University
    Tsinghua University)

  • Kunlei Zhu

    (Qufu Normal University)

  • Shoushan Fan

    (Tsinghua University)

  • Jia Li

    (Tsinghua University)

  • Kai Liu

    (Tsinghua University
    Tsinghua University)

Abstract

The methanol oxidation reaction is the bottleneck for direct methanol fuel cells. Unfortunately, the state-of-the-art Pt-based catalysts suffer heavily from the CO poisoning problem. Isolating Pt atoms in a material can avoid CO poisoning. However, single-atom Pt catalysts alone are inert towards methanol oxidation reaction. Here, we report high-entropy alloyed single-atom Pt catalysts, in which single-atom Pt sites are alloyed with non-noble elements in a high-entropy structure. This catalyst not only possesses active Pt sites but also inherits the ability of single-atom Pt to resist CO poisoning. Consequently, the catalyst shows a notable mass activity of 35.3 A mg−1 at only 2.3 at% Pt and maintains high activity even after operation for 180,000 s. Both experimental and theoretical results reveal that the high-entropy structure induces a synergistic effect, wherein the elements coordinated around single-atom Pt sites effectively remove adsorbed CO from Pt. This mechanism facilitates the key reaction steps of methanol oxidation reaction and avoids CO poisoning. This work presents a high-entropy alloyed single-atom strategy to realize efficient and durable methanol oxidation reaction catalysis with low costs.

Suggested Citation

  • Mingda Liu & Zhichao Zhang & Chenyu Li & Sen Jin & Kunlei Zhu & Shoushan Fan & Jia Li & Kai Liu, 2025. "High-entropy alloyed single-atom Pt for methanol oxidation electrocatalysis," Nature Communications, Nature, vol. 16(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61376-y
    DOI: 10.1038/s41467-025-61376-y
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    References listed on IDEAS

    as
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