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The role of carbon catalyst coatings in the electrochemical water splitting reaction

Author

Listed:
  • William J. V. Townsend

    (University of Nottingham
    University of Nottingham)

  • Diego López-Alcalá

    (Universidad de Valencia)

  • Matthew A. Bird

    (University of Nottingham)

  • Jack W. Jordan

    (University of Nottingham)

  • Graham A. Rance

    (University of Nottingham)

  • Johannes Biskupek

    (Ulm University)

  • Ute Kaiser

    (Ulm University)

  • José J. Baldoví

    (Universidad de Valencia)

  • Darren A. Walsh

    (University of Nottingham
    The Faraday Institution)

  • Lee R. Johnson

    (University of Nottingham
    The Faraday Institution)

  • Andrei N. Khlobystov

    (University of Nottingham)

  • Graham N. Newton

    (University of Nottingham
    The Faraday Institution)

Abstract

Designing inexpensive, sustainable, and high-performance oxygen-evolution reaction (OER) electrocatalysts is one of the largest obstacles hindering the development of new electrolyzers. Carbon-coated metal/metal oxide (nano)particles have been used in such applications, but the role played by the carbon coatings is poorly understood. Here, we use a carbon-coated catalyst comprising metal-oxide nanoparticles encapsulated within single-walled carbon nanotubes (SWNTs), to study the effects of carbon coatings on catalytic performance. Electrolyte access to the encapsulated metal oxides is shut off by plugging the SWNT ends with size-matched fullerenes. Our results reveal that the catalytic activity of the composite rivals that of the metal oxide, despite the fact that the metal oxides cannot access the bulk electrolyte. Moreover, the rate-determining step (RDS) of the OER matches that measured at empty SWNTs, indicating that electrocatalysis occurs on the carbon surface. Synergism between the encapsulated metal oxide and carbon coating was explored using electrochemical Raman spectroscopy and computational analysis, revealing that charge transfer from the carbon host to the metal oxide is key to the high electrocatalytic activity of carbon in this system; decreasing electron density on the carbon surface facilitates binding of –OH, accelerating the rate of the OER on the carbon surface.

Suggested Citation

  • William J. V. Townsend & Diego López-Alcalá & Matthew A. Bird & Jack W. Jordan & Graham A. Rance & Johannes Biskupek & Ute Kaiser & José J. Baldoví & Darren A. Walsh & Lee R. Johnson & Andrei N. Khlob, 2025. "The role of carbon catalyst coatings in the electrochemical water splitting reaction," Nature Communications, Nature, vol. 16(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59740-z
    DOI: 10.1038/s41467-025-59740-z
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    References listed on IDEAS

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    1. Brian W. Smith & Marc Monthioux & David E. Luzzi, 1998. "Encapsulated C60 in carbon nanotubes," Nature, Nature, vol. 396(6709), pages 323-324, November.
    2. Yizhen Lu & Bixuan Li & Na Xu & Zhihua Zhou & Yu Xiao & Yu Jiang & Teng Li & Sheng Hu & Yongji Gong & Yang Cao, 2023. "One-atom-thick hexagonal boron nitride co-catalyst for enhanced oxygen evolution reactions," Nature Communications, Nature, vol. 14(1), pages 1-8, December.
    3. A. M. Rao & P. C. Eklund & Shunji Bandow & A. Thess & R. E. Smalley, 1997. "Evidence for charge transfer in doped carbon nanotube bundles from Raman scattering," Nature, Nature, vol. 388(6639), pages 257-259, July.
    4. Felix T. Haase & Arno Bergmann & Travis E. Jones & Janis Timoshenko & Antonia Herzog & Hyo Sang Jeon & Clara Rettenmaier & Beatriz Roldan Cuenya, 2022. "Size effects and active state formation of cobalt oxide nanoparticles during the oxygen evolution reaction," Nature Energy, Nature, vol. 7(8), pages 765-773, August.
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