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Electronic metal-support interaction enhanced oxygen reduction activity and stability of boron carbide supported platinum

Author

Listed:
  • Colleen Jackson

    (HySA/Catalysis, Catalysis Institute, University of Cape Town, Corner of Madiba Circle and South Lane)

  • Graham T. Smith

    (HySA/Catalysis, Catalysis Institute, University of Cape Town, Corner of Madiba Circle and South Lane
    Engineering Sciences, University of Southampton)

  • David W. Inwood

    (University of Southampton)

  • Andrew S. Leach

    (University of Southampton)

  • Penny S. Whalley

    (University of Southampton)

  • Mauro Callisti

    (Engineering Sciences, University of Southampton)

  • Tomas Polcar

    (Engineering Sciences, University of Southampton)

  • Andrea E. Russell

    (University of Southampton)

  • Pieter Levecque

    (HySA/Catalysis, Catalysis Institute, University of Cape Town, Corner of Madiba Circle and South Lane)

  • Denis Kramer

    (Engineering Sciences, University of Southampton)

Abstract

Catalysing the reduction of oxygen in acidic media is a standing challenge. Although activity of platinum, the most active metal, can be substantially improved by alloying, alloy stability remains a concern. Here we report that platinum nanoparticles supported on graphite-rich boron carbide show a 50–100% increase in activity in acidic media and improved cycle stability compared to commercial carbon supported platinum nanoparticles. Transmission electron microscopy and x-ray absorption fine structure analysis confirm similar platinum nanoparticle shapes, sizes, lattice parameters, and cluster packing on both supports, while x-ray photoelectron and absorption spectroscopy demonstrate a change in electronic structure. This shows that purely electronic metal-support interactions can significantly improve oxygen reduction activity without inducing shape, alloying or strain effects and without compromising stability. Optimizing the electronic interaction between the catalyst and support is, therefore, a promising approach for advanced electrocatalysts where optimizing the catalytic nanoparticles themselves is constrained by other concerns.

Suggested Citation

  • Colleen Jackson & Graham T. Smith & David W. Inwood & Andrew S. Leach & Penny S. Whalley & Mauro Callisti & Tomas Polcar & Andrea E. Russell & Pieter Levecque & Denis Kramer, 2017. "Electronic metal-support interaction enhanced oxygen reduction activity and stability of boron carbide supported platinum," Nature Communications, Nature, vol. 8(1), pages 1-11, August.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15802
    DOI: 10.1038/ncomms15802
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    1. Chenlu Wang & Liping Zhou & Chengzhe Liu & Jiaming Qiao & Xinrui Han & Luyang Wang & Yaxi Liu & Bi Xu & Qinfang Qiu & Zizhuo Zhang & Jiale Wang & Xiaoya Zhou & Mengqi Zeng & Lilei Yu & Lei Fu, 2024. "Pt nanoshells with a high NIR-II photothermal conversion efficiency mediates multimodal neuromodulation against ventricular arrhythmias," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    2. Wenyao Chen & Junbo Cao & Jia Yang & Yueqiang Cao & Hao Zhang & Zheng Jiang & Jing Zhang & Gang Qian & Xinggui Zhou & De Chen & Weikang Yuan & Xuezhi Duan, 2021. "Molecular-level insights into the electronic effects in platinum-catalyzed carbon monoxide oxidation," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
    3. Jiayi Chen & Mohammed Aliasgar & Fernando Buendia Zamudio & Tianyu Zhang & Yilin Zhao & Xu Lian & Lan Wen & Haozhou Yang & Wenping Sun & Sergey M. Kozlov & Wei Chen & Lei Wang, 2023. "Diversity of platinum-sites at platinum/fullerene interface accelerates alkaline hydrogen evolution," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    4. Wu, Zexing & Chen, Zhi & Xu, Kunhan & Li, Bin & Li, Zhenjiang & Xu, Guangrui & Xiao, Weiping & Ma, Tianyi & Fu, Yunlei & Wang, Lei, 2023. "Cationic defects coupled with trace Pt under the assistance of corrosive engineering for efficient hydrogen electrocatalysis with large current density," Renewable Energy, Elsevier, vol. 210(C), pages 196-202.

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