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Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution

Author

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  • Qiang-Qiang Yan

    (University of Science and Technology of China)

  • Dao-Xiong Wu

    (University of Science and Technology of China)

  • Sheng-Qi Chu

    (Chinese Academy of Sciences)

  • Zhi-Qin Chen

    (University of Science and Technology of China)

  • Yue Lin

    (University of Science and Technology of China)

  • Ming-Xi Chen

    (University of Science and Technology of China)

  • Jing Zhang

    (Chinese Academy of Sciences)

  • Xiao-Jun Wu

    (University of Science and Technology of China
    University of Science and Technology of China)

  • Hai-Wei Liang

    (University of Science and Technology of China)

Abstract

Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm−2 and a high mass activity of 26.1 A mg−1 at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts.

Suggested Citation

  • Qiang-Qiang Yan & Dao-Xiong Wu & Sheng-Qi Chu & Zhi-Qin Chen & Yue Lin & Ming-Xi Chen & Jing Zhang & Xiao-Jun Wu & Hai-Wei Liang, 2019. "Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution," Nature Communications, Nature, vol. 10(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12851-w
    DOI: 10.1038/s41467-019-12851-w
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    Cited by:

    1. Ashwani Kumar & Viet Q. Bui & Jinsun Lee & Lingling Wang & Amol R. Jadhav & Xinghui Liu & Xiaodong Shao & Yang Liu & Jianmin Yu & Yosep Hwang & Huong T. D. Bui & Sara Ajmal & Min Gyu Kim & Seong-Gon K, 2021. "Moving beyond bimetallic-alloy to single-atom dimer atomic-interface for all-pH hydrogen evolution," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    2. Xiaowei Shi & Chao Dai & Xin Wang & Jiayue Hu & Junying Zhang & Lingxia Zheng & Liang Mao & Huajun Zheng & Mingshan Zhu, 2022. "Protruding Pt single-sites on hexagonal ZnIn2S4 to accelerate photocatalytic hydrogen evolution," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    3. Yiming Zhu & Jiaao Wang & Toshinari Koketsu & Matthias Kroschel & Jin-Ming Chen & Su-Yang Hsu & Graeme Henkelman & Zhiwei Hu & Peter Strasser & Jiwei Ma, 2022. "Iridium single atoms incorporated in Co3O4 efficiently catalyze the oxygen evolution in acidic conditions," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    4. Jianxin Zhai & Zhanghui Xia & Baowen Zhou & Haihong Wu & Teng Xue & Xiao Chen & Jiapeng Jiao & Shuaiqiang Jia & Mingyuan He & Buxing Han, 2024. "Photo-thermal coupling to enhance CO2 hydrogenation toward CH4 over Ru/MnO/Mn3O4," Nature Communications, Nature, vol. 15(1), pages 1-9, December.
    5. Junsic Cho & Taejung Lim & Haesol Kim & Ling Meng & Jinjong Kim & Seunghoon Lee & Jong Hoon Lee & Gwan Yeong Jung & Kug-Seung Lee & Francesc Viñes & Francesc Illas & Kai S. Exner & Sang Hoon Joo & Cha, 2023. "Importance of broken geometric symmetry of single-atom Pt sites for efficient electrocatalysis," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    6. Justicia, Jéssica & Alberto Baeza, José & de Oliveira, Adriana S. & Calvo, Luisa & Heras, Francisco & Gilarranz, Miguel A., 2022. "Aqueous-phase reforming of water-soluble compounds from pyrolysis bio-oils," Renewable Energy, Elsevier, vol. 199(C), pages 895-907.

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