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Research Article

Interfacial electronic interaction enabling exposed Pt(110) facets with high specific activity in hydrogen evolution reaction

Sicong Qiao1,§Qun He1,§Quan Zhou1,§Yuzhu Zhou1Wenjie Xu1Hongwei Shou1Yuyang Cao1Shuangming Chen1Xiaojun Wu2Li Song1( )
National Synchrotron Radiation Laboratory, CAS Center for Excellence in Nanoscience, University of Science and Technology of China, Hefei 230026, China
Hefei National Laboratory for Physical Science at the Microscale, Collaborative Innovation of Center of Chemistry for Energy Materials (iChEM), School of Chemistry and Materials Sciences, University of Science and Technology of China, Hefei 230026, China

§ Sicong Qiao, Qun He, and Quan Zhou contributed equally to this work.

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Graphical Abstract

The strong interfacial electronic interaction modulates the hydrogen adsorption strength of Pt(110) facets to achieve high specific activity in acidic hydrogen evolution reaction.

Abstract

To achieve a complete industrial chain of hydrogen energy, the development of efficient electrocatalysts for hydrogen evolution reaction (HER) is of great concerns. Herein, a nickel nitride supported platinum (Pt) catalyst with highly exposed Pt(110) facets (Pt(110)-Ni3N) is obtained for catalyzing HER. Combined X-ray spectra and density functional theory studies demonstrate that the interfacial electronic interaction between Pt and Ni3N support can promote the hydrogen evolution on Pt(110) facets by weakening hydrogen adsorption. As a result, the Pt(110)-Ni3N catalyst delivers an obviously higher specific activity than commercial 20 wt.% Pt/C in acidic media. This work suggests that the suitable interface modulation may play a vital role in rationally designing advanced electrocatalysts.

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Nano Research
Pages 174-180
Cite this article:
Qiao S, He Q, Zhou Q, et al. Interfacial electronic interaction enabling exposed Pt(110) facets with high specific activity in hydrogen evolution reaction. Nano Research, 2023, 16(1): 174-180. https://doi.org/10.1007/s12274-022-4654-2
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Received: 15 April 2022
Revised: 21 May 2022
Accepted: 13 June 2022
Published: 27 August 2022
© Tsinghua University Press 2022
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