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Catalytic activity of graphene-covered non-noble metals governed by proton penetration in electrochemical hydrogen evolution reaction.
Hu, Kailong; Ohto, Tatsuhiko; Nagata, Yuki; Wakisaka, Mitsuru; Aoki, Yoshitaka; Fujita, Jun-Ichi; Ito, Yoshikazu.
Affiliation
  • Hu K; Institute of Applied Physics, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba, 305-8573, Japan.
  • Ohto T; Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, 560-8531, Japan. ohto@molectronics.jp.
  • Nagata Y; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
  • Wakisaka M; Graduate School of Engineering, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama, 939-0398, Japan.
  • Aoki Y; PRESTO, Japan Science and Technology Agency, Saitama, 332-0012, Japan.
  • Fujita JI; PRESTO, Japan Science and Technology Agency, Saitama, 332-0012, Japan.
  • Ito Y; Faculty of Engineering, Hokkaido University, N13W8 Kita-ku, Sapporo, 060-8628, Japan.
Nat Commun ; 12(1): 203, 2021 Jan 08.
Article in En | MEDLINE | ID: mdl-33420063
ABSTRACT
Graphene-covering is a promising approach for achieving an acid-stable, non-noble-metal-catalysed hydrogen evolution reaction (HER). Optimization of the number of graphene-covering layers and the density of defects generated by chemical doping is crucial for achieving a balance between corrosion resistance and catalytic activity. Here, we investigate the influence of charge transfer and proton penetration through the graphene layers on the HER mechanisms of the non-noble metals Ni and Cu in an acidic electrolyte. We find that increasing the number of graphene-covering layers significantly alters the HER performances of Ni and Cu. The proton penetration explored through electrochemical experiments and simulations reveals that the HER activity of the graphene-covered catalysts is governed by the degree of proton penetration, as determined by the number of graphene-covering layers.