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Atomic Structural Evolution of Single-Layer Pt Clusters as Efficient Electrocatalysts

  • Bin Wei Zhang
  • , Long Ren
  • , Zhong Fei Xu
  • , Ning Yan Cheng
  • , Wei Hong Lai
  • , Lei Zhang
  • , Weichang Hao
  • , Sheng Qi Chu
  • , Yun Xiao Wang*
  • , Yi Du*
  • , Lei Jiang
  • , Hua Kun Liu
  • , Shi Xue Dou*
  • *Corresponding author for this work
  • University of Wollongong
  • Beihang University
  • CAS - Institute of High Energy Physics
  • CAS - Technical Institute of Physics and Chemistry

Research output: Contribution to journalArticlepeer-review

Abstract

The rational synthesis of single-layer noble metal directly anchored on support materials is an elusive target to accomplish for a long time. This paper reports well-defined single-layer Pt (Pt-SL) clusters anchored on ultrathin TiO2 nanosheets—as a new frontier in electrocatalysis. The structural evolution of Pt-SL/TiO2 via self-assembly of single Pt atoms (Pt-SA) is systematically recorded. Significantly, the Pt atoms of Pt-SL/TiO2 possess a unique electronic configuration with Pt-Pt covalent bonds surrounded by abundant unpaired electrons. This Pt-SL/TiO2 catalyst presents enhanced electrochemical performance toward diverse electrocatalytic reactions (such as the hydrogen evolution reaction and the oxygen reduction reaction) compared with Pt-SA, multilayer Pt nanoclusters, and Pt nanoparticles, suggesting an efficient new type of catalyst that can be achieved by constructing single-layer atomic clusters on supports.

Original languageEnglish
Article number2100732
JournalSmall
Volume17
Issue number26
DOIs
StatePublished - 1 Jul 2021

Keywords

  • HER
  • continuous active sites
  • electrocatalyst
  • single-layer Pt clusters

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