4.8 Article

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

Journal

SMALL
Volume 17, Issue 26, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202100732

Keywords

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

Funding

  1. Australian Research Council (ARC) [DE170100928, DP170101467]
  2. Commonwealth of Australia through the Automotive Australia 2020 Cooperative Research Centre (AutoCRC)
  3. Baosteel-Australia Joint Research and Development Center (Baosteel) [BA14006]
  4. ARC [LE0882813, LE0237478]

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This paper successfully reports the synthesis of well-defined single-layer Pt clusters anchored on ultrathin TiO2 nanosheets as a new frontier in electrocatalysis. The Pt-SL/TiO2 catalyst exhibits unique electronic configuration and enhanced electrochemical performance, suggesting a promising pathway for constructing efficient new types of catalysts.
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.

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