| Literature DB >> 34080772 |
Bin-Wei Zhang1, Long Ren1, Zhong-Fei Xu1,2, Ning-Yan Cheng1, Wei-Hong Lai1, Lei Zhang1, Weichang Hao2,3, Sheng-Qi Chu4, Yun-Xiao Wang1, Yi Du1,2,3, Lei Jiang2,5,6, Hua-Kun Liu1, Shi-Xue Dou1.
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 PtPt 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.Entities:
Keywords: HER; continuous active sites; electrocatalyst; single-layer Pt clusters
Year: 2021 PMID: 34080772 DOI: 10.1002/smll.202100732
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281