4.7 Article

Micro-tailored g-C3N4 enables Ru single-atom loading for efficient photocatalytic H2 evolution

期刊

APPLIED SURFACE SCIENCE
卷 596, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2022.153471

关键词

Single atom catalysts; Hydrogen production; Photocatalyst; Metal-support interaction; Graphitic carbon nitride

资金

  1. Key Technology Research and Development Program of Shandong [2021CXGC010401]
  2. Natural Science Foundation of Shandong Province [ZR2020QB129]
  3. Weifang University of Science and Technology [KJRC2021009]
  4. Key Laboratory of Fuel Cell Technology of Guangdong Province
  5. Shiyanjia Lab

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Loading single atom (SA) cocatalysts onto semiconductors offers great potential for improving photocatalytic performance. In this study, a simple micro-tailoring strategy was used to cut g-C3N4 into small pieces and oligomers, allowing stable confinement of Ru SAs onto the framework. The resulting composite showed significantly enhanced photocatalytic activity for H2 evolution, achieved through metal-support interaction and directional charge transfer.
Loading single atom (SA) cocatalysts onto semiconductors offers great potential for improving the photocatalytic performance. Here, we report a simple micro-tailoring strategy that cuts g-C3N4 into small pieces and oligomers. Defects, boundaries, dopants and terminal groups created could confine Ru SAs stably onto the framework, ensuring uniform dispersion of Ru SAs on the tailored g-C3N4. The as-prepared composite, the tailored g-C3N4 loaded with Ru SAs, showed a dramatic increase photocatalytic activity for H2 evolution (4052.1 mu mol h(-1) g(-1)) compared to the composite of the non-tailored g-C3N4 loaded with Ru (394.3 mu mol h(-1) g(-1)). The enhanced catalytic activity was achieved by the metal-support interaction between the Ru atoms and the tailored g-C3N4, which could manipulate local charge distribution, thus promoting the adsorption of intermediates and enabling efficient charge transfer. In addition, atomic Ru-sites could provide directional charge transfer channels and targeting sites to facilitate rapid photo-introduced charge transfer and water reduction reaction. The proposed strategy provides a facile and feasible way for the construction of atomically dispersed catalysts for efficient photocatalytic H-2 evolution and other reactions.

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