4.7 Article

Anchoring single Pt atoms on hollow Ag3VO4 spheres for improved activity towards photocatalytic H2 evolution reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 44, Pages 22842-22851

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.04.108

Keywords

Single atom; H-2 evolution reaction; Photocatalytic; Ag3VO4; Pt atom; Electron/hole recombination

Funding

  1. National Nature Science Foundation of China [51762042]
  2. Shaanxi Province Science and Technology Resources Open Sharing Platform Project [2019 PT18]
  3. Science and Technology Program of Shaanxi Province [2018GY086, 2020TD032, 2017GY131, 2017JM2039]
  4. Shaanxi Key Laboratory Project [19JS07]
  5. Transverse Research Projects of Yulin [2018HX08]

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The high cost of noble metal catalysts is a bottleneck for the industry, but using single-atom noble metals can reduce costs significantly. Single Pt atoms on Ag3VO4 were investigated for their impact on photocatalytic performance. The presence of Pt atoms on the surface of Ag3VO4 improved H-2 production efficiency under visible light, attributed to enhanced light utilization and reduced charge transfer resistance.
The high cost of noble metal catalysts has been a great bottleneck for the catalyst industry. Using the noble metal at a single-atom level for catalytic applications could dramatically decrease the cost. The impacts of single Pt atoms on the photocatalytic performance of Ag3VO4 have been investigated and reported. In this report, single Pt atoms were anchored on the surface of Ag3VO4 (AVO) as a cocatalyst, and the resultant composite photocatalyst has been studied for photocatalytic H-2 production from water driven by visible light. The as-prepared AVO particles are hollow nanospheres in the monoclinic phase with a bandgap of 2.20 eV. The light absorption edge of AVO/Pt is slightly red-shifted compared to that of the pristine AVO, indicating more visible light absorption of AVO/Pt. The XPS peaks of Ag, V, and Pt exhibit a significant shift after AVO and Pt get into contact, suggesting the strong interaction between the surface Ag and V atoms, and single Pt atoms. After 3-h illumination, the photocatalytic H-2 evolution amount from AVO/Pt is improved up to 1400 mmol, which is 2.8 times that on the bare AVO. Such efficient photocatalytic H-2 evolution on AVO/Pt is still maintained after five reaction cycles. The better photocatalytic performance of AVO/Pt has been attributed to the more efficient visible light utilization and the lower interfacial charge transfer resistance, as demonstrated in the DRS and EIS spectra. The presence of the surface Pt atoms also leads to a higher amount of reactive radicals, which could efficiently promote the surface redox reactions. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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