4.7 Article Proceedings Paper

Tracking charge transfer pathways in SrTiO3/CoP/Mo2C nanofibers for enhanced photocatalytic solar fuel production

Journal

CHINESE JOURNAL OF CATALYSIS
Volume 43, Issue 2, Pages 507-518

Publisher

ELSEVIER
DOI: 10.1016/S1872-2067(21)63898-6

Keywords

Dual cocatalyst; Electron migration; Schottky junction; Electrospinning; In situ irradiation XPS; Photocatalyst; Solar fuel

Funding

  1. National Natural Science Foundation of China [51972287, U2004172, 51502269]
  2. National Natural Science Foundation of Henan Province [202300410368]
  3. Foundation for University Key Teacher of Henan Province [2020GGJS009]

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This study focuses on the synthesis of a dual cocatalysts system for photocatalytic solar fuel generation. The system, composed of cobalt phosphide and molybdenum carbide embedded on strontium titanate nanofibers, showed significant improvement in hydrogen evolution and CO2 reduction performance. The structure of the dual cocatalysts system effectively promoted spatial charge separation and enhanced photocatalytic performance. The research provides a theoretical basis and ideas for subsequent studies.
Photocatalytic solar fuel generation is currently a hot topic because of its potential for solving the energy crisis owing to its low cost and zero-carbon emissions. However, the rapid bulk recombination of photoexcited carrier pairs is a fundamental disadvantage. To resolve this problem, we synthesized a dual cocatalysts system of cobalt phosphide (CoP) and molybdenum carbide (Mo2C) embedded on strontium titanate (SrTiO3) nanofibers. Compared with those of pristine SrTiO3 and binary samples, the dual cocatalysts system (denoted SCM) showed a significant improvement in the hydrogen evolution and CO2 reduction performance. Further, the structure of SCM effectively promoted spatial charge separation and enhanced the photocatalytic performance. In addition, the Schottky junction formed between the SrTiO3 and cocatalysts enabled the rapid transfer of photoexcited electrons from SrTiO3 to the cocatalysts, resulting in effective separation and prolonged photoexcited electron lifetimes. The electron migration route between SrTiO3 and the cocatalysts was determined by in situ irradiation X-ray spectroscopy, and band structures of SrTiO3 and the cocatalysts are proposed based on results obtained from UV-vis diffraction reflection spectroscopy and ultraviolet photoelectron spectroscopy measurements. On the basis of our results, the dual cocatalysts unambiguously boosts charge separation and enhances photocatalytic performance. In summary, we have investigated the flux of photoexcited electrons in a dual cocatalysts system and provided a theoretical basis and ideas for subsequent research. (C) 2022, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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