4.5 Article

MoSe2/g-C3N4 heterojunction coupled with Pt nanoparticles for enhanced photocatalytic hydrogen evolution

期刊

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpcs.2021.110137

关键词

G-C3N4; MoSe2; Photocatalytic hydrogen evolution; Semiconductor photocatalysts

资金

  1. Hebei talent project training funds [A201803003]
  2. Program for the Young Top Talents of Hebei Province
  3. Natural Science Foundation of Hebei Province [B2019402082]
  4. Science and Technology Research and Development Projects of Handan City [19422111008-16]
  5. Ministry of Education, Singapore [MOE2018-T2-1-017, MOE2019-T1-002012, RG102/19]

向作者/读者索取更多资源

The Pt-MoSe2/g-C3N4 heterostructures synthesized through integrating facile solvothermal technique and solution-phase hybridization method exhibit greatly enhanced photocatalytic hydrogen production compared to bare g-C3N4 and Pt/g-C3N4 catalysts. The enhancement factor is directly correlated with the strong photosynergistic effect of charge-carrier generation and separation path coupling heterojunction sensitization on MoSe2/g-C3N4 with Pt nanoparticle.
The inefficiency of charge separation is the major practically limited factor towards high hydrogen evolution reaction (HER) of photocatalysts. Therefore, design and construction of efficient photocatalysts system with efficient charge transfer path is urgently necessary for HER. Herein, we report an effective strategy to construct Pt-MoSe2/g-C3N4 heterostructure through integrating facile solvothermal technique and solution-phase hybridization method. The synthesized ternary Pt-MoSe2/g-C3N4 heterostructures exhibit greatly enhanced photocatalytic hydrogen production than bare g-C3N4 and Pt/g-C3N4 catalyst. The enhancement factor is directly correlated with strong photosynergistic effect of charge-carrier generation and separation path coupling heterojunction sensitization on MoSe2/g-C3N4 with Pt nanoparticle. Moreover, the mechanism of enhanced catalytic activity is fully studied by electrochemical characterizations and photocurrent analysis.

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