4.6 Article

Pyramid-like CdS nanoparticles grown on porous TiO2 monolith: An advanced photocatalyst for H2 production

Journal

ELECTROCHIMICA ACTA
Volume 250, Issue -, Pages 99-107

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2017.08.042

Keywords

Porous TiO2; CdS; H-2 evolution; Photoactivity

Funding

  1. National Natural Science Foundation of China [21273010]
  2. Program for Natural Science of Henan Province [162300410004]
  3. Program for Science and Technology Innovation Talent at the University of Henan Province [13HASTIT014]
  4. Outstanding Youth Innovation Talent of Henan Province [14410051000]
  5. Ministry of Education for returned overseas students

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Efficient production of H-2 via solar-light-driven water splitting by a semiconductor-based photocatalyst without noble metals is crucial owing to increasingly severe global energy and environmental issues. However, many challenges, including the low efficiency of H-2 evolution, low solar light absorption, excited electron-hole pair recombination, and slow transport of photoexcited carriers, must be resolved to enhance the H-2 photoproduction efficiency and photocatalyst stability. Here, a two-step method is used to synthesize advanced H-2-generating photocatalysts consisting of pyramid-like CdS nanoparticles grown on a porous TiO2 monolith, which show promising photocatalytic activity for the hydrogen evolution reaction. Furthermore, the stability of the photocatalysts is examined through long-term tests to verify their good durability. Without noble metals as cocatalysts, the photocatalyst can reach a high H-2 production rate of 1048.7 mu mol h(-1) g(-1) under UV-vis irradiation when the ratio of the CdS nanoparticles to TiO2 is 5 mol%. This unusual photocatalytic activity arises from the wide-region light adsorption due to the narrow band gap of CdS, effective separation of electrons and holes due to conduction band alignment at the CdS-TiO2 interface, and favorable reaction sites resulting from the porous structure. (C) 2017 Elsevier Ltd. All rights reserved.

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