4.7 Article

Three-dimensional ordered macroporous g-C3N4-Cu2O-TiO2 heterojunction for enhanced hydrogen production

Journal

SCIENCE CHINA-MATERIALS
Volume 65, Issue 1, Pages 139-146

Publisher

SCIENCE PRESS
DOI: 10.1007/s40843-021-1714-9

Keywords

noble metal-free cocatalyst; cross pore channels; 3DOM structure; photocatalytic hydrogen evolution

Funding

  1. National Key Research and Development Program of China [2016YFC0300200]
  2. National Natural Science Foundation of China [21975229]
  3. Natural Science Foundation of Zhejiang Province [Y19B060003]

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In this study, a g-C3N4-Cu2O-TiO2 photocatalyst with a novel three-dimensional ordered macroporous (3DOM) structure was prepared successfully. The unique porous structure enabled higher specific surface area and active sites, leading to improved photocatalytic performance. The double p-n heterojunction and robust porous structure of g-C3N4-Cu2O-TiO2 contributed to enhanced photoactivity, with promising implications for developing cost-effective heterojunction photocatalysts.
In this study, a g-C3N4-Cu2O-TiO2 photocatalyst with a novel three-dimensional ordered macroporous (3DOM) structure was successfully prepared using a sacrificial template strategy and a photodeposition method. The influence of the special porous structure with cross pore channels on the photocatalytic properties of the as-prepared sample was studied in detail. Compared with the original photocatalyst (TiO2 with 3 wt% Pt), g-C3N4-Cu2O-TiO2 exhibited a higher specific surface area and more active sites, thus accelerating the separation efficiency of the photogenerated electron-hole pair. Consequently, the as-prepared photocatalyst showed good photocatalytic performance, reaching a maximum hydrogen production rate of 12,108 mu mol g(-1) h(-1) and approximately five times higher than that of the pristine comparison sample. The enhanced photoactivity of the g-C3N4-Cu2O-TiO2 heterojunction can be ascribed to its double p-n heterojunction and robust porous structure, where the photodeposited Cu2O plays a synergistic catalytic role in the photocatalytic process and the outer clad g-C3N4 layer prevents Cu2O oxidation. Additionally, the possible photocatalytic mechanism was briefly discussed based on the experimental results. This work identifies viable pathways for developing low-cost heterojunction photocatalysts with highly efficient photocatalytic activity toward improved solar energy conversion.

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