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2D-2D heterostructured CdS–CoP photocatalysts for efficient H2 evolution under visible light irradiation
Visible-light photocatalytic water splitting for hydrogen evolution has attracted tremendous attention in past decades, but it still suffers from low solar-hydrogen conversion efficiency. In this paper, two-dimensional (2D) CdS was synthesized by the hydrothermal method, and 2D CoP nanosheets were s...
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Published in: | International journal of hydrogen energy 2019-10, Vol.44 (50), p.27412-27420 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Visible-light photocatalytic water splitting for hydrogen evolution has attracted tremendous attention in past decades, but it still suffers from low solar-hydrogen conversion efficiency. In this paper, two-dimensional (2D) CdS was synthesized by the hydrothermal method, and 2D CoP nanosheets were synthesized by successive hydrothermal, oxidation and phosphodation process. Then 2D-2D CdS–CoP photocatalysts were formed by ultrasonically dispersing the mixed solution of CdS and CoP, and their heterostructure was confirmed by transmission electron microscopy, X-ray photoelectron spectroscopy, fluorescence spectrometer and so on. CdS–CoP with 2% CoP loading amounts exhibits a maximum photocatalytic performance of 56.3 mmolg−1h−1 under visible light irradiation, which is 11.3 times as high as bare CdS. The enhanced photocatalytic performance of CdS–CoP should be due to the following two points: (1) high catalytic activity of CoP; (2) highly efficient separation and transfer of electron-hole pairs photogenerated in CdS due to the synthesized 2D-2D heterostructure.
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•2D-2D heterostructured CdS–CoP photocatalysts were synthesized.•CdS–2%CoP exhibits a maximum visible photocatalytic performance of 56.3 mmolg−1h−1.•The activity of CdS–CoP is due to CoP cocatalyst and the 2D-2D heterostructure. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2019.08.196 |