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Co-doped Mo-Mo2C cocatalyst for enhanced g-C3N4 photocatalytic H2 evolution

[Display omitted] •Co doped Mo-Mo2C is an efficient non-noble-metal cocatalyst for visible light photocatalytic H2 production.•H2 production rate of 2.0 wt.% Co(Mo-Mo2C)/g-C3N4 photocatalyst is 1.4 times greater than that of 2.0 wt.% Pt/g-C3N4.•Co doping can suppress charge recombination, thereby im...

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Published in:Applied catalysis. B, Environmental Environmental, 2020-01, Vol.260, p.118220, Article 118220
Main Authors: Zheng, Yaru, Dong, Jie, Huang, Cunping, Xia, Ligang, Wu, Qiang, Xu, Qunjie, Yao, Weifeng
Format: Article
Language:English
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Summary:[Display omitted] •Co doped Mo-Mo2C is an efficient non-noble-metal cocatalyst for visible light photocatalytic H2 production.•H2 production rate of 2.0 wt.% Co(Mo-Mo2C)/g-C3N4 photocatalyst is 1.4 times greater than that of 2.0 wt.% Pt/g-C3N4.•Co doping can suppress charge recombination, thereby improving the activity of Mo-Mo2C/g-C3N4 catalyst. Molybdenum rich molybdenum carbide (Mo-Mo2C) has recently been confirmed as a highly effective non-noble-metal cocatalyst to boost the photocatalytic activity of g-C3N4 for water splitting. However, the activity of Mo-Mo2C is still much lower than that of Pt noble metal based cocatalysts for photocatalytic hydrogen production (PHE). This work reports a highly active cobalt (Co) doped Mo-Mo2C cocatalyst (Co(Mo-Mo2C)) for PHE. The hydrogen production rate of 2.0 wt.% optimal Co(Mo-Mo2C) loaded g-C3N4 (2.0 wt.% Co(Mo-Mo2C)/g-C3N4) photocatalyst can be as high as 11,291 μmol h−1 g−1, at 6.7% apparent quantum efficiency (AQE) at 420 nm, which is 1.4 times greater than that of 2.0 wt.% Pt/g-C3N4 photocatalyst. Catalyst characterizations have pointed out that Co doped Mo-Mo2C cocatalyst is able to efficiently suppress photo-generated charge recombination, thus improving the interfacial charge transfer rate. This research provides novel ideas and technical approaches for designing a noble-metal-free, efficient and environmentally friendly cocatalyst for photocatalytic H2 evolution via water reduction.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2019.118220