CoSe2 modified Se-decorated CdS nanowire Schottky heterojunctions for highly efficient photocatalytic hydrogen evolution
[Display omitted] •CoSe2/CdS0.95Se0.05 Schottky heterojunction were fabricated via simple method.•Se-doping can lower the work function of CdS NWs, availing the electrons escaping.•The highest HER rate of CoSe2/CdS0.95Se0.05 is ~66 times higher than that of CdS NWs.•CoSe2 can efficiently boost the s...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-06, Vol.389, p.124431, Article 124431 |
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Sprache: | eng |
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•CoSe2/CdS0.95Se0.05 Schottky heterojunction were fabricated via simple method.•Se-doping can lower the work function of CdS NWs, availing the electrons escaping.•The highest HER rate of CoSe2/CdS0.95Se0.05 is ~66 times higher than that of CdS NWs.•CoSe2 can efficiently boost the separation and migration of charge carriers.
Novel CoSe2 nanobelts/Se-decorated CdS nanowires heterojunctions were successfully constructed via combining strategies of Se-doping and in situ loading of CoSe2 nanobelts. Under visible-light (λ ≥ 400 nm) irradiation, the CoSe2/CdS0.95Se0.05 nanocomposites exhibit significantly enhanced photocatalytic H2-evolution activities. The peak value of the H2-generation rate of 13894.8 μmol·h−1·g−1 is achieved with an apparent quantum efficiency (AQE) of 76.1%, which is approximate 66.7 times higher than that of pure CdS nanowires. Experimental investigations and theoretical calculations demonstrate that the enhanced photocatalytic H2-evolution performance originates from the synergetic effects of 1) the Se-doping to form CdS0.95Se0.05 nanowires, which can reduce the electrostatic potential energy of CdS catalyst to promote electrons migration for reducing the recombination efficiency of electron/hole pairs; and 2) the in situ loading of CoSe2 co-catalyst to construct the Schottky heterojunction between CoSe2 and CdS0.95Se0.05 nanowires, which can not only efficiently boost the separation of charge carriers, but also provide sufficient active sites for reducing H+ to H2 subsequently. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2020.124431 |