Enhanced Visible-Light Hydrogen-Production Activity of Copper-Modified ZnxCd1−xS

Copper modification is an efficient way to enhance the photocatalytic activity of ZnS‐based materials; however, the mechanisms of Cu2+ surface and bulk modifications for improving the activity are quite different. In this work, two different synthetic pathways were devised to prepare surface and bul...

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Veröffentlicht in:ChemSusChem 2013-10, Vol.6 (10), p.2009-2015
Hauptverfasser: Zhang, Jun, Xu, Quanlong, Qiao, Shi Zhang, Yu, Jiaguo
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Sprache:eng
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Zusammenfassung:Copper modification is an efficient way to enhance the photocatalytic activity of ZnS‐based materials; however, the mechanisms of Cu2+ surface and bulk modifications for improving the activity are quite different. In this work, two different synthetic pathways were devised to prepare surface and bulk Cu2+‐modified ZnxCd1−xS photocatalysts through cation‐exchange and coprecipitation methods, respectively. Different Cu2+ modifications brought different effects on the phase structure, morphology, surface area, optical property, as well as the photocatalytic H2‐production activity of the final products. The optimized Cu2+‐surface‐modified ZnxCd1−xS photocatalyst has a high H2‐production rate of 4638.5 μmol h−1 g−1 and an apparent quantum efficiency of 20.9 % at 420 nm, exceeding that of Cu2+‐bulk‐modified catalyst at the same copper content. Cu2+ surface modification not only brings a new electron‐transferring pathway (interfacial charge transfer), but also produces new surface active sites for H2 evolution, reducing the recombination rate of photogenerated charge carriers. Surface modification: Two different synthetic pathways are devised to prepare surface and bulk Cu2+‐modified ZnxCd1−xS through cation‐exchange and coprecipitation methods, respectively. Cu2+ surface modification can provide a new electron‐transferring pathway (interfacial charge transfer) and also form new surface active sites for H2 evolution, resulting in enhanced visible‐light H2‐production activity (see picture).
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.201300409