کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1269347 | 1497392 | 2016 | 9 صفحه PDF | دانلود رایگان |
• AuPd/Cd0.5Zn0.5S photocatalysts were synthesized via a facile method.
• The AuPd/Cd0.5Zn0.5S shows significantly enhanced H2 evolution activity.
• The intimate interfaces promote the charge transfer and separation.
• The mechanism was proposed and confirmed by SPV result.
In this study, novel AuPd bimetallic co-catalyst decorated Cd0.5Zn0.5S photocatalyst was successfully synthesized via an in-situ chemical deposition method. The physical as well as the photophysical properties of the as-obtained AuPd/Cd0.5Zn0.5S samples were characterized by X-ray diffractometry (XRD), Transmission electron microscope (TEM), UV–vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and surface photovoltage spectroscopy (SPV). The AuPd bimetallic co-catalysts showed dramatic photo-generated charge separation efficiency in Cd0.5Zn0.5S sample, and thus significantly enhance the H2 production activity under visible light irradiation. The AuPd/Cd0.5Zn0.5S sample with 0.5 wt% content had the highest catalytic activity, and the corresponding H2 evolution rate is 3.65 mmol g−1 h−1, which was about 12 times as that of pure Cd0.5Zn0.5S sample under visible light irradiation. The photocatalytic activity of the photocatalyst was stable even after 9 cycling photocatalytic experiments. A possible mechanism on the photocatalytic enhancement of AuPd NPs was systematically investigated, which can provide a novel concept for the synthesis of other desirable photocatalytic materials.
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Journal: International Journal of Hydrogen Energy - Volume 41, Issue 33, 7 September 2016, Pages 14704–14712