Efficient and stable photocatalytic hydrogen production from water splitting over ZnxCd1-xS solid solutions under visible light irradiation

被引:86
作者
Chan, Chih-Chieh [1 ]
Chang, Chung-Chieh [2 ]
Hsu, Chia-Hao [2 ]
Weng, Yu-Ching [1 ]
Chen, Kew-Yu [1 ]
Lin, Hsiao-Han [1 ]
Huang, Wen-Chih [1 ]
Cheng, Sheng-Fa [1 ]
机构
[1] Feng Chia Univ, Dept Chem Engn, Taichung 40724, Taiwan
[2] Acad Sinica, Inst Phys, Taipei 11529, Taiwan
关键词
Photocatalyst; ZnxCd1-xS; Hydrogen; Water splitting; Visible light; ZINC-SULFIDE; ELECTRONIC-STRUCTURE; OPTICAL-PROPERTIES; BOWING PARAMETER; CADMIUM-SULFIDE; H-2; EVOLUTION; CDS-ZNS; CD1-XZNXS; NANOCRYSTALS; LUMINESCENCE;
D O I
10.1016/j.ijhydene.2013.11.059
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
A simple co-precipitation method was employed to synthesize a series of cubic zinc-blende phase of ZnxCd1-xS photocatalysts using Na2S as the S source. Structural, morphological and optical properties of the samples have been investigated by XRD, SEM, EDS, XRF, ICP, N-2 physisorption and UV-vis diffuse reflectance techniques. The ZnxCd1-xS solid solution is not a simple compound mixture of ZnS and CdS, its XRD patterns show new structural peaks instead of mixture of original peaks. The lattice parameter a measured from the XRD patterns of the ZnxCd1-xS samples exhibits a slightly nonlinear relationship with the Zn mole fraction, which is slightly inconsistent with Vegard's law, thus suggesting that a nonhomogeneous alloy structure exists in ZnxCd1-xS solid solution. The photocatalytic H-2 evolution from water splitting in the sacrificial reagents of 0.25 M Na2S/0.35 M K2SO3 under visible light at 30 degrees C and 55 degrees C were also examined in the study. It is found that ZnxCd1-xS solid solution with composition x = 0.4-0.5 shows the highest photocatalytic H-2 production performance. The studied ZnxCd1-xS exhibits at least 50 h stable photocatalytic activity under outdoor sunlight irradiation. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1630 / 1639
页数:10
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