Ni2+-doped ZnxCd1-xS photocatalysts from single-source precursors for efficient solar hydrogen production under visible light irradiation

被引:62
|
作者
Wang, Yabo [1 ]
Wu, Jianchun [1 ]
Zheng, Jianwei [2 ]
Jiang, Rongrong [1 ]
Xu, Rong [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[2] Inst High Performance Comp, Singapore 138632, Singapore
关键词
SOLID-SOLUTION PHOTOCATALYSTS; H-2; EVOLUTION; AQUEOUS-SOLUTIONS; CDS NANORODS; WATER; TIO2; ZNS; NANOCRYSTALS;
D O I
10.1039/c2cy00310d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ni2+-doped photocatalysts Ni(y)-ZnxCd1-xS (where 0 <= x <= 0.80, 0% <= y <= 8%) were prepared by a two-step route, which consisted of a first precipitation of single-source precursors and a subsequent solvothermal treatment of the precursors in ethylenediamine. Structural, morphological and optical properties of the as-prepared samples were characterized by XRD, UV-vis DRS, FESEM, TEM, N-2 physisorption, ICP-AES and XPS techniques. The photocatalytic activity was evaluated for hydrogen evolution from the aqueous solution containing sodium sulfide and sodium sulfite under visible light irradiation. All Ni2+-doped samples exhibit enhanced photocatalytic activity compared with the non-doped sample. Sample Ni(4%)-Zn0.4Cd0.6S gives the highest hydrogen evolution rate of 941 mu mol h(-1) under the optimized reaction conditions without any co-catalysts, with a corresponding quantum efficiency of 22.8% at 420 nm which is much higher compared to those of previously reported Ni2+-doped metal sulfide photocatalysts. It is suggested that good crystallinity, suitable band structure and the accommodation sites introduced by Ni2+ doping for charge carrier separation together contribute to the high activity of such photocatalysts for hydrogen evolution.
引用
收藏
页码:581 / 588
页数:8
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