Dodecylamine coordinated tri-arm CdS nanorod wrapped in intermittent ZnS shell for greatly improved photocatalytic H2 evolution

被引:118
作者
Sun, Guotai [1 ,2 ]
Shi, Jian-Wen [1 ]
Mao, Siman [1 ]
Ma, Dandan [1 ]
He, Chi [3 ]
Wang, Hongkang [1 ]
Cheng, Yonghong [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Elect Engn, Ctr Nanomat Renewable Energy, State Key Lab Elect Insulat & Power Equipment, Xian 710049, Peoples R China
[2] Northwestern Polytech Univ, Sch Mat Sci & Engn, Ctr Nano Energy Mat, State Key Lab Solidificat Proc, Xian 710072, Peoples R China
[3] Xi An Jiao Tong Univ, Sch Energy & Power Engn, State Key Lab Multiphase Flow Power Engn, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Hydrogen evolution; Heterostructure; Dodecylamine; Proton adsorption; HYDROGEN EVOLUTION; H-2; PRODUCTION; OPTICAL-PROPERTIES; QUANTUM DOTS; EFFICIENT; PERFORMANCE; COCATALYSTS; GRAPHENE; WATER; NANOCRYSTALS;
D O I
10.1016/j.cej.2021.132382
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A new photocatalyst, the tri-arm CdS/ZnS core-shell nanorod, is carefully designed for the first time, where triarm CdS nanorods are decorated by dodecylamine (DDA) molecules and then wrapped in an intermittent ZnS shell. The resultant photocatalyst with a CdS/ZnS mole ratio of 0.5 (CZS0.5) presents a significantly improved H2 evolution rate of 726.0 mu mol/h (3 mg of catalysts, equal to 242.0 mmol/g/h) in the absence of co-catalysts, which is currently the highest value in CdS-based catalysts. The apparent quantum efficiency of CZS0.5 reaches 50.61% at 380 nm. The significantly enhanced photocatalytic performance can be attributed to a win-win situation between the analogous type-II mechanism formed in the CdS/ZnS heterojunction and the H+ adsorption resulting from the DDA molecules. Due to the analogous type-II mechanism, photogenerated electrons are transferred from the ZnS shell to the CdS nanorod. Owing to the decoration of DDA, many H+ ions are adsorbed on CdS. Thus, the photogenerated electrons gathered in CdS can be captured quickly and in a timely manner by the adsorbed proton H+ to produce hydrogen, which effectively suppresses the recombination of photogenerated electrons and holes. This study may bring new insights for developing other photocatalysts with high performance by using small organic molecules.
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页数:10
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