Facile ion-exchange synthesis of urchin-shaped CdS/Bi2S3 heterostructures with enhanced photostability and visible light photocatalytic activity

被引:42
作者
Yan, Yunhui [1 ,2 ]
Zhou, Zhaoxian [3 ]
Li, Wuqi [1 ]
Zhu, Yanjie [1 ]
Cheng, Yun [1 ]
Zhao, Fengying [1 ]
Zhou, Jianguo [1 ]
机构
[1] Henan Normal Univ, Sch Environm, Xinxiang 453007, Henan, Peoples R China
[2] Xinxiang Med Univ, Dept Chem, Xinxiang 453003, Henan, Peoples R China
[3] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
基金
美国国家科学基金会; 高等学校博士学科点专项科研基金;
关键词
HYDROGEN EVOLUTION; HETEROJUNCTION PHOTOCATALYSTS; H-2; EVOLUTION; CDS; PERFORMANCE; NANOCRYSTALS; PHOTOREDUCTION; DEGRADATION; COCATALYSTS; NANOHYBRIDS;
D O I
10.1039/c4ra05655h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Blackberry-like CdS microspheres were synthesized by a facile hydrothermal method. Subsequently, through a simple ion-exchange reaction between the CdS microsphere and Bi(NO3)(3)center dot 5H(2)O, novel urchin-shaped CdS/Bi2S3 core/shell heterostructures have successfully been fabricated. The photocatalytic activity and photostability were evaluated by degradation of rhodamine B (RhB) under visible light irradiation. The results show that the content of Bi2S3 had important effects on the photocatalytic activity, and the CdS/Bi2S3 heterostructures with the theoretical molar ratio of Bi/Cd 0.25 exhibited the best photocatalytic activity. The improved photocatalytic activity and photostability were attributed to the visible light absorption enhanced by Bi2S3 and the formation of a heterojunction between CdS and Bi2S3, which can effectively accelerate the charge separation and transfer corrosive holes from CdS to robust Bi2S3. Experimentally and theoretically, Bi2S3 anchored on CdS acts as a corrosion protection agent for CdS and also acts as a co-catalyst.
引用
收藏
页码:38558 / 38567
页数:10
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