Controllable incorporation of CdS nanoparticles into TiO2 nanotubes for highly enhancing the photocatalytic response to visible light

被引:22
作者
Wang ChengLin [1 ]
Sun Lan [1 ]
Xie KunPeng [1 ]
Lin ChangJian [1 ,2 ]
机构
[1] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
来源
SCIENCE IN CHINA SERIES B-CHEMISTRY | 2009年 / 52卷 / 12期
基金
中国国家自然科学基金;
关键词
TiO2; nanotube; CdS; photocatalysis; RhB; ALUMINUM-OXIDE TEMPLATES; RHODAMINE-B; ARRAY PHOTOELECTRODES; NANOWIRE ARRAYS; SOLAR-CELLS; AZO-DYE; TITANIUM; FABRICATION; ELECTRODE; DEGRADATION;
D O I
10.1007/s11426-009-0157-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A constant current electrochemical deposition was employed to incorporate CdS nanoparticles into the TiO2 nanotube arrays (TiO2NTs). The size and amount of CdS nanoparticles in TiO2NTs (CdS@TiO2NTs) were controllable via modulating current, deposition time and electrolyte concentration. It was revealed, from the scanning electron microscopy (SEM) images and X-ray photoelectron spectroscopy (XPS) in depth profile, that CdS nanoparticles were filled into TiO2 nanotubes. A shift of the absorption edge toward the visible region under the optimal electrodeposition condition was observed with the diffuse reflectance spectroscopy (DRS). A 5-fold enhancement in the photocurrent spectrum for TiO2NTs was observed and the photocurrent response range was significantly extended into the visible region because of the CdS incorporation. Compared with pure TiO2NTs, under a visible light irradiation, CdS@TiO2NTs exhibited a 3.5-fold improvement of photocatalytic activity, which was demonstrated by the photocatalytic decomposition of Rhodamine B (RhB).
引用
收藏
页码:2148 / 2155
页数:8
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