Enhancing photocatalytic activity of Sn doped TiO2 dominated with {105} facets

被引:24
|
作者
Jiang, Hai Bo [1 ]
Xing, Jun [1 ]
Chen, Zu Peng [1 ]
Tian, Feng [2 ]
Cuan, Qian [3 ,4 ]
Gong, Xue-Qing [3 ,4 ]
Yang, Hua Gui [1 ,5 ]
机构
[1] E China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] Shanghai Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai 200093, Peoples R China
[3] E China Univ Sci & Technol, Ctr Computat Chem, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[4] E China Univ Sci & Technol, Res Inst Ind Catalysis, Shanghai 200237, Peoples R China
[5] Griffith Univ, Ctr Clean Environm & Energy, Nathan, Qld 4222, Australia
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
High facets; TiO2; Sn doping; Photocatalyst; First-principle calculations; VISIBLE-LIGHT ABSORPTION; SINGLE-CRYSTALS; PHOTOREACTIVITY; PERCENTAGE; NANOSHEETS; PROPERTY; WATER;
D O I
10.1016/j.cattod.2013.08.027
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Electronic structures of semiconductor photocatalysts control the light absorbance, charge-carrier separation and mobility, activation energy and consequently, photocatalytic activity. Ion doping has been widely used to modify the electronic structure of a semiconductor photocatalyst. Here, we successfully synthesized Sn doped single crystalline anatase TiO2 particles dominated with {1 0 5} facets by a gas phase oxidation process, and their structure and composition were thoroughly analyzed by XRD/TEM/FESEM/XPS. The photoluminescence emission spectra measurements reveal that the small amount of doped Sn in TiO2 could suppress the recombination of photogenerated electron-hole pairs. Thus, the Sn doped TiO2 shows a significantly enhanced photocatalytic hydrogen evolution performance, with its hydrogen generation rate being 4.5 times higher than that of pure TiO2. First-principle simulation results suggest the doped Sn at the edge exhibit higher adsorption energy toward H, which could promote the H-2 generation from the splitting of water. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 23
页数:6
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