Development of high efficient visible light-driven N, S-codoped TiO2 nanowires photocatalysts

被引:20
|
作者
Zhang, Yanlin [1 ,2 ,3 ]
Liu, Peihong [1 ]
Wu, Honghai [1 ]
机构
[1] South China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Normal Univ, Key Lab Theoret Chem Environm, Minist Educ, Guangzhou 510006, Guangdong, Peoples R China
[3] South China Normal Univ, Guangdong Technol Res Ctr Ecol Management & Remed, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
关键词
Nanowires; Nitrogen sulfur codoped titania; Visible light irradiation; Quantum efficiency; DOPED TIO2; THIN-FILMS; PHOTODEGRADATION; NANOPARTICLES; DEGRADATION; STABILITY; CATALYSTS; WATER; OXIDE;
D O I
10.1016/j.apsusc.2014.12.043
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
One-dimensional (1D) nanowire material (especially nonmetal doped 1D nanowires) synthesized by a facile way is of great significance and greatly desired as it has higher charge carrier mobility and lower carrier recombination rate. N, S-codoped TiO2 nanowires were synthesized using titanium sulfate as a precursor and isopropanol as a protective capping agent by a hydrothermal route. The obtained doped nanowires were characterized by XRD, SEM, HRTEM, SAED, XPS, BET and UV-vis absorption spectrum. The incorporation of N and S into TiO2 NWs can lead to the expansion of its lattice and remarkably lower its electron-transfer resistance. Photocatalytic activity measurement showed that the N, S-codoped TiO2 nanowires with high quantum efficiency revealed the best photocatalytic performance for atrazine degradation under visible light irradiation compared to N, S-codoped TiO2 nanoparticles and S-doped TiO2 nanowires, which was attributed to (i) the synergistic effect of N and S doping in narrowing the band gap, separating electron-hole pairs and increasing the photoinduced electrons, and (ii) extending the anatase-to-rutile transformation temperature above 600 degrees C. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:335 / 343
页数:9
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