Characterization, activity and kinetics of a visible light driven photocatalyst: Cerium and nitrogen co-doped TiO2 nanoparticles

被引:119
|
作者
Yu, Tao [1 ]
Tan, Xin [1 ,2 ]
Zhao, Lin [1 ]
Yin, Yuxin [2 ]
Chen, Peng [1 ]
Wei, Jing [1 ]
机构
[1] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Chem Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; Cerium doping; Nitrogen doping; Photocatalyst; Visible light; TITANIUM-DIOXIDE PHOTOCATALYSTS; ENHANCED DEGRADATION; OXIDE; IRRADIATION; PERFORMANCE; SOLAR; UV;
D O I
10.1016/j.cej.2009.10.051
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In order to effectively photocatalytically degrade azo dye under solar irradiation, anatase TiO2 that was co-doped with cerium and nitrogen (Ti1-xCexO1-yNy) nanoparticles (NPs) were synthesized using a one-step technique with a modified sol-gel process. The crystal structure and chemical properties were characterized using XRD, BET and XPS. Oxynitride species, Ce4+/Ce3+ pairs, and Ti-O-N and Ti-O-Ce bonds were determined using XPS. The photocatalytic mechanism was investigated through methylene blue (MB) photocatalytic degradation using various filtered wavelengths of light (lambda > 365 nm, lambda > 420 nm, lambda > 500 nm, lambda > 550 nm and lambda > 600 nm) for a period of 10 h. Two experimental parameters were studied systematically, namely the atomic ratio of doped N to Ce and the irradiation wavelength number. The photocatalytic degradation of MB over Ti1-xCexO1-yNy NPs in aqueous suspension was found to follow approximately first-order kinetics according to the Langmuir-Hinshelwood model. The enhanced photocatalytic degradation was attributed to the increased number of photogenerated (OH)-O-center dot radicals. (C) 2009 Elsevier B. V. All rights reserved.
引用
收藏
页码:86 / 92
页数:7
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