Preparation and characterization of Pd/N codoped TiO2 photocatalysts with high visible light photocatalytic activity

被引:13
|
作者
Yu Xinluan [1 ]
Wang Yan [1 ]
Meng Xiangjiang [1 ]
Yang Jianjun [1 ]
机构
[1] Henan Univ, Minist Educ, Key Lab Special Funct Mat, Kaifeng 475004, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Titanium dioxide; Nanotubular titanic acid; Palladium and nitrogen codoping; Oxygen vacancy; Visible light photocatalysis; DOPED TITANIUM-DIOXIDE; OXIDATION; PHOTODEGRADATION; PHOTOREACTIVITY; DEGRADATION; MORPHOLOGY; N-TIO2; STATE;
D O I
10.1016/S1872-2067(12)60597-X
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Pd/N codoped TiO2 photocatalysts were prepared by annealing nanotubular titanic acid, uniformly dispersed urea, and palladium chloride in air or nitrogen atmosphere. The resultant photocatalysts were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, and electron spin resonance spectroscopy. The results showed that the calcination atmosphere played an important role in the morphology, crystal structure, spectral absorption, oxygen vacancy concentration, and visible light photocatalytic performance of the catalysts. The photocatalytic performance of samples calcined in an air atmosphere was better than those calcined in a nitrogen atmosphere. The visible light photocatalytic activity of the samples was investigated by monitoring the photocatalytic oxidation of propylene. It was found that the samples prepared at 400 degrees C in air possessed the highest photocatalytic activity under visible light irradiation (lambda >= 420 nm). The mechanism of the visible light response of the Pd/N codoped TiO2 photocatalysts was discussed in depth, and the origin of the visible light photocatalytic activity was attributed to both the elemental Pt/N dopants and the existence of oxygen vacancies. (C) 2013, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1418 / 1428
页数:11
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