锐钛矿
光催化
光降解
煅烧
材料科学
X射线光电子能谱
金红石
甲基橙
漫反射红外傅里叶变换
热重分析
结晶度
核化学
光化学
化学
化学工程
有机化学
催化作用
工程类
复合材料
作者
Jing Bu,Jun Fang,Fucheng Shi,Zhiquan Jiang,Weixin Huang
出处
期刊:Chinese Journal of Chemical Physics
[American Institute of Physics]
日期:2010-02-01
卷期号:23 (1): 95-101
被引量:17
标识
DOI:10.1088/1674-0068/23/01/95-101
摘要
We developed a novel approach for the preparation of N-doped TiO2 photocatalysts by calcining ammonium titanium oxalate at different temperatures. The structures of N-TiO2 were characterized by powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, diffuse reflectance UV-Vis spectroscopy, and scanning electron microscope. The N-doped TiO2 photocatalysts calcined below 700 °C are the pure anatase phase but that calcined at 700 °C is a mixture of anatase and rutile phases. The doped N locates at the interstitial site of TiO2 which leads to the narrowing of bad gap of pure anatase N-TiO2. Among all photocatalysts, N-TiO2 photocatalysts calcined at 600 and 400 °C exhibit the best performance in the photodegradation of methyl orange under the UV light and all-wavelength light illuminations, respectively; however, because of the perfect crystallinity and the existence of anatase-rutile phase junctions, N-TiO2 photocatalyst calcined at 700 °C exhibits the highest specific photodegradation rate, i.e., the highest quantum yield, under both the UV light and all-wavelength light illuminations.
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