文献类型：期刊文献

英文题名：Synthesis of visible light-driven Eu, N co-doped TiO2 and the mechanism of the degradation of salicylic acid

作者：Ma, Yunfei[1]; Zhang, Jinlong[1]; Tian, Baozhu[1]; Chen, Feng[1]; Bao, Shenyuan[1]; Anpo, Masakazu[2]

机构：[1] Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China; [2] Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Naka Ku 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan

年份：2012

卷号：38

期号：8

起止页码：1947

外文期刊名：Research on Chemical Intermediates

收录：EI(收录号：20125115817379)

语种：英文

外文关键词：X ray diffraction - Photodegradation - Adsorption - Titanium dioxide - Catalysts - High resolution transmission electron microscopy - Light - Salicylic acid - Europium - X ray photoelectron spectroscopy - Doping (additives) - Photocatalysis - Sodium compounds

摘要：Europium and nitrogen co-doped TiO2 was successfully synthesized by the precipitation-peptization method. The structure and properties of the catalysts were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and UV-vis diffuse reflectance spectra. The photocatalytic efficiency was evaluated by monitoring the photocatalytic degradation of salicylic acid under visible light irradiation. It was verified that TiO2 co-doped with nitrogen and 1% europium showed the highest photocatalytic activity. The adsorption isotherms were obtained by measuring the salicylic acid concentration before and after the dark adsorption at different original solution concentrations. The results illustrated that the doping of Eu was beneficial to the adsorption of salicylic acid. The probable degradation mechanism of salicylic acid was examined by the addition of NaF, Na2S2O3, and K2S2O 8 as the probe molecules. It was verified that salicylic acid was first adsorbed on the surface of the catalysts, followed by the degradation by the photogenerated holes (hvb+). ? Springer Science+Business Media B.V. 2012.