Published August 15, 2011 | Version v1
Journal article

Synthesis, characterization and degradation of Bisphenol A using Pr, N co-doped TiO2 with highly visible light activity

  • 1. Department of Physics and Chemistry, Henan Polytechnic University, Henan Jiaozuo 454000 (China)

Description

Praseodymium and nitrogen co-doped titania (Pr/N-TiO2) photocatalysts, which could degrade Bisphenol A (BPA) under visible light irradiation, were prepared by the modified sol-gel process. Tetrabutyl titanate, urea and praseodymium nitrate were used as the sources of titanium, nitrogen and praseodymium, respectively. The resulting materials were investigated by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), UV-vis absorbance spectroscopy, X-ray photoelectron spectroscopy (XPS), N2 adsorption-desorption isotherm and Fourier transform infrared spectra (FTIR). It was found that Pr doping inhibited the growth of crystalline size and the transformation from anatase to rutile. The degradation of BPA under visible light illumination was taken as probe reaction to evaluate the photo-activity of the co-doped photocatalyst. In our experiments, the optimal dopant amount of Pr was 1.2 mol% and the calcination temperature was 500 deg. C for the best photocatalytic activity. Pr/N-TiO2 samples exhibited enhanced visible-light photocatalytic activity compared to N-TiO2, undoped TiO2 and commercial P25. The nitrogen atoms were incorporated into the crystal of titania and could narrow the band gap energy. Pr doping could slow the radiative recombination of photogenerated electrons and holes in TiO2. The improvement of photocatalytic activity was ascribed to the synergistic effects of nitrogen and Pr co-doping.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2011.05.074

Additional details

Identifiers

DOI
10.1016/j.apsusc.2011.05.074;
PII
S0169-4332(11)00776-8;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
257
Journal Issue
21
Journal Page Range
p. 8965-8973
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.