skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Preparation N-F-codoped TiO{sub 2} nanorod array by liquid phase deposition as visible light photocatalyst

Journal Article · · Materials Research Bulletin
;  [1];  [1]; ; ; ;  [1]
  1. CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science, and Engineering, University of Science and Technology of China, Hefei, Anhui 230026 (China)

Research highlights: {yields} The formation of N, F-codoped TiO{sub 2} nanorod arrays via the LPD. {yields} Calcination temperature greatly effects the incorporation of N and F into TiO{sub 2}. {yields} TNRAs calcined at 450 {sup o}C showed highest visible light photocatalytic activity. {yields} A synergetic effect of 1D nanorod arrays and appropriate amount of N and F codoping. -- Abstract: An efficient method for the preparation of N-F-codoped visible light active TiO{sub 2} nanorod arrays is reported. In the process, simultaneous nitrogen and fluorine doped TiO{sub 2} nanorod arrays on the glass substrates were achieved by liquid phase deposition method using ZnO nanorod arrays as templates with different calcination temperature. The as-prepared samples were characterized by Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and UV-vis absorption spectra measurements. It was found that calcination temperature is an important factor influencing the microstructure and the amount of N and F in TiO{sub 2} nanorod arrays samples. The visible light photocatalytic properties were investigated using methylene blue (MB) dye as a model system. The results showed that N-F-codoped TiO{sub 2} nanorod arrays sample calcined at 450 {sup o}C demonstrated the best visible light activity in all samples, much higher than that of TiO{sub 2} nanoparticles and P25 particles films.

OSTI ID:
22210012
Journal Information:
Materials Research Bulletin, Vol. 46, Issue 3; Other Information: Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English