Carbon-Doped TiO<sub>2</sub> and Carbon, Tungsten-Codoped TiO<sub>2</sub> through Sol–Gel Processes in the Presence of Melamine Borate: Reflections through Photocatalysis

Elaine M. Neville(Innovation Cluster (Canada)), Michael J. Mattle, David Loughrey(Innovation Cluster (Canada)), Rajesh Bashyam, Mahfujur Rahman(Innovation Cluster (Canada)), J. M. Don MacElroy(Innovation Cluster (Canada)), James A. Sullivan(Innovation Cluster (Canada)), K. Ravindranathan Thampi
The Journal of Physical Chemistry C
July 13, 2012
Cited by 126Open Access
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Abstract

A series of C-doped, W-doped, and C,W-codoped TiO2 samples have been prepared using modified sol-gel techniques. Reproducible inexpensive C-doping arises from the presence of melamine borate in a sol-gel mixture, whereas W-doping is from the addition of tungstic acid to the sol. The materials have been characterized using elemental analysis, N-2 physisorption (BET), thermogravimetric analysis, X-ray diffraction, Raman, X-ray photoelectron, UV-vis spectroscopies, and photocatalytic activity measurements. Doping C and W independently results in an increased absorbance in the visible region of the spectrum with a synergistic effect in increased absorbance when both elements are codoped. The increased visible-light absorbance of the W-doped or codoped materials is not reflected in photocatalytic activity. Visible-light-induced photocatalytic activity of C-doped material was superior to that of an undoped catalyst, paving the way for its application under only visible-light irradiation conditions. A significant fraction of the spectral red shift commonly observed with doped catalysts might be due to the formation of color centers as a result of defects associated with oxygen vacancies, and bandgap-related narrowing or intragap localization of dopant levels are not the only factors responsible for enhanced visible-light absorption in doped photocatalysts. Furthermore, bandgap narrowing through increases in the energy of the valence band may actually decrease photo-oxidation activity through a curtailment of one route of oxidation.


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