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Light-Driven Preparation, Microstructure, and Visible-Light Photocatalytic Property of Porous Carbon-Doped TiO2
Author(s) -
Xiaoxin Zou,
Guodong Li,
Jun Zhao,
Juan Su,
Wei Xiao,
Kai Wang,
Yuning Wang,
JieSheng Chen
Publication year - 2012
Publication title -
international journal of photoenergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.426
H-Index - 51
eISSN - 1687-529X
pISSN - 1110-662X
DOI - 10.1155/2012/720183
Subject(s) - photocatalysis , visible spectrum , materials science , x ray photoelectron spectroscopy , photochemistry , diffuse reflectance infrared fourier transform , diffuse reflection , absorption edge , absorption (acoustics) , chemical engineering , porosity , electron paramagnetic resonance , catalysis , chemistry , organic chemistry , composite material , optics , band gap , optoelectronics , nuclear magnetic resonance , engineering , physics
Highly porous carbon-doped TiO2 (C-TiO2) has been prepared, for the first time, through a light-driven approach using crystalline titanium glycolate (TG) as the single-source precursor. Although the nonthermally prepared porous C-TiO2 is amorphous, it shows a remarkable visible-light photocatalytic activity higher than that of nitrogen-doped TiO2 (N-TiO2) due to its significant surface area (530 m2/g) and pore-rich structure. X-ray photoelectron, electron paramagnetic resonance, and UV-Vis diffuse reflectance spectroscopy reveal that the as-prepared porous C-TiO2 photocatalyst contains Ti–O–C bonds which result in visible-light absorption of the material at wavelengths less than 550 nm. Furthermore, it is discovered that the Ti–O–C bonds in the as-prepared C-TiO2 is easily transformed to coke-type species under mild thermal treatment (200°C). The resulting coke-containing porous TiO2 is an even better visible-light photocatalyst, almost twice as effective as N-TiO2, because of its stronger visible-light absorption. The Ti–O–C and the coke-containing porous TiO2 materials follow two different mechanisms in the visible-light photocatalysis process for degradation of methylene blue

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