Photocatalytic behaviors and structural characterization of nanocrystalline Fe-doped TiO2 synthesized by mechanical alloying

被引:140
作者
Kim, DH
Hong, HS
Kim, SJ
Song, JS
Lee, KS
机构
[1] Hanyang Univ, Div Engn & Mat Sci, Seoul 133171, South Korea
[2] Sejong Univ, Dept Adv Mat Engn, Seoul 143747, South Korea
[3] KERI, Elect & Magnet Devices Grp, Chang Won 641120, South Korea
关键词
titanium dioxide; Fe-doping; photocatalyst; nanocrystalline; mechanical alloying; oxide materials; nanostructured materials;
D O I
10.1016/j.jallcom.2003.11.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanocrystalline Fe-doped TiO2 powders were synthesized by mechanical alloying (MA) with varying Fe contents from 0 up to 4.8 wt.% to shift the absorption threshold into the visible light region. The photocatalytic feasibility of the Fe-doped TiO2 powder was evaluated by quantifying the visible light absorption capacity using ultraviolet and visible (UV-Vis) spectroscopy and photoluminescence spectroscopy. Effects of Fe additions on the crystal structures and the morphologies of the Fe-doped powders were also investigated as a function of the doping content using transmission electron microscopy-electron diffraction pattern (TEM-EDP), X-ray diffraction (XRD) and energy dispersive X-ray (EDAX) and X-ray photoelectron spectroscopy (XPS). The UV-Vis study showed that the UV absorption for the Fe-doped powder moved to a longer wavelength (red shift) and the photoefficiency was enhanced. Based on the analysis of the photoluminescence spectra, the red shift was believed to be induced by localizing the dopant level near the valence band of TiO2. The UV-Vis absorption depended on the Fe concentration. TEM-EDP and XRD investigations showed that the Fe-doped powder had a rutile phase in which the added Fe atoms were dissolved. The rutile phase was composed of spherical particles and chestnut bur shaped particles, resulting in a larger surface area than the spherical P-25 powder. (C) 2003 Elsevier B.V. All rights reserved.
引用
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页码:259 / 264
页数:6
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