Excimer laser processing as a tool for photocatalytic design of sol-gel TiO2 thin films

被引:16
|
作者
Starbova, K. [1 ]
Yordanova, V. [1 ]
Nihtianova, D. [2 ]
Hintz, W. [3 ]
Tomas, J. [3 ]
Starbov, N. [1 ]
机构
[1] Bulgarian Acad Sci, Cent Lab Photoproc, BU-1113 Sofia, Bulgaria
[2] Bulgarian Acad Sci, Cent Lab Mineral & Crystallog, BU-1113 Sofia, Bulgaria
[3] Otto VonGuericke Univ Magdegurg, Mech Proc Engn Dept, D-39106 Magdeburg, Germany
关键词
Titania; sol-gel; thin films; laser modification; phase transitions; photocatalysis;
D O I
10.1016/j.apsusc.2007.12.036
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
Nanostructured sol-gel TiO2 thin films spin coated on silicate glass plates are subjected to excimer (KrF*) pulsed laser irradiation in order to tailor their structure and photocatalytic properties. The surface morphology of virgin and laser-processed films are followed applying electron optical imaging and atomic force microscopy. The evolution of the surface roughness and pore formation are shown to be accompanied by optical absorption edge shift to infrared wavelength range. Conventional X-ray diffraction analysis and high-resolution transmission electron imaging are applied in order to obtain information on the phase composition. Co-existence of amorphous and anatase TiO2 phases in nonirradiated sol-gel films is found. It is established that after laser processing the most intense XRD anatase peak is shifted to lower 2 theta range. The analysis of high-resolution transmission electron images of film profiles evidences for the laser induced phase transitions. Formation of rutile and brookite TiO2 accompanied by evolution of oxygen deficient TinO2n-1 phases are identified in the subsurface region. The contribution of laser processing for increasing the photocatalytic efficiency of laser-modified films toward the oxidation of methylene blue water solution is demonstrated. The results obtained reveal a novel-processing route for designing sol-gel titania films with improved photocatalytical activity. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:4044 / 4051
页数:8
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