EPR study of the surface characteristics of nanostructured TiO2 under UV irradiation

被引:247
|
作者
Coronado, JM
Maira, AJ
Conesa, JC
Yeung, KL
Augugliaro, V
Soria, J
机构
[1] CSIC, Inst Catalisis & Petr Quim, Madrid 28047, Spain
[2] Hong Kong Univ Sci & Technol, Dept Chem Engn, Kowloon, Hong Kong, Peoples R China
[3] Univ Palermo, Dipartimento Ingn Chim Proc & Mat, I-90128 Palermo, Italy
关键词
D O I
10.1021/la010153f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanostructured TiO2 samples with primary particle size in the 4-20 nm range were prepared by either hydrothermal (H) or thermal (T) treatment of an amorphous precursor, and their behavior under UV illumination at 77 X was studied by means of EPR spectroscopy. The samples of the H series present the smallest crystallite size and after irradiation in a vacuum show some Ti3+ centers. In contrast, under these conditions only weak signals associated with oxygenated radicals are observed for the T samples. However, when oxygen is preadsorbed, several oxygenated complexes (O-, O2-, O2H., and O-3(-)) are photogenerated in proportions that depend on the characteristics of the material. Subsurface O- species are exclusively detected in the case of the samples of the H series, whereas ozonide radicals and surface O- are stabilized on materials with larger crystalline domains. These oxygenated complexes are thermally unstable, and they disappeared after warming to room temperature in the case of the T samples, but they are transformed to O-2(-) on the surface of the hydrothermally treated TiO2. Since adsorbed water and different types of free hydroxyls are present on these materials, as revealed by FTIR, a number of surface reactions have to be considered in order to account for the formation and stability of such photogenerated species.
引用
收藏
页码:5368 / 5374
页数:7
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