Spectral dependences of the activity and selectivity of N-doped TiO2 in photodegradation of phenols

被引:21
作者
Emeline, A. V. [1 ,2 ]
Zhang, X. [2 ]
Jin, M. [2 ]
Murakami, T. [2 ]
Fujishima, A. [2 ]
机构
[1] St Petersburg State Univ, VA Fock Inst Phys, Dept Photon, St Petersburg, Russia
[2] Kanagawa Acad Sci & Technol, Kanagawa, Japan
关键词
Photocatalysis; Visible-light photocatalyst; Quantum yield; Selectivity; Doping; GAP METAL-OXIDES; BAND-GAP; TITANIUM-DIOXIDE; PHOTOCHEMICAL PROCESSES; QUANTUM YIELD; PHOTOELECTROCHEMICAL PROPERTIES; PHOTOCATALYTIC DEGRADATION; SURFACE; 4-CHLOROPHENOL; KINETICS;
D O I
10.1016/j.jphotochem.2009.01.001
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
In present study we report the spectral dependencies of the quantum yield of phenol and 4-chlorophenol photodegradation over N-doped TiO2 and the selectivity of the photocatalyst toward formation the major intermediates. Applying the theoretical model developed earlier [A.V. Emeline, V.K. Ryabchuk, N. Serpone, J. Phys. Chem. B. 103 (1999) 1316; AN. Emeline. AN. Frolov, V.K. Ryabchuk, N. Serpone, J. Phys. Chem. B 107 (2003) 7109] for analysis of the experimental spectral dependencies we conclude that extrinsic N-doped induced absorption is formed by overlapping of several single absorption bands, which presumably correspond to different intrinsic defects (color centers) in TiO2 distinguished by different efficiency of photogeneration of charge carriers. It is also inferred that measurement and corresponding analysis of spectral dependencies of the quantum yield and selectivity of heterogeneous photochemical reactions can be considered as a powerful spectroscopic mean to deconvolve the complex non-resolved absorption spectrum of solids. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 19
页数:7
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