Theoretical Discussion of Electron Interfacial Transfer in Semiconductor Heterogeneous Photocatalysis

被引:2
|
作者
Liu, Baoshun [1 ,2 ]
机构
[1] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Hubei Province, Peoples R China
[2] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Hubei Province, Peoples R China
关键词
SENSITIZED SOLAR-CELLS; DIFFUSION LENGTH; KINETIC-MODEL; HOLE TRANSFER; DISSOLVED POLLUTANTS; LIGHT-INTENSITY; TIO2; DEGRADATION; RECOMBINATION; PHOTOOXIDATION;
D O I
10.1149/2.062309jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A theoretical model was established to discuss the interfacial electron transfer in semiconductor heterogeneous photocatalysis. Two possible electron transfer mechanisms were compared: one is that electrons are firstly trapped by surface defects, and then transfer to O-2 (T-T transfer); another is that electrons directly transfer to O-2 from conduction band (CB) (CB-O-2 transfer). The effects of O-2 diffusion, density of electron traps, speed of electron trapping, and speed of interfacial electron transfer on the photocatalysis were studied. Based on the theoretical calculation, the most probable electron transfer was proposed. It was shown that the filling of traps by electrons plays an important role in the T-T electron transfer. For low light intensity, the quantum yield (QY) of photocatalysis is almost independent on light intensity as the electron traps are almost empty; for high light intensity, the QY decreases sharply to zero as all of traps are filled by electrons. The T-T transfer does not accord to experimental results, while the CB-O-2 electron transfer is reasonable. However, the electron trapping by defects must be important as defects are prevalent in photocatalysts, so we proposed that the most probable interfacial electron transfer is dominated by CB-O-2 transfer, but limited by trapping-detrapping through defects. (C) 2013 The Electrochemical Society. All rights reserved.
引用
收藏
页码:H591 / H596
页数:6
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