Electrochemical investigation of traps in a nanostructured TiO2 film

被引:171
作者
Wang, HL [1 ]
He, JJ [1 ]
Boschloo, G [1 ]
Lindström, H [1 ]
Hagfeldt, A [1 ]
Lindquist, SE [1 ]
机构
[1] Univ Uppsala, Dept Chem Phys, S-75121 Uppsala, Sweden
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2001年 / 105卷 / 13期
关键词
D O I
10.1021/jp0036083
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
Electron traps at the nanostructured TiO2 (anatase)/aqueous electrolyte interface have been studied by means of electrochemical methods. The transient current decays at different potentials positive of the flat band potential clearly illustrate the trap-filling process. The more negative the potential, the shorter the trap-filling period. It is found that most traps locate positive of -0.9 V vs Ag/AgCl at pH 13, or positive of -0.3 V vs Ag/AgCl at pH 4.7. It is proposed that the trap distribution as a function of potential is directly proportional to dQ/dU, i.e., to the current density in a linear sweep voltammetry experiment. The trap densities in aqueous electrolytes are estimated to be 4 x 10(11) cm(-2) (microscopic area) at pH 4.7 and 5 x 10(13) cm(-2) (microscopic area) at pH 13. The pH dependency of the trap density indicates that traps investigated are surface-related.
引用
收藏
页码:2529 / 2533
页数:5
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