Near-IR transient absorption study on ultrafast electron-injection dynamics from a Ru-complex dye into nanocrystalline In2O3 thin films:: Comparison with SnO2,ZnO, and TiO2 films

被引:32
作者
Furube, Akihiro [1 ]
Murai, Miki [1 ]
Watanabe, Sadayuki [1 ]
Hara, Kohjiro [1 ]
Katoh, Ryuzi [1 ]
Tachiya, M. [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan
关键词
transient absorption; electron injection; ultrafast spectroscopy; dye-sensitized semiconductor film; In2O3;
D O I
10.1016/j.jphotochem.2006.05.026
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
We investigated the dynamics of photoinduced ultrafast electron injection from the excited state of cis-di(thiocyanato)bis(2,2'-bipyridyl-4,4'dicarboxylate)ruthenium(II) (N3 dye) into the conduction band of nanocrystalline In2O3 films by measuring transient absorption of N3-sensitized In2O3 films in the wavelength region from 600 nm to 4 mu m at 100-250-fs temporal resolutions, and the results were compared with those for N3-sensitized nanocrystalline ZnO, SnO2, and TiO2 films. Although the reaction kinetics could not be simply described by a single exponential function and the near-IR transient absorption spectral shapes were dependent on the environmental conditions, the predominant injection time for the In2O3 films was 5-10ps. The SnO2 and In2O3 films showed similar injection dynamics, and the injection times for these films were much shorter than the 150-ps injection time reported for ZnO films. The predominant injection time for the TiO2 film was within 100 fs, which is in agreement with reported values. The differences in the injection times are qualitatively explained in terms of the density of acceptor states in the conduction bands at the LUMO level of N3 dye. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
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