Slow cation transfer follows sensitizer regeneration at anatase TiO2 interfaces

被引:52
作者
Staniszewski, Aaron [3 ,4 ]
Ardo, Shane [3 ,4 ]
Sun, Yali [1 ,2 ]
Castellano, Felix N. [1 ,2 ]
Meyer, Gerald J. [3 ,4 ]
机构
[1] Bowling Green State Univ, Dept Chem, Bowling Green, OH 43403 USA
[2] Bowling Green State Univ, Ctr Photochem Sci, Bowling Green, OH 43403 USA
[3] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
基金
美国国家科学基金会;
关键词
D O I
10.1021/ja803668z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
After rapid photoinduced electron injection into TiO(2) and regeneration by a donor, D, such as iodide or phenothiazine, sensitizers are present in an environment distinctly different from that prior to light absorption. Significantly, the absorption spectrum of the Ru(II) sensitizer in this new environment is one that is known to be less favorable for excited-state electron injection. The transient absorption features were found to report on photoinduced variations in the local electronic environment of the Ru(II) sensitizer-TiO(2) interface that were induced by ion transfer. The data demonstrate that slow (mu s to ms) cation transfer follows regeneration to yield the sensitizer that was initially photoexcited.
引用
收藏
页码:11586 / +
页数:3
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