Photoinduced electron transfer reactions of pyranine with benzoquinone and titanium dioxide

被引:4
作者
Kathiravan, A. [1 ]
Jhonsi, M. Asha [2 ]
机构
[1] Univ Madras, Natl Ctr Ultrafast Proc, Taramani Campus, Madras 600113, Tamil Nadu, India
[2] BS Abdur Rahman Univ, Dept Chem, Madras 600048, Tamil Nadu, India
关键词
pyranine; fluorescence quenching; PET; benzoquinone; TCSPC; STATE PROTON-TRANSFER; SENSITIZED SOLAR-CELLS; WATER MIXTURES; EMISSION; DYNAMICS; METHANOL; KINETICS; ACETATE;
D O I
10.1002/bio.3113
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The fluorescence quenching of pyranine by benzoquinone in acetonitrile medium was studied using steady-state and time-resolved fluorescence techniques. The quenching process was characterized by a Stern-Volmer plot, which displayed a linear aspect. From the linear plot, the bimolecular quenching rate constant was obtained. The obtained rate constants are within diffused controlled limits. The results show that benzoquinone can efficiently quench the fluorescence of pyranine with dynamic quenching rate constants in the order of 10(10) M-1 s(-1), suggesting that the pyranine can act as a good electron donor for photoinduced electron transfer in artificial photosynthesis and organic solar cells. In addition, the electron injection dynamics of a pyranine/titanium dioxide semiconductor film was also investigated and electron injection from the excited state pyranine into the conduction band of titanium dioxide is suggested. These preliminary results hold promise for the possibility of using pyranine in dye-sensitized solar cells. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:1344 / 1348
页数:5
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