Luminescence-based assessment of thermodynamic constants for electrostatic binding of non-luminescent dyes and atomic ions to colloidal semiconductor surfaces

被引:15
作者
Dang, XJ [1 ]
Hupp, JT [1 ]
机构
[1] Northwestern Univ, Dept Chem, Ctr Nanofabricat & Mol Self Assembly, Evanston, IL 60208 USA
关键词
binding constant; electrostatic binding; semiconductor surface;
D O I
10.1016/S1010-6030(01)00484-1
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
Steady-state and time-resolved luminescence experiments were employed to study the electrostatic interaction of cationic photosensitizers and negatively charged colloidal semiconductor particles. Electrostatic adsorption of efficient photosensitizers on semiconductor surfaces is known to quench the photosensitizers' luminescence. By monitoring the quenching, either directly or competitively, thermodynamic constants for binding of both luminescent and non-luminescent ruthenium and osmium. complexes to negatively charged SnO2 Particle have been determined. The function of atomic cations, such as Li+, Na+ and K+, in controlling the binding of cationic dyes to colloidal SnO2 has also been studied via competitive luminescence. From the study, semiconductor surface binding constants for these species have also been determined. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:251 / 256
页数:6
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