Characterisation and spectral properties of surface adsorbed phenosafranine dye in zeolite-Y and ZSM-5: Photosensitisation of embedded nanoparticles of titanium dioxide

被引:26
作者
Easwaramoorthi, S. [1 ,2 ]
Natarajan, P. [1 ]
机构
[1] Univ Madras, Natl Ctr Ultrafast Proc, Madras 600113, Tamil Nadu, India
[2] Univ Madras, Dept Inorgan Chem, Madras 600025, Tamil Nadu, India
关键词
Phenosafranine; Titanium dioxide in zeolites; Zeolite-Y; ZSM-5; Photosensitisation; CHARGE-TRANSFER; ELECTRON-TRANSFER; INTRAZEOLITE PHOTOCHEMISTRY; PHOTOPHYSICAL PROPERTIES; ORGANIC-MOLECULES; QUANTUM DOTS; TIO2; RU(BPY)(3)(2+); SYSTEMS; 2,4,6-TRIPHENYLPYRYLIUM;
D O I
10.1016/j.micromeso.2008.07.042
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Synthesis, characterisation and photosensitisation of titanium dioxide nanoparticles by phenosafranine dye adsorbed on the external surfaces of microporous materials were carried out. Titanium dioxide nanoparticles were anchored on the external Surface as well as encapsulated in the cavities of porous zeolites. The composite materials are characterized using powder XRD and UV-visible diffuse reflectance spectroscopy. The organic dye phenosafranine is used as visible light absorbing sensitiser. Photosensitisation of the titanium dioxide nanoparticles deposited on the external surface of the microporous silicates are effected by the singlet excited states of phenosafranine and the mechanism of photosensitization is suggested to be static in nature. Photosensitisation of the TiO2 nanoparticles encapsulated in the cavities of the host is more efficient. In the case of the sensitisation of the TiO2 nanoparticles encapsulated inside the zeolite framework, the process is facilitated by the interaction between the host lattice with adsorbed water molecules and the excited state of the dye molecules at the outer surface of the host. The present investigation for the first time reports on the sensitization of TiO2 nanoparticles by the organic dye separated in space by the insulator host material. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:541 / 550
页数:10
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