Metadata of CSIR Papers
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Creator |
Kar, P
Verma, S Sen, A Das, A Ganguly, B Ghosh, HN |
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Subject |
Chemistry
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Description |
We have synthesized a new photoactive ruthenium(II) complex having a pendant catechol functionality (K(2)[Ru(CN)(4)(L)] (1) (L is 4-[2-(4'-methyl-2,2'-bipyndinyl-4-yl)vinyl]benzene-1,2-diol) for studying the dynamics of the interfacial electron transfer between nanoparticulate TiO(2) and the photoexcited states of this Ru(II) complex using femtosecond transient absorption spectroscopy. Steady-state absorption and emission studies revealed that the complex 1 showed a strong solvatochromic behavior in solvents or solvent mixtures of varying polanty. Our steady-state absorption studies further revealed that 1 is bound to TiO(2) surfaces through the catechol functionality, though 1 has two different types of functionalities (catecholate and cyanato) for binding to TiO(2) surfaces The longer wavelength absorption band tail for 1, bound to TiO(2) through the proposed catecholate functionality, could also be explained on the basis of the DFT calculations Dynamics of the interfacial electron transfer between 1 and TiO(2) nanoparticles was investigated by studying kinetics at various wavelengths in the visible and near-infrared region Electron injection to the conduction band of the nanoparticulate TiO(2) was confirmed by detection of the conduction band electron in TiO(2) ([e(-)](TiO2)(CB)) and cation radical of the adsorbed dye (1(.+)) in real time as monitored by transient absorption spectroscopy A single exponential and pulse-width limited (<100 fs) electron injection was observed Back electron transfer dynamics was determined by monitoring the decay kinetics of 1(.+) and [e(-)](TiO2)(CB) This is the first report on ultrafast ET dynamics on TiO(2) nanoparticle surface using a solvatochromic sensitizer molecule.
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Publisher |
AMER CHEMICAL SOCWASHINGTON1155 16TH ST, NW, WASHINGTON, DC 20036 USA
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Date |
2011-09-20T12:03:17Z
2011-09-20T12:03:17Z 2010 |
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Type |
Article
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Identifier |
INORGANIC CHEMISTRY
0020-1669 http://hdl.handle.net/123456789/12261 |
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Language |
English
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