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Dynamics of luminescence from Ru(bpy)/sub 3/Cl adsorbed on semiconductor surfaces

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100220a013· OSTI ID:6440474

The dynamic spectroscopic properties of the excited state of Ru(bpy)/sub 3//sup 2 +/ adsorbed on powdered semiconductors (TiO/sub 2/,SnO/sub 2/,SrTiO/sub 3/, and ZrO/sub 2/), a powdered insulator (SiO/sub 2/), and microcrystalline methylviologen chloride have been investigated by using a pulsed dye laser (6 ns, 450 nm) or a YAG laser (25 ps, 530 nm) as an exciting light source. The time-resolved luminescence spectra of Ru(byp)/sub 3//sup 2 +/ adsorbed on oxide semiconductors were found to be classified into two components. One is blue shifted compared with the normal spectrum and originates from the tightly bound Ru(byp)/sub 3//sup 2 +/ whose excited state decays with a lifetime of 12-20 ns depending on the substrate. The short lifetime can be explained by an electron-transfer interaction between the excited Ru(byp)/sub 3//sup 2 +/ and the oxide semiconductor. The other originates from loosely bound Ru(byp)/sub 3//sup 2 +/ whose luminescent state has a longer lifetime (40-3500 ns) than that of the tightly bound RU(byp)/sub 3//sup 2 +/. The excited Ru(byp)/sub 3//sup 2 +/ on microcrystalline methylviologen chloride decays very fast with a lifetime of 3.3 ns, indicating a strong electron-transfer interaction. Hydrogen evolved due to the dye sensitization effect on Ru(byp)/sub 3//sup 2 +/ on TiO/sub 2/, although the efficiency was not good. This is explained by the poor adsorption ability of Ru(byp)/sub 3//sup 2 +/ onto TiO/sub 2/ and by recombination of electrons injected into the conduction band with the oxidized dyes.

Research Organization:
Toho Univ., Chiba-ken, Japan
OSTI ID:
6440474
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 86:23; ISSN JPCHA
Country of Publication:
United States
Language:
English

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