Abstract

The luminescence spectra and lifetime of tris(2,2′-bipyridine)ruthenium(II), Ru(bpy)32+, were studied in sol-gel reaction systems of tetramethoxysilane (TMOS) and titanium(IV) isopropoxide (TTIP) with HCl. Luminescence lifetime in the TMOS system increased as the sol-gel reaction proceeded, because diffusion-controlled luminescence quenching such as oxygen and collisional quenching with solvent molecules were suppressed in the rigid matrices. On the other hand, luminescence lifetime in the TTIP system decreased during the sol-gel reaction. The decrease in lifetime was ascribed to electron transfer from photoexcited Ru(bpy)32+ to the conduction band of the TiO2 xerogels. Extended X-ray absorption fine structure (EXAFS) measurements were done to associate lifetime in the Si-Ti xerogels with the structures of Ti4+ sites in the xerogels.

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