The photodynamics of the [Ru(bpy)3]2+ ion dopant in a solvent exposed silica sol-gel thin film

The [Ru(bpy)(3)]2(+) ion was encapsulated in a silica based sol-gel thin film, and the luminescence decay time constant of the photo-excited (MLCT)-M-3 (metal-ligand-charge-transfer) was examined when this thin film was immersed in water, methanol, ethanol, 2-propanol, and glycerol. The luminescence decays of the films in the methanol, 2-propanol, and glycerol were better explained by a KWW model, while the luminescence decay of film immersed in water and ethanol were both well explained by a single exponential decay. Intriguingly, the dynamics of the dopants immersed in water, ethanol as well as in sol-gel bulk deviated from a single exponential fit and began to better explained by the the KWW model as temperature increased. The energy gap, Delta E(sol-gel film) and Delta E(solution), between the lowest (MLCT)-M-3 state and atom localized (3)dd state for dopants under the presence of all solvents tested in this study were extracted from the temperature dependence study of the luminescence decay time constant. Generally, the Delta E(sol-gel film) values of ethanol and water were reduced from Delta E(solution), and Delta E(sol-gel film) value in all solvents matched the value of Delta E for sol-gel bulk. The effect on the dynamics in solvent over three weeks was investigated, and the films immersed in water presented the most remarkable monotonic increase in relaxation rates finally approaching the asymptotic value observed in the water solution. This phenomenon was considered to correspond to a trapping environment change due to a hydrophilic interaction through sequential intrusion of water or ethanol solvent into sol-gel pores.