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Interfacial Electron Transfer Dynamics Following Laser Flash Photolysis of [Ru(bpy)(2)((4,4 '-PO3H2)(2)bpy)](2+) in TiO2 Nanoparticle Films in Aqueous Environments
Brennaman, MK., Patrocinio, AOT., Song, WJ., Jurss, JW., Concepcion, JJ., Hoertz, P., Traub, MC., Iha, NYM., & Meyer, TJ. (2011). Interfacial Electron Transfer Dynamics Following Laser Flash Photolysis of [Ru(bpy)(2)((4,4 '-PO3H2)(2)bpy)](2+) in TiO2 Nanoparticle Films in Aqueous Environments. ChemSusChem, 4(2, Sp. Iss S1), 216-227. https://doi.org/10.1002/cssc.201000356
Nanosecond laser flash photolysis has been used to investigate injection and back electron transfer from the complex [(Ru-(bpy)(2)(4,4'-(PO3H2)(2)bpy)](2+) surface-bound to TiO2 (TiO2-Ru-II). The measurements were conducted under conditions appropriate for water oxidation catalysis by known single-site water oxidation catalysts. Systematic variations in average lifetimes for back electron transfer, <tau(bet)> - were observed with changes in pH, surface coverage, incident excitation intensity, and applied bias. The results were qualitatively consistent with a model involving rate-limiting thermal activation of injected electrons from trap sites to the conduction band or shallow trap sites followed by site-to-site hopping and interfacial electron transfer, TiO2(e(-))-Ru3+ -> TiO2-Ru2+. The appearance of pH-dependent decreases in the efficiency of formation of TiO2-Ru3+ and in incident-photon-to-current efficiencies with the added reductive scavenger hydroquinone point to pH-dependent back electron transfer processes on both the sub-nanosecond and millisecond-microsecond time scales, which could be significant in limiting long-term storage of multiple redox equivalents