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Interfacial electron transfer at titanium dioxide (Ti(O.sub.2)) is investigated for a series of surface bound ruthenium-polypyridyl dyes. The results and detailed analyses incorporating molecular photophysics and semiconductor density of states measurements indicate that the multiexponential behavior is often observed in interfacial injection studies is not due to sample heterogeneity. This work shows that the kinetic heterogeneity results from competition between excited-state relaxation and injection as the photoexcited dye relaxes through the 3MLCT manifold to the thermally equilibrated state.

The first example of excited state electron transfer from cob(I)alamin is reported herein. Vitamin B12 was anchored to a mesoporous TiO2 thin film and electrochemically reduced to the cob(I)alamin form. Pulsed laser excitation resulted in rapid excited state electron transfer, ket > 108 s-1, followed by microsecond interfacial charge recombination to re-form cob(I)alamin. The supernucleophilic cob(I)alamin was found to be a potent photoreductant. The yield of excited state electron transfer was found to be excitation wavelength dependent. The implications of this dependence are discussed. [ABSTRACT FROM AUTHOR]

The first example of excited state electron transfer from cob(I)alamin is reported herein. Vitamin B12 was anchored to a mesoporous TiO2 thin film and electrochemically reduced to the cob(I)alamin form. Pulsed laser excitation resulted in rapid excited state electron transfer, ket > 108 s-1, followed by microsecond interfacial charge recombination to re-form cob(I)alamin. The supernucleophilic cob(I)alamin was found to be a potent photoreductant. The yield of excited state electron transfer was found to be excitation wavelength dependent. The implications of this dependence are discussed. [ABSTRACT FROM AUTHOR]

Interfacial electron transfer at titanium dioxide (TiO2) is investigated for a series of surface bound ruthenium-polypyridyl dyes whose metal-to-ligand charge-transfer state (MLCT) energetics are tuned through chemical modification. The 12 complexes are of the form RuII(bpy-A)(L)22+, where bpy-A is a bipyridine ligand functionalized with phosphonate groups for surface attachment to TiO2. Functionalization of ancillary bipyridine ligands (L) enables the potential of the excited state RuIII/*couple, E+/*, in 0.1 M perchloric acid (HClO4(aq)) to be tuned from -0.69 to -1.03 V vs NHE. Each dye is excited by a 200 fs pulse of light in the visible region of the spectrum and probed with a time-delayed supercontiuum pulse (350-800 nm). Decay of the MLCT excited-state absorption at 376 nm is observed without loss of the ground-state bleach, which is a clear signature of electron injection and formation of the oxidized dye. The dye-dependent decays are biphasic with time constants in the 3-30 and 30-500 ps range. The slower injection rate constant for each dye is exponentially distributed relative to E+/*. The correlation between the exponentially diminishing density of TiO2 sub-band acceptor levels and injection rate is well described using Marcus-Gerischer theory, with the slower decay components being assigned to injection from the thermally equilibrated state and the faster components corresponding to injection from higher energy states within the 3MLCT manifold. These results and detailed analyses incorporating molecular photophysics and semiconductor density of states measurements indicate that the multiexponential behavior that is often observed in interfacial injection studies is not due to sample heterogeneity. Rather, this work shows that the kinetic heterogeneity results from competition between excited-state relaxation and injection as the photoexcited dye relaxes through the 3MLCT manifold to the thermally equilibrated state, underscoring the potential for a simple kinetic model to reproduce the complex kinetic behavior often observed at the interface of mesoporous metal oxide materials. [ABSTRACT FROM AUTHOR]