Parameters affecting electron transfer dynamics from semiconductors to molecular catalysts for the photochemical reduction of protons

The aim of this work is to use transient absorption spectroscopy to study the parameters affecting the kinetics and efficiency of electron transfer in a photocatalytic system for water reduction based on a cobalt proton reduction catalyst (CoP) adsorbed on a nanocrystalline TiO2 film. In the first approach, water is used as the proton and electron source and H-2 is generated after band gap excitation of TiO2 functionalised with CoP. The second system involves the use of a sacrificial electron donor to regenerate the TiO2/CoP system in water at neutral pH. The third system consists of CoP/TiO2 films co-sensitised with a ruthenium-based dye (RuP). In particular, we focus on the study of different parameters that affect the kinetics of electron transfer from the semiconductor to the molecular catalyst by monitoring the lifetime of charge carriers in TiO2. We observe that low catalyst loadings onto the surface of TiO2, high excitation light intensities and small driving forces strongly slow down the kinetics and/or reduce the efficiency of the electron transfer at the interface. We conclude that the first reduction of the catalyst from Co-III to Co-II can proceed efficiently even in the absence of an added hole scavenger at sufficiently high catalyst coverages and low excitation densities. In contrast, the second reduction from Co-II to Co-I, which is required for hydrogen evolution, appears to be at least 10(5) slower, suggesting it requires efficient hole scavenging and almost complete reduction of all the adsorbed CoP to Co-II. Dye sensitisation enables visible light photoactivity, although this is partly offset by slower, and less efficient, hole scavenging.