Photodriven hydrogen evolution by molecular catalysts using Al(2)O(3)-protected perylene-3,4-dicarboximide on NiO electrodes

The design of efficient hydrogen-evolving photocathodes for dye-sensitized photoelectrochemical cells (DSPECs) requires the incorporation of molecular light absorbing chromophores that are capable of delivering reducing equivalents to molecular proton reduction catalysts at rates exceeding those of charge recombination events. Here, we report the functionalization and kinetic analysis of a nanostructured NiO electrode with a modified perylene-3,4-dicarboximide chromophore (PMI) that is stabilized against degradation by atomic layer deposition (ALD) of thick insulating Al(2)O(3) layers. Following photoinduced charge injection into NiO in high yield, films with Al(2)O(3) layers demonstrate longer charge separated lifetimes as characterized via femtosecond transient absorption spectroscopy and photoelectrochemical techniques. The photoelectrochemical behavior of the electrodes in the presence of Co(ii) and Ni(ii) molecular proton reduction catalysts is examined, revealing reduction of both catalysts. Under prolonged irradiation, evolved H(2) is directly observed by gas chromatography supporting the applicability of PMI embedded in Al(2)O(3) as a photocathode architecture in DSPECs.