Nature Communications · 2016 · 200 citations · 45 references
Natural SciencesChemistryMaterials ScienceCatalysisComputational ChemistrySpectroscopyCatalytic MechanismsLight HarvestingNanostructured Energy MaterialsPhotocatalysisPhotochemical KineticsPhotochemistryCatalytic ActivityElectron TransferHydrogen ProductionMetal-organic Framework PhotocatalystsPalladium CatalystsPhotochemical ReactionsTransient Absorption SpectroscopyUltrafast Spectroscopy
Abstract Photocatalytic water splitting is a natural but challenging chemical way of harnessing renewable solar power to generate clean hydrogen energy. Here we report a potential hydrogen-evolving photochemical molecular device based on a self-assembled ruthenium–palladium heterometallic coordination cage, incorporating multiple photo- and catalytic metal centres. The photophysical properties are investigated by absorption/emission spectroscopy, electrochemical measurements and preliminary DFT calculations and the stepwise electron transfer processes from ruthenium-photocentres to catalytic palladium-centres is probed by ultrafast transient absorption spectroscopy. The photocatalytic hydrogen production assessments reveal an initial reaction rate of 380 μmol h −1 and a turnover number of 635 after 48 h. The efficient hydrogen production may derive from the directional electron transfers through multiple channels owing to proper organization of the photo- and catalytic multi-units within the octahedral cage, which may open a new door to design photochemical molecular devices with well-organized metallosupramolecules for homogenous photocatalytic applications.
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Hydrogen Evolution Catalyzed by Cobaloximes
Jillian L. Dempsey, Bruce S. Brunschwig, Jay R. Winkler et al. · Accounts of Chemical Research · 2009 · 1.1K citations · Full text
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