The development of efficient and sustainable electrochemical systems able to provide clean-energy fuels and chemicals is one of the main current challenges of materials science and engineering. Over the last decades, significant advances have been made in the development of robust electrocatalysts for different reactions, with fundamental insights from both computational and experimental work. Some of the most promising systems in the literature are based on expensive and scarce platinum-group metals; however, natural enzymes show the highest per-site catalytic activities, while their active sites are based exclusively on earth-abundant metals.
View Article and Find Full Text PDFUltrathin amorphous silica membranes with embedded organic molecular wires (oligo(-phenylenevinylene), three aryl units) provide chemical separation of incompatible catalytic environments of CO reduction and HO oxidation while maintaining electronic and protonic coupling between them. For an efficient nanoscale artificial photosystem, important performance criteria are high rate and directionality of charge flow. Here, the visible-light-induced charge flow from an anchored Ru bipyridyl light absorber across the silica nanomembrane to CoO water oxidation catalyst is quantitatively evaluated by photocurrent measurements.
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