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- W2740366188 abstract "The visible-light-driven hydrogen evolution reaction (HER) by covalent photosensitizer-catalyst dyads is one of the most elegant concepts in supramolecular homogeneous solar energy conversion. The intricacies of catalyst reactivity and photosensitizer-catalyst interactions require a detailed fundamental understanding of the system to rationalize the observed reactivities. Here, we report three dyads based on the covalent imine-bond linkage of an iridium photosensitizer and an organo-functionalized Anderson polyoxometalate anion [MMo6 O18 {(OCH2 )3 CNH2 }2 ]3- (M=Mn3+ , Fe3+ , Co3+ ). Modification of the central metal ion M is used to modulate the HER activity. Detailed theoretical and experimental studies examine the role of the central metal ion M and provide critical understanding of the redox activity and light-driven HER activity of the novel dyads. Thus, the study enables a knowledge-based optimization of HER dyads by chemical modification of the reactive metal oxide components." @default.
- W2740366188 created "2017-08-08" @default.
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- W2740366188 date "2017-08-30" @default.
- W2740366188 modified "2023-10-17" @default.
- W2740366188 title "Experimental and Theoretical Investigation of the Light-Driven Hydrogen Evolution by Polyoxometalate-Photosensitizer Dyads" @default.
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- W2740366188 doi "https://doi.org/10.1002/chem.201702116" @default.
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