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Chemical and Photochemical Water Oxidation Mediated by an Efficient Single‐Site Ruthenium Catalyst

Water oxidation is a fundamental step in artificial photosynthesis for solar fuels production. In this study, we report a single‐site Ru‐based water oxidation catalyst, housing a dicarboxylate‐benzimidazole ligand, that mediates both chemical and light‐driven oxidation of water efficiently under neu...

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Detalles Bibliográficos
Autores principales: Abdel‐Magied, Ahmed F., Shatskiy, Andrey, Liao, Rong‐Zhen, Laine, Tanja M., Arafa, Wael A. A., Siegbahn, Per E. M., Kärkäs, Markus D., Åkermark, Björn, Johnston, Eric V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680270/
https://www.ncbi.nlm.nih.gov/pubmed/27966290
http://dx.doi.org/10.1002/cssc.201601171
Descripción
Sumario:Water oxidation is a fundamental step in artificial photosynthesis for solar fuels production. In this study, we report a single‐site Ru‐based water oxidation catalyst, housing a dicarboxylate‐benzimidazole ligand, that mediates both chemical and light‐driven oxidation of water efficiently under neutral conditions. The importance of the incorporation of the negatively charged ligand framework is manifested in the low redox potentials of the developed complex, which allows water oxidation to be driven by the mild one‐electron oxidant [Ru(bpy)(3)](3+) (bpy=2,2’‐bipyridine). Furthermore, combined experimental and DFT studies provide insight into the mechanistic details of the catalytic cycle.