| Literature DB >> 26423045 |
Serena Berardi1, Laia Francàs1, Sven Neudeck2, Somnath Maji1, Jordi Benet-Buchholz1, Franc Meyer3, Antoni Llobet4,5.
Abstract
Mastering the light-induced four-electron oxidation of water to molecular oxygen is a key step towards the achievement of overall water splitting to produce alternative solar fuels. In this work, we report two rugged molecular pyrazolate-based diruthenium complexes that efficiently catalyze visible-light-driven water oxidation. These complexes were fully characterized both in the solid state (by X-ray diffraction analysis) and in solution (spectroscopically and electrochemically). Benchmark performances for homogeneous oxygen production have been obtained for both catalysts in the presence of a photosensitizer and a sacrificial electron acceptor at pH 7, and a turnover frequency of up to 11.1 s(-1) and a turnover number of 5300 were obtained after three successive catalytic runs. Under the same experimental conditions with the same setup, the pyrazolate-based diruthenium complexes outperform other well-known water oxidation catalysts owing to both electrochemical and mechanistic aspects.Entities:
Keywords: complexes; photosensitizer; redox chemistry; ruthenium; water oxidation
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Year: 2015 PMID: 26423045 DOI: 10.1002/cssc.201500798
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928