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A molecular ruthenium catalyst with water-oxidation activity comparable to that of photosystem II
Stockholm University, Faculty of Science, Department of Organic Chemistry.
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2012 (English)In: Nature Chemistry, ISSN 1755-4330, E-ISSN 1755-4349, Vol. 4, no 5, 418-423 p.Article in journal (Refereed) Published
Abstract [en]

Across chemical disciplines, an interest in developing artificial water splitting to O-2 and H-2, driven by sunlight, has been motivated by the need for practical and environmentally friendly power generation without the consumption of fossil fuels. The central issue in light-driven water splitting is the efficiency of the water oxidation, which in the best-known catalysts falls short of the desired level by approximately two orders of magnitude. Here, we show that it is possible to close that 'two orders of magnitude' gap with a rationally designed molecular catalyst [Ru(bda)(isoq)(2)] (H(2)bda = 2,2'-bipyridine-6,6'-dicarboxylic acid; isoq = isoquinoline). This speeds up the water oxidation to an unprecedentedly high reaction rate with a turnover frequency of >300 s(-1). This value is, for the first time, moderately comparable with the reaction rate of 100-400 s(-1) of the oxygen-evolving complex of photosystem II in vivo.

Place, publisher, year, edition, pages
2012. Vol. 4, no 5, 418-423 p.
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Chemical Sciences
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URN: urn:nbn:se:su:diva-80761DOI: 10.1038/NCHEM.1301ISI: 000303109700018OAI: oai:DiVA.org:su-80761DiVA: diva2:557798
Funder
Knut and Alice Wallenberg FoundationSwedish Research Council
Note

AuthorCount:7;

Available from: 2012-09-29 Created: 2012-09-27 Last updated: 2017-12-07Bibliographically approved

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