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双核钌配合物实现高效光驱动水氧化催化

Efficient Light-Driven Water Oxidation Catalysis by Dinuclear Ruthenium Complexes.

作者信息

Berardi Serena, Francàs Laia, Neudeck Sven, Maji Somnath, Benet-Buchholz Jordi, Meyer Franc, Llobet Antoni

机构信息

Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007, Tarragona, Spain.

Institute of Inorganic Chemistry, Georg-August-University Göttingen, Tammannstraße 4, 37077, Göttingen, Germany.

出版信息

ChemSusChem. 2015 Nov;8(21):3688-96. doi: 10.1002/cssc.201500798. Epub 2015 Oct 1.

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.

摘要

掌握光诱导水四电子氧化生成分子氧是实现整体水分解以生产替代太阳能燃料的关键一步。在这项工作中,我们报道了两种坚固的基于吡唑酸盐的二钌配合物,它们能高效催化可见光驱动的水氧化反应。这些配合物在固态(通过X射线衍射分析)和溶液中(通过光谱和电化学方法)都得到了全面表征。在pH = 7时,在光敏剂和牺牲电子受体存在的情况下,两种催化剂均获得了均相产氧的基准性能,经过三次连续催化运行后,周转频率高达11.1 s⁻¹,周转数达到5300。在相同的实验条件和相同的装置下,基于吡唑酸盐的二钌配合物在电化学和机理方面均优于其他知名的水氧化催化剂。

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