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铁多吡啶配合物在水溶液中催化析氢反应。

Hydrogen evolution catalyzed by an iron polypyridyl complex in aqueous solutions.

作者信息

Connor G P, Mayer K J, Tribble C S, McNamara W R

机构信息

Department of Chemistry, College of William and Mary , PO Box 8795, Williamsburg, Virginia 23187-8795, United States.

出版信息

Inorg Chem. 2014 Jun 2;53(11):5408-10. doi: 10.1021/ic500069c. Epub 2014 May 21.

Abstract

Iron complexes containing tetradentate monophenolate ligands have been found to be highly active for the electrocatalytic reduction of protons to hydrogen gas. Catalysis occurs at -1.17 V vs SCE in CH3CN with a turnover frequency of up to 1000 s(-1) and a 660 mV overpotential. Interestingly, the catalyst activity is enhanced in the presence of water, achieving turnover frequencies of 3000 s(-1) with an overpotential of 800 mV, making it one of the most active iron electrocatalysts currently reported. The catalyst is also capable of generating hydrogen from purely aqueous buffer solutions of pH 3-5 with Faradaic efficiencies of 98%.

摘要

已发现含有四齿单酚配体的铁配合物对质子电催化还原为氢气具有高活性。在乙腈中相对于饱和甘汞电极(SCE),催化反应在-1.17 V下发生,周转频率高达1000 s⁻¹,过电位为660 mV。有趣的是,在有水存在的情况下催化剂活性增强,在800 mV过电位下实现了3000 s⁻¹的周转频率,使其成为目前报道的活性最高的铁电催化剂之一。该催化剂还能够从pH为3 - 5的纯水性缓冲溶液中产生氢气,法拉第效率为98%。

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