期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 694, 期 17, 页码 2808-2813出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2009.02.003
关键词
Hydrogen; Redox; Cluster; Rhodium; Hydrides; Electrochemistry
资金
- EPSRC
- Universities of Bath and Oxford
- EPSRC [EP/F006675/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/F006675/1] Funding Source: researchfish
Water-insoluble phosphine-surface-stabilised rhodium clusters [Rh-6(PR3)(6)H-12][BAr4F](2) (R = cyclohexyl, Ar-F = (3,5-CF3)(2)C6H3) can be immobilised onto suitable glassy carbon, graphite, or tin-doped indium oxide (ITO) electrode surfaces. When immersed into alcohol/aqueous electrolyte media, they display stable voltammetric responses consistent with the formation of organic microdroplet vertical bar aqueous electrolyte two-phase conditions which are similar to those observed in corresponding anhydrous (CH2Cl2) solution phase. This results in an electrode surface that is straightforwardly modified with cluster materials that can uptake or release dihydrogen depending on their redox-state. The results presented herein lead to a slight re-evaluation of the originally reported hydrogen store and release cycle for this system. (C) 2009 Elsevier B.V. All rights reserved.
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