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A stable electrochemically active copper interface for room-temperature ionic liquidvia surface modification to a metal–organic charge-transfer complex
Yuki Hanyu,Itaru Honma
Journal of Materials Chemistry Pub Date : 05/25/2011 00:00:00 , DOI:10.1039/C1JM00026H
Abstract

A novel electrochemical interface between metal electrode and room-temperature ionic liquid (RTIL) was prepared by a procedurally facile method. A morphologically uniform and stable metal–quinone charge-transfer complex film of copper-2,3-dicyano-5,6-dichloro-1,4-benzo-quinone (Cu-DDQ) was found to possess lithium active interface against 1-ethyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl] imide ([EMIm][Tf2N]), an RTIL. The cyclic voltammetry of the film showed reversible ionic charge transfers occurring across the interface. The electrochemical impedance spectroscopy indicated that the interfacial impedance may become as low as ∼1000 Ω cm−2. The bias-induced reversible transport of lithium ion was further confirmed by the XPS method. These results suggest that metal–organic CT complex salts prepared on metal electrodes by a simple surface modification may become an excellent electrochemically active interface with RTIL.

Graphical abstract: A stable electrochemically active copper interface for room-temperature ionic liquid via surface modification to a metal–organic charge-transfer complex
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