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首页> 外文期刊>Journal of Materials Chemistry: An Interdisciplinary Journal dealing with Synthesis, Structures, Properties and Applications of Materials, Particulary Those Associated with Advanced Technology >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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A stable electrochemically active copper interface for room-temperature ionic liquid via surface modification to a metal-organic charge-transfer complex

机译:通过对金属-有机电荷转移络合物进行表面改性,可为室温离子液体提供稳定的电化学活性铜界面

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摘要

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 l-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.
机译:通过程序上简便的方法制备了金属电极与室温离子液体(RTIL)之间的新型电化学界面。发现具有形态学上稳定的铜-2,3-二氰基-5,6-二氯-1,4-苯并醌(Cu-DDQ)的金属-醌电荷转移复合膜具有针对l-的锂活性界面乙基-3-甲基咪唑鎓双[(三氟甲基)磺酰基]酰亚胺([EMIm] [Tf2N]),RTIL。薄膜的循环伏安法表明,在界面上发生了可逆的离子电荷转移。电化学阻抗谱表明,界面阻抗可能低至〜1000Ωcm〜(-2)。通过XPS方法进一步证实了偏压诱导的锂离子可逆传输。这些结果表明,通过简单的表面修饰在金属电极上制备的金属-有机CT复合盐可能成为与RTIL的优良电化学活性界面。

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