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Electrode Kinetics of Ferrocenium/ferrocene in Room-temperature ionic Liquids

机译:室温离子液体中铁核/二茂铁的电极动力学

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The diffusion coefficients and heterogeneous rate constants of ferrocenium/ferrocene ([Fe(Cp){sub}2]{sup}+/Fe(Cp){sub}2) were investigated in order to elucidate the role of solvent dynamics on the electrode kinetics in hydrophobic room-temperature ionic liquids based on bis(trifluoromethylsulfonyl)imide (TFSΓ). The [Fe(Cp){sub}2]{sup}+/Fe(Cp){sub}2 redox reaction was reversible from cyclic voltammetry of a platinum electrode. The diffusion coefficient of Fe(Cp){sub}2 was inversely proportional to the viscosity of the ionic liquid. The diffusion coefficients of [Fe(Cp){sub}2]{sup}+ in the ionic liquids were smaller than those of Fe(Cp){sub}2 because of the Coulombic interaction between charged species and the ionic liquids. The apparent heterogeneous rate constants of [Fe(Cp){sub}2]{sup}+/Fe(Cp){sub}2 estimated by the electrochemical impedance spectroscopy in the ionic liquids were smaller than those in organic solvents. The heterogeneous rate constants correlate with the viscosity of the electrolytes probably due to the slow dynamics of the ions composing the ionic liquids.
机译:研究了亚铁/二茂烯([Fe(CP){Sub} 2] {Sup} + / Fe(Cp){sub} 2)的扩散系数和异质速率常数,以阐明溶剂动力学在电极上的作用基于双(三氟甲基磺酰基)酰亚胺(TFSγ)的疏水室温离子液中的动力学。 [Fe(CP){Sub} 2] {sup} + / fe(cp){sub} 2氧化还原反应由铂电极的循环伏安法可逆。 Fe(Cp){sub} 2的扩散系数与离子液体的粘度成反比。的[Fe(CP){子} 2] {SUP} +在离子液体中的扩散系数较铁(CP){子} 2的因带电物质和离子液体之间的库仑相互作用的小。通过电化学阻抗光谱法在离子液体中估计的[Fe(Cp){sub} 2] {sup} + / fe(cp){sub} 2的表观异质速率常数小于有机溶剂中的电化学阻抗谱估计。由于组成离子液体的离子的缓慢动态,异质速率常数可能与电解质的粘度相关。

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