Electrochemical Impedance Spectroscopy at Redox-Type LiquidlLiquid Interfaces: The Capacitance Lag

被引:4
作者
Akilavasan, Jeganathan [1 ]
Marlow, Frank [1 ,2 ]
机构
[1] MPI Kohlenforsch, D-45470 Mulheim, Germany
[2] Univ Duisburg Essen, Ctr Nanointegrat Duisburg Essen CENIDE, D-47057 Duisburg, Germany
关键词
IMMISCIBLE ELECTROLYTE-SOLUTIONS; DOUBLE-LAYER; ION ADSORPTION; WATER INTERFACE; CHARGE-TRANSFER; NANOPARTICLES;
D O I
10.1021/acs.jpcc.9b10116
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Liquidlliquid interfaces (LLIs) between redox-type electrolytes are investigated with a 2-electrode technique by the subtraction of the volume effects of the adjacent bulk phases and a correction of equipment errors. In this system, the electron transfer through the LLI turns out to overdominate the ion transfer. Surprisingly, no indication for a barrier in the charge transfer was found. The measured resistances assignable to the LLI are extremely low. The efficient charge transfer through the LLI is ascribed to an ionic adsorption layer acting as a buffer for the electrons and opening a new channel for the charge transport. The impedance spectra show a specific peculiarity: a "capacitance lag" at high frequencies. This lag is interpreted using a new model of delayed transport. Microscopically, such a kind of transport is explained with an adsorbed ion layer with variable charge. It acts as a buffer and causes a time delay in the charge transfer.
引用
收藏
页码:4101 / 4108
页数:8
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