Pettit C M, Goonetilleke P C, Sulyma C M, Roy D
Department of Physics, Clarkson University, Potsdam, New York 13699-5820, USA.
Anal Chem. 2006 Jun 1;78(11):3723-9. doi: 10.1021/ac052157l.
The technique of time-resolved impedance spectroscopy can be combined with dc cyclic voltammetry (CV) to study mechanisms and kinetics of electrochemical reactions at solid-liquid interfaces. Utilization of these techniques in a combined framework, however, is based on a number of specific considerations of measurement procedures and data analysis. The present work discusses certain essential elements of this topic, focusing primarily on the analysis of time-resolved impedance spectra where interdependent dc and ac effects of parallel faradaic and nonfaradaic reactions are present under potentiodynamic conditions. A thin gold film is used as a model experimental system where oxidation and reduction of the sample surface is voltage-controlled both in the presence and in the absence of specifically adsorbing Cl- ions in neutral background electrolytes of NaF. Impedance spectra are recorded under transient conditions of CV, and kinetic parameters based on electrode-equivalent circuit models are obtained as functions of CV scans.
时间分辨阻抗谱技术可与直流循环伏安法(CV)相结合,用于研究固液界面电化学反应的机理和动力学。然而,在组合框架中使用这些技术基于测量程序和数据分析的一些特定考虑。本工作讨论了该主题的某些基本要素,主要侧重于对时间分辨阻抗谱的分析,其中在动电位条件下存在平行的法拉第反应和非法拉第反应的相互依存的直流和交流效应。使用薄金膜作为模型实验系统,在NaF中性背景电解质中,无论有无特异性吸附的Cl-离子,样品表面的氧化和还原均由电压控制。在CV的瞬态条件下记录阻抗谱,并获得基于电极等效电路模型的动力学参数作为CV扫描的函数。