Electrochemical impedance spectroscopy measurements on time-variant systems: the case of the Volmer-Heyrovský corrosion reaction. Part I: theoretical description

Abstract

One of the theoretical requirements of electrochemical impedance spectroscopy measure­ments is that the studied system should not be varying with time. Unfortunately, this is rarely the case of physical systems. In the literature, quite a few methods exist to check and correct a posteriori the effect of time-variance, allowing to use conventional equivalent circuit models to fit and interpret the data. We suggest a different approach where, for a given electro­chemical mechanism and specific experimental conditions, assuming stationarity during each measurement, a time- and frequency-dependent expression of the Faradaic impe­dance is derived from the kinetic equations. The case of a potential relaxation at zero current following an anodic steady-state polarization is considered for a system where a Volmer-Heyrovský corrosion mechanism is supposed to take place.

Keywords

• EIS
• non-stationarity
• Faradaic
• relaxation
• potential decay
• adsorption