Abstract
The redox processes of the [Fe(CN) 6] 3− 4− couple mediated by polyaniline films were studied by steady-state, ac and EHD impedance methods. At pH < 1, charging and discharging of the polymer capacitance in parallel with the faradaic impedance of the substrate reaction, occurring at the polymer-electrolyte interface, are the processes which determine the transient behaviour. Neither the charge transport across the film nor the charge-transfer kinetics of either the substrate or the polymer are experimentally accessible. At less acidic pHs (~ 3), a low frequency phenomenon detected in EHD experiments seems to be associated with surface protonation equilibria.
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