Original scientific paper
https://doi.org/10.5599/jese.508
Electrochemical behaviour of poly(3,4-ethylenedioxytiophene) modified glassy carbon electrodes after overoxidation − the influence of the substrate on the charge transfer resistance
Dora Zalka
; Institute of Chemistry, Laboratory of Electrochemistry and Electroanalytical Chemistry, Eötvös Loránd University, Pázmány P. s. 1/A, H-1117 Budapest, Hungary
Soma Vesztergom
; Institute of Chemistry, Laboratory of Electrochemistry and Electroanalytical Chemistry, Eötvös Loránd University, Pázmány P. s. 1/A, H-1117 Budapest, Hungary
Mária Ujvári
; Institute of Chemistry, Laboratory of Electrochemistry and Electroanalytical Chemistry, Eötvös Loránd University, Pázmány P. s. 1/A, H-1117 Budapest, Hungary
Gyözö G. Láng
; Institute of Chemistry, Laboratory of Electrochemistry and Electroanalytical Chemistry, Eötvös Loránd University, Pázmány P. s. 1/A, H-1117 Budapest, Hungary
Abstract
Time dependence of the electrochemical impedance of an overoxidized glassy carbon|poly(3,4-ethylenedioxytiophene) (PEDOT)|0.1 mol·dm-3 sulfuric acid (aq.) elec-trode has been investigated. To follow the changes occurring at the film/substrate interface after the overoxidation procedure, successive impedance measurements were carried out. Although the system is intrinsically nonstationary, the charge transfer resis-tance (Rct) corresponding to different time instants could be determined by using the so-called 4-dimensional analysis method. The same post-experimental mathematiccal/ana-lytical procedure could be used also for the estimation of the charge transfer resistance corresponding to the time instant just after overoxidation of the PEDOT film. The increase of the charge transfer resistance of the overoxidized system with respect to that of the pristine electrode suggests that during overoxidation the electrochemical activity of the film decreases and the charge transfer process at the metal/film interface beco-mes more hindered. After the overoxidation procedure, when the electrode potential was held in the “stability region” (at E = 0.4 V vs. SSCE in the present case) the Rct decre-ased continuously with experiment time to a value somewhat higher than that of the pristine electrode. By comparing the properties of the GC|PEDOT|0.1 M H2SO4 and the Au|PEDOT|0.1 M H2SO4 electrodes a possible mechanistic explanation for the observed behavior has been proposed. This is based on the assumption that in the case of the GC|PEDOT|0.1 M H2SO4 electrode two processes may occur simultaneously during the impedance measurements: (a) reduction of the oxidized surface of the GC substrate, including the reduction of the oxygen-containing surface functionalities and (b) read-sorption of the polymer chains (polymer chain ends) on the surface.
Keywords
Non-stationary system; 4-dimensional analysis method; substrate-polymer interaction; oxidation of glassy carbon
Hrčak ID:
200266
URI
Publication date:
15.5.2018.
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