Standard

Determination of the charge transfer resistance of poly(3,4-ethylenedioxythiophene)-modified electrodes immediately after overoxidation. / Zalka, D.; Kovács, N.; Szekeres, K.; Ujvári, M.; Vesztergom, S.; Eliseeva, S.; Kondratiev, V.; Láng, G. G.

In: Electrochimica Acta, Vol. 247, 01.09.2017, p. 321-332.

Research output: Contribution to journalArticlepeer-review

Harvard

APA

Vancouver

Author

Zalka, D. ; Kovács, N. ; Szekeres, K. ; Ujvári, M. ; Vesztergom, S. ; Eliseeva, S. ; Kondratiev, V. ; Láng, G. G. / Determination of the charge transfer resistance of poly(3,4-ethylenedioxythiophene)-modified electrodes immediately after overoxidation. In: Electrochimica Acta. 2017 ; Vol. 247. pp. 321-332.

BibTeX

@article{411d362367a54f69ab7f09f7c955d818,
title = "Determination of the charge transfer resistance of poly(3,4-ethylenedioxythiophene)-modified electrodes immediately after overoxidation",
abstract = "Many electrochemical systems are intrinsically nonstationary and are affected by time-dependent phenomena. The requirement of stationarity in the classical version of impedance spectroscopy appears to be in conflict with the essential properties of the object, therefore a post-experimental mathematical/analytical procedure is necessary for the reconstruction of the “true” impedance values. In this study, it has been shown that the 4-dimensional analysis method, originally proposed by Stoynov, can not only be used for the correction of existing (experimentally measured) impedance data, but it also opens up the possibility of the estimation of impedance spectra outside the time interval of the measurements. As an illustrative example the method has been applied for the determination of the charge transfer resistance (Rct) of poly(3,4-ethylenedioxytiophene) (PEDOT) modified electrode as a function of time, including the Rct value corresponding to the time instant just after overoxidation of the polymer film. After the overoxidation the charge transfer resistance decreased continuously with experiment time to a value somewhat higher than the Rct of the pristine electrode. The results imply that a “healing process” may occur at the film/substrate interface. A better understanding of this effect may have an impact on practical applications.",
keywords = "4-dimensional analysis method, charge transfer resistance, instantaneous impedance, non-stationary system, overoxidation of poly(3,4-ethylenedioxytiophene) (PEDOT)",
author = "D. Zalka and N. Kov{\'a}cs and K. Szekeres and M. Ujv{\'a}ri and S. Vesztergom and S. Eliseeva and V. Kondratiev and L{\'a}ng, {G. G.}",
year = "2017",
month = sep,
day = "1",
doi = "10.1016/j.electacta.2017.06.177",
language = "English",
volume = "247",
pages = "321--332",
journal = "Electrochimica Acta",
issn = "0013-4686",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Determination of the charge transfer resistance of poly(3,4-ethylenedioxythiophene)-modified electrodes immediately after overoxidation

AU - Zalka, D.

AU - Kovács, N.

AU - Szekeres, K.

AU - Ujvári, M.

AU - Vesztergom, S.

AU - Eliseeva, S.

AU - Kondratiev, V.

AU - Láng, G. G.

PY - 2017/9/1

Y1 - 2017/9/1

N2 - Many electrochemical systems are intrinsically nonstationary and are affected by time-dependent phenomena. The requirement of stationarity in the classical version of impedance spectroscopy appears to be in conflict with the essential properties of the object, therefore a post-experimental mathematical/analytical procedure is necessary for the reconstruction of the “true” impedance values. In this study, it has been shown that the 4-dimensional analysis method, originally proposed by Stoynov, can not only be used for the correction of existing (experimentally measured) impedance data, but it also opens up the possibility of the estimation of impedance spectra outside the time interval of the measurements. As an illustrative example the method has been applied for the determination of the charge transfer resistance (Rct) of poly(3,4-ethylenedioxytiophene) (PEDOT) modified electrode as a function of time, including the Rct value corresponding to the time instant just after overoxidation of the polymer film. After the overoxidation the charge transfer resistance decreased continuously with experiment time to a value somewhat higher than the Rct of the pristine electrode. The results imply that a “healing process” may occur at the film/substrate interface. A better understanding of this effect may have an impact on practical applications.

AB - Many electrochemical systems are intrinsically nonstationary and are affected by time-dependent phenomena. The requirement of stationarity in the classical version of impedance spectroscopy appears to be in conflict with the essential properties of the object, therefore a post-experimental mathematical/analytical procedure is necessary for the reconstruction of the “true” impedance values. In this study, it has been shown that the 4-dimensional analysis method, originally proposed by Stoynov, can not only be used for the correction of existing (experimentally measured) impedance data, but it also opens up the possibility of the estimation of impedance spectra outside the time interval of the measurements. As an illustrative example the method has been applied for the determination of the charge transfer resistance (Rct) of poly(3,4-ethylenedioxytiophene) (PEDOT) modified electrode as a function of time, including the Rct value corresponding to the time instant just after overoxidation of the polymer film. After the overoxidation the charge transfer resistance decreased continuously with experiment time to a value somewhat higher than the Rct of the pristine electrode. The results imply that a “healing process” may occur at the film/substrate interface. A better understanding of this effect may have an impact on practical applications.

KW - 4-dimensional analysis method

KW - charge transfer resistance

KW - instantaneous impedance

KW - non-stationary system

KW - overoxidation of poly(3,4-ethylenedioxytiophene) (PEDOT)

UR - http://www.scopus.com/inward/record.url?scp=85022323401&partnerID=8YFLogxK

U2 - 10.1016/j.electacta.2017.06.177

DO - 10.1016/j.electacta.2017.06.177

M3 - Article

AN - SCOPUS:85022323401

VL - 247

SP - 321

EP - 332

JO - Electrochimica Acta

JF - Electrochimica Acta

SN - 0013-4686

ER -

ID: 9442693