INIFTA   05425
INSTITUTO DE INVESTIGACIONES FISICO-QUIMICAS TEORICAS Y APLICADAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Effect of the prolonged electrode potential cycling on the impedance response of poly(o-aminophenol) (POAP)
Autor/es:
R. TUCCERI
Lugar:
Sofía
Reunión:
Conferencia; ECIS 2013, 27th Conference of European colloid and Interface Society; 2013
Institución organizadora:
ECIS 2013, 27th Conference of European colloid and Interface Society
Resumen:
Effect of the prolonged
electrode potential cycling on the impedance response of poly(o-aminophenol) (POAP)
film electrodes
Ricardo Tucceri
Instituto de Investigaciones
Fisicoquímicas Teóricas y Aplicadas (INIFTA).
CONICET, Facultad de
Ciencias Exactas, Universidad Nacional de La Plata,
Sucursal 4, Casilla de
Correo 16, (1900) La Plata, Argentina.
corresponding author?s e-mail:
rtucce@gmail.com
The aim of this work
was to study the effect of prolonged potentiodynamic cycling (-0.2 V < E
< 0.5 V vs. SCE) on the conducting properties of poly(o-aminophenol) (POAP)
film electrodes. The Electrochemical Impedance Spectroscopy (EIS) was employed
in this study to obtain dependences of charge-transport parameters on the
degree of deactivation (qcd) of the polymer after prolonged
electrode potential cycling. Impedance diagrams of POAP films were analyzed on
the basis of two different models 1,2. While diffusion coefficients
for electron (De) and ion (Di) transport
decrease, interfacial resistances related to ion (Rif|s) and electron (Rm|f, Ref|s) transfer across the different
interfaces involved in the metal/polymer film/solution system increase as the
degree of deactivation increases. Fig. 1 shows the Rm|f vs. qcd
dependence. The slower electron transport with the increase in the degree of
deactivation was attributed to the increase of the electron hopping distance
between redox sites. Transport parameters, such as, Rif|s and Di, were
associated with proton movements. POAP films maintain their conducting
properties almost unaltered for about 500 potential cycles at a scan rate of
0.010 V s-1. However, a loss of conductivity was observed as the
number of potential cycles was extended beyond 500.
Fig.
1.
Metal-polymer interfacial electron-transfer resistance (Rm/f)
as a function of qcd.
Electrolyte: 0.1 M HClO4 + 0.4 M NaClO4 + 2 x 10-3
M (HQ/Q) solution.
Literature:
1.
Vorotyntsev, M.A., Deslouis, C., Musiani, M.M., Tribollet, B.,
Aoki, K., 1999, Transport across an electroactive polymer film in contact with
media allowing both ionic and electronic interfacial exchange, Electrochim.
Acta, Vol. 44, pp. 2105-2115.
2. Rodríguez Nieto, F.J., Tucceri,
R.I., 1996, The pH effect
on the Charge Transport at Redox
Polymer-Modified Electrodes. An ac Impedance Study applied to Poly (o-aminophenol) Film Electrodes, J. Electroanal. Chem. Vol. 416, pp.
1-24.