TY - JOUR
T1 - Electrochemical polymerization, characterization and in-situ conductivity studies of poly-3,4-ortho-xylendioxythiophene (PXDOT)
AU - Salinas, Gerardo
AU - Del-Oso, José Alfredo
AU - Espinoza-Montero, Patricio Javier
AU - Heinze, Jürgen
AU - Frontana-Uribe, Bernardo A.
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/11
Y1 - 2018/11
N2 - The electrochemical polymerization of 3,4-ortho-xylendioxythiophene (XDOT) in acetonitrile on Pt electrode let to obtain stable and well-adhered conducting polymer films. The voltamperometric response of the poly-3,4-ortho-xylendioxythiophene (PXDOT) showed a mirror-image, indicating fast electron transfer (ΔEp = 60 mV), which is a rare phenomenon in thick layers of conducting polymers. The in-situ electrochemical conductance experiments showed that the maximal conductance for PXDOT is reached at lower potentials and with less hysteresis than the observed for PEDOT, confirming a fast electrochemical response of the polymer. This behavior could be attributed to the presence of the xylen-unit attached to the polymer chain, which generates an internal order on the oligomeric chains, forming channels that facilitate the mobility of the electrolyte ions during the charge/discharge processes. Additionally, PXDOT showed an irreversible cathodic process which does not correspond to an n-doping, nevertheless induce a polymer internal rearrangement, which causes a major change in the p-doping signal. This cathodic process thus, it was attributed to the reduction of intrachain charge-trapped that was produced during electropolymerization.
AB - The electrochemical polymerization of 3,4-ortho-xylendioxythiophene (XDOT) in acetonitrile on Pt electrode let to obtain stable and well-adhered conducting polymer films. The voltamperometric response of the poly-3,4-ortho-xylendioxythiophene (PXDOT) showed a mirror-image, indicating fast electron transfer (ΔEp = 60 mV), which is a rare phenomenon in thick layers of conducting polymers. The in-situ electrochemical conductance experiments showed that the maximal conductance for PXDOT is reached at lower potentials and with less hysteresis than the observed for PEDOT, confirming a fast electrochemical response of the polymer. This behavior could be attributed to the presence of the xylen-unit attached to the polymer chain, which generates an internal order on the oligomeric chains, forming channels that facilitate the mobility of the electrolyte ions during the charge/discharge processes. Additionally, PXDOT showed an irreversible cathodic process which does not correspond to an n-doping, nevertheless induce a polymer internal rearrangement, which causes a major change in the p-doping signal. This cathodic process thus, it was attributed to the reduction of intrachain charge-trapped that was produced during electropolymerization.
KW - 3, 4-dialkoxythiophenes
KW - Charge trapping
KW - Conducting polymers
KW - In-situ conductance-electrochemical analysis
KW - σ-dimers
UR - http://www.scopus.com/inward/record.url?scp=85052753739&partnerID=8YFLogxK
U2 - 10.1016/j.synthmet.2018.08.020
DO - 10.1016/j.synthmet.2018.08.020
M3 - Article
AN - SCOPUS:85052753739
SN - 0379-6779
VL - 245
SP - 135
EP - 143
JO - Synthetic Metals
JF - Synthetic Metals
ER -