Electropolymerization and characterization of COOH-functionalized poly(3,4-ethylenedioxythiophene): Ionic exchanges

► COOH-functionalized EDOT was successfully electropolymerized by different methods. ► Stored specific charges are higher than those stored in PEDOT. ► Both anion and cation ionic exchange are observed by EQCM experiments. ► UV–Vis spectroelectrochemical results are similar to those obtained from PE...

Full description

Saved in:
Bibliographic Details
Published inElectrochimica acta Vol. 56; no. 27; pp. 10238 - 10245
Main Authors Arias-Pardilla, J., Otero, T.F., Yu, Hsiao-hua
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 30.11.2011
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:► COOH-functionalized EDOT was successfully electropolymerized by different methods. ► Stored specific charges are higher than those stored in PEDOT. ► Both anion and cation ionic exchange are observed by EQCM experiments. ► UV–Vis spectroelectrochemical results are similar to those obtained from PEDOT. ► After deep p-dedoping some kind of hysteresis is observed during p-doping. The electropolymerization of COOH-functionalized 3,4-ethylenedioxythipohene was investigated by cyclic voltammetry, by anodic potential steps or by flow of a constant anodic current. Compared with PEDOT, an anodic shift of the oxidation polymerization potential is observed. Nevertheless the polymer film oxidation/reduction is shifted to more cathodic potentials, giving higher stored specific charges than those obtained from PEDOT films generated in similar conditions. The generated polymer shows a stable redox process, E0=−0.04V. EQCM results point to a p-doping process exchanging anions with solution, whereas a second reduction process at −0.77V is related to a p-doping process exchanging cations. The new material is electrochromic: it is colourless in its oxidized state and blue colour in its reduced state. UV–Vis spectroelectrochemical results are similar to those obtained from PEDOT films.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2011.09.020