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...
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Published in | Electrochimica acta Vol. 56; no. 27; pp. 10238 - 10245 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
30.11.2011
Elsevier |
Subjects | |
Online Access | Get full text |
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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. |
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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 |