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Near-Ohmic Behavior for Conducting Polymers: Extension Beyond PEDOT on Gold-Plated Platinum to Other Polymer-Counterion/Substrate Combinations

Conducting polymers constitute a class of materials for which electrochemical and electron transport properties are a function not only of their chemical identity but also of their complex morphology. In this paper, we investigate and compare the frequency dependence behavior of the impedance of pol...

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Bibliographic Details
Published in:ACS applied materials & interfaces 2012-03, Vol.4 (3), p.1601-1607
Main Authors: Kayinamura, Yohani P, Roberts, Julia H, Rubinson, Judith F
Format: Article
Language:English
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Summary:Conducting polymers constitute a class of materials for which electrochemical and electron transport properties are a function not only of their chemical identity but also of their complex morphology. In this paper, we investigate and compare the frequency dependence behavior of the impedance of poly(3,4-ethylenedioxythiophene), or PEDOT, and that of poly(3,4-ethylenedioxypyrrole), or PEDOP, which are doped with a series of polyatomic anions during electrodeposition. We also contrast the behavior of PEDOT on Pt|Au, Pt, glassy carbon, and gold. Initial results for polycarbazole, PCz, electrodes are, in addition, included. Deposition parameters were adjusted to produce morphologically similar films for PEDOT, PEDOP, and PCz. In doing so, we have been successful in producing frequency-independent impedance behavior similar to that previously reported for PEDOT on Pt|Au. Although the impedance behavior of these polymers appears to be primarily determined by morphological features, the impact of counterion identity (beyond ionic charge transport) is also discussed. These studies suggest that choice of polymer/dopant combination and electrodeposition parameters can be manipulated to tune the impedance characteristics of electrodes, thereby optimizing them for capacitive or faradaic charge injection, or some combination of the two.
ISSN:1944-8244
1944-8252
DOI:10.1021/am2017706