Electrochromic properties of conducting polyanilines
- 14 November 1989
- journal article
- Published by IOP Publishing in Journal of Physics D: Applied Physics
- Vol. 22 (11) , 1598-1603
- https://doi.org/10.1088/0022-3727/22/11/005
Abstract
A study has been made of the electrochromic behaviour of polyaniline films of potential use in passive display devices, and a preliminary examination of the properties of substituted polyanilines has also been carried out. Films of 'emeraldine-type' conducting polyanilines have been grown electrochemically from aqueous solutions onto glass substrates coated with gold or indium tin oxide. The authors have studied the electrochemistry of their redox reactions in acidic media to examine the kinetics and reversibility. Cyclic voltammetry was used to determine the electrode potentials for growth and redox switching and to obtain information on the electrode kinetics. The effect of electrode potential on the optical absorption spectra was observed, and was found to be consistent with polaron and bipolaron formation. The electrochromic colour contrast and switching times were measured as a function of pH; the requirements were somewhat conflicting, but a satisfactory compromise could be obtained around pH=0. By switching the electrodes over a constant potential step but from a variety of starting potentials, the influence on switching times of the initial oxidation state, and hence of the film conductivity, was investigated. Under suitable circumstances electronic conductivity, ionic transport or interfacial charge-transfer can limit the switching speed, but response times (for 50% transmission change) as short as 15 ms have been obtained without full optimisation. Of the numerous substituted polyanilines tried, only simple alkyl and alkoxy derivatives formed good polymeric films, and only the 2-ethoxy and 2-methoxy polymers gave good electrochromic behaviour. Switching times for these two were very fast, being less than 2.5 ms for both oxidising and reducing potential changes.Keywords
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