Abstract
Electrochemical copolymerization of 3-methylpyrrole and N-methylpyrrole perchlorate doped has been carried out at two overpotentials and at different electrodeposition times in acetonitrile medium. A mixture of instantaneous and progressive nucleation mechanisms has been established from the current density–time transients. Doping/dedoping reversibility is deduced from the electrochemical study of copolymer films by cyclic voltammetry. Fourier Transform Infrared spectrum analysis shows that electropolymerization time has a great influence on the random monomers proportion in the copolymer obtained. Although the copolymer conductivity is in the range of the measured for poly 3-methylpyrrole and poly N-methylpyrrole obtained in similar conditions, it remains conductive for a much longer time than the homopolymers.
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