Abstract

Electrochemical polymerization of aniline was conducted in constant current mode at different pH ranging from 0.2 to 3.7 in an ITO glass electrode-quartz cell assembly for in situ monitoring of the changes in potential, amount of charge passed through, and u.v.-visible absorption (u.v.-Vis) spectra during polymerization. u.v.-Vis spectra of product polyaniline (PAn) films were determined in different pH solutions to evaluate the apparent acid dissociation constants (p Ka) app from plots of log{ (Abs HAX − Abs obs ) (Abs obs − Abs A ) versus pH, where Abs obs, Abs HAX, and Abs A are the observed absorption strength and those of the fully protonated and deprotonated species, respectively, for a given wavelength light. In PAn films prepared at low pH (< 1.0), emeraldine form PAn chains with relatively long average conjugation length but broad distribution were produced, while in those prepared at high pH (> 1.5), PAn chains with short conjugation length were produced and later deteriorated as the polymerization proceeded, because the polymerization potential eventually exceeded a critical value (+ 0.8 V) beyond which degradation of produced PAn chains took place.

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