Abstract
In this work, we provide electrochemical and spectroscopic evidence of the conducting polymer-heavy metal ion interaction by comparing the electrochemical and spectroscopic behavior (FTIR) of two different conducting polymer-modified electrodes based on 3,4-alkoxythiophenes: 3,4-ethylenedioxythiophene (EDOT) and ortho-xylen-3,4-dioxythiophene (XDOT) during the potentiodynamic stripping of copper. By analyzing the electrochemical and spectroscopic results, it is possible to propose two different copper dissolution processes during the electrochemical stripping process, which depend on the conducting polymer used. With PEDOT matrix, stripping occurs in a two-step pathway, observed as two anodic peaks, involving the formation of the Cu(+)-PEDOT complex and the subsequent oxidation step of the Cu(+) complex to release Cu(2+) ions. On the other side, the experiments carried out let us propose the formation of a poorly stable Cu(2+)-PXDOT complex or a superficial mechanism for the Cu(2+) release, characterized by a single stripping signal for this process. Thus, the incorporation of Cu ions into the matrix and the stripping release are intimately related to the chemical structure of the polymer used.