Electrical impedance spectroscopy investigation of surfactant-magnetite-polypyrrole particles.

ABSTRACT

We report an electrical impedance spectroscopy (EIS) characterization of composite systems formed by emulsion polymerization of polypyrrole (PPY) in concentrated aqueous solutions of sodium dodecyl sulfate (SDS) containing dispersed magnetite particles. SDS-(Fe3O4)-(conducting polymer) microaggregates with different iron contents were prepared by varying in a reciprocal manner the relative amounts of the metal oxide and PPY. We have measured the zeta-potential and the average size of the corresponding dispersed particles and examined their relative composition through energy dispersive X-ray (EDX) microanalysis and Fourier transform infrared (FTIR) spectroscopy. Important aspects of the charge transport in these composite particles can be identified by mapping the real and imaginary parts of their complex impedance as a function of the frequency of the applied external electric field. For instance, for binary composites SDS-(Fe3O4) polarization effects are dominant at the low-frequency regime, with a well-defined dielectric relaxation easily identifiable. On the other hand, when the relative amount of PPY is progressively increased in the ternary SDS-(Fe3O4)-PPY composites, a transition between different charge transport mechanisms is observed at higher frequencies. The EIS results suggest that in these ternary aggregates the PPY chains envelop the metal oxide clusters and effectively shield them from the external field, and that only in binary samples that do not contain PPY is that the surfactant molecules can directly enclose the magnetite particles. These results are consistent with the fact that the average size of the aggregates in the ternary composites is in general larger than those of either SDS-PPY or SDS-magnetite binary particles.