4.5 Article

Electric modulus based relaxation dynamics and ac conductivity scaling of polypyrrole nanotubes

Journal

SYNTHETIC METALS
Volume 198, Issue -, Pages 239-247

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.synthmet.2014.10.009

Keywords

Conducting polymers; Polypyrrole nanotubes; Dielectric permittivity; Electric modulus; ac conductivity

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The relaxation mechanism and ac conductivity of camphorsulfonic acid (CSA) doped polypyrrole (PPy) nanotubes synthesized by self-assembly polymerization method at different molar ratio of dopant/ monomer (CSA/pyrrole) have been studied over a wide frequency range of 42 Hz-5 MHz in the temperature range of 303-373 K. The dielectric permittivity (epsilon') shows saturation at higher frequencies and a strong dispersion at lower frequencies. Higher (epsilon') at lower frequencies is attributed to the interfacial or electrode polarization effects. The dielectric loss (epsilon '') decreases almost linearly with increasing frequency due to the presence of dc conductivity. The frequenCy dependence of imaginary part of modulus (M '') shows a non-Debye conductivity relaxation peal< which has been explained using the Kohlrausch-Williams-Watts (KWW) stretched exponential function. The relaxation time (tau) for charge carriers' motion decreases with increasing both temperature and dopant/monomer ratio. The scaling behavior of (M '') spectra suggests that the relaxation dynamics is independent of both the dopant/monomer ratio and temperature. The frequency dependence of ac conductivity follows a power law, sigma(ac()omega)=A omega(s) with 0 < s < 1. The temperature dependence studies of frequency exponent (s) reveal that charge carriers in PPy nanotubes follow the correlated barrier hopping (CBH) model. The scaling behavior of conductivity spectra indicates the temperature independent electrical conduction in PPy nanotubes. The activation energy for the relaxation has been evaluated and is found to be almost same as that of dc conduction. (C) 2014 Elsevier B.V. All rights reserved.

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