journal article·2018-04

Impedance spectroscopy study of polyester/carbon nanotube composites

Z. Samir, Y. El Merabet, M.P.F. Graça, S. Soreto Teixeira, M.E. Achour, L.C. Costa

Polymer Composites· Volume 39· Issue 4
Publisher page

Abstract

The electrical properties of carbon nanotubes loaded in polyester polymer matrix were studied by using the impedance spectroscopy technique. The study was carried out in the frequency range between 100 Hz and 1 MHz and temperature between 170 and 400 K. Cole–Cole representation was used to interpret the impedance spectra of all the samples. The variation of the electrical conductivity, as a function of temperature, for concentrations higher than the conduction threshold was analyzed. This variation undergoes a significant decrease from a critical temperature that corresponds to the phenomenon known as positive temperature coefficient in resistivity. Tunneling effect is responsible for the change of the conductivity. The carbon particles are not in physical contact and the electrons tunnel through the insulating polymer gap between particles. With the rise of temperature, the gap between particles increases and tunneling becomes less probable. Consequently, above this temperature, the electrical conductivity begins to increase, due to the fact that the temperature dependence of conductivity is mainly related with different thermal expansion of polymer matrix and carbon nanotubes. POLYM. COMPOS., 39:1297–1302, 2018. © 2016 Society of Plastics Engineers
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Research context

OpenAlex topics: Carbon Nanotubes in Composites · Conducting polymers and applications · Advanced Sensor and Energy Harvesting Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

LASTID Laboratory, Department of Physics, Faculty of Sciences University Ibn Tofail, BP 133 Kenitra 14000 Morocco

I3N and Physics Department University of Aveiro Aveiro 3810‐193 Portugal

Funding

FCT-Portuguese Foundation for Science and Technology · FCT-CNRST; FEDER

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