In this study nanocomposites consisting of an epoxy resin and ceramic zinc ferrite nanoparticles have been successfully developed and investigated morphologically and structurally by means of scanning electron microscopy (SEM) images and X-ray diffraction (XRD) spectra. The thermal properties of the nanocomposites were studied via differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The thermomechanical characterization of the fabricated nanocomposites was studied via dynamic mechanical analysis (DMA) and the magneto-dielectric response was assessed by means of a broadband dielectric spectroscopy (BDS) and by employing a superconducting quantum interference device (SQUID) magnetometer. Data analysis demonstrates that the incorporation of nanoinclusions into the matrix improves both the thermomechanical and the dielectric properties of the systems, as indicated by the increase of the storage modulus, the real part of dielectric permittivity and conductivity values with filler content, while at the same time induces magnetic properties into the matrix. Zinc ferrite nanoparticles and their respective nanocomposites exhibit superparamagnetic behavior at room temperature. Three relaxations were recorded in the dielectric spectra of all systems; originating from the filler and the polymer matrix, namely interfacial polarization, glass to rubber transition of the polymer matrix and the reorientation of small polar side groups of the polymer chain.

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In the present study two sets of nanocomposites consisting of an epoxy resin and BaFe12O19 or SrFe12O19 nanoparticles were successfully developed and characterized morphologically and structurally via scanning electron microscopy and X-ray diffraction spectra. The dielectric response of the nanocomposites was investigated by means of broadband dielectric spectroscopy and their magnetic properties were derived from magnetization tests. Experimental data imply that the incorporation of the ceramic nanoparticles enhances significantly the dielectric properties of the examined systems and their ability to store electrical energy. Dielectric spectra of all systems revealed the presence of three distinct relaxation mechanisms, which are attributed both to the polymer matrix and the nanoinclusions: Interfacial polarization, glass to rubber transition of the polymer matrix and the re-orientation of small polar side groups of the polymer chain. The magnetic measurements confirmed the ferromagnetic nature of the nanocomposites. The induced magnetic properties increase with the inclusion of hexaferrite nanoparticles. The nanocomposites with SrFe12O19 nanoparticles exhibit higher values of coercive field, magnetization, magnetic saturation and remanence magnetization. A magnetic transition was detected in the ZFC/FC curves in the case of the BaFe12O19/epoxy nanocomposites.

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In this study, series of nanocomposites consisting of an epoxy matrix and different carbon nanoinclusions (Carbon Black, Multiwall Carbon Nanotubes (MWCNT), Graphene nanoplatelets (GnP) and nanodiamonds) were developed, and their electrical response was examined in wide frequency and temperature ranges. Depending on the filler type and concentration, nanocomposites exhibited either insulator to conductor transitions or dielectric relaxation phenomena. Recorded relaxations were attributed to interfacial polarization, glass to rubber transition and motion of polar side groups. Nanocomposites integrating carbon black or MWCNTs exhibit an abrupt increase in permittivity and conductivity at a critical concentration (or percolation threshold). The insulator to conductor transition is described by means of percolation theory and critical concentration and exponent are determined. Conductance mechanisms are investigated in all sets of nanocomposites, by accounting the influence of temperature on conductivity and by applying the Variable Range Hopping model. Further, analysis reveals hopping conductivity as the main charge migration process below critical concentration, while hopping and metallic-like conduction coexist above it.