Particle Size Dependence of the Dielectric Properties of Polyvinyledene Fluoride/Silver Composites

The dependence of the dielectric properties of micro- (m-) and nano- (n-) silver (Ag)/poly(vinylidene fluoride) (PVDF) composites on the Ag particle size was determined. The magnitude of dielectric constant and conductivity for the PVDF/n-Ag composites was much higher than that of the PVDF/m-Ag composites at the same Ag volume loading. Our results suggest that the percolative behaviors were quite different for the m- and n-systems owing to the Ag particle size effect. The dielectric property depends on the synergistic effects of interfacial area, interparticle distance, and interfacial adhesion, all of which are highly dependent on the Ag particle size. The increased interfacial area, reduced interparticle distance, and improved interfacial adhesion contributed to the better dielectric properties of the PVDF/n-Ag composites.     

Dielectric Loss Suppression of Silver/Poly(vinylidene fluoride) Composite Films with Polydopamine

The preparation and dielectric properties of silver-polydopamine/poly(vinylidene fluoride) (Ag-PDOP/PVDF) composite films with suppressed dielectric loss are reported. The dielectric loss tangents of the composite films were found to be rather low similar to that of pure PVDF over the frequency range 100 Hz to 30 kHz, almost regardless of the Ag content, and even lower than that of pristine PVDF in the relatively high frequency region. The nanoscale structure comprised of Ag nanoparticles (Ag NPs), isolated by the PDOP coating and the PVDF matrix, hindered the formation of percolative networks, resulting in the decreased conduction loss in the composite films, even at a high filler loading. The strong interfacial interaction between the Ag@PDOP particles and the PVDF matrix also contributed to the restrained interfacial loss. Consequently, these composite films had higher permittivity and smaller dielectric loss than the PVDF matrix at relatively high frequencies, and would thus be attractive for physically small capacitor applications in electronics and electric power systems.     

Effects of CNT inclusions on structure and dielectric properties of PVDF/CNT nanocomposites

ABSTRACT

The effects of multiwall carbon nanotube (CNT) inclusions on the crystalline structure of poly(vinylidene fluoride) (PVDF), and on the dielectric properties of PVDF/CNT nanocomposites (NCs), prepared by melt mixing, were investigated by employing X-ray diffraction, differential scanning calorimetry, and dielectric spectroscopy techniques. Our results imply that, in the NCs, the formation of β-phase crystals depends on specific compression treatment in the melt and fast cooling. Dielectric measurements on NCs, with CNT concentrations below the electrical percolation threshold, reveal that the dielectric strength of the two relaxation processes in the amorphous phase and dielectric permittivity, ?′, measured within the broad temperature range from ?150 °C to 60 °C, increase strongly with increasing CNT concentration. This enhancement of amorphous PVDF polarizability has been attributed to the increase of the local electric field, due to local polarization generated at the surface of conductive inclusions/CNT clusters.     

Finely-reconciled high dielectric constant and low dielectric loss in ternary polymer/Cr2C3/montmorillonite composite films by filler-synergy strategy

Polymer/conductive ceramic composites with high dielectric constant have become research hotspot of dielectric capacitor materials. However, the conductivity and dielectric loss increase when high dielectric constant is achieved. In order to reconcile high dielectric constant and low dielectric loss, in this study, poly (vinylidene fluoride) (PVDF)/chromium carbide (Cr₂C₃)/montmorillonite (MMT) ternary composite films were prepared by solution cast. Dielectric response based on interfacial polarization was improved and dielectric constant of composites was increased. MMT ceramic was used to suppress interface leakage current. Compared with PVDF/Cr₂C₃ composites, the conductivity and dielectric loss of ternary composites were reduced.     

Dielectric behavior of TiC–PVDF nanocomposites

TiC/PVDF nanocomposite is prepared via simple blending and hot pressing route. Percolation theory was employed to explain the dielectric behavior of the TiC/PVDF composites. The dependence of the dielectric properties of the composite on both volume fraction of the filler and frequency is investigated. High dielectric constant (? = 540) and low loss (tan δ = 0.48) of the composites at 100 Hz have been observed near the percolation threshold (0.12). The composites show a weak frequency dependence towards the high frequency range (10–100 kHz), regardless of the TiC content. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Giant permittivity of three phase polymer nanocomposites obtained by modifying hybrid nanofillers with polyvinylpyrrolidone

In this work, the combination of graphene decorated with graphene quantum dots (G-D-GQDs) and barium titanate (BaTiO₃) nanoparticles filled poly (vinyledene fluoride) (PVDF) nanocomposites are prepared using solvent casting method. The modification of G-D-GQDs and BaTiO₃ nanoparticles with polyvinyl pyrrolidone (PVP) show finer dispersion in PVDF matrix as compared to unmodified G-D-GQDs and BaTiO₃ nanoparticles in PVDF matrix. XRD of PVDF nanocomposites shows the formation of α and β form of PVDF crystals. The incorporation of the combination of PVP modified BaTiO₃ nanoparticles and G-D-GQDs in PVDF matrix show a decrease in crystallization temperature (T_c), percent crystallinity (X_c) and increase in thermal stability as compared to unmodified PVDF/BaTiO₃/G-D-GQDs nanocomposites, due to interaction of PVP modified nanoparticles with PVDF. Further, the incorporation of the combination of 20 wt.% BaTiO₃ nanoparticles and 3 wt.% G-D-GQDs in PVDF matrix show a giant dielectric constant. The giant dielectric constant is achieved due to accumulation of more charges across conductor-insulator interface, more numbers of microcapacitor formed and enhanced interfacial compatibility between BaTiO₃/G-D-GQDs with PVDF through PVP. The loss tangent (tan δ) of PVP modified G-D-GQDs and BaTiO₃ nanoparticles and its PVDF nanocomposites is low due to lower leakage current, which make the material suitable for various applications.     

Enhanced energy storage in polyvinylidenefluoride (PVDF) + BaZrO<Subscript>3</Subscript> electroactive nanocomposites

PVDF + BaZrO₃ electroactive nanocomposite thin film has been prepared by solution casting method. The structural analysis was carried out by using x-ray diffraction pattern and atomic force microscopy (AFM). Generally, the performance of dielectric capacitors toward higher energy density and higher operating temperatures has been drawing increased interest. In this regard, the present study was focussed on the fabrication and characterization of PVDF + BaZrO₃ electroactive nanocomposites in view of enhancing the energy density at elevated temperature. Cole-Cole plot is an agreement with multiple relaxation process in electroactive nanocomposites. Dielectric energy storage performance is assessed for PVDF nanocomposites with different wt% of BaZrO₃ at different frequencies and temperature. It has been observed that with increase of temperature, the permittivity increased while the energy density slightly decreased but significantly higher than pure polymer PVDF. A high energy density of 6.88 J/cm³ was obtained for BaZrO₃ electroactive nanocomposites at 50 °C and 5.06 J/cm³ at 70 °C. Overall, the testing results indicate that using nanocomposites of PVDF and BaZrO₃ as a dielectric component is promising for implementation to preserve high energy density values up to temperatures of 70 °C.The enhancement of dielectric permittivity and the energy density is attributed due to increase of interracial charge density. The effect of BaZrO₃ nanoparticles in energy density of PVDF is first time reported.     

Temperature- and magnetic field-dependent electrical transport studies of poly(-3,4 ethylenedioxythiophene) nanoparticles

Large-scale silver nanowires (AgNWs) with a width of 50–60 nm and a typical length of 10 ± 5 μm were synthesized conveniently through a simple polyol reduction method, and the weight of obtained AgNWs was close to 10 g in this one-pot reaction with 500 ml of solution. The as-prepared AgNWs were incorporated into polyvinylidene fluoride matrix (PVDF) to fabricate the AgNWs/PVDF composites, and dielectric behaviors of the composites were investigated. The results revealed that a low percolation threshold of 1.8 vol% was observed in the AgNWs/PVDF composites, which was due to the large aspect ratio of one-dimension structured AgNWs. A giant dielectric constant of 80,000 at 1 kHz was obtained with 1.8 vol% of AgNWs mainly caused by the percolation effect. Besides, the large micro-capacitor networks and strong interfacial polarization at percolation threshold contributed to the enhanced dielectric constant.     

Enhanced dielectric properties of polyvinylidene fluoride with addition of SnO2 nanoparticles

In this letter, SnO₂/polyvinylidene fluoride (PVDF) nanocomposites with outstanding dielectric properties were fabricated. The SEM and TEM images showed that SnO₂ nanoparticles with size of 5–7 nm dispersed homogeneously in polymer matrix. The significantly improved dielectric constant was well explained by percolation theory. The nanocompo‐ sites can retain a certain value of breakdown field. The maximum energy density of SnO₂/PVDF nanocomposites was 5.4 J/cm³, two times that of the pure polyvinylidene fluoride. These findings suggest that SnO₂/PVDF nanocomposites are suitable candidates for energy storage applications. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Novel Ag–BaTiO3/PVDF three-component nanocomposites with high energy density and the influence of nano-Ag on the dielectric properties

Novel Ag–BaTiO₃/PVDF (polyvinylidene fluoride) three-component nanocomposites and traditional BaTiO₃/PVDF two-component nanocomposites were prepared by the same procedures. The dielectric properties of these two kinds of composites were compared. The results showed that the kind of three-component nanocomposites had better dielectric properties. The energy density of such kind of composites could reach nearly 10 J/cm³, which indicated that these nanocomposites could be used as the dielectric layers of pulse-power capacitors. The Coulomb blockade effect was used to explain the dielectric breakdown properties and the resistivities under high electric field of such new kind of nanocomposites.