Nanoscale pulverization effect in double-layered MOF-derived hierarchical G/Co@C composites for boosting electromagnetic wave dissipation.

Metal-organic frameworks (MOFs) have drawn a lot of interest as prospective starting points for highly effective electromagnetic wave (EMW) absorbers. However, the inevitable shrinkage and probable densification that occur during pyrolysis significantly reduce the microwave-loss capacity. A dual-layer MOF, ZIF-8@ZIF-67, is created and effectively decorated on graphene sheets as a solution to this problem. The shrinkage and densification were then suppressed by the subsequent pulverization effect between the two MOFs. Due to suitable compositions and specialized microstructures, G/Co@C exhibits excellent impedance matching and dissipates EMW by combining magnetic and dielectric loss. The maximum reflection loss of G/Co@C-7/paraffin is -55.0 dB at 5.8 GHz with just 7% filler. Therefore, the preparation of high-efficiency MOF-derived microwave absorbers by the pulverization effect is demonstrated to be an efficient strategy.

Influences of Thermal Treatment on the Dielectric Performances of Polystyrene Composites Reinforced by Graphene Nanoplatelets.

Dielectric properties of composites near percolation threshold (fc) are often sensitive to thermal treatments, and the annealing temperature is usually associated with a polymer's rheological properties. In this study, the influences of the thermal treatment on dielectric properties are investigated for the polystyrene (PS) matrix composite reinforced by graphene nanoplatelets (GNP) fillers near fc. It can be found that the thermal treatment can not only increase the dielectric constant, but also decrease the dielectric loss for the PS/GNP composite. This interesting phenomenon possibly happens in the interfacial region of PS/GNP with the thickness about 4-6 nm according to the electron energy-loss spectroscopy (EELS) results. The free volumes around the interface can be easily altered by the movement of polymeric segments after annealing at the glass transition temperature.

Design of Electrically Conductive Structural Composites by Modulating Aligned CVD-Grown Carbon Nanotube Length on Glass Fibers.

Function-integration in glass fiber (GF) reinforced polymer composites is highly desired for developing lightweight structures and devices with improved performance and structural health monitoring. In this study, homogeneously aligned carbon nanotube (CNT) shell was in situ grafted on GF by chemical vapor deposition (CVD). It was demonstrated that the CNT shell thickness and weight fraction can be modulated by controlling the CVD conditions. The obtained hierarchical CNTs-GF/epoxy composites show highly improved electrical conductivity and thermo-mechanical and flexural properties. The composite through-plane and in-plane electrical conductivities increase from a quasi-isolator value to ∼3.5 and 100 S/m, respectively, when the weight fraction of CNTs grafted on GF fabric varies from 0% to 7%, respectively. Meanwhile, the composite storage modulus and flexural modulus and strength improve as high as 12%, 21%, and 26%, respectively, with 100% retention of the glass transition temperature. The reinforcing mechanisms are investigated by analyzing the composite microstructure and the interfacial adhesion and wetting properties of CNTs-GF hybrids. Moreover, the specific damage-related resistance variation characteristics could be employed to in situ monitor the structural health state of the composites. The outstanding electrical and structural properties of the CNTs-GF composites were due to the specific interfacial and interphase structures created by homogeneously grafting aligned CNTs on each GF of the fabric.

Influence of Thermal Treatments on the Evolution of Conductive Paths in Carbon Nanotube-Al2O3 Hybrid Reinforced Epoxy Composites.

The conductive path formed by carbon nanotubes (CNTs) in a polymer matrix is one of the most attractive topics for developing multifunctional nanocomposites. In this article, we studied the evolution of conductive paths and interactions in the interfacial regions in epoxy-based composites reinforced by an urchinlike hybrid of CNTs and alumina microparticles (µAl2O3). A homogeneous dispersion of CNTs in the epoxy matrix was achieved thanks to the core-shell structures of CNTs-µAl2O3 hybrids, resulting in the interpenetrated epoxy's cross-linking network that strongly bonds with CNTs. Furthermore, thermal treatments at different temperatures around the glass-transition temperature (Tg) were conducted under vacuum on composites near the percolation threshold. It was found that the dielectric behavior and the Tg were shifted in spite of the constant CNT mass fraction used. This was mainly due to the fact that thermal treatment generated the adjustment of the cross-linking network of epoxy, and the distances between adjacent CNTs were reduced gradually. This study can provide insight into the evolution of conductive paths in the interfacial regions from a more straightforward perspective.

Quantitative Study of Interface/Interphase in Epoxy/Graphene-Based Nanocomposites by Combining STEM and EELS.

A quantitative study of the interphase and interface of graphene nanoplatelets (GNPs)/epoxy and graphene oxide (GO)/epoxy was carried out by combining scanning transmission electron microscopy (STEM) and electron energy-loss spectroscopy (EELS). The interphase regions between GNPs and epoxy matrix were clearly identified by the discrepancy of the plasmon peak positions in the low energy-loss spectra due to different valence electron densities. The spectrum acquisitions were carried out along lines across the interface. An interphase thickness of 13 and 12.5 nm was measured for GNPs/epoxy and GO/epoxy, respectively. The density of the GNPs/epoxy interphase was 2.89% higher than that of the epoxy matrix. However, the density of the GO/epoxy interphase was 1.37% lower than that of the epoxy matrix. The interphase layer thickness measured in this work is in good agreement with the transition layer theory, which proposed an area with modulus linearly varying across a finite width. The results provide an insight into the interphase for carbon-based polymer composites that can help to design the functionalization of nanofillers to improve the composite properties.

Improving dielectric properties of BaTiO3/ferroelectric polymer composites by employing surface hydroxylated BaTiO3 nanoparticles.

Dielectric properties of poly(vinylidene fluoride) (PVDF) based nanocomposites filled with surface hydroxylated BaTiO(3) (h-BT) nanoparticles were reported. The h-BT fillers were prepared from crude BaTiO(3) (c-BT) in aqueous solution of H(2)O(2). Results showed that the dielectric properties of the h-BT/PVDF nanocomposites had weaker temperature and frequency dependences than that of c-BT/PVDF nanocomposites. Meanwhile, the h-BT/PVDF composites showed lower loss tangent and higher dielectric strength. It is suggested that the strong interaction between h-BT fillers and PVDF matrix is the main reason for the improved dielectric properties.