Search

Dielectric materials with superb thermal and electrical properties are highly desired for high-voltage electrical equipment and advanced electronics. Here, we propose a novel strategy to improve the performance of epoxy composites by employing boron nitride nanosheets (BNNSs) and γ-glycidyl ether oxypropyl sesimoxane (G-POSS) as functional fillers. The resultant ternary epoxy composites exhibit high electrical resistivity (1.63 × 1013 Ω·cm) and low dielectric loss (<0.01) due to the ultra-low dielectric constants of cage-structure of G-POSS. In addition, a high thermal conductivity of 0.3969 W·m−1·K−1 is achieved for the epoxy composites, which is 114.66% higher than that of pure epoxy resin. This can be attributed to the high aspect ratio and excellent thermally conductive characteristics of BNNSs, promoting phonon propagation in the composites. Moreover, the epoxy composite simultaneously possesses remarkable dynamic mechanical properties and thermal stability. It is believed that this work provides a universal strategy for designing and fabricating multifunctional composites using a combination of different functional fillers. [ABSTRACT FROM AUTHOR]

The developments in the high-power densities and high integration of electronic devices have put forward higher requirements for advanced thermal management materials (TMMs) to meet the rising demand for heat dissipation. However, it has remained a major challenge to achieve significant enhancement of thermal conductivity (TC) of TMMs without compromising their mechanical and dielectric properties. Here, we report a flexible, thermally conductive composite film that contain aramid nanofiber (ANF) and silver nanoparticles (AgNPs) decorated with boron nitride (BN), the in-plane TC of which is up to 12 W/mK at 40 wt.% filler contents. Such a high TC is attributed to the bridging role of AgNPs, which greatly reduces the interfacial thermal resistance of composites. At the same time, the as-prepared composite films possess outstanding mechanical strength (>126 MPa), owing to the coupling between the ANF network and the favourable hydrogen bonding interaction between the ANF and the functional BN. Moreover, a low dielectric loss (<0.05), high electrical resistivity (~1014 Ω·cm), and high decomposition temperature (>500°C) are simultaneously achieved for the composite films. These findings offer a facile strategy for the design of multifunctional TMMs, which hold great promising for application in electric devices. [ABSTRACT FROM AUTHOR]