Abstract
Hexagonal boron nitride (h-BN)-based heat-spreading materials have drawn considerable attention in electronic diaphragm and packaging fields because of their high thermal conductivity and desired electrical insulation properties. However, the traditional approach to fabricate thermally conductive composites usually suffers from low thermal conductivity, and cannot meet the requirement of thermal management. In this work, novel h-BN/cellulose-nano fiber (CNF) composite films with excellent thermal conductivity in through plane and electrical insulation properties are fabricated via an innovative process, i.e., the perfusion of h-BN into porous three dimensional (3D) CNF aerogel skeleton to form the h-BN thermally conductive pathways by filling the CNF aerogel voids. When at an h-BN loading of 9.51 vol %, the thermal conductivity of h-BN/CNF aerogel perfusion composite film is 1.488 W·m−1·K−1 at through plane, an increase by 260.3%. The volume resistivity is 3.83 × 1014 Ω·cm, superior to that of synthetic polymer materials (about 109~1013 Ω·cm). Therefore, the resulting h-BN/CNF film is very promising to replace the traditional synthetic polymer materials for a broad spectrum of applications, including the field of electronics.
Highlights
The rapid development of miniaturization, integration, and high-power electronic devices brings with it higher requirements for their effective heat-dissipation properties [1,2,3]
It is hard to form thermally conductive pathways between the two sides of the composite because of the barrier between fibers and inorganic metallic compound particles [34,35]. To address this problem, perfusing hexagonal boron nitride (h-Boron nitride (BN)) into cellulose-nano fiber (CNF) (100~2000 nm in length,
When h-BN content was 23.08 wt%, the thermal conductivities of the blended composite film and aerogel perfusion film were 0.678 W·m−1K−1 and 1.488 W·m−1K−1 at 25 ◦C, respectively, 64.2% and 260.3% higher than that of pure CNF film
Summary
The rapid development of miniaturization, integration, and high-power electronic devices brings with it higher requirements for their effective heat-dissipation properties [1,2,3]. It is hard to form thermally conductive pathways between the two sides of the composite because of the barrier between fibers and inorganic metallic compound particles [34,35] To address this problem, perfusing h-BN into cellulose-nano fiber (CNF) (100~2000 nm in length,
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