Isolated graphene sheets were achieved by graphite intercalation and charge-induced exfoliation. The resultant graphene oxide sheets were incorporated into polymer composites and thermal expansion was investigated by a thermo-mechanical analyzer. The test results indicated that inclusion of graphene into composites resulted in low coefficients of thermal expansion (CTEs), and increasing graphene fraction reduced CTEs more significantly. The 5 wt % graphene oxide-based composite shows 31.7% reduction below the glass transition temperature. Preliminary measurement of thermal conductivity also indicated that graphene composites significantly improved the thermal conductivity of polymer matrix. Thermal conductivity of 5% graphene composites showed about 4-fold increment in comparison to the polymer matrix. This finding will provide a solid foundation for graphene-enabled thermal management in microelectronics.
Carbon nanotubes (CNTs) demonstrate extraordinary properties and show great promise
in enhancing out-of-plane properties of traditional polymer composites and enabling
functionality, but current manufacturing challenges hinder the realization of their potential.
This paper presents a method to fabricate multifunctional multiscale composites through
an effective infiltration-based vacuum-assisted resin transfer moulding (VARTM)
process. Multi-walled carbon nanotubes (MWNTs) were infused through and
between glass-fibre tows along the through-thickness direction. Both pristine and
functionalized MWNTs were used in fabricating multiscale glass-fibre-reinforced epoxy
composites. It was demonstrated that the mechanical properties of multiscale
composites were remarkably enhanced, especially in the functionalized MWNT
multiscale composites. With only 1 wt% loading of functionalized MWNTs, tensile
strength was increased by 14% and Young’s modulus by 20%, in comparison with
conventional fibre-reinforced composites. Moreover, the shear strength and short-beam
modulus were increased by 5% and 8%, respectively, indicating the improved
inter-laminar properties. The strain–stress tests also suggested noticeable enhancement in
toughness. Scanning electron microscopy (SEM) characterization confirmed an
enhanced interfacial bonding when functionalized MWNTs were integrated into
epoxy/glass-fibre composites. The coefficient thermal expansion (CTE) of functionalized
nanocomposites indicated a reduction of 25.2% compared with epoxy/glass-fibre
composites. The desired improvement of electrical conductivities was also achieved. The
multiscale composites indicated a way to leverage the benefits of CNTs and opened up
new opportunities for high-performance multifunctional multiscale composites.
Flexible organic−inorganic hybrids are promising thermoelectric materials to recycle waste heat in versatile formats. However, current organic/inorganic hybrids suffer from inferior thermoelectric properties due to aggregate nanostructures. Here we demonstrate flexible organic−inorganic hybrids where size-tunable Bi2Te3 nanoparticles are discontinuously monodispersed in the continuous conductive polymer phase, completely distinct from traditional bi-continuous hybrids. Periodic nanofillers significantly scatter phonons while continuous conducting polymer phase provides favored electronic transport, resulting in ultrahigh power factor of ~1350 μW m−1 K−2 and ultralow in-plane thermal conductivity of ~0.7 W m−1 K−1. Consequently, figure-of-merit (ZT) of 0.58 is obtained at room temperature, outperforming all reported organic materials and organic−inorganic hybrids. Thermoelectric properties of as-fabricated hybrids show negligible change for bending 100 cycles, indicating superior mechanical flexibility. These findings provide significant scientific foundation for shaping flexible thermoelectric functionality via synergistic integration of organic and inorganic components.
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