Abstract:The preparation of three dimensional graphene/polyurethane (3DGP) composites in cross-bite can be achieved through two steps. To begin with, Graphene aerogel (GA) is prepared by hydrothermal reduction and freeze-drying with graphene oxide (GO) as the precursor of network framework. Secondly, it is necessary to employ polyurethane (PU) as a filler of composite material with adjusted hardness and fluidity to impregnate GA in a vacuum state. The structure and morphology of GO、GA and 3DGP were characterized and analyzed with the help of SEM, Raman and FTIR, as the thermal stability and piezoresistive characteristics are tested by means of TGA-DSC and self-made piezoresistive test platform. The results demonstrate that: the 6 g/L aqueous solution of GO is interconnected with GO layers impacted by the action of EDA reducing agent, which can also form a regular honeycomb three-dimensional network with the pore size about 0.8 mm, as PU and GA can be well occluded in 3DGP. Besides, the continuity of the three-dimensional network skeleton provides a good channel for the phonon of the heat transport carrier, which remarkably enhances the thermal stability of 3DGP and increases by 45 degrees centigrade than that of the PU at the weight loss rate of 5%. Additionally, it has low hysteresis (8.7%) and shows two piezoresistive effects in piezoresistive measurement range.