Synergistic enhancement in permittivity and energy storage capacity of epoxy dielectrics via constructing continuous 3D BaTiO3 network collaborated with graphene oxide

Three-dimensional (3D) ceramic network has advantages over conventional ceramic nanoparticles in achieving high-performance flexible polymer dielectrics. However, the energy storage capacity cannot be substantially improved due to the relatively large dielectric loss and low breakdown strength. In this study, hierarchical 3DBT/ EP-GO (GEBT) dielectric hybrid composites with greatly improved permittivity and energy storage density were obtained by reversely introducing a mixed graphene oxide (GO)/epoxy (EP) solution into three-dimensional BaTiO3 (3DBT) network, which was facilely constructed by sol-gel method using cleanroom wiper as the tem-plate. A relatively high dielectric constant (epsilon' = 15.6) and breakdown strength (E-0 = 239.8 kV mm(-1)) were simultaneously achieved for the GEBT-4 system with similar to 15.4 wt% 3DBT and 0.75 wt% GO (to the epoxy). This system was much superior to the GEBT-1 with only 15 wt% 3DBT (epsilon' = 9.2, E0 = 128.8 kV mm-1) and epoxy nanocomposite with 25 wt% BT nanoparticles (epsilon' = 6.3, E0 = 121.0 kV mm(-1)). The continuous 3DBT ceramic network provided an effective polarization pathway within epoxy matrix, in which GO prevented electrical breakdown of the composites, thereby resulting in the significantly enhanced energy storage performance.

Automated summary

By introducing a mixed graphene oxide/epoxy solution into a three-dimensional barium titanate network, hierarchical ceramic network/graphene oxide/epoxy composites with improved dielectric properties were obtained. The addition of graphene oxide prevented electrical breakdown and the ceramic network provided an effective polarization pathway, resulting in significantly enhanced energy storage performance.