Low-temperature carbonization of polyacrylonitrile/graphene carbon fibers: A combined ReaxFF molecular dynamics and experimental study

Graphene inclusion in a polymer matrix is a promising route to significantly enhance the mechanical properties of low-grade carbon fibers (CFs). Using ReaxFF molecular dynamics simulation, the atomistic mechanism leading to this enhancement is investigated. We demonstrate that the graphene edges along with the nitrogen and oxygen functional groups play a catalytic role and act as seeds to expedite alignment of the all-carbon rings, which are starting sites for the growth of graphitic structures. To examine the role of this proposed mechanism that enhances the graphitic structure of PAN/graphene CFs, we discuss the experimental results wherein the PAN/graphene CFs carbonized at 1250 degrees C demonstrate 91% (from 632 to 1207 MPa) increase in strength and 101% (from 88 to 177 GPa) enhancement in Young's modulus compared to PAN-based CFs carbonized at 1500 degrees C. These enhanced mechanical properties of low-grade carbon fibers achieved via graphene inclusion at decreased carbonization temperature provide a means to realize both energy savings and cost reduction. (C) 2020 Elsevier Ltd. All rights reserved.

Automated summary

Incorporating graphene in a polymer matrix is a promising approach to enhance the mechanical properties of low-grade carbon fibers. Molecular dynamics simulations reveal that graphene edges and nitrogen/oxygen functional groups catalyze the alignment of carbon rings, leading to the growth of graphitic structures and improved fiber properties. The experimental results demonstrate significant enhancements in strength and modulus, highlighting the potential for energy savings and cost reduction.