Superior hydrogen permeation resistance via Ni–graphene nanocomposites: Insights from atomistic simulations

Abstract

Designing hydrogen-resistant Ni-based alloys from the perspective of the Ni/graphene interface (NGI) provides the potential to increase hydrogen trapping away from potential fracture paths. Nonetheless, numerous essential mechanisms of hydrogen penetration behaviors in the Ni-graphene nanocomposites are presently not well understood. Here we investigate the influence of Ni/graphene interfaces (NGIs) on the behavior of hydrogen diffusion and trapping in their vicinity using atomistic simulations. Hydrogen diffusion is competitively affected by elevated temperatures and NGIs. The difference in the mean square displacement for hydrogen between the composites and pure Ni can be of two orders of magnitude, highlighting the sluggish diffusion in the composites. As NGIs reduce hydrogen formation energy and diffusion barrier, hydrogen prefers to migrate towards the interfaces. Hydrogen readily forms sp3 C–H bonds with C atoms, thereby impeding its detachment from graphene and subsequent entry into a non-diffusible state. Results of the study will contribute to the use of Ni–graphene nanocomposites as hydrogen-resistant materials for nuclear reactors.