We show from a series of molecular dynamics simulations that the tensile fracture behavior of a nanocrystalline graphene (nc-graphene) nanostrip can become insensitive to a pre-existing flaw (e.g., a hole or a notch) below a critical length scale in the sense that there exists no stress concentration near the flaw, the ultimate failure does not necessarily initiate at the flaw, and the normalized strength of the strip is independent of the size of the flaw. This study is a first direct atomistic simulation of flaw insensitive fracture in high-strength nanoscale materials and provides significant insights into the deformation and failure mechanisms of nc-graphene.
Phase diagrams provide ‘roadmaps' to the possible states of matter. Their determination traditionally rests on the assumption that all phases, even unstable ones, have well-defined free energies under all conditions. However, this assumption is commonly violated in condensed phases due to mechanical instabilities. This long-standing problem impedes thermodynamic database development, as pragmatic attempts at solving this problem involve delicate extrapolations that are highly nonunique and that lack an underlying theoretical justification. Here we propose an efficient computational solution to this problem that has a simple interpretation, both as a topological partitioning of atomic configuration space and as a minimally constrained physical system. Our natural scheme smoothly extends the free energy of stable phases, without relying on extrapolation, thus enabling a formal assessment of widely used extrapolation schemes.
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