Icosahedral quasicrystals spontaneously form from the melt in simulations of Al-Cu-Fe alloys. We model the interatomic interactions using oscillating pair potentials tuned to the specific alloy system based on a database of density functional theory (DFT)-derived energies and forces. Favored interatomic separations align with the geometry of icosahedral motifs that overlap to create face-centered icosahedral order on a hierarchy of length scales. Molecular dynamics simulations, supplemented with Monte Carlo steps to swap chemical species, efficiently sample the configuration space of our models, which reach up to 9846 atoms. Exchanging temperatures of independent trajectories (replica exchange) allows us to achieve thermal equilibrium at low temperatures. By optimizing structure and composition we create structures whose DFT energies reach to within $\sim 2$ meV/atom of the energies of competing crystal phases. Free energies obtained by adding contributions due to harmonic and anharmonic vibrations, chemical substitution disorder, phasons, and electronic excitations, show that the quasicrystal becomes stable against competing phases at temperatures above 600 K. The average structure can be described succinctly as a cut through atomic surfaces in six-dimensional space that reveal specific patterns of preferred chemical occupancy. Atomic surface regions of mixed chemical occupation demonstrate the proliferation of phason fluctuations, which can be observed in real space through the formation, dissolution and reformation of large-scale icosahedral motifs—a picture that is hidden from diffraction refinements due to averaging over the disorder and consequent loss of information concerning occupancy correlations.

• Received 13 August 2019
• Accepted 20 January 2020

DOI:https://doi.org/10.1103/PhysRevResearch.2.013196

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Published by the American Physical Society