The relationship between local density and bond-orientational order during crystallization of the Gaussian core model.

Abstract

Whether nucleation is triggered by density or by bond-orientational order is one of the most hotly debated issues in recent investigations of the crystallization process. Here, we present a numerical study of the relationship between them for soft particles within the isothermal-isobaric ensemble. We compress the system and thus obtain the fluid-solid transition. By investigating locally dense-packed particles and particles with a relatively high bond-orientational order in the compressing process, we find a sharp increase of the spatial correlations for both densely packed particles and highly bond-orientational ordered particles at the phase transition point, which provide new characterization methods for the liquid-crystal transition. We also find that it is the bond-orientational order rather than density that triggers the nucleation process. The relationship between the local density and the bond-orientational order parameter is strongly affected by the characterization methods used. The local bond order parameter (q6) shows clear correlation with the local density (ρ) in the fluid stage, while the coarse-grained form (q[combining macron]6) does not correlate with ρ at all, owing to the comparable spatial scales of q6 and ρ. Nevertheless, q[combining macron]6 shows an obvious advantage in distinguishing between solid and liquid particles in our work. These results may elevate our understanding of the mechanism of the crystallization process.