Direct observations of shape fluctuation in long-time atomistic simulations of metallic nanoclusters

Abstract

Metallic nanoclusters are functional materials whose unique physical and chemical properties are sensitively controlled by their shapes and structures. An in-depth understanding of their morphological stability is therefore of crucial importance. It has been well documented by transmission electron microscopy (TEM) studies that metallic nanoclusters can interconvert between different isomers. However, the relevant mechanisms remain elusive because the timescales of such shape fluctuations are too short to be resolved experimentally and yet too long for conventional atomistic simulations. By employing massively parallel accelerated molecular dynamics (AMD) simulations reaching timescales of milliseconds, we provide a clear description of the dynamical processes leading to shape fluctuation in metallic nanoclusters of platinum, silver, copper, and gold at different sizes and temperatures. In all these materials, direct transformations between face-centered-cubic and fivefold symmetric structures (decahedron or icosahedron) are observed away from the melting point. These transitions occur following either a slip-mediated twinning mechanism or a surface-reconstruction driven process. The identified pathways are shown to be reversible, allowing for genuine shape fluctuation processes that do not involve melting or other external factors.