journal article·2021-03-23Open access

An Artificial Neural Network Reveals the Nucleation Mechanism of a Binary Colloidal AB13 Crystal

Gabriele M. Coli, Marjolein Dijkstra

ACS Nano· Volume 15· Issue 3

Abstract

Colloidal suspensions of two species have the ability to form binary crystals under certain conditions. The hunt for these functional materials and the countless investigations on their formation process are justified by the plethora of synergetic and collective properties these binary superlattices show. Among the many crystal structures observed over the past decades, the highly exotic colloidal icosahedral AB13 crystal was predicted to be stable in binary hard-sphere mixtures nearly 30 years ago, yet the kinetic pathway of how homogeneous nucleation occurs in this system is still unknown. Here we investigate binary nucleation of the AB13 crystal from a binary fluid phase of nearly hard spheres. We calculate the nucleation barrier and nucleation rate as a function of supersaturation and draw a comparison with nucleation of single-component and other binary crystals. To follow the nucleation process, we employ a neural network to identify the AB13 phase from the binary fluid phase and the competing fcc crystal with single-particle resolution and significant accuracy in the case of bulk phases. We show that AB13 crystal nucleation proceeds via a coassembly process where large spheres and icosahedral small-sphere clusters simultaneously attach to the nucleus. Our results lend strong support for a classical pathway that is well-described by classical nucleation theory, even though the binary fluid phase is highly structured and exhibits local regions of high bond orientational order.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Material Dynamics and Properties · Phase Equilibria and Thermodynamics · Crystallization and Solubility Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Soft Condensed Matter, Debye Institute for Nanomaterials Science, Department of Physics, Utrecht University, Princetonplein 1, 3584 CC Utrecht, The Netherlands

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

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