Nucleation and growth of micellar polycrystals under time-dependent volume fraction conditions

TL;DR

This study investigates the crystallization kinetics of micellar colloidal polycrystals under varying temperature conditions, revealing the influence of volume fraction and nanoparticle presence, and demonstrating the applicability of classical nucleation models.

Contribution

The paper introduces a combined experimental and modeling approach to understand micellar polycrystal nucleation and growth under dynamic volume fraction conditions, adapting classical theories to account for nanoparticle effects.

Findings

Crystallization temperature increases with heating rate.

Model predictions align with microscopy data on grain size.

Nucleation rate dependence matches that of colloidal hard spheres.

Abstract

We study the freezing kinetics of colloidal polycrystals made of micelles of Pluronic F108, a thermosensitive copolymer, to which a small amount of silica nanoparticles of size comparable to that of the micelles are added. We use rheology and calorimetry to measure Tc, the crystallization temperature, and find that Tc increases with the heating rate \dot{T} used to crystallize the sample. To rationalize our results, we first use viscosity measurements to establish a linear mapping between temperature T and the effective volume fraction, {\phi}, of the micelles, treated as hard spheres. Next, we reproduce the experimental \dot{T} dependence of the crystallization temperature with numerical calculations based on standard models for the nucleation and growth of hard spheres crystals, classical nucleation theory and the Johnson-Mehl-Avrami-Kolmogorov theory. The models have been adapted to account for the peculiarities of our experiments: the presence of nanoparticles that are expelled in the grain boundaries, and the steady increase of T and hence {\phi} during the experiment. We moreover show that the polycrystal grain size obtained from the calculations is in good agreement with light microscopy data. Finally, we find that the {\phi} dependence of the nucleation rate for the micellar polycrystal is in remarkable quantitative agreement with that found in previous experiments on colloidal hard spheres. These results suggests that deep analogies exist between hard-sphere colloidal crystals and Pluronics micellar crystals, in spite of the difference in particle softness. More generally, our results demonstrate that crystallization processes can be quantitatively probed using standard rheometry.