# Real-time observation of the isothermal crystallization kinetics in a deeply supercooled liquid

Source: [Real-time observation of the isothermal crystallization kinetics in a deeply supercooled liquid](<https://www.sota2.com/research/paper/68fa354d1e209131ce8a01e1>)

Collection index: [llms.txt](<https://www.sota2.com/research/llms.txt>)

Data updated: 2025-10-24T21:10:18.831Z

Authors: M. Zanatta, L. Cormier, L. Hennet, C. Petrillo, F. Sacchetti

Published: 2016-11-11T12:59:47.000Z

## Abstract

Below the melting temperature $T\_m$ crystals are the stable phase of typical elemental or molecular systems. However, cooling down a liquid below $T\_m$, crystallization is anything but inevitable. The liquid can be supercooled, eventually forming a glass below the glass transition temperature $T\_g$. Despite their long lifetimes and the presence of strong barriers that produces an apparent stability, supercooled liquids and glasses remain intrinsically metastable state and thermodynamically unstable towards the crystal. Here we investigated the isothermal crystallization kinetics of the prototypical strong glassformer GeO$\_2$ in the deep supercooled liquid at 1100 K, about half-way between $T\_m$ and $T\_g$. The crystallization process has been observed through time-resolved neutron diffraction for about three days. Data show a continuous reorganization of the amorphous structure towards the alpha-quartz phase with the final material composed by crystalline domains plunged into a low-density, residual amorphous matrix. A quantitative analysis of the diffraction patterns allows determining the time evolution of the relative fractions of crystal and amorphous, that was interpreted through an empirical model for the crystallization kinetics. This approach provides a very good description of the experimental data and identifies a predator-prey-like mechanism between crystal and amorphous, where the density variation acts as blocking barrier.

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## Original sources and implementation

[Original paper](<https://arxiv.org/abs/1611.03687>)

[PDF](<https://arxiv.org/pdf/1611.03687.pdf>)