Anisotropic Crystallization Kinetics and Interfacial Dynamics of Phase-Change Material Sb$_2$S$_3$ from Machine Learning Force Field Simulations

Fuente: arXiv
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Main Authors: Chakraborty, Souvik, Li, Wen-Qing, Liu, Yun
Format: Preprint
Published: 2026
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author Chakraborty, Souvik
Li, Wen-Qing
Liu, Yun
author_facet Chakraborty, Souvik
Li, Wen-Qing
Liu, Yun
contents The phase-change material antimony sulfide (Sb$_2$S$_3$) relies on rapid and reversible phase transitions between crystalline and amorphous states, which are critical for their performance in data storage and photonics applications. In this work, a machine learning force field is developed based on the moment tensor potential approach, allowing us to understand the atomistic origin of the structural evolution and crystallization kinetics in Sb$_2$S$_3$ for the first time, by enabling large-scale molecular dynamics simulations (up to 7680 atoms for 40 ns). Sb$_2$S$_3$ shows anisotropic growth rates with the [100] facet exhibiting the fastest growth due to the strong Sb-S covalent bonding along its quasi-1D ribbon-like structure of its crystalline phase. The activation energy for crystal growth is found to be 0.55-0.57 eV, whereas that for diffusion is around 1.16-1.56 eV. The lower activation energy for crystal growth indicates that its heterogeneous crystallization is interface controlled rather than diffusion limited, unlike GST and GeTe with atomic attachment at the solid-liquid interface being energetically favoured over long range atomic transport. These findings provide key insights into the structural, thermodynamic, and kinetic properties of Sb$_2$S$_3$, paving the way for optimizing its functionality including switching speed, reliability, and energy efficiency.
format Preprint
id arxiv_https___arxiv_org_abs_2605_20785
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Anisotropic Crystallization Kinetics and Interfacial Dynamics of Phase-Change Material Sb$_2$S$_3$ from Machine Learning Force Field Simulations
Chakraborty, Souvik
Li, Wen-Qing
Liu, Yun
Materials Science
Disordered Systems and Neural Networks
The phase-change material antimony sulfide (Sb$_2$S$_3$) relies on rapid and reversible phase transitions between crystalline and amorphous states, which are critical for their performance in data storage and photonics applications. In this work, a machine learning force field is developed based on the moment tensor potential approach, allowing us to understand the atomistic origin of the structural evolution and crystallization kinetics in Sb$_2$S$_3$ for the first time, by enabling large-scale molecular dynamics simulations (up to 7680 atoms for 40 ns). Sb$_2$S$_3$ shows anisotropic growth rates with the [100] facet exhibiting the fastest growth due to the strong Sb-S covalent bonding along its quasi-1D ribbon-like structure of its crystalline phase. The activation energy for crystal growth is found to be 0.55-0.57 eV, whereas that for diffusion is around 1.16-1.56 eV. The lower activation energy for crystal growth indicates that its heterogeneous crystallization is interface controlled rather than diffusion limited, unlike GST and GeTe with atomic attachment at the solid-liquid interface being energetically favoured over long range atomic transport. These findings provide key insights into the structural, thermodynamic, and kinetic properties of Sb$_2$S$_3$, paving the way for optimizing its functionality including switching speed, reliability, and energy efficiency.
title Anisotropic Crystallization Kinetics and Interfacial Dynamics of Phase-Change Material Sb$_2$S$_3$ from Machine Learning Force Field Simulations
topic Materials Science
Disordered Systems and Neural Networks
url https://arxiv.org/abs/2605.20785