Polydispersity-driven dynamical differences between two- and three-dimensional supercooled liquids

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: Pihlajamaa, Ilian, van Gessel, Lotte, Laudicina, Corentin, van Burik, Luc, Janssen, Liesbeth
Format: Preprint
Published: 2025
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866912260501274624
author Pihlajamaa, Ilian
van Gessel, Lotte
Laudicina, Corentin
van Burik, Luc
Janssen, Liesbeth
author_facet Pihlajamaa, Ilian
van Gessel, Lotte
Laudicina, Corentin
van Burik, Luc
Janssen, Liesbeth
contents Previous studies have suggested a conundrum in the relaxation dynamics of polydisperse supercooled liquids. It has been shown that in two dimensions, the relative relaxation times of particles of different sizes become more similar as the material is cooled, whereas the opposite happens in three dimensions: they decouple. Here we resolve this conundrum. First, we show that the coupling observed in two dimensions is an artifact of cage correction introduced to account for Mermin-Wagner fluctuations. Instead, the relative relaxation time of small and large particles in two dimensions remains constant or slightly decouples with temperature, as opposed to the substantial decoupling observed in three dimensions. Investigating these dimensional differences further, we find through mobile cluster analysis that small particles initiate relaxation in both dimensions. As the clusters grow larger, they remain dominated by small particles in three dimensions whereas in two cluster growth becomes particle-size agnostic. We explain these findings with a minimal model by studying the distributions of single-particle barrier heights in the system, showing there is a clear difference in the environments of small and large particles, depending on the dimensionality. These findings highlight the critical role of dimensionality in glass formation, providing new insights into the mechanisms underlying the glass transition in polydisperse supercooled liquids.
format Preprint
id arxiv_https___arxiv_org_abs_2503_03320
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Polydispersity-driven dynamical differences between two- and three-dimensional supercooled liquids
Pihlajamaa, Ilian
van Gessel, Lotte
Laudicina, Corentin
van Burik, Luc
Janssen, Liesbeth
Soft Condensed Matter
Materials Science
Statistical Mechanics
Chemical Physics
Previous studies have suggested a conundrum in the relaxation dynamics of polydisperse supercooled liquids. It has been shown that in two dimensions, the relative relaxation times of particles of different sizes become more similar as the material is cooled, whereas the opposite happens in three dimensions: they decouple. Here we resolve this conundrum. First, we show that the coupling observed in two dimensions is an artifact of cage correction introduced to account for Mermin-Wagner fluctuations. Instead, the relative relaxation time of small and large particles in two dimensions remains constant or slightly decouples with temperature, as opposed to the substantial decoupling observed in three dimensions. Investigating these dimensional differences further, we find through mobile cluster analysis that small particles initiate relaxation in both dimensions. As the clusters grow larger, they remain dominated by small particles in three dimensions whereas in two cluster growth becomes particle-size agnostic. We explain these findings with a minimal model by studying the distributions of single-particle barrier heights in the system, showing there is a clear difference in the environments of small and large particles, depending on the dimensionality. These findings highlight the critical role of dimensionality in glass formation, providing new insights into the mechanisms underlying the glass transition in polydisperse supercooled liquids.
title Polydispersity-driven dynamical differences between two- and three-dimensional supercooled liquids
topic Soft Condensed Matter
Materials Science
Statistical Mechanics
Chemical Physics
url https://arxiv.org/abs/2503.03320