Molecular simulations of phase separation in elastic polymer networks

Fuente: arXiv
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Autori principali: Yokoyama, Takahiro, Qiang, Yicheng, Zwicker, David, Nikoubashman, Arash
Natura: Preprint
Pubblicazione: 2025
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author Yokoyama, Takahiro
Qiang, Yicheng
Zwicker, David
Nikoubashman, Arash
author_facet Yokoyama, Takahiro
Qiang, Yicheng
Zwicker, David
Nikoubashman, Arash
contents Phase separation within polymer networks plays a central role in shaping the structure and mechanics of both synthetic materials and living cells, including the formation of biomolecular condensates within cytoskeletal networks. Previous experiments and theoretical studies indicate that network elasticity can regulate demixing and stabilize finite-sized domains, yet the microscopic origin of this size selection remains elusive. Here, we use coarse-grained molecular dynamics simulations with implicit solvent to investigate how network architecture controls phase separation and limits domain growth. By systematically varying chain contour length, chain rigidity, and network topology, we uncover that finite domains emerge when intrinsic chain- or network-level length scales, such as persistence length or entanglement length, impose local constraints on coarsening. Further, the size of these finite domains is highly correlated with these microscopic network properties, but depends surprisingly little on bulk elasticity. Taken together, our findings establish a molecular basis for understanding droplet formation in polymer networks, and provide guiding principles for engineering materials and interpreting condensate behavior in cells.
format Preprint
id arxiv_https___arxiv_org_abs_2511_22300
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Molecular simulations of phase separation in elastic polymer networks
Yokoyama, Takahiro
Qiang, Yicheng
Zwicker, David
Nikoubashman, Arash
Soft Condensed Matter
Phase separation within polymer networks plays a central role in shaping the structure and mechanics of both synthetic materials and living cells, including the formation of biomolecular condensates within cytoskeletal networks. Previous experiments and theoretical studies indicate that network elasticity can regulate demixing and stabilize finite-sized domains, yet the microscopic origin of this size selection remains elusive. Here, we use coarse-grained molecular dynamics simulations with implicit solvent to investigate how network architecture controls phase separation and limits domain growth. By systematically varying chain contour length, chain rigidity, and network topology, we uncover that finite domains emerge when intrinsic chain- or network-level length scales, such as persistence length or entanglement length, impose local constraints on coarsening. Further, the size of these finite domains is highly correlated with these microscopic network properties, but depends surprisingly little on bulk elasticity. Taken together, our findings establish a molecular basis for understanding droplet formation in polymer networks, and provide guiding principles for engineering materials and interpreting condensate behavior in cells.
title Molecular simulations of phase separation in elastic polymer networks
topic Soft Condensed Matter
url https://arxiv.org/abs/2511.22300