Surface mobility of a glass-forming polymer in an ionic liquid

Fuente: arXiv
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Auteurs principaux: Zhang, Xinyu, Pedersen, Christian, Zhu, Haoqi, Wang, Siming, Fu, Yuchen, Dai, Liang, Carlson, Andreas, Salez, Thomas, Chai, Yu
Format: Preprint
Publié: 2025
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author Zhang, Xinyu
Pedersen, Christian
Zhu, Haoqi
Wang, Siming
Fu, Yuchen
Dai, Liang
Carlson, Andreas
Salez, Thomas
Chai, Yu
author_facet Zhang, Xinyu
Pedersen, Christian
Zhu, Haoqi
Wang, Siming
Fu, Yuchen
Dai, Liang
Carlson, Andreas
Salez, Thomas
Chai, Yu
contents The free surface of glassy polymers exhibits enhanced segmental dynamics compared to the bulk, forming a liquid-like layer that lowers the glass transition temperature (Tg) in nanometersized polymer samples. Recent studies have shown that immersing polymers in ionic liquids can suppress this enhanced surface dynamics. To investigate how ionic liquids influence polymer dynamics near the ionic-liquid-polymer interface, we measure the surface leveling of nanometersized stepped polystyrene films immersed in ionic liquids, and compared the results to the case of films in vacuum. Our results reveal that ionic liquids significantly slow the leveling process both above and below Tg. However, our results indicate that the liquid-like surface layer below Tg does exist in ionic liquids. Numerical solutions of the thin-film equation, incorporating appropriate boundary conditions, show that the surface mobility of PS films in ionic liquids can match that of PS films in vacuum. Thus, while ionic liquids alter the polymer flow process, they do not eliminate the dynamical heterogeneity inherent to glassy polymers.
format Preprint
id arxiv_https___arxiv_org_abs_2505_06008
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Surface mobility of a glass-forming polymer in an ionic liquid
Zhang, Xinyu
Pedersen, Christian
Zhu, Haoqi
Wang, Siming
Fu, Yuchen
Dai, Liang
Carlson, Andreas
Salez, Thomas
Chai, Yu
Soft Condensed Matter
Classical Physics
The free surface of glassy polymers exhibits enhanced segmental dynamics compared to the bulk, forming a liquid-like layer that lowers the glass transition temperature (Tg) in nanometersized polymer samples. Recent studies have shown that immersing polymers in ionic liquids can suppress this enhanced surface dynamics. To investigate how ionic liquids influence polymer dynamics near the ionic-liquid-polymer interface, we measure the surface leveling of nanometersized stepped polystyrene films immersed in ionic liquids, and compared the results to the case of films in vacuum. Our results reveal that ionic liquids significantly slow the leveling process both above and below Tg. However, our results indicate that the liquid-like surface layer below Tg does exist in ionic liquids. Numerical solutions of the thin-film equation, incorporating appropriate boundary conditions, show that the surface mobility of PS films in ionic liquids can match that of PS films in vacuum. Thus, while ionic liquids alter the polymer flow process, they do not eliminate the dynamical heterogeneity inherent to glassy polymers.
title Surface mobility of a glass-forming polymer in an ionic liquid
topic Soft Condensed Matter
Classical Physics
url https://arxiv.org/abs/2505.06008