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Autores principales: Song, Lijian, Gao, Meng, Huo, Juntao, Wang, Li-Min, Yue, Yuanzheng, Wang, Jun-Qiang
Formato: Preprint
Publicado: 2025
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Acceso en línea:https://arxiv.org/abs/2501.11857
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author Song, Lijian
Gao, Meng
Huo, Juntao
Wang, Li-Min
Yue, Yuanzheng
Wang, Jun-Qiang
author_facet Song, Lijian
Gao, Meng
Huo, Juntao
Wang, Li-Min
Yue, Yuanzheng
Wang, Jun-Qiang
contents Glass transition is a reversible transition that occurs in most amorphous materials. However, the nature of glass transition remains far from being clarified. A key to understand the glass transition is to clarify what determines the glass transition temperature (Tg) and liquid fragility (m). Here the glass transition thermodynamics for 150 different glass-forming systems are studied statistically. It is found that the activation characters in the energy landscape are crucial to precisely portray the glass transition and, in particular, both the activation free energy (G*) and the activation entropy (S*) play critical roles. G* determines Tg, Tg=G*/290+25.5, while S* determines m, m=S*/Rln10+15 with R is gas constant. Based on the Boltzmann definition of entropy, the fragility is an indication of the number of the degeneracy of the evolution paths. This explains why the nano-confined, low-dimension or high-pressured glasses exhibit stronger characteristics, which has been a puzzling phenomenon for a long time.
format Preprint
id arxiv_https___arxiv_org_abs_2501_11857
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle The critical role of entropy in glass transition kinetics
Song, Lijian
Gao, Meng
Huo, Juntao
Wang, Li-Min
Yue, Yuanzheng
Wang, Jun-Qiang
Materials Science
Glass transition is a reversible transition that occurs in most amorphous materials. However, the nature of glass transition remains far from being clarified. A key to understand the glass transition is to clarify what determines the glass transition temperature (Tg) and liquid fragility (m). Here the glass transition thermodynamics for 150 different glass-forming systems are studied statistically. It is found that the activation characters in the energy landscape are crucial to precisely portray the glass transition and, in particular, both the activation free energy (G*) and the activation entropy (S*) play critical roles. G* determines Tg, Tg=G*/290+25.5, while S* determines m, m=S*/Rln10+15 with R is gas constant. Based on the Boltzmann definition of entropy, the fragility is an indication of the number of the degeneracy of the evolution paths. This explains why the nano-confined, low-dimension or high-pressured glasses exhibit stronger characteristics, which has been a puzzling phenomenon for a long time.
title The critical role of entropy in glass transition kinetics
topic Materials Science
url https://arxiv.org/abs/2501.11857