Non-equilibrium coexistence between a fluid and a hotter or colder crystal of granular hard disks.

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL Journal of Chemical Physics Pub Date : 2025-03-28 DOI:10.1063/5.0250643
R Maire, A Plati, F Smallenburg, G Foffi
{"title":"Non-equilibrium coexistence between a fluid and a hotter or colder crystal of granular hard disks.","authors":"R Maire, A Plati, F Smallenburg, G Foffi","doi":"10.1063/5.0250643","DOIUrl":null,"url":null,"abstract":"<p><p>Non-equilibrium phase coexistence is commonly observed in both biological and artificial systems, yet understanding it remains a significant challenge. Unlike equilibrium systems, where free energy provides a unifying framework, the absence of such a quantity in non-equilibrium settings complicates their theoretical understanding. Granular materials, driven out of equilibrium by energy dissipation during collisions, serve as an ideal platform to investigate these systems, offering insights into the parallels and distinctions between equilibrium and non-equilibrium phase behavior. For example, the coexisting dense phase is typically colder than the dilute phase, a result usually attributed to greater dissipation in denser regions. In this article, we demonstrate that this is not always the case. Using a simple numerical granular model, we show that a hot solid and a cold liquid can coexist in granular systems. This counterintuitive phenomenon arises because the collision frequency can be lower in the solid phase than in the liquid phase, consistent with equilibrium results for hard-disk systems. We further demonstrate that kinetic theory can be extended to accurately predict phase temperatures even at very high packing fractions, including within the solid phase. Our results highlight the importance of collisional dynamics and energy exchange in determining phase behavior in granular materials, offering new insights into non-equilibrium phase coexistence and the complex physics underlying granular systems.</p>","PeriodicalId":15313,"journal":{"name":"Journal of Chemical Physics","volume":"162 12","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1063/5.0250643","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Non-equilibrium phase coexistence is commonly observed in both biological and artificial systems, yet understanding it remains a significant challenge. Unlike equilibrium systems, where free energy provides a unifying framework, the absence of such a quantity in non-equilibrium settings complicates their theoretical understanding. Granular materials, driven out of equilibrium by energy dissipation during collisions, serve as an ideal platform to investigate these systems, offering insights into the parallels and distinctions between equilibrium and non-equilibrium phase behavior. For example, the coexisting dense phase is typically colder than the dilute phase, a result usually attributed to greater dissipation in denser regions. In this article, we demonstrate that this is not always the case. Using a simple numerical granular model, we show that a hot solid and a cold liquid can coexist in granular systems. This counterintuitive phenomenon arises because the collision frequency can be lower in the solid phase than in the liquid phase, consistent with equilibrium results for hard-disk systems. We further demonstrate that kinetic theory can be extended to accurately predict phase temperatures even at very high packing fractions, including within the solid phase. Our results highlight the importance of collisional dynamics and energy exchange in determining phase behavior in granular materials, offering new insights into non-equilibrium phase coexistence and the complex physics underlying granular systems.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
流体与颗粒状硬盘的较热或较冷晶体之间的非平衡共存。
非平衡相共存在生物系统和人工系统中都很常见,但理解它仍然是一个重大挑战。与平衡系统不同,在平衡系统中自由能提供了一个统一的框架,在非平衡环境中缺乏这样一个量会使它们的理论理解复杂化。颗粒材料在碰撞过程中因能量耗散而失去平衡,是研究这些系统的理想平台,可以深入了解平衡和非平衡相行为之间的相似之处和区别。例如,共存的致密相通常比稀相冷,这一结果通常归因于致密区域的耗散更大。在本文中,我们将证明情况并非总是如此。通过一个简单的数值颗粒模型,我们证明了热固体和冷液体在颗粒系统中可以共存。这种违反直觉的现象之所以出现,是因为碰撞频率在固相中可能比在液相中低,这与硬盘系统的平衡结果一致。我们进一步证明,动力学理论可以扩展到准确地预测相温度,即使在非常高的填料分数,包括在固相。我们的研究结果强调了碰撞动力学和能量交换在确定颗粒材料相行为中的重要性,为非平衡相共存和颗粒系统背后的复杂物理提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Chemical Physics
Journal of Chemical Physics 物理-物理:原子、分子和化学物理
CiteScore
7.40
自引率
15.90%
发文量
1615
审稿时长
2 months
期刊介绍: The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance. Topical coverage includes: Theoretical Methods and Algorithms Advanced Experimental Techniques Atoms, Molecules, and Clusters Liquids, Glasses, and Crystals Surfaces, Interfaces, and Materials Polymers and Soft Matter Biological Molecules and Networks.
期刊最新文献
Fourth-order complex time-dependent Redfield theory for absorption line shapes. Clarifying NH2 + O(3P) reaction dynamics: A full-dimensional MRCI, machine-learned PES unravels high-temperature kinetics. Revisiting photoacidity using R*NH2 photoacids. Probing component segregation and anisotropy for co-deposited glasses of TCTA and Ir(ppy)3 by GIWAXS. Medium-range ordering of interfacial water at charged clay interfaces: From layering to network connectivity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1