中程结构秩序是玻璃态液体活化动力学和复杂性降低的驱动力

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-11-14 Epub Date: 2024-10-31 DOI:10.1021/acs.jpcb.4c05488
Baicheng Mei, Kenneth S Schweizer
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引用次数: 0

摘要

我们深入分析了可变质液体中活化动力学的弹性集合非线性朗格文方程理论,以确定α弛豫时间、局部笼型和集合弹性壁垒、动态局部化长度和剪切模量之间的预测相互关系在理论中与中程阶(MRO)静态相关长度存在因果关系。对于可蜕变硬球液体,后者随密度呈指数增长,而对于等压条件下的过冷液体,则随温度呈非普遍反幂律增长。α时间和其他笼序度量与热力学逆无量纲可压缩性之间的预言联系的物理起源已完全确立。研究发现,虽然来自真实空间第一配位壳的动力学约束对α时间很重要,但与更普遍的 MRO 相关性在适度和深度蜕变体系中的后果相比,它们的重要性是次要的。这种理解为基于无量纲压缩率匹配将化学性质复杂的热液体预测映射为有效的硬球液体(我们称之为 "复杂性还原 "方案)的理论基础和先前的成功提供了新的启示。从本质上讲,后者等同于热液体 MRO 相关性等于其有效硬球类似物的物理要求。研究表明,仅映射就能为 21 种分子液体和聚合物液体的玻璃化转变温度 Tg 提供卓越的定量预测能力。研究还获得了 MRO 相关长度的化学特异性绝对值和随冷却而增长的预测值,这些相关长度在 Tg 时位于 2-6 nm 的窗口范围内。此外,还简要讨论了动态异质性、弹性促进和超越配对结构的问题。并概述了从理论上分析平衡深玻璃体系的未来机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medium-Range Structural Order as the Driver of Activated Dynamics and Complexity Reduction in Glass-Forming Liquids.

We analyze in depth the Elastically Collective Nonlinear Langevin Equation theory of activated dynamics in metastable liquids to establish that the predicted inter-relationships between the alpha relaxation time, local cage and collective elastic barriers, dynamic localization length, and shear modulus are causally related within the theory to the medium range order (MRO) static correlation length. The latter grows exponentially with density for metastable hard sphere fluids and as a nonuniversal inverse power law with temperature for supercooled liquids under isobaric conditions. The physical origin of predicted connections between the alpha time and other metrics of cage order and the thermodynamic inverse dimensionless compressibility is fully established. It is discovered that although kinetic constraints from the real space first coordination shell are important for the alpha time, they are of secondary importance compared to the consequences of the more universal MRO correlations in both the modestly and deeply metastable regimes. This understanding sheds new light on the theoretical basis for, and prior successes of, the predictive mapping of chemically complex thermal liquids to effective hard sphere fluids based on matching their dimensionless compressibilities, a scheme we call "complexity reduction". In essence, the latter is equivalent to the physical requirement that the thermal liquid MRO correlation equals that of its effective hard sphere analog. The mapping alone is shown to provide a remarkable level of quantitative predictive power for the glass transition temperature Tg of 21 molecular and polymer liquids. Predictions for the chemically specific absolute magnitude and growth with cooling of the MRO correlation length are obtained and lie in the window of 2-6 nm at Tg. Dynamic heterogeneity, elastic facilitation, and beyond pair structure issues are briefly discussed. Future opportunities to theoretically analyze the equilibrated deep glass regime are outlined.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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