当物理与化学在动态玻璃转化过程中相遇。

Haibao Lu
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引用次数: 0

摘要

物理定律可以统一吗?最令人费解的挑战之一是如何协调物理学和化学,即分子物理学与凝聚态物理学的关系,这是由玻璃态物质在玻璃转变温度下的动态波动和缩放效应所导致的。1995 年,凝聚态物理学的先驱、诺贝尔物理学奖获得者菲利普-沃伦-安德森将这一差距称为凝聚态物理学中最深奥、最有趣的未决问题。2005 年,《科学》在其 125 周年纪念刊物中强调,"玻璃态的本质是什么?然而,由于物理学和化学分别受凝聚态和分子态物理定律的制约,具有跨学科的复杂性,玻璃态的本质及其与玻璃化转变的联系尚未被完全理解。因此,玻璃态转变的研究对于探索玻璃态物质的缩放效应和动态波动的工作原理,以及进一步协调物理学和化学的跨学科复杂性至关重要。首先,本文提出了微相分离的热力学有序-无序自由能方程,以阐述玻璃化转变过程中相分离和微相分离相互作用产生的动态平衡和波动。其次,采用亚当-吉布斯(Adam-Gibbs,AG)域模型来探索玻璃态物质中的协同动力学和分子纠缠。该模型依赖于配对过渡概率的概念,其中每个畴包含 e+1 个区段,在玻璃化转变温度下,约有 3.718 个区段在一个畴中协同松弛。该模型能够对以前未验证的说法进行理论建模和验证,即 50 到 100 个单体在玻璃化温度下会同步松弛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
When physics meets chemistry at the dynamic glass transition.

Can the laws of physics be unified? One of the most puzzling challenges is to reconcile physics and chemistry, where molecular physics meets condensed-matter physics, resulting from the dynamic fluctuation and scaling effect of glassy matter at the glass transition temperature. The pioneer of condensed-matter physics, Nobel Prize-winning physicist Philip Warren Anderson referred to this gap as the deepest and most interesting unsolved problem in condensed-matter physics in 1995. In 2005, Science, in its 125th anniversary publication, highlighted that the question of "what is the nature of glassy state?" was one of the greatest scientific conundrums for the next quarter century. However, the nature of the glassy state and its connection to the glass transition have not been fully understood owing to the interdisciplinary complexity of physics and chemistry, governed by physical laws at the condensed-matter and molecular scales, respectively. Therefore, the study of glass transition is essential to explore the working principles of the scaling effects and dynamic fluctuations in glassy matter and to further reconcile the interdisciplinary complexity of physics and chemistry. Initially, this paper proposes a thermodynamic order-to-disorder free-energy equation for microphase separation to formulate the dynamic equilibria and fluctuations, which originate from the interplay of the phase and microphase separations during glass transition. Secondly, the Adam-Gibbs (AG) domain model is employed to explore the cooperative dynamics and molecular entanglement in glassy matter. It relies on the concept of transition probability in pairing, where each domain contains e+1 segments, in which approximately 3.718 segments cooperatively relax in a domain at the glass transition temperature. This model enables the theoretical modelling and validation of a previously unverified statement, suggesting that 50 to 100 individual monomers would relax synchronously at glass transition temperature.

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