Suppr超能文献

键取向有序在玻璃化转变和结晶中的作用。

Roles of bond orientational ordering in glass transition and crystallization.

机构信息

Institute of Industrial Science, University of Tokyo, Tokyo, Japan.

出版信息

J Phys Condens Matter. 2011 Jul 20;23(28):284115. doi: 10.1088/0953-8984/23/28/284115. Epub 2011 Jun 27.

Abstract

It is widely believed that crystallization in three dimensions is primarily controlled by positional ordering, and not by bond orientational ordering. In other words, bond orientational ordering is usually considered to be merely a consequence of positional ordering and thus has often been ignored. This one-order-parameter (density) description may be reasonable when we consider an equilibrium liquid-solid transition, but may not be enough to describe a metastable state and the kinetics of the transition. Here we propose that bond orientational ordering can play a key role in (i) crystallization, (ii) the ordering to quasi-crystal and (iii) vitrification, which occurs under rather weak frustration against crystallization. In a metastable supercooled state before crystallization, a system generally tends to have bond orientational order at least locally as a result of a constraint of dense packing. For a system interacting with hard-core repulsions, the constraint is intrinsically of geometrical origin and thus the basic physics is the same as nematic ordering of rod-like particles upon densification. Furthermore, positional ordering is easily destroyed even by weak frustration such as polydispersity and anisotropic interactions which favour a symmetry not consistent with that of the equilibrium crystal. Thus we may say that vitrification can be achieved by disturbing and prohibiting long-range positional ordering. Even in such a situation, bond orientational ordering still survives, accompanying its critical-like fluctuations, which are the origin of dynamic heterogeneity for this case. This scenario naturally explains both the absence of positional order and the development of bond orientational order upon cooling in a supercooled state. Although our argument is speculative in nature, we emphasize that this physical picture can coherently explain crystallization, vitrification, quasi-crystallization and their relationship in a natural manner. For a strongly frustrated system, even bond orientational order can be destroyed. Even in such a case there may still appear a structural signature of dense packing, which is linked to slow dynamics.

摘要

人们普遍认为,三维结晶主要受位置有序控制,而不受键取向有序控制。换句话说,键取向有序通常被认为仅仅是位置有序的结果,因此通常被忽略。当我们考虑平衡液-固转变时,这种一参数(密度)描述可能是合理的,但可能不足以描述亚稳状态和转变的动力学。在这里,我们提出键取向有序可以在以下方面发挥关键作用:(i)结晶、(ii)准晶的有序化和 (iii)玻璃化转变,这在结晶的弱受挫下发生。在结晶前的亚稳过冷状态下,由于密集堆积的约束,系统通常倾向于具有至少局部的键取向有序。对于与硬芯排斥相互作用的系统,约束本质上是几何起源的,因此基本物理与棒状粒子在致密化时的向列有序相同。此外,即使受到像多分散性和各向异性相互作用这样的弱受挫的干扰,位置有序也很容易被破坏,这些相互作用有利于与平衡晶体不一致的对称性。因此,我们可以说玻璃化转变可以通过干扰和禁止长程位置有序来实现。即使在这种情况下,键取向有序仍然存在,伴随着其类似临界的波动,这是这种情况动态异质性的起源。这种情况自然解释了在过冷状态下冷却时位置有序的缺失和键取向有序的发展。虽然我们的论点本质上是推测性的,但我们强调这种物理图像可以以自然的方式连贯地解释结晶、玻璃化转变、准晶及其关系。对于一个强烈受挫的系统,甚至键取向有序也可能被破坏。即使在这种情况下,仍然可能出现密集堆积的结构特征,这与缓慢的动力学有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验