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胶体中形状驱动的固-固转变

Shape-driven solid-solid transitions in colloids.

作者信息

Du Chrisy Xiyu, van Anders Greg, Newman Richmond S, Glotzer Sharon C

机构信息

Department of Physics, University of Michigan, Ann Arbor, MI 48109-1040.

Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109-2136.

出版信息

Proc Natl Acad Sci U S A. 2017 May 16;114(20):E3892-E3899. doi: 10.1073/pnas.1621348114. Epub 2017 May 1.

Abstract

Solid-solid phase transitions are the most ubiquitous in nature, and many technologies rely on them. However, studying them in detail is difficult because of the extreme conditions (high pressure/temperature) under which many such transitions occur and the high-resolution equipment needed to capture the intermediate states of the transformations. These difficulties mean that basic questions remain unanswered, such as whether so-called diffusionless solid-solid transitions, which have only local particle rearrangement, require thermal activation. Here, we introduce a family of minimal model systems that exhibits solid-solid phase transitions that are driven by changes in the shape of colloidal particles. By using particle shape as the control variable, we entropically reshape the coordination polyhedra of the particles in the system, a change that occurs indirectly in atomic solid-solid phase transitions via changes in temperature, pressure, or density. We carry out a detailed investigation of the thermodynamics of a series of isochoric, diffusionless solid-solid phase transitions within a single shape family and find both transitions that require thermal activation or are "discontinuous" and transitions that occur without thermal activation or are "continuous." In the discontinuous case, we find that sufficiently large shape changes can drive reconfiguration on timescales comparable with those for self-assembly and without an intermediate fluid phase, and in the continuous case, solid-solid reconfiguration happens on shorter timescales than self-assembly, providing guidance for developing means of generating reconfigurable colloidal materials.

摘要

固-固相变在自然界中最为普遍,许多技术都依赖于它们。然而,由于许多此类相变发生时的极端条件(高压/高温)以及捕捉转变中间状态所需的高分辨率设备,对其进行详细研究很困难。这些困难意味着一些基本问题仍未得到解答,比如仅发生局部粒子重排的所谓无扩散固-固相变是否需要热激活。在此,我们引入了一类最小模型系统,该系统呈现出由胶体粒子形状变化驱动的固-固相变。通过将粒子形状用作控制变量,我们在熵的作用下重塑了系统中粒子的配位多面体,这种变化在原子固-固相变中是通过温度、压力或密度的变化间接发生的。我们对单个形状家族内一系列等容、无扩散的固-固相变的热力学进行了详细研究,发现既有需要热激活或“不连续”的相变,也有无需热激活或“连续”的相变。在不连续的情况下,我们发现足够大的形状变化能够在与自组装相当的时间尺度上驱动重新构型,且无需中间流体相;而在连续的情况下,固-固重新构型发生的时间尺度比自组装短,这为开发生成可重构胶体材料的方法提供了指导。

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