Liu Iris B, Sharifi-Mood Nima, Stebe Kathleen J
Department of Chemical and Biomolecular Engineering, 220 South 33rd Street, University of Pennsylvania, Philadelphia, PA 19104-6391, USA.
Department of Chemical and Biomolecular Engineering, 220 South 33rd Street, University of Pennsylvania, Philadelphia, PA 19104-6391, USA
Philos Trans A Math Phys Eng Sci. 2016 Jul 28;374(2072). doi: 10.1098/rsta.2015.0133.
Control over the spatial arrangement of colloids in soft matter hosts implies control over a wide variety of properties, ranging from the system's rheology, optics, and catalytic activity. In directed assembly, colloids are typically manipulated using external fields to form well-defined structures at given locations. We have been developing alternative strategies based on fields that arise when a colloid is placed within soft matter to form an inclusion that generates a potential field. Such potential fields allow particles to interact with each other. If the soft matter host is deformed in some way, the potential allows the particles to interact with the global system distortion. One important example is capillary assembly of colloids on curved fluid interfaces. Upon attaching, the particle distorts that interface, with an associated energy field, given by the product of its interfacial area and the surface tension. The particle's capillary energy depends on the local interface curvature. We explore this coupling in experiment and theory. There are important analogies in liquid crystals. Colloids in liquid crystals elicit an elastic energy response. When director fields are moulded by confinement, the imposed elastic energy field can couple to that of the colloid to define particle paths and sites for assembly. By improving our understanding of these and related systems, we seek to develop new, parallelizable routes for particle assembly to form reconfigurable systems in soft matter that go far beyond the usual close-packed colloidal structures.This article is part of the themed issue 'Soft interfacial materials: from fundamentals to formulation'.
控制软物质基质中胶体的空间排列意味着能够控制从系统的流变学、光学和催化活性等各种各样的性质。在定向组装中,通常利用外部场来操纵胶体,使其在给定位置形成明确的结构。我们一直在开发基于当胶体置于软物质中形成内含物从而产生势场时所产生的场的替代策略。这种势场使粒子能够相互作用。如果软物质基质以某种方式变形,该势场会使粒子与整体系统的变形相互作用。一个重要的例子是胶体在弯曲流体界面上的毛细管组装。附着时,粒子会使该界面变形,并产生一个由其界面面积与表面张力的乘积给出的相关能量场。粒子的毛细管能量取决于局部界面曲率。我们在实验和理论上探索这种耦合。在液晶中有重要的类比。液晶中的胶体引发弹性能量响应。当指向矢场通过限制作用而形成时,所施加的弹性能量场可以与胶体的能量场耦合,以确定粒子的路径和组装位点。通过增进我们对这些及相关系统的理解,我们寻求开发新的、可并行化的粒子组装途径,以在软物质中形成远超通常密堆积胶体结构的可重构系统。本文是主题为“软界面材料:从基础到配方”的特刊的一部分。