Miller Daniel S, Wang Xiaoguang, Abbott Nicholas L
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, Wisconsin 53706.
Chem Mater. 2014 Jan 14;26(1):496-506. doi: 10.1021/cm4025028.
This brief perspective focuses on recent advances in the design of functional soft materials that are based on confinement of low molecular weight liquid crystals (LCs) within micrometer-sized droplets. While the ordering of LCs within micrometer-sized domains has been explored extensively in polymer-dispersed LC materials, recent studies performed with LC domains with precisely defined size and interfacial chemistry have unmasked observations of confinement-induced ordering of LCs that do not follow previously reported theoretical predictions. These new findings, which are enabled in part by advances in the preparation of LCs encapsulated in polymeric shells, are opening up new opportunities for the design of soft responsive materials based on surface-induced ordering transitions. These materials are also providing new insights into the self-assembly of biomolecular and colloidal species at defects formed by LCs confined to micrometer-sized domains. The studies presented in this perspective serve additionally to highlight gaps in knowledge regarding the ordering of LCs in confined systems.
本简要观点聚焦于基于将低分子量液晶(LCs)限制在微米级液滴内的功能性软材料设计的最新进展。虽然在聚合物分散液晶材料中已广泛探索了微米级区域内液晶的有序排列,但最近对具有精确界定尺寸和界面化学的液晶区域进行的研究揭示了一些不符合先前报道理论预测的液晶受限诱导有序排列的观察结果。这些新发现部分得益于聚合物壳层包裹液晶制备技术的进步,为基于表面诱导有序转变的软响应材料设计开辟了新机遇。这些材料还为生物分子和胶体物种在由限制在微米级区域的液晶形成的缺陷处的自组装提供了新见解。本观点中呈现的研究还进一步凸显了关于受限系统中液晶有序排列的知识空白。