液晶
材料科学
两亲性
聚合物
稳定器(航空)
化学物理
相(物质)
各向同性
分子
光子晶体
螺旋(腹足类)
纳米技术
化学工程
光学
化学
光电子学
有机化学
物理
共聚物
复合材料
生物
机械工程
生态学
蜗牛
工程类
作者
Xu Ma,Yucen Han,Yan‐Song Zhang,Yong Geng,Apala Majumdar,Jan P. F. Lagerwall
标识
DOI:10.1038/s41467-024-45674-5
摘要
Abstract Multiple emulsions are usually stabilized by amphiphilic molecules that combine the chemical characteristics of the different phases in contact. When one phase is a liquid crystal (LC), the choice of stabilizer also determines its configuration, but conventional wisdom assumes that the orientational order of the LC has no impact on the stabilizer. Here we show that, for the case of amphiphilic polymer stabilizers, this impact can be considerable. The mode of interaction between stabilizer and LC changes if the latter is heated close to its isotropic state, initiating a feedback loop that reverberates on the LC in form of a complete structural rearrangement. We utilize this phenomenon to dynamically tune the configuration of cholesteric LC shells from one with radial helix and spherically symmetric Bragg diffraction to a focal conic domain configuration with highly complex optics. Moreover, we template photonic microparticles from the LC shells by photopolymerizing them into solids, retaining any selected LC-derived structure. Our study places LC emulsions in a new light, calling for a reevaluation of the behavior of stabilizer molecules in contact with long-range ordered phases, while also enabling highly interesting photonic elements with application opportunities across vast fields.
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