Versatile homeotropic liquid crystal alignment with tunable functionality prepared by one-step method

液晶 材料科学 基质(水族馆) 硅烷 顺势排列 图层(电子) 甲基丙烯酸酯 单层 聚合物 丙烯酸酯 粘附 化学工程 纳米技术 复合材料 聚合 光电子学 单体 海洋学 地质学 工程类 硅烷
作者
Yang Zhang,Weiping Yang,Minzhao Gu,Qunmei Wei,Pengrong Lv,Ming Li,Danqing Liu,Wei Zhao,Dirk J. Broer,Guofu Zhou
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:608: 2290-2297 被引量:15
标识
DOI:10.1016/j.jcis.2021.10.159
摘要

Alignment layers are vital to the function of numerous devices based on liquid crystal (LC) materials. The pursue of versatile, effective and even flexible alignment layers, preferably prepared by simple methods, is still actively ongoing. Herein, we propose a facile one-step method by mixing silanes into the starting LC mixtures, which in contact with a glass substrate secede and self-assemble in-situ to form a stable and highly effective homeotropic alignment layer at the interface. Tetradecyldimethyl(3-trimethoxysilylpropyl)ammonium chloride (TDTA) is selected as the example to demonstrate the method, although a number of other silanes can produce similar results. With only 0.05 vol% of TDTA added to a mixture of liquid crystals and reactive mesogens, a uniform monolayer is chemically attached to the substrate, which automatically aligns the LCs homeotropically. Furthermore, by blending the TDTA with acrylate functionalized silanes like 3-(trimethoxysilyl)propyl methacrylate (A174), additional reactive functional groups can be easily introduced into the alignment layer, therefore offering opportunities to adjust the interface properties. An electro-responsive smart window based on the polymer stabilized liquid crystals (PSLCs) is successfully prepared using a one-step method, demonstrating excellent electro-optic performances and notably enhanced adhesion between the substrate and the in-situ formed polymer network. These findings are valuable especially for the development of flexible LC devices.
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