Versatile homeotropic liquid crystal alignment with tunable functionality prepared by one-step method
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Updated: Oct 13, 2025

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
Published on: October 31, 2019
Yang Zhang1, Weiping Yang2, Minzhao Gu3
1SCNU-TUE Joint Lab of Device Integrated Responsive Materials (DIRM), National Center for International Research on Green Optoelectronics, South China Normal University, No 378, West Waihuan Road, Guangzhou Higher Education Mega Center, 510006 Guangzhou, China; Solar Energy Research Institute, Yunnan Normal University, Kunming 650500, China.
Abstract:
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.

