The association of structural chirality and liquid crystal anchoring in polymer stabilized cholesteric liquid crystals

被引:4
作者
Radka, Brian P. [1 ]
Lee, Taewoo [3 ]
Smalyukh, Ivan I. [2 ,3 ,4 ]
White, Timothy J. [1 ,2 ]
机构
[1] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
[2] Univ Colorado, Mat Sci & Engn Program, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Phys, Boulder, CO 80309 USA
[4] Univ Colorado, Renewable & Sustainable Energy Inst, Boulder, CO 80309 USA
关键词
ELECTROOPTIC PERFORMANCE; NETWORK STRUCTURE; COLOR CHANGES; REFLECTION; PITCH; ORIGIN; PHOTOISOMERIZATION; DEFORMATION; MESOPHASES; TEXTURES;
D O I
10.1039/d3sm01558k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polymer stabilized cholesteric liquid crystals (PSCLCs) are electrically reconfigurable reflective elements. Prior studies have hypothesized and indirectly confirmed that the electro-optic response of these composites is associated with the electrically mediated distortion of the stabilizing polymer network. The proposed mechanism is based on the retention of structural chirality in the polymer stabilizing network, which upon deformation is spatially distorted, which accordingly affects the pitch of the surrounding low molar-mass liquid crystal host. Here, we utilize fluorescent confocal polarized microscopy to directly assess the electro-optic response of PSCLCs. By utilizing dual fluorescent probes, sequential imaging experiments confirm that the periodicity of the polymer stabilizing network matches that of the low molar-mass liquid crystal host. Further, we isolate distinct ion-polymer interactions that manifest in certain photopolymerization conditions. Polymer stabilized cholesteric liquid crystals (PSCLCs) are electrically reconfigurable reflective elements. This investigation confirms that the liquid crystal anchors to the structurally chiral polymer network during ion-mediated deformation.
引用
收藏
页码:1815 / 1823
页数:9
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