偏斜
材料科学
聚合
液晶
化学物理
聚合物
结晶学
晶体结构
小旋翼机
凝聚态物理
分子物理学
光学
纳米技术
共聚物
光电子学
物理
复合材料
化学
作者
Monirosadat Sadati,José A. Martínez‐González,Alexander E. Cohen,Sepideh Norouzi,Orlando Guzmán,Juan Pablo
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-10-01
卷期号:15 (10): 15972-15981
被引量:18
标识
DOI:10.1021/acsnano.1c04231
摘要
Liquid crystals are important components of optical technologies. Cuboidal crystals consisting of chiral liquid crystals-the so-called blue phases (BPs), are of particular interest due to their crystalline structures and fast response times, but it is critical that control be gained over their phase behavior as well as the underlying dislocations and grain boundaries that arise in such systems. Blue phases exhibit cubic crystalline symmetries with lattice parameters in the 100 nm range and a network of disclination lines that can be polymerized to widen the range of temperatures over which they occur. Here, we introduce the concept of strain-controlled polymerization of BPs under confinement, which enables formation of strain-correlated stabilized morphologies that, under some circumstances, can adopt perfect single-crystal monodomain structures and undergo reversible crystal-to-crystal transformations, even if their disclination lines are polymerized. We have used super-resolution laser confocal microscopy to reveal the periodic structure and the lattice planes of the strain and polymerization stabilized BPs in 3D real space. Our experimental observations are supported and interpreted by relying on theory and computational simulations in terms of a free energy functional for a tensorial order parameter. Simulations are used to determine the orientation of the lattice planes unambiguously. The findings presented here offer opportunities for engineering optical devices based on single-crystal, polymer-stabilized BPs whose inherent liquid nature, fast dynamics, and long-range crystalline order can be fully exploited.
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