4.8 Article

Control of Monodomain Polymer-Stabilized Cuboidal Nanocrystals of Chiral Nematics by Confinement

Journal

ACS NANO
Volume 15, Issue 10, Pages 15972-15981

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c04231

Keywords

liquid crystals; photonic soft crystals; stabilized blue-phases; confinement; confocal microscopy

Funding

  1. Department of Energy, Office of Basic Energy Sciences, Division of Materials Science and Engineering [DESC0019762]
  2. National Science Foundation under MRI Grant [1828629]
  3. SC EPSCoR [21-GE03]
  4. Laboratorio Nacional de Supercomputo del Sureste de Mexico (LNS)
  5. CONACYT [201901023N]
  6. Division Of Materials Research
  7. Direct For Mathematical & Physical Scien [1828629] Funding Source: National Science Foundation

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This article introduces the concept of strain-controlled polymerization of blue phases under confinement, enabling the formation of strain-correlated stabilized morphologies that can adopt perfect single-crystal monodomain structures and undergo reversible crystal-to-crystal transformations under some circumstances.
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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