4.4 Article

Nucleation and growth of blue phase liquid crystals on chemically-patterned surfaces: a surface anchoring assisted blue phase correlation length

Journal

MOLECULAR SYSTEMS DESIGN & ENGINEERING
Volume 6, Issue 7, Pages 534-544

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1me00044f

Keywords

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Funding

  1. U.S. Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division
  2. DOE Office of Science [DE-AC02-06CH11357]
  3. University of Chicago MRSEC Shared User Facilities [NSF DMR-1420709]
  4. Laboratorio Nacional de Supercomputo del (LNS) [201901023N]

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In this study, liquid epitaxial growth was used to achieve the spontaneous nucleation and growth of blue phase crystal cores. The research focused on measuring the correlation length of crystallographic orientation in blue phase chiral liquid crystals, and the formation process of single crystal BPII blue phase. The results suggest that by using patterned substrates, it is possible to design processes that allow for the formation of macroscopically large single-domain, single-crystal BPs.
In condensed matter, the correlation length is an essential parameter which describes the distance over which a material maintains its structural properties. In liquid crystals, for the orientational order parameter this characteristic length is of the order of nanometers, while in solid crystals it can extend to macroscopic length scales. Here, we report the measurement of the correlation length, or persistence length, of the crystallographic orientation of blue phases (BPs)-chiral liquid crystals with long-range 3D-crystalline structures and submicron-sized lattice-parameters. These materials exhibit phase transformations that have been identified as the liquid analog of crystal-crystal martensitic transformations. In this work, we use liquid epitaxial growth to achieve spontaneous BP-crystal nucleation and subsequent growth. Specifically, we design patterned substrates made of a binary array of regions with different liquid crystal anchoring, which facilitate a uniform nucleation and growth of BP-crystals with (100)-lattice orientation and a simple cubic symmetry. Our results indicate that this simple cubic BP, the so-called blue phase II (BPII), forms first on the patterned surface, thereby propagating the growth of domains in directions parallel or perpendicular to the patterned regions. These results are used to understand the emergence of a surface anchoring assisted BPII-correlation length, taken as the distance over which the BP preserves its lattice orientation, as a function of time and pattern characteristics. We found that BPII single crystals can be achieved on patterned regions whose lateral dimensions are equal to or larger than 10 mu m, consistent with our measurements of the BPII-correlation length. This newly acquired understanding of the role of surfaces on the formation of BPs is then used to design processes that permit formation of macroscopically large mono-domain, single-crystal BPs by relying on significantly reduced patterned areas (only part of the area is patterned), a feature that could benefit the applications of this intriguing class of materials.

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