Reversible Nanoparticle Cubic Lattices in Blue Phase Liquid Crystals
Author(s) -
Mohamed Amine Gharbi,
Sabine Manet,
Julien Lhermitte,
Sarah Brown,
Jonathan Milette,
Violeta Toader,
Mark Sutton,
Linda Reven
Publication year - 2016
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.5b07379
Subject(s) - disclination , materials science , small angle x ray scattering , liquid crystal , nanoparticle , colloidal crystal , synchrotron , crystallography , chemical physics , lattice (music) , cubic crystal system , phase (matter) , phase transition , scattering , gyroid , colloid , nanotechnology , optics , condensed matter physics , polymer , chemical engineering , copolymer , optoelectronics , composite material , chemistry , physics , engineering , organic chemistry , acoustics
Blue phases (BPs), a distinct class of liquid crystals (LCs) with 3D periodic ordering of double twist cylinders involving orthogonal helical director twists, have been theoretically studied as potential templates for tunable colloidal crystals. Here, we report the spontaneous formation of thermally reversible, cubic crystal nanoparticle (NP) assemblies in BPs. Gold NPs, functionalized to be highly miscible in cyanobiphenyl-based LCs, were dispersed in BP mixtures and characterized by polarized optical microscopy and synchrotron small-angle X-ray scattering (SAXS). The NPs assemble by selectively migrating to periodic strong trapping sites in the BP disclination lines. The NP lattice, remarkably robust given the small particle size (4.5 nm diameter), is commensurate with that of the BP matrix. At the BP I to BP II phase transition, the NP lattice reversibly switches between two different cubic structures. The simultaneous presence of two different symmetries in a single material presents an interesting opportunity to develop novel dynamic optical materials.
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