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Phase behaviors of colloidal analogs of bent-core liquid crystals.

ABSTRACT: Bent-core liquid crystal (LC) molecules are known to form mesophases with fascinating polar order and supramolecular chirality despite the achiral nature of the mesogens. The assembly of colloidal particles with geometrical similarity to bent-core molecular mesogens not only provides new insights into the physical behaviors of atoms or molecules but also leads to new materials with broad applications. Despite tremendous progress in colloidal synthesis and assembly, there has been a lack of colloidal model systems of bent-core molecular mesogens for LC property discovery and application development. This article describes a systematic study on the phase behaviors of colloidal analogs of bent-core LC mesogens in both experiments and simulations. We demonstrated that bent rods with controlled bending angle (?) and aspect ratio (L/D, with L and D as the length and diameter of each rod arm, respectively) can spontaneously assemble into several typical banana phases including smectic A, smectic C, synclinic tilted antiferroelectric-like smectic, and twist smectic phases, resembling bent-core LC molecules. The formation and transition of these phases were found to be strongly dependent on the geometric parameters of rods. Phase diagrams were developed to illustrate the existence and stability range of all the LC phases in ? and L/D space. This work opens the door to the development of novel complex types of molecular or colloidal self-organization and new functional materials with electro-optical or nonlinear optical properties.

SUBMITTER: Yang Y

PROVIDER: S-EPMC5947975 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Phase behaviors of colloidal analogs of bent-core liquid crystals.

Yang Yang Y Pei Hanwen H Chen Guangdong G Webb Kyle Thomas KT Martinez-Miranda Luz J LJ Lloyd Isabel K IK Lu Zhongyuan Z Liu Kun K Nie Zhihong Z

Science advances 20180511 5

Bent-core liquid crystal (LC) molecules are known to form mesophases with fascinating polar order and supramolecular chirality despite the achiral nature of the mesogens. The assembly of colloidal particles with geometrical similarity to bent-core molecular mesogens not only provides new insights into the physical behaviors of atoms or molecules but also leads to new materials with broad applications. Despite tremendous progress in colloidal synthesis and assembly, there has been a lack of collo ...[more]

PMID: 29756038

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Project description:This feature article describes recent advances in several areas of research involving the interfacial ordering of liquid crystals (LCs). The first advance revolves around the ordering of LCs at bio/chemically functionalized surfaces. Whereas the majority of past studies of surface-induced ordering of LCs have involved surfaces of solids that present a limited diversity of chemical functional groups (surfaces at which van der Waals forces dominate surface-induced ordering), recent studies have moved to investigate the ordering of LCs on chemically complex surfaces. For example, surfaces decorated with biomolecules (e.g., oligopeptides and proteins) and transition-metal ions have been investigated, leading to an understanding of the roles that metal-ligand coordination interactions, electrical double layers, acid-base interactions, and hydrogen bonding can play in the interfacial ordering of LCs. The opportunity to create chemically responsive LCs capable of undergoing ordering transitions in the presence of targeted molecular events (e.g., ligand exchange around a metal center) has emerged from these fundamental studies. A second advance has focused on investigations of the ordering of LCs at interfaces with immiscible isotropic fluids, particularly water. In contrast to prior studies of surface-induced ordering of LCs on solid surfaces, LC-aqueous interfaces are deformable and molecules at these interfaces exhibit high levels of mobility and thus can reorganize in response to changes in the interfacial environment. A range of fundamental investigations involving these LC-aqueous interfaces have revealed that (i) the spatial and temporal characteristics of assemblies formed from biomolecular interactions can be reported by surface-driven ordering transitions in the LCs, (ii) the interfacial phase behavior of molecules and colloids can be coupled to (and manipulated via) the ordering (and nematic elasticity) of LCs, and (iii) the confinement of LCs leads to unanticipated size-dependent ordering (particularly in the context of LC emulsion droplets). The third and final advance addressed in this article involves interactions between colloids mediated by LCs. Recent experiments involving microparticles deposited at the LC-aqueous interface have revealed that LC-mediated interactions can drive interfacial assemblies of particles through reversible ordering transitions (e.g., from 1D chains to 2D arrays with local hexagonal symmetry). In addition, recent single-nanoparticle measurements suggest that the ordering of LCs about nanoparticles differs substantially from micrometer-sized particles and that the interactions between nanoparticles mediated by the LCs are far weaker than predicted by theory (sufficiently weak that the interactions are reversible and thus enable self-assembly). Finally, LC-mediated interactions between colloidal particles have also been shown to lead to the formation of colloid-in-LC gels that possess mechanical properties relevant to the design of materials that interface with living biological systems. Overall, these three topics serve to illustrate the broad opportunities that exist to do fundamental interfacial science and discovery-oriented research involving LCs.

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Phase behaviors of colloidal analogs of bent-core liquid crystals.

Publications

Phase behaviors of colloidal analogs of bent-core liquid crystals.

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