Directed self-assembly into low-density colloidal liquid crystal phases

Yongxiang Gao, Flavio Romano, Roel P. A. Dullens, Jonathan K. Doye, and Dirk G. A. L. Aarts
Phys. Rev. Materials 2, 015601 – Published 3 January 2018
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Abstract

Alignment of anisometric particles into liquid crystals (LCs) often results from an entropic competition between their rotational and translational degrees of freedom at dense packings. Here we show that by selectively functionalizing the heads of colloidal rods with magnetic nanoparticles this tendency can be broken to direct the particles into novel, low-density LC phases. Under an external magnetic field, the magnetic heads line up in columns whereas the nonmagnetic tails point out randomly in a plane perpendicular to the columns, forming bottle-brush-like objects; laterally, the bottle brushes are entropically stabilized against coalescence. Experiments and simulations show that upon increasing the particle density the system goes from a dilute gas to a dense two-dimensional liquid of bottle brushes with a density well below the zero-field nematic phase. Our findings offer a strategy for self-assembly into three-dimensional open phases that may find applications in switchable photonics, filtration, and light-weight materials.

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  • Received 21 October 2017

DOI:https://doi.org/10.1103/PhysRevMaterials.2.015601

©2018 American Physical Society

Physics Subject Headings (PhySH)

Polymers & Soft Matter

Authors & Affiliations

Yongxiang Gao1,2,*, Flavio Romano2, Roel P. A. Dullens2, Jonathan K. Doye2, and Dirk G. A. L. Aarts2,†

  • 1Institute for Advanced Study, Shenzhen University, Nanhai Avenue 3688, Nanshan District, Shenzhen 518060, China
  • 2Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QZ, England, United Kingdom

  • *Corresponding author: yongxiang.gao@szu.edu.cn
  • Corresponding author: dirk.aarts@chem.ox.ac.uk

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Issue

Vol. 2, Iss. 1 — January 2018

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