Volume 61, Number 3, February 2003
|Page(s)||334 - 340|
|Section||Condensed matter: structure, mechanical and thermal properties|
|Published online||01 January 2003|
Polar order in nanostructured organic materials
Department of Materials Science and Engineering,
Northwestern University Evanston, IL 60208, USA
2 Department of Chemistry, and Feinberg School of Medicine Northwestern University - Evanston, IL 60208, USA
Accepted: 12 November 2002
Achiral multi-block liquid crystals are not expected to form polar domains. Recently, however, films of nanoaggregates formed by multi-block rodcoil molecules were identified as the first example of achiral single-component materials with macroscopic polar properties. By solving an Ising-like model with dipolar and asymmetric short-range interactions, we show here that polar domains are stable in films composed of aggregates as opposed to isolated molecules. Unlike classical molecular systems, these nanoaggregates have large intralayer spacings ( ), leading to a reduction in the repulsive dipolar interactions which oppose polar order within layers. In finite-thickness films of nanostructures, this effect enables the formation of polar domains. We compute exactly the energies of the possible structures consistent with the experiments as a function of film thickness at zero temperature (T). We also provide Monte Carlo simulations at non-zero T for a disordered hexagonal lattice that resembles the smectic-like packing in these nanofilms.
PACS: 61.30.Cz – Molecular and microscopic models and theories of liquid crystal structure / 61.46.+w – Nanoscale materials: clusters, nanoparticles, nanotubes, and nanocrystals
© EDP Sciences, 2003
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