Local-field anisotropy of a light wave in quasi-two-dimensional soft-matter objects

Experimental values of the Lorentz tensor components L j for uniaxial quasi-two dimensional “soft matter” objects on substrates (bilayer lipid membranes, multilayer Langmuir films, smectics A, hexatic smectics B, submicron films of discotics Col hd , micron anisotropic films of liquid-crystal combli...

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Veröffentlicht in:Journal of experimental and theoretical physics 2010-04, Vol.110 (4), p.622-636
1. Verfasser: Aver’yanov, E. M.
Format: Artikel
Sprache:eng
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Zusammenfassung:Experimental values of the Lorentz tensor components L j for uniaxial quasi-two dimensional “soft matter” objects on substrates (bilayer lipid membranes, multilayer Langmuir films, smectics A, hexatic smectics B, submicron films of discotics Col hd , micron anisotropic films of liquid-crystal comblike polymers and macromolecular polymers, submicron films of conjugated conductive polymers), freely suspended submicron films of smectics A, and uniaxially stretched micron films of conjugated conductive polymers have been determined using dispersion of refractive indices in the visible range. The dependences of the components L j on the type of orientation (axial, planar) of uniaxial molecules (structural units of the film) with respect to the optical axis of the film, the film thickness, the substrate type, the chemical structure of molecules, and their long-range orientational order are established. It is revealed that the smectic A-hexatic B phase transition and two-dimensional crystallization of the smectic layer lead to changes in the components L j due to the change in the orientational ordering of molecules as a result of the relation between the orientational and hexatic order parameters. All the above objects are characterized by isotropization of the Lorentz tensor L and the local-field tensor f with a simultaneous decrease in the birefringence of the sample and in the anisotropy of the molecular polarizability due to the change in the electronic structure of molecules. The correction for the anisotropy of the local-field tensor f to the orientational order parameter or the anisotropy of the molecular polarizability increases. The existing model approaches to calculating the components L j for the objects under consideration are compared with the experimental data.
ISSN:1063-7761
1090-6509
DOI:10.1134/S1063776110040102