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1.
Nanomaterials (Basel) ; 14(5)2024 Feb 27.
Artigo em Inglês | MEDLINE | ID: mdl-38470767

RESUMO

We consider the influence of different nanoparticles or micrometre-scale colloidal objects, which we commonly refer to as particles, on liquid crystalline (LC) orientational order in essentially spatially homogeneous particle-LC mixtures. We first illustrate the effects of coupling a single particle with the surrounding nematic molecular field. A particle could either act as a "dilution", i.e., weakly distorting local effective orientational field, or as a source of strong distortions. In the strong anchoring limit, particles could effectively act as topological point defects, whose topological charge q depends on particle topology. The most common particles exhibit spherical topology and consequently act as q = 1 monopoles. Depending on the particle's geometry, these effective monopoles could locally induce either point-like or line-like defects in the surrounding LC host so that the total topological charge of the system equals zero. The resulting system's configuration is topologically equivalent to a crystal-like array of monopole defects with alternating topological charges. Such configurations could be trapped in metastable or stable configurations, where the history of the sample determines a configuration selection.

2.
Nanomaterials (Basel) ; 14(3)2024 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-38334591

RESUMO

We theoretically study the generic mechanisms that could establish critical behavior in nematic liquid crystals (NLCs). The corresponding free energy density terms should exhibit linear coupling with the nematic order parameter and, via this coupling, enhance the nematic order. We consider both temperature- and pressure-driven, order-disorder phase transitions. We derive a scaled effective free energy expression that describes how qualitatively different mechanisms enforce critical behavior. Our main focus is on the impact of nanoparticles (NPs) in homogeneous NP-NLC mixtures. We illustrate that in the case of pressure-driven phase changes, lower concentrations are needed to impose critical point conditions in comparison with pure temperature variations.

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