Pattern Formation During the Growth of Liquid Crystal Phases

MRS Bulletin ◽  
1991 ◽  
Vol 16 (1) ◽  
pp. 38-45 ◽  
Author(s):  
Patrick Oswald ◽  
John Bechhoefer ◽  
Francisco Melo

Liquid crystals, discovered just a century ago, have wide application to electrooptic displays and thermography. Their physical properties have also made them fascinating materials for more fundamental research.The name “liquid crystals” is actually a misnomer for what are more properly termed “mesophases,” that is, phases having symmetries intermediate between ordinary solids and liquids. There are three major classes of liquid crystals: nematics, smectics, and columnar mesophases. In nematics, although there is no correlation between positions of the rodlike molecules, the molecules tend to lie parallel along a common axis, labeled by a unit vector (or director) n. Smectics are more ordered. The molecules are also rodlike and are in layers. Different subtypes of smectics (labeled, for historical reasons, smectic A, smectic B,…) have layers that are more or less organized. In the smectic A phase, the layers are fluid and can glide easily over each other. In the smectic B phase, the layers have hexagonal ordering and strong interlayer corrélations. Indeed, the smectic B phase is more a highly anisotropic plastic crystal than it is a liquid crystal. Finally, columnar mesophases are obtained with disklike molecules. These molecules can stack up in columns which are themselves organized in a two-dimensional array. There is no positional correlation between molecules in one column and molecules in the other columns.

Author(s):  
H. N. W. Lekkerkerker ◽  
G. J. Vroege

A review is given of the field of mineral colloidal liquid crystals : liquid crystal phases formed by individual mineral particles within colloidal suspensions. Starting from their discovery in the 1920s, we discuss developments on the levels of both fundamentals and applications. We conclude by highlighting some promising results from recent years, which may point the way towards future developments.


1989 ◽  
Vol 177 ◽  
Author(s):  
R. Geer ◽  
T. Stoebe ◽  
C. C. Huang ◽  
R. Pindak ◽  
J. Goodby

ABSTRACTA high-resolution differential quasi-adiabatic calorimeter has been developed to investigate the physical properties of freestanding liquid-crystal films. Our recent heat-capacity studies near the smectic-A-hexatic-B transition of both 65OBC and 46OBC freestanding films clearly demonstrate the evolution towards twodimensional limiting behavior in four-layer films. As the film thickness decreases towards four molecular layers, the heatcapacity anomalies first display separate peaks for the surface and interior transitions and then evolve to one dominated by the surface transition.


Crystals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 648 ◽  
Author(s):  
Mamatha Nagaraj

Liquid crystal templating is a versatile technique to create novel organic and inorganic materials with nanoscale features. It exploits the self-assembled architectures of liquid crystal phases as scaffolds. This article focuses on some of the key developments in lyotropic and thermotropic liquid crystals templating. The procedures that were employed to create templated structures and the applications of these novel materials in various fields including mesoporous membranes, organic electronics, the synthesis of nanostructured materials and photonics, are described.


2016 ◽  
Vol 120 (10) ◽  
pp. 2829-2837 ◽  
Author(s):  
Paul J. Repasky ◽  
Deña M. Agra-Kooijman ◽  
Satyendra Kumar ◽  
C. Scott Hartley

The information about liquid crystal phases that can be obtained by light scattering and by high-resolution X-ray scattering is reviewed. Results for the nematic-smectic A transition suggest the de Gennes-McMillan model is correct, but adequate theoretical solutions to the model remain elusive. Recent results on the smectic A to smectic C transition are presented that show unambiguously that it exhibits classic mean-field behaviour and this is explained by a Ginzburg criterion argument. Some preliminary results of a study of a nematic-smectic A transition in a lyotropic material are given and indicate similarity to thermotropic materials.


A thin film of nematic liquid crystal (ZLI 1085) is sandwiched between two horizontally mounted glass blocks, whose faces have been treated to align the molecules of the liquid parallel to the plane of the blocks. By moving one block relative to the other in its own plane, the liquid crystal is subjected to an oscillatory linear shear. Above a certain frequency-dependent amplitude, mechanical Williams domains of alternating bright and dark stripes are observed perpendicular to the direction of shear. A theoretical analysis of this phenomenon is carried out to provide predictions for both the thickness of the stripes and the critical amplitude as a function of frequency. Good agreement is found between the experimental and theoretical results.


2020 ◽  
Vol 98 (7) ◽  
pp. 379-385
Author(s):  
Carson O. Zellman ◽  
Danielle Vu ◽  
Vance E. Williams

Although the impact of individual functional groups on the self-assembly of columnar liquid crystal phases has been widely studied, the effect of varying multiple substituents has received much less attention. Herein, we report a series of dibenzo[a,c]phenazines containing an alcohol or ether adjacent to an electron-withdrawing ester or acid. With one exception, these difunctional mesogens form columnar phases. The phase behavior appeared to be dominated by the electron-withdrawing substituent; transition temperatures were similar to derivatives with these groups in isolation. In most instances, the addition of an electron-donating group ortho to an ester or acid suppressed the melting temperature and elevated the clearing temperature, leading to broader liquid crystal thermal ranges. This effect was more pronounced for derivatives functionalized with longer chain hexyloxy groups. These results suggest a potential strategy for controlling the phase ranges of columnar liquid crystals and achieving room temperature mesophases.


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