scholarly journals Liquid crystals of carbon nanotubes and graphene

Author(s):  
Cécile Zakri ◽  
Christophe Blanc ◽  
Eric Grelet ◽  
Camilo Zamora-Ledezma ◽  
Nicolas Puech ◽  
...  

Liquid crystal ordering is an opportunity to develop novel materials and applications with spontaneously aligned nanotubes or graphene particles. Nevertheless, achieving high orientational order parameter and large monodomains remains a challenge. In addition, our restricted knowledge of the structure of the currently available materials is a limitation for fundamental studies and future applications. This paper presents recent methodologies that have been developed to achieve large monodomains of nematic liquid crystals. These allow quantification and increase of their order parameters. Nematic ordering provides an efficient way to prepare conductive films that exhibit anisotropic properties. In particular, it is shown how the electrical conductivity anisotropy increases with the order parameter of the nematic liquid crystal. The order parameter can be tuned by controlling the length and entanglement of the nanotubes. In the second part of the paper, recent results on graphene liquid crystals are reported. The possibility to obtain water-based liquid crystals stabilized by surfactant molecules is demonstrated. Structural and thermodynamic characterizations provide indirect but statistical information on the dimensions of the graphene flakes. From a general point of view, this work presents experimental approaches to optimize the use of nanocarbons as liquid crystals and provides new methodologies for the still challenging characterization of such materials.

Author(s):  
Cengiz Camci ◽  
Boris Glezer

The liquid crystal thermography can be successfully used in both transient and steady-state heat transfer experiments with excellent spatial resolution and good accuracy. Although most of the past liquid crystal based heat transfer studies are reported in the stationary frame, measurements from the rotating frame of turbomachinery systems exist The main objective of the present investigation is to determine the influence of rotation on the color calibration of encapsulated liquid crystals sprayed on the flat surface of a rotating aluminum disk. The investigation is performed for a rotational speed range from 0 rpm to 7500 rpm using three different liquid crystal coatings displaying red at 30, 35 and 45° C, under stationary conditions. An immediate observation from the present study is that the color response of liquid crystals is strongly modified by the centrifugal acceleration of the rotating environment. It is consistently and repeatedly observed that the hue versus temperature curve is continuously shifted toward lower temperatures by increasing rotational speed. The relative shift of the display temperature of the green can be as high as 7°C at 7500 rpm when compared to the temperature of the green observed under stationary conditions. The present study shows that relative shift of the liquid crystal color has a well-defined functional dependency to rotational speed. The shift is linearly proportional to the centrifugal acceleration. It is interesting to note that the individual shift curves of the green for all three liquid crystal coatings collapse into a single curve when they are normalized with respect to their own stationary green values. When the color attribute is selected as “intensity” instead of “hue”, very similar shifts of the temperature corresponding to the intensity maximum value appearing around green is observed. An interpretation of the observed color shift is made from a thermodynamics energy balance point of view.


Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1262
Author(s):  
Mikhail A. Osipov ◽  
Maxim V. Gorkunov ◽  
Alexander A. Antonov

Density functional theory of rod-coil diblock copolymers, developed recently by the authors, has been generalised and used to study the liquid crystal ordering and microphase separation effects in the hexagonal, lamellar and nematic phases. The translational order parameters of rod and coil monomers and the orientational order parameters of rod-like fragments of the copolymer chains have been determined numerically by direct minimization of the free energy. The phase diagram has been derived containing the isotropic, the lamellar and the hexagonal phases which is consistent with typical experimental data. The order parameter profiles as functions of temperature and the copolymer composition have also been determined in different anisotropic phases. Finally, the spatial distributions of the density of rigid rod fragments and of the corresponding orientational order parameter in the hexagonal phase have been calculated.


The line broadening in the electron resonance spectra of monoradicals dissolved in anisotropic media, such as liquid crystals, provides a valuable probe of both the orientational order and the molecular dynamics. However, the fast-motion relaxation theory employed to extract this information from the linewidths assumes that the nuclear spin is quantized along the direction of the magnetic field. This approximation is only correct when the symmetry axis of a uniaxial liquid crystal is either parallel or perpendicular to the field. We have therefore removed this assumption and have developed a general theory of line broadening valid for all orientations of the liquid crystal. The theory is then used to evaluate the angular dependence of the linewidths and this is compared with the dependence predicted by the approximate theory, for two classes of nitroxide spin probes. These comparisons reveal that for steroidal spin probes the error, introduced by assuming the nuclear spin to be quantized along the field, is confined to the dynamic properties derived from the linewidths. In contrast, significant errors appear in both the dynamic and static properties obtained from an analysis of the linewidth variations for fatty acid spin probes based on the approximate theory. It would seem that the exact theory must be employed to obtain precise information from linewidth investigations of liquid crystals, except when the orientational order is extremely small.


2014 ◽  
Vol 22 (1) ◽  
Author(s):  
T. Devi ◽  
B. Choudhury ◽  
A. Bhattacharjee ◽  
R. Dabrowski

AbstractOptical studies have been carried out on two fluorinated isothiocyanato nematic liquid crystal (LC) compounds 4′-butylcyclohexyl-3, 5-difluoro-4-isothiocyanatobiphenyl and 4′-pentylcyclohexyl-3, 5-difluoro-4-isothiocynatobiphenyl. Transition temperatures of the two samples were confirmed using a polarizing microscope. The two LC compounds were found to exhibit fairly high clearing temperatures. Measurements of refractive indices of the two compounds were done by using thin prism method with He-Ne laser beam of wavelength 630 nm. Birefringence of the two LC compounds was calculated from the measured refractive indices. Both the compounds are found to display fairly high values of birefringence. Validation of a modified four-parameter model, based on Vuks equation describing the temperature dependence of refractive indices of the two liquid crystals, is also presented in this paper. The model is validated by fitting the experimentally measured values of refractive indices, birefringence and average refractive indices of the two nematic LCs with the theoretical values. In this paper, the calculation of order parameters of the LCs is presented by using two methods: direct extrapolation method based solely on the birefringence data and by using modified Vuks method based on Haller’s extrapolation. As observed from the obtained results, this procedure of calculating order parameter gives very reasonable results.


2020 ◽  
Vol 22 (40) ◽  
pp. 23064-23072
Author(s):  
Andraž Rešetič ◽  
Jerneja Milavec ◽  
Valentina Domenici ◽  
Blaž Zupančič ◽  
Alexej Bubnov ◽  
...  

Orientational order parameter of magnetically aligned liquid crystal elastomer particles suspended in a cured silicone matrix is assessed using 2H-NMR spectroscopy. Obtained results correspond well with the composite's thermomechanical response.


2014 ◽  
Vol 22 (3) ◽  
Author(s):  
J. Kędzierski ◽  
K. Garbat ◽  
Z. Raszewski ◽  
M. Kojdecki ◽  
K. Kowiorski ◽  
...  

AbstractOptical properties of a nematic liquid crystal with small refractive index and small birefringence were studied. The ordinary and extraordinary refractive indices and birefringence were measured as functions of temperature by using an Abbe refractometer and wedge nematic cells. From values of these indices the nematic orientational order parameter was calculated by using several methods and corresponding mathematical models. Kuczyński et al. method was found to be suitable for determining the order parameter also for materials featuring small ordinary refractive index, with unknown density.


1981 ◽  
Vol 59 (4) ◽  
pp. 515-520 ◽  
Author(s):  
P. Palffy-Muhoray ◽  
D. A. Balzarini

Using a simple new interferometric technique, the ordinary and extraordinary refractive indices of the nematic liquid crystal p-ethoxybenzilidene-p-n-butylaniline have been measured separately as a function of temperature. Changes in the refractive indices have been measured with an accuracy of ±0.005% and the absolute values with an accuracy of ±0.5%. Thermal expansivity data has been obtained by utilizing a specially constructed thermometer containing the sample. By using a recently developed Clausius–Mossotti relation for anisotropic fluids, the effective molecular polarizability and hence the orientational order parameter have been obtained from refractive index and density measurements as a function of temperature.


1990 ◽  
Vol 45 (1) ◽  
pp. 37-42 ◽  
Author(s):  
A. Scharkowski ◽  
H. Schmiedel ◽  
R. Stannarius ◽  
E. Weißhuhn

AbstractA survey of various methods to measure the elastic constants Ki of nematic liquid crystals is given. To determine K1, K3 and the anisotropy of the diamagnetic susceptibility Δx of two members of the 5n-hexyl-2-[4n-alkyloxy-phenyl]-pyrimidines and a mixture of both, we used a combined electromagneto- optical method, consisting in independent measurements of the optical phase difference in electric and magnetic fields acting on the same cell. The temperature dependence of the K1- and K3-values for these phenylpyrimidines can be explained by common theories. The Δx data show the same temperature dependence as the values of the orientational order parameter S obtained by 1H-NMR.


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