Transient Electro-Optic Kerr Effect in Liquid Crystalline Isothiocyanates
15 Jun 1999-Journal of the Physical Society of Japan (Physical Society of Japan)-Vol. 68, Iss: 6, pp 1939-1942
TL;DR: In this paper, the D.C. Kerr response and the pre-transitional behavior of two liquid crystalline isothiocyanates 4-(4 ′ -n-pentyl phenyl)-phenyl isothIocyanate (5NCS) and 4-( 4 ′ −n-heptylphenyl-phenyl)-isothIOCyanate(7NCS), at temperatures above the smectic-isotropic transition temperatures were investigated.
Abstract: Measurements are reported for the first time on the D.C. Kerr response and the pre-transitional behaviour of two liquid crystalline isothiocyanates 4-(4 ′ -n-pentyl phenyl)-phenyl isothiocyanate (5NCS) and 4-(4 ′ -n-heptyl phenyl)-phenyl isothiocyanate (7NCS) at temperatures above the smectic-isotropic transition temperatures. The Kerr law has been verified and the real part of the third order nonlinear susceptibilities (χ (3) ) above the smectic-isotropic transition are determined for the two liquid crystalline isothiocyanates from the electro-optic Kerr effect (EOKE) experiments. The variation of susceptibility with temperature has also been studied. The results have been compared with the cyanobiphenyls which have been widely studied and are known for their giant optical non-linearities.
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TL;DR: In this article, the authors present an attempt towards a unified picture of the direct transition from the isotropic to smectic-A phase, including structure and nature revealed by experiments, molecular models and Landau-de Gennes theory.
23 citations
TL;DR: The isotropic-nematic phase transition in liquid crystals is described in the context of the slowing of orientational relaxation associated with divergent growth of the orientational correlation length, and the correlation length of the density fluctuations is diverging with the same temperature dependence as the pseudonematic domain correlation length.
Abstract: The isotropic phase of nematogenic liquid crystals has nanometer length scale domains with pseudonematic ordering. As the isotropic to nematic phase transition temperature (TNI) is approached from above, the orientational correlation length, ξ, of the pseudonematic domains grows as (T - T(*))(-1/2), where T(*) is 0.5-1 K below TNI. The orientational relaxation, which is a collective property of the pseudonematic domains, was measured with optical heterodyne detected-optical Kerr effect (OHD-OKE). The orientational relaxation obeys Landau-de Gennes theory, as has been shown previously. To examine the environmental evolution experienced by molecules in the pseudonematic domains, two-dimensional infrared (2D IR) vibrational echo experiments on the CN stretching mode of the non-perturbative vibrational probes 4-pentyl-4(')-selenocyanobiphenyl (5SeCB) and 4-pentyl-4(')-thiocyanobiphenyl (5SCB) in the nematogen 4-cyano-4(')-pentylbiphenyl (5CB) were performed. The 2D IR experiments measure spectral diffusion, which is caused by structural fluctuations that couple to the CN vibrational frequency. Temperature dependent studies were performed just above TNI, where the correlation length of pseudonematic domains is large and changing rapidly with temperature. These studies were compared to 2D IR experiments on 4-pentylbiphenyl (5B), a non-mesogenic liquid that is very similar in structure to 5CB. The time constants of spectral diffusion in 5CB and 5B are practically identical at temperatures ≥5 K above TNI. As the temperature is lowered, spectral diffusion in 5B slows gradually. However, the time constants for spectral diffusion in 5CB slow dramatically and diverge as T(*) is approached. This divergence has temperature dependence proportional to (T - T(*))(-1/2), precisely the same as seen for the correlation length of pseudonematic domains, but different from the observed orientational relaxation times, which are given by the Landau-de Gennes theory. The data and previous results show that spectral diffusion in 5CB has no contributions from orientational relaxation, and the structural dynamics responsible for the spectral diffusion are likely a result of density fluctuations. The results suggest that the correlation length of the density fluctuations is diverging with the same temperature dependence as the pseudonematic domain correlation length, ξ. The isotropic-nematic phase transition in liquid crystals is described in the context of the slowing of orientational relaxation associated with divergent growth of the orientational correlation length. The results presented here show that there is another divergent dynamical process, likely associated with density fluctuations.
22 citations
TL;DR: It is shown that maximum Kerr constants in the order of several 10-11 m V-2 make ionic liquid crystals attractive as new class of functional materials in low-speed Kerr effect applications.
Abstract: The electro-optic Kerr effect in simple dipolar fluids such as nitrobenzene has been widely applied in electro-optical phase modulators and light shutters. In 2005, the discovery of the large Kerr effect in liquid-crystalline blue phases (Y. Hisakado et al., Adv. Mater. 2005, 17, 96-98.) gave new directions to the search for advanced Kerr effect materials. Even though the Kerr effect is present in all transparent and optically isotropic media, it is well known that the effect can be anomalously large in complex fluids, namely in the isotropic phase of liquid crystals or in polyelectrolyte solutions. Herein, it is shown that the Kerr effect in the isotropic phase of ionic liquid crystals combines the effective counterion polarization mechanism found in polyelectrolytes and the unique pretransitional growth of the Kerr constant found in the isotropic phase of nematic liquid crystals. Maximum Kerr constants in the order of several 10-11 m V-2 (ten times higher than the Kerr constant of the toxic nitrobenzene and less temperature sensitive than Kerr constants of nematic liquid crystals) make ionic liquid crystals attractive as new class of functional materials in low-speed Kerr effect applications.
13 citations
TL;DR: A remarkable change in coupling occurs at ∼5 K above TNI, precisely where the rate of spectral diffusion in 5CB was observed to deviate from that of a similar nonmesogenic liquid.
Abstract: Two-dimensional infrared (2D IR) data are presented for a vibrational probe in three nematogens: 4-cyano-4′-pentylbiphenyl, 4-cyano-4′-octylbiphenyl, and 4-(trans-4-amylcyclohexyl)-benzonitrile. The spectral diffusion time constants in all three liquids in the isotropic phase are proportional to [T*/(T – T*)]1/2, where T* is 0.5–1 K below the isotropic–nematic phase transition temperature (TNI). Rescaling to a reduced temperature shows that the decays of the frequency–frequency correlation function (FFCF) for all three nematogens fall on the same curve, suggesting a universal dynamic behavior of nematogens above TNI. Spectral diffusion is complete before significant orientational relaxation in the liquid, as measured by optically heterodyne detected-optical Kerr effect (OHD-OKE) spectroscopy, and before any significant orientational randomization of the probe measured by polarization selective IR pump–probe experiments. To interpret the OHD-OKE and FFCF data, we constructed a mode coupling theory (MCT) sc...
12 citations
TL;DR: The results demonstrate that the presence of local orientational order at temperatures well above TNI does not affect the spectral diffusion (structural evolution) within pseudonematic domains when the correlation lengths are short, and density fluctuations are likely the source of spectral diffusion at temperatures at least 5 Kabove TNI.
Abstract: Nematogen liquids in the isotropic phase are macroscopically homogeneous but on multinanometer length scales have pseudonematic domains with correlation lengths that grow as the isotropic to nematic phase transition temperature (TNI) is approached from above. Orientational relaxation of nematogens in the isotropic phase manifests as two fast power laws and a slow exponential decay when measured by optical heterodyne detected optical Kerr effect (OHD-OKE) experiments. The long time exponential relaxation is associated with complete randomization of pseudonematic domains. We examine the effect of local orientational correlation on spectral diffusion (structural evolution) experienced by a vibrational probe molecule within the pseudonematic domains of 4-cyano-4'-pentylbiphenyl (5CB) using two-dimensional infrared (2D IR) vibrational echo spectroscopy. The addition of low concentration 4-pentyl-4'-thiocyanobiphenyl (5SCB) as a long-lived vibrational probe to 5CB is shown to lower TNI of the sample slightly, but the fast power law dynamics and exponential decays observed by OHD-OKE spectroscopy are unchanged. We compare the complete orientational relaxation and spectral diffusion for samples of 5SCB in 5CB to 5SCB in 4-pentylbiphenyl (5B) at four temperatures above TNI. 5B has a molecular structure similar to 5CB but is not a nematogen. At all but the lowest temperature, the spectral diffusion in 5CB and 5B is described well as a triexponential decay with very similar time constants. The results demonstrate that the presence of local orientational order at temperatures well above TNI does not affect the spectral diffusion (structural evolution) within pseudonematic domains when the correlation lengths are short. However, when the temperature of the sample is held very close to TNI, the spectral diffusion in 5CB slows dramatically while that in 5B does not. It is only as the correlation length becomes very long that its presence impacts the spectral diffusion (structural fluctuations) sensed by the vibrational probes located in pseudonematic domains. The orientational relaxation is modeled with schematic mode coupling theory (MCT). Fitting with MCT provides density and orientational correlation functions. The density correlation decays are similar for 5B and 5CB, but the orientational correlation decays are much slower for 5CB. Additionally, the time dependence of the spectral diffusion in 5CB is strikingly similar to that of the density correlation function decay, while the orientational correlation function decay is far too slow to contribute to the spectral diffusion. Therefore, density fluctuations are likely the source of spectral diffusion at temperatures at least 5 K above TNI.
12 citations
References
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TL;DR: In this paper, a tensor function describing the dependence of the dielectrical impermeability tensor on the electrical field tensor has been calculated for all 32 crystallographic classes.
Abstract: The sixth-rank tensor K describing the nonlinear electro-optical fourth-order effect has been calculated. A relationship between the non-zero components of the above tensor for all 32 crystallographic classes is shown. The calculations were executed with the aid of a tensor function describing the dependence of the dielectrical impermeability tensor on the electrical field tensor. It has been shown that changes in the optical properties of crystals due to the fourth-order electro-optical effect are similar to those brought about by the Kerr effect.
14 citations
TL;DR: In this article, the optical and dc pulsed field Kerr effects have been measured in 5 OCB in the isotropic phase and in dilute solution in terms of the Landau-de Gennes model.
Abstract: The optical and dc pulsed field Kerr effects have been measured in 5 OCB in the isotropic phase and in dilute solution. The pretransitional behaviour has been examined in terms of the Landau-de Gennes model. The constants of this formalism have been given and a possible optical shutter has been suggested.
11 citations
TL;DR: In this paper, an apparatus for the measurement of the optical Kerr effect in liquid samples is described and the authors show how more accurate, reproducible results could be obtained with continuous-wave lasers and how the inherent problems of thermal defocusing effects can be overcome.
Abstract: An apparatus for the measurement of the optical Kerr effect in liquid samples is described. Previously, observations of this effect have used powerful, pulsed lasers as the orienting light field. The authors show how more accurate, reproducible results could be obtained with continuous-wave lasers and how the inherent problems of thermal defocusing effects can be overcome.
10 citations
TL;DR: In this paper, the short range orientational order characteristic of molecular fluids is discussed as a function of the shape of the molecules and of intermolecular interactions, based on experimental results obtained from dielectric relaxation, Kerr effect and X-ray studies.
Abstract: The short range orientational order characteristic of molecular fluids is discussed as a function of the shape of the molecules and of intermolecular interactions. Low molecular weight and polymeric substances exhibiting only an isotropic melt or, in addition, liquid crystalline phases were taken into account. The discussion is based on experimental results obtained from dielectric relaxation, Kerr effect and X-ray studies. The characterization of the short range order is given in terms of correlation parameters, related to the general pair correlation function.
3 citations