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Register a new userCalorimetric study of the nematic to smectic-textit{A} and smectic-textit{A} to smectic-textit{C} phase transitions in liquid-crystal+aerosil dispersions
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Germano Iannacchione
Publication date
2005
fields
Physics
and research's language is
English
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A high-resolution calorimetric study has been carried out on nano-colloidal dispersions of aerosils in the liquid crystal 4-textit{n}-pentylphenylthiol-4-textit{n}-octyloxybenzoate ($bar{8}$S5) as a function of aerosil concentration and temperature spanning the smectic-textit{C} to nematic phases. Over this temperature range, this liquid crystal possesses two continuous XY phase transitions: a fluctuation dominated nematic to smectic-textit{A} transition with $alpha approx alpha_{XY} = -0.013$ and a mean-field smectic-textit{A} to smectic-textit{C} transition. The effective critical character of the textit{N}-Smtextit{A} transition remains unchanged over the entire range of introduced quenched random disorder while the peak height and enthalpy can be well described by considering a cut-off length scale to the quasi-critical fluctuations. The robust nature of the textit{N}-Smtextit{A} transition in this system contrasts with cyanobiphenyl-aerosil systems and may be due to the mesogens being non-polar and having a long nematic range. The character of the Smtextit{A}-Smtextit{C} transition changes gradually with increasing disorder but remains mean-field-like. The heat capacity maximum at the Smtextit{A}-Smtextit{C} transition scales as $rho_S^{-0.5}$ with an apparent evolution from tricritical to a simple mean-field step behavior. These results may be generally understood as a stiffening of the liquid crystal (both the nematic elasticity as well as the smectic layer compression modulus $B$) with silica density.
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Liquid crystals offer many unique opportunities to study various phase transitions with continuous symmetry in the presence of quenched random disorder (QRD). The QRD arises from the presence of porous solids in the form of a random gel network. Experimental and theoretical work support the view that for fixed (static) inclusions, quasi-long-range smectic order is destroyed for arbitrarily small volume fractions of the solid. However, the presence of porous solids indicates that finite-size effects could play some role in limiting long-range order. In an earlier work, the nematic - smectic-A transition region of octylcyanobiphenyl (8CB) and silica aerosils was investigated calorimetrically. A detailed x-ray study of this system is presented in the preceding Paper I, which indicates that pseudo-critical scaling behavior is observed. In the present paper, the role of finite-size scaling and two-scale universality aspects of the 8CB+aerosil system are presented and the dependence of the QRD strength on the aerosil density is discussed.
Ring patterns of concentric 2pi-solitons in molecular orientation, form in freely suspended chiral smectic-C films in response to an in-plane rotating electric field. We present measurements of the zero-field relaxation of ring patterns and of the driven dynamics of ring formation under conditions of synchronous winding, and a simple model which enables their quantitative description in low polarization DOBAMBC. In smectic C_A* TFMHPOBC we observe an odd-even layer number effect, with odd number layer films exhibiting order of magnitude slower relaxation rates than even layer films. We show that this rate difference is due to much larger spontaneous polarization in odd number layer films.
We develop a theory of Smectic A - Smectic C phase transition with anomalously weak smectic layer contraction. We construct a phenomenological description of this transition by generalizing the Chen-Lubensky model. Using a mean-field molecular model, we demonstrate that a relatively simple interaction potential suffices to describe the transition. The theoretical results are in excellent agreement with experimental data.
Using a generalized Landau theory involving orientational, layering, tilt, and biaxial order parameters we analyze the smectic-A* and smectic-C* (Sm-A* -- Sm-C*) transition, showing that a combination of small orientational order and large layering order leads to Sm-A* -- Sm-C* transitions that are either continuous and close to tricriticality or first order. The model predicts that in such systems the increase in birefringence upon entry to the Sm-C* phase will be especially rapid. It also predicts that the change in layer spacing at the Sm-A* -- Sm-C* transition will be proportional to the orientational order. These are two hallmarks of Sm-A* -- Sm-C* transitions in de Vries materials. We analyze the electroclinic effect in the Sm-A* phase and show that as a result of the zero-field Sm-A* -- Sm-C* transition being either continuous and close to tricriticality or first order (i.e for systems with a combination of weak orientational order and strong layering order) the electroclinic response of the tilt will be unusually strong. Additionally, we investigate the associated electrically induced change in birefringence and layer spacing, demonstrating de Vries behavior for each, i.e. an unusually large increase in birefringence and an unusually small layer contraction. Both the induced change in birefringence and layer spacing are shown to scale quadratically with the induced tilt angle.
We study theoretically the smectic A to C phase transition in isotropic disordered environments. Surprisingly, we find that, as in the clean smectic A to C phase transition, smectic layer fluctuations do not affect the nature of the transition, in spite of the fact that they are much stronger in the presence of the disorder. As a result, we find that the universality class of the transition is that of the Random field XY model (RFXY).
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