Morphology and structure of thin liquid-crystalline films at nematic-isotropic transition

We review the main features of very thin nematic liquid-crystalline films on solid substrates, focusing on 5CB on oxidized silicon wafers. By discussing the theoretical aspects of the observed structures, we show that the phenomena at work include isotropic capillary condensation and that the coexistence of isotropic and nematic terraces in thin films is a result of the interplay of several mechanisms. Further theoretical as well as experimental efforts are needed to completely understand the wetting behavior of these systems.Received: 1 August 2003PACS: 68.08.Bc Wetting - 68.15. + e Liquid thin films - 61.30.Hn Surface phenomena in liquid crystals including anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions     

Random anisotropy nematic model: Connection with experimental systems

We study theoretically the phase behavior of the continuum Random Anisotropy Nematic model. A domain-type pattern is assumed to appear in a distorted nematic liquid crystal (LC) phase. We map the model parameters to physical quantities characterizing LCs confined to Controlled-Pore Glasses and LC-aerosil dispersions. The domain size dependence on the disorder strength is obtained in accordance with the Imry-Ma prediction. The model estimates for temperature shifts of the paranematic-nematic phase transition and for the critical point, where this transition ceases to exist, are compared to the available experimental results.Received: 28 March 2004, Published online: 29 June 2004PACS: 61.30.-v Liquid crystals - 61.30.Dk Continuum models and theories of liquid crystal structure - 61.30.Gd Orientational order of liquid crystals; electric and magnetic field effects on order - 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions     

Wetting properties of rare gases on weak substrates

Since the original prediction that liquid He does not wet Cs at low temperatures and the soon after experimental observation of a wetting transition on this system, noble gases on alkalis have become model systems for the study of wetting transitions and of their accompanying line of prewetting transitions off coexistence. Here we review very briefly the theory of wetting and prewetting and discuss some results on the properties of rare gases adsorbed on alkali surfaces obtained with the use of the density functional theory and of accurate adsorbate-substrate potentials.     

Prewetting and layering in athermal polymer solutions

Coexistence conditions for prewetting and layering at a hard surface in additive hard sphere polymer solutions, where the solvent particles are smaller than the monomers, have been calculated by density functional methods. Various chain lengths and pressures have been investigated. An unexpected finding is that prewetting in these systems may proceed below the bulk critical pressure. We rationalize this behavior in terms of local properties of the pressure tensor. For longer chains, a different behavior is observed where the systems display a lower wetting pressure, i.e., a low pressure bound for surface wetting.     

Stability of thin nematic films

We discuss the peculiarity of thin nematic films on solid substrates with a free surface, underlining the differences with what is usually seen in dewetting. We review the thermodynamic basis of the coupled phase/thickness separation that has previously been shown experimentally. We give new experimental evidences for the origin of the coupling force chosen in our previous theoretical model. This additional information contributes to the discussion raised by the article of Ziherl and Zumer in this issue [19].Received: 3 December 2003PACS: 68.15. + e Liquid thin films - 64.70.Md Transitions in liquid crystals - 61.30 Surface phenomena in liquid crystals including anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions and wetting transitions     

Thickening of a smectic membrane in an evanescent X-ray beam

We report an unusual thickening of smectic membranes under the influence of X-ray irradiation below the critical angle. In the case of a four-layer film the thickness was found to grow at the footprint of the beam, reaching within minutes tens of layers. The effect is attributed to the localized energy dissipation of the evanescent wave. The island thus created is not connected to the meniscus and after the beam is switched off the film returns to its original state. A possible explanation is given in terms of a local disrupture of the tension of the smectic membrane.Received: 22 July 2004, Published online: 1 October 2004PACS: 61.30.-v Liquid crystals - 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions - 52.25.Os Emission, absorption, and scattering of electromagnetic radiation     

Surface aided replica exchange algorithm applied to the prewetting transition

A novel algorithm, termed surface aided replica exchange (SARE), was introduced in which the fluid–surface interaction was varied in order to generate different replicas in a particular ensemble. Exchange between replicas was allowed with a probability of acceptance obtained by imposing detailed balance. The method was implemented in a modified isothermal-isobaric ensemble that permitted precise characterization of the prewetting line of a simple adsorbed fluid. The prewetting line for each surface was characterized by computing the adsorption of the fluid as a function of pressure, and the wetting temperature estimated for each surface.     

Stripe instability in thin films of smectic liquid-crystal polymers

Two-dimensional nanostripes are formed in thin films of side-chain liquid-crystalline polymer films when the material enters the smectic phase. The structure is investigated using transmission electron microscopy. Electron diffraction patterns show that the chain molecules are mostly aligned in the film plane and the average molecular director is parallel to the direction of the stripes. We discuss factors affecting the stripe amplitude and periodicity, such as the film thickness and the temperature of annealing in the nematic phase, and suggest a possible mechanism for their formation. We propose that an equilibrium instability occurs due to a competition between the layer-aligning effect of the substrate and the planar director alignment, forcing smectic layers perpendicular to the film surface. The stripes decorate the overall patterns of nematic director in the polymer film and provide a means of high-resolution imaging for observation of textures and disclinations.Received: 10 June 2003, Published online: 19 August 2003PACS: 68.37.Lp Transmission electron microscopy (TEM) (including STEM, HRTEM, etc.) - 61.30.Vx Polymer liquid crystals - 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions - 68.55.Nq Composition and phase identification     

Frustrated rotations in nematic monolayers

Tabe and Yokoyama found recently that the optical axis in a chiral monolayer of a ferronematic rotates when water evaporates from the bath: the chiral molecules act as propellers. When the axis is blocked at the lateral walls of the trough, the accumulated rotation inside creates huge splays and bends. We discuss the relaxation of these tensions, assuming that a single dust particle nucleates disclination pairs. For the simplest geometry, we then predict a long delay time followed by a non-periodic sequence of bursts. These ideas are checked by numerical simulations.PACS: 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions - 61.30.Jf Defects in liquid crystals     

Surface and bulk interchange energy in binary mixtures of chain molecules

The interchange (interaction) parameter, controlling the phase behaviour of a binary mixture, is determined for the bulk and the surface of binary mixtures of different types of chain molecules, using surface tensiometry and a mean-field theory. For all mixtures and concentrations studied an identical behaviour is observed at the surface, depending only on the square of the reduced chain length mismatch , where and are the difference in and average of the number of carbons of the two components.Received: 21 December 2003, Published online: 25 March 2004PACS: 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions - 68.35.Md Surface thermodynamics, surface energies - 68.03.Cd Surface tension and related phenomena     

Grain Boundary Phase Transitions and their Influence on Properties of Polycrystals

Grain boundary (GB) phase transitions can change drastically the properties of polycrystals. The GB wetting phase transition can occur in the two-phase area of the bulk phase diagram where the liquid (L) and solid (S) phases are in equlibrium. Above the temperature of the GB wetting phase transition a GB cannot exist in equlibrium contact with the liquid phase. The experimental data on GB wetting phase transitions in numerous systems are analysed. The GB wetting tie-line can continue in the one-phase area of the bulk phase diagram as a GB solidus line. This line represents the GB premelting or prewetting phase transitions. The GB properties change drastically when GB solidus line is crossed by a change in the temperature or concentration. The experimental data on GB segregation, energy, mobility and diffusivity obtained in various systems both in polycrystals and bicrystals are analysed. In case if two solid phases are in equilibrium, the GB “solid state wetting” can occur. In this case the layer of the solid phase 2 has to substitute GBs in the solid phase 1. Such GB phase transition occurs if the energy of two interphase boundaries is lower than the GB energy in the phase 1.     

Surface phase transitions of multiple-site associating fluids

Surface phase transitions of Lennard–Jones (LJ) based two- and four-site associating fluids have been studied for various associating strengths using grand-canonical transition matrix Monte Carlo simulations. Our results suggest that, in the case of a smooth surface, represented by a LJ 9-3-type potential, multiple-site associating fluids display a prewetting transition within a certain temperature range. However, the range of the prewetting transition decreases with increasing associating strength and increasing number of sites on the fluid molecules. With the addition of associating sites on the surface, a quasi-2D vapor–liquid transition may appear, which is observed at a higher surface site density for weaker associating fluids. The prewetting transition at lower associating strength is found to shift towards the quasi-2D vapor–liquid transition with increasing surface site density. However, for highly associating fluids, the prewetting transition is still intact, but shifts slightly towards the lower temperature range. Adsorption isotherms, chemical potentials and density profiles are used to characterize surface phase transitions.     

Wetting transitions in polydisperse fluids

The properties of the coexisting bulk gas and liquid phases of a polydisperse fluid depend not only on the prevailing temperature but also on the overall parent density. As a result, a polydisperse fluid near a wall will exhibit density-driven wetting transitions inside the coexistence region. We propose a likely topology for the wetting phase diagram, which we test using Monte Carlo simulations of a model polydisperse fluid at an attractive wall, tracing the wetting line inside the cloud curve and identifying the relationship to prewetting.     

Threshold criterion for wetting at the triple point

Grand canonical simulations are used to calculate adsorption isotherms of various classical gases on alkali metal and Mg surfaces. Ab initio adsorption potentials and Lennard-Jones gas-gas interactions are used. Depending on the system, the resulting behavior can be nonwetting for all temperatures studied, complete wetting, or (in the intermediate case) exhibit a wetting transition. An unusual variety of wetting transitions at the triple point is found in the case of a specific adsorption potential of intermediate strength. The general threshold for wetting near the triple point is found to be close to that predicted with a heuristic model of Cheng et al. This same conclusion was drawn in a recent experimental and simulation study of Ar on CO2 by Mistura et al. These results imply that a dimensionless wetting parameter w is useful for predicting whether wetting behavior is present at and above the triple temperature. The nonwetting/wetting crossover value found here is w approximately 3.3.     

Structure and phase transitions in a network-forming associating Lennard-Jones fluid in a slit-like pore: a density functional approach

A study is reported of adsorption of an associating Lennard-Jones fluid with four associative sites per molecule in a slit-like pore. The density distribution of particles in the pore and thermodynamics properties are evaluated by using a density functional method. It is found that at low temperatures the fluid exhibits a set of layering transitions, followed by capillary condensation. Transitions are localized by analysing the grand canonical potential. The density profiles of particles and the distribution of unbound and differently bonded particles demonstrate changes in the structure of the fluid in the pore along the phase coexistence. The critical temperature is lower for a confined fluid, compared with the bulk counterpart. However, an increase in the energy of association increases the critical temperature. The envelope of the capillary condensation is narrower than the bulk liquid-vapour phase diagram. The dependence of the solvation force on the energy of association and on the bulk density is discussed.     

Dynamical behaviour of holographic gratings with a nematic film --Polymer slice sequence structure

We have studied the dynamical response of a new kind of holographic grating to a pulsed electric field. The structure, named POLICRYPS, consists of a sequence of homogeneous polymer slices separated by liquid-crystal films. We have found that both the rise and fall response times depend on the pulse duration and amplitude of the applied electric field. We propose a phenomenological explanation for this behaviour, outlining the possibility of getting response times of the order of 100 s by properly choosing the pulse shape. Results are very interesting for developments in which POLICRYPS gratings could be proposed as basic elements in photonic devices for telecom applications, and induce to a deeper analysis of the microscopic interaction between liquid crystal and polymer interfaces in these samples.Received: 5 February 2004, Published online: 14 September 2004PACS: 61.30.Pq Microconfined liquid crystals: droplets, cylinders, randomly confined liquid crystals, polymer dispersed liquid crystals, and porous systems - 42.40.Eq Holographic optical elements; holographic gratings - 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitions     

Extraordinary wetting phase diagram for mixtures of Bose-Einstein condensates

The possibility of wetting phase transitions in Bose-Einstein condensed gases is predicted on the basis of Gross-Pitaevskii theory. The surface of a binary mixture of Bose-Einstein condensates can undergo a first-order wetting phase transition upon varying the interparticle interactions, using, e.g., Feshbach resonances. Interesting ultra-low-temperature effects shape the wetting phase diagram. The prewetting transition is, contrary to general expectations, not of first order but critical, and the prewetting line does not meet the bulk phase coexistence line tangentially. Experimental verification of these extraordinary results is called for, especially now that it has become possible, using optical methods, to realize a planar "hard wall" boundary for the condensates.     

Observational constraints of modified Chaplygin gas in loop quantum cosmology

We explore the behavior of the holographic superconductors at zero temperature for a charged scalar field coupled to a Maxwell field in higher-dimensional AdS soliton spacetime via analytical way. In the probe limit, we obtain the critical chemical potentials increase linearly as a total dimension d grows up. We find that the critical exponent for condensation operator is obtained as 1/2 independently of d, and the charge density is linearly related to the chemical potential near the critical point. Furthermore, we consider a slightly generalized setup the Einstein–Power–Maxwell field theory, and find that the critical exponent for condensation operator is given as 1/(4?2n) in terms of a power parameter n of the Power–Maxwell field, and the charge density is proportional to the chemical potential to the power of 1/(2?n).     

Holographic Superconductors with Nonlinear Arcsin‐Electrodynamics

Holographic s‐wave superconductors with nonlinear arcsin‐electrodynamics in the background of Schwarzschild anti‐de Sitter black holes are investigated. The analytical Sturm–Liouville eigenvalue problem is explored and the scalar and electromagnetic fields are assumed not to influence the background metric (the probe limit). The critical temperatures of phase transitions depending on the parameter of the model are obtained. It is shown that in this case, the condensation formation becomes easier compared to Born–Infeld nonlinear electrodynamics. The critical exponent near the critical temperature is calculated, which is 1/2. With the help of the matching method, analytic expressions for the condensation value and the critical temperature are derived. The real and imaginary parts of the conductivity in the model, making use of an analytical method, are computed.     

Cross-Over Between First-Order and Critical Wetting at the Liquid-Vapour Interface of n-Alkane/Methanol Mixtures: Tricritical Wetting and Critical Prewetting

A simple mean-field theory is presented which describes the basic observations of recent experiments revealing rich wetting behaviour of n-alkane/methanol mixtures at the liquid-vapour interface. The theory, qualitative and in part heuristic, is based on a microscopic lattice-gas model from which a Cahn–Landau approach is distilled. Besides the physics associated with the short-range components of the intermolecular interactions, effects of the long-range tails of the net van der Waals forces between interfaces are also taken into account. Further, gravitational thinning of the wetting phase is incorporated. The calculation of the spreading coefficient S is extended to the experimentally relevant situation in which the bulk adsorbate is slightly away from two-phase coexistence due to gravity. Analysis of this novel approximation to S for systems with short-range forces leads to the conclusion that the surface specific heat exponents _s =1,1/2, and 0, for first-order wetting, tricritical wetting and critical wetting, respectively, are robust with respect to (weak) gravitational thinning, consistently with experiment. For three different systems the adsorption is calculated as a function of temperature and compared with the experimentally measured ellipticity. Including weak long-range forces which favour wetting in the theory does not visibly alter the critical wetting transition for the nonane/methanol mixture, in contrast with the generic expectation of first-order wetting for such systems, but in good agreement with experiment. For decane/methanol weak long-range forces bring the transition very close to the prewetting critical point, leading to an adsorption behaviour closely reminiscent of short-range tricritical wetting, observed experimentally for alkane chain length between 9.6 and 10. Finally, for undecane/methanol the transition is clearly of first order. First-order wetting is also seen in the experiment.