Free energy of semiflexible polymers and structure of interfaces

The free energy of semiflexible polymers is calculated as a functional of the compositional scalar order parameter and the orientational order parameter of second-rank tensor S_ij on the basis of a microscopic model of wormlike chains with variable segment lengths. We use a density functional theory and a gradient expansion to evaluate the entropic part of the free energy, which is given in a power series of .The interaction term of the free energy is derived with a random phase approximation. For the rigid rod limit, the nematic-isotropic transition point is given by , N and w being the degree of polymerization and the anisotropic interaction parameter, respectively, and the degree of ordering at the transition point is 0.33448. We also find that the contour length of polymer chains becomes larger in a nematic phase than in an isotropic phase. Interface profiles are obtained numerically for some typical cases. In the neighborhood of isotropic-isotropic interfaces, polymer chains tend to align parallel to the interface on the polymer-rich side and perpendicular on the poor side. When an isotropic region and a nematic region coexist, orientational order parallel to the interface is preferred in the nematic region. Received: 28 May 1998 / Revised: 12 August 1998 / Accepted: 8 September 1998     

Core percolation in random graphs: a critical phenomena analysis

We study both numerically and analytically what happens to a random graph of average connectivity α when its leaves and their neighbors are removed iteratively up to the point when no leaf remains. The remnant is made of isolated vertices plus an induced subgraph we call the core. In the thermodynamic limit of an infinite random graph, we compute analytically the dynamics of leaf removal, the number of isolated vertices and the number of vertices and edges in the core. We show that a second order phase transition occurs at α = e = 2.718 ... : below the transition, the core is small but above the transition, it occupies a finite fraction of the initial graph. The finite size scaling properties are then studied numerically in detail in the critical region, and we propose a consistent set of critical exponents, which does not coincide with the set of standard percolation exponents for this model. We clarify several aspects in combinatorial optimization and spectral properties of the adjacency matrix of random graphs. Received 31 January 2001 and Received in final form 26 June 2001     

Simple Landau model of the smectic- A-isotropic phase transition

A simple Landau-type free energy function is presented to describe the smectic-A-isotropic phase transition. Varying the coupling between orientational and positional order parameters, a smectic-A-isotropic or a nematic-isotropic phase transition occurs. Within this model the smectic-A-isotropic phase transition is found to be always more strongly first order than the nematic-isotropic phase transition. The theoretical results are found to be in good agreement with all published experimental results. Received 27 June 2000     

The secondary structure of RNA under tension

We study the force-induced unfolding of random disordered RNA or single-stranded DNA polymers. The system undergoes a second-order phase transition from a collapsed globular phase at low forces to an extensive necklace phase with a macroscopic end-to-end distance at high forces. At low temperatures, the sequence inhomogeneities modify the critical behaviour. We provide numerical evidence for the universality of the critical exponents which, by extrapolation of the scaling laws to zero force, contain useful information on the ground-state (f = 0) properties. This provides a good method for quantitative studies of scaling exponents characterizing the collapsed globule. In order to get rid of the blurring effect of thermal fluctuations, we restrict ourselves to the ground state at fixed external force. We analyze the statistics of rearrangements, in particular below the critical force, and point out its implications for force-extension experiments on single molecules. Received 18 June 2002 and Received in final form 23 September 2002 RID="a" ID="a"e-mail: muller@ipno.in2p3.fr     

DMRG studies on interchain coupling model for quasi-one-dimensional organic magnet

We introduce a solid-on-solid growth process which evolves by random deposition of dimers, surface diffusion, and evaporation of monomers from the edges of plateaus. It is shown that the model exhibits a robust transition from a smooth to a rough phase. The roughening transition is driven by an absorbing phase transition at the bottom layer of the interface, which displays the same type of critical behavior as the pair contact process with diffusion 2A↦3A, 2A↦. Received 14 October 2002 Published online 14 February 2003 RID="a" ID="a"e-mail: Haye.Hinrichsen@physik.uni-wuppertal.de     

Stability of the Haldane state against the antiferromagnetic-bond randomness

Ground-state phase diagram of the one-dimensional bond-random S=1 Heisenberg antiferromagnet is investigated by means of the loop-cluster-update quantum Monte-Carlo method. The random couplings are drawn from a rectangular uniform distribution. We found that even in the case of extremely broad bond distribution, the magnetic correlation decays exponentially, and the correlation length is hardly changed; namely, the Haldane phase continues to be realized. This result is accordant with that of the exact-diagonalization study, whereas it might contradict the conclusion of an analytic theory founded in a power-law bond distribution instead. The latter theory predicts that a second-order phase transition occurs at a certain critical randomness, and the correlation length diverges for sufficiently strong randomness. Received: 31 March 1998 / Revised and Accepted: 7 July 1998     

Fluctuations at the domain edges of nematic liquid crystals in two dimensions

Capillary waves and director fluctuations reduce the surface tension of a non-anchoring unbound nematic surface by comparable amounts. These are relatively small effects in three dimensions, but in two dimensions they become more significant. We examine the conditions in two dimensions under which they dominate explicitly within the framework of a model of the Maier-Saupe type. We find that for reasonable physical parameters of the model the onset of the fluctuation dominated regime generally preempts the nematic-isotropic transition. We conclude that processes which are sensitive to line tension, such as Ostwald ripening during two-dimensional liquid-gas phase separation, are much more strongly coupled to anisotropic molecular interactions and associated nematic ordering than in three dimensions. Received 10 February 1999 and Received in final form 29 March 1999     

Orientation-dependent depletion interaction in rodlike colloid-polymer mixtures

Depletion interaction in a suspension of rodlike colloids with added non-adsorbing polymer coils is theoretically studied. We calculate an overlap volume of depletion zone between two rodlike colloids, based on the second virial approximation. We examine nematic-isotropic phase transition (NIT) and two-phase coexistence between an isotropic and a nematic phase at low polymer concentrations. We find that the depletion interaction is dependent on the orientational order parameter of rodlike colloids and leads to a decrease in the NIT concentration on the addition of polymer. The coexistence curves have a leaning-chimney shape and are shifted to lower rod concentrations on increasing the polymer concentration. Received 23 May 2001 and Received in final form 18 July 2001     

First and second order transition in frustrated XY systems

The nature of the phase transition for the XY stacked triangular antiferromagnet (STA) is a controversial subject at present. The field theoretical renormalization group (RG) in three dimensions predicts a first order transition. This prediction disagrees with Monte-Carlo (MC) simulations which favor a new universality class or a tricritical transition. We simulate by the Monte-Carlo method two models derived from the STA by imposing the constraint of local rigidity which should have the same critical behavior as the original model. A strong first order transition is found. Following Zumbach we analyze the second order transition observed in MC studies as due to a fixed point in the complex plane. We review the experimental results in order to clarify the critical behavior observed. Received: 18 February 1998 / Revised: 24 April 1998 / Accepted: 30 April 1998     

Adsorption of a random heteropolymer with random self-interactions onto an interface

We consider the adsorption of a random heteropolymer onto an interface within the model of Garel et al. [#!gareletal89!#] by taking into account random self-interactions and ternary repulsive interactions between the monomers. Within the replica trick and by using a self-consistent preaveraging procedure we map the adsorption problem onto the problem of binding state of a quantum mechanical Hamiltonian. The analysis of the latter is treated within the variational method based on the 2nd Legendre transform. Our study reveals a complex behaviour of the localization of the heteropolymer. In particular, we predict a reentrant localization transition for moderate values of the asymmetry of the distribution function of the monomer sequences along the heteropolymer. Received 9 October 2001 and Received in final form 27 February 2002 Published online 6 June 2002     

Effect of hydrodynamic flow on kinetics of nematic-isotropic transition in liquid crystals

We investigate kinetics of nematic-isotropic transition by solving the hydrodynamic equations for the nematic tensor order parameter and the fluid velocity in two space dimension (x-y plane). Numerical results indicate that nematic directors tend to align parallel to the x-y plane when hydrodynamic flow is incorporated. Late stage growth exponents, for the correlation length and for the number of topological defects, are not significantly altered by hydrodynamic flow. However, in contrast to the case without flow, the relation holds well, which may indicate the validity of dynamical scaling for the case with hydrodynamic flow. Received: 8 September 1997 / Received in final form: 23 October 1997 /Accepted: 3 November 1997     

Generalized off-equilibrium fluctuation-dissipation relations in random Ising systems

We show that the numerical method based on the off-equilibrium fluctuation-dissipation relation does work and is very useful and powerful in the study of disordered systems which show a very slow dynamics. We have verified that it gives the right information in the known cases (diluted ferromagnets and random field Ising model far from the critical point) and we used it to obtain more convincing results on the frozen phase of four-dimensional spin glasses. Moreover we used it to study the Griffiths phase of the diluted and the random field Ising models. Received 1 December 1998 and Received in final form 17 February 1999     

Shearing of planar smectic C chevrons

We have theoretically investigated chevron formation in smectic C materials and the transformation of this chevron structure to a tilted layer structure as the cell is sheared. We find a series of transition temperatures at which the behaviour of the cell critically changes. As the cell is cooled from the smectic A phase past the first critical temperature there is a second order transition which forms two tilted layer states with lower energy than the smectic A bookshelf structure. Although these low energy tilted structures exist the bookshelf structure is the stable state for zero shear. However, upon further cooling this bookshelf structure becomes unstable to the formation of a chevron state. Now when the cell is sheared the chevron structure smoothly transforms into the tilted layer structure. As each further critical temperature is passed an additional multiple chevron solution is formed which although a high energy, unstable state may be observed transiently. For sufficiently low temperatures the transition from chevron to tilted layer becomes first order. This first order transition occurs as the chevron interface merges with the surface alignment region to form the tilted layer structure. Received 28 December 1998 and Received in final form 8 April 1999     

Stretched exponential relaxation on the hypercube and the glass transition

We study random walks on the dilute hypercube using an exact enumeration Master equation technique, which is much more efficient than Monte Carlo methods for this problem. For each dilution p the form of the relaxation of the memory function q(t) can be accurately parametrized by a stretched exponential over several orders of magnitude in q(t). As the critical dilution for percolation is approached, the time constant tends to diverge and the stretching exponent drops towards 1/3. As the same pattern of relaxation is observed in a wide class of glass formers, the fractal like morphology of the giant cluster in the dilute hypercube appears to be a good representation of the coarse grained phase space in these systems. For these glass formers the glass transition may be pictured as a percolation transition in phase space. Received 16 June 2000 and Received in final form 13 October 2000     

A simple model of DNA denaturation and mutually avoiding walks statistics

Recently Garel, Monthus and Orland [Europhys. Lett. 55, 132 (2001)] considered a model of DNA denaturation in which excluded volume effects within each strand are neglected, while mutual avoidance is included. Using an approximate scheme they found a first order denaturation. We show that a first order transition for this model follows from exact results for the statistics of two mutually avoiding random walks, whose reunion exponent is c > 2, both in two and three dimensions. Analytical estimates of c due to the interactions with other denaturated loops, as well as numerical calculations, indicate that the transition is even sharper than in models where excluded volume effects are fully incorporated. The probability distribution of distances between homologous base pairs decays as a power law at the transition. Received 8 July 2002 / Received in final form 25 July 2002 Published online 17 September 2002     

Investigation of the phase transition at the nematic liquid crystal-wall interface within nonextensivity

In this study, the nematic-isotropic phase transition is investigated for a sample in the shape of a slab of thickness d, using nonextensive formalism. The interaction potential is written as the sum of the direct interaction of a given nematic molecule with the substrate and of its incomplete interaction with the other nematic molecules due to the presence of the limiting surface. In this framework, we show the effects of the nonextensivity on the nematic-isotropic transition at the nematic-wall interface. The generalized model can shed light on the properties of nematic liquid crystal confined in small-scale structures.     

Phase diagram of randomly polymerized membrane

Using a replica formalism, a generalization of a recent mean field model corresponding to the observed wrinkling transition in randomly polymerized membranes is presented. In this model we study the effects of global fluctuations of the surface normals to the flat membrane, which can be introduced by a random local field. In absence of these global fluctuations, we show that, the model exhibits both continuous and discontinuous transitions between flat and wrinkled phases, contrary to what has been predicted by Bensimon et al. and Attal et al. Phase diagrams both in replica symmetry and in breaking of replica symmetry in sense of Almeida and Thouless are given. We have also investigated the effects of global fluctuations on the replica symmetry phase diagram. We show that, the wrinkled phase is favored and the flat phase is unstable. For large global fluctuations, the transition between wrinkled and flat phases becomes first order. Received: 3 December 1997 / Revised: 31 March 1998 / Accepted: 3 August 1998     

Adsorption and localization of random copolymers subject to a force: The Morita approximation

We discuss directed walk models of random copolymers, either adsorbed at a surface or localized at an interface between two immiscible liquids. We consider the response to an applied force which can cause desorption or delocalization into a bulk phase, and calculate the critical force as a function of temperature. The randomness is quenched and, even for directed models, we cannot usually treat the quenched system analytically so we resort to an approximation in which the quenched average is approximated by an annealed average with a side condition which ensures the correct proportion of the types of comonomers. We argue that this approach gives the exact result for the quenched system in some cases and a bound in others.Received: 17 May 2004, Published online: 3 August 2004PACS: 36.20.Ey Conformation (statistics and dynamics) - 05.70.Jk Critical point phenomena in thermodynamics - 64.60.-i General studies of phase transitions