4,374 research outputs found

    Orientations of the lamellar phase of block copolymer melts under oscillatory shear flow

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    We develop a theory to describe the reorientation phenomena in the lamellar phase of block copolymer melt under reciprocating shear flow. We show that similar to the steady-shear, the oscillating flow anisotropically suppresses fluctuations and gives rise to the parallel-perpendicular orientation transition. The experimentally observed high-frequency reverse transition is explained in terms of interaction between the melt and the shear-cell walls.Comment: RevTex, 3 pages, 1 figure, submitted to PR

    Evidence of a Critical time in Constrained Kinetic Ising models

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    We study the relaxational dynamics of the one-spin facilitated Ising model introduced by Fredrickson and Andersen. We show the existence of a critical time which separates an initial regime in which the relaxation is exponentially fast and aging is absent from a regime in which relaxation becomes slow and aging effects are present. The presence of this fast exponential process and its associated critical time is in agreement with some recent experimental results on fragile glasses.Comment: 20 Pages + 7 Figures, Revte

    Derivation of an Abelian effective model for instanton chains in 3D Yang-Mills theory

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    In this work, we derive a recently proposed Abelian model to describe the interaction of correlated monopoles, center vortices, and dual fields in three dimensional SU(2) Yang-Mills theory. Following recent polymer techniques, special care is taken to obtain the end-to-end probability for a single interacting center vortex, which constitutes a key ingredient to represent the ensemble integration.Comment: 18 pages, LaTe

    Orientational phase transitions in the hexagonal phase of a diblock copolymer melt under shear flow

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    We generalize the earlier theory by Fredrickson [J. Rheol. v.38, 1045 (1994)] to study the orientational behaviour of the hexagonal phase of diblock copolymer melt subjected to steady shear flow. We use symmetry arguments to show that the orientational ordering in the hexagonal phase is a much weaker effect than in the lamellae. We predict the parallel orientation to be stable at low and the perpendicular orientation at high shear rates. Our analysis reproduces the experimental results by Tepe et al. [Macromolecules v.28, 3008 (1995)] and explains the difficulties in experimental observation of the different orientations in the hexagonal phase.Comment: 21 pages, 6 eps figures, submitted to Physical Review

    Reactions at polymer interfaces: A Monte Carlo Simulation

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    Reactions at a strongly segregated interface of a symmetric binary polymer blend are investigated via Monte Carlo simulations. End functionalized homopolymers of different species interact at the interface instantaneously and irreversibly to form diblock copolymers. The simulations, in the framework of the bond fluctuation model, determine the time dependence of the copolymer production in the initial and intermediate time regime for small reactant concentration ρ0Rg3=0.163...0.0406\rho_0 R_g^3=0.163 ... 0.0406. The results are compared to recent theories and simulation data of a simple reaction diffusion model. For the reactant concentration accessible in the simulation, no linear growth of the copolymer density is found in the initial regime, and a t\sqrt{t}-law is observed in the intermediate stage.Comment: to appear in Macromolecule

    Surface states in nearly modulated systems

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    A Landau model is used to study the phase behavior of the surface layer for magnetic and cholesteric liquid crystal systems that are at or near a Lifshitz point marking the boundary between modulated and homogeneous bulk phases. The model incorporates surface and bulk fields and includes a term in the free energy proportional to the square of the second derivative of the order parameter in addition to the usual term involving the square of the first derivative. In the limit of vanishing bulk field, three distinct types of surface ordering are possible: a wetting layer, a non-wet layer having a small deviation from bulk order, and a different non-wet layer with a large deviation from bulk order which decays non-monotonically as distance from the wall increases. In particular the large deviation non-wet layer is a feature of systems at the Lifshitz point and also those having only homogeneous bulk phases.Comment: 6 pages, 7 figures, submitted to Phys. Rev.

    Cutoff for the East process

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    The East process is a 1D kinetically constrained interacting particle system, introduced in the physics literature in the early 90's to model liquid-glass transitions. Spectral gap estimates of Aldous and Diaconis in 2002 imply that its mixing time on LL sites has order LL. We complement that result and show cutoff with an O(L)O(\sqrt{L})-window. The main ingredient is an analysis of the front of the process (its rightmost zero in the setup where zeros facilitate updates to their right). One expects the front to advance as a biased random walk, whose normal fluctuations would imply cutoff with an O(L)O(\sqrt{L})-window. The law of the process behind the front plays a crucial role: Blondel showed that it converges to an invariant measure ν\nu, on which very little is known. Here we obtain quantitative bounds on the speed of convergence to ν\nu, finding that it is exponentially fast. We then derive that the increments of the front behave as a stationary mixing sequence of random variables, and a Stein-method based argument of Bolthausen ('82) implies a CLT for the location of the front, yielding the cutoff result. Finally, we supplement these results by a study of analogous kinetically constrained models on trees, again establishing cutoff, yet this time with an O(1)O(1)-window.Comment: 33 pages, 2 figure

    Simple model with facilitated dynamics for granular compaction

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    A simple lattice model is used to study compaction in granular media. As in real experiments, we consider a series of taps separated by large enough waiting times. The relaxation of the density exhibits the characteristic inverse logarithmic law. Moreover, we have been able to identify analytically the relevant time scale, leading to a relaxation law independent of the specific values of the parameters. Also, an expression for the asymptotic density reached in the compaction process has been derived. The theoretical predictions agree fairly well with the results from the Monte Carlo simulation.Comment: 15 pages, 4 figures, REVTeX file; no changes except for single-spacing to save paper (previous version 22 pages

    Steady State of microemulsions in shear flow

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    Steady-state properties of microemulsions in shear flow are studied in the context of a Ginzburg-Landau free-energy approach. Explicit expressions are given for the structure factor and the time correlation function at the one loop level of approximation. Our results predict a four-peak pattern for the structure factor, implying the simultaneous presence of interfaces aligned with two different orientations. Due to the peculiar interface structure a non-monotonous relaxation of the time correlator is also found.Comment: 5 pages, 3 figure

    Determination of complex dielectric functions of ion implanted and implanted‐annealed amorphous silicon by spectroscopic ellipsometry

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    Measuring with a spectroscopic ellipsometer (SE) in the 1.8–4.5 eV photon energy region we determined the complex dielectric function (ϵ = ϵ1 + iϵ2) of different kinds of amorphous silicon prepared by self‐implantation and thermal relaxation (500 °C, 3 h). These measurements show that the complex dielectric function (and thus the complex refractive index) of implanted a‐Si (i‐a‐Si) differs from that of relaxed (annealed) a‐Si (r‐a‐Si). Moreover, its ϵ differs from the ϵ of evaporated a‐Si (e‐a‐Si) found in the handbooks as ϵ for a‐Si. If we use this ϵ to evaluate SE measurements of ion implanted silicon then the fit is very poor. We deduced the optical band gap of these materials using the Davis–Mott plot based on the relation: (ϵ2E2)1/3 ∼ (E− Eg). The results are: 0.85 eV (i‐a‐Si), 1.12 eV (e‐a‐Si), 1.30 eV (r‐a‐Si). We attribute the optical change to annihilation of point defects
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