113 research outputs found

    Memory in an aging molecular glass

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    The dielectric susceptibility of the molecular liquid sorbitol below its calorimetric glass transition displays memory strikingly similar to that of a variety of glassy materials. During a temporary stop in cooling, the susceptibility changes with time, and upon reheating the susceptibility retraces these changes. To investigate the out-of-equilibrium state of the liquid as it displays this memory, the heating stage of this cycle is interrupted and the subsequent aging characterized. At temperatures above that of the original cooling stop, the liquid enters a state on heating with an effective age that is proportional to the duration of the stop, while at lower temperatures no effective age can be assigned and subtler behavior emerges. These results, which reveal differences with memory displayed by spin glasses, are discussed in the context of the liquid's energy landscape.Comment: 5 pages, 4 figures. Significant revisions made to tex

    Evolution of particle-scale dynamics in an aging clay suspension

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    Multispeckle x-ray photon correlation spectroscopy was employed to characterize the slow dynamics of a colloidal suspension formed by highly-charged, nanometer-sized disks. At scattering wave vectors qq corresponding to interparticle length scales, the dynamic structure factor follows a form f(q,t)exp[(t/τ)βf(q,t) \sim \exp[-(t/\tau)^{\beta}], where β\beta \approx 1.5. The characteristic relaxation time τ\tau increases with the sample age tat_a approximately as τta1.8\tau \sim t_a^{1.8} and decreases with qq approximately as τq1\tau \sim q^{-1}. Such a compressed exponential decay with relaxation time that varies inversely with qq is consistent with recent models that describe the dynamics in disordered elastic media in terms of strain from random, local structural rearrangements. The amplitude of the measured decay in f(q,t)f(q,t) varies with qq in a manner that implies caged particle motion at short times. The decrease in the range of this motion and an increase in suspension conductivity with increasing tat_a indicate a growth in the interparticle repulsion as the mechanism for internal stress development implied by the models.Comment: 4 pages, includes 4 postscript figures; accepted for publication in Phys Rev Let

    Frequency-domain study of relaxation in a spin glass model for the structural glass transition

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    We have computed the time-dependent susceptibility for the finite-size mean-field Random Orthogonal model (ROM). We find that for temperatures above the mode-coupling temperature the imaginary part of the susceptibility χ(ν)\chi''(\nu) obeys the scaling forms proposed for glass-forming liquids. Furthermore, as the temperature is lowered the peak frequency of χ\chi'' decreases following a Vogel-Fulcher law with a critical temperature remarkably close to the known critical temperature TcT_c where the configurational entropy vanishes.Comment: 7 pages, 4 figures, epl LaTeX packag

    Wrinkling of a bilayer membrane

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    The buckling of elastic bodies is a common phenomenon in the mechanics of solids. Wrinkling of membranes can often be interpreted as buckling under constraints that prohibit large amplitude deformation. We present a combination of analytic calculations, experiments, and simulations to understand wrinkling patterns generated in a bilayer membrane. The model membrane is composed of a flexible spherical shell that is under tension and that is circumscribed by a stiff, essentially incompressible strip with bending modulus B. When the tension is reduced sufficiently to a value \sigma, the strip forms wrinkles with a uniform wavelength found theoretically and experimentally to be \lambda = 2\pi(B/\sigma)^{1/3}. Defects in this pattern appear for rapid changes in tension. Comparison between experiment and simulation further shows that, with larger reduction of tension, a second generation of wrinkles with longer wavelength appears only when B is sufficiently small.Comment: 9 pages, 5 color figure

    Critical dynamics of a spin-5/2 2D isotropic antiferromagnet

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    We report a neutron scattering study of the dynamic spin correlations in Rb2_2MnF4_4, a two-dimensional spin-5/2 antiferromagnet. By tuning an external magnetic field to the value for the spin-flop line, we reduce the effective spin anisotropy to essentially zero, thereby obtaining a nearly ideal two-dimensional isotropic antiferromagnet. From the shape of the quasielastic peak as a function of temperature, we demonstrate dynamic scaling for this system and find a value for the dynamical exponent zz. We compare these results to theoretical predictions for the dynamic behavior of the two-dimensional Heisenberg model, in which deviations from z=1z=1 provide a measure of the corrections to scaling.Comment: 5 pages, 4 figures. Submitted to Physical Review B, Rapid Communication

    High-resolution x-ray study of the nematic - smectic-A and smectic-A - smectic-C transitions in 8barS5-aerosil gels

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    The effects of dispersed aerosil nanoparticles on two of the phase transitions of the thermotropic liquid crystal material 4-n-pentylphenylthiol-4'-n-octyloxybenzoate 8barS5 have been studied using high-resolution x-ray diffraction techniques. The aerosils hydrogen bond together to form a gel which imposes a weak quenched disorder on the liquid crystal. The smectic-A fluctuations are well characterized by a two-component line shape representing thermal and random-field contributions. An elaboration on this line shape is required to describe the fluctuations in the smectic-C phase; specifically the effect of the tilt on the wave-vector dependence of the thermal fluctuations must be explicitly taken into account. Both the magnitude and the temperature dependence of the smectic-C tilt order parameter are observed to be unaffected by the disorder. This may be a consequence of the large bare smectic correlation length in the direction of modulation for this transition. These results show that the understanding developed for the nematic to smectic-A transition for octylcyanobiphenyl (8CB) and octyloxycyanobiphenyl (8OCB) liquid crystals with quenched disorder can be extended to quite different materials and transitions.Comment: 7 pages, 8 figure

    Evidence for glass and spin-glass phase transitions from the dynamic susceptibility

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    We present evidence that there is a phase transition, with a diverging static susceptibility, underlying the transformation of a liquid into a glass. The dielectric susceptibility, at frequencies above its characteristic value, shows a power-law tail extending over many decades to higher frequencies. An extrapolation of this behavior to the temperature where the dynamics becomes arrested indicates a diverging susceptibility. We present evidence for analogous behavior in the magnetic susceptibility of a paramagnet approaching the spin-glass transition. The similarity of the response in these two glassy systems suggests that some conventional lore, such as that the spin glass shows evidence for a diverging correlation length only in a nonlinear but not in the linear susceptibility, may be invalid

    Calorimetric study of the isotropic to nematic phase transition in an aligned liquid crystal nano-colloidal gel

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    A high-resolution calorimetric study of the specific heat (C p ) has been carried out for the isotropic to nematic phase transition in an aligned liquid crystal (octylcyanobiphenyl -8CB) and aerosil nano-colloid gel. A stable alignment was achieved by repeated thermal cycling of the samples in the presence of a strong uniform magnetic field, which introduces anisotropy to the quenched random disorder of the silica gel. In general, the specific heat features of the I2N transition in aligned (anisotropic) gel samples are consistent with those seen in random (isotropic) gel samples, namely the observance of two C p peaks and non-monotonic transition temperature shifts with increasing silica concentration. However, larger transition temperature shifts with silica density, modification of the phase conversion process in the two-phase coexistence region, and a larger effective transition enthalpy are observed for the aligned samples. The lower-temperature aligned C p peak is larger and broader while exhibiting less dispersion than the equivalent peak for the random gel. This may be a consequence of the alignment altering the evolution from random-dilution-dominated to random-field-dominated effects. The exact origin of the larger transition temperature shifts is uncertain but the larger enthalpy suggests that the nematic state is different in the aligned system than in random gels. The general non-monotonic behaviour of the transition temperature is interpreted using dimensional analysis as a combination of an effective elastic stiffening of the liquid crystal combined with a liquid crystal and aerosil surface interaction energy

    Smectic ordering in liquid crystal - aerosil dispersions II. Scaling analysis

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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.Comment: 14 pages, 10 figures, 1 table. Companion paper to "Smectic ordering in liquid crystal - aerosil dispersions I. X-ray scattering" by R.L. Leheny, S. Park, R.J. Birgeneau, J.-L. Gallani, C.W. Garland, and G.S. Iannacchion
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