arXiv subjects

Th. Voigtmann

Publications and source records attributed to Th. Voigtmann.

30 records · Page 2Linked to original sources

arXiv2006

Sensitivity of arrest in mode-coupling glasses to low-q structure

We quantify, within mode coupling theory, how changes in the liquid structure affect that of the glass. Apart from the known sensitivity to the structure factor $S(q)$ at wavevectors around the first sharp diffraction peak $q_0$, we find a strong (and inverted) response to structure at wavevectors \emph{below} this peak: an increase in $S(q_0/2)$ {\em lowers} the degree of arrest over a wide $q$-range. This strong sensitivity to `caged cage' packing effects, on length scales of order 2d, is much weaker in attractive glasses where short-range bonding dominates the steric caging effect.

cond-mat.soft↗

arXiv2004

Tagged-particle dynamics in a hard-sphere system: mode-coupling theory analysis

The predictions of the mode-coupling theory of the glass transition (MCT) for the tagged-particle density-correlation functions and the mean-squared displacement curves are compared quantitatively and in detail to results from Newtonian- and Brownian-dynamics simulations of a polydisperse quasi-hard-sphere system close to the glass transition. After correcting for a 17% error in the dynamical length scale and for a smaller error in the transition density, good agreement is found over a wide range of wave numbers and up to five orders of magnitude in time. Deviations are found at the highest densities studied, and for small wave vectors and the mean-squared displacement. Possible error sources not related to MCT are discussed in detail, thereby identifying more clearly the issues arising from the MCT approximation itself. The range of applicability of MCT for the different types of short-time dynamics is established through asymptotic analyses of the relaxation curves, examining the wave-number and density-dependent characteristic parameters. Approximations made in the description of the equilibrium static structure are shown to have a remarkable effect on the predicted numerical value for the glass-transition density. Effects of small polydispersity are also investigated, and shown to be negligible.

cond-mat.stat-mech↗

arXiv2003

Alpha-Relaxation Processes in Binary Hard-Sphere Mixtures

Molecular-dynamics simulations are presented for two correlation functions formed with the partial density fluctuations of binary hard-sphere mixtures in order to explore the effects of mixing on the evolution of glassy dynamics upon compressing the liquid into high-density states. Partial-density-fluctuation correlation functions for the two species are reported. Results for the alpha-relaxation process are quantified by parameters for the strength, the stretching, and the time scale, where the latter varies over almost four orders of magnitude upon compression. The parameters exhibit an appreciable dependence on the wave vector; and this dependence is different for the correlation function referring to the smaller and that for the larger species. These features are shown to be in semi-quantitative agreement with those calculated within the mode-coupling theory for ideal liquid-glass transitions.

cond-mat.soft↗

arXiv2003

Mixing effects for the structural relaxation in binary hard-sphere liquids

We report extensive molecular-dynamics simulation results for binary mixtures of hard spheres for different size disparities and different mixing percentages,for packing fractions up to 0.605 and over a characteristic time interval spanning up to five orders in magnitude. We explore the changes in the evolution of glassy dynamics due to mixing and discover two opposite scenarios: for large size disparity, increasing the mixing percentage of small particles leads to a speed-up of long-time dynamics, while small disparity leads to a slowing down. These results agree with predictions based on the mode coupling theory for ideal glass transitions.

cond-mat.soft↗

arXiv2002

Effect of Composition Changes on the Structural Relaxation of a Binary Mixture

Within the mode-coupling theory for idealized glass transitions, we study the evolution of structural relaxation in binary mixtures of hard spheres with size ratios $δ$ of the two components varying between 0.5 and 1.0. We find two scenarios for the glassy dynamics. For small size disparity, the mixing yields a slight extension of the glass regime. For larger size disparity, a plasticization effect is obtained, leading to a stabilization of the liquid due to mixing. For all $δ$, a decrease of the elastic moduli at the transition due to mixing is predicted. A stiffening of the glass structure is found as is reflected by the increase of the Debye-Waller factors at the transition points. The critical amplitudes for density fluctuations at small and intermediate wave vectors decrease upon mixing, and thus the universal formulas for the relaxation near the plateau values describe a slowing down of the dynamics upon mixing for the first step of the two-step relaxation scenario. The results explain the qualitative features of mixing effects reported by Williams and van Megen [Phys. Rev. E \textbf{64}, 041502 (2001)] for dynamical light-scattering measurements on binary mixtures of hard-sphere-like colloids with size ratio $δ=0.6$.

cond-mat.soft↗

arXiv2002

Completely monotone solutions of the mode-coupling theory for mixtures

We establish that a mode-coupling approximation for the dynamics of multi-component systems obeying Smoluchowski dynamics preserves a subtle yet fundamental property: the matrices of partial density correlation functions are completely monotone, i.e. they can exactly be written as superpositions of decaying exponentials only. This statement holds, no matter what further approximations are needed to calculate the theory's coupling parameters. The long-time limit of these functions fulfills a maximum property, and an iteration scheme for its numerical determination is given. We also show the existence of a unique solution to the equations of motion for which power series both for short times and small frequencies exist, the latter except at special points where ergodic-to-nonergodic transitions occur. These transitions are bifurcations that are proven to be of the cuspoid family.

cond-mat.soft↗

arXiv2001

Stiff-Glass Approximation of Mode-Coupling Theory

The stiff-glass approximation of the mode-coupling theory of the glass-transition--as introduced in a recent paper by Götze and Mayr for a discussion of phenomena resembling the Boson Peak and High-Frequency Sound observations made in real glass-formers--is examined in detail. It amounts to a neglection of two-phonon processes and thus provides a clear physical picture for the MCT solutions deep in the glass. In addition, the effect of additional symplifying approximations and the combination of these approximations is studied.

cond-mat.soft↗

arXiv2000

Higher order glass-transition singularities in colloidal systems with attractive interactions

The transition from a liquid to a glass in colloidal suspensions of particles interacting through a hard core plus an attractive square-well potential is studied within the mode-coupling-theory framework. When the width of the attractive potential is much shorter than the hard-core diameter, a reentrant behavior of the liquid-glass line, and a glass-glass-transition line are found in the temperature-density plane of the model. For small well-width values, the glass-glass-transition line terminates in a third order bifurcation point, i.e. in a A_3 (cusp) singularity. On increasing the square-well width, the glass-glass line disappears, giving rise to a fourth order A_4 (swallow-tail) singularity at a critical well width. Close to the A_3 and A_4 singularities the decay of the density correlators shows stretching of huge dynamical windows, in particular logarithmic time dependence.

cond-mat.soft↗

arXiv2000

Reorientational relaxation of a linear probe molecule in a simple glassy liquid

Within the mode-coupling theory (MCT) for the evolution of structural relaxation in glass-forming liquids, correlation functions and susceptibility spectra are calculated characterizing the rotational dynamics of a top-down symmetric dumbbell molecule, consisting of two fused hard spheres immersed in a hard-sphere system. It is found that for sufficiently large dumbbell elongations, the dynamics of the probe molecule follows the same universal glass-transition scenario as known from the MCT results of simple liquids. The $α$-relaxation process of the angular-index-j=1 response is stronger, slower and less stretched than the one for j=2, in qualitative agreement with results found by dielectric-loss and depolarized-light-scattering spectroscopy for some supercooled liquids. For sufficiently small elongations, the reorientational relaxation occurs via large-angle flips, and the standard scenario for the glass-transition dynamics is modified for odd-j responses due to precursor phenomena of a nearby type-A MCT transition. In this case, a major part of the relaxation outside the transient regime is described qualitatively by the $β$-relaxation scaling laws, while the $α$-relaxation scaling law is strongly disturbed.

cond-mat.soft↗

arXiv2000

Universal and non-universal features of glassy relaxation in propylene carbonate

It is demonstrated that the susceptibility spectra of supercooled propylene carbonate as measured by depolarized-light-scattering, dielectric-loss, and incoherent quasi-elastic neutron-scattering spectroscopy within the GHz window are simultaneously described by the solutions of a two-component schematic model of the mode-coupling theory (MCT) for the evolution of glassy dynamics. It is shown that the universal beta-relaxation-scaling laws, dealing with the asymptotic behavior of the MCT solutions, describe the qualitative features of the calculated spectra. But the non-universal corrections to the scaling laws render it impossible to achieve a complete quantitative description using only the leading-order-asymptotic results.

cond-mat.soft↗

arXiv1999

Colloidal gelation and non-ergodicity transitions

Within the framework of the mode coupling theory (MCT) of structural relaxation, mechanisms and properties of non-ergodicity transitions in rather dilute suspensions of colloidal particles characterized by strong short-ranged attractions are studied. Results building on the virial expansion for particles with hard cores and interacting via an attractive square well potential are presented, and their relevance to colloidal gelation is discussed.

cond-mat.soft↗

arXiv1999

Equations of structural relaxation

In the mode coupling theory of the liquid to glass transition the long time structural relaxation follows from equations solely determined by equilibrium structural parameters. The present extension of these structural relaxation equations to arbitrarily short times on the one hand allows calculations unaffected by model assumptions about the microscopic dynamics and on the other hand supplies new starting points for analytical studies. As a first application, power-law like structural relaxation at a glass-transition singularity is explicitly proven for a special schematic MCT model.

cond-mat.soft↗