Vortex lattice melting in layered superconductors with periodic columnar pins

The melting transition of the vortex lattice in highly anisotropic, layered superconductors with commensurate, periodic columnar pins is studied in a geometry where magnetic field and columnar pins are normal to the layers. Thermodynamic properties and equilibrium density distributions are obtained from numerical minimizations of an appropriate free-energy functional. We find a line of first-order transitions that ends at a critical point as the pin concentration is increased. A simple Landau theory providing a semi-quantitative explanation of the numerical results is proposed.Comment: Four pages, 3 Figure

Phase diagram of randomly pinned vortex matter in layered superconductors: dependence on the details of the point pinning

We study the thermodynamic and structural properties of the superconducting vortex system in high temperature layered superconductors, with magnetic field normal to the layers, in the presence of a small concentration of strong random point pinning defects via numerical minimization of a model free energy functional in terms of the time-averaged local density of pancake vortices. Working at constant magnetic induction and point pinning center concentration, we find that the equilibrium phase at low temperature ($T$) and small pinning strength ($s$) is a topologically ordered Bragg glass. As $T$ or $s$ is increased, the Bragg glass undergoes a first order transition to a disordered phase which we characterize as a ``vortex slush'' with polycrystalline structure within the layers and interlayer correlations extending to about twenty layers. This is in contrast with the pinned vortex liquid phase into which the Bragg glass was found to melt, using the same methods, in the case of a large concentration of weak pinning centers: that phase was amorphous with very little interlayer correlation. The value of the second moment of the random pinning potential at which the Bragg glass melts for a fixed temperature is very different in the two systems. These results imply that the effects of random point pinning can not be described only in terms of the second moment of the pinning potential, and that some of the unresolved contradictions in the literature concerning the nature of the low $T$ and high $s$ phase in this system are likely to arise from differences in the nature of the pinning in different samples, or from assumptions made about the pinning potential.Comment: 13 pages including 11 figures. Typos in HTML abstract corrected in v

Non-classical Rotational Inertia in a Two-dimensional Bosonic Solid Containing Grain Boundaries

We study the occurrence of non-classical rotational inertia (NCRI) arising from superfluidity along grain boundaries in a two-dimensional bosonic system. We make use of a standard mapping between the zero-temperature properties of this system and the statistical mechanics of interacting vortex lines in the mixed phase of a type-II superconductor. In the mapping, the liquid phase of the vortex system corresponds to the superfluid bosonic phase. We consider numerically obtained polycrystalline configurations of the vortex lines in which the microcrystals are separated by liquid-like grain boundary regions which widen as the vortex system temperature increases. The NCRI of the corresponding zero-temperature bosonic systems can then be numerically evaluated by solving the equations of superfluid hydrodynamics in the channels near the grain boundaries. We find that the NCRI increases very abruptly as the liquid regions in the vortex system (equivalently, superfluid regions in the bosonic system) form a connected, system-spannig structure with one or more closed loops. The implications of these results for experimentally observed supersolid phenomena are discussed.Comment: Ten pages, including figure

Dynamics of Glass Forming Liquids with Randomly Pinned Particles

It is frequently assumed that in the limit of vanishing cooling rate, the glass transition phenomenon becomes a thermodynamic transition at a temperature $T_{K}$. However, with any finite cooling rate, the system falls out of equilibrium at temperatures near $T_g(>T_{K})$, implying that the very existence of the putative thermodynamic phase transition at $T_{K}$ can be questioned. Recent studies of systems with randomly pinned particles have hinted that the thermodynamic glass transition may be observed in simulations and experiments carried out for liquids with randomly pinned particles. This expectation is based on the results of approximate calculations that suggest that the temperature of the thermodynamic glass transition increases as the concentration of pinned particles is increased and it may be possible to equilibrate the system at temperatures near the increased transition temperature. We test the validity of this prediction through extensive molecular dynamics simulations of two model glass-forming liquids in the presence of random pinning. We fit the temperature-dependence of the structural relaxation time to the Vogel-Fulcher-Tammann form that predicts a divergence of the relaxation time at a temperature $T_{VFT}$ and identify this temperature with the thermodynamic transition temperature $T_K$. We find that $T_{VFT}$ does not show any sign of increasing with increasing concentration of pinned particles. The main effect of pinning is found to be a rapid decrease in the kinetic fragility of the system with increasing pin concentration. Implications of these observations for current theories of the glass transition are discussed.Comment: submitted to scientific repor

Theoretical approaches to the glass transition in simple liquids

Theoretical approaches to the development of an understanding of the behaviour of simple supercooled liquids near the structural glass transition are reviewed and our work on this problem, based on the density functional theory of freezing and replicated liquid state theory, are summarized in this context. A few directions for further work on this problem are suggested

Growing length and time scales in glass forming liquids

We study the growing time scales and length scales associated with dynamical slow down for a realistic glass former, using computer simulations. We perform finite size scaling to evaluate a length scale associated with dynamical heterogeneity which grows as temperature decreases. However, relaxation times which also grow with decreasing temperature, do not show the same kind of scaling behavior with system size as the dynamical heterogeneity, indicating that relaxation times are not solely determined by the length scale of dynamical heterogeneity. We show that relaxation times are instead determined, for all studied system sizes and temperatures, by configurational entropy, in accordance with the Adam-Gibbs relation, but in disagreement with theoretical expectations based on spin-glass models that configurational entropy is not relevant at temperatures substantially above the critical temperature of mode coupling theory. The temperature dependence of the heterogeneity length scale shows significant deviations from theoretical expectations, and the length scale one may extract from the system size dependence of the configurational entropy has much weaker temperature dependence compared to the heterogeneity length scale at all studied temperatures. Our results provide new insights into the dynamics of glass-forming liquids and pose serious challenges to existing theoretical descriptions

Short-time β\beta-relaxation in glass-forming liquids is cooperative in nature

Temporal relaxation of density fluctuations in supercooled liquids near the glass transition occurs in multiple steps. The short-time $\beta$-relaxation is generally attributed to spatially local processes involving the rattling motion of a particle in the transient cage formed by its neighbors. Using molecular dynamics simulations for three model glass-forming liquids, we show that the $\beta$-relaxation is actually cooperative in nature. Using finite-size scaling analysis, we extract a growing length-scale associated with $\beta$-relaxation from the observed dependence of the $\beta$-relaxation time on the system size. Remarkably, the temperature dependence of this length scale is found to be the same as that of the length scale that describes the spatial heterogeneity of local dynamics in the long-time $\alpha$-relaxation regime. These results show that the conventional interpretation of $\beta$-relaxation as a local process is too simplified and provide a clear connection between short-time dynamics and long-time structural relaxation in glass-forming liquids

Vanishing of configurational entropy may not imply an ideal glass transition in randomly pinned liquids

Ozawa et. al [1] presented numerical results for the configurational entropy density, $s_c$, of a model glass-forming liquid in the presence of random pinning. The location of a "phase boundary" in the pin density ($c$) - temperature ($T$) plane, that separates an "ideal glass" phase from the supercooled liquid phase, is obtained by finding the points at which $s_c(T,c) \to 0$. According to the theoretical arguments by Cammarota et. al. [2], an ideal glass transition at which the $\alpha$-relaxation time $\tau_\alpha$ diverges takes place when $s_c$ goes to zero. We have studied the dynamics of the same system using molecular dynamics simulations. We have calculated the time-dependence of the self intermediate scattering function, $F_s(k,t)$ at three state points in the $(c-T)$ plane where $s_c(T,c) \simeq 0$ according to Ref. [1]. It is clear from the plots that the relaxation time is finite [$\tau_\alpha \sim \mathcal{O}(10^6)]$ at these state points. Similar conclusions have been obtained in Ref.[3] where an overlap function was used to calculate $\tau_\alpha$ at these state points