Can the jamming transition be described using equilibrium statistical mechanics?

When materials such as foams or emulsions are compressed, they display solid behaviour above the so-called `jamming' transition. Because compression is done out-of-equilibrium in the absence of thermal fluctuations, jamming appears as a new kind of a nonequilibrium phase transition. In this proceeding paper, we suggest that tools from equilibrium statistical mechanics can in fact be used to describe many specific features of the jamming transition. Our strategy is to introduce thermal fluctuations and use statistical mechanics to describe the complex phase behaviour of systems of soft repulsive particles, before sending temperature to zero at the end of the calculation. We show that currently available implementations of standard tools such as integral equations, mode-coupling theory, or replica calculations all break down at low temperature and large density, but we suggest that new analytical schemes can be developed to provide a fully microscopic, quantitative description of the jamming transition.Comment: 8 pages, 6 figs. Talk presented at Statphys24 (July 2010, Cairns, Australia

Structure and dynamics in glass-formers: predictability at large length scales

Dynamic heterogeneity in glass-formers has been related to their static structure using the concept of dynamic propensity. We re-examine this relationship by analyzing dynamical fluctuations in two atomistic glass-formers and two theoretical models. We introduce quantitative statistical indicators which show that the dynamics of individual particles cannot be predicted on the basis of the propensity, nor by any structural indicator. However, the spatial structure of the propensity field does have predictive power for the spatial correlations associated with dynamic heterogeneity. Our results suggest that the quest for a connection between static and dynamic properties of glass-formers at the particle level is vain, but they demonstrate that such connection does exist on larger length scales.Comment: 7 pages; 4 figs - Extended, clarified versio

Electronic Correlations in CoO2, the Parent Compound of Triangular Cobaltates

A 59Co NMR study of CoO2, the x=0 end member of AxCoO2 (A = Na, Li...) cobaltates, reveals a metallic ground state, though with clear signs of strong electron correlations: low-energy spin fluctuations develop at wave vectors q different from 0 and a crossover to a Fermi-liquid regime occurs below a characteristic temperature T*~7 K. Despite some uncertainty over the exact cobalt oxidation state n this material, the results show that electronic correlations are revealed as x is reduced below 0.3. The data are consistent with NaxCoO2 being close to the Mott transition in the x -> 0 limit.Comment: 4 pages, submitte

Novel Crossover in Coupled Spin Ladders

We report a novel crossover behavior in the long-range-ordered phase of a prototypical spin-$1/2$ Heisenberg antiferromagnetic ladder compound $\mathrm{(C_7H_{10}N)_2CuBr_4}$. The staggered order was previously evidenced from a continuous and symmetric splitting of $^{14}$N NMR spectral lines on lowering temperature below $T_c\simeq 330$ mK, with a saturation towards $\simeq 150$ mK. Unexpectedly, the split lines begin to further separate away below $T^*\sim 100$ mK while the line width and shape remain completely invariable. This crossover behavior is further corroborated by the NMR relaxation rate $T_1^{-1}$ measurements. A very strong suppression reflecting the ordering, $T_1^{-1}\sim T^{5.5}$, observed above $T^*$, is replaced by $T_1^{-1}\sim T$ below $T^*$. These original NMR features are indicative of unconventional nature of the crossover, which may arise from a unique arrangement of the ladders into a spatially anisotropic and frustrated coupling network.Comment: 5 pages, 3 figure

Attractive Tomonaga-Luttinger Liquid in a Quantum Spin Ladder

We present NMR measurements of a strong-leg spin-1/2 Heisenberg antiferromagnetic ladder compound (C7H10N)2CuBr4 under magnetic fields up to 15 T in the temperature range from 1.2 K down to 50 mK. From the splitting of NMR lines we determine the phase boundary and the order parameter of the low-temperature (3-dimensional) long-range-ordered phase. In the Tomonaga-Luttinger regime above the ordered phase, NMR relaxation reflects characteristic power-law decay of spin correlation functions as 1/T1 T^(1/2K-1), which allows us to determine the interaction parameter K as a function of field. We find that field-dependent K varies within the 1<K<2 range which signifies attractive interaction between the spinless fermions in the Tomonaga-Luttinger liquid

Compressing nearly hard sphere fluids increases glass fragility

We use molecular dynamics to investigate the glass transition occurring at large volume fraction, phi, and low temperature, T, in assemblies of soft repulsive particles. We find that equilibrium dynamics in the (phi, T) plane obey a form of dynamic scaling in the proximity of a critical point at T=0 and phi=phi_0, which should correspond to the ideal glass transition of hard spheres. This glass point, `point G', is distinct from athermal jamming thresholds. A remarkable consequence of scaling behaviour is that the dynamics at fixed phi passes smoothly from that of a strong glass to that of a very fragile glass as phi increases beyond phi_0. Correlations between fragility and various physical properties are explored.Comment: 5 pages, 3 figures; Version accepted at Europhys. Let

A random walk description of the heterogeneous glassy dynamics of attracting colloids

We study the heterogeneous dynamics of attractive colloidal particles close to the gel transition using confocal microscopy experiments combined with a theoretical statistical analysis. We focus on single particle dynamics and show that the self part of the van Hove distribution function is not the Gaussian expected for a Fickian process, but that it reflects instead the existence, at any given time, of colloids with widely different mobilities. Our confocal microscopy measurements can be described well by a simple analytical model based on a conventional continuous time random walk picture, as already found in several other glassy materials. In particular, the theory successfully accounts for the presence of broad tails in the van Hove distributions that exhibit exponential, rather than Gaussian, decay at large distance.Comment: 13 pages, 5 figs. Submitted to special issue "Classical and Quantum Glasses" of J. Phys.: Condens. Matter; v2: response to refere

Field-induced magnetic behavior in quasi-one-dimensional Ising-like antiferromagnet BaCo2V2O8: A single-crystal neutron diffraction study

BaCo2V2O8 is a nice example of a quasi-one-dimensional quantum spin system that can be described in terms of Tomonaga-Luttinger liquid physics. This is explored in the present study where the magnetic field-temperature phase diagram is thoroughly established up to 12 T using single-crystal neutron diffraction. The transition from the N\'eel phase to the incommensurate longitudinal spin density wave (LSDW) phase through a first-order transition, as well as the critical exponents associated with the paramagnetic to ordered phase transitions, and the magnetic order both in the N\'eel and in the LSDW phase are determined, thus providing a stringent test for the theory.Comment: 17 pages with 15 figure

Magnetic structure of azurite above the 1/3 magnetization plateau

The transition from the 1/3 magnetization plateau towards the saturation magnetization in azurite has been studied by low-temperature, high-magnetic-field, high-frequency proton nuclear magnetic resonance (NMR). The observed symmetrical splitting of the NMR spectra is incompatible with the longitudinal incommensurate order appearing when the longitudinal correlation function becomes dominant over the transverse one, which is the expected framework for the existence of the 2/3 magnetization plateau. The spectra are rather interpreted in terms of a more standard transverse antiferromagnetic (canted) order