A novel particle tracking method with individual particle size measurement and its application to ordering in glassy hard sphere colloids

Particle tracking is a key to single-particle-level confocal microscopy observation of colloidal suspensions, emulsions, and granular matter. The conventional tracking method has not been able to provide accurate information on the size of individual particle. Here we propose a novel method to localise spherical particles of arbitrary relative sizes from either 2D or 3D (confocal) images either in dilute or crowded environment. Moreover this method allows us to estimate the size of each particle reliably. We use this method to analyse local bond orientational ordering in a supercooled polydisperse colloidal suspension as well as the heterogeneous crystallisation induced by a substrate. For the former, we reveal non-trivial couplings of crystal-like bond orientational order and local icosahedral order with the spatial distribution of particle sizes: Crystal-like order tends to form in regions where very small particles are depleted and the slightly smaller size of the central particle stabilizes icosahedral order. For the latter, on the other hand, we found that very small particles are expelled from crystals and accumulated on the growth front of crystals. We emphasize that such information has not been accessible by conventional tracking methods

Importance of many-body correlations in glass transition: an example from polydisperse hard spheres

Most of the liquid-state theories, including glass-transition theories, are constructed on the basis of two-body density correlations. However, we have recently shown that many-body correlations, in particular bond orientational correlations, play a key role in both the glass transition and the crystallization transition. Here we show, with numerical simulations of supercooled polydisperse hard spheres systems, that the lengthscale associated with any two-point spatial correlation function does not increase toward the glass transition. A growing lengthscale is instead revealed by considering many-body correlation functions, such as correlators of orientational order, which follows the lengthscale of the dynamic heterogeneities. Despite the growing of crystal-like bond orientational order, we reveal that the stability against crystallization with increasing polydispersity is due to an increasing population of icosahedral arrangements of particles. Our results suggest that, for this type of systems, many-body correlations are a manifestation of the link between the vitrification and the crystallization phenomena. Whether a system is vitrified or crystallized can be controlled by the degree of frustration against crystallization, polydispersity in this case.Comment: To appear in J. Chem. Phys. for a special issue on the Glass Transitio

Local Oscillatory Rheology from Echography

Local Oscillatory Rheology from Echography (LORE) consists in a traditional rheology experiment synchronized with high-frequency ultrasonic imaging which gives access to the local material response to oscillatory shear. Besides classical global rheological quantities, this method provides quantitative time-resolved information on the local displacement across the entire gap of the rheometer. From the local displacement response, we compute and decompose the local strain in its Fourier components and measure the spatially-resolved viscoelastic moduli. After benchmarking our method on homogeneous Newtonian fluids and soft solids, we demonstrate that this technique is well suited to characterize spatially heterogeneous samples, wall slip, and the emergence of nonlinearity under large amplitude oscillatory stress in soft materials.Comment: 10 pages, 5 figures, submitted to Phys. Rev. Applie

コロイド過冷却液体における構造的不均一性と動的不均一性：共焦点顕微鏡による研究

The glass transition is often thought as decoupled from any structural change. I show in this thesis that two types of local order can be detected in a simple experimental glass former. This order increases when approaching the glass transition and is spatially correlated with the dynamic heterogeneities of the supercooled liquid.On envisage souvent la transition vitreuse comme découplée de tout changement structurel. Dans cette thèse, je montre que deux types d'ordre local peuvent être détectée dans un système vitreux expérimental simple. Cet ordre croit à l'approche de la transition vitreuse et est corrélé spatialement avec les hétérogénéités dynamiques du liquide surfondu

Creep and Fracture of a Protein Gel under Stress

International audienceBiomaterials such as protein or polysaccharide gels are known to behave qualitatively as soft solids and to rupture under an external load. Combining optical and ultrasonic imaging to shear rheology we show that the failure scenario of a protein gel is reminiscent of brittle solids: after a primary creep regime characterized by a power-law behavior whose exponent is fully accounted for by linear viscoelasticity, fractures nucleate and grow logarithmically perpendicularly to shear, up to the sudden rupture of the gel. A single equation accounting for those two successive processes nicely captures the full rheological response. The failure time follows a decreasing power law with the applied shear stress, similar to the Basquin law offatigue for solids. These results are in excellent agreement with recent fiber-bundle models that include damage accumulation on elastic fibers and exemplify protein gels as model, brittlelike soft solids

Active glass: ergodicity breaking dramatically affects response to self-propulsion

We study experimentally the response of a dense sediment of Brownian particles to self-propulsion. We observe that the ergodic supercooled liquid relaxation is monotonically enhanced by activity. By contrast the nonergodic glass shows an order of magnitude slowdown at low activities with respect to passive case, followed by fluidization at higher activities. Our results contrast with theoretical predictions of the ergodic approach to glass transition summing up to a shift of the glass line. We propose that nonmonotonicity is due to competing effects of activity: (i) extra energy that helps breaking cages (ii) directionality that hinders cage exploration. We call it "Deadlock from the Emergence of Active Directionality" (DEAD). It suggests further theoretical works should include thermal motion.Comment: 5 pages, 3 figures + supplementary materials (3 pages, 5 figures