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Huaguang Wang

Publications and source records attributed to Huaguang Wang.

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Glass Transition in Monolayers of Rough Colloidal Ellipsoids

Structure-dynamics correlation is one of the major ongoing debates in the glass transition, although a number of structural features have been found connected to the dynamic heterogeneity in different glass-forming colloidal systems. Here using colloidal experiments combined with coarse-grained molecular dynamics simulations, we investigate the glass transition in monolayers of rough colloidal ellipsoids. Compared with smooth colloidal ellipsoids, the surface roughness of ellipsoids is found to significantly change the nature of glass transition. In particular, we find that the surface roughness induced by coating only a few small hemispheres on the ellipsoids can eliminate the existence of orientational glass and the two-step glass transition found in monolayers of smooth ellipsoids. This is due to the surface roughness-induced coupling between the translational and rotational degrees of freedom in colloidal ellipsoids, which also destroys the structure-dynamics correlation found in glass-forming suspensions of colloidal ellipsoids. Our results not only suggest a new way of using surface roughness to manipulate the glass transition in colloidal systems, but also highlight the importance of detailed particle shape on the glass transition and structure-dynamics correlation in suspensions of anisotropic colloids.

cond-mat.soft

Structural Origin of the Two-Step Glass Transition

The glass transition is a long-standing problem in physics. Identifying the structural origin of the transition may lead to the ultimate solution to the problem. Here, for the first time, we discover such a structural origin by proposing a novel method to analyze structure-dynamics relation in glasses. An interesting two-step glass transition, with rotational glass transition preceding translational one, is identified experimentally in 2D colloidal rod systems. During the transition, parallel and perpendicularly packed rods are found to form local free energy minima in configurational space, separated by an activation barrier. This barrier increases significantly when rotational glass transition is approached; thereby the rotational motion is frozen while the translational one remains diffusive. We argue that the activation barrier for rotation is the origin of the two-step glass transition. Such an activation barrier between well-defined local configurations holds the key to understand the two-step glass transition in general.

cond-mat.soft