Dynamics of polydisperse hard-spheres under strong confinement. (1st June 2020)

• Record Type: Journal Article
• Authors: Roberts, Ryan C.; Marioni, Nico; Palmer, Jeremy C.; Conrad, Jacinta C.
• Is Part Of: Molecular physics. Volume 118:Number 9/10(2020)
• Publication Date: 2020-06-01
• Subjects: Glass transition -- molecular dynamics -- confinement -- hard spheres -- correlation length; Molecules -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Molécules -- Périodiques; Chimie physique et théorique -- Périodiques; 539.6.05
• DOI: 10.1080/00268976.2020.1728407
• Languages: English
• ISSNs: 0026-8976

Abstract

Abstract : We use molecular simulation to probe the connection between local structure and the unusual re-entrant dynamics observed for polydisperse hard-sphere liquids confined in thin slit pores. The local structure is characterised by calculating 2-D bond-orientational order parameters associated with square and hexatic order for particles in the layer adjacent to the confining walls. When the wall separation is commensurate with the average particle size, the particles primarily exhibit local hexatic order, whereas local square order increases in prevalence for incommensurate geometries. The relaxation time extracted from the ensemble-averaged mean-square displacement increases exponentially with the static correlation length associated with hexatic local order in strongly confined commensurate geometries, in agreement with theoretical predictions for dynamical slowing. Square order, by contrast, is not associated with a growing length scale for either commensurate or incommensurate geometries, indicating that it is strongly geometrically frustrated. Our results suggest that the influence of bond-orientational order on dynamical slowing may be altered by changing the extent of confinement. GRAPHICAL ABSTRACT: