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Nicholas W. Hackney

Publications and source records attributed to Nicholas W. Hackney.

3 recordsLinked to original sources

Shear and crystallization in deformable granular packings: why don't auxetics order?

Shear of three-dimensional, highly compressed granular packings is simulated using a bonded particle approach that explicitly resolves elastic deformation. Varying Poisson's ratio $\nu$ produces significant changes in rheology, packing structure, and grain morphology. During flow, conventional systems ($\nu > 0$) readily crystallize while auxetics ($\nu < 0$) resist ordering. This duality reflects the fact that conventional grains develop polyhedral-like facets but conserve volume while auxetics behave oppositely, demonstrating an unexpected interaction between elasticity, geometry, and crystallization.

cond-mat.soft

Shape Elasticity in Colloidal Bent-Core Liquid Crystals

Curved particles have been shown to stabilize a range of states with unique order in dense suspensions of colloidal bent core liquid crystals. The shape of the colloidal rods encourages the formation of curved director fields. However, states of constant bend cannot uniformly fill either two or three dimensional Euclidean space and are therefore geometrically frustrated. As a result, curved rods are forced to couple their preference for bend with additional twist and splay deformations, giving rise to twist-bend and splay-bend states of nematic and smectic order. In this article, we study the effect of rod curvature on these diverse states of liquid crystalline order using molecular dynamics simulations of a bonded particle model of curved rods with tunable shape elasticity. Focusing on the case of intermediately curved rods, we find that curved rods go through a sequence of isotropic, nematic twist-bend and smectic splay-bend ordering as the density is increased from the dilute limit, in agreement with previous studies of rigid rods. As the rods become more elastic, the critical concentration separating these phases is shifted to higher density. Lastly, we find that flexibility weakens the first-order phase transition separating the isotropic and nematic twist-bend phases.

cond-mat.soft

Dispersed, condensed and self-limiting states of geometrically frustrated assembly

In self-assembling systems, geometric frustration leads to complex states characterized by internal gradients of shape misfit. Frustrated assemblies have drawn recent interest due to the unique possibility that their thermodynamics can sense and select the finite size of assembly at length scales much larger than constituent building blocks or their interactions. At present, self-limitation is chiefly understood to derive from zero-temperature considerations, specifically the competition between cohesion and scale-dependent elastic costs of frustration. While effects of entropy and finite temperature fluctuations are necessarily significant for self-assembling systems, their impact on the self-limiting states of frustrated assemblies is not known. We introduce a generic, minimal model of frustrated assembly, and establish its finite-temperature and concentration dependent thermodynamics by way of simulation and continuum theory. The phase diagram is marked by three distinct states of translation order: a dispersed vapor; a defect-riddled condensate; and the self-limiting aggregate state. We show that, at finite temperature, the self-limiting state is stable at intermediate frustration. Further, in contrast to the prevailing picture, its thermodynamic boundaries with the macroscopic disperse and bulk states are temperature controlled, pointing to the essential importance of translational and conformational entropy in their formation.

cond-mat.soft