Condensed Matter Theory

Abstract:

These notes provide an introduction to phase ordering in dry, scalar active matter. We first briefly review Model A and Model B, the long-standing continuum descriptions of ordering in systems with a non-conserved and conserved scalar order parameter. We then contrast different ways in which the field theories can be extended so that the phase ordering persists, but in systems that are active and do not reach thermodynamic equilibrium. The active models allow a wide range of dynamical steady states not seen in their passive counterparts. These include microphase separation, active foams and travelling density bands.

Abstract:

Chemically active colloids or enzymes cluster into dense droplets driven by their phoretic response to collectively generated chemical gradients. Employing Brownian dynamics simulation techniques, our study of the dynamics of such a chemically active droplet uncovers a rich variety of structures and dynamical properties, including the full range of fluidlike to solidlike behavior, and non-Gaussian positional fluctuations. Our work sheds light on the complex dynamics of the active constituents of metabolic clusters, which are the main drivers of nonequilibrium activity in living systems.

Abstract:

We study the defect solutions of the nonreciprocal Cahn-Hilliard model. We find two kinds of defects, spirals with unit magnitude topological charge, and topologically neutral targets. These defects generate radially outward traveling waves and thus break the parity and time-reversal symmetry. For a given strength of nonreciprocity, spirals and targets with unique asymptotic wave number and amplitude are selected. We use large-scale simulations to show that at low nonreciprocity α, disordered states evolve into quasistationary spiral networks. With increasing α, we observe networks composed primarily of targets. Beyond a critical threshold α_{c}, a disorder-order transition from defect networks to traveling waves emerges. The transition is marked by a sharp rise in the global polar order.

Abstract:

Magnetic gels with embedded micro-/nano-sized magnetic particles in cross-linked polymer networks can be actuated by external magnetic fields, with changes in their internal microscopic structures and macroscopic mechanical properties. We investigate the responses of such magnetic gels to an external magnetic field, by means of coarse-grained molecular dynamics simulations. We find that the dynamics of magnetic particles are determined by the interplay of magnetic dipole-dipole interactions, polymer elasticity, and thermal fluctuations. The corresponding microscopic structures formed by the magnetic particles, such as elongated chains, can be controlled by the external magnetic field. Furthermore, the magnetic gels can exhibit reinforced macroscopic mechanical properties, where the elastic modulus increases algebraically with the magnetic moments of the particles in the form of ∝(m-mc)2 when magnetic chains are formed. This simulation work can not only serve as a tool for studying the microscopic and the macroscopic responses of the magnetic gels, but also facilitate future fabrications and practical controls of magnetic composites with desired physical properties.