Searcharxiv⌕ Search

arXiv subjects

Sara Jabbari Farouji

Publications and source records attributed to Sara Jabbari Farouji.

2 recordsLinked to original sources

General perturbative framework for kinetics of rare transitions in 1-dimensional active particle systems

We present a theoretical framework that enables investigating rare transitions in a general model of an active particle in an external potential, with the thermal Active Ornstein-Uhlenbeck Particle (AOUP) appearing as a special case. Using a projection-operator formalism, we compute transition rates perturbatively in two distinct asymptotic regimes. In the regime of small persistence times-where the activity evolves much faster than the particle's position-integrating out the activity reproduces the rates previously reported in the literature. In the opposite regime of large persistence times, we instead integrate out the position and obtain the corresponding rates analytically. Together, these asymptotic expansions uniquely specify a rational approximation that remains accurate across intermediate persistence times. As a result, we obtain an analytic expression for the rate valid across all persistence times and activity strengths in the rare-event limit, which are in excellent agreement with numerical simulations. The presented framework applies to rare transitions in a broad class of driven systems.

cond-mat.stat-mech↗

Active string fluids and gels formed by dipolar active Brownian particles in 3D

Self-propelled particles possessing permanent magnetic dipole moments occur naturally in magnetotactic bacteria and in man-made systems like active colloids or micro-robots. Yet, the interplay between self-propulsion and anisotropic dipole-dipole interactions on dynamic self-assembly in three dimensions (3D) remains poorly understood. We conduct Brownian dynamics simulations of active dipolar particles in 3D, focusing on the low-density regime, where dipolar hard spheres tend to form chain-like aggregates and percolated networks with increasing dipolar coupling strength. We find that strong active forces override dipolar attractions, effectively inhibiting chain-like aggregation and network formation. Conversely, activating particles with low to moderate forces results in a fluid composed of active chains and rings. At strong dipolar coupling strengths, this active fluid transitions into an active gel, consisting of a percolated network of active chains. Although the overall structure of the active gel remains interconnected, the network experiences more frequent configurational rearrangements due to the reduced bond lifetime of active dipolar particles. Consequently, particles exhibit enhanced translational and rotational diffusion within the active fluid of strings and active gels compared to their passive counterparts. We quantify the influence of activity on aggregates topology, as they transition from branched structures to unconnected chains and rings. Our findings are summarized in a state diagram, delineating the impact of dipolar coupling strength and active force magnitude on the system.

cond-mat.soft↗