arXiv subjects

S. A. Mallory

Publications and source records attributed to S. A. Mallory.

9 recordsLinked to original sources

arXiv2025

Single-File Diffusion of Active Brownian Particles

Single-file diffusion (SFD) is a key mechanism underlying transport phenomena in confined physical and biological systems. In a typical SFD process, microscopic particles are restricted to moving in a narrow channel where they cannot pass one another, resulting in constrained motion and anomalous long-time diffusion. In this study, we use Brownian dynamics simulations and analytical theory to investigate the SFD of athermal active Brownian particles (ABPs), a minimal model of active colloids. Building on prior work (Phys. Rev. E 108, 064601 (2023)), where the kinetic temperature, pressure, and compressibility of the single-file ABP system were derived, we develop an accurate analytical expression for the mean square displacement (MSD) of a tagged particle. We find that the MSD exhibits ballistic behavior at short times, governed by the reduced kinetic temperature of the system. At long times, the characteristic subdiffusive scaling of SFD, $\langle (Δx)^2 \rangle \sim t^{1/2}$, is preserved. However, self-propulsion introduces significant changes to the 1D mobility, which we directly relate to the system's compressibility. Furthermore, we demonstrate that the generalized 1D mobility, originally proposed by Kollmann for equilibrium systems (Phys. Rev. Lett. 90, 180602 (2003)), can be extended to active systems with minimal modification. These findings provide a framework for understanding particle transport in active systems and for tuning transport properties at the microscale, particularly in geometries where motion is highly restricted.

cond-mat.soft↗

arXiv2021

Self-assembly of active amphiphilic Janus particles

In this article, we study the phenomenology of a two dimensional dilute suspension of active amphiphilic Janus particles. We analyze how the morphology of the aggregates emerging from their self-assembly depends on the strength and the direction of the active forces. We systematically explore and contrast the phenomenologies resulting from particles with a range of attractive patch coverages. Finally, we illustrate how the geometry of the colloids and the directionality of their interactions can be used to control the physical properties of the assembled active aggregates and suggest possible strategies to exploit self-propulsion as a tunable driving force for self-assembly.

cond-mat.soft↗

arXiv2021

An active approach to colloidal self-assembly

In this review we discuss recent advances in the self-assembly of self-propelled colloidal particles and highlight some of the most exciting results in this field with a specific focus on dry active matter. We explore this phenomenology through the lens of the complexity of the colloidal building blocks. We begin by considering the behavior of isotropic spherical particles. We then discuss the case of amphiphilic and dipolar Janus particles. Finally, we show how the geometry of the colloids and/or the directionality of their interactions can be used to control the physical properties of the assembled active aggregates, and suggest possible strategies on how to exploit activity as a tunable driving force for self-assembly. The unique properties of active colloids lend promise for the design of the next generation of functional, environment-sensing microstructures able to perform specific tasks in an autonomous and targeted manner.

cond-mat.soft↗

arXiv2020

Universal reshaping of arrested colloidal gels via active doping

Colloids that interact via a short-range attraction serve as the primary building blocks for a broad range of self-assembled materials. However, one of the well-known drawbacks to this strategy is that these building blocks rapidly and readily condense into a metastable colloidal gel. Using computer simulations, we illustrate how the addition of a small fraction of purely repulsive self-propelled colloids, a technique referred to as active doping, can prevent the formation of this metastable gel state and drive the system toward its thermodynamically favored crystalline target structure. The simplicity and robust nature of this strategy offers a systematic and generic pathway to improving the self-assembly of a large number of complex colloidal structures. We discuss in detail the process by which this feat is accomplished and provide quantitative metrics for exploiting it to modulate self-assembly. We provide evidence for the generic nature of this approach by demonstrating that it remains robust under a number of different anisotropic short-ranged pair interactions in both two and three dimensions. In addition, we report on a novel microphase in mixtures of passive and active colloids. For a broad range of self-propelling velocities, it is possible to stabilize a suspension of fairly monodisperse finite-size crystallites. Surprisingly, this microphase is also insensitive to the underlying pair interaction between building blocks. The active stabilization of these moderately-sized monodisperse clusters is quite remarkable and should be of great utility in the design of hierarchical self-assembly strategies. This work further bolsters the notion that active forces can play a pivotal role in directing colloidal self-assembly.

cond-mat.soft↗

arXiv2016

Activity-assisted self-assembly of colloidal particles

We outline a basic strategy of how self-propulsion can be used to improve the yield of a typical colloidal self-assembly process. The success of this approach is predicated on the thoughtful design of the colloidal building block as well as how self-propulsion is endowed to the particle. As long as a set of criteria are satisfied, it is possible to significantly increase the rate of self-assembly, and greatly expand the window in parameter space where self-assembly can occur. In addition, we show that by tuning the relative on/off time of the self-propelling force it is possible to modulate the effective speed of the colloids allowing for further optimization of the self-assembly process.

cond-mat.soft↗

arXiv2015

Anomalous dynamics of an elastic membrane in an active fluid

Using numerical simulations, we characterized the behavior of an elastic membrane immersed in an active fluid. Our findings reveal a nontrivial folding and re-expansion of the membrane that is controlled by the interplay of its resistance to bending and the self-propulsion strength of the active components in solution. We show how flexible membranes tend to collapse into multi-folded states, whereas stiff membranes oscillates between an extended configuration and a singly folded state. This study provides a simple example of how to exploit the random motion of active particles to perform mechanical work at the micro-scale.

cond-mat.soft↗

arXiv2014

The role of particle shape in active depletion

Using numerical simulations, we study how a solution of small active disks, acting as depletants, induces effective interactions on large passive colloids. Specifically, we analyze how the range, strength, and sign of these interactions are crucially dependent on the shape of the colloids. Our findings indicate that while colloidal rods experience a long-ranged predominantly attractive interaction, colloidal disks feel a purely repulsive force that is short-ranged in nature and grows in strength with the size ratio between the colloids and active depletants. For colloidal rods, simple scaling arguments are proposed to characterize the strength of these induced interactions.

cond-mat.soft↗

arXiv2014

Curvature Induced Activation of a Passive Tracer in an Active Bath

We use numerical simulations to study the motion of a large asymmetric tracer immersed in a low density suspension of self-propelled nanoparticles in two dimensions. Specifically, we analyze how the curvature of the tracer affects its translational and rotational motion in an active environment. We find that even very small amounts of curvature are sufficient for the active bath to impart directed motion to the tracer which results in its effective activation. We propose simple scaling arguments to characterize this induced activity in terms of the curvature of the tracer and the strength of the self-propelling force. Our results suggest new ways of controlling the transport properties of passive tracers in an active medium by carefully tailoring their geometry.

cond-mat.soft↗

arXiv2014

Anomalous Thermomechanical Properties of a Self-propelled Colloidal Fluid

We use numerical simulations to compute the equation of state of a suspension of spherical, self-propelled nanoparticles. We study in detail the effect of excluded volume interactions and confinement as a function of the system temperature, concentration and strength of the propulsion. We find a striking non-monotonic dependence of the pressure with the temperature, and provide simple scaling arguments to predict and explain the occurrence of such an anomalous behavior. We conclude the paper by explicitly showing how our results have an important implications for the effective forces exerted by fluids of self-propelled particles on passive, larger components.

cond-mat.soft↗