Searcharxiv⌕ Search

arXiv · 2610.26657

Dynamic clustering of active chemotactic Janus particles

Abstract

Modeling self-propulsion as an emergent diffusiophoretic effect, we come back to the dynamic clustering experiment of active Janus colloids. Working in the original three-dimensional geometry, and using the chemical solute concentration as a control parameter, we find that the dynamic clustering region occupies a robust fraction of the phase diagram. This behavior is rationalized using a linear stability analysis that efficiently captures the instability of the gas phase to dynamic clusters. We also find that dynamic clustering results from the combined effects of a Keller-Segel collapse and of a motility-induced phase separation, either being arrested by the orientational coupling to the chemical field in agreement with previous work.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Joël Mabillard, Frédéric van Wijland, Jean-Baptiste Fournier. 2026-10-19. Dynamic clustering of active chemotactic Janus particles. https://arxiv.org/abs/2610.26657

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Dense granular rheology from fluctuations

A governing equation for the granular temperature of flows past the jamming point is proposed and validated term-by-term with discrete element simulation. We measure and construct models for transport coefficients that do not diverge near the jamming fraction. As a limiting case of our equation, we derive the granular fluidity equation and find disagreement between the preexisting parametrizations of nonlocal granular fluidity, extended kinetic theory, and our discrete element simulations that is resolved by our continuum model.

cond-mat.soft↗

Hydrogel mechanics below swelling equilibrium

Hydrogels are versatile soft materials whose behavior arises from complex polymer-network-fluid interactions. Combining theory and experiments, we show that their mechanics simplify greatly below swelling equilibrium. In this regime, mixing and pore pressures effectively control local hydration, relegating polymer-network elasticity to accommodate the deformed shape. This mechanical hierarchy renders partially-dried hydrogels analogous to incompressible solids with environment-driven target volumes, enabling a staggered mechanical description that accurately captures their state and behavior.

cond-mat.soft↗

Nonlocal Electrostatic Field Theory from Microscopic Description

The study of electric fields in soft materials converges either to the study of point-like particles (local) in nonlinear theories or to the use of particles with finite sizes in nonlocal linear theories. In this work, we start from the microscopic equations of motion and construct a unified mean field Fokker-Planck equation that describes the non-equilibrium electrostatics of nonlocal nonlinear systems. We obtain a generalized Poisson-Boltzmann equation for such systems, as well as their electrostatic free energy expression. In the linear approximation, we obtain an anisotropic susceptibility in an isotropic fluid, which allows for local linear response inversion in electrostatics.

cond-mat.soft↗