Related Experiment Video
Updated: Jan 13, 2026

Taking Advantage of Reduced Droplet-surface Interaction to Optimize Transport of Bioanalytes in Digital Microfluidics
Published on: November 10, 2014
Effective interactions in active Brownian particles
Clare R Rees-Zimmerman1, C Miguel Barriuso Gutierrez2,3, Chantal Valeriani2,3
1Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QZ, UK. clare.rees-zimmerman@chch.ox.ac.uk.
Abstract:
We report an approach to obtain effective pair potentials which describe the structure of two-dimensional systems of active Brownian particles. The pair potential is found by an inverse method, which matches the radial distribution function found from two different schemes. The inverse method, previously demonstrated via simulated equilibrium configurations of passive particles, has now been applied to a suspension of active particles. Interestingly, although active particles are inherently not in equilibrium, we still obtain effective interaction potentials which accurately describe the structure of the active system. Treating these effective potentials as if they were those of equilibrium systems, furthermore allows us to measure effective chemical potentials and pressures. Both the passive interactions and active motion of the active Brownian particles contribute to their effective interaction potentials.
Related Concept Videos
Van der Waals Interactions
Equilibrium Conditions for a Particle
To understand the concept of equilibrium, let us first consider the forces acting on an object. When different forces act on an object, they can...
Noncovalent Attractions in Biomolecules
Noncovalent Attractions in Biomolecules
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Passive Diffusion: Overview and Kinetics
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting...

