Dynamic nonlinear electrophoretic velocity of a spherical colloid
Phys. Rev. Fluids 10, 063702 – Published 12 June, 2025
DOI: https://doi.org/10.1103/759z-ngl6
Abstract
We develop a numerical scheme to compute the dynamic electrophoretic velocity of a uniformly charged, dielectric, spherical colloidal particle under an unsteady electric field, for, in principle, arbitrary imposed electric field strength, . Here, is the characteristic size of the particle, is the applied field strength, and the factor corresponds to the thermal voltage. We focus our computations on Debye lengths comparable to the particle size; i.e., , where is the Debye length, and moderately-charged particles, i.e., , where is the surface charge density on the colloid and is the permittivity of the medium. For a suddenly applied field, the initial growth of the electrophoretic mobility (i.e., ratio of particle speed to field strength) occurs on the momentum diffusion time and is independent of in the practically relevant case of large Schmidt number, , where is the kinematic viscosity and is the mean ion diffusion coefficient. Subsequently, the Debye cloud deforms on the ion diffusion timescale, leading to the mobility approaching its steady-state in a -dependent manner. For the stopping problem, where the field is suddenly switched off, most of the change in the particle speed occurs on the momentum diffusion timescale, and the particle fully stops after the Debye cloud regains its equilibrium spherical shape. Under an oscillatory field, the field frequency has a large influence on both the amplitude and phase lag of the mobility, as it determines if the Debye cloud has sufficient time to deform within an oscillation cycle. The time-average flow about the particle resembles a stresslet.