Electrodiffusiophoretic motion of a charged spherical particle in a nanopore.

The electrodiffusiophoretic motion of a charged spherical nanoparticle in a nanopore subjected to an axial electric field and electrolyte concentration gradient has been investigated using a continuum model, composed of the Poisson-Nernst-Planck equations for the ionic mass transport and the Navier-Stokes equations for the flow field. The charged particle experiences electrophoresis in response to the imposed electric field and diffusiophoresis caused solely by the imposed concentration gradient. The diffusiophoretic motion is induced by two different mechanisms, an electrophoresis driven by the generated electric field arising from the difference of ionic diffusivities and the double layer polarization and a chemiphoresis due to the induced osmotic pressure gradient around the charged nanoparticle. The electrodiffusiophoretic motion along the axis of a nanopore is investigated as a function of the ratio of the particle size to the thickness of the electrical double layer, the imposed concentration gradient, the ratio of the surface charge density of the nanopore to that of the particle, and the type of electrolyte. Depending on the magnitude and direction of the imposed concentration gradient, one can accelerate, decelerate, and even reverse the particle's electrophoretic motion in a nanopore by the superimposed diffusiophoresis. The induced electroosmotic flow in the vicinity of the charged nanopore wall driven by both the imposed and the generated electric fields also significantly affects the electrodiffusiophoretic motion.