Electrophoretic Migration and Axial Diffusion of Individual Nanoparticles in Cylindrical Nanopores

Abstract

Membranes with straight, vertical nanopores have found widespread applications in chemical and biological sciences, including separation, detection, catalysis, and drug delivery. They can also serve as a model system to understand molecular behavior and fundamental mechanisms of separation, bridging the gap between conventional model systems such as flat surfaces and real chromatographic stationary phases such as micrometer-sized porous particles. We recently found that the axial motion of individual biomolecules inside nanopores can be significantly slower than in bulk solution. This suggests that either chromatographic adsorption was present and/or the viscosity inside the nanopores was unusually high. In this study, we measured the electrophoretic motion as well as the axial diffusion of individual nanoparticles in cylindrical alumina nanopores. We found that the electrophoretic mobilities and the diffusion coefficients of polystyrene nanoparticles were both substantially smaller compared to bulk solution independent of particle size or pore diameter. The results imply that the apparent solution viscosity in nanodomains is anomalous