Electrokinetic behavior of a pH-regulated dielectric cylindrical nanopore

A continuum model is adopted to describe the electrokinetic behavior of a pH-regulated cylindrical nanopore, the surface of which has charge-regulated carboxyl groups. We focus on the influences of the permittivity of the nanopore material, nanopore size, salt concentration, and solution pH on this behavior, and the underlying mechanisms. The influence of the nanopore permittivity becomes significant when a nanopore is shorter than ca. 50 nm. It is interesting to observe that if it is longer than ca. 100 nm, the nanopore conductance decreases with increasing permittivity. If it is sufficiently short, the conductance increases with increasing permittivity. If the nanopore length takes a medium level, the conductance is insensitive to the variation in the permittivity. For a short nanopore (~20 nm), the conductivity increases with increasing permittivity. However, if pH is sufficiently high, it becomes insensitive to permittivity. Although the larger the permittivity the greater the conductivity, in general, this effect becomes insignificant when the bulk salt concentration is sufficiently high, implying that the effect of membrane polarization is important only if the bulk salt concentration is sufficiently low.