A nanopore’s response to an electrical potential
drop is
characterized by its electrical conductance,
. For the last two decades, it has been
thought that at low electrolyte concentrations,
, the conductance is concentration-independent
such that
. It has been recently demonstrated that
surface charge regulation changes the dependency to
, whereby the slope typically takes the
values α = 1/3 or 1/2. However, experiments have observed slopes
of 2/3 and 1 suggesting that additional mechanisms, such as convection
and slip-lengths, appear. Here, we elucidate the interplay between
three mechanisms: surface charge regulation, convection, and slip
lengths. We show that the inclusion of convection does not change
the slope, and when the effects of hydrodynamic slip are included,
the slope is doubled. We show that when all effects are accounted
for, α can take any value between 0 and 1 where the exact value
of the slope depends on the material properties. This result is of
utmost importance in designing any electro-kinetically driven nanofluidic
system characterized by its conductance.