Abstract

Ionic transport through a charged nanopore at low ion concentration is governed by the surface conductance. Several experiments have reported various power-law relations between the surface conductance and ion concentration, i.e., Gsurf c0α. However, the physical origin of the varying exponent, α, is not yet clearly understood. By performing extensive coarse-grained Molecular Dynamics simulations for various pore diameters, lengths, and surface charge densities, we observe varying power-law exponents even with a constant surface charge and show that α depends on how electrically "perfect"the nanopore is. Specifically, when the net charge of the solution in the pore is insufficient to ensure electroneutrality, the pore is electrically "imperfect"and such nanopores can exhibit varying α depending on the degree of "imperfectness". We present an ionic conductance theory for electrically "imperfect"nanopores that not only explains the various power-law relationships but also describes most of the experimental data available in the literature.

Original languageEnglish (US)
Pages (from-to)10518-10526
Number of pages9
JournalACS Nano
Volume14
Issue number8
DOIs
StatePublished - Aug 25 2020

Keywords

  • ion conductance
  • ion selectivity
  • ion transport
  • molecular dynamics
  • nanopore
  • power-law
  • surface charge

ASJC Scopus subject areas

  • Materials Science(all)
  • Engineering(all)
  • Physics and Astronomy(all)

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