AI Article Synopsis

  • The ionic conductance in charged nanopores exhibits a power-law behavior at low salinity, influenced by surface charges that affect zeta potential and ion distributions.
  • Accurately measuring surface charge density in single-digit nanopores poses challenges, leading researchers to develop new methodologies to investigate these effects.
  • Through experiments with silicon nitride nanopores, a modified conductance model was established to analyze the relationship between pore concentration, surface charges, and potential leakage, allowing for a better understanding of ion mobility in nanopores.

Article Abstract

The ionic conductance in a charged nanopore exhibits a power-law behavior in low salinity-as has been verified in many experiments (G0∝c0α)-which is governed by surface charges. The surface charge inside a nanopore determines the zeta potential and ion distributions, which have a significant impact on ion transport, especially in a single-digit nanopore with potential leakage. However, precisely measuring surface charge density in a single-digit nanopore remains a challenge. Here, we propose a methodology for exploring the power-law variation of ionic conductance, with potential leakage taken into account. We conducted experiments to measure the ionic current using silicon nitride nanopores and employed a continuous theory to explore the relationship between pore-bound concentration and surface charges. Considering that the influence of potential leakage on concentration follows a power-law relationship, we established a coefficient (α) to examine the controlling factors of potential leakage and modified the conductance model to obtain the ion mobility inside a nanopore.

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Source
http://dx.doi.org/10.3390/molecules30010191DOI Listing

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