Pith. sign in

REVIEW

Ionic Current Rectification in Nanopores: Effects of Nanopore Material, Electrolyte and Surface Treatment

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2402.01321 v1 pith:IKKSJ3ZF submitted 2024-02-02 physics.app-ph

Ionic Current Rectification in Nanopores: Effects of Nanopore Material, Electrolyte and Surface Treatment

classification physics.app-ph
keywords differentnanoporeschannelchargecurrentmaterialnanoporesurface
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

Ionic Current Rectification (ICR) can appear in nanopores, causing a diode-like behavior that originates from different efficiency of ion transport through the pore channel with respect to the applied voltage bias polarity. This effect is particularly interesting for nanopores with a short channel length, that is smaller than 500 nm, because then the dependence of the ion current on the direction along which the ions pass through the channel is determined by the geometry and material of the nanopore, and by the ion concentration in the electrolyte. Surface charges can play an important role, and therefore nanopores consisting of multiple materials can induce ICR because of different charge distributions at the nanopore-electrolyte interface for the different material sections. In this work, we study four solid-state nanopore designs considering different geometries of charge distributions along the inner and outer surfaces of nanopores, and evaluate their impact on ICR with six different electrolytes. The direct comparison between experimental data and modeling enables to understand how the different surface charge configurations impact the ICR.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.