Electrokinetic behavior of conical nanopores functionalized with two polyelectrolyte layers: effect of pH gradient

The behavior of ionic current rectification of a conical nanopore functionalized with two polyelectrolyte (PE) layers via layer-by-layer deposition subject to an extra applied pH gradient is investigated theoretically. The applied pH, the electric potential, the half-cone angle of the conical nanopo...

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Bibliographic Details
Published inSoft matter Vol. 18; no. 44; pp. 8427 - 8435
Main Authors Liu, Tien Juin, Hsu, Jyh-Ping
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 16.11.2022
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Summary:The behavior of ionic current rectification of a conical nanopore functionalized with two polyelectrolyte (PE) layers via layer-by-layer deposition subject to an extra applied pH gradient is investigated theoretically. The applied pH, the electric potential, the half-cone angle of the conical nanopore, and the fixed charge densities of the PE layers are examined in detail for their influence on the ionic current rectification (ICR) behavior of the nanopore. We found that this behavior depends highly on the direction of the pH gradient, which arises because the associated electroosmotic flow plays a significant role. The mechanisms of ionic transport in the present pH asymmetric system are discussed. The results gathered reveal that the ICR behavior of a nanopore can be tuned effectively by applying an extra pH gradient. We also examine the case where two PE layers are uniformly merged into one layer. In this case, both the fixed charge density and the concentration profile are quite different from those when two PE layers are present. The behavior of ionic current rectification of a conical nanopore functionalized with two polyelectrolyte (PE) layers via layer-by-layer deposition subject to an extra applied pH gradient is investigated theoretically.
Bibliography:https://doi.org/10.1039/d2sm01172g
Electronic supplementary information (ESI) available. See DOI
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ISSN:1744-683X
1744-6848
1744-6848
DOI:10.1039/d2sm01172g