Interionic Interactions in Conducting Nanoconfinement

Interionic interactions in conducting nanopores determine how counterions may be packed in the pores subject to the applied voltage. In ideal metals, interactions are exponentially screened by metallic electrons. However, modern nanoporous electrodes are predominantly made of carbon materials. To wh...

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Published inChemphyschem Vol. 14; no. 18; pp. 4121 - 4125
Main Authors Rochester, Christopher C., Lee , Alpha A., Pruessner, Gunnar, Kornyshev, Alexei A.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 16.12.2013
WILEY‐VCH Verlag
Wiley
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Summary:Interionic interactions in conducting nanopores determine how counterions may be packed in the pores subject to the applied voltage. In ideal metals, interactions are exponentially screened by metallic electrons. However, modern nanoporous electrodes are predominantly made of carbon materials. To what extent is this screening affected by a different mode of dielectric response in such materials? To answer this question we study Coulomb interaction of charges in cylindrical and slit pores that allow finite electric field penetration into the pore walls, as well as the Coulomb interaction in a nanogap between two thin walls of graphene modeled by a non‐local dielectric function. In all cases studied the screening was found to be subtly different than in metallic nanopores, but still strong enough to support realization of the so called superionic state in such pores. Screening factor: Interionic interactions in a metallic nanopore are exponentially screened by electrons of the metal, with the screening length proportional to the pore width or diameter. This article investigates how such screening would look in non‐ideally metallic electrodes, typical for semi‐metallic carbons.
Bibliography:ArticleID:CPHC201300834
istex:050687FCE97B349A0D9A8F5F27F0C3E7A8C0F607
ark:/67375/WNG-JG9DQ9GX-R
Engineering and Physical Sciences Research Council (EPRSC) - No. EP/H004319/1
EPSRC - No. EP/G036888/1
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ISSN:1439-4235
1439-7641
1439-7641
DOI:10.1002/cphc.201300834