Traditionally, ion selectivity in nanopores and nanoporous membranes is understood to be a consequence of Debye overlap, in which the Debye screening length is comparable to the nanopore radius somewhere along the length of the nanopore(s). This criterion sets a significant limitation on the size of ion-selective nanopores, as the Debye length is on the order of 1-10 nm for typical ionic concentrations. However, the analytical results we present here demonstrate that surface conductance generates a dynamical selectivity in ion transport, and this selectivity is controlled by so-called Dukhin, rather than Debye, overlap. The Dukhin length, defined as the ratio of surface to bulk conductance, reaches values of hundreds of nanometers for typical surface charge densities and ionic concentrations, suggesting the possibility of designing large-nanopore (10-100 nm), high-conductance membranes exhibiting significant ion selectivity. Such membranes would have potentially dramatic implications for the efficiency of osmotic energy conversion and separation techniques. Furthermore, we demonstrate that this mechanism of dynamic selectivity leads ultimately to the rectification of ionic current, rationalizing previous studies, showing that Debye overlap is not a necessary condition for the occurrence of rectifying behavior in nanopores.
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http://dx.doi.org/10.1021/acs.jpcb.8b11202 | DOI Listing |
J Phys Chem C Nanomater Interfaces
December 2024
Department of Chemical Engineering, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Hybrid nanoplasmonic structures composed of subwavelength apertures in metallic films and nanoparticles have recently been demonstrated as ultrasensitive plasmonic sensors. This work investigates the electrokinetically driven propagation of the assembly mechanism of the metallic nanoparticles through nanoapertures. The Debye-Hückel approximation for a symmetric electrolyte solution with overlapping electrical double layers (EDLs) is used to obtain an analytical solution to the problem.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Université de Lorraine, CNRS, Laboratoire Interdisciplinaire des Environnements Continentaux (LIEC), UMR7360, 54000 Nancy, France. Electronic address:
Hypothesis: Electrostatic interactions between colloids are governed by the overlap of their electric double layers (EDLs) and the ionic screening of the structural charges distributed at their core surface and/or in their peripheral ion-permeable shell, relevant to soft particles like polymer colloids and microorganisms. Whereas ion size-mediated effects on the organization of isolated EDLs have been analysed, their contribution to the electrostatic energy of interacting soft particles has received less attention THEORY AND SIMULATIONS: Herein, we elaborate a formalism to evaluate the electrostatic interaction energy profile between spherical core/shell particles, building upon a recent Poisson-Boltzmann theory corrected for the sizes of ions and particle structural charges, for ion correlations and dielectric decrement. Interaction energy is derived from pairwise disjoining pressure and exact Surface Element Integration method, beyond the Derjaguin approximation.
View Article and Find Full Text PDFNat Commun
August 2024
State Key Laboratory of Analytical Chemistry for Life Science, State Key Laboratory of Pollution Control and Resource Reuse, School of Chemistry and Chemical Engineering, School of Environment, Nanjing University, 163 Xianlin Ave, Nanjing, 210023, China.
C-C coupling is of utmost importance in the electrocatalytic reduction of CO, as it governs the selectivity of diverse product formation. Nevertheless, the difficulties to directly observe C-C coupling pathways at a specific nanocavity hinder the advances in catalysts and electrolyzer design for efficient high-value hydrocarbon production. Here we develop a nano-confined Raman technology to elucidate the influence of the local electric field on the evolution of C-C coupling intermediates.
View Article and Find Full Text PDFJ Chem Phys
August 2024
Department of Pure and Applied Chemistry, Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
For both dielectric spectroscopy and light scattering spectra, the relaxation modes in the microwave region have been characterized by the Debye relaxation model, which is determined by the peak frequency, or by an empirically extended model (e.g., Cole-Davidson and Kohlrausch-Williams-Watts), which has the appropriate line shape.
View Article and Find Full Text PDFHeliyon
July 2024
Industrial Engineering Department, College of Engineering, King Saud University, P.O. Box 800, Riyadh, 11421, Saudi Arabia.
In the present study, the frequency-dependent dielectric relaxation and electrical conduction mechanisms in sol-gel-derived ZnCdFeO (ZCFO) spinel ferrite were studied in the temperature range of 343-438 K. The formation of the ZCFO spinel ferrite phase with space group Fd3m was confirmed by X-ray diffraction analysis. The dielectric relaxation and electrical conduction mechanisms were studied using complex impedance spectroscopy (CIS).
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