Because of their asymmetry, conical nanochannels/nanopores exhibit various attractive electrokinetic features, including ion selectivity, ionic concentration polarization, and ionic current rectification. The polyelectrolyte layer (PEL)-covered (soft) conical nanochannels have recently attracted significant attention because of their unique rectification characteristics. In the modeling of soft nanochannels, it is usually assumed that the properties of the PEL and the electrolyte are the same, an assumption that is not true, especially for dense PELs. In the present work, the influence of the PEL-electrolyte property difference on the ionic current rectification in conical soft nanochannels is studied. To this end, adopting a finite-element approach, the Poisson-Nernst-Planck and Navier-Stokes equations are numerically solved for a steady-state by considering different values of permittivity, diffusivity, and dynamic viscosity for the PEL and the electrolyte. The model is validated by comparing the results with the available theoretical and experimental data. The results show that the PEL-electrolyte property difference leads to a significant improvement of the rectification behavior, especially at low and moderate salt concentrations. This not only highlights the importance of considering different properties for the PEL and the electrolyte but also implies that the rectification behavior of soft nanochannels/nanopores may be improved considerably by utilizing denser PELs.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.aca.2020.05.011DOI Listing

Publication Analysis

Top Keywords

ionic current
12
current rectification
12
pel electrolyte
12
conical nanochannels
8
soft nanochannels
8
properties pel
8
pel-electrolyte property
8
property difference
8
rectification behavior
8
rectification
6

Similar Publications

Carving Metal-Organic-Framework Glass Based Solid-State Electrolyte Via a Top-Down Strategy for Lithium-Metal Battery.

Angew Chem Int Ed Engl

January 2025

KU Leuven, Materials engineering, Kasteelpark Arenberg 44 bus 2450, 3001 LEUVEN Belgium, LEUVEN, BELGIUM.

Traditional polymer solid electrolytes (PSEs) suffer from low Li conductivity, poor kinetics and safety concerns. Here, we present a novel porous MOF glass gelled polymer electrolyte (PMG-GPE) prepared via a top-down strategy, which features a unique three-dimensional interconnected graded-aperture structure for efficient ion transport. Comprehensive analyses, including time-of-flight secondary ion mass spectrometry (TOF-SIMS), Solid-state 7Li magic-angle-spinning nuclear magnetic resonance (MAS-NMR), Molecular Dynamics (MD) simulations, and electrochemical tests, quantify the pore structures, revealing their relationship with ion conductivity that increases and then decreases as macropore proportion rises.

View Article and Find Full Text PDF

Using Energetic Information Quantities from Density Functional Theory to Simultaneously Identify Both Covalent and Noncovalent Interactions.

Chemphyschem

January 2025

University of North Carolina, Research Computing Center, 211 Manning Drive, 27599-3420, Chapel Hill, UNITED STATES OF AMERICA.

Covalent bonding and noncovalent interactions are important chemical concepts and how to identify them has been of current interest in the literature. Within the framework of density functional theory (DFT), we recently proposed a few qualitative descriptors to categorize different types of interactions with Pauli energy and its derivatives. In this work, we expand the scope by including the quantities derived from energetic information, which were recently proposed and thoroughly investigated by us from the framework of information-theoretic approach (ITA) in DFT.

View Article and Find Full Text PDF

The poor reversibility of the zinc anode caused by interfacial side reactions and dendritic growth poses significant constraints on the practical application of aqueous zinc-ion batteries. Herein, a co-solute, acesulfame potassium, with strongly polar, zincophilic guest anions is introduced into a conventional low-concentration aqueous electrolyte. This regulation enhances the electrolyte's ionic conductivity and accelerates the desolvation process of zinc ions at the electrode/electrolyte interface.

View Article and Find Full Text PDF

Li-CO2 batteries demonstrate promising prospects in terms of high-density energy storage and efficient CO2 fixation. However, their practical application is impeded by sluggish reaction kinetics and leakage of volatile and flammable organic electrolytes, especially for high temperature application scenarios, leading to large polarization and limited cycling stability. Herein, we fabricate a highly rechargeable and stable Li-CO2 battery with high temperature adaptability by employing fluorine-substituted graphdiyne (FGDY) as cathode catalysts and imidazolium-based ionic liquid as electrolyte solvents.

View Article and Find Full Text PDF

Green extraction and IC analysis of trace impurities in TATB through deep eutectic solvents.

J Chromatogr A

January 2025

School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang, 621010, PR China; Institute of Chemical Materials, China Academy of Engineering Physics, Mianyang, 621900, PR China. Electronic address:

1,3,5-trinamino-2,4,6-trinitrobenzene (TATB) as an important insensitive high explosive has excellent safety performance due to strong hydrogen bonds. Ionic impurities including sulfate ions (SO), nitrate ions (NO) and chloride ions (Cl) formed during the preparation of TATB have negative effects on TATB-based explosives. However, strong hydrogen bonds result in extremely low solubility of TATB in traditional solvents, which poses a huge obstacle to extract and detect the impurities in TATB for quality control.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!