Poisson-Boltzmann thermodynamics of counterions confined by curved hard walls.

Phys Rev E

LPTMS, CNRS, Université Paris-Sud, Université Paris-Saclay, F-91405 Orsay, France.

Published: January 2016

AI Article Synopsis

Article Abstract

We consider a set of identical mobile pointlike charges (counterions) confined to a domain with curved hard walls carrying a uniform fixed surface charge density, the system as a whole being electroneutral. Three domain geometries are considered: a pair of parallel plates, the cylinder, and the sphere. The particle system in thermal equilibrium is assumed to be described by the nonlinear Poisson-Boltzmann theory. While the effectively one-dimensional plates and the two-dimensional cylinder have already been solved, the three-dimensional sphere problem is not integrable. It is shown that the contact density of particles at the charged surface is determined by a first-order Abel differential equation of the second kind which is a counterpart of Enig's equation in the critical theory of gravitation and combustion or explosion. This equation enables us to construct the exact series solutions of the contact density in the regions of small and large surface charge densities. The formalism provides, within the mean-field Poisson-Boltzmann framework, the complete thermodynamics of counterions inside a charged sphere (salt-free system).

Download full-text PDF

Source
http://dx.doi.org/10.1103/PhysRevE.93.012601DOI Listing

Publication Analysis

Top Keywords

thermodynamics counterions
8
counterions confined
8
curved hard
8
hard walls
8
surface charge
8
contact density
8
poisson-boltzmann thermodynamics
4
confined curved
4
walls consider
4
consider set
4

Similar Publications

Viridium: A Stable Radical and Its π-Dimerization.

J Am Chem Soc

January 2025

Institut de Chimie de Strasbourg, CNRS UMR 7177, Université de Strasbourg, 4, rue Blaise Pascal, Strasbourg 67000, France.

The discovery of a stable organic radical formed under mild, clean, and efficient light-mediated conditions is reported. The structure of the stable acridinium-based radical photoproduct was unambiguously established by single-crystal X-ray diffraction, mass spectrometry, and in solution by EPR, UV/vis, and NMR spectroscopies. The photochemical mechanism of its formation has been elucidated by photophysical experiments coupled with EPR experiments and theoretical investigations.

View Article and Find Full Text PDF

The highly anisotropic and nonadditive nature of nanoparticle surfaces restricts their characterization by limited types of techniques that can reach atomic or molecular resolution. While small-angle neutron scattering (SANS) is a unique tool for analyzing complex systems, it has been traditionally considered a low-resolution method due to its limited scattering vector range and wide wavelength spread. In this article, we present a novel perspective on SANS by showcasing its exceptional capability to provide molecular-level insights into nanoparticle interfaces.

View Article and Find Full Text PDF

In the present study, the mixed micellization behavior of gemini surfactant-1, 5-bis (N-hexadecyl- N, N-dimethylammonium) pentane dibromide (G5) with non-ionic surfactant triton X-100 (TX-100) was investigated in the micellar phase by utilizing the conductometric technique. The deviation of ideal critical micelle concentration (cmc*) from experimental critical micelle concentration (cmc) has been estimated using well-known Clint's theory of mixed micelles. The regular solution approximation was used to determine the interaction parameter (β) and found to be negative.

View Article and Find Full Text PDF

Understanding the mechanism of a CO-responsive surfactant is essential for enhancing its industrial applications. Conventional experimental methods face challenges in pinpointing the exact location of proton transfer within the system and in accurately describing the impact of intermolecular and intramolecular interactions on the CO responsiveness of such substances. To address this gap, this study employs molecular dynamics simulations and free energy perturbation methods to investigate the proton transfer process between a CO-responsive cationic surfactant '-dodecyl-,-dimethylacetamidinium (DMAAH) and its counterion bicarbonate ion at the oil-water interface and micelle surface and in the bulk aqueous phase.

View Article and Find Full Text PDF

General and Versatile Nanoarchitectonics for Amino Acid-Based Glasses via Co-Assembly of Organic Counterions.

Angew Chem Int Ed Engl

December 2024

Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Lab of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

Amino acid-based biomolecular glasses represent an emerging material to meet the demand for sustainable development. However, most amino acids are difficult to vitrify due to their strong crystallization tendency, limiting further advancements of this field. In this study, we demonstrate that the introduction of counterions effectively suppresses crystallization, as hydrogen bonds within the system stabilize the disordered structures.

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!