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The charge inversion phenomenon is studied by molecular dynamics simulations, focusing on size and valence asymmetric salts, and a threshold of surface charge density for charge inversion. The charge inversion criteria by the…

软凝聚态物质 · 物理学 2009-11-10 Motohiko Tanaka

For binary solvent mixtures composed of ions and two kinds of polar solvents, electric double layer near a charged object is strongly affected by not only the binary solvent composition but also nature of solvents such as volume and dipole…

软凝聚态物质 · 物理学 2022-02-11 Jun-Sik Sin , Chung-Sik Sin

Charge-stabilized colloidal spheres dispersed in deionized water are supposed to repel each other. Instead, artifact-corrected video microscopy measurements reveal an anomalous long-ranged like-charge attraction in the interparticle pair…

软凝聚态物质 · 物理学 2009-11-11 Marco Polin , David G. Grier , Yilong Han

The free energy of ion solvation can be decomposed into enthalpic and entropic contributions. This helps to understand the connection between the dielectric properties and the underlying forces. We present a simple linear-response model of…

软凝聚态物质 · 物理学 2024-06-24 Alec Wills , Anthony Mannino , Isidro Losada , Sara G. Mayo , Jose M. Soler , Marivi Fernandez-Serra

We consider the interactions between two uncharged planar macroscopic surfaces immersed in an electrolyte solution which are induced by interfacial selectivity. These forces are taken into account by introducing a depletion free-energy…

软凝聚态物质 · 物理学 2009-10-31 M. N. Tamashiro , P. Pincus

We present a theory of effective electrostatic interactions in polydisperse suspensions of charged macroions, generalizing to mixtures a theory previously developed for monodisperse suspensions. Combining linear response theory with a…

软凝聚态物质 · 物理学 2013-08-20 Jun Kyung Chung , Alan R. Denton

Colloidal systems present exciting opportunities to study clusters. Unlike atomic clusters, which are frequently produced at extremely low density, colloidal clusters may interact with one another. Here we consider the effect of such…

软凝聚态物质 · 物理学 2011-01-20 Alex Malins , Stephen R. Williams , Jens Eggers , Hajime Tanaka , C. Patrick Royall

We investigate, within a local density functional theory formalism, the interactions between like-charged polyions immersed in a confined electrolyte. We obtain a simple condition for a repulsive effective pair potential, that can be…

软凝聚态物质 · 物理学 2009-10-31 E. Trizac

Over the past few decades the experimental literature has consistently reported observations of attraction between like-charged colloidal particles and macromolecules in solution. Examples include nucleic acids and colloidal particles in…

软凝聚态物质 · 物理学 2020-04-22 Alzbeta Kubincova , Philippe H. Hunenberger , Madhavi Krishnan

The subtle interplay between critical phenomena and electrostatics is investigated by considering the effective force acting on two parallel walls confining a near-critical binary liquid mixture with added salt. The ion-solvent coupling can…

软凝聚态物质 · 物理学 2011-09-13 Markus Bier , Andrea Gambassi , Martin Oettel , S. Dietrich

A simple model is presented to calculate the potential of mean force between a polyion and a multivalent counterion inside a polyelectrolite solution. We find that under certain conditions the electrostatic interactions can lead to a strong…

统计力学 · 物理学 2009-11-11 Jürgen F. Stilck , Yan Levin

The solvation of charged, nanometer-sized spherical solutes in water, and the effective, solvent-induced force between two such solutes are investigated by constant temperature and pressure Molecular Dynamics simulations of model solutes…

软凝聚态物质 · 物理学 2009-11-10 J. Dzubiella , J. -P. Hansen

We investigate effective interactions between a colloidal particle, immersed in a binary mixture of smaller spheres, and a semipermeable membrane. The colloid is modeled as a big hard sphere and the membrane is represented as an infinitely…

软凝聚态物质 · 物理学 2007-05-23 Pawel Bryk

Within a dipolar Poisson-Boltzmann theory including electrostatic correlations, we consider the effect of explicit solvent structure on solvent and ion partition confined to charged nanopores. We develop a relaxation scheme for the solution…

软凝聚态物质 · 物理学 2015-10-28 Sahin Buyukdagli

We study the ionic equilibria and interactions of neutral semi-permeable spherical shells immersed in electrolyte solutions, including polyions. Although the shells are uncharged, only one type of ions of the electrolyte can permeate them,…

软凝聚态物质 · 物理学 2012-07-24 Vladimir Lobaskin , Artem N. Bogdanov , Olga I. Vinogradova

We show that the interaction of an oil-dispersed colloidal particle with an oil-water interface is highly tunable from attractive to repulsive, either by varying the sign of the colloidal charge via charge regulation, or by varying the…

软凝聚态物质 · 物理学 2016-08-25 Jeffrey Everts , Sela Samin , René van Roij

We perform computational investigations of electrolyte-mediated interactions of charged colloidal particles confined within nanochannels. We investigate the role of discrete ion effects, valence, and electrolyte strength on colloid-wall…

软凝聚态物质 · 物理学 2023-02-28 Inderbir S. Sidhu , Amalie L. Frischknecht , Paul J. Atzberger

Using computer simulations, the electrophoretic motion of a positively charged colloid (macroion) in an electrolyte solution is studied in the framework of the primitive model. Hydrodynamic interactions are fully taken into account by…

软凝聚态物质 · 物理学 2015-06-25 Apratim Chatterji , Jürgen Horbach

The forces between charged macromolecules, usually given in terms of osmotic pressure, are highly affected by the intervening ionic solution. While in most theoretical studies the solution is treated as a homogeneous structureless…

软凝聚态物质 · 物理学 2014-04-22 Dan Ben-Yaakov , David Andelman , Daniel Harries , Rudi Podgornik

Suspensions of hard colloidal particles frequently serve as model systems in studies on fundamental aspects of phase transitions. But often colloidal particles that are considered as ``hard'' are in fact weakly charged. If the colloids are…

软凝聚态物质 · 物理学 2014-03-24 Sven Dorosz , Nikhilesh Shegokar , Tanja Schilling , Martin Oettel