arXiv subjects

David Ribar

Publications and source records attributed to David Ribar.

6 recordsLinked to original sources

arXiv2026

Polarisation-mediated underscreening from weakly bonded ion clusters

We explore the hypothesis that ions form loosely connected clusters at high ionic strength in aqueous solutions, and that these clusters have relevance to the experimentally observed phenomenon usually referred to as "anomalous underscreening". Cluster formation lowers the ionic strength below its nominal value, slowing the decay of the screening length but not reversing it. Here we focus on an additional contribution, cluster polarisation. We demonstrate that this effect produces longer-ranged repulsive interactions between like-charged surfaces or particles in concentrated salt solutions. We derive an analytical bulk relation in which the entire architecture of a cluster enters through a single quantity, the charge-weighted second moment of its intramolecular charge structure factor, which quantifies the polarisation response of an arbitrary cluster topology. We also make numerical calculations using classical polymer Density Functional Theory, cDFT, for a model based on star-like clusters in which satellite ions are weakly bonded by a harmonic spring to a common central ion. The corona of satellite ions is assumed to be net neutral, since the formation of highly charged clusters would be accompanied by a significant self-energy cost. Using this model, we calculate surface interactions and screening lengths at various overall salt concentrations. We show that, under the assumption that the fraction of ions belonging to clusters increases with salt concentration, one may qualitatively arrive at "anomalous underscreening", i.e., an effective screening length that displays a minimum at an overall (monovalent) salt concentration of about 1 M. Quantitatively, we note that the predicted growth of the screening length beyond this threshold value is weaker than typically found by experimental surface force measurements.

cond-mat.soft↗

arXiv2025

Classical density functional treatment of polydisperse polarisable clusters

Ion clustering has been proposed as a mechanism leading to the peculiar 'anomalous underscreening' phenomenon seen for electrostatic interactions between charge surfaces immersed in concentrated electrolytes. These interactions have been measured using the Surface Force Apparatus, according to which there are strong repulsive interactions between like-charged surfaces, with a range that increases upon further addition of salt, above some threshold concentration. A common suggestion is that ionic aggregates, if they form in sufficient numbers, will reduce the concentration of free ions and thereby increase the nominal Debye length. In previous work, we investigated a cluster model using classical Density Functional Theory (cDFT) and a polymer-like description of the ion clusters. These clusters were monodisperse and of either a linear or branched architecture, and a fixed charge sequence along the chains. In this work, we generalise the cDFT to treat 'living polymers' with variable chain lengths and charge arrangements along the chain. This approach allows clusters to become polarised by the presence of charged surfaces, manifested by like-charged bonding. We find that even with a small degree of like-charged bonding a full equilibrium treatment of our model predicts only weak repulsion between like-charged surfaces. When a global constraint is applied so that the charged surfaces are neutralised only by the dissociated ions, while the clusters contribute overall zero charge, even a very small fraction of clustering ions generate strong and long-ranged forces. Moreover, if the cluster fraction increase substantially upon the addition of further salt, then the strength of the surface forces will also increase, although the range remains roughly constant.

cond-mat.soft↗

arXiv2025

Polyampholyte model of ion clusters: double-layer interactions in the presence of dissociated simple salt

We explore interactions between equally charged surfaces, in the presence of simple salt and either neutral or monovalently charged polyampholytes. We consider the possibility of using these charged polymers as crude models of ion clusters. The latter have been hypothesised to form in concentrated aqueous salt solutions, and are possibly related to anomalous underscreening. This phenomenon usually manifests itself by unexpectedly strong and long-ranged effective forces at very high ionic strengths. If ion clusters are formed, they are expected to carry at most a weak net charge. Keeping this in mind, we investigate how polyampholyte chains mediate interactions between charged surfaces. A significant amount of simple salt is also present, in most cases. We highlight that if the charges of the polyampholytes are unevenly distributed, there is a polarisation response that in turn can generate very strong and long-ranged surface forces, even at rather high concentrations of simple salt. Aside from their possible relevance to ion clusters and underscreening phenomena, these results also suggest the possibility of tailoring synthetic polyampholytes, in order to regulate colloidal stability.

cond-mat.soft↗

arXiv2024

Exceptionally strong double-layer barriers generated by polyampholyte salt

Experiments using the Surface Force Apparatus (SFA) have found anomalously long-ranged interactions between charged surfaces in concentrated salt solutions. Ion clustering have been suggested as a possible origin of this behaviour. In this work, we demonstrate that if such stable clusters indeed form, they are able to induce remarkably strong free energy barriers, under conditions where a corresponding solution of simple salt provide negligible forces. Our cluster model is based on connected ions producing a polyampholyte salt, containing a symmetric mixture of monovalent cationic and anionic polyampholytes. Ion distributions and surface interactions are evaluated utilising statistical-mechanical (classical) polymer Density Functional Theory, cDFT. In the Supporting Information, we briefly investigate a range of different polymer architectures (connectivities), but in the main part of the work a polyampholyte ion is modelled as a linear chain with alternating charges, in which the ends carry an identical charge (hence, a monovalent net charge). These salts are able to generate repulsions, between similarly charged surfaces, of a remarkable strength - exceeding those from simple salts by orders of magnitude. The underlying mechanism for this is the formation of brush-like layers at the surfaces, i.e. the repulsion is strongly related to excluded volume effects, in a manner similar to the interaction between surfaces carrying grafted polymers. We believe our results are relevant not only to possible mechanisms underlying anomalously long-ranged underscreening in concentrated simple salt solutions, but also for the potential use of synthesised polyampholyte salt as extremely efficient stabilisers of colloidal dispersions.

cond-mat.soft↗

arXiv2024

Solvent-induced ion clusters generate long-ranged double-layer forces at high ionic strengths

Recent experimental results by the Surface Force Apparatus (SFA) have identified a dramatic deviation from previously established theories of simple electrolytes. This deviation, referred to as anomalous underscreening, suggests that the range of electrostatic interactions increase upon a further addition of salt, beyond some threshold concentration (usually about 1M). In this theoretical work, we explore an extension of the Restricted Primitive Model (RPM) wherein a short-ranged pair potential of mean force (sPMF) is added to the usual Coulombic interactions so as to mimic changes of the hydration as two ions approach one another. The strength of this potential is adjusted so that the modified RPM saturates at a realistic concentration level (within a range 4-7M, typical to aqueous 1:1 salts). We utilise grand canonical simulations to establish surface forces predicted by the model and compare them directly with SFA data. We explore different sPMF models, which in all cases display significant clustering at concentrations above about 1M. In these models, we find significant double-layer repulsion at separations that significantly exceed those expected from standard RPM predictions. We do not, however, observe an increase of the screening length with salt concentration, but rather that this screening length seemingly saturates at a (rather high) value. The simulated long-ranged interactions are shown to correlate with ion cluster formation, implicating the important role of accompanying {\em cluster-cluster} interactions. In particular, steric interactions between clusters (manifested in density-density correlations) are quite relevant in these systems.

cond-mat.soft↗

arXiv2024

Cluster Formation induced by local dielectric saturation in Restricted Primitive Model Electrolytes

Experiments using the Surface Force Apparatus (SFA) have found anomalously long ranged charge-charge underscreening in concentrated salt solutions. Meanwhile, theory and simulations have suggested ion clustering to be the possible origin of this behaviour. The popular Restricted Primitive Model of electrolyte solutions, in which the solvent is represented by a uniform relative dielectric constant, $\varepsilon_r$, is unable to resolve the anomalous underscreening seen in experiments. In this work, we modify the Restricted Primitive Model to account for local dielectric saturation within the ion hydration shell. The dielectric constant in our model locally decreases from the bulk value to a lower saturated value at the ionic surface. The parameters for the model are deduced so that typical salt solubilities are obtained. Our simulations for both bulk and slit geometries show that our model displays strong cluster formation and these give rise to long-ranged interactions between charged surfaces at distances similar to what has been observed in SFA measurements. An electrolyte model wherein the dielectric constant remains uniform does not display similar clusters, even with $\varepsilon_r$ equal to the saturated value at ion contact. Hence, the observed behaviours are not simply due to an enhanced Coulomb interaction.

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