arXiv subjects

Emily Krucker-Velasquez

Publications and source records attributed to Emily Krucker-Velasquez.

3 recordsLinked to original sources

arXiv2025

Potential of mean force and underscreening of polarizable colloids in concentrated electrolytes

This study uses advanced numerical methods to estimate the mean force potential (PMF) between charged, polarizable colloidal particles in dense electrolytes. We observe that when the Debye screening length, $λ_{\mathrm{D}}$, is below the hydrated ion size, the PMF shows discernible oscillations of purely electrostatic origin as opposed to chemical affinity, in addition to the expected decay in DLVO theory. Moreover, our findings suggest concentrated electrolytes are significantly less efficient at muting electrostatic interactions in electrostatically stabilized colloidal suspensions, potentially having significant implications for our understanding of colloidal stability and the forces that govern the behavior of concentrated charged soft matter systems beyond DLVO theory.

cond-mat.soft↗

arXiv2024

Immersed boundary method for dynamic simulation of polarizable colloids of arbitrary shape in explicit ion electrolytes

We develop a computational method for modeling electrostatic interactions of arbitrarily-shaped, polarizable objects on colloidal length scales, including colloids/nanoparticles, polymers, and surfactants, dispersed in explicit ion electrolytes and nonionic solvents. Our method computes the nonuniform polarization charge distribution induced in a colloidal particle by both externally applied electric fields and local electric fields arising from other charged objects in the dispersion. This leads to expressions for electrostatic energies, forces, and torques that enable efficient molecular dynamics and Brownian dynamics simulations of colloidal dispersions in electrolytes, which can be harnessed to accurately predict structural and transport properties. We describe an implementation in which colloidal particles are modeled as rigid composites of small spherical beads that tessellate the surface of the particle. The electrostatics calculations are accelerated using a spectrally-accurate particle-mesh-Ewald technique implemented on a graphics processing unit (GPU) and regularized such that the electrostatic calculations are well-defined even for overlapping bodies. We demonstrate the effectiveness of this approach through a series of calculations, including the induced dipole moments and forces for one, two, and lattices of spherical colloids in an electric field; the induced dipole moment and torque for anisotropic particles in an electric field; the equilibrium distribution of ions in the double layer around charged colloids; the dynamics of charged colloids; and ions in the double layer around a polarizable colloid exposed to an electric field.

cond-mat.soft↗

arXiv2021

Underscreening and hidden ion structures in large scale simulations of concentrated electrolytes

The electrostatic screening length predicted by Debye-Hückel theory decreases with increasing ionic strength, but recent experiments have found that the screening length can instead increase in concentrated electrolytes. This phenomenon, referred to as underscreening, is believed to result from ion-ion correlations and short-range forces such as excluded volume interactions among ions. We use Brownian Dynamics to simulate a version of the Restrictive Primitive Model for electrolytes over a wide range of ion concentrations, ionic strengths, and ion excluded volume radii for binary electrolytes. We measure the decay of the charge-charge correlation among ions in the bulk, and compare it against scaling trends found experimentally and determined in certain weak coupling theories of ion-ion correlation. Moreover, we find that additional large scale ion structures emerge at high concentrations. In this regime, the frequency of oscillations computed from the charge-charge correlation function is not dominated by electrostatic interactions but rather by excluded volume interactions and with oscillation periods on the order of the ion diameter. We also find that the nearest neighbor correlation of ions sharing the same charge transitions from negative at small concentrations to positive at high concentrations, representing the formation of small, like-charge ion clusters. We conclude that the increase in local charge density due to the formation of these clusters and the topological constraints of macroscopic charged surfaces can help explain the degree of underscreening observed experimentally.

cond-mat.soft↗