Correlated dynamics of weakly charged silica spheres at an air-water interface

TL;DR

This study investigates how weakly charged silica spheres at an air-water interface exhibit correlated motion influenced by Coulomb interactions, revealing a scaling law and effective surface viscosity that depend on particle concentration.

Contribution

It demonstrates that Coulomb interactions significantly affect particle correlations and introduces a scaling law for correlated motion across different concentrations and particle sizes.

Findings

Correlation decay rates decrease with increasing particle concentration.

Coulomb interactions enhance cross-correlations among particles.

A universal scaling law relates correlated motion to particle size and surface viscosity.

Abstract

Optical microscopy and multi-particle tracking are used to investigate the spatially correlated motion of weakly charged silica spheres at an air-water interface for different area fraction $n$ occupied by the particles. When the area fraction is very small, e.g. $n=0.03$, the correlation function along the line joining the centers of particles $D_{rr}$ decays with inter-particle distance $R$ as $1/R^{0.86\pm0.02}$, and the function perpendicular to this line $D_{\theta\theta}$ decays with $R$ as $1/R^{1.45\pm0.03}$, which differs from the results of [Phys. Rev. Lett. 97, 176001 (2006)] with low surface viscosity (where $D_{rr}\propto 1/R$, $D_{\theta\theta}\propto 1/R^2$). We argue that the differences arise from the Coulomb interaction between particles. The Coulomb interaction enhances the correlated motion of particles. Experimental results show that with the increase of $n$, the decay rate of $D_{rr}$ and $D_{\theta\theta}$ with $R$ decreases and the cross-correlation enhances for the Coulomb interaction increases. The Coulomb interaction between colloidal particles should serve as an effective surface viscoelastical role in our system. With the scaled separation $\frac R {d}(\frac {\eta_{w}d} {\eta_{es,2p}})^{3/2}$, the correlated motions for various values of $n$ and different particles can be scaled onto a single master curve, where $d$ is particles' diameter, $\eta_{w}$ is the viscosity of the water, and $\eta_{es,2p}$ is the effective surface viscosity whose measurements agree well with that of one-particle surface viscosity $\eta_{es,1p}$. The effective surface viscosity $\eta_{es,2p}$ as a function of the area fraction $n$ for different silica spheres is presented.