Diffusivity and Hydrodynamic Drag of Nanoparticles at a Vapor-liquid Interface
Joel Koplik, Charles Maldarelli

TL;DR
This study investigates the surface diffusivity and hydrodynamic drag of nanoparticles at vapor-liquid interfaces, revealing that contact line fluctuations do not cause increased drag, contrary to previous hypotheses, and showing consistent drag behavior across experiments.
Contribution
Molecular dynamics simulations demonstrate that contact line fluctuations do not lead to anomalous drag increases, resolving a paradox in nanoparticle interfacial dynamics.
Findings
Drag decreases as particles move further into vapor.
Surface drag is less than bulk liquid drag due to partial submersion.
Contact line fluctuations do not cause increased drag.
Abstract
Measurements of the surface diffusivity of colloidal spheres translating along a vapor/liquid inter- face show an unexpected decrease in diffusivity, or increase in surface drag (from the Stokes-Einstein relation) when the particles situate further into the vapor phase. However, direct measurements of the surface drag from the colloid velocity due to an external force find the expected decrease with deeper immersion into the vapor. The paradoxical drag increase observed in diffusion experiments has been attributed to the attachment of the fluid interface to heterogeneities on the colloid surface, which causes the interface, in response to thermal fluctuations, to either jump or remain pinned, creating added drag. We have performed molecular dynamics simulations of the diffusivity and force experiments for a nanoparticle with a rough surface at a vapor/liquid interface to examine the…
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