Polyelectrolyte adsorption: Chemical and electrostatic interactions

Adi Shafir*, David Andelman

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Mean-field theory is used to model polyelectrolyte adsorption and the possibility of overcompensation of charged surfaces. For charged surfaces that are also chemically attractive, the overcharging is large in high salt conditions, amounting to 20–40?% of the bare surface charge. However, full charge inversion is not obtained in thermodynamical equilibrium for physical values of the parameters. The overcharging increases with addition of salt, but does not have a simple scaling form with the bare surface charge. Our results indicate that a more evolved explanation is needed in order to understand polyelectrolyte multilayer buildup. For strong polymer-repulsive surfaces, we derive simple scaling laws for the polyelectrolyte adsorption and overcharging. We show that the overcharging scales linearly with the bare surface charge, but its magnitude is very small in comparison to the surface charge. In contrast with the attractive surface, here the overcharging is found to decrease substantially with addition of salt. In the intermediate range of weak repulsive surfaces, the behavior with addition of salt crosses over from increasing overcharging (at low ionic strength) to a decreasing one (at high ionic strength). Our results for all types of surfaces are supported by full numerical solutions of the mean-field equations.

Original languageEnglish
Article number061804
Pages (from-to)061804-1-061804-12
Number of pages12
JournalPhysical Review E - Statistical, Nonlinear, and Soft Matter Physics
Volume70
Issue number6
DOIs
StatePublished - Dec 2004

Funding

FundersFunder number
U.S.-Israel Binational Foundation
United States-Israel Binational Science Foundation287/02
Israel Science Foundation210/01

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