Spherical polyelectrolyte brushes in the presence of multivalent counterions: The effect of fluctuations and correlations as determined by molecular dynamics simulations

被引:63
作者
Mei, Yu [1 ]
Hoffmann, Martin [1 ]
Ballauff, Matthias [1 ]
Jusufi, Arben [1 ,2 ]
机构
[1] Univ Bayreuth, D-95440 Bayreuth, Germany
[2] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
来源
PHYSICAL REVIEW E | 2008年 / 77卷 / 03期
关键词
D O I
10.1103/PhysRevE.77.031805
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
We consider the interaction of multivalent counterions with spherical polyelectrolyte brushes (SPBs). SPBs result if linear polyelectrolyte chains (contour length 60 nm) are densely grafted to colloidal spheres of 116 nm in diameter. When dispersed in water the surface layer, consisting of chains of the strong polyelectrolyte poly(styrene sulfonic acid), will swell. Recent work [Mei et al., Phys. Rev. Lett. 97, 158301 (2006)] has demonstrated that spherical polyelectrolyte brushes undergo a collapse in the presence of a mixture of monovalent and multivalent counterions. The collapse crossover could be well described by a mean-field approach. Here we demonstrate that the application of a mean-field approach is well founded by simulation results done with molecular dynamics (MD). MD simulations show that over a wide range of multivalent counterion concentration the effects of ion correlation and fluctuations can be neglected. Higher-valent counterions are shown to interact strongly with the polyelectrolyte chains of the SPBs and thus exhibit a much reduced osmotic activity in the system. This reduction is the driving force for the collapse.
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页数:10
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