Morphology of Polymer Brushes Infiltrated by Attractive Nanoinclusions of Various Sizes

被引:41
作者
Opferman, Michael G. [1 ]
Coalson, Rob D. [2 ]
Jasnow, David [1 ]
Zilman, Anton [3 ]
机构
[1] Univ Pittsburgh, Dept Phys & Astron, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
[3] Univ Toronto, Dept Phys, Toronto, ON M5S 1A7, Canada
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
NUCLEAR-PORE COMPLEX; COLLAPSE-STRETCHING TRANSITION; GRAFTED POLYMERS; PROTEIN ADSORPTION; MIXED-SOLVENTS; TRANSPORT; LAYERS; MODEL; NUCLEOPORINS; SOLVATION;
D O I
10.1021/la4013922
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Addition of nanoparticles can control the morphologies of grafted polymer layers that are important in a variety of natural and artificial systems. We study the morphologies of grafted polymer layers interacting attractively with nanoparticle inclusions, as a function of particle size and the interaction strength, using self-consistent field theory and Langevin dynamics simulations. We find that the addition of nanoparticles causes distinctive changes in the layer morphology. For sufficiently strong interaction/binding, increasing the concentration of nanoparticles causes a compression of the polymer layer into a compact, low height state, followed by a subsequent rebound and swelling at sufficiently high concentrations. For nanoparticles of small size, the compression of the layer is sharp and occurs over a narrow range of nanoparticle concentrations. The transition region widens as the nanoparticle size increases. The transition is initiated via a dense layer of tightly bound monomers and nanoparticles near the grafting surface, with a low density region above it. For nanopartides much larger than the characteristic graft spacing in the brush, the behavior is reversed: the nanoparticles penetrate only the dilute region near the top of the polymer layer without causing the layer to collapse.
引用
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页码:8584 / 8591
页数:8
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