Dynamics of solvent-free grafted nanoparticles

被引:41
|
作者
Chremos, Alexandros [1 ]
Panagiotopoulos, Athanassios Z. [1 ]
Koch, Donald L. [2 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 136卷 / 04期
基金
美国国家科学基金会;
关键词
SURFACE-FUNCTIONALIZED NANOPARTICLES; LIQUID-LIKE BEHAVIOR; COMPUTER-SIMULATIONS; LIGHT-SCATTERING; NEWTONIAN FLOW; POLYMER; TRANSITION; RHEOLOGY; MODEL; ARRAY;
D O I
10.1063/1.3679442
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The diffusivity and structural relaxation characteristics of oligomer-grafted nanoparticles have been investigated with simulations of a previously proposed coarse-grained model at atmospheric pressure. Solvent-free, polymer-grafted nanoparticles as well as grafted nanoparticles in a melt were compared to a reference system of bare (ungrafted) particles in a melt. Whereas longer chains lead to a larger hydrodynamic radius and lower relative diffusivity for grafted particles in a melt, bulk solvent-free nanoparticles with longer chains have higher relative diffusivities than their short chain counterparts. Solvent-free nanoparticles with short chains undergo a glass transition as indicated by a vanishing diffusivity, diverging structural relaxation time and the formation of body-centered-cubic-like order. Nanoparticles with longer chains exhibit a more gradual increase in the structural relaxation time with decreasing temperature and concomitantly increasing particle volume fraction. The diffusivity of the long chain nanoparticles exhibits a minimum at an intermediate temperature and volume fraction where the polymer brushes of neighboring particles overlap, but must stretch to fill the interparticle space. (C) 2012 American Institute of Physics. [doi:10.1063/1.3679442]
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页数:9
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