Structure and Entanglement Factors on Dynamics of Polymer-Grafted Nanoparticles

被引:45
作者
Liu, Siqi [1 ]
Senses, Erkan [1 ]
Jiao, Yang [1 ]
Narayanan, Suresh [2 ]
Akcora, Pinar [1 ]
机构
[1] Stevens Inst Technol, Dept Chem Engn & Mat Sci, Hoboken, NJ 07030 USA
[2] Argonne Natl Lab, Adv Photon Source, 9700 S Cass Ave, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
VISCOSITY;
D O I
10.1021/acsmacrolett.6b00089
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Nanoparticles functionalized with long polymer chains at low graft density are interesting systems to study structure-dynamic relationships in polymer nanocomposites since they are shown to aggregate into strings in both solution and melts and also into spheres and branched aggregates in the presence of free polymer chains. This work investigates structure and entanglement effects in composites of polystyrene-grafted iron oxide nanoparticles by measuring particle relaxations using X-ray photon correlation spectroscopy. Particles within highly ordered strings and aggregated systems experience a dynamically heterogeneous environment displaying hyperdiffusive relaxation commonly observed in jammed soft glassy systems. Furthermore, particle dynamics is diffusive for branched aggregated structures which could be caused by less penetration of long matrix chains into brushes. These results suggest that particle motion is dictated by the strong interactions of chains grafted at low density with the host matrix polymer.
引用
收藏
页码:569 / 573
页数:5
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