Covalent polymer functionalization of graphene nanosheets and mechanical properties of composites

被引:1089
|
作者
Fang, Ming [1 ]
Wang, Kaigang [1 ]
Lu, Hongbin [1 ]
Yang, Yuliang [1 ]
Nutt, Steven [2 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Minist Educ, Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Univ So Calif, Dept Chem Engn & Mat Sci, Los Angeles, CA 90089 USA
关键词
TRANSFER RADICAL POLYMERIZATION; GRAPHITE OXIDE; RAMAN-SPECTRA; CARBON NANOTUBES; SINGLE-LAYER; NANOCOMPOSITES; STRENGTH; BRUSHES; NANOPARTICLES; DISPERSIONS;
D O I
10.1039/b908220d
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
For developing high performance graphene-based nanocomposites, dispersal of graphene nanosheets in polymer hosts and precise interface control are challenging due to their strong interlayer cohesive energy and surface inertia. Here we report an efficient method to functionalize graphene nanosheets. The initiator molecules were covalently bonded to the graphene surface via a diazonium addition and the succeeding atom transfer radical polymerization linked polystyrene chains (82 wt% grafting efficiency) to the graphene nanosheets. The prominent confinement effect arising from nanosheets resulted in a 15 degrees C increase in the glass transition temperature of polystyrene compared to the pure polymer. The resulting polystyrene nanocomposites with 0.9 wt% graphene nanosheets revealed around 70% and 57% increases in tensile strength and Young's modulus. The protocol is believed to offer possibilities for optimizing the processing properties and interface structure of graphene-polymer nanocomposites.
引用
收藏
页码:7098 / 7105
页数:8
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