Entropy-driven segregation of nanoparticles to cracks in multilayered composite polymer structures

被引:299
|
作者
Gupta, S
Zhang, QL
Emrick, T [1 ]
Balazs, AC
Russell, TP
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[2] Univ Pittsburgh, Dept Chem & Petr Engn, Pittsburgh, PA 15261 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nmat1582
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
Multilayer composites, which combine ductile polymers with brittle films, constitute vital components for optical communications, microelectronics and bio-engineering applications. However, crack formation is a critical problem in these materials; thus, designing layered systems that can respond to environmental changes and undergo self-healing is particularly important for a range of technologies. Here, nanoparticles dispersed in a polymer matrix were found to migrate to a crack generated at the interface between the polymer and a glassy layer. Segregation of the nanoparticles to the crack depended on both the enthalpic and entropic interactions between the polymer and nanoparticles. In particular, poly( ethylene oxide)- covered 5.2-nm spherical nanoparticles in a poly( methyl methacrylate) matrix diffused to cracks in the adjoining silicon oxide layer, whereas tri-n-octylphosphine oxide-covered nanoparticles did not. These results point to a simple means of fabricating systems that can self-heal, improving the durability of multilayered systems, or form the basis for auto-responsive materials.
引用
收藏
页码:229 / 233
页数:5
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