单层
材料科学
聚合物
纳米颗粒
自组装
纳米尺度
蒸发
纳米技术
化学工程
双层
化学物理
表面能
膜
化学
复合材料
生物化学
物理
工程类
热力学
作者
Shisheng Xiong,Darren R. Dunphy,Dan Wilkinson,Zhang Jiang,Joseph Strzalka,Jin Wang,Yongrui Su,Juan Pablo,C. Jeffrey Brinker
出处
期刊:Nano Letters
[American Chemical Society]
日期:2013-01-29
卷期号:13 (3): 1041-1046
被引量:23
摘要
The pathway of interfacial self-assembly of large-scale, highly ordered 2D nanoparticle/polymer monolayer or bilayer arrays from a toluene solution at an air/water interface was investigated using grazing-incidence small-angle scattering at a synchrotron source. Interfacial-assembly of the ordered nanoparticle/polymer array was found to occur through two stages: formation of an incipient randomly close-packed interfacial monolayer followed by compression of the monolayer to form a close-packed lattice driven by solvent evaporation from the polymer. Because the nanoparticles are hydrophobic, they localize exclusively to the polymer-air interface during self-assembly, creating a through thickness asymmetric film as confirmed by X-ray reflectivity. The interfacial self-assembly approach can be extended to form binary NP/polymer arrays. It is anticipated that by understanding the interfacial self-assembly pathway, this simple evaporative procedure could be conducted as a continuous process amenable to large area nanoparticle-based manufacturing needed for emerging energy technologies.
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