Nanoparticle assembly at fluid interfaces:: Structure and dynamics

被引:229
作者
Lin, Y
Böker, A
Skaff, H
Cookson, D
Dinsmore, AD
Emrick, T [1 ]
Russell, TP
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[2] Australian Nucl Sci & Technol Org, Menai, NSW 2234, Australia
[3] Univ Massachusetts, Dept Phys, Amherst, MA 01003 USA
关键词
D O I
10.1021/la048000q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The self-assembly of nanoparticles at fluid interfaces, driven by the reduction in interfacial energy, was investigated. With spherical, tri-n-octyl-phosphine-oxide covered cadium selenide (CdSe) nanoparticles (1-8 nm), thermal fluctuations compete with the interfacial segregation giving rise to a size-dependent self-assembly of the particles. The structure of the nanoparticle assembly was studied using electron microscopy, atomic force microscopy, and X-ray scattering in situ, which indicate that the particles form a densely packed monolayer. The energetics of the adsorption of nanoparticles onto the interface was revealed by time-dependent fluorescence studies on a mixture of two different sized nanoparticles at the interface. The dynamics of the nanoparticles at the fluid interface, probed using fluorescence photobleaching methods, suggests a liquid-like behavior. The results have implications in the design of hierarchical self-assemblies of nanoparticles for the one-step fabrication of devices on multiple length scales.
引用
收藏
页码:191 / 194
页数:4
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