4.6 Article

Control of nanoparticle dispersion in thin polymer films

Journal

SOFT MATTER
Volume 4, Issue 12, Pages 2441-2447

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b807565d

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Funding

  1. U.S. Department of Energy [DEFG02-05ER46211]

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We have found larger (>5 nm) nanoparticles are uniformly distributed in a polymer film immediately after spin-coating. However, using the same thin film fabrication process leads to C-60 nanoparticle segregation to the substrate, resulting in a kinetically trapped state that resists dispersion. The additional processing steps introduced here are found to yield uniform dispersion of these small nanoparticles in polymer films. Moreover, we show that although very small nanoparticles, such as C-60 fullerenes, can be homogeneously distributed in the film, larger organic nanoparticles subsequently phase separate to the solid substrate. Both processes, dispersion and segregation in thin films, are primarily driven through entropic terms dictated by the relative size of the nanoparticle and polymer statistical segment. This is in agreement with a simple theory and supported by density functional theory calculations that predict uniform dispersion in thin films when the nanoparticle diameter is less than similar to 1.5 times the size of a polymer statistical segment. This is despite the fact that both the larger and C-60 nanoparticles are miscible in the bulk, demonstrating the thermodynamic influence of a hard substrate. Morphologies are characterized via neutron reflectivity measurements throughout the study to accurately characterize nanoparticle dispersion.

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