Journal
POLYMERS
Volume 10, Issue 6, Pages -Publisher
MDPI
DOI: 10.3390/polym10060598
Keywords
polymer; nanoparticle composite; nanoparticle diffusion; interfacial structure and dynamics
Categories
Funding
- National Natural Science Foundation of China [21522401, 21534004, 91630201, 21374043]
- Program for JLU Science and Technology Innovative Research Team
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The diffusion dynamics of fullerene (C-60) in unentangled linear atactic polystyrene (PS) and polypropylene (PP) melts and the structure and dynamic properties of polymers in interface area are investigated by performing all-atom molecular dynamics simulations. The comparison of the results in two systems emphasises the influence of local interactions exerted by polymer side group on the diffusion dynamics of the nanoparticle. In the normal diffusive regime at long time scales, the displacement distribution function (DDF) follows a Gaussian distribution in PP system, indicating a normal diffusion of C-60. However, we observe multiple peaks in the DDF curve for C-60 diffusing in PS melt, which indicates a diffusion mechanism of hopping of C-60. The attractive interaction between C-60 and phenyl ring side groups are found to be responsible for the observed hopping diffusion. In addition, we find that the C-60 is dynamically coupled with a subsection of a tetramer on PS chain, which has a similar size with C-60. The phenyl ring on PS chain backbone tends to have a parallel configuration in the vicinity of C-60 surface, therefore neighbouring phenyl rings can form chelation effect on the C-60 surface. Consequently, the rotational dynamics of phenyl ring and the translational diffusion of styrene monomers are found to be slowed down in this interface area. We hope our results can be helpful for understanding of the influence of the local interactions on the nanoparticle diffusion dynamics and interfacial properties in polymer/nanoparticle composites.
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