Abstract
Polymer nanocomposites (PNCs) are important materials that are widely used in many current technologies and potentially have broader applications in the future due to their excellent property tunability, light weight, and low cost. However, expanding the limits in property enhancement remains a fundamental scientific challenge. Here, we demonstrate that well-dispersed, small (diameter ∼1.8 nm) nanoparticles with attractive interactions lead to unexpectedly large and qualitatively different changes in PNC structural dynamics in comparison to conventional nanocomposites based on particles of diameters ∼10-50 nm. At the same time, the zero-shear viscosity at high temperatures remains comparable to that of the neat polymer, thereby retaining good processability and resolving a major challenge in PNC applications. Our results suggest that the nanoparticle mobility and relatively short lifetimes of nanoparticle-polymer associations open qualitatively different horizons in the tunability of macroscopic properties in nanocomposites with a high potential for the development of advanced functional materials.
Original language | English |
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Pages (from-to) | 752-759 |
Number of pages | 8 |
Journal | ACS Nano |
Volume | 11 |
Issue number | 1 |
DOIs | |
State | Published - Jan 24 2017 |
Funding
This work was supported by the U.S. Department of Energy Office of Science, Basic Energy Sciences, Materials Science and Engineering Division. This research used resources of the Oak Ridge Leadership Computing Facility at Oak Ridge National Laboratory, which is supported by the Office of Science of the Department of Energy under Contract DE-AC05-00OR22725.
Keywords
- apparent disentanglement
- fragility
- glass transition
- polymer nanocomposites
- small nanoparticles