posted on 2014-12-10, 00:00authored byChristopher A. Grabowski, Hilmar Koerner, Jeffrey
S. Meth, Alei Dang, Chin Ming Hui, Krzysztof Matyjaszewski, Michael R. Bockstaller, Michael F. Durstock, Richard A. Vaia
Demands
to increase the stored energy density of electrostatic capacitors
have spurred the development of materials with enhanced dielectric
breakdown, improved permittivity, and reduced dielectric loss. Polymer
nanocomposites (PNCs), consisting of a blend of amorphous polymer
and dielectric nanofillers, have been studied intensely to satisfy
these goals; however, nanoparticle aggregates, field localization
due to dielectric mismatch between particle and matrix, and the poorly
understood role of interface compatibilization have challenged progress.
To expand the understanding of the inter-relation between these factors
and, thus, enable rational optimization of low and high contrast PNC
dielectrics, we compare the dielectric performance of matrix-free
hairy nanoparticle assemblies (aHNPs) to blended PNCs in the regime
of low dielectric contrast to establish how morphology and interface
impact energy storage and breakdown across different polymer matrices
(polystyrene, PS, and poly(methyl methacrylate), PMMA) and nanoparticle
loadings (0–50% (v/v) silica). The findings indicate that the
route (aHNP versus blending) to well-dispersed morphology has, at
most, a minor impact on breakdown strength trends with nanoparticle
volume fraction; the only exception being at intermediate loadings
of silica in PMMA (15% (v/v)). Conversely, aHNPs show substantial
improvements in reducing dielectric loss and maintaining charge/discharge
efficiency. For example, low-frequency dielectric loss (1 Hz–1
kHz) of PS and PMMA aHNP films was essentially unchanged up to a silica
content of 50% (v/v), whereas traditional blends showed a monotonically
increasing loss with silica loading. Similar benefits are seen via
high-field polarization loop measurements where energy storage for
∼15% (v/v) silica loaded PMMA and PS aHNPs were 50% and 200%
greater than respective comparable PNC blends. Overall, these findings
on low dielectric contrast PNCs clearly point to the performance benefits
of functionalizing the nanoparticle surface with high-molecular-weight
polymers for polymer nanostructured dielectrics.