4.8 Article

Performance of Dielectric Nanocomposites: Matrix-Free, Hairy Nanoparticle Assemblies and Amorphous Polymer-Nanoparticle Blends

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 6, 期 23, 页码 21500-21509

出版社

AMER CHEMICAL SOC
DOI: 10.1021/am506521r

关键词

polymer-grafted nanoparticles; colloidal silica; dielectric breakdown; permittivity; energy storage; capacitor

资金

  1. Air Force Office of Scientific Research (AFOSR)
  2. Air Force Research Laboratory Materials & Manufacturing Directorate
  3. National Science Foundation (NSF) [DMR 0969301, CMMI-1234263]
  4. AFOSR [FA9550-09-1-0169]
  5. Direct For Mathematical & Physical Scien
  6. Division Of Materials Research [969301] Funding Source: National Science Foundation

向作者/读者索取更多资源

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 similar to 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.

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