Scinovex
articleTop 1% cited

Exploring Strategies for High Dielectric Constant and Low Loss Polymer Dielectrics

The Journal of Physical Chemistry Letters · 2014 · Vol. 5(21) · pp. 3677–3687
Lei Zhu

Abstract

Polymer dielectrics having high dielectric constant, high temperature capability, and low loss are attractive for a broad range of applications such as film capacitors, gate dielectrics, artificial muscles, and electrocaloric cooling. Unfortunately, it is generally observed that higher polarization or dielectric constant tends to cause significantly enhanced dielectric loss. It is therefore highly desired that the fundamental physics of all types of polarization and loss mechanisms be thoroughly understood for dielectric polymers. In this Perspective, we intend to explore advantages and disadvantages for different types of polarization. Among a number of approaches, dipolar polarization is promising for high dielectric constant and low loss polymer dielectrics, if the dipolar relaxation peak can be pushed to above the gigahertz range. In particular, dipolar glass, paraelectric, and relaxor ferroelectric polymers are discussed for the dipolar polarization approach.

Dielectric materials and actuatorsFerroelectric and Piezoelectric MaterialsAdvanced Sensor and Energy Harvesting MaterialsDielectricMaterials scienceHigh-κ dielectricDipoleCapacitorPolarization (electrochemistry)Dielectric lossCondensed matter physicsPolymerFerroelectricity

Funding

  • National Science Foundation
  • Office of Naval Research
Citations
706
FWCI
17.27
field-weighted impact
References
83
Percentile
100%
vs. same field & year
Citations per year
References
High-field deformation of elastomeric dielectrics for actuators
Materials Science and Engineering C · 2000 · 681 citations
Surface plasmons in metallic nanoparticles: fundamentals and applications
Journal of Physics D Applied Physics · 2011 · 878 citations
Materials for electrochemical capacitors
Nature Materials · 2008 · 15,889 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.