RESUMO
Ultra-high volumetric performance electrochemical double layer capacitors based on high density aligned nano-porous microwave exfoliated graphite oxide have been studied. Elimination of macro-, meso-, and larger micro-pores from electrodes and controlling the nano-morphology results in very high volumetric capacitance, energy, and power density values.
Assuntos
Grafite/química , Nanoestruturas/química , Óxidos/química , Capacitância Elétrica , Técnicas Eletroquímicas/instrumentação , Eletrodos , Líquidos Iônicos/química , Micro-Ondas , PorosidadeRESUMO
Electromechanical properties of the relaxor ferroelectric poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene) [P(VDF-TrFE-CFE)] terpolymer blended with a small amount of poly(vinylidene fluoride-chlorotrifluoroethylene) [P(VDF-CTFE)] copolymer, which possesses a much higher elastic modulus than that of the neat terpolymer, were investigated. It was observed that the presence of small amount of P(VDF-CTFE) does not affect the microstructure of the crystalline phase. However, the uniaxially stretched blended films show a slight increase in the crystallinity and increased or similar induced polarization at high electric fields compared with the neat terpolymer, likely caused by the interface effect. Consequently, for blends with P(VDF-CTFE) less than 5 wt%, the transverse strains S1 along the stretching direction for uniaxially stretched blended films are nearly the same as those of neat P(VDF-TrFE-CFE), whereas the elastic modulus along the S1-direction increases with the P(VDF-CTFE) content. As a result, the blended films exhibit a higher elastic energy density and electromechanical coupling factor k31 compared with the neat terpolymer.
RESUMO
The promise of aromatic, amorphous, polar polymers containing high dipolar moments with very low defect levels is demonstrated for future dielectric materials with ultrahigh electric-energy density, low loss at high applied fields, and ultrahigh breakdown strengths. Specifically, aromatic polythiourea films exhibit an ultrahigh breakdown field (>1 GV m(-1)), which results in an energy density of ≈22 J cm(-3), as well as a low loss.
RESUMO
Dielectric polymers with high dipole density have the potential to achieve very high energy density, which is required in many modern electronics and electric systems. We demonstrate that a very high energy density with fast discharge speed and low loss can be obtained in defect-modified poly(vinylidene fluoride) polymers. This is achieved by combining nonpolar and polar molecular structural changes of the polymer with the proper dielectric constants, to avoid the electric displacement saturation at electric fields well below the breakdown field. The results indicate that a very high dielectric constant may not be desirable to reach a very high energy density.