Highly Efficient Piezoelectrets through Ultra-Soft Elastomeric Spacers

Piezoelectrets are artificial ferroelectrics that are produced from non-polar air-filled porous polymers by symmetry breaking through high-voltage-induced Paschen breakdown in air. A new strategy for three-layer polymer sandwiches is introduced by separating the electrical from the mechanical response. A 3D-printed grid of periodically spaced thermoplastic polyurethane (TPU) spacers and air channels was sandwiched between two thin fluoroethylene propylene (FEP) films. After corona charging, the air-filled sections acted as electroactive elements, while the ultra-soft TPU sections determined the mechanical stiffness. Due to the ultra-soft TPU sections, very high quasi-static (22,000 pC N–1) and dynamic (7500 pC N–1) coefficients were achieved. The isothermal stability of the coefficients showed a strong dependence on poling temperature. Furthermore, the thermally stimulated discharge currents revealed well-known instability of positive charge carriers in FEP, thereby offering the possibility of stabilization by high-temperature poling. The dependences of the dynamic coefficient on seismic mass and acceleration showed high coefficients, even at accelerations approaching that of gravity. An advanced analytical model rationalizes the magnitude of the obtained quasi-static coefficients of the suggested structure indicating a potential for further optimization.

Nanoscale ordering of planar octupolar molecules for nonlinear optics at higher temperatures

We develop scenarios for orientational ordering of an in-plane system of small flat octupolar molecules at the low-concentration limit, aiming towards nonlinear-optical (NLO) applications at room temperatures. The octupoles interact with external electric poling fields and intermolecular interactions are neglected. Simple statistical-mechanics models are used to analyze the orientational order in the very weak poling limit, sufficient for retrieving the NLO signals owing to the high sensitivity of NLO detectors and measurement chains. Two scenarios are discussed. Firstly, the octupolar poling field is imparted by a system of point charges; the setup is subject to cell-related constraints imposed by mechanical strength and dielectric breakdown limit. The very weak octupolar order of benchmarking TATB molecules is shown to emerge at Helium temperatures. The second scenario addresses the dipoling of octupolar molecules with a small admixture of electric dipolar component. It requires a strong field regime to become effective at Nitrogen temperature range. An estimation of the nonlinear susceptibility coefficient matrix for both scenarios is done in the high-temperature (weak interaction) limit formalism. We argue that moderate modifications of the system like, e.g., an increase of the size of the octupole, accompanied by dipole-assisted octupoling, can increase the poling temperature above Nitrogen temperatures.

Ferroelectric behavior in paracrystalline poly(vinyl trifluoroacetate)

Dielectric behavior in paracrystalline poly(vinyl trifluoroacetate) was investigated from the viewpoint of ferroelectricity. This polymer has a large CF3 dipole moment (2.3 Debye) and structural defects due to the atactic sequence in its chain conformation. It is possible to rotate the dipoles in paracrystals with defects under high electric field. The dielectric behavior was measured from 20 to 200 °C. A large dielectric constant and dielectric relaxation strength (Δε = 17 at 110 °C) were observed in the α-relaxation region. Corona poling on the samples was carried out at DC field 80 MV/m and 80 °C. Ferroelectric D–E hysteresis loop was observed under high electric field, and the remanent polarization and coercive field at 40 °C were 15 mC/m2 and 155 MV/m, respectively. Pyroelectric response and thermally stimulated current were measured from the current through the electrode irradiated by a pulsed semiconductor laser. A pyroelectric constant of about 6 μC/m2K was observed, which was stable up to near the poling temperature. The ferroelectricity in poly(vinyltrifluoroacetate) stems from the rotation of molecular chains in its paracrystals and orientation of the CF2 dipoles. Poly(vinyltrifluoroacetate) dielectrics can be used for capacitors with high power density, artificial skins, muscles and other flexible electronics.

Thermally stimulated depolarization current characteristic of EVA–conductive PPy composites

Thermally stimulated depolarization current in pure poly(ethylene-co-vinyl acetate) and poly(ethylene-co-vinyl acetate) composites with different amounts of polypyrrole/carbon nanoparticles (of various weight ratios, 100:0, 95:5, 90:10, 85:15, 80:20, and 70:30) have been investigated at poling temperature 363 K using different polarizing voltage. Thermograms of pure and composite samples have two or three peaks over all temperature ranges depending on the polarizing voltage. The decrease in peak height with increased polarized voltage is observed in pure poly(ethylene-co-vinyl acetate) samples loaded with 5%, 10%, 15%, and 30% polypyrrole due to the detrapping of the large amounts of charge results in electrode blocking and decrease in thermally stimulated depolarization current in those samples. The molecular parameters, such as activation energy E, charge released Q, and relaxation times τ0 and τ m for thermally stimulated depolarization current peaks have been estimated.