Facile preparation and charge retention mechanism of polymer-based deformable electret.

Electret materials with high deformability largely extend their applications such as wearable devices and actuators. Meanwhile, the deformability of currently reported electrets is somewhat limited except for a liquid electret that requires synthetic procedures with relatively low product yield. Here, we report a polymer-based electret with infinite deformability, which is simply prepared by corona-discharging on the mixture of two commercially available polymers, , polybutenes (PB) as a liquid polyolefin and polypropylene--maleic anhydride (MPP) as a solute. The charge retention mechanism of the PB/MPP electret was both experimentally and computationally elucidated from the views of molecular and nanoscale structures, and transport properties. Contrary to the ease of the preparation, the charge retention mechanism was complicated. The results of quantum chemical calculations and X-ray scattering indicated that the succinic anhydride polar moieties in MPP act as a charge trap site while how they distribute in the non-polar matrix also matters. Transport property measurements revealed the strong connection between complex viscosity and the relaxation time of the charge decay of the PB/MPP electret. Finally, we fabricated a simple piezoelectric device consisting of the PB/MPP electret. It was demonstrated that the piezoelectric performance of the PB/MPP electret is comparable to that of a conventional solid electret.