Multi-layer ferroelectrets consisting of fluoroethylenepropylene (FEP) copolymer and open-porous expanded polytetrafluoroethylene (ePTFE) films exhibit stable internal electret charges, high piezoelectric coefficients and heat resistance, making them promising candidates for wearable sensors or nanogenerators in body-area networks. Here, three- and five-layer (FEP/ePTFE/FEP and FEP/ePTFE/FEP/ePTFE/FEP) ferroelectret stacks were laminated and poled in a corona discharge. The resulting charge distributions were measured by use of the pulsed electro-acoustic (PEA) method and revealed that charges of opposite polarity were trapped at the interfaces between the FEP and ePTFE layers. Thus, the existence of one macro-dipole in the three-layer structure and of two macro-dipoles in the five-layer structure was directly shown for the first time. Moreover, electric-displacement-versus-electric-field (D-E) loops revealed that remnant polarization is given by the number of macro-dipoles in the respective stack. Due to the addition of the macro-dipoles, the piezoelectric d 33 coefficient of the FEP/ePTFE/FEP/ePTFE/FEP stack reaches 200 pC/N even under a potentially non-uniform compression of the soft ePTFE layers. The results should be useful for a better understanding and a performance optimization of ferroelectrets in self-powered intelligent devices.@en

In contrast to molecular-dipole polymers, such as PVDF, ferroelectrets are a new class of flexible spatially heterogeneous piezoelectric polymers with closed or open voids that act as deformable macro-dipoles after charging. With a spectrum of manufacturing processes being developed to engineer the heterogeneous structures, ferroelectrets are made with attractive piezoelectric properties well-suited for applications, such as pressure sensors, acoustic transducers, etc. However, the sources of the macro-dipole charges have usually been the same, microscopic dielectric barrier discharges within the voids, induced when the ferroelectrets are poled under a large electric field typically via a so-called corona poling, resulting in the separation and trapping of opposite charges into the interior walls of the voids. Such a process is inherently self-limiting, as the reverse internal field from the macro-dipoles eventually extinguishes the microdischarges, resulting in limited density of ions and not too high overall piezoelectric performance. Here, a new method to form ferroelectrets with gigantic electroactivity is proposed and demonstrated with the aid of an external ion booster. A laminate consisting of expanded polytetrafluoroethylene (ePTFE) and fluorinated-ethylene-propylene (FEP) was prefilled with bipolar ions produced externally by an ionizer and sequentially poled to force the separation of positive and negative ions into the open fibrous structure, rendering an impressive piezoelectric d33 coefficient of 1600 pC/N an improvement by a factor of 4 in comparison with the d33 of a similar sandwich poled with nonenhanced corona poling. The (pre)filling clearly increases the ion density in the open voids significantly. The charges stored in the open-cell structure stays at a high level for at least 4 months. In addition, an all-organic nanogenerator was made from an ePTFE-based ferroelectret, with conducting poly(3,4-ethylene dioxythiophene): poly(styrenesulfonate) (PEDOT: PSS) coated fabric electrodes. When poled with this ion-boosting process, it yielded an output power twice that of a similar sample poled in a conventional corona-only process. The doubling in output power is mainly brought about by the significantly higher charge density achieved with the aid of external booster. Furthermore, aside from the bipolar ions, extra monopolar ions can during the corona poling be blown into the open pores by using for instance a negative ionic hair dryer to produce a unipolar ePTFE-based ferroelectret with its d33 coefficient enhanced by a factor of 3. Ion-boosting poling thus unleashes a new route to produce bipolar or unipolar open-cell ferroelectrets with highly enhanced piezoelectric response.@en