ABSTRACT
Lead-free BiFeO3-BaTiO3 (BF-BT) piezoceramics have sparked considerable interest in recent years due to their high piezoelectric performance and high Curie temperature. In this paper, we show how the addition of highly aligned porosity (between 40 and 60 vol %) improves the piezoelectric performance, sensing, and energy harvesting figures of merit in freeze-cast 0.70BiFeO3-0.30BaTiO3 piezoceramics compared to conventionally processed, nominally dense samples of the same composition. The dense and porous BF-BT ceramics had similar longitudinal piezoelectric coefficients (d33) immediately after poling, yet the dense samples were observed to age faster than those of porous ceramics. After 24 h, for example, the porous samples had significantly higher d33 values ranging from 112 to 124 pC/N, compared to 85 pC/N for the dense samples. Porous samples exhibited 3 and 5 times higher longitudinal piezoelectric voltage coefficient g33 and energy harvesting figure of merit d33g33 than dense samples due to the unexpected increase in d33 and decrease in relative permittivity with porosity. Spontaneous polarization (Ps) and remnant polarization (Pr) decrease as the porosity content increased from 37 to 59 vol %, as expected due to the lower volume of active material; however, normalized polarization values with respect to porosity level showed a slight increase in the porous materials relative to the dense BF-BT. Furthermore, the porous ceramics showed improved temperature-dependent strain-field response compared to the dense. As a result, these porous materials show excellent potential for use in high temperature sensing and harvesting applications.
ABSTRACT
While the consequences of humidity during solid-state processing of sodium potassium niobate-based lead-free piezoelectric powders are well established, the effect of humidity at later fabrication steps is less known. This study assesses the effect of humidity on the sintering and functional properties of 0.06LiNbO3-0.94(K0.5Na0.5)NbO3 (LKNN). Samples sintered in high-humidity air display a higher density, lower dielectric losses, and an increased mechanical quality factor. The observed properties persisted even after five months of storage with marginal reduction in the measured piezoelectric parameters. While the improvements shown with the high-humidity sintering method might be too small to justify investments in special atmosphere sintering, it more importantly indicates that no special equipment or atmosphere control is required to avoid adverse effects of humidity during sintering of sodium potassium niobate-based piezoceramics.
ABSTRACT
The electrical properties of pristine fluoropolymers are inferior due to their low polar crystalline phase content and rigid dipoles that tend to retain their fixed moment and orientation. Several strategies, such as electrospinning, electrohydrodynamic pulling, and template-assisted growing, have been proven to enhance the electrical properties of fluoropolymers; however, these techniques are mostly very hard to scale-up and expensive. Here, a facile interfacial engineering approach based on amine-functionalized graphene oxide (AGO) is proposed to manipulate the intermolecular interactions in poly(vinylidenefluoride-trifluoroethylene) (PVDF-TrFE) to induce ß-phase formation, enlarge the lamellae dimensions, and align the micro-dipoles. The coexistence of primary amine and hydroxyl groups on AGO nanosheets offers strong hydrogen bonding with fluorine atoms, which facilitates domain alignment, resulting in an exceptional remnant polarization of 11.3 µC cm-2 . PVDF-TrFE films with 0.1 wt.% AGO demonstrate voltage coefficient, energy density, and energy-harvesting figure of merit values of 0.30 Vm N-1 , 4.75 J cm-3 , and 14 pm3 J-1 , respectively, making it outstanding compared with state-of-the-art ceramic-free ferroelectric films. It is believed that this work can open-up new insights toward structural and morphological tailoring of fluoropolymers to enhance their electrical and electromechanical performance and pave the way for their industrial deployment in next-generation wearables and human-machine interfaces.
ABSTRACT
The characteristic functionality of ferroelectric materials is due to the symmetry of their crystalline structure. As such, ferroelectrics lend themselves to design approaches that manipulate this structural symmetry by introducing extrinsic strain. Using in situ dark-field X-ray microscopy to map lattice distortions around deeply embedded domain walls and grain boundaries in BaTiO3, we reveal that symmetry-breaking strain fields extend up to several micrometres from domain walls. As this exceeds the average domain width, no part of the material is elastically relaxed, and symmetry is universally broken. Such extrinsic strains are pivotal in defining the local properties and self-organization of embedded domain walls, and must be accounted for by emerging computational approaches to material design.
