ABSTRACT
A bit more than a decade after the first report of ferroelectric switching in hafnium dioxide-based ultrathin layers, this family of materials continues to elicit interest. There is ample consensus that the observed switching does not obey the same mechanisms present in most other ferroelectrics, but its exact nature is still under debate. Next to this fundamental relevance, a large research effort is dedicated to optimizing the use of this extraordinary material, which already shows direct integrability in current semiconductor chips and potential for scalability to the smallest node architectures, in smaller and more reliable devices. Here we present a perspective on how, despite our incomplete understanding and remaining device endurance issues, the lessons learned from hafnium dioxide-based ferroelectrics offer interesting avenues beyond ferroelectric random-access memories and field-effect transistors. We hope that research along these other directions will stimulate discoveries that, in turn, will mitigate some of the current issues. Extending the scope of available systems will eventually enable the way to low-power electronics, self-powered devices and energy-efficient information processing.
ABSTRACT
Ba0.92Ca0.08Ti0.95Zr0.05O3 (BCZT8-5) ceramic materials have been scarcely studied as lead-free piezo/ferroelectrics despite their enhanced Curie temperature (>100 °C) with respect to most studied BCZT compositions. In this work, homogeneous dense BCZT8-5 ceramics with grain size in the range of 20 µm, and optimum ferroelectric, dielectric, and electromechanical performance, were prepared by the mixed oxides route using moderate synthesis (1250 °C-2 h) and sintering (1400 °C-2 h) conditions. Thickness-poled thin disks and monomodal shear plate resonators were used for the determination of piezoelectric coefficients, coupling factors, elastic, and dielectric permittivity coefficients, including all losses, by iterative analysis of impedance curves at resonance. Furthermore, the thermal evolution of the piezoelectric characteristics at resonance was determined to assess the enhanced working range of the ceramics (≈100 °C). Ferroelectric hysteresis loops and strains vs. electric-field butterfly loops were also measured and showed soft behavior with Ec = 2 kV/cm, Pr = 12 µC/cm2 after a maximum applied field of 3 kV was used. The ceramics showed a high endurance of P-E cycles to electrical fatigue up to 107 cycles. Moreover, dielectric properties as a function of temperature were also accomplished and showed nearly normal ferroelectric behavior, characteristic of samples with low crystallographic disorder. Overall, these ceramics showed high sensitivity and higher stability than other currently studied BCZT compositions.
ABSTRACT
Ferroelectric polymers represent one of the key building blocks for the preparation of flexible electronic devices. However, their lack of functionality and ability to simply tune their ferroelectric response significantly diminishes the number of fields in which they can be applied. Here we report an effective way to introduce functionality in the structure of ferroelectric polymers while preserving ferroelectricity and to further tune the ferroelectric response by incorporating functional insulating polymer chains at the chain ends of ferroelectric polymer in the form of block copolymers. The block copolymer self-assembly into lamellar nanodomains allows confined crystallization of the ferroelectric polymer without hindering the crystallinity or chain conformation. The simple adjustment of block polarity leads to a significantly different switching behavior, from ferroelectric to antiferroelectric-like and linear dielectric. Given the simplicity and wide flexibility in designing molecular structure of incorporated blocks, this approach shows the vast potential for application in numerous fields.
ABSTRACT
A facile ferroelectric nanostructures preparation method is developed based on the self-assembly of poly(2-vinylpyridine)-b-poly(vinylidene fluoride-co-trifluoroethylene)-b-poly(2-vinylpyridine) triblock copolymers (P2VP-b-P(VDF-TrFE)-b-P2VP), and the effect of morphological characteristics of the block copolymers on the ferroelectric response has been investigated for the first time. By simple adjustment of the ratio between the blocks, lamellar, cylindrical, and spherical morphologies are obtained in the melt and preserved upon crystallization of P(VDF-TrFE). However, at high P(VDF-TrFE) content, crystallization becomes dominant and drives the self-assembly of block copolymers. The crystallization study of the block copolymers reveals the preservation of the high degree of crystallinity inside the confined nanodomains as well as the reduction of the crystalline size and the Curie transition temperature with the confinement level. Only a small difference in the coercive field and the shape of the hysteresis loop is observed for block copolymers with a lamellar morphology produced either by crystallization-driven self-assembly or by confinement inside preformed lamellar domains. In contrast, delayed spontaneous polarization or the absence of dipole switching is demonstrated for the confinement of ferroelectric crystals inside both isolated cylindrical and spherical domains, exemplifying the influence of dimensionality on the critical size for ferroelectric order.
