An applied electric field can reversibly change the temperature of an electrocaloric material under adiabatic conditions, and the effect is strongest near phase transitions. We demonstrate a giant electrocaloric effect (0.48 kelvin per volt) in 350-nanometer PbZr(0.95)Ti(0.05)O3 films near the ferroelectric Curie temperature of 222 degrees C. A large electrocaloric effect may find application in electrical refrigeration.
The physics of pyroelectric detectors is reviewed, including a discussion of response and electronic noise and their dependence on device design and material parameters. Other sources of noise are described, particularly as generated by environmental effects such as microphony, together with techniques for their minimisation. The range of ferroelectric materials which have been assessed for use in pyroelectric detectors is reviewed and their properties compared, particularly from the aspect of application to different types of device. Finally, an account is given of the wide range of applications for which pyroelectric detectors have been used, including a detailed description of both the pyroelectric vidicon and pyroelectric arrays and their application to thermal imagers.
Rietveld refinements using neutron powder profiles are reported for a series of samples (commonly known as PZT), with x ranging from to . Cation shifts, octahedral distortion and tilts are determined with varying composition across the ferroelectric rhombohedral regions, and , of the PZT phase diagram. These parameters are then used in conjunction with a simple Landau-Devonshire model to investigate the nature of the phase transition.
It is found that the cation shifts, octahedral distortion and tilt angles decrease with increasing Ti content, but, surprisingly, the octahedral strain, as indicated by the rhombohedral angle, increases. This is in contrast to the case for all other known rhombohedral perovskites. Furthermore, the refined anisotropic displacement parameters of the cations are anomalous and cannot be accounted for by the average crystal structure. A model is presented in which a domain-type `local' structure is considered, containing `ordered' additional cation displacements, consistently with the reports of extra reflections observed in electron microscopy studies by Viehland et al, Dai et al and Ricote et al.
Single-phase multiferroic materials are of considerable interest for future memory and sensing applications. Thin films of Aurivillius phase Bi7Ti3Fe3O21 and Bi6Ti2.8Fe1.52Mn0.68O18 (possessing six and five perovskite units per half-cell, respectively) have been prepared by chemical solution deposition on c-plane sapphire. Superconducting quantum interference device magnetometry reveal Bi7Ti3Fe3O21 to be antiferromagnetic (TN = 190 K) and weakly ferromagnetic below 35 K, however, Bi6Ti2.8Fe1.52Mn0.68O18 gives a distinct room-temperature in-plane ferromagnetic signature (Ms = 0.74 emu/g, μ0Hc =7 mT). Microstructural analysis, coupled with the use of a statistical analysis of the data, allows us to conclude that ferromagnetism does not originate from second phase inclusions, with a confidence level of 99.5%. Piezoresponse force microscopy (PFM) demonstrates room-temperature ferroelectricity in both films, whereas PFM observations on Bi6Ti2.8Fe1.52Mn0.68O18 show Aurivillius grains undergo ferroelectric domain polarization switching induced by an applied magnetic field. Here, we show for the first time that Bi6Ti2.8Fe1.52Mn0.68O18 thin films are both ferroelectric and ferromagnetic and, demonstrate magnetic field-induced switching of ferroelectric polarization in individual Aurivillius phase grains at room temperature
The crystal structure of the perovskite lead zirconate PbZrO 3 has been redetermined using single-crystal X-ray diffraction (MoKct radiation, 2--0.71069A).Single-crystal data at 100 K: space group. Pbam, a=5.884(1), b=11.787(3), c=8.231(2) (1). An investigation is made into previous contradicting reports of a possible disorder in the oxygens and their origin by examining the crystal pseudo-symmetry. Information distinguishing an ordered and disordered oxygen substructure is shown to reside in weak l odd reflections. Because of their extremely low intensities these reflections have not contributed sufficiently in previous X-ray structure investigations and hence, to date, conclusive evidence differentiating between ordered and disordered models has not been possible. By collecting single-crystal X-ray data at low temperature and by using exceptionally long scans on selected hkl, l odd, reflections, a new accurate structure determination is presented and discussed, showing the true ordered oxygen positions. Because of the large difference in scattering factors between lead and oxygen when using X-rays, a neutron diffraction Rietveld refinement using polycrystalline samples (D1A instrument, ILL, 2-1.90788 A) is also reported as further evidence to support the true ordered oxygen structure revealed by the low-temperature X-ray analysis.
Nanostructured materials are central to the evolution of future electronics and information technologies. Ferroelectrics have already been established as a dominant branch in the electronics sector because of their diverse application range such as ferroelectric memories, ferroelectric tunnel junctions, etc. The on-going dimensional downscaling of materials to allow packing of increased numbers of components onto integrated circuits provides the momentum for the evolution of nanostructured ferroelectric materials and devices. Nanoscaling of ferroelectric materials can result in a modification of their functionality, such as phase transition temperature or Curie temperature (TC), domain dynamics, dielectric constant, coercive field, spontaneous polarisation and piezoelectric response. Furthermore, nanoscaling can be used to form high density arrays of monodomain ferroelectric nanostructures, which is desirable for the miniaturisation of memory devices. This review article highlights some research breakthroughs in the fabrication, characterisation and applications of nanoscale ferroelectric materials over the last decade, with priority given to novel synthetic strategies
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