Role of Microstructures in the Dielectric Properties of PVDF-Based Nanocomposites Containing High-Permittivity Fillers for Energy Storage.

Polymer-based nanocomposites containing inorganic ferroelectric inclusions, typically ABO3 perovskites, have emerged as innovative dielectric materials for energy storage and electric insulation, potentially coupling the high breakdown strength (BDS) and easy processing of polymers with the enhancement of dielectric constant provided by the ferroelectric phase. In this paper, experimental data and three-dimensional finite element method (3D FEM) simulations were combined to shed some light on the effect of microstructures on the dielectric properties of poly(vinylidene fluoride) (PVDF)-BaTiO3 composites. The existence of particle aggregates or touching particles has a strong effect on the effective dielectric constant and determines an increase of the local field in the neck region of the ferroelectric phase with a detrimental effect on the BDS. The distribution of the field and the effective permittivity are very sensitive to the specific microstructure considered. The degradation of the BDS can be overcome by coating the ferroelectric particles with a thin shell of an insulating oxide with a low dielectric constant, such as SiO2 (εr = 4). The local field is highly concentrated on the shell, while the field in the ferroelectric phase is reduced almost to zero and that on the matrix is close to the applied one. The electric field in the matrix becomes less homogeneous with increasing the dielectric constant of the shell material, as happens with TiO2 (εr = 30). These results provide a solid background to explain the enhanced dielectric properties and the superior BDS of composites containing core-shell inclusions.

Audiological Risk Factors, Referral Rates and Dropouts: 9 Years of Universal Newborn Hearing Screening in North Sardinia.

Background: Objectives of the present work were to analyze the prevalence of hearing loss in our population of screened newborns during the first 9 years of the universal newborn hearing screening (UNHS) program at University Hospital Sassari (Italy) (AOU Sassari), to analyze the risk factors involved, and to analyze our effectiveness in terms of referral rates and dropout rates. Methods: Monocentric retrospective study whose target population included all the newborns born or referred to our hospital between 2011 and 2019. Results: From 2011 to 2019, a total of 11,688 babies were enrolled in our screening program. In total, 3.9‱ of wellborn babies and 3.58% of neonatal intensive care unit (NICU) babies had some degree of hearing loss. The most frequently observed risk factors among non-NICU babies were family history of hearing loss (3.34%) and craniofacial anomalies (0.16%), among NICU babies were low birth weight (54.91%) and prematurity (24.33%). In the multivariate analysis, family history of hearing loss (p < 0.001), NICU (p < 0.001), craniofacial anomalies (p < 0.001), low birth weight (<1500 g) (p = 0.04) and HIV (p = 0.03) were confirmed as risk factors. Conclusions: Our data are largely consistent with the literature and most results were expected, one relevant exception being the possible role of NICU as a confounding factor and the limited number of risk factors confirmed in the multivariate analysis.

The local and average structure of Ba(Ti, Ce)O3 perovskite solid solution: effect of cerium concentration and particle size.

The amazing properties of ferroelectric perovskite BaTiO3 (BT) and its solid solutions make them indispensable for many technological applications (e.g. multilayer capacitors). Unfortunately, the so-called `size effect' limits their use. Indeed, under a certain critical particle size, these materials show a suppression of the spontaneous polarization and thus of the ferroelectric properties. In pure nanometric BaTiO3, this is related to a certain local structural disorder. However, only a few studies have explored BT solid solutions, where the doping effect, coupled to the reduced particle size, can play an important role. Therefore, in this work, the structure of BaCexTi1-xO3 (x = 0.02-0.20) was explored by traditional Rietveld method and Pair Distribution Function. Samples present a particle size from 80-160 nm to 400-1000 nm depending on increasing x. The carbox approach was applied, investigating the evolution of the local structure, its modifications and the structural coherent correlation length, as a function of cerium amount. Results demonstrate a cooperative effect of composition and reduced size in the ferroelectricity loss. The two, in fact, contribute to intensify the local structural disorder, decreasing the structural coherent correlation length. The local structural disorder is thus confirmed to be a relevant factor in the ferroelectric properties degradation.

Revealing the Role of the Intermediates during the Synthesis of BaTi5O11.

BaTi5O11 has been extensively studied because of their microwave dielectrics properties. Traditionally, it is difficult to achieve this material as single-phase. Here, we report an effective method to obtain BaTi5O11 powder with nanometer-scale crystals, by solid-state reaction at moderate temperatures and using as precursors nanostructured particles consisting of BaTiO3 and TiO2. The main advantage is the intimate contact between the BaTiO3 and TiO2 that ensure, when the solid-state reaction takes place, the formation of complex solid compounds from three or more constituents. The formation mechanism of BaTi5O11 has been studied as a function of both the thermal treatment and the time reaction. The reaction was monitored by Raman spectroscopy combined with Confocal microscopy, the aim of this characterization technique is to provide the description of the general strategy and design principles to obtain BaTi5O11 powder. Consequently, this work is a challenging task for the compositional and structural study of complex inorganic nanoparticles.

Ferroelectric order driven Eu3+ photoluminescence in BaZrxTi1-xO3 perovskite.

The ability to tune and enhance the properties of luminescent materials is essential for enlarging their application potential. Recently, the modulation of the photoluminescence emission of lanthanide-doped ferroelectric perovskites by applying an electric field has been reported. Herein, we show that the ferroelectric order and, more generally the polar order, has a direct effect on the photoluminescence of Eu3+ in the model BaZrxTi1-xO3 perovskite even in the absence of an external field. The dipole arrangement evolves with increasing x from long-range ferroelectric order to short-range order typical of relaxors until the non-polar paraelectric BaZrO3 is achieved. The cooperative polar interactions existing in the lattice (x < 1) promote the off-center displacement of the Eu3+ ion determining a change of the lanthanide site symmetry and, consequently, an abrupt variation of the photoluminescence emission with temperature. Each type of polar order is characterized by a distinct photoluminescence behaviour.

Cation Diffusion and Segregation at the Interface between Samarium-Doped Ceria and LSCF or LSFCu Cathodes Investigated with X-ray Microspectroscopy.

The chemical compatibility between electrolytes and electrodes is an extremely important aspect governing the overall impedance of solid-oxide cells. Because these devices work at elevated temperatures, they are especially prone to cation interdiffusion between the cell components, possibly resulting in secondary insulating phases. In this work, we applied X-ray microspectroscopy to study the interface between a samarium-doped ceria (SDC) electrolyte and lanthanum ferrite cathodes (La0.4Sr0.6Fe0.8Cu0.2O3 (LSFCu); La0.9Sr0.1Fe0.85Co0.15O3 (LSCF)), at a submicrometric level. This technique allows to combine the information about the diffusion profiles of cations on the scale of several micrometers, together with the chemical information coming from space-resolved X-ray absorption spectroscopy. In SDC-LSCF bilayers, we find that the prolonged thermal treatments at 1150 °C bring about the segregation of samarium and iron in micrometer-sized perovskite domains. In both SDC-LSCF and SDC-LSFCu bilayers, cerium diffuses into the cathode perovskite lattice A-site as a reduced Ce3+ cation, whereas La3+ is easily incorporated in the ceria lattice, reaching 30 atom % in the ceria layer in contact with LSFCu.