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Using first-principles calculations based on density functional theory, this work investigated the mechanical, magnetic, elastic, electrical, and optical characteristics of the halide-based perovskite FrGeX3 (X = Cl, Br, I) at different hydrostatic pressures ranging from 0 to 9 GPa. It was determined that the compound FrGeX3 (X = Cl, Br, I) is stable and ductile in nature by calculating its thermodynamic and mechanical stability using the parameters of its formation enthalpy and elastic constant. When no hydrostatic pressure is applied, the band computations reveal that FrGeCl3, FrGeBr3, and FrGeI3 all remain in the semiconductor region with bandgaps of 1.14, 0.8, and 0.645 eV, respectively. The study examined how increasing induced pressure affects the bandgap and density of states of the structure for all three halides. The bandgap of FrGeCl3, FrGeBr3, and FrGeI3 fell to 0 eV at 9, 6, and 5 GPa, respectively. In addition, the optical absorption, reflectivity, refractive index, and imaginary and real components of dielectric functions were all studied in detail for cubic perovskites FrGeX3 (X = Cl, Br, I) under varying hydrostatic pressures, from 0 to 9 GPa. Due to increased pressure, the compound transitioned into a conductor and improved its absorption capabilities for all compounds within the 8–14 eV range, making it suitable for use in the UV spectrum. Cl has the largest absorption among all compounds, whereas I displays the lowest. Reflectivity ranges from around 14% to 18% for all compounds and increases w%ith pressure. The actual component of the refractive index ranges from around 2.25 to 2.7 at 0 eV and increases with pressure. Chlorine has a low refractive index, whereas iodine demonstrates the greatest. The highest fluctuation is shown for Br. The dielectric characteristics vary from around 5 to 7.5 F/m. Chlorine (Cl) has the least charge storage capacity, while iodine (I) demonstrates the most, of which both increase with pressure in all compounds. Structure FrGeX3 (X = Cl, Br, I) is hardened and made more ductile by applying hydrostatic pressure, as seen by the increasing bulk, Young's, and shear modulus values, as well as the elastic constants (C11 and C12). While the electrons were in a co-linear position, the magnetic property was also studied by optimizing the band structure and density of states. The diamagnetic property of the combination FrGeX3 (where X = Cl, Br, I) remained unchanged even when subjected to increased pressure. According to the findings, this perovskite material has remarkable absorption properties, which point to a change in its behavior from semiconductor to metal. Their potential uses in solar cells, UV absorbers, and optoelectronic devices are highlighted by these computational results. [ABSTRACT FROM AUTHOR]

Here, we report on the structural, vibrational phonon, electrical, and magnetic properties of undoped strontium titanate SrTiO3, Ce doped Sr1−xCexTiO3, and (Ce, Fe) co-doped Sr1−xCexTi1−yFeyO3 samples synthesized through solid state reaction route. The Rietveld refined powder x-ray diffraction analysis confirmed the cubic Pm-3m phase in our as-synthesized samples. We observed grain size reduction in SrTiO3 from scanning electron micrographs due to the incorporation of Ce and Fe dopants. The sample purity in terms of chemical species identification has been confirmed from energy-dispersive x-ray spectroscopy. The characteristic phonon modes in our samples are identified using room temperature Raman spectroscopy and benchmarked against existing relevant experimental observations. The incorporation of Ce and Fe as substitutional dopants in SrTiO3 unit cell was confirmed from the absence of absorption at 480, 555, 580, and 1635 cm−1 band in Fourier transform infrared spectra. The 3% Ce doping in Sr0.97Ce0.03TiO3 sample may have induced ferroelectric order, whereas the undoped SrTiO3 (STO) revealed lossy paraelectric nature. In the case of (Ce = 3%, Fe = 10%) co-doped Sr0.97Ce0.03Ti0.90Fe0.10O3 sample, we observed ferromagnetic hysteresis with orders of magnitude enhancement in remnant magnetization and coercivity as compared to undoped STO sample. This long range robust ferromagnetic order may have originated from F-center mediated magnetic interaction. [ABSTRACT FROM AUTHOR]

A significant structural modification and enhancement of the electrical and magnetic properties with dilute substitution of Zr (≤1mol.%) in the Bi0.8La0.2Fe1-xZrxO3 system has been reported. A mixture of rhombohedral and orthorhombic phases was detected in these conventionally sintered ceramics. Transition from a leaky state to an insulating state was observed upon Zr substitution. This is the first time that a drop in the electrical conductivity as large as 6 orders of magnitude for doping as small as 0.25mol. % in bismuth ferrite systems has been reported. An investigation on the nature of this abrupt transition revealed the dominant role of defects. A proper consideration of possible defect reactions taking place during and after sintering satisfactorily accounts for the observed modulation in the electrical properties. Both AC and DC measurements indicate that, before Zr substitution, ptype hopping conduction prevails with an activation energy as low as ~0.57 eV, whereas the Zr substitution makes oxide ion migration the central mechanism for conduction with the activation energy of ~0.96-1.08 eV. In contrast to that, the magnetic properties of the compounds experience a more subtle effect; a gradual modification of saturation magnetization and coercivity with Zr substitution is observed. Curve fitting of the magnetic hysteresis loops not only allowed extraction of three separate contributions from the magnetic response but also helped to explain the effects of Zr on the magnetic properties. Modifications of structural characteristics and magnetic anisotropy of the samples are believed to be the primary driving force behind the improvement in the magnetic properties. [ABSTRACT FROM AUTHOR]

Flexible materials embedded with hard magnetic particles have recently gained widespread recognition as small-scale actuators due to their capacity to be a rapid and precise shape-shifting material. Strontium ferrite (SrFe12O19) particles have been shown as a great candidate for such applications, since it is an inert hard magnetic material that, in contrast to barium ferrite and neodymium, is also biocompatible. The preparation of such material is done by mixing the magnetic particles into the uncured elastomer (polydimethylsiloxane (PDMS)), in liquid form, and then pouring the mixture in a mold for curing. If the samples are subjected to a magnetic field during the curing process, chains of particles are formed in the direction of the applied field, thus creating an easy axis in this same direction. The magnetic properties of such composite cannot yet be found in literature. In this study, we analyzed three concentrations of strontium ferrite particles in PDMS under three field configurations, resulting in 9 different samples. The concentrations used were 1:1, 2:1, and 4:1 ratios of PDMS to strontium ferrite per weight. All three types of samples were cured either in a zero magnetic field, or over the north pole of a neodymium permanent magnet, or over the side of said magnet. A biaxial vibrating sample magnetometer (VSM) was used to measure hysteresis curves parallel and perpendicular to the curing field. The samples cured in a field show a squareness ratio of up to 0.94 while the samples cured in zero field, only close to 0.5. The samples cured in a field show a magnetic anisotropy with an easy axis parallel to the curing field. Harvesting these modified properties, a mobile robot manufacturing method is proposed that bypasses the need of applying a high intensity magnetic field. [ABSTRACT FROM AUTHOR]

Improvement in magnetic and electrical properties of multiferroic BiFeO3 in conjunction with their dependence on particle size is crucial due to its potential applications in multifunctional miniaturized devices. In this investigation, we report a study on particle size dependent structural, magnetic and electrical properties of sol-gel derived Bi0.9Ba0.1FeO3 nanoparticles of different sizes ranging from ~ 12 to 49 nm. The substitution of Bi by Ba significantly suppresses oxygen vacancies, reduces leakage current density and Fe2+ state. An improvement in both magnetic and electrica properties is observed for 10% Ba-doped BiFeO3 nanoparticles compared to its undoped counterpart. The saturation magnetization of Bi0.9Ba0.1FeO3 nanoparticles increase with reducing particle size in contrast with a decreasing trend of ferroelectric polarization. Moreover, a first order metamagnetic transition is noticed for ~ 49 nm Bi0.9Ba0.1FeO3 nanoparticles which disappeared with decreasing particle size. The observed strong size dependent multiferroic properties are attributed to the complex interaction between vacancy induced crystallographic defects, multiple valence states of Fe, uncompensated surface spins, crystallographic distortion and suppression of spiral spin cycloid of BiFeO3. [ABSTRACT FROM AUTHOR]

FeSiB based soft magnetic flakes (SMFs; ϕ: 63-106 µm, t: 2-5 µm) coated with optimally thick (∼10 nm) SiO2 were fabricated as the potential magnetic material for pressed cores suitable for use in power inductors operating beyond 10 MHz. Such thin SMFs were produced by mechanical ball milling of commercially available thick (∼27 µm) ribbons followed by an optimized sol-gel coating in presence of a silane coupling agent. Milling helped to reduce ribbon thickness below the skin depth to minimize eddy current loss at high frequencies. The effect of milling (medium, duration, rotation speed, and ball-to-powder ratio) and coating conditions on the soft magnetic properties of the SMFs were investigated. An optimally tiny fraction of the milled flakes was allowed to become nanocrystalline, which augments saturation flux density (BS) and permeability (µ) without incurring additional losses. The results from X-Ray photoelectron spectroscopy and magnetization measurement confirm that a stress-releasing post-annealing process reduced coercivity from ∼62 Oe to ∼6 Oe and enhanced the magnetic saturation moment from 126 emu/g to 142 emu/g without affecting the thin yet robust insulating SiO2 layer. [ABSTRACT FROM AUTHOR]

This article highlights the preparation of NiFe2O4 nanoparticles by adopting a sol–gel auto-combustion route. The prime focus of this study is to investigate the impact of γ-irradiation on the microstructural, morphological, functional, optical, and magnetic characteristics. The resulting NiFe2O4 products have been characterized employing numerous instrumental techniques such as Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction (XRD), UV–visible spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), and Physical Properties Measurement System for a variety of γ-ray doses (0, 25, and 100 kGy). FESEM micrographs illustrate the aggregation of ferrite nanoparticles in the pristine NiFe2O4 product having an average particle size of 168 nm, and the surface morphology is altered after exposure to γ-irradiation. XRD spectra have been analyzed employing the Rietveld method, and the results of the XRD investigation reveal the desired phases (cubic spinel phases) of NiFe2O4 with the observation of other transitional phases. The values of the crystallite size are in the range of 34.04–34.71 nm investigated by the Debye–Scherrer (D–S) method. Several microstructural parameters, such as bond length, bond angle, and hopping length, have been determined from the analysis of the Rietveld method. This study reports that γ-irradiations demonstrate a great influence on optical bandgap energy, and it varies from 1.80 to 1.89 eV evaluated via the Kubelka–Munk function. The FTIR measurement depicts a proof for the persistence of Ni–O and Fe–O stretching vibrations within the respective products at positions 365 and 547 cm−1, respectively, thus indicating the successful development of NiFe2O4. The saturation magnetization (MS) of the pristine Ni ferrite product is noticed to be 28.08 emu/g. A considerable increase in MS is observed in the case of low γ-dose (25 kGy), and a decrement nature is disclosed after the result of high dose of γ-irradiation (100 kGy). [ABSTRACT FROM AUTHOR]

Polycrystalline ceramics, Bi1-2xBa2xFe1-xNbxO3 (x = 0.00-0.15), were synthesized by solid state reactions method. X-ray diffraction data have revealed elimination of impurity phases and an increase in unit cell volume with Ba and Nb substitution. Diffraction peak splitting is found to be suppressed which indicates a decrease in octahedral distortion. The Mössbauer spectra demonstrate the suppression of spiral spin modulation of the magnetic moments resulting in enhanced ferromagnetism with increasing dopant concentration. The leakage current density of the sample with x = 0.10 is found to be greatly reduced up to six orders of magnitude as compared to the undoped sample. Ohmic conduction is found to be dominant mechanism in all the samples, however, undoped sample showed space charge limited conduction in high electric filed region, while the sample with x = 0.15 exhibited grain boundary limited conduction in low electric field region. [ABSTRACT FROM AUTHOR]

Materials showing reversible resistance switching between high-resistance state and low-resistance state at room temperature are attractive for today’s semiconductor technology. In this letter, the reproducible hysteresis and resistive switching characteristics of metal-CuxO-metal (M-CuxO-M) heterostructures driven by low voltages are demonstrated. The fabrication of the M-CuxO-M heterostructures is fully compatible with the standard complementary metal-oxide semiconductor process. The hysteresis and resistive switching behavior are discussed. The good retention characteristics are exhibited in the M-CuxO-M heterostructures by the accurate controlling of the preparation parameters. [ABSTRACT FROM AUTHOR]