Thermal Stability and Non-Linear Optical and Dielectric Properties of Lead-Free K0.5Bi0.5TiO3 Ceramics.

Lead-free K0.5Bi0.5TiO3 (KBT) ceramics with high density (~5.36 g/cm3, 90% of X-ray density) and compositional purity (up to 90%) were synthesized using a solid-state reaction method. Strongly condensed KBT ceramics revealed homogenous local microstructures. TG/DSC (Thermogravimetry-differential scanning calorimetry) techniques characterized the thermal and structural stability of KBT. High mass stability (>0.4%) has proven no KBT thermal decomposition or other phase precipitation up to 1000 °C except for the co-existing K2Ti6O13 impurity. A strong influence of crystallites size and sintering conditions on improved dielectric and non-linear optical properties was reported. A significant increase (more than twice) in dielectric permittivity (εR), substantial for potential applications, was found in the KBT-24h specimen with extensive milling time. Moreover, it was observed that the second harmonic generation (λSHG = 532 nm) was activated at remarkably low fundamental beam intensity. Finally, spectroscopic experiments (Fourier transform Raman and far-infrared spectroscopy (FT-IR)) were supported by DFT (Density functional theory) calculations with a 2 × 2 × 2 supercell (P42mc symmetry and C4v point group). Moreover, the energy band gap was calculated (Eg = 2.46 eV), and a strong hybridization of the O-2p and Ti-3d orbitals at Eg explained the nature of band-gap transition (Γ â†’ Γ).

Mechanical Properties of Nano-Crystalline Glass-Carbomer Cements Used in Dentistry.

The main aim of this study was to assess the impact of the environment on the mechanical and tribological properties of glass-carbomer cements used in dentistry. The properties of the Glass Cements Polyalkene (GCP) Glass Fill material, belonging to glass-polyalkene cements, were tested after placing it in various environments: air, distilled water, artificial saliva simulating a neutral environment (pH = 7), and simulating inflammation (pH = 4). The research material included four samples and a two-year reference material. The analysis of volumetric consumption and the assessment of the impact of solubility on the stability of glass-carbomer cements were carried out using tribological measurements and Vickers hardness measurements. In addition, microstructural characterization of the materials was performed using scanning electron microscopy (SEM). It was observed that the lowest wear (0.04%), the most stable microstructure, and the lowest average hardness (21.52 HV 0.1) were exhibited by the material stored in artificial saliva simulating a neutral environment (pH = 7). The least stable microstructure and statistically the highest hardness (77.3 HV 0.1) was observed in the test sample, which was stored in air for two years and then in distilled water. The highest consumption (0.11%) was recorded in the case of cement placed in artificial saliva simulating inflammation (pH = 4). The results obtained in this study indicate specific trends in the influence of the environment in which the tested cement is located, such as air, distilled water, air/distilled water, artificial saliva simulating a neutral environment, and simulating inflammation, on its structure, hardness, and wear.

Magnetic and Electrical Properties of CuCr2Se4 Nanoparticles.

CuCr2Se4 nanoparticles were obtained by the high-energy ball milling of CuCr2Se4 single crystals, which had a size of approximately 32 nm after 5 h of milling. Structural, magnetic, and electrical studies have shown that a reduction in CuCr2Se4 single crystals to the nanosize leads to (1) a weakening of ferromagnetic interactions, both long and short range, (2) a lack of saturation of magnetization at 5 K and 70 kOe, (3) a change in the nature of electrical conductivity from metallic to semiconductor, and (4) a reduction in the thermoelectric power factor S2σ by an order of magnitude of 400 K. The above results were considered in terms of the parameters of the band model, derived from the high-temperature expansion of magnetic susceptibility and from the diffusive component of thermoelectric power. Theoretical calculations showed a significant weakening of both the superexchange and double exchange mechanisms, a reduction in the [Cr3+,Cr4+] band width from 0.76 to 0.19 eV, and comparable values of the Fermi energy and the activation energy (0.46 eV) in the intrinsic region of electrical conductivity. The main advantage of high-energy ball milling is the ability to modify the physicochemical properties of already existing compounds for desired applications.

Hybrid Mesoporous TiO2/ZnO Electron Transport Layer for Efficient Perovskite Solar Cell.

In recent years, perovskite solar cells (PSCs) have gained major attention as potentially useful photovoltaic technology due to their ever-increasing power-conversion efficiency (PCE). The efficiency of PSCs depends strongly on the type of materials selected as the electron transport layer (ETL). TiO2 is the most widely used electron transport material for the n-i-p structure of PSCs. Nevertheless, ZnO is a promising candidate owing to its high transparency, suitable energy band structure, and high electron mobility. In this investigation, hybrid mesoporous TiO2/ZnO ETL was fabricated for a perovskite solar cell composed of FTO-coated glass/compact TiO2/mesoporous ETL/FAPbI3/2D perovskite/Spiro-OMeTAD/Au. The influence of ZnO nanostructures with different percentage weight contents on the photovoltaic performance was investigated. It was found that the addition of ZnO had no significant effect on the surface topography, structure, and optical properties of the hybrid mesoporous electron-transport layer but strongly affected the electrical properties of PSCs. The best efficiency rate of 18.24% has been obtained for PSCs with 2 wt.% ZnO.

Characteristics of Mg-Based Sintered Alloy with Au Addition.

The magnesium-based alloys produced by mechanical alloying (MA) are characterized by specific porosity, fine-grained structure, and isotropic properties. In addition, alloys containing magnesium, zinc, calcium, and the noble element gold are biocompatible, so they can be used for biomedical implants. The paper assesses selected mechanical properties and the structure of the Mg63Zn30Ca4Au3 as a potential biodegradable biomaterial. The alloy was produced by mechanical synthesis with a milling time of 13 h, and sintered via spark-plasma sintering (SPS) carried out at a temperature of 350 °C and a compaction pressure of 50 MPa, with a holding time of 4 min and a heating rate of 50 °C∙min-1 to 300 °C and 25 °C∙min-1 from 300 to 350 °C. The article presents the results of the X-ray diffraction (XRD) method, density, scanning electron microscopy (SEM), particle size distributions, and Vickers microhardness and electrochemical properties via electrochemical impedance spectroscopy (EIS) and potentiodynamic immersion testing. The obtained results reveal the compressive strength of 216 MPa and Young's modulus of 2530 MPa. The structure comprises MgZn2 and Mg3Au phases formed during the mechanical synthesis, and Mg7Zn3 that has been formed during the sintering process. Although MgZn2 and Mg7Zn3 improve the corrosion resistance of the Mg-based alloys, it has been revealed that the double layer formed because of contact with the Ringer's solution is not an effective barrier; hence, more data and optimization are necessary.

Magnetization Processes in Metallic Glass Based on Iron of FeSiB Type.

In the present paper, the magnetization processes in amorphous alloys based on iron are discussed in detail. Our main goal was to measure the stabilization energy connected with the presence of microvoids (frozen during rapid cooling from the liquid phase) and to determine the interaction energy of relaxators with spontaneous magnetization vector (the so-called wN Neel) for amorphous Fe78Si13B9 alloys. A structural analysis of the alloys using X-ray measurements at the subsequent stages of crystallization was also performed.

Influence of Milling Time on Phase Composition and Product Structure of Mg-Zn-Ca-Ag Alloys Obtained by Mechanical Synthesis.

Magnesium-based alloys are widely used in the construction of automotive, aviation, and medical applications. The solutions presently used for the production of biodegradable materials are characterized by considerable energy consumption and limitations resulting from the use of different devices and technologies. The proposed material is easier to manufacture due to mechanical alloying (MA). Thanks to the MA process, it is possible to carefully tailor the desired chemical composition and microstructure. There are many parameters that can be modified during synthesis in order to obtain an alloy with the desired microstructure and specific expected alloy properties. The duration of grinding of the alloy, the size and number of balls, and the protective atmosphere have a great influence on the process of mechanical alloying and the properties of the obtained products. So, the aim of this work was to determine the influence of milling time on the phase composition and structure of Mg-based alloy synthesis products. The tested samples were milled for 5, 8, 13, 20, 30, 50, and 70 h. X-ray diffraction analysis (XRD) and scanning electron microscopy studies (SEM) with energy-dispersive spectroscopy (EDS) were performed to obtain the powder morphology and chemical composition of Mg66-xZn30Ca4Agx (where x = 1, 2) powders. Structure characterization based on the Rietveld refinement and crystallite size determination based on the Williamson-Hall theory of milling products were also carried out.

Characteristics of the Mg-Zn-Ca-Gd Alloy after Mechanical Alloying.

Magnesium-based materials are interesting alternatives for medical implants, as they have promising mechanical and biological properties. Thanks to them, it is possible to create biodegradable materials for medical application, which would reduce both costs and time of treatment. Magnesium as the sole material, however, it is not enough to support this function. It is important to determine proper alloying elements and methods. A viable method for creating such alloys is mechanical alloying, which can be used to design the structure and properties for proper roles. Mechanical alloying is highly influenced by the milling time of the alloy, as the time of the process affects many properties of the milled powders. X-ray diffraction (XRD) and scanning electron microscopy (SEM) with energy-dispersive spectroscopy (EDS) were carried out to study the powder morphology and chemical composition of Mg65Zn30Ca4Gd1 powders. Moreover, the powder size was assessed by granulometric method and the Vickers hardness test was used for microhardness testing. The samples were milled for 6 min, 13, 20, 30, 40, and 70 h. The hardness correlated with the particle size of the samples. After 30 h of milling time, the average value of hardness was equal to 168 HV and it was lower after 13 (333 HV), 20 (273 HV), 40 (329 HV), and 70 (314 HV) h. The powder particles average size increased after 13 (31 µm) h of milling time, up to 30 (45-49 µm) hours, and then sharply decreased after 40 (28 µm) and 70 (12 µm) h.

Influence of Crystallite Size on the Magnetic Order in Semiconducting ZnCr2Se4 Nanoparticles.

Structural, electrical, magnetic, and specific heat measurements were carried out on ZnCr2Se4 single crystal and on nanocrystals obtained from the milling of this single crystal after 1, 3, and 5 h, whose crystallite sizes were 25.2, 2.5, and 2 nm, respectively. For this purpose, the high-energy ball-milling method was used. The above studies showed that all samples have a spinel structure, and are p-type semiconductors with less milling time and n-type with a higher one. In turn, the decrease in crystallite size caused a change in the magnetic order, from antiferromagnetic for bulk material and nanocrystals after 1 and 3 h of milling to spin-glass with the freezing temperature Tf = 20 K for the sample after 5 h of milling. The spin-glass behavior for this sample was derived from a broad peak of dc magnetic susceptibility, a splitting of the zero-field-cooling and field-cooling susceptibilities, and from the shift of Tf towards the higher frequency of the ac susceptibility curves. A spectacular result for this sample is also the lack of a peak on the specific heat curve, suggesting a disappearance of the structural transition that is observed for the bulk single crystal.