Search Results (568)

The effects of Cu content on the microstructure, texture, precipitates, and magnetic and mechanical properties of 0.20 mm-thick non-oriented silicon steel (3.0% Si-0.8% Al-0.5% Mn) were systematically investigated using optical microscopy, X-ray diffraction, electron backscatter diffraction, and transmission electron microscopy. The strengthening mechanisms of Cu-bearing high-strength non-oriented silicon steel were further elucidated. Increasing Cu content inhibited grain growth and suppressed the development of the α*-fiber texture in annealed sheets, while promoting the formation of γ-fiber texture. As a result, the P_1.0/400 and B₅₀ values deteriorated. The P_1.0/400 and B₅₀ values of 1.47% Cu non-oriented silicon steel were 13.930 W/kg and 1.614 T, respectively. However, due to the solid solution strengthening effect of 0.5% Cu and partial precipitation strengthening, the R_p0.2 increased by 43 MPa. After aging treatment at 550 °C for 20 min, the P_1.0/400 values of the aged sheets slightly increased, while the B₅₀ values remained almost unchanged. In the aged sheets containing 1.0–1.5% Cu, clustered Cu-rich precipitates with average sizes of 2.71 nm and 13.28 nm were observed. The crystal structure of these precipitates transitioned from the metastable B2-Cu to the stable FCC-Cu. These precipitates enhanced the R_p0.2 of the non-oriented electrical steel to 241 MPa and 269 MPa through cutting and bypass mechanisms, respectively. A high-strength non-oriented silicon steel with balanced magnetic and mechanical properties was developed for driving motors of new energy vehicles by utilizing nanoscale Cu-rich precipitates formed through aging treatment. The optimized steel exhibits a yield strength of 708 MPa, a magnetic induction B₅₀ of 1.639 T, and high-frequency iron loss P_1.0/400 of 14.77 W/kg. Full article

The present study concentrates on the role and underlying mechanisms of in situ crystallization (employed for nanocrystal formation) in influencing the solidification microstructure and properties of aluminum alloys. By systematically analyzing the effects on α-Al refinement, silicon phase modification, and secondary phase control, as well as exploring the impact on room-temperature mechanical properties, high-temperature deformation behavior, and fatigue performance, this work reveals the potential physical mechanisms of improving mechanical properties by providing nucleation sites and inhibiting grain growth, such as fine-grain strengthening and dispersion strengthening. Moreover, stabilization of the second phase optimizes high-temperature deformation behavior, and a reduction in stress concentration improves fatigue performance. Compared with traditional microstructure control methods, in situ crystallization can achieve deeper grain refinement from micron to nanometer scale, ensuring high uniformity of grain distribution and showing good compatibility with existing processes. By defining the regulation of in situ crystallization on the microstructure and properties of aluminum alloy, the existing research provides a feasible material solution for high stress, high temperature, and high reliability. Its core significance lies in breaking through the performance bottlenecks of traditional modification technology, such as unstable refining effect, element segregation, and so on. The co-promotion of “strength–plasticity–stability” of aluminum alloys and the consideration of process compatibility and cost controllability lay a theoretical and technical foundation for the industrialization of high-performance aluminum alloys. Full article

Ice nucleation temperatures and associated ice growth rates are critical parameters in defining the initial ice morphology template, which governs dry layer resistance during sublimation and therefore impacts primary drying kinetics and overall process time. In this study, we developed a through-vial impedance spectroscopy (TVIS) method to determine both ice nucleation temperature and average ice growth rate, from which future estimation of average ice crystal size may be possible. Whereas previous TVIS applications were limited to solutions containing simple, uncharged solutes such as sugars, our adapted approach enables the analysis of conductive solutions (5% sucrose with 0%, 0.26%, and 0.55% NaCl), covering osmolarities below and above isotonicity. We established that the real part capacitance at low and high frequencies—either side of the dielectric relaxation of ice—provides the following: (i) a temperature-sensitive parameter for detecting the onset of ice formation, and (ii) a temperature-insensitive parameter for determining the end of the ice growth phase (unaffected by temperature changes in the frozen solution). This expanded capability demonstrates the potential of TVIS as a process analytical technology (PAT) for non-invasive, in situ monitoring of freezing dynamics in pharmaceutical freeze-drying. Full article

Ascorbic Acid (AA), an important biomolecule present in relatively high concentrations in blood and other biological fluids, has been rarely investigated with reference to its effect on the biological mineralization–demineralization processes. To our knowledge, the present work is one of an extremely limited few found in the literature in which the effect of the presence of AA in mineralizing or demineralizing electrolyte solutions is addressed in a quantitative way. We have used the constant saturation method for the accurate measurement of the rates of crystal growth of hydroxyapatite (HAP, Ca₅(PO₄)₃OH), the model compound of the inorganic component of the hard tissues of higher mammals. It was found that both crystal growth and dissolution were accelerated significantly. The increase in crystal growth rates showed stronger dependence on the solution supersaturation (120% increase for the highest and 460% for the lowest) in the presence of 0.1 mM of AA, pH 7.40, 37 °C, 0.15 M NaCl. The dissolution rate increase was less dependent (average of ca. 300% increase). It was concluded from the detailed characterization of the solid that the acceleration effect was due to the uptake of AA on the HAP surface. Full article

Regulating the crystallization dynamics of perovskite films is key to improving the efficiency and operational stability of (FA_0.83MA_0.17Cs_0.05)Pb(I_0.85Br_0.15)₃ perovskite solar cells (PSCs). However, precise regulation of the crystallization process remains challenging. Here, we introduce a reactive anti-solvent strategy based on the Kornblum reaction to modulate crystallization via in-situ chemical transformation. Specifically, trans-cinnamoyl chloride (TCC) is employed as a single-component anti-solvent additive that reacts with dimethyl sulfoxide (DMSO) in the perovskite precursor solution. The resulting acylation reaction generates carbonyl-containing products and sulfur ions. The carbonyl oxygen coordinates with Pb²⁺ ions to form Pb–O bonds, which retard rapid crystallization, suppress heterogeneous nucleation, and facilitate the growth of larger perovskite grains with improved film uniformity. Additionally, the exothermic nature of the reaction accelerates local supersaturation and nucleation. This synergistic crystallization control significantly enhances the film morphology and device performance, yielding a champion power conversion efficiency (PCE) of 23.02% and a markedly improved fill factor (FF). This work provides a new pathway for anti-solvent engineering through in-situ chemical regulation, enabling efficient and scalable fabrication of high-performance PSCs. Full article

This study introduces novel experimental systems that facilitate the nucleation, growth, aggregation, and agglomeration of ionic salt solutions, leading to structurally and functionally distinctive crystal formations. Through evaporative crystallization in hanging drops—including layered binary solutions—a range of macroscopic agglomerates were produced, such as hollow spheroidal NaCl/NiSO₄ structures, octahedral NaCl films, pentagonally arranged CdSO₄ spherulites, and NH₄Cl dendritic shells. Additionally, NaCl spheroids were used as templates to fabricate carbon-based morphologies and colloidal photonic crystals with convex or concave geometries, which were subsequently analyzed optically. The study reveals that crystallization and self-assembly, whether independently or synergistically applied, can yield complex architectures with potential applications in advanced device manufacturing beyond conventional processing methods. Full article

A novel behavior of fluid inclusions (FIs) in crystals is reported in this study. Typically, at “high” temperature, FIs in molecular crystals become faceted, adopting the morphology of a single crystal. Usually, upon cooling, these faceted FIs develop into rounded cavities containing the mother solution with a retreat gas bubble. After annealing at low temperature, the FIs reshape back into a negative-crystal morphology, but the gas bubble remains. This latter process can take from minutes to very long times depending on the storage temperature and solubility. Investigations into the behavior of FIs of dicumyl peroxide (DCP) under fast cooling rates have revealed a morphological transition from negative crystals to FIs with a holly-leaf shape. The spikes of the holly-leaf-shaped FIs point toward the corners of the former negative crystal, and the sizes of the gas bubbles exceed those of conventional retreat bubbles. Therefore, it is likely that this phenomenon is linked to rapid cooling and an excess of CO₂ dissolved in the mother solution from which the DCP single crystals were grown. The concentration of the solution inside the FIs rapidly increases after the nucleation of this large gas bubble. This is consistent with a sharp acceleration of inward crystal growth immediately after its appearance. Interestingly, FIs in pyroclastic olivine crystals grown from CO₂-rich lava can also present a holly-leaf shape. Thus, this non-equilibrium morphological transition may be relatively common. Full article

This paper presents the preparation of Z-cut near-stoichiometric lithium niobate (NSLN) wafers using a combined process of the lithium-rich Czochralski growth and diffusion methods. The fabricated Z-cut NSLN wafers exhibited outstanding comprehensive performance, including a high Curie temperature of up to 1200 °C, a refractive index gradient in the diameter direction below 1.5 × 10⁻⁴ cm⁻¹, and a UV absorption edge shifted 14 nm toward the ultraviolet region compared to congruent lithium niobate crystals, with a coercive field of 1268 V/mm. Additionally, the wafers demonstrated excellent processing characteristics, with the bow of 4-inch wafers controlled within 55 μm, surpassing the machining standards of traditional lithium niobate wafers of the same size. These results indicated the highly uniform chemical stoichiometry and crystallization quality of the wafers. Leveraging the high uniformity and low coercive field of the wafers, periodic triangular domain structure arrays were successfully fabricated, laying the foundation for domain engineering design in electro-optic deflectors and switching devices. This study not only achieves the scalable preparation of NSLN wafers but also provides a reliable technical solution for their practical applications in high-performance electro-optic devices. Full article

In this work, ZnO nanorods were grown on vertically aligned and randomly aligned silica nanosprings using the hydrothermal method. The initial step was the deposition of a ZnO seed layer by atomic layer deposition to promote nucleation. For hydrothermal growth, equimolar (0.2 M) solutions of Zinc nitrate hexahydrate and hexamethylene tetraamine prepared in DI water were used. The ZnO NR grown on the VANS were flower-like clusters, while for the RANS, the ZnO NR grew radially outward from the individual nanosprings. The lengths and diameters of ZnO NR grown on VANS and RANS were 175 and 650 nm, and 35 and 250 nm, respectively. Scanning electron microscopy confirmed the formation of ZnO nanorods, while X-ray diffraction and Raman spectroscopy verified that they have a hexagonal wurtzite crystal structure with preferential growth along the c-axis. X-ray photoelectron spectroscopy, in conjunction with in vacuo annealing, was used to examine the surface electronic structure of ZnO nanorods and defect healing. Photoluminescence of the ZnO nanorods indicates high crystal quality, as inferred from the weak defect band relative to strong excitonic band edge emission. Full article

We calculate the Doniach phase diagram of heavy-fermion systems containing Ce and Eu ions, using the scaling solution of the periodic Anderson model, and compare the results with the experimental data on CeRu₂Ge₂ and EuCu₂(Ge_1−xSi_x)₂. The temperature–pressure (T–p) phase diagram emerges from the competition between the pressure-dependent Kondo interaction and the temperature- and pressure-dependent RKKY interaction. Both are derived using scaling equations in the presence of crystal-field effects: Kondo temperature $T_K$ is related to the coupling constant g(p), where p is the control parameter, and the temperature-dependent renormalized coupling $g(T,T_K(g))$. For comparison with the experiment, we assume a linear dependence of g on the control parameter, which could be pressure or composition. The Néel temperature $T_N(p)$ is obtained by comparing the free energies of the system in the antiferromagnetic and paramagnetic states. The resulting asymmetric $T_N(p)$ arises naturally from the exponential growth of $T_K(p)$ and a much slower polynomial growth of the RKKY interaction. Phase diagrams for CeRu₂Ge₂ and EuCu₂(Ge_1−xSi_x)₂ successfully capture key experimental features: pressure-induced suppression of magnetic order, the peak of RKKY interaction energy, and crossover to a heavy-Fermi-liquid regime at high coupling strength. Our work provides the first quantitative, material-specific construction of Doniach diagrams, clarifies the entropy removal at low temperatures and offers predictive insight for future experiments under extreme conditions. Full article

Crystalline products with a narrow and uniform distribution of crystals by size (CSD), characterized by a desired average size, are necessary in many practices. Therefore, extensive, but mostly experimental, research is devoted to the problem of obtaining such CSDs. Alternatively, this manuscript presents a theoretical approach for calculating CSD resulting from crystallization in unstirred solutions. First, classical equations for the rates of diffusion-controlled and kinetically controlled growth of crystals are used to discuss the size-dependent growth of the nucleated crystals and the initial CSD (which arises from the non-simultaneous nucleation of crystals). Then, applying the law of conservation of matter, it is proved that the CSD continues to expand during the growth stage. Furthermore, it is substantiated that, due to their uneven spatial distribution, crystals of the same size can grow at different rates. This depends on whether the crystals are outside the diffusion fields of other crystals or are clustered together in “nests”. Moreover, by calculating the growth rates of crystals in “nests”, an explanation is given for the observation that closely spaced crystals are smaller in size than the separately growing crystals. Finally, the CSD established during the Ostwald ripening is discussed quantitatively, step-by-step. Full article

Salbutamol sulfate is a selective β2-receptor agonist used to treat asthma and chronic obstructive pulmonary disease. The crystals of salbutamol sulfate usually appear as needles with a relatively large aspect ratio, showing poor powder properties. In this study, spherical particles of salbutamol sulfate were obtained via antisolvent crystallization. Four different antisolvents, including ethanol, n-propanol, n-butanol, and sec-butanol, were selected, and their effects on crystal form and morphology were compared. Notably, a new solvate of salbutamol sulfate with sec-butanol has been obtained. The novel crystal form was characterized by single-crystal X-ray diffraction, revealing a 1:1 stoichiometric ratio between solvent and salbutamol sulfate in the crystal lattice. In addition, the effects of crystallization temperature, solute concentration, ratio of antisolvent to solvent, feeding rate, and stirring rate on the morphology of spherical particles were investigated in different antisolvents. We have found that crystals grown from the n-butanol–water system at optimal conditions (25 °C, antisolvent/solvent ratio of 9:1, and drug concentration of 0.2 g·mL⁻¹) could be developed into compact and uniform spherulites. The morphological evolution process was also monitored, and the results indicated a spherulitic growth pattern, in which sheaves of plate-like crystals gradually branched into a fully developed spherulite. This work paves a feasible way to develop new crystal forms and prepare spherical particles of pharmaceuticals. Full article

This study presents a comprehensive case analysis of pyrite-hosted solid inclusions and their metallogenic significance in the Bainaimiao porphyry Cu deposit in NE China, which is genetically linked to the early Silurian granodiorite intrusion and porphyry dykes. Solid inclusions in pyrite from the deposit’s southern ore belt were analyzed across distinct mineralization stages. Using Electron Probe Micro-Analysis (EPMA) and in situ sulfur isotope analysis (MC-ICP-MS), inclusion assemblages in pyrite were identified, including pyrrhotite-chalcopyrite solid solutions, biotite, and dolomite. The results demonstrate that these inclusions primarily formed through coprecipitation with pyrite during crystal growth. Early-stage mineralizing fluids exhibited extreme temperatures exceeding 700 °C, coupled with low oxygen fugacity (fO₂) and low sulfur fugacity (fS₂). Sulfur isotope compositions (δ³⁴S: −5.85 to −4.97‰) indicate a dominant mantle-derived magmatic sulfur source, with contributions from reduced sulfur in sedimentary rocks. Combined with regional geological evolution, the Bainaimiao deposit is classified as a porphyry-type deposit. Its ore-forming materials were partially derived from Mesoproterozoic submarine volcanic exhalative sedimentary source beds, which were later modified and enriched by granodiorite porphyry magmatism. Full article

The emergence of antimicrobial resistance and the increasing demand for a healthier lifestyle have set new goals for science and industry. In the search for new, more effective, and environmentally friendly antimicrobial agents, special attention is being paid to natural resources. In this regard, essential oils derived from plants, which are widely used in the cosmetic, food, and pharmaceutical industries, are one of the solutions. In view of the above, this study aims to investigate the biological effects of Abies alba essential oil (AAEO). The chemical profile of AAEO was evaluated by GC/MS analysis, which revealed a high abundance of limonene (52.2%) and α-pinene (36.2%). Antioxidant activity evaluation showed a higher potential of AAEO in scavenging ABTS radical species with an IC₅₀ value of 1.18 ± 0.05 mg/mL. In vitro antimicrobial activity was determined by disc diffusion and minimum inhibitory concentration assays and showed that AAEO was more efficient in inhibiting the growth of G⁺ bacterial species. On contrary, in situ evaluations of antimicrobial effects of AAEO on different food models (strawberry, kiwi, white radish, and beetroot) resulted in more efficient suppression of G⁻ bacterial species. Although AAEO showed low effects on yeasts determined by in vitro methods, in situ investigations showed its higher potential in eradication of Candida yeast. The antibiofilm properties of the AAEO matrix were determined by means of crystal violet assay and MALDI-TOF MS Biotyper analysis against biofilm-forming Salmonella enterica. The analysis performed led to the conclusion that AAEO, when applied prior to biofilm formation, may contribute to the removal of planktonic cells and alter the abiotic surface, thereby reducing the suitability of Salmonella enterica for microbial attachment. Full article

As a contactless physical field, a steady magnetic field (SMF) is capable of acting on substances, which leads to changes in physical and/or chemical properties and to further influencing thermodynamic and kinetic behaviors at macroscopic, mesoscopic, and microscopic scales. The application of the SMF to material science has evolved into an important interdisciplinary field—the Electromagnetic Processing of Materials (EPM). Therein, the implementation of the SMF for the solidification of metals and alloys has been increasingly given attention. The SMF was found to regulate nucleation, crystal growth, the distribution of solutes and structure morphology during alloy solidification via various magnetic effects, such as magnetic damping, the thermoelectric magnetic effect, magnetic orientation and magnetically controlled diffusion. In this review, we briefly summarize the main SMF effects and review recent progress in magnetic field-assisted solidification processing, including nucleation, dendritic growth, solute segregation and interfacial phenomena. Finally, future perspectives regarding controlling alloys’ solidification using an SMF are discussed. Full article