Search Results (143)

This paper presents the results of a comprehensive study of the structure, phase composition, thermal corrosion, and tribological properties of multilayer gradient coatings based on YSZ/NiCrAlY obtained using detonation spraying. X-ray phase analysis showed that the coatings consist entirely of metastable tetragonal zirconium dioxide (t’-ZrO₂) phase stabilized by high temperature and rapid cooling during spraying. SEM analysis confirmed the multilayer gradient phase distribution and high density of the structure. Wear resistance, optical profilometry, wear quantification, and coefficient of friction measurements were used to evaluate the operational stability. The results confirm that the structural parameters of the coating, such as porosity and phase gradient, play a key role in improving its resistance to thermal corrosion and CMAS melt, which makes such coatings promising for use in high-temperature applications. It is shown that a dense and thick coating effectively prevents the penetration of aggressive media, providing a high barrier effect and minimal structural damage. Tribological tests in the temperature range from 21 °C to 650 °C revealed that the best characteristics are observed at 550 °C: minimum coefficient of friction (0.63) and high stability in the stage of stable wear. At room temperature and at 650 °C, there is an increase in wear due to the absence or destabilization of the protective layer. Full article

High-Cu-content (Cu-content > 1.3 at.%) nanocrystalline alloys exhibit wide heat-treatment windows and favorable soft magnetic properties due to the presence of pre-existing α-Fe nanocrystals. By fabricating ribbons with varying thicknesses to tailor cooling rates, distinct structural characteristics were achieved in Fe₈₂B_16.5Cu_1.5 alloy ribbons. Notably, the face-centered cubic (fcc) γ-Fe phase was identified in Fe-based nanocrystalline alloys. The precipitation of the fcc γ-Fe phase originates from a phase-selection mechanism under specific cooling conditions, while its retention in the as-quenched ribbon with a thickness of 27 μm is attributed to kinetic suppression during rapid cooling and the nanoscale stabilization effect. The formation of the fcc γ-Fe phase significantly reduced the saturation flux density (B_s) and increased coercivity (H_c), concurrently destabilizing the residual amorphous matrix. By suppressing the precipitation of the γ-Fe and Fe₃B phases through precise control of ribbon thickness and annealing parameters, the alloy ribbon with a thickness of 16 μm achieved an optimal combination of B_s (1.82 T) and H_c (8.3 A/m). These findings on anomalous fcc γ-Fe phase precipitation provide novel insights into metastable phase engineering and offer structural design guidelines for alloys containing pre-existing α-Fe nanocrystals. Full article

The performance degradation of sodium-ion batteries (SIBs) in extremely low-temperature conditions has faced significant challenges for energy storage applications in extreme environments. This review systematically establishes failure mechanisms that govern the performance of low-temperature SIBs, including significantly increased electrolyte viscosity, lattice distortion and adverse phase transitions in electrodes, and sluggish desolvation kinetics at the solid electrolyte interface. Herein, we specifically summarize a series of multi-scale optimization strategies to address these low-temperature challenges: (1) optimizing low-freezing-point solvent components and regulating solvation structures to increase ionic diffusion conductivity; (2) enhancing the hierarchical structure of electrodes and optimizing electron distribution density to improve structural stability and capacity retention at low temperatures; and (3) constructing an inorganic-rich solid electrolyte interphase to induce uniform ion deposition, reduce the desolvation barrier, and inhibit side reactions. This review provides a comprehensive overview of low-temperature SIB applications coupled with advanced characterization and first-principles simulations. Furthermore, we highlight solvation-shell dynamics, charge transfer kinetics, and metastable-phase evolution at the atomic scale, along with the critical pathways for overcoming low-temperature limitations. This review aims to establish fundamental principles and technological guidelines for deploying advanced SIBs in extreme low-temperature environments. Full article

The structural integrity of viral envelopes is a critical determinant of infectivity for enveloped viruses, directly influencing vector stability, functional accuracy of surface-displayed epitopes, and preservation of native conformational states required for membrane protein studies. However, conventional purification methods often disrupt envelope integrity and cause envelope proteins to lose their activity. Here, we systematically compared discontinuous, continuous, and optimized continuous sucrose density gradient centrifugation protocols for purifying Autographa californica multiple nucleopolyhedrovirus (AcMNPV). Through cryo-EM, we demonstrated that our optimized continuous sucrose gradient protocol significantly increased the proportion of AcMNPV budded virions with intact envelopes from 36% to 81%, while preserving the metastable prefusion conformation of the fusion protein GP64. This advancement should prove useful for structural studies of viral envelope proteins and may enhance applications in gene therapy and vaccine development utilizing enveloped viruses. Full article

Hydrogen embrittlement is a critical issue for zirconium alloys, which receives long-term attention in their applications. The formation of brittle hydrides facilitates crack initiation and propagation, thereby significantly reducing the material’s ductility. This study investigates the tensile properties and hydride morphology of a novel zirconium alloy under different hydrogen-charging current densities ranging from 0 to 300 mA/cm², aiming to clarify the influence of hydrides on the fracture behavior of the alloy. The mechanical property results reveal that, as the hydrogen-charging current density increases from 0 to 100 mA/cm², the maximal elongation decreases from 24.99% to 21.87%. When the current density is further increased from 100 mA/cm² to 200 mA/cm², the maximal elongation remains basically unchanged. However, a substantial drop in elongation is observed as the hydrogen-charging current density rises from 200 mA/cm² to 300 mA/cm², decreasing from 20.77% to 15.18%, which indicates a marked deterioration in hydrogen embrittlement resistance. Subsequently, phase compositions, fracture morphology, and hydride types in the fracture region of tensile specimens were characterized. The morphology and quantity of hydrides change with increasing hydrogen-charging current density. When the hydrogen-charging current density reaches 100 mA/cm², the δ-phase hydrides form, which significantly reduces the ductility of the zirconium alloy. At a hydrogen-charging current density of 200 mA/cm², metastable ζ-phase hydrides are formed, resulting in negligible variations in the alloy’s mechanical properties. However, when it comes to 300 mA/cm², stable δ-phase hydrides with diverse morphologies form, leading to a pronounced degradation in tensile performance. Finally, by integrating mechanical tests with microstructural characterization, the influence of hydrides formed under different hydrogen-charging current densities on the zirconium alloy was analyzed. With increasing hydrogen-charging current density, the maximal elongation of the specimens gradually decreases, while the tensile strength steadily increases. At a hydrogen-charging current density of 300 mA/cm², a larger amount of hydrides is formed, and the hydride type transitions completely from a mixture of δ-phase and ζ-phase hydrides to entirely δ-phase hydrides. The formation of lath-like δ-phase hydrides induces twinning structures, resulting in further lattice mismatch, which significantly reduces the maximal elongation of the zirconium alloy. Additionally, the morphology of the δ-phase hydrides changes from slender needle-like structures to lath-like structures, leading to a notable increase in internal stress, which in turn further enhances the tensile strength of the specimens. Full article

Fe₂B is a potentially promising electrocatalyst for the oxygen evolution reaction (OER) due to its excellent electronic conductivity, which is superior to that of traditional oxide catalysts. However, the activity of Fe₂B is still not satisfactory. In this study, meta-stable microstructure stacking faults (SFs) were incorporated into Fe₂B through a one-step high-pressure and high-temperature (HPHT) method. Pressure suppressed atomic diffusion but formed SFs when the grain grew. Fe₂B with SFs exhibited remarkable OER activity, with low overpotential values of only 269 and 344 mV required to reach current densities of 10 and 100 mA cm⁻², respectively; because of the presence of SFs, the overpotential for the OER was reduced to only 67.7% of that of Fe₂B without SFs at 10 mA cm⁻². Theoretical and experimental investigations confirmed that these SFs regulate the d-band center of Fe₂B toward the Fermi level, optimizing the catalytic site activity. Furthermore, SFs reduced the charge transfer between Fe atoms and boron (B) atoms, increasing the number of free electrons in the structure and thereby increasing conductivity. Finally, this study suggests a strategy to construct microstructures in crystals, providing new insights into designing excellent catalysts via microstructure engineering. Full article

Lithium carbonate is an important material in the lithium battery. The materials can be obtained from a reactive crystallization process. To prepare the higher-quality crystals, such as purity, crystal size distribution, and desired morphology, it needs to be controlled effectively in the crystallization process. Therefore, a study of crystallization kinetics was required. Here, the metastable region was explored first. Subsequently, a LiCl-K₂CO₃-H₂O reaction system in a continuous stirred-tank crystallizer with controlling pH was used to study the crystallization kinetics, such as nucleation rate (B⁰), agglomeration kernel (β), and crystal growth rate (G), which can be determined with measured crystal size distribution at a steady-state condition using an agglomeration population balance model. The process variables include lithium chloride solution flow rate, potassium carbonate solution flow rate, and stirring speed. The results show that B⁰, β, and G were in the range of 3.47 × 10⁹–5.98 × 10¹² no/m³·s, 1.78 × 10⁻¹⁹–1.20 × 10⁻¹² m³-slurry/no·s, and 3.00 × 10⁻¹¹–2.11 × 10⁻¹⁰ m/s, respectively, depending on the operating conditions. All relative supersaturations were in the range of 1.22–2.04. In addition, the crystal size observed was found to be in the range of 1.28–32.7 μm, with irregular platelet forms in most cases. In addition, more slurry density can be obtained at the feed rate of 40 mL/min. A linear regression for crystallization kinetics was also discussed in this work. Finally, this process demonstrated that the recycling of lithium was possible for a circular economy. Therefore, the result can be used as a reference for larger-scale operations in industry. Full article

Single crystals of the new modification of copper pyrovanadate, δ-Cu₂V₂O₇, were prepared using the chemical vapor transport reaction method. The crystal structure (monoclinic, P2₁/n, a = 5.0679(3), b = 11.4222(7), c = 9.4462(6) Å, β = 97.100(6)°, V = 542.61(6) ų, Z = 4) was solved by direct methods and refined to R₁ = 0.029 for 1818 independent observed reflections. The crystal structure contains two Cu sites: the Cu1 site in [4 + 2]-octahedral coordination and the Cu2 site in [4 + 1]-tetragonal pyramidal coordination. There are two V⁵⁺ sites, both tetrahedrally coordinated by O atoms. Two adjacent V1O₄ and V2O₄ tetrahedra share the O4 atom to form a V₂O₇ dimer. The crystal structure of δ-Cu₂V₂O₇ can be described as based upon layers of V₂O₇ dimers of tetrahedra parallel to the (001) plane and interlined by chains of the edge-sharing Cu1O₆ and Cu2O₅ polyhedra running parallel to the a axis and arranged in the layers parallel to the (001) plane. The crystal chemical analysis of the three other known Cu₂V₂O₇ polymorphs indicates that, by analogy with δ-Cu₂V₂O₇, they are based upon layers of V₂O₇ groups interlinked by layers consisting of chains of CuO_n coordination polyhedra (n = 5, 6). The crystal structures of the Cu₂V₂O₇ polymorphs can be classified according to the mutual relations between the Cu-O chains, on the one hand, and the V₂O₇ groups, on the other hand. The analysis of the literature data and physical density values suggests that, at ambient pressure, α- and β-Cu₂V₂O₇ are the low- and high-temperature polymorphs, respectively, with the phase transition point at 706–710 °C. The β-phase (ziesite) may form metastably under temperatures below 560 °C and, under heating, transform into the stable α-phase (blossite) at 605 °C. The δ- and γ-polymorphs have the highest densities and most probably are the high-pressure phases. The structural complexity relations among the polymorphs correspond to the sequence α = β < γ < δ; i.e., the δ phase described herein possesses the highest complexity, which supports the hypothesis about its stability under high-pressure conditions. Full article

Gallium nitride (GaN) semiconductors and their broadband InGaN alloys in their hexagonal phase have been extensively studied over the past 30 years and have allowed the development of blue-ray lasers, which are essential disruptive developments. In addition to high-efficiency white light-emitting diodes, which have revolutionized lighting technologies and generated a great industry around these semiconductors, several transistors have been developed that take advantage of the characteristics of these semiconductors. These include power transistors for high-frequency applications and high-power transistors for power electronics, among other devices, which have far superior achievements. However, less effort has been devoted to studying GaN and InGaN alloys grown in the cubic phase. The metastable or cubic phase of III-N alloys has superior characteristics compared to the hexagonal phase, mainly because of the excellent symmetry. It can be used to improve lighting technologies and develop other devices. Indium gallium nitride, In_xGa_1−xN alloy, has a variable band interval of 0.7 to 3.4 eV that covers almost the entire solar spectrum, making it a suitable material for increasing the efficiencies of photovoltaic devices. In this study, we successfully synthesized high-quality cubic InGaN films on MgO (100) substrates using plasma-assisted molecular beam epitaxy (PAMBE), demonstrating tunable emissions across the visible spectrum by varying the indium concentration. We significantly reduced the defect density and enhanced the crystalline quality by using an intermediate cubic GaN buffer layer. We not only developed a heterostructure with four GaN/InGaN/GaN quantum wells, achieving violet, blue, yellow, and red emissions, but also highlighted the immense potential of cubic InGaN films for high-efficiency light-emitting diodes and photovoltaic devices. Achieving better p-type doping levels is crucial for realizing diodes with excellent performance, and our findings will pave the way for this advancement. Full article

This article studies the influence of solid-phase (type 1 samples) and melt-quenching (type 2 samples) technological modes of obtaining Na₃Fe₂(PO₄)₃ polycrystals on their structures and ion-conducting properties. α-Na₃Fe₂(PO₄)₃ polycrystals of the 1st type are formed predominantly under an isothermal firing regime, and the synthesis of the 2nd type is carried out under sharp temperature gradient conditions, contributing to the formation of glassy precursors possessing a reactive and deformed structure, in which the crystallization of crystallites occurs faster than in precursors obtained under isothermal firing. The elemental composition of α-Na₃Fe₂(PO₄)₃ type 2 polycrystals is maintained within the normal range despite the sharp non-equilibrium thermodynamic conditions of synthesis. The microstructure of the type 1 Na₃Fe₂(PO₄)₃ polycrystals is dominated by chaotically arranged crystallites of medium (7–10 μm) and large (15–35 μm) sizes, while the polycrystals of type 2 are characterized by the preferential formation of small (3–4 μm) and medium (7–10 μm) crystallites, causing uniaxial deformations in their structure, which contribute to a partial increase in their symmetry. The advantage of type 2 polycrystals is that they have higher density and conductivity and are synthesized faster than type 1 samples by a factor of 4. The article also considers the issues of crystallization in a solid-phase precursor from the classical point of view, i.e., the process of the formation of small solid-phase nuclei in the metastable phase and their growth to large particles due to association with small crystallites using phase transitions. Possible variants and models of crystallite growth in Na₃Fe₂(PO₄)₃ polycrystals, as well as distinctive features of crystallization between two types of samples, are discussed. Full article

A systematic study was conducted on the influence of silicon on the microstructure, stress distribution, and martensitic nucleation and transformation of 301 metastable austenitic stainless steel during cold-rolling deformation. When the deformation amount of conventional 301 stainless steel is ≤20%, the amount of martensite transformation is very small. When the deformation amount is ≥30%, the amount of martensite transformation significantly increases. The introduction of Si significantly improves the amount of martensite transformation and the uniformity of deformation. 301Si-H has a significantly higher amount of martensite in the same deformation microstructure than conventional 301Si-L with a lower silicon content. Increasing the Si content decreases the stacking fault energy of 301 stainless steel. During deformation, Si tends to cluster at the grain boundaries, reducing stacking fault width and increasing dislocation density, creating sites for shear martensite nucleation at the grain boundaries. Simultaneously, significant deformation encourages the formation of deformation twins and facilitates martensite nucleation. Full article

The car-following model (CFM) utilizes intelligent transportation systems to gather comprehensive vehicle travel information, enabling an accurate description of vehicle driving behavior. This offers valuable insights for designing autonomous vehicles and making control decisions. A novel extended CFM (ECFM) is proposed to accurately characterize the micro car-following behavior in traffic flow, expanding the stable region and improving anti-interference capabilities. Linear stability analysis of the ECFM using perturbation methods is conducted to determine its stable conditions. The reductive perturbation method is used to comprehensively describe the nonlinear characteristics of traffic flow by solving the triangular shock wave solution, described by the Burgers equation, in the stable region, the solitary wave solution, described by the Korteweg–de Vries (KdV) equation, in the metastable region, and the kink–antikink wave solution, described by the modified Korteweg–de Vries (mKdV) equation, in the unstable region. These solutions depict different traffic density waves. Theoretical analysis of linear stability and numerical simulation indicate that considering both the lateral gap and the optimal velocity of the preceding vehicle, rather than only the lateral gap as in the traditional CFM, expands the stable region of traffic flow, enhances the anti-interference capability, and accelerates the dissipation speed of disturbances. By improving traffic flow stability and reducing interference, the ECFM can decrease traffic congestion and idle time, leading to lower fuel consumption and greenhouse gas emissions. Furthermore, the use of intelligent transportation systems to optimize traffic control decisions supports a more efficient urban traffic management, contributing to sustainable urban development. Full article

The effect of temperature on the localized corrosion resistance and passive film characteristics of laser powder-bed fusion (LPBF) 316L (UNS S31603) was studied in a buffered 3.5 wt% NaCl solution at 25, 50, and 75 °C. DC techniques such as cyclic potentiodynamic polarization showed lower passive current densities, high breakdown potentials, and a higher resistance to initial breakdown compared with wrought 316L samples at all temperatures. However, LPBF 316L was more susceptible to metastable pitting at potentials before film breakdown and higher damage accumulation post film breakdown. AC techniques, such as Mott–Schottky analysis and electrochemical impedance spectroscopy, showed that the formed passive film was more robust on the LPBF 316L samples at all temperatures, accounting for the higher initial resistance to pitting. However, with increasing temperatures, the film formed had an increasing concentration of defect density. Passive compositions at the various test temperatures studied using X-ray photoelectron spectroscopy (XPS) showed that the LPBF samples showed higher amounts of Cr and Fe oxides and hydroxides compared with the wrought samples, which made the passive films on the LPBF samples more compact and protective. Investigation of the pits formed on the LPBF showed the preferential regions of attack were the melt-pool boundaries and cell interiors due to their being depleted of Cr and Mo when compared with the boundaries and matrix. Full article

Due to the rare earth supply shortage, ThMn₁₂-type RFe₁₂-based (R is the rare earth element) magnets with lean rare earth content are gaining more concern. Most ThMn₁₂-type RFe₁₂ structures are thermodynamically metastable and require doping of the stabilizing element Ti. However, the Ti-doping effects on the hard magnetic properties of RFe₁₁Ti have not been thoroughly investigated. Herein, based on density functional theory calculations, we report the Ti-doping effects on the phase stability, intrinsic hard magnetic properties and electronic structures of RFe₁₁Ti (R = La, Ce, Pr, Nd, Sm, Y, Zr). Our results indicate that Ti-doping not only increases their phase stability, but also enhances the magnetic hardness of ground-state RFe₁₂ phases. Particularly, it leads to the transition of CeFe₁₁Ti and PrFe₁₁Ti from easy-plane to easy-axis anisotropy. Charge density distributions demonstrate that Ti-doping breaks the original symmetry of the R-site crystal field, which alters the magnetic anisotropy of RFe₁₁Ti. Projected densities of states reveal that the addition of Ti results in the shift of occupied and unoccupied f-electron energy levels of rare earth elements, affecting their magnetic exchange. This study provides an insight into regulating the hard magnetic properties of RFe₁₂-based magnets by Ti-doping. Full article

Measurements of atmosphere density in the upper thermosphere and exosphere are of great significance for studying space–atmosphere interactions. However, the region from 200 km to 1000 km has been a blind area for traditional ground-based active remote sensing techniques due to the limitation of facilities and the paucity of neutral atmosphere. To fulfill this gap, the University of Science and Technology of China is developing a powerful metastable helium resonance fluorescent lidar incorporating a 2 m aperture telescope, a high-energy 1083 nm pulsed laser, as well as a superconducting nanowire single-photon detector (SNSPD) with high quantum efficiency and low dark noise. The system is described in detail in this work. To evaluate the performance of the lidar system, numerical simulation is implemented. The results show that metastable helium density measurements can be achieved with a relative error of less than 20% above 370 km in winter and less than 200% in 270–460 km in summer, demonstrating the feasibility of metastable helium lidar. Full article