Search Results (287)

In this study, we investigate the phase transition process during high-alumina, low-lithium glass-ceramics (ZnO-MgO-Li₂O-SiO₂-Al₂O₃) crystallization. The differential scanning calorimetry and high-temperature X-ray diffraction results show that approximately 10 wt.% of (Zn, Mg)Al₂O₄ crystals precipitated when the heat treatment temperature reached 850 °C, indicating that a large number of nuclei had already formed during the earlier stages of heat treatment. Field emission transmission electron microscopy used to observe the microstructure of glass-ceramics after staged heat treatment revealed that cation migration occurred during the nucleation process. Zn and Mg aggregated around Al to form (Zn, Mg)Al₂O₄ nuclei, which provided sites for crystal growth. Moreover, high-valence Zr aggregated outside the glass network, leading to the formation of nanocrystals. Raman spectroscopy analysis of samples at different stages of crystallization revealed that during spinel precipitation, the Q³ and Q⁴ structural units in the glass network increased significantly, along with an increase in the number of bridging oxygens. Highly coordinated Al originally present in the network mainly participated in spinel nucleation, effectively suppressing the subsequent formation of Li_xAl_xSi_1−xO₂, which eventually resulted in the successful preparation of glass-ceramics with (Zn, Mg)Al₂O₄ and ZrO₂ as the main crystalline phases. The grains in this glass-ceramic are all nanocrystals. Its Vickers hardness and flexural strength can reach up to 875 Hv and 350 MPa, respectively, while the visible light transmittance of the glass-ceramic reaches 81.5%. This material shows potential for applications in touchscreen protection, aircraft and high-speed train windshields, and related fields. Full article

The scalable synthesis of high-quality single-crystal diamond films remains pivotal for next-generation extreme-performance devices. Iridium substrates offer exceptional promise for heteroepitaxy, yet early-stage growth mechanisms limiting crystal quality are poorly understood. An integrated multiscale investigation combining first-principles DFT calculations, molecular dynamics simulations, and experimental validation is presented to resolve the oriented attachment process governing diamond growth on Ir(100). Robust interfacial bonding at the interface and optimal carbon coverage are revealed to provide thermodynamic driving forces for primary nucleation. A critical angular tolerance enabling defect-free coalescence through crystallographic realignment is identified by molecular dynamics. Concurrent nucleation growth pathways are experimentally confirmed through SEM, AFM, and Raman spectroscopy, where nascent crystallites undergo spontaneous orientational registry to form continuous epitaxial domains. Grain boundary annihilation is observed upon lattice rotation aligning adjacent grains below the critical angle. Crucially, intrinsic atomic steps are generated on the resultant coalesced layer, eliminating conventional etching requirements for homoepitaxial thickening. This work advances fundamental understanding of single-crystal diamond growth mechanisms, facilitating enhanced quality control for semiconductor device manufacturing and quantum applications. Full article

Ga₂O₃ is an ultra-wide bandgap semiconductor material that has attracted significant attention for deep ultraviolet photodetector applications due to its excellent UV absorption capability and reliable stability. In this study, a novel plasma-enhanced thermal oxidation (PETO) method has been proposed to fabricate Ga₂O₃ thin films on the GaN/sapphire substrate in the gas mixture of Ar and O₂. By adjusting the O₂-to-Ar ratio (2:1, 4:1, and 8:1), the structural, morphological, and photoelectric properties of the synthesized Ga₂O₃ films are systematically studied as a function of the oxidizing atmosphere. It is demonstrated that, at an optimal O₂-to-Ar ratio of 4:1, the synthesized Ga₂O₃ thin film has the largest grain size of 31.4 nm, the fastest growth rate of 427.5 nm/h, as well as the lowest oxygen vacancy concentration of 16.61%. Furthermore, the nucleation and growth of Ga₂O₃ thin films on the GaN/sapphire substrate by PETO is proposed. Finally, at the optimized O₂-to-Ar ratio of 4:1, the metal–semiconductor–metal-structured Ga₂O₃-based photodetector achieves a specific detectivity of $2.74\times {10}^{13}$ Jones and a solar-blind/visible rejection ratio as high as 116 under a 10 V bias. This work provides a promising approach for the cost-effective fabrication of Ga₂O₃ thin films for UV photodetector applications. 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

This study aimed to optimize the grain structure of complex thin-walled nickel-based superalloy castings by investigating the influence of key casting parameters using both cellular automaton–finite element (CAFE) simulations and experimental validation. The main problem addressed was the inhomogeneous grain morphology arising from complex mold geometries and uneven thermal conditions during investment casting. The solidification process was simulated using the ProCAST software, incorporating the CAFE method to model temperature fields and grain growth dynamics. The results revealed that the molten metal flow pattern during mold filling significantly affected the local temperature field and subsequent grain formation. Specifically, simultaneous bidirectional filling minimized thermal gradients and suppressed coarse columnar grain formation, promoting finer, more uniform equiaxed grains. Lowering the pouring temperature (to 1430 °C) in combination with reduced shell temperature (600–800 °C) enhanced nucleation and improved grain uniformity in thin-walled regions. Higher cooling rates also refined the grain structure by increasing undercooling and limiting grain growth. Experimental castings confirmed these simulation outcomes, demonstrating that the proposed optimization strategies can significantly improve grain homogeneity in critical structural areas. These findings provide a practical approach for controlling microstructure in large, intricate superalloy components through targeted process parameter tuning. 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

Solid-state lithium batteries (SSLBs) have emerged as a promising alternative to conventional lithium-ion systems due to their superior safety profile, higher energy density, and potential compatibility with lithium metal anodes. However, a major challenge hindering their widespread deployment is the formation and growth of lithium dendrites, which compromise both performance and safety. This review provides a comprehensive and structured overview of recent advances in dendrite suppression strategies, with special emphasis on the role played by the nature of the solid electrolyte. In particular, we examine suppression mechanisms and material innovations within the three main classes of solid electrolytes: sulfide-based, oxide-based, and polymer-based systems. Each electrolyte class presents distinct advantages and challenges in relation to dendrite behavior. Sulfide electrolytes, known for their high ionic conductivity and good interfacial wettability, suffer from poor mechanical strength and chemical instability. Oxide electrolytes exhibit excellent electrochemical stability and mechanical rigidity but often face high interfacial resistance. Polymer electrolytes, while mechanically flexible and easy to process, generally have lower ionic conductivity and limited thermal stability. This review discusses how these intrinsic properties influence dendrite nucleation and propagation, including the role of interfacial stress, grain boundaries, void formation, and electrochemical heterogeneity. To mitigate dendrite formation, we explore a variety of strategies including interfacial engineering (e.g., the use of artificial interlayers, surface coatings, and chemical additives), mechanical reinforcement (e.g., incorporation of nanostructured or gradient architectures, pressure modulation, and self-healing materials), and modifications of the solid electrolyte and electrode structure. Additionally, we highlight the critical role of advanced characterization techniques—such as in situ electron microscopy, synchrotron-based X-ray diffraction, vibrational spectroscopy, and nuclear magnetic resonance (NMR)—for elucidating dendrite formation mechanisms and evaluating the effectiveness of suppression strategies in real time. By integrating recent experimental and theoretical insights across multiple disciplines, this review identifies key limitations in current approaches and outlines emerging research directions. These include the design of multifunctional interphases, hybrid electrolytes, and real-time diagnostic tools aimed at enabling the development of reliable, scalable, and dendrite-free SSLBs suitable for practical applications in next-generation energy storage. Full article

This study systematically investigates the homogenization-induced Laves phase dissolution kinetics and recrystallization mechanisms in laser powder bed fusion (L-PBF) processed IN718 superalloy. The as-built material exhibits a characteristic fine dendritic microstructure with interdendritic Laves phase segregation and high dislocation density, featuring directional sub-grain boundaries aligned with the build direction. Laves phase dissolution demonstrates dual-stage kinetics: initial rapid dissolution (0–15 min) governed by bulk atomic diffusion, followed by interface reaction-controlled deceleration (15–60 min) after 1 h at 1150 °C. Complete dissolution of the Laves phase is achieved after 3.7 h at 1150 °C. Recrystallization initiates preferentially at serrated grain boundaries through boundary bulging mechanisms, driven by localized orientation gradients and stored energy differentials. Grain growth kinetics obey a fourth-power time dependence, confirming Ostwald ripening-controlled boundary migration via grain boundary diffusion. Such a study is expected to be helpful in understanding the microstructural development of L-PBF-built IN718 under heat treatments. Full article

This study systematically evaluates the influence of copper (Cu) addition in gas-shielded solid wires on the microstructure and cryogenic toughness of X80 pipeline steel welds. Welds were fabricated using solid wires with varying Cu contents (0.13–0.34 wt.%) under identical gas metal arc welding (GMAW) parameters. The mechanical capacities were assessed via tensile testing, Charpy V-notch impact tests at −20 °C and Vickers hardness measurements. Microstructural evolution was characterized through optical microscopy (OM), scanning electron microscopy (SEM) and electron backscatter diffraction (EBSD). Key findings reveal that increasing the Cu content from 0.13 wt.% to 0.34 wt.% reduces the volume percentage of acicular ferrite (AF) in the weld metal by approximately 20%, accompanied by a significant decline in cryogenic toughness, with the average impact energy decreasing from 221.08 J to 151.59 J. Mechanistic analysis demonstrates that the trace increase in the Cu element. The phase transition temperature and inclusions is not significant but can refine the prior austenite grain size of the weld, so that the total surface area of the grain boundary increases, and the surface area of the inclusions within the grain is relatively small, resulting in the nucleation of acicular ferrite within the grain being weak. This microstructural transition lowers the critical crack size and diminishes the density for high-angle grain boundaries (HAGBs > 45°), which weakens crack deflection capability. Consequently, the crack propagation angle decreases from 54.73° to 45°, substantially reducing the energy required for stable crack growth and deteriorating low-temperature toughness. Full article

The effects of trace Ce on the microstructure and texture of non-oriented silicon steel during recrystallization and grain growth were examined using X-ray diffraction and electron backscatter diffraction. Additionally, this study focused on investigating the mechanisms by which trace Ce influences the evolution of the {114} <481> and γ-fiber textures. During the recrystallization process, as the recrystallization fraction of annealed sheets increased, the intensity of α-fiber texture decreased, while the intensities of α*-fiber and γ-fiber textures increased. The {111} <112> grains preferentially nucleated in the deformed γ-grains and their grain-boundary regions and tended to form a colony structure with a large amount of nucleation. In addition, the {100} <012> and {114} <481> grains mainly nucleated near the deformed α-grains, which were evenly distributed but found in relatively small quantities. The hindering effect of trace Ce on dislocation motion in cold-rolled sheets results in a 2–7% lower recrystallization ratio for the annealed sheets, compared to conventional annealed sheets. Trace Ce suppresses the nucleation and growth of γ-grains while creating opportunities for α*-grain nucleation. During grain growth, trace Ce reduces γ-grain-boundary migration rate in annealed sheets, providing growth space for {114} <418> grains. Consequently, the content of the corresponding {114} <481> texture increased by 6.4%, while the γ-fiber texture content decreased by 3.6%. Full article

This study focuses on S32654 super austenitic stainless steel (SASS) and systematically characterizes the morphology of the sigma (σ) phase and the segregation behavior of alloying elements in its as-cast microstructure. High-temperature confocal scanning laser microscopy (HT-CSLM) was employed to investigate the effect of the rare earth element yttrium (Y) on the solidification microstructure and σ phase precipitation behavior of SASS. The results show that the microstructure of SASS consists of austenite dendrites and interdendritic eutectoid structures. The eutectoid structures mainly comprise the σ phase and the γ₂ phase, exhibiting lamellar or honeycomb-like morphologies. Regarding elemental distribution, molybdenum displays a “concave” distribution pattern within the dendrites, with lower concentrations at the center and higher concentrations at the sides; when Mo locally exceeds beyond a certain threshold, it easily induces the formation of eutectoid structures. Mo is the most significant segregating element, with a segregation ratio as high as 1.69. The formation mechanism of the σ phase is attributed to the solid-state phase transformation of austenite (γ → γ₂ + σ). In the late stages of solidification, the concentration of chromium and Mo in the residual liquid phase increases, and due to insufficient diffusion, there are significant compositional differences between the interdendritic regions and the matrix. The enriched Cr and Mo cause the interdendritic austenite to become supersaturated, leading to solid-state phase transformation during subsequent cooling, thereby promoting σ phase precipitation. The overall phase transformation process can be summarized as L → L + γ → γ → γ + γ₂ + σ. Y microalloying has a significant influence on the solidification process. The addition of Y increases the nucleation temperature of austenite, raises nucleation density, and refines the solidification microstructure. However, Y addition also leads to an increased amount of eutectoid structures. This is primarily because Y broadens the solidification temperature range of the alloy and prolongs grain growth perio, which aggravates the microsegregation of elements such as Cr and Mo. Moreover, Y raises the initial precipitation temperature of the σ phase and enhances atomic diffusion during solidification, further promoting σ phase precipitation during the subsequent eutectoid transformation. Full article

The prediction of microstructure evolution during thermal processing plays a crucial role in tailoring the mechanical properties of metallic components. Therefore, this work presents a comprehensive, multiscale modelling approach to simulating phase transformations in large-diameter steel rings during cooling. A finite-element-based thermal model was first used to simulate transient temperature distributions in a large-diameter ring under different cooling conditions, including air and water quenching. These thermal histories were subsequently employed in two complementary phase transformation models of different levels of complexity. The Avrami model provides a first-order approximation of the evolution of phase volume fractions, while a complex full-field cellular automata approach explicitly simulates the nucleation and growth of ferrite grains at the microstructural level, incorporating local kinetics and microstructural heterogeneities. The results highlight the sensitivity of final grain morphology to local cooling rates within the ring and initial austenite grain sizes. Simulations demonstrated the formation of heterogeneous microstructures, particularly pronounced in the ring’s surface region, due to sharp thermal gradients. This approach offers valuable insights for optimising heat treatment conditions to obtain high-quality large-diameter ring products. Full article

In this study, we have explored the thermomechanical processing on 0.1C3Mn steel to produce an ultrafine-grained (UFG) dual-phase (DP) microstructure. The composition was designed to allow a decrease in temperature for the warm deformation of austenite. It was found that the warm deformation of austenite induced a dramatic ferrite transformation, in contrast to the absence of the formation of ferrite in the well-annealed state. Compression by 60% at 650 °C resulted in the generation of a UFG-DP microstructure with a ferrite grain size of 1.4 μm and a ferrite volume fraction of 62%. The UFG-DP 0.1C3Mn steel presents a good combination of strength, ductility and fracture resistance, and the fracture strain of the UFG-DP is higher than the as-quenched low-carbon martensite. The high fracture strain of the UFG-DP could be attributed to delayed void nucleation and constrained void growth, as revealed by the quantitative X-ray tomography. Full article

Electroless nickel deposition (ELD) on polymer substrates enables the fabrication of flexible, conductive fibres for wearable and functional textiles. However, achieving uniform, low-defect coatings on synthetic fibres such as nylon-6,6 remains challenging due to their chemical inertness, hydrophobicity, and poor interfacial compatibility with metal coatings. This study presents a solvent-assisted approach using dimethyl sulfoxide (DMSO) in a conventional aqueous ELD bath to control both polymer–metal interfacial chemistry and nickel coating microstructure. The modified surface supports dense catalytic sites, triggering spatially uniform Ni nucleation. The combination of scanning electron microscopy and transmission electron microscopy confirms the difference in coarse grains with fully aqueous baths to a nanocrystalline shell with DMSO-modified baths. This refined microstructure relieves residual stress and anchors firmly to the swollen polymer, delivering +7 °C higher onset decomposition temperature and 45% lower creep strain at 50 °C compared with aqueous controls. The fabric strain sensor fabricated by 1 wt.% DMSO-modified ELD shows a remarkable sensitivity against strain, demonstrating a 1400% resistance change under 200% stain. Electrochemical impedance and polarisation tests confirm a two-fold rise in charge transfer resistance and negligible corrosion current drift after accelerated ageing. By clarifying how a polar aprotic co-solvent couples polymer swelling with metal growth kinetics, the study introduces a scalable strategy for tuning polymer–metal interfaces and advances solvent-assisted ELD as a route to mechanically robust, thermally stable, and corrosion-resistant conductive textiles. Full article

In this study, we investigated the formation mechanism of organo-metal halide perovskite nanostructures through a two-step process categorized as dissolution–recrystallization. It is proposed that the initial formation of nanostructures is governed by the generation of seed grains, whereas the Ostwald ripening model explains only the subsequent growth stage of these structures. We suggest that newly generated grains—formed adjacent to pre-positioned grains—experience compressive stress arising from volume expansion during the phase transition from PbI₂ to the MAPbI₃ perovskite phase. Owing to their unstable state, these grains may serve as effective seeds for the nucleation and growth of nanostructures. Depending on the dipping time, diverse morphologies such as nanorods, plates, and cuboids were observed. The morphology, including the aspect ratio and growth direction of these nanostructures, appears to be strongly influenced by the residual compressive stress within the seed grains. These findings suggest that the shape and aspect ratio of perovskite nanostructures can be tailored by carefully regulating nucleation, dissolution, and growth dynamics during the two-step process. Full article