Search Results (600)

As a potential strategic resource of critical metals, deep-sea cobalt-rich crusts represent one of the most promising metal reservoirs within oceanic seamount systems, and their metallogenic mechanism constitutes a frontier topic in deep-sea geoscience research. This review focuses on the cobalt-rich crusts from the Magellan Seamount region in the northwestern Pacific and synthesizes existing geological, mineralogical, and geochemical studies to systematically elucidate their mineralization processes and metal enrichment mechanisms from a microstructural perspective, with particular emphasis on cobalt enrichment and its controlling factors. Based on published observations and experimental evidence, the formation of cobalt-rich crusts is divided into three stages: (1) Mn/Fe colloid formation—At the chemical interface between oxygen-rich bottom water and the oxygen minimum zone (OMZ), Mn²⁺ and Fe²⁺ are oxidized to form hydrated oxide colloids such as δ-MnO₂ and Fe(OH)₃. (2) Key metal adsorption—Colloidal particles adsorb metal ions such as Co²⁺, Ni²⁺, and Cu²⁺ through surface complexation and oxidation–substitution reactions, among which Co²⁺ is further oxidized to Co³⁺ and stably incorporated into MnO₆ octahedral vacancies. (3) Colloid deposition and mineralization—Mn–Fe colloids aggregate, dehydrate, and cement on the exposed seamount bedrock surface to form layered cobalt-rich crusts. This process is dominated by the Fe/Mn redox cycle, representing a continuous evolution from colloidal reactions to solid-phase mineral formation. Biological processes play a crucial catalytic role in the microstructural evolution of the crusts. Mn-oxidizing bacteria and extracellular polymeric substances (EPS) accelerate Mn oxidation, regulate mineral-oriented growth, and enhance particle cementation, thereby significantly improving the oxidation and adsorption efficiency of metal ions. Tectonic and paleoceanographic evolution, seamount topography, and the circulation of Antarctic Bottom Water jointly control the metallogenic environment and metal sources, while crystal defects, redox gradients, and biological activity collectively drive metal enrichment. This review establishes a conceptual framework of a multi-level metallogenic model linking macroscopic oceanic circulation and geological evolution with microscopic chemical and biological processes, providing a theoretical basis for the exploration, prediction, and sustainable development of potential cobalt-rich crust deposits. Full article

Magnesium hydride (MgH₂) is a promising solid-state hydrogen storage material owing to its high hydrogen capacity and low cost, yet its practical application is limited by sluggish kinetics, high operating temperatures, and poor cycling stability. Among various catalytic approaches, Fe-based catalysts have emerged as attractive candidates due to their abundance, compositional tunability, and effective promotion of hydrogen sorption reactions in MgH₂ systems. This review critically summarizes recent progress in Fe-based catalysts for MgH₂ hydrogen storage, encompassing elemental Fe, iron oxides, Fe-based alloys, and advanced composite catalysts with nanostructured and multicomponent architectures. Mechanistic insights into catalytic enhancement are discussed, with particular emphasis on interfacial electron transfer, catalytic phase evolution, hydrogen diffusion pathways, and synergistic effects between Fe-containing species and MgH₂, supported by experimental and theoretical studies. In addition to catalytic activity, key stability challenges—including catalyst agglomeration, phase segregation, interfacial degradation, and performance decay during cycling—are analyzed in relation to structural evolution and kinetic–thermodynamic trade-offs. Finally, a roadmap for the scalable design of Fe-based catalysts is proposed, highlighting rational catalyst selection, interface engineering, and compatibility with large-scale synthesis. This review aims to bridge fundamental mechanisms with practical design considerations for developing durable and high-performance MgH₂-based hydrogen storage materials. Full article

SiC/Al matrix composites are prone to forming brittle Al₄C₃ phase via interfacial reactions during fabrication, which severely limits their mechanical properties and engineering applications. Microalloying is an effective method to inhibit this brittle phase, yet the interfacial mechanism of alloying elements at the atomic scale remains unclear. Centered on molecular dynamics simulation combined with experimental verification, this study systematically investigates the laws of Fe and Ni microalloying on the interface regulation and mechanical property optimization of SiC/Al composites. Simulation results show that Fe and Ni atoms tend to segregate at the SiC/Al interface, which can suppress interfacial reactions, promote dislocation nucleation and proliferation, induce new dislocation types, and achieve the synergistic improvement of strength and ductility—with Ni exhibiting a more prominent strengthening effect. Composites prepared by the pressure infiltration-hot extrusion process show no Al₄C₃ phase in phase detection. Mechanical property tests confirm that Fe and Ni microalloying can effectively enhance the comprehensive performance of the materials, among which Ni increases the strength–ductility product by 54%. This study clarifies the interfacial regulation mechanism of Fe and Ni microalloying at the atomic scale, providing theoretical guidance and experimental support for the microalloying design of SiC/Al composites. Full article

Rechargeable lithium-, sodium-, and potassium-ion batteries are utilized as essential energy storage devices for portable electronics, electric vehicles, and large-scale energy storage systems. In these systems, anode materials play a vital role in determining energy density, cycling stability, and safety of various batteries. However, the complex electrochemical reactions and dynamic changes that occur in anode materials during charge–discharge cycles generate major challenges for performance optimization and understanding failure mechanisms. In situ characterization techniques, capable of real-time tracking of microstructures, composition, and interface dynamics under operating conditions, provide critical insights that bridge macroscopic performance and microscopic mechanisms of anodes. This review systematically summarizes the applications of such techniques in studying anodes for lithium-, sodium-, and potassium-ion batteries, with a focus on their contributions across different anode types. It also indicates current challenges and future directions of these techniques, aiming to offer valuable references for relevant applications and the design of high-performance anodes. Full article

In situ preparation routes have become central to advancing lead sulfide (PbS) quantum dots (QDs) for solar-energy conversion, owing to their ability to create strongly coupled QD/oxide interfaces that are difficult to achieve with ex situ colloidal methods, along with their simplicity and potential for low-cost, scalable processing. This review systematically examines the fundamental mechanisms, processing levers, and device implications of the dominant in situ approaches successive ionic layer adsorption and reaction (SILAR), voltage-assisted SILAR (V-SILAR), and chemical bath deposition (CBD). These methods enable conformal QD nucleation within mesoporous scaffolds, improved electronic coupling, and scalable low-temperature fabrication, forming the materials foundation for high-performance PbS-based architectures. We further discuss how these in situ strategies translate into enhanced solar-energy applications, including quantum-dot-sensitized solar cells (QDSSCs) and photoelectrochemical (PEC) hydrogen production, highlighting recent advances in interfacial passivation, scaffold optimization, and bias-assisted growth that collectively suppress recombination and boost photocurrent utilization. Representative device metrics reported in recent studies indicate that in-situ-grown PbS quantum dots can deliver photocurrent densities on the order of ~5 mA cm⁻² at applied potentials around 1.23 V versus RHE in photoelectrochemical systems, while PbS-based quantum-dot-sensitized solar cells typically achieve power conversion efficiencies in the range of ~4–10%, depending on interface engineering and device architecture. These performances are commonly associated with conformal PbS loading within mesoporous scaffolds and quantum-dot sizes in the few-nanometer regime, underscoring the critical role of morphology and interfacial control in charge transport and recombination. Recent studies indicate that performance improvements in PbS-based solar-energy devices are primarily governed by interfacial charge-transfer kinetics and recombination suppression rather than QD loading alone, with hybrid heterostructures and inorganic passivation layers playing a key role in modifying band offsets and surface trap densities at the PbS/oxide interface. Remaining challenges are associated with defect-mediated recombination, transport limitations in densely loaded porous scaffolds, and long-term chemical stability, which must be addressed to enable scalable and durable PbS-based photovoltaic and photoelectrochemical technologies. Full article

The interfacial behavior between lattice reinforcement and aluminum matrix plays an important role in determining the mechanical and tribological properties of lattice-reinforced aluminum matrix composites. In this study, 316L lattices with different aspect ratios were prepared by laser powder bed elting (LPBF) technology, and LY12 aluminum alloy was infiltrated under vacuum conditions. The effects of lattice aspect ratio on the interfacial reaction, microstructure, hardness, compressive strength, and wear resistance of the composites were systematically studied. First-principles calculations show that FeAl₂ and FeAl₃ intermetallic compounds are preferentially formed at the interface, showing good thermodynamic stability and mechanical properties. The microstructure analysis shows that the increase in aspect ratio promotes the formation of coarse FeAl₃ phase and network AlCu, while a too-large aspect ratio leads to the instability of microstructure and the generation of microcracks. When the lattice constant is 10 mm and the diameter of the support is 1 mm (BCC-10-1), the composite material has the best wear resistance, and the specific wear rate is 3.07 × 10⁻⁴ mm³/(N·m). These findings provide valuable insights into the design of high-performance lattice-reinforced aluminum matrix composites with customized interface properties. Full article

Mechanical forces, chemical and electrochemical reactions, and environmental variables can all lead to surface degradation of parts. Composite coatings can be applied to these materials to enhance their surface characteristics. Recently, nickel-based composite coatings have gained greater attention because of their remarkable wear resistance. The efficiency, precision, and affordability of this process make it a popular method. In addition, electroplating nickel-based composites offers a more environmentally friendly alternative to traditional dangerous coatings such as hard chrome. Tribological and wear characteristics are highly dependent on several variables, such as particle parameters, deposition energy, fluid dynamics, and bath composition. Mass loss, coefficient of friction, hardness, and roughness are quantitative properties that provide useful information for coating optimization and selection. Under optimized electrodeposition conditions, the Ni-SiC-graphite coatings achieved a 57% reduction in surface roughness (Ra), a 38% increase in microhardness (HV), and a 25% reduction in wear rate (Ws) compared to pure Ni coatings, demonstrating significant improvements in tribological performance. Overall, the incorporation of SiC nanoparticles was found to consistently improve microhardness while graphite or MoS₂ reduces friction. Differences in wear rate among studies appear to result from variations in current density, particle size, or test conditions. Furthermore, researchers run tribology studies and calculate the volume percentage using a variety of techniques, but they fall short in providing a sufficient description of the interface. This work primarily contributes to identifying gaps in tribological research. With this knowledge and a better understanding of electrodeposition parameters, researchers and engineers can improve the lifespan and performance of coatings by tailoring them to specific applications. Full article

Photocatalytic processes have emerged as an efficacious strategy for the removal of organic pollutants from wastewater. In the present investigation, a BiVO₄ nanorod supported on Bi₂O₂S nanosheet catalyst (referred to as BiVO₄/Bi₂O₂S) was meticulously synthesized via a straightforward synthetic approach, aimed explicitly at the photodegradation of tetracycline (TC). The optimized BiVO₄/Bi₂O₂S composite, with a theoretical weight ratio of BiVO₄ to Bi₂O₂S at 2:1 (designated as 2BVO/BOS), demonstrated a significant improvement in tetracycline degradation efficiency, achieving up to 82.9% under visible light irradiation for 90 min. This result stands in stark contrast to the relatively low degradation rates of 42.9% and 50.7% observed for pure BiVO₄ and Bi₂O₂S, respectively. Furthermore, the apparent reaction rate of 2BVO/BOS (approximately 0.01894 min⁻¹) was 3.19-fold and 2.66-fold higher than those of BiVO₄ (0.00594 min⁻¹) and Bi₂O₂S (0.00713 min⁻¹), respectively. This significant improvement in photocatalytic efficacy can be ascribed to the composite’s superior capacity for visible light absorption, as well as its remarkable proficiency in charge carrier separation and transfer. Comprehensive experimental analyses, corroborated by extensive characterization techniques, revealed the formation of a distinctive S-scheme charge transfer mechanism at the interface between BiVO₄ and Bi₂O₂S. This mechanism effectively suppresses charge recombination and optimizes the redox potentials of the photogenerated carriers, thereby enhancing the overall photocatalytic performance. The current study underscores the remarkable potential and promising application of BiVO₄/Bi₂O₂S composite in the realm of wastewater treatment. Full article

Ni–ySiC system (where y = 0.001, 0.005, and 0.015 wt.%) composite materials with enhanced mechanical properties have been fabricated and comprehensively investigated. The composites were synthesized using a combined technology involving preliminary mechanical activation of powder components in a planetary mill followed by consolidation via spark plasma sintering (SPS) at 850 °C. The microstructure and phase composition were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The physico-mechanical properties were evaluated by density measurements (hydrostatic weighing), three-point bending tests (25 °C and 400 °C), and Young’s modulus measurement using an ultrasonic method (25–750 °C). It was found that the introduction of ultralow amounts of SiC nanoparticles (0.001 wt.%) leads to an extreme increase in flexural strength: by 115% at 20 °C (up to 1130 MPa) and by 86% at 400 °C (up to 976 MPa) compared to pure nickel. Microstructural analysis revealed the formation of an ultrafine-grained structure (0.15–0.4 µm) with the presence of pyrolytic carbon and probable nickel silicide interlayers at the grain boundaries. Thermodynamic and kinetic modeling, including the calculation of chemical potentials and diffusion coefficients, confirmed the possibility of reactions at the Ni/SiC interface with the formation of nickel silicides (Ni₂Si, NiSi) and free carbon. The scientific novelty of the work lies in establishing a synergistic strengthening mechanism combining the Hall–Petch, Orowan (dispersion), and solid solution strengthening effects, and in demonstrating the property extremum at an ultralow content of the dispersed phase (0.001 wt.%), explained from the standpoint of quantum-chemical analysis of phase stability. The obtained results are of practical importance for the development of high-strength and thermally stable nickel composites, promising for application in aerospace engineering. Full article

Unconventional shale oil reservoirs, characterized by ultra-low porosity and permeability, severely constrain oil recovery. CO₂-enhanced oil recovery (CO₂-EOR) following hydraulic fracturing is an effective approach that combines incremental oil recovery with long-term CO₂ storage. However, CO₂ transport in the fracture–matrix system is complex, especially when molecular diffusion and geochemical reactions are coupled. This study conducts numerical simulations on a representative shale reservoir in the Ordos Basin, incorporating both mechanisms under post-fracturing injection–soaking conditions. The results show that molecular diffusion enhances CO₂ mass transfer across the fracture–matrix interface, increasing the final CO₂ sweep efficiency by 0.17 percentage points relative to convection alone, whereas geochemical reactions reduce it by about 0.3 percentage points. When both mechanisms coexist, the net effect is a decrease of approximately 0.2 percentage points in CO₂ sweep efficiency. In contrast, pressure sweep efficiency differs by less than 0.5 percentage points among all cases and stabilizes near 47%, suggesting that pressure propagation is only weakly affected by diffusion and reactions. Sensitivity analysis reveals that, among operational parameters, injection pressure and injection rate strongly affect CO₂ sweep efficiency, whereas soaking time governs pressure propagation. Among reservoir parameters, permeability has the most pronounced influence on both CO₂ and pressure sweep efficiencies, followed by temperature, while initial reservoir pressure has minimal impact. This work quantitatively elucidates the coupled roles of molecular diffusion and geochemical reactions in shale reservoirs and provides practical guidance for optimizing post-fracturing CO₂-EOR operations. Full article

In this study, novel, high-strength polymer blends were synthesized using poly(butylene succinate) (PBS) modified with grafted polyrotaxane (GPR). Then, their mechanical properties and morphologies were evaluated. A unique, two-step, reactive kneading method was developed to substantially improve the mechanical properties of PBS, which promoted transesterification reaction using an organo-titanium catalyst (Ti) in the first step and a urethanization reaction using hexamethylene diisocyanate (HDI) in the second step. The optimized blend material, [PBS/GPR10/Ti]-HDI, achieved remarkable toughening, and its Izod impact strength increased approximately seven-fold compared with that of unmodified PBS. Scanning electron microscopy (SEM) of the fracture surfaces confirmed a transition from brittle to ductile fracture, attributed to the controlled reaction sequence. First, strong chemical bonds formed at the PBS/GPR interface via Ti-catalyzed transesterification. Then, HDI induced simultaneous internal crosslinking (gelation) of the GPR domains and chain extension of the PBS matrix. This modification strategy maintained the excellent inherent soil biodegradability of PBS while improving its degradability in marine environments. This study presents a new guideline for designing materials that can considerably enhance the mechanical properties of biodegradable plastics. Full article

In order to address the urgent demand for high-performance materials in the field of automotive lightweighting, there is a need for solutions to the interface instability and performance degradation of traditional reinforcing phases (e.g., SiC, CNT) at elevated temperatures. The present study prepared BNNTs/Al composites via the stirred casting method for automotive connecting rods. The microstructure, interface characteristics, phase evolution, and high-temperature wettability were systematically characterised using a range of analytical techniques, including SEM, TEM, XRD, and DSC. A study was conducted to assess the mechanical properties of the composites in comparison to those of conventional 40Cr steel. This investigation enabled an evaluation of the material’s comprehensive performance for use in automotive connecting rods. The study successfully achieved uniform dispersion of BNNTs within the aluminium matrix, forming tightly bonded, semi-coherent interfaces such as Al/AlN and Al/AlB₂. It was found that complete wetting was achieved at 675 °C, with interface reactions generating AlN and AlB₂ phases that significantly enhanced performance. The prepared connecting rod demonstrates a specific strength that significantly exceeds that of 40Cr steel. The experimental investigation conducted in a controlled setting yielded notable outcomes. The empirical evidence demonstrated a 6.5% enhancement in braking performance and a 5.8% reduction in fuel consumption. Through the optimisation of interface design and process control, the BNNTs/Al composite achieves a balanced compromise between high strength, low density, and excellent thermal stability. The material’s potential for use in lightweight automotive connecting rods is significant, offering a novel approach to the eco-friendly manufacturing of related components. Full article

Carbon-fiber-reinforced thermoset polyimide composites have found wide applications in various aerospace areas. In this paper, the influence of carbon-fiber sizing on the thermal properties of polyimide composites was studied. Nonlinear detriment of the epoxy sizing was found to affect the composite’s thermal resistance. Furtherly, the mechanism, possibly responsible for the nonlinear detrimental effect of the epoxy sizing, was investigated through curing kinetics analysis and chemical structure characterization. Thermal curing activation energy change was found, possibly arising from the insertion of a flexible segment into the polyimide chain by epoxy–amine reaction. Based on the proposed mechanism, a strategy to manipulate the thermal resistance was established and verified. By the precuring of the carbon-fiber sizing, the polyimide composite exhibited obvious thermal resistance improvement, indicated by an enhancement of the glass transition temperature by 20 °C, and a weight-loss reduction under thermal aging at 400 °C by 25%. Simultaneously, a good fiber-matrix interface was maintained. This strategy provides a new route to enhance the thermal properties of polyimide composites from the viewpoint of carbon-fiber-matrix compatibility. Full article

Two-dimensional materials and their van der Waals heterostructures have shown great potential in quantum physics, flexible electronics, and optoelectronic devices. However, interfacial bubbles originated from trapped air, solvent residues, adsorbed molecules and reaction byproducts remain a key limitation to performance. This review provides a comprehensive overview of the formation mechanisms, characteristics, impacts, and optimization strategies related to bubbles in 2D heterostructures. We first summarize common fabrication approaches for constructing 2D heterostructures and discuss the mechanisms of bubble formation together with their physicochemical features. Then, we introduce characterization techniques ranging from macroscopic morphological observation to atomic-scale interfacial analysis, including optical microscopy, atomic force microscopy, transmission electron microscopy, and spectroscopic methods systematically. The effects of bubbles on the mechanical, electrical, thermal, and optical properties of 2D materials are subsequently examined. Finally, we compare key interface optimization strategies—such as thermal annealing, chemical treatments, AFM-based cleaning, electric field-driven approaches, clean assembly and AI-assisted methods. We demonstrate that, although substantial advances have been made in understanding interfacial bubbles, key fundamental challenges persist. Future breakthroughs will require the combined advancement of mechanistic insight, in situ characterization, and process engineering. Moreover, with the rapid adoption of AI and autonomous experimental platforms in materials fabrication and data analysis, AI-enabled process optimization and real-time characterization are emerging as key enablers for achieving high-cleanliness and scalable van der Waals heterostructures. Full article

This review explores the pervasive role of water in generating, storing, and mediating electric charge across natural and artificial systems. Far from being a passive medium, water actively participates in electrostatic and electrochemical processes through its intrinsic ionization, interfacial polarization, and charge separation mechanisms. The Maxwell–Wagner–Sillars (MWS) effect is presented as a unifying framework explaining charge accumulation at air–water, water–ice, and water–solid interfaces, forming dynamic “electric mosaics” across Earth’s environments. The authors integrate diverse phenomena—triboelectricity, hygroelectricity, hydrovoltaic effects, elastoelectricity, and electric-field-driven phase transitions—showing that ambient water continually shapes the planet’s electrical landscape. Electrostatic shielding by humid air and hydrated materials is described, as well as the spontaneous electrification of sliding or dripping water droplets, revealing new pathways for clean energy generation. In addition, the review highlights how electric fields and interfacial charges alter condensation, freezing, and chemical reactivity, underpinning discoveries such as microdroplet chemistry, “on-water” reactions, and spontaneous redox processes producing hydrogen and hydrogen peroxide. Altogether, the paper frames water as a universal electrochemical medium whose interfacial electric imprint influences atmospheric, geological, and biological phenomena while offering novel routes for sustainable technologies based on ambient charge dynamics and water-mediated electrification. Full article