Search Results (1,342)

Ammonia decomposition over non-precious metal thermos-catalysts offers a viable and cost-effective pathway for sustainable hydrogen production. In this study, LaCeO₃ perovskite was synthesized using a citric acid complexation method and employed as a support for mono- and bimetallic catalysts prepared by incipient wetness impregnation, maintaining a total metal loading of 10 wt%. Structural and surface properties were systematically investigated using BET, XRD, H₂-TPR, SEM, TEM, and CO₂-TPD. Among the monometallic catalysts (Ni, Co, and Fe), 10%Ni/LaCeO₃ exhibited the highest activity, which is attributed to its enhanced reducibility and optimal surface basicity, facilitating NH₃ activation. Bimetallic systems (Ni-Co, Ni-Fe, and Co-Fe) with equal metal loadings (5 wt% each) showed better activity compared to their monometallic counterparts following the order: 5%Ni–5%Co/LaCeO₃ > 5%Ni–5%Fe/LaCeO₃ > 5%Co–5%Fe/LaCeO₃. The improved performance of the Ni-Co system is due to structural interactions between Ni and Co, which promote hydrogen desorption and accelerate N–H bond cleavage, while suppressing nitrogen recombination as the rate-limiting step. Further systematic optimization of the Ni/Co ratio showed that 8%Ni–2%Co/LaCeO₃ had the highest catalytic activity with consistent performance over 50 h. This optimal composition provides a balanced distribution of active metallic sites and moderate-to-strong basic sites, enhancing NH₃ adsorption and intermediate transformation. These findings show that LaCeO₃-supported Ni-Co catalysts are promising candidates for efficient hydrogen production from ammonia without using noble metals. Full article

The sluggish kinetics of alkaline hydrogen oxidation reaction (HOR) and high cost of Pt–based catalysts have long hindered large–scale deployment of alkaline membrane fuel cells. Via first–principles calculations, we designed a series of 3d transition metal single atoms anchored on PdN₂ monolayer (TM–PdN₂, TM = Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn) and evaluated their alkaline HOR performance. Ti-, Cr-, Fe-, Co-, Ni-modified systems exhibit excellent thermodynamic and electrochemical stability under operating conditions. Single-atom doping tunes the p-band center of N and d-band center of metal sites, enabling precise modulation of H and OH adsorption strengths. Mechanistic analysis reveals HOR follows H₂ + 2OH* → H* + OH* + H₂O → 2H₂O, with the final step as rate-determining step. H adsorption contributes 3.45 times more to HOR activity than OH adsorption. Fe–PdN₂ delivers the best performance, with an ultra–low barrier of 0.11 eV and a rate constant of 2.82 × 10¹⁰ s^–1·site⁻¹, values that significantly outperform those of Pt(111) (0.22 eV, 4.5 × 10⁹ s⁻¹·site⁻¹). This work provides theoretical guidance for rational design of high–performance alkaline HOR electrocatalysts. Full article

Nickel ferrite (NiFe₂O₄) is one of the most studied inverse-spinel ferrites because it combines moderate saturation magnetization, comparatively high electrical resistivity, chemical stability, and broad synthesis flexibility. Yet the literature shows that the measured structure and magnetism of NiFe₂O₄ are not intrinsic constants; they evolve strongly with dimensionality, size, thickness, strain state, cation distribution, surface spin disorder, and synthesis pathway. This review develops a unified theoretical and literature-based interpretation of how dimensionality reshapes the structural and magnetic behavior of NiFe₂O₄ across bulk ceramics, nanoparticles, one-dimensional nanostructures, polycrystalline thin films, and ultrathin epitaxial films. The review is anchored in the two uploaded nickel ferrite attachments and expanded using internet-sourced journal literature on spinel inversion, surface effects, mechanochemical synthesis, sputtered and pulsed laser deposited thin films, and epitaxial ultrathin-film anomalies. The central novelty of this article is the formulation of a dimensionality-dependent framework in which the observed magnetic response is governed by a competition among three coupled factors: (i) the cation-distribution function, which controls the A–B superexchange balance and therefore the net ferrimagnetic moment; (ii) the microstructural coherence function, which measures how crystallinity, strain, defects, and anti-phase boundaries preserve or degrade exchange continuity; and (iii) the surface/interface spin-order parameter, which quantifies the loss or reconfiguration of magnetic order at free surfaces and buried interfaces. Within this framework, bulk NiFe₂O₄ behaves as a near-equilibrium inverse spinel with relatively stable magnetization, whereas nanoscale NiFe₂O₄ experiences strong spin canting and finite-size suppression due to the growing fraction of disordered surface spins. Thin films introduce a distinct regime in which strain, texture, anti-phase boundaries, substrate mismatch, and growth kinetics determine both anisotropy and magnetization. In ultrathin epitaxial films, off-equilibrium cation redistribution and interface-controlled electronic reconstruction may even generate magnetization values far above bulk expectations. The review also compares major synthesis routes—solid-state reaction, sol–gel, co-precipitation, hydrothermal growth, reactive milling, combustion, pulsed laser deposition, and radio-frequency sputtering—and explains why each route biases the final dimensionality-dependent properties differently. A set of word-style equations is provided to formalize spinel inversion, finite-size suppression, anisotropy scaling, coercivity trends, and superparamagnetic crossover. Beyond summarizing the field, the review proposes a regime map linking dimensionality to characteristic structural defects and magnetic signatures, and it identifies unresolved questions concerning the true origin of enhanced magnetization in ultrathin NiFe₂O₄, the interplay between anti-phase boundaries and strain, and the distinction between intrinsic inversion changes and extrinsic substrate artifacts. The resulting article offers a submission-ready, originality-focused review that positions dimensionality as the master variable governing structure–magnetism correlations in nickel ferrite. Full article

Next-generation wastewater treatment and recycling rely on membrane-based processes, but they face a trade-off among permeability, selectivity, and fouling resistance. In the present study, thin-film nanocomposite (TFN) membranes were fabricated by incorporating a ternary TiO₂-SiO₂-biochar nanofiller into a polysulfone (PSf) support using nonsolvent-induced phase separation, after which m-phenylenediamine and trimesoyl chloride were used via interfacial polymerization to produce a selective polyamide layer. The membrane compositions were M1 (22 wt.% PSf), M2 (22 wt.% PSf/0.5 wt.% TiO₂/0.5 wt.% SiO₂/0.5 wt.% biochar), and M3 (polyamide-coated M2). FTIR, XRD, SEM, contact-angle, porosity, and mechanical analyses supported successful membrane formation and changes in morphology, wettability, and structural strength after nanofiller incorporation and TFC coating. The addition of a nanofiller increased the hydrophilicity of the membranes by decreasing the water contact angle from 98.6 ± 0.8° for pristine PSf to 35.6 ± 1.5° for the nanocomposite membrane. Consequently, the pure-water permeability increased from 21 to 37 L m⁻² h⁻¹ bar⁻¹. After polyamide layer formation, the optimized TFN membrane maintained a contact angle of 55.4 ± 3.8° and achieved a high Congo red rejection of 98% with permeate flux of 7–9 L m⁻² h⁻¹ bar⁻¹. The membrane also showed good antifouling performance, with flux recovery ratios exceeding 90%. For heavy-metal-containing solutions, the optimized membrane showed apparent removal efficiencies of 78–98% for multivalent heavy metals (Pb²⁺, Hg²⁺, Cd²⁺, Mn²⁺, Zn²⁺, Cu²⁺, Ni²⁺, Fe³⁺, As³⁺, and Cr⁶⁺). Static adsorption tests showed the order M2 > M3 > M1, confirming that exposed TiO₂-SiO₂-biochar sites contribute to pollutant uptake, while the superior filtration performance of M3 is attributed to the combined effect of the polyamide selective layer and adsorption-assisted interactions. Overall, the TiO₂-SiO₂-biochar-based TFN membrane provides a promising platform for dye removal and preliminary heavy-metal attenuation from contaminated water. Full article

Gadolinium is a rare-earth element that is promising for the field of biomedicine due to its unique properties that enhance image quality, giving it high potential in targeted cancer therapy, antimicrobial treatments, etc. The disadvantage of Gd-containing materials is their high toxicity. In this work, ensembles of Fe and Al₂O₃ nanoparticles were fabricated by the electric explosion of wire and Gd ribbons using rapid quenching techniques. Stable Fe, Fe/Gd and Fe/Gd/Al₂O₃ aqueous suspensions with a Z-potential of about –54 mV were fabricated by the ball-milling mechanosynthesis of Fe (100%), Fe and Gd (70 and 30 wt. % accordingly) and Fe, Al₂O_3, and Gd (69, 30 and 1 wt.% accordingly). Fillers from suspensions were used for the synthesis of epoxy composites mimicking natural tissue with embedded magnetic particles. The concentration range for synthesized epoxy composites (0, 5, 10, and 15 wt.% of the filler) corresponded to the biomedical range of interest. Thin-film magnetoimpedance (MI) elements were prepared by a sputtering technique: conventional [FeNi/Cu]₅/Cu/[Cu/FeNi]₅ (NP) element and [FeNi/Cu]₅/Cu/[Cu/P{FeNi]₅} element with patterned top multilayer (SqP). They showed a maximum MI ratio of about 160% for NP and about 60% for SqP. MI sensor response was affected by the presence of filled magnetic composites in the shape of cylinders (5 mm × 4 mm) situated at about 1 mm due to the stray fields in the filler. MI response showed a linear dependence on the filler concentration for each selected position. These results open the possibility to develop new iron- and gadolinium-containing materials for simultaneous magnetic imaging and detection by magnetic field sensors, extending the functional properties of Fe/Gd materials for biomedical devices and therapies. Full article

In this study, Fe₇₀Ni₃₀ metal was deposited onto continuous glass fiber composites via magnetron sputtering, followed by surface coating with SiO₂. The effects of key process parameters-including Fe₇₀Ni₃₀ sputtering duration (2, 5, 10, 20, and 30 min) and SiO₂ surface coating-on the electromagnetic properties and microwave absorption performance of the materials were systematically investigated. Scanning electron microscopy (SEM) characterization revealed that as sputtering time increased, the metal coating evolved from discrete small particles into a continuous film. Cross-sectional SEM analysis further demonstrated the formation of a bilayer structure after SiO₂ introduction. X-ray diffraction (XRD) patterns confirmed the presence of diffraction peaks corresponding to the Fe₇₀Ni₃₀ alloy solid solution. Electromagnetic parameter measurements indicated that the influence of sputtering time on electromagnetic properties was primarily pronounced during the metal layer growth stage; once a continuous film was formed, the variation in electromagnetic parameters diminished. Concurrently, the SiO₂ coating exhibited a significant regulatory effect on dielectric parameters. Reflection coefficient calculations showed that the optimal absorption thickness for the single-layer material ranged from 2.5 to 3.0 mm, with the absorption peak shifting toward lower frequencies as thickness increased. However, the effective absorption bandwidth (EAB) was only 3–5 GHz, failing to meet wideband requirements. In contrast, the three-layer composite structure (total thickness: 3.8 mm) optimized via genetic algorithm achieved impedance gradient and loss synergy, expanding the EBW (R < −10 dB) from 4.8 GHz (single layer) to 10 GHz (8–18.0 GHz)-a substantial improvement over the single-layer configuration. This work provides experimental evidence and technical support for the structural design and process optimization of lightweight, high-efficiency, wideband microwave-absorbing materials. Full article

This study investigates the modulation of coercivity and magnetodielectric coupling in heat-treated, nickel-substituted lanthanum ferrite. LaFe_0.7Ni_0.3O₃ samples were synthesized by high-energy ball milling and sintered at temperatures between 1073 and 1473 K. Chemical composition, crystalline structural evolution, surface morphology, magnetic, dielectric, and electrical properties, as well as magnetodielectric coupling, were analyzed. The XPS spectra revealed the presence of adsorbed oxygen, associated with the high oxygen affinity of the material. This behavior is interpreted as a charge-compensation mechanism, related both to the formation of oxygen vacancies and to the partial oxidation of Fe³⁺ to Fe⁴⁺. XRD and Rietveld refinement confirmed a single-phase orthorhombic Pnma structure, and structural simulations revealed progressive octahedral distortions with increasing temperature, affecting the octahedral tilting and electronic bandwidth. Magnetic characterization revealed that thermal processing modifies the magnetic behavior, inducing weak ferromagnetism and a significant increase in coercivity, correlating with progressive densification, greater domain stability, and reduced microstrain. Impedance measurements revealed magnetodielectric coupling, the Maxwell–Wagner interfacial polarization mechanism, and reduced dielectric losses. These findings demonstrate that the coercivity and magnetodielectric response in cationic nickel-substituted lanthanum ferrite can be tuned through thermal processing. A semi-empirical magnetocrystalline anisotropy model is proposed to explain the coercivity evolution and associated multiferroic behaviors, thus contributing to the study of functional ferrites as sustainable alternatives to rare-earth magnetic materials with potential in sensors and memory devices. Full article

The electrochemical co-conversion of CO₂ and H₂O into valuable products is a promising approach toward carbon-neutral energy systems. Alloy exsolution from perovskite lattices has emerged as an effective strategy to engineer catalytic interfaces, yet the mechanistic influence of exsolved bimetallic species on CO₂/H₂O co-electrolysis remains insufficiently clarified. To address this gap, density functional theory (DFT) calculations were performed in this study to systematically examine how NiFe alloy clusters exsolved from the LSFNO (La_0.7Sr_0.3Fe_0.9Ni_0.1O_3-δ) (111) surface modify the electronic structure of the interfacial region and promote the RWGS reaction in CO₂/H₂O co-electrolysis. Our work highlights bimetallic alloy exsolution as a powerful strategy for improving co-electrolysis catalysts and offers valuable guidance for the rational design of next-generation high-entropy oxide systems. Full article

Due to the increased anthropogenic load, crops are polluted with heavy metals, including nickel (Ni). This is a serious environmental problem, as Ni penetrates barrier-free into cereal crops and accumulates in the grains used by humans and animals for food. Wheat is one of the main staple crops, cultivated in many countries. This study suggested that plant growth promoting bacteria (PGPB) with varying enzymatic activities could help wheat plants to cope with Ni stress by reducing Ni toxicity and regulating the metal’s homeostasis. PGPB Bacillus megaterium AFI1 has a strong phosphate-solubilizing activity and produces siderophores, while Paenibacillus nicotianae AFI2 has nitrogen-fixing and silicate-solubilizing activities. Both strains produce indole and polysaccharides and have 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity. PGPB under Ni exposure (100 mg/kg of soil) significantly increased grain yield (by 34–42%) and decreased (by 20–33%) Ni content in wheat grains. PGPB also decreased malondialdehyde (MDA) and H₂O₂ levels in wheat plants under Ni stress. The contents of iron (Fe), boron (B), nitrogen (N) and phosphorus (P) decreased significantly and potassium (K) and zinc (Zn) oppositely increased significantly in all plant organs under Ni exposure. The inoculation with AFI1 mainly increased P and Fe, and the inoculation with AFI2 increased N and silica (Si) in wheat grains under Ni stress. In our experiments, under nickel exposure PGPB Bacillus megaterium AFI1 and Paenibacillus nicotianae AFI2 increased antioxidant protection of plants by decreasing the level of stress ethylene and regulating the homeostasis of nutrients in wheat plants. These PGPB can be considered as promising candidates for the development of biologicals to be used for growing plants in soils with low levels of nickel contamination. Full article

Electrochemical water splitting stands as a feasible approach for sustainable hydrogen production, but its industrial implementation is restricted by sluggish oxygen evolution reaction (OER) kinetics and excessive dependence on freshwater resources. As a widely existing alternative, seawater contains a high concentration of chloride ions (Cl⁻), which give rise to serious electrode corrosion and catalyst deactivation, bringing great challenges to actual electrolysis applications. Herein, we report a facile room-temperature two-step soaking strategy to fabricate sulfur-modified NiFe layered double hydroxide (S-NiFe-LDH) catalysts for efficient OER in both alkaline freshwater and seawater electrolytes. The introduction of sulfur not only optimizes the electronic structure of NiFe-LDH to strengthen intrinsic catalytic activity and speed up charge transfer, but also promotes the formation of a Cl⁻-resistant layer, thus significantly improving corrosion resistance. In addition, DFT calculations show sulfur modification in NiFe layered double hydroxide upshifts the O 2p-band center to activate lattice oxygen, switches the oxygen evolution reaction pathway to the lattice oxygen mechanism with reduced thermodynamic barriers, and realizes the selective adsorption of OH⁻ over Cl⁻. As a result, the as-prepared S-NiFe-LDH catalyst exhibits exceptional OER performance, requiring overpotentials (η) of 250, 270, and 290 mV to reach current densities of 50, 100, and 200 mA·cm⁻² in 1 M KOH, respectively, with a Tafel slope of 22.3 mV·dec⁻¹. Moreover, it maintains remarkable stability for more than 200 h in alkaline seawater electrolytes and achieves nearly 100% Faradaic efficiency for water splitting, effectively avoiding the parasitic chlorine evolution reaction (CER). This work provides a scalable and energy-efficient synthetic route for designing advanced non-noble metal catalysts, paving the way for industrial-scale hydrogen production from seawater. Full article

This study investigates the production behavior of Fe–Ni–S matte from synthetic nickel ore designed to simulate low-grade saprolitic laterite. The synthetic feed was formulated based on XRF and XRD analyses of magnetically upgraded laterite concentrate. Thermodynamic modeling, including phase stability analysis, Ellingham evaluation, viscosity prediction, and sulfidation equilibria, was employed to define optimal smelting conditions. Carbothermic reduction at 1550 °C enabled selective reduction in NiO and FeO, leading to the formation of Fe–Ni alloy droplets, which subsequently reacted with FeS to produce Fe–Ni–S matte. The carbon ratio played a critical role in controlling FeO content in slag, thereby influencing slag basicity and viscosity. An optimal carbon ratio of 0.2–0.4 mol maintained slag viscosity within the industrially favorable range (2–5 poise) and minimized crucible dissolution. Thermodynamic analysis confirmed that FeS is the only stable sulfide phase at high temperature and dissolves into the Fe–Ni melt, promoting stable matte formation. Under optimized carbon and FeS addition conditions, a maximum nickel recovery of approximately 88% was achieved, attributed to improved slag composition, controlled viscosity, and enhanced matte–slag separation. These results demonstrate that simultaneous carbothermic reduction and sulfidation is an effective route for Fe–Ni–S matte production from saprolite-derived oxide feed. Control of carbon ratio, FeS addition, and Al₂O₃ flux is essential for achieving stable matte formation and efficient metal–slag separation. Full article

Metal accumulation in cacao (Theobroma cacao L.) cultivation represents an important agronomic and food-safety concern, particularly in acidic tropical soils where cadmium (Cd) and other trace metals can become bioavailable and translocate to plant tissues. Green magnetic nanomaterials offer a potential strategy for reducing metal mobility in agricultural substrates, but their performance depends on surface chemistry, dose, and plant genotype. In this study, we synthesized and evaluated MCRES, defined here as a maghemite–Citrus reticulata extract system, a biofunctionalized γ-Fe₂O₃-based nanosystem prepared by coupling iron oxide nanoparticles (NPs) with a 3% (w/v) Citrus reticulata peel extract. The objective was to determine whether citrus-mediated biofunctionalization could produce a scalable magnetic nanoamendment capable of modifying Cd and naturally occurring Ni partitioning in cacao seedlings. MCRES was recovered magnetically and dried, yielding 8.44 g of product from 10 g of precursor. Rietveld analysis performed in X ray diffractograms confirmed phase-pure cubic γ-Fe₂O₃ with a lattice parameter of 0.8332 nm, a crystallite size of 11.3(1) nm, and satisfactory refinement quality (χ² ≈ 1.34). Transmission electron microscope images showed quasi-spherical NPs with a log-normal size distribution centered at 7.5 nm. Magnetic measurements showed superparamagnetic-like behavior at 300 K, high saturation magnetization values of 62 emu g⁻¹ at 300 K and 71 emu g⁻¹ at 5 K, and elevated effective anisotropy values obtained from the Law of Approach to Saturation fitting. MCRES was applied at 0, 1, 2, 4, and 6 g pot⁻¹ to cacao seedlings containing Cd-amended Ultisol with naturally occurring Ni. Plant responses were genotype and dose dependent: TSH-1188 genotype showed limited dose sensitivity for most biometric variables, whereas ICS-95 genotype showed significant dose effects, with maximum growth at the 2 g pot⁻¹ treatment. Metal-partitioning results indicated that Cd remained comparatively mobile toward shoots, whereas Ni was preferentially retained in roots. In TSH-1188 genotype, the Ni translocation factor decreased from 3.07 in the control to 0.85–1.00 at higher MCRES doses. Compared with previous work on non-biofunctionalized nanomaghemite, these results suggest that citrus-mediated biofunctionalization produces a distinct Cd/Ni partitioning response. Overall, MCRES is recommended as a promising nursery-scale green nanoamendment for reducing metal mobility in cacao cultivation, but its agronomic use should be optimized according to genotype and dose. Future work should include side-by-side comparisons with unfunctionalized γ-Fe₂O₃, Citrus reticulata extract alone, and non-contaminated controls under field conditions to validate its long-term effectiveness and environmental safety. Full article

The widespread accumulation of ampicillin (AMP) poses significant ecological and health risks, demanding rapid and portable monitoring tools. Herein, a Fe-Ni bimetallic-doped polydopamine (FeNi@PDA) nanozyme with exceptional peroxidase-like activity was synthesized for the visual and on-site monitoring of AMP. Optimized through bimetallic electronic coupling, FeNi@PDA exhibited enhanced catalytic efficiency (K_M = 0.051 mmol/L for H₂O₂ and 0.049 mmol/L for 3,3′,5,5′-tetramethylbenzidine) and generated ¹O₂ and ·O₂⁻ via H₂O₂ activation. Leveraging the competitive consumption of reactive oxygen species (ROS) by electron-rich AMP, a colorimetry detection mode was developed where AMP concentration inversely correlated with oxidized 3,3′,5,5′-tetramethylbenzidine (oxTMB) formation. This strategy achieved a good linear relationship of between 0.05 to 100 μg/mL, with a limit of detection (LOD) of 10.38 ng/mL. Furthermore, a smartphone-integrated paper-based detection mode was fabricated by immobilizing FeNi@PDA on filter paper. The color gradient of test papers, analyzed via smartphone imaging, enabled on-site AMP quantification with a LOD of 340 ng/mL. This work not only developed a novel Fe-Ni bimetallic nanozyme with enhanced peroxidase-like activity and established a competitive ROS-consumption sensing mechanism but also pioneered a dual-mode detection platform for low-cost, user-friendly ampicillin monitoring in environmental samples. Full article

This study proposes a novel synergistic design strategy to enhance the oxidation resistance of FeNiCuAl-based high-entropy alloys by integrating multi-element alloying (Cr-Co-Mn), trace Y modification, and laser-cladding-induced nanocrystallization. While the Base Alloy exhibited a mass gain of approximately 15 mg/cm² after oxidation at 900 °C for 120 h, the addition of Cr_2.5Co_2.5Mn_2.5 promoted the formation of a multilayered oxide scale (outer MnCr₂O₄/inner Al₂O₃), reducing the parabolic oxidation rate constant to 1.7 × 10⁻⁵ mg²·cm⁻⁴·s⁻¹. The originality of this work lies in the coupling of compositional and microstructural engineering; further addition of 0.5 at.% Y decreased this constant to 1.7 × 10⁻⁶ mg²·cm⁻⁴·s⁻¹—a three-order-of-magnitude reduction relative to the Base Alloy, while increasing the apparent oxidation activation energy to ~350 kJ/mol. After 100 thermal cycles at 1000 °C, the designed alloy showed a mass change of only 0.05 ± 0.02 mg/cm², with its critical load and interfacial fracture energy reaching 78 N and 14.8 J/m², respectively. Furthermore, the alloy retained a hardness of 310 HV, an elastic modulus of 135 GPa, and a tensile strength of 240 MPa at elevated temperature. These results demonstrate that the synergistic integration of chemical and structural optimization provides a new paradigm for designing low-cost, high-performance FeNiCuAl-based protective coatings. Full article

This work investigated the effect of yttrium addition on the pre-oxidation behavior of Fe–25Ni–20Cr–4Al–1Nb–1Mn–1.5Si-based alloys at 1000 °C in a 4% H₂ + 0.2% CH₄ + Ar + 0.25% H₂O atmosphere. The oxidation resistance and oxide scale adhesion were evaluated through cyclic oxidation tests and micro-scratch measurements. Results show that the Y-free alloy formed a discontinuous oxide layer, whereas all Y-containing alloys formed a continuous and dense Al₂O₃ scale. Incorporating 0.2 wt.% Y increased the work of adhesion by approximately 7 to 9 times relative to the Y-free sample, indicating a pronounced interfacial strengthening effect. The role of yttrium content and oxygen partial pressure in promoting alumina-scale formation was discussed based on thermodynamic considerations and microstructural evidence. Full article