Search Results (5,109)

The microstructure, phase composition, and high-temperature oxidation behavior of Al_0.5CoCr_0.5NiPt_0.1 and AlCoCr_0.5NiPt_0.1 multi-principal element alloys (MPEAs) at 1100 °C in air were investigated. Depending on the content of aluminum, the microstructure of as-cast samples contains FCC and BCC solid solutions. Similarly, the ratio of two solid solutions varies depending on the aluminum content in the alloy. When the content of aluminum is x = 0.5, the microstructure is dominated by the FCC solid solution, while a BCC solid solution is dominated when the concentration of aluminum is increased to x = 1.0. Moreover, in both MPEAs, platinum exists as a part of solid solutions rather than a separate phase. High-temperature oxidation was carried out in a Plavka.Pro PM-1 SmartKiln muffle furnace under isothermal conditions at 1100 °C for 100 h exposure in air, and weighing was performed every 10 h. The maximum specific weight gain for the Al_0.5CoCr_0.5NiPt_0.1 alloy was 0.965 mg/cm², and 0.675 mg/cm² for the AlCoCr_0.5NiPt_0.1 alloy. Based on the high-temperature oxidation experiment results, it was established that AlCoCr_0.5NiPt_0.1 MPEA exhibits greater resistance towards high-temperature dry air corrosion with the formation of an exclusive Al₂O₃ scale on the surface with 3–5 μm thickness; the parabolic oxidation rate constant for this alloy is k_p = 20.2 × 10^–13 (g²/cm⁴s). Introduction of platinum into the composition of the Fe-free AlCoCr_0.5Ni alloy reduces the value of the parabolic oxidation rate constant by half. Full article

Accurate and robust battery health prognostics are critical for reliable battery management in electronic devices and electric vehicles. Previous studies have demonstrated that combining electrochemical impedance spectroscopy (EIS) with machine learning enables accurate health-state forecasting in LiCoO₂ coin cells. However, the applicability of this EIS-AI paradigm across diverse chemistries and industrial-grade battery formats remains unvalidated, limiting its practical deployment in energy storage systems. Here, we develop an EIS–AI battery prognostic framework and validate its performance on LiNi_1/3Mn_1/3Co_1/3O₂ (NMC111) cylindrical cells and LiNi_0.8Mn_0.1Co_0.1O₂ (NMC811) pouch cells. A hybrid Convolutional Neural Network–Bidirectional Long Short-Term Memory (CNN–BiLSTM) architecture is developed to estimate state of health (SoH) and predict remaining useful life (RUL) from EIS spectra. Trained on an in-house dataset comprising over 13,000 impedance spectra from 22 cells (8 NMC111 and 14 NMC811), the model achieves robust performance, with average coefficients of determination (R²) exceeding 0.92 for SoH estimation and 0.90 for RUL prediction across various batteries and cycling protocols. Salient feature analysis further reveals chemistry- and protocol-dependent frequency regimes associated with degradation. These results demonstrate that impedance spectra constitute physically informative descriptors for data-driven battery prognostics and provide a scalable and interpretable pathway for deploying EIS-AI frameworks in real-world battery management systems (BMSs). Full article

This study investigates how the initial oxygen fraction in a confined space affects post-vent combustion, gas composition, and pressure hazards during thermal runaway (TR) of 58 Ah prismatic Li(Ni_0.8Co_0.1Mn_0.1)O₂ lithium-ion cells. Thermal abuse experiments were conducted in a 250 L sealed chamber under five initial oxygen fractions (20%, 15%, 10%, 5%, and 0% O₂), with synchronized measurements of cell temperature, vent-jet temperature, chamber pressure, voltage, and post-event gas composition. A first-vent event occurred reproducibly at a cell surface temperature of approximately 155 °C, followed by TR onset at about 170 °C. Although the onset temperatures were only weakly affected by ambient oxygen concentration, the post-vent hazard escalation depended strongly on oxygen availability. As the initial oxygen fraction increased from 0% to 20%, the peak vent-jet temperature increased from 353 °C to 1172 °C, and the peak chamber pressure rose from 90.7 kPa to 523.1 kPa. Gas chromatography showed that H₂, CO₂, CO, CH₄, and C₂H₄ were the dominant gaseous products. Lower oxygen fractions promoted retention of combustible species, whereas higher oxygen fractions enhanced oxidation and increased the CO₂/CO ratio. An oxygen-participation parameter, η, was introduced to quantify the fraction of initially available chamber oxygen consumed during post-vent oxidation. The increase in η was positively associated with oxygen-involved heat release and chamber overpressure. When the accessible oxygen fraction was limited to 10% or below, secondary combustion and pressure buildup were markedly suppressed, although a localized near-field thermal hazard remained significant around 10% O₂. These results provide quantitative guidance for enclosure inerting, vent management, and post-vent hazard mitigation in high-energy lithium-ion battery systems. Full article

Polycrystalline La_2−xBi_xNiMnO₆ (x = 0.2, 0.5, 1.0) samples were synthesized via a high-temperature and high-pressure method, with their structural, magnetic, and electrical properties systematically characterized. X-ray diffraction (XRD) confirms a monoclinic double perovskite structure (space group P2₁/n) for all samples, while Bi³⁺ induces a lattice volume expansion trend inferred from XRD peak shifts due to its larger ionic radius than La³⁺. Magnetically, all exhibit ferromagnetism and soft magnetic features, with magnetization decreasing as Bi content increases. The x = 0.2 and 0.5 samples show two distinct Curie temperatures, both decreasing with Bi substitution, whereas the higher Curie temperature vanishes in the x = 1.0 sample, likely due to Bi-induced structural changes. Electrically, all display semiconducting behavior (resistivity: x = 0.5 > x = 0.2 > x = 1.0) and negative magnetoresistance (MR) at 200 K, peaking at 12% (x = 0.5) and 7.5% (x = 1.0). For the x = 1.0 sample, negative magnetoresistance strengthens with decreasing temperature (130–200 K), with magnetoresistance-field (MR-H) curves showing herringbone and arc shapes. Full article

To improve the surface properties of 40Cr steel, Ni45/Y₂O₃ laser-cladded coatings (L-CCs) were fabricated on the surface of 40Cr steel. The effects of Y₂O₃ addition (0.5%, 1.0%, and 1.5%) on the microstructure, microhardness, residual stress, wear resistance, and corrosion resistance of the L-CCs were systematically investigated. The results indicate that Y₂O₃ has a significant effect on enhancing the corrosion resistance and suppressing the residual stress of the L-CCs, whereas its contribution to the improvement of microhardness and wear resistance is relatively limited. Compared with the single Ni45 L-CC, the L-CC containing 1.0% Y₂O₃ exhibited a 45.9% reduction in corrosion current density and a 79.3% reduction in residual stress. At a Y₂O₃ addition of 0.5%, the microhardness increased by 4.0%, while the average friction coefficient and wear mass loss decreased by 4.8% and 2.6%, respectively, relative to the single Ni45 L-CC. Excessive Y₂O₃ addition reduces the fluidity of materials in the molten pool and deteriorates the microstructural uniformity, thereby weakening or even impairing the surface properties of the L-CCs. Full article

A comparative study was undertaken to examine the V_TH stability of p-GaN gate high electron mobility transistors (HEMTs) without the p-NiO reduced surface field (RESURF) terminal and with the RESURF terminal under off-state drain voltage stress and negative gate stress, involving in-depth analyses of the net negative charge accumulation processes in the gate region and buffer layer, thereby revealing the degradation mechanisms of the devices. The findings indicate that the p-NiO RESURF terminal effectively enhances the stability of V_TH under off-state drain voltage stress by injecting holes into the buffer layer and hence initiating a light-pumping effect, and simultaneously also by flattening the electric field peak on the drain side beneath the gate and thus significantly mitigating hole loss in the gate region and electron capture in the buffer layer. This study provides a theoretical basis for the application of the p-NiO RESURF terminal in p-GaN HEMTs. Full article

The catalytically supported upgrading of green ethanol and green methanol mixtures can produce higher alcohols, such as iso-butanol, in a sustainable manner. Iso-butanol can be used as a feedstock to defossilize the chemical and transportation sectors. MgO-Al₂O₃ hydrotalcite-based catalysts are a promising option for this purpose. In this paper, samples were synthesized using co-precipitation and urea methods with different Mg/Al molar ratios with Ni acting as the active catalytic component. Thereby, the catalysts synthesized using the urea method exhibited the greatest activity, producing iso-butanol concentrations of up to 170 mmol L⁻¹ at 185 °C, with selectivities towards iso-butanol of 85–89% and a maximum space–time yield of 8.2 mmol g⁻¹ h⁻¹. The most active catalyst among all samples from this paper was characterized by 100% proportions of strong basic and medium acidic catalyst sites and the largest specific surface area. XRD analysis revealed the presence of NiO, MgO and the spinels Al₂NiO₄ and Al₂MgO₄ in both synthesis variants as well as elemental Ni in one sample from the urea synthesis. CO₂-TPD and NH₃-TPD experiments showed the dominance of strong basic and medium/strong acidic catalyst sites in both synthesis pathways. Full article

Intensive nitrogen (N) fertilization in Phyllostachys edulis (Carrière) J.Houz. forests increases productivity but also accelerates nitrous oxide (N₂O) emissions, posing a challenge to balancing forest yield with environmental sustainability. Silicon (Si), a beneficial element for bamboo, has emerged as a potential regulator of soil nitrogen (N) cycling, but its role in controlling N₂O emissions in forest ecosystems is not fully understood. In this study, we conducted a factorial pot experiment using P. edulis forest soil, with data collected over two years, but only the second-year results were analyzed, with controlled N (0, 80, and 160 mg kg⁻¹) and Si (0, 25, and 50 mg kg⁻¹) additions. The experiment lasted two years, but only the second-year data were used for analysis. We investigated how Si affected soil inorganic N dynamics, enzyme activities, plant growth, and cumulative N₂O emissions. Si addition significantly reduced N-induced N₂O emissions by up to 53%, with the strongest mitigation observed under moderate N input (p < 0.05, two-way ANOVA). This effect was associated with lower activities of AMO, NaR, and NiR, together with reduced availability of oxidized N substrates, indicating that Si mitigated N₂O emissions mainly by constraining upstream N transformation processes rather than by directly suppressing N₂O fluxes. Si addition also tended to promote plant biomass accumulation. These findings suggest that integrating Si fertilization into bamboo forest management may help improve nutrient use efficiency while mitigating greenhouse gas emissions. Full article

Layered sodium transition-metal oxides are promising cathode materials for sodium-ion batteries due to their high theoretical capacity; however, their practical application is often limited by sluggish Na⁺ diffusion kinetics and structural instability during cycling. P2/O3 phase coexistence has been proposed as an effective strategy to balance capacity and stability, yet it is typically achieved through precise Na-content tuning or complex synthesis conditions, which restrict compositional flexibility. Herein, we demonstrate a phase-engineering approach that induces stable P2/O3 phase coexistence without adjusting the overall Na stoichiometry by controlling the dopant incorporation pathway. Using Na_0.8(Ni_0.25Fe_0.33Mn_0.33Cu_0.07)O₂ (NaNFMC) as a model system, Mg doping via a wet chemical route enables homogeneous dopant distribution, which triggers local stacking rearrangement and the formation of prismatic Na⁺ diffusion channels characteristic of the P2 phase. In contrast, dry-doped samples with identical Mg content retain a predominantly O3-type structure, highlighting the decisive role of dopant incorporation in governing phase evolution. As a result of the phase-engineered P2/O3 coexisting framework, the Mg wet-doped cathode exhibits enhanced initial reversibility, superior rate capability, and improved long-term cycling stability compared to pristine and dry-doped counterparts. Voltage-resolved dQ/dV and cyclic voltammetry analyses reveal stabilized redox behavior with reduced polarization, while electrochemical impedance spectroscopy confirms suppressed impedance growth and improved Na⁺ transport kinetics after cycling. This study establishes that phase engineering through controlled dopant incorporation provides an effective alternative to conventional Na-content tuning strategies for layered sodium cathodes. The findings offer a scalable and versatile design principle for optimizing the electrochemical performance and structural durability of next-generation sodium-ion battery cathode materials. Full article

The influence of zirconia incorporation and template type on the physicochemical properties of NiMo/Al₂O₃-ZrO₂ catalysts was investigated for the hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT) and the hydrogenation (HYD) of naphthalene (N). Catalysts were prepared by co-impregnation on supports synthesized via a sol-gel method using starch (A) and activated carbon (C) as structure-directing templates, followed by zirconium incorporation through a grafting procedure. The resulting materials were characterized by SEM–EDX, N₂ physisorption, H₂-TPR, XPS, HRTEM, and pyridine-FTIR. SEM-EDX confirmed homogeneous metal distributions and compositions close to nominal values (Mo = 20 wt%, Ni = 5 wt%, Zr = 11 wt%) with Ni/(Ni + Mo) = 0.30. N₂ adsorption–desorption isotherms correspond to type IV(a) with H3-H4 hysteresis loops, characteristic of mesoporous structures. After metal incorporation, surface areas decreased to 96 m² g⁻¹ for NiMo/Al₂O₃ and 81 m² g⁻¹ for Zr-modified catalysts, while the activated carbon-templated sample preserved a larger mesoporous volume (0.335 cm³ g⁻¹) and higher macroporosity (72%). H₂-TPR profiles indicated improved reducibility for Zr-containing catalysts. XPS revealed an increase of MoS₂ species from 45% in NiMo/Al₂O₃ to 75% in NiMo/Al₂O₃-ZrO₂(C), accompanied by a higher degree of sulfidation index (DSI) from 47.1% to 73.9%. HRTEM analysis of Zr-modified catalysts revealed longer MoS₂ slabs (11.8–12.1 nm) and higher edge-to-corner ratios (17–17.4) compared with NiMo/Al₂O₃ (6.2 nm; fe/fc = 8.2). Pyridine-FTIR showed a substantial increase in total acidity from 91 to 421 μmol g⁻¹ upon Zr addition. Catalytically, NiMo/Al₂O₃-ZrO₂(C) exhibited the highest HDS conversion (40%), reaction rate (10.5 × 10⁻⁹ mol s⁻¹ g⁻¹), and TOF (4.69 × 10⁻⁵ s⁻¹), whereas NiMo/Al₂O₃-ZrO₂(A) reached the highest naphthalene conversion (97.18%), with a reaction rate of 27.4 × 10⁻⁷ mol s⁻¹ g⁻¹ and TOF of 12.9 × 10⁻³ s⁻¹. These results demonstrate that Zr incorporation and the activated carbon template favored hydrodesulfurization, whereas the starch template promoted hydrogenation performance. Full article

The growing importance of renewable energy sources and the implementation of circular economy principles highlight the need for the rational management of biomass combustion by-products. The aim of this study was to assess the chemical composition of ash produced through the combustion of various biomass fractions from four varieties of common hazel (Corylus avellana L.) in the context of its potential for secondary use. The analysis covered the shells, husks, leaves, and shoots of the following varieties: Kataloński, Olbrzymi z Halle, Olga, and Webba Cenny. Combustion was carried out under laboratory conditions at a temperature of 550 °C, and the content of macro- and micro-element oxides (P₂O₅, K₂O, CaO, SO₃, Cl, SiO₂, MnO, Fe₂O₃, NiO, CuO) and potentially toxic elements (ZnO, TiO₂, Cr₂O₃) was determined using the EDXRF method. The results showed significant variation in the chemical composition of the ash depending on the biomass fraction and variety. The highest P₂O₅ content was found in the leaves of the Kataloński variety (5.02), whilst the highest K₂O concentration was found in the husk of the Olga variety (47.33%). The maximum CaO content was found in the leaves of the Webba Cenny variety (32.60). The leaf and husk fractions were characterised by the highest content of nutrients of fertilising importance, whilst the shells exhibited the lowest values for most macronutrients. The content of potentially toxic elements was low. The results obtained indicate that the selective utilisation of specific fractions of hazel biomass can increase the efficiency of mineral recovery whilst maintaining environmental safety, in line with the principles of the circular economy. Full article

As a result of the high safety, low cost, and environmental benignity, aqueous zinc-ion batteries are regarded as one of the most promising candidates for next-generation large-scale energy storage systems. However, their further development is constrained by performance bottlenecks in existing cathode materials, including capacity, cycle life, and reaction kinetics. In this study, a high-entropy design strategy is employed to synthesize the metal oxide (FeNiMnMgCuCo)₃O₄ with a cubic spinel structure, and its electrochemical performance as a cathode for zinc-ion batteries is systematically evaluated. The prepared (FeNiMnMgCuCo)₃O₄ high-entropy cathode exhibits high reversible capacity (341.3 mA h g⁻¹ at 0.1 A g⁻¹) and remarkable long-term cycling stability (76.1% retention after 1000 cycles at 3 A g⁻¹). This work not only demonstrates a high-entropy cathode material with practical potential but also provides new research insights for optimizing zinc-ion storage performance through composition design and entropy regulation. Full article

Atmospheric plasma spraying (APS) represents a critical solution for enhancing the durability of agricultural components, such as harrow discs, which are subjected to synergistic wear and corrosion during soil cultivation. This study presents experimental results evaluating the electrochemical corrosion behavior and thermal shock resistance of discs coated via atmospheric plasma thermal spraying. Both metallic and ceramic materials, in powder form, from established manufacturers were used to produce the coatings, and the three types of coatings (two metallic and one ceramic) have the following chemical compositions and trade names: W₂C/WC12Co (Metco71NS), Cr₂O₃-4SiO₂-3TiO (Metco136F) and Co25.5Cr10.5Ni7.5W0.5C (Metco45C-NS). The coatings were analyzed using electron microscopy to evaluate the surfaces following corrosion testing. The ceramic coating based on the Cr₂O₃-4SiO₂-3TiO demonstrated the highest protective efficiency by increasing the charge transfer resistance from 307 Ω/cm² to 2213 Ω/cm² for the ceramic coating. It provided a superior physical barrier, reducing the corrosion current density from 0.140 mA/cm² for unprotected substrate to 0.004 mA/cm², representing an improvement of nearly two orders of magnitude. These findings demonstrate that implementing Cr₂O₃-4SiO₂-3TiO ceramic systems can significantly extend the operational lifespan of soil-engaging components, providing a cost-effective strategy for reducing maintenance intervals and material loss in aggressive agricultural environments. Full article

The rational design of electrode materials with tailored composition and architecture is crucial for advancing high-capability electrochemical energy storage systems. This study reports that gadolinium-modified NiFe₂O₄ nanosheet electrodes were effectively synthesized on nickel foam via a hydrothermal approach followed by thermal treatment. A series of compositions (NiFe, NiFe–Gd1, NiFe–Gd2, and NiFe–Gd3) were prepared to systematically examine the effect of Gd incorporation on structural features and electrochemical properties. X-ray diffraction (XRD) analysis confirmed the formation of the cubic spinel NiFe₂O₄ phase without detectable secondary phases, indicating that the crystal structure remains intact after Gd introduction. X-ray photoelectron spectroscopy (XPS) further verified the presence of Ni²⁺, Fe³⁺, and Gd³⁺ species within the lattice environment. Morphological analysis using field-emission scanning electron microscopy (FESEM) revealed a nanosheet-based architecture, where the optimized NiFe–Gd2 electrode exhibited a porous and interconnected nanosheet framework with abundant exposed edges. This structural configuration improves electrolyte penetration and facilitates efficient ion transport during charge storage processes. Electrochemical measurements demonstrated that the NiFe–Gd2 electrode delivers an areal capacitance of 5235 mF cm⁻² at 10 mA cm⁻², along with improved reaction kinetics and low internal resistance. An asymmetric supercapacitor assembled using NiFe–Gd2 as the positive electrode and activated carbon as the negative electrode operated stably within a 0–1.5 V potential window, achieving an energy density of 0.136 mWh cm⁻² and a power density of 3.14 mW cm⁻², while retaining 86.55% of its initial capacitance after 7000 cycles. These results highlight the potential of rare-earth engineering as a viable strategy for designing advanced spinel ferrite electrodes and pave the way for the development of high-performance, durable, and scalable supercapacitor systems for practical energy storage applications. Full article

The redox mechanisms of silica-supported Ni particles were investigated using their in situ X-ray absorption fine structure, providing mechanistic insights into partially reduced NiO and partially oxidized metallic Ni. The results of surface oxidation of partially reduced NiO particles at room temperature revealed that the surface was not fully covered with metallic Ni and that metallic Ni had also formed within the particle interior. During NiO particle reduction, the process initiates at specific surface sites, and before the metallic Ni phase fully covers the surface, O²⁻ ions are expelled from the particle. Conversely, the oxidation of metallic Ni particles progresses inward from the surface, with an accompanying increase in the thickness of the NiO layer that forms upon O₂ exposure at room temperature. This mechanism is supported by observations that the reduction of a thin NiO shell on metallic Ni particles was completed below 200 °C, while reduction temperatures shifted to higher values as the NiO layer thickness increased. The distinct oxidation and reduction mechanisms are attributed to differences in the migration direction of O²⁻ ions. During reduction, it is proposed that O²⁻ ions within the particles migrate to the surface along the interface between the NiO phase and the metallic Ni phase. This study elucidates the detailed mechanism behind the redox interconversion between NiO and metallic Ni in solid catalyst particles. Full article