Search Results (5,114)

Monolithic ceramic catalysts are a key technology for the industrial treatment of coal mine ventilation air methane (VAM). The preparation of straight-channel NiO/CeO₂ monolithic ceramic catalysts via phase inversion addresses critical bottlenecks for industrial VAM abatement. However, high-temperature sintering leads to irreversible NiO agglomeration and coarsening, severely reducing catalytic activity. In this study, an in situ reduction–oxidation reconstruction method is developed to regenerate sinter-degraded NiO. The reconstructed catalyst increases methane conversion from below 70% after sintering to over 95% at 550 °C and achieves full conversion at 600 °C. The catalyst maintains near 100% conversion during 400 h of continuous operation at 600 °C and shows no performance degradation over 15 thermal cycles. Moreover, the reconstructed catalyst exhibits excellent steam tolerance with fully reversible deactivation. The reconstructed catalyst presents a refined porous structure with BET surface area rising from 4.5 to 11.4 m² g⁻¹, an elevated Ni³⁺/Ni²⁺ ratio (1.47 to 1.97), a higher surface adsorbed oxygen proportion (36.8% to 48.7%) and significantly strengthened NiO-CeO₂ interfacial interaction. This work provides a facile and efficient in situ regeneration strategy, greatly enhancing the VAM oxidation activity and stability of sinter-degraded monolithic ceramic catalysts. Full article

Controlling the microstructure of electroless nickel coatings is crucial for optimizing the interfacial properties of carbon fibers. However, a systematic understanding of how dispersants can effectively leverage the refining effect of nanoparticles in composite plating systems remains lacking. This paper proposes the use of a composite dispersant, comprising polyethylene glycol (PEG) and sodium methylene bis-naphthalene sulfonate (NNO) at a 1:1 mass ratio, for nano-Al₂O₃ to achieve microstructure refinement of nickel coatings on carbon fiber surfaces. The results demonstrate that the composite dispersant modifies the surface state and dispersion stability of Al₂O₃ particles through synergistic adsorption, thereby regulating the nucleation and growth behavior of the Ni-P alloy. At an optimal composite dispersant concentration of 3 g/L, the coating exhibits the most compact structure, with Ni-P particle size refined to approximately 181 nm. The coating consists of two phases: crystalline Ni₃P and amorphous Ni-P. The dual adsorption effect of the dispersant—inhibiting Al₂O₃ agglomeration while improving the surface wettability of carbon fibers—is key to enhancing the refinement efficiency. Conversely, excessive dispersant addition leads to deteriorated coating quality. This study provides experimental evidence for understanding the multiphase interfacial interaction mechanism involving organic additives, nanoparticles, and metal deposition, and offers a novel strategy for controlling the surface functionalization of carbon fibers. Full article

Understanding the development characteristics and controlling factors of organic-rich shales in carbonate platform settings is essential for predicting their distribution and assessing their natural gas exploration potential. However, the mechanisms governing the accumulation of such shales in these specific sedimentary environments remain poorly constrained, and the lack of integrated petrological and geochemical studies limits accurate evaluation of their resource potential. The key objective of this study is to investigate the development characteristics and formation mechanisms of organic-rich shales within intraplatform depressions. To address this objective, we conducted a comprehensive petrological and geochemical analysis of the Cambrian Shuijingtuo Formation organic-rich shale deposits deposited in a carbonate platform setting, particularly from Well EYY3 in Western Hubei, Central Yangtze region. The obtained results indicate that total organic carbon (TOC) contents in the Shuijingtuo Formation can reach up to 4.77%, with a thickness of approximately 9.5 m for shales containing over 2% TOC. Vertically, TOC content exhibits a rapid increase at the base, followed by a gradual decline toward the top, reflecting the evolution of depositional environments. The characteristics of organic-rich shale indicate a significant presence of carbonate minerals, which increase in concentration, alongside tuff lenticular bodies and lithological transition surfaces between tuff and shale. While the longitudinal variation of SiO₂ content in shale is subtle, there is a slight increase in land-sourced clasts and excess silica, and TOC has a significant positive correlation. At the base of the Shuijingtuo Formation, redox parameters, including U-EF and Mo-EF, display a rapid increase followed by a gradual decrease. Conversely, changes in Ni-EF, which indicate paleoproductivity, are less pronounced, and their correlation with TOC is relatively poor. These findings suggest that rapid sea-level rise associated with Cambrian transgressions was the main factor influencing organic matter enrichment in the carbonate platform depressions. This rise supplied nutrients and silica-rich organisms, altering the biological landscape and fostering anoxic conditions in the intraplatform depressions, promoting organic-rich shale formation. As sea levels declined, water circulation became restricted, leading to oxidation of shallow water bodies, decreased paleoproductivity, and shale deposits transitioned to tuff. Therefore, organic-rich shale can also be developed on carbonate platforms, with its formation primarily controlled by fluctuations in sea level. During highstand periods, intraplatform depressions may serve as favorable zones for shale gas exploration. Full article

Water electrolysis has emerged as a strategically appealing route for the sustainable production of green hydrogen (H₂) via the hydrogen evolution reaction (HER), though the sluggish kinetics of the oxygen evolution reaction (OER) remains a bottleneck hindering large-scale practical applications. In this regard, an attractive solution is offered by the integration of the ethanol oxidation reaction (EOR) into hybrid water-splitting systems, favorably reducing anodic overpotentials. Nonetheless, an open challenge is related to the fabrication of eco-friendly and economically viable catalysts free from noble metals, combining efficiency and stability. Herein, we explore nickel-oxide-based nanostructures grown onto porous Ni foam scaffolds by a scalable hydrothermal (HT) approach as EOR electrocatalysts. Material properties arising from modulation of the sole HT growth time are investigated by complementary structural, microscopic, and spectroscopic techniques. Electrochemical tests demonstrate good durability and very attractive EOR performances, mainly influenced by the morphology and the NiOOH surface content of the target systems. Overall, the present work advances an attractive route to transition-metal-based electrocatalysts for efficient alcohol-oxidation-assisted water electrolysis. Full article

To address the application requirements of energy storage devices for new energy electric vehicles—including high energy density, high-power density, fast charging and discharging, and long-term cycling stability—traditional symmetric supercapacitors are often limited by low energy density and poor compatibility between the anode and cathode, making it difficult to meet the high-efficiency energy storage demands under the dynamic operating conditions of electric vehicles. This study focuses on the regulation of hierarchical thin-film structures and the innovative heterogeneous coating interface engineering with precise slurry coating and film-forming optimization and designs and fabricates NiCo₂O₄/NiFeO composite thin-film electrodes and Mn-doped porous carbon (Mn-PC) thin-film electrodes. The uniform, compact and stable coating formation on nickel foam substrates via controllable slurry coating facilitates the efficient integration of active materials and conductive supports. The electrode slurries were coated onto conductive nickel foam substrates, and high-performance aqueous supercapacitors were assembled using an asymmetric configuration. A systematic study was conducted covering material preparation, structural characterization, electrochemical testing, and full-device performance evaluation. Using techniques such as XRD, XPS, SEM, TEM, BET, and an electrochemical workstation, the study revealed the structure–activity relationships among material morphology, crystalline phases, pore structure, and electrochemical performance, elucidating the charge storage mechanisms of the composite electrode films and the principles of synergistic adaptation between the anode and cathode. The results indicate that NiCo₂O₄ nanowires decorated with in situ-grown NiFeO nanosheets to form a composite structure; when coated onto nickel foam, this forms a uniform, porous electrode film with a specific surface area of 171.3 m²/g, a specific capacitance as high as 1746 F/g at 1 A/g, and a capacity retention rate of 94.0% after 10,000 cycles. After coating and film formation, the Mn-PC anode introduced pseudocapacitive active sites through uniform Mn doping, resulting in a film electrode specific capacitance of 348 F/g and significantly improved rate and cycling performance. The assembled NiCo₂O₄/NiFeO//Mn-PC asymmetric supercapacitor exhibits a thin-film electrode specific capacitance of 153 F/g at 1 A/g, with a maximum energy density of 52 Wh/kg. Even at a power density of 9000 W/kg, it maintains 45 Wh/kg, and retains 89.5% of its capacity after 10,000 cycles, with overall performance outperforming most previously reported transition metal-based devices. This coating-engineered electrode fabrication strategy breaks through the interface mismatch and structural instability bottlenecks of traditional thin-film electrodes, providing a novel material system and an efficient coating assembly strategy for high-performance supercapacitor thin-film electrodes in new energy electric vehicles, and offers experimental evidence and technical references for the development and application of high-power energy storage coating devices for automotive use, as well as the innovative design of electrode coating engineering in energy storage fields. Full article

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