Search Results (126)

In this study, amorphous Fe₆₀Nb₃B₁₇Si₆Cr₆Ni₄Mo₄ coatings were prepared using the high-velocity air fuel method. The microstructure, wear resistance, and corrosion resistance of the Fe₆₀Nb₃B₁₇Si₆Cr₆Ni₄Mo₄ coatings were examined for various levels of nanocrystallization. In contrast to the as-sprayed coating, the samples that were heat-treated formed partial α-Fe and crystalline Cr₂O₃. The generated nanocrystals exerted a dispersion-strengthening effect on the coatings, leading to enhanced hardness and fracture toughness. When the annealing temperature was below the initial crystallization temperature, the wear resistance improved by approximately 1.65 times, the wear rate decreased to half of that in the as-sprayed state, and the depth of the wear scar reduced. However, the resistance of the coatings to corrosion deteriorated as the degree of crystallization increased. X-ray photoelectron spectroscopy analysis revealed that heat treatment modified the composition of the passive film, thereby influencing its corrosion resistance. These results provide crucial insights into the application of Fe-based amorphous coatings in wear- and corrosion-resistant environments. Full article

This study examined the effects of phosphoric acid (H₃PO₄), polyimide (PI), and lubricants (MoS₂, graphite) on the phase stability, microstructure, and magnetic performance of Fe-5.0 wt.%Si soft magnetic composites (SMCs). Warm compaction (≤550 °C) and annealing at 700 °C were applied to samples prepared under a full factorial design. X-ray diffraction confirmed stable α-Fe(Si) phases without secondary phases. SEM and TEM–EDS revealed interfacial insulating layers mainly composed of Si-O, with localized phosphorus and carbon. Additive composition strongly influenced magnetic and physical properties. Increasing H₃PO₄ and PI reduced the density from 7.50 to 7.27 g/cm³ and lowered the permeability (from 189 at 1 kHz to 156), due to thicker interparticle layers that restricted metallic contact and domain wall motion. In contrast, Q-values rose significantly with frequency: for H₃PO₄ 0.25 wt.% + PI 0.25 wt.% + graphite 0.3 wt.%, Q increased from 0.39 (1 kHz) to 2.91 (10 kHz), reflecting effective eddy current suppression. Lubricant type further influenced performance: graphite consistently outperformed MoS₂, with 0.3 wt.% graphite providing the best balance of high density, permeability, and a frequency-stable Q-value. Overall, Fe-5.0 wt.%Si performance is governed not by bulk phase changes but by the trade-off between densification and insulation at particle interfaces. The optimal combination of low H₃PO₄ and PI with 0.3 wt.% graphite offers practical guidelines for designing high-frequency, high-efficiency motor materials. Full article

Growing interest in sustainable hydrogen production has brought renewed attention to photoelectrochemical (PEC) water splitting as a promising route for direct solar-to-chemical energy conversion. This study explores how integrating hematite (α-Fe₂O₃) and cupric oxide (CuO) photoelectrodes with a series of nickel-based co-catalysts can improve photoelectrochemical activity. Photoanodic (NiO_x, NiFeO_x, NiWO₄) and photocathodic (Ni, NiCu, NiMo) co-catalysts were synthesized via co-precipitation and mechanochemical methods and characterized through X-ray Diffraction (XRD), X-ray Fluorescence (XRF), Transmission Electron Microscopy–Energy Dispersive X-ray Spectroscopy (TEM-EDX), Scanning Electron Microscopy–Energy Dispersive X-ray Spectroscopy (SEM-EDX), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmett–Teller (BET) gas-adsorption analyses to clarify their crystallographic, morphological, and compositional properties, as well as their surface chemistry and textural properties (surface area and porosity). Electrochemical tests under 1 SUN illumination showed that NiO_x significantly improves the photocurrent of hematite photoanodes. Among the cathodic co-catalysts, NiMo demonstrated the best performance when combined with CuO photocathodes. For both photoelectrodes, an optimal co-catalyst loading was identified, beyond which performance declined due to potential charge transfer limitations and light attenuation. These findings highlight the critical role of co-catalyst composition and loading in optimizing the efficiency of PEC systems based on earth-abundant materials, offering a pathway toward scalable and cost-effective hydrogen production. Full article

The use of molybdenum-based alloys as materials for components operating under high temperatures and significant mechanical loads is widely recognized due to their excellent mechanical properties. However, their low high-temperature resistance remains a critical limitation, which can be effectively mitigated by applying protective coatings. In this study, we investigate the influence of a two-step coating process on the properties and performance of the TZM molybdenum alloy. In the first step, pack cementation was performed. Simultaneous surface saturation with aluminum and silicon, a process known as aluminosiliconizing, was conducted at 1000 °C for 6 h. The saturating mixture comprised powders of aluminum, silicon, aluminum oxide, and ammonium chloride. The second step involved the application of a pre-ceramic coating based on polyhydrosiloxane modified with silicon and boron. This treatment effectively eliminated pores and cracks within the coating. Thermodynamic calculations were carried out to evaluate the likelihood of aluminizing and siliconizing reactions under the applied conditions. Aluminosiliconizing of the TZM alloy resulted in the formation of a protective layer 20–30 µm thick. The multiphase structure of this layer included intermetallics (Al₆₃Mo₃₇, MoAl₃), nitrides (Mo₂N, AlN, Si₃N₄), oxide (Al₂O₃), and a solid solution α-Mo(Al). Subsequent treatment with silicon- and boron-modified polyhydrosiloxane led to the development of a thicker surface layer, 130–160 µm in thickness, composed of crystalline Si, amorphous SiO₂, and likely amorphous boron. A transitional oxide layer ((Al,Si)₂O₃) 5–7 µm thick was also observed. The resulting coating demonstrated excellent structural integrity and chemical inertness in an argon atmosphere at temperatures up to 1100 °C. High-temperature stability at 800 °C was observed for both coating types: aluminosiliconizing, and aluminosiliconizing followed by the pre-ceramic coating. Moreover, additional oxide layers of SiO₂ and B₂O₃ formed on the two-step coated TZM alloy during heating at 800 °C for 24 h. These layers acted as an effective barrier, preventing the evaporation of the substrate material. Full article

The sustainable development of our society faces significant challenges, including the need for environmentally friendly energy storage devices. Our work is concerned with the conversion of Mo-based recycled industrial waste into active nanocatalysts for energy storage applications. To reach this goal, we employed hydrothermal synthesis, a low-cost and temperature-scalable method. The proposed synthesis produces MoO₃ nanobelts (50–200 nm in width and 2–5 µm in length) with a high yield, about 74%. The synthesized nanostructures were characterized in 1 M KOH and 1 M NH₄OH, as alkaline environments are a promising choice for the development of eco-friendly devices. To investigate the material’s behaviour cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS) measurements were carried out. From CV curves, it was possible to evaluate the specific capacitance values of 290 and 100 Fg⁻¹ at 5 mVs⁻¹ in 1 M KOH and 1 M NH₄OH, respectively. Also, GCD was employed to evaluate the specific capacitance of the material, resulting in 75 and 60 Fg⁻¹ in 1 M KOH and 1 M NH₄OH, respectively. CV and GCD analyses revealed that MoO₃ nanobelts act as two different types of energy storage devices: supercapacitors and pseudocapacitors. Additionally, EIS allowed us to distinguish between the resistive and capacitive behaviour contributions depending on the electrolyte. Furthermore, it provided a comprehensive electrochemical characterization in different alkaline electrolytes, with the intention of conjugating waste management and sustainable energy storage device production. Full article

Water pollution caused by increasing industrial and human activity remains a serious environmental challenge, especially due to the persistence of organic contaminants in aquatic systems. Photocatalysis offers a promising and eco-friendly solution, but in the case of bismuth oxide (Bi₂O₃) there is still a limited understanding of how structural and morphological features influence photocatalytic performance. In this work, a straightforward hydrothermal synthesis method followed by controlled calcination was developed to produce phase-pure α- and β-Bi₂O₃ with tunable morphologies. By varying the hydrothermal temperature and reaction time, distinct structures were successfully obtained, including flower-like, broccoli-like, and fused morphologies. XRD analyses showed that the final crystal phase depends solely on the calcination temperature, with β-Bi₂O₃ forming at 350 °C and α-Bi₂O₃ at 500 °C. SEM and BET analyses confirmed that morphology and surface area are strongly influenced by the hydrothermal conditions, with the flower-like β-Bi₂O₃ exhibiting the highest surface area. UV–Vis spectroscopy revealed that β-Bi₂O₃ also has a lower bandgap than its α counterpart, making it more responsive to visible light. Photocatalytic tests using Rhodamine B showed that the flower-like β-Bi₂O₃ achieved the highest degradation efficiency (81% in 4 h). Kinetic analysis followed pseudo-first-order behavior, and radical scavenging experiments identified hydroxyl radicals, superoxide radicals, and holes as key active species. The catalyst also demonstrated excellent stability and reusability. Additionally, Methyl Orange (MO), a more stable and persistent azo dye, was selected as a second model pollutant. The flower-like β-Bi₂O₃ catalyst achieved 73% degradation of MO at pH = 7 and complete removal under acidic conditions (pH = 2) in less than 3 h. These findings underscore the importance of both phase and morphology in designing high-performance Bi₂O₃ photocatalysts for environmental remediation. Full article

Two-dimensional (2D) material-based resistive random-access memory (RRAM) has emerged as a promising solution for neuromorphic computing and computing-in-memory architectures. Compared to conventional metal-oxide-based RRAM, the novel 2D material-based RRAM devices demonstrate lower power consumption, higher integration density, and reduced performance variability, benefiting from their atomic-scale thickness and ultra-flat surfaces. Remarkably, 2D layered metal oxides retain these advantages while preserving the merits of traditional metal oxides, including their low cost and high environmental stability. Through a multi-step dry transfer process, we fabricated a Pd-MoO₃-Ag RRAM device featuring 2D α-MoO₃ as the resistive switching layer, with Pd and Ag serving as inert and active electrodes, respectively. Resistive switching tests revealed an excellent operational stability, low write voltage (~0.5 V), high switching ratio (>10⁶), and multi-bit storage capability (≥3 bits). Nevertheless, the device exhibited a limited retention time (~2000 s). To overcome this limitation, we developed a Gr-MoO₃-Ag heterostructure by substituting the Pd electrode with graphene (Gr). This modification achieved a fivefold improvement in the retention time (>10⁴ s). These findings demonstrate that by controlling the type and thickness of 2D materials and resistive switching layers, RRAM devices with both high On/Off ratios and long-term data retention may be developed. Full article

In this work, the influences of the Ar flow-rate and sublimation temperature on the phase composition and morphological structure of the sublimation products of analytical reagent MoO₃ are investigated. The results show that the sublimation products are always composed of thermodynamically stable orthorhombic molybdenum trioxide (α-MoO₃) and metastable monoclinic molybdenum trioxide (β-MoO₃) under different reaction conditions, among which the proportion of β-MoO₃ gradually increases with the increase in Ar flow-rate and the decrease in sublimation temperature. The formation temperature of α-MoO₃ is mainly between 780 K and 847 K, with the particles exhibiting an obvious sheet-like morphology. This work also finds that β-MoO₃ is mainly generated below 500 K; however, due to the co-actions of the deposition of gaseous MoO₃ molecules, the adsorption of Ar molecules, and the collision effect between the different particles, the newly formed β-MoO₃ is more inclined to take a spherical-shaped morphology in order to maintain its lowest energy state. Full article

To probe the properties of single atoms is a challenging task, especially from the experimental standpoint, due to sensitivity limits. Nevertheless, it is sometimes possible to achieve this by making corresponding choices and adjustments to the experimental technique and sample under investigation. In the present case, the absolute value of the electronic charge the Fe atoms acquire when they are adsorbed on the surface of aluminum oxide α-Al₂O₃(0001) was measured by a set of surface-sensitive techniques: low-energy ion scattering (LEIS), Auger electron spectroscopy (AES), low-energy electron diffraction (LEED), and work function (WF) measurements, in combination with density functional theory (DFT) calculations. The main focus was the submonolayer coverage of Fe atoms in situ deposited on the well-ordered stoichiometric α-Al₂O₃(0001) 7 nm thick film formed on a Mo(110) crystal face. An analysis of the evolution of the Fe LVV Auger triplet upon variation of the Fe coverage shows that there is electronic charge transfer from Fe to alumina and that its value gradually decreases as the Fe coverage grows. The same trend is also predicted by the DFT results. Extrapolation of the experimental Fe charge value versus coverage plot yields an estimated value of a single Fe atom adsorbed on α-Al₂O₃(0001) of 0.98e (electron charge units), which is in reasonable agreement with the calculated value (+1.15e). The knowledge of this value and the possibility of its adjustment may be important points for the development and tuning of modern sub-nanometer-scale technologies of diverse applied relevance and can contribute to a more complete justification and selection of the corresponding theoretical models. Full article

As a candidate material for turbine blades in aerospace engines, Nb-Si-based alloys have attracted significant research attention due to their high melting point and low density. However, their poor high-temperature oxidation resistance limits practical applications. Different alloying elements, including Ti, Mo, and Hf, were added to Nb-Si-based alloys to study the microstructural evolution of alloys. Additionally, the oxidation behavior and the oxidation kinetics of different alloys, as well as the morphology and microstructure of oxide scale and interior alloys at 1523 K from 1 h to 20 h were analyzed systematically. The current findings indicated that the Mo element is more conducive to promoting the formation of high-temperature precipitates of β-Nb₅Si₃ than the Ti and Hf elements. Inversely, the Ti element tends to cause the transition from high-temperature-phase β-Nb₅Si₃ to low-temperature-phase α-Nb₅Si₃, while the Hf element improves the appearance of the γ-Nb₅Si₃ phase but inhibits the other phases and refines the primary Nbss effectively. Noteworthily, compared with the oxidation weight gain of different alloys, Nb-16Si-20Ti-5Mo-3Hf-2Al-2Cr alloy has excellent high-temperature oxidation resistance, in which the oxidation products are TiNb₂O₇, Nb₂O₅, SiO₂, TiO₂, and HfO₂. It can be determined that in the oxidation process, the Ti element will preferentially form an oxide film of TiO₂, thereby wrapping around the matrix phases, protecting the matrix, and improving the antioxidant capacity, while the Hf element can form an infinite solid solution with the matrix and consume the small number of oxygen atoms entering the matrix, so as to achieve the effect of improving the oxidation resistance. Full article

Two modifications of ZnMoO₄ were successfully obtained by mechanochemical treatment with two milling speeds applied at 500 and 850 rpm. The phase formation was monitored by XRD analysis. The metastable monoclinic ß-ZnMoO₄ was directly synthesized at room temperature using the higher milling speed of 850 rpm. The thermodynamically stable triclinic α-ZnMoO₄ was obtained by combining heat treatment t 600 °C and ball milling at the lower milling speed of 500 rpm. The IR spectra contain typical vibration bands and confirm the formation of both ZnMoO₄ polymorphs. UV-Vis absorption and photoluminescence (PL) spectroscopy are used to study the optical properties of the as-prepared samples. The calculated optical band gaps for α- and ß-ZnMoO₄ are 4.09 and 3.02 eV. The photoluminescence emission spectrum of both samples shows peaks with different maximum intensity at 615 and 403 nm for α and ß phase, respectively. CIE co-ordinates are located in the orange and blue range of the color diagram. Full article

The key to selectively cleaving C–O bonds in lignin to produce high-value aromatic chemicals lies in the development of efficient and stable catalysts. In this study, a heterostructured catalyst with N-doped carbon-supported Co and dual-phase Mo_xC nanoparticles was prepared via the in situ pyrolysis of a Co–Mo–N precursor. The dual-phase α-MoC/β-Mo₂C heterostructure is adjusted by varying the Co:Mo ratio to affect the structure and electronic properties of the catalyst. The heterostructures bring about enhanced electron transfer from Co to Mo, which promotes hydrogen dissociation over the Co sites, significantly improving the catalyst’s hydrogenolysis activity and stability. The optimal catalyst with Co₁Mo_xC@NC exhibits excellent hydrogenolysis activity; under the optimal reaction conditions (260 °C, 1 MPa H₂, 3 h), the yield of aromatic monomers reaches 28.5%. Such prominent performance not only benefits from the numerous α-MoC/β-Mo₂C hetero-interfaces that offer abundant active sites for hydrogen dissociation, but also should be ascribed to the strong synergistic effect between Co and Mo. Full article

Developing more effective gold–support synergy is essential for enhancing the catalytic performance of supported gold nanoparticles (AuNPs) in the gas-phase oxidation of ethanol to acetaldehyde (AC) at lower temperatures. This study demonstrates a significantly improved Au–support synergy achieved by copper doping in LaMO₃ (M = Mn, Fe, Co, Ni) perovskites. Among the various Au/LaMCuO₃ catalysts, Au/LaMnCuO₃ exhibited exceptional catalytic activity, achieving an AC yield of up to 91% and the highest space-time yield of 764 g_AC g_Au⁻¹ h⁻¹ at 225 °C. Notably, this catalyst showed excellent hydrothermal stability, maintaining performance for at least 100 h without significant deactivation when fed with 50% aqueous ethanol. Comprehensive characterization reveals that Cu doping facilitates the formation of surface oxygen vacancies on the Au/LaMCuO₃ catalysts and enhances Au–support interactions. The LaMnCuO₃ perovskite stabilizes the crucial Cu⁺ species, resulting in a stable Au-Mn-Cu synergy within the Au/LaMnCuO₃ catalyst, which facilitates the activation of O₂ and ethanol at lower temperatures. The optimization of the reaction conditions further improves AC productivity. Kinetic studies indicate that the cleavages of both the O-H bond and the α-C-H bond of ethanol are the rate-controlling steps. Full article

The ultrafine MoO₃ powders were prepared by the combination of centrifugal spray drying and calcination in this work. The thermal decomposition behavior of the spherical precursor was studied. The phase constituents, morphologies, particle size, and specific surface areas of MoO₃ powders were characterized at different temperatures. It is found that the decomposition of the precursor is subjected to five stages, and forms different intermediate products, including (NH₄)₈Mo₁₀O₃₄, (NH₄)₂Mo₃O₁₀, (NH₄)₂Mo₄O₁₃, h-MoO₃, and the final product α-MoO₃. Moreover, the decomposition rate equation is established based on the thermal decomposition kinetic parameters of the precursor. With an increase in decomposition temperature, the morphology changes from unclear boundary particles to dispersed flake particles, and the flaky particles exhibit larger sizes, higher crystallinity, and better dispersion, which can be attributed to the mass transfer of gaseous MoO₃ products. Additionally, the MoO₃ particle size decreases progressively, and the specific surface area increases and then decreases. At 500 °C, it can achieve ultrafine flaky MoO₃ powder with the size of thick sheets, with a thickness of about 300 nm and a length of about 1–3 μm. This research can offer an innovative strategy for preparing ultrafine MoO₃ powder. Full article

α-Hydroxy ketones are a crucial class of organic compounds prevalent in natural products and pharmaceutical molecules. The CO₂-promoted hydration of propargylic alcohols is an efficient method for the synthesis of α-hydroxy ketones. Herein, an ionic liquid (IL) was designed to catalyze this reaction individually under atmospheric CO₂ pressure, volatile organic solvents, and additives. This IL, constructed from the molybdate anion, can be recycled from industrial (NH₄)₂MoO₄ production wastewater, demonstrating its high tolerance to catalytic environments and significant potential for practical applications. To our knowledge, this is the first instance of an oxometallate-based IL catalyst being utilized for the CO₂-promoted hydration of propargylic alcohols. Further mechanistic studies revealed the bifunctionality of this IL in activating both CO₂ and substrates. Full article