Search Results (157)

This study presents the development of Cu-doped NiMo/TiO₂ photoelectrocatalysts for simultaneous green hydrogen production and pharmaceutical pollutant removal under simulated solar irradiation. The catalysts were synthesized via wet impregnation (15 wt.% total metal loading with 0.6 wt.% Cu) and thermally treated at 400 °C and 900 °C to investigate structural transformations and catalytic performance. Comprehensive characterization (XRD, BET, SEM, XPS) revealed phase transitions, enhanced crystallinity, and redistribution of redox states upon Cu incorporation, particularly the formation of NiTiO₃ and an increase in oxygen vacancies. Crystallite sizes for anatase, rutile, and brookite ranged from 21 to 47 nm at NiMoCu400, while NiMoCu900 exhibited only the rutile phase with 55 nm crystallites. BET analysis showed a surface area of 44.4 m²·g⁻¹ for NiMoCu400, and electrochemical measurements confirmed its higher electrochemically active surface area (ECSA, 2.4 cm²), indicating enhanced surface accessibility. In contrast, NiMoCu900 exhibited a much lower BET surface area (1.4 m²·g⁻¹) and ECSA (1.4 cm²), consistent with its inferior photoelectrocatalytic performance. Compared to previously reported binary NiMo/TiO₂ systems, the ternary NiMoCu/TiO₂ catalysts demonstrated significantly improved hydrogen production activity and more efficient photoelectrochemical degradation of paracetamol. Specifically, NiMoCu400 showed an anodic peak current of 0.24 mA·cm⁻² for paracetamol oxidation, representing a 60% increase over NiMo400 and a cathodic current of −0.46 mA·cm⁻² at −0.1 V vs. RHE under illumination, nearly six times higher than the undoped counterpart (–0.08 mA·cm⁻²). Mott–Schottky analysis further revealed that NiMoCu400 retained n-type behavior, while NiMoCu900 exhibited an unusual inversion to p-type, likely due to Cu migration and rutile-phase-induced realignment of donor states. Despite its higher photosensitivity, NiMoCu900 showed negligible photocurrent, confirming that structural preservation and surface redox activity are critical for photoelectrochemical performance. This work provides mechanistic insight into Cu-mediated photoelectrocatalysis and identifies NiMoCu/TiO₂ as a promising bifunctional platform for integrated solar-driven water treatment and sustainable hydrogen production. Full article

In the wake of global energy transition and the “dual-carbon” goal, the rapid growth of electric vehicles has posed challenges for large-scale lithium-ion battery decommissioning. Retired batteries exhibit dual attributes of strategic resources (cobalt/lithium concentrations several times higher than natural ores) and environmental risks (heavy metal pollution, electrolyte toxicity). This paper systematically reviews pyrometallurgical and hydrometallurgical recovery technologies, identifying bottlenecks: high energy/lithium loss in pyrometallurgy, and corrosion/cost/solvent regeneration issues in hydrometallurgy. To address these, an integrated recycling process is proposed: low-temperature physical separation (liquid nitrogen embrittlement grinding + froth flotation) for cathode–anode separation, mild roasting to convert lithium into water-soluble compounds for efficient metal oxide separation, stepwise alkaline precipitation for high-purity lithium salts, and co-precipitation synthesis of spherical hydroxide precursors followed by segmented sintering to regenerate LiNi_1/3Co_1/3Mn_1/3O₂ cathodes with morphology/electrochemical performance comparable to virgin materials. This low-temperature, precision-controlled methodology effectively addresses the energy-intensive, pollutive, and inefficient limitations inherent in conventional recycling processes. By offering an engineered solution for sustainable large-scale recycling and high-value regeneration of spent ternary lithium ion batteries (LIBs), this approach proves pivotal in advancing circular economy development within the renewable energy sector. Full article

Defluoridation of water was investigated in an adsorption column study using Al-Mg-Ca-coated sand (AMCCS), a ternary metal oxide adsorbent with eco-friendly components that were shown to be effective for water defluoridation, in a batch adsorption study. A packed column of the AMCCS sorbent was evaluated as function of column flow rate, solution type, and sorbent recyclability. Adsorption column experiments included two column flow rates of 2 mL/min and 10 mL/min using two different solutions: deionized water and a synthetic solution representative of groundwater. Greater fluoride column adsorption capacity was obtained at the lower flow rate for both solutions, mainly due to longer contact times between solution and AMCCS sorbent. Adsorption of fluoride occurred through physical adsorption, which followed the Langmuir adsorption model and second-order kinetics for deionized water and synthetic solution. A lower AMCCS column fluoride adsorption capacity was observed for the synthetic solution due to the competition from adsorption of other ions in the synthetic solution, whereas fluoride adsorption by the AMCCS column was influenced by interphase mass transfer to a lesser extent using the synthetic solution than deionized water. The re-coating of spent AMCCS sorbent in the adsorption column resulted in effective recycling and reuse of the AMCCS adsorption column for both deionized water and the synthetic solution, rendering the AMCCS adsorption column a recyclable and sustainable flow through water defluoridation system. Full article

This study presents the fabrication and characterization of highly selective, room-temperature gas sensors based on ternary zinc oxide–molybdenum disulfide–titanium dioxide (ZnO-MoS₂-TiO₂) nanoheterostructures. Integrating two-dimensional (2D) MoS₂ with oxide nano materials synergistically combines their unique properties, significantly enhancing gas sensing performance. Comprehensive structural and chemical analyses, including scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and Fourier transform infrared spectroscopy (FTIR), confirmed the successful synthesis and composition of the ternary nanoheterostructures. The sensors demonstrated excellent selectivity in detecting low concentrations of nitrogen dioxide (NO₂) among target gases such as ammonia (NH₃), methane (CH₄), and carbon dioxide (CO₂) at room temperature, achieving up to 58% sensitivity at 4 ppm and 6% at 0.1 ppm for NO₂. The prototypes demonstrated outstanding selectivity and a short response time of approximately 0.51 min. The impact of light-assisted enhancement was examined under 1 mW/cm² weak ultraviolet (UV), blue, yellow, and red light-emitting diode (LED) illuminations, with the blue LED proving to deliver the highest sensor responsiveness. These results position ternary ZnO-MoS₂-TiO₂ nanoheterostructures as highly sensitive and selective room-temperature NO₂ gas sensors that are suitable for applications in environmental monitoring, public health, and industrial processes. Full article

Zinc cobaltite (ZnCo₂O₄) is a ternary metal oxide found in spinel with promising properties for various applications. Optimizing its catalytic activity requires an understanding of its electrochemical behavior. The electrochemical properties of ZnCo₂O₄ have significantly improved due to recent developments in nanostructuring, doping, surface modification, hybridization, structural engineering, and electrochemical activation. These improvements have inspired and motivated researchers by presenting the latest developments in the field. The spinel structure, coupled with the redox properties of cobalt ions, semiconducting characteristics, and electrocatalytic potential, positions ZnCo₂O₄ as a versatile material for several electrochemical energy storage and conversion systems. This review explores these advancements; the notable properties of ZnCo₂O₄; and its applications in sensors, batteries, photovoltaics, and supercapacitors. Full article

Black-odorous water (BOW) in urban areas poses significant risks to water safety and human health. Chemical oxygen demand (COD) is a critical parameter for the control and monitoring of BOW. However, traditional methods for COD determination are expensive, time-consuming, and involve the use of hazardous chemicals. In this study, reduced graphene oxide (rGO) and transitional metal particles (Cu, Ni) were used as working electrode materials for facile on-site determination of COD in BOW. Three composite materials (rGO/Cu, rGO/Ni, and rGO/Cu/Ni) were synthesized by one-step chemical reduction with different ratios, and their microstructure and chemical composition were characterized. Glucose solution and real water were used to evaluate the electrocatalytic performance of the different sensors. The ternary composite (rGO/Cu/Ni) screen-printed electrode sensor demonstrated excellent performance in COD analysis, with a low limit of detection (18.9 mg L⁻¹), a broad linear detection range from 53 to 1500 mg L⁻¹, and a 1.61% relative error for real water samples. The testing results were highly consistent with those obtained using the standard chromium sulfate method. This study offers promising prospects for the mass production of cost-effective COD electrochemical sensors, facilitating real-time, on-site monitoring of water bodies in major urban areas. Full article

The effects of a small addition of Ag and Ti on the thermal stability, mechanical properties, and tribological behavior of Zr-Co-Al bulk metallic glass (BMG) were investigated. A 5 at.% addition of Ag and Ti to the Zr-Co-Al base alloy improved the thermal stability and had no significant effect on the mechanical properties but considerably improved the wear behavior. The coefficient of friction decreased while the wear rate increased with increasing normal loads for all three alloys. Zr-Co-Al-Ti showed the best tribological performance among the studied alloys, with coefficient of friction and wear rate lower by a factor of four compared to Zr-Co-Al BMG. Predominantly oxidative wear was seen for the quaternary Zr-Co-Al-Ag and Zr-Co-Al-Ti BMGs at higher loads in contrast to abrasive and adhesive wear for the ternary Zr-Co-Al base alloy. These results highlight the potential of Ag and Ti micro-alloying for improving the mechanical and tribological properties of Zr-based amorphous alloys. Full article

Today, the machining of heat-resistant alloys based on triple, quad, or penta equilibria high-entropy alloy systems of elements (ternary, quaternary, quinary iron-, titanium-, or nickel-rich alloys), including dual-phase by Gibb’s phase rule, steels of the austenite class, and nickel- and titanium-based alloys, are highly relevant for the airspace and aviation industry, especially for the production of gas turbine engines. Cutting tools in contact with those alloys should withstand intensive mechanical and thermal loads (tense state of 1.38·10⁸–1.54·10⁸ N/m², temperature up to 900–1200 °C). The most spread material for those tools is cutting ceramics based on oxides, nitrides of the transition and post-transition metals, and metalloids. This work considers the wear resistance of the cutting insert of silicon nitride with two unique development coatings — titanium–zirconium nitride coating (Ti,Zr)N and complex quad nitride coating with TiN content up to 70% (Ti,Al,Cr,Si)N with a thickness of 3.8–4.0 µm on which microtextures were produced by the assisted electric discharge machining with the electrode-tool of ø0.25 mm. The microtextures were three parallel microgrooves of R0.13^+0.02 mm at a depth of 0.025₋₀.₀₅. The operational life was increased by ~1.33 when the failure criterion in turning nickel alloy was 0.4 mm. Full article

The hydrogen economy, as an emerging paradigm for sustainable energy, relies on efficient hydrogen oxidation (HOR) and hydrogen evolution reactions (HER). These reactions require effective catalysts to enhance reaction kinetics and reduce costs. Platinum (Pt) is widely used but faces issues such as high cost and CO poisoning. Non-precious metal catalysts, particularly Ni-based alloys, are being explored as viable alternatives. This study introduces a ternary MoWNi alloy catalyst synthesized via microwave-assisted methods and annealing. The MoWNi alloy catalyst achieves a current density of 3.5 mA·cm⁻² at an overpotential of 100 mV in HOR and requires only 25 mV overpotential to reach a current density of 10 mA·cm⁻² in HER, making it comparable to commercial 20% Pt/C catalysts. Notably, the catalyst also exhibits superior stability and resistance to CO toxicity. These findings underscore the potential of MoWNi alloy catalysts in advancing hydrogen-based energy systems. Full article

The increasing demand for zinc resources and the declining availability of sulfide zinc ore reserves have made the efficient utilization of zinc oxide a topic of considerable interest. In this study, a ternary composite collector ABN (Al-BHA-NaOL system) was applied to the direct flotation of smithsonite. Micro-flotation studies showed that at pH 9, ABN exhibited better adsorption on smithsonite, achieving a recovery rate of 80.62%. Visual MINTEQ 3.1 and zeta potential analysis confirmed that ABN predominantly reacted with Zn(OH)₂(aq) on the surface of smithsonite. Furthermore, X-ray photoelectron spectroscopy (XPS) analysis results elucidated the formation of Al-O bonds through chemical adsorption on the smithsonite surface. Additionally, powder contact angle measurements indicated that ABN enhances the surface contact angle of smithsonite. These results illuminate that ABN is adsorbed by reacting with O sites on hydroxylated metal ions on the smithsonite surface, with Al serving as the adsorption center, thereby achieving separation and purification. Due to ABN’s adsorption characteristics, smithsonite can achieve efficient and clean direct flotation recovery without sulfidization. Full article

This study presents the synthesis of a CuO-TiO₂–saponite ternary nanocomposite via a hydrothermal method, designed to efficiently remove bromocresol green dye. Characterization techniques, including X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy, confirmed significant interactions between metal oxide nanoparticles and the clay mineral matrix. Diffuse reflectance and photoluminescence analyses revealed a narrow band gap and surface defects, such as oxygen vacancies, enhancing the material’s photocatalytic properties. Under UV irradiation, the nanocomposite achieved 83% discoloration of bromocresol green dye within 150 min. The inhibitor studies identified hydroxyl and superoxide radicals as key species in the degradation mechanism. This work underscores the potential of clay-mineral-based nanocomposites, where clay minerals function both as structural support and as enhancers of the semiconductor’s photocatalytic activity. Full article

In this study, magnetic binary/ternary Zn_xCo_1−xFe₂O₄ (x = 0, 0.5, 1) nanoparticles were synthesized using a straightforward one-step microwave technique. To produce the Zn_xCo_1−xFe₂O₄ nanoparticles, iron (III) nitrate nonahydrate, zinc nitrate hexahydrate, and cobalt nitrate hexahydrate were used as metal sources, with urea used as the fuel and ammonium nitrate as the oxidizer. These materials were combined in an alumina crucible covered by a CuO jacket to absorb microwave energy and facilitate calcination. The thermal treatment involved placing the alumina crucible in a domestic microwave oven at 450 W for 30 min. The key strengths of this experimental strategy include its simplicity, cost-effectiveness, and rapidity, aligning with green chemistry principles. The synthesized nanoparticles were characterized using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, a vibrating sample magnetometer (VSM), and Brunauer–Emmett–Teller (BET) analysis. XRD analysis confirmed the presence of the pure ferrite nanocrystalline phase. Scanning electron microscopy (SEM), employed with energy-dispersive X-ray spectroscopy (EDS), was used to study the surface morphology and analyze the elemental composition. The SEM analysis revealed that the synthesized magnetic nanoparticles had particle sizes ranging from 30 to 50 nm. Furthermore, we explored the potential use of these magnetic nanoparticles as photocatalysts for degrading organic pollutants such as methylene blue in aqueous solutions. Full article

NH₃ selective catalytic reduction (NH₃-SCR) is the most prevalent and effective method for removing nitrogen oxides. Over the past few decades, manganese (Mn)-based catalysts have demonstrated strong catalytic activity and have been extensively studied for low-temperature NH₃-SCR reactions. This paper provides an in-depth introduction to four forms of Mn-based catalysts: single manganese oxide-based catalysts, binary Mn-based metal oxide catalysts, ternary and multivariate Mn-based metal oxide catalysts, and nano-Mn-based catalysts. Advances have been made in enhancing Mn-based catalysts’ redox performance and acidity, increasing the active component’s dispersion, lowering binding energy, enlarging specific surface area, raising the Mn⁴⁺/Mn³⁺ ratio, and enriching surface adsorbed oxygen by optimizing preparation methods, altering the oxidation state of active components, modifying crystal phases, and adjusting morphology and dispersion, along with various metal modifications. The mechanism of low-temperature NH₃-SCR reactions has been elucidated using various characterization techniques. Finally, the research directions and future prospects of Mn-based catalysts for low-temperature NH₃-SCR reactions are discussed, aiming to accelerate the commercial application of new Mn-based catalysts. Full article

A mixed-metal ternary chalcogenide, cobalt molybdenum telluride (CMT), has been identified as an efficient tri-functional electrocatalyst for seawater splitting, leading to enhanced oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and oxygen reduction reaction (ORR). The CMT was synthesized by a single step hydrothermal technique. Detailed electrochemical studies of the CMT-modified electrodes showed that CMT has a promising performance for OER in the simulated seawater solutions, exhibiting a small overpotential of 385 mV at 20 mA cm⁻², and superior catalyst durability for prolonged period of continuous oxygen evolution. Interestingly, while gas chromatography analysis confirmed the evolution of oxygen in an anodic chamber, it showed that there was no chlorine evolution from these electrodes in alkaline seawater, highlighting the novelty of this catalyst. CMT also displayed remarkable ORR activity in simulated seawater as indicated by its four-electron reduction pathway forming water as the dominant product. One of the primary challenges of seawater splitting is chlorine evolution from the oxidation of dissolved chloride salts. The CMT catalyst successfully and significantly lowers the water oxidation potential, thereby separating the chloride and water oxidation potentials by a larger margin. These results suggest that CMT can function as a highly active tri-functional electrocatalyst with significant stability, making it suitable for clean energy generation and environmental applications using seawater. Full article

The potential of photocatalytic CO₂ conversion is significant for the production of fuels and chemicals, while simultaneously mitigating CO₂ emissions and addressing environmental concerns. Despite the current drawbacks of single metal-based photocatalysts, such as lower performance, uncontrollable selectivity, and instability, this study focuses on the synthesis of Ag₃VO₄ nanorods using the sol–gel method. The goal is to create a highly effective catalyst for visible light-responsive CO₂ conversion. The successful synthesis of Ag₃VO₄ nanorods with a nanorod structure, functional under visible light, resulted in the highest yields of CH₄ and dimethyl ether (DME) at 271 and 69 µmole/g-cat, respectively. The optimized Ag₃VO₄ nanorods demonstrated performance improvements, with CH₄ and DME production 6.4 times and 4.5 times higher than when using V₂O₅ samples. This suggests that Ag₃VO₄ nanorods facilitate electron transfer to CO₂, offer short pathways for electron transfer, and create empty spaces within the nanorods as electron reservoirs, enhancing the photoactivity. The prolonged stability of Ag₃VO₄ in the CO₂ conversion system confirms that the nanorod structure provides controllable selectivity and stability. Therefore, the fabrication of nanorod structures holds promise in advancing high-performance photocatalysts in the field of photocatalytic CO₂ conversion to solar fuels. Full article