Search Results (127)

The microstructures and oxidation behavior of the NbSiTiAlHf alloys doped with rare earth elements at 1300 °C were investigated. The nominal compositions of the selected alloys are Nb-13.5Si-23Ti-37Al-5Hf-0.5X (at.%), where X = Y, Dy, and La, respectively. It was shown that the whole scales were mainly composed of the major phases of Al₂O₃ and the minor phases of TiO₂, where the TiO₂ formed on the surface or in the upper layer of scales, for the undoped, Y, and Dy-doped alloy. But, for the 0.5 at.% La-doped alloys, the whole scales were constituted with the major phases of both Al₂O₃ and TiO₂, and contained plenty of large voids. The 0.5 at.% Dy-doped alloys exhibited the lowest scale growth rate with the value of 1.87 × 10⁻¹¹ cm²/s, and the benefits of Y on the oxidation rates were short-term, while 0.5 at.% La-doped alloys had the highest scale growth rate of 4.55 × 10⁻¹⁰ cm²/s compared with those of all the selected alloys. Then, the effects of Y, Dy, and La on the oxidation behavior of the alumina-scale-forming NbSiTiAlHf alloys were discussed. Full article

Acetone necessitates reliable detection for the sake of both industrial and environmental safety. Metal oxides are widely used as functional materials for the development of gas sensors because techniques like nanostructure modification, doping, and solid solution formation can enhance their sensitivity and selectivity by tuning structural and electronic properties. This study developed PrFeTiO₅ nanostructures, synthesized via the solid-state reaction for acetone sensing. The sensor demonstrated a high response to acetone at an operating temperature of 400 °C, with a low influence of humidity, displaying outstanding selectivity towards acetaldehyde, NH₃, H₂, CO, and CO₂, making it suitable across various applications. Full article

This review summarizes the recent developments in titanium suboxide (TSO) doping and the application of doped materials in pollutant degradation and electrochemistry. Doping is mainly limited to transition and rare-earth metals, with some exceptions, of similar ionic radii and charge, that can replace Ti ions in TSO without too much disturbance to the lattice. Consequently, doping is limited to below 10 at%, which predominantly induces oxygen vacancy formation. Doping mechanisms are weighted, and their effect on conductivity, stability, and catalytic activity is overviewed. High-temperature H₂ reduction of TiO₂ is still the dominant preparation method, with carbothermal reduction and Ti reduction gaining ground due to safety and energy concerns. Doping predominantly increases the conductivity 2–5 times, while the stability can be both improved or worsened, depending on the size and charge of the doping ion. Electrochemical oxidation, at positive overpotentials, of per- and polyfluoroalkyl substances (PFAS), antibiotics, and other water pollutants, is the main avenue of application. Doping almost exclusively leads to complete selected pollutant degradation and improvement of the pristine TSO, which is summarized in detail. New niche applications of peroxide, hydrogen, and chlorine production are also viable on doped TSO and are touched upon. Complementing experimental results are theoretical calculations, and we give an overview of density functional theory (DFT) results of transition metal-doped TSOs, identifying active centers, degradation trends, and potential new doping candidates. Full article

Rare-earth barium copper oxide (REBCO) high-temperature superconductors, owing to their ability to maintain high critical current density (J_c) under liquid-nitrogen-temperature and high-magnetic-field conditions, are widely regarded as one of the most promising material systems among all superconductors. This review systematically summarizes fabrication strategies for REBCO coated conductors, with a focus on pulsed laser deposition (PLD) for achieving high-quality epitaxial growth with precise composition control. To enhance in-field performance, strategies for introducing artificial pinning centers (APCs) are examined, including rare-earth element doping, substrate surface decoration, and nanoscale secondary phase incorporation. The mechanisms of vortex pinning from different dimensional defects and their synergistic effects are compared. Finally, we suggest potential future directions aimed at further enhancing the superconducting properties. Full article

The rational design of transition metal oxides with tailored electronic structures and defect chemistries is critical for advancing high-performance supercapacitors. Herein, we report the engineering of cobalt oxide (Co₃O₄) gels through controlled sol–gel synthesis and rare earth (RE) incorporation using neodymium (Nd), gadolinium (Gd), and dual neodymium/gadolinium (Nd/Gd) doping. X-ray diffraction (XRD) confirmed the preservation of the cubic spinel structure with systematic peak shifts and broadening, evidencing lattice strain, oxygen vacancy generation, and defect enrichment. Field-emission scanning electron microscopy (FE-SEM) analyses revealed distinct morphological evolution from compact nanoparticle assemblies in pristine Co₃O₄ to highly porous, interconnected frameworks in Nd/Gd–Co₃O₄ (Nd/Gd-Co). X-ray photoelectron spectroscopy (XPS) verified the stable incorporation of RE ions, accompanied by electronic interaction with the Co–O matrix and enhanced oxygen defect states. Electrochemical measurements demonstrated that the Nd/Gd–Co electrode achieved a remarkable areal capacitance of 25 F/cm² at 8 mA/cm², superior ionic diffusion coefficients, and the lowest equivalent series resistance (0.26 Ω) among all samples. Long-term cycling confirmed 84.35% capacitance retention with 94.46% coulombic efficiency after 12,000 cycles. Furthermore, the asymmetric pouch-type supercapacitor (APSD) constructed with Nd/Gd–Co as the positive electrode and activated carbon as the negative electrode delivered a wide operational window of 1.5 V, an areal capacitance of 140 mF/cm², an energy density of 0.044 mWh/cm², and 89.44% retention after 7000 cycles. These findings establish Nd/Gd-Co gels as robust and scalable electrode materials and demonstrate that RE co-doping is an effective strategy for bridging high energy density with long-term electrochemical stability in asymmetric supercapacitors. Full article

Zinc oxide (ZnO) thin films have attracted increasing attention as promising materials for sensing applications due to their wide band gap, high exciton binding energy, and remarkable chemical stability. However, the inherent limitations of pure ZnO, such as moderate sensitivity, selectivity, and relatively high operating temperatures, limit its widespread use in advanced sensing technologies. Co-doping, or dual doping with two distinct elements, has emerged as an effective strategy to overcome these challenges by synergistically tailoring the structural, electronic, and surface properties of ZnO thin films. This review provides a comprehensive overview of recent advances in the development of co-doped ZnO thin films for sensing applications. The focus is on the role of different combinations of dopants, including transition metals, rare earth elements, and non-metals, in modulating the charge carrier concentration, oxygen vacancy density, and adsorption dynamics. These effects collectively enhance the sensing properties and long-term stability and reduce detection limits. The analysis highlights the correlations between synthesis methods, dopant incorporation mechanisms, and resulting sensor performance. Key challenges such as dopant clustering, reproducibility, and scalability are discussed, along with emerging opportunities in flexible room-temperature sensor platforms. Overall, it has been demonstrated that co-doped ZnO thin films represent a versatile and tunable class of sensing materials with strong potential for next-generation environmental and biomedical monitoring. Full article

Dry reforming of methane and ethanol is a promising catalytic process for the conversion of carbon dioxide and hydrocarbon feedstocks into synthesis gas (H₂/CO), which serves as a key platform for the production of fuels and chemicals. Over the past decade, substantial progress has been achieved in the design of catalysts with enhanced activity and stability under the demanding conditions of these strongly endothermic reactions. This review summarizes the latest developments in catalyst systems for DRM and EDR, including Ni-based catalysts, perovskite-type oxides, MOF-derived materials, and high-entropy alloys. Particular attention is given to strategies for suppressing carbon deposition and preventing metal sintering, such as oxygen vacancy engineering in oxide supports, rare earth and transition metal doping, strong metal–support interactions, and morphological control via core–shell and mesoporous architectures. These approaches have been shown to improve coke resistance, maintain metal dispersion, and extend catalyst lifetimes. The review also highlights emerging concepts such as multifunctional hybrid systems and innovative synthesis methods. By consolidating recent findings, this work provides a comprehensive overview of current progress and future perspectives in catalyst development for DRM and EDR, offering valuable guidelines for the rational design of advanced catalytic materials. Full article

The long-term corrosion behavior of Al₂O₃-3%TiO₂ (AT3) coatings doped with1%, 5% and 8% CeO₂ prepared by plasma spraying was studied in 5% NaCl solution. The results showed that the protective performance of CeO₂-doped coatings was significantly higher than that of undoped coatings, primarily due to the reduction in coating porosity caused by the addition of rare-earth elements. Among the doped coatings, the 5% CeO₂-doped coating exhibited the best protective performance. The addition of rare-earth oxides CeO₂ reduced the content of γ-Al₂O₃ in the coating, but when the concentration of CeO₂ increased to 8%, the Ce element was rich in the gap of the coating. Excessive CeO₂ enriched in the gaps and coexisted more with Ti, and prevented the formation of the AlTi phase, which affected the performance of the coating. Electrochemical and XPS results revealed that an appropriate amount of Ce atoms or CeO₂ particles could fill the pores of the coating. During long-term immersion, Ce (IV) was converted to Ce (III), which demonstrated that Ce atoms have high chemical activity in coatings. The thermodynamic calculation results show that more CeO₂ particles improved the adsorption of corrosive ions. It indicated that the content of doped rare-earth oxides exceeding 5% would be utilized as an active material in the corrosive process. Full article

A pyrochlore-type crystal structure photocatalytic nanomaterial, Ho₂FeSbO₇, was successfully synthesized using a hydrothermal method. Additionally, a fluorite-structured Bi_0.5Yb_0.5O_1.5 was prepared via rare earth Yb doping. Finally, a novel Ho₂FeSbO₇/Bi_0.5Yb_0.5O_1.5 heterojunction photocatalyst (HBHP) was fabricated using a solvothermal method. The crystal structure, surface morphology, and physicochemical properties of the samples were characterized using XRD, a micro-Raman spectrometer, FT-IR, XPS, ultraviolet photoelectron spectroscopy (UPS), TEM, and SEM. The results showed that Ho₂FeSbO₇ possessed a pyrochlore-type cubic crystal structure (space group Fd-3m, No. 227), while Bi_0.5Yb_0.5O_1.5 featured a fluorite-type cubic structure (space group Fm-3m, No. 225). The results of the degradation experiment indicated that when HBHP, Ho₂FeSbO₇, or Bi_0.5Yb_0.5O_1.5 was employed as a photocatalytic nanomaterial, following 140 min of visible light irradiation, the removal efficiency of ciprofloxacin (CIP) reached 99.82%, 86.15%, or 73.86%, respectively. This finding strongly evidenced the remarkable superiority of HBHP in terms of photocatalytic performance. Compared to the individual catalyst Ho₂FeSbO₇, Bi_0.5Yb_0.5O_1.5, or N-doped TiO₂, the removal efficiency of CIP by HBHP was 1.16 times, 1.36 times, or 2.52 times higher than that by Ho₂FeSbO₇, Bi_0.5Yb_0.5O_1.5, or N-doped TiO₂, respectively. The radical trapping experiments indicated that in the CIP degradation process, the hydroxyl radical owned the strongest oxidation ability, followed by the superoxide anion and the photoinduced hole. These studies are of great significance for the degradation of antibiotics and environmental protection. Full article

In this paper, high-strength W-1%La₂O₃ alloy wire was obtained by solid-state doping using tungsten powder and lanthanum oxide, large deformation rotary forging and wire drawing, which solved the disadvantages of traditional tungsten alloy wire processing such as the uneven distribution of rare earth oxides. The effects of rotary forging and annealing on the microstructure and properties of tungsten alloy were studied, which provided some basis for preparing high-strength tungsten alloy wire. The results indicate that tungsten alloy undergoes recovery at relative high temperatures (1480–1380 °C) during the rotary forging process. After large deformation, subgrains and uneven microstructures appear, so annealing is required before tungsten alloys wire drawing processing. With increasing annealing temperature, the recrystallization degree gradually increases and the hardness of tungsten alloy gradually decreases. When the deformation is less than 81.2%, tungsten alloy wire exhibits brittle fracture. When the deformation increases to 88.4% (ø0.8 mm), the fracture surface of the wire exhibits a plastic–brittle mixed fracture mechanism. Full article

Rare-earth (RE) doping has been found to be a potent method to improve the structural, optical, electronic, and magnetic properties of ZnO, positioning it as a versatile material for future optoelectronic devices. This review herein thoroughly discusses the latest developments in RE-doped ZnO based on the role of the dopant type, concentration, synthesis method, and consequences of property modifications. The 4f electronic states of rare-earth elements create strong visible emissions, control charge carriers, and design defects. These structural changes lead to tunable bandgap energies and increased light absorption. Also, RE doping considerably enhances ZnO’s performance in electronic devices, like UV photodetectors, LEDs, TCOs, and gas sensors. Though, challenges like solubility constraints and lattice distortions at higher doping concentrations are still key challenges. Co-doping methodologies and new synthesis techniques to further optimize the incorporation of RE into ZnO matrices are also reviewed in this article. By showing a systematic comparison of different RE-doped ZnO systems, this paper sheds light on their future optoelectronic applications. The results are useful for the design of advanced ZnO-based materials with customized functionalities, which will lead to enhanced device efficiency and new photonic applications. Full article

A Yb³⁺-doped BiOI 3D nanosheet array composite was successfully fabricated through a solvothermal deposition strategy on flexible carbon cloth (CC). This composite was subsequently integrated with high-chlorine fly ash (FA) blocks to form the Yb-BiOI/CC/FA hybrid material. Comprehensive characterization was performed using multiple analytical techniques for crystalline phase identification, morphological analysis, valence state, band structure evaluation, and charge carrier separation assessment. Electrochemical measurements were conducted to evaluate the material’s electronic properties. Experimental results demonstrated superior photocatalytic performance under visible light irradiation, with the Yb-BiOI/CC/FA composite achieving 52.87% methylene blue degradation efficiency. The reaction rate constant of this modified nanomaterial was approximately 2.1 times higher than that of pristine BiOI/CC/FA. Radical trapping experiments revealed that superoxide radicals (·O₂⁻) served as the predominant oxidative species. This study presents a dual-benefit strategy for environmental remediation by simultaneously achieving sustainable waste valorization of industrial byproducts (FA) and developing high-efficiency photocatalytic materials. The successful integration of rare-earth metal modification with substrate engineering provides valuable insights for designing advanced photocatalytic systems for pollutant degradation. Full article

Gas-sensing technology is crucial for the detection of toxic and harmful gases to ensure environmental safety and human health. Gas sensors convert the changes in the conductivity of the sensing material resulting from the adsorption of gas molecules into measurable electrical signals. Rare earth orthoferrite-based perovskite oxides have emerged as promising candidates for gas-sensing technology owing to their exceptional structural, optical, and electrical properties, which enable the detection of various gases. In this article, we review the latest developments in orthoferrite-based gas sensors in terms of sensitivity, selectivity, stability, operating temperature, and response and recovery times. It begins with a discussion on the gas-sensing mechanism of orthoferrites, followed by a critical emphasis on their nanostructure, doping effects, and the formation of nanocomposites with other sensing materials. Additionally, the role of the tunable bandgap and different porous morphologies with a high surface area of the orthoferrites on their gas-sensing performance were explored. Finally, we identified the current challenges and future perspectives in the gas-sensing field, such as novel doping strategies and the fabrication of miniaturized gas sensors for room-temperature operation. Full article

From the lanthanide group, part of the rare earth elements (REEs), lanthanum is one of the most important elements given its application potential. Although it does not have severe toxicity to the environment, its increased usage in advanced technologies and medical fields and scarce natural reserves point to the necessity also of recovering lanthanum from diluted solutions. Among the multiple methods for separation and purification, adsorption has been recognized as one of the most promising because of its simplicity, high efficiency, and large-scale availability. In this study, a xerogel based on silicon and iron oxides doped with zinc oxide and polymer (SiO₂@Fe₂O₃@ZnO) (SFZ), obtained by the sol–gel method, was considered as an adsorbent material. Micrography indicates the existence of particles with irregular geometric shapes and sizes between 16 μm and 45 μm. Atomic force microscopy (AFM) reveals the presence of dimples on the top of the material. The specific surface area of the material, calculated by the Brunauer–Emmet–Teller (BET) method, indicates a value of 53 m²/g, with C constant at a value of 48. In addition, the Point of Zero Charge (pH_pZc) of the material was determined to be 6.7. To establish the specific parameters of the La(III) adsorption process, static studies were performed. Based on experimental data, kinetic, thermodynamic, and equilibrium studies, the mechanism of the adsorption process was established. The maximum adsorption capacity was 6.7 mg/g, at a solid/liquid ratio = 0.1 g:25 mL, 4 < pH < 6, 298 K, after a contact time of 90 min. From a thermodynamic point of view, the adsorption process is spontaneous, endothermic, and occurs at the adsorbent–adsorbate interface. The Sips model is the most suitable for describing the observed adsorption process, indicating a complex interaction between La(III) ions and the adsorbent material. The material can be reused as an adsorbent material, having a regeneration capacity of more than 90% after the first cycle of regeneration. The material was reused 3 times with considerable efficiency. Full article

Zr-4 alloy tubes, as the primary cladding material in nuclear reactor cores, face the critical challenge of oxidative attack in 1200 °C steam environments. To address this issue, high-temperature oxidation-resistant coatings fabricated via extreme high-speed laser cladding (EHLA) present a promising mitigation strategy. In this study, Y₂O₃-modified (0.0–5.0 wt.%) Cr/FeCrAl composite coatings were designed and fabricated on Zr-4 substrates using the EHLA process, followed by systematic investigation of Y doping effects on coating microstructures and steam oxidation resistance (1200 °C, H₂O atmosphere). Experimental results demonstrate that Y₂O₃ doping remarkably enhanced the oxidation resistance, with optimal performance achieved at 2.0 wt.% Y₂O₃ (31% oxidation mass gain compared to the substrate after 120-min exposure). Microstructural analysis reveals that the dense grain boundary network facilitates rapid surface diffusion of Al, promoting continuous Al₂O₃ protective film formation. Additionally, Y segregation at grain boundaries suppressed outward diffusion of Cr³⁺ cations, effectively inhibiting void formation at the oxide-coating interface and improving interfacial stability. The developed rare-earth-oxide-doped composite coating via extreme high-speed laser cladding process shows promising applications in surface-strengthening engineering for nuclear reactor Zr-4 alloy cladding tubes, providing both theoretical insights and technical references for the design of high-temperature oxidation-resistant coatings in nuclear industry. Full article