Search Results (203)

The interface between high-performance thermoelectric materials and electrodes critically governs the conversion efficiency and long-term reliability of thermoelectric generators under high-temperature operation. Here, we propose Al_xCoCrFeNi high-entropy alloys (HEA) as barrier layers to bond Cu-W electrodes with p-type skutterudite (p-SKD) thermoelectric materials. The HEA/p-SKD interface exhibited excellent chemical bonding with a stable and controllable reaction layer, forming a dense, defect-free (Fe,Ni,Co,Cr)Sb phase (thickness of ~2.5 μm) at the skutterudites side. The interfacial resistivity achieved a low value of 0.26 μΩ·cm² and remained at 7.15 μΩ·cm² after aging at 773 K for 16 days. Moreover, the interface demonstrated remarkable mechanical stability, with an initial shear strength of 88 MPa. After long-term aging for 16 days at 773 K, the shear strength retained 74 MPa (only 16% degradation), ranking among the highest reported for thermoelectric materials/metal joints. Remarkably, the joint maintained a shear strength of 29 MPa even after 100 continuous thermal cycles (623–773 K), highlighting its outstanding thermo-mechanical stability. These results validate the Al_xCoCrFeNi high-entropy alloys as an ideal interfacial material for thermoelectric generators, enabling simultaneous optimization of electrical and mechanical performance in harsh environments. Full article

This study addresses the efficiency and cost challenges of hydrogen evolution reaction (HER) catalysts in the context of carbon neutrality strategies by employing a synergistic approach that combines cation vacancy anchoring and transition metal doping on two-dimensional (2D) MXenes. Using an in situ LiF/HCl etching process, the aluminum layers in Ti₃AlC₂ were precisely removed, resulting in a few-layer Ti₃C₂T_x MXene with an increased interlayer spacing of 12.3 Å. Doping with the transition metals Fe, Co, Ni, and Cu demonstrated that Fe@Ti₃C₂ provided the optimal HER performance, characterized by an overpotential (η₁₀) of 81 mV at 10 mA cm⁻², a low Tafel slope of 33.03 mV dec⁻¹, and the lowest charge transfer resistance (R_ct = 5.6 Ω cm²). Mechanistic investigations revealed that Fe’s 3d⁶ electrons induce an upward shift in the d-band center of MXene, improving hydrogen adsorption free energy and reducing lattice distortion. This research lays a solid foundation for the design of non-precious metal catalysts using MXenes and highlights future avenues in bimetallic synergy and scalability. Full article

Electrochemical devices on solid electrolytes are closely considered from the point of view of efficient utilization of environmental resources in order to obtain a variety of products, including those with high added cost. This study provides insight into the functionality of electrochemical cells that have been designed with a specific configuration. These cells have the same ionic composition of the anode, cathode, and electrolyte. This was achieved by iron doping of highly conductive (La,Sr)(Ga,Mg)O_3−δ electrolyte, and gallium and magnesium doping of the electrode material based on (La,Sr)FeO_3−δ. The main focus in this study is on the electrochemical behavior of such cells depending on the oxygen partial pressure in the gas phase, as well as the stability of the electrochemical performance over time for more than 950 h of testing. According to the obtained results, the electrochemical cell with a completely identical ionic composition of electrodes La_0.6Sr_0.4Fe_0.85Ga_0.1Mg_0.05O_3−δ and electrolyte (La_0.8Sr_0.2)_0.98Ga_0.7Fe_0.1Mg_0.2O_3−δ demonstrated the best set of optimal performances. This consists of excellent chemical compatibility, high electrochemical activity (0.08 Ω cm² in air at 800 °C), and a minor degradation rate. Full article

Metal sulfides are promising anode candidates for sodium–ion batteries (SIBs) due to their high theoretical capacities. However, their practical application is limited by significant volume extension and sluggish Na⁺ diffusion during cycling, which lead to rapid capacity degradation and poor long-term stability. In this work, we report the rational design of a hollow triple-shelled high-entropy sulfide (NaFeZnCoNiMn)₉S₈, synthesized through sequential templating method under hydrothermal conditions. Transmission electron microscopy confirms its well-defined three-shelled architecture. The inter-shell voids effectively buffer Na⁺ insertion/desertion-induced volume extension, while the tailored high-entropy matrix enhances electronic conductivity and accelerates Na⁺ transport. This synergistic design yields outstanding performance, including a high initial Coulombic efficiency (ICE) of 94.1% at 0.1 A g⁻¹, low charge-transfer resistance (0.32~2.54 Ω), fast Na⁺ diffusion efficiency (10^−8.5–10^−10.5 cm² s⁻¹), and reversible capacity of 582.6 mAh g⁻¹ after 1600 cycles at 1 A g⁻¹ with 91.2% capacity retention. These results demonstrate the potential of high-entropy, multi-shelled architectures as a robust platform for next-generation durable SIB anodes. Full article

Ti-2Al-9.2Mo-2Fe (2A2F) alloy is a low-cost β-Ti alloy in which the expensive β-stabilizing elements (Ta, Nb, W, Ni) are replaced with relatively inexpensive Mo and Fe for use in low-cost applications in various industries. The 2A2F alloy exhibits excellent mechanical properties such as high specific strength and low elastic modulus compared to conventional steel alloys but is prone to brittleness owing to the formation of the ω phase when heat-treated at relatively low temperatures. Therefore, an appropriate aging treatment should be performed to control the precipitation of the isothermal ω phase and secondary α phase. This study aims to derive the appropriate aging-treatment conditions following a solution treatment at 790 °C for 1 h, which is below the β-transus temperature of 815 °C. The aging treatments are conducted at holding temperatures in the range of 450–600 °C and holding times between 1 and 18 h. At relatively low aging temperatures of 450 °C and 500 °C, the precipitation of the isothermal ω phase resulted in significantly high hardness and compressive strength. As the aging temperature and holding time increased, the ω phase gradually transformed into the secondary α phase, leading to a balanced combination of strength and ductility. However, at excessively high aging temperatures and prolonged durations, excessive precipitation and growth of secondary α phases occurred, which caused a reduction in hardness and compressive strength, accompanied by an increase in ductility. In this study, the effects of precipitation evolution on mechanical properties such as tensile strength and hardness under various heat treatment conditions were comparatively analyzed. Full article

The enzyme ω-transaminase (ω-TA) has garnered significant attention due to its capacity to catalyze the synthesis of chiral amines with high efficiency. Nevertheless, the lack of stability of ω-TA and the difficulty of recycling and reuse are still challenges that limit its application. This study developed a novel magnetic nanocellulose composite carrier (NNC@Fe₃O₄@Ni), synthesized from microcrystalline cellulose via low-eutectic solvent treatment, amine modification, and metal hybridization. The NNC@Fe₃O₄@Ni was characterized by FTIR, XPS, XRD, BET, and VSM. Additionally, the performance and catalytic behavior of the immobilized enzyme were investigated. The results revealed that NNC@Fe₃O₄@Ni exhibited a high specific surface area, superparamagnetism, and dual-site functionality (amine/Ni²⁺). Response Surface Methodology (RSM) optimized the carrier-enzyme interaction parameters, yielding optimal immobilization conditions: a mass ratio of 50.8 mg g⁻¹, temperature of 12.5 °C, and duration of 58.6 min, achieving 82.91% enzyme activity recovery. Compared to free enzymes, the immobilized variant demonstrated enhanced catalytic stability, with expanded optimal pH (9.0) and temperature (30 °C). Thermal stability assessments showed 84.39% activity retention after 5 h at 30 °C and 90.30% residual activity post-120 h storage. The catalyst maintained >80% efficiency over 10 reuse cycles. These findings confirm the efficacy of magnetic nanocellulose carriers in enhancing ω-TA stability, reusability, and catalytic performance, offering a viable strategy for industrial biocatalytic processes. Full article

The low-symmetry Weyl semimetallic Td-phase WTe₂ exhibits both a distinct out-of-plane damping torque (${\tau }_{\mathrm{DL}}$) and exceptional charge–spin interconversion efficiency enabled by strong spin-orbit coupling, positioning it as a prime candidate for spin–orbit torque (SOT) applications in two-dimensional transition metal dichalcogenides. Herein, we report on thickness-dependent unconventional out-of-plane ${\tau }_{\mathrm{DL}}$ in chemically vapor-deposited (CVD) polycrystalline Td-WTe₂ (t)/Ni₈₀Fe₂₀/MgO/Ti (Td-WTN-t) heterostructures. Angle-resolved spin-torque ferromagnetic resonance measurements on the Td-WTN-12 structure showed significant spin Hall conductivities of σ_SH,y = 4.93 × 10³ (ℏ/2e) Ω⁻¹m⁻¹ and σ_SH,z = 0.81 × 10³ (ℏ/2e) Ω⁻¹m⁻¹, highlighting its potential for wafer-scale spin–orbit torque device applications. Additionally, a detailed examination of magnetotransport properties in polycrystalline few-layer Td-WTe₂ films as a function of thickness revealed a marked amplification of the out-of-plane magnetoresistance, which can be ascribed to the anisotropic nature of charge carrier scattering mechanisms within the material. Spin pumping measurements in Td-WTN-t heterostructures further revealed thickness-dependent spin transport properties of Td-WTe₂, with damping analysis yielding an out-of-plane spin diffusion length of λ_SD ≈ 14 nm. Full article

NiFe₂O₄ and TiO₂ are widely studied for photoelectrochemical (PEC) applications due to their unique properties. Nitrogen-doped graphene (NG) and metal–organic frameworks (MOFs), such as MIL-100(Fe) (where MIL stands for Materials of Lavoisier Institute), are commonly incorporated to enhance PEC performance by offering a high surface area and facilitating efficient charge transport. Composite systems are commonly employed to overcome the limitations of individual PEC catalysts. In this study, a highly efficient NiFe₂O₄/NG@MIL-100(Fe)/TiO₂ photoanode was developed to enhance photoelectrochemical water-splitting performance. The composite was synthesized via a hydrothermal method with a two-step heating process. X-ray diffraction confirmed the expected crystal structures, with peak broadening in NiFe₂O₄ indicating reduced crystallite size and increased lattice strain. X-ray photoelectron spectroscopy of the Ni 2p and Fe 2p regions validated the successful integration of NiFe₂O₄ into the composite. Electrochemical analysis demonstrated excellent performance, with linear sweep voltammetry achieving a peak photocurrent density of 3.5 mA cm⁻² at 1.23 V (vs RHE). Electrochemical impedance spectroscopy revealed a reduced charge-transfer resistance of 50 Ω, indicating improved charge transport. Optical and electronic properties were evaluated using UV-Vis spectroscopy and Tauc plots, revealing a direct bandgap of 2.1 eV. The composite exhibited stable photocurrent under amperometric J-t testing for 2000 s, demonstrating its durability. These findings underscore the potential of NiFe₂O₄/NG@MIL-100(Fe)/TiO₂ as a promising material for renewable energy applications, particularly in photoelectrochemical water splitting. Full article

Duck eggs are rich in essential nutrients, such as amino acids, vitamins, and polyunsaturated fatty acids. However, their application in the food industry is hindered by glucose, which contributes to undesirable darkening during the Maillard reaction in processing. The present study examined the effect of the desugarization of duck eggs using baker’s yeast on their chemical composition. The results showed that the desugarization process reduces the content of glucose and minerals (Cu, Fe, and Zn) and alters the vitamin composition depending on the treatment conditions. Changes were also observed in the fatty acid profile, including increased levels of oleic acid (C18:1), palmitoleic acid (C16:1), and linoleic acid (C18:2, ω − 6). A high intragroup correlation among saturated fatty acids indicates the stability of their distribution. An increase in the content of essential amino acids—glycine, leucine, valine, and phenylalanine—was also recorded. Correlation analysis of the amino acid composition revealed significant relationships among both essential and non-essential amino acids. Overall, the desugarization process using baker’s yeast not only improves the nutritional profile of duck egg powder but also enhances its functional properties, positioning it as a promising ingredient for the food processing industry. Full article

Enhancing the stability of oxygen evolution reaction (OER) catalysts is a critical challenge for realizing efficient water splitting. In this work, we introduce an innovative approach by applying an electric field during the annealing of a CoFe₂O₄/C catalyst. By controlling the electric field strength (100 mV) and treatment duration (1 h), we achieved dual optimization of the catalyst’s microstructure and electronic environment, resulting in a significant improvement in catalytic stability. The experimental results demonstrate that the electric field-treated catalyst exhibits a reduced overpotential decay (only 0.8 mV) and enhanced stability (retaining 89.1% of its initial activity after 24 h) during extended OER testing. This performance significantly surpasses that of the untreated sample, which showed an overpotential decay of 1.5 mV and retained only 72.5% of its activity after 24 h. X-ray photoelectron spectroscopy (XPS) analysis confirmed that the electric field treatment promoted the formation of oxygen vacancies, substantially improved electron transfer efficiency, and optimized the local electronic environment of Co²⁺/Co³⁺ and Fe²⁺/Fe³⁺, leading to a decrease in charge transfer resistance (Rct) from 58.2 Ω to 42.9 Ω. This study not only presents a novel strategy for modulating catalyst stability via electric fields but also broadens the design concepts for OER catalytic materials by establishing a structure–activity relationship between electric field strength, microstructure, and catalytic performance, ultimately providing a theoretical foundation and experimental guidance for the development of highly efficient and stable water splitting catalysts. Full article

The development of efficient and sustainable electrocatalysts for optimizing methanol oxidation reactions (MORs) in direct methanol fuel cells (DMFCs) is crucial for the innovation of clean electrode energy technologies. This study highlights the synthesis and characterization of magnesium ferrite (MgFe₂O₄) and magnesium-based metal–organic framework (Mg-MOF) composites, utilizing cost-effective and scalable methods such as co-precipitation and ultrasound-assisted synthesis. The composite material, prepared in a 1:1 ratio, demonstrated enhanced catalytic performance due to the synergistic integration of MgFe₂O₄ and Mg-MOF. Comprehensive structural and morphological analyses, including X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), the Brunauer–Emmett–Teller (BET) technique, and X-ray photoelectron spectroscopy (XPS), confirmed the successful formation of the composite. Also, the modification of magnetic properties, particularly the values of coercive force (Hc), led to a significant enhancement in electrical and catalytic performance. The material exhibited mesoporous characteristics and an improved surface area. Electrochemical evaluations revealed superior MOR activity for the composite electrode, achieving a current density of 31.5 mA∙cm⁻² at 1 M methanol with an onset potential of 0.34 V versus Ag/AgCl, measured at a scan rate of 100 mV/s. Remarkably, the composite electrode showed a 75% improvement in current density compared to its components. Additionally, the composite exhibited a low overpotential of 350 mV and favorable Tafel slopes of 22.54 and 4.27 mV∙dec⁻¹ at high and low potentials, respectively, confirming rapid methanol oxidation kinetics on this electrode. It also demonstrated excellent stability, retaining 97.4% of its current density after 1 h. Electrochemical impedance spectroscopy (EIS) further revealed a reduced charge transfer resistance of 9.26 Ω, indicating enhanced conductivity and catalytic efficiency. These findings underscore the potential of MgFe₂O₄/Mg-MOF composites as cost-effective and high-performance anode materials for DMFCs, paving the way for sustainable energy solutions. Full article

High-chromium white iron (HCWI) alloys are often used in industries such as mining which require a high wear resistance. Whilst nitrogen is known as a good austenitic stabiliser, the effects of nitrogen on corrosion properties for welded HCWI have not been studied. Chromium hardfacing alloys were deposited via gas metal arc welding using nitrogen as a shielding gas at flow rates of 5 L/min, 10 L/min, and 15 L/min. The corrosion behaviour of these modified alloys was studied using electrochemical techniques such as potentiodynamic measurements and electrochemical impedance spectroscopy. Higher gas flow rates were found to increase the volume fraction of the eutectic austenite while reducing the amounts of eutectic carbides. Nitrogen did not transform the M₇C₃ (M = Cr, Fe) carbides into any other form of carbides. The sample without nitrogen as a shielding gas was found to display the worst corrosion resistance after electrochemical testing, such as corrosion resistance parameters in EIS tests. Higher nitrogen shielding gas flow rates were found to produce higher levels of corrosion resistance; this was especially true for the 15 L/min sample with a corrosion resistance parameter to EIS that was more than double that of the sample without nitrogen shielding gas (e.g., 4700 vs. 2325 Ω·cm² respectively). Full article

This study examines the microstructure and corrosion resistance of FeCrNiAl_0.7Cu_0.3Si_x (x = 0, 0.1, 0.3, and 0.5) high-entropy alloys (HEAs) in a 3.5% NaCl solution. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and electrochemical testing were employed to systematically analyze the alloys’ microstructures and corrosion behavior. The XRD results indicate that the addition of Si affects the phase structure of the alloy. At Si = 0, the alloy exhibits a single BCC phase. By increasing the Si content to 0.1 and 0.3, a BCC₂ phase appears. At Si = 0.5, Si-containing intermetallic compounds form. SEM observations reveal that as the Si content increases, the alloy develops a distinct dendritic structure. Polarization tests in the 3.5% NaCl solution show that the corrosion current density first decreases and then increases with increasing Si content. At Si contents of 0.1, 0.3, and 0.5, the corrosion current densities are 4.275 × 10⁻⁶ A·cm⁻², 4.841 × 10⁻⁷ A·cm⁻², and 2.137 × 10⁻⁶ A·cm⁻², respectively. FeCrNiAl_0.7Cu_0.3S_0.3 HEA exhibits the lowest corrosion current density, indicating a lower corrosion rate. Electrochemical impedance spectroscopy (EIS) tests show that at Si = 0.3, the alloy has the largest capacitive arc radius. The charge-transfer resistance (RCT) for the alloys with the Si contents of 0.1, 0.3, and 0.5 are 2.532 × 10⁵ Ω·cm², 4.088 × 10⁵ Ω·cm², 4.484 × 10⁵ Ω·cm², and 2.083 × 10⁵ Ω·cm², respectively. FeCrNiAl_0.7Cu_0.3Si_0.3 HEA has the highest RCT, which indicates a more stable passivation film and better resistance to chloride ion intrusion. The corrosion morphology observed after polarization testing shows that all alloys exhibit intergranular corrosion characteristics. The Si content alters the distribution of passivation film-forming elements, Cr and Ni. Compared to other alloys, the corrosion morphology of FeCrNiAl_0.7Cu_0.3Si_0.3 HEA is more complete. Combining the polarization, EIS, and corrosion morphology results, it can be concluded that FeCrNiAl_0.7Cu_0.3Si_0.3 HEA exhibits the best corrosion resistance in the 3.5% NaCl solution. Full article

The effect of chlorides on the corrosion activities of SS304 and carbon steel A36 was investigated during immersion in a hybrid pumice–Portland cement extract solution, containing high concentration of chlorides (5 g ${\mathrm{L}}^{-1}$ NaCl), in order to simulate the concrete–pore marine environment. The hybrid pumice–Portland cement (HB1) has been considered an alternative “green” cement system. The initial pH of the extract (12.99) decreased to 9.5 after 14 days, inducing a severe corrosion risk for A36, as suggested by the very negative corrosion potential (OCP ≈ −363 mV). Meanwhile, the SS304 tended to passivate and its OCP shifted to positive values (≈+72 mV). Consequently, the surface of the A36 presented a corrosion layer mainly of $\mathrm{FeOOH}$, while that of the SS304 was composed of ${\mathrm{Cr}}_2{\mathrm{O}}_3$, ${\mathrm{Fe}}_3{\mathrm{O}}_4$ and $\mathrm{NiO}$, according to the SEM-EDS and XPS analysis. An extended area of an almost uniform corrosion attack was observed on the A36 surface, due to the less protective Fe-corrosion products, while the SS304 surface presented some small pits of ≈1 µm. Based on electrochemical impedance measurements, the polarization resistance (Rp) and thickness of the passive layer were calculated. The Rp of the SS304 surface increased by two orders of magnitude up to ≈11,080 $\mathrm{k}\mathsf{\Omega } {\mathrm{cm}}^2$, and the thickness of the layer reached ≈1.5 nm after 30 days of immersion. The Rp of carbon steel was ≈2.5 $\mathrm{k}\mathsf{\Omega } {\mathrm{cm}}^2$ due to the less protective properties of its corrosion products. Full article

Red mullet (Mullus barbatus), a prominent fish species in the Mediterranean Sea, is a fish with a particular abundance of unsaturated fatty acids and other nutrients, including a substantial quantity of minerals. The nutritive quality parameters (lipid quality indices, fatty acid profiles, and mineral content, along with proximate composition) of 75 red mullet samples collected from five distinct locations (L1–L5) in the North and South Euboean Gulf, Euboea Island (Evia), Greece, were examined. It was hypothesized that the different habitats may have an impact on each fish’s chemical composition. Proximate composition (protein, ash, moisture, fat, and minerals) and bioactive compound determination (total carotenoids, and vitamins A, E, and C) were conducted on the lyophilized fish samples. The protein and lipid content of the wet fillet varied substantially from 10.8 to 14.3 and 13.2 to 16.8% w/w, respectively. The samples exhibited statistically non-significant variation in the total SFAs and MUFAs (p > 0.05). The level of total PUFAs was above 30% in all the samples and no significant differences were observed between them. However, arachidonic acid (20:4 ω-6) was only detected in fish samples from two locations (i.e., L1 and L3). The concentrations of Fe, Na, Mg, K, Ca, Ag, Sr, Li, and Zn varied significantly (p < 0.05) in relation to the size of the fish samples. The highest concentrations of heavy metals were detected at the northern location (L5), indicating a possible negative correlation between size and arsenic concentration. The varied mineral composition and fatty acid content of the samples can be attributed to their distinctive biological characteristics (i.e., length and weight) and dietary environments. Full article