Search Results (1,532)

Silver is a promising electrocatalyst for electrochemical CO₂ reduction reaction owing to its high selectivity and efficiency for CO production. However, it still faces a fundamental trade-off between reaction activity and stability. Here, we developed a three-dimensional coral-like porous silver (CP-Ag) catalyst through seed-assisted nanoparticle attachment synthesis, which creates a unique architecture featuring interconnected pores and stable grain boundaries (GBs) between constituent Ag nanoparticles (Ag NPs). Compared to normal Ag NPs, CP-Ag demonstrates superior catalytic performance, maintaining >90% Faradaic efficiency (FE) for CO across a wide potential range (−0.6 to −1.0 V vs. RHE) while achieving 2-times higher current density. Importantly, CP-Ag demonstrated an impressive long-term stability by sustaining nearly 90% FE for CO approximately 40 h at a current density of −50 mA cm⁻² in a flow cell. The enhanced catalytic performance arises from three factors: (1) the three-dimensional coral-like morphology increases accessible active sites and promotes charge transfer efficiency; (2) stable GBs between interconnected nanoparticles increase reaction activity; (3) more moderate binding on Ag (100) preferentially promotes *CO intermediate formation. Our findings highlight the importance of simultaneously engineering both morphological and crystallographic features to optimize silver catalysts for CO₂ conversion. Full article

Beryl is classified as a cyclosilicate mineral, and its color is primarily determined by the type and oxidation state of trace elements. In this study, natural yellow-green beryl was used as the research subject, and heat treatment experiments were performed at various temperatures under both oxidizing and reducing atmospheres. A combination of analytical techniques, including electron probe microanalysis (EPMA), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and ultraviolet-visible spectroscopy (UV-Vis), were employed to systematically investigate the composition, structure, and chromogenic mechanisms of beryl before and after heat treatment. The experimental results indicate that heat treatment under both atmospheres can lead to the transformation of yellow-green beryl into blue, with 500–600 °C under a reducing atmosphere identified as the optimal treatment condition. With increasing temperature, beryl gradually dehydrates, resulting in a faded blue color and reduced transparency. Even after treatment at 700 °C, no significant changes in unit cell parameters were observed, and both type I and type II water were retained, indicating that the color change is not attributed to crystal structure transformation or phase transitions. The study reveals that the essential mechanism of color modification through heat treatment lies in the valence change between Fe²⁺ and Fe³⁺ occupying channel and octahedral sites. The observed color variation is attributed to changes in absorption band intensity resulting from charge transfers of O²⁻ → Fe³⁺ and Fe²⁺ → Fe³⁺. This study provides theoretical insights and technical references for the color enhancement of beryl through heat treatment. Full article

Electrochemical water splitting for hydrogen production is considered a key pathway for achieving sustainable energy conversion. However, the sluggish reaction kinetics of the oxygen evolution reaction (OER) and high overpotentials severely hinder the large-scale application of water electrolysis technology. Nickel–iron layered double hydroxide (NiFe-LDH) has gained attention as a promising non-precious metal OER catalyst due to its abundant active sites and good intrinsic activity. However, its relatively low conductivity and charge transfer efficiency limit the improvement of catalytic performance. Therefore, this study used a simple hydrothermal method to generate a NiFe-LDH/Cs_0.32WO₃ heterojunction composite catalyst, relying on the excellent electronic conductivity of Cs_0.32WO₃ to improve overall charge transfer efficiency. According to electrochemical testing results, the modified NiFe-LDH/Cs_0.32WO₃-20 mg achieved a low overpotential of 349 mV at a current density of 10 mA cm⁻², a Tafel slope of 67.0 mV dec⁻¹, and a charge transfer resistance of 65.1 Ω, which represent decreases of 39 mV, 23.1%, and 40%, respectively, compared to pure NiFe-LDH. The key to performance improvement lies in the tightly bonded heterojunction interface between Cs_0.32WO₃ and NiFe-LDH. X-ray photoelectron spectroscopy (XPS) shows a distinct interfacial charge transfer phenomenon, with a notable negative shift of the W4f peak (0.85 eV), indicating the directional transfer of electrons from Cs_0.32WO₃ to NiFe-LDH. Under the influence of the built-in electric field within the heterojunction, this interfacial charge redistribution improved the electronic structure of NiFe-LDH, increased the proportion of high-valent metal ions, and significantly enhanced the OER reaction kinetics. This study provides new insights for the preparation of efficient heterojunction electrocatalysts. Full article

To mitigate the consumption of active sites on co-catalysts by H₂O₂ and to enhance the efficiency and stability of co-catalytic Fenton reactions, an external circulation two-stage packed-bed reactor (ECTPBR) was developed using DPW (diatomite plate@polydopamine@WC) as a co-catalyst to degrade 4-nitrophenol (4-NP). Under suitable conditions, the ECTPBR could achieve over 91.97% 4-NP degradation, with low iron sludge production (11.97 mg/L) and minimal tungsten leaching (3.6363 mg/L). The two-stage strategy enabled spatial separation of Fe³⁺ reduction and Fenton reactions, minimizing the loss of active sites on DPW, ensuring long-term system stability, and reducing the toxicity of 4-NPdegradation products. In addition, external circulation enhanced mass transfer and improved resistance to shock loads. These advantages suggest that the ECTPBR may serve as an effective strategy for applying co-catalytic Fenton reactions in the treatment of toxic and refractory organic wastewater. Full article

In this paper, we aimed to evaluate whether simple, low molecular mass benzoquinone derivatives, featuring different substituents in para- and meta-position relative to the tert-butyl group, possess biological activities against major targets associated with Alzheimer’s disease. The 1,4-benzoquinone derivatives studied herein inhibited both cholinesterases in the micromolar concentration range, generally showing a preference for butyrylcholinesterase over acetylcholinesterase; formed complexes with biometal ions Fe²⁺, Cu²⁺ and Zn²⁺; and displayed a certain BACE1 inhibition. Moreover, the tested compounds displayed certain antioxidant activity via either electron transfer or hydrogen atom transfer mechanisms. The antioxidant capacity of the unsubstituted tert-butyl-1,4-benzoquinone (compound 1) was three times lower than that of the standard antioxidant BHT, while 2,6-disubstituted derivatives (compounds 15 and 7) exhibited peroxyl radical scavenging activity comparable to that of Trolox. Taken together with in silico-predicted low toxicity, good intestinal absorption and favorable oral bioavailability, the presented 1,4-benzoquinone derivatives are promising scaffolds for the design of more complex molecules with enhanced cholinesterase and BACE1 inhibitory activity. Furthermore, they could serve as functional substituents in other structural scaffolds to combine and enhance their biological activities. Full article

This study assessed the effects of NiFe-based metal catalysts on CO₂ conversion to methane (CH₄) and carboxylic acids in microbial electrosynthesis (MES) cells. A NiFeBi alloy, when electrodeposited on a conductive bioring cathode, significantly decreased CH₄ production from 0.55 to 0.12 L (Lc d)⁻¹ while enhancing acetate production to 1.0 g (Lc d)⁻¹, indicating suppressed methanogenic activity and improved acetogenic activity. On the other hand, NiFeMn and NiFeSn catalysts showed varied effects, with NiFeSn increasing both CH₄ and acetate production and suggesting potential in promoting both chain elongation and CO₂ uptake. When these alloys were electrodeposited on a 3D-printed conductive polylactide (cPLA) lattice, the production of longer-chain carboxylic acids like butyrate and caproate increased significantly, indicating enhanced biocompatibility and nutrient delivery. The NiFeSn-coated cPLA lattice increased caproate production, which was further enhanced using an acetogenic enrichment. However, the overall throughput remained low at 0.1 g (Lc d)⁻¹. Cyclic voltammetric analysis demonstrated improved electrochemical responses with catalyst coatings, indicating better electron transfer. These findings underscore the importance of catalyst selection and cathode design in optimizing MES systems for efficient CO₂ conversion to value-added products, contributing to environmental sustainability and industrial applications. Full article

This study investigates the effect of copper (Cu) and silver (Ag) additions on the electrochemical behavior of the Fe40Al intermetallic alloy in artificial saliva, aiming to evaluate its potential for biomedical applications such as dental implants. Alloys with varying concentrations of Ag (0.5, 1.0, and 3.0 wt%) and Cu (1.0, 3.0, and 5.0 wt%) were synthesized and exposed to a biomimetic electrolyte simulating oral conditions. Electrochemical techniques, including open circuit potential (OCP), linear polarization resistance (LPR), potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS), were employed to assess corrosion performance. Results show that unmodified Fe40Al exhibits good corrosion resistance, attributed to the formation of a stable passive oxide layer. The addition of Cu, particularly at 3.0 wt%, significantly improved corrosion resistance, yielding lower corrosion current densities and higher polarization resistance and charge transfer resistance values, surpassing even 316L stainless steel in some metrics. Conversely, Ag additions led to a degradation of corrosion resistance, especially at 3.0 wt%, due to microstructural changes and the formation of metallic Ag precipitates, AgSCN, and galvanic cells, which promoted localized corrosion. EIS results revealed that Cu- and Ag-modified alloys developed less homogeneous and less protective passive layers over time, as indicated by increased double-layer capacitance (C_dl) and reduced constant phase element exponent (n_dl) values. Overall, the Fe40Al alloy shows intrinsic corrosion resistance in simulated physiological environments, and Cu additions can enhance this performance under controlled conditions. However, Ag additions negatively affect the protective behavior of the passive layer. These findings offer critical insight into the design of Fe-Al-based biomaterials for dental or biomedical applications where corrosion resistance and electrochemical stability are paramount. Full article

Transition metal sulfides have found a popular spot in research for super capacitive materials due to their enhanced power density and conductivity. This study reports the preparation of a hybrid iron copper sulfide, Fe_0.5Cu_0.5S/rGO, composite via the co-precipitation method. The structural and morphological characterization was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM), which confirmed the successful integration of Fe_0.5Cu_0.5S with rGO. The composite exhibited a high specific capacitance of 416.91 F/g at 1 A/g, 330.65% higher than 96.81 F/g of Fe_0.5Cu_0.5S and outstanding cyclic stability. The enhanced performance can be attributed to the synergistic effects of Fe_0.5Cu_0.5S and rGO, facilitating efficient charge transfer kinetics, ion diffusion, and structural stability, making it a promising candidate for high-performing supercapacitor applications. Full article

Petroleum hydrocarbon (PH) contamination in groundwater necessitates sustainable remediation solutions. This study develops a novel co-encapsulated composite by embedding steel slag (SS) and sodium persulfate (SPS) within an ethyl cellulose (EC) matrix ((SS + SPS)/EC) for permeable reactive barrier applications. The EC matrix enables controlled release of SPS oxidant and gradual leaching of alkaline components (Ca²⁺/OH⁻) and Fe²⁺/Fe³⁺ activators from SS, synergistically sustaining radical generation while buffering pH extremes. Optimized at a 10:7 SS:SPS mass ratio, the composite achieves 66.3% PH removal via dual pathways: (1) sulfate radical (${\mathrm{S}\mathrm{O}}_4^{-}$•) oxidation from Fe²⁺-activated persulfate (S₂${\mathrm{O}}_8^{2-}$ + Fe²⁺→${\mathrm{S}\mathrm{O}}_4^{-}$• + ${\mathrm{S}\mathrm{O}}_4^{2-}$ + Fe³⁺), and (2) direct electron transfer by surface-bound Fe³⁺. In situ material evolution enhances functionality—nitrogen physisorption reveals a 156% increase in surface area and 476% pore volume expansion, facilitating contaminant transport while precipitating stable sulfate minerals (Na₂SO₄, Na₃Fe(SO₄)₃) within pores. Crucially, the composite maintains robust performance under groundwater-relevant conditions: 54% removal at 15 °C (attributed to pH-buffered activation) and >55% efficiency with common interfering anions (Cl⁻, ${\mathrm{H}\mathrm{C}\mathrm{O}}_3^{-}$, 50 mg·L⁻¹). This waste-derived design demonstrates a self-regulating system that concurrently addresses oxidant longevity (≥70 h), geochemical stability (pH 8.5→10.4), and low-temperature activity, establishing a promising strategy for sustainable groundwater remediation. Continuous-flow column validation (60 d, 5 mg·L⁻¹ gasoline) demonstrates sustained >80% removal efficiency and systematically stable effluent pH (9.8–10.2) via alkaline leaching. Full article

This study introduces an efficient and sustainable catalytic system utilizing cobalt ferrite nanoparticles (CoFe₂O₄-NPs) for the synthesis of valuable 6-amino-2-oxo-4-phenyl (or 4-chlorophenyl)-1,2,3,4-tetrahydropyrimidine-5-carbonitrile derivatives. Recognizing the limitations of traditional methods for the Biginelli reaction, we thoroughly characterized CoFe₂O₄-NPs, alongside individual iron oxide nanoparticles (Fe₂O₃-NPs) and cobalt oxide nanoparticles (CoO-NPs), using FTIR, XRD, TEM, SEM, XPS, TGA, and BET analysis. These characterizations revealed the unique structural, morphological, and physicochemical properties of CoFe₂O₄-NPs, including an optimized porous structure and significant bimetallic synergy between Fe and Co ions. Catalytic studies demonstrated that CoFe₂O₄-NPs significantly outperformed individual Fe₂O₃-NPs and CoO-NPs under mild conditions. While the latter only catalyzed the Knoevenagel condensation, CoFe₂O₄-NPs uniquely facilitated the complete Biginelli reaction. This superior performance is attributed to the synergistic electronic environment within CoFe₂O₄-NPs, which enhances reactant activation, intermediate stabilization, and proton transfer during the multi-step reaction. This work highlights the potential of CoFe₂O₄-NPs as highly efficient and selective nanocatalysts for synthesizing biologically relevant 1,2,3,4-tetrahydropyrimidines, offering a greener synthetic route in organic chemistry. Full article

Anion exchange membrane (AEM) water electrolysis is a potentially inexpensive and efficient source of hydrogen production as it uses effective low-cost catalysts. The catalytic activity and performance of nickel iron oxide (NiFeO_x) catalysts for hydrogen production in AEM water electrolyzers were investigated. The NiFeO_x catalysts were synthesized with various iron content weight percentages, and at the stoichiometric ratio for nickel ferrite (NiFe₂O₄). The catalytic activity of NiFeO_x catalyst was evaluated by linear sweep voltammetry (LSV) and chronoamperometry for the oxygen evolution reaction (OER). NiFe₂O₄ showed the highest activity for the OER in a three-electrode system, with 320 mA cm⁻² at 2 V in 1 M KOH solution. NiFe₂O₄ displayed strong stability over a 600 h period at 50 mA cm⁻² in a three-electrode setup, with a degradation rate of 15 μV/h. In single-cell electrolysis using a X-37 T membrane, at 2.2 V in 1 M KOH, the NiFe₂O₄ catalyst had the highest activity of 1100 mA cm⁻² at 45 °C, which increased with the temperature to 1503 mA cm⁻² at 55 °C. The performance of various membranes was examined, and the highest performance of the tested membranes was determined to be that of the Fumatech FAA-3-50 and FAS-50 membranes, implying that membrane performance is strongly correlated with membrane conductivity. The obtained Nyquist plots and equivalent circuit analysis were used to determine cell resistances. It was found that ohmic resistance decreases with an increase in temperature from 45 °C to 55 °C, implying the positive effect of temperature on AEM electrolysis. The FAA-3-50 and FAS-50 membranes were determined to have lower activation and ohmic resistances, indicative of higher conductivity and faster membrane charge transfer. NiFe₂O₄ in an AEM water electrolyzer displayed strong stability, with a voltage degradation rate of 0.833 mV/h over the 12 h durability test. Full article

Dry Turkish oak (Quercus cerris) sawdust, untreated and treated with three activators, (H₃PO₄, NaOH and H₂O₂) was pyrolyzed under limited-oxygen conditions to obtain biochar samples. The electrochemical properties of these samples were tested and compared to the properties of several commercial carbon blacks. The electrochemical characterization was performed via cyclic voltammetry, analyzing the response toward two commonly used redox probes, [Fe(CN)₆]^3−/−4− and [Ru(NH₃)₆]^2+/3+. The influence of the scan rate on this response was investigated, and the resulting data were used to obtain the values of the heterogenous charge transfer constant, k₀. Higher k₀ values were observed for carbon blacks than for investigated biochar samples. The detection of 4-nitrophenol and heavy metal ions was used to assess the applicability of biochars for electroanalytical purposes. The response of untreated biochar was comparable with the response of Vulcan carbon black, which showed the best response of all analyzed carbon blacks. Full article

Fe³⁺-incorporated hydrogels are particularly valuable for wearable devices due to their tunable mechanical properties and ionic conductivity. However, conventional immersion-based fabrication fundamentally limits hydrogel performance because of heterogeneous ion distribution, ionic leaching, and scalability limitations. To overcome these challenges, we report a novel one-pot strategy where controlled amounts of Fe³⁺ are directly added to polyacrylamide-sodium acrylate (PAM-SA) precursor solutions, ensuring homogeneous ion distribution. Combining this with Photoinduced Electron/Energy Transfer Reversible Addition–Fragmentation Chain Transfer (PET-RAFT) polymerization enables efficient hydrogel fabrication under open-vessel conditions, improving its scalability. Fe³⁺ concentration achieves unprecedented modulation of mechanical properties: Young’s modulus (10 to 150 kPa), toughness (0.26 to 2.3 MJ/m³), and strain at break (800% to 2500%). The hydrogels also exhibit excellent compressibility (90% strain recovery), energy dissipation (>90% dissipation efficiency at optimal Fe³⁺ levels), and universal adhesion to diverse surfaces (plastic, metal, PTFE, and cardboard). Finally, these Fe³⁺-incorporated hydrogels demonstrated high effectiveness as strain sensors for monitoring finger/elbow movements, with gauge factors dependent on composition. This work provides a scalable, oxygen-tolerant route to tunable hydrogels for advanced wearable devices. Full article

Hydrogen energy is a pivotal carrier for achieving carbon neutrality, requiring green and efficient production via water electrolysis. However, the anodic oxygen evolution reaction (OER) involves a sluggish four-electron transfer process, resulting in high overpotentials, while the prohibitive cost and complex preparation of precious metal catalysts impede large-scale commercialization. In this study, we develop a FeCo-based bimetallic deep eutectic solvent (FeCo-DES) as a multifunctional reaction medium for engineering a three-dimensional (3D) coral-like FeOOH-Co₂(OH)₃Cl/NF composite via a mild one-step impregnation approach (70 °C, ambient pressure). The FeCo-DES simultaneously serves as the solvent, metal source, and redox agent, driving the controlled in situ assembly of FeOOH-Co₂(OH)₃Cl hybrids on Ni(OH)₂/NiOOH-coated nickel foam (NF). This hierarchical architecture induces synergistic enhancement through geometric structural effects combined with multi-component electronic interactions. Consequently, the FeOOH-Co₂(OH)₃Cl/NF catalyst achieves a remarkably low overpotential of 197 mV at 100 mA cm⁻² and a Tafel slope of 65.9 mV dec⁻¹, along with 98% current retention over 24 h chronopotentiometry. This study pioneers a DES-mediated strategy for designing robust composite catalysts, establishing a scalable blueprint for high-performance and low-cost OER systems. Full article

To address the low selectivity in the electrocatalytic conversion of furfural (FFR) to furfuryl alcohol (FFA) under alkaline conditions, a Zn-based metal–organic framework (MBON-2) featuring a 3D hierarchical flower-like architecture self-assembled from nanosheets was synthesized via a simple hydrothermal method. Under optimal conditions, MBON-2 exhibited an extremely high selectivity of FFA (100%) and a high Faradaic efficiency (FE) of 93.19% at −0.2 V vs. RHE. Electrochemical impedance spectroscopy (EIS) revealed the excellent electron transfer and mass transport properties of MBON-2. In addition, in situ Fourier transform infrared (FTIR) spectroscopy studies confirmed the adsorption of FFR molecules onto the Zn and B sites of MBON-2 during the ECH of FFR, providing key insights into the hydrogenation mechanism. The numerous exposed B and Zn sites of the MBON-2, as well as its robust structural stability contributed to its outstanding catalytic performance in the electrochemical hydrogenation (ECH) of FFR. This work provides valuable guidelines for developing efficient Zn-based catalysts for the ECH of FFR. Full article