Search Results (85)

Background: Traditional methods exhibit an extremely low removal efficiency for antibiotics in water, making an efficient and energy-saving approach urgently needed. Methods and Results: In this study, a novel catalytic approach based on the in situ generation of high-valent iron (Fe(IV)/Fe(V)) has been developed by adding biochar instead of modifying the electrode materials (in previous studies) for the efficient removal of sulfamethoxazole (SMX) from water. Fe(IV)/Fe(V) was produced by the anodic oxidation of low concentrations of Fe(III) and subsequently activated by nitrogen-doped corn stalk biochar (NBC). The results showed that the degradation efficiency increased from 50.83% to 90.67% within 60 min after the addition of nitrogen-modified biochar. The abundant defect structures, graphitic N and oxygen-containing functional groups in NBC endowed the catalyst with excellent activation capability. Quenching experiments and methyl phenyl sulfoxide (PMSO) probe experiments revealed that singlet oxygen (¹O₂) and Fe(IV)/Fe(V) were the main contributors to SMX degradation. Degradation pathways were inferred based on transformation products (TPs) and density functional theory (DFT) calculations. Ecotoxicity prediction using the ECOSAR program indicated that the TPs formed in the E/Fe(III)/NBC system exhibited markedly lower toxicity to aquatic organisms than the parent SMX. Furthermore, the E/Fe(III)/NBC system maintained a high degradation efficiency for SMX in real aquatic environments. Additionally, the E/Fe(III)/NBC system showed high removal rates for other sulfonamides such as sulfadiazine (SDZ), sulfamethoxypyridazine (SMP), sulfathiazole (STZ) and sulfadoxine (SDX). Conclusions: Overall, the E/Fe(III)/NBC system was demonstrated to be a highly efficient and sustainable technology for removing various antibiotics from water. Full article

This study presents a straightforward strategy for producing novel, effective and inexpensive functional non-noble metal-supported carbon materials made from abundant natural biomass. These materials offer a cost-effective alternative to noble metals for the oxidation of hydrazine (HzOR) and demonstrate the potential for widespread adoption of green, energy-saving hydrazine-based technologies in energy applications. Highly efficient and cost-effective iron (Fe) and manganese–iron (MnFe)-supported nitrogen-doped carbon (N–C) materials were developed using hydrothermal synthesis. Meanwhile, the N–C material was obtained from biomass—birch-wood chips—using hydrothermal carbonisation (HTC), followed by activation and nitrogen doping of the resulting hydrochar. The morphology, structure, and composition of the MnFe, MnFe/N–C, and Fe/N–C catalysts were determined using scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy dispersive X-ray spectroscopy (EDS). The activity of the catalysts for HzOR in an alkaline medium was evaluated using cyclic voltammetry (CV). Depositing MnFe particles onto N–C was shown to significantly enhance electrocatalytic activity for HzOR compared to the Fe/N–C catalyst and especially to the MnFe particles catalyst in terms of highly developed porous structure, which offers the largest surface area, lowest onset potential, and highest current density response, resulting in the strongest catalytic activity. These results suggest that the MnFe/N–C catalyst could be a highly promising anode material for HzOR in direct hydrazine fuel cells (DHFCs). Full article

The field of electrochemical devices, encompassing energy storage, fuel cells, electrolysis, and sensing, is fundamentally reliant on the electrode materials that govern their performance, efficiency, and sustainability. Traditional materials, while foundational, often face limitations such as restricted reaction kinetics, structural deterioration, and dependence on costly or scarce elements, driving the need for continuous innovation. Emerging electrode materials are designed to overcome these challenges by delivering enhanced reaction activity, superior mechanical robustness, accelerated ion diffusion kinetics, and improved economic feasibility. In energy storage, for example, the shift from conventional graphite in lithium-ion batteries has led to the exploration of silicon-based anodes, offering a theoretical capacity more than tenfold higher despite the challenge of massive volume expansion, which is being mitigated through nanostructuring and carbon composites. Simultaneously, the rise of sodium-ion batteries, appealing due to sodium’s abundance, necessitates materials like hard carbon for the anode, as sodium’s larger ionic radius prevents efficient intercalation into graphite. In electrocatalysis, the high cost of platinum in fuel cells is being addressed by developing Platinum-Group-Metal-free (PGM-free) catalysts like metal–nitrogen–carbon (M-N-C) materials for the oxygen reduction reaction (ORR). Similarly, for the oxygen evolution reaction (OER) in water electrolysis, cost-effective alternatives such as nickel–iron hydroxides are replacing iridium and ruthenium oxides in alkaline environments. Furthermore, advancements in materials architecture, such as MXenes—two-dimensional transition metal carbides with metallic conductivity and high volumetric capacitance—and Single-Atom Catalysts (SACs)—which maximize metal utilization—are paving the way for significantly improved supercapacitor and catalytic performance. While significant progress has been made, challenges related to fundamental understanding, long-term stability, and the scalability of lab-based synthesis methods remain paramount for widespread commercial deployment. The future trajectory involves rational design leveraging advanced characterization, computational modeling, and machine learning to achieve holistic, system-level optimization for sustainable, next-generation electrochemical devices. Full article

Zinc and its alloys have been regarded as an alternative option for biodegradable implant materials to magnesium and iron-based alloys due to their promising degradation rate. However, poor osseointegration with bone tissue limits their further clinical application. Considering the biofunction of strontium (Sr), namely promoting the formation of bone tissue, in this work, a ZnO-Sr composite coating was prepared on pure Zn via anodic oxidation to boost bioactivity. Surface morphology and composition of the layer were examined via scanning electron microscopy (SEM) and X-ray diffraction (XRD). Electrochemical measurements were carried out to assess the corrosion behaviour. Long-term immersion tests in simulated body fluid (SBF) for up to 21 days were conducted to evaluate the in vitro bioactivity. Corrosion morphology and corrosion products were studied to reveal the corrosion mechanism. The results demonstrated that the Sr-ZnO coating optimized the corrosion rate and enhanced the bioactivity of the substrate, improving its potential for orthopedic applications. Full article

Electrolysis and biological processes, such as fermentation and microbial electrolysis cells, offer efficient hydrogen production alongside wastewater treatment. This study presents a novel microbial electrolyzer (ME) comprising a titanium dioxide (TiO₂) anode, a nickel–iron–carbon (NiFeC) cathode, and a cellulose nanocrystal proton exchange membrane (CNC-PEM) designed to generate hydrogen from palm oil mill effluent (POME). The system is powered by a 12 V electric double-layer organic supercapacitor (EDLOSC) integrated with a ZnO/PVA-based solar thin film. Power delivery to the TiO₂-NiFeC-PEM electrolyzer is optimized using an Adaptive Neuro-Fuzzy Inference System (ANFIS). Laboratory-scale pilot tests demonstrated effective degradation of POME’s organic content, achieving a hydrogen yield of approximately 60%. Additionally, the nano-structured ZnO/CuO–ZnO/PVA solar film facilitated stable power supply, enhancing in situ hydrogen production. These results highlight the potential of the EDLOSC-encased ZnO/PVA-powered electrolyzer as a sustainable solution for hydrogen generation and industrial wastewater treatment. Full article

Computed tomography (CT) imaging has proven to be effective for detecting and visualizing a wide range of inhomogeneities and defects. Applying computer vision (CV)-based image processing enables detailed feature measurements on selected CT image slices, which could be of benefit as cells of the same type often show variations in electrical properties. When combined with electrical testing, CT imaging could provide valuable insights into the battery cell, helping to identify potential sources of electrical deviations. However, it remains unclear to what extent CT-based measurements, especially for larger prismatic cells, e.g., those used in automotive applications, can explain electrical deviations aside from identifying significant or latent defects. Therefore, this study performs a correlative analysis and compares the electrical measurement results with CT-based measurements of the cell’s physical features, specifically the anode and cathode sizes. Electrical and CT measurements from ten lithium iron phosphate/graphite (LFP/C) cells of the same type are analyzed. The results indicate that while CT imaging has the potential to help identify the sources of electrical deviations, it also shows that cell-level CT measurements alone cannot fully explain electrical performance deviations. Measurement uncertainty, the potential overlapping impact of other cell features, and the actual influence of the measured physical properties on the cell’s electrical performance limit the correlation between CT-based measurements and electrical parameters. Full article

Phosphorus (P) discharge from onsite wastewater treatment systems (OWTSs) poses a significant threat to water quality, contributing to eutrophication in nutrient-sensitive aquatic environments. In treated effluents, P predominantly exists as orthophosphate (PO₄³⁻), a highly bioavailable and reactive form that requires targeted removal. This study evaluates the performance of electrocoagulation (EC) as a polishing step for PO₄³⁻ removal from OWTS effluents using 12 anode/cathode combinations comprising aluminum (Al), iron (Fe), magnesium (Mg), and stainless steel (SS). Key operational parameters, including treatment time, mixing speed, current density, pH, and initial PO₄³⁻ concentration, were systematically investigated when synthetic denitrified effluent (20 mg P/L) was treated. Based on the performance, the four most effective electrode combinations (Al/Al, Al/Mg, Fe/Al, and Mg/Mg), along with a commercial benchmark (Fe/Fe), were further tested under extended hydraulic retention times (up to 48 h) in both synthetic and real (denitrified) wastewater. To date, none of the studies have systematically evaluated all possible anode/cathode combinations involving multiple electrode materials under uniform operational conditions. The Al/Al and Mg/Mg EC systems achieved rapid and high PO₄³⁻ removal efficiencies (>95%), while Mg-based systems demonstrated sustained performance over prolonged treatment durations, especially in real wastewater. Bimetallic pairs such as Al/Mg and Fe/Al exhibited synergistic effects through enhanced coagulant generation and pH stabilization. The results indicated that PO₄³⁻ removal efficiency was strongly influenced by electrode material selection, hydrodynamic conditions, and wastewater compositions, underscoring the need to design EC systems based on site-specific water quality conditions in OWTSs. Full article

By modulating the mass ratio of hydrothermal agents to cobalt/iron precursors, Co₃O₄ nanowires were successfully integrated into spinel-type Co/Fe@NF, forming a heterojunction anode for alkaline water electrolysis (AWE) hydrogen production. This Co₃O₄ nanowire-assembled CoFe₂O₄ nanosheet anode (Co/Fe(5:1)@NF) exhibits exceptional electrochemical oxygen evolution reaction (OER) performance, requiring only 221 mV overpotential to achieve 10 mA cm⁻². Sulfamethoxazole (SMX) was employed as a model pollutant to investigate the anode sacrificial material; it achieved approximately 95% SMX degradation efficiency, reducing the OER potential of 50 mV/10 mA cm⁻². SMX oxidation coupled with Co/Fe heterojunction structure partially substitutes the OER. Co/Fe heterojunction generates an internal magnetic field, which induces the formation of novel active species within the system. ·O₂⁻ is the newly formed active oxygen species, which enhanced the proportion of indirect SMX oxidation. Quantitative analysis reveals that superoxide radical-mediated indirect oxidation of SMX accounts for approximately 38.5%, Fe(VI) for 9.4%, other active species for 6.1%, and direct oxidation for 46.0%. The nanowire–nanosheet assembly stabilizes a high-spin configuration on the catalyst surface, redirecting oxygen intermediate pathways toward triplet oxygen (³O₂) generation. Subsequent electron transfer from nanowire tips facilitates rapid ³O₂ reduction, forming superoxide radicals (·O₂⁻). This study effectively driven by indirect oxidation, with cathodic hydrogen production, providing a novel strategy for utilizing renewable electricity and reducing OER while offering insights into the design of Co/Fe-based catalyst. Full article

Sb-based anodes have great potential in lithium-ion batteries because of their relatively high theoretical capacities. However, in general, their volume changes (>150%) during charge and discharge process have a significant impact, which affects their electrochemical performances. In this paper, nano-alloy FeSb wrapped in three-dimensional honeycomb graphite carbon (FeSb@C) was prepared by the freeze-drying method using sodium chloride as a template. The three-dimensional carbon can buffer the volume change in the reaction process, increasing the contact area between the electrode and electrolyte. Furthermore, the addition of metallic iron also increases the overall specific capacity and improves its electrochemical performance. As the anode of a lithium-ion battery, the optimized FeSb@C shows excellent electrochemical performance with a specific capacity of 193.0 mAh g⁻¹ at a high current density of 5 A g⁻¹, and a reversible capacity of 607.8 mAh g⁻¹ after 600 cycles of 1 A g⁻¹. It provides an effective strategy for preparing high-performance lithium-ion batteries anode materials. Full article

This study reports the synthesis and evaluation of iron molybdate (Fe₂(MoO₄)₃) and iron tungstate (FeWO₄) as photocatalysts for the degradation of a real industrial effluent from aluminum anodizing processes under visible light irradiation. The oxides were synthesized via a co-precipitation method in an aqueous medium, followed by microwave-assisted hydrothermal treatment. Structural and morphological characterizations were performed using X-ray diffraction, field-emission scanning electron microscopy, Raman spectroscopy, ultraviolet–visible (UV–vis), and photoluminescence (PL) spectroscopies. The effluent was characterized by means of ionic chromatography, total organic carbon (TOC) analysis, physicochemical parameters (pH and conductivity), and UV–vis spectroscopy. Both materials exhibited well-crystallized structures with distinct morphologies: Fe₂(MoO₄)₃ presented well-defined exposed (001) and (110) surfaces, while FeWO₄ showed a highly porous, fluffy texture with irregularly shaped particles. In addition to morphology, both materials exhibited narrow bandgaps—2.11 eV for Fe₂(MoO₄)₃ and 2.03 eV for FeWO₄. PL analysis revealed deep defects in Fe₂(MoO₄)₃ and shallow defects in FeWO₄, which can influence the generation and lifetime of reactive oxygen species. These combined structural, electronic, and morphological features significantly affected their photocatalytic performance. TOC measurements revealed degradation efficiencies of 32.2% for Fe₂(MoO₄)₃ and 45.3% for FeWO₄ after 120 min of irradiation. The results highlight the critical role of morphology, optical properties, and defect structures in governing photocatalytic activity and reinforce the potential of these simple iron-based oxides for real wastewater treatment applications. Full article

This work aims to clarify whether the individual advantages of the two commonly used silicate- and aluminate-based electrolytes for the plasma electrolytic oxidation (PEO) of steel can be combined in a two-step process. The first PEO step was carried out in an aluminate–phosphate electrolyte with pulsed voltage and anodic amplitudes between 150 V and 200 V. The second PEO step was carried out at an increased anodic voltage amplitude of 400 V in a silicate–phosphate electrolyte. As a reference, PEO was conducted in a single step in the same silicate–phosphate electrolyte at an increased anodic voltage amplitude of up to 400 V. The microstructural layer analysis was carried out using SEM and EDX analyses, Raman spectroscopy and XRD analysis. Heterogeneous layers containing iron oxide and iron phosphate form in the silicate–phosphate electrolyte at anodic voltage amplitudes up to 300 V by electrochemical reactions. Further increasing the anodic voltage amplitude up to 400 V results in heterogeneous layers, too. PEO in the aluminate–phosphate electrolyte at 150 V causes the formation of thin, amorphous layers mainly consisting of aluminum and iron oxides. At 200 V amplitude, a PEO layer with pronounced open porosity is formed, which primarily consists of the crystalline phases corundum and hercynite. During subsequent PEO in the silicate–phosphate electrolyte, the previously formed layers were replaced by a macroscopically homogeneous layer that is mostly nanocrystalline and may contain amorphous iron(-aluminum) phosphates and oxides as well as silicon oxide. It can be concluded that the two-step PEO process is suitable for the production of more homogeneous PEO layers. Full article

In this study, we synthesized anode materials based on iron oxide (Fe₂O₃), titanium dioxide (TiO₂), and reduced graphene oxide (rGO) via the electrophoretic deposition technique. The structural and morphological characteristics of electrodes were examined through various methods including SEM, XRD, Raman, and XPS. Among the investigated compositions, the three-component Fe₂O₃/TiO₂/rGO electrode displayed superior electrochemical characteristics in comparison to the binary Fe₂O₃/rGO and TiO₂/rGO electrodes. Specific capacities of 571, 683, and 729 mAh/g were achieved at 0.5 mA for the respective Fe₂O₃:TiO₂ molar ratios of 1:1, 2:1, and 3:1. The 2:1 ratio configuration offered the most promising balance between cycling stability and capacity, highlighting its potential as a high-performance anode in lithium-ion batteries. This work contributes valuable insights into the synergistic behavior of dual-transition metal oxides in composite electrode design using a low-cost and scalable method. Full article

The anodic stability of tungsten carbide (WC) and iron oxide with a spinel structure (Fe₃O₄) were compared against similar data for nanostructured, boron-doped diamond (BDD), and the benchmark Vulcan XC72 carbon, in view of their eventual application as alternative supports for the anion exchange membrane electrolyzer anode. To this end, metal oxide composites were prepared by the in situ autocombustion (ISAC) method, and the anodic behavior of materials (composites as well as supports alone) was investigated in 1 M NaOH electrolyte by the rotating ring–disc electrode method, which enables the separation oxygen evolution reaction and materials’ degradation currents. Among all supports, BDD has proven to be the most stable, while Vulcan XC72 is the least stable under the anodic polarization, with Fe₃O₄ and WC demonstrating intermediate behavior. The Co₃O₄-BDD, -Fe₃O₄, -WC, and -Vulcan composites prepared by the ISAC method were then tested as catalysts of the oxygen evolution reaction. The Co₃O₄-BDD and Co₃O₄-Fe₃O₄ composites appear to be competitive electrocatalysts for the OER in alkaline medium, showing activity comparable to the literature and higher support stability towards oxidation, either in cyclic voltammetry or chronoamperometry stability tests. On the contrary, WC- and Vulcan-based composites are prone to degradation. 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

Sodium dual-ion batteries combine economic and environmental benefits by using carbon materials in both electrodes and sodium compounds in the electrolyte. Among other factors, their successful implementation for energy storage relies on optimization of the properties of the carbon electrode materials. To this end, carbon materials with a wide range of textural and structural properties were prepared by simply heat treating a single porous carbon in the absence or presence of a low-cost highly effective iron-based catalyst. These materials were investigated as anode or cathode in the sodium dual-ion batteries by prolonged galvanostatic cycling. The optimal textural and structural properties for carbon materials to achieve the best performance as electrodes in sodium dual-ion batteries were identified as having a high degree of graphitic structural order combined with minimal microporosity in the cathode and a non-graphitic structure with a layer spacing of around 0.37 nm and moderate microporosity in the anode. Full article