Search Results (5,759)

Developing cost-effective yet high-performance hard carbon anodes is critical for advancing the commercialization of sodium-ion batteries (SIBs), as they offer a balance of low cost, high capacity, and compatibility with Na⁺ storage mechanisms. Herein, waste towels, an abundant, low-cost precursor with a high carbon yield (>49%), were utilized to synthesize hard carbons via a two-step process: pre-oxidation at 250 °C to stabilize the fibrous structure, followed by carbonization at 1100 °C (THC-1100), 1300 °C (THC-1300), or 1500 °C (THC-1500). Electrochemical evaluations revealed that THC-1300, carbonized at an intermediate temperature, exhibited superior Na⁺ storage performance compared to its counterparts: it delivered a high reversible specific capacity of ~320 mAh/g at 1.0 C (1 C = 320 mA/g), with 78% capacity retention after 200 cycles, demonstrating excellent long-term cyclic stability. Its rate capability was equally impressive, achieving specific capacities of 341.5, 331.2, 302.0 and 234.8 mAh/g at 0.2, 0.5, 2.0 and 5.0 C, respectively, indicating efficient Na⁺ diffusion even at high current densities. Notably, THC-1300 also showed an improved initial Coulombic efficiency (ICE) of 75.4%, reflecting reduced irreversible Na⁺ consumption during the first cycle. These enhancements are attributed to the synergistic effects of THC-1300’s optimized structural and textural properties: a balanced interlayer spacing (d₍₀₀₂₎ = 0.387 nm) that facilitates rapid Na⁺ intercalation, a low BET surface area (1.62 m²/g) helps to minimize electrolyte side reactions. The combined advantages of high specific capacity, improved ICE, and remarkable cycling stability position this waste-towel-derived hard carbon as a highly viable and sustainable candidate for anode materials in next-generation SIBs, addressing both performance and cost requirements for large-scale energy storage applications. Full article

Developing electrocatalysts that are efficient and durable for the oxygen evolution reaction (OER) is essential for improving the energy efficiency of alkaline water splitting. Spinel-type transition-metal oxides have emerged as promising non-noble alternatives; however, their catalytic performance is often limited by sluggish charge transport and insufficient utilization of active sites. Herein, we present a systematic comparative study of electrodeposited Co₃O₄ (CO-300) and Cu-substituted Co₂CuO₄ (CCO-300) nanosheet films directly grown on Ni foam. Structural, morphological, and spectroscopic analyses reveal that Cu²⁺ integration into Co-oxide spinel lattice modifies the local electronic environment and produces a more open and interconnected nanosheet architecture, thereby enhancing conductivity and increasing the density of accessible redox-active sites. As a result, the optimized CCO-300 exhibits superior catalytic performance at higher current densities, along with a smaller Tafel slope (44 mV dec^–1), a larger electrochemically active surface area (ECSA), and reduced charge-transfer resistance compared to CCO-300, indicating accelerated reaction kinetics and improved electron-ion transport. Furthermore, the multistep chronopotentiometry measurements and long-term stability tests over 100 h at current densities of 10 and 250 mA cm^–2 highlight the excellent operational stability of the CCO-300 catalyst. Full article

In this study, the influence of the electrochemical oxidation process on Ti-Grad 23 alloy (Ti6Al4V ELI) in 1 M H₃PO₄, under applied voltages between 200 and 275 V, at a constant time of 1 min, is analyzed. The structural, morphological, and wettability properties of the TiO₂ anodic layers obtained were investigated by X-ray diffraction (XRD), energy dispersive electron microscopy (SEM-EDS), contact angle measurements, and chemical corrosion. XRD analysis showed the development and intensification of anatase and brookite phases, with increased crystallite size after electrochemical oxidation. SEM/EDS characterization confirmed the formation of an inhomogeneous porous TiO₂ layer, with pore diameters ranging from 98 to 139 nm and a significant increase in oxygen content. Contact angle measurements demonstrate enhanced hydrophilicity for all oxidized samples, with progressively lower values as the applied voltage increased. Chemical corrosion tests in Ringer solution and Ringer + 40 g/L H₂O₂ indicated that oxidized surfaces maintain structural stability in physiological media, whereas exposure to oxidizing environments induces partial pore closure and crack formation due to localized corrosion. The optimal anodizing condition was identified at 200 V for 1 min, yielding a uniform distribution of pores and improved morpho-functional characteristics suitable for biomedical applications. The optimal electrochemical oxidation conditions were identified at 200 V for 1 min, ensuring a uniform pore distribution. Full article

High-entropy ceramic (HEC) thin films generally refer to multi-component solid solutions composed of multiple metallic and non-metallic elements, existing in forms such as carbides, nitrides, and borides. Benefiting from the high-entropy effect, lattice distortion, sluggish diffusion, and cocktail effect of high-entropy systems, HEC thin films form simple amorphous or nanocrystalline structures while exhibiting high hardness/elastic modulus, excellent tribological properties, and thermal stability. Although the mixing entropy increases with the number of elements in the system, a higher number of elements does not guarantee improved performance. In addition to system configuration, the regulation of preparation methods and processes is also a key factor in enhancing performance. Arc ion plating (AIP) has emerged as one of the mainstream techniques for fabricating high-entropy ceramic (HEC) thin films, which is attributed to its high ionization efficiency, flexible multi-target configuration, precise control over process parameters, and high deposition rate. Through rational design of the compositional system and optimization of key process parameters—such as the substrate bias voltage, gas flow rates, and arc current—HEC thin films with high hardness/toughness, wear resistance, high-temperature oxidation resistance, and electrochemical performance can be fabricated, and several of these properties can even be simultaneously achieved. Against the backdrop of AIP deposition, this review focuses on discussions grounded in the thermodynamic principles of high-entropy systems. It systematically discusses how process parameters influence the microstructure and, consequently, the mechanical, tribological, electrochemical, and high-temperature oxidation behaviors of HEC thin films under various complex service conditions. Finally, the review outlines prospective research directions for advancing the AIP-based synthesis of high-entropy ceramic coatings. Full article

This work addresses the influence of Ni on the natural passivation process of stainless steels (SSs) in alkaline media simulating concrete pore solution by a combination of electrochemical and X-ray photoelectron spectroscopy (XPS) surface analysis. It was found that the involvement of Ni in the passive film on the SS promoted Fe depletion at the passive film/substrate interface and increased the content of Cr oxide during natural passivation, thereby enhancing the corrosion resistance of the passive film. The passive film with Ni has a higher breakdown potential and can be more easily re-passivated compared with a passive film without Ni. Full article

Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li₇La₃Zr₂O₁₂ (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO₃) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials. Full article

Microplastics (MPs) have emerged as persistent environmental pollutants with adverse effects on ecosystems and human health. Conventional removal methods, such as filtration and sedimentation, primarily rely on physical separation without addressing the degradation of MPs, leading to their accumulation and the risk of secondary pollution. This review explores the potential of advanced oxidation processes (AOPs), including photocatalysis, electrochemical oxidation, Fenton processes, sulfate radical-based oxidation, sonochemical treatment, ozonation, and plasma technologies, which generate reactive oxygen and nitrogen species capable of promoting polymer chain scission, microbial biodegradation, and the oxidative fragmentation and mineralization of MPs into non-toxic byproducts. Hybrid AOP systems combined with biological treatments or membrane-based filtration are also examined for their effectiveness in degrading MPs, as well as for scalability and the environmental impacts of their byproducts when integrated into existing wastewater treatment systems. The review further discusses challenges related to operational parameters, energy consumption, and the formation of secondary pollutants. By identifying current knowledge gaps and future research directions, this review provides insights into optimizing AOPs and integrations of AOPs with biological treatments or membrane-based processes for sustainable MP remediation and water treatment applications. Full article

In recent years, biomass utilization has attracted extensive attention. Herein, hexagonal/cubic ZnIn₂S₄ (ZIS) heterojunction catalysts were synthesized via a solvothermal method for the selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran (DFF). The results demonstrated that the constructed heterojunctions effectively promoted carrier separation. The optimal catalyst achieved an HMF conversion rate of 88.8% and a DFF yield of 86.6% within 1 h in the open air. X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) characterizations confirmed the successful fabrication of the composite phase structure and revealed a porous spherical morphology. Equivalent circuit fitting of electrochemical impedance spectroscopy (EIS) data indicated that the hexagonal/cubic heterojunctions possessed the lowest charge transfer resistance (Rct = 5825 Ω), which effectively reduced interfacial charge transfer resistance and accelerated the transport of photoinduced carriers. Radical quenching experiments and electron paramagnetic resonance (EPR) spectroscopy identified superoxide radicals (·O₂⁻) as the primary reactive species. Meanwhile, density functional theory (DFT) calculations elucidated the formation of the built-in electric field and the charge transfer mechanism. This work’s construction of Type-II ZIS heterojunctions effectively addressed the issue of rapid carrier recombination in pristine ZIS materials, providing a feasible strategy for biomass valorization. Full article

Poly(ethylene oxide) (PEO)-based solid polymer electrolytes typically suffer from limited ionic conductivity at near-room temperature and often require inorganic reinforcement. Halide solid-state electrolytes such as Li₃InCl₆ (LIC) offer fast Li⁺ transport but are moisture-sensitive and typically require pressure-assisted densification. Here, we fabricate a flexible LIC–PEO composite electrolyte via slurry casting in acetonitrile with a small amount of LiPF₆ additive. The free-standing membrane delivers an ionic conductivity of 1.19 mS cm⁻¹ at 35 °C and an electrochemical stability window up to 5.15 V. Compared with pristine LIC, the composite shows improved moisture tolerance, and its conductivity can be recovered by mild heating after exposure. The electrolyte enables stable Li|LIC–PEO|Li cycling for >620 h and supports Li|LIC–PEO|NCM111 cells with capacity retentions of 84.2% after 300 cycles at 0.2 C and 80.6% after 150 cycles at 1.2 C (35 °C). Structural and surface analyses (XRD, SEM/EDX, XPS) elucidate the composite microstructure and interfacial chemistry. Full article

To reduce CO₂ emissions into the environment, the automotive sector uses microalloyed structural steels coated with electrophoretic paint in various components, such as the chassis, to reduce weight and increase corrosion resistance. AHSSs are coated with electrophoretic paint (E-coat). Still, to improve adhesion, they undergo a pretreatment, such as zinc phosphate or zirconium oxide. This research will analyze the effects and behavior of these coatings during corrosion on a complex-phase (CP) 780 AHSS using different electrochemical techniques, including cyclic potentiodynamic polarization (CPP), electrochemical noise (EN), and electrochemical impedance spectroscopy (EIS). The CP 780 AHSS was immersed in a 3.5 wt. % sodium chloride solution. Results show that AHSS CP 780 presented a mixed corrosion mechanism due to the heterogeneity of the surface of the zinc phosphate and zirconium oxide pretreatments. On the other hand, the samples with an E-coat paint coating and pretreatment (Zn₃(PO₄)₂/E-coat and ZrO₂/E-coat) have the lowest current densities with values of 6.44 × 10⁻¹¹ 1.02 × 10⁻⁹ A/cm² and also do not show a tendency towards localized corrosion or negative hysteresis. Full article

In this study, oxide coatings with layered double hydroxide (LDH) nanosheets were prepared on AZ91 magnesium alloy by a one-step low-voltage microarc oxidation (MAO) process. The microstructure and composition of the coatings were characterized using SEM, EDS, XRD, FT-IR, and XPS. The corrosion protection performance of the coatings was evaluated by electrochemical analysis and hydrogen evolution tests. The results showed that oxide coatings with Mg-Al-LDH nanosheets are successfully produced by microarc oxidation at a voltage of less than 100 V. The coating with a higher density of Mg-Al LDH nanosheets exhibited enhanced corrosion resistance. Moreover, after modification with stearic acid, the coatings displayed high hydrophobicity and corrosion resistance. Full article

Tannery wastewater from textile-related industries poses treatment challenges due to its high load of recalcitrant pollutants. Various advanced hybrid treatments, such as electro-oxidation (EO), have been proposed but mainly focus on electrode material development. Several studies on EO using multiple electrode pairs with large electroactive surface areas exist, however, none have reported on mass transfer characterization. This study addresses these gaps by investigating the electro-degradation performance of active (mixed-metal oxide, MMO) and non-active (boron-doped diamond, BDD) anodes paired with carbonaceous (graphite) and non-carbonaceous (stainless steel, SS) cathodes under applied current densities of 2 to 6 mA/cm². A 2 L volume of simulated tannery wastewater containing recalcitrant tannic acid was treated using three electrode pairs with a total surface area of 500 cm². Results showed optimal condition was identified at 4 mA/cm² across all electrode combinations and better degradation using BDD anodes and SS cathodes, with total organic carbon (TOC) removed up to 500 mg/L (98% removal). Adopting the 3-electrode configuration, mass transfer coefficients ranged from 4.15 to 5.18 × 10⁻⁶ m/s. Energy consumption evaluation suggested MMO as a more cost-effective option, while BDD remained preferable for highly recalcitrant waste. Higher currents show diminishing returns due to mass transfer and parasitic reactions. Full article

Copper has become more important owing to its eco-friendliness and persistent efficacy against infections. Furthermore, copper has benefits such as safety in use and durability. This study aimed to develop and assess the antibacterial efficacy of stainless steel coated with a composite layer, which is nanostructured and incorporates copper, to create antibacterial surfaces with good adherence and good corrosion resistance. The composite coating was produced using anodic oxidation, with an external copper layer applied via pulse electroplating. The homogenous cauliflower-like covering showed important characteristics, like increased surface roughness, boosted surface free energy, reduced contact angle, and higher hardness. Additionally, the adherence between the composite covering and the substrate was exceptional. Electrochemical experiments indicated aggressive corrosion behavior in chloride-containing settings. Antibacterial tests were conducted on four prevalent bacterial strains: Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Salmonella typhimurium—microorganisms often linked to healthcare and environmental pollution. The coating exhibited enhanced antibacterial efficacy relative to untreated steel and anodized steel. Results indicated that the composite coating is an effective and possibly cost-efficient method for controlling the surface proliferation of the mentioned pathogens. Full article

Pharmaceutical contamination poses growing environmental risks, yet industrial adoption of advanced oxidation processes (AOPs) remains limited by high costs and the environmental impacts associated with specialized electrodes. This study demonstrates that unmodified aluminum electrodes achieve pharmaceutical degradation performance comparable to precious metal systems at dramatically reduced cost and carbon footprint. An aluminum-based electro-Fenton (EF) system was optimized for amlodipine (AML) removal through systematic evaluation of operational parameters. Under optimized conditions (pH 2.7, 35 mg L⁻¹ FeCl₃, 1.3 mM NaCl, 5 V), the system achieved 97% AML degradation within 15 min, following pseudo-first-order kinetics ($k=0.15$ min⁻¹). The mechanism combines hydroxyl radical oxidation with synergistic electrocoagulation resulting from anodic Al³⁺ release and cathodic Fe²⁺ regeneration. Sustainability assessment revealed exceptional performance: an energy consumption of 0.32 kWh m⁻³, a carbon footprint of 0.53 kg CO₂-eq m⁻³ (60–75% lower than conventional AOPs), and operational costs of $0.71–1.05 m⁻³. Aluminum electrodes cost 100× less than platinum alternatives, with the generated Al(OH)₃ sludge offering valorization potential. This work demonstrates that high-performance electrochemical remediation is achievable using Earth-abundant materials, providing a scalable and cost-effective alternative for pharmaceutical wastewater treatment in resource-constrained settings. Full article

Two amide-preformed aromatic diamine monomers, N,N-bis(4-(3-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (m-6) and N,N-bis(4-(4-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (p-6), were synthesized and utilized to prepare two series of electroactive poly(amide-imide)s (PAIs) through a two-step polycondensation reaction with commercially available aromatic tetracarboxylic dianhydrides. The obtained polymers exhibited solubility in various polar organic solvents, and most of them could form transparent, flexible films via solution casting. Thermal analysis indicated glass transition temperatures (T_g) ranging from 250 °C to 277 °C, as measured by DSC, with no significant weight loss observed before 400 °C in TGA tests. Cyclic voltammograms (CV) of the polymer films on ITO-coated glass substrates revealed two reversible oxidation redox pairs between 0.67 and 1.04 V vs. Ag/AgCl in an electrolyte-containing acetonitrile solution. The PAI films showed stable redox activity with high optical contrast both in the visible and near-infrared regions, transitioning from colorless in the neutral state to green and blue in the oxidized states. Furthermore, the polymer films retained good electrochemical and electrochromic stability even after more than 100 cyclic switching operations. The PAIs displayed outstanding electrochromic performance, including high optical contrast (up to 95%), rapid response times (below 4.6 s for coloring and 5.7 s for bleaching), high coloration efficiency (up to 240 cm²/C), and low decay in optical contrast (less than 5% after 100 switching cycles for most PAIs). Full article