Search Results (3,587)

This study introduces a synergistic drop-casting, sonication, and thermal treatment (DSTT) method for fabricating multi-walled carbon nanotube (MWCNT)-coated conductive cotton fabrics. The process produced uniform MWCNT networks with a minimum sheet resistance of 0.072 ± 0.004 kΩ/sq. at ~30 wt.% loading. Scanning electron microscopy confirmed an improved MWCNT network. Reproducibility was demonstrated for different fabric sizes, with resistance values remaining consistent within experimental errors. Stability tests showed only minor changes in sheet resistance after 16 weeks of ambient storage and periodic manual bending. Compared to conventional methods such as room-temperature drying, vacuum drying, and sonication alone, DSTT consistently performed better, yielding fabrics with lower resistance and more reliable conductivity. These results highlight DSTT as a reproducible and scalable method for producing conductive cotton fabrics suitable for smart textiles and wearable electronics. Full article

This study evaluated powdered activated carbon (PAC) pre-coating as a pretreatment strategy to enhance dissolved organic matter (DOM) removal and control fouling during microfiltration of surface water. Two PAC types (one is coal-based and the other is wood-based), divided into three different particle size ranges (22–44, 44–63, 63–88 μm) using sieves and coating weights ranging from 0.6 to 1.2 and 2.4 mg/cm², were systematically compared. Coating PAC improved the quality of water after filtration and stabilized filtration flux, with smaller PAC particle size ranges exhibiting higher DOM removal efficiencies, achieving maximum removals of approximately 30–35% for DOC and over 50% for UV260 at the highest coating weight, whereas uncoated membranes showed negligible DOM removal. The resulting PAC layer on the membrane increased filtration resistance. Fluorescence EEM and Mw distribution results showed that aromatic and high molecular weight DOM was preferentially adsorbed by PAC before reaching the membrane surface; therefore, their contribution to membrane fouling could be reduced. SEM observations showed differences in the images of deposits formed on the PAC layer. These results indicate that the PAC layer acted as a protective interception zone that reduced direct contact between DOM and the membrane surface, thereby contributing to improved flux stability. The coating effect varied with the weight, type and size range of PAC, highlighting the importance of PAC selection. The findings of this study could contribute to more efficient and sustainable urban water supply system operation and management through water quality improvement and process configuration. Full article

Carbon–metal composite NiCrFeC coatings, prepared with and without controlled oxygen addition, were investigated to evaluate the influence of oxygen on the structure, mechanical response, and tribological performance. X-ray diffraction revealed that oxygen-containing films (NiCrFeC + O₂) exhibit a mixed metallic–oxide microstructure with CrNi, CrO, and NiO phases, whereas oxygen-free coatings show only CrNi crystalline peaks. The incorporation of oxygen led to a substantial increase in nano-hardness, from 0.84 GPa for NiCrFeC to 1.59 GPa for NiCrFeC + O₂. Scratch testing up to 100 N indicated improved adhesion and higher critical loads for the oxygen-rich coatings. Tribological measurements performed under dry sliding conditions using a sapphire ball showed a significant reduction in friction: NiCrFeC + O₂ stabilized at ~0.20, while NiCrFeC exhibited values between 0.25 and 0.35 at 0.5 N and 0.4–0.5 at 1 N, accompanied by non-uniform sliding due to coating failure. Wear-track analysis confirmed shallower penetration depths and narrower wear scars for NiCrFeC + O₂, despite similar initial roughness (~35 nm). These findings demonstrate that oxygen incorporation enhances hardness, adhesion, and wear resistance while substantially lowering friction, making NiCrFeC + O₂ coatings promising for low-friction dry-sliding applications. Full article

Fire-retardant intumescent coatings offer an effective means of enhancing the fire resistance of combustible substrates such as wood. These coatings have a complex chemical composition and, when exposed to temperatures above 200 °C, undergo an intumescent reaction accompanied by the release of non-flammable gases, forming an expanded, charred layer with low thermal conductivity. This provides thermal insulation and acts as a physical barrier against heat, oxygen, and flammable volatiles. In this study, the applicability of several thermoanalytical techniques for evaluating the performance of three different intumescent coatings applied to spruce wood was investigated. Simultaneous thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) showed that coating No. 3 was the most efficient, initiating substrate protection at the lowest temperature and reducing the combustion enthalpy by approximately 50% compared to uncoated wood. DSC-microscopy visualization enabled direct observation of the intumescent expansion, degradation of the carbonized protective layer, and delayed thermal decomposition of coated wood. Furthermore, a comparison between TGA-MS and TGA-IST16-GC-MS demonstrated the superiority of chromatographic separation for identifying evolved gaseous products. While TGA-MS is effective for detecting small gaseous species (e.g., H₂O, CO₂, formaldehyde), TGA-IST16-GC-MS enables the deconvolution of many degradation products evolving simultaneously, allowing for distinction between flame-retardant-related species, polymer backbone fragments, nitrogen-rich heterocycles, and small oxygenated molecules in the most effective coating. Full article

AISI 1045 steel often undergoes premature failure under combined corrosive-wear conditions due to its insufficient surface durability. To address this, a hot-dip aluminum (HDA) coating was deposited on the steel substrate. The microstructure, corrosion behavior, and tribological properties of the coating were systematically characterized using scanning electron microscopy (SEM), electrochemical techniques, and tribometry. The results reveal that the coating exhibits a continuous triple-layer structure, consisting of the steel substrate, an intermediate Fe-Al intermetallic compound layer, and an outer aluminum-rich layer. In a 3.5 wt.% NaCl solution, the coating formed a protective Al₂O₃ film, demonstrating clear passivation behavior. It significantly enhanced the substrate’s performance, achieving an approximately 90% reduction in wear rate and a substantial increase in charge transfer resistance. The coated sample showed a lower friction coefficient (0.24) compared to the bare substrate (0.34). Herein, this work demonstrates that a straightforward and industrially viable hot-dip aluminizing process can effectively improve the corrosion and wear resistance of medium-carbon steel. The findings provide a practical surface-hardening strategy for such steels operating in aggressive environments. Full article

This study aimed to examine the influence of sputtering temperature on the bonding structure and properties of non-hydrogenated chromium/nickel co-doped diamond-like carbon (DLC) films synthesized via direct current magnetron sputtering. The Cr/Ni doping levels in the coatings were regulated by varying the shield opening above a chromium-nickel (20/80 at.%) target, resulting in a total metal co-doping concentration ranging from 6.1 to 8.9 at.%. The thickness of the Cr/Ni-DLC films ranged from 160 to 180 nm. Meanwhile, the deposition temperatures of 185 °C and 235 °C were achieved by adjusting the substrate-to-target distance. The XPS and Raman spectroscopy results indicated enhanced graphitization of the Cr/Ni-DLC films with a decrease in the synthesis temperature. XPS results indicated the formation of carbon-oxide and metal-oxide bonds, with no evidence of metal carbide formation in the doped DLC films. Furthermore, both the nanohardness and Young’s modulus demonstrated significant improvement, while the friction coefficient was reduced more than twice as the deposition temperature increased. These findings provide valuable insights into the influence of deposition temperature on Cr/Ni co-doped DLC films, highlighting their potential as advanced functional coatings. Full article

Zeolite imidazolate frameworks (ZIFs)-derived carbon materials have garnered widespread attention as peroxymonosulfate (PMS) activators in removing antibiotics because of their excellent catalytic performance. However, most carbon materials derived from ZIFs exhibit limited efficacy in treating high-concentration (>10 ppm) antibiotic wastewater, and their synthesis methods are environmentally unfriendly. Herein, we develop a simple and environmentally friendly preparation method to synthesize a new type of nitrogen-doped carbon-supported carbon nanotubes coated with cobalt nanoparticle (Co-CNTs@NC) composites via high-temperature calcination of cobalt–zinc bimetallic ZIFs. The material characterization results confirm the successful preparation of Co-CNTs@NC composites featuring a high specific surface area (512.13 m²/g) and a Co content of 5.38 wt%. Across an initial pH range of 3.24–9.00, the Co-CNTs@NC/PMS catalytic system achieved over 84.17% degradation of 20 mg/L tetracycline hydrochloride within 90 min, demonstrating its favorable pH tolerance. The singlet oxygen-dominated degradation mechanism was confirmed by quenching experiments and electron paramagnetic resonance characterization. This work can provide technical guidance and reference significance for the preparation of metal–carbon materials derived from ZIFs with excellent efficiency of removal of high-concentration antibiotics. Full article

Graphene oxide (GO) is a carbon-based nanomaterial explored for agricultural and forestry uses, but plant responses are strongly subject to both the dose and the route of exposure. We summarized recent studies with defined graphene oxide (GO) exposures by seed priming, foliar delivery, and root or soil exposure, while comparing annual crops with woody forest plants. Mechanistic progress points to a shared physicochemical basis: surface oxygen groups and sheet geometry reshape water and ion microenvironments at the soil–seed and soil–rhizosphere interfaces, and many reported shifts in antioxidant enzymes and hormone pathways likely represent downstream stress responses. In crops, low-to-moderate doses most consistently improve germination, root architecture, and tolerance to salinity or drought stress, whereas high doses or prolonged root exposure can cause root surface coating, oxidative injury, and photosynthetic inhibition. In forest plants, evidence remains limited and often relies on seedlings or tissue culture. For forest plants with long life cycles, processes such as soil persistence, aging, and multi-seasonal carry-over become key factors, especially in nurseries and restoration substrates. The available data indicate predominant root retention with generally limited root-to-shoot translocation, so residues in edible and medicinal organs remain insufficiently quantified under realistic-use patterns. This review provides a scenario-based framework for crop- and forestry-specific safe-dose windows and proposes standardized endpoints for long-term fate and ecological risk assessment. Full article

Low work function (LWF) materials are essential for enabling efficient systems’ behavior in applications ranging from vacuum electronics to energy conversion devices and next-generation opto-electronic interfaces. Recent advances in theory, characterization, and materials engineering have dramatically expanded the candidates for LWF systems, including alkali-based compounds, perovskites, borides, nitrides, barium and scandium oxides, 2D materials, MXenes, functional polymers, carbon materials, and hybrid architectures. This review provides a comprehensive overview of the fundamental mechanisms governing the work function (WF) and discusses the state-of-the-art measurement techniques, as well as the most used computational approaches for predicting and validating WF values. The recent breakthroughs in engineering LWF surfaces through different methods are discussed. Special emphasis is placed on the relationship between predicted and experimentally measured WF values, highlighting the role of surface contamination, reconstruction, and environmental stability. Performance, advantages, and limitations of major LWF material families are fully analyzed, identifying emerging opportunities for next applications. Finally, current and fundamental challenges in achieving scalable, stable, and reproducible LWF surfaces are considered, presenting promising research directions such as high-throughput computational discovery and in situ surface engineering with protective coatings. This review aims to provide a unified framework for understanding, achieving, and advancing LWF materials toward practical and industrially relevant technologies. Full article

Interactions between alkaline solutions and the surface of pyrolytically coated graphite tubes (PCGTs) with/without a platform for determination of vanadium using high-resolution continuum source graphite furnace atomic absorption spectrometry (HR CS GFAAS) are discussed. Changes on the surface of tubes, lifetime of tubes, and formation of memory effect in the determination of vanadium in alkaline solutions (NaOH, Na₂CO₃, and real alkaline slag leachates) were investigated. Based on the results obtained, it is possible to state that HR CS GFAAS determination of vanadium content in alkaline solutions reveals that PCGTs with a platform are more susceptible than those without a platform to the formation of deposits and degradation of the platform surface, especially after the application of hydroxide environments. More marked and faster formation of deposits leads to shortening of the analytical lifetime of PCGTs with a platform (approx. 70 atomization/analytical cycles (ACs)) compared to PCGTs without a platform (approx. 290 ACs). The mechanical life of both types of tubes is comparable (approx. 500 ACs). Deposits formed on the internal surface of PCGTs can be removed in the presence of a carbonate environment and higher temperatures. Damage to the PCGT surface leads to the formation of scaled shapes and cavities, which can result in decreased absorbance due to losses of vanadium in the cavities (negative measurement error), or in increased absorbance by washing out of vanadium from the cavities (positive measurement error, and formation of memory effect). It was found that more frequent cleaning of PCGTs by performing ACs in an environment of 4 mol L⁻¹ HNO₃ can eliminate these unfavourable phenomena. Our results have shown that in the case of samples analysed with different sample environments (acidic vs. alkaline), the surface material of the tube/platform wears out more quickly, and therefore it is necessary to include a cleaning stage after changing the nature of the environment. 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

Hydrogenated tetrahedral amorphous carbon (ta-C:H) thin films were modified using 266 nm picosecond laser pulses to investigate structural transformations at low and moderate fluences. Nitrogen-doped hydrogenated tetrahedral amorphous carbon layers 20–40 nm thick were deposited on silicon (Si) and silicon dioxide on silicon (SiO₂/Si) substrates and irradiated with picosecond pulses at 0.5–1.6 J cm⁻² using a raster-scanned beam. Structural changes in morphology, composition, and bonding were evaluated via optical microscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Even below 1.0 J cm⁻², localized color shifts and slight swelling indicated early structural rearrangements without significant material removal. Above 1.0–1.2 J cm⁻², the films were largely ablated, although a persistent 3–6 nm carbon layer remained on both substrate types. XPS showed an increase in sp²-bonded carbon by roughly 15%–20% in optimally modified regions, and Raman spectroscopy revealed defect-activated D-bands and the formation of multilayer defective graphene or reduced-graphene-oxide-like flakes at ablation boundaries. These results indicate that picosecond ultraviolet irradiation enables controllable graphitization and thinning of ta-C:H films while maintaining uniform processing over centimeter-scale areas, providing a route to thin, conductive, partially graphitized carbon coatings for optical and electronic applications. Full article

Coral aggregate concrete (CAC) serves as a critical material for sustainable development in marine engineering, effectively addressing the shortage of aggregate resources in the construction of offshore islands and reefs. In this paper, the aggregate characteristics, static and dynamic mechanical properties and modification technology of CAC are systematically reviewed. Research indicates that the coral aggregates (CAs), due to its high porosity (approximately 50%), low bulk density (900–1100 kg/m³), and rough, porous surface, results in relatively low static compressive strength (20–40 MPa), insufficient elastic modulus, and significant brittleness in CAC. However, its dynamic performance shows the opposite advantage. Under impact loads, the energy absorption capacity is enhanced by 32.6–140.3%, compared to ordinary concrete (OC) due to the energy dissipation mechanism of pore platic deformation. Through the modification techniques, such as aggregate pre-treatment (acid washing/coating), incorporation of auxiliary cementitious materials (silica fume increases strength by 16.4%), fibre reinforcement (carbon fibres enhance flexural strength by 33.3%), and replacement with novel cementitious materials (magnesium sulphate cement improves chloride ion binding capacity by 90.7%), the mechanical properties and durability of CAC can be significantly optimised. This paper highlights gaps in current research regarding the high strain rate (>200 s⁻¹) dynamic response, multi-factor coupled durability in marine environments, and the engineering application of alkali-activated materials, providing theoretical basis for future research directions. Full article

Resin curing coating is an effective approach to mitigate the intrinsic defects of lignocellulosic biomass-derived hard carbon, which facilitates its large-scale application in sodium-ion batteries due to their improved specific capacity, initial coulombic efficiency, and carbon yield. However, current traditional curing processes suffer from issues such as uneven cross-linking encapsulation and long curing cycles, significantly affecting the electrochemical performance of the derived carbon and production efficiency/cost. In this study, a phenolic resin solution impregnation combined with microwave-accelerated curing has been employed, and its curing process, along with the electrochemical performance of the derived carbon, was investigated. The results show that uniformly phenolic resin-coated bamboo could be achieved within 120 s. A dense cross-linked network not only leads to a high hard carbon yield and low specific surface area but also creates an abundant pseudographene-like structure with more closed pores. Under optimal crosslinking conditions, the obtained hard carbon sample shows a significantly enhanced reversible capacity (371.73 mAh g⁻¹) and high initial coulombic efficiency of 84.54%, far exceeding the bamboo-derived hard carbon (229.23 mAh g⁻¹, 74.90%) and the hard carbon sample prepared by traditional heating curing (304.31 mAh g⁻¹, 80.63%). Additionally, the designed sample displays excellent structural stability, maintaining 80% of their capacity after 500 cycles at a high current density of 300 mA g⁻¹. This fast and simple resin coating strategy shows great potential for the scalable synthesis of high-performance hard carbon anode materials. Full article

The rapid commercialization of next-generation photovoltaic (PV) technologies, particularly perovskite, thin-film roll-to-roll (R2R) architectures, and tandem devices, requires robust assessment of environmental performance at the level of industrial manufacturing processes. Environmental impacts can no longer be evaluated solely at the device or module level. Although many life-cycle assessment (LCA) studies compare silicon, cadmium telluride (CdTe), copper indium gallium selenide (CIGS), and perovskite technologies, most rely on aggregated indicators and database-level inventories. Few studies systematically compile and harmonize process-level life-cycle inventories (LCIs) for the manufacturing steps that differentiate emerging industrial routes, such as solution coating, R2R processing, atomic layer deposition, low-temperature annealing, and advanced encapsulation–metallization strategies. In addition, inconsistencies in functional units, system boundaries, electricity-mix assumptions, and scale-up modeling continue to limit meaningful cross-study comparison. To address these gaps, this review (i) compiles and critically analyzes process-resolved LCIs for innovative PV manufacturing routes across laboratory, pilot, and industrial scales; (ii) quantifies sensitivity to scale-up, yield, throughput, and electricity carbon intensity; and (iii) proposes standardized methodological rules and open-access LCI templates to improve reproducibility, comparability, and integration with techno-economic and prospective LCA models. The review also synthesizes current evidence on recycling, circularity, and critical-material management. It highlights that end-of-life (EoL) benefits for emerging PV technologies are highly conditional and remain less mature than for crystalline-silicon systems. By shifting the analytical focus from technology class to manufacturing process and life-cycle configuration, this work provides a harmonized evidence base to support scalable, circular, and low-carbon industrial pathways for next-generation PV technologies. Full article