Search Results (169)

This study investigates the effect of the surface functionalization of tungsten disulfide (WS₂) nanoparticles with aminoacetic acid (glycine) on the structure, curing behavior, and mechanical performance of epoxy nanocomposites. Aminoacetic acid, as a non-toxic, bio-based modifier, enables a sustainable approach to producing more efficient nanofillers. Functionalization, as confirmed by FTIR, EDS, and XRD analyses, led to elevated surface polarity and greater chemical affinity between WS₂ and the epoxy matrix, thereby promoting uniform nanoparticle dispersion. The strengthened interfacial bonding resulted in a notable decrease in the curing onset temperature—from 51 °C (for pristine WS₂) to 43 °C—accompanied by an increase in polymerization enthalpy from 566 J/g to 639 J/g, which reflects more extensive crosslinking. The SEM examination of fracture surfaces revealed tortuous crack paths and localized plastic deformation zones, indicating superior fracture resistance. Mechanical testing showed marked improvements in flexural and tensile strength, modulus, and impact toughness at the optimal WS₂ loading of 0.5 phr and a 7.5 wt% aminoacetic acid concentration. The surface-modified WS₂ nanoparticles, which perform dual functions, not only reinforce interfacial adhesion and structural uniformity but also accelerate the curing process through chemical interaction with epoxy groups. These findings support the development of high-performance, environmentally sustainable epoxy nanocomposites utilizing amino acid-modified 2D nanofillers. Full article

Tungsten-doped vanadium dioxide (W-VO₂) shows semiconductor-to-metal phase transition properties at room temperature, which is an ideal thermo-chromic smart window material. However, low visual transmittance and solar modulation limit its application in building energy saving. In this paper, a W-VO_2−x@AA core-shell nanoparticle is proposed to improve the thermo-chromic performance of W-VO₂. Oxygen vacancies were used to promote the connection of W-VO_2−x nanoparticles with L-ascorbic acid (AA) molecules. Oxygen vacancies were tuned in W-VO₂ nanoparticles by thermal annealing temperatures in vacuum, and W-VO_2−x@AA nanoparticles were synthesized by the hydrothermal method. A smart window was formed by dispersing W-VO_2−x@AA core-shell nanoparticles into PVP evenly and spin-coating them on the surface of glass. The visual transmittance of this smart window reaches up to 67%, and the solar modulation reaches up to 12.1%. This enhanced thermo-chromic performance is related to the electron density enhanced by the AA surface molecular coordination effect through W dopant and oxygen vacancies. This work provides a new strategy to enhance the thermo-chromic performance of W-VO₂ and its application in the building energy-saving field. Full article

In the “dual carbon” objective, the preparation of non-precious metal catalysts with low cost and high activity is essential for the study of hydrogen evolution reactions (HERs). This study employed biomass pomelo peel powder as the carbon source and ammonium metatungstate (AMT) as the tungsten source and, through a facile one-step method in molten salt, fabricated a biomass carbon-based nanocatalyst featuring carbon flakes adorned with tungsten carbide (WC) nanoparticles. Dicyandiamide and cysteine were introduced as nitrogen and sulfur sources, respectively, to explore the impacts of N-S elemental doping on the structure, composition, and HER performance of the WC/C catalyst. The experimental results showed that N-S doping changed the electronic structure of WC and increased the electrochemically active surface area, resulting in a significant increase in the HER activity of WC/C@N-S catalysts. The WC/C@N-S catalyst was evaluated with hydrogen evolution performance in a 0.5 mol/L H₂SO₄ solution. When the cathodic current density reached 10 mA/cm², the overpotential was 158 mV, and the Tafel slope was 68 mV/dec, underscoring its excellent HER performance. The outcomes offer novel insights into the high-value utilization of agricultural biomass resources, and pave the way for the development of cost-effective, innovative hydrogen evolution catalysts. Full article

Pd-WO₃ coatings on porous silicon (PSi) substrates are engineered to enhance interfacial charge transfer and surface reactivity through atomic-scale structural tailoring. This study combines first-principles calculations and experimental characterization to elucidate how Pd nanoparticles (NPs) optimize the coating’s electronic structure and environmental stability. The hierarchical PSi framework with uniform nanopores (200–500 nm) serves as a robust substrate for WO₃ nanorod growth (50–100 nm diameter), while Pd decoration (15%–20% surface coverage) strengthens Pd–O–W interfacial bonds, amplifying electron density at the Fermi level by 2.22-fold. Systematic computational analysis reveals that Pd-induced d-p orbital hybridization near the Fermi level (−2 to +1 eV) enhances charge delocalization, optimizing interfacial charge transfer. Experimentally, these modifications enhance the coating’s response to environmental degradation, showing less than 3% performance decay over 30 days under cyclic humidity (45 ± 3% RH). Although designed for gas sensing, the coating’s high surface-to-volume ratio and delocalized charge transport channels demonstrate broader applicability in catalytic and high-stress environments. This work provides a paradigm for designing multifunctional coatings through synergistic interface engineering. Full article

Protective garments for the medical radiation shielding of healthcare professionals must ensure flexibility and shielding performance. As such, process technologies for density enhancement are required when manufacturing shielding sheets to ensure the reproducibility of flexibility and shielding performance. Although previous efforts commonly reduced particle size to minimize porosity, nanoparticle production cost is significant. Therefore, this study aimed to improve the density of the shielding sheet by controlling the spacing between internal particles. The proposed improvement method is based on polydisperse particle packing. Particle sizes can be adjusted using process techniques such as sintering, pressing, and mixing. The study materials used are tungsten and bismuth oxide (eco-friendly alternatives to lead), with polyethylene as the polymer matrix. First, the shielding performance improved by 4% in the sintering process when the tungsten content reached 90 weight percent (wt%). The solvent removal process, used to eliminate the solvent added for polymer utilization, increased the density by 13.18%; however, it was lower than that of the compression process. The shielding performance improved by approximately 10% in the compression molding process when the tungsten content was 90 wt%. This study confirms that optimizing density enhancement strategies for radiation shielding materials can significantly improve shielding performance. Full article

Cesium tungsten bronzes (Cs_xWO₃), as functional materials with excellent near-infrared shielding properties, demonstrate significant potential for applications in smart windows. However, traditional synthesis methods, such as solid-state reactions and solvothermal/hydrothermal approaches, typically require harsh conditions, including high temperatures (above 200 °C), high pressure, inert atmospheres, or prolonged reaction times. In this study, we propose an optimized microwave-assisted solvothermal synthesis strategy that significantly reduces the severity of reaction conditions through precise parameter control. When benzyl alcohol was employed as the solvent, Cs_xWO₃ nanoparticles could be rapidly synthesized within a relatively short duration of 15 min at 180 °C, or alternatively obtained through 2 h at a low temperature of 140 °C. However, when anhydrous ethanol, which is cost-effective and environmentally friendly, was substituted for benzyl alcohol, successful synthesis was also achieved at 140 °C in 2 h. This method overcomes the limitations of traditional high-pressure reaction systems, achieving efficient crystallization under low-temperature and ambient-pressure conditions while eliminating safety hazards and significantly improving energy efficiency. The resulting materials retain excellent near-infrared shielding performance and visible-light transparency, providing an innovative solution for the safe, rapid, and controllable synthesis of functional nanomaterials. Full article

E. coli O157:H7 contamination in food and the environment poses a serious threat to human health. Rapid and sensitive identification of foodborne pathogens remains challenging. Here, we prepared tungsten disulfide (WS₂)–Au nanocomposites coupled with the Raman signal molecule 5,5′-dithio-bis-(2-nitrobenzoic acid) (DTNB) and antibodies to replace the conventional colloidal gold nanoparticles and applied SERS-active nanotags in the SERS-ICA method for highly sensitive detection of E. coli O157:H7. The large surface area and numerous effective SERS hotspots of WS₂-Au nanotags provide superior SERS signals. Under optimized conditions, this ICA achieves the quantitative detection of E. coli O157:H7 in a broad linear range of 8 × 10²–8 × 10⁷ CFU/mL and at a low detection limit of 175 CFU/mL. In addition, the test strip indicates high specificity for E. coli O157:H7 identification, favorable reproducibility, and shows good accuracy in the detection of actual food samples, such as milk and pork. The proposed assay can be used for rapid qualitative and quantitative detection of E. coli O157:H7 and has great potential for field application. Full article

Tungsten disulfide (WS₂) is attractive for the development of chemiresistive sensors due to its favorable band gap, as well as its mechanical strength and chemical stability. In this work, we elaborate a procedure for the synthesis of thin films consisting of vertically and/or horizontally oriented WS₂ nanoparticles by sulfurizing nanometer-thick tungsten layers deposited on oxidized silicon substrates using magnetron sputtering. According to X-ray photoelectron spectroscopy and Raman scattering data, WS₂ films grown in an H₂-containing atmosphere at 1000 °C are almost free of tungsten oxide. The WS₂ film’s thickness is controlled by varying the tungsten sputtering duration from 10 to 90 s. The highest response to nitrogen dioxide (NO₂) at room temperature was demonstrated by the film obtained using a tungsten layer sputtered for 30 s. The increased sensitivity is attributed to the high surface-to-volume ratio provided by the horizontal and vertical orientation of the small WS₂ nanoparticles. Based on density functional calculations, we conclude that the small in-plane size of WS₂ provides many high-energy sites for NO₂ adsorption, which leads to greater charge transfer in the sensor. The detection limit of NO₂ calculated for the best sensor (WS₂-30s) is 15 ppb at room temperature and 8 ppb at 125 °C. The sensor can operate in a humid environment and is significantly less sensitive to NH₃ and a mixture of H₂, CO, and CO₂ gases. Full article

We report the successful synthesis of amorphous titanium-engineered tungsten oxide (WTi) films via a facile and cost-effective electrodeposition method. Unlike conventional high-temperature or vacuum-based techniques, our approach enables a scalable, all-solution process, ensuring efficiency and sustainability. X-ray diffraction (XRD) confirmed the amorphous nature of all films, a key factor in enhancing ion diffusion for superior electrochromic (EC) performance. Field-emission scanning electron microscopy (FESEM) revealed that an optimized nanoparticle network facilitates rapid charge transport and ion intercalation, while uncontrolled nucleation and grain growth hinder EC efficiency. By precisely tuning the Ti concentration, the optimized 3 at% WTi-3 film achieved outstanding EC properties, including an impressive optical modulation of 85% at 600 nm, exceptional reversibility of 95.61%, and a high coloration efficiency of 51.55 cm²/C. This study underscores the pivotal role of amorphous engineering and dopant concentrations in advancing high-performance EC materials, paving the way for next-generation smart windows and energy-efficient displays. Our findings highlight a transformative strategy for low-cost, high-efficiency EC devices, demonstrating unprecedented performance through precision-engineered material design. Full article

The electrocatalytic reduction of nitric oxide and nitrogen dioxide (NOx) remains a significant challenge due to the need for stable, efficient, and cost-effective materials. This study presents a novel support system for NOx reduction in alkaline media, composed of ZrO₂-WO₃-C (ZWC), synthesized via coprecipitation. Platinum nanoparticles (10 wt.%) were loaded onto ZWC and Vulcan carbon support, using similar methods for comparison. Comprehensive physicochemical and electrochemical analyses (N₂ physisorption, XRD, XPS, SEM, TEM, and cyclic and linear voltammetry) revealed that PtZWC outperformed PtC and commercial PtEtek in NOx electrocatalysis. Notably, PtZWC exhibited the highest total electric charge for NOx reduction. At the same time, the hydrogen evolution reaction (HER) was shifted to more negative cathodic potentials, indicating reduced hydrogen coverage and a modified dissociative Tafel mechanism on platinum. Additionally, the combination of WO₃ and ZrO₂ in ZWC enhanced electron transfer and suppressed HER by reducing NO and hydrogen atom adsorption competition. While the incorporation of WO₃ and ZrO₂ lowered the surface area to 96 m²/g, it significantly improved pore properties, facilitating better Pt nanoparticle dispersion (3.06 ± 0.85 nm, as confirmed by SEM and TEM). XRD analysis identified graphite and Pt phases, with monoclinic WO₃ broadening PtZWC peaks (20–25°). At the same time, XPS confirmed oxidation states of Pt, W, and Zr and tungsten-related oxygen vacancies, ensuring chemical stability and enhanced catalytic activity. Full article

Tungsten disulfide (WS₂) nanoparticles have emerged in the biomedical field as potential theranostic agents due to their unique properties, including biocompatibility. However, their impact on the immune response remains unexplored. This study aimed to evaluate the effects of inorganic fullerene-like WS₂ (IF-WS₂) nanostructures on human peripheral blood mononuclear cells (PBMCs) in vitro. The study investigated several parameters to evaluate the effects of IF-WS₂ nanoparticles. Cytotoxicity was assessed by measuring cell viability, apoptosis, and necrosis. Internalization of IF-WS₂ by PBMCs was analyzed using morphological and flow cytometric techniques. Proliferation was studied in CellTrace Far Red-prestained total PBMCs stimulated with phytohemagglutinin (PHA) and in isolated T cell cultures stimulated with CD3/CD28-coated beads. Additionally, the production of cytokines and chemokines was measured in culture supernatants of total PBMCs and T cells. IF-WS₂ nanoparticles were non-cytotoxic up to a concentration of 200 µg/mL. Concentrations ≥25 µg/mL inhibited PHA-stimulated PBMC proliferation but did not affect T cell proliferation. Morphological and flow cytometric analysis demonstrated dose- and time-dependent internalization of IF-WS₂ by macrophages. Additionally, IF-WS₂ significantly reduced the production of pro-inflammatory cytokines (IL-1β, TNF-α, IL-8, MCP-1, and GRO-α) in PHA-stimulated PBMCs. Th1, Th17, and Th21 cytokines were downregulated, while Th2, Th9, and T regulatory cytokines were upregulated. In conclusion, this study demonstrated for the first time that pristine IF-WS₂ nanoparticles, at non-cytotoxic concentrations, exhibit notable anti-inflammatory and immunomodulatory properties on activated PBMCs in vitro. Full article

Detecting multiple tumor markers is of great importance. It helps in early cancer detection, accurate diagnosis, and monitoring treatment. In this work, gold nanoparticles–toluidine blue–graphene oxide (AuNPs-TB–GO) and gold nanoparticles–carboxyl ferrocene–tungsten disulfide (AuNPs–FMC–WS₂) nanocomposites were prepared for labeling Carcinoembryonic antigen (CEA) antibody and Carbohydrate antigen 72–4 (CA72-4) antibody, respectively, and used as two kinds of probes with different electrochemical signals. With the excellent magnetic performance of biotin immune magnetic beads (IMBs), the biofunctional IMBs were firmly deposited on the magnetic glassy carbon electrode (MGCE) surface by applying a constant magnetic field, and then the CEA and CA72-4 antibody were immobilized on the IMBs by the avidin–biotin conjugation. The assay was based on the change in the detection peak current. Under the optimum experimental conditions, the linear range of detection of CEA is of the two-component immunosensor is from 0.01 to 120 ng/mL, with a low detection limit of 0.003 ng/mL, and the linear range of detection of CA72-4 is from 0.05 to 35 U/mL, with a detection limit of 0.016 U/mL. The results showed that the proposed immunosensor enabled simultaneous monitoring of CEA and CA72-4 and exhibited good reproducibility, excellent high selectivity, and sensitivity. In particular, the proposed multiplexed immunoassay approach does not require sophisticated fabrication and is well-suited for high-throughput biosensing and application to other areas. Full article

This study investigates the chemical and structural modifications of vertically aligned tungsten disulfide–tungsten trioxide (WS₂-WO₃) nanosheets decorated with silver nanoparticles (Ag(NPs)) under nitrogen plasma conditions. The synthesized vertically aligned WS₂-WO₃ nanosheets were functionalized through direct-current (DC) magnetron sputtering, forming silver-decorated samples. Structural changes, as well as the size and distribution of Ag(NPs), were characterized using scanning electron microscopy (SEM). Chemical state analysis was conducted via X-ray photoelectron spectroscopy (XPS), while Raman spectroscopy was employed to investigate vibrational modes. The findings confirmed the successful decoration of Ag(NPs) and identified unexpected compound transformations that were dependent on the duration of functionalization. The synthesized and functionalized samples were evaluated for their sensing capabilities towards Rhodamine B (RhB) through surface-enhanced resonance Raman scattering (SERRS). This study discusses the impact of substrate morphology and the shape and size of nanoparticles on the enhancement of SERRS mechanisms, achieving an enhancement factor (EF) of approximately 1.6 × 10⁶ and a limit of detection (LOD) of 10⁻⁹ M. Full article

Metal–organic framework (MOF)-derived carbon, which contains metal nanoparticles embedded in a carbon matrix, is becoming an important group of catalysts. We report the synthesis of tungsten carbide–carbon nanocomposites using a similar concept, i.e., by pyrolysis of organotungsten compounds under high-temperature and high-pressure conditions. We characterized the product using various analytical techniques and examined its electrocatalytic activity. Two precursors, Bis(cyclopentadienyl)tungsten (IV) dichloride (Cp₂WCl₂) and Bis(cyclopentadienyl)tungsten (IV) dihydride (Cp₂WH₂) were pyrolyzed at 4.5 GPa and 600 °C. Tungsten carbide (β-WC_1−x) crystals with a size of 2 nm embedded in graphitic carbon were formed from Cp₂WH₂-derived samples. Electrochemical measurements showed that all samples were active in the oxygen reduction reaction (ORR), with the Cp₂WH₂-derived sample having the best catalytic performance. Full article

In this work, within the framework of a self-consistent model of arc discharge, a simulation of plasma parameters in a mixture of argon and methane was carried out, taking into account the evaporation of the electrode material in the case of a refractory and non-refractory cathode. It is shown that in the case of a refractory tungsten cathode, almost the same methane conversion rate is observed, leading to similar values in the density of the main methane conversion products (C, C₂, H) at different values of the discharge current density. However, with an increase in the current density, the evaporation rate of copper atoms from the anode increases, and a jump in the I–V characteristic is observed, caused by a change in the plasma-forming ion. This is due to the lower ionization energy of copper atoms compared to argon atoms. In this mode, an increase in metal–carbon nanoparticles is expected. It is shown that, in the case of a cathode made of non-refractory copper, the discharge characteristics and the component composition of the plasma depend on the field enhancement factor near the cathode surface. It is demonstrated that increasing the field enhancement factor leads to more efficient thermal field emission, lowering the cathode’s surface temperature and the gas temperature in the discharge gap. This leads to the fact that, in the arc discharge mode with a cathode made of non-refractory copper, the dominant types of particles from which the synthesis of a nanostructure can begin are, in descending order, copper atoms (Cu), carbon clusters (C₂), and carbon atoms (C). Full article