Search Results (161)

Excessive Zn(II) ions in aquatic environments pose significant risks to both human health and ecological systems due to their toxic effects, bioaccumulation potential, and interference with essential biological processes. To address this issue, a novel analcime@calcium aluminate@polyethylene glycol 400 (ACP) nanocomposite was fabricated using the hydrothermal technique, alongside an analcime@calcium aluminate (AC) nanocomposite for the efficient elimination of Zn(II) ions from aqueous media. X-ray diffraction (XRD) analysis affirmed the successful formation of crystalline phases, revealing average crystallite sizes of 72.93 nm for AC and 63.60 nm for ACP. Energy-dispersive X-ray spectroscopy (EDX) confirmed the elemental composition of the nanocomposites, showing that AC primarily contained oxygen, sodium, aluminum, silicon, and calcium, whereas ACP incorporated 19.3% carbon due to the polyethylene glycol 400. Field emission scanning electron microscopy (FE-SEM) revealed that AC exhibited hexagonal and platelet-like structures, whereas ACP displayed more dispersed and layered morphologies. High-resolution transmission electron microscopy (HR-TEM) confirmed the presence of stacked platelet-like structures in AC and more defined, separated nanosheets in ACP. The maximum adsorption capacities of AC and ACP were 149.93 and 230.95 mg/g, respectively. The adsorption pathway of Zn(II) ions onto ACP nanocomposite involved three primary interactions: electrostatic attraction facilitated by calcium aluminate, ion exchange provided by analcime, and complexation promoted by polyethylene glycol 400. Thermodynamic analysis indicated that the adsorption process was exothermic, spontaneous, and primarily chemical in nature. Kinetic modeling confirmed that adsorption followed the pseudo-second-order model, while isotherm studies demonstrated adherence to the Langmuir model, indicating monolayer adsorption on homogeneous sites. Full article

Crystal violet dye poses significant environmental and human health risks due to its toxicity, persistence, and bioaccumulative nature. It contributes to potential carcinogenicity, cytotoxicity, and systemic toxicity upon human exposure. To address this issue, a novel SrCO₃/MgO/CaO/CaCO₃ nanocomposite was synthesized using the Pechini sol-gel method, producing AE500 and AE700 at 500 and 700 °C, respectively, for the efficient removal of crystal violet dye from aqueous media. X-ray diffraction (XRD) analysis confirmed the formation of crystalline phases, with average crystallite sizes of 64.53 nm for AE500 and 75.34 nm for AE700. Energy-dispersive X-ray spectroscopy (EDX) revealed elemental compositions with variations in carbon, oxygen, magnesium, calcium, and strontium percentages influenced by synthesis temperature. Field-emission scanning electron microscopy (FE-SEM) showed morphological differences, where AE500 had irregular polyhedral structures, while AE700 exhibited more compact spherical formations, with average grain sizes of 99.98 and 132.23 nm, respectively. High-resolution transmission electron microscopy (HR-TEM) confirmed the structural integrity and nano-scale morphology, showing aggregated irregularly shaped particles in AE500, while AE700 displayed well-defined polyhedral and nearly spherical nanoparticles. The calculated average particle diameters were 21.67 nm for AE500 and 41.19 nm for AE700, demonstrating an increase in particle size with temperature. Adsorption studies demonstrated maximum capacities of 230.41 mg/g for AE500 and 189.39 mg/g for AE700. The adsorption process was exothermic, spontaneous, and physical, following the pseudo-first-order kinetic model and Langmuir isotherm, indicating monolayer adsorption onto a homogenous surface. Full article

Residual stresses in multilayer thin coatings represent a complex multiscale phenomenon arising from the intricate interplay of multiple factors, including the number and thickness of layers, material properties of the layers and substrate, coefficient of thermal expansion (CTE) mismatch, deposition technique and growth mechanism, as well as process parameters and environmental conditions. A multiscale approach to residual stress measurement is essential for a comprehensive understanding of stress distribution in such systems. To investigate this, two AlGaN/GaN multilayer coatings with distinct layer architectures were deposited on sapphire substrates using metalorganic vapor phase epitaxy (MOVPE). High-resolution X-ray diffraction (HRXRD) was employed to confirm their epitaxial growth and structural characteristics. Focused ion beam (FIB) cross-sectioning and transmission electron microscopy (TEM) lamella preparation were performed to analyze the coating structure and determine layer thickness. Residual stresses within the multilayer coatings were evaluated using two complementary techniques: High-Resolution Scanning Transmission Electron Microscopy—Graphical Phase Analysis (HRSTEM-GPA) and Focused Ion Beam—Digital Image Correlation (FIB-DIC). HRSTEM-GPA enables atomic-resolution strain mapping, making it particularly suited for investigating interface-related stresses, while FIB-DIC facilitates microscale stress evaluation. The residual strain values obtained using the FIB-DIC and HRSTEM-GPA methods were −3.2 × 10⁻³ and −4.55 × 10⁻³, respectively. This study confirms that residual stress measurements at different spatial resolutions are both reliable and comparable at the required coating depths and locations, provided that a critical assessment of the characteristic scale of each method is performed. Full article

Zirconium sulfide nanoparticles (Zr_xS_y) are prepared on a flexible substrate of carbon cloth (CC) via a one-step synthesis approach using the low-pressure chemical vapor deposition (LPCVD) technique. The scanning electron microscopy (SEM) image reveals that the particle sizes are in the range of ca. 3~23 nm with an average value of ~13.02 nm. The synthesized Zr_xS_y nanoparticles are composed of ZrS₃ and Zr₉S₂ phases, which is verified by X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HR-TEM). By using the Zr_xS_y/CC as a supercapacitor flexible electrode, the capacitance extracted from the cyclic voltammetry measurement is 406 C g⁻¹ at a scan rate of 5 mV s⁻¹; the capacitance values obtained from GCD curves at a current density of 0.5 A g⁻¹ and 1 A g⁻¹ are 151 and 134 C g⁻¹, respectively. These results highlight the promising potential of Zr_xS_y as a supercapacitor material for future energy-storage technology. Full article

Methylene blue dye, commonly used in various industries, poses significant risks to both human health and the environment due to its persistence, toxicity, and potential to disrupt aquatic ecosystems. Exposure can cause severe health conditions such as methemoglobinemia, while its stability and solubility allow it to persist in natural water systems, reducing oxygen levels and harming aquatic life. In this study, novel analcime/sodium magnesium aluminum silicon silicate nanocomposites (Z1 and Z2) were synthesized via a controlled hydrothermal method, where Z1 and Z2 were synthesized in the absence and presence of polyethylene glycol as a template, respectively. X-ray diffraction (XRD) analysis confirmed the formation of crystalline phases of analcime and sodium magnesium aluminum silicon silicate. The average crystallite size of the Z1 nanocomposite is 75.30 nm, whereas the Z2 nanocomposite exhibits a smaller average crystallite size of 60.27 nm due to the template effect. Field emission scanning electron microscopy (FE-SEM) revealed that Z2 exhibited more uniform and well-dispersed particles compared to Z1. Energy-dispersive X-ray spectroscopy (EDX) confirmed the elemental composition, showing higher sodium content and optimized incorporation of aluminum and silicon in Z2. High-resolution transmission electron microscopy (HR-TEM) demonstrated that Z2 had well-defined spherical particles, indicating improved structural control. The maximum adsorption capacities were 230.95 mg/g for Z1 and 290.69 mg/g for Z2. The adsorption process was exothermic, spontaneous, and chemical in nature, following the pseudo-second-order kinetic model and Langmuir isotherm, confirming monolayer adsorption on homogeneous surfaces. Full article

Excessive levels of Zn(II) ions in aquatic environments pose significant risks to both ecosystems and human health. In aquatic systems, Zn(II) ions disrupt metabolic functions in organisms, leading to toxicity and bioaccumulation. For humans, prolonged exposure can result in gastrointestinal distress, immune system dysfunction, and neurological complications, necessitating effective removal strategies. This study reports the synthesis and characterization of CoFe-MgO-C-M600 (CoFe₂O₄@MgO@(Mg_0.23Co_0.77)(Mg_0.35Co_1.65)O₄@C) and CoFe-MgO-C-M800 (CoFe₂O₄@MgO@C) nanocomposites for the efficient removal of Zn(II) ions from aqueous media. The nanocomposites were synthesized using the Pechini sol-gel method and characterized through X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), field emission scanning electron microscopy (FE-SEM), and high-resolution transmission electron microscopy (HR-TEM). XRD analysis confirmed the crystalline structure of both nanocomposites, with CoFe-MgO-C-M600 exhibiting a smaller average crystallite size (38.67 nm) than CoFe-MgO-C-M800 (75.48 nm). EDX results verified the elemental composition of the nanocomposites, ensuring the successful incorporation of key elements. FE-SEM analysis revealed significant morphological differences, with CoFe-MgO-C-M600 displaying smaller and more uniform grains compared to CoFe-MgO-C-M800. The results show that CoFe-MgO-C-M600 possesses a highly porous and interconnected structure, enhancing its surface area and adsorption potential. In contrast, CoFe-MgO-C-M800 demonstrates larger and more compact grains, which may affect its adsorption performance. HR-TEM further confirmed these findings, demonstrating that CoFe-MgO-C-M600 had a smaller average particle diameter (35.45 nm) than CoFe-MgO-C-M800 (321.14 nm). Adsorption studies indicated that CoFe-MgO-C-M600 and CoFe-MgO-C-M800 achieved maximum adsorption capacities of 276.24 and 200.00 mg/g, respectively. The adsorption process was determined to be exothermic, spontaneous, and physical in nature, following the pseudo-second-order kinetic model and the Langmuir isotherm. Full article

This study reports the synthesis, characterization, and catalytic performance of a series of catalysts of Ru supported on CeO₂-Y₂O₃ composites (Ru/CeYX; X = 0, 33, 66, and 100 wt.% Y₂O₃) for CO₂ hydrogenation. Supported material modification (Y₂O₃-CeO₂), by the Y₂O₃ incorporation, allowed a change in selectivity from methane to RWGS of the CO₂ hydrogenation reaction. This change in selectivity is correlated with the variation in the physicochemical properties caused by Y₂O₃ addition. X-ray diffraction (XRD) analysis confirmed the formation of crystalline fluorite-phase CeO₂ and α-Y₂O₃. High-resolution transmission electron microscopy (HR-TEM) and energy-dispersive X-ray spectroscopy (EDS) elemental mapping revealed the formation of a homogeneous CeO₂-Y₂O₃ nanocomposite. As the Y₂O₃ content increased, the specific surface area, measured by BET, showed a decreasing trend from 106.3 to 51.7 m² g⁻¹. X-ray photoelectron spectroscopy (XPS) of Ce3d indicated a similar Ce³⁺/Ce⁴⁺ ratio across all CeO₂-containing materials, while the O1s spectra showed a reduction in oxygen vacancies with increasing Y₂O₃ content, which is attributed to the decreased surface area upon composite formation. Catalytically, the addition of Y₂O₃ influenced both conversion and selectivity. CO₂ conversion decreased with increasing Y₂O₃ content, with the lowest conversion observed for Ru/CeY100. Regarding selectivity, methane was the dominant product for Ru/CeY0 (pure CeO₂), while CO was the main product for Ru/CeY33, Ru/CeY66, and Ru/CeY100, indicating a shift towards the reverse water–gas shift (RWGS) reaction. The highest RWGS reaction rate was observed with the Ru/CeY33 catalyst under all tested conditions. The observed differences in conversion and selectivity are attributed to a reduction in active sites due to the decrease in surface area and oxygen vacancies, both of which are important for CO₂ adsorption. In order to verify the surface species catalytically active for RWGS, the samples were characterized by FTIR spectroscopy under reaction conditions. Full article

Landfill leachate, a complex wastewater generated from municipal solid waste (MSW) landfills, presents significant environmental challenges due to its high organic content and toxic pollutants. This study proposes a sustainable solution by employing the green synthesis of copper oxide nanoparticles (CuO NPs) using durian (Durio zibethinus) husk extract, which serves as a natural reducing and stabilizing agent. This approach transforms agricultural waste into a valuable resource for environmental remediation. The synthesis was carried out under mild conditions, avoiding harmful chemicals and reducing energy consumption. The CuO NPs were characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR), and UV-Vis spectroscopy to examine their morphology, crystallinity, purity, and optical properties. SEM and HR-TEM analyses revealed mainly spherical nanoparticles with an average size of 35–50 nm and minimal aggregation. XRD analysis confirmed the presence of a highly crystalline monoclinic phase of CuO, while the EDX spectrum showed distinct peaks corresponding to copper (72%) and oxygen (28%) by weight, confirming the high purity of the material. Preliminary tests demonstrated the photocatalytic efficiency of the CuO NPs, achieving up to a 79% reduction in chemical oxygen demand (COD) in landfill leachate. These findings underscore the potential of green-synthesized CuO NPs for environmental applications, offering an innovative, sustainable method for wastewater treatment and supporting the advancement of solid waste management practices. Full article

High-quality 2-inch aluminum nitride (AlN) crystals were grown using a double-zone resistance heating system, and the growth mechanism of AlN bulk crystals was further investigated. It was found that during the growth process, the vapor pressure at the growth interface, as well as the quality and structure of the seed crystal, was closely related to the growth conditions. The 2-inch AlN crystals were characterized using high-resolution X-ray diffraction (HRXRD) and optical microscopy. Optical microscopy observations of different regions on the native surface of the crystals revealed several morphologies, including regular step flow, irregular step flow, and domain-like structures. Comparisons showed that areas of the crystal surface with regular step-flow morphology exhibited high crystal quality, whereas the crystal quality decreased progressively as the step-flow morphology diminished. Therefore, the crystal quality can be preliminarily assessed through the surface morphology, providing guidance for improving the crystal growth process. Full article

We studied specially designed InAs/GaSb/AlSb/GaSb M-structures, a type-II superlattice (T2SL), that can serve as active materials for short-wavelength infrared (SWIR) applications. To obtain the dispersion relation of the investigated M-structures, k·p perturbation theory based on the eight-band model implemented in the nextnano++ v1.18.1 (nextnano GmbH, Munich, Germany) software was used. Numerical band-gap engineering and dispersion calculations for the investigated M-structures (composed of 6/1/5/1 monolayers, with InSb interfaces included) revealed the presence of an additional energy level within the energy gap. This energy level originates from the InSb-like interfaces and does not appear in structures with different layer or interface thicknesses. Its properties strongly depend on interface thickness, temperature, and strain. Numerical calculations of the probability density function ${|\Psi |}^2$, absorption coefficients, and optical absorption spectra at varying temperatures demonstrate that, under specific conditions, such as an optimised interface thickness and temperature, optical absorption increases significantly. These theoretical results are based on structures fabricated using molecular-beam epitaxy (MBE) technology. High-resolution X-ray diffraction (HRXRD) measurements confirm the high crystallographic quality of these M-structures. Full article

Reducing dehydrogenation temperature while preserving high hydrogen generation capacity obstructs the hydrolysis of sodium borohydrides (NaBH₄). The two-dimensional (2D) MAX phase of titanium aluminum carbide (Ti₃AlC₂) and MXene (Ti₃C₂T_x) multilayers was investigated for hydrogen generation via NaBH₄ hydrolysis with and without light. The material was characterized using X-ray diffraction (XRD), Fourier transform infrared (FT-IR), transmission electron microscopy (TEM), high-resolution TEM (HR-TEM), scanning electron microscopy (SEM), and diffuse reflectance spectroscopy (DRS). The activity of Ti₃AlC₂ was significantly enhanced by the integration of UV light radiation during hydrolysis. Ti₃AlC₂/Ti₃C₂T_x improved the dehydrogenation rates of NaBH₄ at ambient conditions and maintained high hydrogen generation rates (HGRs) over time compared to a conventional method. It exhibited a HGR of 200–300 mL·min⁻¹·g⁻¹. Photo-assisted hydrolysis over the catalyst can be maintained for several times at ambient temperature. The catalyst demonstrated effective performance even after five cycles of usage. Full article

The design of efficient and cost-effective electrocatalysts to replace Pt in an oxygen reduction reaction (ORR) is crucial for advancing proton exchange membrane fuel cell (PEMFC) technologies. This study synthesized Pd-Co bimetallic alloy nanoparticles supported on reduced graphene oxide (rGO) through a simple chemical-reduction method, making it suitable for low-cost, large-scale fabrication and significantly reducing the need for Pt. The nanostructures were systematically characterized using various analytical techniques, including X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray spectroscopy (EDX), and cyclic voltammetry (CV). Electrochemical investigations revealed that the Pd-Co/rGO catalyst exhibits remarkable ORR performance in an alkaline environment, with an electrode-area-normalized activity rivaling that of the commercial Pt/C catalyst. Remarkably, Pd-Co/rGO demonstrated an onset potential (E_onset) of 0.944 V (vs. RHE) and a half-wave potential (E_1/2) of 0.782 V (vs. RHE), highlighting its excellent ORR activity. Furthermore, the Pd-Co/rGO catalyst displayed superior methanol-tolerant ORR activity, outperforming Pt/C and monometallic Pd/rGO and Co/rGO systems. The enhanced electrocatalytic performance is attributed to the smallest size, consistent shape, and good dispersion of the alloy structure on the RGO surface. These findings establish Pd-Co/rGO as a promising alternative to Pt-based catalysts, addressing key challenges such as methanol crossover while advancing PEMFC technology in alkaline media. Full article

A GaN layer with a thickness of 2 µm was grown on a sapphire substrate using atmospheric pressure metal–organic chemical vapor deposition (AP-MOCVD). Subsequently, the layer was annealed under a nitrogen atmosphere at temperatures ranging from 1000 °C to 1120 °C. High-resolution X-ray diffraction (HRXRD) analysis reveals the impact of thermal annealing on the mosaic structure of the GaN, specifically the tilt and twist variations in four planes: (00.2), (10.3), (10.2), and (10.1). Interestingly, the observed trends suggest a differential effect of annealing on screw and edge dislocation densities. The annealing process reduces the edge and screw dislocation density. Lower values (D_screw = 1.2 × 10⁸ cm⁻²; D_edge = 1.6 × 10⁹ cm⁻²) were obtained for the sample annealed at 1050 °C. Notably, both tilt and twist angles exhibited a minimum at 1050 °C (tilt = 252 arcsecs, and twist = 558 arcsecs), indicating improved crystal quality at this specific temperature. Photoluminescence (PL) spectroscopy further complemented the structural analysis. The intensity and broadening of the yellow band (YL) in the PL spectra progressively increased with the increasing annealing temperature, suggesting the presence of additional defect states. The near band edge PL emission (3.35 and 3.41 eV) variation upon thermal annealing was correlated with the mosaic structure evolution. Full article

The use of biomass feedstocks for producing high-value-added chemicals is gaining significant attention in the academic community. In this study, near-infrared carbon dots (NIR-CDs) with antimicrobial and bioimaging functions were prepared from Epigynum auritum branches and leaves using a novel green synthesis approach. The spectral properties of the synthesized NIR-CDs were characterized by ultraviolet–visible (UV-Vis) absorption and fluorescence spectroscopy. The crystal structures of the NIR-CDs were further characterized by high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), and X-ray diffraction (XRD). The NIR-CDs exhibited minimal toxicity, excellent biocompatibility, and high penetrability in both in vivo and in vitro environments, making them ideal luminescent probes for bioimaging applications. Moreover, the antimicrobial activity of NIR-CDs was tested against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), showing significant bacterial growth inhibition. The antimicrobial effect is likely attributed to the NIR-CDs disrupting the cell membrane integrity, leading to the leakage of the intracellular contents. Therefore, NIR-CDs hold promise as fluorescent bioimaging probes and antimicrobial agents. Full article

In this paper, we report the growth of high-quality ${\mathrm{In}}_{0.59}{\mathrm{Ga}}_{0.41}\mathrm{As}/{\mathrm{In}}_{0.37}{\mathrm{Al}}_{0.63}\mathrm{As}$ strain-balanced quantum cascade lasers (QCLs) in the low-pressure MOCVD production type multi-wafer planetary reactor addressing, in particular, quality and scaled manufacturing issues. Special attention was given to achieving the sharp interfaces (IFs), by optimizing the growth interruptions time and time of exposure of InAlAs layer to oxygen contamination in the reactor, which all result in extremely narrow IFs width, below 0.5 nm. The lasers were designed for emission at $7.7\mu$m. The active region was based on diagonal two-phonon resonance design with 40 cascade stages. For epitaxial process control, the High Resolution X-Ray Diffraction (HR XRD) and Transmission Electron Microscopy (TEM) were used to characterize the structural quality of the QCL samples. The grown structures were processed into mesa Fabry-Perot lasers using dry etching RIE ICP processing technology. The basic electro-optical characterization of the lasers is provided. We also present results of Green’s function modeling of QCLs and demonstrate the capability of non-equilibrium Green’s function (NEGF) approach for sophisticated, but still computationally effective simulation of laser’s characteristics. The sharpness of the grown IFs was confirmed by direct measurements of their chemical profiles and as well as the agreement between experimental and calculated wavelength obtained for the bandstructure with ideally abrupt (non-graded) IFs. Full article