Selected Area Electron Diffraction Patterns Research Articles

Effects of CaCO3/MgO on Fe-Co-Mo catalyst in the reprocessing of recycled polypropylene to carbon nanotubes

In recent times, there has been a global discourse on the menace of plastic waste (PW) materials on the ecosystem and ways for effective management of PW. This has resulted in the utilization of PW in the research arena in the synthesis of smart nanomaterials of high value as a sustainable solution. In this study, the catalytic-pyrolysis procedure was used to develop carbon nanotubes (CNTs) from recycled polypropylene (PP) plastic in a one-step chemical vapour deposition (CVD) reactor. The impacts of CaCO3 and MgO as supports for Fe-Co-Mo catalysts in the production of CNTs were studied. Kinetic and thermodynamic parameters were determined from the thermal profile of the catalysts to establish the nature of the reaction in CNTs synthesis. Transmission electron microscopy (TEM), energy Dispersive X-ray (EDX), selected area electron diffraction pattern, particle size distribution (PSD), thermogravimetric analysis (TGA), Raman spectroscopy, Fourier transforms infrared (FTIR) and X-ray diffraction (XRD) were employed to characterize the catalysts and CNTs. The results obtained showed the impact of the supports on the yield, quality, and morphology of the synthesized CNTs. The CNTs yield from catalysts supported with CaCO3 and MgO were 35.12 % and 37.24% respectively. The average outer diameters of CNTs produced over the catalyst with CaCO3 and MgO supports were 36 and 29 nm respectively. The ID/IG ratio for CaCO3 and MgO supports were 0.6724 and 0.8401 respectively. The change in entropy for all phases were −274.41 and −1032.97 J/mol/K and −213.0, −318.48 and −1022.13 J/mol/K for CaCO3 and MgO supported catalyst respectively which confirmed non-spontaneous endothermic reaction. It was observed that MgO support showed better catalytic activity toward CNTs growth in terms of yield while those with CaCO3 support showed higher graphitization.

Structural refinement, dielectric and ferroelectric properties of Cr modified Ba0·90Sr0·10TiO3 ceramics

In this study, we investigated the impact of Chromium substitution on the structural, dielectric and ferroelectric characteristics of Ba0·90Sr0·10Ti1-3x/4CrxO3 (x = 0, 0.005, 0.010, 0.015 and 0.020) ceramics fabricated by solid state reaction method. Rietveld refinement of X-ray diffraction pattern confirmed tetragonal perovskite structure for all the samples. Based on the crystal structure and the lattice parameter obtained through XRD measurement, the Madelung energy of each sample was computed. SEM images revealed a reduction in grain size with rising Cr concentration. TEM, HRTEM, SAED and EDS analysis was carried out for BST-Cr3 sample. Diffused rings observed in Selective Area Electron Diffraction (SAED) patterns indicate the crystallinity of the sample. EDS analysis indicated the presence of Ba, Sr, Ti, O and Cr elements. In the temperature range of 30 °C–150 °C, dielectric measurements (dielectric constant ‘ε’ and tangent loss ‘tanδ’) have been made at different frequencies (1, 10, 50, 100 and 1000 kHz). The samples displayed a diffused phase transition, with noticeable reduction in Curie temperature ‘Tc’ and tangent loss ‘tanδ’ with the substitution of Cr. Polarization versus electric field loops were recorded at different electric fields (5, 10, 15, 20 and 25 kV/cm) and improved values of remnant polarization ‘Pr’ and coercive field ‘Ec’ were observed. A lower Ec value facilitates easier domain movement within the unit cell, leading to enhanced ferroelectric properties. Temperature dependent P-E loops indicated that as the temperature increased, the material became softer accompanied by simultaneous reduction in Pr and Ec values.

Sustainable production of graphene quantum dots from rice husk for photo‐degradation of organochlorine pesticides

AbstractThe controlled synthesis of two‐dimensional nanocrystals of graphene particles instead of amorphous carbon quantum dots is highly challenging and requires tremendous efforts to optimize the reaction conditions. It has been observed that as a significant bio‐compatible zero‐dimensional material, graphene quantum dots are considered as a novel material for opto‐electronics, energy, biological and environmental applications. However, very few are known about their utilization in photocatalytic degradation of pesticides, especially organochlorine pesticides which are resistant to removal by conventional wastewater treatment methods. In this work, graphene quantum dots were produced from rice husk at relatively low temperatures, resulting in an average particle size of 3.3 nm. The high resolution transmission electron microscopy clearly showed the formation of spherical quantum dots having lattice fringes and the selected area electron diffraction pattern showed the crystallinity of the graphene quantum dots. A study of photodegradation of three highly toxic organochlorine pesticides namely, dichlorodiphenyl trichloro ethane, cypermethrin and fenvalerate were carried out using as‐synthesized graphene quantum dots from rice husk. Interestingly, all these pesticides were found to be degraded around 60 % to 70 % under visible light conditions. It confirmed that synthesized graphene quantum dots from rice husk can act as prominent photocatalyst for the degradation of pesticides and other pollutants.

Effect of oxidation temperature on physical properties of polycrystalline β-Ga2O3 grown by thermal oxidation of GaN in O2 ambient from 900 to 1400 °C

This study aimed to investigate the effect of oxidation temperature on the physical properties of β-Ga2O3 grown by thermal oxidation of GaN in the O2 ambient at high oxidation temperatures from 900 to 1400 °C. Notably, the analysis of the oxidation temperatures ranging from 1100 to 1400 °C remains unexplored in the other studies. The effects of the oxidation temperature on the physical properties were investigated via X-ray diffraction, X-ray photoelectron spectroscopy, and field-emission scanning electron microscopy (FESEM). At all oxidation temperatures, XPS results revealed oxygen deficiency. The top FESEM images indicated disordered nanocolumn structures on the surface of the oxide layer, which increased in abundance with oxidation temperatures exceeding 1100 °C. Energy-filtered high-resolution transmission electron microscopy images and the selected area electron diffraction patterns revealed that the top nanocolumns and the oxidized layer comprised polycrystalline β-Ga2O3. Additionally, the cross-sectional lamellae prepared through focused ion beam milling revealed an increase in the thickness of the β-Ga2O3 layer with oxidation temperature. To account for the variations in the oxide layer thickness, the oxidation temperatures were classified into two ranges of 900–1100 °C and 1100–1400 °C for calculating the activation energy. Moreover, this study assumed that the activation energy required for the oxidation process remained constant within each temperature interval. According to Arrhenius's model, the activation energy from 900 to 1100 °C was calculated to be 286.15 kJ/mol (2.97 eV). Furthermore, the activation energy from 1100 to 1400 °C was determined to be 111.33 kJ/mol (1.15 eV).

Magnetic suppression for a possible Fe-poor organic–inorganic hybrid superconductor Fe14Se16(tepa)0.8 (tepa = tetraethylenepentamine) with a superconducting transition at ∼42 K

Composition/structure-dependent superconductivity for FeSe-based superconductors attracted great attention not only due to their high superconducting transition temperatures (TC), but also for understanding the origin of iron-based superconductivity. Here, we report a new Fe-poor organic-inorganic hybrid material Fe14Se16(tepa)0.8 with a paramagnetic-diamagnetic transition at ∼42 K grown by a high-temperature organic-solution-phase method with soluble iron/selenium sources in a tepa solution, alternative to previous intercalation strategies. The Fe14Se16(tepa)0.8 phase is in a tetragonal layered hybrid structure with a nanoplate shape. Composition analyses reveal a Fe-poor characteristic of the hybrid in contrast to previous FeSe-intercalated superconductor, and selected area electron diffraction pattern is featured by Fe3Se4 superstructures with a √2 × √2 of Fe vacancy order. Ab initio density functional calculations show that minus Fe3Se4 ions are stable in the hybrid and ∼0.25e−/Fe0.75Se is obviously larger than the reported values of approximately 0.2e−/FeSe in other FeSe-intercalated superconductors. Typical hysteresis loops and temperature dependence of dc/ac susceptibilities of the Fe14Se16(tepa)0.8 measured below ∼42 K suggest a presence of the Meissner effect in this material. Effects of synthesis conditions on structures and magnetic properties of the hybrids show a magnetic evolution from a long-range ferrimagnetic (FIM) order of Fe14Se16(tepa) to a coexistence of FIM and superconducting (SC) orders of Fe14Se16(tepa)0.9 and an SC order of Fe14Se16(tepa)0.8. X-ray absorption spectrum (XAS) confirms the presence of ferric/ferrous irons. Mössbauer studies reveal that the high-TC superconductivity originates from a suppression of the FIM order through tuning the spin states of irons from high-spin Fe3+ (S = 5/2) and Fe2+ (S = 2) in the Fe14Se16(tepa) to low-spin Fe3+ (S = 1/2) and Fe2+ (S = 0) in the Fe14Se16(tepa)0.8. Although no zero resistance is detected even at a temperature of 2 K, the resistivity at 2 K decreases by more than 1600 times compared to that in a normal state calculated by a variable range hopping (VRH) model, suggesting that the high-TC superconductivity of Fe14Se16(tepa)0.8 is possible.

Pressure-induced phase transition and metallization in zirconium disulfide under different hydrostatic environments up to 25.3 GPa

The pressurized behaviours of structure, vibration and electrical transport in zirconium disulfide have been systematically investigated in a diamond anvil cell (DAC) under different hydrostatic environments up to 25.3 GPa utilizing in-situ Raman spectroscopy, electrical conductivity measurement, high-resolution transmission electron microscopy (HRTEM) and first-principles theoretical calculations. Upon compression, our experimental results showed that ZrS2 underwent a phase transition accompanied by a semiconductor-to-metal transformation at 15.4 GPa under non-hydrostatic condition. Under hydrostatic condition, the corresponding phase transition occurred at a higher pressure of 17.5 GPa, indicating that the high-pressure phase transition is sensitive to the hydrostaticity in the sample chamber of DAC. Upon decompression, some absolutely new Raman peaks emerged at the pressures below 4.8 GPa and 2.9 GPa under non-hydrostatic and hydrostatic environments, respectively, which revealed an irreversible phase transition in ZrS2. Furthermore, our observations from selected-area electron diffraction patterns confirmed the irreversibility of the high-pressure phase transformation.

Improved photoluminescence stability and defect passivation in SbBr3 post-treated CsPbBr3 quantum dots under ambient conditions.

Inorganic cesium lead halide perovskites have evoked wide popularity because of their excellent optoelectronic properties, high photoluminescence (PL) quantum yield (PLQY), and narrowband emission. Here, cesium lead bromide (CsPbBr3 ) quantum dots (QDs) were synthesized via the ligand-assisted re-precipitation method. Post-synthesis treatment of CsPbBr3 QDs using antimony tribromide improved the PL stability and optoelectronic properties of the QDs. In addition, the PLQY of the post-treated sample was enhanced to 91% via post-treatment, and the luminescence observed was maintained for 8 days. The post-synthesis treatment ensured defect passivation and improved the stability of CsPbBr3 perovskite QDs. High-resolution transmission electron microscopy revealed the presence of more ordered, uniform-sized CsPbBr3 QDs after post-synthesis treatment, and the uniformity of the sample improved as the day passed. The formation of a mixed crystal phase was observed from X-ray diffraction in both as-synthesized, as well as post-treated QDs samples with the possibility of a polycrystalline nature in the post-treated CsPbBr3 QDs as per the selected area electron diffraction pattern. The X-ray photoelectron spectroscopy spectra confirmed the presence of antimony and the possibility of defect passivation in the post-treated samples. These QDs can act as potential candidates in various optoelectronic applications such as photodetectors and light-emitting diodes due to their high PLQY and longer lifetime.

Eco-friendly innovation: harnessing nature’s blueprint for enhanced photocatalysis and antimicrobial potential in multi-structured PN/ZnO nanoparticles

This research unveils an innovative approach to green synthesis, detailed characterization, and multifunctional exploration of bio-functionalized zinc oxide nanoparticles (PN/ZnO NPs) adorned with phytochemicals from Piper nigrum (PN). Employing an extensive suite of spectroscopic techniques and physicochemical methods, including UV–vis spectroscopy, field emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), energy dispersive x-ray (EDX) spectroscopy, Fourier-transform infrared (FTIR), x-ray diffraction (XRD), and Brunauer–Emmett–Teller (BET) analysis, the study delves into the unique properties of PN/ZnO NPs. XRD confirms the development of the wurtzite phase with a crystallite diameter of 47.77 nm. FTIR reveals ZnO functionalization by PN’s phytochemicals, while FESEM and HRTEM suggest diverse architectural features. Selected area electron diffraction patterns authenticate the crystalline structure. BET analysis showcases a large specific surface area of 80.72 m2 g−1 and a mesoporous structure. The absorption peak at 372 nm and an energy band gap (E g) of 3.44 eV validate ZnO NP formation. The catalytic performance is demonstrated through the degradation of commercial reactive yellow-17 (RY-17) dye, with PN/ZnO (dosage 300 mg l−1) achieving 94.72% removal at a dose of 120 mg l−1. Pseudo-first-order kinetics govern the photodegradation process. PN-ZnO NPs showcase potent antimicrobial efficacy against both gram-negative and gram-positive bacteria, with varying clearance zones. This study stands as an impactful exploration, integrating green synthesis, detailed characterization, and versatile functionalities of PN/ZnO NPs.

Corrosion resistance and conductivity behavior of Cr-Al-N MAX phase coatings prepared by magnetron sputtering technology

Chromium aluminum nitride (CrAlN) coatings containing Cr2AlN phase were prepared by unbalanced magnetron sputtering followed by annealing at 1000 °C. The crystal structures, X-ray diffraction patterns, and selected area electron diffraction patterns of the Cr2AlN phase were modeled using computer software and compared with experimental observations. A good agreement was found between the two sets of results, thereby confirming the presence of Cr2AlN phase in the coatings. While previous studies have demonstrated the formation of Cr2AlN phase theoretically, this study presents experimental evidence of its physical existence. The potentiodynamic polarization results and interfacial contact resistance measurements show that the CrAlN coating with Cr2AlN phase has excellent corrosion resistance (a corrosion current density of 5.35 × 10−7 A/cm2 and electrical conductivity of 5.5 mΩ·cm2) and is thus a promising candidate for the protection of fuel cell bipolar plates.

Properties and antibacterial activity of MnFe2O4 nanoparticles obtained by pulsed laser ablation in liquid

In this study, MnFe2O4 nanoparticles (NPs) were fabricated via pulsed laser ablation in liquid. Chemical and structural composition, microstructure, magnetic and antibacterial properties were characterized. Spinel was found as the main crystalline phase, while Fe2O3 and Mn2O3 were observed as the major secondary phases, all identified by X-ray diffractometry (XRD). Observation by Transmission Electron Microscopy (TEM) indicated that most of the nanoparticles were spherical in shape and found in agglomerates, most likely because of their magnetic nature. Moreover, Fast Fourier Transform of selective area electron diffraction patterns pointed at the existence of crystalline particles. The coercive field (Hc) and saturation magnetization (Ms) values determined for these NPs were found to increase with decreasing temperature. Their antibacterial properties were evaluated using the viable bacteria counting technique (colony) for MnFe2O4 concentrations of 100 and 300 μg/mL with Bacillus subtilis, Salmonella typhimurium, Pseudomonas aeruginosa, Klebsiella pneumoniae and Escherichia coli strains.

Revealing the influence of aerosol particle state on the high-quality α-Ga2O3 single crystal thin film growth by Mist CVD epitaxy

There is little research on α-Ga2O3 single crystal film because it is a metastable phase of Ga2O3 crystal and difficult for controllable fabrication. In this paper, highly crystallized Ga2O3 thin films of poly-crystalline, α-Ga2O3 and β-Ga2O3 were prepared by modulating the growth temperature from 400 °C to 700 °C by mist-assisted CVD (Mist CVD) method. The results show that films grown at 525 °C owes the best crystalline quality of α-Ga2O3 film. To further improve the crystallinity of α-Ga2O3 thin film, a systematic simulation revealing the distribution changes of aerosol particle size, flow field, and temperature gradient in the reaction chamber were explored. The optimal growth region C with uniform particle size, well-distribute temperature gradient and stable flow field is determined. Meanwhile, the experimental results of α-Ga2O3 thin films grown at different positions in the reaction chamber was proved to consistent with the simulation results. Furthermore, the optimal single crystallized α-Ga2O3 thin films with smooth surface morphology and optical property were obtained. The PL spectrum operated at room temperature show the α-Ga2O3 film with low defect density and high crystalline quality. It shows that the single crystallized α-Ga2O3 is orientated grown on sapphire substrate with epitaxial relationship of α-Ga2O3 (0006)//c-Al2O3 (0006). Although, slight lattice mismatch is observed on the selected area electron diffraction pattern of the interface between sapphire and α-Ga2O3 film, it is ideal for further application in devices. This work reveals the key point for α-Ga2O3 single crystal film growth by mist CVD is to construct a steady and orderly environment through controlling aerosol particle state.

Effect of cobalt addition on structural, optical, morphological and magnetic properties of NiO nanoparticles prepared by chemical precipitation method

The modification in the microstructural, functional group, optical, morphological and magnetic properties of pure and different concentrations (0.01 M to 0.04 M) of cobalt doped NiO nanoparticles synthesized by chemical precipitation method is examined using X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, UV–Vis absorption spectroscopy (UV–Vis), Photoluminescence (PL), Scanning Electron Microscopy (SEM), and Energy dispersive X-ray spectroscopy (EDX), Transmission Electron Microscopy (TEM), High-Resolution Transmission Electron Microscopy (HR-TEM), Selected Area Electron Diffraction pattern (SAED) and vibrating sample magnetometer (VSM). The average grain size of pure NiO and cobalt doped NiO nanoparticles are 16.37 nm, 18.36 nm, 21.42 nm, 16.83 nm and 18.36 nm respectively. The UV absorbance study shows a strong absorption peak in ultraviolet visible region. The band gap values of pure NiO and cobalt doped NiO nanoparticles are 2.32 eV, 3.14 eV, 3.08 eV, 3.03 eV and 3.06 eV respectively. The incorporation of cobalt into NiO nanoparticles have strongly influenced the magnetic behaviour and the material got converted from weak ferromagnetic into ferromagnetic material.

Twisting two-dimensional iron sulfide layers into coincident site superlattices via intercalation chemistry.

Layered van der Waals (vdW) materials are susceptible not only to various stacking polymorphs through translations but also twisted structures due to rotations between layers. Here, we study the influence of such layer-to-layer twisting through the intercalation of ethylenediamine (EDA) molecules into tetragonal iron sulfide (Mackinawite FeS). Selected area electron diffraction patterns of intercalated FeS display reflections corresponding to multiple square lattices with a fixed angle between them, contrary to a single square lattice seen in the unintercalated phase. The observed twist angles of 49.13° and 22.98° result from a superstructure formation well described by the coincident site lattice (CSL) theory. According to the CSL theory, these measured twist angles lead to the formation of larger coincident site supercells. We build these CSL models for FeS using crystallographic group-subgroup transformations and find simulated electron diffraction patterns from the model to agree with the experimentally measured data.

Probing the influence of strontium doping and annealing temperature on the structure and biocompatibility of hydroxyapatite nanorods.

Among numerous biologically important metal cations, strontium (Sr2+) has received much attention in bone tissue regeneration because of its osteoinductive properties combined with its ability to inhibit osteoclast activity. In this study, strontium-doped hydroxyapatite (Sr-HAp) nanorods with varying molar ratios of Ca : Sr (10 : 0, 9 : 1, 5 : 5, 3 : 7 and 0 : 10) were synthesized using the chemical precipitation technique. The synthesized Sr-HAp nanostructures were characterized using powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy, energy dispersive X-ray spectroscopy, and Raman and Fourier transform infrared (FTIR) spectroscopies to understand their structural and morphological features, and composition. XRD results revealed the formation of HAp nanostructures, whose unit cell volume increased as a function of the dopant level. The reaction process investigation showed the formation of hydroxyapatite (HAp), strontium apatite (SAp) and various Sr-HAp phases. FESEM micrographs displayed the morphological transformation of Sr-HAp from nanorods to nanosheets upon increasing the dopant level. In the FTIR spectra, the bands of the PO43- group shifted towards a lower wavenumber upon increasing the dopant concentration in Sr-HAp that signifies the structural distortion due to the presence of a large amount of strontium ions. The peaks of PO43- and OH- vibrations in the Raman spectra were further analysed to corroborate the structural distortion of Sr-HAp. Selected area electron diffraction patterns obtained using TEM reveal the reduced crystallinity of Sr-HAp due to Sr-doping, which is in line with the XRD results. Finally, the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay showed that the synthesized Sr-HAp has no toxic effect on the survival and growth of mesenchymal stem cells. In summary, the synthesized novel Sr-HAp nanorods exhibit great promise for bone tissue engineering applications.

Ordering transformation in Nb<sub>0.8</sub>CoSb induced by <i>in situ</i> heating-induced Nb diffusion

This study focused on the investigation of Nb<sub>0.8</sub>CoSb half-Heusler alloy covered with Nb films. By employing <i>in-situ</i> heating transmission electron microscopy (TEM) technique, diffusion of Nb was observed at high temperature, resulting in the ordering transformation from Nb<sub>0.8</sub>CoSb to Nb<sub>0.8+<i>δ</i></sub>CoSb. Through observations of high-angle annular dark-field (HAADF) images and selected-area electron diffraction (SAED) patterns, it was found that under elevated temperatures, the diffuse streaks representing short-range disorder in Nb<sub>0.8</sub>CoSb samples transitioned into superlattice diffraction spots representing long-range order. The modulation wave vector of this superstructure was determined to be <i>q</i>=1/3(<i>a</i><sup>*</sup> + <i>b</i><sup>*</sup>-<i>c</i><sup>*</sup>). This structural evolution primarily arised from the diffusion of Nb atoms from the Nb film into the Nb<sub>0.8</sub>CoSb sample at high temperature, leading to compositional changes in Sb and Nb. Further comparative analysis revealed significant differences between <i>in-situ</i> synthesized Nb<sub>0.8+<i>δ</i></sub>CoSb samples and <i>ex-situ</i> synthesized Nb<sub>0.84</sub>CoSb samples despite both exhibiting superstructures. In the <i>ex-situ</i> synthesized Nb<sub>0.84</sub>CoSb, the modulation wave vector of the superstructure was <<i>q</i>=1/3(2<i>a</i><sup>*</sup>-2<i>c</i><sup>*</sup>), mainly attributed to Nb compositional variations. Moreover, the superstructure in Nb<sub>0.84</sub>CoSb samples could remain stable from room temperature tor high temperature, whereas in Nb<sub>0.8+<i>δ</i></sub>CoSb samples, it only existed at elevated temperatures and gradually weakened as the temperature decreased, suggesting it might be a metastable structure between Nb<sub>0.8</sub>CoSb and Nb<sub>0.84</sub>CoSb. In summary, this study reveals the diversity of superstructures induced by compositional variations and the complexity of structural phase transitions in half-Heusler alloys, enriching the understanding of these materials and providing important guidance for the design and functional control of phase-change materials

In Situ Liquid Cell Transmission Electron Microscopy Study of Studtite Particle Formation and Growth via Electron Beam Radiolysis.

This study presents in situ observations of studtite (UO2O2(H2O)2·2H2O) crystal growth utilizing liquid phase transmission electron microscopy (LP-TEM). Studtite was precipitated from a uranyl nitrate hexahydrate solution using hydrogen peroxide formed by the radiolysis of water in the TEM electron beam. The hydrogen peroxide (H2O2) concentration, directly controlled by the electron beam current, was varied to create local environments of low and high concentrations to compare the impact of the supersaturation ratio on the nucleation and growth mechanisms of studtite particles. The subsequent growth mechanisms were observed in real time by TEM and scanning TEM imaging. After the initial precipitation reaction, a post-mortem TEM analysis was performed on the samples to obtain high-resolution TEM images and selected area electron diffraction patterns to investigate crystallinity as well as energy-dispersive X-ray spectroscopy spectra to ensure that studtite was produced. The results reveal that studtite particles form through various mechanisms based on the concentration ratio of uranyl to H2O2 and that studtite is initially produced through an amorphous intermediary prior to formation of the crystalline material commonly reported in the literature.

Mycosynthesis of silver nanoparticles from endophytic Aspergillus flavipes AUMC 15772: ovat-statistical optimization, characterization and biological activities

BackgroundMycosynthesis of silver nanoparticles (SNPs) offers a safe, eco-friendly, and promising alternative technique for large-scale manufacturing. Our study might be the first report that uses mycelial filtrate of an endophytic fungus, Aspergillus flavipes, for SNPs production under optimal conditions as an antimicrobial agent against clinical multidrug-resistant (MDR) wound pathogens.ResultsIn the present study, among four different endophytic fungi isolated from leaves of Lycium shawii, the only one isolate that has the ability to mycosynthesize SNPs has been identified for the first time as Aspergillus flavipes AUMC 15772 and deposited in Genebank under the accession number OP521771. One variable at a time (OVAT) and Plackett Burman design (PBD) were conducted for enhancing the production of mycosynthesized SNPs (Myco-SNPs) through optimization using five independent variables. The overall optimal variables for increasing the mycosynthesis of SNPs from mycelial filtrate of A. flavipes as a novel endophytic fungus were a silver nitrate concentration of 2 mM, a pH of 7.0, an incubation time of 5 days, and a mycelial filtrate concentration of 30% in dark conditions. UV–visible spectroscopy (UV–Vis), Fourier transform infrared spectroscopy (FT-IR), X-ray spectroscopy (XRD), Transmission electron microscopy (TEM), and Selected-Area Electron Diffraction (SAED) patterns were used to characterize Myco-SNPs, which showed the peak of absorbance at 420 nm, and FTIR showed the bands at 3426.44, 2923.30, 1681.85, 1552.64, and 1023.02 cm-1, respectively, which illustrated the presence of polyphenols, hydroxyl, alkene, nitro compounds, and aliphatic amines, respectively. The XRD pattern revealed the formation of Myco-SNPs with good crystal quality at 2θ = 34.23° and 38.18°. The TEM image and SAED pattern show the spherical crystalline shape of Myco-SNPs with an average size of 6.9232 nm. High antibacterial activity of Myco-SNPs was recorded against MDR wound pathogens as studied by minimum inhibitory concentrations ranging from 8 to 32 µg/mL, time kill kinetics, and post-agent effects. Also, in vitro cell tests indicated that Myco-SNPs support the cell viability of human skin fibroblast cells as a nontoxic compound.ConclusionThe obtained results revealed the successful production of Myco-SNPs using the mycelial filtrate of A. flavipes, which may be a promising nontoxic alternative candidate for combating MDR wound pathogens.

Establishment of a facile technique to fabricate bulk AA6061/CNT composite with improved mechanical properties using combined stir-casting and squeeze-casting

Three dispersion techniques were investigated for fabricating AA6061–0.5 wt% CNT composites by combined stir-casting and squeeze-casting - direct drop of CNT (DD), mixed Al and CNT pellet drop (PD), and direct drop of ultrasonicated CNT (USDD). Al-20Mg alloy was added to enhance CNT wettability. The PD samples resulted in the highest retention of CNTs in the matrix along with a uniform distribution, confirmed by detailed transmission electron microscope analysis. The selected area electron diffraction pattern and X-ray diffraction confirmed the formation of Mg2Si. The hardness of all composite samples increased significantly over AA6061, predominantly due to a reduction in crystallite size and an increase in dislocation density. The best combination of tensile properties was achieved in the PD composite, yielding an improvement of ultimate tensile strength and yield strength by 40% and 33%, respectively, compared to as-cast AA6061 without sacrificing the ductility. Well-developed serrations were observed in the stress-strain plots of the samples, which have been attributed to the pinning-unpinning action of mobile dislocations by the Mg solute atoms. The fracture surface of the PD composite displays features of ductile fracture along with CNT bridging and rupture, confirming the presence of a strong interface and effective load transfer strengthening.

CeO2-CePO4 and Ag@CeO2-CePO4 nanocomposites from Penaeus semisulcatus for heavy metals sensing, UV shielding and cytotoxic applications

CeO2-CePO4 and Ag@CeO2-CePO4 nanocomposites (NCs) were prepared using Penaeus semisulcatus and characterized by various analytical techniques. The NCs exhibited spherical morphology, with average particle sizes measuring 2.36 nm, 3.30 nm and 29.64 nm for the samples air dried, annealed at 550 °C and 800 °C respectively, and the Selected Area Electron Diffraction patterns from HR-TEM revealed their crystalline nature. In 3d X-ray Photoelectron Spectra (XPS) of NCs, the highest binding energies were observed at 916.46 eV (3d3/2) and 898.16 eV (3d5/2) with spin–orbit splitting of 18.3 eV. The X-Ray Diffraction (XRD) patterns of the NCs showed peaks typical of both CeO2 and CePO4 phases. The Fourier Transform-Infra Red (FT-IR) spectrum contained bands due to Ce-O stretching at 560 cm−1 and PO43- groups at 1008 and 711 cm−1, which was further substantiated by Raman spectrum, which had an intense peak at 468 cm−1 corresponding to F2g band of CeO2 and another peak at 976 cm−1 due to PO43- tetrahedron. In the Ultraviolet-Visible Diffuse Reflectance Spectra (UV-Vis DRS), the broad absorption peak at 352 nm and minor peaks around 300 nm confirmed the formation of CeO2-CePO4 NCs. The green synthesized NCs were excellent fluorescence sensors for Pb2+, Cd2+ and Hg2+ in a wide range of concentrations, from 5.0x10-9 M to 4.0x10-5 M. The concentration Vs. emission fitting plot had three distinctive linear ranges. At a low concentration range (5x10-9 to 3.5x10-7 M), the limit of detection for Pb2+, Cd2+ and Hg2+ was found to be 2.41x10-8, 2.56x10-8 and 3.11x10-8 M. The sensitive detection of a mixture of heavy metal ions in ppb levels by biocompatible NCs gained insight in treating aqueous industrial wastes. Further, NCs showed cytotoxicity and UV shielding properties.

Discovery of Environmental Nanoparticles in a Mineral Water Spring from Yiyuan County, Shandong Province, Eastern China: A New Form of Elements in Mineral Water

Environmental nanoparticles are known to be present in various aquatic environments, exerting significant influences on water quality, particularly in water distribution systems. However, there has been a notable dearth of research on the presence and impact of environmental nanoparticles in mineral water, a unique water resource. In this study, we employed Nanoparticle Tracking Analysis (NTA) and conducted High-Resolution Transmission Electron Microscopy (HRTEM) to address this research gap. This groundbreaking study represents the first comprehensive exploration of environmental nanoparticles within natural mineral water from Zibo City, Shandong Province, China. The results of the NTA showed that the concentration of the particles was 5.5 × 105 particles/mL and the peak diameter of the size distribution was 180 nm. The HRTEM showed that the nanoparticles were granular, pinniform, rodlike, and flakey in shape, and some of the nanoparticles existed in aggregation. The energy-dispersive spectrometry results showed that most of the nanoparticles contained O, Mg, Ca, Si, Fe, Ti, and P, and some of them also contained F, V, S, and Mn. When combined with the characteristics of the selected area electron diffraction pattern, the nanoparticles were confirmed to be Ca-bearing nanoparticles, attapulgite nanorods, MnO2 nanosheets, and TiO2 nanoparticles. These findings shed light on a novel manifestation of elemental compositions in mineral water. Furthermore, considering the chemical and physical attributes of both the nanoparticles and mineral water, it is highly plausible that these environmental nanoparticles result from the weathering of minerals. The presence of these nanoparticles within mineral water offers a unique opportunity to advance our comprehension of nanoparticle behavior across diverse systems. Significantly, the realm of environmental nanoparticle science holds paramount importance for ongoing endeavors in ensuring water safety, enhancing treatment processes, and facilitating effective remediation procedures.