Field Emission Scanning Electron Microscopy Research Articles

Investigation of Bi2MoO6/MXene nanostructured composites for photodegradation and advanced energy storage applications

This study presents nanostructured composite Bi2MoO6/MXene heterostructure by using hydrothermal method for photodegradation of the congo-red dye and also for energy storage devices. X-ray diffractometer (XRD), High Resolution Transmission Electron Microscopy (HRTEM), Field emission scanning electron microscope (FESEM) and X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET) were performed to examine the structural properties along with surface area and porosity of the material. Due to addition of MXene the larger surface area and improved pore size help to quickly break down additional organic pollutants by adsorbing them. The band gap of Bi2MoO6/MXene nanostructured composite reduced to 2.4 eV suggesting transfer of electrons from VB to CB. Bi2MoO6/MXene exhibits a high (92.3%) photocatalytic degradation rate for a duration of 16 min which was verified using UV-visible spectroscopy, also scavenger test was conducted to ascertain the reactive agent along with the degradation pathway was confirmed by LCMS. Elemental content was also established by using inductively coupled plasma mass spectrometry (ICP-MS). For estimating energy storage capacity cyclic voltammetry (CV) was performed. It was observed Bi2MoO6/MXene nanostructured composite electrodes had specific capacitance of 642.91Fg− 1, power density of 1.24 kWkg− 1, and energy density of 22.32 Whkg− 1 at a current density of 5Ag− 1 also it exhibited 64.42% capacity retention having current density 20 Ag− 1 throughout 10,000 Galvanostatic charge discharge (GCD) cycles. High electrical conductivity of Bi2MoO6/MXene electrode was again examined by Electrochemical impedance spectroscopy (EIS). These findings demonstrate the potential of Bi2MoO6/MXene nanostructured composites in both photodegradation and energy storage applications.

Computational supported experimental insights in adsorption of Congo Red using ZnO/doped ZnO in aqueous solution

The rapid growth of industrialisation has led to the discharge of harmful effluents into water bodies, severely disrupting the balance of ecosystems. The detection and removal of dyes from wastewater remains a significant challenge. In this study, we report the synthesis of zinc oxide (ZnO) and its doped derivatives through a facile chemical method, followed by comprehensive characterisation and analysis to assess their potential in various applications. The structural properties of the synthesised materials were confirmed by X-ray diffraction (XRD), which verified their crystalline nature and phase purity. Morphological analysis using field emission scanning electron microscopy (FE-SEM) coupled with energy dispersive X-ray analysis (EDAX) revealed well-defined nanostructures and uniform elemental distribution. The adsorption ability of the synthesized adsorbents was investigated through electrochemical methods, cyclic voltammetry and Tafel plots, which demonstrated enhanced conductivity and charge transfer characteristics. Additionally, theoretical studies through molecular modelling and molecular dynamic simulations were employed to elucidate the interactions between Congo red molecules and the surface of the synthesized compounds. Adsorption experiments were conducted to evaluate the efficacy of ZnO and its doped variants as adsorbents. To investigate any structural or functional changes after dye adsorption FTIR and XRD were compared, provided a deeper insight into the adsorption mechanism. This multi-faceted approach highlights the potential of ZnO-based materials for effective wastewater treatment and other environmental applications.

A zinc oxide–tin oxide–nerolidol hybrid nanomaterial: Efficacy against esophageal squamous cell carcinoma

Abstract The sixth most common cancer in the world, esophageal cancer, requires aggressive treatment such as surgery, chemotherapy, radiotherapy, and immunotherapy. Phytochemicals and medicinal plants are being used in the green synthesis of nanoparticles. Our study aimed to synthesize ZnO–SnO2 nerolidol nanocomposite and study its effects on esophageal squamous cell carcinoma cells. UV spectroscopy showed significant absorbance at 288 nm, transmission electron microscopy and DLS showed spherical shapes, and transmission electron microscopy also showed 108 nm average diameters. The ZnO–SnO2 nerolidol nanocomposite was also investigated using energy-dispersive X-ray analysis, Fourier transform infrared spectroscopy, photoluminescence, and field emission scanning electron microscopy. A cytotoxic effect was observed against KYSE-150 cells with an IC50 concentration of 14.9 μg/mL. The ZnO–SnO2 nerolidol nanocomposite inhibited cancer cell proliferation in KYSE-150 cells and enhanced apoptosis by altering its mitochondrial membrane potential. The ZnO–SnO2 nerolidol nanocomposite also enhanced oxidative stress, leading to a decrease in superoxide dismutase, catalase, and glutathione and an increase in lipid peroxidation. Ultimately, ZnO–SnO2 nerolidol nanocomposite enhanced the caspase cascade by inducing caspases 3, 8, and 9 in KYSE-150 cells. On the whole, we suggest that the ZnO–SnO2 nerolidol nanocomposite can be an effective treatment strategy against esophageal squamous cell carcinoma in KYSE-150 cells. However, understanding molecular circuits is still warranted.

Voltammetric Determination of Pyridoxine in Pharmaceutical Samples Using Phosphorus-Doped Copper Oxide Pencil Graphite Electrode

Abstract A phosphorus-doped copper oxide/pencil graphite electrode (P-doped CuO/PGE) was developed to determine pyridoxine selectively. The phosphorus doped into the copper has revealed a large number of defects that can provide active sites for the reaction to take place, thus contributing to the improvement of the electrical conductivity of copper oxide. Cyclic voltammetry, electrochemical impedance spectroscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy were employed for the characterization of the P-doped CuO/PGE. Surface morphology was analyzed by field emission scanning electron microscopy. Electrochemical measurements were performed by differential pulse voltammetry, and the limit of detection (LOD) and limit of quantification values for pyridoxine were calculated. The LOD value was 0.33 μmol L-1 with a linear range of 1.0 and 100 μmol L-1. The developed sensor showed a remarkable anti-interference effect against interference from ascorbic acid, dopamine, glucose, uric acid, and lactate. Potential interference effects of species that may coexist with pyridoxine in pharmacological samples were also investigated. The applicability of the developed sensor to real samples was examined, and satisfactory recovery values were obtained.

Efficiency Improvement on Indium Tin Oxide Films for Dye-Sensitized Solar Cell Using Oxygen Plasma by Bias-Magnetron RF Sputtering Process

Dye-sensitized solar cells (DSSCs) are among the most widely studied thin-film solar cells because of their cost-effectiveness, low toxicity, and simple fabrication method. However, there is still much scope for replacing current DSSC materials due to their high cost, low volume, and lack of long-term stability. Accordingly, indium tin oxide (ITO)-nanorod films were fabricated by electron (E)-beam evaporation using the glancing angle deposition method in this study. Then, the ITO-nanorod was treated with oxygen plasma via a bias-magnetron radio-frequency (RF) sputtering process to improve the efficiency of DSSCs under a varying gas flow rate of 20, 40, 60, 80, and 100 sccm. The field emission scanning electron microscopy (FE-SEM) investigation of the ITO film structure revealed that the obtained nanorod structures have slightly different diameters. At the same time, an increase in the oxygen flow rate resulted in a rougher film surface structure. In this, the lower sheet resistance was received because of rougher morphology. When comparing the DSSCs efficiency (η) test results, we found that at a gas flow rate of 100 sccm, the highest efficiency value showed 9.5%. On the other hand, the ITO-nanorod without plasma treatment exhibited the lowest η. Hence, plasma technology can be practically applied to improve the η of DSSC devices. This study will be a prototype of a highly advanced solar cell manufacturing method for the solar cell industry.

Nanostructure of TiO\(_{2}\) and WO\(_{3}\) multilayer films deposited on ITO glass for electrochromic enhanced photocatalytic activity

The photocatalytic activity (PA) by electrochromic (EC) enhancement of single and multilayer films of TiO2, WO3, TiO2/WO3, and WO3/TiO2 was investigated. All films were deposited from metal on an ITO glass substrate using direct current (DC) magnetron sputtering via an oblique angle deposition (OAD) technique at 85°. Subsequently, a thermal oxidation (TO) process at 500℃ was applied for the samples to form metal oxide films. The morphology, elemental composition, crystal structure, and optical properties were studied by using field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffractometry (XRD), and UV-vis spectroscopy, respectively. The photocatalytic properties were investigated by showing the degradation rate of methylene blue (MB) solution as an organic pollutant that was examined under ultraviolet irradiation of 300 µW∙cm‒2. The film samples were investigated by comparing the pre-color and colored states that were achieved through the EC process. The EC properties of WO3 led to increased charge insertion on the film surface. This observation was further supported by cyclic voltammetry (CV) testing, which revealed a higher current density for the thin film samples. The photodegradation results showed that the samples in the colored state exhibited a significantly higher degradation rate of MB compared to the pre-color state.

A semiconducting supramolecular Co(II)-metallogel based resistive random access memory (RRAM) design with good endurance capabilities.

A highly efficient approach for synthesizing a supramolecular metallogel of Co(II) ions, denoted as CoA-TA, has been established under room temperature and atmospheric pressure conditions. This method employs the metal-coordinating organic ligand benzene-1,3,5-tricarboxylic acid as a low molecular weight gelator (LMWG) in DMF solvent. A comprehensive analysis of the mechanical properties of the resulting supramolecular Co(II)-metallogel was conducted through rheological investigation, considering angular frequency and thixotropic study. The hierarchical rocky network structure of the supramolecular Co(II)-metallogel was unveiled using field emission scanning electron microscopy (FESEM). Transmission electron microscopic (TEM) analysis showed rod-shaped structures via low-magnification high angle annular dark field (HAADF) bright field scanning transmission electron microscopic (STEM) imaging, while energy dispersive X-ray (EDX) elemental mapping confirmed its primary chemical constituents. The formation mechanism of the metallogel was examined via fourier transform infrared spectroscopy (FTIR) spectroscopy. The nature of the synthesized CoA-TA metallogel was affirmed through powder X-ray diffraction (PXRD) analysis. Furthermore, this study involved fabrication of Schottky diode structures in a metal-semiconductor-metal geometry based on cobalt(II) metallogel (CoA-TA), enabling observation of charge transport behavior. Remarkably, a resistive random access memory (RRAM) device utilizing cobalt(II) metallohydrogel (CoA-TA) demonstrated bipolar resistive switching at room temperature and under ambient conditions. The switching mechanism was investigated, revealing the formation and rupture of conductive filaments between metal electrodes that govern the resistive switching behavior. This RRAM device exhibited an impressive ON/OFF ratio (~ 414) and exceptional endurance over 5000 switching cycles. These structures offer great potential for diverse applications such as non-volatile memory design, neuromorphic computing, flexible electronics and optoelectronics. Their advantages lie in their fabrication process, reliable resistive switching behavior and overall performance stability.

ZnS Thin Films Prepared Using Spray Pyrolysis Technique

It is well known that spray pyrolysis of an aqueous solution of thiourea and zinc acetate onto a glass substrate at spray rates of (3 mlmin-1) may successfully synthesize thin coatings of zinc sulfide. The impact of several substrate temperatures (150, 200, 300, and 400 oC) on the structural and optical characteristics was also discussed in this research. Field emission scanning electron microscopy (FESEM), UV-Vis-NIR spectrometry, and X-ray diffraction (XRD) were used to characterize the films. On each one of the deposited ZnS sheets, a cubic structure was seen. On the other hand, the temperature of the substrate appeared to affect the crystallinity and morphology. It was discovered that as the substrate temperature was lowered, the bandgap value of ZnS films somewhat rose. Furthermore, it is most likely that the Zn(S,O) production inside the solid solution is responsible for the fluctuations seen in the 3.5-3.8 eV region.

Wear properties of Al6061/SiC + B4C + TiC hybrid composites produced by vacuum infiltration method

Abstract In the study, hybrid metal matrix composite (HMMC) structures were produced by vacuum infiltration method (VIM) using Al6061 alloy and varying amounts of SiC, B4C, and TiC ceramic powder pairs. Age-hardening processes were applied to these HMMCs. After heat treatment, wear behavior was examined under different loads using the pin-on-disc test method. All Al6061 hybrid composites exhibited better wear performance than unreinforced Al6061. In the wear tests of composite samples, the lowest volume loss and therefore the highest wear resistance were obtained in Al6061 3 wt.% B4C + SiC composites under 5 N force. The lowest wear resistance due to the highest volume loss was determined in Al6061/1 wt.% TiC + B4C composites under 15 N force. Abrasive and adhesive wear characteristics were observed in field emission scanning electron microscopy(FESEM) images of worn surfaces. Additionally, wear debris, smearing, and deep grove formations were determined on the surface. In the EDS analysis performed on the worn surface, O and Fe elements were found in addition to the elements that are likely to be in the structure (such as Al, B, C, Ti, Si, and Mg). The wear tests caused the formation of oxide layers on the sample surfaces.

Layer-by-Layer Deposition of Hollow TiO2 Spheres with Enhanced Photoelectric Conversion Efficiency for Dye-Sensitized Solar Cell Applications

Fabricating photoanodes with a strong light-scattering effect can improve the photoconversion efficiency of dye-sensitized solar cells (DSSCs). In this work, a facile microwave hydrothermal process was developed to prepare Au@TiO2 core–shell nanostructures, and then the Au core was removed by etching, resulting in hollow TiO2. Morphological characterizations such as field emission scanning and transmission electron microscopy measurements have been used for the successful formation of core–shell and hollow TiO2 nanostructures. Next, we attempted to deposit the different-sized hollow TiO2-based microspheres simultaneously on the surface of small-sized TiO2 nanoparticles-based compact film as light-scattering layers via electrophoretic deposition. The deposited hollow TiO2 microspheres constitute bi- and tri-layers that not only improve the light-harvesting properties but also speed up the photogenerated charge transfer. Compared to commercial TiO2 compact film (4.75%), the resulting bi-layer and tri-layered films-based DSSCs displayed power conversion efficiencies of 6.33% and 8.08%, respectively. It is revealed that the deposited bi- and tri-layered films can enhance the light absorption ability via multiple photon reflection. This work validates a novel and controllable strategy to develop light-scattering layers with increased light-harvesting properties for highly efficient dye-sensitized solar cells.

Synthesis and characterization of p-CuO/n-ZnO heterostructured composite thin films for the detection of formaldehyde gas.

We report the synthesis and characterization of pure CuO and CuO-ZnO nanostructured composite thin films sprayed on particle-free glass substrates using chemical spray pyrolysis method. The films were systematically analyzed through microstructural, morphological, chemical, and gas-sensing studies. X-ray diffraction (XRD) studies confirmed the polycrystalline nature of the films, with a predominant monoclinic phase along the (002) direction. Key structural parameters, such as crystallite size, dislocation density, strain, and the number of crystallites per unit area, were reported from XRD analysis. Field emission scanning electron microscopy (FESEM) revealed a bundled-like morphology with uniform particle distribution, enhancing the surface area for effective gas interaction. X-ray photoelectron spectroscopy (XPS) results indicated that Cu and Zn ions existed predominantly in the 2+ oxidation state, contributing to the films' reactivity. Significantly, the gas sensing studies were investigated with static liquid distribution method, highlighting the remarkable performance of the 30 wt.% CuO-ZnO composite thin film. This composite exhibited a substantial response to 5 ppm formaldehyde at ambient conditions, showing a recovery time of 22 seconds and a response time of 15 seconds. These findings underscore the potential of CuO-ZnO composites for efficient formaldehyde gas sensing applications, marking a notable advancement in the field of environmental monitoring.

Effect of Iodine Doped Pentacene Thin Film on the Performance of Organic Light Emitting Diode

The study investigated the effect of iodine-doped pentacene film as a buffer layer in an organic light-emitting diode (OLED). In this study, an ITO (indium tin oxide)-based sample is used as a reference device for comparative purposes. In OLED devices, the buffer layers were deposited using the doping of iodine vapor with the pentacene materials under proper conditions. The thermal treatment of the doped pentacene film results in increasing the conductivity of the buffer layer. Surface morphology for the bilayer anode was carried out by FESEM (Field Emission Scanning Electron Microscope) analysis. In our work, maximum luminance of 2345 cd/m2 and current efficiency of 5.4 cd/A are obtained, along with more stability performance under annealing treatment in the device structure of FTO/iodine-doped pentacene (30 nm)/TPD [N, N′-Bis(3-methyl phenyl)-N, N′-diphenylbenzidine] (44 nm)/Alq3 [Tris(8-hydroxyquinoline)aluminum(III)] (52 nm)/LiF (lithium fluoride) (5 nm)/Al (aluminum) (110 nm).

Hydrodeoxygenation of Isoeugenol-Derived Model Compound over Carbon-Supported Pt and Pt-SnS Catalysts for the Production of Sustainable Jet Fuel.

This study focuses on the sustainable production of bio-jet fuel through the catalytic hydrodeoxygenation (HDO) of isoeugenol (IE). Sucrose-based activated carbon supported bimetallic Platinum-Tin metal sulphides (PtO-SnS/AC) catalyst was prepared for HDO process. Physicochemical properties of catalysts with different spraying synthesis methods (in situ and ex situ metal doping) and Pt loading (0.1-1.0 %) were further investigated. The PtO-SnS/AC catalysts were characterised using various techniques such as X-ray absorption spectroscopy (XAS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), field-emission scanning electron microscopy (FESEM) and thermogravimetric analysis (TGA). Both HRTEM and FESEM results show the successful preparation of a spherical nanoparticles doped over activated carbon, and Pt was dispersed on the outer shell of the particles. The catalytic HDO of IE was evaluated in a batch system and showed a high yield and conversion as follows: IE conversion of 100 %, liquid-phase mass balance of 95.92 %, dihydroeugenol (DH) conversion of 99.32 %, propylcyclohexane (PCH) yield of 88.94 % and 2-methoxy-4-propylcyclohexanol (HYD) yield of 76.19 %. Moreover, the PtO-SnS/AC catalyst exhibited high reusability with low metal leaching and high coke resistance for 10 cycles. The catalyst was evaluated in a continuous flow reactor for 100 h at different reaction temperatures, and interestingly, the catalyst showed low deactivation with a high half-time.

Utilization of coalmine overburden-furnace slag and fly ash mixed cement-treated subbase/base course material for sustainable flexible pavements: mechanical performance and environmental impact.

The scarcity of conventional aggregates with tremendous growth in highway construction and the indiscriminate dumping of industrial waste materials in precious landfills has become a huge global concern. This study is aimed at utilizing wastes from various industries, including coalmine overburden (OB) dump, basic oxygen furnace (BOF) slag, and fly ash to produce suitable and sustainable cement-treated subbase/base course layers (CBSB/CTB) for flexible pavement construction. Response surface methodology was used to optimize the composition of the blended material considering unconfined compressive strength (UCS) and Poisson's ratio. Results demonstrated that 50% OB dump, 40% slag, 5% fly ash, and 5% cement achieved a 7-day UCS of 4.84MPa and Poisson's ratio of 0.25, in line with IRC:37-2018 guidelines. X-ray diffraction (XRD) and field emission scanning electron microscope (FESEM) analysis confirmed the presence of ettringite crystals, calcium-silicate-hydrate (C-S-H), and calcium-aluminosilicate-hydrate (C-A-S-H) gels which are the source of strength development in the blend. Further, a soaked California bearing ratio (CBR) of 136.08% and flexural strength of 2.06MPa after 7days and 28days of curing, respectively, demonstrates the overall strength of the stabilized waste. Approximately 4% weight loss was observed after wet-dry durability tests, indicating exceptional performance of the optimal blend in inclement weather conditions. Furthermore, the environmental impact of the blended material was studied through a leaching study. Fly ash had a high zinc (Zn) level, while BOF slag showed a rich concentrationof chromium (Cr), manganese (Mn), and iron (Fe) in the acid digestion test. In spite of this, the toxicity characteristics leaching procedure (TCLP) test indicated that the levels of heavy metals that leached from the stabilized material stayed considerably below the permissible limits set forth in Indian Standard, IS:10500 (2012). Finally, cost analysis showed a 51.6% reduction in construction cost with cement-treated industrial wastes instead of granular base/subbase made with conventional aggregates. The study recommends the suitability of the stabilized waste material as an alternate construction material for large-scale field applications, which could encourage the construction of flexible pavements that are environmentally benign, economical, and sustainable.

Enhanced photocatalytic degradation of organic pollutants by randomly oriented 2D SnS2 nanostructures

Abstract In this study, we present a bottom-up solvothermal technique using tin tetrachloride pentahydrate (SnCl4.5H2O) and thioacetamide as precursors to synthesize SnS2 nanostructures. Different solvents including isopropyl alcohol, ethanol (EN), and ethylene glycol were used in the reaction to enhance the photodegradation efficiency of organic pollutants, Methylene Blue (MB), and Tetracycline (TC) in an aqueous medium under simulated solar light irradiation. The SnS2 nanostructures synthesized with these solvents were characterized using various structural, morphological, and optical techniques, including x-ray diffraction, RAMAN, field emission scanning electron microscope, x-ray photoelectron spectroscopy, UV–Vis, and Brunauer–Emmett–Teller analysis. The choice of solvent was found to significantly affect the structural, morphological, and optical properties of the SnS2 nanostructures. Notably, the sample synthesized with EN as the solvent displayed a unique morphology, enhanced light-harvesting ability, efficient charge carrier separation, and a larger specific surface area, all of which contributed to its superior photocatalytic activity. This sample achieved 99.9% degradation of MB and 95% degradation of TC within 20 and 40 min, respectively. The kinetic analysis revealed maximum rate constant (k) values of 0.15242 min−1 for MB and 0.060 95 min−1 for TC, as determined by the pseudo-first-order kinetic model. We also discuss the plausible mechanism involving visible light-induced electron–hole pairs that generate reactive species, leading to the mineralization of dyes into H2O, CO2, and other gaseous products. The synthesized SnS2 nanostructures demonstrate significant potential for enhanced photocatalytic activity in organic pollutant degradation, underscoring their promise in addressing water pollution challenges.

MgAl-Layered Double Hydroxide-Coated Bio-Silica as an Adsorbent for Anionic Pollutants Removal: A Case Study of the Implementation of Sustainable Technologies

The adsorption efficiency of Cr(VI) and anionic textile dyes onto MgAl-layered double hydroxides (LDHs) and MgAl-LDH coated on bio-silica (b-SiO2) nanoparticles (MgAl-LDH@SiO2) derived from waste rice husks was studied in this work. The material was characterized using field-emission scanning electron microscopy (FE-SEM/EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopic (XPS) techniques. The adsorption capacities of MgAl-LDH@SiO2 were increased by 12.2%, 11.7%, 10.6%, and 10.0% in the processes of Cr(VI), Acid Blue 225 (AB-225), Acid Violet 109 (AV-109), and Acid Green 40 (AG-40) dye removal versus MgAl-LDH. The obtained results indicated the contribution of b-SiO2 to the development of active surface functionalities of MgAl-LDH. A kinetic study indicated lower intraparticle diffusional transport resistance. Physisorption is the dominant mechanism for dye removal, while surface complexation dominates in the processes of Cr(VI) removal. The disposal of effluent water after five adsorption/desorption cycles was attained using enzymatic decolorization, photocatalytic degradation of the dyes, and chromate reduction, satisfying the prescribed national legislation. Under optimal conditions and using immobilized horseradish peroxidase (HRP), efficient decolorization of effluent solutions containing AB-225 and AV-109 dyes was achieved. Exhausted MgAl-LDH@SiO2 was processed by dissolution/precipitation of Mg and Al hydroxides, while residual silica was used as a reinforcing filler in polyester composites. The fire-proofing properties of composites with Mg and Al hydroxides were also improved, which provides a closed loop with zero waste generation. The development of wastewater treatment technologies and the production of potentially marketable composites led to the successful achievement of both low environmental impacts and circular economy implementation.

Antibacterial and Photocatalytic Applications of Silver Nanoparticles Synthesized from Lacticaseibacillus rhamnosus

The biosynthesis of silver nanoparticles (AgNPs) presents an innovative and sustainable approach in nanotechnology with promising applications in fields such as medicine, food safety, and pharmacology. In this study, AgNPs were successfully synthesized using the probiotic strain Lacticaseibacillus rhamnosus (BCRC16000), addressing challenges related to stability, biocompatibility, and scalability that are common in conventional nanoparticle production methods. The formation of AgNPs was indicated by a color change from yellow to brown, and UV–visible spectrophotometry confirmed their presence with a characteristic absorption peak at 443 nm. Furthermore, Fourier transform infrared (FTIR) spectroscopy revealed the involvement of biomolecules in reducing silver ions, which suggests their role in stabilizing the nanoparticles. In addition, field emission scanning electron microscopy (FE-SEM) showed significant morphological and structural changes. At the same time, dynamic light scattering (DLS) and zeta potential analyses provided valuable insights such as average size (199.7 nm), distribution, and stability, reporting a polydispersity index of 0.239 and a surface charge of −36.3 mV. Notably, the AgNPs demonstrated strong antibacterial activity and photocatalytic efficiency, underscoring their potential for environmental and biomedical applications. Therefore, this study highlights the effectiveness of Lacticaseibacillus rhamnosus in the biosynthesis of AgNPs, offering valuable antibacterial and photocatalytic properties with significant industrial and scientific implications.

Morphological and structural analysis of monodispersive silica nanoparticles fabricated by Stober method for self-cleaning applications

Abstract In this work, silica nanoparticles have been synthesized via the Stober process on a p-type silicon substrate by spin coating method. Structural and morphological study has been carried out by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Microstructural analysis by Raman spectroscopy displays a prominent peak at 521 cm-1 which corresponds to crystalline silicon. Further, the elemental study by using energy dispersive x-ray spectroscopy (EDX) confirms the presence of silica with no other impurities. Besides, the wettability property has been studied by contact angle measurement and found to be around 130ο for the 6-layer coated thin film which is quasi-super-hydrophobic. The wettability results obtained signify promising properties for the development of self-cleaning devices and applications.

Investigation of the Microstructure, Electrical and Mechanical Properties of Al-CNTs-B4C Composite Prepared by Double-Step Stir Casting for Power Transmission Conductor

Abstract Monolithic aluminium alloy is a modern engineering material that is in high demand owing to its excellent performance and versatility. It has a high electrical conductivity, low density, high strength- to- weight ratio, and high resistance to corrosion. However, it lacks adequate resistance to creep, fatigue, stable microstructure, and strength at elevated temperatures. To overcome these deficiencies, aluminium matrix composites are developed. This work focuses on an experimental investigation of the microstructure, mechanical strength, and electrical conductivity of Al-CNTs-B4C composite consolidated by a double-step stir casting technique. An X-ray diffractometer, transmission electron microscopy, and a field-emission scanning electron microscope fitted with energy dispersive X-ray spectroscopy were used to characterize the start-up powders and the cast samples. A Brinell tester was used to measure the microhardness of the cast samples. A four-point probe meter was used to determine the electrical conductivity. The microstructural results revealed formation of Al4C3 and Al3BC intermetallics, B4C phase and amorphous carbon precipitate. Marginally improved electrical conductivity of 33.33 x 107 S/m (65.1% IACS) was obtained with Al-5CNTs-15B4C, together with high microhardness of 725.72 MPa. The microhardness improved by 94.7% over monolithic pure Al. The double-step stir casting enhanced the homogenous dispersion of the reinforcements. The improvements in the mechanical properties and electrical conductivity were attributed to the synergy between B4C and CNTs which induced Orowan looping, load transfer effect, plastic deformation and dislocation pinning in the composite. It is recommended that this composite will perform creditably in power transmission.

Analysis of the factors influencing movable fluid in shale oil reservoirs: a case study of Chang 7 in the Ordos Basin, China

Shale oil in the Ordos Basin is one of the most important areas for further exploration. In this paper, the relationships between the organic geochemistry, physical properties, micropore structure and mobile fluid composition of the Chang7 shale were studied via field emission scanning electron microscopy field emission scanning electron microscopy, nuclear magnetic resonance and computed tomography. The results indicate that the shales are mainly composed of quartz, clay and feldspar. The micro/nanopores are composed of mineral intergranular pores, dissolution pores and intercrystalline pores. The pore size of the mobile fluid ranges from 10 to 30 nm and from 0.1 to 10 μm, and a higher temperature is associated with a better fluidity of 10–30 nm. Based on the fractal turning point method, the shale reservoirs are classified as moderate or high heterogeneity. The mobile liquid was mainly controlled by the brittleness index, permeability, permeability, radius of the throat, radius of the pore throat, and volume ratio of the pore throat. The second factor was the heterogeneity strength and burial depth, but the relationship with TOC content and maturity was not obvious.