Field Emission Scanning Electron Microscopy Research Articles

Development of hydrophilic multilayer structures for energy saving window applications using sol-gel spin coating

This study is centered on analyzing the microstructural and optical reflectivity properties of multilayers composed of dielectric titania and silica. The goal is to investigate their potential application as energy-efficient windows on glass surfaces in different modern building projects. Nevertheless, the creation of these coatings can be quite expensive due to their complex structure. This study focuses on the development of a cost-effective method to produce a multilayer structure made of titania and silica. This structure has the remarkable ability to reflect approximately 100 % of UV light and 70 % of infrared light, all achieved with just three layers. The X-ray diffraction (XRD) analysis was conducted to examine the crystallinity of the coatings. The results indicated the presence of an anatase phase, as evidenced by the Bragg angle of 25O. Empirical support was obtained through the use of Fourier transform infrared spectroscopy (FTIR), which revealed the presence of functional bonds at specific wavenumbers. Titania and silica were identified at wave numbers of 596 cm−1 and 1246 cm−1, respectively. The FTIR investigation was further supported by energy dispersive spectrum analysis (EDAX), which verified the existence of titania and silica in the multilayer structure. Through the use of field emission scanning electron microscopy (FESEM), the analysis of the multilayer structure unveiled the existence of layers composed of titania, silica, and titania. These layers were found to have thicknesses of approximately 286 nm, 315 nm, and 222 nm, respectively. The coatings were analyzed for reflectance using a UV–VIS-NIR spectrophotometer, which showed a full reflection of 100 % in the far ultraviolet range and a reflection of 70 % in the infrared region. Furthermore, the analysis of the coatings’ wetting behavior with a contact angle meter revealed their hydrophilic nature, suggesting their potential use in self-cleaning applications.

Novel magnetic hybrid bio-mixture with two types of nano powders for the targeted drug delivery systems: Characterize, prepare, stability, ultra-sonicated and the thermal management

By systematically evaluating the thermal conductivity (TC) and viscosity of Fe₃O₄ + TiO₂ and Fe₃O₄ + ZnO nanofluids, this study aims to identify key differences in their performance and behavior, particularly in biomedical applications. The investigation is conducted in a simulated body fluid (SBF) to closely replicate physiological conditions, providing a realistic assessment of their potential for use in hyperthermia therapy and targeted drug delivery. The study employs X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR) to analyze the crystal structure and chemical composition of the nanomaterials, while field emission scanning electron microscopy (FESEM) characterizes the size, shape, and dispersion of nanoparticles within the fluid matrix. The results indicated that Fe₃O₄ + ZnO exhibits superior thermal conductivity, whereas Fe₃O₄ + TiO₂ shows higher viscosity due to its tendency to form denser aggregates. These findings are crucial for selecting the appropriate nanofluid formulation for specific biomedical applications. Additionally, the study highlights that the observed differences in thermal and rheological behavior between the two hybrid nanofluids could be leveraged to tailor them for optimized performance in different therapeutic contexts. Ultimately, this comparative analysis offers valuable insights into the design and development of magnetic hybrid bio-nanofluids (BNs), guiding future research efforts toward their potential optimization for cutting-edge biomedical technologies.

Performance of yellow and pink oyster mushroom dyes in dye sensitized solar cell

A solar photovoltaic (PV) cell, is an electrical device that uses the PV effect to convert light energy into electricity. The application of oyster mushroom dyes in dye sensitized solar cell (DSSC) is a novel strategy to substitute the costly chemical production process with easily extractable, environmentally acceptable dyes. Both dyes of yellow and pink oyster mushrooms were extracted using the same process but dried into powder form using two techniques, warm drying and freeze drying. The characterization was carried out utilizing current-voltage (I-V) characterization for electrical properties, Ultraviolet-Visible (UV-Vis) spectrophotometer for optical properties, Field Emission Scanning Electron Microscopy (FESEM), and Atomic Force Microscopy (AFM) for the structural properties. It was found that freeze-dried pink and yellow oyster mushroom had shown the good properties for DSSC application as it produced energy bandgap which lies within the range of efficient dye sensitizer; 1.7 eV and 2.2 eV, the most uniform distribution of pores and a nearly spherical form in FESEM analysis, and AFM result obtained with the highest root mean square (RMS) roughness value (26.922 and 34.033) with stereoscopic morphologies. The data proved that mushroom dyes can be incorporated in DSSC with the optimization of drying method in the extraction process, dilution of dye and the layer of deposition on the glass substrate. The current density-voltage (J–V) characteristics of fabricated DSSC was characterized using Newport Oriel Sol3A solar simulator under AM 1.5 Sun condition (100 mW/cm2, 25 oC). From the result obtained by solar simulator, the fabricated FTO/TiO2/Pleurotus djamor dye/Pt indicated the Voc of 0.499 V and Jsc of 0.397 mA/cm2.

Slow release of surfactant by smart thermosensitive polymer-functionalized mesoporous silica for enhanced oil recovery: Synthesis and characterization

The efficiency of surfactant flooding can be improved through slow-release technology, which enables stimuli-sensitive and gradual release of surfactant. In this study, we synthesized a novel nanocomposite capsule composed of mesoporous silica functionalized with thermosensitive poly N-vinyl caprolactam (PNVCL). Well-optimized nanocarriers were synthesized by conducting sensitivity analyses on key synthesis parameters such as pH, reaction duration, and hydrophobic phase, resulting in hydrodynamic diameters ranging from 47 to 109 nm. Characterization of the nanocarrier structure was performed using dynamic light scattering (DLS), Brunauer–Emmett–Teller (BET) analysis, and field emission scanning electron microscopy (FESEM), while Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and energy-dispersive X-ray spectroscopy (EDS) were employed to analyze the nanocarrier composition. Poly N-vinyl caprolactam (NVCL)-functionalized mesoporous silica exhibited high surfactant loading (approximately 52 % w/w) and a large specific surface area (542.88 m2/g), featuring ink-bottle pores. Additionally, it demonstrated thermosensitive behavior, with the lower critical solution temperature of 39 °C. Gradual release of cetyltrimethylammonium bromide (CTAB) was observed in both deionized water and formation brine, with release rates increasing with temperature. Overall, the synthesized nanocomposite carrier holds significant potential as an ideal candidate for effectively controlling the release of surfactants in reservoirs subjected to high-temperature and high-salinity conditions.

Cytocompatible Hyperbranched Polyesters Capable of Altering the Ca2+ Signaling in Neuronal Cells In Vitro.

Synthetic hyperbranched polyesters with potential therapeutic properties were synthesized using the bifunctional polyethylene glycol or PEG with different molecular weights, ca., 4000, 6000, and 20,000 g/mol, and the trifunctional trans-aconitic acid or TAA. During polycondensation, a fixed amount of PEG was allowed to react with varying amounts of TAA (1:1 and 1:3) to control the branching extents. It was found that the synthetic polyesters had a considerable yield and were highly water soluble. Spectroscopic data (Fourier transform infrared and 1H NMR) confirmed the polyester formation; the branching percentages were determined from 1H NMR spectroscopy which varied from 73% to 22% among the synthesized samples. As the molecular weight of PEG was increased, the branching percentage drastically dropped. All polyesters were found to be negatively charged due to the ionization of unreacted -COOH in the branched ends at the working pH (7.4). Both the hydrodynamic size and intrinsic viscosity were found to reduce as the branching extent increased. Among the sets of polyesters, the one with the highest branching percentage (73%) showed the core-shell morphology (evident from field emission scanning electron microscopy and transmission electron microscopy studies). It also exhibited the highest efficiency toward Ca2+ influx in neuronal cells due to the unique morphology and the negatively charged surface. Nevertheless, this particular grade of polyester along with all the other grades was cytocompatible and induced reactive oxygen species generation. Since the maximally branched grade was highly efficient in altering the Ca2+ signaling through stronger influx, it may well be tested for treating neuronal disorders in vivo in future.

Designing nano-heterostructured nickel doped tin sulfide/tin oxide as binder free electrode material for supercapattery

New generation of electrochemical energy storage devices (EESD) such as supercapattery is being intensively studied as it merges the ideal energy density of batteries and optimal power density of supercapacitors in a single device. A multitude of parameters such as the method of electrodes preparation can affect the performance of supercapattery. In this research, nickel doped tin sulfide /tin oxide (SnS@Ni/SnO2) heterostructures were grown directly on the Ni foam and subjected to different calcination temperatures to study their effect on formation, properties, and electrochemical performance through X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and electrochemical tests. The optimized SnS@Ni/SnO2 electrode achieved a maximum specific capacity of 319 C g− 1 while activated carbon based capacitive electrode exhibited maximum specific capacitance of 381.19 Fg− 1. Besides, capacitive electrodes for the supercapattery were optimized by incorporating different conductive materials such as acetylene black (AB), carbon nanotubes (CNT) and graphene (GR). Assembling these optimized electrodes with the aid of charge balancing equation, the assembled supercapattery was able to achieve outstanding maximum energy density and power density of 36.04 Wh kg− 1 and 12.48 kW kg− 1 with capacity retention of 91% over 4,000 charge/discharge cycles.

Impact of sol-gel synthesized α-aluminium oxide nanoparticles for the enhancement of transformer oil insulation properties

Transformers require advanced insulating materials that outperform mineral oil in terms of cooling, insulation effectiveness, eco-friendliness, and operational efficiency in extreme operational and weather conditions. As a result, emphasis has shifted to renewable and ecologically friendly materials. This change in emphasis is motivated by worries about the environment, fuel shortages, and the disposal of waste oil. Transformers have historically employed solid insulators like paper and pressboard as well as mineral or synthetic oil. However, the development of ecologically friendly insulating materials has been spurred by new environmental regulations as well as economic benefits. This research investigates the use of sol-gel synthesized aluminium oxide (Al2O3) nanoparticles to improve the insulation properties of host transformer oil. The synthesized aluminium nanoparticles were characterized with X-ray diffractometer (XRD) and found rhombohedral structure, whose chemical composition was studied by energy dispersive X-ray spectrum (EDAX). Investigation using Fourier transform infrared spectroscopy (FTIR) also revealed the production of AlOOH and hydroxyl vibrational bands at wavenumbers of 690 and 2976 cm−1, respectively. Studies using field emission scanning electron microscopy (FESEM) showed that the nanoparticles are spherical in form and have a diameter of around 38 nm. Additionally, the incorporation of α-aluminium oxide nanoparticles into the host oil showed an improvement in the breakdown voltage and suggested a possible use for better transformer oil insulation.

Mechanochemical synthesis and characterization of poly[(aniline-co-N-(4-sulfophenyl) aniline] nanofibers and its nanocomposite with titanium dioxide nanoparticles and study of their efficiency in hybrid solar cell

The advantages of polyaniline for application in new generation solar cells include its cost-effectiveness, environmentally friendly synthesis, remarkable stability, and the ability to modify the bandgap through the synthesis of its nanocomposites. But a challenge for its nanostructures is the limited solubility in non-toxic solvents, including water, which limits their processability in coating techniques. We overcame this challenge by synthesizing its copolymer with diphenylamine-4-sulfonate and its nanocomposite with titanium dioxide nanoparticles (TiO2NPs). So through a solid-state and template-free technique and using sodium diphenylamine-4-sulfonate, aniline hydrochloride salt, TiO2NPs, and FeCl3∙6 H2O as an oxidant, poly(N-(sulfophenyl)aniline) nanoflowers (PSANFLs), poly [(aniline-co-N-(4-sulfophenyl) aniline] nanofibers (PAPSANFs), poly(N-(sulfophenyl)aniline) nanofibers/titanium dioxide nanoparticles (PSANFs/TiO2NPs), and poly (aniline-co-N-(4-sulfophenyl)aniline nanofibers/titanium dioxide nanoparticles (PAPSANFs/TiO2NPs) were synthesized. Characterization of the synthesized samples was carried out through field emission scanning electron microscopy (FE-SEM), Fourier-transform infrared spectra, ultraviolet-visible spectra (UV-Vis), cyclic voltammetry (CV), and elemental analysis (CHNS). The FE-SEM images clearly illustrate that the synthesized samples are of nanoscale dimensions. The band gap values of 2.23 eV for PSANFs/TiO2NPs and 1.96 eV for PAPSANFs/TiO2NPs nanocomposites were determined through electrochemical calculations based on cyclic voltammetry curves, showcasing the complementary properties of n and p semiconductors. Using doctor blade method to prepare films from synthesized materials and the architectural pattern of ITO│TiO2NPs│semiconductor sample│Al, all hybrid solar cells are fabricated. The I-V characteristics and power conversion efficiency (PCE) of the samples were examined and discussed. The PCE values for the four samples were found to be in the range of 0.20–0.82 %.

Investigating the structural and electromagnetic properties of ZnFe2O4@MWCNTs nanocomposites

This study introduces ZnFe2O4@MWCNTs nanocomposites (ZF@MWCNTs NCs), developed using ZnFe2O4 magnetic nanoparticles (ZFNPs) and multi-walled carbon nanotubes (MWCNTs) via a simple, cost-effective, and scalable ultrasonic process. The design involves ZFNPs acting as an electromagnetic (EM) skeleton or magnetic shell surrounding a conductive MWCNT core, optimizing microwave absorption. By combining the magnetic properties of ZFNPs and the electrical conductivity of MWCNTs, the quasi-core-shell structure achieves excellent impedance matching and synergistic dielectric/magnetic loss. Comprehensive characterization was performed, including X-ray diffraction (XRD) for crystal structure, field emission scanning electron microscopy (FESEM) with energy-dispersive X-ray spectroscopy (EDS) for morphology and elemental analysis, Fourier transform infrared (FT-IR) spectroscopy for structural identification, vibrating sample magnetometers (VSM) for magnetic properties, and vector network analyzers (VNA) for dielectric properties. Among the five synthesized weight ratios, M4 sample exhibited the best reflection loss (RL) under the X-band at −47.16 dB with a thickness of 2.33 mm and under the Ku-band at −24.40 dB with a thickness of 1.53 mm. These nanocomposites demonstrated 99.99 % wave dissipation under both X- and Ku-bands, making them highly effective microwave absorbers. This work provides a promising approach for developing high-performance microwave-absorbing materials.

Eco-friendly synthesis of curcumin-loaded ZnO nanoparticles encapsulated in Pluronic F-127: Implications for bacterial and breast cancer therapies

The development of a nanomaterials production process that is both economical and environmentally friendly is a result of the growing importance placed on people’s health. The Zinc oxide (ZnO)-Pluronic F127 (PF127)-Curcumin (CUR) nanoparticles (NPs) were synthesized through a green method using Senna auriculata flower extracts. These NPs were characterized using a variety of techniques, such as ultraviolet–visible spectroscopy (UV), Fourier transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FESEM), Energy Dispersive X-ray analysis (EDAX), X-ray diffraction (XRD), photoluminescence (PL), and dynamic light scattering (DLS). From the XRD studies, synthesized ZnO-PF127-CUR NPs exhibit a wurtzite hexagonal crystal structure. The antimicrobial activity of ZnO-PF127-CUR NPs and Amoxicillin was tested against Staphylococcus aureus, Klebsiella pneumoniae, Shigella dysenteriae, Staphylococcus pneumoniae, Bacillus subtilis, proteus vulgaris, and candida albicans, respectively. The anticancer activity of ZnO-PF127-CUR NPs was tested against human breast cancer cell line (MDA-MB-237), and ZnO-PF127-CUR exhibits potential anticancer activity. These results support using ZnO-PF127-CUR NPs in healthcare manufacturing environments to improve human health.

Thermodynamics and Kinetic Study for Removal of Orange-G Dye from Aqueous Solution by Nano Composite

In this study, where graphene oxide was prepared by Hummer method, while copper oxide was prepared in the green way using (capparies spinosa) plant extract as a reducing agent, these oxides were diagnosed as well as the binary nanocomposite by several techniques including Fourier Transform Infrared Spectroscopy (FTIR), X-rays diffraction , and field Emission scanning electron microscopy (FESEM), after that the superimposed (GO/CuO) was used to adsorbent the orange G dye ( Orange - G) from its aqueous solutions, A number of factors affecting adsorption were studied (equilibrium time, surface weight, pH, concentration effect, temperature). The results showed that the ideal time for adsorption of the orange dye (orange-G) on the surface of the nanocomposite (GO/CuO) was (30min), the best ideal weight for dye removal was (0.05gm), the best concentration was (20ppm), and the best acid function was (pH=2). After that, the adsorption kinetics were also studied by applying the pseudo first and second order of adsorption. The results showed that the adsorption process follows the false second-order kinetics. The thermodynamic functions of the removal process were also studied, and it was found that the value of (DH) is negative for the surface of the composite (GO/CuO) with dye. Meaning the adsorption process is exothermic, and that the DG0 has negative value, meaning that the adsorption processes occur spontaneously. positive DS0 values indicate that the molecules are becoming less bound

Effect of substrate temperature on In2S3 thin films using nebulizer spray pyrolysis method for photodetector applications

In this work, Indium Sulfide (In2S3) thin films were prepared using an economical nebulizer spray pyrolysis technique by various substrate temperatures from 250 °C to 375 °C in steps of 25 °C to evaluate their photo sensing properties. X-ray diffraction (XRD) patterns confirm the presence of In2S3 with face centered cubic structure for all substrate temperatures. The densely packed small spherical grain-sized particles were observed for In2S3 films deposited at 350 °C using Field emission scanning electron microscope (FESEM) analysis. The optical bandgap values were decreased from 3.16 eV to 2.28 eV, with increment in coating temperatures from 250 °C to 350 °C. The high intensity Photoluminescence (PL) peak is observed at 480 nm for the film coated at 350 °C is due to higher rate of electron–hole pair recombination. The photo sensing analysis revealed that the In2S3 thin films deposited at 350 °C, has the maximum responsivity (R) of 9.09 × 10−2 A W−1, detectivity (D*) of 8.25 × 1010 Jones, and external quantum efficiency (EQE) of 21.2%. Increasing the substrate temperature results in a significant enhancement of photo sensing characteristics.

Development of cellulose-supported Pd-nanocatalyst for the heck coupling and michael addition reactions

The development of reusable, bio-resource based nanocatalysts with high turnover numbers (TONs) is essential for increased sustainability in the chemical sector. Herein, cellulose-supported bio-resourced poly(hydroxamic acid) is employed as a ligand in the synthesis of a palladium nanocomposite (PdNc-PHA) that exhibits higher TONs that previously reported similar systems for the Mizoroki-Heck and Michael addition reactions. The PdNc-PHA catalyst was characterised using Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectrometry (EDX), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) analyses. Results showed that the PdNc-PHA catalyst exhibits excellent durability and high catalytic activity in the Mizoroki-Heck and Michael addition reactions, leading to high yields of the desired corresponding products. The Mizoroki-Heck reaction of aryl/heteroaryl chlorides with olefins resulted in the production of cross-coupled products, while the Michael addition reaction of phenol/thiophenol and aliphatic cyclic/alicyclic amines with a variety of olefins synthesised the corresponding O-, S-, and N-alkylated products. The recycle and reusability of the catalyst were tested using 4-nitrochlorobenzene and butyl acrylate. The results demonstrated that the catalyst maintained its catalytic activity effectively for up to ten cycles without any noticeable loss in performance. This research represents a promising strategy for efficient catalysis based on bio-waste as a wealth material.

Photocatalyst immobilisation on cylindrical surface: Scale-up potential of continuous photocatalytic reactor

The use of continuous photocatalytic reactor is important for sustainable water treatment technology. Photocatalyst immobilisation on supports (of varying shapes and sizes) having the desired degree of uniformity and smoothness is challenging, and is evolving. The major concerns are the geometry of the surface (which restricts the scalability of such systems) and the appropriate adhesion of the photocatalyst. Flat surface has an inherent limitation of low photocatalyst area per floor space, and poor light distribution, whereas cylindrical surfaces can overcome all these limitations. In this work, we have developed and assessed the photocatalyst coating methodology over cylindrical (quartz) surface and have prepared a modular (continuous) photocatalytic reactor. We have immobilised titanium-dioxide on the outer surface of a cylindrical quartz tube using a rotating (coating) mechanism, using the viscous sol prepared from the sol-gel method followed by heat treatment, and not with any binder to the as-synthesized powder. Various characterization techniques, including ultraviolet-diffuse reflectance spectroscopy, energy-dispersive spectroscopy, x-ray diffraction, field-emission scanning electron microscopy, optical surface profilometry, and ultraviolet–visible spectroscopy, are used to evaluate the impact of process conditions – number of layers, rotational speed, and sol viscosity, on the coating uniformity, smoothness, and layer thickness. The performance of the custom-made (modular-type) reactor is evaluated for degradation of the model molecule (pollutant). The reactor performance and capacity can be easily scaled up by parallel connections or introducing multiple coated tubes (to increase the photocatalyst area). The outcome of the work will be of immense value in scaling up the continuous large scale photocatalytic operation and treatment process.

Synthesis, structure, I–V characteristics, and optical properties of chromium oxide thin films for optoelectronic applications

Abstract Improving coating technology and thin film formation by optimizing the experimental parameters has become essential for various industrial and technological fields. This work aims to study the influence of the precursor materials on the physical and electro-optical properties of Cr2O3 thin films. The solutions were prepared using the sol–gel route and deposited on glass slides using the spin coating technique. The structure and morphology of the films were studied using XRD, FT-infrared (IR), and field-emission scan-electron microscope. The results indicated the formation of a high-purity Cr2O3 (Eskolaite) phase in the form of spherical nanoparticles with sizes of 17–25 nm. Three bands appear at 490, 765, and 889 cm − 1 {{\rm{cm}}}^{-1} in the FTIR spectra, which are attributed to Cr – O {\rm{Cr}}{\rm{\mbox{--}}}{\rm{O}} / Cr ═ O {\rm{Cr}}{\rm{═}}{\rm{O}} vibrations. The I–V curves showed linear behavior and good ohmic features. Ultraviolet-visible-near infrared spectra showed that the films are highly transparent, with band gaps in the range of 2.60–2.90 eV, and refractive indices in the range of 1.92–2.25. The sheet resistances, the new figure of merit, the real and fictional dielectric constants, and the optical conductivity were discussed. The Cr2O3 thin films are the best candidates for various utilizations, including solar cells, sensors in the IR region, and energy storage.

Low magnetic field alignment of carbon fibers in a polymer matrix for high-performance thermal interface materials

Carbon-based materials like carbon nanotubes, graphene nanoplatelets, graphite, and carbon fibers (CF) are highly promising fillers for enhancing the thermal conductivity of thermal interface materials (TIMs) due to their high thermal conductivity and low thermal expansion. Aligning these fillers can further improve thermal conductivity, but current alignment methods using high magnetic fields are impractical for industrial use. In this study, we investigated the enhancement of the thermal conductivity of CF–polymer composites by aligning CF fillers with a low magnetic field. We observed up to 17 times enhancement of the thermal conductivity (from 3.1 to 52.8 W/mK) in a CF–graphene–polymer composite film by vertically aligning the CF fillers with a magnetic field of 0.75 T. The analysis of the structural properties of the films using X-ray diffraction and field-emission scanning electron microscopy imaging confirmed that the crystalline c-axis of the graphite plates in the CF was oriented perpendicular to the magnetic field direction. The large anisotropy in the diamagnetic susceptibility of the laminated graphene structure of the CF flakes is at the origin of the filler alignment. Furthermore, the thermal conductivity of the composites showed a strong correlation with the degree of filler alignment, which was dependent on the CF–graphene hybridization and the type of polymer matrix. This study provides a scalable and cost-effective method for enhancing the physical properties of carbon composites by controlling their microarchitecture using a low magnetic field.

Green Synthesis and Characterization of Apple Peel‐Derived Selenium Nanoparticles for Anti‐Fungal Activity and Effects of MexA Gene Expression on Efflux Pumps in Acinetobacter baumannii

ABSTRACTSelenium nanoparticles (Se‐NPs) were produced adopting an environmentally benign green synthetic approach from the waste biomaterial obtained from the apple peel extract (APE). The produced NPs were characterized through UV–Visible spectroscopy (UV–Vis), atomic force microscopy (AFM), Fourier‐transform infrared spectroscopy (FT‐IR), X‐ray diffraction (XRD), field emission‐scanning electron microscopy (FE‐SEM), and transmission electron microscopy (TEM). The UV–Visible spectra exhibited the absorption peak λmax at 295 nm, confirming the formation of Se‐NPs. The AFM examination revealed the roughness and distribution of the nanoparticles, and FT‐IR ascertained the surface‐contained functional groups presence. The XRD confirmed the crystalline nature of the sample, and FE‐SEM validated the surface morphology and the size range of 52 to 84 nm. The TEM demonstrated the spherical shapes of the Se‐NPs with a face‐centered cubic crystal nature, whereas the size distribution analysis showed mean size of 70 nm. The minimum inhibitory concentration (MIC) at 500 μg mL−1 against Candida spp., namely, C. albicans, C. guilliermondii, and C. ciferrii, confirmed their anti‐fungal activity with the in control and minor statistical difference (p < 0.05) in the dissemination mean zones of inhibition for the Se‐NPs treatment against these fungi. The Se‐NPs effects on MexA gene expression demonstrated the efflux pump role in the anti‐fungal activity and gene's down regulation for the treated fungal strains. The Se‐NPs exhibited their anti‐fungal activity against the multi‐drug resistant microbes.

Synthesis and Characterization of Acacia-Stabilized Doxorubicin-Loaded Gold Nanoparticles for Breast Cancer Therapy.

The targeted delivery of drugs is vital in breast cancer treatment due to its ability to produce long-lasting therapeutic effects with minimal side effects. This study reports the successful development of doxorubicin hydrochloride (DOX)-loaded colloidal gold nanoparticles stabilized with acacia gum (AG). Optimization studies varied AG concentrations (0.25% to 3% w/v) to determine optimal conditions for nanoparticle synthesis. The resulting acacia stabilized gold nanoparticles (AGNPs) were characterized using various techniques including high-resolution transmission electron microscopy (HR-TEM), powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FE-SEM), and selected area electron diffraction (SAED). In vitro drug release studies demonstrated a higher release rate of DOX in sodium acetate buffer (pH 5.0) compared to phosphate buffer saline (pH 7.4), suggesting an enhanced therapeutic efficacy in acidic tumor environments. Cytotoxicity of DOX-AGNPs and free DOX was assessed in human breast cancer cells (MDA-MB-231). The DOX-AGNPs exhibited significantly greater cytotoxicity, indicating enhanced efficacy in targeting cancer cells. This enhancement suggests that adsorbing DOX on the surface of gold nanoparticles can improve drug delivery and effectiveness, potentially reducing side effects compared to pure DOX and traditional delivery methods. Stability tests conducted over six months at 25±1°C showed significant changes in particle size and PDI, suggesting limited stability under these conditions. Overall, the acacia-stabilized gold nanoparticles synthesized in this study exhibit promising characteristics for drug delivery applications, particularly in cancer therapy, with effective drug loading, controlled release, and favorable physicochemical properties.

Exposing graphene oxide’s function in enhancing dye sensitized solar cell efficiency

This study aims to explore the potential for increasing the efficiency of the Dye sensitized solar cells through the incorporation of graphene oxide into the titanium dioxide matrix. The presence of defects was observed by Raman spectra. The structural properties and crystallite size of TiO2, GO, and GO/TiO2 composite were investigated using X-ray diffraction analysis, whereas the changes in morphology of graphene oxide and GO/TiO2 were assessed by Field Emission Scanning Electron Microscopy. The presence of functional groups were analyzed by Fourier Transform Infrared Spectroscopy. UV-Visible spectroscopy revealed a reduction in optical bandgap from 3.25 eV for TiO2 to 2.89 eV for GO/TiO2 and optical conductivity were observed increasing from 5.49 × 107 S/cm to 1.19 × 108 S/cm. The efficiency of the fabricated DSSCs was determined through I-V measurement, which showed that the addition of 0.2 wt% of graphene oxide in TiO2 significantly increased the short-circuit current from 0.38 milliampere to 0.75 milliampere, fill factor from 0.71 to 0.82, resulting in a substantial efficiency improvement from 3.99% to 9.11%.

High Sensitivity Of Nanocrystalline SnO2-Y2O3 Thin Films Based UV-Detector Prepared Using Chemical Bath Deposition

Nanocrystalline Tin dioxide - Yttrium oxide (NC SnO2-Y2O3) thin film was effectively created by employing the chemical bath deposition approach on SiO2/Si substrates. X-ray diffraction, field emission scanning electron microscopy [FESEM], and energy-dispersive X-ray spectroscopy were used to analyze the structural and the surface morphology of the annealed sample at 500°C for two hours in air. When annealed at 500°C, the SnO2-Y2O3 film crystallized was accomplished with a tetragonal rutile structure. The nanocrystalline SnO2 thin film was effectively employed as a UV photodetector device (UV PDs). A UV photo detector based on nanocrystalline SnO2-Y2O3 film showed 2988% sensitivity when exposed to a 360 nm wavelength (6 mW/cm2) at an applied voltage of 3 V. In contrast, the responsivity value was 3.247 A/W. The rise and full times were determined by calculating to be 0.663 s and 0.436 s, respectively. The excellent performance of the device could be correlated with high surface-to-volume proportions including its elevated crystal performance. Given its outstanding stability and reliability, the nanocrystalline SnO2-Y2O3 thin film sensor is the optimum option for commercially photo-electronic applications.