Field Emission Scanning Electron Microscopy Images Research Articles

Improved water purification by PVDF ultrafiltration membrane modified with GO-PVA-NaAlg hydrogel

This work presents a modified polyvinylidene fluoride (PVDF) ultrafiltration membrane blended with graphene oxide-polyvinyl alcohol-sodium alginate (GO-PVA-NaAlg) hydrogel (HG) and polyvinylpyrrolidone (PVP) prepared by the immersion precipitation induced phase inversion approach. Characteristics of the membranes with different HG and PVP concentrations were analyzed by field emission scanning electron microscopy (FESEM), Atomic force microscopy (AFM), contact angle measurement (CA), and Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). The FESEM images showed an asymmetric structure of the fabricated membranes, and possessing a thin dense layer over the top and a layer finger-like. With increasing HG content, membrane surface roughness increases so that highest surface roughness for the membrane containing 1wt% HG is with a Ra value of 281.4 nm. Also, the contact angle of the membrane reaches from 82.5° in bare PVDF membrane to 65.1° in the membrane containing 1wt% HG. The influences of adding HG and PVP to the casting solution on pure water flux (PWF), hydrophilicity, anti-fouling ability, and dye rejection efficiency were evaluated. The highest water flux reached 103.2 L/m2 h at 3 bar for the modified PVDF membranes containing 0.3 wt% HG and 1.0wt% PVP. This membrane exhibited a rejection efficiency of higher than 92%, 95%, and 98% for Methyl Orange (MO), Conge Red (CR), and Bovine Serum Albumin (BSA), respectively. All nanocomposite membranes possessed a flux recovery ratio (FRR) higher than bare PVDF membranes, and the best anti-fouling performance of 90.1% was relevant to the membrane containing 0.3 wt% HG. The improved filtration performance of the HG-modified membranes was due to the enhanced hydrophilicity, porosity, mean pore size, and surface roughness after introducing HG.

Multi-susceptible single-phased hexaferrite with significant magnetic switching properties by selectively doping

An effective combustion technique is used to synthesize Sr0.8La0.2Fe12-xCuxO19 (x = 0,1) M-type strontium hexagonal ferrite nanoparticles (SHFNPs). The impact of La and La-Cu substitution on the structural, microstructural, and magnetic characteristics of SHFNPs is scrutinized. The samples are characterized using several experimental techniques, such as x-ray diffraction (XRD), Raman spectroscopy (RS), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), and vibrating sample magnetometer (VSM). The obtained results reveal that the single lattice structure of the substituted strontium hexaferrite can be acquired by transforming Fe3+ to Fe2+ on the 2a site. Raman spectroscopy (RS) verifies the formation of all crystallographic sites of hexaferrite. The broadening of 4f2 and 12k peaks indicates the presence of disorder at the crystal sites resulting from the change in the chemical environment after doping with Cu2+ ions. FESEM images reveal flat hexagonal facets of the particle that signify the magneto-plumbite structure. The magnetic results provide high values of both intrinsic coercivity and (BH)max. The obtained data constitute good magnetic characteristics for perpetual magnet applications. Furthermore, the reduced coercivity of the Sr0.8La0.2Fe11CuO19 (SLCHF) sample with high magnetizations can be used to create microwave absorbing and data storage materials.

Optical, structural, electrical and photocatalytic properties of aluminum doped zinc oxide nanostructures

The Al-doped ZnO (Zn1-xAlxO, x = 0.00, 0.02, 0.04, 0.06, and 0.08) nanostructures were synthesized by the chemical vapor deposition technique. Analysis by X-ray diffraction reveals that both undoped and Al-doped ZnO nanostructures are crystallized in a single-phase wurtzite structure with a preferred orientation along the (101) plane. The addition of Al was studied to see how it influenced bond length, crystallite size, unit cell volume, lattice strain, and dislocation density. Field-emission scanning electron microscope imaging showed a significant variation in the morphology with increasing the Al doping level. Absorption spectra in the UV–Visible range revealed that introducing Al3+ ions into the ZnO lattice causes a blue shift in the optical band gap, which was explained according to Burstein-Moss effect and variation of the electronic structure. The direct electrical conductivity measurement showed a transformation between two conduction mechanisms upon variation of the temperature. Transition of the charge carriers from shallow and deep donor levels dominated in the low and high temperature ranges, respectively. The photodegradation rate constants and degradation efficiency were determined as well as the photocatalytic mechanism was described. Upon reaching the x = 0.08 Al doping level, the photocatalytic efficiency of the examined samples increased by 1.7-fold. The obtained results demonstrate that Al doping can tune the electrical, optical, and photocatalytic properties of ZnO nanostructures that make them applicable for many optoelectronic applications.

Enhanced Thermal Stability of Sputtered TiN Thin Films for Their Applications as Diffusion Barriers against Copper Interconnect

In this work, the deposition of titanium nitride (TiN) thin film using direct current (DC) sputtering technique and its application as diffusion barriers against copper interconnect was presented. The deposited film was analyzed by using X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), and X-ray photoelectron spectroscopy (XPS) techniques. XRD patterns showed the face-centered cubic (FCC) structure for the TiN/SiO2/Si film, having (111) and (200) peaks and TiN (111), Cu(111), and Cu(200) peaks for Cu/TiN/SiO2/Si film. FESEM images revealed that the grains were homogeneously dispersed on the surface of the TiN film, having a finite size. XPS study showed that Ti2p doublet with peaks centered at 455.1 eV and 461.0 eV for TiN film was observed. Furthermore, the stoichiometry of the deposited TiN film was found to be 0.98. The sheet resistance of the TiN film was analyzed by using a four-point probe method, and the resistivity was calculated to be 11 μΩ cm. For the utilization, TiN film were tested for diffusion barrier performance against Cu interconnect. The results exhibited that TiN film has excellent performance in diffusion barrier for copper metallization up to a temperature of 700 °C. However, at a higher annealing temperature of 800 °C, the formation of Cu3Si and TiSi2 compounds were evident. Thus, stoichiometric TiN film with high thermal stability and low resistivity produced in this study could be applied for the fabrication of microelectronic devices.

Facile synthesis and characterization of Fe3O4/analcime nanocomposite for the efficient removal of Cu(II) and Cd(II) ions from aqueous media

In the water purification field, heavy metal pollution is a problem that causes severe risk aversion. This study aimed to examine the disposal of cadmium and copper ions from aqueous solutions by a novel Fe3O4/analcime nanocomposite. A field emission scanning electron microscope (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction were used to characterize the synthesized products. The FE-SEM images showed that the analcime and Fe3O4 samples consist of polyhedral and quasi-spherical shapes with average diameters of 923.28 and 28.57 nm, respectively. Besides, the Fe3O4/analcime nanocomposite consists of polyhedral and quasi-spherical shapes with average diameters of 1100.00 nm. The greatest uptake capability of the Fe3O4/analcime nanocomposite toward the copper and cadmium ions is 176.68 and 203.67 mg/g, respectively. The pseudo-second-order kinetic model and Langmuir equilibrium isotherm best describe the uptake of copper and cadmium ions using the Fe3O4/analcime nanocomposite. The uptake of copper and cadmium ions using the Fe3O4/analcime nanocomposite is exothermic and chemical in nature.

Photocatalytic Denitrification of Nitrate Using Fe-TiO2-Coated Clay Filters

In this work, 3D-structured clay filters were prepared and coated with iron-doped titanium dioxide (Fe-TiO2) using 3D printing and sol–gel soaking and calcination techniques. Three-dimensional printing was employed to mold and shape the clay filters before annealing. The coated and uncoated filters were characterized for different properties, i.e., morphology, optical properties, and crystalline structure, using field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), UV/Vis diffused reflectance spectroscopy (DRS), and X-ray diffraction (XRD). The FESEM images show uniform coatings of round-shaped Fe-TiO2 on the tiny pore of the clay filter. The optical energy band gap of the obtained coating was around 2.8 eV, estimated by Tauc’s plot, compared with 3.2 eV of pristine anatase TiO2. The XRD spectra data processed through XRD software revealed the coatings of TiO2 on the filter surface with the obtained phase of anatase. The photocatalytic performance of bare and coated filters was initially tested for the degradation of indigo carmine (IC) dye and the obtained results suggested the photocatalytic degradation of IC dye by the Fe-TiO2 clay filter compared with the bare filter. Afterward, the denitrification of nitrate NO3 at various concentrations was performed using Fe-TiO2-coated clay filters and analyzing the total nitrogen (TN) analysis and reduction of NO3 to nitrite (NO2−), nitrogen monoxide (NO), and nitrogen gas (N2). The TN analysis revealed up to 81% denitrification efficiency of the 30 ppm NO3 solution with the photocatalytic response of the Fe-TiO2-coated filter. The results revealed that the Fe-TiO2-coated clay filter has a high potential for denitrification applications under natural sunlight.

Preparation and characterization of titania supported on layered double hydroxide precipitated on glass fiber cloth

Support of titania nanoparticles on platy particles of a layered double hydroxide (LDH) on glass fiber cloth (GFC) is demonstrated. MgAl-LDH was deposited onto the GFC surface via homogenous precipitation using urea hydrolysis in the presence of GFC. X-ray diffraction (XRD) patterns, field-emission scanning electron microscopy (FE-SEM) images, and elemental analyses revealed that MgAl-LDH platy particles were deposited and vertically aligned on the GFC surfaces, forming MgAl-LDH-coated GFC. The resultant specimen was soaked in a water dispersion of P25 standard, a well-known titania photocatalyst, for 5 min at room temperature and then extensively washed with an excess of water. The presence of P25 nanoparticles on the MgAl-LDH platy particles on GFC surfaces was evidenced by FE-SEM imaging, elemental analyses, and MB decomposition experiments in which an MB solution showed a greater decrease in concentration under 365 nm irradiation in the presence of the supported P25 than in the presence of MgAl-LDH-coated GFC and GFC subjected to the P25 deposition procedure without MgAl-LDH deposition. In addition, FE-SEM images and elemental analysis of the supported P25 specimen showed only small differences before and after the MB experiment. Therefore, the results mentioned above show the facile support of P25 on MgAl-LDH supported on a GFC surface.

Optical and structural properties of H-BN@Gd2O3 nanoflake prepared by laser–induced ablation in liquid

In this paper, we reported the synthesis of hexagonal BN, Gd2O3 nanoparticles, and BN@Gd2O3 hybrid nanocomposites by novel laser ablation in liquid. Several analytical techniques including x-ray diffraction (XRD), UV–vis spectroscopy, Fluorescence spectroscopy, Field Emission Scanning electron Microscopy (FE-SEM) with Energy dispersive spectroscopy (EDS), High-resolution transmission electron microscope (HR-TEM), and map imaging were used to investigate the structural and optical properties of synthesized nanoparticles. According to FE-SEM and TEM results, FE-SEM images show the formation of h-BN NPs, sheet-like, and spherical nanoparticles, hexagonal-type nanoflake of Gd2O3, and needle-like shapes. High-resolution transmission electron microscopy images confirm that the average diameter of all samples is ∼40 nm. However, the length of the nanorods is found to vary from 50 nm to 240 nm. The optical properties studies show that the optical energy gap of h-BN, Gd2O3, and h-BN@Gd2O3 is in the range of (4.5–5.5) eV.

Investigation of the metal–semiconductor interface by equivalent circuit model in zinc phthalocyanine (ZnPc) based Schottky diodes and its charge transport properties

In this report, the ZnPc-based metal–semiconductor (MS) junction Schottky devices (Al/ZnPc/ITO) were fabricated using an effusion cell coating unit. To study the formation of the MS junction, the surface morphology of the deposited ZnPc thin film was investigated using field-emission scanning electron microscope (FESEM) images. The interfacial properties of the MS junction of the Al/ZnPc/ITO configuration were studied using the ac impedance spectroscopy technique within the frequency range of 50 Hz–10 MHz at room temperature (300 K). The bias-dependent impedance spectroscopy was carried out within the voltage range of ±1 V to establish the equivalent circuit of the MS junction Schottky diodes (SDs). The current vs. voltage (I-V) measurements of the fabricated SDs were also conducted to deduce the diode parameters, namely on/off ratio, photosensitivity, ideality factor, barrier height, and series resistance. The charge transport parameters including dc conductivity, mobility and transit time of the charge carriers were also estimated employing the spatial-charge limited current (SCLC) theory, which illustrates the enhanced carrier’s mobility and consequently, the device performance after light irradiation.

Marble waste reinforced composite with tunable physico-mechanical and thermal properties: micromechanical simulation assisted experimental investigation

ABSTRACT This paper investigates the development of waste marble dust-reinforced particulate composites through an integrated approach of investigation. Samples of marble-epoxy composites were prepared with systematic variations in filler content to achieve tunable mechanical, physical, and thermal properties. Increasing ceramic filler's loading level resulted in superior properties of composite samples, as demonstrated by macroscale characterization such as compressive and flexural strength. Microstructural characterizations such as Fourier transform infrared spectroscopy (FT-IR), Field emission scanning electron microscopy (FE-SEM), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) analysis were used to better understand the results. FT-IR results indicate chemical linkages forming between the epoxy resin and marble dust in the composite, while FE-SEM images suggest strong interfacial bonding between filler and matrix. TGA analysis shows enhancement of thermal properties with increasing filler content, while XRD indicates enhancement of crystallinity. Micro-mechanical modeling using the representative volume element (RVE) approach was also carried out using a commercial simulation package, determining Young’s modulus and comparing it with experimental results.

Light and scanning electron microscopy of aecia and aeciospores of Cronartium ribicola on Pinus koraiensis branch tissues

Morphological characteristics of aecia and aeciospores of Cronartium ribicola on Pinus koraiensis branch tissues were investigated using light and field emission scanning electron microscopy (FESEM). Mature P. koraiensis trees in Jeongseon, Korea, showed yellowish aecia on stems and branches. Aecia and surrounding tissues were excised from the lesions and vapor-fixed for FESEM imaging, which revealed morphology including intact blister-shaped, flattened, and burst forms. Light microscopy revealed yellowish aeciospores having surface projections. Aeciospores were mostly ovoid and measured approximately 20 µm long. The FESEM showed irregularly shaped cracks on the aecia that had erupted through the bark of P. koraiensis. Some aeciospores had germinated, producing two germ tubes from a spore in a burst aecium. Aeciospores had both smooth and verrucose regions on the surface, and some had concave or convex regions. Aeciospore layers and underlying fungal matrices including aecial columns were obvious in the cross-sections of aecia. Approximately 1 µm-high wart-like surface projections could be resolved and comprised less than 10 angular platelets stacked in vertical rows. Remains of the primary spore wall were present between surface projections. These results provide insights into the morphology of the heteroecious rust fungus with the help of vapor fixation and high-resolution surface imaging.

CdO Nanostructures: Synthesis, Characterization, and Photocatalytic Degradation of Malachite Green Dye in Aqueous Media

Cadmium oxide (CdO) nanoparticles were prepared by using co-precipitation method and applied on photodegradation of malachite green (MG) dye in an aqueous solution. The as-prepared CdO nanoparticles were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), High-resolution transmission electron microscopy (HR-TEM) and (SAED), and Fourier transform infrared (FTIR) techniques. The XRD pattern confirmed the formation of crystalline CdO nanoparticles with cubic structure while the FESEM image validated the preparation of disc-like spherical irregular shape nanostructures agglomerated with the size of 10-30 nm. The as- prepared CdO nanoparticles exhibited 98 % photodegradation efficiency against the MG dye in 165 min of visible light irradiation at 0.05 g of dose. The experimental data has followed the pseudo-first-order kinetic model, and the rate constant value obtained is 0.002 min-1. Thus, the synthesized CdO nanoparticles degraded MG dye effectively and may be used for environmental remediation purposes.

PbS quantum dots-sensitized ZnO nanorods-based third generation solar cells

PbS quantum dots (QDs) and PbS QDs-sensitized ZnO nanostructures of rod-like shape have been synthesized by the successive ionic layer adsorption and reaction method. The optical absorption spectra PbS QDs indicate that the prepared sample exhibits significant visible light absorption. The light absorption of PbS QDs-sensitized ZnO nanorods (NRs) was higher than bare ZnO NRs. X-ray diffraction pattern of PbS QDs exhibits diffraction peaks corresponding to (200), (112), and (202) planes of PbS. A Uniform development of ZnO nanostructures of rod-like shape and the PbS QDs deposition over its surface was witnessed from the field-emission scanning electron microscope and transmission electron microscope images. The small ring pattern confirming the polycrystalline nature of the prepared PbS thin film was observed from the selected area electron diffraction pattern. Solar cells were made using PbS QDs-sensitized ZnO NRs as photoanodes and it exhibited a power conversion efficiency of 1.2%.

Back to the Basics: Probing the Role of Surfaces in the Experimentally Observed Morphological Evolution of ZnO.

Although the physics and chemistry of materials are driven by exposed surfaces in the morphology, they are fleeting, making them inherently challenging to study experimentally. The rational design of their morphology and delivery in a synthesis process remains complex because of the numerous kinetic parameters that involve the effective shocks of atoms or clusters, which end up leading to the formation of different morphologies. Herein, we combined functional density theory calculations of the surface energies of ZnO and the Wulff construction to develop a simple computational model capable of predicting its available morphologies in an attempt to guide the search for images obtained by field-emission scanning electron microscopy (FE-SEM). The figures in this morphology map agree with the experimental FE-SEM images. The mechanism of this computational model is as follows: when the model is used, a reaction pathway is designed to find a given morphology and the ideal step height in the whole morphology map in the practical experiment. This concept article provides a practical tool to understand, at the atomic level, the routes for the morphological evolution observed in experiments as well as their correlation with changes in the properties of materials based solely on theoretical calculations. The findings presented herein not only explain the occurrence of changes during the synthesis (with targeted reaction characteristics that underpin an essential structure-function relationship) but also offer deep insights into how to enhance the efficiency of other metal-oxide-based materials via matching.

Eco-Friendly Synthesis of Ni/NiO Nanoparticles Using Gymnema sylvestre Leaves Extract for Antifungal Activity

The invention of an easy synthetic approach for extremely impactful nanomaterials (NMs) is one of the crucial research areas in modern science and engineering. In the present work, we describe a cost-effective, simple, rapid and environmentally gracious biogenic fabrication of nickel/nickel oxide nanoparticles (Ni/NiO NPs) using Gymnema sylvestre as a natural fuel. The textural characteristics of as-prepared Ni/NiO NPs were explored using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), diffuse reflectance spectra (DRS), photoluminescence spectroscopy (PL), field-emission scanning electron microscope (FESEM), energy dispersive X-ray analysis (EDX), and high-resolution transmission electron microscopy (HRTEM). XRD affirmed the crystalline nature and phase formation of Ni/NiO NPs. The FTIR spectrum ascertains the formation of Ni/NiO NPs, and the band gap of 4.29 eV is revealed from DRS studies. Ni/NiO NPs display an intense emission peak at 576.2 nm in their PL spectrum. The fabrication of pseudo-spherical Ni/NiO NPs was displayed by FESEM and HRTEM images. The particle size obtained from HRTEM was 21 nm, which resembles the median crystallite size ascertained from the XRD data. Additionally, the plausible mechanism for Ni/NiO NPs formation is illustrated. Moreover, as-synthesized Ni/NiO NPs displayed considerable antifungal potential against Candida albicans and Aspergillus niger. Results revealed that the Gymnema sylvestre leaves extract can synthesize Ni/NiO NPs with appealing biological effectiveness for application in the nanomedicine sector.

A Biophysical Research on the Determination of Morphological and Structural Properties of Coumarin-Loaded Liposomes

The major goal of this research was to examine how coumarin affects lipid model membranes. For this reason, liposome membranes were formed using dimyristoyl phosphatidylcholine (DMPC) as zwitterionic lipid. The influence of coumarin on the morphology, packing order, fluidity, and hydration state of lipid membranes was specifically investigated by means of microscopic (field emission scanning electron microscopy (FE-SEM)) and spectroscopic (attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy) techniques. Taken into account the results obtained with FE-SEM images and analysis, liposomes without and with coumarin have uniform structures and spherical shapes in appearance. However, coumarin-loaded liposomes are observed with an increase in size when compared to a mean diameter of unloaded-liposomes. Considering ATR-FTIR analysis, the investigation of the vibrational bands which belong to the hydrophobic and hydrophilic parts of DMPC lipid reveals that coumarin alters the physical features of the DMPC liposomes by decreasing the order and increasing the fluidity of the system and making hydrogen bonding with the interfacial and headgroup regions of zwitterionic lipid DMPC. Finally, performing more biophysical studies on the interactions of biologically active compounds with model membranes plays an important role in determining the molecular action mechanisms of these compounds in drug discovery and formulations.

Fabricating Antibacterial Polyethylene Terephthalate Substrates Through an Industrial Approach by Applying Emulsions of Copper-Based Nanoparticles

In this research, various emulsions of copper-based nanoparticles were synthesized through the chemical reduction method followed by utilizing the pad–dry–cure technique as an industrial approach to manufacturing bactericidal polyethylene terephthalate (PET) substrates. Copper sulfate/copper acetate, sodium hypophosphite (SHP)/ascorbic acid, and cetyltrimethylammonium bromide were employed as salts, reducing agents, and stabilizers, respectively. Also, a spin finish oil was used for forming an emulsion. The effects of type and amount of copper salt and reductant as well as the use of resin and stabilizer were investigated concerning antibacterial activities, weight, and color changes of coated samples to find optimum formulation. Field-emission scanning electron microscope (FESEM) images, mapping/energy-dispersive spectroscopy (EDX), X-ray diffraction (XRD) pattern, Raman spectroscopy, and UV–visible spectrophotometer was proved successful in synthesis and loading of copper-based emulsions on the PET substrates. The results revealed that change of copper salt, substituting SHP with ascorbic acid, the addition of resin, and the use of surfactant yielded negligible effect, enhancing impact, reducing the influence, and improving efficacy on bactericidal characteristics of the treated samples, respectively. Based on findings, the samples coated by emulsion containing only copper sulfate/SHP and emulsion including only copper acetate were considered optimum samples indicating 100% bactericidal properties against both S. aureus and E. coli pathogenic bacteria. Despite showing bactericidal activities, it was further found that the treated samples exhibited cell toxicity toward human skin cells implying their applications in indirect contact usages. Coated samples further indicated a good washing fastness even after 20 washing cycles. This route can be considered as a facile industrially applicable method for imparting bactericidal properties to polymeric substrates. Furthermore, such emulsions can potentially be consumed as an antibacterial spin finish oil in melt-spinning to develop antibacterial textiles.

Photocatalytic Degradation of Methyl blue by TiO2 Nanoparticles Incorporated in Cement

In this study, titanium dioxide (TiO2) nanoparticles incorporated with cement were synthesis by a simple casting method as a function concentration of TiO2 (0.2, 0.4, 0.8, 1, and 2 wt%). The prepared samples were characterized using the technique of Field Emission Scanning Electron Microscope (FESEM) and UV-Visible spectrophotometer, which was used to measure the adsorption spectra. The observed photocatalytic efficiency of TiO2 nanoparticles (NP) incorporated with cement was investigated by decomposing the dye methyl blue (MB) solution under sunlight irradiation. According to the slope, the value of the k constant at the best sample is 0.8wt%, k=0.8265 min-1. FESEM image of the TiO2/cement with 0.8 wt% content show the TiO2 NPs were well-attached to cement particles, and they covered the cement surface. The increase in photocatalytic (PC) activity was due to an increase of TiO2 concentration in the cement, which best occur of 0.8 wt% of TiO2 in cement. The degradation at the MB (5ppm) was 98.864 % after 120 min under sunlight irradiation. The method involves easily and simply preparing TiO2/cement that is used in self-cleaning and studying the effect of different festive factors, including the concentration of the dye. The preparation of TiO2/cement was successful as a photocatalyst for a self-cleaning surface.

Influence of Mg2+ and Ce3+ substituted on synthesis, structural, morphological, electrical, and magnetic properties of cobalt nano ferrites

Mg2+ and Ce3+ doped Cobalt ferrites Co1-xMgxFe2-yCeyO4 (x = 0.0, 0.25, 0.5 and 0.75; y = 0.0, 0.03, 0.06, and 0.09) were synthesized chemically through the sol-gel auto combustion method. The structural analysis was done using X-ray diffraction (XRD) analysis, Field Emission Scanning Electron Microscopy (FESEM), and Fourier Transform Infrared Spectroscopy (FTIR) analysis. XRD study showed the ferrite’s formation of spinel cubic structure. The outcomes of FESEM images show that the particles are homogenous with minor agglomeration. The formation of peak ϑ 1 around 600 cm-1 and ϑ 2 around 400 cm-1 is shown by FTIR, confirming the formation of the spinel structure. High dopant concentrations result in increased DC electrical resistance. High-resistance materials with a decreased dielectric constant and loss are obtained by substituting Mg2+ and Ce3+ cations at the Co2+ and Fe3+ sites. These materials are suited for high-frequency devices. Additionally, it was observed that the AC conductivity was dispersed across the applied frequency ranges and exhibited a lower value than the parent material. The effect of the substituted on magnetic studies was examined systematically using a VSM at a temperature in the room. The magnetization measurements show that the synthesized contents increases, magnetization values decrease, and coercivity increases.

Biosynthesis of pure and MnSO4 (II) doped CeO2 nanoparticles: Electrochemical studies and its antibacterial activity

Cerium oxide (Nanoceria) nanoparticles were synthesized by green synthesis method using Manganese Sulphate (MnSO4)as a dopant with various concentrations. Different physicochemical methods were used to analyse the nanoparticles, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Field emission scanning electron microscopy (FE-SEM), Energy dispersive X-ray analysis (EDAX), UV–Visible spectrophotometer (UV–Vis), and Photoluminescence (PL) investigations for optical activity. The cubic fluorite structures of the CeO2 nanoparticles were determined by XRD with a typical crystallite size of 18 nm for undoped CeO2 and 12 nm for MnSO4/CeO2. FTIR spectroscopy analysis the presence of CeO2 phase by examining structural bond vibrations with intense bands. FE-SEM images divulges the prepared nanoparticles have a cubic structure and are uniformly allocated with small clusters. The optical activity of the synthesised sample was evaluated, and it reveals UV absorption from 200 to 1200 nm. The band value was estimated using the optical spectrum. While PL Studies reveals a broad intensity peak at 340 nm with increase in doping concentration. Furthermore, the aim of the present study is capacitive characteristics were analysed by Cyclic voltammetry (CV) which deliver prominent capacitance value of 479 F/g at a scan rate 10 mV/s. Antibacterial activity of MnSO4/CeO2 nanoparticles have also been demonstrated against E. coli and Enterobacter (gram. −ve) bacteria were comparatively subjected than Bacillus subtilis (gram +ve) pathogenic bacteria.