X-ray Diffraction Patterns Research Articles

Novel Syntheses of Wide-Band Gap Semiconducting CdxZnx−1Co2O4 of Spinel Nanostructure: Characterization and Optical Properties

AbstractCadmium doped zinc cobaltite spinel structure in the form of CdxZnx-1Co2O4 (0 ≤ x ≤ 1) are synthesized by sol-gel method. The energy dispersive X-ray spectra confirm the synthesis of pure ZnCo2O4 and Cd doped samples nanoparticles. Scanning and transmission electron microscopes images of Cd ZnCo2O4 samples show the cubic crystal structure of the nanoparticles. A good crystallinity of the ZnCo2O4 and its dopants samples are indicated by the sharpness and strong peaks of X-ray diffraction patterns. The particle size is independent of the ratio of incorporated Cd into the ZnCo2O4 matrix. The FT-IR transmission spectrum of each Cdx Zn1-xCo2O4 complex shows two strong vibration peaks that are ascribed to the spinel structure’s octahedral and tetrahedral. The absorption spectra reveal three distinct absorption characteristics for Cdx Znx-1Co2O4 peaking at 268, 532 and 778 nm due to the photoexcitation of electrons from O 2p to Co 3d transitions and d-d transition of Co 3d. N2 adsorption–desorption isotherms for Cdx Znx-1Co2O4 indicate are carried out.

Comparison of ZnO Nanoparticles Prepared by Spray Pyrolysis and Consecutive Method for UV-Driven Photocatalytic Degradation of Methylene Blue

ZnO is a semiconductor material that is widely used for many applications in industries such as solar cells, dye-sensitized solar cells, food packaging, photocatalytic, anti-microbial, light-emitting diode devices, and gas sensors. In this study, ZnO nanoparticles (NPs) have been successfully synthesized using two methods, namely spray pyrolysis and a consecutive method. The consecutive method is a combination of sol-gel and spray drying methods. The objective of this study is to investigate the photocatalytic performance of ZnO fabricated using those methods. Both methods used the same precursor, zinc acetate dehydrate as a source of zinc, but with different solvents and additives. Based on the X-ray diffraction pattern, the ZnO NPs synthesized using spray pyrolysis and a consecutive method exhibited similar polycrystalline hexagonal wurtzite structures. The large crystal sizes of ZnO NPs were obtained using a consecutive method, sol-gel followed by spray drying, in comparison with those from the ZnO spray pyrolysis. In contrast, the particle size of ZnO prepared by the consecutive method was in a smaller range. The SEM analysis implied that the ZnO structures had surface defects. In the UV-driven photocatalytic degradation of methylene blue, ZnO produced by the consecutive method exhibited slightly higher degradation performance than ZnO spray pyrolysis. This performance was attributed to the larger crystal size of ZnO NPs, which provided a longer carrier movement at semiconductor surfaces and reduced electron-hole recombination. Additionally, ZnO NPs produced using the consecutive method underwent agglomeration that leads to a smaller contact surface with methylene blue, obstructing the degradation process.

Effect of Annealing Temperature on the Structural Properties and Performance of ZnO/SnO<sub>2</sub> Nanostructure of AZO-Based Humidity Sensor

Advanced research in metal oxide-based nanotechnology has led to its broad applications, which include humidity sensors as well as electronic devices. Meanwhile, zinc oxide (ZnO)/tin oxide (SnO2) composite nanostructure has established a presence in many electronic devices, and their performance can be further enhanced by electrospraying at high annealing temperatures. This paper explores how annealing temperature influences the structural properties and performance of ZnO/SnO2 nanostructures in AZO-based humidity sensors. The ZnO/SnO2 nanostructures were fabricated on AZO glass utilising electrospraying and then subjected to annealing at various temperatures: 100°C, 200°C, 300°C, 400°C as well as 500°C. The structural characteristics of the synthesized films were analysed utilising Field-Emission Scanning Electron Microscopy (FESEM) as well as X-ray Diffraction (XRD). Additionally, the humidity sensing performance of the films was evaluated based on their response time, sensitivity as well as recovery time. Following the results, a higher annealing temperature resulted in smaller crystallites and smaller diameters within the 71.6–91.9 nm range. Besides, the XRD patterns demonstrate a shift in the (002) peaks towards a higher angle value with incremental annealing temperature. In terms of the humidity sensing performance, the sensitivity level increased with increasing annealing temperature, while the recovery period and response time were reduced. In summary, the annealing temperature significantly influenced the performance of the ZnO/SnO2 composite nanostructures, which recorded the best sensitivity of 173.10, 234 seconds response time, and 80 seconds recovery time after annealing at 500°C.

Combining graph deep learning and London dispersion interatomic potentials: A case study on pnictogen chalcohalides.

Machine-learning interatomic potential models based on graph neural network architectures have the potential to make atomistic materials modeling widely accessible due to their computational efficiency, scalability, and broad applicability. The training datasets for many such models are derived from density-functional theory calculations, typically using a semilocal exchange-correlation functional. As a result, long-range interactions such as London dispersion are often missing in these models. We investigate whether this missing component can be addressed by combining a graph deep learning potential with semiempirical dispersion models. We assess this combination by deriving the equations of state for layered pnictogen chalcohalides BiTeBr and BiTeI and performing crystal structure optimizations for a broader set of V-VI-VII compounds with various stoichiometries, many of which possess van der Waals gaps. We characterize the optimized crystal structures by calculating their x-ray diffraction patterns and radial distribution function histograms, which are also used to compute Earth mover's distances to quantify the dissimilarity between the optimized and corresponding experimental structures. We find that dispersion-corrected graph deep learning potentials generally (though not universally) provide a more realistic description of these compounds due to the inclusion of van der Waals attractions. In particular, their use results in systematic improvements in predicting not only the van der Waals gap but also the layer thickness in layered V-VI-VII compounds. Our results demonstrate that the combined potentials studied here, derived from a straightforward approach that neither requires fine-tuning the training nor refitting the potential parameters, can significantly improve the description of layered polar crystals.

Synergistic Integration of α-Ag2WO4 into PLA/PBAT for the Development of Electrospun Membranes: Advancing Structural Integrity and Antimicrobial Efficacy.

The rising resistance of various pathogens and the demand for materials that prevent infections drive the need to develop broad-spectrum antimicrobial membranes capable of combating a range of microorganisms, thereby enhancing safety in biomedical and industrial applications. Herein, we introduce a simple and efficient technique to engineer membranes composed of polylactic acid (PLA) and polybutylene adipate terephthalate (PBAT) biopolymers and α-Ag2WO4 particles using an electrospinning technique. The corresponding structural, thermal, mechanical, and antimicrobial properties were characterized. X-ray diffraction (XRD) patterns confirmed the integration of crystalline α-Ag2WO4 within the polymer matrix. Scanning electron microscopy (SEM) and Raman confocal microscopy revealed uniformly dispersed α-Ag2WO4 particles in the electrospun fibers, influencing their diameter and surface roughness. Thermal analysis indicated adjustments in the thermal stability and crystallinity of the composites with an increasing α-Ag2WO4 content. Dynamic mechanical analysis (DMA) highlighted variations in storage modulus and glass transition temperatures due to interactions between α-Ag2WO4 and polymer chains, with tensile tests showing an increase in elastic modulus and ultimate tensile strength as the α-Ag2WO4 content increased. Antimicrobial assessments revealed that PLA/PBAT membranes with α-Ag2WO4 showed pronounced antibacterial activity, forming inhibition halos across all samples against Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus, and Mycobacterium smegmatis (a surrogate for Mycobacterium tuberculosis). These membranes also exhibited potent antiviral activity against bacteriophage phi 6, a surrogate for SARS-CoV-2, suggesting potential applications in combating infections caused by enveloped viruses. The antimicrobial activities are attributed to the generation of reactive oxygen species (ROS) and the controlled release of Ag+ ions. This work underscores the multifaceted capabilities of α-Ag2WO4-enhanced PLA/PBAT membranes in combating bacterial and viral growth, where both durability and microbial resistance are critical. Taken together, our findings provide a solution for obtaining advanced materials to be applied in a wide range of industrial applications, such as filtration systems, food preservation, antimicrobial coatings, protective textiles, and cleaning products.

Structural, magnetic and dielectric properties in double perovskite La2-xScxCoMnO6 (x = 0.0, 0.1, and 0.2)

The effect of Sc doping on structural, magnetic, and dielectric properties of double perovskite La2CoMnO6 synthesized by solid-state method was investigated. Crystal structure of La2-xScxCoMnO6 (x = 0.0, 0.1, and 0.2) compounds confirmed through X-ray diffraction patterns (XRD). Rietveld refinement of the XRD revealed the monoclinic phase with P21/n space group and the structural properties such as lattice parameter, bond lengths, and bond angles were obtained. Field emission scanning electron microscopy images revealed a uniform grain distribution, and the grain size was increased with increasing Sc content. The elemental mapping confirms the stoichiometry of the compounds. The room temperature Raman spectra confirm the monoclinic crystal structure and reveal two broad peaks viz., Ag, and Bg which were attributed to specific vibrational modes within the (Co/Mn)O6 octahedra. Magnetic measurements show that Curie temperature (Tc1) decreases with Sc substitution of 206 K for x = 0.0–193 for x = 0.2 due to the Co2+-Mn4+ FM coupling and it follows Curie–Weiss law in the paramagnetic region. Impedance spectroscopy studies show that the conductivity in these materials is predominantly due to the intrinsic bulk grains.

Effect of anisotropy field on the resonance frequency and reflection loss shift characteristics of barium hexaferrite ceramics

Abstract For this study, a modified barium hexaferrite based microwave and radar absorbing material was used. Synthesis and characterization of BaFe(12-2x)(MnTi)xO19 (0.1 ≤ x ≤ 1.0) have been prepared by solid state reaction method. The X-ray diffraction patterns reveal that all samples only crystallized into M-type barium hexaferrite after calcination at 1200 °C. Surface morphology images show that the hexagonal flake-like particle is formed at the initial stages of the Mn-Ti substitution level. The magnetic properties measurement reveals that the variation of magnetization values may vary based on preferable site occupation of Mn4+-Ti2+ cations to replace Fe3+ cations. The significant decrease in field coercivity (Hc) from 3.18 kOe to 0.51 kOe with the increase of Mn-Ti substitution affected the lowering values of field anisotropy (Ha). The maximum reflection loss (RL) positions of BaFe(12-2x)(MnTi)xO19 compositional series are shifted to lower frequency range following the Ha trendlines. The maximum RL value equals to 98.42% microwave absorption at 10.5 GHz has been obtained in x = 1.0 (BaFe10Mn0.5Ti0.5O19) composition.

Synthesis and Characterization of Cu-Co Substituted Strontium Hexaferrite for Magnetic Applications

In this study, the structural and magnetic characterizations of a series of SrCoxCuxFe12-2xO19; 0.0 ≤ x ≤ 0.5 samples, which were produced by the conventional ceramic method, were carried out. The structure was examined by X-ray diffraction (XRD) technique and optical microscopy. A vibrating sample magnetometer (VSM) was used to characterize the ferrimagnetic properties. XRD patterns confirmed the presence of a single phase as Sr-hexaferrite while there were not any peaks of unreacted Fe2O3 phase. The densities varied between 92 – 98 %. XRD patterns of the Sr-hexaferrite samples were slightly modified because of the co-substitution of Cu-Co; however, the magnetic properties changed remarkably. The sample with Cu-Co of x = 0.1 content had the highest saturation magnetization (33.52 emu/g), remanence (19.74 emu/g), and coercivity (4.3 kOe). The synthesized magnetic samples were found to be suitable for the development of attractive ferrimagnetic properties for the current ferrite magnets.

NaW2S4 and RbxWS2: Alternative Sources for 2M-WS2 and 1T'-WS2 Monolayers.

With the recent strive to develop novel quantum materials, including two-dimensional nanosheets, alkali-layered intercalated materials have found a new purpose as starting materials for such compounds. Enriching the library of alkali materials, we present a solid-state synthesis for preparing NaW2S4 (P1̅, No. 2) and RbxWS2 (C2/m, No. 12). Solving their crystal structure from their powder X-ray diffraction patterns, we show that both materials are layered, the former being a slightly distorted version of the latter. We compare the two structures and find that the main difference is the interlayer spacing in the a-direction. We further show that, like their cousin, KxWS2, both compounds can be deintercalated with dilute acid to form superconducting 2M-WS2, with structural and property characterization showing similar behavior, regardless of the starting material. Lastly, we find that both materials can be exfoliated in the same manner as KxWS2 to form superconducting 1T'-WS2 monolayers. We describe an easy one-step method for preparing two new layered materials and, thus, provide more opportunities to access valuable superconducting materials.

Study of Pure and Mixed-Phase TiO2 Nanomaterials Synthesized via a Modified Solvothermal Method and Their Optical Properties

The modified-solvothermal method has been used to synthesize pure anatase and anatase-rutile mixed-phase TiO2 nanomaterials using titanium isopropoxide, sodium hydroxide, and triethylamine as primary sources with different calcination temperatures (500 °C and 700 °C). The effect of the precipitating agent, capping agent, and calcination temperatures on the properties, such as structural, morphological, and optical of the resultant nanomaterials has been investigated through several techniques including X-ray diffraction (XRD), Raman spectroscopy, Transmission electron microscopy (TEM), UV–Vis absorption spectroscopy, Scanning electron microscopy (SEM), selected area electron diffraction (SAED), and high-resolution transmission electron microscopy (HRTEM). XRD and Raman spectra confirmed the pure anatase and anatase-rutile mixed structures of the prepared nanomaterials at 500 °C and 700 °C. Furthermore, the Raman active modes confirmed the formation of TiO2. It is noticed that the crystallite size of the nanomaterials increased with increasing calcination temperature of the XRD pattern. The morphologies of the prepared samples were displayed using SEM and TEM micrographs, which are almost the same in shape (cubic and cubic rod mixed). The particle size increased with an increase in calcination temperature and was found to be between 10 and 20 nm, which is similar to the crystallite size. The lattice fringes (d) from HRTEM images are assigned to the XRD plane (101) and (110) plane of anatase and anatase-rutile TiO2, respectively. The SAED exhibited well crystalline nature and confirmed the polycrystalline nature of the prepared nanomaterials by the bright points and the ring patterns. The optical band gap decreased with an increase in temperature and the optical properties are affected by calcination temperature and triethylamine.

Variations in the optical and thermoelectric behavior of ZnCo2O4 nanostructures as a function of synthesis temperature

Zinc cobalt oxide nanostructures were synthesized by electrochemical deposition of zinccobalt alloy at various bath temperatures (15, 30, 45 and 60 ˚C) and its hydrothermal oxidation at 100 ˚C. X-ray diffraction pattern and Raman spectroscopy data reveals the formation of spinal structure of ZnCo2O4. Photoluminescence spectra of the samples exhibit broad peaks with a red shift in the emission energy. Diffused reflectance spectroscopy measured the band gap of the synthesized materials; band gap is 3.06, 3.03, 3.02 and 2.99 eV, for samples electrodeposited at 15, 30, 45 and 60 ˚C, respectively. Optical conductivity of synthesized materials decreases with increasing deposition layers while reflectance shows opposite trend. Thermoelectric set up measures the change in potential difference through synthesized materials when different temperatures are applied and an increment in potential were observed. Seebeck co-efficient and power factor are also studied as function of bath temperature.

Innovative dilute magnetic compositions for spin-electronics field: Room temperature ferromagnetism of Sr0.98Gd0.02Ti0.98X0.02O (X = Ru, Mn, Fe)

An interesting new dilute magnetic compositions have been synthesized by solid-state reaction from (Gd, Ru), (Gd, Mn) and (Gd, Fe) codoped SrTiO3 semiconductors. The X-ray diffraction (XRD) patterns of pure, (Gd, Ru), (Gd, Mn) and (Gd, Fe) codoped SrTiO3 samples verified the formation of cubic SrTiO3 structure. The morphological analysis using scanning electron microscope (SEM) showed that the addition of (Gd, Ru), (Gd, Mn) and (Gd, Fe) ions obviously effect on the grains size and shape of SrTiO3 powder. The band gap energy of SrTiO3 powder was found to be 3.22 eV, and when (Gd, Ru), (Gd, Mn) and (Gd, Fe) ions incorporated into its lattice a blue shift to 3.28, 3.29 and 3.295 eV were detected, respectively. The X-Ray photoelectron spectroscopy (XPS) analysis of (Gd, Mn) codoped SrTiO3 composition (best ferromagnetic sample) ruled out the presence of Gd and Mn metals and confirmed the existence of Gd3+ and Mn2+ oxidation states. The measured magnetic results indicated that (Gd, Ru), (Gd, Mn) and (Gd, Fe) dopants strongly advance the ferromagnetic nature of SrTiO3 structure. The H-M loop of (Gd, Mn) codoped SrTiO3 composition gives the best ferromagnetic order with detected saturation magnetization (MS), coercivity (HC) and retentivity (Mr) of 0.52 emu/g, 177 Oe and 0.054 emu/g, respectively. These outcomes established the promising room temperature ferromagnetic order of the fabricated compositions, especially Sr0.98Gd0.02Ti0.98Ru0.02O3 semiconductor for spin-electronics applications.

Multifunctional bacterium induced carbonate precipitation with low nitrogen effectively remediates cadmium polluted water

Microorganism Induced Carbonate Precipitation (MICP) has emerged as an efficacious approach to address the issue of cadmium (Cd) contamination in water bodies. However, the associated production of ammonium nitrogen (NH4+-N) poses a significant challenge to the MICP. To tackle this, our research has developed a novel bacterium (UN-1), with dual MICP and NH4+-N degradation capabilities. We have elucidated the biogeochemical pathways of Cd2+ precipitation and NH4+-N degradation, characterized the micromorphology, phase composition, and crystallization of the MICP products, and identified the key factors influencing the MICP reaction. Our findings indicate that The UN-1-mediated MICP effectively removes Cd2+ at concentrations below 20 mg/L, reducing NH4+-N levels to 50 mg/L within 120 h. The predominant strains in UN-1 are Sporosarcina (24.35 %), Bacillus (31.36 %), Tumebacillus (6.89 %), Nitrospira (11.09 %), and Alkaliphilus (8.16 %). The bacterium employs urea enzymes UreA, UreB, and UreC for urea hydrolysis, thereby facilitating carbonate production, while the degradation of NH4+-N is mediated by hydroxylamine oxidase (HAO), nitrite reductase (NIR), and nitrate reductase (NAR). The resultant MICP products after Cd2+ removal are irregular spherical minerals, 200–300 nm in diameter, exhibiting well-developed single-crystal structures and high crystallinity. Their X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) patterns align with the characteristics of cadmium carbonate (CdCO3) minerals. Optimal conditions for the UN-1-led MICP reaction are identified as a pH range of 5.0 to 9.0 and a temperature range of 20 to 40 °C, the dissolved oxygen (DO) concentration in the water does not significantly impact the MICP. Furthermore, the study demonstrates that NH4+-N concentrations can be maintained at low levels under most conditions. This research introduces an innovative solution to the NH4+-N by-product challenge during Cd removal via MICP, laying a solid theoretical foundation for the development of a rapid, efficient, and eco-friendly remediation technology for Cd-contaminated waters.

Comprehensive approach on La1-xPbxMnO3 (0.2 ≤ x ≤ 0.5) perovskites synthesized by solid state reaction technique

We have synthesized Pb concentrated La manganites La1-xPbxMnO3 (0.2 ≤ x ≤ 0.5) using solid state reaction route to investigate several physical properties such as structural, thermal, magnetic, electronic and elastic properties via both the experimental characterizations and the first principles calculations under the framework of density functional theory (DFT). The structures of the studied perovskites are examined by X-ray diffraction (XRD) pattern and also compared with the crystallographic data obtained by computations. The crystallization and formation of the studied phase of manganites are confirmed by analyzing the thermogravimetric (TG) curve. The temperature dependence of magnetization of all the samples exhibits a ferromagnetic metal phase with the Curie temperatures TC ranging from 334 to 338K. Although a metal-semiconductor transition is expected at around TC for the measurement of electrical resistivity with temperature but we observe semiconducting behavior because of the resistivity data started from room temperature. The calculated energy dispersion of all the manganites shows metallic conduction in conformity with the available experimental results. All the studied perovskites under investigation possess mechanical stability, malleability as well as anisotropy. The calculated Debye temperatures of all the Pb-doped La manganites show excellent correspondence with the other thermophysical parameters like melting point, phonon thermal conductivity and hardness as well.

One-pot synthesis of graphene nanosheets‑nickel cobalt LDHs nanocomposite for electrocatalysis of oxygen evolution reaction

Oxygen evolution reaction (OER) is known as a bottleneck for the overall water-splitting process due to its slow kinetics. In this regard, constructing a high-performance, cost-effective electrode material may act as a game changer. Here, a 2D/2D nanocomposite has prepared out of graphene nanosheets and nickel‑cobalt layered double hydroxide (NiCo LDH) by a simple solvothermal method. The 2D flower-like structures of NiCo LDH attached to graphene nanosheets have observed in field-emission scanning (FE-SEM) and transmission (TEM) electron microscopy images. The X-ray diffraction (XRD) patterns have revealed the formation of Ni(OH)2 and Co(OH)2 lattices along with hexagonal graphene crystals. X-ray energy dispersive spectroscopy (EDS) has noted the 2.2:1 ratio of nickel to cobalt in the graphene/NiCo LDH nanocomposite. X-ray elemental maps have shown the uniform distribution of elements in the sample, and the corresponding functional groups have observed in the Fourier-transform infrared (FTIR) and Raman spectra. X-ray photoelectron spectroscopy (XPS) has determined the coexistence of divalent and trivalent metals in the nanocomposite. The N2 adsorption-desorption study has shown signs of slit-shaped ion-accessible micro and mesopores with high specific surface area for the nanocomposite. It has benefited the ion diffusion process during the exposure of the modified electrode to the electrolyte. The graphene/NiCo LDH nanocomposite has provided the onset potential of 1.56 V, overpotential of 338 mV at 10 mA cm−2, Tafel slope of 69 mV dec−1, charge-transfer resistance (Rct) of 27 Ω, double layer capacitance (Cdl) of 24 μF, electrochemically surface area (ECSA) of 0.6 cm2, and roughness factor (RF) of 20. The electrode has maintained 98.3 % of its initial signal after 10 h continuous measurement at OER potential. This electrocatalytic activity refers to the sheet-like morphology, effective hydroxide ion transfer through interlayer spaces, enhanced conductivity, and high chemical stability achieved by a constructive synergy between graphene nanosheets and NiCo LDH.

HTXRD based lattice thermal expansion and specific heat capacity modelling of C15-Fe2Zr Laves phase

Crystallographic phase pure C15-Fe2Zr was obtained through arc melting technique. X-ray Diffraction (XRD), scanning electron microscope (FESEM) along with energy-dispersive X-ray analysis (EDS) and differential scanning calorimetry (DSC)were employed to study the single phase in Fe-33.3at.% Zr alloy. Rietveld refinement of the high-temperature XRD patterns (from 298K-873 K) revealed the average linear and volumetric coefficients of thermal expansion of the alloys as αai= 0.3643 × 10−5 K−1 and αVi = 1.0916 × 10−5 K−1, respectively. The experimental heat capacity and enthalpy increment of the C15-Fe2Zr phase from 310K to 890K was modelled employing Quasi-harmonic Debye Grüneisen theoretical modelling by identifying the vibrational, electronic, anharmonic and magnetic contributions. Curie temperature(~625K) was determined from the magnetic contribution of the heat capacity.

Preparation of ZnO nanoparticles from Juglans regia dry husk extract for biomedical applications

The worldwide problem of antibiotic resistance threatens public health, necessitating the search for antimicrobial agents that are not only effective against antibiotic-resistant bacteria but also harmless to the environment. Metal nanoparticles and their oxides are promising agents for battling antibiotic-resistant bacteria, and nanoparticles (NPs) of any size or form can be manufactured in high quality using low-cost and simple-to-follow processes that are friendly to theenvironment. The purpose of this study was to evaluate the antimicrobial activity of zinc oxide nanoparticles (ZnO NPs) that were synthesized using the extract of Juglans regia dried husk, a waste product. Extract components wereused as capping and reducing agents in reactions with zinc acetate salt. The properties of ZnO NPs were examined using Fourier-transform infrared spectroscopy (FTIR), UV–visible spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray diffraction (XRD). The antibacterial activity ZnO NPs against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, and Candida albicans, which were isolated from patients with urinary tract infection, was assessed using the agar well diffusion method.ZnO NPs produced using the aqueous extract of Juglans regia dried husk had a band gap of 3.5 eV, which was determined using UV–visible spectra in the wavelength range of 200–1100 nm. The FTIR spectra of ZnO NPs, acquired in the range of 400–4000 cm-1, contained bands corresponding to specific functional groups of biomolecules and metal oxides. X-ray patterns were acquired in the range of 2θ = 20° to 80°. The crystallite size of produced ZnO NPs, calculated using Scherrer’s formula, was 8.7 nm. The wurtzite hexagonal structure of ZnO NPs was confirmed by the presence of the wide band at 495 to 850 cm-1. The peaks in the XRD pattern corresponded to the (100), (002), (101), (110), (103), and (201) planes. Prepared nanoparticles were semispherical, with a grain diameter of approximately 23 nm and mean roughness (Sa) of 1.65 nm. According to the results of antibacterial testing, ZnO NPs exhibited the greatest growth inhibition effect against Staphylococcus epidermidis, followed by Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Candida albicans (diameter of inhibition zones of 37 ± 0.89, 35.6 ± 0.52, 33.3 ± 1.36, and 35 ± 0.89 mm, respectively). ZnO NPs exhibited significant antibacterial activity owing to their distinct toxicity toward microorganisms. Hence, they can be applied as antimicrobial agents in medicine, surgery, diagnostics, and nanomedicine.

Formamidinium Lead Iodide‐Based Perovskite Solar Cell Fabrication With an Electrospun‐Reduced Graphene Oxide Back Electrode: A Novel Approach

AbstractIn this work, low‐cost and simple structure perovskite solar cells (PSCs) were fabricated using formamidinium lead iodide (FAPbI3) as the light absorber and reduced graphene oxide nanofibers (rGO NFs) as the counter electrode (CE). The FAPbI3 light absorber was prepared using a two‐step solution process, whereas the rGO NFs were synthesized through a simple electrospinning method. The as‐prepared FAPbI3 and rGO NFs were characterized by high‐resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), and X‐ray diffraction (XRD) pattern analysis. The surface morphology of the as‐prepared FAPbI3 and rGO NFs showed crystalline and bead‐free fiber structures, as confirmed by HRTEM and FESEM image analysis. The AFM topographical images of FAPbI3 and rGO NFs further reveal the crystalline and fiber structures. XRD pattern analysis confirmed the cubic crystalline phase of FAPbI3 and the graphitic nature of rGO NFs. From the electrochemical impedance spectroscopy studies, the PSC assembled with the FAPbI3 light absorber and rGO NFs‐based CE demonstrated an electrical conductivity of 3.64 × 10−4 S cm−1. The fabricated PSC device achieved an efficiency of 8.78% compared to the 7.49% efficiency of the device with a sputtered gold CE. This work uniquely integrates advanced materials, cost‐effective manufacturing, and enhanced efficiency in PSCs using FAPbI3 light absorbers and rGO NFs, addressing key challenges in cost and sustainability in solar technology.

Fabrication of Cerium Oxide-Graphene Oxide Nanocomposite using Ultrasound-Assisted Precipitation Method

<p class="Abstract">The cerium oxide-graphene oxide nanocomposite was fabricated by ultrasound-assisted precipitation method and characterized using Fourier transform infrared, UV-Vis spectroscopy, X-ray diffractometer, and transmission electron microscope. The Fourier transform infrared spectra displayed the vibrations of O-H, C=C, and C-H indicating the interaction between cerium oxide and graphene oxide. The broad absorption of around 300 nm is ascribed to the superposition of cerium oxide and graphene oxide absorption peaks. X-ray diffraction pattern analysis suggests the creation of graphene oxide nanosheets with an interlayer spacing of 0.821 nm. The transmission electron microscope image showed that the cerium oxide nanoparticles dispersed on the graphene oxide nanosheet. These findings exhibit the useful ultrasound-assisted precipitation method for fabricating cerium oxide-graphene oxide nanocomposite.</p>

High pressure and high temperature synthesis of a new boron carbide phase

The dense boron carbide (B-C) phases with diamond structure are predicted to be superhard, with hardness close to that of a cubic boron nitride (c-BN). At ambient conditions, graphite-like BC3 is well characterized, firstly reported by Kouvetakis et al. In this work, we have synthesized a new B-C phase from the graphite-like BC3 in a laser-heated diamond anvil cell. Interestingly, this phase could be recoverable to ambient pressure due to dynamic stabilities. The Raman spectrum and X-ray diffraction patterns give the possible structure of this new phase.