The Synthesis and Characterization of a Novel One-Dimensional Bismuth (III) Coordination Polymer as a Precursor for the Production of Bismuth (III) Oxide Nanorods

A novel Bi (III) coordination compound, [Bi(HQ)(Cl)4]n ((Q = pyridine-4-carbaldehyde thiosemicarbazone), was prepared in this research using a sonochemical technique. SEM, infrared spectroscopy (IR), XRD, and single-crystal X-ray analysis were utilized to analyze the Bi(III) coordination compound. The structure determined using single-crystal X-ray crystallography indicates that the coordination compound is a 1D polymer in solid state and that the coordination number of bismuth (III) ions is six, (BiSCl5), with one S donor from the organic ligand and five Cl donors from anions. It is equipped with a hemidirectional coordination sphere. It is interesting that the ligand has been protonated in the course of the reaction with a Cl- ion balancing the charge. This compound’s supramolecular properties are directed and regulated by weak directional intermolecular interactions. Through π–π stacking interactions, the chains interact with one another, forming a 3D framework. Thermolysis of the compound at 170 °C with oleic acid resulted in the formation of pure phase nanosized Bi (III) oxide. SEM technique was used to examine the morphology and size of the bismuth (III) oxide product produced.

Efficient, scalable, closed-loop synthesis of highly crystalline pure phase MgAl-layered double hydroxides intercalated with hydroxyl anions

Layered double hydroxides (LDH) can play an important part in a variety of areas. But conventional LDH synthesis often causes product agglomeration and plenty of high-salt wastewater, and need a...

Optimizing ZnO/CdS Nano Composite Controlled by Fe Doping Towards Efficiency in Water Treatment and Antimicrobial Activity

Nanocrystalline composite zinc oxide (ZnO) and CdS with Fe doping thin films grown on glass substrate by chemical method. The parameters like temperature of the solution, UV exposure, pH of solution, immersion time, immersion cycles, have been controlled and standardized for nanocrystalline film. The synthesis NPs were analyzed by X-ray diffraction (XRD). Rietveld method shows that Fe-doped composite ZnO/CdS is a single pure phase and wurtzite structure. Samples were analyzed by sophisticated various instrument like XRD, UV- Visible spectrometer, HRTEM, HRSEM and composition was analyzed by EDX attached with HRTEM. The band gap was calculated by absorption spectroscopy and found that absorption was blue-shifted. The electron structure shows that doping changes the crystal structure and transition level create better efficiency and creates octahedral symmetry. The antibacterial studies showed that the 5.0 wt% Fe-doped exhibited maximum antibacterial effect.

Microwave-Assisted Hydrothermal Synthesis of Zinc-Aluminum Spinel ZnAl2O4

The drawback of the hydrothermal technique is driven by the fact that it is a time-consuming operation, which greatly impedes its commercial application. To overcome this issue, conventional hydrothermal synthesis can be improved by the implementation of microwaves, which should result in enhanced process kinetics and, at the same time, pure-phase and homogeneous products. In this study, nanometric zinc aluminate (ZnAl2O4) with a spinel structure was obtained by a hydrothermal method using microwave reactor. The average ZnAl2O4 crystallite grain size was calculated from the broadening of XRD lines. In addition, BET analysis was performed to further characterize the as-synthesized particles. The synthesized materials were also subjected to microscopic SEM and TEM observations. Based on the obtained results, we concluded that the grain sizes were in the range of 6–8 nm. The surface areas measured for the samples from the microwave reactor were 215 and 278 m2g−1.

Structural and magnetic variations in Ba0.5Sr0.5Fe9Ce1Al2O19 hexaferrites at different sintering temperatures

M-type hexaferrites has attracted researchers due to their ordinary magnetic properties and utilization as media for magnetic recording and microwave devices. In this study we have synthesized Ba0.5Sr0.5Fe9Ce1Al2O19 via conventional ceramic route. The synthesized material is treated against different temperatures and investigated structurally and magnetically by using several techniques such as X-ray diffraction, Scanning electron microscopy, and VSM respectively. Morphology of samples confirms the absence of secondary phases and uniform distribution of particles. X-ray diffraction patterns confirms the formation of pure phase of Hexaferrites. Microstructural analyses show the decrease in porosity and dislocations among sintered samples. Magnetic properties for the samples show a decrease in Ms and Mr with increasing temperature from 1225 °C to 1310 °C, while coercivity shows an increase with increasing temperature and maximum coercivity is observed at 1290 °C. The trends and occurrences can be well-linked to the structural variations and sintering effects. The results suggest that material can be used in various magnetic applications such as Recording media, and memory devices.

MnO, Co and Ni Nanoparticle Synthesis by Oleylamie and Oleic Acid

Background: Magnetic nanoparticles are attracting much attention toward easy operation and size controlable synthesis methods. We develop a method to synthesize MnO, Co, CoO, and Ni nanoparticles by thermal decomposition of metal 2,4-pentanedionates in the presence of oleylamine (OLA), oleic acid (OA), and 1‐octadecene (ODE). Methods: Similar experimental conditions are used to prepare nanoparticles except for the metal starting materials (manganese 2,4-pentanedionate, nickel 2,4-pentanedionate, and cobalt 2,4-pentanedionate), leading to different products. For the manganese 2,4-pentanedionate starting material, MnO nanoparticles are always obtained as the reaction is controlled with different temperatures, precursor concentrations, ligand ratios, and reaction time. For the cobalt 2,4-pentanedionate starting material, only three experimental conditions can produce pure phase CoO and Co nanoparticles. For the nickel 2,4-pentanedionate starting material, only three experimental conditions lead to the production of pure phase Ni nanoparticles. Results: The nanoparticle sizes increase with the increase of reaction temperatures. It is observed that the reaction time affects nanoparticle growth. The nanoparticles are studied by XRD, TEM, and magnetic measurements. Conclusion: This work presents a facile method to prepare nanoparticles with different sizes, which provides a fundamental understanding of nanoparticle growth in solution.

Impact of Annealing Temperature on the Morphological, Optical and Photoelectrochemical Properties of Cauliflower-like CdSe0.6Te0.4 Photoelectrodes; Enhanced Solar Cell Performance

We are reporting on the impact of air annealing temperatures on the physicochemical properties of electrochemically synthesized cadmium selenium telluride (CdSe0.6Te0.4) samples for their application in a photoelectrochemical (PEC) solar cell. The CdSe0.6Te0.4 samples were characterized with several sophisticated techniques to understand their characteristic properties. The XRD results presented the pure phase formation of the ternary CdSe0.6Te0.4 nanocompound with a hexagonal crystal structure, indicating that the annealing temperature influences the XRD peak intensity. The XPS study confirmed the existence of Cd, Se, and Te elements, indicating the formation of ternary CdSe0.6Te0.4 compounds. The FE-SEM results showed that the morphological engineering of the CdSe0.6Te0.4 samples can be achieved simply by changing the annealing temperatures from 300 to 400 °C with intervals of 50 °C. The efficiencies (ƞ) of the CdSe0.6Te0.4 photoelectrodes were found to be 2.0% for the non-annealed and 3.1, 3.6, and 2.5% for the annealed at 300, 350, and 400 °C, respectively. Most interestingly, the PEC cell analysis indicated that the annealing temperatures played an important role in boosting the performance of the photoelectrochemical properties of the solar cells.