We report the detailed analysis of electrochemical investigation of honeycomb structured Na$_{2}$Ni$_{2}$TeO$_{6}$ material as a cathode for sodium-ion batteries using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), galvanostatic charge-discharge (GCD)...
We use the x-ray diffraction, magnetic susceptibility, isothermal magnetization, and photoelectron spectroscopy to study the structural, magnetic and electronic properties of La (1−x) AxCoO3 (A = Sr, Ca; x = 0 -0.2) nanoparticles. The Rietveld refinements of room temperature powder x-ray diffraction data confirm the single phase and the rhombohedral crystal structure with R3C space group. We find drastic changes in the magnetic properties and spin-states with Sr/Ca substitution (hole doping). For x = 0 sample, the magnetic measurements show a ferromagnetic transition at TC≈85 K, which shifted significantly to higher temperatures with hole doping; simultaneously a significant increase in the spontaneous magnetic moment has been observed. Whereas, the coercive field HC values are 7, 4.4 and 13.2 kOe for x = 0, 0.2 (Sr), and 0.2(Ca) samples. Furthermore, the FC magnetization shows a ferromagnetic Brillouin function like behavior at low temperatures for Ca samples. We demonstrate that the Sr/Ca substitution increases the population of IS (Co 3+ ) and LS (Co 4+ ) states and tune the ferromagnetism in nanoparticles via double-exchange interactions between Co 3+ -Co 4+ . Our results suggest an important role of hole carriers and nano-size effect in controlling the spin-state and magnetism in La (1−x) AxCoO3 nanoparticles.
We present a combined stress and structural analysis of the growth of epitaxial NiO monolayers on Ag(001). Our experimental results indicate an unexpectedly complex interface formation, where a fraction of the first NiO monolayer (ML) is embedded into the Ag surface. This interface formation induces a tensile surface stress change. Subsequent deposition leads to a layer-by-layer growth of NiO up to 5 ML. Here, the average film stress is compressive −5.8 GPa, and it corresponds quantitatively to the misfit-induced stress. Our density functional calculations complement the experimental results by identifying the proper O-Ag bonding geometry in the ML regime from two indistinguishable options as provided by the analysis of surface x-ray diffraction data.
The biogenic synthesis of silver nanoparticles (AgNPs) and their potent application against dye degradation and phytopathogens are attracting many scientists to nanotechnology. An attempt was made to synthesize silver nanoparticles using Plantago ovata leaf extract and test their effectiveness in removing organic dyes and antifungal activity. In the present study, stable AgNPs were synthesized from 0.1 mM AgNO3 and authenticated by observing the color change from yellow to red-brown, which was confirmed with wavelength UV-Vis spectrophotometer detection. The crystalline nature of the particles was characterized by x-ray diffraction (XRD) patterns. Furthermore, the AgNPs were characterized by high-resolution transmission electron microscope and scanning electron microscope investigations. Atomic force microscopy (AFM) and Raman spectra were also used to confirm the size and structure of the synthesized AgNPs. The elemental analysis and functional groups responsible for the reduction of AgNPs were analyzed by electron dispersive spectroscopy and fourier transform infra-red spectroscopy Fourier transforms infrared, respectively. A new biological approach was taken by breaking down organic dyes such as methylene blue and congo red. The AgNPs effectively inhibit the fungal growth of Alternaria alternata. This could be a significant achievement in the fight against many dynamic pathogens and reduce dye contamination from waste water.
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