This study explored the structural, optical, and dielectric properties of Pure and Mn+2 doped ZnO nano-particles (Zn1−xMnxO) with x ≥ 20%, synthesized by co-precipitation method followed by annealing at 4500C. Different characterization techniques were conducted to characterize the as-prepared nano-particles. X-ray Diffraction analysis of the pure and Mn+2 doped presented a hexagonal wurtzite structure and a decreased crystallite size with increasing doping concentration. Morphological analysis from SEM revealed finely dispersed spherical nanoparticles with particle size of 40–50 nm. Compositional analysis from EDX confirmed the incorporation of Mn+2ions in ZnO structure. The Results of UV spectroscopy showed that changing the doping concentration affects the band gap, and a red shift is observed as the doping concentration is increased. The band gap changes from 3.3 to 2.75 eV. Dielectric measurements exhibited decrease in the relative permittivity, dielectric loss factor and ac conductivity by increasing Mn concentration.
La1-xCaxMnO3 nanoparticles (x = 0.1, 0.2, 0.3) (LCMO NPs) were synthesized using the coprecipitation method. The prepared samples were investigated using x-ray diffraction (XRD), which confirmed the single-phase structure. The nanoparticle’s crystallite size was determined using Debye–Scherrer’s formula. Scanning electron microscopy showed that the size of the nanoparticles was between 33 nm and 55 nm. Energy-dispersive x-ray spectroscopy (EDX) was used to determine the elemental composition of samples. The four-probe method was used to measure the temperature-dependent electrical resistivity. Magnetic properties, such as hysteresis loop, magnetoresistance, and magnetization versus temperature, were measured using a vibrating sample magnetometer. The study of magnetization versus applied magnetic field M(H) showed that, at 77 K, all the loops exhibit ferromagnetism. DC magnetization versus temperature at a 70-Oe-applied field for all samples showed a paramagnetic-ferromagnetic phase transition. A decrease in Curie temperature Tc after increasing the concentration of x was observed. The real and imaginary parts of temperature-dependent ac magnetic susceptibility were measured and revealed a transition from the ferromagnetic to the paramagnetic phase at a particular temperature Tc, with DC magnetization behavior.
In the present study, pure, Co, Gd, and Co/Gd di-doped ZnO nanoparticles were synthesized via the co-precipitation synthesis route. The prepared samples were characterized through different techniques such as the X-ray diffraction method (XRD), scanning electron microscopy (SEM), UV-Vis spectroscopy, photoluminescence (PL)spectroscopy, and an impedance analyzer and vibrating sample magnetometer (VSM). The XRD pattern shows ZnO’s wurtzite hexagonal crystal structure; moreover, the shifting of characteristic peaks toward the lower angle indicates the inclusion of Co and Co/Gd in the ZnO host lattice. SEM micrographs show various morphologies such as rods, the agglomeration of particles, and spherical nanoparticles. The UV-Vis spectroscopy reveals that the absorption increased in the visible region and there was a substantial redshift for the doped samples. The bandgap decreased from 3.34 to 3.18 eV for the doped samples. The PL spectra show near-edge and inter-band transitions; the origin of inter-band transitions is attributed to the defect states present within the bands. The dielectric constant is strongly frequency dependent and decreases with Co and Co/Gd doping, while the electrical conductivity increases. A VSM study indicates that pure ZnO is diamagnetic, while the Co and Co/Gd doped ZnO nanoparticles showed ferromagnetic behavior. Under UV-visible light irradiation, the Co/Gd-ZnO nanoparticles showed higher photocatalytic activity than the ZnO nanoparticles. The enhanced photocatalytic activity may be attributed to a decreased bandgap with doping.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.