arXiv subjects

Shalendra Kumar

Publications and source records attributed to Shalendra Kumar.

4 recordsLinked to original sources

arXiv2011

Structural and magnetic properties of Ni doped CeO2 nanoparticles

We report room temperature ferromagnetism in Ni doped CeO2 nanoparticles using X-ray diffraction (XRD), high resolution transmission electron microscopy (HR-TEM), and dc magnetization measurements. Nanoparticles of Ce1-xNixO2 (0.0 \leq x \leq 0.10) were prepared by using a co-precipitation method. XRD measurements indicate that all samples exhibit single phase nature with cubic structure and ruled out the presence of any secondary phase. Lattice parameters, strain and particle size calculated from XRD data have been found to decrease with increase in Ni doping. Inter-planner distance measured from HR-TEM images for different Ni doped samples indicate that Ni ions are substituting Ce ions in CeO2 matrix. Magnetization measurements performed at room temperature display weak ferromagnetic behavior of Ce1-xNixO2 (0.0 \leq x \leq 0.10) nanoparticles. Magnetic moment calculated from magnetic hysteresis loop was found to increases with Ni doping up to 7% and then start decreasing with further doping.

cond-mat.mes-hall↗

arXiv2009

Room temperature ferromagnetism in chemically synthesized ZnO rods

We report structural and magnetic properties of pure ZnO rods using X-ray diffraction (XRD), magnetization hysteresis (M-H) loop and near edge x-ray fine structure spectroscopy (NEXAFS) study at O K edge. Sample of ZnO was prepared by co-precipitation method. XRD and selective area electron diffraction measurements infer that ZnO rods exhibit a single phase polycrystalline nature with wurtzite lattice. Field emission transmission electron microscopy, field emission scanning electron microscopy micrographs infers that ZnO have rod type microstructures with dimension 200 nm in diameter and 550 nm in length. M-H loop studies performed at room temperature display room temperature ferromagnetism in ZnO rods. NEXAFS study reflects absence of the oxygen vacancies in pure ZnO rods.

cond-mat.mtrl-sci↗

arXiv2009

Structural and magnetic study of a dilute magnetic semiconductor: Fe doped CeO2 nanoparticles

This paper reports the effect of Fe doping on the structure and room temperature ferromagnetism of CeO2 nanoparticles. X-ray diffraction and selective area electron diffraction measurement reflects that Ce1-xFexO2 (x = 0.0 - 0.07) nanoparticles exhibit single phase nature with cubic structure and none of the sample showed the presence of any secondary phase. The mean particle size calculated by using a transmission electron microscopy measurement was found to increase with increase in Fe content. DC magnetization measurements performed at room temperature indicates that all the samples exhibit ferromagnetism. The saturation magnetic moment has been found to increase with an increase in the Fe content.

cond-mat.mtrl-sci↗

arXiv2009

Electronic structure and magnetic properties of Ni0.2Cd0.3Fe2.5-xAlxO4 (x = 0.0 - 0.4) ferrite nanoparticles

Structural, magnetic and electronic structural properties of Ni0.2Cd0.3Fe2.5-xAlxO4 ferrites nanoparticles have been studied x-ray diffraction (XRD), transmission electron microscopy (TEM), dc magnetization, and near edge x-ray absorption fine structure spectroscopy (NEXAFS) measurements. Nanoparticles of Ni0.2Cd0.3Fe2.5-xAlxO4 (x = 0.0 - 0.4) ferrite were synthesized using sol-gel method. The XRD and TEM measurements show that all samples have single phase nature with cubic structure and have nanocrystalline behavior. From the XRD and TEM analysis, it is observed that particle size increases with Al doping. DC magnetization measurements infer that magnetic moment decreases whereas blocking temperature increases with increase in Al doping. It is observed that the magnetic moment decreases with Al doping which may be due to the dilution of the sublattice by the doping of Al ions. The NEXAFS measurements performed at room temperature indicates that Fe exist in mixed valence state.

cond-mat.mtrl-sci↗