Structural, optical, and magnetic properties of V-doped ZnO nanoparticles and the onset of ferromagnetic order

Pure and vanadium (V) doped ZnO nanoparticles (NPs) were successfully synthesized via a modified sol-gel method. The wurtzite crystal structure of ZnO remained intact with the vanadium doping concentrations under the present synthesis environment as confirmed by an array of advanced analytical techniques; such as Rietveld refined X-ray diffraction (XRD) pattern, as well as bond valence sum (BVS) analysis. SEM and TEM techniques were used to examine the morphology of the samples. UV-Vis-NIR spectra showed an absorption band in the UV range with reduction in the band gap from 3.23 eV to 3.20 eV when V content increases. Photoluminescence (PL) shows that doping with V causes the creation of some defects in the band gap of ZnO. The energy position of the obtained PL emission introduces a blue shift when the measurement temperature increases. The M-T curve is successfully fitted using both three dimensional (3D) spin wave model and Curie-Weiss law which attests to the mixed state existence of ferromagnetic (FM) and paramagnetic (PM) phases. The electron paramagnetic resonance (EPR) analysis supports the XRD results and provides evidence of oxygen vacancies (V-O). Magnetic interaction is quantitatively studied and explained by polaronic percolation of bound magnetic polarons (BMP) produced by V-O defects. (C) 2022 Elsevier B.V. All rights reserved.

Automated summary

Pure and doped ZnO nanoparticles were synthesized via a modified sol-gel method. The crystal structure of ZnO remained intact with vanadium doping, as confirmed by various analytical techniques. SEM and TEM were used to examine the morphology of the samples. UV-Vis-NIR spectra showed changes in the band gap and absorption band with increased vanadium content. Photoluminescence analysis revealed the creation of defects in the band gap due to vanadium doping. Magnetic studies indicated a mixed state of ferromagnetic and paramagnetic phases, with magnetic interaction explained by defects-induced magnetic polarons.