{"title":"Investigations on the structural, magnetic and spin interactions of Mn0.5Zn0.5ErxFe2-xO4 ferrites synthesized by co-precipitation method","authors":"Lakshita Phor , Swati Saini , Mohd Afzal , Vandana Meena , Amanpreet Singh , Ashok Kumar , Surjeet Chahal","doi":"10.1016/j.mseb.2025.118234","DOIUrl":null,"url":null,"abstract":"<div><div>This study investigates the impact of Er<sup>3+</sup> doping on the structural and magnetic properties of Mn<sub>0.5</sub>Zn<sub>0.5</sub>Er<sub>x</sub>Fe<sub>2−x</sub>O<sub>4</sub> (x = 0.0–0.1) nanoparticles synthesized by co-precipitation. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) confirm the formation of a single cubic spinel phase. Er<sup>3+</sup> substitution leads to a lattice parameter increase from 8.3827 to 8.4197 Å, attributed to Er<sup>3+</sup>’s larger ionic radius relative to Fe<sup>3+</sup>. SEM analysis reveals a reduction in nanoparticle size from 33.1 to 25.1 nm with increased Er<sup>3+</sup> content. Magnetic measurements show a decline in maximum magnetization from 32.46 to 15.04 emu/g at 10,000 Oe, indicating a decrease in net magnetization with Er<sup>3+</sup> doping, accompanied by negligible coercivity and retentivity. Electron paramagnetic resonance (EPR) spectroscopy further characterizes spin dynamics, including peak-to-peak line width, resonance field, Lande’s g-factor, spin concentration, and relaxation time, highlighting significant changes in magnetic properties due to Er<sup>3+</sup> doping.</div></div>","PeriodicalId":18233,"journal":{"name":"Materials Science and Engineering: B","volume":"317 ","pages":"Article 118234"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Science and Engineering: B","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0921510725002570","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
This study investigates the impact of Er3+ doping on the structural and magnetic properties of Mn0.5Zn0.5ErxFe2−xO4 (x = 0.0–0.1) nanoparticles synthesized by co-precipitation. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) confirm the formation of a single cubic spinel phase. Er3+ substitution leads to a lattice parameter increase from 8.3827 to 8.4197 Å, attributed to Er3+’s larger ionic radius relative to Fe3+. SEM analysis reveals a reduction in nanoparticle size from 33.1 to 25.1 nm with increased Er3+ content. Magnetic measurements show a decline in maximum magnetization from 32.46 to 15.04 emu/g at 10,000 Oe, indicating a decrease in net magnetization with Er3+ doping, accompanied by negligible coercivity and retentivity. Electron paramagnetic resonance (EPR) spectroscopy further characterizes spin dynamics, including peak-to-peak line width, resonance field, Lande’s g-factor, spin concentration, and relaxation time, highlighting significant changes in magnetic properties due to Er3+ doping.
期刊介绍:
The journal provides an international medium for the publication of theoretical and experimental studies and reviews related to the electronic, electrochemical, ionic, magnetic, optical, and biosensing properties of solid state materials in bulk, thin film and particulate forms. Papers dealing with synthesis, processing, characterization, structure, physical properties and computational aspects of nano-crystalline, crystalline, amorphous and glassy forms of ceramics, semiconductors, layered insertion compounds, low-dimensional compounds and systems, fast-ion conductors, polymers and dielectrics are viewed as suitable for publication. Articles focused on nano-structured aspects of these advanced solid-state materials will also be considered suitable.