4.7 Article

Sol-gel synthesis of MnxNi1-xCo2O4 spinel phase materials: Structural, electronic, and magnetic properties

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 742, 期 -, 页码 78-89

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2018.01.139

关键词

Nanostructured materials; Oxide materials; Sol-gel processes; Magnetic measurements; Photoelectron spectroscopies; X-ray diffraction

资金

  1. Department of Applied Chemistry
  2. Centre for Nanomaterials Science Research
  3. Department of Physics
  4. Faculty of Science at the University of Johannesburg
  5. School of Chemistry at the University of the Witwatersrand
  6. National Research Foundation (South Africa) [88080, 109623, 93620]

向作者/读者索取更多资源

A series of spinel-type MnxNi1-xCo2O4 (x = 0, 0.3, 0.5, 0.7, 1) oxides were synthesized by using a citrate sol-gel technique. The structural, magnetic and electronic properties of the oxides with different Mn content were investigated using X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), vibrating sample magnetometer (VSM) and X-ray photoelectron spectroscopy (XPS). The XRD and FTIR studies revealed that MnxNi1-xCo2O4 formed in a cubic structure for all the compositions synthesized. Transmission electron microscopy (TEM) studies show cubic nano-plates for x = 0 and on increasing Mn concentration, agglomerated nanoparticles with sphere-like shape are observed with a particle size in the range of 11.7 nm-22.1 nm. This is in close agreement with the results of XRD analysis. The Mn 2p, Ni 2p, and Co 2p XPS spectra reveal the coexistence of Mn2+, Mn3+, Ni2+, Ni3+, Co2+, and Co3+ species on the surface of MnxNi1-xCo2O4 samples in differing proportions. The measurements of magnetic properties at room temperature show that the samples have some ferromagnetic behaviour. The saturation magnetization, remnant magnetization, and coercivity of the nanoparticles vary significantly with a concentration of Mn, which tends to be distributed in both tetrahedral and octahedral positions of the spinel lattice. (C) 2018 Elsevier B.V. All rights reserved.

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