4.5 Article

Room temperature ferromagnetism in Eu-doped ZnO nanoparticulate powders prepared by combustion reaction method

期刊

JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS
卷 355, 期 -, 页码 325-330

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jmmm.2013.12.028

关键词

Zinc oxide; Diluted magnetic semiconductors (DMS); Room temperature ferromagnetism (RTFM); Combustion reaction

资金

  1. CNPq (Brazilian Financial Agency)
  2. FAPEG
  3. CNPq [308183/2012-6]

向作者/读者索取更多资源

Nanoparticulate powders of Eu-doped ZnO with 1.0, 1.5, 2.0 and 3.0 at% Eu were synthesized by combustion reaction method using zinc nitrate, europium nitrate and urea as fuel without subsequent heat treatments. X-ray diffraction patterns (XRD) of all samples showed broad peaks consistent with the ZnO wurtzite structure. The absence of extra reflections in the diffraction patterns ensures the phase purity, except for x=0.03 that exhibits small reflection corresponding to Eu2O3 phase. The average crystallite size determined from the most prominent (1 0 1) peak of the diffraction using Scherrer's equation was in good agreement with those determined by transmission electron microscopy (TEM); being similar to 26 nm. The magnetic properties measurements were performed using a vibrating sample magnetometer (VSM) in magnetic fields up to 2.0 kOe at room temperature. The hysteresis loops, typical of magnetic behaviors, indicating that the presence of an ordered magnetic structure can exist in the Eu-doped ZnO wurtzite structure at room temperature. The room temperature ferromagnetism behavior increases with the Eu3+ doping concentration. All samples exhibited the same Curie temperature (T-C) around similar to 726 K, except for x=0.01; T-C similar to 643 K. High resolution transmission electron microscopy (HRTEM) images revealed defects/strain in the lattice and grain boundaries of Eu-doped ZnO nanoparticulate powders. The origin of room temperature ferromagnetism in Eu-doped ZnO nanoparticulate powders was discussed in terms of these defects, which increase with the Eu3+ doping concentration. (C) 2013 Elsevier B.V. All rights reserved,

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