纳米晶材料
材料科学
纤锌矿晶体结构
X射线光电子能谱
结构精修
兴奋剂
反铁磁性
矫顽力
磁化
分析化学(期刊)
铁磁性
磁矩
结晶学
凝聚态物理
核磁共振
纳米技术
化学
晶体结构
磁场
锌
光电子学
物理
量子力学
冶金
色谱法
作者
M. Shatnawi,A. M. Alsmadi,Ibrahim Bsoul,B. Salameh,G. Alna’Washi,Feras M. Aldweri,F. El Akkad
标识
DOI:10.1016/j.jallcom.2015.09.166
摘要
We carried out a systematic study on the effect of Co doping on the structural, magnetic and optical properties of ZnO nanocrystalline particles, using x-ray diffraction, x-ray photoelectron spectroscopy (XPS), Quantum Design PPMS-9 magnetometry, and Ultra Violet-Visible spectroscopy. The Zn1-xCoxO nanoparticles with 0≤x≤0.1 were successfully prepared by the formal solid-state reaction method. The XPS results and the XRD analysis with full structural Rietveld refinement reveals that all Zn1-xCoxO nanocrystalline particles in this Co-doping range have hexagonal wurtzite structure. Co atoms have been successfully incorporated in tetrahedral sites and no secondary phases or Co rich clusters were detected. For all Co-doped ZnO nanoparticles under investigation, the field dependence of the magnetization curves exhibits ferromagnetic behavior with relatively small coercive fields at room temperature. The coercive fields increased with Co-doping and decreased with temperature, as expected. In addition, we found a signature for antiferromagnetic ordering between the Co ions. We also observed a strong correlation between the magnetic and optical behavior of the Co-doped ZnO nanoparticles. Optical diffuse reflectance and absorption spectra exhibit a red shift at room temperature in the absorption band edge with increasing Co-doping. The red shift is attributed to the sp-d exchange interaction between free charge carriers in ZnO band and the localized magnetic moments.
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