Synthesis, Structural and Magnetic Characterization of Ni-Doped ZnO Diluted Magnetic Semiconductor

R. Elilarassi, G. Chandrasekaran
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引用次数: 40

Abstract

In the present work, Zn1−xNixO (x = 0.02, 0.04, 0.06 and 0.08) nanoparticles have been synthesized using sol-gel auto-combustion method. The structural and magnetic properties of the Ni-doped ZnO samples annealed at 800oC were characterized by Thermogravimetry/Differential thermal analysis (TG/DTA), X-ray diffractometer (XRD), Scanning electron microscope (SEM), FTIR spectrophotometer, Vibrating sample magnetometer (VSM) and Electron paramagnetic resonance (EPR) spectroscopy. Thermal analysis of as–prepared Zn0.98Ni0.02O sample shows that the synthesis process undergoes two stage weight losses before yielding Zn0.98Ni0.02O nanoparticles. Structural analysis using XRD reveals the formation of hexagonal wurtzite structure. SEM micrographs of Zn0.98Ni0.02O show the presence of spherical nanoparticles and the formation of well defined pores in the sample. FTIR study confirms the formation of ZnO with the stretching vibrational mode around 525 cm-1. VSM measurement of sample (Zn0.96Ni0.04O) shows the hysteresis loop at room temperature confirms the ferromagnetic property of the sample. EPR spectra of the nickel doped ZnO samples suggest that the exchange interaction between Ni2+ ions results in the ferromagnetic nature of the samples.
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ni掺杂ZnO稀释磁性半导体的合成、结构及磁性表征
本文采用溶胶-凝胶自燃烧法合成了Zn1−xNixO (x = 0.02, 0.04, 0.06和0.08)纳米颗粒。采用热重/差热分析(TG/DTA)、x射线衍射仪(XRD)、扫描电镜(SEM)、红外光谱(FTIR)、振动样品磁强计(VSM)和电子顺磁共振(EPR)等手段表征了800℃退火后ni掺杂ZnO样品的结构和磁性能。对制备的Zn0.98Ni0.02O样品的热分析表明,在制备出Zn0.98Ni0.02O纳米粒子之前,合成过程经历了两个阶段的失重。XRD结构分析揭示了六方纤锌矿结构的形成。zn0.98 ni0.020的SEM显微图显示,样品中存在球形纳米颗粒,并形成了清晰的孔隙。FTIR研究证实ZnO在525 cm-1附近以拉伸振动模式形成。样品(zn0.96 ni0.040 o)在室温下的磁滞回线证实了样品的铁磁性。镍掺杂ZnO样品的EPR光谱表明,Ni2+离子之间的交换相互作用导致了样品的铁磁性。
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