溶液共沉淀法制备的掺铁氧化锌纳米粒子的摩斯鲍尔和磁学研究

Li Liu, Qifu Bao, Tiangui Zhao, Kun Liu, Detai Shi, Siyu Li, Wei Zhu, Xiaolong Li, Jianer Zhou
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引用次数: 0

摘要

采用溶液共沉淀法合成了一系列 Zn[式:见正文]FexO([式:见正文], 0.015, 0.045, 0.075)纳米粒子,并研究了它们的结构和性质特征。X 射线衍射(XRD)分析表明,所有 Zn[式中:见正文]FexO 样品都呈现出 P63mc 空间群的六方菱锰矿晶体结构。铁的掺入导致样品出现轻微的晶格畸变。扫描电子显微镜(SEM)和透射电子显微镜(TEM)检测了纳米颗粒的形态,包括多分散和团聚,以及第二相 ZnFe2O4 的存在。紫外-可见漫反射光谱显示,Zn[式:见正文]FexO 的带隙在 3.152 和 3.163[式:见正文]eV 之间。随着铁离子掺杂量的增加,带隙呈轻微下降趋势。莫斯鲍尔光谱显示,纳米粒子中的铁离子以三价态存在,并呈现出两种不同的构型:一种是铁取代锌而不产生空位,另一种是铁取代锌而产生空位。掺铁样品的铁磁性可归因于由 F 中心机制介导的两个铁[式:见正文]离子之间的交换相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mössbauer and magnetic studies of Fe-doped ZnO nanoparticles prepared by solution co-precipitation method
A series of Zn[Formula: see text]FexO ([Formula: see text], 0.015, 0.045, 0.075) nanoparticles were synthesized using the solution co-precipitation method, and their structural and property characteristics were investigated. X-ray diffraction (XRD) analysis revealed that all Zn[Formula: see text]FexO samples exhibited a hexagonal wurtzite crystal structure with the P63mc space group. The introduction of Fe doping led to a slight lattice distortion in the samples. The morphology of the nanoparticles, including polydispersion and agglomeration, as well as the presence of the second phase ZnFe2O4, was examined by scanning electron microscope (SEM) and transmission electron microscope (TEM). UV–Vis diffuse reflectance spectroscopy demonstrated that the band gap of Zn[Formula: see text]FexO lies between 3.152 and 3.163[Formula: see text]eV. With the increase in Fe ion doping, the band gap shows a slight decreasing trend. Mössbauer spectroscopy revealed that iron ions in the nanoparticles existed in a trivalent state and exhibited two different configurations: One involved iron replacing zinc without creating a vacancy, while the other involved iron substituting zinc with a vacancy. The ferromagnetic nature of the Fe-doped samples can be attributed to the exchange interaction between two Fe[Formula: see text] ions mediated by the F-center mechanism.
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