共沉淀
煅烧
矫顽力
微晶
材料科学
化学工程
粒径
聚乙烯吡咯烷酮
纳米颗粒
分散剂
反铁磁性
纳米尺度
粒子(生态学)
矿物学
剩磁
纳米技术
色散(光学)
磁化
冶金
化学
磁场
有机化学
凝聚态物理
高分子化学
地质学
催化作用
量子力学
海洋学
工程类
光学
物理
作者
Xuemin He,D.-G. Chen,Kun-Yu Su,Zhen-Fei Yu,Yi Zhang,Wei Zhong
摘要
Different morphologies and sizes of α-Fe2O3 were prepared by a coprecipitation method using polyvinylpyrrolidone as a dispersant. In the preparation process, homogeneous and dispersed nanoscale FeOOH particles were first obtained by the coprecipitation method, and then the FeOOH particles were calcined at high temperature to form α-Fe2O3. The growth and aggregation of the α-Fe2O3 particles at different calcination temperatures resulted in α-Fe2O3 powders with diversiform morphologies (nanoscale microsphere, pinecone ellipsoidal, polyhedral, and quasi-spherical structures). By analyzing the SEM images, it was inferred that the polyhedral structure of α-Fe2O3 particles was formed by the accumulation of rhomboid sheet structures and high-temperature growth. In terms of the magnetic properties, the samples belonged to the class of canted antiferromagnetic materials, and the morphology, particle size, and crystallite size of the α-Fe2O3 particles were important factors affecting the coercivity. Among these, when the calcination temperature was increased from 700 °C to 800 °C, the growth rate of the particle size was significantly faster than that of the crystallite size, and the coercivity increased substantially from 1411 Oe to 2688 Oe.
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