磁矩
结晶学
扫描透射电子显微镜
材料科学
磁各向异性
透射电子显微镜
矫顽力
铁磁性
扫描电子显微镜
分析化学(期刊)
核磁共振
磁化
化学
凝聚态物理
磁场
纳米技术
物理
量子力学
色谱法
复合材料
作者
Syed Kamran Haider,Min‐Chul Kang,Jisang Hong,Young Soo Kang,Cheol‐Woong Yang,Dong-Soo Kim
标识
DOI:10.1038/s41598-021-85713-5
摘要
Abstract Nd 2 Fe 14 B and Nd 2−x Dy x Fe 14 B (x = 0.25, 0.50) particles were prepared by the modified co-precipitation followed by reduction–diffusion process. Bright field scanning transmission electron microscope (BF-STEM) image revealed the formation of Nd–Fe–B trigonal prisms in [− 101] viewing zone axis, confirming the formation of Nd 2 Fe 14 B/Nd 2−x Dy x Fe 14 B. Accurate site for the Dy substitution in Nd 2 Fe 14 B crystal structure was determined as “f” site by using high-angle annular dark field scanning transmission electron microscope (HAADF-STEM). It was found that all the “g” sites are occupied by the Nd, meanwhile Dy occupied only the “f” site. Anti-ferromagnetic coupling at “f” site decreased the magnetic moment values for Nd 1.75 Dy 0.25 Fe 14 B (23.48 μB) and Nd 1.5 Dy 0.5 Fe 14 B (21.03 μB) as compared to Nd 2 Fe 14 B (25.50 μB). Reduction of magnetic moment increased the squareness ratio, coercivity and energy product. Analysis of magnetic anisotropy at constant magnetic field confirmed that “f” site substitution did not change the patterns of the anisotropy. Furthermore, magnetic moment of Nd 2 Fe 14 B, Nd 2−x Dy x Fe 14 B, Nd (“f” site), Nd (“g” site) and Dy (“f” site) was recorded for all angles between 0° and 180°.
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