新化合物 Mn1.2Co0.05Fe0.7P0.45Si0.5B0.05的机械合成、结构、热和磁性行为

N. Khitouni, Maha M. Almoneef, Amira Mili, M. Khitouni, A. Wederni, J. Sunol
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引用次数: 0

摘要

通过机械合金化 15 小时,然后在 1373 K 下加热 2 小时和在 1073 K 下加热 24 小时两次退火,系统地合成了 Mn1.2Co0.05Fe0.7P0.45Si0.5B0.05 化合物。同一粉末在 1373 K 退火 2 小时和 1073 K 退火 24 小时后,精炼相为独特的(Mn, Fe)2(P, Si)型六方结构。机械合金粉末的最终晶粒大小约为 20 nm,在退火过程中上升到 95 nm。此外,高能研磨(约 0.75%)产生了大量晶格微应变。在 373 至 923 K 的整个温度范围内,热分析显示了几个重叠的放热峰,这表明在结构松弛和重排过程后,微观结构得到了改善。此外,合金的居里温度约为 675 K。根据磁性能分析,机械合金粉末在研磨 15 小时后呈现出特殊的软铁磁状态,而退火合金则显示出超顺磁特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechano-Synthesis, Structure, and Thermal and Magnetic Behaviors of the New Compound Mn1.2Co0.05Fe0.7P0.45Si0.5B0.05
The Mn1.2Co0.05Fe0.7P0.45Si0.5B0.05 compound has been systematically synthesized by mechanical alloying for 15 h, followed by annealing with two heating cycles at 1373 K for 2 h and 1073 K for 24 h. The powder that was milled for 15 h revealed the main hexagonal-Mn2P-type phase and the minor cubic-Mn3Fe2Si phase through X-ray diffraction examination. After annealing the same powder at 1373 K for 2 h and again at 1073 K for 24 h, the refined phase was the unique (Mn, Fe)2(P, Si) type with a hexagonal structure. For the mechanically alloyed powder, the final crystallite size was approximately 20 nm, and it rose to 95 nm during the annealing process. Further, a large amount of lattice microstrain was achieved as a result of high-energy milling (about 0.75%). Over the whole temperature range of 373 to 923 K, the thermal analysis showed several overlapping exothermic peaks, which indicated the improvement of the microstructure after the structural relaxation and reordering process. Moreover, the Curie temperature of the alloy was retrieved at approximately 675 K. According to an analysis of the magnetic properties, the mechanically alloyed powder exhibited an exceptional soft ferromagnetic state after 15 h of milling, and the annealed alloy showed superparamagnetic characteristics.
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