-
YTi(Fe1-xCox)11在012型四方结构,居里温度随Co含量的增加而提高,本文为了揭示YTi(Fe1-xCox)11磁性与微观结构的联系,对这一系列化合物进行穆斯堡尔谱研究,在室温下,测量YTi(Fe1-xCox)11(其中x=0.0,0.2,0.4)的穆斯堡尔谱,最佳拟合结果证实在这种化合物中,Co原子优先占据j和f晶位,在所测样品中,超精细场在x=0.2处出现极值,这与YTi(Fe1-xCox)11饱和磁化强度测量结果相符合。并对YTi(Fe1-xCox)11,Y2(Fe1-xCox)14和YTi(Fe1-xCox)11的穆斯堡尔谱的实验结果进行比较,分析在YTiFe11中与Y2Fe14B中的3d电子能带结构的差异。YTi(Fe1-xCox)11 crystallizes in the ThMn12-type tetragonal structure, with x ranging from 0.0 to 1.0, the Curie temperature increases with the increase of Co content. In order to understand the relation between magnetic properties and microst-ructure of these compounds, we studied their M?ssbauer spectra. The M?ssbauer effect measurements were carried out at room temperature on YTi(Fe1-xCox)11, with x equal to 0.0, 0.2 and 0.4. The best fits confirm that Co atoms preferentially occupy the j and f sites. The hyperfine fields of the measured samples reach a maximum at x = 0.2,which is in agreement with the results of magnetic measurements. By comparing the experimental results of M?ssbauer spectra of YTi(Fe1-xCox)11, Y2(Fe1-xCox)14B and YTi(Fe1-xNix)11, we analyze the difference of the 3d band structure between YTiFe11, and Y2Fe14B.
计量
- 文章访问数: 7238
- PDF下载量: 459
- 被引次数: 0