Miyanaga T, Okazaki T, Murako R, Takegahara K, Nagamatsu S, Fujikawa T, Kon H, Sakisaka Y
Faculty of Science and Technology, Hirosaki University, Hirosaki Aomori, Japan.
J Synchrotron Radiat. 2003 Mar 1;10(Pt 2):113-9. doi: 10.1107/s0909049502022549. Epub 2003 Feb 27.
Magnetic X-ray absorption fine-structure (XAFS) spectra have been measured for Ni-Mn alloys. The magnetic XAFS in the near-edge region (X-ray absorption near-edge structure, XANES) and X-ray magnetic circular dichroism (XMCD) of the Mn and Ni K-edge for Ni(1-x)Mn(x) (x = 0.25, 0.24 and 0.20) show that (i) the local magnetic structure around the Mn atom is quite different from that around the Ni atom, and (ii) the peak intensity in the magnetic XANES of the Mn K-edge depends on the magnetization of the sample in contrast to the Ni K-edge. The Mn K-edge magnetic EXAFS (extended XAFS) for Ni(0.76)Mn(0.24) is also measured. The second and fourth peaks in the Fourier transform are observed to be enhanced in comparison with the non-magnetic EXAFS, indicating that the second- and fourth-shell Ni atoms are replaced by Mn atoms due to heat treatment (atomic ordering). Semi-relativistic theoretical calculation explains the observed magnetic EXAFS.
已对镍锰合金测量了磁性X射线吸收精细结构(XAFS)光谱。对于Ni(1-x)Mn(x)(x = 0.25、0.24和0.20),锰和镍K边的近边区域磁性XAFS(X射线吸收近边结构,XANES)以及X射线磁圆二色性(XMCD)表明:(i)锰原子周围的局部磁性结构与镍原子周围的局部磁性结构有很大不同;(ii)与镍K边相比,锰K边磁性XANES中的峰强度取决于样品的磁化强度。还测量了Ni(0.76)Mn(0.24)的锰K边磁性扩展X射线吸收精细结构(EXAFS)。观察到傅里叶变换中的第二和第四峰与非磁性EXAFS相比有所增强,这表明由于热处理(原子有序化),第二和第四壳层的镍原子被锰原子取代。半相对论理论计算解释了观察到的磁性EXAFS。