Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439, USA.
Phys Rev Lett. 2010 Nov 19;105(21):216407. doi: 10.1103/PhysRevLett.105.216407.
The electronic structure and magnetism of Ir 5d5 states in nonmetallic, weakly ferromagnetic BaIrO3 are probed with x-ray absorption techniques. Contrary to expectation, the Ir 5d orbital moment is found to be ~1.5 times larger than the spin moment. This unusual, atomiclike nature of the 5d moment is driven by a strong spin-orbit interaction in heavy Ir ions, as confirmed by the nonstatistical large branching ratio at Ir L(2,3) absorption edges. As a consequence, orbital interactions cannot be neglected when addressing the nature of magnetic ordering in BaIrO3. The local moment behavior persists even as the metallic-paramagnetic phase boundary is approached with Sr doping or applied pressure.
利用 X 射线吸收技术研究了非金属弱铁磁 BaIrO3 中 Ir5d5 态的电子结构和磁性。与预期相反,Ir5d 轨道磁矩被发现比自旋磁矩大约 1.5 倍。这种不寻常的原子态 5d 矩是由重 Ir 离子中的强自旋轨道相互作用驱动的,这一点在 Ir L(2,3)吸收边的非统计大分支比中得到了证实。因此,在研究 BaIrO3 中磁有序的性质时,不能忽略轨道相互作用。即使在 Sr 掺杂或施加压力接近金属-顺磁相界时,局域磁矩行为仍然存在。