London Centre for Nanotechnology and Department of Physics and Astronomy, University College London, London, UK.
J Phys Condens Matter. 2012 Aug 8;24(31):312202. doi: 10.1088/0953-8984/24/31/312202. Epub 2012 Jul 9.
This report presents azimuthal dependent and polarization dependent x-ray resonant magnetic scattering at the Ir L(3) edge for the bilayered iridate compound Sr(3)Ir(2)O(7). The two magnetic wave vectors, k1 = (1/2, 1/2, 0) and k2 = (1/2, -1/2, 0), result in domains of two symmetry-related G-type antiferromagnetic structures, denoted A and B, respectively. These domains are approximately 0.02 mm(2) and are independent of the thermal history. An understanding of this key aspect of the magnetism is necessary for an overall picture of the magnetic behaviour in this compound. The azimuthal and polarization dependence of the magnetic reflections, relating to both magnetic wavevectors, show that the Ir magnetic moments in the bilayer compound are oriented along the c axis. This contrasts with single layer Sr(2)IrO(4) where the moments are confined to the ab plane.
这份报告介绍了在 Ir L(3) 边缘的双层铱酸盐化合物 Sr(3)Ir(2)O(7)的方位角相关和偏振相关的 X 射线共振磁散射。两个磁向量 k1 = (1/2, 1/2, 0) 和 k2 = (1/2, -1/2, 0),导致了两个具有对称性相关 G 型反铁磁结构的畴,分别表示为 A 和 B。这些畴大约为 0.02 平方毫米,并且与热历史无关。对于这种化合物的磁行为的整体描述,理解这一关键方面是必要的。与两个磁向量都相关的磁反射的方位角和偏振依赖性表明,双层化合物中的 Ir 磁矩沿 c 轴取向。这与单层 Sr(2)IrO(4)形成对比,其中磁矩局限在 ab 平面内。