London Centre for Nanotechnology and Department of Physics and Astronomy, University College London, London WC1E 6BT, United Kingdom and Diamond Light Source Ltd, Diamond House, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE, United Kingdom.
Royal Commission for the Exhibition of 1851 Research Fellow, Interface Analysis Centre, University of Bristol, Bristol BS2 8BS, United Kingdom.
Phys Rev Lett. 2013 Mar 15;110(11):117207. doi: 10.1103/PhysRevLett.110.117207. Epub 2013 Mar 13.
The magnetic structure and electronic ground state of the layered perovskite Ba(2)IrO(4) have been investigated using x-ray resonant magnetic scattering. Our results are compared with those for Sr(2)IrO(4), for which we provide supplementary data on its magnetic structure. We find that the dominant, long-range antiferromagnetic order is remarkably similar in the two compounds and that the electronic ground state in Ba(2)IrO(4), deduced from an investigation of the x-ray resonant magnetic scattering L(3)/L(2) intensity ratio, is consistent with a J(eff)=1/2 description. The robustness of these two key electronic properties to the considerable structural differences between the Ba and Sr analogues is discussed in terms of the enhanced role of the spin-orbit interaction in 5d transition metal oxides.
使用 X 射线共振磁散射研究了层状钙钛矿 Ba(2)IrO(4)的磁结构和电子基态。我们的结果与 Sr(2)IrO(4)的结果进行了比较,我们为其提供了有关其磁结构的补充数据。我们发现,两种化合物中占主导地位的长程反铁磁有序非常相似,并且从 X 射线共振磁散射 L(3)/L(2)强度比的研究中推断出的 Ba(2)IrO(4)的电子基态与 J(eff)=1/2 描述一致。讨论了这些两个关键电子性质对 Ba 和 Sr 类似物之间相当大的结构差异的稳健性,这是由于 5d 过渡金属氧化物中自旋轨道相互作用的增强作用。