期刊
NEW JOURNAL OF PHYSICS
卷 21, 期 -, 页码 -出版社
IOP PUBLISHING LTD
DOI: 10.1088/1367-2630/aaff1b
关键词
epitaxial strain; iridates; spin-orbit; electronic structure; Gamma-X crossover; optical anisotropy
资金
- U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-FG02-00ER45818]
- US Department of Energy
We study the modification of the electronic structure in the strong spin-orbit coupled Sr2IrO4 by epitaxial strain using density-functional methods. Structural optimization shows that strain changes the internal structural parameters such as the Ir-O-Ir bond angle, which has an important effect on the band structure. An interesting prediction is the G-X crossover of the valence band maximum with strain, while the conduction minimum at M remains unchanged. This in turn suggests strong strain dependence of the transport properties for the hole-doped system, but not when the system is electron doped. Taking the measured value of the Gamma-X separation for the unstrained case, we predict the Gamma-X crossover of the valence band maximum to occur for the tensile epitaxial strain e(xx) approximate to 3%. A minimal tight-binding model within the J(eff) = 1/2 subspace is developed to describe the main features of the band structure. The optical absorption spectra under epitaxial strain are computed using density-functional theory, which explains the observed anisotropy in the optical spectra with the polarization of the incident light. We show that the optical transitions between the Ir (d) states, which are dipole forbidden, can be explained in terms of the admixture of Ir (p) orbitals with the Ir (d) bands.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据