Electronic structure and optical properties of Sr2IrO4 under epitaxial strain

• Published in: New journal of physics Vol. 21; no. 1; pp. 013036 - 13051
• Main Authors: Bhandari, Churna, Popovi, Zoran S, Satpathy, S
• Format: Journal Article
• Language: English
• Published: Bristol IOP Publishing 31.01.2019
• Subjects: Absorption spectra; Admixtures; Anisotropy; Band structure of solids; crossover; Density functional theory; Dipoles; Electron spin; Electronic structure; Electronics; epitaxial strain; Epitaxy; Incident light; iridates; optical anisotropy; Optical properties; Optimization; Physics; spin-orbit; Transport properties; Valence band; Γ–X crossover
• ISSN: 1367-2630
• DOI: 10.1088/1367-2630/aaff1b

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 Γ−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 Γ−X separation for the unstrained case, we predict the Γ−X crossover of the valence band maximum to occur for the tensile epitaxial strain exx 3%. A minimal tight-binding model within the Jeff = 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.