Publication Detail / Abstract

Distortions of the oxygen octahedra influence the fundamental electronic structure of perovskite oxides, such as their bandwidth and exchange interactions. Utilizing a fully ab initio methodology based on density functional theory plus dynamical mean field theory (DFT+DMFT), we study the crystal and magnetic structure of ₃. Comparing our results with DFT+U performed on the same footing, we find that DFT+U overestimates the propensity for magnetic ordering, as well as the octahedral rotations, leading to a different ground-state structure. This demonstrates that structural distortions can be highly sensitive to electronic correlation effects and to the considered magnetic state, even in a moderately correlated metal such as SrMoO₃. Moreover, by comparing different downfolding schemes, we demonstrate the robustness of the DFT+DMFT method for obtaining structural properties, highlighting its versatility for applications to a broad range of materials.