Spin–orbit coupling, orbitally entangled antiferromagnetic order, and collective spin–orbital excitations in Sr2VO4

Abstract

Abstract With electron filling n = 1 in the Sr 2 VO 4 compound, the octahedrally coordinated t 2 g orbitals are strongly active when the tetragonal distortion induced crystal field is tuned by external agent such as pressure. Considering the full range of crystal field induced tetragonal splitting in a realistic three-orbital model, collective spin–orbital excitations are investigated using the generalized self-consistent plus fluctuation approach. At ambient pressure, an entangled orbital + antiferromagnetic order is found to be stabilized beyond a critical value (∼30 meV) of spin–orbit coupling which is in the realistic range for 3d ions. The behavior of the calculated energy scales of collective excitations with crystal field is consistent with that of the transition temperatures with pressure as obtained from susceptibility and resistivity anomalies in high-pressure studies.