Unraveling the Mn L3-edge RIXS spectrum of lightly manganese doped Sr3Ru2O7

Abstract

Resonant inelastic x-ray scattering (RIXS) experiment was performed at the Mn L3 edge. A 10 \% Mn-doped Sr3Ru2O7 compound, where the Mn3+ ions are in the 3d4 state, were probed for dd excitations. The dilute doping concentration allows one to treat the dopant Mn3+ ions as effectively free in the host ruthenium compound. The local nature of dd RIXS spectroscopy permits one to use a single-site model to simulate the experimental spectra. The simulated spectra reproduces the in-plane [100] experimental RIXS spectrum. We also predict the intensity for the in-plane [110] direction and the out-of-plane spin orientation configuration [001]. Based on our single-ion model we were able to fit the experimental data to obtain the crystal field parameters, the 10Dq value, and the intra-orbital spin-flip energy 2J(or 3JH, where JH is the Hund's energy) of the Mn3+ ion. Utilizing our computed RIXS quantum transition amplitudes between the various d orbitals of the Mn3+ ion, the expression for the Kramers-Heisenberg cross section, and a self-consistent fitting procedure we also identify the energy boundaries of the non-spin-flip and spin-flip dd excitations present in the experimental data. From our fitting procedure we obtain 2J (3JH)=2.06 eV, a value which is in excellent agreement with that computed from the free ion Racah parameters. We also identified the charge transfer boundary. In addition to predicting the microscopic parameters, we find a quantum spin-flip transition in the non-cross (σin-σout, πin-πout) x-ray polarization channels of the dd RIXS spectra. A similar transition, was previously predicted to occur in the π-π channel of the magnon spectrum in the non-collinear non-coplanar Kagome compound composed of Cu2+ 3d9 ion.

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