Theory of resonant inelastic X-ray scattering in vanadium oxides: how to detect $d$-$d$ excitations?

TL;DR

This paper develops a theoretical framework for interpreting resonant inelastic X-ray scattering (RIXS) spectra in vanadium oxides, focusing on $d$-$d$ excitations, by combining model Hamiltonians, ab initio calculations, and symmetry-group methods.

Contribution

It introduces a detailed theoretical approach to analyze RIXS in vanadium oxides, including symmetry considerations and analytical calculations for specific resonant states.

Findings

Predicts low-energy spectral features related to $d$-$d$ excitations in vanadium perovskites.

Provides a method to calculate RIXS amplitudes beyond the fast collision approximation.

Simplifies analysis for particular resonant states using symmetry-group approach.

Abstract

Generic low-energy spectral features related to $d$-$d$ excitations in nearly cubic vanadium perovskites are predicted for the expected $L$-edge resonant inelastic X-ray scattering (RIXS) measurements. Model Hamiltonian describing local electronic properties, including crystal-field effects, of vanadium 3d orbitals in the basic $t_{2g}^2$ configuration is formulated with the help of complementary {\it ab initio} quantum-chemical cluster calculations. In the presence of 2p-core hole, the local Hamiltonian includes strong 2p-3d electron interactions. As a prerequisite for evaluating RIXS transition amplitudes beyond the fast collision approximation, a symmetry-group approach is applied to generate a basis set of many-electron wavefunctions of the intermediate core-hole states accessible in RIXS processes. Although a comprehensive description of the core-hole multiplets still remains a formidable task and requires using specially designed numerical codes, for particular resonant states the analysis is simplified and the calculation of RIXS amplitude can be carried out analytically to the end.