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Methodological advents for the calculation of the multiplet energy levels arising from multiple-open-shell 2p 5 3d n+1 electron configurations, with n = 0, 1, 2,… and 9, are presented. We use the Ligand-Field Density Functional Theory (LFDFT) program, which has been recently implemented in the Amsterdam Density Functional (ADF) program package. The methodology consists of calculating the electronic structure of a central metal ion together with its ligand coordination by means of the Density Functional Theory code. Besides, the core-hole effects are treated by incorporating many body effects and corrections via the configuration interaction algorithm within the active space of Kohn-Sham orbitals with dominant 2p and 3d characters of the transition metal ions, using an effective ligand-field Hamiltonian. The Slater-Condon integrals (F 2 (3d,3d), F 4 (3d,3d), G 1 (2p,3d), G 3 (2p,3d) and F 2 (2p,3d)), spin-orbit coupling constants (ζ 2p and ζ 3d ) and parameters of the ligand-field potential (represented within the Wybourne formalism) are therefore determined giving rise to the multiplet structures of systems with 3d n and 2p 5 3d n+1 configurations. The oscillator strengths of the electric-dipole allowed 3d n → 2p 5 3d n+1 ransitions are also calculated allowing the theoretical simulation of the absorption spectra of the 2p core-electron excitation. This methodology is applied to transition metal ions in the series Sc 2+ , Ti 2+ ,…, Ni 2+ and Cu 2+ but also to selective compounds, namely SrTiO 3 and MnF 2 . The comparison with available experimental data is good. Therefore, a non-empirical ligand-field treatment of the 2p 5 3d n+1 configurations is established and available in the ADF program package illustrating the spectroscopic details of the 2p core-electron excitation that can be valuable in the further understanding and interpretation of the transition metal L 2,3 -edge X-ray absorption spectra.

physical chemistry chemical physics

A non-empirical calculation of 2p core-electron excitation in compounds with 3d transition metal ions using ligand-field and density functional theory (LFDFT)