Crystal-field effects competing with spin-orbit interactions in NaCeO${}_2$

Abstract

Ce compounds feature a remarkable diversity of electronic properties, which motivated extensive investigations over the last decades. Inelastic neutron scattering represents an important tool for understanding their underlying electronic structures but in certain cases a straightforward interpretation of the measured spectra is hampered by the presence of strong vibronic couplings. The latter may give rise to extra spectral features, which complicates the mapping of experimental data onto standard multiplet diagrams. To benchmark the performance of embedded-cluster quantum chemical computational schemes for the case of $4f$ systems, we here address the Ce 4$f^1$ multiplet structure of NaCeO${}_2$, an antiferromagnet with $D_{2d}$ magnetic-site symmetry for which neutron scattering measurements indicate only weak vibronic effects. Very good agreement with the experimental results is found in the computations, which validates our computational approach and confirms NaCeO${}_2$ as a 4$f$ magnet in the intermediate coupling regime with equally strong 4$f$-shell spin-orbit and crystal-field interactions.

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Cited by in corpus (3)

• Electronic and structural properties of RbCeX${}_2$ (X${}_2$: O${}_2$, S${}_2$, SeS, Se${}_2$, TeSe, Te${}_2$)
• Yb${}^{3+}$ $f$-$f$ excitations in NaYbSe${}_2$: benchmarking embedded-cluster quantum chemical schemes for 4$f$ insulators
• Explaining the extra crystal field mode in ACeX2