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• W2003637679 abstract "The electronic structure of the low-dimensional 4d(5) oxides Sr2RhO4 and Ca3CoRhO6 is herein investigated by embedded-cluster quantum chemistry calculations. A negative tetragonal-like t2g splitting is computed in Sr2RhO4 and a negative trigonal-like splitting is predicted for Ca3CoRhO6, in spite of having positive tetragonal distortions in the former material and cubic oxygen octahedra in the latter. Our findings bring to the foreground the role of longer-range crystalline anisotropy in generating noncubic potentials that compete with local distortions of the ligand cage, an issue not addressed in standard textbooks on crystal-field theory. We also show that sizable t2g(5)-t2g(4)eg(1) couplings via spin-orbit interactions produce in Sr2RhO4 ⟨Z⟩ = ⟨Σ(i)l(i)·s(i)⟩ ground-state expectation values significantly larger than 1, quite similar to theoretical and experimental data for 5d(5) spin-orbit-driven oxides such as Sr2IrO4. On the other hand, in Ca3CoRhO6, the ⟨Z⟩ values are lower because of larger t2g-eg splittings. Future X-ray magnetic circular dichroism experiments on these 4d oxides will constitute a direct test for the ⟨Z⟩ values that we predict here, the importance of many-body t2g-eg couplings mediated by spin-orbit interactions, and the role of low-symmetry fields associated with the extended surroundings." @default.
• W2003637679 created "2016-06-24" @default.
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• W2003637679 date "2014-04-29" @default.
• W2003637679 modified "2023-10-09" @default.
• W2003637679 title "Electronic Structure of Low-Dimensional 4d⁵ Oxides: Interplay of Ligand Distortions, Overall Lattice Anisotropy, and Spin–Orbit Interactions" @default.
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• W2003637679 doi "https://doi.org/10.1021/ic402653f" @default.
• W2003637679 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24779549" @default.
• W2003637679 hasPublicationYear "2014" @default.
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