Fig. 1: Competing interactions in Pr4+ oxides. | Nature Communications

Fig. 1: Competing interactions in Pr4+ oxides.

From: Chemical design of electronic and magnetic energy scales of tetravalent praseodymium materials

Fig. 1: Competing interactions in Pr4+ oxides.The alternative text for this image may have been generated using AI.

a Hierarchy of single-ion energy scales for Pr4+ ions in octahedral oxygen environments starting from a 2F, (S = 1/2, L = 3) free-ion state. For spin-orbit coupling (SOC) as the dominant energy scale (Jeff = 1/2 limit, left, brown), the low-symmetry crystal field (CF) lifts the degeneracy of the ground-state 2F5/2 and excited 2F7/2 multiplets into seven Kramers doublets (KDs, with selected radial squared wave-functions represented). For approximate Oh symmetry, the Γ7 doublet, in the \(\left|J,{m}_{J}\right\rangle\) basis, is given by \({\Gamma }_{7}^{\pm }=\sin \theta \left|\frac{5}{2},\pm \frac{5}{2}\right\rangle+\cos \theta \left|\frac{5}{2},\mp \frac{3}{2}\right\rangle\), where \({\sin }^{2}\theta \, \approx \, 1/6\) (See SI). For CF as the dominant energy scale (Seff = 1/2 limit, right, blue), SOC and distortion from Oh symmetry lift the 2A2u ground state and the triply degenerate 2T2u and 2T1u excited states into seven KDs. The ground-state doublet is given in the \(\left|{m}_{l},{m}_{s}\right\rangle\) basis by \(\left|\pm \right\rangle=A\,\left|\mp 3,\pm \frac{1}{2}\right\rangle -\,B\,\left|\mp 2,\mp \frac{1}{2}\right\rangle \,+\,C\,\left|\pm 1,\pm \frac{1}{2}\right\rangle -\,D\,\left|\pm 2,\mp \frac{1}{2}\right\rangle\), where \({({A}^{2}/{B}^{2})}^{{\Gamma }_{7}} \, \approx \, 2.6\) and \({({C}^{2}/{D}^{2})}^{{\Gamma }_{7}} \, \approx \, 0.33\) for the \(\left|{\Gamma }_{7}\right\rangle\) doublet62 (See SI). In the intermediate limit, the competition between ΔCF and ζSOC scales in Pr4+ yields seven KD (indicated by the mix of brown/blue lines) with magnetic properties that are distinct from the Jeff = 1/2 and Seff = 1/2 limits, such as large magnetic super-exchange achievable by tuning the ligand field. bd Crystal structure, magnetic lattice dimensionality, and Pr4+ coordination environment for the oxides studied in this work: Na2PrO3 (2-Pr), Sr2PrO4 (1-Pr), and Li8PrO6 (0-Pr), respectively.

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