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Coexistence of magnetic order and valence fluctuations in the Kondo lattice system Ce2Rh3Sn5

MPG-Autoren
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Gamża,  M. B.
Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Gumeniuk,  R.
Roman Gumeniuk, Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Burkhardt,  U.
Ulrich Burkhardt, Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Schnelle,  W.
Walter Schnelle, Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Rosner,  H.
Physics of Quantum Materials, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Leithe-Jasper,  A.
Andreas Leithe-Jasper, Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Zitation

Gamża, M. B., Gumeniuk, R., Burkhardt, U., Schnelle, W., Rosner, H., Leithe-Jasper, A., et al. (2017). Coexistence of magnetic order and valence fluctuations in the Kondo lattice system Ce2Rh3Sn5. Physical Review B, 95(16): 165142, pp. 1-12. doi:10.1103/PhysRevB.95.165142.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002D-498F-E
Zusammenfassung
We report on the electronic band structure, structural, magnetic, and thermal properties of Ce2Rh3Sn5. Ce LIII-edge XAS spectra give direct evidence for an intermediate valence behavior. Thermodynamic measurements reveal magnetic transitions at T-N1 approximate to 2.9 K and T-N2 approximate to 2.4 K. Electrical resistivity shows behavior typical for the Kondo lattices. The coexistence of magnetic order and valence fluctuations in a Kondo lattice system we attribute to a peculiar crystal structure in which Ce ions occupy two distinct lattice sites. Analysis of the structural features of Ce2Rh3Sn5, together with results of electronic band structure calculations and thermodynamic and spectroscopic data indicate that at low temperatures only Ce ions from the Ce1 sublattice adopt a stable trivalent electronic configuration and show local magnetic moments that give rise to the magnetic ordering. By contrast, our study suggests that Ce2 ions exhibit a nonmagnetic Kondo-singlet ground state. Furthermore, the valence of Ce2 ions estimated from the Ce LIII-edge XAS spectra varies between +3.18 at 6 K and +3.08 at room temperature. Thus our joined experimental and theoretical investigations classify Ce2Rh3Sn5 as a multivalent charge-ordered system.