Spectroscopy and electronic structure of Sr2YRuO6 and Sr2YRu0.75Ir0.25O6

E. B. Guedes, M. Abbate, F. Abud, R. F. Jardim, F. C. Vicentin, and R. J. O. Mossanek
Phys. Rev. B 94, 045109 – Published 11 July 2016

Abstract

We study the electronic structure of the Sr2YRuO6 and Sr2YRu0.75Ir0.25O6 compounds using x-ray (resonant) photoemission and absorption spectroscopies. The experimental results are interpreted with first-principles calculations, which give a good agreement with all the spectra. These results show that, although the spin-orbit coupling does not induce orbital anisotropies in these systems, it is responsible for the reduction of magnetic moments within the the Ir5+O6 octahedra, weakening the magnetic ordering in the substituted system. Finally, our findings support the idea that the canting of Ru5+ magnetic moments actually plays an important role in the stabilization of the intriguing magnetic ordering in the Sr2YRuO6 compound.

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  • Received 15 February 2016
  • Revised 18 May 2016

DOI:https://doi.org/10.1103/PhysRevB.94.045109

©2016 American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied Physics

Authors & Affiliations

E. B. Guedes1,*, M. Abbate1, F. Abud2, R. F. Jardim2, F. C. Vicentin3, and R. J. O. Mossanek1

  • 1Departamento de Física, Universidade Federal do Paraná, Caixa Postal 19044, 81531-990 Curitiba-PR, Brazil
  • 2Instituto de Física, Universidade de São Paulo, 05315-970 São Paulo-SP, Brazil
  • 3Laboratório Nacional de Luz Síncrotron, Caixa Postal 6192, 13083-970 Campinas-SP, Brazil

  • *guedes@fisica.ufpr.br

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Issue

Vol. 94, Iss. 4 — 15 July 2016

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