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Unveiling complex magnetic structures of the 4f−4d exchange coupled antiferromagnets Ba3RRu2O9 (R=Tb,Er)

Deepak Garg1,*, C. Ritter2, M. Skoulatos3, S. Nandi4,5, and Yixi Su1

  • *Contact author: deepak1.phy@gmail.com

Phys. Rev. B 113, 144435 – Published 28 April, 2026

DOI: https://doi.org/10.1103/pbtn-g5wz

Abstract

The magnetic structures of Ba3RRu2O9 (R=Tb,Er) have been investigated using high-intensity neutron powder diffraction (NPD) supported by dc and ac susceptibility studies. The NPD data reveal antiferromagnetic (AFM) ground states below TN ∼9.8 and 6 K in Ba3TbRu2O9 and Ba3ErRu2O9, respectively, consistent with the magnetic transitions observed in dc and ac susceptibility measurements. In Ba3TbRu2O9, the magnetic structure is characterized by a propagation vector, k=(0,0,0), where Tb and Ru order ferromagnetically in the ab plane. Neighboring planes of Tb are coupled antiferromagnetically along the c direction as are neighboring planes of Ru, which leads to an AFM order between Tb and Ru as well. In contrast, the magnetic structure of Ba3ErRu2O9 is characterized by k=(0.5,0,0), with Er and Ru moments exhibiting a canted AFM ordering. Interestingly, the collinear (noncollinear) AFM order of Tb (Er) accompanied by the collinear (noncollinear) magnetic order of Ru in Ba3TbRu2O9 (Ba3ErRu2O9) along with the concurrent ordering of the rare earth and Ru in both compounds suggests a strong coupling between 4f and 4d electrons. Both compounds show weak magnetic ordering above TN similar to that reported for Ba3HoRu2O9. We have understood this intriguing feature by preparing a Ba3ErRu2O9 sample with 3% excess RuO2. Our analysis suggests that the weak magnetic ordering above TN is strongly dependent on the excess RuO2; however, and interestingly, the magnetic structure below TN is robust against this RuO2 surplus. Our detailed study provides insights into the magnetic ground states of these two compounds, thereby enhancing the understanding of magnetic ordering in this fascinating family.

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