Pseudospin versus magnetic dipole moment ordering in the isosceles triangular lattice material K3Er(VO4)2

Danielle R. Yahne, Liurukara D. Sanjeewa, Athena S. Sefat, Bradley S. Stadelman, Joseph W. Kolis, Stuart Calder, Kate A. Ross

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Spin-1/2 antiferromagnetic triangular lattice models are paradigms of geometrical frustration, revealing very different ground states and quantum effects depending on the nature of anisotropies in the model. Due to strong spin orbit coupling and crystal field effects, rare-earth ions can form pseudospin-1/2 magnetic moments with anisotropic single-ion and exchange properties. Thus, rare-earth-based triangular lattices enable the exploration of this interplay between frustration and anisotropy. Here we study one such case, the rare-earth double vanadate glaserite material K3Er(VO4)2, which is a quasi-two-dimensional (2D) isosceles triangular antiferromagnet. Our specific heat and neutron powder diffraction data from K3Er(VO4)2 reveal a transition to long range magnetic order at TN=155±5 mK which accounts for all Rln2 entropy. We observe what appears to be a coexistence of three-dimensional (3D) and quasi-2D order below TN. The quasi-2D order leads to an anisotropic Warren-like peak profile for (hk0) reflections, while the 3D order is best-described by layers of antiferromagnetic b-aligned moments alternating with layers of zero moment. Our magnetic susceptibility data reveal that Er3+ takes on a strong XY single-ion anisotropy in K3Er(VO4)2, leading to vanishing moments when pseudospins are oriented along c. Thus, the magnetic structure, when considered from the pseudospin point of view could comprise of alternating layers of b-axis and c-axis aligned antiferromagnetism.

Original languageEnglish
Article number104423
JournalPhysical Review B
Volume102
Issue number10
DOIs
StatePublished - Sep 2020

Funding

We thank Gang Chen and Ovidiu Garlea for useful discussions. This research used resources at the High Flux Isotope Reactor, a DOE Office of Science User Facility operated by the Oak Ridge National Laboratory. Work performed on synthesis, crystal growth, and x-ray diffraction at Clemson University was funded by DOE BES Grant No. DE-SC0014271. D.R.Y., K.A.R., and J.W.K. acknowledge funding from the Department of Energy Award No. SC0020071 during the preparation of this manuscript.

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