Crystal structure and magnetic properties of the Ba3TeCo3P2O14, Pb3TeCo3P2O14, and Pb3TeCo3V2O14 langasites

J.W. Krizan, C. de la Cruz, Niels Hessel Andersen, R.J. Cava

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

We report the structural and magnetic characterizations of Ba3TeCo3P2O14, Pb3TeCo3P2O14, and Pb3TeCo3V2O14, compounds that are based on the mineral dugganite, which is isostructural to langasites. The magnetic part of the structure consists of layers of Co2+ triangles. Nuclear and magnetic structures were determined through a co-refinement of synchrotron and neutron powder diffraction data. In contrast to the undistorted P321 langasite structure of Ba3TeCo3P2O14, a complex structural distortion yielding a large supercell is found for both Pb3TeCo3P2O14 and Pb3TeCo3V2O14. Comparison of the three compounds studied along with the zinc analog Pb3TeZn3P2O14, also characterized here, suggests that the distortion is driven by Pb2+ lone pairs; as such, the Pb compounds crystallize in a pyroelectric space group, P2. Magnetic susceptibility, magnetization, and heat capacity measurements were performed to characterize the magnetic behavior. All three compounds become antiferromagnetic with Néel temperatures TN≈21K (Ba3TeCo3P2O14), ≈13K (Pb3TeCo3P2O14), and ≈8K (Pb3TeCo3V2O14), and they exhibit magnetic transitions at high applied magnetic fields, suggesting intrinsically complex magnetic behavior for tetrahedrally coordinated d7 Co2+ in this structure type.

Original languageEnglish
JournalJournal of Solid State Chemistry
Volume203
Pages (from-to)310-320
ISSN0022-4596
DOIs
Publication statusPublished - 2013

Keywords

  • Langasite
  • Dugganite
  • Frustrated magnetism
  • Neutron diffraction
  • Magnetic structure
  • Rietveld co-refinement

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