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Phys. Rev. B 79, 045102 (2009) [9 pages]

Determination of the single-ion anisotropy energy in a S=5/2 kagome antiferromagnet using x-ray absorption spectroscopy

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M. A. de Vries1,2,*, T. K. Johal3, A. Mirone4, J. S. Claydon5, G. J. Nilsen1,2, H. M. Rønnow1, G. van der Laan3,6, and A. Harrison2,7
1Laboratory for Quantum Magnetism, École Polytechnique Fédérale de Lausanne, Station 3, CH-1015 Lausanne, Switzerland
2CSEC and School of Chemistry, The University of Edinburgh, Edinburgh EH9 3JZ, United Kingdom
3Daresbury Laboratory, Warrington WA4 4AD, United Kingdom
4ESRF, 6 rue Jules Horowitz, F-38000 Grenoble, France
5Department of Engineering Materials, University of Sheffield, Sheffield S1 3JD, United Kingdom
6Diamond Light Source, Chilton, Didcot OX11 0DE, United Kingdom
7Institut Laue-Langevin, 6 rue Jules Horowitz, F-38000 Grenoble, France

Received 14 August 2008; revised 30 November 2008; published 6 January 2009

We report x-ray absorption and x-ray linear dichroism measurements at the Fe L2,3 edges of the geometrically frustrated systems of potassium and hydronium iron jarosite. Comparison with simulated spectra, involving ligand-field multiplet calculations modeling the 3d-2p hybridization between the iron ion and the oxygen ligands, has yielded accurate estimates for the ligand metal-ion hybridization and the resulting single-ion crystal-field anisotropy energy. Using this method we provide an experimentally verified scenario for the appearance of a single-ion anisotropy in this nominally high-spin 3d5 orbital singlet 6S system, which accounts for features of the spin-wave dispersion in the long-range-ordered ground state of potassium iron jarosite.

© 2009 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.79.045102
DOI:
10.1103/PhysRevB.79.045102
PACS:
75.25.+z, 71.70.Ch, 71.70.Ej, 75.10.Dg

*markadevries@googlemail.com