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Dresden 2009 – wissenschaftliches Programm

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MA: Fachverband Magnetismus

MA 40: Poster II: Bio- and Molecular Magnetism (1-9); Magnetic Coupling Phenomena/Exchange Bias (10-15); Magnetic Particlicles and Clusters (16-29); Micro and Nanostructured Magnetic Materials (30-51); Multiferroics (52-64); Spin Injection in Heterostructures (65-67); Spin-Dyn./Spin-Torque (68-93); Spindependent Transport (94-108)

MA 40.59: Poster

Freitag, 27. März 2009, 11:00–14:00, P1A

Investigation of the magnetic configuration of LuFe2O4 by means of XMCD and multiplet calculations — •Christine Derks1, Michael Raekers1, Christian Taubitz1, Karsten Kuepper2, Stephen J. Blundell3, Dharmalingam Prabhakaran3, and Manfred Neumann11Universität Osnabrück, FB Physik, Osnabrück — 2FZ Dresden-Rossendorf, Dresden — 3Clarendon Laboratory, University of Oxford, Oxford, UK

The use of magneto electric coupling and multi ferroics in spintronics has led to an intense research of ferro electric magnets. The spinel LuFe2O4 is a very promising candidate for such applications. This compound exhibits giant room temperature magneto dielectric response, which suggests a strong coupling between spin moment und electric dipole. The resulting giant magneto capacitance is due to charge ordering of mixed valent iron ions. A complex two dimensional ferri magnetism plays an important role for the multi ferroic properties of LuFe2O4. We determine the magnetic configuration by means of XMCD. Experimental data are compared with multiplet calculations, which are performed with the TT multiplet program [1]. The trigonal bipyramidal crystal symmetry was included in these calculations. We suggest a local charge order with a ferrimagnetic structure as found by Mössbauer and neutron diffraction; The minority spin sub lattice exhibits 2/3 of total Fe3+ ions whereas the majority spin subband contains 1/3 of Fe3+ and all the Fe2+ ions. [1] F.M.F. de Groot, High resolution x-ray emission and x-ray absorption spectroscopy, Chem. Rev., vol. 101, pp. 1779-1808, (2001).

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