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Phys. Rev. B 78, 174406 (2008) [5 pages]

Near-zero-moment ferromagnetism in the semiconductor SmN

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C. Meyer1,2, B. J. Ruck1,*, J. Zhong1, S. Granville1, A. R. H. Preston1, G. V. M. Williams3, and H. J. Trodahl1,4
1The MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University, P.O. Box 600, Wellington 6140, New Zealand
2Institut Néel, CNRS-UJF, BP 166, 38042 Grenoble, France
3The MacDiarmid Institute for Advanced Materials and Nanotechnology, Industrial Research Ltd., P.O. Box 31310, Lower Hutt 5040, New Zealand
4Ceramics Laboratory, EPFL-Swiss Federal Institute of Technology, Lausanne 1015, Switzerland

Received 16 October 2008; published 6 November 2008

The magnetic behavior of SmN has been investigated in stoichiometric polycrystalline films. All samples show ferromagnetic order with Curie temperature (TC) of 27±3 K, evidenced by the occurrence of hysteresis below TC. The ferromagnetic state is characterized by a very small moment and a large coercive field, exceeding even the maximum applied field of 6 T below about 15 K. The residual magnetization at 2 K, measured after cooling in the maximum field, is 0.035μB per Sm. Such a remarkably small moment results from a near cancellation of the spin and orbital contributions for Sm+3 in SmN. Coupling to an applied field is therefore weak, explaining the huge coercive field. The susceptibility in the paramagnetic phase shows temperature-independent Van Vleck and Curie-Weiss contributions. The Van Vleck contribution is in quantitative agreement with the field-induced admixture of the J=7/2 excited state and the 5/2 ground state. The Curie-Weiss contribution returns a Curie temperature that agrees with the onset of ferromagnetic hysteresis, and a conventional paramagnetic moment with an effective moment of 0.4μB per Sm ion, in agreement with expectations for the crystal-field modified effective moment on the Sm+3 ions.

© 2008 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.78.174406
DOI:
10.1103/PhysRevB.78.174406
PACS:
75.50.Pp, 75.30.Cr, 74.70.Ad

*ben.ruck@vuw.ac.nz