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Appl. Phys. Lett. 97, 232501 (2010); http://dx.doi.org/10.1063/1.3520488 (3 pages)

CoIr-carbon complexes with magnetic anisotropies larger than 0.2 eV: A density-functional-theory prediction

Ruijuan Xiao, Michael D. Kuz’min, Klaus Koepernik, and Manuel Richter

IFW Dresden e.V., P.O. Box 270116, D-01171 Dresden, Germany

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(Received 27 October 2010; accepted 5 November 2010; published online 6 December 2010)

We report a density-functional study of the heteronuclear CoIr dimer adsorbed on benzene or graphene. In either case, CoIr prefers an upright position above the center of a carbon hexagon with the Co atom next to it. The Ir atom stays away from the carbon ring and thus preserves its free-atom-like properties. This results in a very large magnetic anisotropy of more than 0.2 eV per dimer. So high a value should suffice for long-term data storage at the temperature of liquid nitrogen.

© 2010 American Institute of Physics

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KEYWORDS and PACS

PACS

  • 75.30.Gw

    Magnetic anisotropy

  • 31.15.es

    Applications of density-functional theory (e.g., to electronic structure and stability; defect formation; dielectric properties, susceptibilities; viscoelastic coefficients; Rydberg transition frequencies)

ARTICLE DATA

PUBLICATION DATA

ISSN

0003-6951 (print)  
1077-3118 (online)

For access to fully linked references, you need to log in.
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    R. Xiao, D. Fritsch, M. D. Kuz'min, K. Koepernik, M. Richter, K. Vietze, and G. Seifert, Phys. Rev. B 82, 205125 (2010).

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