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Impact on Interface Spin Polarization of Molecular Bonding to Metallic Surfaces

Source: Phys. Rev. Lett. 105, 077201 (2010); doi:10.1103/PhysRevLett.105.077201

Published 13 August 2010

PACS
  • 85.75.-d
    Magnetoelectronics; spintronics
  • 31.10.+z
    Theory of electronic structure, electronic transitions, and chemical binding in atoms and molecules
  • 75.70.-i
    Magnetic properties of thin films, surfaces, and interfaces
  • 78.70.Dm
    X-ray absorption spectra (condensed matter)
  • YEAR: 2010
PUBLICATION DATA
ISSN:
1553-9644 (online)
Publisher:
AIP is a member of CrossRef APS
S. Javaid,1 M. Bowen,1 S. Boukari,1 L. Joly,1,2 J.-B. Beaufrand,1 Xi Chen,1 Y. J. Dappe,1 F. Scheurer,1 J.-P. Kappler,1 J. Arabski,1 W. Wulfhekel,3 M. Alouani,1 and E. Beaurepaire1
1IPCMS UMR 7504 CNRS, Université de Strasbourg, 23 rue du Loess, BP 43, 67034 Strasbourg Cedex 2, France
2Swiss Light Source, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland
3Physikalisches Institut, Karlsruhe Institute of Technology, Wolfgang-Gaede-Strasse 1, 76131 Karlsruhe, Germany

We have studied the repercussion of the molecular adsorption mechanism on the electronic properties of the interface between model nonmagnetic or magnetic metallic surfaces and metallo-organic phthalocyanines molecules (Pcs). Our intertwined x-ray absorption spectroscopy experiments and computational studies reveal that manganese Pc (MnPc) is physisorbed onto a Cu(001) surface and retains the electronic properties of a free molecule. On the other hand, MnPc is chemisorbed onto Co(001), leading to a dominant direct exchange interaction between the Mn molecular site and the Co substrate. By promoting an interfacial spin-polarized conduction state on the molecule, these interactions reveal an important lever to tailor the spintronic properties of hybrid organic-metallic interfaces.
History: Received 20 January 2010; published 13 August 2010
Permalink: http://link.aps.org/abstract/PRL/v105/e077201
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