Dynamic spin filtering at the Co/Alq3 interface mediated by weakly coupled second layer molecules

Spin filtering at organic-metal interfaces is often determined by the details of the interaction between the organic molecules and the inorganic magnets used as electrodes. Here we demonstrate a spin-filtering mechanism based on the dynamical spin relaxation of the long-living interface states forme...

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Veröffentlicht in:Nature communications 2016-08, Vol.7 (1), p.12668-12668, Article 12668
Hauptverfasser: Droghetti, Andrea, Thielen, Philip, Rungger, Ivan, Haag, Norman, Großmann, Nicolas, Stöckl, Johannes, Stadtmüller, Benjamin, Aeschlimann, Martin, Sanvito, Stefano, Cinchetti, Mirko
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Sprache:eng
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Zusammenfassung:Spin filtering at organic-metal interfaces is often determined by the details of the interaction between the organic molecules and the inorganic magnets used as electrodes. Here we demonstrate a spin-filtering mechanism based on the dynamical spin relaxation of the long-living interface states formed by the magnet and weakly physisorbed molecules. We investigate the case of Alq 3 on Co and, by combining two-photon photoemission experiments with electronic structure theory, show that the observed long-time spin-dependent electron dynamics is driven by molecules in the second organic layer. The interface states formed by physisorbed molecules are not spin-split, but acquire a spin-dependent lifetime, that is the result of dynamical spin-relaxation driven by the interaction with the Co substrate. Such spin-filtering mechanism has an important role in the injection of spin-polarized carriers across the interface and their successive hopping diffusion into successive molecular layers of molecular spintronics devices. At the hybrid interface between an organic molecular layer and a metallic magnetic surface, spin-filtering effects may be exploited for the generation of spin polarization. Here, the authors demonstrate a dynamic spin-filtering effect across the Co/Alq 3 interface, mediated via a second Alq 3 layer.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms12668