Spectroscopic Fingerprints of Work-Function-Controlled Phthalocyanine Charging on Metal Surfaces (Articolo in rivista)

Type
Label
  • Spectroscopic Fingerprints of Work-Function-Controlled Phthalocyanine Charging on Metal Surfaces (Articolo in rivista) (literal)
Anno
  • 2014-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/nn5060333 (literal)
Alternative label
  • Borghetti, Patrizia; Ei-Sayed, Afaf; Goiri, Elizabeth; Rogero, Celia; Lobo-Checa, Jorge; Floreano, Luca; Ortega, Jose Enrique; de Oteyza, Dimas G. (2014)
    Spectroscopic Fingerprints of Work-Function-Controlled Phthalocyanine Charging on Metal Surfaces
    in ACS nano
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Borghetti, Patrizia; Ei-Sayed, Afaf; Goiri, Elizabeth; Rogero, Celia; Lobo-Checa, Jorge; Floreano, Luca; Ortega, Jose Enrique; de Oteyza, Dimas G. (literal)
Pagina inizio
  • 12786 (literal)
Pagina fine
  • 12795 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 8 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 10 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 12 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Donostia Int Phys Ctr; Ctr Phys Mat; University of Basque Country; Lab Nazl TASC (literal)
Titolo
  • Spectroscopic Fingerprints of Work-Function-Controlled Phthalocyanine Charging on Metal Surfaces (literal)
Abstract
  • The electronic character of a p-conjugated molecular overlayer on a metal surface can change from semiconducting to metallic, depending on how molecular orbitals arrange with respect to the electrodes Fermi level. Molecular level alignment is thus a key property that strongly influences the performance of organic-based devices. In this work, we report how the electronic level alignment of copper phthalocyanines on metal surfaces can be tailored by controlling the substrate work function. We even show the way to finely tune it for one fixed phthalocyaninemetal combination without the need to intercalate substrate-functionalizing buffer layers. Instead, the work function is trimmed by appropriate design of the phthalocyanines supramolecular environment, such that charge transfer into empty molecular levels can be triggered across the metalorganic interface. These intriguing observations are the outcome of a powerful combination of surface-sensitive electron spectroscopies, which further reveal a number of characteristic spectroscopic fingerprints of a lifted LUMO degeneracy associated with the partial phthalocyanine charging. (literal)
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