The electronic structure of carbon overlayers on Ni(111) has been investigated by using photoemission, energy-loss, and ionization-loss spectroscopy techniques. The combined use of these spectroscopies gives a detailed picture of these surfaces which have important catalytic implications. The carbidic carbon overlayer shows states at ∼1-, 4.2-, and 13-eV binding energy. Of particular significance is the detection (both in photoemission and in ionization-loss spectroscopy) of a carbon-derived state very near the Fermi level, in excellent agreement with recent theoretical predictions. The graphitic overlayer has an electronic structure very close to the electronic structure of pure graphite. We detect, however, an almost rigid shift of both valence and conduction bands which points to a charge transfer of about 0.02 electrons per carbon atom between the nickel substrate and the graphitic overlayer.

Electronic structure of carbidic and graphitic carbon on Ni(111)

MODESTI, SILVIO;
1984-01-01

Abstract

The electronic structure of carbon overlayers on Ni(111) has been investigated by using photoemission, energy-loss, and ionization-loss spectroscopy techniques. The combined use of these spectroscopies gives a detailed picture of these surfaces which have important catalytic implications. The carbidic carbon overlayer shows states at ∼1-, 4.2-, and 13-eV binding energy. Of particular significance is the detection (both in photoemission and in ionization-loss spectroscopy) of a carbon-derived state very near the Fermi level, in excellent agreement with recent theoretical predictions. The graphitic overlayer has an electronic structure very close to the electronic structure of pure graphite. We detect, however, an almost rigid shift of both valence and conduction bands which points to a charge transfer of about 0.02 electrons per carbon atom between the nickel substrate and the graphitic overlayer.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2559469
 Avviso

Registrazione in corso di verifica.
La registrazione di questo prodotto non è ancora stata validata in ArTS.

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 85
  • ???jsp.display-item.citation.isi??? ND
social impact