• Medientyp: E-Artikel
  • Titel: Characterization of as‐grown and adsorbate‐covered N‐polar InN surfaces using in situ photoelectron spectroscopy
  • Beteiligte: Eisenhardt, Anja; Himmerlich, Marcel; Krischok, Stefan
  • Erschienen: Wiley, 2012
  • Erschienen in: physica status solidi (a), 209 (2012) 1, Seite 45-49
  • Sprache: Englisch
  • DOI: 10.1002/pssa.201100098
  • ISSN: 1862-6300; 1862-6319
  • Schlagwörter: Materials Chemistry ; Electrical and Electronic Engineering ; Surfaces, Coatings and Films ; Surfaces and Interfaces ; Condensed Matter Physics ; Electronic, Optical and Magnetic Materials
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>The surface electronic properties and adsorption behaviour of as‐grown and oxidized N‐polar InN films are characterized by photoelectron spectroscopy (XPS, UPS). The epitaxial growth of the InN layers was performed by plasma‐assisted molecular beam epitaxy on GaN/6H‐SiC(000‐1). After growth and <jats:italic>in situ</jats:italic> characterization the InN surfaces were exposed to molecular oxygen to evaluate the adsorption behaviour of O<jats:sub>2</jats:sub> on N‐polar InN and to study its impact on the surface electronic properties of the III‐nitride material. The results are compared with studies on In‐polar InN on GaN/sapphire templates. The as‐grown N‐polar InN surface exhibits a pronounced surface state at a binding energy of ∼1.6 eV. The valence band minimum lies about 0.8–1.0 eV below the surface Fermi level. Additionally, the XPS core level binding energies for InN(000‐1) are reduced compared to InN(0001) films, indicating different surface band bending for clean N‐polar and In‐polar InN, respectively. The interaction of molecular oxygen with the InN(000‐1) surface leads to a downward band bending by 0.1 eV compared to the initial state. Additional adsorption of species from the residual gas of the UHV chamber increases the surface downward band bending. Furthermore two pronounced oxygen related states with an energy distance of ∼5 eV could be detected in the valence band region. The adsorbed oxygen results in an additional component in the N1s core level spectra, which is interpreted as formation of NO<jats:sub><jats:italic>x</jats:italic></jats:sub> bonds.</jats:p>