The
oxidation mechanism of hafnium overlayers on an Si(111) substrate
[Hf–Si(111), including the outermost metallic Hf overlayers
and interfacial Hf silicides (HfSi and HfSi4)] was investigated
via high-resolution synchrotron radiation X-ray photoelectron spectroscopy
(SR-XPS) of Hf 4f5/2,7/2, Si 2p1/2,3/2, and
O 1s core levels. The atomic-scale interaction of O2 molecules
with Hf–Si(111) is discussed by comparing the results obtained
following thermal O2 exposures [translational energy (E
t) ≈ 0.03 eV] with those obtained following
supersonic O2 molecular beam (SOMB) irradiation (E
t ≈ 2.2 eV). Metallic Hf and interfacial
HfSi were immediately oxidized to HfO2 and Hf (sub)silicates
(Hf–O–Si configurations) via trapping-mediated dissociative
adsorption. Upon excessive SOMB irradiation, the other interfacial
HfSi4 was oxidized via direct dissociation. When oxidation
proceeded at the Si(111) substrate via excess SOMB irradiation, volatile
Si atoms were emitted from the interfacial SiO2/Si-strained
layers. When the volatile Si atoms were trapped in the overlayers,
the HfO2 overlayers were converted into completely oxidized
Hf silicate layers. However, when the volatile Si atoms passed through
the HfO2 overlayers, they reacted with the impinging O2, and the outermost SiO2 deposition layers were
formed on HfO2 (or Hf silicate) layers.