P. Marcus et al., DETERMINATION OF ATTENUATION LENGTHS OF PHOTOELECTRONS IN ALUMINUM AND ALUMINUM-OXIDE BY ANGLE-DEPENDENT X-RAY PHOTOELECTRON-SPECTROSCOPY, Surface and interface analysis, 20(11), 1993, pp. 923-929
Angle-dependent x-ray photoelectron spectroscopy (AD-XPS) measurements
have been carried out on thin aluminium oxide layers formed on pure a
luminium by oxidation in oxygen at 25-degrees-C and at 250-degrees-C.
The amounts of oxygen of the oxide overlayers were measured by nuclear
reaction analysis (NRA). The equivalent thicknesses of the oxide laye
rs were 14 angstrom and 21.5 angstrom for the oxides formed at 25-degr
ees-C and at 250-degrees-C, respectively. The AD-XPS measurements were
carried out in the range of take-off angles 12-122-degrees. The signa
ls emitted by Al3+ in the oxide and by Al(m) in the metal versus take-
off angle can be, within experimental error, fitted by an exponential
function in the range of take-off angles approximately 30-120-degrees.
This confirms the applicability of an exponential law for the attenua
tion of photoelectrons for the studied system in the range of take-off
angles approximately 30-120-degrees. The AD-XPS measurements were use
d to determine the attenuation lengths of the electrons emitted by alu
minium (kinetic energy approximately 1180 eV) in the oxide (lambda(ox)
) and in the metal (lambda(m)). The attenuation lengths derived from t
he experiments are: lambda(ox) = 20 angstrom and lambda(m) = 18 angstr
om. These values are lower than the theoretical inelastic mean free pa
ths owing to the contribution of elastic scattering. For the lowest in
vestigated take-off angles (<30-degrees) the measurements deviate from
the exponential law. The deviation is attributed to the effects of el
astic scattering and of the angle of acceptance of the photoelectrons.
As a complement to this work, an intercomparison of AD-XPS measuremen
ts was performed in four laboratories on the two reference samples. In
the range of take-off angles 40-120-degrees, the results can be fitte
d by the exponential law for the attenuation of the photoelectrons. Ho
wever, differences of 10-20% were observed in the apparent overlayer t
hickness. Careful analysis of the data revealed that this was primaril
y caused by a systematic error introduced in the peak fitting when a s
ymmetrical peak is used, instead of an asymmetrical peak, for the Al(m
) signal.