Rk. Schulze et al., AL DEPOSITION ON FE - FORMATION OF AN IRON ALUMINIDE SURFACE ALLOY, Journal of vacuum science & technology. A. Vacuum, surfaces, and films, 12(6), 1994, pp. 3054-3061
Citations number
15
Categorie Soggetti
Physics, Applied","Materials Science, Coatings & Films
An investigation has been made of the formation of a surface iron-alum
inum alloy through aluminum adsorption (and subsequent reaction) on Fe
(100) single-crystal and polycrystalline Fe surfaces. On the Fe(100) s
urface, Auger electron spectroscopy and low-energy ion scattering spec
troscopy (LEISS) studies indicate that at low Al coverages (<1 ML), an
d a very low Al deposition rate (<0.03 ML/min), a surface alloy grows
uniformly at 25 degrees C to yield an aluminide with an approximate av
erage stoichiometry of FeAl3. At higher Al exposures the surface becom
es more aluminum rich. This Al enrichment is due to a kinetic limitati
on in the formation of the surface alloy. Heating the surface (300 deg
rees C during or after Al deposition) partially overcomes this kinetic
limitation, and the topmost surface layer changes to a stable stoichi
ometry with some reduction in the relative aluminum concentration. Low
-energy electron diffraction observations made during the Al depositio
n (or subsequent heating experiments) gave no indication of long-range
order, suggesting the formation of a disordered surface alloy. LEISS
experiments show that at 25 degrees C, the final stoichiometric config
uration of the surface is highly dependent on the average arrival rate
of Al at the surface. A higher deposition rate ultimately leads to a
more aluminum-rich surface than for an equivalent dose at a lower rate
. This may be rationalized by noting that at higher deposition rates t
he Al atoms are more likely to encounter other Al atoms at the surface
and may proceed to form two-dimensional microclusters of Al instead o
f reacting to form a surface or subsurface aluminide alloy. The thermo
dynamic implications of these observations in the context of the forma
tion of intermetallic alloy phases seen here will be discussed.