J. Im et al., IN-SITU ANALYSIS OF THIN-FILM DEPOSITION PROCESS USING TIME-OF-FLIGHT(TOF) ION-BEAM ANALYSIS-METHODS, Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms, 118(1-4), 1996, pp. 772-781
The use of non-destructive, in situ methods for the characterization o
f thin film growth phenomena is the key both to obtaining a better und
erstanding of thin film growth processes and to the development of mor
e reliable deposition procedures, especially for complex layered struc
tures involving multi-phase materials. However, surface characterizati
on methods that utilize tither electrons (e.g. AES or XPS) or low ener
gy ions (SIMS) for the signal require an ultra-high vacuum (UHV) envir
onment and utilize instrumentation which obstructs line of sight acces
s to the substrate. These methods are therefore incompatible with line
of sight deposition methods and thin film deposition processes which
introduce gas, either as an intrinsic part of the deposition procedure
or in order to produce the desired composition. We have developed a m
eans of differentially pumping both the ion beam source and detectors
of a TOF ion beam surface analysis spectrometer that does not interfer
e with the deposition process and permits compositional and structural
analysis of the growing film in the present system, at pressures up t
o several mTorr. Higher pressures are feasible with modified source-de
tector geometry. In order to quantify the sensitivity of Ion Scatterin
g Spectroscopy (ISS) and Direct Recoil Spectroscopy (DRS), we have mea
sured the signal intensity for stabilized clean metals in a variety of
gas environments as a function of the ambient gas species and pressur
e, and ion beam species and kinetic energy. The results are: interpret
ed in terms of collision cross sections which are compared with known
gas phase scattering data and provide an apriori basis for the evaluat
ion of time-of-flight ion scattering and recoil spectroscopies (ToF-IS
ARS) for various industrial processing environments which involve both
inert and reactive gases. The cross section data for primary ion-gas
molecule and recoiled atom-gas molecule interactions are also provided
, from which the maximum operating pressure in any experimental config
uration can be obtained.