Sims analysis of residual gas elements.
Dep.
Ingeneria Electrica – SEES, CINVESTAV-IPN, Av. IPN # 2508,
Mexico
D.F. 07300, Mexico
SIMS is the most sensitivity method of the elemental
analysis of solid surface and thin films with the detection limit (DL)
of 1014 atoms/cm3 for the most elements. But in the case
of elements like H, C, N and O, which form atmospheric gases, the DL is
essentially worse. The reason is presence of these gases in the residual
atmosphere of an analytical instrument. The gases adsorb continuous on the
analyzed sample surface and become re-sputtered by an ion beam and registered
as the background signal. Therefore the SIMS signal for these elements (
negative ions in our study) consists of the two components: particles,
presented in the bulk of the target and the same particles, adsorbed and
re-sputtered than:
, (1)
here s is the analyzed surface area, jo
is the primary ion current density, Yx is the partial yield
of element x, bx is the ionization probability
of element x, Rx is the transmission coefficient of the
instrument, Nad is the flux of molecules on analyzed surface
from residual atmosphere, ax is the sticking coefficient
and n is the number of x atoms in the adsorbed molecules.
Under the typical SIMS regime the adsorption rate is
almost 4 order less than the sputtering rate. And we can conclude that a
balance between adsorbed and target atoms depends on the sputtering regime,
only. Moreover, all adsorbed atoms will be re-sputtered back (in time unit).
Eq.(1) gives a method of experimental determination of
both adsorbed and target atoms. Indeed, eq.(1) can be considered as a simple
linear function (
) of the primary ion current density jo.
So, both component of eq.(1) can be found from a linear extrapolation of
experimental dependence of SIMS signal on jo.
We have applied described before technique for
analysis of H, C, O, N, and F in Si and GaAs targets. The DL for the elements
was found almost one order more than for the “standard” SIMS measurements. We
estimated the residual gas composition in the sample chamber, basing on
experimentally found adsorbed component in eq.(1) - Nad.