As the CASYMS chamber only provides an ion beam, the needed neutral
particles had to be produced in the setup itself. A polished tungsten(110)
surface of 25x30mm was chosen to neutralize the ion beam from the
CASYMS source [33]. The beam hits the neutralization
surface (NS) at grazing incidence (11
). This neutralizes
almost 100% of the ions (see also Section 3.2.1).
The neutralization of the positive ions is also associated with dissociation
of molecules making it possible to use CO
primary ions
to produce neutral oxygen atoms and N
ions to produce
nitrogen atoms. Molecular beams have a far higher intensity than corresponding
atomic ion beams at CASYMS. The drawback of using molecules is that
at the low energies used a considerable fraction of molecules might
have survived and hit the conversion surface in the actual instrument
as molecules instead of atoms. But these surviving molecules would
have been easily be identifiable by the time-of-flight (CODIF). The
measurements showed no substantial molecule fraction even at the lowest
energies investigated. Thus the dissociation was assumed to be very
effective even at lower energies (< 200eV per oxygen atom) contrary
to results reported in [37,38]. The high dissociation
yield might be due to the different material used (W instead of Pd)
and also due to a possible overlayer on the surface most probably
water as the NS was not heated or cleaned as described in [33].
Figure 6.2 depicts a schematic view of
the neutralizer including the beam path.
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The primary ion beam flux impinging on the neutralizer is estimated
in Equation 6.1. denotes
the primary molecular ion flux measured using the beam scanner in
CASYMS. This scanner has a sensitive area
of 10mm
and is realized with a channeltron. The neutralization surface has
a active area
of 30x25mm
and is tilted
to an angle
of 11
. The total primary ion
flux
is given by
The neutral particle intensity after the charged particles deflection
plates is estimated in Equation 6.2.
denotes the fraction of neutral particles either molecules or atom
pairs) after reflection (
0.95 for tungsten),
the reflection efficiency into an solid angle of 22.5
x22.5
(see Chapter 4.2.2). The reflection efficiency
is estimated to be 0.2 for tungsten at an incidence angle of 11
.
denotes the fraction of the into the 22.5
x22.5
cone reflected particles that are within a solid angle of 9
x1.3
(this is the effective beam divergence after the exit aperture). The
latter angle was selected such that the neutral beam covers the conversion
surface (CS) completely even when the CS is moved around using the
x-translation table.
was estimated using angular
scattering images from tungsten single crystals and has a value of
0.16. An additional factor
accounts for the possible
misalignment of the into three tungsten crystal pieces divided neutralizer
surface. This loss was estimated to be of the order of 0.5. Additional
loss
is due to the fact that only particles scattered
from the middle of the conversion surface would make it through the
exit aperture when scattered inside the 9
x1.3
solid angle. Particles impinging near the edge of the neutralization
surface are more likely to be absorbed by the exit aperture. Although
more accurate calculations should be done to estimate the loss due
to this effect, a value of 0.5 was used for
. The
neutral flux
at the exit of the neutralizer is then given
by
The factor of 2 accounts for the dissociation of molecules yielding
two usable particles (either two nitrogen atoms when using a N
primary beam or an oxygen and a carbon monoxide molecule when using
a CO
primary beam [39]). With typical
count rates
at the beam scanner of 30kHz this yields
a neutral beam intensity
of about 6000 neutral particles
per second.
March 2001 - Martin Wieser, Physikalisches Institut, University of Berne, Switzerland