International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XXXV, Part B5. Istanbul 2004
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Split Photodiode Duo
Detector Cantilever & Tip
Sample
Figure 1. AFM contact and non-contact mode. In contact
mode, the change of the cantilever deflection is monitored
with the split photodiode detector. A feedback loop tries to
keep the cantilever deflection constant by moving the z-
scanner in order to maintain a constant photodetector
difference signal. The topographic information is related to
this movement of the z-scanner. When in non-contact mode,
the scanning tip oscillates close to the sample surface. Here
the oscillation amplitude is kept constant and used for
topographic information.
The probe head is a tip mounted on the top of a flexible
cantilever (Figure 1), which scans across the sample surface.
For high resolution, the tip has to be very sharp, usually
between 2nm to 20nm. A piezoelectric tube scanner performs
the scan. Thereby, either the tip is moved or the sample
itself, depending on the device used. The tip surface
interaction is monitored by the reflection of a laser beam at
the cantilever. The laser is detected by a split photodetector,
where the difference in the photodetector output voltage is
related to either the cantilever deflection or the oscillation
amplitude.
In order to use scanning probe methods for the spatial
measurement of surfaces, the measured values (Current) have
to be transformed into metric measures. This involves
special complications, because of the non-linearity of the
scanning motion and the measurement errors due to the
complex probe and sample geometry, which are hard to
determine. A solution of this problem is provided by the
development of metrological AFM (MAFM). These combine
a high vertical measuring accuracy of AFM with the exact
lateral measuring, for instance by controlling the motion of
the AFM with interferometric methods. Because of the
combination of several sophisticated instruments, these
devices are custom-made and therefore very expensive. They
are used mainly for calibration purposes.
2.3 Volumetric measurement
Confocal Laser Scanning Microscopy
Confocal Laser Scanning Microscopy (CLSM) is a 3D light
microscopy technique. The CLSM is based on conventional
microscopes, but the light source is a laser. The laser beam is
focused on a sample in a way, that only one object point is
illuminated. A detector pinhole discriminates against
scattered light that is not emitted in the plane of focus. The
resulting signal information from every object point
represents a data cube. The CLSM can be used in reflection
mode to characterize topographies. In order to achieve
higher resolutions, a laser beam is applied in combination
with a 3D scanner. The resolution of a CLSM is then
restricted by the wavelength of the used laser and the
resolution of the scanning system. CLSM images can be
acquired of a wide range of samples, if only the minimum
requirements concerning reflection are fulfilled. But, since
most objects do not behave as perfect mirrors, data from
reflection mode have to be carefully interpreted. The use of
CLSM in life science is well established for a broad range of
research activities {sce Pawley, 1990], whereas the
application in technical and material science is rather new
[Wendt, 1995, Tiziani et al., 2000].
3. A VERSATILE CALIBRATION OBJECT
In the first place, it has been our aim to create a method for
the quantitative 3D reconstruction of SEM data. This task
could be achieved by using an appropriate tilting stage and
a suitable calibration object [Sinram et al., 2002b]. But, more
and more it became clear that there is a general wish to
combine existing data with additional specific information
provided only by other micro-range measurement methods.
The correlation of complementary information from samples
of interest offers new characteristics and a more precise
analysis of surface features, e.g. if scanning electron
microscopy and confocal laser scanning microscopy are
combined [Al Nawas et al., 2001, Wessel et al., 2003]. Yet, in
order to be able to correlate additional data with existing 3D
datasets, the accuracy of all methods involved has to be
determined. To us, the easiest and most accurate way to
accomplish this task is the calibration of all the micro-
measurement methods involved with one calibration object.
Since every sensor used for analytic purposes has its
specific optical and mechanical peculiarities, the calibration
object has to be carefully designed in order to cope with a
variety of requirements. Most important was the decision to
use gas assisted focused ion beam (FIB) metal deposition to
produce the 3D micro-object. This method allowed the
fabrication of 3D objects of various shape and structure.
However, the precision to be achieved with this kind of
technique has its limits and up to now, can only be roughly
estimated. Considering all of the above facts, we found a
possibility, which is not simply a compromise but a new
methodological approach. It allows correlative 3D
microscopy by using a flexible calibration technique.
3.1 Fabrication by gas assisted ion beam deposition
The most suitable way for the fabrication of the calibration
object was found in the technique of gas assisted focused
ion beam deposition [see Steckl et al., 1988]. Focused ion
beam (FIB) systems operate similar to scanning electron
microscopes, though a focused beam of gallium ions (Ga)
instead of an electron beam is used. The FIB technique
allows imaging or patterning of structures. Patterning in this
case either means the process of specific removal of material
as the beam scans along the sample surface, or the process of
specific deposition of metal (by gas assisted deposition)
onto the surface (Figure 3).
When the gallium ions of the primary beam hit the sample
surface, a small amount of material is sputtered, leaving the
surface as either ions or neutral atoms. This process is called
milling. Additionally, the primary beam produces secondary
electrons (SE). The secondary electrons can be used for
imaging or for gas assisted deposition. If an organometallic
gas, e.g. W(CO)s is introduced into the sample chamber of
the microscope, it interacts with the secondary electrons of
the ion beam as well as the beam itself and forms a nof-
volatile product that adsorbs on the surface. Lateral
deposition and structure formation can be controlled by
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