The sulfur-gold bond has several advantages and was, therefore, the
first bond tested in this thesis. One advantage is that it is a strong
covalent bond with a high bond enthalpy of kJ/mol
[135]. Because nearly all bonds between biomolecules are
weaker, this would be a good proof of principle for the method.
Furthermore, this bond is well known, e.g. GRANDBOIS et al.
presented AFM experiments in 1999 [54] where they
measured a bond-force of
nN at loading-rates of 10nN/sec
for the sulfur-gold bond.
Another key advantage is the
simplified setup shown in
figure 4.2. Magnetic markers
functionalised
with a SH-group on the surface can directly
bind to the patterned gold lines. The fabrication of the sample is much
easier, because there is no surface preparation involved and even the
SiO protection layer is
omitted. Suitable magnetic markers are
commercially available in a wide variety. The SICASTAR-SH
particles from MICROMOD (with a diameter of 1.5m) were used
because these particles passed some important tests.
The most important property is that the markers only bind specifically
to gold and not on the SiO surface of the wafer. To ensure this, we
tested the SICASTAR-SH markers on SiO
surface and
MICROMOD SICASTAR markers without a SH-group on a gold
surface. In both tests, the markers did not bind to the surface.
During the experiments, it became apparent that the binding only works
good when the sample was freshly made. Even an ultrasonic bath in
acetone didn't change this behaviour. This was very much unexpected,
because the gold lines, buried in SiO, should not change over time,
and the magnetic markers are always the same. So, we examined whether
the gold surface changes over time. Auger measurements of a freshly made
gold surface and of a 6 weeks old gold surface are compared in
figure 4.3.