DISSERTATION
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_____________________________________________________________ Results and Discussion<br />
(bare) and pzc (DNA). Namely, all pulse profiles have an upper potential equal to the pzc (bare).<br />
Furthermore, they all relate differently to the pzc (DNA). For the 300 mV pulse profile both<br />
potentials are always positive with respect to the pzc (DNA). For the 500 mV pulse profile<br />
pulsing occurs between positive and slightly negative potentials with respect to the pzc (DNA)<br />
and in the 700 mV pulse profile both positive and negative potentials with similar amplitude<br />
with respect to the pzc (DNA) are applied.<br />
Figure 3.21. Selected potential pulse profiles with respect to the pzc (bare) and pzc (DNA):<br />
ΔE = 300 mV (pulse profile 0.5/0.2 V), ΔE = 500 mV (pulse profile 0.5/0 V) and ΔE = 700<br />
mV (pulse profile 0.5/-0.2 V). Figure adapted from ref. 5 .<br />
By applying a 300 mV pulse profile a small increase in Rct as compared to the Rct of the MCHmodified<br />
electrode is observed showing that obviously only a very small amount of DNA was<br />
immobilized (Figure 3.22, blue curve). However, the amount of immobilized DNA still exceeds<br />
the amount of DNA immobilized by means of the incubation method after the same time (Figure<br />
3.22, black curve). This shows that the investigated pulse profile accelerates the immobilization<br />
of DNA. After the initial immobilization of a minor amount of DNA, the pzc shifts from pzc<br />
(bare) to a more negative value (pzc (DNA)). Therefore, since the pulsing occurs only between<br />
positive potentials relative to pzc (DNA) and the potential difference is small, only a minor ion<br />
stirring effect is achieved and upon initial DNA immobilization, the DNA strands remain lying<br />
on the electrode surface. The electrode is physically blocked by the initially immobilized DNA<br />
strands and the access of additional DNA molecules is impeded.<br />
3.3 Importance of controlling the surface 56