DISSERTATION
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________________________________________________________________ Experimental Work<br />
Figure 5.4. Scheme of the electrochemical setup used for determination of the pzc. The<br />
implemented capacitive bridge (Cb) is shown in the figure. CE – counter electrode, RE –<br />
reference electrode, WE – working electrode.<br />
Determination of the pzc of the DNA modified surface was done by initially immobilizing<br />
ssDNA (from 1 µM solution in 10 mM PB with 450 mM K2SO4) on a clean electrode surface<br />
for 5 min via potential-assisted immobilization (0.5/-0.2 V (vs. Ag/AgCl/3 M KCl) following<br />
a pulse profile with 10 ms pulse duration (procedure explained in detail in Section 5.7.2).<br />
Afterwards the electrode was thoroughly rinsed with the immobilization buffer and water,<br />
respectively to remove any loosely bound DNA strands, and placed in an appropriate solution<br />
for pzc determination. PDEIS was performed for a potential range of -0.4 V to 0.5 V vs.<br />
Ag/AgCl (3 M KCl) with 30 mV potential steps. EIS measurements for discrete potential values<br />
were done as in the case of the bare electrode.<br />
5.5 Potential-assisted formation of self-assembled monolayers<br />
Preparation of gold electrodes for thiol self-assembling was done as explained in Chapter 5.3.<br />
After characterization with EIS and CV (see Sections 5.9.1 and 5.9.2) gold electrodes were<br />
immediately used for potential-assisted SAM formation of thiols of different length – MCH,<br />
MCU and MCHD (1 mM in phosphate buffer, 20 mM K2SO4 with 30 % ethanol), using several<br />
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