Scheme 1. Schematic illustration of the formation of mixed SAMs and immobilization of Fc-D on Au electrodes.
Fig. 1. Cyclic voltammograms of (a) SAMs and Fc-D-modified Au UME (10 μm diameter) or (b) Au electrode (4.5 mm diameter) and (c) 11-Fc-thiol mixed SAMs modified Au UME (10 μm diameter) or (d) Au electrode (4.5 mm diameter), by varying the scan rate from 50 to 500 mV/s in electrolyte solution. (Inset box) Plot of anodic peak currents vs. potential sweep rates.
Fig. 2. Cyclic voltammograms of (a) Fc-D modified Au UME and (b) Fc-D modified Au electrode in electrolyte solution with (red)/without (black) 0.5 mM p-AP. Scan rate was 50 mV/s.
Fig. 3. Cyclic voltammograms of (a) Fc-D modified Au UME and (b) Fc-D modified Au electrode in electrolyte solution containing various concentrations of p-AP. Scan rate was 50 mV/s.
Fig. 4. Calibration plot corresponding to change (a) in anodic limiting current for Fc-D modified Au UME and (b) in anodic peak current for Fc-D modified Au electrode upon different concentration of p-AP. The detecting limit (dashed line) was determined by multiplying the standard deviation of zero concentration results by 3.
Fig. 5. Cyclic voltammogram of SAMs and Fc-D modifiedAu UME in electrolyte solution containing 0.5 mM of p-AP by varying the scan rate from 50 to 500 mV/s.
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