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The peak potential of peak Ia shifted to less positive potential when pH was increased.
Table 2 shows the current density response at the peak potential of the glycerol oxidation reaction.
The separation of anodic peak potential of dopamine and ascorbic acid reaches 250 mV.
It was proved with shifted peak potential of IP to a less positive potential rather than bare GCE.
Figure 6 gives the variation of the anodic peak potential of the S30 alloy as function of log (v).
SOX exhibits a pair of well-defined reversible redox peaks in 0.1 M pH 7.0 phosphate buffer solution (PBS) with the oxidation peak potential of −0.446 V and the reduction peak potential of −0.496 V.
The peak potential of palladous oxide reduction shifts to a less positive value with decreasing its hydration degree.
The peak potential of the peak was linearly dependent on pH with dEp/dpH as 42 mV/pH.
Open image in new window Fig. 6 Variation of the anodic peak potential of cyclic voltammograms of S30 sample as function of log v).
However, the peak current density at the oxidation peak potential of MOR increases in accordance to the catalyst support on D14, D16, and D18.
The reduction peak potential of the electrode is close to −0.12 V, which enables high selective amperometric detection of H2O2 at a low applied potential.
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