Abstract
Kinetics of the V5+/V4+ redox reaction on Vulcan XC-72 modified glassy carbon disk electrode is investigated in a three-electrode configuration. Cyclic voltammograms of V5+/V4+ redox couple suggest that the overpotential range for the kinetic analysis is limited to ±300 mV, after excluding V4+/V3+ redox reaction at the negative overpotential and the oxygen evolution reaction at the positive overpotential. The linear sweep-voltammograms (LSVs) are corrected for potential drop due to solution resistance (iR s ), mass-transfer resistance, and most importantly, for the back reaction current. These corrections are imperative to estimate the Tafel slope in the limited range of overpotential for V5+/V4+ redox reaction. The charge-transfer coefficient (α) estimated from the Tafel slope deviates significantly from the expected value of 0.5 for the single electron-transfer reaction. Moreover, the instantaneous slope of the Tafel plot suggests that the α is overpotential dependent. Therefore, Marcus theory of electrochemical kinetics is applied to estimate the α. The reorganization energy (λ) calculated from the Arrhenius plots is in the range of values reported in the literature for the other redox couples.
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