(561d) Effect of Hydrogen Diffusion on Hydrogen Oxidation/Evolution Kinetics (Invited) | AIChE

(561d) Effect of Hydrogen Diffusion on Hydrogen Oxidation/Evolution Kinetics (Invited)

Authors 

Xu, B. - Presenter, University of Delaware
Yan, Y., University of Delaware
Wang, J., University of Delaware
Yang, X., University of Delaware
Nash, J., University of Delaware
Zheng, J., University of Delaware
Rotating disk electrode (RDE) method is widely employed in studies on the hydrogen oxidation/evolution reaction (HOR/HER) owing to its well-defined mass transport behaviors. While it is accepted that the measured HOR current is controlled by both the electrode kinetics and the diffusion of H2, HER is typically assumed to be free of diffusion limitation. We demonstrate that HER could also be diffusion limited when the electrode kinetics is fast, as evidenced by the rotation speed dependent HER current on Pt in acid (pH = 1) and the overlap of the HER polarization curve with the concentration overpotential curve. The HER diffusion limitation originates from the insufficient mass transport of produced H2 from the electrode surface to the bulk electrolyte and the highly reversible nature of HOR/HER. Kinetic analyses based on HER polarization curves on Pt in acid without correcting for the diffusion limitation could lead to inaccurate Tafel slopes and mechanistic interpretations, and significantly underestimated HER activities. A general data analysis protocol based on the reversible Koutecky-Levich equation is developed to obtain accurate kinetic information of HOR/HER even when electrode kinetics is facile. This new method is compared with other existing methods on Pt disk electrodes at different pHs and thin-film electrodes with different Pt loadings.