Bubbles are known to hinder electrochemical processes in water-splitting electrodes. In this study, we present a novel method to promote gas evolution away from the electrode surface. We consider a ring microelectrode encircling a hydrophobic microcavity from which a succession of bubbles grows. The ring microelectrode, tested under alkaline water electrolysis conditions, does not suffer from bubble coverage. Consequently, the chronopotentiometric fluctuations of the cell are weaker than those associated with conventional microelectrodes. Herein, we provide fundamental understanding of the mass transfer processes governing the transient behaviour of the cell potential. With the help of numerical transport models, we demonstrate that bubbles forming at the cavity reduce the concentration overpotential by lowering the surrounding concentration of dissolved gas, but may also aggravate the ohmic overpotential by blocking ion-conduction pathways. The theoretical and experimental insight gained have relevant implications in the design of efficient gas-evolving electrodes.
AbstractBubbles are known to hinder electrochemical processes in water-splitting electrodes. In this study, we present a novel method to promote gas evolution away from the electrode surface. We consider a ring microelectrode encircling a hydrophobic microcavity from which a succession of bubbles grows. The ring microelectrode, tested under alkaline water electrolysis conditions, does not suffer from bubble coverage. Consequently, the chronopotentiometric fluctuations of the cell are weaker than those associated with conventional microelectrodes. Herein, we provide fundamental understanding of the mass transfer processes governing the transient behaviour of the cell potential. With the help of numerical transport models, we demonstrate that bubbles forming at the cavity reduce the concentration overpotential by lowering the surrounding concentration of dissolved gas, but may also aggravate the ohmic overpotential by blocking ion-conduction pathways. The theoretical and experimental insight gained have relevant implications in the design of efficient gas-evolving electrodes.