📝 SummarXiv

Abstract

Bubble formation in electrochemical system often hinders reaction efficiency by reducing active surface area and obstructing mass transfer, yet the mechanisms governing their nanoscale nucleation dynamics and impact remains unclear. In this study, we used molecular dynamics simulations to explore nanobubble nucleation and reaction rates during water electrolysis on planar- and nano-electrodes, with systematically tuning electrode wettability through water-electrode and gas-electrode interactions. We identified distinct nucleation regimes: gas layers, surface nanobubbles, bulk nanobubbles, and no nanobubbles, and revealed a volcano-shaped relationship between wettability and reaction rate, where optimal wettability strikes a balance between suppressing bubbles and ensuring sufficient reactant availability to maximize performance. Nanoelectrodes consistently exhibit higher current densities compared to planar electrodes with the same wettability, due to pronounced edge effects. Furthermore, moderate driving forces enhance reaction rates without triggering surface bubble formation, while excessive driving forces induce surface nanobubble nucleation, leading to suppressed reaction rates and complex dynamics driven by bubble growth and detachment. These findings highlight the importance of fine-tuning wettability and reaction driving forces to optimize gas-evolving electrochemical systems at the nanoscale and underscore the need for multiscale simulation frameworks integrating atomic-scale reaction kinetics, nanoscale bubble nucleation, and microscale bubble dynamics to fully understand bubble behavior and its impact on performance.