Electrocatalysis
is considered promising in renewable
energy conversion
and storage, yet numerous efforts rely on catalyst design to advance
catalytic activity. Herein, a hydrodynamic single-particle electrocatalysis
methodology is developed by integrating collision electrochemistry
and microfluidics to improve the activity of an electrocatalysis system.
As a proof-of-concept, hydrogen evolution reaction (HER) is electrocatalyzed
by individual palladium nanoparticles (Pd NPs), with the development
of microchannel-based ultramicroelectrodes. The controlled laminar
flow enables the precise delivery of Pd NPs to the electrode–electrolyte
interface one by one. Compared to the diffusion condition, hydrodynamic
collision improves the number of active sites on a given electrode
by 2 orders of magnitude. Furthermore, forced convection enables the
enhancement of proton mass transport, thereby increasing the electrocatalytic
activity of each single Pd NP. It turns out that the improvement in
mass transport increases the reaction rate of HER at individual Pd
NPs, thus a phase transition without requiring a high overpotential.
This study provides new avenues for enhancing electrocatalytic activity
by altering operating conditions, beyond material design limitations.