Journal
ANALYTICAL CHEMISTRY
Volume 93, Issue 36, Pages 12337-12345Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c02099
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Funding
- National Science Foundation of China [NSFC-21804018]
- National Science Foundation of Shanghai [19ZR1470800]
- Fundamental Research Funds for the Central Universities [2232020A-09, 2232021G-04]
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In this study, the individual gas bubble nucleation and dynamics on nanoscale electrodes were investigated using scanning electrochemical cell microscopy (SECCM). The nanostructured catalyst surface showed significantly less supersaturation for gas bubble nucleation and a notable increase of bubble detachment compared to its flat counterpart. The results suggest that deliberate microstructure design on a catalyst surface is a promising strategy for improving electrocatalytic gas evolution in terms of both bubble nucleation and elimination.
Electrocatalytic gas evolution reactions, where gaseous molecules are electrogenerated by reduction or oxidation of a species, play a central role in many energy conversion systems. Superaerophobic electrodes, usually constructed by their surface microstructures, have demonstrated excellent performance for electrochemical gas evolution reactions due to their bubble-repellent properties. Understanding and quantification of the gas bubble behavior including nucleation and dynamics on such micro-structured electrodes is an important but underexplored issue. In this study, we reported a scanning electrochemical cell microscopy (SECCM) investigation of individual gas bubble nucleation and dynamics on nanoscale electrodes. A classic Pt film and a nonconventional transition-metal dichalcogenide MoS2 film with different surface topologies were employed as model substrates for both H-2 and N-2 bubble electrochemical studies. Interestingly, the nanostructured catalyst surface exhibit significantly less supersaturation for gas bubble nucleation and a notable increase of bubble detachment compared to its flat counterpart. Electrochemical mapping results reveal that there is no clear correlation between bubble nucleation and hydrogen evolution reaction (HER) activity, regardless of local electrode surface microstructures. Our results also indicate that while the hydrophobicity of the nanostructured MoS2 surface promotes bubble nucleation, it has little effect on bubble dynamics. This work introduces a new method for nanobubble electrochemistry on broadly interesting catalysts and suggests that the deliberate microstructure on a catalyst surface is a promising strategy for improving electrocatalytic gas evolution both in terms of bubble nucleation and elimination.
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