Abstract
The oxygen evolution reaction involves complex interplay among electrolyte, solid catalyst, and gas-phase and liquid-phase reactants and products. Monitoring catalysis interfaces between catalyst and electrolyte can provide valuable insights into catalytic ability. But it is a challenging task due to the additive solid supports in traditional measurement. Here we design a nanodevice platform and combine on-chip electrochemical impedance spectroscopy measurement, temporary I-V measurement of an individual nanosheet, and molecular dynamic calculations to provide a direct way for nanoscale catalytic diagnosis. By removing O2 in electrolyte, a dramatic decrease in Tafel slope of over 20% and early onset potential of 1.344 V vs. reversible hydrogen electrode are achieved. Our studies reveal that O2 reduces hydroxyl ion density at catalyst interface, resulting in poor kinetics and negative catalytic performance. The obtained in-depth understanding could provide valuable clues for catalysis system design. Our method could also be useful to analyze other catalytic processes.
Highlights
The oxygen evolution reaction involves complex interplay among electrolyte, solid catalyst, and gas-phase and liquid-phase reactants and products
Efficiency of water catalysis is severely limited by poor kinetics of the oxygen oxidation reaction, namely oxygen evolution reaction (OER)[3, 4]
A significant decrease in Tafel slope over 20% and an early onset potential of 1.344 Vxayrgeeonbasedrsvoerdptbioynreamt coavtianlgytOic2ininteerlfeaccterowlyotuel.dOruedr ustcuedOy Hre−veioalns concentration in the double layer (DL) and result in a poor kinetics and negative catalytic performance
Summary
The oxygen evolution reaction involves complex interplay among electrolyte, solid catalyst, and gas-phase and liquid-phase reactants and products. During an OER process, chemical reactions mainly take place at catalysts/electrolyte interface. We propose and use concurrent measurement of electrical conductivity of the electrode materials to probe the effects of O2 at the reaction interface during the OER.
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