Cation Effects on the Acidic Oxygen Reduction Reaction at Carbon Surfaces.
J L HübnerL E B LucchettiH N NongDmitry I SharapaB PaulM KroschelJ KangDetre TeschnerSilke BehrensFelix StudtA Knop-GerickeS SiahrostamiPeter StrasserPublished in: ACS energy letters (2024)
Hydrogen peroxide (H 2 O 2 ) is a widely used green oxidant. Until now, research has focused on the development of efficient catalysts for the two-electron oxygen reduction reaction (2e - ORR). However, electrolyte effects on the 2e - ORR have remained little understood. We report a significant effect of alkali metal cations (AMCs) on carbons in acidic environments. The presence of AMCs at a glassy carbon electrode shifts the half wave potential from -0.48 to -0.22 V RHE . This cation-induced enhancement effect exhibits a uniquely sensitive on/off switching behavior depending on the voltammetric protocol. Voltammetric and in situ X-ray photoemission spectroscopic evidence is presented, supporting a controlling role of the potential of zero charge of the catalytic enhancement. Density functional theory calculations associate the enhancement with stabilization of the *OOH key intermediate as a result of locally induced field effects from the AMCs. Finally, we developed a refined reaction mechanism for the H 2 O 2 production in the presence of AMCs.
Keyphrases
- ionic liquid
- density functional theory
- hydrogen peroxide
- molecular dynamics
- high glucose
- diabetic rats
- nitric oxide
- randomized controlled trial
- electron transfer
- drug induced
- molecular docking
- high resolution
- oxidative stress
- magnetic resonance imaging
- reduced graphene oxide
- computed tomography
- staphylococcus aureus
- highly efficient
- climate change
- cystic fibrosis
- simultaneous determination