Anodic H<sub>2</sub>O<sub>2</sub> Generation in Carbonate‐Based Electrolytes—Mechanistic Insight from Scanning Electrochemical Microscopy
Lejing Li, Rajini P. Antony, Carla Santana Santos, Ndrina Limani, Stefan Dieckhöfer, Wolfgang Schuhmann
Abstract
Abstract For the anodic H 2 O 2 generation, it has been shown that the electrolyte composition can steer the reaction pathway toward increased H 2 O 2 generation. Previous efforts made on composition optimization found that the impact of the molar fraction of carbonate species varies for different anodes, and therefore, controversies remain concerning the reaction pathways as well as the species involved in H 2 O 2 formation. Considering that water oxidation results in the liberation of protons within the anode microenvironment, the corresponding acidification would cause an equilibrium shift between carbonate species, which in turn may modulate the reaction pathway. We determined the changes in the fraction of carbonate species in the vicinity of an anode by performing local pH measurements using a Au nanoelectrode positioned in close proximity to an operating anode by shear‐force scanning electrochemical microscopy (SECM). It could be confirmed that the main anionic species at the interface is HCO 3 − , at potentials where H 2 O 2 is preferentially formed, regardless of the pH value in the bulk. The simultaneous use of a Au−Pt double barrel microelectrode in generator‐collector SECM measurements demonstrates that the local HCO 3 − concentration is collectively determined by the oxidation current, buffer capacity, and bulk pH of the electrolyte.