During the electrochemical reduction of oxygen, platinum catalysts are often (partially) oxidized. While these platinum oxides are thought to play a crucial role in fuel cell degradation, their... Show moreDuring the electrochemical reduction of oxygen, platinum catalysts are often (partially) oxidized. While these platinum oxides are thought to play a crucial role in fuel cell degradation, their nature remains unclear. Here, we studied the electrochemical oxidation of Pt nanoparticles using in situ XPS. When the particles were sandwiched between a graphene sheet and a proton exchange membrane that is wetted from the back, a confined electrolyte layer was formed, allowing us to probe the electrocatalyst under wet conditions. We show that the surface oxide formed at the onset of Pt oxidation has a mixed Pt delta+/Pt2+/Pt4+ composition. The formation of this surface oxide is suppressed when a Br-containing membrane is chosen due to adsorption of Br on Pt. Time-resolved measurements show that oxidation is fast for nanoparticles: even bulk PtO2 center dot nH(2)O growth occurs on the subminute time scale. The fast formation of Pt4+ species in both surface and bulk oxide form suggests that Pt4+-oxides are likely formed (or reduced) even in the transient processes that dominate Pt electrode degradation. Show less
Iridium oxide-based catalysts are uniquely active and stable in the oxygen evolution reaction. Theoretical work attributes their activity to oxyl or mu(1)-O species. Verifying this intermediate... Show moreIridium oxide-based catalysts are uniquely active and stable in the oxygen evolution reaction. Theoretical work attributes their activity to oxyl or mu(1)-O species. Verifying this intermediate experimentally has, however, been challenging. In the present study, these challenges were overcome by combining theory with new experimental strategies. Ab initio molecular dynamics of the solid-liquid interface were used to predict spectroscopic features, whereas sample architecture, developed for surface-sensitive X-ray spectroscopy of electrocatalysts in confined liquid, was used to search for these species under realistic conditions. Through this approach, we have identified mu(1)-O species during oxygen evolution. Potentiodynamic X-ray absorption additionally shows that these mu(1)-O species are created by electrochemical oxidation currents in a deprotonation reaction. Show less
Velasco-Velez, J.J.; Jones, T.E.; Streibel, V.; Havecker, M.; Chuang, C.H.; Frevel, L.; ... ; Knop-Gericke, A. 2019
An electrode for the oxygen evolution reaction based on a conductive bi-layered free standing graphene support functionalized with iridium nanoparticles was fabricated and characterized by means of... Show moreAn electrode for the oxygen evolution reaction based on a conductive bi-layered free standing graphene support functionalized with iridium nanoparticles was fabricated and characterized by means of potentiometric and advanced X-ray spectroscopic techniques. It was found that the electrocatalytic activity of iridium nanoparticles is associated to the formation of Ir 5d electron holes. Strong Ir 5d and O 2p hybridization, however, leads to a concomitant increase O 2p hole character, making oxygen electron deficient and susceptible to nucleophilic attack by water. Consequently, more efficient electrocatalysts can be synthesized by increasing the number of electron-holes shared between the metal d and oxygen 2p. Show less
