Photoelectron spectroscopy offers detailed information about the electronic structure and chemical composition of surfaces, owing to the short distance that the photoelectrons can escape from a... Show morePhotoelectron spectroscopy offers detailed information about the electronic structure and chemical composition of surfaces, owing to the short distance that the photoelectrons can escape from a dense medium. Unfortunately, photoelectron based spectroscopies are not directly compatible with the liquids required to investigate electrochemical processes, especially in the soft X-ray regime. To overcome this issue, different approaches based on photoelectron spectroscopy have been developed in our group over the last few years. The performance and the degree of information provided by these approaches are compared with those of the well established bulk sensitive spectroscopic approach of total fluorescence yield detection, where the surface information gained from this approach is enhanced using samples with large surface to bulk ratios. The operation of these approaches is exemplified and compared using the oxygen evolution reaction on IrOx catalysts. We found that all the approaches, if properly applied, provide similar information about surface oxygen speciation. However, using resonant photoemission spectroscopy, we were able to prove that speciation is more involved and complex than previously thought during the oxygen evolution reaction on IrOx based electrocatalysts. We found that the electrified solid-liquid interface is composed of different oxygen species, where the terminal oxygen atoms on iridium are the active species, yielding the formation of peroxo species and, finally, dioxygen as the reaction product. Thus, the oxygen-oxygen bond formation is dominated by peroxo species formation along the reaction pathway. Furthermore, the methodologies discussed here open up opportunities to investigate electrified solid-liquid interfaces in a multitude of electrochemical processes with unprecedented speciation capabilities, which are not accessible by one-dimensional X-ray spectroscopies. Show less
Mom, R.; Frevel, L.; Velasco-Velez, J.J.; Plodinec, M.; Knop-Gericke, A.; Schlogl, R. 2019
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
Manganese oxide (MnOx) electrocatalysts are examined herein by in situ soft X-ray absorption spectroscopy (XAS) and resonant inelastic X-ray scattering (RIXS) during the oxidation of water buffered... Show moreManganese oxide (MnOx) electrocatalysts are examined herein by in situ soft X-ray absorption spectroscopy (XAS) and resonant inelastic X-ray scattering (RIXS) during the oxidation of water buffered by borate (pH 9.2) at potentials from 0.75 to 2.25 V vs. the reversible hydrogen electrode. Correlation of L-edge XAS data with previous mechanistic studies indicates Mn-IV is the highest oxidation state involved in the catalytic mechanism. MnOx is transformed into birnessite at 1.45 V and does not undergo further structural phase changes. At potentials beyond this transformation, RIXS spectra show progressive enhancement of charge transfer transitions from oxygen to manganese. Theoretical analysis of these data indicates increased hybridization of the Mn-O orbitals and withdrawal of electron density from the O ligand shell. In situ XAS experiments at the O K-edge provide complementary evidence for such a transition. This step is crucial for the formation of O-2 from water. 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
