Hard X‑ray Photoelectron Spectroscopy Probing Fe Segregation during the Oxygen Evolution Reaction

• Published in: ACS applied materials & interfaces Vol. 16; no. 43; pp. 59516 - 59527
• Main Authors: Longo, Filippo, Lloreda-Jurado, Pedro Javier, Gil-Rostra, Jorge, Gonzalez-Elipe, Agustin R., Yubero, Francisco, Thomä, Sabrina L. J., Neels, Antonia, Borgschulte, Andreas
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 30.10.2024
• Subjects: catalysts; electrochemistry; electrodes; electrolytes; oxygen production; porosity; species; Surfaces, Interfaces, and Applications; X-ray photoelectron spectroscopy; NiFe-oxyhydroxide; oxygen evolution reaction; HAXPES; Fe surface segregation; nondestructive in-depth chemical profiles; nanostructured thin film catalysts
• ISSN: 1944-8244; 1944-8252; 1944-8252
• DOI: 10.1021/acsami.4c11902

NiFe electrocatalysts are among the most active phases for water splitting with regard to the alkaline oxygen evolution reaction (OER). The interplay between Ni and Fe, both at the surface and in the subsurface of the catalyst, is crucial to understanding such outstanding properties and remains a subject of debate. Various phenomena, ranging from the formation of oxides/(oxy)­hydroxides to the associated segregation of certain species, occur during the electrochemical reactions and add another dimension of complexity that hinders the rational design of electrodes for water splitting. In this work, we have developed the procedure for the quantification of chemical depth profiling by XPS/HAXPES measurements and applied it to two NiFe electrodes with different porosities. The main outcome of this study is related to the surface reconstruction of the electrodes during the OER, followed at two different depths by means of X-ray photoelectron spectroscopy. We find that Fe initially segregates at the surface when exposed to ambient conditions, resulting in the formation of an inactive FeO x phase. In addition, the porosity of the catalyst plays a significant role in the segregation process and thus in the performance of the electrode. In particular, the higher porosity of the nanostructured sample is responsible for a more pronounced diffusion of Fe from the subsurface to the surface with a more effective suppression of the activity of the Ni1–x Fe x OOH phase. These results highlight the importance of the fact that the chemical state of the surface of a multielement system is a snapshot in time, dependent on both external parameters, such as the applied potential and the adjacent electrolyte, and the underlying bulk properties accessible with HAXPES.