Unraveling the Evolution of Dynamic Active Sites of LaNi<sub><i>x</i></sub>Fe<sub>1–<i>x</i></sub>O<sub>3</sub> Catalysts During OER
Haritha Cheraparambil, Miquel Vega‐Paredes, Christina Scheu, Claudia Weidenthaler
Abstract
High Resolution Image Download MS PowerPoint Slide Perovskites have attracted tremendous attention as potential catalysts for the oxygen evolution reaction (OER). It is well-known that the introduction of Fe into rare earth perovskites such as LaNiO 3 enhances the intrinsic OER activity. Despite numerous studies on structure–property relationships, the origin of the activity and the nature of the active species are still elusive and unclear. In this work, we study a series of LaNi x Fe 1– x O 3 perovskites using in situ electrochemical surface-enhanced Raman spectroscopy and electron energy loss spectroscopy to decipher the surface evolution and formation of active species during OER. While the origin of the activity arises from NiOOH species formed from the active Ni centers in LaNiO 3, our work shows that Fe serves as the active center in LaNi 0.5 Fe 0.5 O 3 and forms Fe–O–Ni and FeOOH species during OER. The OER activity of LaFeO 3 originates from FeOOH species, which interact with the soluble Ni species in the electrolyte forming an active electrode–electrolyte interface with high-valent stable surface iron species (Fe 4+ ) and thereby improving the performance. Our work provides deeper insights into the synergistic effects of Ni and Fe on the catalytic activity, which in turn provides new design principles for perovskite catalysts for the OER.