No abstract

Identifying real active sites and understanding the mechanism of oxygen evolution reaction (OER) are still a big challenge today for developing efficient electrochemical catalysts in renewable energy technologies. Here, using a combined in situ/operando experiments and theory, the catalytic mechanism of the ordered OER active Co and Ir ions in Sr2CoIrO6−δ is studied, which exhibits an unprecedented low overpotential 210 mV to achieve 10 mA cm–2, ranking the highest performance among perovskite‐based solid‐state catalysts. Operando X‐ray absorption spectroscopies as a function of applied voltage indicates that Ir4+ ion is gradually converted into extremely high‐valence Ir5+/6+, while the part of Co3+ ion is transferred into Co4+ under OER process. Density functional theory calculations explicitly reveal the order Co‐O‐Ir network as an origin of ultrahigh OER activity. The work opens a promising path to overcome the sluggish kinetics of OER bottleneck for water splitting via proper arrangements of the multi‐active sites in catalyst.

Understanding proton transport in Ruddlesden–Popper (RP) oxides, as attractive electrode materials for protonic ceramic fuel cells, is challenging because of the complexity of intrinsic oxygen defects in first-series RP oxides (A2BO4). We investigated the processes of intrinsic oxygen defects in proton transportation, such as formation of defects, incorporation of dissociative water into the defective lattice, transfer of a proton along the oxygen sites, and electronic properties of the transition state (TS) in A2BO4. The coexistence of oxygen vacancies (VO) and interstitial oxygen (Oi), VO+Oi defect pair, presents advantageous hydration energies and lattice distortions efficiently accelerating proton transport in the lattice. Moreover, the inherent driving force for proton transport is related to the O 2p band level by O–H···O bond interactions in the TS. Our findings elucidate the fundamental mechanism of proton conduction affected by intrinsic oxygen defects, which will motivate the community to focus more on defect engineering to enhance performance.