P‐Incorporation Induced Enhancement of Lattice Oxygen Participation in Double Perovskite Oxides to Boost Water Oxidation

Abstract

AbstractActivating the lattice oxygen in the catalysts to participate in the oxygen evolution reaction (OER), which can break the scaling relation–induced overpotential limitation (> 0.37 V) of the adsorbate evolution mechanism, has emerged as a new and highly effective guide to accelerate the OER. However, how to increase the lattice oxygen participation of catalysts during OER remains a major challenge. Herein, P‐incorporation induced enhancement of lattice oxygen participation in double perovskite LaNi0.58Fe0.38P0.07O3‐σ (PLNFO) is studied. P‐incorporation is found to be crucial for enhancing the OER activity. The current density reaches 1.35 mA cmECSA−2 at 1.63 V (vs RHE), achieving a sixfold increase in intrinsic activity. Experimental evidences confirm the dominant lattice oxygen participation mechanism (LOM) for OER pathway on PLNFO. Further electronic structures reveal that P‐incorporation shifts the O p‐band center by 0.7 eV toward the Fermi level, making the states near the Fermi level more O p character, thus facilitating LOM and fast OER kinetics. This work offers a possible method to develop high‐performance double perovskite OER catalysts for electrochemical water splitting.