“Breaking the O═O Bond”: Deciphering the Role of Each Element in Highly Durable CoPd₂Se₂ toward Oxygen Reduction Reaction

Abstract

In-depth insight into oxygen reduction reaction (ORR) electrocatalyst with high figures of merit (activity, stability, and selectivity) is highly crucial to rationally design electrocatalyst with a potential to replace state-of-the-art Pt/C. This work reports the synthesis of CoPd2Se2 nanoparticles that show remarkably high stability of 50000 electrochemical cycles toward ORR. Morphology of the particles is characterized using SEM and TEM microscopy techniques and simulated using Bravais–Friedel–Donay–Harker (BFDH) morphology calculation method. A deconvoluted approach was used to understand the role of each element in the compound. DFT calculation was performed to have an in-depth analysis of the active site. Co and Pd provided an active site for the O2 adsorption and Pd dissociates the O═O bond. The back-donation of substantial electron density to the π* antibonding orbital of the molecule expedites the 4e- reduction of O2 throughout the entire potential range. During the electrochemical stability test, Se forms a protective layer and prevents the active Co and Pd sites from OH poisoning.