Pd “Kills Two Birds with One Stone” for the Synthesis of Catalyst: Dual Active Sites of Pd Triggers the Kinetics of O₂ Electrocatalysis

Abstract Noble metal‐based catalyst, despite their exorbitant cost, are the only successful catalyst for bifunctional oxygen electrocatalysis owing to their capability to drive forward the reaction rate kinetically. Therefore, it is desirable to diminish the noble metal loading without any compromise in the catalyst performance. In this study, the aim to achieve two goals with one action via a single‐step route to have ultra‐low loading of Pd in the catalyst. The Pd is used as a catalyst for C─C bond formation followed by complexation reactions or vice versa, in conventional Suzuki‐Miyaura cross‐coupling (SMCC) reaction, which yields a Pd‐based porous organic polymer. Interestingly, it is found that dispersed Pd nanocluster (Pd_NC) is present together with Pd single atom doped into nanocarbon (Pd‐NC) matrix in the catalyst (Pd_NC/Pd‐NC₈₀₀) that obtained after pyrolysis of the porous polymer. The catalyst exhibits remarkable bifunctional activity and durability towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Further, it is studied that the in situ attenuated total reflection infrared (ATR‐IR) spectroscopy at different electrochemical potentials during ORR and OER to observe the reaction intermediates. The homemade zinc‐air battery with the catalyst displayed great performance, establishing the significance of Pd_NC/Pd‐NC₈₀₀ as a bifunctional oxygen electrocatalyst.