In/Outside Catalytic Sites of the Pore Walls in One‐Dimensional Covalent Organic Frameworks for Oxygen Reduction Reaction

Pore channels play a decisive for mass transport in catalytic systems. However, the influences of the location of catalytic sites inside or outside of the pore walls on the performance were still under‐explored due, because it is difficult to construct sites anchored in or outside of pore walls. Herein, one‐dimensional covalent organic frameworks (COFs) with precisely anchored active sites were used to explore the effects of channels on a typical oxygen reduction reaction (ORR) catalysis. Electrocatalytic evaluations showed that single Pt sites located inside of the channels exhibited higher kinetic activity compared to those anchored outside. The in situ spectroscopic analysis revealed that local reconstruction of Pt–Cl breaking and potential‐induced anion transport occurred more effectively inside the channels. The superior anion transportability and kinetic activity of the inside‐channel active sites also facilitated *OH desorption during the ORR process outperforming their outside‐channel counterparts. The results of this study provide strategies for designing active sites in porous catalysts for heterogeneous catalysis.