Dual‐Atom Catalysts Derived from a Preorganized Covalent Organic Framework for Enhanced Electrochemical Oxygen Reduction

Abstract

Dual-atom catalysts (DAC) are deemed as promising electrocatalysts due to the abundant active sites and adjustable electronic structure, but the fabrication of well-defined DAC is still full of challenges. Herein, bonded Fe dual-atom catalysts (Fe 2 DAC) with Fe 2 N 6 C 8 O 2 configuration were developed through onestep carbonization of a preorganized covalent organic framework with bimetallic Fe chelation sites (Fe 2 COF). The transition from Fe 2 COF to Fe 2 DAC involved the dissociation of the nanoparticles and the capture of atoms by carbon defects. Benefitting from the optimized d-band center and enhanced adsorption of OOH* intermediates, Fe 2 DAC exhibited outstanding oxygen reduction activity with a half-wave potential of 0.898 V vs. RHE. This work will guide more fabrication of dualatom and even cluster catalysts from preorganized COF in the future.