Rational Design of Covalent Organic Frameworks-Based Single Atom Catalysts for Oxygen Evolution Reaction and Oxygen Reduction Reaction

Abstract

The rational design of high-performance catalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is essential for the development of clean and renewable energy technologies, particularly in fuel cells and metal-air batteries. Two-dimensional (2D) covalent organic frameworks (COFs) possess numerous hollow sites, which contribute to the stable anchoring of transition metal (TM) atoms and become promising supports for single atom catalysts (SACs). Herein, the OER and ORR catalytic performance of a series of SACs based on TQBQ-COFs were systematically investigated through density functional theory (DFT) calculations, with particular emphasis on the role of the coordination environment in modulating catalytic activity. The results reveal that Rh/TQBQ exhibits the most effective OER catalytic performance, with an overpotential of 0.34 V, while Au/TQBQ demonstrates superior ORR catalytic performance with an overpotential of 0.50 V. A critical mechanistic insight lies in the distinct role of boundary oxygen atoms in TQBQ, which perturb the adsorption energetics of reaction intermediates, thereby circumventing conventional scaling relationships governing OER and ORR pathways. Furthermore, we established the adsorption energy of TM atoms (Ead) as a robust descriptor for predicting catalytic activity, enabling a streamlined screening strategy for SAC design. This study emphasizes the significance of the coordination environment in determining the performance of catalysts and offers a new perspective on the design of novel and effective OER/ORR COFs-based SACs.