Axial heteroatom (P, S and Cl)-decorated Fe single-atom catalyst for the oxygen reduction reaction: a DFT study.

An FeN 4 single-atom catalyst (SAC) embedded in a graphene matrix is considered an oxygen reduction reaction (ORR) catalyst for its good activity and durability, and decoration on the Fe active site can further modulate the performance of the FeN 4 SAC. In this work, the axial heteroatom (L = P, S and Cl)-decorated FeN 4 SAC (FeN 4 L) and pure FeN 4 were comparatively studied using density functional theory (DFT) calculations. It was found that the rate-determining step (RDS) in the ORR on pure FeN 4 is the reduction of OH to H 2 O in the last step with an overpotential of 0.58 V. However, the RDS of the ORR for the axial heteroatom-decorated FeN 4 L is the reduction of O 2 to OOH in the first step. The axial P and S heteroatom-decorated FeN 4 P and FeN 4 S exhibit lower activity than pure FeN 4 since the overpotentials of the ORR on FeN 4 P and FeN 4 S are 1.02 V and 1.09 V, respectively. Meanwhile, FeN 4 Cl exhibits the best activity towards the ORR since it possesses the lowest overpotential (0.51 V). The main reason is that the axial heteroatom decoration alleviates the adsorption of all the species in the whole ORR, thus modulating the free energy in every elementary reaction step. A volcano relationship between the d band center and the ORR activity can be determined among the axial heteroatom-decorated FeN 4 L SACs. The d band center of the Fe atom in various FeN 4 L SACs follows the order of FeN 4 > FeN 4 Cl > FeN 4 S > FeN 4 P, whereas the overpotential of the ORR on various catalysts follows the order of FeN 4 Cl > FeN 4 > FeN 4 S ≈ FeN 4 P. Δ G (*OH) is a simple descriptor for the prediction of the ORR activity of various axial heteroatom-decorated FeN 4 L, although the RDS in the ORR is either the first step or the last step. This paper provides a guide to the design and selection of the ORR over SACs with different axial heteroatom decorations, contributing to the rational design of more powerful ORR electrocatalysts and achieving advances in electrochemical conversion and storage devices.