Constructing N,S and N,P Co‐Coordination in Fe Single‐Atom Catalyst for High‐Performance Oxygen Redox Reaction
Xiaoqing Lü, Lifang Jiao, Shoufu Cao, Yuying Hu, Chunyu Yang, Zengxuan Chen, Shuxian Wei, Siyuan Liu, Zhaojie Wang
Abstract
Abstract Single‐atom catalysts (SACs) are promising electrocatalysts for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER), in which the coordination environment plays a crucial role in activating the intrinsic activity of the central metal. Taking the FeN 4 SAC as a probe, this work investigates the effect of introducing S or P atoms into N coordination (FeS x N 4− x and FeP x N 4− x ( x =1–4)) on the electronic structure optimization of Fe center and its catalytic performance. Attributing to the optimal Fe 3d orbitals, FePN 3 can effectively activate O 2 and promote ORR with a low overpotential of 0.29 V, surpassing FeN 4 and most reported catalysts. FeSN 3 is beneficial to H 2 O activation and OER, proceeding with an overpotential of 0.68 V, which is superior to FeN 4 . Both FePN 3 and FeSN 3 exhibit outstanding thermodynamic and electrochemical stability with negative formation energies and positive dissolution potentials. Hence, the N,P and N,S co‐coordination might provide better catalytic environment than regular N coordination for SACs in ORR and OER. This work demonstrates FePN 3 /FeSN 3 as high‐performance ORR/OER catalysts and highlights N,P and N,S co‐coordination regulation as an effective approach to fine tune high atomically dispersed electrocatalysts.