Transition Metal (Co, Ni, Fe, Cu) Single‐Atom Catalysts Anchored on 3D Nitrogen‐Doped Porous Carbon Nanosheets as Efficient Oxygen Reduction Electrocatalysts for Zn–Air Battery

Abstract

Exploring highly active and cost-efficient single-atom catalysts (SACs) for oxygen reduction reaction (ORR) is critical for the large-scale application of Zn-air battery. Herein, density functional theory (DFT) calculations predict that the intrinsic ORR activity of the active metal of SACs follows the trend of Co > Fe > Ni ≈ Cu, in which Co SACs possess the best ORR activity due to its optimized spin density. Guided by DFT calculations, four kinds of transition metal single atoms embedded in 3D porous nitrogen-doped carbon nanosheets (MSAs@PNCN, M = Co, Ni, Fe, Cu) are synthesized via a facile NaCl-template assisted strategy. The resulting MSAs@PNCN displays ORR activity trend in lines with the theoretical predictions, and the Co SAs@PNCN exhibits the best ORR activity (E_1/2 = 0.851 V), being comparable to that of Pt/C under alkaline conditions. X-ray absorption fine structure (XAFS) spectra verify the atomically dispersed Co-N₄ sites are the catalytically active sites. The highly active CoN₄ sites and the unique 3D porous structure contribute to the outstanding ORR performance of Co SAs@PNCN. Furthermore, the Co SAs@PNCN catalyst is employed as cathode in Zn-air battery, which can deliver a large power density of 220 mW cm^-2 and maintain robust cycling stability over 530 cycles.