Over recent years,catalytic materials of Fe-N-C species have been recognized being active for oxygen reduction reaction(ORR).However,the identification of active site remains challenging as it generally involves a pyrolysis process and mixed components being obtained.Herein Fe3C/C and Fe2N/C samples were synthesized by temperature programmed reduction of Fe precursors in 15%CH4/H2 and pure NH3,respectively.By acid leaching of Fe2N/C sample,only single sites of FeN4 species were presented,providing an ideal model for identification of catalytic functions of the single sites of FeN4 in ORR.A correlation was conducted between the concentration of FeⅡN4 in low spin state by M?ssbauer spectra and the kinetic current density at 0.8 V in alkaline media,and such a structure-performance correlation assures the catalytic roles of low spin FeⅡ N4 species as highly active sites for the ORR.