Synergistic effect of well-defined dual sites boosting the oxygen reduction reaction

Herein, we construct a novel electrocatalyst with Fe-Co dual sites embedded in N-doped carbon nanotubes ((Fe,Co)/CNT), which exhibits inimitable advantages towards the oxygen reduction reaction. The electrocatalyst shows state-of-the-art ORR performance with an admirable onset potential (E-onset, 1.15 V vs. 1.05 V) and half-wave potential (E-1/2, 0.954 V vs. 0.842 V), outperforming those of the commercial Pt/C. The ORR test reveals that the performance of the (Fe,Co)/CNT is superior to most of the reported non-precious catalysts in alkaline electrolytes. Furthermore, when employed as a cathode catalyst in a Zn-air battery, the (Fe,Co)/CNT exhibits high voltages of 1.31 V and 1.23 V at discharge current densities of 20 mA cm(-2) and 50 mA cm(-2), respectively. In addition, the power density and the specific energy density reach 260 mW cm(-2) and 870 W h kg(Zn)(-1). We discover that the Fe-Co dual sites embedded in N-doped porous carbon are beneficial for the activation of oxygen by weakening the O=O bonds.