Hierarchical Core-Shell Co2 N/CoP Embedded in N, P-doped Carbon Nanotubes as Efficient Oxygen Reduction Reaction Catalysts for Zn-air Batteries.

Abstract

Projecting a cost-effective and highly efficient electrocatalyst for the oxygen reaction reduction (ORR) counts a great deal for Zn-air batteries. Herein, a hierarchical core-shell ORR catalyst (Co2 N/CoP@PNCNTs) is developed by embedding cobalt phosphides and/or cobalt nitrides as the core into N, P-doped carbon nanotubes (PNCNTs) as the shell via one-step carbonization, nitridation, and phosphorization of pyrolyzing Co-MOF precursor. The globally N, P-doped structure of Co2 N/CoP@PNCNTs demonstrates an outstanding electrocatalytic activity in the alkaline solution with the onset and half-wave potentials of 1.07and 0.85V respectively. Moreover, a Zn-air battery assembled from Co2 N/CoP@PNCNTs as the air cathode delivers an open circuit potential of 1.49V, a maximum power density of 151.1mW cm-2 and a specific capacity of 823.8 mAh kg-1 . It is reflected that Co2 N/CoP@PNCNTs provides a long-term durability with a slight decline of 15 h in the chronoamperometry measurement and an excellent charge-discharge stability with negligible voltage decay for 150 h at 10mA cm-2 in Zn-air batteries. The results reveal that Co2 N/CoP@PNCNTs has superiority over most Co-Nx -C or Cox P@C catalysts reported so far. The excellent catalytic properties and stability of Co2 N/CoP@PNCNTs derive from synergistic effects between Co2 N/CoP and mesoporous N, P-doped carbon nanotubes.