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Published on: December 6, 2021
Hierarchical Core-Shell Co2 N/CoP Embedded in N, P-doped Carbon Nanotubes as Efficient Oxygen Reduction Reaction
Chongchao Yao1,2, Jiaxin Li1,2,3, Zhihao Zhang4
1National Engineering Laboratory for VOCs Pollution Control Material and Technology, Research Center for Environmental Material and Pollution Control Technology, University of Chinese Academy of Sciences, Beijing, 101408, P. R. China.
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 1.07 and 0.85 V respectively. Moreover, a Zn-air battery assembled from Co2 N/CoP@PNCNTs as the air cathode delivers an open circuit potential of 1.49 V, a maximum power density of 151.1 mW 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 10 mA 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.
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