4.7 Article

Atomic iron coordinated by nitrogen doped carbon nanoparticles synthesized via a synchronous complexation-polymerization strategy as efficient oxygen reduction reaction electrocatalysts for zinc-air battery and fuel cell application

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 440, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.135721

Keywords

Transition mental-nitrogen-carbon catalysts; Fe-N-C; Oxygen reduction reaction; Complexation-polymerization strategy; Zn-air battery; Proton exchange membrane fuel cell

Funding

  1. National Natural Science Foundation of China [22075055]
  2. Guangxi Science and Technology Project [AB16380030]

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A general method of synthesizing transition metal coordinated by nitrogen doped carbon (M-N-C) using a synchronous complexation-polymerization strategy was developed, showing excellent ORR activity and durability of Fe-N-C for metal-air batteries and fuel cells.
Developing atomic transition metal coordinated by nitrogen doped carbon (M-N-C) eletrocatalysts for oxygen reduction reaction (ORR) is critical to achieve low cost metal-air batteries and fuel cells. Herein, a general method of synthesizing M-N-C was developed via a synchronous complexation-polymerization strategy, in which nitrogen-containing ligand was coordinated with specific transition metal ions and diamino aromatic compound was simultaneously polymerized by the metal ion as initiator; by the following pyrolysis in a molten NaCl bath, M-N-C was finally synthesized. Fe-N-C was synthesized by this strategy using 2, 4, 6-Tri (2-pyridyl)1, 3, 5-triazine (TPTZ) as ligand for FeCl2, and 1, 8-Diaminonaphthalene (DAN) as monomer of polymerization. Results demonstrate that introducing DAN into TPTZ-Fe-2} significantly affect the derived carbon structure and electrochemical performance of corresponding Fe-N-C. The Fe-N-C prepared by TPTZ and DAN with the molar ratio of 1:1 shows excellent ORR activity and durability, whose initial half-wave potential is 0.90 V in 0.1 M KOH and 0.80 V in 0.5 M H2SO4 respectively, after 10 K cycles, the potential is only 14 mV loss in 0.1 M KOH and 20 mV decay in 0.5 M H2SO4. And the ORR performance as cathode is further proved by a single practical Zn-air battery with a maximum power density of 192 mW cm(-2) and a specific capacity of 800 mAh gZn-1, much higher than 137 mW cm(-2) and 735 mAh gZn(-1) of the same loading of commercial Pt/C catalyst and proton exchange membrane fuel cell with a high power output of 640 mW cm(-2). Attributed to the vast kinds of ligands, metal ions and polymerizing monomers, this strategy provides a flexible platform of synthesizing advanced M-N-C catalysts, compared with other reported methods.

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