Highly AccessibleCo–N_x Active Sites-Doped CarbonFramework with Uniformly DispersedCobalt Nanoparticles for the Oxygen Reduction Reaction in Alkalineand Neutral Electrolytes

Abstract

Porous carbon materials with nitrogen-coordinated transition metal active sites have been widely regarded as appealing alternatives to replace noble metal catalysts in oxygen-based electrochemical reaction activities. However, improving the electrocatalytic activity of transition-metal-based catalysts remains a challenge for widespread application in renewable devices. Herein, we use a simple one-step pyrolysis method to construct a Co nanoparticles/Co–N_x-decorated carbon framework catalyst with a near-total external surface structure and uniform dispersion nanoparticles, which displays promising catalytic activity and superior stability for oxygen reduction reactions in both alkaline and neutral electrolytes, as evidenced by the positive shift of half-wave potential by 44 and 11 mV compared to 20% Pt/C. Excellent electrochemical performance originates from highly accessible Co nanoparticles/Co–N_x active sites at the external surface structure (this is, exposing active sites). The thus-assembled liquid zinc–air battery using the synthesized electrocatalyst as the cathode material delivers a maximum power density of 178 mW cm^–2 with an open circuit potential of 1.48 V and long-term discharge stability over 150 h.