Unravelling Temperature Ramping Rates in Fabricating NaCl‐Induced Porous Co/N‐C Electrocatalysts for Oxygen Reduction Reaction

Abstract

Pyrolysis is a necessary procedure for synthesizing carbon‐based nonprecious metal electrocatalysts via stimulating interaction and carbonization of precursors. In this work, ramping rates that correlated with thermal gradient has been investigated to reveal the configuration evolution of the precursors. Spectra characterizations demonstrated that ramping rates affected decomposition and aromatization of precursors. Increasing ramping rates improved the percentage of doped nitrogen and defects, promoting dispersion of Co atoms in the carbonaceous matrix and increasing density of active sties. In addition, the size variation of NaCl template under different ramping rates modifies the porous structure of Co/N−C electrocatalysts, greatly increasing the percentage of macropores and micropores at rapid ramping rates. As a result, electrocatalysts obtained at 5 °C min−1 exhibit comparable catalytic activity to that of Pt/C due to highly dispersed active sites and rational percentage of porosity, facilitating the sufficient reaction of oxygen along the catalysts. These results shed lights on regulating physical properties of carbonaceous electrocatalysts.

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“…In these works, it is also concluded that the pyrolysis temperature affects the geometry of the above M–N–C (M = Fe or Co) active sites and the corresponding ORR kinetics. In another report of Co–N–C catalyst synthesis, it was found that the decomposition and aromatization of precursors are affected by the ramping rates 36 . Increasing the ramping rates improved the percentage of doped nitrogen and defects in the carbon matrix and promoted dispersion of Co atoms in the catalyst, increasing the density of active sites (Figure 2).…”

“…In another report of Co-N-C catalyst synthesis, it was found that the decomposition and aromatization of precursors are affected by the ramping rates. 36 Increasing the ramping rates improved the percentage of doped nitrogen and defects in the carbon matrix and promoted dispersion of Co atoms in the catalyst, increasing the density of active sites (Figure 2).…”