Hierarchical‐Pore‐Stabilization Strategy for Fabricating 18.3 wt% High‐Loading Single‐Atom Catalyst for Oxygen Reduction Reaction

Abstract

AbstractMetal single‐atom catalysts (M‐SACs) attract extraordinary attention for promoting oxygen reduction reaction (ORR) with 100% atomic utilization. However, low metal loading (usually less than 2 wt%) limits their overall catalytic performance. Herein, a hierarchical‐structure‐stabilization strategy for fabricating high‐loading (18.3%) M‐SACs with efficient ORR activity is reported. Hierarchical pores structure generated with high N content by SiO2 can provide more coordination sites and facilitate the adsorption of Fe3+ through mesoporous and confinement effect of it stabilizes Fe atoms in micropores on it during pyrolysis. High N content on hierarchical pores structure could provide more anchor sites of Fe atoms during the subsequent secondary pyrolysis and synthesize the dense and accessible Fe‐N4 sites after subsequent pyrolysis. In addition, Se power is introduced to modulate the electronic structure of Fe‐N4 sites and further decrease the energy barrier of the ORR rate‐determining step. As a result, the Fe single atom catalyst delivers unprecedentedly high ORR activity with a half‐wave potential of 0.895 V in 0.1 M KOH aqueous solution and 0.791 V in 0.1 M HClO4 aqueous solution. Therefore, a hierarchical‐pore‐stabilization strategy for boosting the density and accessibility of Fe‐N4 species paves a new avenue toward high‐loading M‐SACs for various applications such as thermocatalysis and photocatalysis.