Tunable Synthesis of Hollow Metal-Nitrogen-Carbon Capsules for Efficient Oxygen Reduction Catalysis in Proton Exchange Membrane Fuel Cells.

Abstract

Atomically dispersed metal catalysts anchored on nitrogen-doped (N-doped) carbons demand attention due to their superior catalytic activity relative to that of metal nanoparticle catalysts in energy storage and conversion processes. Herein, we introduce a simple and versatile strategy for the synthesis of hollow N-doped carbon capsules that contain one or more atomically dispersed metals (denoted as H-M-N_<i>x</i>-C and H-M^mix-N_<i>x</i>-C, respectively, where M = Fe, Co, or Ni). This method utilizes the pyrolysis of nanostructured core-shell precursors produced by coating a zeolitic imidazolate framework core with a metal-tannic acid (M-TA) coordination polymer shell (containing up to three different metal cations). Pyrolysis of these core-shell precursors affords hollow N-doped carbon capsules containing monometal sites (<i>e.g.</i>, Fe-N<i>_<i>x</i></i>, CoN_<i>x</i>, or Ni-N_<i>x</i>) or multimetal sites (Fe/Co-N_<i>x</i>, Fe/Ni-N_<i>x</i>, Co/Ni-N_<i>x</i>, or Fe/Co/Ni-N_<i>x</i>). This inventory allowed exploration of the relationship between catalyst composition and electrochemical activity for the oxygen reduction reaction (ORR) in acidic solution. H-Fe-N_<i>x</i>-C, H-Co-N_<i>x</i>-C, H-FeCo-N_<i>x</i>-C, H-FeNi-N_<i>x</i>-C, and H-FeCoNi-N_<i>x</i>-C were particularly efficient ORR catalysts in acidic solution. Furthermore, the H-Fe-N_<i>x</i>-C catalyst exhibited outstanding initial performance when applied as a cathode material in a proton exchange membrane fuel cell. The synthetic methodology introduced here thus provides a convenient route for developing next-generation catalysts based on earth-abundant components.