A pyridinic Fe-N₄ macrocycle models the active sites in Fe/N-doped carbon electrocatalysts.

ABSTRACT: Iron- and nitrogen-doped carbon (Fe-N-C) materials are leading candidates to replace platinum catalysts for the oxygen reduction reaction (ORR) in fuel cells; however, their active site structures remain poorly understood. A leading postulate is that the iron-containing active sites exist primarily in a pyridinic Fe-N₄ ligation environment, yet, molecular model catalysts generally feature pyrrolic coordination. Herein, we report a molecular pyridinic hexaazacyclophane macrocycle, (phen₂N₂)Fe, and compare its spectroscopic, electrochemical, and catalytic properties for ORR to a typical Fe-N-C material and prototypical pyrrolic iron macrocycles. N 1s XPS and XAS signatures for (phen₂N₂)Fe are remarkably similar to those of Fe-N-C. Electrochemical studies reveal that (phen₂N₂)Fe has a relatively high Fe(III/II) potential with a correlated ORR onset potential within 150?mV of Fe-N-C. Unlike the pyrrolic macrocycles, (phen₂N₂)Fe displays excellent selectivity for four-electron ORR, comparable to Fe-N-C materials. The aggregate spectroscopic and electrochemical data demonstrate that (phen₂N₂)Fe is a more effective model of Fe-N-C active sites relative to the pyrrolic iron macrocycles, thereby establishing a new molecular platform that can aid understanding of this important class of catalytic materials.

SUBMITTER: Marshall-Roth T 

PROVIDER: S-EPMC7572418 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature