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Pyrolysis-free Fe–PIPhen catalyzes alkaline ORR

An Fe2+ coordination polymer of a nitrogen-rich phenanthroline ligand on carbon reduces O2 near 0.85 V with a four-electron pathway.

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How is PIPhen made?

Condensation of 1,10-phenanthroline-5,6-dione with 2,2′-bipyridyl-5,5′-dialdehyde.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified

Is pyrolysis used?

No; Fe-PIPhen is loaded on carbon powder without pyrolysis.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified

N 1s components?

398.6 eV pyridinic N, 400.2 eV =N– (imidazole), 401.1 eV graphitic N.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified

What XRD extra peak marks the polymer?

A diffraction near 11.9° from microcrystalline Fe-PIPhen.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified

Carbon support particle size?

Vulcan XC-72 spheres 35–60 nm; composite 40–60 nm after coating.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified

Ligand condensation conditions?

Reflux 120 °C, 12 h under argon, then ethanol/water wash.

Source: Supramolecular Iron Complex Formed Between Nitrogen Riched Phenanthroline Derivative and Iron With Improved Oxygen Reduction Activity in Alkaline Electrolyte · DOI · quote verified