DFT modeling of the oxygen electroreduction reaction on SiN3-doped carbon nanotubes

Abstract

The thermodynamic features and mechanism of the electrocatalytic oxygen reduction reaction were studied using the revPBE0-D3(BJ)/Def2-TZVP method on the example of (6,6)-armchair carbon nanotube doped with a tricoordinated silicon atom and nitrogen atoms of pyridinic and graphitic nature. Irreversible oxidation of the silicon center as a result of the formation of stable oxygen-containing adsorbates was shown. It was found that Si-poisoned structures are capable of participating in the catalysis of the target reaction along two- and four-electron routes at high overpotentials. For a nanotube doped simultaneously with pyridinic and graphitic nitrogens the potential possibility of eliminating the silicon atom from the catalyst composition in the form of orthosilicic acid and the participation of a silicon-free nitrogen-doped framework in the oxygen electroreduction reaction, for which the stage of tautomerization of pyridin-2(1H)-one to pyridin-2-ol is the limiting step was shown.