Pd/Pt embedded CN monolayer as efficient catalysts for CO oxidation

TL;DR

This study uses density functional theory to explore Pd/Pt embedded carbon nitride monolayers as stable, efficient catalysts for CO oxidation, revealing distinct reaction mechanisms and electronic interactions that enhance catalytic activity.

Contribution

It introduces Pd/Pt embedded CN monolayers as effective single atom catalysts for CO oxidation, analyzing their stability and reaction pathways via computational methods.

Findings

Pd/Pt are firmly anchored in CN monolayer due to strong orbital hybridization.

Pd@CN favors the less common TER mechanism with a low reaction barrier.

Pt@CN predominantly follows the LH mechanism with a moderate barrier.

Abstract

Single atom catalysts (SACs) based on 2D materials are identified to be efficient in many catalytic reaction. In this work, the catalytic performance of Pd/Pt embedded planar carbon nitride (CN) for CO oxidation, has been investigated via spin$-$polarized density functional theory calculations. We find that Pd/Pt can be firmly anchored in the porous CN monolayer due to the strong hybridization between Pd/Pt-d orbitals and adjacent N-2p orbitals. The resulting high adsorption energy and large diffusion barrier of Pd/Pt, ensuring the remarkable stability of the catalyst Pd/Pt@CN during CO oxidation reaction. The three distinct CO reaction mechanisms, namely, Eley-Rideal (ER), Langmuir-Hinshelwood (LH), and Tri-molecular Eley-Rideal (TER), are taken into consideration comparatively. Intriguingly, the oxidation reaction on Pd@CN prefers to proceed through the less common TER mechanism, where two CO molecules and one O2 molecule need to cross a small reaction barrier of 0.48 eV, and finally dissociate into two CO2 molecules. However, the LH mechanism is the most relevant one on Pt@CN with a rate-limiting reaction barrier of 0.68 eV. Moreover, the origin of SAC's reactivity enhancement is the electronic "acceptance$-$donation" interaction caused by orbital hybridization between Pd/Pt and preadsorbed O2/CO. Our findings are expected to widen the catalytic application of carbon based 2D materials.