Reaction Mechanism of Rapid CO Electroreduction to Propylene and Cyclopropane (C<sub>3+</sub>) over Triple Atom Catalysts
Mohsen Tamtaji, Soonho Kwon, Charles B. Musgrave, William A. Goddard, GuanHua Chen
Abstract
The carbon monoxide reduction reaction (CORR) toward C 2+ and C 3+ products such as propylene and cyclopropane can not only reduce anthropogenic emissions of CO and CO 2 but also produce value-added organic chemicals for polymer and pharmaceutical industries. Here, we introduce the concept of triple atom catalysts (TACs) that have three intrinsically strained and active metal centers for reducing CO to C 3+ products. We applied grand canonical potential kinetics (GCP-K) to screen 12 transition metals (M) supported by nitrogen-doped graphene denoted as M3N7, where M stands for Mn, Fe, Co, Ni, Cu, Ru, Rh, Pd, Ag, Ir, Pt, and Au. We sought catalysts with favorable CO binding, hydrogen binding, and C–C dimerization energetics, identifying Fe3N7 and Ir3N7 as the best candidates. We then studied the entire reaction mechanism from CO to C 3 H 6 and C 2 H 4 as a function of applied potential via, respectively, 12-electron and 8-electron transfer pathways on Fe3N7 and Ir3N7. Density functional theory (DFT) predicts an overpotential of 0.17 V RHE for Fe3N7 toward propylene and an overpotential of 0.42 V RHE toward cyclopropane at 298.15 K and pH = 7. Also, DFT predicts an overpotential of 0.15 V RHE for Ir3N7 toward ethylene. This work provides fundamental insights into the design of advanced catalysts for C 2+ and C 3+ synthesis at room temperature.