Single‐Atom Molybdenum‐N₃ Sites for Selective Hydrogenation of CO₂ to CO

Abstract

The design of efficient non-noble metal catalysts for CO₂ hydrogenation to fuels and chemicals is desired yet remains a challenge. Herein, we report that single Mo atoms with a MoN₃ (pyrrolic) moiety enable remarkable CO₂ adsorption and hydrogenation to CO, as predicted by density functional theory studies and evidenced by a high and stable conversion of CO₂ reaching about 30.4 % with a CO selectivity of almost 100 % at 500 °C and very low H₂ partial pressure. Atomically dispersed MoN₃ is calculated to facilitate CO₂ activation and reduces CO₂ to CO* via the direct dissociation path. Furthermore, the highest transition state energy in CO formation is 0.82 eV, which is substantially lower than that of CH₄ formation (2.16 eV) and accounts for the dominant yield of CO. The enhanced catalytic performances of Mo/NC originate from facile CO desorption with the help of dispersed Mo on nitrogen-doped carbon (Mo/NC), and in the absence of Mo nanoparticles. The resulting catalyst preserves good stability without degradation of CO₂ conversion rate even after 68 hours of continuous reaction. This finding provides a promising route for the construction of highly active, selective, and robust single-atom non-precious metal catalysts for reverse water-gas shift reaction.