Structure-Performance Descriptors and the Role of the Axial Oxygen Atom on M-N4-C Single-Atom Catalysts for Electrochemical CO2 Reduction

Revealing and characterizing the catalytic sites, along with elucidating a convenient activity descriptor, can provide essential guidance in determining efficient electrocatalytic catalysts for the CO2 reduction reaction (CO2RR). In this work, the mechanism of CO2 reduction to methane (CH4) on catalysts (SACs) was studied by density functional theory calculations, a step forward to revealing the effects of the axial O atom (M-N4O-C) on their catalytic activity. The electrocatalytic reduction activity of CO2 over M-N4-C SACs is strongly dependent on the outmost d-shell electron numbers and electronegativity of the selected metals. The introduction of the axial O atom changes the coordination structure of the central metal atoms, which not only improves the stability of M-N4O-C SACs (especially electrochemical stability) but also affects the adsorption strength of intermediate species and then improves or reduces the catalytic activity, which depends on the intrinsic properties of the metal atoms. More importantly, by considering the comprehensive effects of the number of outmost d-shell electrons, the electronegativity, coordinate numbers, and bonding length of the central metal atom and the nearest neighbor atom, a descriptor (q)) based on the intrinsic properties of materials was developed to correlate the catalytic activity. The volcano-shaped relationships between the q) and limiting potentials were well established. In particular, five SACs (Mn-N4-C, Cr-N4-C, Os- N4O-C, Ru-N4O-C, and Rh-N4O-C) close to the summit of the volcano were screened. Based on this descriptor, the catalyst activity can be predicted directly from the characteristics of the material instead of the expensive calculation of adsorption energies. This work is of great significance for understanding the mechanism of electrocatalytic CO2RR and the design of efficient and stable electrocatalysts.

Automated summary

In this study, the mechanism of CO2 reduction to methane on catalysts was investigated using density functional theory calculations. The introduction of an axial O atom was found to affect the catalytic activity by changing the coordination structure of the metal atoms. A descriptor based on the intrinsic properties of materials was developed to correlate the catalytic activity, allowing for direct prediction of catalyst activity. This work is important for understanding the mechanism of electrocatalytic CO2 reduction and designing efficient and stable electrocatalysts.