Single-atom catalysts (SACs) have emerged as an excellent platform for enhancing catalytic performance. Inspired by the recent experimental synthesis of nitrogenated holey 2D graphene (C2N-h2D) (Mahmood et al., Nat. Commun., 2015, 6, 6486-6493), we report density functional theory calculations combined with computational hydrogen electrode model to show that C2N-h2D supported metal single atoms (M@C2N) are promising electrocatalysts for CO2 reduction reaction (CO2 RR). M confined at pyridinic N6 cavity promotes activation of inert O[double bond, length as m-dash]C[double bond, length as m-dash]O bonds and subsequent protonation steps, with *COOH → *CO → CHO predicted to be the primary pathway for producing methanol and methane. It is found that *CO + H+ + e- → *CHO is most likely to be the potential determining step; breaking the scaling relation of *CO and *CHO binding on M@C2N SACs may simply be a rare event that is sensitively controlled by the detailed geometry of the adsorbate. Among twelve metals screened, M@C2N SACs where M = Ti, Mn, Fe, Co, Ni, Ru were identified to be effective in catalyzing CO2 RR with lowered overpotentials (0.58 V-0.80 V).

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Small means big: DFT-calculated C–O bond length of adsorbed intermediates can serve as a good descriptor for predicting the C–O bond scission reactivity of phenolics over metal catalysts.

For many years, experimental and theoretical studies have investigated the solubility of CO2 in a variety of ionic liquids (ILs), but the overarching absorption mechanism is still unclear. Currently, two...