The interaction of CO 2 with nitride MXenes of different thickness is investigated using periodic density functional theorybased calculations and kinetic simulations carried out in the framework of transition state theory, the ultimate goal being predicting their possible use in Carbon Capture and Storage (CCS). We consider the basal (0001) surface plane of nitride MXenes with M n + 1 N n (n = 1-3; M=Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, and W) stoichiometry and also compare to equivalent results for extended (001) and ( 111) surfaces of the bulk rock-salt transition metal nitride compounds. The present results show that the composition of MXenes has a marked influence on the CO 2 -philicity of these substrates, whereas the thickness effect is, in general, small, but not negligible. The largest exothermic activation is predicted for Ti-, Hf-, and Zr-derived MXenes, making them feasible substrates for CO 2 trapping. From an applied point of view, Cr-, Mo-, and W-derived MXenes are especially well suited for CCS as the interaction with CO 2 is strong enough but molecular dissociation is not favored. Newly developed kinetic phase diagrams are introduced supporting that Cr-, Mo-, and W-derived MXenes are appropriate CCS substrates as they are predicted to exhibit easy capture at mild conditions and easy release by heating below 500 K.