The rate-limiting step for ammonia (NH 3 ) production via the Haber-Bosch process is known to be the dissociation of molecular nitrogen (N 2 ), which requires quite harsh working conditions, even when using appropriate heterogeneous catalysts. Here, motivated by the demonstrated enhanced chemical activity of MXenes a new class of two-dimensional inorganic materials towards the adsorption of quite stable molecules such as CO 2 and H 2 O, we use density functional theory including dispersion to investigate the suitability of such MXene materials to catalyze the N 2 dissociation. Results show that MXenes exothermically adsorb N 2 , with rather large adsorption energies ranging from -1.11 to -3.45 eV and elongation of the N 2 bond length by ~20%, greatly facilitating its dissociation with energy barriers below 1 eV, reaching 0.28 eV in the most favorable studied case of W 2 N. Microkinetic simulations indicate that the first hydrogenation of adsorbed atomic nitrogen is feasible at low pressures and moderate temperatures, and that the production of NH 3 may occur above 800 K on most studied MXenes, in particular in W 2 N. These results reinforce the promising capabilities of MXenes to dissociate nitrogen and suggest combining them co-catalytically with Ru nanoparticles to further improve the efficiency of ammonia synthesis.