Separation Properties of Porous MoS Membranes Decorated with Small Molecules.

Using first-principles simulations, we surveyed the interactions between porous MoS monolayers in the 2H phase and 15 small molecules (H, O, HO, HS, CO, CO, SO, N, NO, NO, NH, HF, HCl, CH, and CHOH). Four types of molecules including H, O, HS, and NO directly dissociate and saturate the corners of the most common S-rimmed triangular pores, while other molecules only molecularly adsorb. The trisublayered structure of a MoS monolayer allows a new in-pore stable adsorption configuration in addition to the most studied above-pore adsorption configuration. Furthermore, the gas penetration pathways through the MoS membranes are no longer the conventional single-peak curve with one transition state like in the case of porous graphenes but are the "M"-shaped curve featuring two transition states connected by a stable in-pore adsorption state. The irreversible pore passivation via dissociative adsorption and reversible pore decoration by molecular adsorption will lead to very different separation performances of the MoS membranes, largely by changing the effective pore size. For example, the S-rimmed pores in the pore-3Mo2S membrane allow free pass of CH and CO molecules. If passivated by H atoms, the membrane can be used to separate gas mixtures like H/CH and H/CO with selectivities of 10:1 and 10:1, respectively. The permeance value of H is estimated to be about 0.15 mol m s Pa at room temperature and 0.1 bar pressure drop across the membrane. In contrast, the medium strong adsorption of a SO molecule in the center of the pore will completely block the passage of CO and CH, whose removal only needs heating. Our work reveals the complex behaviors of porous transition metal dichalcogenides (TMDs) toward guest molecules.