Adsorption and molecular siting of CO, water, and other gases in the superhydrophobic, flexible pores of FMOF-1 from experiment and simulation.

FMOF-1 is a flexible, superhydrophobic metal-organic framework with a network of channels and side pockets decorated with -CF groups. CO adsorption isotherms measured between 278 and 313 K and up to 55 bar reveal a maximum uptake of 6.16 mol kg (11.0 mol L) and unusual isotherm shapes at the higher temperatures, suggesting framework expansion. We used neutron diffraction and molecular simulations to investigate the framework expansion behaviour and the accessibility of the small pockets to N, O, and CO. Neutron diffraction experiments on the crystalline powder show that CO molecules are favourably adsorbed at three distinct adsorption sites in the large channels of FMOF-1 and cannot access the small pockets in FMOF-1 at 290 K and oversaturated pressure at 61 bar. Stepped adsorption isotherms for N and O at 77 K can be explained by combining Monte Carlo simulations in several different crystal structures of FMOF-1 obtained from neutron and X-ray diffraction under different conditions. A similar analysis is successful for CO adsorption at 278 and 283 K up to 30 bar; however, at 298 K and pressures above 30 bar, the results suggest even more substantial expansion of the FMOF-1 framework. The measured contact angle for water on an FMOF-1 pellet is 158°, demonstrating superhydrophobicity. Simulations and adsorption measurements also show that FMOF-1 is hydrophobic and water is not adsorbed in FMOF-1 at room temperature. Simulated mixture isotherms of CO in the presence of 80% relative humidity predict that water does not influence the CO adsorption in FMOF-1, suggesting that hydrophobic MOFs could hold promise for CO capture from humid gas streams.