A new microporous cadmium metal-organic framework was synthesized both mechanochemically and in solution by using a sulfonyl-functionalized dicarboxylate linker and an acylhydrazone colinker. The three-dimensional framework is highly stable upon heating to 300 °C as well as in aqueous solutions at elevated temperatures or acidic conditions. The thermally activated material exhibits steep water vapor uptake at low relative pressures at 298 K and excellent recyclability up to 260 °C as confirmed by both quasi-equilibrated temperature-programmed desorption and adsorption (QE-TPDA) method as well as adsorption isotherm measurements. Reversible isotherms and hysteretic isobars recorded for the desorption-adsorption cycles indicate the maximum uptake of 0.19 g/g (at 298 K, up to p/p = 1) or 0.18 g/g (at 1 bar, within 295-375 K range), respectively. The experimental isosteric heat of adsorption (48.9 kJ/mol) indicates noncoordinative interactions of water molecules with the framework. Exchange of the solvent molecules in the as-made material with water, performed in the single-crystal to single-crystal manner, allows direct comparison of both X-ray crystal structures. The single-crystal X-ray diffraction for the water-loaded framework demonstrates the orientation of water clusters in the framework cavities and reveals their strong hydrogen bonding with sulfonyl, acyl, and carboxylate groups of the two linkers. The grand canonical Monte Carlo (GCMC) simulations of HO adsorption corroborate the experimental findings and reveal preferable locations of guest molecules in the framework voids at various pressures. Additionally, both experimental and GCMC simulation insights into the adsorption of CO (at 195 K) on the activated framework are presented.

Proton-conducting metal–organic frameworks (MOFs) have been gaining attention for their role as solid-state electrolytes in various devices for energy conversion and storage. Here, we present a convenient strategy for inducing and tuning of superprotonic conductivity in MOFs with open metal sites via postsynthetic incorporation of charge carriers enabled by solvent-free mechanochemistry and anion coordination. This scalable approach is demonstrated using a series of CPO-27/MOF-74 [M 2 (dobdc); M = Mg 2+ , Zn 2+ , Ni 2+ ; dobdc = 2,5-dioxido-1,4-benzenedicarboxylate] materials loaded with various stoichiometric amounts of NH 4 SCN. The modified materials are not achievable by conventional immersion in solutions. Periodic density functional theory (DFT) calculations, supported by infrared (IR) spectroscopy and powder X-ray diffraction, provide structures of the modified MOFs including positions of inserted ions inside the [001] channels. Despite the same type and concentration of proton carriers, the MOFs can be arranged in the increasing order of conductivity (Ni < Zn < Mg), which strongly correlates with amounts of water vapor adsorbed. We conclude that the proton conductivity of CPO-27 materials can be controlled over a few orders of magnitude by metal selection and mechanochemical dosing of ammonium thiocyanate. The dosing of a solid is shown for the first time as a useful, simple, and ecological method for the control of material conductivity.

A series of three layered cadmium–organic frameworks containing acylhydrazone and (un)substituted isophthalates have been prepared and characterised.

Proton-conducting solids operating in both anhydrous and humid conditions are of paramount importance for the development of fuel cells. We demonstrate that incorporating formamidinium or methylammonium ions in CPO-27/MOF-74 metal−organic frameworks renders them highly conductive under the two conditions. Highest proton conductivities reach 8 × 10 −4 S/ cm under anhydrous conditions, exceed 10 −3 S/cm already at low relative humidity (30−50% RH) and low temperatures (25−60 °C), and reach 10 −2 S/cm at 60 °C and 70% RH. The dense pore filling with the protic cations is enabled by solvent-free mechanochemistry and stoichiometric saturation of open metal sites (Mg, Ni) with thiocyanate ligands. DFT modeling reveals that high anhydrous proton conductivity is associated with the presence of water-free extended networks of hydrogen bonds along the [001] channel and together with electrochemical impedance measurements (EIS) shed light on the mechanism of proton transport.