Salt Confined in MIL-101(Cr)-Tailoring the Composite Sorbents for Efficient Atmospheric Water Harvesting.

The adsorption method for atmospheric water harvesting (AWH) is considered as a promising heat-driven technology for potable water supply in arid regions. This research is focused on novel composite sorbents based on hygroscopic salts loaded in the pores of MIL-101(Cr) developed for AWH. The composites based on LiCl, LiBr, CaCl2 , and Ca(NO3 )2 were synthesized and comprehensively studied by SEM, XRD, N2 adsorption, and thermogravimetric methods. We evidence that the CaCl2 /MIL-101(Cr) composite demonstrates a high net water uptake of 0.52-0.59 g_(H2 O)/g_(composite) per cycle under conditions of Saudi Arabia and the Sahara desert as the reference regions with extra-dry climate, which exceeds the appropriate values for other adsorbents. It is shown that water adsorption on the composite cannot be presented as a combination of the adsorption on the components, thus indicating a synergistic effect. A detailed characterization of water coordination, mobility, and hydrogen bonding within the confined CaCl2 hydrates and salt solution using solid-state 2 H NMR spectroscopy has been performed. It is established that pore confinement promotes a prolonged transition to a dynamically melted state of the hydrated salt and a notable decrease of the melting temperature, which facilitates the molecular transport of water and causes the alteration of sorption properties of CaCl2 inside MIL-101 pores. Finally, the performance of AWH employing CaCl2 /MIL-101(Cr) was evaluated in terms of the fractions of water extracted and collected, and the specific energy consumption, demonstrating its high potential for AWH.

The impact of framework flexibility and defects on the water adsorption in CAU-10-H.

Aluminum-based metal-organic framework (MOF) CAU-10-H is a promising candidate for heat transformation and water harvesting applications due to its hydrothermal stability, beneficial step-wise water adsorption isotherm and low toxicity. In this study, the effects of the framework flexibility and structural defects on the mechanism of water sorption in CAU-10-H were studied by grand canonical Monte Carlo (GCMC) methods. It was shown by the simulations that the rigid ideal MOF framework is hydrophobic. The account of the linker "flapping" motion during the simulations made the framework more hydrophilic due to unblocking of hydroxyl groups that are inaccessible to water molecules for the rigid structure model. However, this model cannot predict the experimental pressure, at which the step on the adsorption isotherm is observed. Based on this result, we suggested that the presence of structural defects could increase the MOF hydrophilicity. The investigation of the water adsorption using several models of defective structures demonstrated that even a small number of defects shift the calculated position of the step on the adsorption isotherm towards the experimental values. The results obtained in this study emphasize that the controlled synthesis of defective structures is one of the most efficient methods of regulating the MOF adsorption properties.

Water Vapor Adsorption on CAU-10-X: Effect of Functional Groups on Adsorption Equilibrium and Mechanisms.

Metal-organic frameworks (MOFs) possess unique flexibility of structure and properties, which drives them toward applications as water adsorbents in many emerging technologies, such as adsorptive heat transformation, water harvesting from the air, dehumidification, and desalination. A deep understanding of the surface phenomena is a prerequisite for the target-oriented design of MOFs with the required adsorption properties. In this work, we comprehensively study the effect of functional groups on water adsorption on a series CAU-10-X substituted with both hydrophilic (X = NH2) and hydrophobic (X = NO2) groups in the linker. The adsorption equilibrium is measured at P = 7.6-42 mbar and T = 5-100 °C. The study of water adsorption by a set of mutually complementary physicochemical methods (TG, XRD in situ, FTIR, and 1H NMR relaxometry) elucidates the nature of primary adsorption sites and water adsorption mechanisms.

A close view of the organic linker in a MOF: structural insights from a combined 1H NMR relaxometry and computational investigation.

The organic linker in a metal organic framework (MOF) affects its adsorption behavior and performance, and its structure and dynamics play a role in the modulation of the adsorption properties. In this work, the combination of 1H nuclear magnetic resonance (NMR) longitudinal relaxometry and theoretical calculations allowed details of the structure and dynamics of the organic linker in the NH2-MIL-125 MOF to be obtained. In particular, fast field cycling (FFC) NMR, applied here for the first time on MOFs, was used to disclose the dynamics of the amino group and its electronic environment through the analysis of the 14N quadrupole relaxation peaks, observed in the frequency interval 0.5-5 MHz, at different temperatures from 25 to 110 °C. The line width of the peaks allowed a lower boundary on the rotational correlation time of the N-H bonds to be set, whereas relevant changes in the amplitudes were interpreted in terms of a change in the orientation of the 14N averaged electric field gradient tensor. The experimental findings were complemented by quantum chemistry calculations and classical molecular dynamics simulations.