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The quest for understanding the structure-property correlation in porous materials has remained a persistent focus across various research domains, particularly within the sorption realm. Molecular metal oxide clusters, owing to their precisely tunable atomic structures and long-range order, exhibit significant potential as versatile platforms for sorption investigations. This study presents a series of isostructural Ti8Ce2-oxo clusters with subtle variations in coordinated linkers and explores their gas sorption behavior. Notably, Ti8Ce2-BA (where BA denotes benzoic acid) manifests a distinctive twostep profile during CO2 adsorption, accompanied by a hysteresis loop. This observation marks a pioneering instance within the metal oxide cluster field. Of particular intrigue, the presence of unsaturated Ce(Ⅳ) sites was found to be correlated with the stepped sorption property. Moreover, the introduction of an electrophilic fluorine atom, positioned ortho or para to the benzoic acid, facilitated precise control over gate pressure and stepped sorption quantities. Advanced in-situ techniques systematically unraveled the underlying mechanism behind this unique sorption behavior. The findings elucidate that robust Lewis base-acid interactions are established between CO2 molecules and Ce ions, consequently altering the conformation of coordinated linkers. Conversely, the F atoms primarily contribute to gate pressure variation by influencing the Lewis acidity of the Ce sites. This research advances the understanding in fabricating geometrically "flexible" metal-oxo clusters and provides profound insights into their host-guest interaction motifs. These insights hold substantial promise across diverse fields, particularly in CO2 gas capture and gas-phase catalysis, and offer valuable guidance for future adsorbent designs grounded in fundamental theories of structure-property relationships. 

A huge challenge facing scientists is the development of adsorbent materials that exhibit ultrahigh porosity but maintain balance between gravimetric and volumetric surface areas for the onboard storage of hydrogen and methane gas—alternatives to conventional fossil fuels. Here we report the simulation-motivated synthesis of ultraporous metal–organic frameworks (MOFs) based on metal trinuclear clusters, namely, NU-1501-M (M = Al or Fe). Relative to other ultraporous MOFs, NU-1501-Al exhibits concurrently a high gravimetric Brunauer−Emmett−Teller (BET) area of 7310 m 2 g −1 and a volumetric BET area of 2060 m 2 cm −3 while satisfying the four BET consistency criteria. The high porosity and surface area of this MOF yielded impressive gravimetric and volumetric storage performances for hydrogen and methane: NU-1501-Al surpasses the gravimetric methane storage U.S. Department of Energy target (0.5 g g −1 ) with an uptake of 0.66 g g −1 [262 cm 3 (standard temperature and pressure, STP) cm −3 ] at 100 bar/270 K and a 5- to 100-bar working capacity of 0.60 g g −1 [238 cm 3 (STP) cm −3 ] at 270 K; it also shows one of the best deliverable hydrogen capacities (14.0 weight %, 46.2 g liter −1 ) under a combined temperature and pressure swing (77 K/100 bar → 160 K/5 bar). 

Abstract The fabrication of MOF polymer composite materials enables the practical applications of MOF‐based technology, in particular for protective suits and masks. However, traditional production methods typically require organic solvent for processing which leads to environmental pollution, low‐loading efficiency, poor accessibility, and loss of functionality due to poor solvent resistance properties. For the first time, we have developed a microbial synthesis strategy to prepare a MOF/bacterial cellulose nanofiber composite sponge. The prepared sponge exhibited a hierarchically porous structure, high MOF loading (up to ≈90 %), good solvent resistance, and high catalytic activity for the liquid‐ and solid‐state hydrolysis of nerve agent simulants. Moreover, the MOF/ bacterial cellulose composite sponge reported here showed a nearly 8‐fold enhancement in the protection against an ultra‐toxic nerve agent (GD) in permeability studies as compared to a commercialized adsorptive carbon cloth. The results shown here present an essential step toward the practical application of MOF‐based protective gear against nerve agents.