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Herein, we describe a new class of porous composites comprising metal–organic framework (MOF) crystals confined in single spherical matrices made of packed covalent‐organic framework (COF) nanocrystals. These MOF@COF composites are synthesized through a two‐step method of spray‐drying and subsequent amorphous (imine‐based polymer)‐to‐crystalline (imine‐based COF) transformation. This transformation around the MOF crystals generates micro‐ and mesopores at the MOF/COF interface that provide far superior porosity compared to that of the constituent MOF and COF components added together. We report that water sorption in these new pores occurs within the same pressure window as in the COF pores. Our new MOF@COF composites, with their additional pores at the MOF/COF interface, should have implications for the development of new composites. [ABSTRACT FROM AUTHOR]

Herein, we describe a new class of porous composites comprising metal–organic framework (MOF) crystals confined in single spherical matrices made of packed covalent‐organic framework (COF) nanocrystals. These MOF@COF composites are synthesized through a two‐step method of spray‐drying and subsequent amorphous (imine‐based polymer)‐to‐crystalline (imine‐based COF) transformation. This transformation around the MOF crystals generates micro‐ and mesopores at the MOF/COF interface that provide far superior porosity compared to that of the constituent MOF and COF components added together. We report that water sorption in these new pores occurs within the same pressure window as in the COF pores. Our new MOF@COF composites, with their additional pores at the MOF/COF interface, should have implications for the development of new composites. [ABSTRACT FROM AUTHOR]

Adsorptive heat transformation systems such as adsorption thermal batteries and chillers can provide space heating and cooling in a more environmental friendly way. However, their use is still hindered by their relatively poor performances and large sizes due to the limited properties of solid adsorbents. Here, the spray-drying continuous-flow synthesis of a new type of solid adsorbents that results from combining metal-organic frameworks (MOFs), such as UiO-66, and hygroscopic salts, such as CaCl2 has been reported. These adsorbents, commonly named as composite salt in porous matrix (CSPM) materials, allow improving the water uptake capabilities of MOFs while preventing their dissolution in the water adsorbed; a common characteristic of these salts due to the deliquescence effect. It is anticipated that MOF-based CSPMs, in which the percentage of salt can be tuned, are promising candidates for thermal batteries and chillers. In these applications, it is showed that a CSPM made of UiO-66 and CaCl2 (38% w/w) exhibits a heat storage capacity of 367 kJ kg−1 , whereas a second CSPM made of UiO-66 and CaCl2 (53% w/w) shows a specific cooling power of 631 W kg−1 and a coefficient of performance of 0.83, comparable to the best solid adsorbents reported so far. [ABSTRACT FROM AUTHOR]

New functional TiO 2 -clay nanoarchitectures based on layered and fibrous silicates and incorporating Pd and Pt noble metal nanoparticles (NPs) have been synthesized by applying a sol–gel methodology that involves the use of commercial organoclays. The incorporation of the noble metal NPs can be done using two different approaches: i) direct addition to the synthesis medium of a noble metal precursor (typically acetylacetonate) during the generation of the nanoarchitecture, and ii) selective photodeposition of the noble metal NPs in a post-treatment of the TiO 2 -clay nanoarchitecture. The resulting materials have been characterized by means of XRD, FTIR, Raman, 29 Si-NMR, FE-SEM, TEM and N 2 adsorption–desorption isotherms. The efficiency of these nanoarchitectures in the photocatalytic hydrogen production has been tested in the photoreforming of methanol. The higher rate in the hydrogen production corresponds to the nanoarchitectures containing Pt and TiO 2 NPs derived from sepiolite. [ABSTRACT FROM AUTHOR]

This work reports on the synthesis of nanosheets of layeredtitanosilicateJDF-L1 supported on commercial E-type glass fibers with the aim ofdeveloping novel nanoarchitectures useful as robust and easy to handlehydrogen adsorbents. The preparation of those materials is carriedout by hydrothermal reaction from the corresponding gel precursorin the presence of the glass support. Because of the basic characterof the synthesis media, silica from the silicate-based glass fiberscan be involved in the reaction, cementing its associated titanosilicateand giving rise to strong linkages on the support with the resultof very stable heterostructures. The nanoarchitectures built up bythis approach promote the growth and disposition of the titanosilicatenanosheets as a house-of-cards radially distributed around the fiberaxis. Such an open arrangement represents suitable geometry for potentialuses in adsorption and catalytic applications where the active surfacehas to be available. The content of the titanosilicate crystallinephase in the system represents about 12 wt %, and this percentageof the adsorbent fraction can achieve, at 298 K and 20 MPa, 0.14 wt% hydrogen adsorption with respect to the total mass of the system.Following postsynthesis treatments, small amounts of Pd (<0.1 wt%) have been incorporated into the resulting nanoarchitectures inorder to improve their hydrogen adsorption capacity. In this way,Pd-layered titanosilicate supported on glass fibers has been testedas a hydrogen adsorbent at diverse pressures and temperatures, givingrise to values around 0.46 wt % at 298 K and 20 MPa. A mechanism ofhydrogen spillover involving the titanosilicate framework and thePd nanoparticules has been proposed to explain the high increase inthe hydrogen uptake capacity after the incorporation of Pd into thenanoarchitecture. [ABSTRACT FROM AUTHOR]

Abstract: JDF-L1 and AM-4 are porous layered titanosilicates that can be modified by ion exchange while keeping the crystallinity. In this study, JDF-L1 and AM-4 were exchanged with Ag+, Zn2+ and Cu2+ ions and characterized by XRD and TEM. JDF-L1 exchanged titanosilicate preserved the crystalline structure while AM-4 exchanged titanosilicate showed a certain loss of crystallinity. In the case of Ag-exchanged samples, the Ag nanoparticles were distributed at the edges of the JDF-L1 crystals whereas they were distributed around the AM-4 particles. The antimicrobial activity was tested with Staphylococcus aureus. All the exchanged titanosilicates showed good antimicrobial activity against the bacteria and the most active was Ag–AM-4. [Copyright &y& Elsevier]

Adsorption‐based cooling systems, which can be driven by waste heat and solar energy, are promising alternatives to conventional, compression‐based cooling systems, as they demand less energy and emit less CO2. The performance of adsorption‐based cooling systems relates directly to the performance of the working pairs (sorbent–water). Accordingly, improvement of these systems relies on the continual discovery of new sorbents that enable greater mass exchange while requiring less energy for regeneration. Here, it is proposed that covalent‐organic frameworks (COFs) can replace traditional sorbents for adsorption‐based cooling. In tests mimicking standard operating conditions for industry, the imine‐based COF TpPa‐1 exhibits a regeneration temperature below 65 °C and a cooling coefficient of performance of 0.77 – values which are comparable to those reported for the best metal–organic framework sorbents described to date. Moreover, TpPa‐1 exhibits a photothermal effect and can be regenerated by visible light, thereby opening the possibility for its use in solar‐driven cooling. [ABSTRACT FROM AUTHOR]

Herein, we exploit the well‐known swelling behaviour of metal–organic frameworks (MOFs) to create a self‐folding polymer film. Namely, we show that incorporating crystals of the flexible MOF MIL‐88A into a polyvinylidene difluoride (PVDF) matrix affords a polymer composite film that undergoes reversible shape transformations upon exposure to polar solvents and vapours. Since the self‐folding properties of this film correlate directly with the swelling properties of the MIL‐88A crystals, it selectively bends to certain solvents and its degree of folding can be controlled by controlling the relative humidity. Moreover, it shows a shape‐memory effect at relative humidity values from 60 % to 90 %. As proof of concept, we demonstrate that these composite films can lift cargo and can be used to assemble 3D structures from 2D patterns. Our strategy is a straightforward method for designing autonomous soft materials with folding properties that can be tuned by judicious choice of the constituent flexible MOF. [ABSTRACT FROM AUTHOR]

Herein, we exploit the well‐known swelling behaviour of metal–organic frameworks (MOFs) to create a self‐folding polymer film. Namely, we show that incorporating crystals of the flexible MOF MIL‐88A into a polyvinylidene difluoride (PVDF) matrix affords a polymer composite film that undergoes reversible shape transformations upon exposure to polar solvents and vapours. Since the self‐folding properties of this film correlate directly with the swelling properties of the MIL‐88A crystals, it selectively bends to certain solvents and its degree of folding can be controlled by controlling the relative humidity. Moreover, it shows a shape‐memory effect at relative humidity values from 60 % to 90 %. As proof of concept, we demonstrate that these composite films can lift cargo and can be used to assemble 3D structures from 2D patterns. Our strategy is a straightforward method for designing autonomous soft materials with folding properties that can be tuned by judicious choice of the constituent flexible MOF. MOF‐n‐Fold: The swelling behaviour of the metal–organic framework MIL‐88A is used to impart self‐folding properties to a polymer film upon exposure to polar solvents and vapours. The degree of folding of the resulting film can be controlled by changing the relative humidity, showing a shape memory effect. [ABSTRACT FROM AUTHOR]

Porous metal–organic frameworks (MOFs) are attracting great attention from industry, thanks to their myriad potential applications in areas such as catalysis and gas storage. Zr-MOFs (also known as UiO-type MOFs) are especially promising, owing to their large surface areas, high chemical versatility and remarkable hydrothermal, chemical and thermal stabilities. However, among the challenges currently precluding the industrial exploitation of MOFs is the lack of green methods for their synthesis. Herein we describe a continuous-flow spray-drying method for the simultaneous synthesis and shaping of spherical MOF microbeads in a mixture of water and acetic acid. We used this approach to build two archetypical Zr-MOFs: UiO-66-NH2 and Zr-fumarate. By tuning the concentration of acetic acid in water, we were able to produce, by a scalable process, UiO-66-NH2 and Zr-fumarate beads with SBET and water-sorption values comparable to the literature values obtained with other methods. [ABSTRACT FROM AUTHOR]

The synthesis, X-ray crystallographic structure, and water uptake measurements of the first coordination polymer made of a cyclodextrin and a transition metal ion (in this case, Cu2+) are shown. This coordination polymer is made by connecting paddle-wheel Cu2+ units through a γ-cyclodextrin functionalized with eight carboxylate groups, is stable in water, and shows selective water-induced reversible structural transformations. [ABSTRACT FROM AUTHOR]

Here, a two-step method is reported that enables imparting new functionalities to covalent organic frameworks (COFs) by nanoparticle confinement. The direct reaction between 1,3,5-tris(4-aminophenyl)benzene and 1,3,5-benzenetricarbaldehyde in the presence of a variety of metallic/metal-oxide nanoparticles resulted in embedding of the nanoparticles in amorphous and non-porous imine-linked polymer organic spheres ( NP@a-1). Post-treatment reactions of NP@a-1 with acetic acid under reflux led to crystalline and porous imine-based COF-hybrid spheres ( NP@c-1). Interestingly, Au@c-1 and Pd@c-1 were found to be catalytically active. [ABSTRACT FROM AUTHOR]

Materials with surfaces that can be switched from high/superhydrophobicity to superhydrophilicity are useful for myriad applications. Herein, we report a metal-organic framework (MOF) assembled from ZnII ions, 1,4-benzenedicarboxylate, and a hydrophobic carborane-based linker. The MOF crystal-surface can be switched between hydrophobic and superhydrophilic through a chemical treatment to remove some of the building blocks. [ABSTRACT FROM AUTHOR]

Materials with surfaces that can be switched from high/superhydrophobicity to superhydrophilicity are useful for myriad applications. Herein, we report a metal-organic framework (MOF) assembled from ZnII ions, 1,4-benzenedicarboxylate, and a hydrophobic carborane-based linker. The MOF crystal-surface can be switched between hydrophobic and superhydrophilic through a chemical treatment to remove some of the building blocks. [ABSTRACT FROM AUTHOR]

Herein we report a study on water adsorption/desorption-triggered single-crystal to single-crystal transformations in a MOF, by single-crystal and humidity-controlled powder X-ray diffraction and water-sorption measurements. We identified a gate-opening effect at a relative humidity of 85% upon water adsorption, and a gate-closure effect at a relative humidity of 55 to 77% upon water desorption. This reversible breathing effect between the “open” and the “closed” structures of the MOF involves the cleavage and formation of several coordination bonds. [ABSTRACT FROM AUTHOR]