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Development in patterning technique of metal–organic frameworks (MOFs) will facilitate their integration in microelectronics, but controlling the structure of MOFs at the nanoscale remains a major ...

Modification of the gas permeation properties of ZIF-8 membranes using electron beam irradiation is reported. 3.8 and 3.2 fold enhancements in ideal selectivity for CO2/N2 and CO2/CH4 can be achieved with less than 1 min exposure time.

ConspectusMetal-organic framework solids (MOFs) are synthetic nanoporous materials that have drawn intense efforts in synthesis and characterization of chemical properties, most notably for their ability to adsorb liquids and gases. They are constructed as "node-spacer" nanostructured materials: metal centers (ions or clusters) connected by organic linkers (commonly containing carboxylate or imidazolate groups) to form crystalline, extended, often highly nanoporous structures. MOFs exhibit a variety of advantages over conventional porous materials: rationally designed synthesis of desired crystal structures and crystal engineering become feasible; great synthetic versatility and ease of incorporating different chemical functionalities are realized; and the use of lightweight organic linkers allows for ultrahigh surface area and porosity previously not accessible to conventional materials (i.e., zeolites and porous carbon). As a consequence, MOFs show great promise for a rapidly expanding collection of applications such as gas storage, separations, catalysis, sensing, and drug delivery.The mechanochemistry of MOFs and their response to shock waves, which we discuss in this Account, have been only partially explored. Mechanochemistry, the connection between the mechanical and the chemical worlds, has ancient origins. Rubbing sticks together to start a fire is mechanochemistry. Only in the past decade or so, however, has mechanochemistry gained a notable focus in the chemical community. In the following discussion, we present a general introduction to the complex mechanochemical behavior of MOFs both under quasi-static compression and under shock loading created by high-speed impact. During elastic deformation, MOFs undergo reversible structural or phase transitions. Plastic deformation of MOFs can result in mechanochemistry and can permanently modify the crystal structure, the pore dimensions and configuration, and the chemical bonding. The large energies required to induce bond rearrangement during plastic deformation suggest an interesting potential of MOFs for shock wave mitigation applications.MOFs are promising materials for shock energy dissipation because of the high density of nanopores which can absorb shock energy as they collapse. We have recently developed a platform to assess shock wave energy attenuation by MOFs and other powdered materials. It uses a tabletop laser-driven flyer plate to impact MOF samples at velocities of up to 2.0 km/s. The pressure of the shock waves that break out from the MOF sample can be measured by photon Doppler velocimetry. By measuring the shock profiles of MOF layers with different thicknesses, we can determine the shock pressure attenuation by the MOF layer. We have identified the two-wave structure of shocks in MOFs caused by nanopore collapse. Electron micrographs of recovered shocked MOFs show distinct zones in the shocked material corresponding to shock powder compaction, nanopore collapse, and chemical bond destruction.

Formation of thick, high energy density, flexible solid supercapacitors is challenging because of difficulties infilling gel electrolytes into porous electrodes. Incomplete infilling results in a low capacitance and poor mechanical properties. Here we report a bottom-up infilling method to overcome these challenges. Electrodes up to 500 μm thick, formed from multi-walled carbon nanotubes and a composite of poly(3,4-ethylenedioxythiophene), polystyrene sulfonate and multi-walled carbon nanotubes are successfully infilled with a polyvinyl alcohol/phosphoric acid gel electrolyte. The exceptional mechanical properties of the multi-walled carbon nanotube-based electrode enable it to be rolled into a radius of curvature as small as 0.5 mm without cracking and retain 95% of its initial capacitance after 5000 bending cycles. The areal capacitance of our 500 μm thick poly(3,4-ethylenedioxythiophene), polystyrene sulfonate, multi-walled carbon nanotube-based flexible solid supercapacitor is 2662 mF cm–2 at 2 mV s–1, at least five times greater than current flexible supercapacitors., The development of high performance flexible solid supercapacitors calls for an effective approach to infill gel electrolytes into porous electrodes. Here the authors report a bottom-up method to address this technical challenge, which leads to enhanced areal capacitance and durability.

Recent investigations into the mechanical properties and mechanochemical reactions of metal-organic frameworks (MOFs) have suggested the potential for energy dissipation by multiple mechanisms. Although the possibility of efficient multifunctional shock dissipation by MOFs was suggested by static high pressure studies, there is little known about MOFs under shock compression. Here, we measure the attenuation of shock wave by the MOF denoted zeolitic-imidazolate framework (ZIF-8) in its desolvated, porous state. We find that shock wave dissipation by ZIF-8 occurred by multiple processes: powder compaction, nanopore-collapse, and chemical bond-breakage. The shock energy absorbance in ZIF-8 is proportional to ZIF-8 thickness, allowing the prediction of the thickness of MOF layer needed to attenuate shock waves to a desired lower energy. Compared with PMMA, often used as a standard, ZIF-8 attenuates 7 times more shock energy per unit mass for impacts at a lower velocity of 0.75 km/s and 2.5 times more at a higher velocity of 1.6 km/s. This research illustrates how to improve the ability to attenuate shock waves for personnel and equipment protection by engineering multifunctionality into the shock wave absorbing armor material.

The internal free volume of porous materials diminishes upon mechanical compression, and such volume collapse can have chemical consequences., The internal free volume of porous materials diminishes upon mechanical compression, and such volume collapse can have chemical consequences. We report here the endothermic bond breakage in a metal-organic framework (MOF) during compression-induced collapse. Upon bulk compression at 1.9 GPa, the effective number for Zr–O bonds between Zr(iv) ions and carboxylate groups in UiO-66 decreased from 4.0 to 1.9, as determined by EXAFS, and the internal free volume was synchronously collapsed. Consistent with the EXAFS data, IR spectra confirmed conversion of syn–syn bridging carboxylates to monodentate ligation, thus establishing mechanochemical reactions induced by external compression of MOFs. Substantial mechanical energy (∼4 kJ g–1) was absorbed by UiO-66 nanocrystals during compression, as demonstrated from nanocompression of single crystals (600 nm) in situ during scanning electron microscopy, which establishes the potential application of MOFs as mechanical energy absorbers for hydrostatic and shock compression.

Metal–organic frameworks (MOFs) have potential applications as energy absorbing materials for shock wave energy mitigation due to their nanoporosity. Here we have examined km/s laser-driven flyer plate impacts on a prototypical MOF, ZIF-8. We observed particle fragmentation and morphological changes in microcrystals of ZIF-8 at lower shock pressures (≈2.5 GPa), and amorphization and structural collapse at higher pressures (≈8 GPa). High-speed emission spectroscopy revealed that 50 ns after flyer plate impacts, an emission pulse was generated by ZIF-8 resulting from chemical bonds that were broken and subsequently reformed. MOFs may prove useful in the dissipation of shock wave energy through large structural changes (free volume collapse and endothermic bond breakage).

Porous materials provide a plethora of technologically important applications that encompass molecular separations, catalysis, and adsorption. The majority of research in this field involves network solids constructed from multitopic constituents that, when assembled either covalently or ionically, afford macromolecular arrangements with micro- or meso-porous apertures. Recently, porous solids fabricated from discrete organic cages have garnered much interest due to their ease of handling and solution processability. Although this class of materials is a promising alternative to network solids, fundamental studies are still required to elucidate critical structure-function relationships that govern microporosity. Here, we report a systematic investigation of the effects of building block shape-persistence on the porosity of molecular cages. Alkyne metathesis and edge-specific postsynthetic modifications afforded three organic cages with alkynyl, alkenyl, and alkyl edges, respectively. Nitrogen adsorption experiments conducted on rapidly crystallized and slowly crystallized solids illustrated a general trend in porosity: alkynylalkenylalkyl. To understand the molecular-scale origin of this trend, we investigated the short and long time scale molecular motions of the molecular cages using ab initio molecular dynamics (AIMD) and classical molecular dynamics (MD) simulations. Our combined experimental and computational results demonstrate that the microporosity of molecular cages directly correlates with shape persistence. These findings discern fundamental molecular requirements for rationally designing porous molecular solids.

Conversion of cellulosic biomass to renewable chemicals such as 5-hydroxymethylfurfural (HMF) is of high current interest. Herein, we report a rare example of one-pot synthesis of HMF from glucose by tandem catalysis. The system is composed of a thermophilic glucose isomerase enzyme for glucose isomerization to fructose and a solid acid catalyst for fructose dehydration to HMF. A base (−NH2) functionalized mesoporous silica (aminopropyl-FMS) with large pore size was deployed successfully to immobilize and protect the thermophilic glucose isomerase in organic solvents at high temperature. The combination of this catalyst with a Bronsted acid (−SO3H) functionalized mesoporous silica (propylsulfonic acid-FMS) allowed us to conduct a one-pot transformation of glucose to HMF directly in a monophasic solvent system composed of tetrahydrofuran (THF) and H2O (4:1 v/v) with 61% yield of fructose and 30% yield of HMF at temperatures >363 K in 24 h.

Two manganese sulfates, [C2H6O2][MnSO4] (1) and [C4N2H12][Mn(SO4)2(H2O)] (2), were solvothermally synthesized in the presence of ethylene glycol and piperazine. Both compounds are constructed from 4-membered ring ladder chains made of MnO6 and SO4 units, with 1 displaying a 3D zeolite gismondine (GIS) framework and 2 possessing a 1D chain structure, respectively.

The deformation and mechanical behavior of individual zeolitic–imidazolate framework (ZIF-8) micro- and sub-microcrystals were observed under compression. Young’s modulus and volume changes as a function of applied pressure were determined on individual single crystals, offering insights in the relationship among structure, morphology, and mechanical properties. Dramatic volume decreases and amorphization were detected during compression over a pressure range of 0–4 GPa for individual 1.2 μm ZIF-8 microcrystals, and the deformed microcrystals partially recovered after pressure release. The orientation and size effects on the mechanical behavior of ZIF-8 nano- and microcrystals were also investigated. The presence of solvates within the pores of the ZIF-8 has a dramatic effect on the mechanical properties of the single crystals. Methanol-solvated ZIF-8 microcrystals are much less deformable than the desolvated microcrystals and shatter completely at very low applied force.