Metal-organic Framework Nanocrystals Research Articles

Cobalt nanoparticles packaged into nitrogen-doped porous carbon derived from metal-organic framework nanocrystals for hydrogen production by hydrolysis of sodium borohydride

Efficient safe transportation and generation of hydrogen are the key technologies for the hydrogen economy development in future. Sodium borohydride (NaBH4) features highly volumetric density and environmentally benign hydrolysis products, which making it a promising candidate for chemical hydrogen storage. Cobalt nanoparticles packaged into nitrogen-doped porous carbon were successfully prepared by pyrolysis of MOFs. The addition of Zn in MOFs as a “fence” expanded the distance of adjacent Co atoms in space and simultaneously, the leaving Zn2+ sites generated free N sites during pyrolysis. These are beneficial to reduce the sizes of Co nanoparticles and enhance the dispersity of active sites. The modification method allows the cobalt nanoparticles to be uniformly and finely confined within the porous carbon. Contributed by highly dispersed Co nanoparticles and confinement effect, the catalyst showed excellent catalytic activity with hydrogen production rate of 1807 mL (H2) min−1·gCo−1 and lower activation energy (20 kJ/mol) than ever reported. The stability test confirmed that deactivation of catalyst occurred due to deposition of borate species at the surface of catalyst. This observation may provide an idea to modify and upgrade stability of catalyst.

Synergistic Effect of Co-Ni Hybrid Phosphide Nanocages for Ultrahigh Capacity Fast Energy Storage.

Rational design of metal compounds in terms of the structure/morphology and chemical composition is essential to achieve desirable electrochemical performances for fast energy storage because of the synergistic effect between different elements and the structure effect. Here, an approach is presented to facilely fabricate mixed‐metal compounds including hydroxides, phosphides, sulfides, oxides, and selenides with well‐defined hollow nanocage structure using metal–organic framework nanocrystals as sacrificial precursors. Among the as‐synthesized samples, the porous nanocage structure, synergistic effect of mixed metals, and unique phosphide composition endow nickel cobalt bimetallic phosphide (NiCo‐P) nanocages with outstanding performance as a battery‐type Faradaic electrode material for fast energy storage, with ultrahigh specific capacity of 894 C g−1 at 1 A g−1 and excellent rate capability, surpassing most of the reported metal compounds. Control experiments and theoretical calculations based on density functional theory reveal that the synergistic effect between Ni and Co in NiCo‐P can greatly increase the OH− adsorption energy, while the hollow porous structure facilitates the fast mass/electron transport. The presented work not only provides a promising electrode material for fast energy storage, but also opens a new route toward structural and compositional design of electrode materials for energy storage and conversion.

Quasi-thresholdless Photon Upconversion in Metal-Organic Framework Nanocrystals.

Photon upconversion based on sensitized triplet-triplet annihilation ( sTTA) is considered asa promising strategy for the development of light-managing materials aimed to enhance the performance of solar devices by recovering unused low-energy photons. Here, we demonstrate that, thanks to the fast diffusion of excitons, the creation of triplet pairs in metal-organic framework nanocrystals ( nMOFs) with size smaller than the exciton diffusion length implies a 100% TTA yield regardless of the illumination condition. This makes each nMOF a thresholdless, single-unit annihilator. We develop a kinetic model for describing the upconversion dynamics in a nanocrystals ensemble, which allows us to define the threshold excitation intensity Ithbox required to reach the maximum conversion yield. For materials based on thresholdless annihilators, Ithbox is determined by the statistical distribution of the excitation energy among nanocrystals. The model is validated by fabricating a nanocomposite material based on nMOFs, which shows efficient upconversion under a few percent of solar irradiance, matching the requirements of real life solar technologies. The statistical analysis reproduces the experimental findings, and represents a general tool for predicting the optimal compromise between dimensions and concentration of nMOFs with a given crystalline structure that minimizes the irradiance at which the system starts to fully operate.

Lectin-Recognizable MOF Glyconanoparticles: Supramolecular Glycosylation of ZIF-8 Nanocrystals by Sugar-Based Surfactants.

A strategy toward the integration of highly functional microporous materials, such as metal-organic frameworks (MOFs), in composites via biochemical recognition interactions is presented. Postsynthetic modification of zeolitic-imidazolate framework-8 MOF nanocrystals with a maltose-exposing biocompatible surfactant (the so-called “Glyco-MOFs”) was performed to confer affinity toward lectin protein concanavalin A. The addition of small amounts of concanavalin A to the colloidal Glyco-MOF dispersion triggers the aggregation of these units into self-limited size supramolecular architectures directed by specific sugar–lectin binding interactions.

Size control over metal-organic framework porous nanocrystals.

Porous nanocrystals of metal-organic frameworks (MOFs) offer greater bioavailability, higher surface-to-volume ratios, superior control over MOF membrane fabrication, and enhanced guest-sorption kinetics compared to analogous bulk phases, but reliable synthesis of uniformly sized particles remains an outstanding challenge. Here, we identify the smallest and most probable sizes of known MOF nanocrystals and present an exhaustive comparative summary of nano- versus bulk-MOF syntheses. Based on critical analysis of reported size data and experimental conditions, an alternate to the LaMer model is proposed that describes nanocrystal formation as a kinetic competition between acid-base and metal-ligand reactivity. Particle growth terminates when ligands outcompete metal-ion diffusion, thereby arresting polymerization to produce kinetically trapped particle sizes. This model reconciles disparate trends in the literature and postulates that minimum particle sizes can be achieved by minimizing the relative ratios of metal-to-linker local concentrations. By identifying conditions that disfavor small nanocrystal sizes, this model also provides routes towards macroscopic MOF single crystals. A universal "seesaw" relationship between nanocrystal sizes and the concentrations of acidic surface-capping ligands provides a roadmap for achieving precise synthetic control. Best practices in synthesis, characterization, and data presentation are recommended for future investigations so that MOF nanocrystals may achieve their full potential as advanced nanomaterials.

Investigating the origin of high efficiency in confined multienzyme catalysis.

Biomimetic strategies have successfully been applied to confine multiple enzymes on scaffolds to obtain higher catalytic efficiency of enzyme cascades than freely distributed enzymes. However, the origin of high efficiency is poorly understood. We developed a coarse-grained, particle-based model to understand the origin of high efficiency. We found that a reaction intermediate is the key in affecting reaction kinetics. In the case of unstable intermediates, the confinement of multiple enzymes in clusters enhanced the catalytic efficiency and a shorter distance between enzymes resulted in a higher reaction rate and yield. This understanding was verified by co-encapsulating multiple enzymes in metal-organic framework (MOF) nanocrystals as artificially confined multienzyme complexes. The activity enhancement of multiple enzymes in MOFs depended on the distance between enzymes, when the decay of intermediates existed. The finding of this study is useful for designing in vitro synthetic biology systems based on artificial multienzyme complexes.

2D Metal Organic Framework‐Graphitic Carbon Nanocomposites as Precursors for High‐Performance O2‐Evolution Electrocatalysts

AbstractThe development of effective and precious‐metal‐free electrocatalysts for the oxygen evolution reaction (OER) represents a major bottleneck to unlock a renewable energy scenario based on water splitting technologies. Materials uniting the electrical conductivity of conjugated graphitic nanomaterials with the chemical regularity of metal‐organic‐framework (MOF) crystals are promising precursors for such electrocatalysts. Nanoscale integration of these two materials is challenging. A new synthesis route is developed that integrates 2D MOF nanocrystals and graphitic carbon nanolamellae into layered composites. The graphitic carrier contributes excellent charge–transport properties, and the 2D macromolecular MOF precursor provides a suitable shuttle for introducing highly dispersed metal species. Furthermore their direct chemical environment can be controlled via selection of organic linker. Thermal decomposition of 2D cobalt tetrafluoro benzene‐dicarboxylate MOF nanocrystals within such composites enables the stabilization of cobalt oxyhydroxyfluoride nanoparticles on the graphitic carrier, which display an extraordinary activity for the OER in alkaline media, with low onset overpotential (310 mVRHE) and current densities >104 mA cm−2 μmolCo−1 at an operating overpotential of 450 mV, alongside excellent operational stability. The wide compositional array of MOFs makes this synthesis approach versatile toward advanced (electro)catalysts and other functional materials for applications from sensing to energy storage and conversion.

Zirconium metal-organic framework nanocrystal as microwave sensitizer for enhancement of tumor therapy

Although surgical resection and chemotherapy were widely applied in tumor therapy, the dysfunction of normal cells resulted in the side effects (such as anorexia, nausea). MW thermal therapy is a non-invasive anticancer strategy under the help of MW sensitizer, with the safety and higher efficacy. Zirconium metal-organic framework nanocubes (ZrMOF NCs) modified with polyethylene glycol, were prepared via one pot method and carbodiimide technique, resulting in their large specific surface area and porosity. Our results showed that non-ion-loaded ZrMOF NCs in 0.9% NaCl solution exhibited better heating effect, higher than that in pure water, due to the robust collision among the ions under MW irradiation. The in vivo experiments confirmed that ZrMOF-PEG NCs+MW group exhibited the higher temperature in the tumor region than that of only MW treatment, suggesting a better MW thermal therapeutic anticancer efficacy. This work provides a new preparation strategy of biosafety nanomaterial as MW sensitizer for enhancing MW thermal anticancer therapy.

Enhanced CO2/CH4 separation performance of mixed-matrix membranes through dispersion of sorption-selective MOF nanocrystals

Mixed matrix membranes (MMMs) derived from metal-organic frameworks (MOFs) nanocrystals represent a promising alternative for overcoming the trade-off between permeability and selectivity derived from the pristine polymeric membrane. The selection of MOFs fillers are mainly focused on their diffusion-selectivity property for gas-pairs. However, the improvement of both gas-permeability and selectivity through addition of sorption-selective MOFs are rarely reported. Herein, the incorporation of CO2-philic KAUST-7 (also referred to as NbOFFIVE-1-Ni) nanocrystals makes the neat 6FDA-Durene polyimide membrane more permeable and more selective, surpassing the state-of-the-art 2008 Robeson upper bound for CO2/CH4. Nano-sized (~ 80 nm) KAUST-7 crystals with sharp particle size distribution were first fabricated through a co-solvent synthesis method. The explored gas transportation mechanism indicates that the improvement of CO2/CH4 selectivity on MMMs are attributed to the significant raise of the sorption-selectivity rather than the diffusion-selectivity. The favorable interfacial interaction between the imide groups of the 6FDA and the H of the pyrazine in the KAUST-7 enhances plasticization resistance of the neat polymer membrane. The developed MMMs exhibit a promising application in CO2 capture from natural- and bio-gas.

Facile Synthesis of MgAl-Layered Double Hydroxide Supported Metal Organic Framework Nanocomposite for Adsorptive Removal of Methyl Orange Dye

In this work, we report the fabrication of MgAl- layered double hydroxide (LDH) supported copper based metal organic framework (MOF) nanocomposite via a facile solvothermal method. Reaction of pre-synthesized benzene-1,4-dicarboxylate ions (BDC) intercalated MgAl-LDH with Cu(II) ions produce paddle-wheel like Cu-(BDC) MOF nanocrystals on the surface of MgAl-LDHs. The structures and morphology of the synthesized new materials have been investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), UV–visible and photo luminescent spectroscopy, Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The adsorption characteristics of the synthesized material showed the dye removal efficiency over 99% after 20 min with an adsorption capacity of 600 mg/g.

Cysteamine-modified ZIF-8 colloidal building blocks: Direct assembly of nanoparticulate MOF films on gold surfaces via thiol chemistry

Chemical modification of metal organic framework (MOF) nanocrystal colloids was used to endow them with chemical affinity for gold substrates. Modified nanocrystals were then used as building blocks for rapid and selective self-assembly of porous films. Cysteamine (Cys, 2-aminoetanethiol) was chosen as both chemical modulator and functionalizing agent of Zeolite Imidazolate Framework-8 (ZIF-8) MOF nanocrystals. Important parameters such as the impact of the modulator on the range of nanocrystals stability, size, polydispersity, morphology, and crystalline structure were assessed via both, small and wide angle x-ray scattering (SAXS and WAXS). Cysteamine modified ZIF-8 nanocrystals were assembled into films over conductive Au substrates and film growth was followed in-situ with Quartz Crystal Microbalance (QCM). Thiol moieties exposed out of the ZIF-8 surface after cysteamine modification, results in the formation of thiol bonds with Au conductive substrates as shown via Cyclic Voltammetry experiments. The strategy here presented allows for the synthesis of pre-designed building blocks for MOF films on metal surfaces.

Nanocoating of Hydrophobic Mesoporous Silica around MIL-101Cr for Enhanced Catalytic Activity and Stability.

The metal-organic framework (MOF) MIL-101Cr was readily encapsulated by a very thin shell (around 30 nm) of hydrophobic mesoporous silica, which replicates the irregular shape of the MOF nanocrystals. Such a silica shell facilitates the diffusion of hydrophobic reactants with enhancement of the catalytic activity of the MOF and significantly improved catalytic stability of the MOF in the oxidation of indene.

Synthesis of Metal-Organic Framework Nanocrystals and Research on Its Adsorption of Dye

Synthesis of Metal-Organic Framework Nanocrystals and Research on Its Adsorption of Dye

Highly Fluorescent Metal-Organic-Framework Nanocomposites for Photonic Applications.

Metal-organic frameworks (MOFs) are porous hybrid materials built up from organic ligands coordinated to metal ions or clusters by means of self-assembly strategies. The peculiarity of these materials is the possibility, according to specific synthetic routes, to manipulate both the composition and ligands arrangement in order to control their optical and energy-transport properties. Therefore, optimized MOFs nanocrystals (nano-MOFs) can potentially represent the next generation of luminescent materials with features similar to those of their inorganic predecessors, that is, the colloidal semiconductor quantum dots. The luminescence of fluorescent nano-MOFs is generated through the radiative recombination of ligand molecular excitons. The uniqueness of these nanocrystals is the possibility to pack the ligand chromophores close enough to allow a fast exciton diffusion but sufficiently far from each other preventing the aggregation-induced effects of the organic crystals. In particular, the formation of strongly coupled dimers or excimers is avoided, thus preserving the optical features of the isolated molecule. However, nano-MOFs have a very small fluorescence quantum yield (QY). In order to overcome this limitation and achieve highly emitting systems, we analyzed the fluorescence process in blue emitting nano-MOFs and modeled the diffusion and quenching mechanism of photogenerated singlet excitons. Our results demonstrate that the excitons quenching in nano-MOFs is mainly due to the presence of surface-located, nonradiative recombination centers. In analogy with their inorganic counterparts, we found that the passivation of the nano-MOF surfaces is a straightforward method to enhance the emission efficiency. By embedding the nanocrystals in an inert polymeric host, we observed a +200% increment of the fluorescence QY, thus recovering the emission properties of the isolated ligand in solution.

A Metal-Organic-Framework-Based Electrolyte with Nanowetted Interfaces for High-Energy-Density Solid-State Lithium Battery.

Solid-state batteries (SSBs) are promising for safer energy storage, but their active loading and energy density have been limited by large interfacial impedance caused by the poor Li+ transport kinetics between the solid-state electrolyte and the electrode materials. To address the interfacial issue and achieve higher energy density, herein, a novel solid-like electrolyte (SLE) based on ionic-liquid-impregnated metal-organic framework nanocrystals (Li-IL@MOF) is reported, which demonstrates excellent electrochemical properties, including a high room-temperature ionic conductivity of 3.0 × 10-4 S cm-1 , an improved Li+ transference number of 0.36, and good compatibilities against both Li metal and active electrodes with low interfacial resistances. The Li-IL@MOF SLE is further integrated into a rechargeable Li|LiFePO4 SSB with an unprecedented active loading of 25 mg cm-2 , and the battery exhibits remarkable performance over a wide temperature range from -20 up to 150 °C. Besides the intrinsically high ionic conductivity of Li-IL@MOF, the unique interfacial contact between the SLE and the active electrodes owing to an interfacial wettability effect of the nanoconfined Li-IL guests, which creates an effective 3D Li+ conductive network throughout the whole battery, is considered to be the key factor for the excellent performance of the SSB.

Pore Breathing of Metal-Organic Frameworks by Environmental Transmission Electron Microscopy.

Metal-organic frameworks (MOFs) have emerged as a versatile platform for the rational design of multifunctional materials, combining large specific surface areas with flexible, periodic frameworks that can undergo reversible structural transitions, or "breathing", upon temperature and pressure changes, and through gas adsorption/desorption processes. Although MOF breathing can be inferred from the analysis of adsorption isotherms, direct observation of the structural transitions has been lacking, and the underlying processes of framework reorganization in individual MOF nanocrystals is largely unknown. In this study, we describe the characterization and elucidation of these processes through the combination of in situ environmental transmission electron microscopy (ETEM) and computer simulations. This combined approach enables the direct monitoring of the breathing behavior of individual MIL-53(Cr) nanocrystals upon reversible water adsorption and temperature changes. The ability to characterize structural changes in single nanocrystals and extract lattice level information through in silico correlation provides fundamental insights into the relationship between pore size/shape and host-guest interactions.

Boosting the Catalytic Performance of Metal-Organic Frameworks for Steroid Transformations by Confinement within a Mesoporous Scaffold.

Solid-state crystallization achieves selective confinement of metal-organic framework (MOF) nanocrystals within mesoporous materials, thereby rendering active sites more accessible compared to the bulk-MOF and enhancing the chemical and mechanical stability of MOF nanocrystals. (Zr)UiO-66(NH2 )/SiO2 hybrid materials were tested as efficient and reusable heterogeneous catalysts for the synthesis of steroid derivatives, outperforming the bulk (Zr)UiO-66(NH2 ) MOF. A clear correlation between the catalytic activity of the dispersed Zr sites present in the confined MOF, and the loading of the mesoporous SiO2 , is demonstrated for steroid transformations.

Boosting the Catalytic Performance of Metal–Organic Frameworks for Steroid Transformations by Confinement within a Mesoporous Scaffold

AbstractSolid‐state crystallization achieves selective confinement of metal–organic framework (MOF) nanocrystals within mesoporous materials, thereby rendering active sites more accessible compared to the bulk‐MOF and enhancing the chemical and mechanical stability of MOF nanocrystals. (Zr)UiO‐66(NH2)/SiO2 hybrid materials were tested as efficient and reusable heterogeneous catalysts for the synthesis of steroid derivatives, outperforming the bulk (Zr)UiO‐66(NH2) MOF. A clear correlation between the catalytic activity of the dispersed Zr sites present in the confined MOF, and the loading of the mesoporous SiO2, is demonstrated for steroid transformations.

Enhanced Charge Collection in MOF-525-PEDOT Nanotube Composites Enable Highly Sensitive Biosensing.

With the aim of a reliable biosensing exhibiting enhanced sensitivity and selectivity, this study demonstrates a dopamine (DA) sensor composed of conductive poly(3,4‐ethylenedioxythiophene) nanotubes (PEDOT NTs) conformally coated with porphyrin‐based metal–organic framework nanocrystals (MOF‐525). The MOF‐525 serves as an electrocatalytic surface, while the PEDOT NTs act as a charge collector to rapidly transport the electron from MOF nanocrystals. Bundles of these particles form a conductive interpenetrating network film that together: (i) improves charge transport pathways between the MOF‐525 regions and (ii) increases the electrochemical active sites of the film. The electrocatalytic response is measured by cyclic voltammetry and differential pulse voltammetry techniques, where the linear concentration range of DA detection is estimated to be 2 × 10−6–270 × 10−6 m and the detection limit is estimated to be 0.04 × 10−6 m with high selectivity toward DA. Additionally, a real‐time determination of DA released from living rat pheochromocytoma cells is realized. The combination of MOF5‐25 and PEDOT NTs creates a new generation of porous electrodes for highly efficient electrochemical biosensing.

Confining Metal–Organic Framework Nanocrystals within Mesoporous Materials: A General Approach via “Solid-State” Synthesis

Here we report the selective growth of well-dispersed metal–organic framework (MOF) nanocrystals within mesoporous materials via novel “solid-state” synthesis. The ability to control and direct the growth of MOFs on confined surfaces (pores) paves the way for new prospective applications of such hybrid systems and could unlock the full potential of these materials. As confirmed by a combination of different characterization techniques, an outstanding high loading of mesoporous cavities (≤40 wt %) by the smallest MOF crystals yet reported (4.5 ± 1 nm) leads to several improved properties, including diffusion, attrition resistance, and handling.