Lanthanide-Doped Nanoparticles Anchoring on Metal-Organic Frameworks with Thermally Enhanced Upconversion Luminescence for Sensitive Nanothermometers.

Nanothermometers can detect changes in the local temperature in living cells and in vivo, revealing fundamental biological properties. Despite the exploration of different temperature-responsive materials, the design and development of temperature-sensing probes with high brightness and high sensitivity remain a daunting challenge. Here, we employed the UiO-66 type metal-organic frameworks (MOFs) to anchor UNCPs on the surface of the MOFs for constructing MOF@UCNPs nanohybrids. The in situ composite method with MOFs leads to the coordination interaction between the ligands and the surface of UCNPs, enabling controlled composite formation between different MOFs and UCNPs. Remarkably, the surface interaction favors the anomalous thermo-enhanced luminescence, achieving a 35-fold enhancement of UiO-66@NaYF4:Yb/Tm at 413 K. Furthermore, these MOF@UCNPs nanohybrids with thermo-enhanced luminescence are developed as multifunctional biological probes for bioimaging and intracellular temperature sensing, demonstrating a high thermal sensitivity of 1.92% K-1 in the physiological temperature range. Based on these findings, temperature monitoring of the local position was successfully carried out by the designed MOF@UCNPs nanoprobes in vivo. These findings underscore the potential of MOF@UCNPs nanohybrids, opening up new avenues for the development of a multifunctional platform for biological analysis.

Engineering microporous ethane-trapping metal-organic frameworks for boosting ethane/ethylene separation.

Realization of ethane-trapping materials for separating ethane (C2H6) from ethylene (C2H4) by adsorption, to potentially replace the energy-intensive cryogenic distillation technology, is of prime importance in the petrochemical industry. It is still very challenging to target C2H6-selective adsorbents with both high C2H6 capture capacity and gas selectivity. Herein, we report that a crystal engineering or reticular chemistry strategy enables the control of pore size and functionality in a family of isomorphic metal-organic frameworks (MOFs) for boosting the C2H6 uptake and selectivity simultaneously. By altering the carboxylic acid linker in Ni(bdc)(ted)0.5, we developed two novel isoreticular MOFs, Ni(ndc)(ted)0.5 and Ni(adc)(ted)0.5 (termed ZJU-120 and ZJU-121, respectively), in which the pore sizes and nonpolar aromatic rings can be finely engineered. We discover that activated ZJU-120a with the optimized pore size (4.4 Å) and aromatic rings exhibits both a very high C2H6 uptake (96 cm3 g-1 at 0.5 bar and 296 K) and C2H6/C2H4 selectivity (2.74), outperforming most of the C2H6-selective MOFs reported. Computational studies indicate that the suitable pore size and more nonpolar aromatic rings on the pore surfaces of ZJU-120a mainly contribute to its exceptional C2H6 uptake and selectivity. The breakthrough experiments demonstrate that ZJU-120a can efficiently separate C2H6 from 50/50 and 10/90C2H6/C2H4 mixtures under ambient conditions.

Rational design of copper(I)-doped metal-organic frameworks as dual-functional nanocarriers for combined chemo-chemodynamic therapy.

Combination therapies are an increasingly important part of the antitumor medicine armamentarium. However, developing desirable nanomaterials for combination therapies is still a great challenge. Herein, a biocompatible Cu(I)-doped metal-organic framework (MOF) (denoted as CuZn-ZIF) is designed as a novel dual-functional nanocarrier. Doxorubicin molecules are covalently bound to the surface of the CuZn-ZIF and released by the cleavage of chemical bonds in an acidic environment, demonstrating the capacity of controlled drug release. More importantly, CuZn-ZIF nanocarriers can simultaneously play the role of nanocatalysts, capable of catalyzing H2O2 into a highly reactive intracellular toxic hydroxyl radical (˙OH). An in vivo study reveals that nanoparticles exhibit high antitumor efficacy through the combined performance of DOX and Cu(I), proving the great potential of this copper(I)-based MOF for combined chemo-chemotherapy to improve therapeutic efficacy.

Photo-Stimuli-Responsive Dual-Emitting Luminescence of a Spiropyran-Encapsulating Metal-Organic Framework for Dynamic Information Encryption.

The development of photo-stimuli-responsive luminescent materials is essential to address emerging demands in encryption security. Here, a novel photo-stimuli-responsive dual-emitting luminescent material ZJU-128⊃SP (SP = spiropyran) is reported, which is obtained by encapsulating spiropyran molecules into a cadmium-based metal-organic framework (MOF), [Cd3 (TCPP)2 ]·4DMF·4H2 O (ZJU-128, H4 TCPP = 2,3,5,6-tetrakis (4-carboxyphenyl)pyrazine). This MOF/dye composite ZJU-128⊃SP exhibits a blue emission from the ligand of ZJU-128 at 447 nm and a red emission around 650 nm from spiropyran. Utilizing the photoisomerization of spiropyran from ring-closed to ring-open form under UV-light irradiation, significant fluorescence resonance energy transfer (FRET) process between ZJU-128 and spiropyran is achieved. As a result, the blue emission of ZJU-128 is gradually decreased while the red emission of spiropyran increases. This dynamic fluorescent behavior can fully recover to the original state following exposure to visible light (>405 nm). By taking advantage of the time-dependent fluorescence, dynamical anti-counterfeiting patterns and multiplexed coding are successfully developed based on ZJU-128⊃SP film. This work provides an inspiring point for the design of information encryption materials with higher security requirements.

Precise Design and Deliberate Tuning of Turn-On Fluorescence in Tetraphenylpyrazine-Based Metal-Organic Frameworks.

The manipulation on turn-on fluorescence in solid state materials attracts increasing interests owing to their widespread applications. Herein we report how the nonradiative pathways of tetraphenylpyrazine (TPP) units in metal-organic frameworks (MOFs) systems could be hindered through a topological design approach. Two MOFs single crystals of different topology were constructed via the solvothermal reaction of a TPP-based 4,4',4″,4‴-(pyrazine-2,3,5,6-tetrayl) tetrabenzoic acid (H4TCPP) ligand and metal cations, and their mechanisms of formation have been explored. Compared with the innate low-frequency vibrational modes of flu net Tb-TCPP-1, such as phenyl ring torsions and pyrazine twists, Tb-TCPP-2 adopts a shp net, so the dihedral angle of pyrazine ring and phenyl arms is larger, and the center pyrazine ring in TPP unit is coplanar, which hinders the radiationless decay of TPP moieties in Tb-TCPP-2. Thereby Tb-TCPP-2 exhibits a larger blue-shifted fluorescence and a higher fluorescence quantum yield than Tb-TCPP-1, which is consistent with the reduced nonradiative pathways. Furthermore, Density functional theory (DFT) studies also confirmed aforementioned tunable turn-on fluorescence mechanism. Our work constructed TPP-type MOFs based on a deliberately topological design approach, and the precise design of turn-on fluorescence holds promise as a strategy for controlling nonradiative pathways.

Abundant Dislocation Layered Double Hydroxides Synthesis by Molten Salt with Bound Water Boosting Oxygen Evolution.

Optimizing the adsorption free energy and promoting the active phase transition to further enhance the oxygen evolution reaction (OER) activity remain significant challenges. The adsorption free energy can be optimized by modulating the electronic structure and adjusting the crystal configuration. Meanwhile, the transformation of the active phase can be promoted by introducing strain energy. The theoretical calculations are conducted to verify the rational envisage. However, it is still a great obstacle to introducing strain into the electrocatalysts and avoiding destruction. The stress field caused by dislocation can realize both of the above. Hence, the molten salt with the bound water method is proposed and the abundant dislocation layered double hydroxides (D-NiFe LDH) are constructed. The in situ characterizations further verify the dislocations significantly affect the generation of the active phase and the state of electronic structure. Consequently, the D-NiFe LDH exhibits outstanding OER activity and obtains 10 mA cm-2 , only requiring 199 mV overpotential with fabulous stability (100 mA cm-2 more than 24 h). The work paves a new avenue for the rational introduction dislocations to optimize the crystal configuration and boost the active phase formation, significantly enhancing the OER performance.

Polarized Laser Switching with Giant Contrast in MOF-Based Mixed-Matrix Membrane.

Nonlinear optical (NLO) switch materials have attracted considerable attention in photonics. Although various materials based on complex structural transitions have been developed extensively, the studies on light-driven up-conversion laser switches are rare, which have advantages including easy operations at room temperature and high contrasts. Here, the concept of photoswitch building unit is proposed to construct a novel sandwich-like mixed-matrix membrane. Dye@metal-organic framework (MOF) crystals and spirooxazine are regarded as the laser emission and absorption units, followed by their hierarchical encapsulation into the polydimethylsiloxane carrier unit. Excited MOF microcrystals exhibit two-photon pumped lasing anisotropy, with an ultrahigh degree of linear polarization (≈99.9%). Photochromic molecules can be interconverted by the external ultraviolet stimulus, causing sharp absorption-band variations and inducing the laser emission or quenching. Such up-conversion polarized laser switch material is reported for the first time. Record-high NLO contrast (≈6.1 × 104 ) among the solid-state NLO switch materials can be obtained through simultaneously controlling the ultraviolet irradiation and the emission-detected polarization direction at room temperature.

Cationic Metal-Organic Framework-Based Mixed-Matrix Membranes for Fast Sensing and Removal of Cr2O7 2- Within Water.

Considering that metal-organic framework (MOF)-polymer mixed-matrix membranes (MMMs) can overcome the drawbacks of intrinsic fragility and poor processability of pure-MOF membranes, we designed MOF-based MMMs for efficient removal and fast fluorescence sensing of heavily toxic ions within water systems simultaneously. In this work, a series of MOF-based MMMs are prepared by mixing a hydrolytically stable cationic [Eu7 (mtb)5(H2O)16]·NO3 8DMA·18H2O (denoted as Eu-mtb) MOF material into poly (vinylidene fluoride) with high loadings up to 70%. The free volume at the interface between the polymer and Eu-mtb particles, combined with the permanent porosity and uniform distribution of Eu-mtb particles, enables these MMMs to show fast enrichment of Cr2O7 2- from solutions and consequently have a full contact between the analyte and MOFs. The developed Eu-mtb MMM (70wt% loading) thus shows both efficient removal and exceptional fluorescence sensing of Cr2O7 2- in aqueous media. The overall adsorption capacity of the Eu-mtb MMM (70 wt% loading) for Cr2O7 2- reaches up to 33.34 mg/g, which is 3.4 times that of powder-form Eu-mtb. The detection limit of the Eu-mtb MMM (70 wt% loading) for Cr2O7 2- is around 5.73 nM, which is lower than that of the reported powder-form Eu-mtb. This work demonstrates that it is feasible to develop flexible luminescent MOF-based MMMs as a significant platform for efficient removal and sensitive sensing of pollutants from water systems simultaneously.

Boosting Hydrogen Evolution through the Interface Effects of Amorphous NiMoO4-MoO2 and Crystalline Cu.

The rational design and synthesis of a highly efficient and cost-effective electrocatalyst for hydrogen evolution reaction (HER) are of great importance for the efficient generation of sustainable energy. Herein, amorphous/crystalline heterophase Ni-Mo-O/Cu (denoted as a/c Ni-Mo-O/Cu) was synthesized by a one-pot electrodeposition method. Thanks to the introduction of metallic Cu and the formation of amorphous Ni-Mo-O, the prepared electrocatalyst exhibits favorable conductivity and abundant active sites, which are favorable to the HER progress. Moreover, the interfaces consisting of Cu and Ni-Mo-O show electron transfers between these components, which might modify the absorption/desorption energy of H atoms, thus accelerating HER activity. As expected, the prepared a/c Ni-Mo-O/Cu possesses excellent HER performance, which affords an ultralow overpotential of 34.8 mV at 10 mA cm-2, comparable to that of 20 wt % Pt/C (35.0 mV), and remarkable stability under alkaline conditions.

Dense Packing of Acetylene in a Stable and Low-Cost Metal-Organic Framework for Efficient C2 H2 /CO2 Separation.

Porous materials for C2 H2 /CO2 separation mostly suffer from high regeneration energy, poor stability, or high cost that largely dampen their industrial implementation. A desired adsorbent should have an optimal balance between excellent separation performance, high stability, and low cost. We herein report a stable, low-cost, and easily scaled-up aluminum MOF (CAU-10-H) for highly efficient C2 H2 /CO2 separation. The suitable pore confinement in CAU-10-H can not only provide multipoint binding interactions with C2 H2 but also enable the dense packing of C2 H2 inside the pores. This material exhibits one of the highest C2 H2 storage densities of 392 g L-1 and highly selective adsorption of C2 H2 over CO2 at ambient conditions, achieved by a low C2 H2 adsorption enthalpy (27 kJ mol-1 ). Breakthrough experiments confirm its exceptional separation performance for C2 H2 /CO2 mixtures, affording both large C2 H2 uptake of 3.3 mmol g-1 and high separation factor of 3.4. CAU-10-H achieves the benchmark balance between separation performance, stability, and cost for C2 H2 /CO2 separation.

Highly Efficient Encapsulation of Doxorubicin Hydrochloride in Metal-Organic Frameworks for Synergistic Chemotherapy and Chemodynamic Therapy.

Iron-based metal-organic frameworks (MOFs) have been reported to have great potential for encapsulating doxorubicin hydrochloride (DOX), which is a frequently used anthracycline anticancer drug. However, developing a facile approach to realize high loading capacity and efficiency as well as controlled release of DOX in MOFs remains a huge challenge. Herein, we synthesized water-stable MIL-101(Fe)-C4H4 through a microwave-assisted method. It was found the nano-MOFs acted as nanosponges when soaked in a DOX alkaline aqueous solution with a loading capacity experimentally up to 24.5 wt %, while maintaininga loading efficiency as high as 98%. The mechanism of the interaction between DOX and nanoMOFs was investigated by absorption spectra and density functional theory (DFT) calculations, which revealed that the deprotonated DOX was electrostatically adsorbed to the unsaturated Fe3OCl(COO)6·H2O (named Fe3 trimers). In addition, the as-designed poly(ethylene glycol-co-propylene glycol) (F127) modified nanoparticles (F127-DOX-MIL) could be decomposed under the stimulation of glutathione (GSH) and ATP. As a result, DOX and Fe(III) ions were released, and they could undergo a Fenton-like reaction with the endogenous H2O2 to generate the highly toxic hydroxyl radical (·OH). The in vitro experiments indicated that F127-DOX-MIL could cause remarkable Hela cells inhibition through chemotherapy and chemodynamic therapy. Our study provides a new strategy to design a GSH/ATP-responsive drug-delivery nanosystem for chemo/chemodynamic therapy.

Benchmark C2 H2 /CO2 Separation in an Ultra-Microporous Metal-Organic Framework via Copper(I)-Alkynyl Chemistry.

Separation of acetylene from carbon dioxide remains a daunting challenge because of their very similar molecular sizes and physical properties. We herein report the first example of using copper(I)-alkynyl chemistry within an ultra-microporous MOF (CuI @UiO-66-(COOH)2 ) to achieve ultrahigh C2 H2 /CO2 separation selectivity. The anchored CuI ions on the pore surfaces can specifically and strongly interact with C2 H2 molecule through copper(I)-alkynyl π-complexation and thus rapidly adsorb large amount of C2 H2 at low-pressure region, while effectively reduce CO2 uptake due to the small pore sizes. This material thus exhibits the record high C2 H2 /CO2 selectivity of 185 at ambient conditions, significantly higher than the previous benchmark ZJU-74a (36.5) and ATC-Cu (53.6). Theoretical calculations reveal that the unique π-complexation between CuI and C2 H2 mainly contributes to the ultra-strong C2 H2 binding affinity and record selectivity. The exceptional separation performance was evidenced by breakthrough experiments for C2 H2 /CO2 gas mixtures. This work suggests a new perspective to functionalizing MOFs with copper(I)-alkynyl chemistry for highly selective separation of C2 H2 over CO2 .

Structural Variation and Switchable Nonlinear Optical Behavior of Metal-Organic Frameworks.

Two europium metal-organic frameworks (MOFs) based on the same ligand, named as ZJU-23-Eu and ZJU-24-Eu, are selectively synthesized by fine-tuning solvent contents to tailor the coordination modes. Eu atoms are eight-coordinated and nine-coordinated in ZJU-23-Eu and ZJU-24-Eu respectively, and their frameworks vary in both spatial connectivity and symmetry. The ligand not only has multiphoton response but also suitable triplet energy level (19 998 cm-1 ) to sensitize Eu3+ . Thus ZJU-23-Eu exhibits characteristic emission of Eu3+ peaking at 614 nm via the energy transfer from the two-/three-photon excited ligand to Eu3+ , with its bidimensional layered structure benefiting this process. In contrast, the changed spatial connectivity in tridimensional ZJU-24-Eu narrows the distances between adjacent Eu3+ ions and reduces the density, resulting in poor two-photon excited fluorescence. Besides, noncentrosymmetric ZJU-24-Eu shows second harmonic generation (SHG) response with an intensity of ≈6.2 times relative to KH2 PO4 (KDP) microcrystalline powder while centrosymmetric ZJU-23-Eu cannot. These results have established two nonlinear optical (NLO) models based on MOFs to synchronously analyze the effects of two structural variables on different NLO behaviors, and provide ingenious ways to design MOF-based NLO devices with function on demand.

Boosting hydrogen generation by anodic oxidation of iodide over Ni-Co(OH)2 nanosheet arrays.

For overall water electrolysis, the hydrogen evolution reaction (HER) is severely limited by the sluggish kinetics of the anodic oxygen evolution reaction (OER). Therefore, replacing the OER with a more favorable anodic oxidation reaction with remarkable kinetics is of paramount significance, especially the one that can produce value-added chemicals. Moreover, time-saving and cost-effective strategies for the fabrication of electrodes are helpful for the wide application of electrolysis. Herein, thermodynamically more favorable iodide electrooxidation over Ni doped Co(OH)2 nanosheet arrays (NSAs) in alkaline solution is presented as the alternative to the OER to boost the HER. And the active species are determined to be the reverse redox of the Co(iv)/Co(iii) couple. Remarkably, a negative shift of voltage of 320 mV is observed at a current density of 10 mA cm-2 after using iodide electrolysis to replace ordinary water splitting. The synthetic strategy and iodide oxidation in this work expand the application of Co-based materials in the field of energy-saving hydrogen production.

Controllable broadband multicolour single-mode polarized laser in a dye-assembled homoepitaxial MOF microcrystal.

Multicolour single-mode polarized microlasers with visible to near-infrared output have very important applications in photonic integration and multimodal biochemical sensing/imaging but are very difficult to realize. Here, we demonstrate a single crystal with multiple segments based on the host-guest metal-organic framework ZJU-68 hierarchically hybridized with different dye molecules generating controllable single-mode green, red, and near-infrared lasing, with the lasing mode mechanism revealed by computational simulation. The segmented and oriented assembly of different dye molecules within the ZJU-68 microcrystal causes it to act as a shortened resonator, enabling us to achieve dynamically controllable multicolour single-mode lasing with a low three-colour-lasing threshold of ~1.72 mJ/cm2 (approximately seven times lower than that of state-of-the-art designed heterostructure alloys, as reported by Fan F et al. (Nat. Nanotechnol. 10:796-803, 2015) considering the single pulse energy density) and degree of polarization >99.9%. Furthermore, the resulting three-colour single-mode lasing possesses the largest wavelength coverage of ~186 nm (ranging from ~534 to ~720 nm) ever reported. These findings may open a new route to the exploitation of multicolour single-mode micro/nanolasers constructed by MOF engineering for photonic and biochemical applications.

Lanthanide metal-organic frameworks with nitrogen functional sites for the highly selective and sensitive detection of NADPH.

A series of isostructural Ln-MOFs, namely Eu(BPDC-xN)(x = 0, 1, 2), with different numbers of nitrogen atoms were designed and synthesized. Due to the strong affinity between the bare phosphate group of NADPH and nitrogen functional sites, the highly selective and sensitive detection of NADPH was realized. Furthermore, as the number of sites was increased, the sensitivity significantly increased, with a detection limit as low as 0.43 µM.

A Chemically Stable Hofmann-Type Metal-Organic Framework with Sandwich-Like Binding Sites for Benchmark Acetylene Capture.

The realization of porous materials for highly selective separation of acetylene (C2 H2 ) from various other gases (e.g., carbon dioxide and ethylene) by adsorption is of prime importance but challenging in the petrochemical industry. Herein, a chemically stable Hofmann-type metal-organic framework (MOF), Co(pyz)[Ni(CN)4 ] (termed as ZJU-74a), that features sandwich-like binding sites for benchmark C2 H2 capture and separation is reported. Gas sorption isotherms reveal that ZJU-74a exhibits by far the record C2 H2 capture capacity (49 cm3 g-1 at 0.01 bar and 296 K) and thus ultrahigh selectivity for C2 H2 /CO2 (36.5), C2 H2 /C2 H4 (24.2), and C2 H2 /CH4 (1312.9) separation at ambient conditions, respectively, of which the C2 H2 /CO2 selectivity is the highest among all the robust MOFs reported so far. Theoretical calculations indicate that the oppositely adjacent nickel(II) centers together with cyanide groups from different layers in ZJU-74a can construct a sandwich-type adsorption site to offer dually strong and cooperative interactions for the C2 H2 molecule, thus leading to its ultrahigh C2 H2 capture capacity and selectivities. The exceptional separation performance of ZJU-74a is confirmed by both simulated and experimental breakthrough curves for 50/50 (v/v) C2 H2 /CO2 , 1/99 C2 H2 /C2 H4 , and 50/50 C2 H2 /CH4 mixtures under ambient conditions.

Boosting Ethylene/Ethane Separation within Copper(I)-Chelated Metal-Organic Frameworks through Tailor-Made Aperture and Specific π-Complexation.

The development of new materials for separating ethylene (C2H4) from ethane (C2H6) by adsorption is of great importance in the petrochemical industry, but remains very challenging owing to their close molecular sizes and physical properties. Using isoreticular chemistry in metal-organic frameworks (MOFs) enables the precise design and construction of target materials with suitable aperture sizes and functional sites for gas separations. Herein, it is described that fine-tuning of pore size and π-complexation simultaneously in microporous copper(I)-chelated MOFs can remarkably boost the C2H4/C2H6 adsorption selectivity. The judicious choice of organic linkers with a different number of carboxyl groups in the UiO-66 framework not only allows the fine tuning of the pore size but also immobilizes copper(I) ions onto the framework. The tailor-made adsorbent, CuI@UiO-66-(COOH)2, thus possesses the optimal pore window size and chelated Cu(I) ions to form π-complexation with C2H4 molecules. It can rapidly adsorb C2H4 driven by the strong π-complexation interactions, while effectively reducing C2H6 uptake due to the selective size-sieving. Therefore, this material exhibits an ultrahigh C2H4/C2H6 selectivity (80.8), outperforming most previously described benchmark materials. The exceptional separation performance of CuI@UiO-66-(COOH)2 is validated by breakthrough experiments for 50/50 v/v C2H4/C2H6 mixtures under ambient conditions.

Controlled dye release from a metal-organic framework: a new luminescent sensor for water.

By introducing the dye Rhodamine 6G (R6G) into a metal-organic framework (MOF), Mn-sdc-2 (H2sdc = 4,4'-stilbenedicarboxylic acid), with a pore size of 20 × 9.8 Å2, the composite R6G@Mn-sdc-2 was obtained. Subsequently, the MOF Mn-sdc-1 with a smaller pore size of 7.5 × 7.5 Å2 can be formed through a single-crystal to single-crystal transformation from Mn-sdc-2, thus tightly locking the dye R6G within the pores. Compared with R6G@Mn-sdc-2, R6G@Mn-sdc-1 exhibits a stronger fluorescence emission of R6G. Because the MOF Mn-sdc-1 can reversibly transform back to Mn-sdc-2 in the presence of trace water, the dye R6G can be released. This enables R6G@Mn-sdc-1 to be used as a new luminescent sensor for trace water in organic solvents by monitoring the fluorescence intensity of released R6G. The limit of detection can reach 0.035% in ethanol (v : v), which is among the most sensitive fluorescent water probes.

Tailoring the pore geometry and chemistry in microporous metal-organic frameworks for high methane storage working capacity.

We realized that tailoring the pore size/geometry and chemistry, by virtue of alkynyl or naphthalene replacing phenyl within a series of isomorphic MOFs, can optimize methane storage working capacities, affording an exceptionally high working capacity of 203 cm3 (STP) cm-3 at 298 K and 5-80 bar.