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Well‐Defined Cu <sub/>2</sub> O/Cu <sub/>3</sub> (BTC) <sub/>2</sub> Sponge Architecture as Efficient Phenolics Scavenger: Synchronous Etching and Reduction of MOFs in confined‐pH NH <sub/>3</sub> ?H <sub/>2</sub> O
摘要： Fabrication of low-dimensional nano-MOFs as well as nanoparticles/metal-organic frameworks (MOFs) hybrids has sparked new scientific interests but remains a challenging task. Taking Cu3(BTC)2 as a proof of concept, it is demonstrated thats NH3?H2O solution of a confined pH value can readily shape the bulk Cu3(BTC)2 into nanoscale Cu3(BTC)2, beyond the need to control the crystal growth kinetics of MOFs. Adjusting the pH of NH3?H2O within a much small range (10–11) allows fine tuning over the size and shape of nanoscale Cu3(BTC)2. Particularly at pH = 11, NH3?H2O exhibits weak reducibility that triggers a reduction of part of Cu3(BTC)2 into Cu2O, while shaping the other into Cu3(BTC)2 nanowires. Benefiting from the coincidence of reduction and etching effects, the newly generated Cu2O dots can in situ anchor onto adjacent Cu3(BTC)2 nanowires at highly dispersive state, forming a well-defined sponge-like architecture built of Cu2O dots and nano-Cu3(BTC)2. The CuOx derived from annealing of the Cu2O dots/nano-Cu3(BTC)2 hybrid preserves the sophisticated sponge architecture and high porosity, and exhibits promising applications in phenol scavenging, with efficiency outperforming its counterparts and many other Cu-based catalysts reported in literature. It is anticipated that the findings here pave the way for the rational design of intricate nano-MOFs in a more efficient way.
关键词： nanoparticles/MOF,etching and reduction,sponge architecture,synergistic effect,low-dimensional MOFs
更新于2025-11-14 17:03:37
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On-demand CO release for amplification of chemotherapy by MOF functionalized magnetic carbon nanoparticles with NIR irradiation
摘要： Carbon monoxide (CO) gas therapy combined with chemotherapy and photothermal therapy (PTT) is a promising treatment mode for malignant tumor. Herein, we firstly reported doxorubicin (DOX) loaded Mn carbonyl modified Fe (III)-based nanoMOFs (MIL-100) coated PEGylated magnetic carbon nanoparticles (denoted as MCM@PEG-CO-DOX NPs) as theranostics nanoplatforms for near-infrared (NIR)-responded CO-DOX combination therapy. MIL-100 as a good nanocarrier of DOX with high loading capacity can also chelate the Mn carbonyl after a smart modification. Meanwhile, magnetic carbon core possessed photothermal effect, which can convert the NIR light to heat by an 808 nm laser irradiation, resulting in the on-demand release of CO and DOX. As a result, combining with PTT, MCM@PEG-CO-DOX NPs killed tumor efficiently. Moreover, our synthesized MCM@PEG-CO-DOX NPs were capable of realizing tumor dual-mode imaging including magnetic resonance imaging (MRI) and photoacoustic imaging (PAI).
关键词： synergistic treatment,dual-mode imaging,MOFs,CO gas therapy,carbon nanoparticles
更新于2025-09-23 15:23:52
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Identification performance of two luminescent lanthanide–organic frameworks
摘要： By the reaction of organic ligands, 2-(3,4-dimethylphenyl)-1H-imidazole-4,5-dicarboxylic acid (H3DMPhIDC) and terephthalic acid (H2DCB) with Eu3+ or Tb3+ ions, respectively, two luminescent metal-organic frameworks (MOFs) [Ln(H2DMPhIDC)(DCB)]n [Ln = Eu (1); Tb (2)] have been constructed. Both MOFs 1 and 2 are isostructural and show two-dimensional structures, which were fully characterized by single crystal X-ray diffraction, elemental analysis, and infrared spectroscopy. Both MOFs have excellent thermal and water stability, and indicate characteristic lanthanide metallic luminescence. Importantly, they can significantly recognize Fe3+ cation in aqoues solutions. Their sensing mechanisms have been suggested according to structural analyses, PXRD data and UV-Vis determinations.
关键词： recognition,crystal structure,luminescent MOFs,fluorescence quenching
更新于2025-09-23 15:23:52
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Luminescence properties of a family of lanthanide metal-organic frameworks
摘要： Two isostructural series of lanthanide metal-organic frameworks denoted as SUMOF-7II (Ln) and SUMOF-7IIB (Ln) ( Ln = La, Ce, Pr, Nd, Sm, Eu, and Gd) were synthesized using4,4',4''-(pyridine-2,4,6-triyl)tris(benzoic acid) (H3L2) and a mixture of H3L2 and 4,4′,4′′-(benzene-1,3,5-triyl)tris(benzoic acid) (H3BTB) as linkers, respectively. Both series were characterized usingpowder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), thermal analysis (TGA), and photoluminescence spectroscopy. Photoluminescence measurements show that Eu-MOFs demonstrate a red emission while Pr- and Nd-MOFs display an emission in the near-infrared (NIR) range. On the other hand, La-, Ce-, Sm- and Gd-MOFs exhibit only a ligand-centered emission. The average luminescence lifetimes in the SUMOF-7IIBseries are 1.3-1.4-fold longer than the corresponding ones in the SUMOF-7II series. SUMOF-7IIs show a good photo- and thermal stability. Altogether, the properties of SUMOF-7II and SUMOF-7IIB render them promising materials for applications including sensing, biosensing, and telecommunications.
关键词： Lanthanide MOFs,Antenna Effect,Photostability,Photophysical Properties.,Metal-Organic Frameworks,Luminescence
更新于2025-09-23 15:23:52
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Activated carbon/metal-organic framework nanocomposite: Preparation and photocatalytic dye degradation mathematical modeling from wastewater by least squares support vector machine
摘要： Herein, Kiwi peel activated carbon (AC), Materials Institute Lavoisier (MIL-88B (Fe), and AC/MIL-88B (Fe) composite were synthesized and used as catalysts to degrade Reactive Red 198. The material properties were analyzed by the FTIR, BET-BJH, XRD, FESEM, EDX, TGA, and UV–Vis/DRS. The BET surface area of AC, MIL-88B (Fe) and AC/MIL-88B (Fe) was 1113.3, 150.7, and 199.4 m2/g, respectively. The band gap values (Eg) estimated by Tauc plot method, were obtained 5.06, 4.19 and 3.79 eV for AC, MIL-88B (Fe) and AC/MIL-88B (Fe), respectively. The results indicated that the AC/MIL-88B (Fe) composite had higher photocatalytic activity (99%) than that of pure AC (79%) and MIL-88B (Fe) catalysts (87%). The decolorization kinetic was matched well with the second-order model. Moreover, the data were modeled using least squares support vector machine which optimized with Cuckoo optimization algorithm. The optimal parameters were found 0.837 and 3.49e+02 based on σ2 and γ values, respectively. The mean square error (MSE) and correlation coefficient (R2) values were obtained 3.97 and 0.948. Therefore, the attained data, materials characterization and prediction of modeling validate the composite form of MIL-88B(Fe) with new AC, had better photocatalytic activity in comparison with the individual form.
关键词： Metal-organic frameworks (MOFs),Synthesis,AC/MIL-88B (Fe) composite,COA-LSSVM modeling,Photocatalytic degradation
更新于2025-09-23 15:23:52
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Mixed-metal organic framework-coated ZnO nanowires array for efficient photoelectrochemical water oxidation
摘要： Designing of high-performance photoanodes is essential for efficient solar energy conversion in photoelectrochemical (PEC) water splitting. Herein, we report an effective approach to synthesize three dimensional (3D) mixed-metal organic framework-coated ZnO nanowires array (ZnNi MOF@ZnO) for the effective PEC performance. The ZnO nanowires act as photon absorber as well as rapid charge transporter; whilst the ZnNi MOF provides the active sites for PEC process by lowering the energy barrier of water oxidation and suppressing electron-hole recombination. The 3D nanostructure of ZnNi MOF@ZnO nanowires array provides intimate interfacial contact through covalent interactions between the ZnNi MOF and ZnO nanowires which facilitates the rapid charge transfer during photocatalytic oxygen evolution reactions. As a result, the ZnNi MOF@ZnO nanowires array exhibited excellent photoelectrochemical water oxidation with very low onset potential (0.31 V vs. RHE) and high photocurrent density (1.40 mA/cm2) as compared to the Zn MOF @ZnO and ZnO nanowires array. This facile strategy provides a promising direction towards high performance photoanode design for adequate solar energy conversion.
关键词： Metal organic frameworks (MOFs),Photoelectrocatalyst,Nanowires array,Photoelectrochemical water oxidation,Photoanodes
更新于2025-09-23 15:22:29
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"Two-in-One" Strategy of o-Amino and Aromatic Nitrogen in Biomimetic Metal-Organic Frameworks for Efficient CO2 Photoconversion
摘要： Visible-light driven photoconversion of CO2 into energy carriers is highly important to the natural carbon balance and sustainable development. Herein, we demonstrate the biological nucleobase adenine-dependent CO2 photoreduction performance in green biomimetic metal-organic frameworks. Photocatalytic results indicate that AD-MOF-2 exhibited a very high HCOOH production rate of 443.2 μmol g-1 h-1 in pure aqueous solution, which is more than two times higher than that of AD-MOF-1 (179.0 μmol hour?1 g?1) in acetonitrile solution. Significantly, experimental and theoretical evidences reveal that CO2 photoreduction reaction mainly takes place on biological adenine molecules by unique o-amino assisted active aromatic nitrogen atom rather than traditional metal center. This work not only serves as an important case study for the development of green biomimetic photocatalysts used for artificial photosynthesis, but also proposes a new catalytic strategy for efficient CO2 photoconversion.
关键词： photosensitivity,hydrophobicity,biomimetic catalysis,green MOFs,artificial photosynthesis
更新于2025-09-23 15:22:29
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Post-synthetic platinum complex modification of a triazine based metal organic frameworks for enhanced photocatalytic H2 evolution
摘要： A triazine-based MOFs [PCN-9(Co)] was synthesized and its photoelectrical, photophysical properties were studied. As a new photocatalyst, PCN-9(Co) displays photocatalytic hydrogen evolution from water under UV–Visible light irradiation. With the introduction of platinum complex, PCN-9-Pt was obtained and platinum complex was believed to coordinate with the N in triazine. The H2 evolution rate of PCN-9-Pt is greatly improved, about 6.8 times higher than that of PCN-9(Co). The reason is due to the fact that platinum complex plays an important role in improving the separation efficiency of photogenerated charge carriers, as verified by PL and EIS results. This result provides a new kind of idea of modifying MOFs materials with molecular complex to improve the photocatalytic activity.
关键词： Post-synthetic,Platinum complex,Photocatalysis,Triazine-based MOFs
更新于2025-09-23 15:22:29
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Ratiometric Luminescent Sensor of Picric Acid based on the Dual-Emission Mixed-Lanthanide Coordination Polymer
摘要： Powerful explosive sensors play a key role in public security and environmental protection. Herein we report a series of isostructural lanthanide coordination polymers [Ln2L1.5(NMP)2]n (LnL, Ln = Eu , Gd, Tb, Dy, Ho and Er, H4L = [1,1′:4′,1″-terphenyl]-2′,4,4″,5′-tetracarboxylic acid, NMP = N-methyl-2-pyrrolidone) and mixed-Ln LnL (EuxTb1-xL, EuxGd1-xL, TbxGd1-xL and EuxTb0.02-xGd0.98L). Luminescence studies show that both H4L and GdL emit strong fluorescence and phosphorescence at 77 K while only fluorescence at room temperature, and TbL exhibits strong Tb3+ characteristic emission though the energy difference between the triplet excited state of H4L (20661 cm-1) and the 5D4 energy level of Tb3+ (20500 cm-1) is very small. By doping Eu3+ and Tb3+ into GdL, we obtained EuxTb0.02-xGd0.98L emitting warm white light. For TbL and Tb0.01Gd0.99L showing the dual-emission, upon addition of picric acid (PA) into their suspensions in Tris-HCl buffer, Tb3+ emission decreases slowly, however, the ligand-based emission is sharply quenched, rendering TbL and Tb0.01Gd0.99L excellent single-lanthanide and mixed-lanthanide ratiometric luminescence PA sensor materials, respectively.
关键词： picric acid (PA),ratiometric luminescence sensors,white light emission,metal-organic frameworks (MOFs),Coordination polymers (CPs)
更新于2025-09-23 15:21:21
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Dual-mode light-emitting lanthanide metal-organic frameworks with high water and thermal stability and its application in white LEDs
摘要： It is well known that the up-conversion luminescence from lanthanide metal-organic frameworks (Ln-MOFs) is difficult to achieve, and thus, there are few reports on dual luminescence-based MOFs. Here, dual-mode light-emitting Ln-MOFs are synthesized using a low-cost hydrothermal method. Our results show that the obtained Ln-MOFs not only have high thermal stability (up to 420 degrees) but also are stable in deionized water. The dual-mode up and down-conversion luminescence is simultaneously observed from Er-Eu-MOFs. The temperature-dependent fluorescence decay time is calculated to be ranged from 0.46 ms to 0.36 ms for temperatures from100 K to 300 K. We suggested that this phenomenon was because the number of phonons participating in the MOF matrix increases with temperature during the luminescence process, and the phonons interact with the electrons in the material. The values of the J-O parameters calculated from the emission spectra indicated that the symmetry around Eu3+ ions in Eu-MOF is the highest, which was also higher than that of Er-Eu-MOF. To explore the potential applications of Eu-MOFs in white light-emitting diodes (LEDs), red emission from Eu-MOFs was combined with blue, green, and yellow emissions from metal halide perovskites to achieve white light emission. The white light with excellent color quality and vision performance was obtained. These findings demonstrate that the Ln-MOFs are potentially successful materials for the applications in white LEDs.
关键词： high thermal stability,Dual-mode luminescence,LEDs,MOFs,lanthanide
更新于2025-09-23 15:21:01