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RSC Advances · 2015 ·Vol. 6 ·期 5 ·3671-3679 · IF 3.84

Titanium incorporated with UiO-66(Zr)-type Metal–Organic Framework (MOF) for photocatalytic application

Aoning Wang,Yingjie Zhou,Zhoulu Wang,Miao Chen,Luyi Sun,Xiang Liu

A UiO-66-type metal–organic framework (MOF) fabricated with titanium was successfully prepared via a facial modified post-grafting method. The as-prepared samples were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), ultraviolet-visible adsorption spectroscopy (UV-vis), and photoluminescence spectroscopy (PL) techniques. The introduction of titanium enhanced the optical properties of UiO-66 via the formation of oxo-bridged hetero-Zr–Ti clusters, but led to a sacrifice in crystallinity. The removal of methylene blue (MB) over these samples could be attributed to the dual function of the adsorption and photo-degradation mechanisms. The highest MB removal efficiency of 87.1% was achieved over UiO-66(1.25Ti) under simulated sun-light irradiation.

研究领域: 材料科学 · 环境科学
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SENSORS AND ACTUATORS B-CHEMICAL · 2022 · IF 9.221

Two-stage ligand exchange in Mn(III)-based porphyrinic metal−organic frameworks for fluorescence water sensing

Kun Yu,Guangyao Zhang,Huining Chai,Lijun Qu,Dan Shan,Xueji Zhang

Metal−organic frameworks (MOFs) have emerged as promising materials for smart sensing and imaging applications. Here, a novel micron-biscuit Mn(III)-based porphyrinic MOF is synthesized with the modulation of 4,4′-biphenyldicarboxylic acid (BPDC). The anisotropic growth of MOF is induced by the increased steric hindrance , yielding micron-biscuit Mn-TCPP(BPDC) MOF crystals. Mn(III), as a sealer, quenched the intrinsic fluorescence of porphyrin because of the ligand-to-metal charge transfer (LMCT) effect, and this disappeared fluorescence can be regularly restored and enhanced due to LMCT effect inhibition and release of free porphyrin derived from the water-induced two-stage ligand exchange (TSLE) between BPDC, porphyrin and water. The as-prepared MOF acts as an excellent “signal-on” luminescent water-sensing probe with low amount (2.5 μg/mL) that can efficiently realize the trace detection of water in various organic media with high sensitivity, especially in dimethyl sulfoxide (DMSO), the detection limit is as low as 0.04% (v/v). Moreover, Mn-TCPP(BPDC) was successfully used for sensing water content in real commercial samples. This MOF with the guest-induced TSLE not only provides inspiration for the design of new luminescent materials, but also widens the path for smart sensing.

CAS / MDL: 787-70-2 65-85-0
研究领域: 材料科学 · 化学
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Nanomaterials · 2021 ·Vol. 11 ·期 10 ·2488 · IF 5.076

Rapid Removal of Mercury from Water by Novel MOF/PP Hybrid Membrane

Jian Gao,Ziming Li,Ziqi Deng,Meihua Liu,Wei Wei,Chunbai Zheng,Yifan Zhang,Shusen Chen,Pengyang Deng

Mercury is one of the most toxic heavy metals that can cause terrible disease for human beings. Among different absorption materials, MOF (metal–organic framework) materials show potential as very attractive materials for the rapid removal of mercury. However, the instability and difficulty for regeneration of MOF crystals limit their applications. Here, a continuous sulfur-modified MOF (UiO-66-NHC(S)NHMe) layer was synthesized in situ on polymeric membranes (PP non-woven fabrics) by post-synthetic modification and used for rapid mercury removal. The MOF-based membrane (US-N) showed high selectivity for mercury in different aqueous systems, which is better than sulfur-modified MOF powders. A thinner MOF layer on US-N showed a much better mercury ion removal performance. US-N with a 59.3 nm MOF layer could remove more than 85% of mercury in 20 min from an aqueous solution. In addition, the US-N can simply regenerate several times for mercury removal and maintain the initial performance (removal ratio > 98%), exhibiting excellent durability and stability. This work promotes the application of MOF materials in the rapid removal of hazardous heavy metal ions from practical environments.Keywords:metal–organic frameworks;membrane;mercury removal;rapid;regenerable

研究领域: 环境科学 · 材料科学
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2022 ·Vol. 23 ·期 24 ·16121 · IF 6.208

Zr-Based Metal−Organic Frameworks with Phosphoric Acids for the Photo-Oxidation of Sulfides

Zhenghua Zhao,Mingjie Liu,Kai Zhou,Hantao Gong,Yajing Shen,Zongbi Bao,Qiwei Yang,Qilong Ren,Zhiguo Zhang

Heterogeneous Brønsted acidic catalysts such as phosphoric acids are the conventional activators for organic transformations. However, the photocatalytic performance of these catalysts is still rarely explored. Herein, a novel Zr-based metal−organic frameworkZr-MOF-Pwith phosphoric acids as a heterogeneous photocatalyst has been fabricated, which shows high selectivity and reactivity towards the photo-oxidation of sulfides under white light illumination. A mechanism study indicates that the selective oxygenation of sulfides occurs with triplet oxygen rather than common reactive oxygen species (ROS). WhenZr-MOF-Pis irradiated, the hydroxyl group of phosphoric acid is converted into oxygen radical, which takes an electron from the sulfides, and then the activated substrates react with the triplet oxygen to form sulfoxides, avoiding the destruction of the catalysts and endowing the reaction with high substrate compatibility and fine recyclability.Keywords:metal−organic frameworks;phosphoric acid;photo-oxidation;oxygen radical

CAS / MDL: 150-78-7
研究领域: 化学 · 材料科学
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Materials · 2023 ·Vol. 16 ·期 18 ·6212 · IF 3.4

Co(II)-Based Metal-Organic Framework Derived CA-CoNiMn-CLDHs with Peroxidase-like Activity for Colorimetric Detection of Phenol

Wenjie Tan,Rui Xin,Jiarui Zhang,Lilin Yang,Min Jing,Fukun Ma,Jie Yang

Given the serious harm of toxic phenol to human health and the ecological environment, it is urgent to develop an efficient, low-cost and sensitive nanoenzyme-based method to monitor phenol. MOF-derived nanozyme has attracted wide interest due to its hollow polyhedra structure and porous micro-nano frameworks. However, it is still a great challenge to synthesize MOF-derived multimetal synergistic catalytic nanoenzymes in large quantities with low cost. Herein, we reported the synthetic strategy of porous hollow CA-CoNiMn-CLDHs with ZIF-67 as templates through a facile solvothermal reaction. The prepared trimetallic catalyst exhibits excellent peroxidase-like activity to trigger the oxidative coupling reaction of 4-AAP and phenol in the presence of H2O2. The visual detection platform for phenol based on CA-CoNiMn-CLDHs is constructed, and satisfactory results are obtained. The Kmvalue for CA-CoNiMn-CLDHs (0.21 mM) is lower than that of HRP (0.43 mM) with TMB as the chromogenic substrate. Because of the synergistic effect of peroxidase-like activity and citric acid functionalization, the built colorimetric sensor displayed a good linear response to phenol from 1 to 100 μM with a detection limit of 0.163 μM (3σ/slope). Additionally, the CA-CoNiMn-CLDHs-based visual detection platform possesses high-chemical stability and excellent reusability, which can greatly improve economic benefits in practical applications.Keywords:metal organic framework;nanozyme;colorimetric detection;phenol

研究领域: 生物化学 · 环境科学
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MOLECULES · 2023 ·Vol. 28 ·期 2 ·877 · IF 4.6

Reversible Regulation of Polar Gas Molecules by Azobenzene-Based Photoswitchable Metal–Organic Framework Thin Films

Xuan Chen,Siyu Fang,Ping Xue,Jiming Huang,Mi Tang,Zhengbang Wang

The development of tunable molecule separation membranes requires materials with remote controllability and ultra-high separation capability. In this paper, a novel photoswitchable metal organic framework (MOF) thin film (Cu2(AzoBPDC)2) was prepared by liquid phase epitaxial layer-by-layer assembly to realize the reversible remote-controlled switching. The azobenzene side groups in the Cu2(AzoBPDC)2thin film showed excellent reversible photoswitching performance under UV (365 nm) and Vis (450 nm) irradiation, achieving the remote-controlled mode of the diffusion flux of polar gas molecules in the MOF thin film.Keywords:metal–organic frameworks;azobenzene;photoswitchable;gas separation

研究领域: 材料科学 · 化学工程 · 光化学
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FARADAY DISCUSSIONS · 2017 ·Vol. 201 ·63-70 · IF 3.588

Facile synthesis of an ultra-stable metal–organic framework with excellent acid and base resistance

Nian Zhao,Ping Li,Xin Mu,Chuanfang Liu,Fuxing Sun,Guangshan Zhu

A novel ultra-stable metal–organic framework, MCIF-1, [Cu2(DCI)2](MeCN), based on dicyanoimidazole and Cu(I), has been synthesized at room temperature successfully. MCIF-1 shows excellent water stability and can retain crystallinity after soaking in water for about one week. In addition, MCIF-1 also shows exceptional resistance under both acidic and basic conditions within a large pH range from 0 to 13.5. What is more, after modifying the synthesis procedure slightly, we can produce this material in a large scale during a very short time. Mild synthesis conditions, excellent stability and ease of large scale production give MCIF-1 great potential for practical use.

研究领域: 材料科学 · 无机化学 · 纳米技术
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DALTON TRANSACTIONS · 2025 · IF 3.3

Application of a reversible thermochromic Co-MOF in smart windows

Xuan Yang,Zesen Yu,Hedong Jiang,Huanhuan Guo,Jian Sun,Jiake Li,Hua Zhu,Yanxiang Wang,Pingchun Guo

Metal–organic frameworks (MOFs) are promising candidates for thermochromic materials. In this study, a hydrogen-bonded 3D porous metal–organic framework, Co-BTC (Co3(BTC)2·12H2O, BTC = 1,3,5-benzenetricarboxylate), exhibited a pink color at room temperature, attributed to the d–d transition of Co2+ ions within the framework, and displayed reversible thermochromic behavior due to alterations in the coordination environment of Co2+ ions. Additionally, Co-BTC/PVB thermochromic film was successfully designed and fabricated as a smart window with a monolayer structure. The window exhibited reversible thermochromic behavior comparable to Co-BTC, with visible transmittance modulation of 10.73%, near-infrared transmittance modulation of 25.87%, and solar transmittance modulation of 12.63%. Compared to a pure PVB window, the smart window reduced indoor temperatures by 5.7 °C in field tests, indicating a significant energy-saving effect. This research presents a potential application for the rational design of MOFs in the development of advanced smart windows.

研究领域: 材料科学 · 能源工程 · 建筑技术
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

A pillar-layered MOF bearing N/O sites for one-step purification of C2H4 from the mixtures with C2H6 or C3H6

Qiang-Qiang Yang,Zhi-Han Ma,Qiang Zhang,Zi-Han Song,Hong-Xiang Nie,Jing-Jing Pang,Zhao-Quan Yao,Hongliang Huang,Min Feng,Tong-Liang Hu,Jian Xu

One-step adsorptive separation of high-purity ethylene (C 2 H 4 ) from the mixtures with ethane (C 2 H 6 ) or propylene (C 3 H 6 ) is of crucial importance in the petrochemical industry. Nevertheless, the development of porous materials that possess both high adsorption capacities and selectivities of C 2 H 6 and C 3 H 6 over C 2 H 4 is still a formidable challenge. Herein, we present a microporous pillar-layered metal–organic framework (MOF) that exhibits excellent uptake capacities of C 2 H 6 (4.73 mmol g −1 ) and C 3 H 6 (8.05 mmol g −1 ) at 298 K and 1 bar, leading to high adsorption selectivities for equimolar mixtures of C 2 H 6 /C 2 H 4 (1.6) and C 3 H 6 /C 2 H 4 (16.4), respectively. Breakthrough column experiments demonstrate that the MOF could achieve one-step acquisition of polymer-grade C 2 H 4 (> 99.9 %) during C 2 H 6 /C 2 H 4 and C 3 H 6 /C 2 H 4 separations. Noteworthily, for a C 3 H 6 /C 2 H 4 mixture (2/5, v / v ), high-purity C 2 H 4 (> 99.9 %) and C 3 H 6 (> 99.5 %) can be directly harvested or recovered upon desorption, with high productivities of 86.23 and 31.05 L kg −1 , respectively, surpassing many well-developed adsorbents for C 3 H 6 /C 2 H 4 separation. Theoretical calculations reveal that the nonpolar pore surface bearing accessible N and O atoms affords more hydrogen bonding interactions with C 2 H 6 and C 3 H 6 than C 2 H 4 , accounting for the adsorption affinity in the order of C 3 H 6  > C 2 H 6  > C 2 H 4 . This work may offer valuable insights into the design and construction of high-performance MOFs for one-step C 2 H 4 purification.

CAS / MDL: 13478-00-7
研究领域: 材料科学 · 化学工程
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MOLECULES · 2024 ·Vol. 29 ·期 8 ·1721 · IF 4.2

Study of CHF3/CH2F2 Adsorption Separation in TIFSIX-2-Cu-i

Shoudong Wang,Lei Zhou,Hongyun Qin,Zixu Dong,Haoyuan Li,Bo Liu,Zhilu Wang,Lina Zhang,Qiang Fu,Xia Chen

Hydrofluorocarbons (HFCs) have important applications in different industries; however, they are environmentally unfriendly due to their high global warming potential (GWP). Hence, reclamation of used hydrofluorocarbons via energy-efficient adsorption-based separation will greatly contribute to reducing their impact on the environment. In particular, the separation of azeotropic refrigerants remains challenging, such as typical mixtures of CH2F2(HFC-23) and CHF3(HFC-32), due to a lack of adsorptive mechanisms. Metal–organic frameworks (MOFs) can provide a promising solution for the separation of CHF3–CH2F2mixtures. In this study, the adsorption mechanism of CHF3–CH2F2mixtures in TIFSIX-2-Cu-i was revealed at the microscopic level by combining static pure-component adsorption experiments, molecular simulations, and density-functional theory (DFT) calculations. The adsorption separation selectivity of CH2F2/CHF3in TIFSIX-2-Cu-i is 3.17 at 3 bar under 308 K. The existence of similar TiF62−binding sites for CH2F2or CHF3was revealed in TIFSIX-2-Cu-i. Interactions between the fluorine atom of the framework and the hydrogen atom of the guest molecule were found to be responsible for determining the high adsorption separation selectivity of CH2F2/CHF3. This exploration is important for the design of highly selective adsorbents for the separation of azeotropic refrigerants.

CAS / MDL: 16962-40-6 67-56-1
研究领域: 材料科学 · 环境科学 · 化学工程
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COMBUSTION AND FLAME · 2025 · IF 6.2

Improve energy release of boron by tunable metal-organic frameworks via synergetic micro-explosion and catalysis

Kang Xue,Huaiyu Li,Lun Pan,Chongjun Li,Minhua Ai,Chengxiang Shi,Xiangwen Zhang,Ji-Jun Zou

Boron is considered as one of the most promising high energy additives to improve the energy density of aerospace propellants and energetic materials. However, the low energy release properties restrict its practical applications. Herein, three kinds of boron-based composite energetic particles (nB@MOF) were prepared by encapsulating nano boron (nB) in metal-organic frameworks (MOFs) by a self-assembly method with Zn, Co and Mo as metal nodes, and 2-methylimidazole and ethylenediamine as organic ligands. The characterization and dynamics results show that the combustion of organic ligands can induce micro-explosion to destroy the surface oxidation layer of agglomeration and promote the oxidation efficiency of boron. Furthermore, the metal oxide catalyst generated in-situ on nB surface by metal nodes can reduce the initial oxidation temperature and improve the mass transfer distance and interface contact of the oxidation reaction. Compared with nB, the maximum pressurization rate of nB@MOF with 2-methylimidazole as the organic ligand is increased by 31.1 times, the initial oxidation temperature of nB@MOF with Mo as the metal node is reduced by 185.9°C, and the combustion heat of all nB@MOF are increased by more than 1.2 times. This work demonstrates that the energy release properties of boron can be effectively improved by synergistic effect of micro-explosion process and interfacial catalysis.

CAS / MDL: 10026-22-9 10196-18-6
研究领域: 材料科学 · 能源化学
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2020 · IF 3.232

A turn-on luminescence probe based on amino-functionalized metal-organic frameworks for the selective detections of Cu2+, Pb2+ and pyrophosphate

Xuanxuan An,Qin Tan,Shuang Pan,Hui Liu,Xiaoli Hu

A “turn-on” fluorescent probe based on amino-functionalized metal-organic frameworks (MOF-5-NH 2 ) is developed for the detection of Cu 2+ , Pb 2+ and pyrophosphate (P 2 O 7 4− , PPi). The fluorescence emission of fluorescent materials obtained by one-step synthesis is attributed to organic ligands. Cu 2+ and Pb 2+ coordinate with the amino group on the surface of the MOF-5-NH 2 , which is ascribed to the host-guest electron transfer between analyte and probe, giving rise to the fluorescence quenching . After adding PPi, the intense affinity between Cu 2+ and PPi remove Cu 2+ from the MOF-5-NH 2 , blocking of the electron transfer process, and the fluorescence can be recovered. The limit of detection is 0.057, 0.25 and 0.32 μmol L −1 for the detection of Cu 2+ , Pb 2+ and PPi, respectively. This turn-on mode based fluorescent probe shows preferable sensitivity and specificity to detect Cu 2+ , Pb 2+ and PPi. These results demonstrate that the fluorescent MOF-5-NH 2 as a sensing platform displays remarkably performance.

CAS / MDL: 10312-55-7 100-21-0
研究领域: 分析化学 · 材料科学
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