GREEN CHEMISTRY
·
2025
·
IF 9.2
Tian Zhao,Pengcheng Xiao,Saiqun Nie,Jiangrong Yu,Shilin Peng,Jiayao Chen,Fuli Luo,Yi Chen
Aqueous zinc-ion batteries (AZIBs) face challenges such as Zn dendrite formation and poor cycle stability. Here, we report an ambient-temperature in situ growth strategy to fabricate a bacterial cellulose-metal organic framework composite separator (BC@UiO-66) for AZIBs. In this approach, UiO-66 (a Zr-based MOF) grows uniformly on BC nanofibers, forming a 95 μm-thick film with hierarchical porosity and abundant Lewis acid sites. The resulting BC@UiO-66 separator facilitates Zn2+ diffusion through interconnected nanochannels and promotes uniform Zn deposition, thereby suppressing dendrite growth. A Zn||Zn symmetric cell using BC@UiO-66 operates stably for over 2400 h at 1 mA cm−2 and a Zn||MnO2 full cell retains 162.98 mAh g−1 after 1000 cycles at 1 A g−1 with ∼100% coulombic efficiency. These results demonstrate the efficacy of MOF-cellulose composite separators in extending AZIB cycle life.
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产品关联
DOI
高影响因子
INORGANICA CHIMICA ACTA
·
2022
·
IF 3.118
Mingyan Chen,Dehua Zhang,Ziying Wang,Yao Zhang,Yucheng Liu
UiO-66 loading carboxyl and phosphotungstic acid has a good affinity to thiophene (TH). The synthesized catalyst, changed its original structure, which can increase its reactive site and enhance the interaction with thiophene (TH) in order to improve the adsorption performance. Then the structural changes were analyzed by XRD, FT-IR, SEM, BET, EDS and other characterization methods. Through static experiments of adsorption desulfurization, it is found that when the adsorption time is 240 min, the adsorption temperature is 30 ℃ and the oil-to-agent ratio is 100:1, the adsorption effect: UiO-66-(COOH) 2 (UC2) > UiO-66, the highest adsorption capacity can reach 89.99 mg/g; while PTA@UiO-66 (PAU) can reach adsorption equilibrium at 210 min, it has better desulfurization performance than UiO-66. After being recycled for 5 times, the adsorption effect is only slightly decreased: the adsorption capacity of UC2 was still 78.02% of the initial adsorption capacity, while that of PAU was 76.07% of the initial adsorption capacity. According to the adsorption kinetics, the adsorption process of thiophene on the adsorbent UC2 is more consistent with W-M model, and the adsorption of PAU is more in line with the pseudo-first order kinetic equation. In addition, it also includes the process of intraparticle diffusion and liquid film diffusion.
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DOI
高影响因子
KEY ENGINEERING MATERIALS
·
2022
·
IF 0
Pan Pan Liu,Peng Bai
In this study, the magnetic UiO-66 composite was prepared and used as an adsorbent to effectively remove Rhodamine B (RhB) from water. The as-prepared magnetic MOFs composites not only retain the unique structure and properties of MOFs materials, but also can be quickly recovered and separated from aqueous solution by applying a magnetic field. The effects of contact time, initial concentration on the adsorption properties were studied. For RhB, pseudo-second-order model and Langmuir model could well explain the adsorption process of magnetic UiO-66 composite, indicating that the adsorption process of the RhB was mainly performed by chemisorption on uniform surface, and the maximum adsorption capacity is 188.68 mg/g. The possible mechanism for RhB was further proposed, revealing that electrostatic interactions, π-π stacking interactions mainly affected the adsorption process.
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DOI
INORGANIC CHEMISTRY COMMUNICATIONS
·
2021
·
IF 2.495
Yanan Ding,Feng Wei,Changchang Dong,Jiadong Li,Chang Zhang,Xiaojun Han
Heavy metal ion pollution has been a potential threat to human health. Herein, a sensitive electrochemical sensor for simultaneously detection of Cd(II) and Pb(II) was developed using a metal–organic framework material UiO-66. UiO-66 before and after carbonization was used to modify the GCE electrodes, respectively. The carbonized UiO-66 modified GCE electrode (CUiO-66/Bi/GCE) showed good detection ability with the linear detection range of 10–50 μg/L and detection limit of 1.16 and 1.14 μg/L for Cd(II) and Pb(II), respectively. Compared with UiO-66, carbonized UiO-66 provided more active sites for Bi ions and heavy metal ions to co-deposit and facilitated the electron transfer, leading to better detection performance. The decoration strategy was applied to disposable screen-printed carbon electrodes (SPCEs) to obtain the linear detection range of 20–120 μg/L and detection limit of 4.67 and 1.24 μg/L for Cd(II) and Pb(II) respectively. The prepared electrochemical sensors hold great potential in real water sample detections.
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DOI
高影响因子
ECS Journal of Solid State Science and Technology
·
2021
·Vol. 10
·期 10
·106011
·
IF 2.07
Jie Yang,Bo Ruan,Wang Ni,Lung-Chang Tsai,Ning Ma,Dean Shi,Tao Jiang,Fang-Chang Tsai
Carbon dots (CDs) has been widely applied in LED diodes, sensing and bioimaging. However, the fluorescence property of CDs is limited because of the solid-state aggregation-caused quenching (ACQ). Metal-organic frameworks (MOFs), due to their high surface area, porosity and tunable pore size, are considered suitable hosts to inhibit the ACQ of CDs. Herein, the Zr-MOFs (UiO-66-(OH)2) is chosen as a host to encapsulate CDs. The dual-emitting CDs@MOFs system is constructed, which overcomes the problem of solid-state aggregation-caused quenching of carbon dots to gain the blue-emitting CDs@UiO-66-(OH)2. With the volume of CDs increased, the fluorescence of CDs@UiO-66-(OH)2 has changed simultaneously. When the volume reaches 3 ml, CDs@UiO-66-(OH)2 begin to cause fluorescence quenching. The correlated color temperatures (CCT) of CDs@UiO-66-(OH)2 are transformed from cold light to warm light. That can be further researched in electroluminescent diodes, ion-sensor, environmental monitoring, biological imaging and developments in other related biochemical fields.
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Yuling Ma,Airong Li,Cheng Wang,Xingbo Ge
Phosphotungstic acid (H 3 PW 12 O 40 , HPW) exhibits a good desulfurization performance towards the oxidative desulfurization (ODS) of oil-derived fuels. However, it presents two drawbacks: a small specific surface area and poor recovery. In this work, HPW was loaded on the support UiO-66 with a stable structure and large specific surface area, and a family of HPW@UiO-66 catalysts was prepared. Based on the structure and property analyses of powder FT-IR, ICP-OES, XRD, SEM, TG and BET, 0.5-HPW@UiO-66 with defects possessed a high crystallinity, regular morphology, stable structure and dispersed HPW clusters. The removal efficiency of DBT reached 100% and was maintained at 94.70% after 12 times of repeated use under the optimal reaction conditions. The results showed that the catalytic performance of HPW@UiO-66 catalyst for model oil desulfurization was improved when the defects existed.
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2020
·Vol. 44
·期 26
·11164-11171
·
IF 3.288
Zhuo Wang,Jin Liu,Zhen Li,Xianbiao Wang,Ping Wang,Di Wang,Fengjun Zhang
A crosslinkable UIO-66 type MOF material denoted UIO-66-DETA composed of Zr(IV) metal ions and 2,5-diallyl ether terephthalic acid (DETA) was synthesized, and then by initiating double bond crosslinking, a new crosslinking MOF material denoted UIO-66-DETA-CL was obtained. UIO-66-DETA and UIO-66-DETA-CL were characterized by FTIR spectroscopy, PXRD, 1H solid-state NMR spectroscopy, SEM, nitrogen sorption, thermogravimetric analysis and hydrogen storage tests to analyze their structure and properties. The results showed that a crosslinked structure has been formed, and UIO-66-DETA-CL can maintain its structure below 340 °C, compared with UIO-66-DETA; its carbon residual rate is improved, which shows that the crosslinking modification enhances the thermal stability. Meanwhile, the hydrogen uptake capacity of UIO-66-DETA-CL reaches 5.36 wt% at 77 K and 4 MPa. Furthermore, the hydrogen adsorption enthalpy of UIO-66-DETA-CL (ΔHUIO-66-DETA-CL) calculated using the Arrhenius equation reaches −0.889 kJ mol−1, which is significantly improved by crosslinking modification. The crosslinked structure changes the pore size and increases the active adsorption sites in organic ligands. The framework of UIO-66-DETA-CL can provide more polar charges to cause some hydrogen molecules to be negatively charged because of a small HOMO–LUMO gap, and a lower LUMO energy level of UIO-66-DETA-CL enables stronger negative charge acceptability. Therefore, crosslinking modification enhances the material's hydrogen storage capacity. This result provides a new idea for the crosslinking modification of MOFs.
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DOI
高影响因子
Surfaces and Interfaces
·
2025
·
IF 6.3
Yanghao Yan,Mingxing Shi,Qin Zhong,Jie Zhong,Yuling Wang,Fengyun Wang,Mingzhu Xia
In this study, UiO-66/Cotton composite adsorbents with varied UiO-66 loadings were fabricated via a coupling strategy and applied for the adsorption of quinolone antibiotics (QNs)—including norfloxacin (NOR), ciprofloxacin (CIP), pefloxacin (PEF), and moxifloxacin (MFX)—from aqueous media. Under optimal conditions ( T = 298 K, pH=8.0, dosage=1 g/L, contact time=2 h, C 0 =100 mg/L), the maximum adsorption capacities followed the order: PEF (106.29 mg/g) > MFX (85.30 mg/g) > NOR (83.64 mg/g) > CIP (75.53 mg/g). Adsorption was enhanced by increased UiO-66 loading, though utilization efficiency decreased. Optimal performance was observed under pH 6.0–10.0 and in the presence of divalent cations. The process followed pseudo-second-order and Freundlich models, involving coordination, hydrogen bonding, electrostatic attraction, and π–π interactions. The UiO-66/Cotton composite (18.63 % loading) exhibited excellent reusability, maintaining 81.25 % removal efficiency for PEF after five cycles. Moreover, its solid–liquid separation and washing efficiency improved by approximately 40.1-fold and 44.3-fold, respectively, compared to pristine UiO-66. This work highlights the potential of MOF-based composite materials for effective QNs removal in water treatment applications.
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产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Zai-Dong Shao,Peng Wu,Fang Liu,Qi-Jun Zhang,Chao-Yang Guo,Rui-Sang Liu,Jiang Lu,Xiao-Meng Ren,Yu-Ming Zheng
Sulfur dioxide (SO 2 ) emissions present significant environmental and health risks, yet efficiently capturing SO 2 remains challenging due to its corrosive nature and the limited performance of conventional adsorbents. In this study, we developed multivariate metal-organic frameworks (MTV-MOFs) based on UiO-66(Zr) for effective SO 2 capture. Through systematic ligand functionalization with -OH, -NH 2 , -SO 3 H, and -(NH 2 ) 2 groups on terephthalic acid linker, we developed a series of MTV-UiO-66 materials with tailored pore environments and adsorption characteristics. UiO-66-NH 2 exhibited superior performance with an SO 2 uptake of 252.9 mL g −1 at 298 K and 1 bar. Ideal adsorbed solution theory (IAST) calculations demonstrated improved selectivity for SO 2 over N 2 (847) and CO 2 (31), surpassing that of the parent UiO-66. Dynamic breakthrough experiments further confirmed the practical viability of MTV-UiO-66 materials for SO 2 capture under both dry and humid (50 % RH) conditions, with UiO-66-NH 2 retaining a capacity of 30.73 mL g −1 in dry settings and exhibiting robust performance in moisture-rich environments. Grand Canonical Monte Carlo (GCMC) simulations and density functional theory (DFT) calculations provided molecular-level insights into the adsorption mechanisms, revealing that functional groups play a crucial role in modulating binding interactions through hydrogen bonding, dipole-dipole interactions, and spatial confinement effects. The computational binding energies corroborated the experimental isosteric heats of adsorption, validating the integrated experimental-computational approach.
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DOI
高影响因子
Materials
·
2021
·Vol. 14
·期 9
·2419
·
IF 3.623
Mingfei Chen,Yingxue Tu,Songhai Wu
There is an urgent need to develop catalytic degradation technologies for chemical warfare agents (CWAs) that are environmentally friendly and do not require secondary treatment. UiO-66-NH2and other metal–organic frameworks (MOFs) based on zirconium have been shown to promote the catalytic degradation of CWAs. At the same time, MOFs have been studied, and they have shown interesting properties in CWA removal because of their ultrahigh surface area, tunable structures, and periodically distributed abundant catalytic sites. However, MOFs synthesized by conventional methods are mostly powdery crystals that are difficult to process and have poor mechanical stability, which largely limit the development of MOFs in practical applications. An emerging trend in MOF research is hybridization with flexible materials. Polymers possess a variety of unique attributes, such as flexibility, thermal and chemical stability, and process ability, and these properties can be combined with MOFs to make a low-cost and versatile material that also provides convenience for the subsequent integration of such MOFs into independent substrates or textiles. In this article, we used a green and simple method to coat the surface of UiO-66-NH2with polydopamine (PDA), PDA can promote the catalytic hydrolysis of UiO-66-NH2to DMNP (a simulant of chemical warfare agents). Additionally, it can adsorb the toxic hydrolysis product p-nitrophenol, avoiding the trouble of secondary treatment. The half-life of UiO-66-NH2coated with polydopamine (UiO-66-NH2@PDA) for catalytic hydrolysis is 8.9 min, and that of pure UiO-66-NH2is 20 min. We speculate that the surface coated with PDA can improve the diffusion of DMNP to the active sites of UiO-66-NH2.
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DOI
高影响因子
ECS Journal of Solid State Science and Technology
·
2024
·Vol. 13
·期 5
·057004
·
IF 1.8
Yu Ding,Yaru Li,Soufian Chakir,Jun Mei,Xianbiao Wang
Phosphate pollution leads to deterioration in water quality, posing a serious threat to human health. Therefore, it is important to develop a highly selective and sensitive fluorescent probe for phosphate detection. Here, we report a novel ratiometric fluorescent probe, Fluorescein@NH2-UiO-66 (denoted as Flu@NH2-UiO-66), for the trace detection of phosphate in water. Specifically, during the in situ solvothermal synthesis of Flu@NH2-UiO-66, fluorescein molecules were encapsulated into the cavities of the metal-organic framework. Furthermore, the encapsulation amount of fluorescein was controlled by adjusting the acidity of the system. The Flu@NH2-UiO-66 (60 H+) sample, prepared with a 60:1 molar ratio of acetic acid to the metal center exhibited distinct dual fluorescence signal peaks. The probe showed a highly selective fluorescence response to phosphate. Within a range of 0–20 μM phosphate concentration, the probe demonstrated excellent linear detection capability with a detection limit of 0.37 μM. Moreover, the mechanism of fluorescence enhancement can be attributed to the addition of phosphate, which greatly increases the UV absorbance of the probe. This study developed a novel ratiometric fluorescent probe capable of rapid, sensitive, and stable detection of trace phosphate, which is of great significance for environmental management.
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DOI
高影响因子
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY
·
2024
·Vol. 30
·期 3
·377-387
·
IF 3
Ma Yuling,Li Airong,Wang Zhihong,Wang Cheng
There is an urgent need to address sulfur dioxide (SO 2 ) from the burning of fossil fuels, which poses a serious hazard to the surrounding environment due to its emission. In this work, UiO-66-type metal–organic framework materials (MOFs) were prepared by hydrothermal method and applied to flue gas desulfurization. Through characterization analysis, it was found that UiO-66 sample had high crystallinity and good thermal stability. Besides, UiO-66 sample had a large specific surface area (1423 m 2 /g) and a large pore volume (0.69 cm 3 /g). In the desulfurization experiments of SO 2 /CO 2 /O 2 /N 2 gas mixture (0.3/10.0/5.5/84.2 vol.%), UiO-66 had a breakthrough time of 137.6 min/g for SO 2 , the high selectivity of SO 2 /CO 2 (36.0), and strong acid resistance. Besides, the adsorption thermodynamic analysis can confirm that the adsorption process of UiO-66 for SO 2 was a combination of physical adsorption and chemical adsorption. At 1.0 bar and 298 K, the adsorption capacity of SO 2 on UiO-66 reached 8.12 mmol/g.
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DOI
高影响因子
危险品化学品经营许可证（带存储）