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MIL-53
JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Highly luminescent CsPbX3@MIL-53(Al) nanoarchitectonics with anomalous stability towards flexible emitting films

Cong Xie,Xiao Zhang,Wenbin Shi,Ping Yang

The poor stability of perovskite nanomaterials exposed in high temperature, moisture, light radiation, and polar solvent conditions severely restrict their commercial application. To address this issue, the growth in situ of CsPbX 3 (X = Cl, Br, I) nanocrystals (NCs) is carried out by using the stable aluminum (Al)-based metal-organic frameworks to create CsPbX 3 @MIL-53(Al) composites. Compared with pristine CsPbX 3 NCs prepared using room temperature ligand assisted re-precipitation synthesis, the CsPbX 3 @MIL-53(Al) composites exhibit narrow photoluminescence (PL) spectra and greatly improved stability. The green emitting CsPbBr 3 @MIL-53(Al) composite exhibit narrowed PL spectrum (the full width at half-maximum of PL spectra: 20 nm for the composite and 28 nm for CsPbBr 3 NCs) and a blue-shifted PL peak wavelength (517.6 nm for the composite and 527.6 nm for the CsPbBr 3 NCs). The relationship of microstructure, components, PL, fluorescence lifetime, and stability are discussed systematically. Anomalous stability against heat-treatment, polar solvent and humidity conditions indicated the composites retained their initial PL intensity after storge more than 4 months in ambient conditions and heat-treated to 120ºC for 5 cycles. The emitting color of CsPbBr 3 @MIL-53(Al) composites are easily adjusted from blue, green to red by controlling the halide components of precursors. The composite was used to create emitting coating and highly bright flexible emitting films which also reveal high stability, suggesting that in situ encapsulation of CsPbX 3 NCs in MIL-53(Al) would supply a novel platform for various emitting devices.

研究领域: 材料科学 · 纳米技术 · 光电技术
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Pebax-based membrane filled with photo-responsive Azo@NH2-MIL-53 nanoparticles for efficient SO2/N2 separation

Qingping Xin,Shuo Li,Faxin Ma,Jianping Guo,Shaofei Wang,Guangyu Xuan,Xiaoli Ding,Lei Zhang,Yuzhong Zhang

The preparation of mixed matrix membranes (MMMs) using metal–organic framework (MOF) as fillers is one of the simple and effective methods to improve the gas permeability and selectivity of membranes, and it has an attractive prospect to achieve controllable gas separation process. Herein, NH 2 -MIL-53 nanoparticles are synthesized by hydrothermal method and modified by aminoazobenzene (Azo) by decompression loading technology. The multifunctional Azo@NH 2 -MIL-53 nanoparticles are incorporated into the Pebax matrix to fabricate MMMs for efficient and controllable SO 2 separation. Pebax/Azo@NH 2 -MIL-53–20% membrane exhibits the maximum SO 2 permeability of 2570 Barrer with a SO 2 /N 2 selectivity of 717 and the separation process of SO 2 /N 2 has dynamic photo-responsive characteristics under different light conditions, which is attributed to the incorporation of the Azo@NH 2 -MIL-53. First, the NH 2 -MIL-53 nanoparticles with high specific surface area of 637 m 2 .g −1 and pore size of 1.50 nm are introduced into MMMs to construct rich SO 2 transport channels, increasing the diffusivity selectivity. Second, the inherent –NH 2 groups and introduced -N = N- groups in Azo@NH 2 -MIL-53 increase the affinity of SO 2 , enhancing the solubility selectivity. Third, by artificially changing the light conditions to accurately control the conformation of Azo and the pore structure of NH 2 -MIL-53 is changed, which significantly changes the SO 2 adsorption capacity of NH 2 -MIL-53. Due to light is available in abundance in the form of sunlight, the mixed matrix membrane coupled with photo-responsive MOF can achieve more efficient and energy-saving gas separation process.

研究领域: 材料科学 · 环境工程
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LANGMUIR · 2020 · IF 3.557

Polydopamine-Assisted Surface Coating of MIL-53 and Dodecanethiol on a Melamine Sponge for Oil–Water Separation

Xiaoxu Dong,Mei Cui,Renliang Huang,Rongxin Su,Wei Qi,Zhimin He

A superhydrophobic and superoleophilic porous composite was successfully prepared via a polydopamine-assisted surface coating of MIL-53(Fe) and 1-dodecanethiol (DDT) on a melamine formaldehyde (MF) sponge. The as-prepared sponge composite (MIL-DDT@MF) has a high water contact angle (WCA) of 151.8°, which is probably attributed to both the rough surface derived from in situ growth of MIL-53 nanocrystals and the low surface energy due to grafting of hydrophobic 1-dodecanethiol. The MIL-DDT@MF sponge can effectively absorb oil or organic solvent with an absorption capacity of up to 54.1 (for petroleum) to 120.2 (for chloroform) times its own weight. In addition, the MIL-DDT@MF sponge retained a high absorption capacity and maintained approximately 78% of its original value after 50 cycles of reuse. Moreover, the MIL-DDT@MF sponge can selectively absorb the oil/organic solvent from water and achieve continuous oil–water separation. The separation efficiency of n-hexane, dichloromethane, and crude oil from water or seawater can reach above 95%. The superhydrophobic and superoleophilic MIL-DDT@MF sponge has potential as a promising absorbent for treatment of oily wastewater.

研究领域: 材料科学 · 环境科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2020 ·Vol. 31 ·期 6 ·4822-4835 · IF 2.22

Fabrication of Z-scheme Bi5O7I/MIL-53(Fe) hybrid with improved photocatalytic performance under visible light irradiation

Zhou Nan,Tan Junjie,Li Xi,Wang Lu,Jin Chenglong,Chen Ming,Yu Zhengsong,Liang Yani,Qiu Zhidong,Li Wenlong,Dong Yulin,Xie Zhizhong,Lin Yawei,Qu Deyu,Zhang Chaocan

A series of Bi 5 O 7 I/MIL-53(Fe) (BOI/MIL- w ) composites were successfully prepared by a facile in-situ solvothermal approach. The matched energy bands enabled Bi 5 O 7 I and MIL-53(Fe) to form a Z-scheme heterojunction which resulted in an efficient separation of the photo-induced electron–hole pairs. The photocatalytic activity of BOI/MIL- w was evaluated by the degradation of Rhodamine B (RhB) in water under the visible light irradiation. Compared with Bi 5 O 7 I, photocatalytic performances of BOI/MIL- w notably boosted. When the content of added MIL-53(Fe) was 3 wt%, BOI/MIL-3 presented the highest activity with a degradation efficiency of 99.7% only after 60 min of irradiation. The reaction rate constant k could reach 0.0992 min −1 which was nearly 12.6 times as high as that of Bi 5 O 7 I. Moreover, BOI/MIL- w had a good stability and reusability, which could ensure its practical application. Trapping experiments confirmed that h + and ·O 2 − were the dominant active species during the photocatalytic process, and further demonstrated the formation of the Z-scheme heterojunction facilitated the photocatalytic performance of BOI/MIL- w .

研究领域: 材料科学 · 环境科学
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Journal of Materials Chemistry C · 2017 ·Vol. 5 ·期 36 ·9465-9471 · IF 5.256

A highly selective and fast-response photoluminescence humidity sensor based on F− decorated NH2-MIL-53(Al) nanorods

Ting Lu,Hongjie Song,Xiaoqun Dong,Jianyu Hu,Yi Lv

NH2-MIL-53(Al) nanorods studded with F− were successfully synthesized via coordination modulation with HF as a modulator. The investigation of the growth mechanism pointed out that F− plays a key role in the formation process. The incorporation of F− into the framework of NH2-MIL-53(Al) not only made the crystal morphology tunable but also magnified the fluorescence enhancement performance of NH2-MIL-53(Al) in water vapor, based on which a highly efficient humidity sensor was fabricated. Among different kinds of humidity sensors, the present sensing system stood out due to its fast response rate, good sensitivity and high selectivity with a low detection limit of 0.6 μg mL−1 (S/N = 3) and a wide detection range from 4 to 40 μg mL−1. On the other hand, a majority of the conventional electronic humidity sensors seriously suffered from temperature dependence, while the present sensing system got over this disadvantage. Therefore, the NH2-MIL-53(Al) nanorod layer-based fluorescence sensing system has the potential for application in the real-time monitoring of humidity under ambient conditions.

CAS / MDL: 10312-55-7
研究领域: 材料科学 · 化学工程
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2019 · IF 3.261

Visible-light-driven MIL-53(Fe)/BiOCl composite assisted by persulfate: Photocatalytic performance and mechanism

Shengchao Miao,Zhenxing Zha,Ying Li,Xinxiang Geng,Jiahui Yang,Shihai Cui,Jing Yang

The novel semiconductor heterojunction of MIL-53(Fe)/BiOCl composite was first prepared through the solvothermal reaction. The prepared materials were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Brunner-Emmet-Teller (BET) and ultraviolet-visible diffuse reflectance spectroscopy (DRS). MIL-53(Fe)/BiOCl heterojunction is a kind of photoexcited materials and it accelerates the photoreactivity of BiOCl under the visible light irradiation. It was used to remove Rhodamine B (RhB) with the existence of persulfate (PS). The UV–vis spectrophotometer and the TOC detector show that the degradation rate and TOC removal efficiency of RhB (20 mg/L) are 99.5% and 69.4%within 30 min visible-light irradiation, respectively. Due to the proper band gap of material and the presence of electron acceptor, PS, the survival time of active radicals are increased. The active species h + , ·SO 4 − and ·OH are found to play the important roles during the reaction system. The possible mechanism for the RhB degradation of MIL-53(Fe)/BiOCl/PS is also proposed. Furthermore, the results of the material reusability for the degradation of RhB indicate that the MIL-53(Fe)/BiOCl has a good stability and can be used in the environmental water sample treatment.

CAS / MDL: 10035-06-0
研究领域: 环境科学 · 材料科学
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NEW JOURNAL OF CHEMISTRY · 2023 ·Vol. 47 ·期 17 ·8334-8346 · IF 3.3

An adsorptive photo-Fenton-like removal of 1,2-benzisothiazolin-3-one by NH2-MIL-53(Fe) under simulated solar light

Peifu Sun,Xiao Zhang,Zhiren Guo,Xinyue Liu,Yuanming Lan,Dongxiang Zhang,Hansheng Li,Jinying Li,Helei Liu,Xiyan Xu

The excessive discharge of isothiazolinone bacteriostatic agent-containing wastewater has posed serious threats to human health and environmental safety. As 1,2-benzisothiazolin-3-one (BIT) is one of the most commonly used isothiazolinones, its effective degradation is necessary and urgent. In the current study, a NH2-MIL-53(Fe)-based adsorptive photo-Fenton-like system was constructed for efficiently adsorbing and photodegrading BIT under solar light. The equilibrium BIT adsorption capacity Qe of NH2-MIL-53(Fe) reached 1140.89 mg g−1. The adsorptive photo-Fenton-like system has achieved more than 90% removal of BIT using NH2-MIL-53(Fe) in the presence of H2O2 under solar light irradiation, and the band gap of NH2-MIL-53(Fe) was calculated by UV-Vis analysis to be 2.10 eV. The influences of pH, dosage of photocatalysts and H2O2 were also assessed. It was found that H2O2 reduced the recombination of electron–hole pairs, and the radical quenching experiments and EPR testing result confirmed that h+, ˙OH and O2˙− played a crucial role in the photocatalytic process. This study supports the application of Fe-based MOF materials for simultaneous adsorption and the solar light photocatalytic degradation of BIT.

研究领域: 环境科学 · 化学工程
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NEW JOURNAL OF CHEMISTRY · 2022 ·Vol. 46 ·期 23 ·11158-11165 · IF 3.925

Histidine functionalized MIL-53(Al) for lead(II) removal from aqueous solution

Jipeng Li,Yanzhi Sun,Yongmei Chen,Yang Tang,Junqing Pan,Pingyu Wan

In the present study, the preparation of a new MOF material His-MIL-53(Al) and its performance in the adsorption of Pb(II) from aqueous solution were investigated. The original material MIL-53(Al) was directly grafted with histidine to obtain the modified MOF material His-MIL-53(Al). The results show that His-MIL-53(Al) has excellent adsorption performance for Pb(II), and the adsorption process is in accordance with the pseudo first-order kinetics and the Langmuir adsorption model, with a maximum adsorption capacity of 50.13 mg g−1, which is much larger than the adsorption capacity of the original material MIL-53(Al). The experimental results also show that the prepared material has good recoverability. Our work demonstrates the applications of His-MIL-53(Al) as a promising material in the adsorption of heavy metals.

CAS / MDL: 7784-27-2 10312-55-7
研究领域: 环境科学 · 材料科学 · 化学工程
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

Removal of MC-LR using the stable and efficient MIL-100/MIL-53 (Fe) photocatalyst: The effect of coordinate immobilized layers

Hailin Tian,Tirusew Araya,Ruiping Li,Yanfen Fang,Yingping Huang

Microcystin-LR (MC-LR), which is produced from cyanobacteria, is the common microcystin with a serious threat to aquatic life and human beings. And the efficient removal method of MC-LR is urgent needed. In this work, the MIL-100/MIL-53 (Fe) photocatalysts, which were successfully prepared by the electrostatic interaction with each other, were applied for the photocatalytic degradation of MC-LR. The structure and optical properties of the MIL-100/MIL-53 (Fe) photocatalysts were characterized by using SEM, XRD, XPS, FT-IR and UV–vis DRS. The very low dosage of the MIL-100/MIL-53 (Fe) photocatalysts achieved the degradation of MC-LR, and the optimized loading was the 50% MIL-100/MIL-53 (Fe) photocatalyst. Compared to MIL-100 (Fe) and MIL-53 (Fe), the MC-LR degradation was up to 96.5% after 3 h under visible light illumination with the 50% MIL-100/MIL-53 (Fe) photocatalyst due to the pore-effect adsorption and the effective separation of photogenerated carriers. The effect of coordinate immobilized layers between MIL-100 (Fe) and MIL-53 (Fe) contributed to the stable and efficient removal of MC-LR for the 50% MIL-100/MIL-53 (Fe) photocatalyst. The MC-LR photocatalytic mechanism and degradation pathway, which the photogenerated holes (h + ) were the main active species, were proposed by radical capture experiments and LC-MS analysis.

研究领域: 环境科学 · 生物学
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JOURNAL OF MOLECULAR STRUCTURE · 2024 · IF 4

Defective MIL-53(Al)-NH2: A bifunctional Lewis-Brønsted acid catalyst for efficient 5-HMF production from glucose

Mengjiao Yu,Xiong-Fei Zhang,Siting Yang,Yunhua Bai,Zhongguo Wang,Jianfeng Yao

Developing functional catalysts with both Lewis and Brønsted acid sites is an essential task for achieving the direct conversion of glucose to 5-hydroxymethylfurfural (5-HMF), a process that is crucial for the sustainable production of renewable fuels and chemicals. In this work, a mixed-linker strategy is proposed to prepare defective MIL-53(Al)-NH 2 by introducing trifluoroacetic acid into the MIL-53(Al)-NH 2 synthesis process. The creation of defects facilitates the exposure and accessibility of Al 3+ centers, as well as changes the coordination environment within the MIL-53(Al)-NH 2 skeleton. Both the number of Lewis and Brønsted acid sites are boosted, which is beneficial for glucose activation and 5-HMF generation. Through optimizing the reaction conditions, a glucose conversion of 98.3 % with a 5-HMF yield of 59.3 % was achieved by using defective 6d-MIL-53(Al)-NH 2 in a biphasic tetrahydrofuran/H 2 O NaCl system. Moreover, the 6d-MIL-53(Al)-NH 2 catalyst showed excellent recyclability and reusability, with its catalytic efficiency maintained almost unchanged for consecutive 10 cycles. The catalytic mechanism was elucidated and the acidity of the Lewis and Brønsted acid was modulated by defect engineering to achieve exceptional performance.

CAS / MDL: 10312-55-7 100-21-0
研究领域: 化学工程 · 催化科学 · 可再生资源
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Plasma Tailoring of NH2-MIL-53 with Enhanced Fluorescence Emission for Simultaneous Detection of Multiple Heavy Metals in Water

Yu Ding,Yuyang Hu,Yangyang Zhao,Yaru Li,Ziteng Huang,Soufian Chakir,Yongfei Xu,Daosheng Sun,Songqin Liu,Huanting Wang,Xianbiao Wang

Indium, copper, and mercury are important raw materials in the electronics industry and often coexist in factory wastewater. Therefore, the development of a highly sensitive and selective method for the simultaneous detection of these heavy metal ions is of great significance for water quality monitoring and environmental protection. Herein, we report a NH2-MIL-53 fluorescent probe for the simultaneous detection of trace In3+, Cu2+, and Hg2+ in water. After a low-temperature NH3 plasma tailoring treatment for grafting electron-donor amine groups, the obtained NH2-MIL-53-M exhibited enhanced fluorescence emission intensity (∼6 times) coupled with selective adsorption of In3+, Cu2+, and Hg2+. This quenched the NH2-MIL-53-M fluorescence and allowed to significantly increase the selectivity and sensitivity for detection of In3+, Cu2+, and Hg2+. The fluorescence quenching constant (Ksv) values were 2.23 × 105, 1.00 × 105, and 2.74 × 104 M–1, while the limit of detection (LODs) values were 0.06, 0.14, and 0.53 μM, for In3+, Cu2+, and Hg2+, respectively. The concentrations of In3+, Cu2+, and Hg2+ in real environmental samples could be determined by addition of appropriate masking agents, and the recoveries were within the range of 94–110%. This study not only supplied a strategy for constructing a highly sensitive and selective fluorescent probe but also established a platform for simultaneous detection of multiple heavy metal ions in water.

研究领域: 环境科学 · 材料科学 · 分析化学
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ANALYST · 2011 ·Vol. 137 ·期 1 ·133-139 · IF 3.913

High-performance liquid chromatographic separation of position isomers using metal–organic framework MIL-53(Al) as the stationary phase

Cheng-Xiong Yang,Shan-Shan Liu,He-Fang Wang,Shan-Wei Wang,Xiu-Ping Yan

Metal–organic framework MIL-53(Al) was explored as the stationary phase for high-performance liquid chromatographic separation of position isomers using a binary and/or polar mobile phase. Baseline separations of xylene, dichlorobenzene, chlorotoluene and nitrophenol isomers were achieved on the slurry-packed MIL-53(Al) column with high resolution and good precision. The effects of mobile phase composition, injected sample mass and temperature were investigated. The separation of xylene, dichlorobenzene, chlorotoluene and nitrophenol isomers on MIL-53(Al) were controlled by entropy change.

研究领域: 化学 · 分析化学
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