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MIL-53
IONICS · 2020 ·Vol. 26 ·期 4 ·1787-1795 · IF 2.394

Enhanced electrochemical performance of all-solid-state sodium-sulfur batteries by PEO-NaCF3SO3-MIL-53(Al) solid electrolyte

Ge Zhi,Li Jie,Liu Jin

A flexible PEO-NaCF 3 SO 3 -MIL-53(Al) solid electrolyte is fabricated for all-solid-state sodium-sulfur batteries (ASSBs). When the mole ratio of EO (ethylene oxide of PEO):Na (sodium ion of NaCF 3 SO 3 ) is 20 and MIL-53(Al) is 3.24 wt%, high ionic conductivities of 6.87 × 10 −5  S cm −1 at 60 °C and 6.52 × 10 −4  S cm −1 at 100 °C are achieved. And the sodium ion transference number is significantly increased to 0.40 from 0.13 compared to the PEO-NaCF 3 SO 3 solid electrolyte without MIL-53(Al). When it is assembled to ASSBs, the batteries obtain high capacity retention and reversible current-rate capability. At 0.1 C and 60 °C, the solid-state battery delivers the first discharge capacity of 897.7 mAh g −1 and 674.9 mAh g −1 after 50 cycles with a coulombic efficiency near 100%. The enhanced electrochemical performances of the solid electrolyte, as well as ASSBs, are benefited from MIL-53(Al) filler.

研究领域: 材料科学 · 电化学
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LANGMUIR · 2024 · IF 3.7

In Situ Synthesis of NH2-MIL-53-Al/PAN Nanofibers for Removal Co(II) through an Electrospinning Process

Yinyin Peng,Ting Pan,Chuang Chen,Yuchen Zhang,Guoyuan Yuan,Derong Liu,Xiaoqin Pu,Wei Xiong

In this study, researchers developed a novel composite material called NH2-MIL-53-Al/PAN, which consists of metal–organic frameworks (MOFs) grown on electrospun PAN nanofibers (NFs). The successful formation of the composite was confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR), and the hydrophilicity of NH2-MIL-53-Al/PAN was demonstrated by the water contact angle (WCA). Batch experiments were conducted to investigate the adsorption performance of Co(II) under different conditions. The maximum adsorption capacity reached 58.72 mg/g, and almost 95% of the adsorption was achieved within the first 6 h. The adsorption process was found to be spontaneous and endothermic and followed the pseudo-second-order kinetics and Langmuir models. Chemisorption and molecular layer adsorption are the main mechanisms of adsorption, and X-ray photoelectron spectroscopy (XPS) analysis further reveals that the interaction between the adsorbent and cobalt is a coordination interaction. In this study, NH2-MIL-53-Al was grown in situ on PAN to ensure effective loading of MOFs and prevent agglomeration during the NF mixing process. This approach successfully addressed the challenge of exposing active sites within the embedded MOF crystals. Additionally, it overcame the difficulty of recycling traditional MOF adsorbents. As a result, the exceptional performance of MOF NFs offers a promising solution for the efficient removal of cobalt-containing wastewater.

研究领域: 材料科学 · 环境科学 · 化学工程
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INORGANIC CHEMISTRY COMMUNICATIONS · 2021 · IF 2.495

Microwave ultrasound-assisted synthesis of NH2-MIL-53(Al) for fluorescence detection of organosulfur compounds in model fuel

Ying-yue Qin,Qiao-ying Wang,Jin-Long Ge,Fang Wu

Amino-MIL-53(Al) (NH 2 -MIL-53(Al)) nanocrystals were successfully obtained through microwave ultrasound-assisted method. The structure and morphology of the as-synthesized NH 2 -MIL-53(Al) nanocrystals were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and N 2 adsorption–desorption isotherms, respectively. Upon excitation at 388 nm, the as-synthesized NH 2 -MIL-53(Al) nanocrystals show strong emission peak at 454 nm in n-octane solution at room temperature. Meanwhile, the fluorescence explorations revealed that NH 2 -MIL-53(Al) can selectively detect organosulfur compounds, including thiophene and benzothiophene through quenching effect in model fuel, with high quenching constant and low detection limit. This work presents a facile platform for the detection of organosulfur compounds in model fuel.

研究领域: 材料科学 · 化学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Enhancing degradation of norfloxacin using chrysanthemum-shaped bimetallic NH2-MIL-53(Fe/Ti) photocatalysts under visible light irradiation

Wen Gao,Fangyuan Wang,Meilin Ou,Qianqian Wu,Lei Wang,Haonan Zhu,Yuanyuan Li,Ning Kong,Jianping Qiu,Shanshan Hu,Shuang Song

The presence of elevated levels of norfloxacin (NOR) in the aquatic environment presents a serious risk to both human health and environmental organisms due to its extremely toxic and persistent characteristics. Herein, a series of Fe/Ti bimetallic composites (NH 2 -MIL-53(Fe/Ti)) were prepared using a one-step hydrothermal method to assess their capability for NOR degradation and investigate degradation mechanisms. It was observed that the well-organized nanosheets interconnected to form chrysanthemum clusters contained a significant number of exposed edges and open pores, which facilitated the enrichment of NOR. Notably, the optimum NH 2 -MIL-53(Fe/Ti) (1.5:1) demonstrated excellent degradation performance for NOR under visible light, owing to an electronic interaction between Fe 3+ and Ti 4+ metal centers. Efficient NOR degradation by NH 2 -MIL-53(Fe/Ti) (1.5:1) was achieved at 84.6% after 120 min of irradiation. Furthermore, the NH 2 -MIL-53(Fe/Ti) (1.5:1) maintained excellent reusability and stability even after five cycles tests. Active species trapping experiments confirmed that the pivotal role of •O 2 − and h + in photodegradation of NOR pollutants. A plausible photocatalytic mechanism was suggested according to various performance characterization and experimental results. Defluorination and ring opening were the main degradation pathways. This work advanced our understanding of photogenerated carriers transfer and energy conversion in bimetallic MOFs . Additionally, a novel strategy was presented for visible light catalytic degradation of NOR, which were highly relevant for the field of environmental treatment.

CAS / MDL: 10312-55-7 1310-73-2
研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Functionalized MIL-53 and its derivatives modified Bi2WO6 as effective piezocatalysts and membranes for adsorption and decomposition of organic pollutants

Zihan Kang,Mengshi Chen,Enzhu Lin,Jiang Wu,Kanghui Ke,Ni Qin,Dinghua Bao

Carbon-based composites with high activity and selectivity have broad prospects in the field of synthesis and catalysis. This work describes the controllable encapsulation of Bi 2 WO 6 (BWO) piezocatalysts with the mixture of derivatives and frameworks obtained by calcining MIL-53 metal–organic frameworks (MOFs). The mesoporous carbon and multi-functional groups of C/Fe 3 O 4 derived from the pyrolysis of MIL-53(Fe) can mediate the magnetic recyclability of catalysts and act as electron transfer units. Due to the high thermal stability, MIL-53(Al) mixed together still retains the frameworks and shows ameliorated hydrophobicity induced by porous carbon , which ensures the continuous generation of active radicals. The MOFs-assembled BWO nanoflowers possess the characteristics of complete adsorption-release and piezocatalytic degradation of organic pollutants, and the piezocatalytic degradation efficiency reaches 3.7 times higher than that of pure BWO nanoflowers. We also proposed a magnetic modulation method to obtain efficient macroporous MOFs/BWO-PVDF membranes. The magnetic composite powders can be highly exposed to the membrane surface to form more active sites for piezocatalytic reaction, which can overcome the problem of catalysts embedding in the membrane. This work not only proposes a novel way of synthesizing carbon composite piezocatalysts, but also provides the possibility to obtain more convenient, recyclable and high-performance piezocatalytic membrane, which is of great significance to explore the extensive application of piezocatalyst in sewage treatment.

研究领域: 环境科学 · 材料科学 · 催化化学
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CHEMICAL ENGINEERING JOURNAL · 2016 · IF 5.31

Simple fabrication of flake-like NH2-MIL-53(Cr) and its application as an electrochemical sensor for the detection of Pb2+

Hongxu Guo,Dongfang Wang,Jianhua Chen,Wen Weng,Minqiang Huang,Zishan Zheng

A novel metal-organic framework (MOF) material, flake-like NH 2 -MIL-53(Cr), was prepared by a simple reflux method and then characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The as-prepared MOF was found to be an effective material for the selective electrochemical detection of microgram levels of Pb 2+ in aqueous solution. Detection was performed by square wave anodic stripping voltammetry. The NH 2 -MIL-53(Cr)-modified electrode showed excellent selectivity and stability for Pb 2+ detection. The electrochemical properties and applications of the modified electrode were studied. Operational parameters such as pH, deposition potential, and deposition time, were also optimized to detect trace amounts of metal ions. This method offers a new strategy for heavy metal detection using MOF materials.

研究领域: 材料科学 · 环境科学 · 分析化学
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Reaction Chemistry & Engineering · 2021 ·Vol. 7 ·期 1 ·84-100 · IF 4.239

Facile synthesis of novel NH2-MIL-53(Fe)/AgSCN heterojunction composites as a highly efficient photocatalyst for ciprofloxacin degradation and H2 production under visible-light irradiation

Jungang Yi,Xianghui Wu,Huadong Wu,Jia Guo,Kun Wu,Linfeng Zhang

With the aim of solving the increasingly serious problem of environmental pollution and the energy crisis, in this work a novel NH2-MIL-53(Fe)/AgSCN (NMFA) composite photocatalyst was successfully prepared through a one-step chemical precipitation method. The prepared composites demonstrate an excellent photocatalytic performance for ciprofloxacin (CIP) and rhodamine B (RhB) degradation under visible-light irradiation. Within 60 min, the degradation rate for CIP and RhB reached 90% and 100%, respectively, which was 1.84/3.33 times and 1.79/2.04 times greater than that of the single NH2-MIL-53(Fe) and AgSCN samples. Furthermore, the H2 production rate of the NMFA-5 composite was 4742 μmol g−1 h−1, which was 5.25 and 17.37 times greater than that of the pure samples. Owing to the combination of NH2-MIL-53(Fe) and AgSCN, the separation and transmission efficiency of the photon-generated carriers in the composites was improved, which was demonstrated using optical characterization and a series of electrochemical characterization techniques. In addition, a possible mechanism for the excellent photocatalytic performance of the NMFA composites is discussed. The work in this paper may provide a technical reference for the application of silver modified metal organic frameworks (MOFs)-based composite photocatalysts for the treatment of environmental remediation.

研究领域: 环境科学 · 材料科学 · 化学工程
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RSC Advances · 2015 ·Vol. 5 ·期 50 ·40094-40102 · IF 3.84

Reverse-phase high performance liquid chromatography separation of positional isomers on a MIL-53(Fe) packed column

Zhiming Yan,Wenmin Zhang,Jia Gao,Yifen Lin,Jianrong Li,Zian Lin,Lan Zhang

The application of the metal–organic framework (MOF) MIL-53(Fe) as a novel stationary phase for reverse-phase high performance liquid chromatography (HPLC) separation of positional isomers is described for the first time. Under the optimized conditions, baseline separation of xylene, dichlorobenzene, chlorotoluene and nitroaniline isomers was achieved on the MIL-53(Fe) packed column within a short time. The retention mechanisms of these isomers on the MIL-53(Fe) packed column were discussed in detail, and a typical reverse-phase behavior can describe the results. The thermodynamic characteristics of the HPLC separation of positional isomers were also evaluated. It was confirmed that the HPLC separation of positional isomers was controlled by the Gibbs free energy change (ΔG). In addition, reverse-phase HPLC separation of the tested isomers was also carried on MIL-53(Al, Cr) packed columns to investigate the influence of the metal centre of the MIL-53 framework on their chromatographic behaviors. The results showed that the MIL-53(Fe) packed column exhibited better separation performance than the MIL-53(Al, Cr) packed columns. Moreover, the MIL-53(Fe) packed column also gave efficient HPLC separation of alkylbenzene and naphthalene, aniline compounds and polycyclic aromatic hydrocarbons (PAHs). These successful applications suggest the potential of MIL-53(Fe) as a novel stationary phase for efficient reverse-phase HPLC separation.

CAS / MDL: 100-21-0
研究领域: 分析化学 · 材料科学
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ACS Applied Materials & Interfaces · 2015 · IF 6.723

Preparation of MIL-53(Fe)-Reduced Graphene Oxide Nanocomposites by a Simple Self-Assembly Strategy for Increasing Interfacial Contact: Efficient Visible-Light Photocatalysts

Ruowen Liang,Lijuan Shen,Fenfen Jing,Na Qin,Ling Wu

In this work, MIL-53(Fe)-reduced graphene oxide (M53-RGO) nanocomposites have been successfully fabricated by a facile and efficient electrostatic self-assembly strategy for improving the interfacial contact between RGO and the MIL-53(Fe). Compared with D-M53-RGO (direct synthesis of MIL-53(Fe)-reduced graphene oxide nanocomposites via one-pot solvothermal approach), M53-RGO nanocomposites exhibit improved photocatalytic activity compared with the D-M53-RGO under identical experimental conditions. After 80 min of visible light illumination (λ ≥ 420 nm), the reduction ratio of Cr(VI) is rapidly increased to 100%, which is also higher than that of reference sample (N-doped TiO2). More significantly, the M53-RGO nanocomposites are proven to perform as bifunctional photocatalysts with considerable activity in the mixed systems (Cr(VI)/dyes) under visible light, which made it a potential candidate for industrial wastewater treatment. Combining with photoelectrochemical analyses, it could be revealed that the introduction of RGO would minimize the recombination of photogenerated electron–hole pairs. Additionally, the effective interfacial contact between MIL-53(Fe) and RGO surface would further accelerate the transfer of photogenerated electrons, leading to the enhancement of photocatalytic activity of M53-RGO toward photocatalytic reactions. Finally, a possible photocatalytic reaction mechanism is also investigated in detail.

CAS / MDL: 10025-77-1
研究领域: 材料科学 · 环境科学 · 化学
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TALANTA · 2025 · IF 6.1

Fabrication of BSA-protected AgNPs modified MIL-53(Al) as SERS substrate for trace determination of diquat and dipterex

Xin Liu,Shiyue Niu,Bin Yang,Jia Liu,Liqian Niu,Xian Wang,Daqian Song,Shuyun Bi

Ultrasensitive Surface-enhanced Raman spectroscopy (SERS) method for the detection of diquat/dipterex was established using bovine serum albumin (BSA)-protected silver nanoparticles (AgNPs) modified MIL-53(Al) (named as BSA/MIL-53(Al)/AgNPs). Compared with unmodified AgNPs, BSA/MIL-53(Al)/AgNPs significantly enhanced the Raman signals of diquat and dipterex and the enhancement factors (EFs) were 1.58 × 10 7 and 2.34 × 10 7 , respectively. The TEM, XRD, TGA, XPS, UV–vis and FT-IR were utilized to characterize BSA/MIL-53(Al)/AgNPs and the binding of the substrate with diquat/dipterex. The optimal measurement conditions were investigated in detail by single factor experiment and response surface model. The impacts of common pesticides and coexisting substances on the determination of diquat/dipterex were studied. Under optimum conditions, linear calibration curves for detecting diquat/dipterex were established with a limit of detection (LOD) of 0.17/0.89 pmol L −1 (3 S 0 / S ). The SERS approaches were used to detect diquat and dipterex in several fruits and vegetables. The recovery was 97.10 %–104.82 % with the relative standard deviation (RSD) of 1.04 %–4.15 % ( n  = 5).

研究领域: 分析化学 · 环境科学
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LANGMUIR · 2025 · IF 3.9

Nanozyme Colorimetric Sensor Array Based on Bimetal–Organic Framework MIL-53 (Fe, Mn) for the Discrimination of Biological Antioxidants

Huining Lan,Jingge Niu,Tianshu Luo,Louqun Wang,Xiaohong Hou

Biological antioxidants play a crucial role in numerous disease-related biological processes, which has led to significant interest in their identification. In this research, a colorimetric sensor array was created. It uses MIL-53 (Fe, Mn) nanozymes to simultaneously detect multiple antioxidants. The bimetallic nanozymes, MIL-53(Fe, Mn), were synthesized by using a solvent-thermal method. This framework demonstrated notable oxidase-like catalytic ability. In particular, it facilitates the conversion of colorless TMB to a blue compound under different pH conditions. When antioxidants were introduced into the reaction system, the sensor array exhibited cross-reactivity, resulting in distinct color signals. Linear discriminant analysis (LDA) was successfully utilized to precisely identify the different concentrations of cysteine (CYS), glutathione (GSH), dopamine (DA), and ascorbic acid (AA) and their combinations. This method enabled accurate determination of the amounts of these substances both individually and in mixtures, providing a reliable way to analyze their concentrations in an experimental context. Furthermore, the prepared sensor array combined with the smartphone successfully distinguished the target antioxidants in the serum. The proposed sensing method would be expected to have practical applications in diagnosis.

CAS / MDL: 51-61-6
研究领域: 生物化学 · 医学诊断
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Water · 2025 ·Vol. 17 ·期 9 ·1309 · IF 3

Novel MIL-53(Fe)@C Magnetic Composite Electrode for Efficient Dechlorination of Disinfection By-Product Trichloroacetic Acid in Water Treatment

Xiaoyan Ma,Rongbin Quan,Wenqing Cao,Weijie Zhang,Su Jiang,Jiao Feng,Jiulong Wang,Stefanos Giannakis

Electrochemical reduction is a promising strategy for the dechlorination of halogenated organic compounds, offering advantages such as enhanced electron transfer efficiency and increased hydrogen atom concentration. It has garnered significant attention for application in mitigating halogenated disinfection by-products (DBPs) in drinking water, owing to its high efficiency and simple operation. In this study, trichloroacetic acid (TCAA), a representative DBP, was selected as the target contaminant. A novel composite cathode comprising a metal–organic framework MIL-53(Fe)@C supported on an Nd magnet (MIL-53(Fe)@C-MAG) and its dechlorination performance for TCAA were systematically investigated. The innovative aspect of this study is the magnetic attachment of the MOF catalyst to the carbonized cathode surface treated through carbonization, which fundamentally differs from conventional solvent-based adhesion methods. Compared to the bare electrode, the MIL-53(Fe)@C-MAG achieved a TCAA removal efficiency exceeding 96.03% within 8 h of contact time. The structural characterization revealed that the α-Fe0crystalline phase serves as the primary active center within the MIL-53(Fe)@C catalyst, facilitating efficient electron transfer and TCAA degradation. The scavenger experiments revealed that TCAA reduction involves a dual pathway: direct electron transfer and atomic hydrogen generation. The modified MIL-53(Fe)@C-MAG electrode exhibited robust electrolytic performance over a broad pH range of 3–7, with TCAA removal efficiency showing a positive correlation with current density within the range of 10–50 mA/cm2. Furthermore, the electrode maintained exceptional stability, retaining more than 90% removal efficiency after five consecutive operational cycles. The versatility of the system was further validated by the rapid and efficient dechlorination of various chlorinated DBPs, demonstrating the broad applicability of the electrode. The innovative magnetic composite electrode demonstrates a significant advancement in electrochemical dechlorination technology, offering a reliable and efficient solution for the purification of drinking water contaminated with diverse halogenated DBPs. These results provide valuable insights into the development of electrolysis for dechlorination in water treatment applications.

研究领域: 环境科学 · 材料科学 · 水处理工程
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