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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

In situ growth of UIO-66-NH2 on thermally stabilized electrospun polyacrylonitrile nanofibers for visible-light driven Cr (VI) photocatalytic reduction

Meimei Zhou,Wei Zou,Xuemei Zhu,Huachen Ma,Pengbo Wang,Jiaxin Shang,Pingping Luo

UIO-66-NH 2 was successfully deposited on electrospun polyacrylonitrile (PAN) nanofibers treated by thermal oxidative stabilization (TOS) via a simple and effective in situ growth method. Owing to the formation of acridone rings, naphthyridinering rings and hydronaphthyridine rings during the TOS process, the thermally stabilized electrospun PAN (TSPAN) nanofibers were greatly improved in stability and heat resistance and could provide adequate nucleation points for MOFs growth, indicating an ideal MOFs deposition support without additional surface modifications. The results demonstrated that UIO-66-NH 2 crystals distributed relatively uniform and dense on the TSPAN nanofibers with mass loading up to 28.1 ​wt%. Compared with powdered UIO-66-NH 2 , the formed UIO-66-NH 2 @TSPAN nanofibers showed enhanced visible light driven photocatalytic activity towards reduction of Cr(VI) due to the improvement of visible light response, more excellent photothermal conversion ability and the increase of exposed active sites. The photocatalytic reduction rate of Cr(VI) over UIO-66-NH 2 @TSPAN was up to 93% within 180 ​min and the rate constant (k ​= ​0.1362) was 2.3 times that of powdered UIO-66-NH 2 (k ​= ​0.00576). Significantly, the mechanical flexibility and structural stability endowed the nanofibrous photocatalyst easy operation and outstanding reusable capability. The photocatalytic activity for Cr(VI) reduction still preserved 90% after five cycles. This work proposes a facile strategy for preparation of free-standing MOFs nanofibers and provides MOFs-based photocatalysts a new opportunitie for broad applications in water treatment.

研究领域: 材料科学 · 环境催化 · 纳米材料 · 光化学 · 水处理技术
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Journal of Materials Chemistry B · 2021 ·Vol. 9 ·期 43 ·9031-9040 · IF 6.331

Development of Au–Pd@UiO-66-on-ZIF-L/CC as a self-supported electrochemical sensor for in situ monitoring of cellular hydrogen peroxide

Jilin Zheng,Peng Zhao,Shiying Zhou,Sha Chen,Yi Liang,Fengchun Tian,Jun Zhou,Danqun Huo,Changjun Hou

Integrating metal–organic frameworks (MOFs) of different components or structures together and exploiting them as electrochemical sensors for electrochemical sensing has aroused great interest. Furthermore, the incorporation of noble metals with MOFs is conducive to the improvement of catalytic performance. In this work, Pd@UiO-66-on-ZIF-L nanomaterials were successfully synthesised onto a self-supported flexible carbon cloth (Pd@UiO-66-on-ZIF-L/CC) through a novel strategy called MOF-on-MOF. Then, Au nanoparticles were electrodeposited onto Pd@UiO-66-on-ZIF-L/CC to obtain Au–Pd@UiO-66-on-ZIF-L/CC, which can serve as an excellent electrocatalyst for the reduction of hydrogen peroxide (H2O2). The obtained flower-like Pd@UiO-66-on-ZIF-L/CC hybrid MOF changes the structure of the monomeric MOF alone and adds more attachment sites. The synergy of the bimetals greatly improved the catalytic performance of the as-developed sensor. Electrochemical experiment results show that the proposed sensor based on Au–Pd@UiO-66-on-ZIF-L/CC has an extended linear range from 1 μM to 19.6 mM with a sensitivity of 390 μA mM−1 cm−2, and a low limit of detection (LOD) of 21.2 nM (S/N = 3). Moreover, it has good anti-interference, reproducibility, repeatability and excellent stability. Furthermore, the real-time in situ detection of H2O2 secreted from human adenocarcinomic alveolar basal epithelial cells (A549 cells) was achieved by culturing cells on Au–Pd@UiO-66-on-ZIF-L/CC, which indicates the potential of the sensor for applications in cancer pathology. Both the synthesis strategy and the sensor design provide new methods and ideas for the production of ultrasensitive H2O2 electrochemical sensors.

研究领域: 材料科学 · 电化学 · 生物传感器 · 癌症病理学
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CHEMOSPHERE · 2025 · IF 8.1

Efficient degradation of aflatoxin B1 and ochratoxin A using dual Z-scheme Sr2MgSi2O7: Eu2+, Dy3+/BiVO4/NH2-UiO-66 heterojunctions with round-the-clock photocatalytic activity

Si-yuan He,Wei Wen,Peng Wu,Zhe Meng

Developing a green and efficient technology for decomposing aflatoxin B 1 (AFB 1 ) and ochratoxin A (OTA) in grains has important theoretical value and application prospects for ensuring food safety. A dual Z-scheme ternary heterojunction photocatalyst, Sr 2 MgSi 2 O 7 :Eu 2+ ,Dy 3+ /BiVO 4 /NH 2 -UiO-66 (SBN), was prepared via a self-assembling hydrothermal approach. The SBN heterojunction photocatalyst exhibits round-the-clock photocatalytic activity due to the intrinsic light source of Sr 2 MgSi 2 O 7 : Eu 2+ , Dy 3+ (SMS). Dual Z-scheme mechanism was proposed and validated through detailed analysis of quenching experiments, ESR spectra, band arrangement, and charge transfer processes. The dual Z-scheme mechanism not only promotes the effective transfer and separation of photo generated charge carriers during charge carrier transport, but also maintains significant reduction and oxidation potentials. SBN photocatalyst exhibits stable and persistent photocatalytic performance, significantly enhancing the degradation efficiency of AFB 1 and OTA under all-weather conditions. Experimental data shows that the removal rate of AFB 1 increased from 69.60 % after 60 min of illumination to 83.9 % after 4 h of turning off the light source; At the same time, the removal rate of OTA increased from 64.8 % to 78.1 %. •O 2 − and •OH were identified as key active species in photocatalytic reactions. Based on the analysis of AFB 1 and OTA degradation intermediates and the prediction of degradation sites using density functional theory (DFT), degradation pathways for AFB 1 and OTA were proposed. Collectively, these findings suggest a highly promising practical approach for the detoxification of mycotoxins in grain commodities.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2019 · IF 3.571

Dispersive Solid-Phase Extraction Using Microporous Sorbent UiO-66 Coupled to Gas Chromatography–Tandem Mass Spectrometry: A QuEChERS-Type Method for the Determination of Organophosphorus Pesticide Residues in Edible Vegetable Oils without Matrix Interference

Xuejin Mao,Aiping Yan,Yiqun Wan,Dongmei Luo,Hongshun Yang

A QuEChERS-type method without matrix interference was designed and developed to determine organophosphorus pesticide residues in edible vegetable oils, based on dispersive solid-phase extraction with cleanup using UiO-66 as sorbent. Microporous UiO-66 directly and selectively adsorbed organophosphorus pesticides and excluded interfering compounds. Clean analytes were obtained by elution and analyzed using gas chromatography–tandem mass spectrometry. The dispersive solid-phase extraction conditions (amount of adsorbent, extraction time, desorption solvent volume, and elution time) were optimized. The limits of detection of the pesticides in vegetable oils were 0.16–1.56 ng/g. Under optimized conditions, the average pesticide recoveries were 81.1–113.5%. The intraday and interday relative standard deviations for analyte recovery were <8.2 and <13.9%, respectively. Thus, the method is reliable and could detect organophosphorus pesticide residues in edible vegetable oils. Furthermore, UiO-66 can be easily recycled and reused at least 10 times, reducing the cost of analysis.

研究领域: 分析化学 · 食品安全 · 环境科学
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JOURNAL OF HAZARDOUS MATERIALS · 2022 · IF 14.224

Ferrocene-modified Uio-66-NH2 hybrids with g-C3N4 as enhanced photocatalysts for degradation of bisphenol A under visible light

Zhikun Huang,Haojie Yu,Li Wang,Xiaowei Liu,Shuning Ren,Jinyi Liu

Designing graphitic carbon nitride (CN) based heterostructured photocatalysts with high catalytic activity is highly desired for peroxymonosulfate (PMS) activation to degrade organic pollutants from water. Herein, a novel heterostructured composite (U-F@CN) consisting of ferrocene-modified Uio-66-NH 2 (U-F) and CN was synthesized. The U-F@CN exhibited superior photocatalytic performance to degrade bisphenol A (BPA) in the presence of PMS under visible light. The experimental results indicated that BPA could be removed entirely by U-F@CN within 60 min under visible light irradiation. In addition, the outstanding photocatalytic activity could be maintained at high level in a wide pH range, appropriate temperature region and natural water condition. Benefiting from the good chemical stability, outstanding optical property and in-situ generation of interfacial heterojunction of U-F@CN, the interfacial transport of photogenerated charges could follow the Z-scheme mechanism, which can accelerate the charge separation and transport to yield abundant reactive active species (ROS) to efficiently active PMS and under visible light. This work provides a novel approach to design CN-based heterostructured photocatalysts with high stability and superior photocatalytic activity for environmental remediation.

研究领域: 材料科学 · 环境科学 · 化学 · 光催化
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Materials Today Chemistry · 2023 · IF 7.3

Flexible core-shell PAN/CNTs@PVDF-HFP/Uio-66-NH2 hybrid nanofibers membrane for advanced lithium-ion batteries separator

Mao Guo,Siyang Dong,Jing Xiong,Xuanyang Jin,Pengfei Wan,Shengjun Lu,Yufei Zhang,Jian Xu,Haosen Fan

Flexible core-shell polyacrylonitrile (PAN)/carbon nanotubes (CNTs)@Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)/Uio-66-NH 2 (PC@PU) hybrid nanofiber membrane was prepared by coaxial electrospinning technology. PAN polymer and CNTs particles were used as core to improve the membrane structure stability for further ensuring the thermal stability of the separator. PVDF-HFP and Uio-66-NH 2 nanoparticles were applied to reinforce the affinity of separator to electrolyte. The PC@PU composite membrane delivered high thermal stability and fantastic electrolyte affinity (545.76%). Furthermore, compared with Celgard 2325 commercial membrane, the PC@PU composite membrane exhibited higher porosity (80.22%) and higher Li + conductivity (3.43 mS/cm), leading to superior rate performance and long-term cycle stability. The cell with the PC@PU hybrid membrane displayed high specific capacity of 143 mAh/g at 1C and only 0.0259% capacity attenuation of each cycle after 1000 cycles. In addition, the PC@PU composite membrane demonstrated remarkable flexibility, and the cells with bent separators exhibited outstanding electrochemical performance. Hence, the PC@PU hybrid nanofiber membrane can pave a way for the further application in the field of secondary batteries separator.

研究领域: 材料科学 · 电化学 · 纳米技术 · 能源存储
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BIOSENSORS & BIOELECTRONICS · 2018 · IF 8.173

Ultrasensitive competitive method-based electrochemiluminescence immunosensor for diethylstilbestrol detection based on Ru(bpy)32+ as luminophor encapsulated in metal–organic frameworks UiO-67

Xue Dong,Guanhui Zhao,Li Liu,Xuan Li,Qin Wei,Wei Cao

In this work, Ru(bpy) 3 2+ encapsulated in metal–organic frameworks (MOFs) UiO-67 (Ru(bpy) 3 2+ /UiO-67) as luminophor was easily prepared and firstly applied in constructing an electrochemiluminescence (ECL) immunosensor to efficiently estimate diethylstilbestrol (DES). The competitive method-based ECL immunosensor platform was fabricated by amino-silicon dioxide which possesses large surface area . The poriness of UiO-67 was splendid so that Ru(bpy) 3 2+ could be easily encapsulated. Ru(bpy) 3 2+ /UiO-67 with excellent ECL luminescence signal existed large specific surface area for easily labeled with antibodies. DES competed with bovine serum albumin-diethylstilbestrol (BSA-DES) for binding to antibody-specific sites in the constructed immunosensor. However DES was micromolecule, which was easier to bond to antibodies than BSA-DES. The ECL signal was gradually decreases with the increase of the concentration of DES. Under optimal conditions, the proposed immunosensor exhibited a wide linear range from 0.01 pg mL −1 to 50 ng mL −1 with a low detetion limit of 3.27 fg mL −1 (S/N = 3). The novel fabricated immunosensor with interference immunity and high stability may cause an attractive approach for the other targets determination.

研究领域: 分析化学 · 环境科学 · 生物技术
✓ 已验证 DOI 高影响因子
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Nano Research · 2024 · IF 9.5

Defect engineering and Ni promoter synergistically accelerating electron transfer to Ru0 sites in UiO-66(Ce) for dicyclopentadiene hydrogenation under mild condition

Li Rushuo,Ban Tao,Zhao Danfeng,Lin Jing,Liu Zhiyuan,Wang Linmeng,Huang Xiubing,Tao Zhiping,Wang Ge

Olefin hydrogenation under mild condition is crucial and challenging for industrial applications. Herein, defective UiO-66(Ce) was constructed by using cyanuric acid as the molecular etching “scissors” and further to synthesize heterogeneous catalyst with highly dispersed RuNi nanoparticles (Ru 1 Ni 1.5 @UiO-66(Ce)-12 h). The construction of Ce-O-Ru/Ni heterogeneous interfaces and Ni–Ru bonds provide electron transfer channels from Ce-oxo clusters and Ni species to Ru species. Furthermore, the microenvironment and electronic structure of Ru 0 active sites were synergistically regulated by adjusting the content of metal-organic frameworks (MOFs) defects and Ni promoter, thereby enhancing the adsorption and activation ability of H–H and C=C bonds. Therefore, Ru 1 Ni 1.5 @UiO-66(Ce)-12 h achieved dicyclopentadiene saturated hydrogenation (100% conversion) to tetrahydrodicyclopentadiene (∼ 100% selectivity) under mild condition (35 °C, 1 MPa) with only 25 min. Meanwhile, the sample exhibited excellent structural stability after 6 cycles test. This study provides a promising strategy for the rational design of remarkable noble metal-based catalysts for practical applications.

研究领域: 催化 · 化学工程 · 材料科学 · 纳米技术
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Particuology · 2021 · IF 3.067

Adsorption removal of sulfamethoxazole from water using UiO-66 and UiO-66-BC composites

Jinbo Ouyang,Jian Chen,Shaoqing Ma,Xiaohong Xing,Limin Zhou,Zhirong Liu,Chuntao Zhang

The adsorption removal of anti-inflammatory drugs from water by diverse materials has drawn great attention. This study investigated the adsorption of sulfamethoxazole (SMX) by two types of materials, UiO-66 and UiO-66-BC composites. Highly porous MOF composites with functional groups were synthesized by combining UiO-66 with corncob-based biochar at different molar ratios. SEM results showed that macroporosity of UiO-66-BC composites was increased by increasing the ratio of biochar. It was found that UiO-66-BC composites displayed highly improved adsorption performance of SMX relative to pristine UiO-66. UiO-66-BC (5%) had the highest SMX adsorption capacity, about 2.4 times those of pristine UiO-66. It was the high surface area of UiO-66 and redundant functional groups of biochar that increased the adsorption performance of composites. Moreover, UiO-66-BC can be reused and displayed the competitive adsorption efficiency after successive adsorption, which made it a potential adsorbent for the removal of SMX from water.

CAS / MDL: 100-21-0 723-46-6
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PROGRESS IN ORGANIC COATINGS · 2024 · IF 6.5

UiO-66 and UiO-66-NH2 membranes-based superhydrophobic coatings for enhanced corrosion protection

Jiaxuan Zhou,Zhitao Wang,Ran Liu,Kai Qi,Yubing Qiu,Xingpeng Guo

Fabricating metal-organic frameworks (MOFs) membranes directly onto metal surfaces as anticorrosive coatings is a feasible approach for the application of MOFs in corrosion protection . The MOFs membranes with specific organic groups can be further customized as versatile platforms for developing various functional coatings. Herein, UiO-66 and UiO-66-NH 2 membranes are synthesized onto aluminum surfaces through a polydopamine-assisted method, which are then grafted with superhydrophobic molecules of perfluorodecyltriethoxysilane (PFDTES). The -COOH groups in UiO-66 and -COOH/-NH 2 groups in UiO-66-NH 2 can serve as firm anchor sites for covalently grafting with PFDTES, enabling robust superhydrophobicity of the as-prepared coatings. The superhydrophobic surfaces exhibit water repellency (water contact angle of ∼165 o ), chemical (pH and salinity) and wear-resisting robustness, and long-term service durability. They also perform decent anti-fouling, self-cleaning, and anti-icing properties. Notably, sustainable corrosion protection can be provided by both coatings during immersion in saline solution (3.5 wt% NaCl) for one month and during a two-week salt spray test. Compared with UiO-66, the -NH 2 groups on UiO-66-NH 2 as extra grafting sites for firmer immobilization of more PFDTES molecules facilitate more durable superhydrophobicity and corrosion protection. We believe that this work could offer valuable insights into the multi-functional development of MOFs membranes-based coatings.

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MICROCHIMICA ACTA · 2019 ·Vol. 187 ·期 1 ·1-8 · IF 5.479

An amino-functionalized zirconium-based metal-organic framework of type UiO-66-NH2 covered with a molecularly imprinted polymer as a sorbent for the extraction of aflatoxins AFB1, AFB2, AFG1 and AFG2 from grain

Liang Yutao,He Juan,Huang Zhipeng,Li Huayu,Zhang Yunxia,Wang Huige,Rui Chaofan,Li Yuanyuan,You Liqin,Li Kai,Zhang Shusheng

A surface imprinted polymer of type UiO-66-NH2@MIP was prepared by combining molecular imprinted polymers (MIPs) and an amino-functionalized zirconium-based metal-organic framework. Quercetin is used as the virtual template, UiO-66-NH 2 acts as the carrier to which the monomer acrylamide can be copolymerized. The material was characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. It was used as a sorbent in a solid-phase extraction column. The extraction conditions were optimized. The adsorption capacities for aflatoxins AFB1, AFB2, AFG1 and AFG2 by this SPE and by the commercial SPE were compared. The method was successfully applied to quantify the aflatoxins in grain. Figures of merit include (a) good linearity (range from 0.20–45 μg·kg −1 ) with R 2 (range from 0.9986–0.9994), (b) low detection limits (90–130 ng·kg −1 ), (c) acceptable reproducibility (1.0–5.9%; for n  = 6), and (d) relatively satisfactory recovery rates (74.3–98.6%). The new sorbent has good selectivity and reusability. UiO-66-NH 2 @MIPs were synthesized with modified UIO-66-NH 2 as core and quercetin as pseudo template. A cartridge was prepared with the polymers as the sorbent, and its performance was compared with different commercial SPE cartridges.

研究领域: 分析化学 · 食品科学 · 材料科学
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RSC Advances · 2023 ·Vol. 13 ·期 50 ·35078-35087 · IF 3.9

Metal–organic framework (UiO-66 and UiO-66-NH2)-based adsorbents for bilirubin removal used in hemoperfusion

Yi Liu,Zhipeng Yuan,Yanrong Chen

Excessive accumulation of bilirubin in patients with hyperbilirubinemia can lead to tissue and organ damage and neurological diseases, and is even life-threatening in severe cases. Hemoperfusion is an effective method for removing bilirubin, but clinically used hemoperfusion adsorbents have unsatisfactory adsorption capacity and kinetics. In order to obtain a safe and efficient bilirubin adsorbent, Zr-based Metal–Organic Framework (MOF) material UiO-66 with high specific surface area and aqueous medium stability was prepared and modified with varying degrees of amination to improve its adsorption capacity. According to adsorption experiments in aqueous solution and simulated plasma, it was confirmed that the unsaturated coordinated zirconium in UiO-66 can effectively induce the aggregation and precipitation of free bilirubin unbound to albumin and the amino group on UiO-66-NH2 has a strong affinity for albumin bound bilirubin. The adsorption effect of UiO-66-NH2 with a high degree of amino modification is significantly stronger than that of UiO-66-NH2 with a low degree of modification. In simulated plasma with a bilirubin concentration of 40 mg dL−1, the adsorption capacities of UiO-66 and UiO-66-NH2-1.9 can reach 69.08 mg g−1 and 81.13 mg g−1. The adsorption isotherm fitting and adsorption kinetics fitting results also show that UiO-66 and UiO-66-NH2 are good adsorbents for bilirubin. In dynamic adsorption, the adsorbents also showed good performance and did not affect the protein in the plasma. The hemolysis test, coagulation time test, and cytotoxicity test confirmed that the bilirubin adsorbents based on UiO-66 and UiO-66-NH2 have good blood compatibility and biocompatibility. This study provides new ideas for the development of a novel bilirubin adsorbent and a theoretical basis for the study of bilirubin adsorption mechanisms.

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