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UIO-66
JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2025 · IF 4.1

Enhancing safety and electrochemical performance of lithium-ion batteries with P/N-IL@NH2-UIO-66 functionalized PVDF separators

Hua Yu,Xuan Wang,Lijun Yang,Qirui Wu,Houming Shen,Geming Wang,Peng Fan

The development of high-performance separator materials has become crucial with the ever-increasing demands for enhanced safety and energy density of lithium-ion batteries in electric vehicles and large-scale energy storage systems. Here, a novel high-safety functionalized separator was prepared by synthesizing a composite material that encapsulates phosphorus‑nitrogen-containing ionic liquid (P/N-IL) within NH 2 -UIO-66-Zr metal-organic framework (MOF), and then combining this composite with a polyvinylidene fluoride (PVDF) P/N-IL@NH 2 -UIO-66/PVDF separator. This functionalized P/N-IL@NH 2 -UIO-66/PVDF separator significantly improves the flame-retardant performance of NCM811 batteries, effectively mitigating the risks of electrolyte combustion and explosion. Meanwhile, the porous structure of P/N-IL@NH 2 -UIO-66 material optimizes the Li + transport pathways, resulting in an increase in the ionic conductivity of NCM811 battery o 3.1 × 10 −4  S/cm (compared to only 3.4 × 10 −6  S/cm for the pure PVDF separator). The Li + transference number is also elevated to 0.68. Moreover, after 600 cycles at a 1C current density, the capacity retention rate reaches as high as 71 %, with an average coulombic efficiency of 96 %, substantially enhancing the electrochemical performance and cycling stability of the battery. This work offers a novel technological pathway for the development of high-safety, high-performance lithium-ion batteries, as well as for the application of ionic liquids and MOFs.

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ANALYTICAL SCIENCES · 2024 · IF 1.8

Sandwich-like voltametric immunosensing of interleukin-8 based on β-cyclodextrin/carbon nanotubes and methylthionine chloride@UIO-66 framework

Zhou Zhihua,Lin Jiajia,Yue Daoping,Chen Huaiyu,Chen Sheng

The level of interleukin-8 (IL-8) in the body is an effective factor for the early diagnosis of acute tubular necrosis and oral tumor. In this work, a novel sandwich-like voltametric immunosensor (SVS) of IL-8 was constructed by preparing β-cyclodextrin/carbon nanotube (CD/CNT) to immobilize primary antibody (PAb) of IL-8 and UIO-66-NH 2 MOFs structure to immobilize second antibody (SAb) and methylene blue (Mb) probe. In this designed SVS, the prepared CD/CNT nanohybrid with large surface area and conductivity can immobilize PAb via simple host–guest recognition, and UIO-66-NH 2 provided an ideal platform to accommodate SAb and a large number of Mb molecules as signal-amplifier. In the existence of target IL-8, the current peak of Mb from the SVS assay increases with the increasement of IL-8 level. Through optimizing and adjusting various factors, a wide linearity (0.001–2.5 ng mL −1 ) and low analytical limit (0.2 pg mL −1 ) of IL-8 were realized, so it’s expected the developed SVS strategy has significant applications for the detection of IL-8. Graphical abstract

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Membranes · 2021 ·Vol. 11 ·期 1 ·35 · IF 4.106

Preparation of Amino-Functional UiO-66/PIMs Mixed Matrix Membranes with [bmim][Tf2N] as Regulator for Enhanced Gas Separation

Jiangfeng Lu,Xu Zhang,Lusheng Xu,Guoliang Zhang,Jiuhan Zheng,Zhaowei Tong,Chong Shen,Qin Meng

Development of mixed matrix membranes (MMMs) with excellent permeance and selectivity applied for gas separation has been the focus of world attention. However, preparation of high-quality MMMs still remains a big challenge due to the lack of enough interfacial interaction. Herein, ionic liquid (IL)-modified UiO-66-NH2filler was first incorporated into microporous organic polymer material (PIM-1) to prepare dense and defect-free mixed matrix membranes via a coating modification and priming technique. IL [bmim][Tf2N] not only improves the hydrophobicity of UiO-66-NH2and facilitates better dispersion of UiO-66-NH2nanoparticles into PIM-1 matrix, but also promotes the affinity between MOFs and polymer, sharply reducing interface non-selective defects of MMMs. By using this strategy, we can not only facilely synthesize high-quality MMMs ignoring non-selective interfacial voids, but also structurally regulate MOF nanoparticles in the polymer substrate and greatly improve interface compatibility and stability of MMMs. The method also gives suitable level of generality for fabrication of versatile defect-free MMMs based on different combination of MOFs and PIMs. The prepared UiO-66-NH2@IL/PIM-1 membrane exhibited outstanding gas separation behavior with large CO2permeation of 8283.4 Barrer and high CO2/N2selectivity of 22.5.Keywords:mixed matrix membrane;amino-functional UiO-66;PIM-1;[bmim][Tf2N];gas separation

CAS / MDL: 10026-11-6
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

UiO-66(Zr) MOF enhances pH sensitivity of carboxymethyl fiber colorimetric films incorporated with anthocyanins for monitoring fish freshness

Weibo Lu,Huangwei Ye,Yike Zhu,Yuhan Li,Huan Li,Qing Shen,Jian Chen

The non-destructive, real-time, and visual assessment of fish freshness is crucial for maintaining food quality and safeguarding public health. In this study, a pH-sensitive and colorimetric enhancement film was developed using a carboxymethyl cellulose/anthocyanin/metal-organic framework (CMC-BA-UIO). The concentration of UIO-66 in the film-forming solution significantly influences the mechanical properties and ammonia responsiveness of the indicator film, with the CMC-BA/2.5%UIO-66 variant exhibiting optimal performance. When utilized for real-time fish freshness monitoring at 4 °C, the CMC-BA/2.5%UIO-66 indicator film demonstrated a distinct color transition from purple to yellow, which exhibited a strong correlation with the rot index (TVB-N) of the fish. These findings indicate that the developed indicator film has potential applications in intelligent packaging for monitoring food shelf life, providing a visual alert to producers and consumers regarding food spoilage.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Construction of greenly biodegradable bacterial cellulose/UiO-66-NH2 composite separators for efficient enhancing performance of lithium-ion battery

Shuaitian Jia,Zan Chen,Yinhui Li,Claudia Li,Cuijia Duan,Kang Hui Lim,Sibudjing Kawi

The disposal of waste lithium batteries , especially waste separators, has always been a problem, incineration and burial will cause environmental pollution, therefore, the development of degradable and high-performance separators has become an important challenge. Herein, UiO-66-NH 2 particles were successfully anchored onto bacterial cellulose (BC) separators by epichlorohydrin (ECH) as a crosslinker, then a BC/UiO-66-NH 2 composite separator was prepared by vacuum filtration. The ammonia groups (−NH 2 ) from UiO-66-NH 2 can form hydrogen bonds with PF 6 − in the electrolyte, promoting lithium-ion transference. Additionally, UiO-66-NH 2 can store the electrolyte and tune the porosity of the separator. The lithium ion migration number (0.62) of the battery assembled with BC/UiO-66-NH 2 composite separator increased by 50 % compared to the battery assembled with commercial PP separator (0.45). The discharge specific capacity of the battery assembled with BC/UIO-66-NH 2 composite separator after 50 charge and discharge cycles is 145.4 mAh/g, which is higher than the average discharge specific capacity of 114.3 mAh/g of the battery assembled with PP separator. When the current density is 2C, the minimum discharge capacity of the battery assembled with BC/UiO-66-NH 2 composite separator is 85.3 mAh/g. The electrochemical performance of the BC/UiO-66-NH 2 composite separator is significantly better than that of the commercial PP separator. In addition, -NH 2 can offer a nitrogen source to facilitate degradation of the BC separators, whereby the BC/UiO-66-NH 2 composite separator could be completely degraded in 15 days.

✓ 已验证 DOI PubMed 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

“Corn-like” APT@UiO-66-NH₂/PEG composite membrane with excellent anti-fouling performance for oil/water emulsions separation

Ruirui Jin,Jingling Gong,Zhaoyang Li,Bin Xiang,Weimin Liu,Jian Li

The increase in oily wastewater exacerbates global water scarcity, triggering ecological damage and health risks. Although membrane separation technology was widely adopted in oily wastewater treatment due to its high efficiency and energy savings, membrane fouling issues lead to flux decline, increased energy consumption, and reduced membrane lifespan, thereby limiting its application. Therefore, this study proposed an advanced “water absorption-storage” strategy by in-situ growing UiO-66-NH₂ nanoparticles on attapulgite (APT) through carefully designed micro-nano-scale rough structures and chemical interactions, forming a unique biomimetic “corn-like” structure. The APT@UiO-66-NH₂/PEG composite membrane prepared in this study establishes a robust hydration barrier through synergistic interactions between its components, thereby exhibiting both outstanding anti-oil fouling capability and highly efficient, stable oil-water emulsion separation performance. Meanwhile, the in-situ growth of UiO-66-NH₂ on APT effectively resolved the issue of easy detachment between APT and UiO-66-NH₂. Moreover, the abundant hydrophilic functional groups (–OH) in polyethylene glycol (PEG) form hydrogen bonds with UiO-66-NH₂ and APT, further enhancing the structural stability. The obtained APT@UiO-66-NH₂/PEG composite membrane achieved separation efficiencies exceeding 99.8 % for various oil-in-water emulsions, with a separation flux reaching 3020 LMH/bar. After 10 separation cycles and 60 min of continuous operation, the separation performance remained essentially stable. The composite membrane demonstrated excellent chemical durability and mechanical stability in high-concentration acid, alkali, and salt solutions, as well as during bending and abrasion tests. Therefore, this study presents a simple and effective purification solution for practical oily wastewater, with the associated strategies and preparation techniques demonstrating broad application prospects.

CAS / MDL: 10026-11-6 10312-55-7
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Catalysis Science & Technology · 2025 · IF 4.2

Thermal Switching of Brønsted Acid Sites in Defective UiO-66 Governs the Activity of Fructose Dehydration to 5-Hydroxymethylfurfural

Kai Yan,Zhihao Yu,Yingqing Li,Mengyan Guo,Yuanyu Wang,Xuebin Lu

The efficient dehydration of fructose to 5-hydroxymethylfurfural (HMF) is a crucial step in biomass valorization, requiring solid acids with precisely balanced Brønsted acidity. Defect engineering in Zr-based metal–organic frameworks (MOFs), such as UiO-66, is well known to enhance Lewis acidity; however, its impact on tailoring Brønsted acid sites remains insufficiently understood. Here, we demonstrate that defective UiO-66 possesses a dual-origin Brønsted acid system, comprising intrinsic μ3–OH groups and water molecules coordinated to defect-generated Lewis acidic Zr centers (Zr–H2O). The concentration of these Brønsted acid sites can be finely regulated by thermal activation treatment. A volcano-shaped dependence of catalytic activity on activation temperature is observed, with an optimum at 200 °C. At moderate activation temperatures below 200 °C, the removal of physisorbed water exposes both μ3–OH and Zr–H2O sites, maximizing Brønsted acid density and HMF yield. Activation beyond 200 °C reduces both types of Brønsted acid sites, resulting in diminished catalytic performance. This study reveals the cooperative effect of defect engineering and thermal activation in tuning the Brønsted acidity of MOFs, providing a rational strategy for designing highly selective catalysts for the sustainable production of platform chemicals.

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INORGANIC CHEMISTRY · 2025 · IF 4.7

Dual Functions of Fluorescence and Peroxidase Mimics for Hemin@NH2-UiO-66 and Ratiometric Fluorescence Sensing to l-Cysteine

Jin Chai,Chunpeng Liu,Hongtian Yang,Yide Han,Yufeng Liu,Ying Zhang,Xia Zhang

The bifunctions of fluorescence activity and peroxidase mimics were well-integrated by a hemin chloride-modified Zr-based metal–organic framework (Hemin@NH2-UiO-66), which can catalyze the oxidation of o-phenylenediamine (OPD) to generate 2,3-diaminophenazine (DAP), presenting typical peroxidase mimic properties. The influence of the introduction of hemin chloride upon the enhanced peroxidase mimic activity was clarified, and the nanozyme catalytic parameters were optimized. Interestingly, the oxidized product of DAP presents strong fluorescence emission at 564 nm; combining it with the intrinsic fluorescence emission of NH2-UiO-66 at 452 nm, a dual-emission system could be built up by the resulting Hemin@NH2-UiO-66 in the presence of definite OPD and H2O2. Moreover, the fluorescence quenching effect (564 nm) was observed by adding l-cysteine (l-Cys); based on that, a straight-line dependence of the fluorescence intensity ratio (I452/I564) upon the concentrations of l-Cys was established. The detection limit was 0.21 μmol, and the analytical selectivity for l-Cys was also demonstrated. The work highlights the idea of combining the intrinsic fluorescence property and nanozyme catalytic activity in a functional MOF, and its special usability is found in the ratiometric fluorescence sensing analyses.

CAS / MDL: 7722-84-1
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Journal of Environmental Chemical Engineering · 2025 ·Vol. 13 ·期 6 ·120451 · IF 7.2

Synergistic effect of Z-scheme heterojunction and Cu-doping in ZnIn2S4/UiO-66-NH2 for enhanced photocatalytic hydrogen evolution

Yang Li,Guozhe Sui,Mingna Chu,Yan Zhuang,Dongxuan Guo,Shuang Meng,Dantong Zhang,Yue Li,Jinlong Li

Photocatalytic water splitting is a highly promising approach for sustainable hydrogen production. However, a critical challenge lies in developing photocatalysts that simultaneously achieve efficient charge separation and abundant catalytic active sites. Herein, a novel heterojunction system composed of ZnIn 2 S 4 integrated with copper-modified UiO-66-NH 2 (ZnIn 2 S 4 /Cu-UiO-66-NH 2 ) is developed as an efficient photocatalyst for hydrogen production. The optimal ZnIn 2 S 4 /Cu-UiO-66-NH 2 exhibits a hydrogen evolution rate of 630.25 μmol g −1 h −1 under visible-light irradiation, demonstrating a remarkable 114-fold enhancement compared to pristine UiO-66-NH 2 . The excellent photocatalytic performance originates from the novel Z-scheme charge transfer mechanism between ZnIn 2 S 4 and Cu-UiO-66-NH 2 , which facilitates efficient charge separation while maintaining strong redox capabilities. Furthermore, the incorporated Cu species serve as highly efficient active sites for hydrogen evolution. This work provides a rational design strategy for constructing Z-scheme heterojunctions, advancing the development of efficient artificial photosynthesis systems for sustainable energy applications.

CAS / MDL: 13746-66-2 13943-58-3
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JOURNAL OF CHROMATOGRAPHY A · 2018 · IF 3.716

Electrospun UiO-66/polyacrylonitrile nanofibers as efficient sorbent for pipette tip solid phase extraction of phytohormones in vegetable samples

Zhiming Yan,Mei Wu,Biqing Hu,Minna Yao,Lan Zhang,Qiaomei Lu,Jie Pang

In this work, metal-organic framework particles incorporated fibers (UiO-66/PAN nanofibers) were used as adsorbent in pipette tip solid phase extraction (PT-SPE) for the first time. The UiO-66/PAN nanofibers were fabricated by a facile electrospinning method and characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction and nitrogen adsorption-desorption experiments. The UiO-66/PAN nanofibers were applied to assemble a novel PT-SPE cartridge for determination of four phytohormones followed by high performance liquid chromatography (HPLC). Several experimental parameters such as kinds of UiO-66/PAN nanofibers, the amount of UiO-66/PAN nanofibers, the effect of solution pH, ionic strength and desorption conditions were intensively investigated. Under the optimal conditions, the linear ranges of the phytohormones were in the range of 0.06–60 ng/mL with correlation coefficients above 0.992. The limits of detection were between 0.01 ng/mL to 0.02 ng/mL. The interday and intraday precision (RSD) for three replicate extractions of the four phytohormones (15 ng/mL for each) was in the range of 1.5–5.6%. The established method was successfully applied for the determination of phytohormones in watermelon and mung bean sprouts samples. The results showed that the electrostatic interaction between the positively charged UiO-66 and anionic forms of phytohormones played an important role in the extraction of the phytohormones.

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MICROCHEMICAL JOURNAL · 2017 · IF 3.034

Preconcentration on metal organic framework UiO-66 for slurry sampling hydride generation-atomic fluorescence spectrometric determination of ultratrace arsenic

Jin Luo,Fujian Xu,Jing Hu,Ping Lin,Jiping Tu,Xi Wu,Xiandeng Hou

In this work, metal organic framework (MOF) UiO-66 with strong stability in water was synthesized and used for the preconcentration of ultratrace arsenic in environment water and the precipitated UiO-66 was converted to slurry for direct determination with hydride generation-atomic fluorescence spectrometry (HG-AFS). Factors affecting the adsorption of arsenic by UiO-66, including pH, adsorption time, stability of UiO-66, masking agents together with the optimum conditions of HG-AFS were investigated in detail. The performance of UiO-66 for adsorbing arsenic was excellent at room temperature over a wide range of pH from 1 to 11, and adsorption efficiencies of >   95% could be achieved within only 5   min. Meanwhile, since conventional digestion process is avoided, the slurry sampling method is fast and convenient with greatly reduced matrix interference. Under the optimum conditions, it shows a good linear relationship between AFS intensities (I) and the concentrations of arsenic (C) (I   =   547C   +   61) with linear correlation coefficients better than 0.99. A precision of 3% (RSD%, n   =   11) at 1   ng/mL and a limit of detection (LOD) of 0.0002   ng/mL were obtained.

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MICROCHEMICAL JOURNAL · 2022 · IF 5.304

UiO-66-NH2: An easily attainable and label-free turn-on probe for facile fluorescence sensing of alkaline phosphatase

Fujian Xu,Jinyi Zhang,Xiaoliang Zeng,Zhou Long,Xiandeng Hou

Alkaline phosphatase (ALP) is now a well acknowledged indicator for diverse clinical diseases correlated with its abnormal expression. Compared to the assays by traditional and lately emerging methods, the fluorescent (FL) sensing, especially in the turn-on mode, has become more favored due to its simplicity, low cost, and high sensitivity and precision. However, the feasible FL probes are still limited and suffering from poor biological compatibility, complex preparation, additional modification or function-alization. Herein, we found that one common metal–organic framework, UiO-66-NH 2 at nanoscale, could act as a new and label-free FL probe for facile sensing of ALP in the turn-on mode, based on the simple aid by phenyl phosphate which could be hydro-lyzed by ALP, with the product of phosphate ion enhancing the FL emission of UiO-66-NH 2 via simple adsorption. Unlike many other FL probes in the turn-on mode, it was unnecessary to quench the FL of the probes in advance, greatly simplifying the sensor design. Moreover, by use of a new method based on dielectric barrier discharge (DBD), the UiO-66-NH 2 could be prepared in 10 min, much shorter than that (usually hours) for preparing most other FL probes for ALP assay. The limit of detection was 0.4 U L -1 , superior or at least rivalrous to the previously reported ones, and the ALP assay was also accomplished for real serum samples, with the analytical results highly consistent with those obtained by the clinical procedures, revealing its high practical utility.

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