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Journal of Water Process Engineering · 2022 · IF 7.34

A novel Zr-MOF modified by 4,6-Diamino-2-mercaptopyrimidine for exceptional Hg (II) removal

Xu Chai,Huaqi Dong,Zenggao Zhang,Zhaoyang Qi,Jie Chen,Zhixian Huang,Changshen Ye,Ting Qiu

Due to natural and production activities, mercury contamination has become one of the major environmental problems in the world. Adsorption is one of the important means to solve this problem. However, most of the commercially available adsorbents exhibit relatively low adsorption capacity and slow kinetics. Therefore, a novel 4,6-diamino-2-mercaptopyrimidine-functionalised Zr-based metal-organic framework (UiO-66-DMP) was synthesised in this study. The UiO-66-DMP was characterised through X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry , X-ray photoelectron spectroscopy, Fourier-transform infrared spectrometry, and thermogravimetric analysis . The potential of the UiO-66-DMP as a superior adsorbent for Hg(II) removal and the corresponding mechanisms were evaluated through batch experiments under different conditions and density functional theory calculations. Benefitting from its high specific surface area and multiple adsorption sites, the maximum Hg(II) adsorption capacity achieved in this study was 822.00 mg·g-1, which is the highest Hg(II) adsorption capacity reported to date. In addition, under the interference of Ca(II), Cd(II), Co(II), Mg(II), Mn(II), Ni(II), Cr(III), Cu(II), Zn(II) and other coexisting ions, the UiO-66-DMP could still maintain the high selective adsorption capacity for Hg(II). According to the characterization analysis and DFT calculation results, the adsorption of Hg(II) onto the UiO-66-DMP was dependent on electrostatic and covalent interactions between metal ions and abundant functional groups on the UiO-66-DMP surface.

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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2022 · IF 4.598

A “signal off” aptasensor based on AuNPs/Ni-MOF substrate-free catalyzed for detection Enrofloxacin

Lina Lv,Baozhong Zhang,Panpan Tian,Lingling Xie,Wenhao Wei,Jintao He,Min Lin,Huina Zhu,Hanyu Chen,Baoshan He

In this project, we developed an electrochemical aptamer sensor based on the coordinated catalysis toward thionine (Thi) of nickel metal-organic framework (Ni-MOF) and gold nanoparticles (AuNPs) to sensitively detect the enrofloxacin (ENR), which belonged to a third-generation quinolone antibiotic for treat diseases caused by bacteria. In order to improve the analytical performance of the sensor, Ni-MOF and gold AuNPs, as the substrate material, could increase the load of the aptamer (Apt) and synergistically catalyze thionine (Thi). Therefore, ultrathin sheets of gold triangular nanosheets (AuTNSs) were prepared as signal labeling materials, which were loaded with a large amount of Thi and complementary deoxyribonucleic acid (cDNA). With the help with Ni-MOF and AuNPs catalysis toward Thi, under optimal conditions, the aptasensor exhibited a massive detection range of 1×10 −2 pg·mL −1 to 1×10 3 pg·mL −1 (S/N = 3) and a detection limit of 5.6×10 −3 pg·mL −1 for ENR. Meanwhile, the proposed sensor has a high sensitivity, satisfactory repeatability and long-time stability, and could be well applied to the detection of food samples.

CAS / MDL: 50-81-7 16961-25-4
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Polarization-induced efficient charge separation in an electromagnetic coupling MOF for enhancing CO2 photocatalytic reduction

Tingting Wei,Liyang Wang,Kaihui Mao,Jian Chen,Jun Dai,Zhiyong Zhang,Lizhe Liu,Xinglong Wu

Rapid recombination of photogenerated carriers severely impairs the performance of photocatalysts , while polarization is an effective driving force for increasing the charge separation and hence improving the photocatalytic activity . In this work, a series of magnetoelectric-coupled layered metal–organic framework (MOF) catalysts with different Co-doped contents (denoted as Ni-MOF and Co x Ni 1-x -MOF) are fabricated with different polarities and employed as novel photocatalysts for CO 2 photocatalytic reduction reaction. Our experiments show that the highest charge separation efficiency occurs in the Co 0.1 Ni 0.9 -MOF sample which has a maximal polarization. This Co 0.1 Ni 0.9 -MOF material has a best CO 2 reduction performance of 38.74 μmol g −1 h −1 which is at a high level in the currently reported layered materials. Meanwhile, it is found that a series of Co x Ni 1-x -MOF samples all display selectivity close to 100% for CO 2 reduction to CO, which is desirable for industrial applications. Theoretical analysis shows that Co doping alters the degree of distortion of the asymmetrical Ni-centered octahedron {NiN 2 O 4 } in Ni-MOF by replacing Ni due to the magnetoelectric coupling effect and Jahn-Teller effect, which results in adjustable polarity of Co x Ni 1-x -MOF. This work provides new insights on how to improve photogenerated charge separation in MOF by enhancing polarization.

CAS / MDL: 920-66-1
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MICROCHEMICAL JOURNAL · 2022 · IF 5.304

Two-dimensional MoS2/Mn-MOF/multi-walled carbon nanotubes composite material for high-performance supercapacitors

Wenhao Peng,Ningning Song,Zilong Su,Jiajun Wang,Kaixuan Chen,Shuji Li,Bingyan Wei,Shiping Luo,Aijuan Xie

A series of MoS 2 and Mn metal organic frameworks (Mn-MOF) were synthesized by hydrothermal method, and then MoS 2 , Mn-MOF and multi-walled carbon nanotubes (MWCNT) were mixed in different mass ratios and applied for supercapacitor. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge (GCD) are used to investigate the electrochemical performance of MoS 2 /Mn-MOF/MWCNT materials with different mass ratios. The experimental results show that when the mass ratio of m(MoS 2 ): m(Mn-MOF): m(MWCNT) is 1:4:1, the electrochemical performance of the MoS 2 /Mn-MOF/MWCNT composite is the best. The specific capacitance of optimal MoS 2 /Mn-MOF/MWCNT (1:4:1) reaches 862.73F g −1 , which is noticeable higher than that of MoS 2 (42.29F g −1 ), Mn-MOF (70.23F g −1 ) and MWCNT (347.27F g −1 ) materials. Moreover, the EIS test manifests that the MoS 2 /Mn-MOF/MWCNT (1:4:1) composite has a lower R ct value (2.566 Ω). Therefore, MoS 2 /Mn-MOF/MWCNT (1:4:1) has the best electrochemical performance among the all as-fabricated supercapacitor materials. This research provides an effective method for the development of Mn-based supercapacitor materials and improves the capacitance performance of MOFs materials.

CAS / MDL: 308068-56-6 62-55-5
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2022 · IF 10.319

Catalytic effect of MOF-derived transition metal catalyst FeCoS@C on hydrogen storage of magnesium

Yaokun Fu,Lu Zhang,Yuan Li,Sanyang Guo,Zhichao Yu,Wenfeng Wang,Kailiang Ren,Qiuming Peng,Shumin Han

The introduction of the heterogeneous catalysts with high activity can significantly improve hydrogen storage performance of MgH 2 , therefore, in this paper, we synthesize a carbon-supported transition metal compound, FeCoS@C derivative from ZIF-67, by utilizing the in situ formed C dispersive multiphase Mg 2 Co, α-Fe, Co 3 Fe 7 , and MgS to implement catalysis to MgH 2 . Noteworthily, MgH 2 -FeCoS@C rapidly absorbs 6.78 wt% H 2 within 60 s at 573 K and can also absorb 4.56 wt% H 2 in 900 s at 473 K. Besides, the addition of FeCoS@C results in decreasing of the initial dehydrogenation temperatures of MgH 2 from 620 to 550 K. The dehydrogenation activation energy of MgH 2 decreases from 160.7 to 91.9 kJ mol –1 . Studies show that the Mg 2 Co, α-Fe, and Co 3 Fe 7 act as “hydrogen channels” to accelerate hydrogen transfer due to the presence of transition metals, and MgS with excellent catalytic effect formed from MgH 2 -FeCoS@C provides a strong and stable catalytic effect. Besides, the carbon skeleton obtained by the carbonization of ZIF-67 not only serves as a dispersion for the multiphase catalytic system, but also provides more active sites for the catalysts. Our study shows that the multiphase and multiscale catalytic system provides an effective strategy for improving the hydrogen storage performance of MgH 2 .

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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Facile fabrication of 2D MOF-Based membrane with hierarchical structures for ultrafast Oil-Water separation

Xuan-Ting He,Bo-Yu Li,Jia-Xiang Liu,Wen-Quan Tao,Zhuo Li

The surface chemical composition and building unit structures of membrane are the key factors to realize highly-efficient oil–water separation. Here we report the synthesis of Cu-CAT-1 metal–organic frameworks (MOFs) with unique two-dimensional (2D) hierarchical structures grown directly on copper mesh (Cu-CAT-1@CM) for oil–water separation. The Cu-CAT-1@CM membrane with micro/nano- architecture exhibits robust superhydrophilicity and underwater superoleophobicity characteristics, allowing gravity-driven oil–water separation by achieving ultrahigh flux up to 329 kL∙m −2 ∙h −1 . The membrane shows excellent separation performances by testing various oils, particularly actual crude oil and xylene, which are considered as the notorious pollutants in the water. The residual oil contents of six samples are all less than 24.6 mg∙L -1 . The mechanism analysis demonstrated that the appropriate hierarchical structures of the membrane surface is the code for the extreme wettability that remarkably improved the separation efficiency. Moreover, such a membrane with high performance can be readily synthesized by electrochemical method at room temperature in only 20 min, which shows the advantages of facile and environmentally friendly fabrication process as well as low cost. Overall, the membrane with energy-saving of gravity-driven and ultra-high permeability allows the rapid separation of oil–water mixture, showing the potential applications for resolving the problem of oil pollution.

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RSC Advances · 2022 ·Vol. 12 ·期 23 ·14707-14715 · IF 4.036

Construction and evaluation of detachable bone-targeting MOF carriers for the delivery of proteasome inhibitors

Hongbing Yang,Zhenyan Yu,Shuaishuai Ji,Jie Yan,Lei Han,Yang Liu,Yanjuan Wang,Yimin Niu,Qiang Huo,Ming Xu

Tumor bone metastasis is an important cause of tumor recurrence and death. Although bone-targeting nanoparticles decorated with targeting ligands have shown good affinity for bone tissues with the properties of adhesion to the bone matrix, it is not easy to detach from the surface of the bone matrix in the tumor-bone microenvironment, attributed to the robust coordination force between the targeting ligands, such as bisphosphates with bone-deposited calcium. This may hinder the transport of nanoparticles from bone tissue to bone metastatic tumors. In this research, we designed a bone-targeting nanocarrier with detachable bone-targeting character for the therapy of bone metastases. The nanoparticles were constructed by using ZIF-8 and bone-targeting and MMP enzyme sensitive polypeptide-modified hyaluronic acid as a carrier and proteasome inhibitor Bortezomib (BTZ) as cargo. The results show that the constructed D8-M3-HA-ZIF8@BTZ nanoparticles possessed several favorable properties such as good colloidal stability, acid-sensitive drug release, D8 peptide mediated bone targeting and MMP enzyme-responsive desorption. Besides, nanoparticle endocytosis and cytotoxicity were enhanced through HA-mediated targeting to CD44 over-expressing tumor cells. Altogether, this study provides a potential cascade targeting strategy for improving the delivery effects of bone targeted nanoparticles for the delivery of proteasome inhibitors.

CAS / MDL: 1469277-96-0
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Peroxydisulfate activation by 2D MOF-derived Ni/Fe3O4 nanoparticles decorated in 3D graphene oxide network

Minjun Liu,Ying Liu,Xinru Liu,Chengcheng Chu,Ducheng Yao,Shun Mao

Metal organic framework (MOF)-derived materials normally have three-dimensional (3D) structure, while little attention has been paid to two-dimensional (2D) MOF-derived materials with high catalytic activity. Nevertheless, the underlying agglomeration and metal leaching issues of 2D MOF-derived catalysts hinder their real applications. In this work, we report a bimetallic nanocomposite (Ni-Fe-C-600-acid/GO) derived from 2D Ni-Fe-MOF and graphene oxide (GO) network. Employing Ni(0) and Fe 3 O 4 as active site, the Ni-Fe-C-600-acid/GO shows high efficiency in peroxydisulfate (PDS) activation for the removal of p-chloroaniline (PCA), and the catalyst/PCA dosage ratio (0.8) is substantially lower than those of the previous studies (3.9–156.9). The prepared catalysts demonstrate high catalytic activity over a wide pH range of 3–9 and maintain high efficiency after five cycles with good tolerance to inorganic anions. The singlet oxygen is identified as the predominant active species and relatively weak contributions from sulfate free radicals and hydroxyl radicals are confirmed. This catalysis system presents new insights in 2D MOF-derived catalysts in advanced oxidation processes .

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JOURNAL OF HAZARDOUS MATERIALS · 2022 · IF 14.224

Novel colorimetric aptasensor based on MOF-derived materials and its applications for organophosphorus pesticides determination

Zheng Shen,Deyan Xu,Guangxian Wang,Lingjun Geng,Rui Xu,Guanjie Wang,Yemin Guo,Xia Sun

For the visual detection of four organophosphorus pesticides (OPs), a colorimetric aptasensor was developed based on aptamer-mediated bimetallic metal-organic frameworks (MOFs) nano-polymers. Fe-Co magnetic nanoparticles (MNPs) and Fe-N-C nanozymes were prepared based on pyrolytic reaction, and were labeled with broad spectrum aptamers and complementary chains of organophosphorus pesticides respectively. The hybridization of aptamers and complementary chains led to the formation of nano-polymers. In the presence of target pesticides, they competed with complementary chains for aptamers on Fe-Co MNPs, resulting in a large number of Fe-N-C nanozymes signal labels being released into the supernatant. Fe-N-C nanozymes showed similar activity to peroxidase and catalyzed the 3,3′,5,5′-tetramethylbenzidine-hydrogen peroxide (TMB-H 2 O 2 ) color system to turn the solution blue-green under mild conditions. The magnetic probes had good selectivity and sensitivity, and were easily separated by magnetic absorption . The sensor functioned well under optimal conditions, demonstrating good stability and specificity for four pesticides: phorate, profenofos , isocarbophos and omethoate, and the detection limits of four pesticides were as low as 0.16 ng/mL, 0.16 ng/mL, 0.03 ng/mL and 1.6 ng/mL respectively, and the recovery rate of OPs residue in vegetable samples was satisfactory. The work described here provided a simple, rapid and sensitive way to construct a biosensor .

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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Synergistic interface-pillared Fe-MOF on 2D Ti3C2TX MXene electrode coupling toward high energy density

Bingzhe Jia,Huailin Yang,Lei Wang,Zhiqi Zhao,Xinming Wu

Compared with most transition metal based electrode materials, 2D M n+1 X n T x has high conductivity and good solvent compatibility. However, its low energy density hinders its application as supercapacitior electrode for electrochemical energy storage applications. Herein, the interface-pillared of Fe-MOF (MIL-100(Fe)) onto Ti 3 C 2 T x MXene layer, which provide rich electrochemical active sites, is achieved, and the MOF nanospheres with MXene nanosheets are subsequently converser into three dimensional multilayer porous nanostructures through the chemical bond couping. Therefore, the MOF nanospheres are anchored between the nansheets of MXene, enabling the fast ion transportation in the three dimensional nanostructures. Menanwhile, the MOF nanospheres prevent the aggregation of MXene nanosheets, and the laminar structure is maintained for more redox reaction sites within the hybrid electrodes through fast charge–discharge cycles. As a result, the MIL-100(Fe)/Ti 3 C 2 T x MXene electrode displays superior energy density (85.53 Wh kg −1 ), which is much higher than the other MXene-based electrodes as far as we know. This design strategy of 2D hybrid electrodes opens up a new way for the commercial application of high perfermance supercapacitor.

CAS / MDL: 554-95-0
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ChemSusChem · 2022 ·Vol. 15 ·期 19 ·e202201386 · IF 9.14

MOF-Incorporated Binuclear N-Heterocyclic Carbene-Cobalt Catalyst for Efficient Conversion of CO2 to Formamides

Zhenzhen Zhou,Xiao Liu,Jian-Gong Ma,Peng Cheng

Graphical It's a trap ! Through a new “ligand-in-dimer-trap” strategy, the host–guest composites featuring metal–organic framework-encapsulated binuclear NHC−Co complex ( Co 2 @MOF) is prepared and used as a double-sites catalyst, which combines and surpasses the advantages of homo- and heterogeneous catalysis and exhibits prime performance in converting CO 2 into widely used formamides under ambient conditions. Environmental problem caused by carbon emission is of widespread concern. Involving CO 2 as C 1 resource into chemical synthesis is one of the most attractive ways for carbon recycling. Herein, the first example of host–guest composites featuring metal–organic framework (MOF)-encapsulated binuclear N-heterocyclic carbene (NHC) complex, Co 2 @MIL101, was developed with the molecularly dispersed [Co(IPr)Br] 2 (μ-Br) 2 ( Co 2 ) loading in the cage of MIL-101(Cr) via a “ligand-in-dimer-trap” strategy, which was comprehensively investigated through various techniques including synchrotron X-ray absorption, electron microscopy, X-ray diffraction, solid-state nuclear magnetic resonance spectroscopy, and others. The noble-metal-free double-sites catalyst Co 2 @MIL101 exhibited promising stability, activity, efficiency, reusability, and substrate adaptability for converting CO 2 into various formamides with amines and hydrosilanes and achieved the best performance for one of the most useful formamides, N -methyl- N -phenylformamide (MFA), among the recyclable catalysts at ambient conditions, providing a reliable approach to successfully unify the advantages of both homo- and heterogeneous catalysts. Density functional theory calculations were applied to illustrate the superior activity of the binuclear NHC complex center as double-sites catalyst toward the activation of CO 2 .

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ANALYST · 2021 ·Vol. 147 ·期 2 ·282-292 · IF 4.616

MOF-assisted antifouling material: application in rapid determination of TB gene in whole-serum specimens

Chenhui Wu,Yunkang Ma,Yingxia Zhou,Wenjie Yang,Lihua Chen

Biofouling is a nuisance in the practical applications of biosensors, which seriously affects the reliability and accuracy of detection. The utilization of antifouling interface materials is a promising option for mitigating biofouling. Only highly accumulated antifouling polymeric surfaces tend to offer “zero” nonspecific protein adsorption. Herein, superior antifouling coatings based on chondroitin sulfate (CS) were prepared by the NH2-MIL-53 (Al) assisted strategy. This is a novel design to improve the antifouling property of material by taking advantage of the high specific surface area of the three-dimensional MOF to increase the accumulation degree of antifouling functional groups per unit area. And the related chemical technology is simple and easy to operate. As expected, this novel CS-loaded MOF demonstrated an excellent antifouling performance in various biological samples, even in 100% goat serum. Only 8.48% changes of differential pulse voltammetry (DPV) were found. Furthermore, this antifouling interface material is successfully applied for the specific detection of the tuberculosis (TB) gene in undiluted biofluids. This developed TB biosensor showed a high analytical performance with a wide linear range (1.00 × 10−16 M to 1.00 × 10−11 M) and a low detection limit, indicating that it may open new avenues for direct biosensing of disease markers for clinical samples.

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