DALTON TRANSACTIONS
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2023
·Vol. 52
·期 42
·15447-15455
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IF 4
Xianliang Li,Diwei Deng,Lufang He,Yan Xu
Exploration of credible non-enzymatic glucose sensors with high selectivity and sensitivity is of great significance for early clinical monitoring of glucose concentration and preventing the threat of diabetes to human health. Here, mesoporous carbon (MC) sphere immobilized Co-MOF-74 nanorods (NRs), denoted as Co-MOF-74 NRs/MC, were successfully prepared, in which the nanostructural porous carbon sphere was obtained using cobalt glycolate as the built-in template followed by a subsequent carbonization and acid treatment, and the MC spheres were then in situ deposited on the surface of Co-MOF-74 NRs via a solvothermal method. Benefiting from the good conductivity of the grafted porous carbon spheres and the abundant active sites, as well as the permeability of microporous MOF-74 nanocrystals, the Co-MOF-74 NRs/MC modified glassy carbon electrode (GCE) exhibited effective non-enzymatic glucose sensing performance with a fast response time (less than 3 s) and a glucose sensitivity of 98.0 μA cm−2 mM−1. Furthermore, the Co-MOF-74 NRs/MC/GCE showed a favourable anti-interference capability in the presence of various interferents and good long-term reusability. The applicability of Co-MOF-74 NRs/MC/GCE for glucose sensing in real serum samples was also investigated, verifying the applicability of the electrode for targeted glucose monitoring in practical applications.
研究领域:
生物医学工程
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材料科学
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DOI
PubMed
高影响因子
CARBOHYDRATE POLYMERS
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2021
·
IF 9.381
Chen Hou,Linhui Fu,Yang Wang,Wenqiang Chen,Fang Chen,Sufeng Zhang,Jianzhi Wang
Smart nanomaterials that can simultaneously detect and eliminate contaminants in water environment are significant for health protection. To achieve such goal, Co-MOF-74 was in-situ assembled on regenerated cellulose membranes followed by calcination process, thus achieving dual-functional Co 3 O 4 /cellulose derivative membrane (Co 3 O 4 /CDM) catalyst. The Co 3 O 4 morphology was readily controlled by further recrystallization of the deposited MOF precursor. Combining the high enrichment ability of cellulose membrane and outstanding peroxidase-active of Co 3 O 4 , the fast color reaction for phenol was accomplished within 10 min by Co 3 O 4 /CDM with the assistance of H 2 O 2 and 4-aminoantipyrine (4-AAP). Moreover, the Co 3 O 4 /CDM also portrayed an excellent degradation property for phenol elimination via sulfate radical-advanced oxidation processes (SR-AOPs). The degradation efficiency of phenol reached 93% in 20 min, and the possible mineralization mechanism was proposed based on the XPS and LC-MS analysis. Thus, Co-MOF-74 derived Co 3 O 4 /CDM shows excellent properties in aiding the colorimetric detection and degradation of phenol in aqueous solutions.
研究领域:
环境科学
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材料科学
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DOI
PubMed
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
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2021
·
IF 5.455
Xiaowu Liang,Pengfei Wang,Congli Li,Min Yuan,Qi Shi,Jinxiang Dong
CO is an important raw material and the separation of CO/N 2 in blast furnace gas can supply an abundant source of CO. Metal organic frameworks (MOFs) containing open metal sites are capable of selectively binding to CO over N 2 . However, the open metal sites easily bind to guest molecules during the preparation and activation process. In this study, typical MOFs containing open metal sites (Co-MOF-74) were used to investigate the activation behavior and corresponding CO/N 2 adsorptive separation performance. To characterize the removal and decomposition of guest molecules, TG-MS and NMR analysis of MOF-74 prepared under different activation conditions were performed. During the heat and vacuum process, the guest H 2 O and methanol (MeOH) molecules in Co-MOF-74 were first removed at 150 °C under vacuum. The aim of high temperature activation at 300 °C is the decomposition of a small amount of bind N,N-dimethylformamide (DMF) and terminal ligands occupying the open metal sites in Co-MOF-74. In addition, H 2 O molecules occupy the open metal sites of Co-MOF-74 during the filtration and MeOH wash steps under air, which is accompanied by the removal of a portion of DMF. The CO adsorption (298 K and 1 bar) and the CO/N 2 selectivity (Ideal adsorbed solution theory: 50:50, v/v) of Co-MOF-74 activated at 300 °C was 6.07 mmol/g and 384, respectively, which was higher than that of the other activated Co-MOF-74 samples and was attributed to the effective removal of guest molecules. Our results may guide the activation of MOFs, which contain open metal sites.
研究领域:
材料科学
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化学工程
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DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
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2019
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IF 6.393
Ya Xiong,Xiao Chang,Xurong Qiao,Kun Li,Lei Zhu,Fujun Xia,Xiaofang Li,Qingbin Zheng,Wei Xing,Qingzhong Xue
For the first time, Co-MOF-74 derived Co 3 O 4 /graphene heterojunction nanoscrolls (Co 3 O 4 /GNS) structure is synthesized by a simple one-step hydrothermal strategy and subsequent calcination process. Theoretically, the growth mechanism of Co 3 O 4 /GNS is revealed by molecular dynamic simulation, demonstrating that a high loading of Co-MOF-74 nanoparticles is needed for effective rolling of GO. The sensor based on Co 3 O 4 /GNS exhibits high response of 58.1 (34-fold enhancement compared with that of Co 3 O 4 ), short response/recovery time of 12 s/66 s (157 s/200 s for Co 3 O 4 ) toward 1 ppm acetone at 190 °C and superior selectivity, which are much better than those of most reported acetone sensors. Moreover, the Co 3 O 4 /GNS can even detect as low as 50 ppb acetone with a notable response (1.24). The appreciable response together with rapid response/recovery of Co 3 O 4 /GNS is attributed to the large heterojunction interface between Co 3 O 4 and graphene nanoscroll and high-speed gas transfer pathways provided by nanoscroll. This unique structure design is believed to offer guidance for generalizable synthesis of metal oxide/GNS that can be effectively applied in the fields of ppb-level gas detection.
研究领域:
材料科学
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化学传感器
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纳米技术
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
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2023
·Vol. 47
·期 18
·8507-8514
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IF 3.3
Jianxia Gu,Jingting He,Haiyan Zheng,Chunyi Sun
The novel composite electrocatalysts [Mo3S13]2−/Co-MOF-74 have been successfully prepared by using a simple solvothermal method. The morphology of composite catalysts can be effectively controlled by regulating the amount of [Mo3S13]2− because the addition of [Mo3S13]2 can affect the nucleation rate of Co-MOF-74. After the optimization, [Mo3S13]2−/Co-MOF-74 with spindle-like morphology displays remarkable OER electrocatalytic activity with a low overpotential (368 mV) to afford the current density of 10 mA cm−2 and a small Tafel slope of 90.6 mV dec−1, which is almost on a par with IrO2/C (358 mV, 89.1 mV dec−1). Besides, this composite catalyst can continuously work for about 17 h with almost negligible attenuation in current density. Such an excellent electrocatalytic OER performance of [Mo3S13]2−/Co-MOF-74 benefits from the good morphology obtained by the introduction of a moderate amount of [Mo3S13]2− as well as the synergistic effect between the [Mo3S13]2− and Co-MOF-74. This work provides new insight into the development of MOF-based electrocatalysts for the OER.
研究领域:
材料科学
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电化学
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DOI
高影响因子
Nano Hybrids and Composites
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2022
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IF 0
Yue Zhang,Tao Li,Shi Yu Tang,Xin Yue Xie,Ru Zeng Liang,Xiao Xiao Chu
Increasing demands of microwave absorbents require new approaches to enhance the absorbing performance. Metal−organic frameworks (MOFs) could be developed as effective absorbers owing to their outstanding features including intrinsic porosity and high specific area. Herein, novel nanostructured Co-MOF-74 composites have been successfully fabricated via a simple solvothermal method. Excellent absorption performance was achieved for the composite with a minimum reflection loss (RL) of −25.5 dB at 2.5 mm and a broad absorption bandwidth (RL < −10 dB) of 6.7 GHz. Such absorber could be developed as lightweight and high-efficiency absorbing materials, and this work provides inspiration for the design of advanced absorbers with strong dissipation capacity and broad effective bandwidth.
研究领域:
材料科学
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电磁工程
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纳米技术
✓ 已验证
DOI
ANALYTICA CHIMICA ACTA
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2023
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IF 6.2
Yuheng Lu,Chenghui Li,Yunfei Tian,Jing Hu,Xiandeng Hou
The determination of trace tellurium in real samples with complicated matrix can be rather challenging due to the low abundance and interferences. Herein, we report a new method for the highly sensitive detection of Te(IV) by photochemical vapor generation-atomic fluorescence spectrometry (PVG-AFS), utilizing Co-MOF-74 as an adsorbent and a precursor of Co 2+ ion sensitizer for preconcentration and enhanced PVG efficiency. The synthesized Co-MOF-74 can completely adsorb Te(IV) within 10 min in a wide pH range. Following filtration and re-suspension in a dilute solution of formic and acetic acid, the adsorbed Te(IV) was converted to volatile compounds under the UV irradiation and swept to AFS for detection. A limit of detection of 0.08 ng/mL for Te(IV) was obtained after a 50-fold preconcentration. The proposed method was used for analysis of various natural water samples for trace Te(IV), with satisfactory spike recoveries achieved.
研究领域:
分析化学
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环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
POLYHEDRON
·
2024
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IF 2.4
Meng Zhao,Yun Yang,Xue-Song Gu,Lanlan Sun
The separation and purification of light hydrocarbons are performed by energy-intensive distillation processes. Microporous metal–organic framework based absorbents acting as alternative technology gains focus. Open metals sites (OMSs) enriched MOF-74 show great potential in light hydrocarbons but its separation selectivity is low and difficult to regenerate. To address this issue, we introduced N -donor ligands into open sites of Co-MOF-74 by post modification. Structure was determined by powder X-ray diffraction, element analysis, infrared spectroscopy and thermogravimetric analyses. As-synthesized modified Co-MOF-74 display potential in C 2 H 4 /C 2 H 6 , C 3 H 6 /C 3 H 8 , C 3 H 8 /CH 4 and C 2 H 6 /CH 4 separation for N -donor ligands placeholder.
研究领域:
材料科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2023
·
IF 9.9
Yi-Shan Ouyang,Qing-Yuan Yang
Photocatalyst systems generally consist of catalysts and cocatalysts to realize light capture, charge carrier migration, and surface redox reactions. Developing a single photocatalyst that performs all functions while minimizing efficiency loss is extremely challenging. Herein, rod-shaped photocatalysts Co 3 O 4 /CoO/Co 2 P are designed and prepared using Co-MOF-74 as a template, which displays an outstanding H 2 generation rate of 6.00 mmol·g −1 ·h −1 when exposed to visible light irradiation. It is 12.8 times higher than pure Co 3 O 4 . Under light excitation, the photoinduced electrons migrate from the catalysts of Co 3 O 4 and CoO to the cocatalyst Co 2 P. The trapped electrons can subsequently undergo a reduction reaction to produce H 2 on the surface. Density functional theory calculations and spectroscopic measurements reveal that enhanced performance results from the extended lifetime of photogenerated carriers and higher charge transfer efficiency. The ingenious structure and interface design presented in this study may guide the general synthesis of metal oxide/metal phosphide homometallic composites for photocatalysis.
研究领域:
材料科学
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能源化学
✓ 已验证
DOI
PubMed
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2026
·
IF 4.1
Wang Ying,Yan Yiting,Zhang Jun,Yang Lin,Liu Fanghua,Tan Chao,Jiang Xue
p-Benzoquinone (PBQ), as a key toxic derivative of benzene, is widely present in industrial wastewater and the production and manufacturing of daily chemicals. Long-term exposure poses a serious health threat, making the development of rapid and sensitive on-site detection technologies highly significant. Electrochemical methods, due to their simple operation, high sensitivity, and ease of miniaturization, are an ideal approach for detecting PBQ. Co-MOF-74 is extensively used in the electrochemical field because of its structural stability, tunable metal nodes, and large surface area, but its low conductivity limits further applications. In this study, Co-MOF-74 was rapidly synthesized using dielectric barrier discharge (DBD) microplasma technology, and then the large π-conjugated organic ligand HATP was introduced for ligand engineering to successfully prepare Co-MOF-74-HATP. This synthesis strategy is not only efficient, but also the introduction of HATP effectively regulates the material’s electronic structure, significantly enhancing its conductivity and electrocatalytic activity. The electrochemical sensor employs chronoamperometric detection at −0.15 V (vs. Ag/AgCl) and exhibits excellent performance for PBQ, featuring two wide linear ranges (17–1602 µM and 1602–5602 µM) with corresponding sensitivities of 1440 µA·mM −1 ·cm −2 and 497.8 µA·mM −1 ·cm −2 , a low limit of detection (LOD) of 3.43 µM ( S / N = 3), and good reproducibility (RSD < 3.0%). It was successfully applied to the detection of PBQ in actual water samples with recoveries ranging from 90.5% to 102.32%. This work expands the synthesis of ligand-functionalized MOFs through DBD microplasma technology and applies them to the electrochemical detection of PBQ in water samples. Graphical abstract
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高影响因子