ACS Applied Nano Materials
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2022
·
IF 6.14
Sehrish Mehdi,Yanyan Liu,Huijuan Wei,Hao Wen,Ruofan Shen,Zhikun Peng,Huanhuan Zhang,Xianli Wu,Chengming Wang,Shuyan Guan,Tao Liu,Baojun Li
Zeolitic imidazole framework (ZIF-67)-derived Co metal catalysts have gained attention as competitive catalysts due to their high metal loading and superior metal dispersion. However, the problems of Co cluster aggregation during use and difficulty in collection of the powder catalyst from the reaction system need to be solved. In this work, Co-based nanoparticles (NPs) are fabricated on a Ni foam. The monolithic catalyst, Co–NC/NF, has been prepared by the pyrolysis of the ZIF-67/NF precursor using manual coating. The characterization confirms the embedding and uniform distribution of Co NPs (10–20 nm) in the N-doped C matrix. The optimized Co–NC/NF600 reveals satisfactory catalytic activity upon hydrolysis of ammonia borane with a hydrogen evolution (rB = 1176 mL min–1 g–1Co), a turn over frequency (TOF = 180 h–1), and an apparent activation energy (Ea = 64 kJ mol–1). The catalytic activity of Co–NC/NF600 with Co and CoOx as active sites has the best rank among the previously reported Co monolithic catalysts. The superior stability and reusability of the catalyst with ∼ 90% retention after five uses are demonstrated under mild NH3BH3 hydrolysis conditions, originating from the high antiaggregation ability of the active sites and the easy recollection of the catalyst. The adopted novel strategy has the potential to synthesize monolithic catalysts applicable in other fields of heterogeneous catalysis in industrial applications such as energy storage and conversion.
研究领域:
材料科学
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催化
·
能源存储与转换
·
化学工程
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ENVIRONMENTAL RESEARCH
·
2023
·
IF 8.3
Fan Wang,Yueying Zheng,Xinggang Wei,Dawei Lan,Jintao Zhu,Yingjie Chen,Ziquan Wo,Tao Wu
This study designed a composite material with internal synergistic effects among multiple components to achieve highly selective adsorption of Cu (II). Through controlled synthesis, the Fe 3 O 4 /MnO 2 (3 1 0)/ZIF-67 composite was successfully fabricated, leading to significant improvement in adsorption selectivity , capacity, and adsorption rate. The experimental results showed that the composite is of outstanding selectivity in the adsorption of Cu (II), with a partition coefficient K of Cu (II) that was 2.2–5.3 times higher than that of other coexisting ions. Moreover, the composite exhibited a remarkable adsorption capacity of 1261.0 mg g −1 and a fast adsorption rate of 840.7 mg g −1 h −1 at 298 K. Additionally, its magnetic property facilitated easy separation from wastewater, thereby enhancing its potential for commercial applications. The synergetic effect mechanism was analyzed through characterizations and DFT calculations. Furthermore, the recyclability of the composite was investigated, which showed that after seven cycles, the adsorption efficiency remained at 85% of its initial efficiency. It can be concluded that Fe 3 O 4 /MnO 2 (3 1 0)/ZIF-67 has potential to address challenges posed by heavy metal pollution in copperplating effluents.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Jin Zhang,Hanxuan Zeng,Lingjun Bu,Shiqing Zhou,Zhou Shi,Lin Deng
In this study, zero valent copper (Cu 0 ) was incorporated into ZIF-67 to construct Cu 0 and cobalt/nitrogen doped carbonaceous frameworks x -Cu@Co N C y . The obtained Cu@Co N C was employed to activate PMS to degrade naproxen (NPX) in aqueous phase. Influencing factors on NPX degradation were investigated, including mole ratio of Cu/Co, pyrolysis temperature, pH, catalyst dosage, PMS concentration, and coexisting inorganic anions. In the presence of 0.5 mM PMS and 25 mg/L 1:3-Cu@Co N C 900, complete degradation of NPX (50 μM) could be achieved in 20 min within a wide pH range of 3 to 10. The superior catalytic activity of Cu@Co N C 900 for PMS activation was related to the increased surface –OH groups, accelerated electron transfer rate induced by Cu 0 with strong conductivity, formed surface PMS complexes with high oxidation activity, and synergistic effect between Cu and Co. EPR analysis, radical scavenging and probe tests excluded the participation of SO 4 − and OH in NPX degradation. Nonradical pathways of electron transfer from NPX to PMS and 1 O 2 oxidation contributed to the excellent degradation. The 1:3-Cu@Co N C 900 demonstrated a decent degradation performance even after five consecutive recycles with low cobalt and copper ions leaching due to the encapsulation of Co and Cu on N -doped porous carbon. Further, the intermediates of NPX degradation were identified, and three possible degradation pathways were proposed. Overall, this work provides a feasible strategy to improve the stability and catalytic activity of ZIF-67 by the incorporation of Cu 0 .
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MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 10
·1-11
·
IF 5.705
Tang Jing,Jiang Sixun,Liu Yu,Zheng Shengbiao,Bai Lei,Guo Jiahao,Wang Jianfei
A composite was prepared from a Co(II)-based zeolitic imidazolate framework (ZIF-67) and graphene oxide (GO) by an in situ growth method. The material was electrodeposited on a glassy carbon electrode (GCE). The modified GCE was used for the simultaneous voltammetric determination of dopamine (DA) and uric acid (UA), typically at working potentials of 0.11 and 0.25 V (vs. SCE). The morphology and structure of the nanocomposite were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. The modified electrode exhibits excellent electroanalytical performance for DA and UA owing to the synergistic effect of the high electrical conductivity of GO and the porosity of ZIF-67. By applying differential pulse voltammetry, a linear response is found for DA in the 0.2 to 80 μM concentration range, and for UA between 0.8 and 200 μM, with detection limits of 50 and 100 nM (at S/ N = 3), respectively. Further studies were performed on the effect of potential interferents, and on electrode stability and reproducibility. The modified GCE was applied to the simultaneous detection of DA and UA in spiked human urine and gave satisfying recoveries.
Schematic of the preparation procedure of GO-ZIF67 and electrochemical reaction mechanisms of UA and DA at the GO-ZIF67-modified glassy carbon electrode (GCE). GO: graphene oxide; ZIF-67: Co(II)-based zeolitic imidazolate framework.
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MICROCHEMICAL JOURNAL
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2025
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IF 5.1
Jie Cao,Jingge Niu,Yizhuo Pang,Tianshu Luo,Jiayi Peng,Xiaohong Hou
Nitrite is a kind of frequently detected inorganic pollutants in water. In order to sensitively and conveniently monitor the nitrite anytime and anywhere, colorimetric sensing method-based nanoenzymes and portably immediate detection devices become urgent. Herein, we utilized L-arginine as a catalyst and a linker to mediate the synthesis of CeO 2 on bimetallic MOFs (CeO 2 @Mn/ZIF-67), with Co and Mn were set as the central metals. Its enzyme-activated performance ( K m : 0.054 mM and V max : 64.00 μMs −1 ) was superior to most reported materials. Nitrite can diazotize with oxTMB, causing a change in the ratio of absorbance at 652 nm to absorbance at 450 nm (A 652 /A 450 ). Thus, a rapid and sensitive platform for the colourimetric detection of nitrite was established. A portable glass tube hydrogel sensor was designed inspired by the principle of disposable alcohol swabs for the first time to achieve the nitrite monitoring. When the glass tube was cut to introduce TMB and nitrite into the nanoenzymes, a noticeable colour change occurred. Attributed to the high activity of the nanoenzymes and the clever design of the detection device, the proposed method overcame the shortcomings of the traditional sensing methods such as long detection time and poor portability.
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RSC Advances
·
2025
·Vol. 15
·期 58
·49875-49888
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IF 4.6
Yangyi Cai,Xiaocan Liu,Weiye Yang,Hongyan Peng,Lijian Meng,Shihua Zhao
Persistent organic pollutants pose significant long-term risks to environmental and human health due to their carcinogenic, mutagenic, and teratogenic properties. This study focuses on the efficient activation of peroxymonosulfate (PMS) through the rational design of a cobalt-based metal–organic framework (ZIF-67) catalyst, enabling rapid degradation of high-concentration dye pollutants. By optimizing the molar ratio of 2-methylimidazole (2-MeIM) to Co(NO3)2·6H2O and employing a hydrothermal synthesis method, we fabricated ZIF-67 (4 : 1) with high crystallinity, large specific surface area (1656.68 m2 g−1), and stable degradation performance. The ZIF-67 (4 : 1)/PMS system achieved complete degradation of 20 mg L−1 and 100 mg per L Rhodamine B (RhB) within 60 seconds and 6 minutes, respectively, surpassing recent reported efficiencies. The system also maintained high activity over a broad pH range (3–9). Radical quenching experiments and electron paramagnetic resonance (EPR) analysis identified sulfate radicals (˙SO4−4) and singlet oxygen (1O2) as the dominant reactive species. Furthermore, the catalyst exhibited excellent recyclability with no significant loss in activity after five consecutive cycles. This work provides a facile and scalable strategy for preparing highly active cobalt-based catalysts, demonstrating great potential for practical applications in industrial wastewater treatment and environmental remediation.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2023
·
IF 6.2
Xiaofei Wang,Ganfan Zhang,Qian Wang,Yue Li,Shouwu Guo
Transition metal phosphides capture wide attention as electrocatalysts in lithium-sulfur (Li-S) batteries due to their unique electrocatalytic activity, and metal-organic framework (MOF) is well suited as precursor due to the inherent advantages such as structural/morphology diversity, tunable composition and distribution of internal elements. However, the relationship of the fabrication process, the phase and actual catalytic activity have been controversial. Herein, based on a facile morphological engineering of ZIF-67 (a classic MOF), three kinds of cobalt phosphide (polyhedron, cube and flake-like) are fabricated and different from traditional delicate strategies such as adopt surfactant and methanol to fabricate three-dimensional ZIF-67 (polyhedron or cube), two-dimensional flake ZIF-67 can be obtained just in aqueous solution without any agent. Besides, CoP/Co 2 P heterostructure is regularly induced although they are fabricated under the same condition, especially for flake cobalt phosphide. Furthermore, the flake cobalt phosphide exhibits improved redox reaction kinetics of polysulfides than that of other cobalt phosphides. After modifying commercial separator using the obtained flake cobalt phosphide, the Li-S battery exhibits a high initial capacity of 1253.6 mAh g −1 at 0.2 C and 858.7 mAh g −1 at 2 C. Meanwhile, the battery can also deliver a capacity of 1064.2 mAh g −1 even under a high sulfur loading of 4.0 mg cm −2 . Furthermore, a capacity retention can reach 67.1% after 110 cycles. This work emphasizes the importance of morphology design of multifunctional catalysts for high performance Li-S battery.
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FOOD CHEMISTRY
·
2024
·
IF 8.5
Jing Jiang,Min Liu,Dalun Xu,Tao Jiang,Jinjie Zhang
As a hypertoxic natural toxin, the risk of Microcystin-leucine-arginine (MC-LR) residues in Bellamya aeruginosa deserves more attention. Herein, employing the conventional thin-layer chromatography (TLC) technology and a novel surface-enhanced Raman scattering (SERS) substrate, a TLC-SERS chip was fabricated for the purification and quantitative detection of MC-LR in complex samples. The substrate exhibited excellent SERS performance with an enhancement factor of 6.6 × 10 7 , a low detection limit of 2.27 × 10 −9 mM for MC-LR, excellent uniformity and reproducibility, as well as a wide linear range. With the application of TLC, the MC-LR was efficiently purified and the concentration was increased to >3 times. Ultimately, recovery rates fluctuated between 93.28% and 101.66% were obtained from the TLC-SERS chip. On balance, the TLC-SERS chip has a robust capacity for achieving rapid and stable quantitative detection of MC-LR, which promises to improve the efficiency of food safety monitoring.
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FOOD CHEMISTRY
·
2025
·
IF 9.8
Linchun Nie,Jiazhi Xia,Jiawei Liao,Na Liu,Meiling Xu,Dejing Meng,Wenjing Liu,Qingxiang Zhou,Chunmao Chen
In this work, polypyrrole-coated Cu, Ni co-doped ZIF-67 (PPy@CuNi-ZIF-67) was designed and prepared via a facile method. Calcined PPy@CuNi-ZIF-67 exhibited highly efficient oxidase-like activity and possessed excellent capacity to oxidize colorless 3,3′,5,5′-tetramethyl benzidine (TMB) into blue oxidation products (oxTMB) within 4 min. Glutathione (GSH) and sulfur-containing compounds can inhibit its oxidase-like activity. Based on this principle, an effective colorimetric method was developed in combination with a smartphone for efficient, sensitive, and visual detection of GSH. Under optimal conditions, good linearity was achieved in the range of 0.83–33.33 μM, and the visual detection limit was 0.27 μM. Moreover, based on the response difference of different sulfur-containing compounds to different chromogenic substrates, a new array sensor was constructed with three chromogenic substrates. The array sensor was proven to quickly distinguish five sulfur-containing compounds at a concentration as low as 8.3 μM in combination with principal component analysis and hierarchical clustering analysis.
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CARBON
·
2023
·
IF 10.9
Qingfu Ban,Luwei Li,Huimin Liu,Dong Zhou,Yaochen Zheng,Yusheng Qin,Ruizhe Xing,Jie Kong
Hollow engineering is an effective approach to optimize impedance matching and modify magnetic-dielectric synergy for enhanced wave absorption capability, but the composition and microstructure manipulation of metal-organic frameworks (MOFs)-derived absorbers remains a challenge. Herein, a novel and facile polymerization-induced assembly-etching strategy is proposed for the manufacture of wrinkled zeolitic imidazolate framework-67@polypyrrole (ZIF-67@PPy) microcages using ammonium persulfate catalyzed pyrrole polymerization and concomitant acid etching. Then, hollow cobalt@N-doped carbon microcages (Co@NCMs) with distorted carbon shells, rich core-shell heterojunctions , highly dispersive Co nanoparticles , and abundant heterogeneous interfaces are produced via high-temperature pyrolysis process , which eliminates the need for additional templates and etching agents. Moreover, the hollow microcage structure with interior cavities and mesopores provides superior impedance matching and lightweight characteristics to the absorbers. Therefore, the hollow absorbers demonstrate a minimum reflection loss of −50.4 dB and an effective absorption bandwidth (EAB) of 3.85 GHz at 2.7 mm with a 10 wt% filler loading. In general, the polymerization-indued assembly-etching strategy inspires the hollow engineering of MOF derivatives, and facilitates the development of superior electromagnetic wave absorption (EMA) materials.
研究领域:
材料科学
·
电磁材料
·
纳米技术
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MICROCHIMICA ACTA
·
2019
·Vol. 186
·期 9
·1-9
·
IF 5.479
Chen Han,Wu Xingxing,Zhao Rui,Zheng Zhou,Yuan Qunhui,Dong Zhijun,Gan Wei
The integration of derivatives of granular metal-organic frameworks (MOFs) and an electrically conductive carbon substrate is an effective way to circumvent the deficiency of powdered pristine MOFs or MOF-derived carbon in practical application. The authors describe the use of graphite oxide (GO) as a substrate for in-situ assembly with the zeolitic imidazole framework ZIF-67. The GO and ZIF-67 composites were converted, via pyrolysis, into reduced graphite oxide loaded with Co/N-co-doped carbon polyhedrons (ZIF-67C@rGO). By using various amounts of GO, a series of ZIF-67C@rGO- x with different fractions of GO were synthesized and utilized as electrode modifiers for the detection of the antibiotic metronidazole (MNZ). The results revealed that the ZIF-67C@rGO-0.06 display best sensing performance. This is likely to be due to its hierarchically open pores, abundant active sites and good electrical conductivity. The sensor, best operated near a working potential around −0.6 V (vs. SCE), has a linear response in the 0.5 to 1000 μM MNZ concentration range and a 0.05 μM detection limit. The sensor was applied to the analysis of pharmaceutical samples where it showed excellent selectivity, good repeatability and satisfying recoveries.
Schematic representation of preparation and application of ZIF-67C@rGO- x .
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JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2023
·
IF 4.3
Mohammad Nazari Kalojeh,Roghayeh Hassanpour Sabet,Mir Ali Farajzadeh,Mohammad Reza Afshar Mogaddam,Elnaz Marzi Khosrowshahi,Mustafa Tuzen
A dispersive solid phase extraction procedure was established for the extraction of some pesticides from fruit juices and then it was combined with dispersive liquid-liquid microextraction for more enrichment of the analytes. For this purpose, 40 mg of zeolitic imidazolate framework-carbon dot composite was dispersed into the sample solution as the sorbent via vortex agitation. After that, the sorbent was collected by centrifugation and the supernatant was wasted. Then, 1 mL of a water-soluble organic solvent (acetone) was added onto the sorbent as the elution solvent. After desorption of the analytes from the sorbent surface, the eluate was mixed with a water-immiscible organic solvent (1,1,2-trichloro-1,2,2 trifluoroethane) at µL-level (45 µL) and the mixture was quickly injected into 5 mL deionized water. The resulting cloudy mixture was centrifuged and 1 µL of the sedimented phase was injected into a gas chromatography-flame ionization detection system. After the optimization of the method, its validation was evaluated. The data showed that the limits of detection and quantification obtained by this method were in the ranges of 0.22–0.72 and 0.73–2.40 ng mL −1 , respectively. The plotted calibration curves were linear in the range of 0.73–1000 µg L −1 for all analytes. High enrichment factors (375−445), and extraction recoveries (75–89%), and negligible matrices effect were obtained for the investigated analytes by the introduced method. Also, the obtained data showed that all samples were free of the analytes.
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