JOURNAL OF CHEMICAL SCIENCES
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2020
·Vol. 132
·期 1
·1-10
·
IF 1.406
Huang Kai,Yu Sibing,Li Xiaoxin,Cai Zhenyu
Abstract A series of novel bimetallic organic framework materials (Cu x -Co y -MOF) have been successfully prepared by a simple one-pot synthetic method, and their characters were evaluated via means of various techniques. The tested data showed a series of Cu x -Co y -MOFs displayed good crystallinity and the doping of Co in original Cu-based framework would not change the morphology of the MOF catalysts. The catalytic activity of prepared materials was tested in the catalytic oxidation of styrene in the presence of TBHP. The effects of reaction time, reaction temperature and other reaction conditions on catalytic performance were systematically studied. The results revealed that the introduction of Co can improve the selectivity to form epoxides and reduce the yield of benzaldehyde without affecting the conversion rate of catalytic oxidation reaction of styrene. Excitingly, the Cu 0.25 -Co 0.75 -MOF showed better catalytic performance than Cu-MOF and Co-MOF under the optimal reaction conditions, the conversion rate of styrene reached 97.81%, and styrene oxide selectivity reached 83.04%, which indicated a significant synergistic effect of the Cu/Co bimetallic MOF. Furthermore, the Cu 0.25 -Co 0.75 -MOF catalyst exhibited good reusability that could be reused at least four times without significant inactivation. Graphic abstract A series of novel bimetallic organic framework materials (Cu x -Co y -MOF) have been successfully prepared via a simple one-pot synthetic method, and they exhibited high activity and selectivity as catalyst towards for oxidation of styrene.
研究领域:
化学
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材料科学
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催化反应
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DOI
高影响因子
MICROCHIMICA ACTA
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2020
·Vol. 187
·期 9
·1-9
·
IF 6.232
Wang Meng,Wang Jingjing,Wang Kangkang,Chen Tingxiang,Wang Jide
A novel magnetic porous carbon with a high specific surface and magnetization saturation, derived from a Zn/Co-MOF-5, was fabricated by direct carbonization of Zn/Co-MOF-5 without the need of additional carbon precursors under optimum pyrolysis temperature. The material was employed as an adsorbent for magnetic solid-phase extraction of four carbamates from water and tomato samples prior to high-performance liquid chromatography–tandem quadrupole mass spectrometry analysis. Under optimum conditions, the method displayed good linearity ( r > 0.9987) within the concentration range 0.05–20 ng mL −1 for water samples and 0.1–40 ng g −1 for tomato samples. The limits of detection (S/ N = 3) for the four carbamate pesticides were in the range 0.0006–0.013 ng mL −1 for water samples and 0.001–0.01 ng g −1 for tomato samples and satisfactory spiked recoveries in the range 86.1 to 109.1% were obtained with the relative standard deviation values from 2.1 to 14.0%.
Graphical abstract
研究领域:
分析化学
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环境科学
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DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2025
·
IF 13.2
Wei Wang,Jianguo Si,Liguo Yue,Weicai Zhang,Qingqing Chen,Haoliang Huang,Fei Lin,Yang Zhao,Sheng Meng,Lifeng Liu
The shuttle effect and sluggish redox kinetics of lithium polysulfides (LiPSs) are generally regarded as main obstacles to practical applications of the promising high energy density lithium-sulfur batteries (LSBs). Using electrocatalysts to expedite LiPSs conversion during charge/discharge has recently become an effective approach to improving LSB performance, but developing highly efficient catalysts active for bidirectional LiPSs conversion both involving multiple electron transfer steps remains a great challenge. Herein, we report the synthesis of a new composite electrocatalyst consisting of bimetallic nickel/cobalt metal–organic frameworks (Ni/Co-MOF) anchored on highly dispersed amino-modified MXene (Ti 3 C 2 -NH 2 , i.e., TCN) supports through a simple one-step hydrothermal method. Density functional theory (DFT) calculations demonstrate that incorporating both Ni and Co species into MOF results in significant electronic coupling effect, making the d-band centers of Ni and Co sites in Ni/Co-MOF@TCN become comparable and the composite catalyst shows similar adsorption and dissociation capability toward LiPSs. Such a synergy between Ni and Co sites has been validated by comprehensive experimental characterization, which confirms that Ni/Co-MOF@TCN has moderate binding strength for LiPSs adsorption/dissociation, so that both Ni and Co can effectively boost the kinetics and thermodynamics of the bidirectional conversion of LiPSs. Consequently, LSBs containing Ni/Co-MOF@TCN as sulfur hosts exhibit a high specific capacity of 1465 mAh g −1 at 0.1 C and excellent stability at 1 C for 600 cycles with a low decay rate of 0.052 % per cycle. Even with a high sulfur loading of 6.8 mg cm −2 and a low electrolyte/sulfur (E/S) ratio of only 5 μL mg −1 , the Ni/Co-MOF@TCN-containing LSBs can still deliver an initial areal capacity of 6.81 mAh cm −2 at 0.1 C. Moreover, Ni/Co-MOF@TCN also shows outstanding performance in single-layer Li-S pouch cells.
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
SENSORS AND ACTUATORS B-CHEMICAL
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2025
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IF 7.7
Meng Tian,Baijing Li,Jianbo Sun
Triethylamine (TEA) finds extensive and critical applications across diverse domains including industrial manufacturing, pharmaceutical research and development, and agricultural cultivation. However, owing to its hazardous attributes such as toxicity and flammability, the detection of TEA has emerged as a pivotal step in safeguarding personal safety, mitigating environmental pollution, and elevating food safety standards. In the present study, Fe-doped cobalt-based metal-organic framework (MOF)-derived nanomaterials were successfully synthesized via a facile and efficient hydrothermal approach. Gas-sensing measurements reveal that the 5 at% Fe-doped Co 3 O 4 exhibits optimal performance, featuring an optimal operating temperature of 220°C and a response value sixfold that of the pure Co 3 O 4 sensor (21). Notably, the 5 at% Fe-doped Co 3 O 4 demonstrates rapid response and recovery time (32 s/34 s). Utilizing characterization techniques such as XPS and Fe-doped infrared spectroscopy for intermediate analysis, this work investigates the mechanism by which doping-induced charge transfer effects modulate the gas-sensing properties of the materials. Fe doping significantly enhances the gas-sensing activity, selectivity, and stability of cobalt-based MOF-derived materials by tailoring their local electronic structures. This discovery provides valuable theoretical underpinnings and experimental insights for the design of high-performance TEA gas sensors.
研究领域:
材料科学
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传感器技术
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纳米材料
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环境监测
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食品安全
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产品关联
DOI
高影响因子
DALTON TRANSACTIONS
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2025
·
IF 3.3
Xuan Yang,Zesen Yu,Hedong Jiang,Huanhuan Guo,Jian Sun,Jiake Li,Hua Zhu,Yanxiang Wang,Pingchun Guo
Metal–organic frameworks (MOFs) are promising candidates for thermochromic materials. In this study, a hydrogen-bonded 3D porous metal–organic framework, Co-BTC (Co3(BTC)2·12H2O, BTC = 1,3,5-benzenetricarboxylate), exhibited a pink color at room temperature, attributed to the d–d transition of Co2+ ions within the framework, and displayed reversible thermochromic behavior due to alterations in the coordination environment of Co2+ ions. Additionally, Co-BTC/PVB thermochromic film was successfully designed and fabricated as a smart window with a monolayer structure. The window exhibited reversible thermochromic behavior comparable to Co-BTC, with visible transmittance modulation of 10.73%, near-infrared transmittance modulation of 25.87%, and solar transmittance modulation of 12.63%. Compared to a pure PVB window, the smart window reduced indoor temperatures by 5.7 °C in field tests, indicating a significant energy-saving effect. This research presents a potential application for the rational design of MOFs in the development of advanced smart windows.
研究领域:
材料科学
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能源工程
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建筑技术
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DOI
PubMed
高影响因子
ChemNanoMat
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2021
·Vol. 7
·期 8
·906-909
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IF 3.154
Jin Yu,Yang Cao,Qian Liu,Yonglan Luo,Yang Liu,Xifeng Shi,Abdullah M. Asiri,Tingshuai Li,Xuping Sun
It's highly desirable to devise and develop non-precious metal catalysts for efficient water oxidation catalysis in alkaline solution. Herein, we report Co-MOF nanosheet arrays grown on the three dimensional conductive nickel foam (Co-MOF/NF) through a hydro-thermal process for efficient alkaline oxygen evolution electrocatalysis. Such catalyst displays an excellent electrochemical performance by achieving an overpotential of 290 mV at 20 mA cm −2 in 1.0 M KOH. Besides, it possesses both a good electrochemical stability and a high turnover frequency of 0.14 s −1 at the overpotential of 400 mV.
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
JOURNAL OF POWER SOURCES
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2020
·
IF 8.247
Xixi Wang,Lei Ge,Qian Lu,Jie Dai,Daqin Guan,Ran Ran,Shih-Chang Weng,Zhiwei Hu,Wei Zhou,Zongping Shao
Constructing catalysts with a low overpotential for the oxygen evolution reaction (OER) is critical for the increased application of rechargeable Zn-air batteries. Herein, an in-situ cobalt extraction and simultaneous coordination growth strategy is adopted to develop an active and robust interface between nanostructural Co-metal-organic framework (Co-MOF) pillars and perovskite LaCoO 3-δ (LC). Moreover, the multi-active cobalt sites, including Co 3+ in the LC and coordinatively unsaturated cobalt sites in the Co-MOF, could promote the deprotonation of oxygen adsorption intermediates and act as catalytic active centres. Therefore, the optimal sample exhibits excellent OER activity with a low overpotential of 330 mV. Notably, the Zn-air battery with Co-MOF/LC-0.5 as the OER catalyst exhibits a low charge potential of 2.03 V and excellent cycling stability. This work illustrates efficient electrochemical catalysts based on perovskites with low overpotentials that are prepared by an in-situ growth strategy, and have great potential in rechargeable Zn-air batteries.
研究领域:
材料科学
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电化学
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能源存储
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DOI
高影响因子
ENERGY & FUELS
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2022
·
IF 4.654
Weijun Zhang,Fen Li,Zhinan Fu,Sheng Dai,Fenghongkang Pan,Jinxia Li,Lihui Zhou
The appearance of mixed-metal MOF materials with abundant metal active sites, high porosity, large surface area, and, particularly, the synergistic effect between different metals which show prominent catalytic activity for oxygen evolution reaction (OER) has motivated profound research. Most of the related reports focus on the hydrothermal methods to prepare the mixed-metal MOFs containing metal ions such as Co, Ni, and Cr, etc. In this work, we proposed a facile impregnation method through an ion-exchange process to fabricate Fe-doped Co-BDC nanosheets (Fe@Co-BDC NSs) that represented significant enhancement for electrocatalytic OER. The tuning mechanism of the ion-exchange method was investigated by the morphology change and electronic structure of Fe@Co-BDC NSs, which should be important for an efficient OER catalyst. The optimized Fe@Co-BDC NSs (5 mM, 60 min) exhibited a significantly lower overpotential of 307 mV with a smaller Tafel slope of 34.1 mV·dec–1, as compared with the pure Co-BDC NSs.
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
ACS Omega
·
2026
·
IF 4.3
Yutong Feng,Hui Sun,Xinyu Liu,Huiping Wu,Gaoyuan Chen,Afang Gao,Shijie Wang,Jiahui Zhou,Bin Yu
Flexible electrochemical sensors based on noninvasive materials can continuously monitor blood glucose levels in sweat, making them ideal for personal diabetes management intelligent devices. It is necessary to construct sweat glucose electrochemical sensors that have the ability to both adjust to human skin and reliably monitor. We first synthesized nickel/cobalt metal–organic framework material (Ni/Co-MOF) nanosheets via a solvent-thermal approach. Then, an oil-based polyurethane (OPU)/polypropylene spun-bonded nonwoven fabric (PPSF) was obtained by coating the surface of PPSF. Silver/silver chloride (Ag/AgCl) paste and conductive carbon (C) paste were printed layer-by-layer on the surface of the OPU/PPSF by screen printing, followed by the immobilization of Ni–Co/MOF nanosheets on the working area using a Nafion solution to form a Ni/Co-MOF@OPU/PPSF flexible glucose sensor for continuous monitoring of glucose in sweat. This Ni/Co-MOF@OPU/PPSF flexible glucose sensor retained the high electrocatalytic activity of Ni/Co-MOF for glucose oxidation and exhibited high sensitivity (159.9 μA/mM·cm2), low limit of detection (LOD) (2 μM), and a wide linearly glucose-monitoring range (10 μM–1 mM). Compared to other nonenzymatic sensors, our Ni/Co-MOF@OPU/PPSF flexible glucose sensor has better immunity than other substances present in sweat. Meanwhile, the Ni/Co-MOF@PPSF flexible glucose sensor not only monitors the glucose in sweat at different body temperatures but also maintains good mechanical flexibility and stable electrochemical properties under bending conditions. It is suggested that our flexible glucose sensor can be used for continuous monitoring of glucose in human sweat. Overall, our glucose sensor can be used for the continuous monitoring of glucose in human sweat.
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DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
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2021
·Vol. 45
·期 45
·21350-21358
·
IF 3.591
Zhen-Zhen Ma,Yao Ma,Bing Liu,Ling Xu,Huan Jiao
Two cobalt metal–organic frameworks (Co-MOFs), [Ch]2[Co3(BDC)3Cl2] (1) and [Ch]2[Co3(BDC)4]·2DMU (2) (Ch+ = choline cation; H2BDC = terephthalic acid; DMU = 1,3-dimethylurea), were prepared through ionothermal reactions with deep eutectic solvents (DESs) of ChCl and DMU as the reaction media. The 1/GCE electrode with better current response was selected as the electrocatalyst. The detection performance of the 1/GCE electrode towards glucose is excellent with a wide linear range of 10–1200 μmol L−1, a detection limit of 3.2 μmol L−1 (S/N = 3), and a rapid response less than 3 s in 0.01 mol L−1 NaOH. 1 also exhibits high anti-interference with the existence of D-Man, D-Fru, DL-AA, and BA, long-term stability of 15 days and reproducibility for glucose detection. 1 was utilized to detect glucose in human serum and orange juice. The found glucose concentrations are very close to the added glucose concentrations in the selected situations with low RSD and high recoveries. This demonstrates that as a non-enzymatic glucose sensor, 1/GCE can detect glucose with high accuracy and reliability in different environments.
研究领域:
生物医学工程
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分析化学
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DOI
高影响因子
Nanomaterials
·
2025
·Vol. 15
·期 17
·1356
·
IF 4.3
Jingchao Zhang,Yingping Bu,Jia Hao,Wenjun Zhang,Yao Xiao,Naihui Zhao,Renchun Zhang,Daojun Zhang
Among various H2production methods, splitting water using renewable electricity for H2production is regarded as a promising approach due to its high efficiency and zero carbon emissions. The oxygen evolution reaction (OER) is an important part of splitting water, but also the main bottleneck. The anodic oxygen evolution reaction (OER) for water electrolysis technology involves multi-electron/proton transfer and has sluggish reaction kinetics, which is the key obstacle to the overall efficiency of electrolyzing water. Therefore, it is necessary to develop highly efficient and cheap OER electrocatalysts to drive overall water splitting. Herein, a series of efficient RuO2-Co3O4composites were synthesized via a straightforward three-step process comprising solvothermal synthesis, ion exchange, and calcination. The results indicate that using 10 mg of RuCl3·xH2O and 15 mg of Co-MOF precursor in the second ion exchange step is the most effective way to acquire the Co3O4-RuO2-10 (RCO-10) composite with the largest specific area and the best electrocatalytic performance after the calcination process. The optimal Co3O4-RuO2-10 composite powder catalyst displays low overpotential (η10= 272 mV), a small Tafel slope (64.64 mV dec−1), and good electrochemical stability in alkaline electrolyte; the overall performance of Co3O4-RuO2-10 surpasses that of many related cobalt-based oxide catalysts. Furthermore, through integration with a carbon cloth substrate, Co3O4-RuO2-10/CC can be directly used as a self-supporting electrode with high stability. This work presents a straightforward method to design Co3O4-RuO2composite array catalysts for high-performance electrocatalytic OER performance.
研究领域:
电化学
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材料科学
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催化
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可再生能源
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纳米材料
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产品关联
DOI
PubMed
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Dan Sun,Qilong Chen,Yi He,Yang Bai,Changhua Li,Rui Gou,Chuanfang Zhang,Xinbo Xu,Haichao Zhang
The main aim of this study was to exploit the advantages of dopamine and tetraaniline (TA) to enhance the physical barrier properties and active anti-corrosion performance of composite coatings ; in this study, the growth of polydopamine on the surface of Co-MOF enhanced its compatibility with waterborne epoxy, and Co-MOF-PDA-TA (MP-TA) was successfully synthesised by adding dopamine and tetraaniline via Michael addition , confirmed through characterisation methods such as Fourier-transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy. MP-TA can be added as a nanofiller additive to water-based epoxy coatings, and a detailed study on the corrosion resistance of the prepared composite coatings showed that the composite coating containing 0.50wt% MP-TA/WEC exhibits good anti-corrosion performance with an impedance modulus at low frequency (0.01 Hz) of 7.253 × 10 9 Ω cm 2 because TA not only prolongs the time required for corrosion ions to reach the interface but also forms a passivation film on the steel surface. Moreover, the reduced TA can be oxidised to EB or even LEB by releasing two electrons, which further promotes the formation of a passivation film, providing a good pathway for the application of MP-TA as a multifunctional additive.
研究领域:
材料科学
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腐蚀与防护
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DOI
高影响因子
危险品化学品经营许可证（带存储）