ANALYTICA CHIMICA ACTA
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2023
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IF 6.2
DanDan Yang,Jingqi Chen,Yuting Huang,Ganghui Chen,Xueliang Liu,Xuan Wang,Like Yang,Zhaohui Li,Jie Hu,Qi Zhou,Jia Ge,Yu Yang
The development of cost-effective and easy-to-use strategies for the detection of ascorbic acid (AA) and acid phosphatase (ACP) is in high demand but challenging. Thus, we report a novel colorimetric platform based on Fe–N/C single atom nanozyme with efficient oxidase mimicking activity for their highly sensitive detection . The designed Fe–N/C single atom nanozyme can directly oxidize 3,3′,5,5′-tetramethylbenzidine (TMB) to produce a blue oxidation product (oxTMB) in the absence of H 2 O 2 . In addition, L-ascorbic acid 2-phosphate can be hydrolyzed to ascorbic acid in the presence of ACP, which inhibits the oxidation reaction and results in a significant bleaching of the blue color. Based on these phenomena, a novel colorimetric assay with high catalytic activity was developed for the determination of ascorbic acid and acid phosphatase with detection limits of 0.092 μM and 0.048 U/L, respectively. Notably, this strategy was successfully applied to the determination of ACP in human serum samples and evaluate ACP inhibitors, indicating its potential as a valuable tool for clinical diagnosis and research.
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PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 23
·11051-11062
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IF 3.3
Chengzhi Hu,Changyan Zhou,Huiping Zhang,Ying Yan
Chemical vapor deposition (CVD) and impregnation (IM) methods were applied in the preparation of novel Fe/LTA (Linde Type A) zeolite membrane/paper-like sintered stainless steel fiber (Fe/LTA/PSSF) catalysts for acetone oxidation. The catalysts were characterized using various techniques, such as actual iron loading (AAS), surface morphology (SEM), phase composition and crystallite size (XRD), specific surface area (BET), valence state (XPS) and reducibility (H2-TPR), to investigate the effects of the calcination process, iron loading, preparation methods and supports on their catalytic activity. The calcined catalysts were more active than the non-calcined catalysts in the catalytic oxidation of acetone due to the different oxidation states of the deposited metal species. The catalysts prepared by CVD with an Fe loading of 2.29% exhibited similar activity to the IM-prepared catalysts with Fe loadings of 4.42% and 9.69%, which may be attributed to the superior dispersion of the active Fe2O3 phases, the smaller size of metal oxide and the increased ability for oxygen storage. Among the IM-prepared catalysts, Fe/LTA/PSSF-IM-2 with an Fe loading of 4.42% exhibited the lowest T90 of 230 °C. Additionally, the catalysts coated on LTA/PSSF showed higher activity and contact efficiency (T90 of 249 °C) compared to those on granular zeolite (T90 of 318 °C).
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Sustainable Materials and Technologies
·
2023
·
IF 9.6
Chao Wang,Jingyi Zhang,Li Wang,Jianmin Feng,Liqun Wang,Lei Dong,Conglai Long,Dejun Li,Feng Hou,Ji Liang
The crucial step for splitting water is the oxygen evolution reaction . The key to promote this reaction lies in the catalyst. Molybdenum disulfide , as a two-dimensional material with molybdenum and sulfur atoms stacked, is especially suitable as a doping platform to develop high-performance OER catalysts. Fe/Co/Ni ternary transition metal combination has always been a highly active catalytic site for OER. Heteroelement of Fe/Co/Ni doping is expected to effectively modify the local electronic configuration of matrix materials and thus enhances their electrocatalytic OER capability. With this in mind, we report a simple in-situ hydrothermal doping of MoS x nanowires on iron‑nickel alloy foam with ternary transition metal of Fe/Co/Ni. This ternary transition metal of Fe/Co/Ni doped f self-supported electrode (denoted Fe/Co/Ni-MoS x /INF) displays outstanding OER performance in terms of small overpotentials of 214 and 263 mV at current densities of 10 and 100 mA/cm 2 , respectively, in alkaline solution. It was far better than the commercial Ir/C catalysts (253 and 434 mV@10 and 100 mA/cm 2 ). The Tafel slope is about 48.1 mV/dec. Moreover, Fe/Co/Ni-MoS x /INF also has an excellent catalytic stability without any obvious performance decay after 20 h operation. This work contributes to the investigation of high-efficiency OER catalysts based on transition metal-doped MoS x and offers a substitute for noble metal catalysts.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2023
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IF 7.2
Fushan Wen,Le Pang,Tao Zhang,Xiaoli Huang,Yuan Xu,Yajie Li
The exploitation of the superior oxygen evolution reaction (OER) electrocatalysts is of great paramount importance to the investigation of developing hydrogen production from water splitting to alleviate the energy crisis. Herein, Fe 3+ ion doped NiS 2 for OER electrocatalysts obtained from a metal-organic framework (MOF) as a self-template, with the graphitic phase carbon nitride (g-C 3 N 4 ) as a chain armor, was prepared by the two-step solvothermal-pyrolysis method. The MOF-derived Fe–NiS 2 @g-C 3 N 4 composite achieves a current density of 10 mA cm −2 at a tiny OER overpotential (280 mV) and shows good stability in duration tests over 60 h. Compared with the undoped sample, the overpotential is significantly lower by 60 mV and the stability is substantially improved. In this study, two strategies, iron ion doping and g-C 3 N 4 coating, were implemented to target the defects of NiS 2 , promoting its catalytic activity and achieving a significant improvement in stability at the cost of a bit of activity. Balancing activity and stability maximized has been achieved by our work. This study presents a potential approach to improve the catalyst activity and stability in an integrated strategy.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Haiying Li,Shishuai Sun,Wen Cui,Xiaolan Li,Chuanjia Kou,Zhihui Xu,Zhihui Zhang
Reasonably regulating the dimensionality and interface of an electrode material can effectively improve its surface chemical reactivity, charge transfer rate, and ion transport performance, which is crucial to solving several problems with supercapacitors , including low energy density and poor cycle stability. The multidimensional hybrid morphology of Co-Fe carbonate hydroxide (CH) coupled with Co-Mn layered double hydroxide (LDH) is generated directly on the nickel foam substrate by a two-stage process. The prepared multidimensional hybrid materials with pore morphology with the synergistic effect of 1D nanorods , 2D nanosheets , and 3D “porous coral” not only ensure sufficient contact between the electrolyte and electrode material but also enhance the charge transfer and ion diffusion of the electrolyte. The strong coupling effect of Co, Fe, and Mn metals between the heterojunction surface can produce various ionic valence states and high conductivities, resulting in increased redox activity, which thus improves the electrochemical performance. The results of the electrochemical performance test show that when the current density is 10 mA cm −2 , the high area-specific capacitance of 7.33 F cm −2 is two times (3.85 F cm −2 ) that of a Co-Fe CH electrode and five times that of a Co CH electrode. The quasi-solid state asymmetric supercapacitor with a Co-Fe-Mn positive electrode and an active carbon negative electrode displays an energy density of 0.723 mWh cm −2 at a power density of 8.53 mW cm −2 . After 5500 cycles, the apparatus exhibits 101.72 % of the initial capacitance, which can effectively drive small electrical appliances. The results indicate that the supercapacitor exhibits excellent cycle stability and application potential in energy storage.
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高影响因子
APPLIED CATALYSIS A-GENERAL
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2022
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IF 5.723
Xin Jin,Yajun Huang,Song He,Guanyu Chen,Xinyu Liu,Chunxiang He,Chunhua Du,Qilin Chen
Sulfate radical-based advanced oxidation processes (SR-AOPs) were frequently utilized for the degradation of various organic pollutants due to their efficient and clean advantages. In this work, Co-Fe based Prussian blue analogues (PBA) nanoparticles were firmly immobilized on nickel foam (NF) as a novel activator for peroxymonosulfate (PMS), and the complete degradation of tetracycline (TC) was achieved within 20 min under optimal conditions. The TC degradation efficiency of samples were investigated under various factors including Co loading, PMS dosage, initial TC concentration, pH, and inorganic anions. The mechanism for PMS activation indicated that reactive oxygen species including sulfate radicals, hydroxyl radicals, superoxide radicals and singlet oxygen contributed to TC degradation. The possible pathway of TC degradation was investigated by liquid chromatography-mass spectroscopy. This work presented a new combination of efficient and easily recoverable supported catalysts and provided useful information for the wastewater treatment .
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高影响因子
COMPOSITE STRUCTURES
·
2022
·
IF 6.603
Chanyuan Wu,Yibo Qu,Yifan Wen,Shen Gong,Zhenghong Zhu
Blindly increasing the content of conductive fillers is difficult to meet the requirements of flexibility and efficient shielding at the same time. In this paper, Cu and Fe bimetallic heterostructure nanoparticles are formed on the surface of CNTs by liquid-phase co-deposition. By taking into account the electrical conductivity of Cu and the magnetic conductivity of Fe, the electromagnetic properties of CNTs are greatly improved. By controlling the temperature gradient to realize the directional solidification of ice crystals combined with freeze-drying process, the flexible (Cu/Fe)@CNT/SA/CNF/PDMS composites with three-dimensional layered structure are successfully prepared. Adding only 1 wt% of (Cu/Fe)@CNT, the EMI-SE of the composite can reach 21 dB (the absorption loss ratio reaches 85.25 %), which is nearly 50 % higher than that of CNT/SA/CNF/PDMS composite. In addition, multi-scale modeling confirms that the introduction of Cu and Fe bimetallic heterostructure nanoparticles and three-dimensional multilayer structure greatly increase the absorption loss of the composites.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2022
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IF 4.326
Jiakang Wan,Ling Wang,Wentao Xu,Zehai Xu,Junsheng Yuan,Guoliang Zhang
Design and synthesis of high-efficiency and stable heterogeneous catalysts for the electro-Fenton process remain challenging. In this study, a co-doped Ce and N metal–organic framework MIL-101(Fe) heterogeneous catalyst (Ce/N-MIL-101(Fe) was synthesized by a facile one-step solvothermal method. Polyvinyl pyrrolidone played dual roles during the fabrication process, which not only acted as a nitrogen source for doping but also prevented MIL-101(Fe) molecules from aggregating and reinforcing the formation crystal with a complete polyhedral crystal shape. The introduction of Ce significantly enhanced the density of active sites and promoted the Fe3+/Fe2+ cycle of the reaction system. Owing to the specific structure and properties, the rate of electron transfer in the catalytic process was significantly promoted. The synthesized Ce/N-MIL-101(Fe) catalyst exhibited a high degradation rate for dyes (>98%) with competitive stability and reusability. Moreover, compared with common electro-Fenton catalysts usually operated in a limited pH range of 3.0–6.0, the working pH range of Ce/N-MIL-101(Fe) was widened up to 10.0. The design concept for producing abundant active sites with co-doping into frameworks can be extended to more heterogeneous electro-Fenton catalysts constituted by other porous materials.
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高影响因子
Molecular Catalysis
·
2022
·
IF 5.089
Nan Li,Changping Jian,Yaping Song,Li Wang,Ata Ur Rehman,Yanghe Fu,Fumin Zhang,De-Li Chen,Weidong Zhu
Herein, we reported a facile and scalable approach for the synthesis of Fe-based MOF MIL-88A(Fe) via a simple liquid-phase route at atmosphere pressure, and its application as a heterogeneous catalyst for the efficient aerobic oxidation of cyclohexene to value-added 2-cyclohexene-1-ol. Over 130 g of spindle-shaped MIL-88A(Fe) nanocrystals with high crystallinity, monodispersed particle size, and large specific surface area were easily synthesized per batch according to our method. The resultant MIL-88A(Fe) exhibited a high catalytic activity (conversion: 81%) with 70% selectivity for 2-cyclohexene-1-ol in the aerobic oxidation of cyclohexene with O 2 as the sole oxidant under mild reaction conditions (0.5 MPa of O 2 , 353 K for 8 h), outperforming the analogues reported in the literatures. The combined experimental and theoretical approach support the reaction mechanism of the oxidation of cyclohexene via both the free radical reaction pathway and Fe-mediated reaction pathway, resulting in the selective formation of 2-cyclohexene-1-ol.
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高影响因子
JOURNAL OF MOLECULAR STRUCTURE
·
2023
·
IF 3.8
Xiyue Wang,Shang Gao,Junfu Wang,Xinying Fan,Chi Song,Chuanwei Zhou,Shuyun Shi,Dandan Wang,Hongji Li
In this work, a novel sensor for selective detection of 2,6-dichlorophenol (2,6-DCP) is developed by combining the selectivity of molecular imprinting technology (MIPs) with the sensitivity of SERS technology. In order to enhance SERS activity of the substrate, Ag nanoparticles are loaded on Ta 2 O 5 particles by means of photodeposition. The synthesized Ta 2 O 5 @Ag is combined with MIL-101 (Fe) to enrich more target molecules and reduce the limit of detection. Finally, Ta 2 O 5 /Ag/MIL-101(Fe)@MIPs (TAM@MIPs) is synthesized by precipitation polymerization for selective detection of 2,6-DCP. When the concentration of 2,6-DCP changes between the range of 10 −2 ∼ 10 −9 M, the Raman intensity and concentration present a good linear relationship. The correlation coefficient (R 2 ) is 0.9969 and the limit of detection (LOD) of 2,6-DCP is 10 −9 M. Furthermore, Under UV-irradiation, the TAM@MIPs also presents photocatalytic performance, which can effectively degrade the organic interfering molecule adsorbed on its surface and present high-efficiency reproducibility. This method broadens the application field of SERS detection and provides a new procedure for the phenolic pollutant detection.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Xueying Cheng,Renquan Guan,Yunning Chen,Yudan Qian,Qingkun Shang,Yingnan Sun
In this study, the adsorption and photocatalytic degradation of oxytetracycline (OTC) were systematically investigated using different metal-doped anatase-phase mesoporous TiO 2 nanocatalysts (M−TiO 2 , M = Fe, Co, Ni, Cr). The results showed that doping with different metals had a significant effect on the ability of TiO 2 to adsorb and degrade OTC . Comparing the photoelectric properties of four photocatalysts (Fe-TiO 2 , Co-TiO 2 , Ni-TiO 2 and Cr-TiO 2 ), it was observed that the mutual synergy between the separation ability of the photogenerated carriers and the adsorption ability of pollutants was the fundamental reason for the excellent photocatalytic performance of Fe-TiO 2 . The relative intensities of the high-resolution mass spectrometry (HRMS) peaks were used to track and analyse the degradation products of pollutants at different adsorption or light-irradiation times during the photocatalytic process. The ability of the pollutants to undergo dark-state adsorption significantly influenced their degradation paths and products. The possible mechanism of the photocatalytic decomposition of pollutants using Fe-TiO 2 along different paths was proposed according to the Fukui function calculation and MS results. To the best of our knowledge, this is the first time that quantitative HRMS results have been used to assess the degradation pathways of pollutants.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Tong Qi,Miao Jia,Qiong Yuan,Xu Zhang,Mengqiu Jia
Metal selenides have excellent theoretical capacity when used to store sodium . Compared with single metal selenides, bimetallic selenides stand out with excellent theoretical capacity, sufficient electrochemical reaction sites and good conductivity. In this work, Zn 3 [Fe(CN) 6 ] 2 prussian blue analogue nanospheres are prepared by a static method with PVP as dispersant, and then heterostructure ZnSe/FeSe nanospheres (ZnSe/FeSe NS) composite are prepared by gas-phase selenation. PVP is conducive to the formation of loose and porous structures and alleviate the volume expansion during sodium storage. In this structure, heterostructures can create abundant active sites and increase the electrochemical capacity. Therefore, the ZnSe/FeSe NS show high sodium storage capacity with a reversible capacity of 549.0 mAh g −1 at 100 mA g −1 and 436.8 mAh g −1 even after 100 cycles at 1 A g −1 . It also shows excellent rate performance with high stable capacities of 524.6, 486.1, 447.3, 431.1, 417.9 mAh g −1 in a series of current densities of 100, 200, 500, 1000, 2000 mA g −1 separately. The excellent capacity of the ZnSe/FeSe NS composite comes from the active sites provided by the heterostructure and the high conductivity provided by the built-in electric field.
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高影响因子
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