MATERIALS CHEMISTRY AND PHYSICS
·
2026
·
IF 5.2
Rawiyah Alkahtani,Ahmad Iqbal,M.S. Al-Buriahi,Muhammad Ali Hamza Shahbaz,Amir Muhammad Afzal,Nora Mobark Farhan,Sohail Mumtaz,Abhinav Kumar
A MIL-53(Al)@KTi 2 (PO 4 ) 3 @rGO was successfully synthesized through hydrothermal and modified Hummers' methods. • The integration of porous MIL-53(Al) and conductive rGO enhanced charge transport and electroactive site accessibility. • The MIL-53(Al)@KTi 2 (PO 4 ) 3 @rGO electrode delivered a high specific capacity of 1189.23C g −1 . • The hybrid SC achieved an energy density of 45 Wh kg −1 and a power density of 2773 W kg −1 . • The ternary electrode showed a low overpotential of 46 mV and a Tafel slope of 49 mV dec −1 . The rising requirement of sustainable and multifunctional electrodes for energy storage and production has stimulated significant interest in advanced electrode architectures. In this study, a MIL-53(Al)@KTi 2 (PO 4 ) 3 @rGO composite was fabricated by means of combined hydrothermal and modified Hummers approach. The composite was rationally designed by integrating the MIL-53(Al), the favorable ionic transport characteristics of NASICON-type KTi 2 (PO 4 ) 3 , and the highly conductive network of rGO, there by promoting efficient charge and ion transport. Electrochemical evaluation in a three-electrode cell demonstrated a high specific capacity of 1189.23C g −1 . When assembled into a two-electrode supercapacitor device, the material delivered an energy density of 45 Wh kg −1 at a power density of 2773 W kg −1 . The device also maintained 92% of its initial capacity with a Coulombic efficiency of 97% after 10,000 consecutive charge–discharge cycles, indicating strong electrochemical durability. In addition to its energy storage performance, the MIL-53(Al)@KTi 2 (PO 4 ) 3 @rGO electrode demonstrated promising catalytic activity for the hydrogen evolution reaction, requiring only 46 mV overpotential to achieve the targeted current density and exhibiting a Tafel slope of 49 mV dec −1 . These results highlight the synergistic contribution of the MOF, NASICON phosphate, and rGO components and establish MIL-53(Al)@KTi 2 (PO 4 ) 3 @rGO as a promising multifunctional platform for advanced supercapacitor systems and electrocatalytic hydrogen production.
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DOI
高影响因子
JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2019
·
IF 2.994
Chunhua Li,Li Zhu,Weixia Yang,Xie He,Haiping Zhao,Wenzhi Tang,Tianli Yue,Zhonghong Li
It is imperative to exploit simple and rapid methods for the detection of total iron in foods to ensure food quality and human health. Herein, we construct the MIL-53(Al)-NH 2 -MPA nanosensor synthesized by post-synthetic modification process for fluorescent detection of total iron in food matrix. The nanosensor emits intense blue fluorescence with excellent stability. The fluorescence can be efficiently quenched by Fe(III) due to the fact that Fe(III) can preferentially bind with O-quinone bands or –NH 2 of MIL-53(Al)-NH 2 -MPA to form strong coordination complex, and that the heteroatoms (N, O and S) in MIL-53(Al)-NH 2 -MPA can donate lone-pair electrons to Fe(III) to promote the electron transfer. Moreover, the competitive absorption of excitation energy of MIL-53(Al)-NH 2 -MPA by Fe(III) endows the nanosensor with superior sensitivity. The fluorescent sensor exhibits excellent anti-interference performances toward other metal ions, and reveals a LOD of 0.36 μM with the broad linear range of 0–110 μM for the detection of Fe(III). Satisfactory recoveries of 92.90–112.70% with RSDs of 0.54–2.48% have been achieved in water and food samples, which are well agreement with inductively coupled plasma mass spectrometry (ICP-MS) (P > 0.05), indicating that MIL-53(Al)-NH 2 -MPA is applicable for detecting total iron in food matrix.
研究领域:
分析化学
·
食品科学
·
材料科学
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产品关联
DOI
高影响因子
ChemSusChem
·
2023
·Vol. 16
·期 23
·e202300699
·
IF 8.4
Cong-Hua Yang,Xiao-Chen Liu,Youcong Li,Shuai Yuan,Tao Wang,Zhi-You Zhou,Shi-Gang Sun
Graphical Combining electrosynthesis with thermocatalysis : A strategy for efficient conversion of propane to high value-added C 3 oxygenated products is developed by coupling the electrosynthesis of H 2 O 2 on oxygen-doped carbon electrocatalyst for 2e − oxygen reduction reaction with thermocatalysis of propane oxidation over MIL-53 (Al, Fe) active sites in the proton exchange membrane fuel cell. Electrochemical conversion of alkanes to high value-added oxygenated products under a mild condition is of significance. Herein, we effectively couple the electrocatalysis of H 2 O 2 with the thermo-catalysis of propane oxidation in the cathode of proton exchange membrane fuel cell. Specifically, H 2 O 2 is in-situ generated on the nitric acid-treated carbon black (C-acid) via 2e − process of oxygen reduction reaction, and then transports to the Fe active sites of MIL-53 (Al, Fe) metal–organic frameworks for propane oxidation. Based on this strategy, the space-time yield of C 3 oxygenated products of propane oxidation reaches 2.65 μmol h −1 cm −2 , which represents a new benchmark for electrochemical alkane oxidation in the fuel-cell-type electrolyzer. This study highlights the importance of multifunctional composite catalysts in the field of electrosynthesis.
研究领域:
化学工程
·
电化学
·
催化
·
能源材料
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DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2018
·
IF 11.698
He Xiao,Wenyao Zhang,Qiushi Yao,Liulian Huang,Lihui Chen,Bruno Boury,Zhongwei Chen
Metal organic frameworks (MOFs) are exploited in many applications of materials science and very recently were investigated as precursors or reagents for material synthesis. In a new way different from previous approaches, here we introduce for the first time the synthesis of metal oxide M x O y in the presence of M-free MOF acting partially as a sacrificial template and as a provider of doping metal atom. We demonstrate this approach in the case of ZnO prepared by a simple hydrothermal method in the presence of a Zn-free MOF like MIL-53(Al) or MIL-125(Ti). The resulting ZnO show low content of Al or Ti < 2% and properties are significantly different depending on whether MIL-53(Al) or MIL-125(Ti) are used or if no MOF is present. The nature and presence of MOF has different major effects on the morphology, the specific surface area of as prepared ZnO and also on the oxygen defects in its crystal structure. Corroborating the XPS, UV–vis DRS, PL, EPR and DFT studies evidence the role of such O-defects on band gap narrowing for samples calcined at 400 °C. These exhibit high efficiency in photodegradation of methyl orange (MO) compared to ZnO prepared in MOF-free conditions or previous literatures. The kinetics of MO degradation is different depending on the morphology, the specific surface and oxygen defects. The present data open the door to a new approach of the synthesis of metal oxides and a control of their properties.
研究领域:
材料科学
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环境科学
·
化学工程
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Guiming Xie,Xingyang Bai,Yi Man,Pengju Ren,Rongrong Jin,Runduo Zhang,Kostya (Ken) Ostrikov,Zhou-jun Wang,Qingyuan Yang
Innovative catalyst design and in-depth mechanism understanding are imperative for industrialization of CO 2 hydrogenation to methanol. Herein, Al-doped Cu/ZnO catalysts, Cu/Al-ZnO-x (x = 1/32, 1/16 and 1/8, denoting Al/Zn molar ratio), were creatively synthesized using MIL-53(Al) as Al sources and reactive templates. The Cu/Al-ZnO-1/16 catalyst exhibited the highest methanol production rate among the Cu/Al-ZnO-x catalysts, which was 1.93 times as active as the conventional Cu/Al-ZnO-1/16-C catalyst using Al(NO 3 ) 3 ·9H 2 O as Al source. Structural characterizations reveal that the use of MIL-53(Al) led to higher S BET , more uniform Al distribution, more abundant oxygen vacancies, more appropriate metal-support interactions and larger amount of medium basic sites. Mechanism studies demonstrate that Al doping would markedly induce oxygen vacancy formation on Cu-ZnO interfaces and thus significantly boost methanol synthesis activity. This work offers a facile approach to develop efficient methanol synthesis catalysts and provides new insights into the nature of Al promotion in Cu/ZnO-based catalysts.
研究领域:
催化化学
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材料科学
·
环境科学
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DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2023
·
IF 10.9
Huan Yao,Ruifeng Zhang,Yu Wen,Yue Liu,Gang Yu,Zhi-Hui Xie
Metal-organic framework [MOF, i.e., NH 2 -MIL-53(Al)] modified TiO 2 (NMT) composite photoanodes were successfully prepared by hydrothermal synthesis and were used for the photoelectrochemical cathodic protection (PECCP) of nickel-plated magnesium alloy (Mg/Ni). Results showed that the synthesis temperature significantly impacted the morphology and PECCP performance of the NMT photoanodes. The NMT@150 photoanode prepared at a reaction temperature of 150 °C exhibited the best PECCP performance and produced a current density of 1980 μA cm −2 under visible light irradiation, which was 19.8 times higher than that of a single TiO 2 photoanode. The composite photoanode could polarize the open circuit potential of the coupled Mg/Ni electrode to -876 mV and remain relatively stable within 35 h. XPS and EPR tests showed that a Z -scheme heterojunction was formed between the NH 2 -MIL-53(Al) and TiO 2 nanotubes, allowing the photogenerated electrons to accumulate mainly on the conduction band of NH 2 -MIL-53(Al). The heterojunction greatly promoted the separation and transfer of photogenerated electron-hole in the NMT composite photoanode, significantly enhancing the PECCP performance for Mg/Ni.
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DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2018
·
IF 2.746
Guihua Gao,Yanyan Xing,Tingting Liu,Jian Wang,Xiaohong Hou
Four water stable metal-organic frameworks (MOFs), MIL-101(Cr), MIL-100(Fe), MIL-53(Al), and UiO-66(Zr), were used as adsorbents for concentration of four androgens and progestogens from water. The adsorption abilities of target analytes on the four MOFs were investigated by experimental and molecular simulation strategies, and UiO-66(Zr) was ultimately selected as the sorbent to develop a porous membrane protected micro-solid-phase extraction (μ-SPE) method for simultaneous extraction androgens and progestogens in environmental water samples followed by LC-MS/MS detection. Several variables affecting the extraction efficiency were systematically investigated, including pH, salt concentration, extraction time, kind of desorption solvent, and desorption time. Under the optimized conditions, excellent linearity was obtained in the range of 20.32–2032 ng/L for T, 10.24–1024 ng/L for P, 7.624–762.4 ng/L for TP , and 8.376–837.6 ng/L for MPA . Limits of detection (LODs) and limits of quantification (LOQs) were 10 ng/L and 20 ng/L for T, 4.0 ng/L and 10 ng/L for P, 2.0 ng/L and 7.0 ng/L for TP, and 3.0 ng/L and 8.0 ng/L for MPA, respectively. The recoveries were ranged from 80.5% to 102.4%. Furthermore, the μ-SPE device could be used for at least 10 extractions (RSD < 10.0%). Meanwhile, comparison was made with solid-phase extraction, and the developed method was demonstrated to be a convenient and eco-friendly pretreatment method for water samples.
研究领域:
环境科学
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分析化学
·
材料科学
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DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Jiang Chang,Ying Qin,Weimin Guo,Jingyuan Zhang,Kuo Zhang,Jianhua Zheng,Lijian Sun,Qiu Fu
The facile and eco-friendly fabrication of a fabric with remarkable flame retardancy, anti-ultraviolet (UV), and superhydrophobic properties is of significant interest for multitask requirements. In this regard, herein, a nonfluorine, facile, and green method is reported for in situ synthesis of metal-organic frame (NH 2 -MIL-53(Al)) on hemp fabric (HF) for the preparation of multifunctional textiles. A homogeneous and compact coating of NH 2 -MIL-53(Al) crystals was deposited on HF, followed by modification with triethoxyoctylsilane (TEOS) to manufacture superhydrophobic NH 2 -MIL-53(Al)@hemp fabric (SM(Al)HF-9), significantly enhancing its water stability. The SM(Al)HF-9 exhibited superior superhydrophobicity properties, with a water contact angle (WCA) up to 156°. Furthermore, the surface of SM(Al)HF-9 cannot be adhered by dye solution and powder, indicating its good self-cleaning and anti-fouling abilities. The SM(Al)HF-9, characterized by a porous structure, effectively separates tetrachloromethane and n-hexane from water mixtures with a separation efficiency exceeding 97 %. The SM(Al)HF-9 has excellent UV-blocking properties, and the UV protection factor is as high as 105.44. Encouragingly, the SM(Al)HF-9 exhibited outstanding flame retardancy, as demonstrated by its self-extinguishing capability and a substantially improved limiting oxygen index (LOI) of 32.4 %. In comparison to raw HF, the peak heat release rate (PHRR) and total heat rate (THR) of the modified HF are reduced by 76.15 % and 54.32 %, respectively. Meanwhile, the NH 2 -MIL-53(Al) has a significant advantage over other MOFs (e.g., ZIF-67, Ce-MOF, Ag-MOF, Fe-MOF and MIL-53(Al)) in improving the flame retardancy of HF. The highly efficient flame-retardant, anti-UV, and superhydrophobic fabric is promising in home and public decoration, and fire protection fields.
研究领域:
材料科学
·
纺织工程
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产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
·
2025
·
IF 9.8
Hongbo Li,Hao Wang,Meiyi Cao,Xing Tong,Shuo Wang,Mingfei Pan
The fluoroquinolone-enrofloxacin (ENR) residue in animal-derived foods poses a significant threat to human health, thereby necessitating developing precise, efficient, and user-friendly detection methods. This study developed a dual-mode fluorescence-colorimetric immunosensing platform using the composite of bimetallic nanoparticles integrated with metal-organic frameworks (Au/Pt NPs@NH 2 -MIL-53(Al)). The Au/Pt NPs with biocompatibility and peroxidase-like activity were modified onto fluorescent NH 2 -MIL-53(Al) and conjugated with Ab 2 to construct signal probes. The platform enables dual-mode quantitative analysis through the competitive binding of ENR and ENR-BSA conjugate to signal probes. It demonstrated a wider linear range (0.08–180 ng/mL) and high sensitivity [LOD: 0.068 ng/mL (fluorescence), 0.066 ng/mL (colorimetric), and 0.074 ng/mL (smartphone-assisted color recognition)]. In real sample analyses, the recoveries ranged from 86.7 % to 106.7 %, with satisfactory stability (RSD ≤ 4.4 %, n = 3). The dual-signal mode facilitates results self-calibration, enhancing reliability, while smartphone-assisted color recognition enables on-site, convenient screening, offering great potential for ENR detection in complex food matrices.
研究领域:
食品科学与技术
·
分析化学
·
纳米技术
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生物传感器
·
环境与健康监测
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产品关联
DOI
PubMed
高影响因子
ANALYST
·
2012
·Vol. 137
·期 22
·5411-5419
·
IF 4.23
Xiang-Feng Chen,Hao Zang,Xia Wang,Jian-Guang Cheng,Ru-Song Zhao,Chuan-Ge Cheng,Xiao-Qing Lu
In this paper, the potential applications of metal–organic framework (MOF) materials as fiber coatings for the solid-phase microextraction (SPME) of polycyclic aromatic hydrocarbons (PAHs) in water samples were explored. Fibers coated with MIL-53(Al, Cr, Fe) materials were fabricated by an adhesive method for SPME. The quantitation was performed by gas chromatography–tandem mass spectrometry (GC–MS/MS) using the multiple reaction monitoring mode. Among the three MIL-53(M) coatings, MIL-53(Al) showed the highest extraction efficiency towards PAHs under the current fabrication procedure. Under optimized conditions, the MIL-53(Al)-coated fiber showed good precision (relative standard deviation <12.5%), low detection limits (0.10 ng L−1 to 0.73 ng L−1, S/N = 3), and good linearity (R2 > 0.98) for aqueous solutions containing 16 PAH . The fiber also offered high thermal and chemical stability. The method developed based on MIL-53(Al) SPME–GC–MS/MS was successfully applied in the analysis of real water samples. Based on the simulation results, the PAHs were adsorbed on MIL-53(Al) primarily through the hydrophobic and π–π interactions between PAHs and the organic linker of the material. The results presented in this paper indicate that water-stable MOF materials have great potential for the SPME of aromatic compounds in water samples.
研究领域:
环境科学
·
分析化学
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产品关联
DOI
PubMed
高影响因子
Biomaterials Science
·
2024
·Vol. 12
·期 19
·5091-5104
·
IF 5.8
Yamin Chai,Wenyan Han,Yanjia Zhang,Yunzheng Du,Biao Wang,Mengya Chen,Nan Li,Wei Luo,Xiaoyu Zha,Lichun Wang,Lailiang Ou
Due to their rapid spread, high variability, and drug-resistant strains, new viral infections are continuously emerging. A lack of effective antiviral drugs and vaccines, resulting in disease and death, has significant socioeconomic consequences. Hemoperfusion can effectively adsorb and remove toxins from the blood, thus purifying the blood and serving as an acute treatment. Therefore, the aim of this study was to construct adsorbents to selectively remove viruses from the blood to quickly treat pathogen infection. We reported on new metal–organic framework (MOF)-polymer beads based on MIL-53(Al) and cellulose acetate (CNC), which were prepared by a one-step phase inversion method and applied as a viral hemo-adsorbent for the first time. The characterization results demonstrated that MIL-53(Al) was well dispersed in the CNC matrix. The adsorption results demonstrated that the capture efficiency of the human immunodeficiency virus (HIV) could exceed 99.93%, and the corresponding infectious titer decreased by approximately 103 times in clinical application. Moreover, CNC/MIL-53 exhibited low hemolysis ratios and good anticoagulant properties. Furthermore, molecular dynamics simulations revealed that the interplay of hydrogen bonding was the governing physisorption mechanism. Overall, CNC/MIL-53 could serve as a new type of hemoperfusion adsorbent for virus removal from blood and provide a new treatment pathway to mitigate epidemics.
研究领域:
生物医学工程
·
材料科学
·
病毒学
·
医疗器械
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产品关联
DOI
PubMed
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2020
·
IF 7.1
Yingxia Zhou,Lai Wei,Lihua Chen
Herein, a small molecule, hemin/G-quadruplex (G4-hemin), was physically embedded into NH 2 -MIL-53 (Al) to construct a novel metal-organic framework (MOF)-based enzyme ( [email protected] ). Its catalytic activity and stability were investigated in detail by catalyzing a reaction of 3,3′,5,5′-Tetramethylbenzidine (TMB) in the presence of H 2 O 2 . The results show that the activity and stability of this new enzyme is better than that of traditional hemin or G4-hemin, and even stronger than that of [email protected] ( [email protected] > G4-hemin > [email protected] > hemin). No significant loss in catalytic activity was observed for at least one day. Even after eight days, only a 13.8 % decrease in activity was recorded. An electrochemical biosensor was successfully developed based on a signal amplification strategy utilizing the catalysis of [email protected] The sensor was able to sensitively detect TB in buffer, even in a diluted solution of many proteins. The proposed method offers high selectivity against mismatch sequences of TB, a good linear response range of 10 −18 moL L -1 to 10 -14 moL L -1 and a low minimum detection limit of 0.330 aM.
研究领域:
生物化学
·
分析化学
·
材料科学
·
生物医学工程
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）