APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
·
2022
·Vol. 194
·期 11
·5167-5184
·
IF 3.094
An Peide,Zhu Fenfen,Liu Shiji,Zhou Xiaolin,Wang Chunfang,Liu Yufeng,Meng Hao,Zhang Xia
Recently, metal–organic frameworks (MOFs) are considered to be the moderate hosts for the bio-enzymes owing to their unique 3D pores and controllable surface affinity to the target molecules. In this work, the benzoic acid (BA)–modulated UiO-66-NO 2 was introduced, and cytochrome c (Cyt C) was chosen as the target enzyme to evaluate the immobilization efficiency of the resulting UiO-66-NO 2 -BA. The immobilization conditions including pH, adsorption time, and temperature and the initial concentrations of BA were optimized. The adsorption kinetics and thermodynamics were analyzed to further explore the enhanced adsorption mechanism. It is worth noted that all the UiO-66-NO 2 -BA exhibited evidently enhanced adsorption capacities in comparison with the unmodified UiO-66-NO 2 due to the formation of the chemical bonds between the UiO-66-NO 2 -BA and cytochrome C, indicating the positive roles of BA modification. Finally, the activities of the immobilized cytochrome C were assessed by using the catalytic oxidation of ABTS in the presence of H 2 O 2 , which reactions were also conducted over the free cytochrome C for comparison. The evidently improved stability under definite pH range, prolonged durability against the organic solvents, and the good reusability of the immobilized cytochrome C highlight the prospect applications of functional MOF immobilized enzymes in the practical catalytic reactions. Graphical abstract
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ACS Applied Nano Materials
·
2021
·
IF 5.097
Nadia Batool,Waseem Iqbal,Xiao-Feng Han,Wen-Tao Wang,Hao-Tian Teng,Xiang Hao,Ruizhi Yang,Jing-Hua Tian
Pt/C is one of the most favorable catalysts with high catalytic activity used in the oxygen reduction reaction (ORR). However, the synthesis of Pt/C with superior durability is still a significant challenge. Here, we introduced a simple technique to fabricate a Pt/N-C catalyst, having ultrasmall Pt nanocrystals encapsulated inside a nitrogen-doped carbon support, which is derived by the UiO-66-NH2 (MOF) using an impregnation technique, followed by a pyrolysis process. This Pt/N-C displays ORR activity and durability in alkaline solution with a half-wave potential of 0.90 V (vs RHE), limited diffusion current density of 5.5 mA cm–2, and only 5 mV deterioration in half-wave potential after testing 20,000 cyclic voltammetry (CV) cycles. In addition, it also shows good performance in acidic solution. In addition, Zn–air batteries (ZABs) assembled using the Pt/N-C air electrode display a high specific capacity of 825 mAh g–1, a high peak power density of 372 mW cm–2, and 208 h long cycle life. This offers an innovative approach for developing noble metal-based catalysts with unusual activity, stability, and a promising future for applications in metal–air batteries and fuel cells.
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OPTICAL MATERIALS
·
2025
·
IF 4.2
Haoran Zhang,Tianxi Feng,Song Ye,Deping Wang
In this research, the modified upconversion nanocrystals NaYF 4 :Yb,Er were adopted as the precursors for the synthesis of the NaYF 4 :Yb,Er@UiO-66 composite. The XRD, XPS and TEM characterizations indicated that the composite has good crystallinity and uniform morphology. Under 980 nm excitation, the NaYF 4 :Yb,Er@UiO-66 composite exhibits bright upconversion emission that characterized of Er 3+ : 2 H 11/2 → 4 I 15/2 , 4 S 3/2 → 4 I 15/2 , and 4 F 9/2 → 4 I 15/2 radiative transitions. After modified with BPEI (branched polyethyleneimine), the NaYF 4 :Yb,Er@UiO-66/BPEI fluorescence probe was constructed and was used for the detection of Cu 2+ . The results revealed that the integrated emission intensity of Er 3+ displayed a linear relationship with the concentration of Cu 2+ within the range of 5 to 45 μM with a LOD of 0.9615 μM. This study offered a feasible method for constructing UCNC@UiO-66 composites with regular morphology,which may have a potential application as fluorescent probes for the detection of various metal ions by adjusting the doping luminescent center.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2025
·
IF 2.8
Shuaiyang Jiang,Ya Liu,Yulu Liu,Dongfang Wang,Xiaofeng Wang,Qian Li
A portable home hemodialysis device is a miniaturized and easy-to-operate medical apparatus designed for patients with chronic kidney disease, enabling them to conveniently perform hemodialysis at home or while traveling. However, it imposes high requirements on the dialysis membrane in terms of dialysis efficiency, adsorption capacity, and blood compatibility. In this study, the composite membrane was fabricated through electrospinning, which is an in situ synthesis of carbon nano tube (CNT) bridged UiO 66 (COOH) 2 on PTFE fibers. UiO 66 (COOH) 2 increased the adsorption site by association with CNT, and achieved the adsorption of creatinine by hydrogen bond and π bond, which greatly reduced the usage of dialysis solution. UiO 66 (COOH) 2 and CNT were first combined for creatinine adsorption, and its maximum static adsorption capacity was 66 mg/g. During the dialysis, the yielding membrane showed a creatinine clearance of 64.89% and a resistance protein rate of more than 98%. Compared with pure PTFE dialysis membrane, the amount of dialysate used to achieve the same dialysis effect was merely 1/10. Furthermore, the membrane has a hemolysis rate of 2% and a low platelet adhesion rate, which shows excellent blood compatibility. Therefore, the dialysis membrane prepared in this study is expected to promote the development of portable home hemodialysis devices.
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JOURNAL OF SOLID STATE CHEMISTRY
·
2025
·
IF 3.5
Gao Shuang,Yu Yue,Li Yun-heng,Yao Sheng-yi,Song Ya-kai,Niu Lu-hao,Chen Xiao-lu
A series of molybdenum-based catalysts were prepared using UiO-66 modified with functional ligands as a carrier. The catalyst structure was characterised using XRD, FT-IR, N 2 adsorption desorption isotherms, TEM and XPS. The introduction of -F atom expanded the pore structure of catalyst and increased the specific surface area, resulting in a greater number of active site and more dispersion. The introduction of functional ligands (-F, -NO 2 ) enhanced the electron attraction capacity of catalyst, and improved the microenvironment around the active centre of the catalyst, which contributed to enhance the catalytic performance. The effect of catalyst structure on catalytic activity was investigated using the removal of dibenzothiophene (DBT) from simulated oils as a probe reaction. Under the optimum reaction conditions, the catalyst (UiO-66-NO 2 -F-MoO 3 ) was found to be the most effective for the DBT conversion, reached 99.1%. After 5 desulfurization experiments, the desulfurization activity of the catalyst cound still reach 90.6 %, indicating that the catalyst had good cyclic stability, which was closely connected to the hydrophobicity of the -F atom. The introduction of -F atom improved the hydrophobicity of the catalyst so that the generated sulfone was not easy to be adsorbed on the active site and improved the cyclic stability of the catalyst. Furthermore, the increase in the number of Mo active species was important in improving the cyclic stability of the catalyst.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2020
·
IF 5.774
Yucheng Liu,Dong Gan,Mingyan Chen,Lili Ma,Bing Yang,Lingli Li,Meng Zhu,Wenwen Tu
A composite material constructed by intercalating super-hydrophilic UiO-66 into the graphene oxide (GO) nanosheets was synthesized under the modification of polydopamine (PDA), and the PDA/RGO/UiO-66 hybrid membranes with enhanced water permeability, favorable dye separation performance and anti-fouling property were prepared on the cellulose acetate (CA) substrate by vacuum-assisted filtration method. In this work, UiO-66 nanoparticles (NPs) were introduced into the GO interlayers to inhibit their accumulation, while PDA was used to partially reduce GO and ensure the stability of the composite material. The prepared powder samples and composite membranes were subjected to PXRD, FT-IR, SEM, AFM, XPS, WCA characterizations and zeta potential tests, respectively. The results indicated that PDA/RGO/UiO-66 complex films presented more hydrophilicity with a pure water flux as high as 167.14 L/(m 2 ·h), which increased by 256.91% compared to the PDA/RGO membrane and maintained a high dye separation performance (99.54% for MB and 87.36% for CR). Also, the improvement in surface hydrophilicity of the membrane was advantageous for heightening its fouling resistance. In general, the PDA/RGO/UiO-66 composite membranes synthesized in this paper have great potential for efficient separation and purification of dye wastewater.
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FOOD CHEMISTRY
·
2025
·
IF 9.8
Wenjing Li,Mengqing Xu,Zhuoyun Xia,Zheng Wang,Yingying Feng,Hui Li,Chuang Jiang,Yingnan Liu
The highly selective and sensitive detection of paraoxon residues at low environmental concentrations remains challenging. Herein, a novel fluorescent metal-organic framework composite (Ce 4+ @UiO-66-NH 2 ) with excellent phosphatase-like activity was developed to catalyze the hydrolysis of paraoxon into yellow p -nitrophenol ( p -NP), which quenched the composite's blue fluorescence via the inner filter effect. Based on this mechanism, a simple, portable, non-biological colorimetric/fluorescent hydrogel nanosensor (CM-SA spheres) was constructed by incorporating red fluorescent Mn-CDs with aggregation-induced emission as an internal reference. Upon increasing paraoxon concentration, the spheres showed visible color changes from colorless to yellow under daylight and blue to red under UV light. The sensor demonstrated a visual detection sensitivity of 0.05 μg mL −1 and limits of detection of 0.013 μg mL −1 (daylight) and 0.027 μg mL −1 (UV). In real sample analyses of tea and water, the CM-SA spheres exhibited strong anti-interference capability and reliability, offering a practical strategy for paraoxon degradation and detection.
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PubMed
高影响因子
CHINESE JOURNAL OF CHEMICAL PHYSICS
·
2020
·Vol. 33
·期 4
·394-400
·
IF 1.067
Liu Jia,Jiang Shen-long,Zhang Qun
We constructed two types of copper-doped metal-organic framework (MOF), i.e ., Cu@UiO- 66-NH 2 and Cu-UiO-66-NH 2 . In the
former, Cu 2+ ions are impregnated in the pore space of the
amine-functionalized, Zr-based UiO-66-NH 2 ; while in the latter, Cu 2+ ions are in-corporated to form a bimetal-center MOF, with Zr 4+ being partially
replaced by Cu 2+ in the Zr−O oxo-clusters. Ultrafast spectroscopy revealed that
the photoinduced relaxation kinetics associated with the ligand-to-cluster charge-transfer
state is promoted for both Cu-doped MOFs relative to undoped one, but in a sequence of
Cu-UiO-66-NH 2 >Cu@UiO-66-NH 2 >UiO-66-NH 2 . Such a
sequence turned to be in line with the trend observed in the visible-light photocatalytic
hydrogen evolution activity tests on the three MOFs. These findings highlighted the subtle
effect of copper-doping location in this Zr-based MOF system, further suggesting that
rational engineering of the specific metal-doping location in alike MOF systems to promote
the photoinduced charge separation and hence suppress the detrimental charge recombination
therein is beneficial for achieving improved performances in MOF-based photocatalysis.
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JOURNAL OF POWER SOURCES
·
2018
·
IF 6.945
Liang Shao,Qian Wang,Zhonglei Ma,Zhanyou Ji,Xiaoying Wang,Doudou Song,Yuguo Liu,Ni Wang
Metal-Organic Frameworks (MOFs) attract increasing attention in the field of energy storage, however, poor conductivity in most MOFs largely hinders their electrical properties. In this work, an effective strategy is developed to make the polyaniline (PANI) molecular chains grow in the pores of UiO-66 as one of the MOFs (labeled as PANI/UiO-66) to form a fixed interpenetrating network structure by using the highly stable porous MOFs , through a variety of synergistic effects to enhance the conductivity and electrochemical properties . Moreover, the design and analysis about PANI/UiO-66 is reported for the first time to our knowledge. In addition, PANI/UiO-66 exhibits an extraordinary capacitance of 1015 F g −1 at 1 A g −1 by electrochemical test. At the same time, the symmetric flexible solid-state supercapacitors is also assembled and tested. The resultant supercapacitor shows a favorable specific capacitance of 647 F g −1 at 1 A g −1 and a high cycling stability (91% capacitance retention after 5000 cycles). The bending test indicates that the obtained supercapacitor is flexible and its performance is only decreased 10% after 800 bending cycles with a bending angle of 180. This flexible solid-state supercapacitor shows great potential in energy storage device.
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JOURNAL OF MEMBRANE SCIENCE
·
2025
·
IF 9
Doudou Dong,Weiliang Xu,Yuanhang Jin,Huan Yu,Rui Yao,Guining Chen,Yanan Guo,Haipeng Zhu,Gongping Liu,Yanshuo Li,Wanqin Jin
Currently, separation of ester/alcohol azeotropes such as methyl methacrylate (MMA)/methanol is a typical energy-intensive process using distillation technology. In principle, pervaporation membrane technology can separate azeotropes with higher energy efficiency, while the membrane performance could not meet the application requirement. We reported a new type of MOF ligand side group regulated UiO-66/PDMS mixed-matrix membranes (MMMs) to selectively separate MMA from the its methanol azeotrope. The incorporation of UiO-66 fillers improved the MMA/methanol performance of PDMS membrane. The results of molecular simulation and characterizations revealed that compared with the pristine UiO-66 and UiO-66-CH 3 , amino groups of UiO-66-NH 2 showed stronger interaction energy and thus higher affinity towards MMA molecule. Therefore, although the pore size of UiO-66-NH 2 is larger than the molecular kinetic diameters of MMA and methanol, the tunable chemical environment and molecular interaction promoted the selective transport of MMA. The optimal UiO-66-NH 2 /PDMS MMM displayed an outstanding separation performance with a total flux of 2.07 kg m −2 h −1 and a separation factor of 5.7 for 18 wt% MMA/methanol azeotrope at 40 °C. The membrane exhibited an excellent long-term performance during continuous separation process of ∼3400 h, and showed potential in scale-up fabrication and separation of other ester/alcohol azeotropes. The proposed MOF ligand side group regulation offers a promising strategy to develop high-performance membranes for azeotropic separation.
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高影响因子
MATERIALS RESEARCH BULLETIN
·
2025
·
IF 5.7
Jiazhuang Chen,Yonglian Zhang,Yingjie Guo,Zan Chen,Cuijia Duan,Claudia Li,Sibudjing Kawi,Yinhui Li
To address the low visible-light absorption of titanium oxide (TiO 2 ) and the agglomeration tendency of covalent-organic-framework (COF), UiO-66 modified by amination was combined with acyl chloride covalent organic framework (AC COF) synthesized by ultrasonic assisted method to successfully form AC COF@UiO-66 core-shell structure. Subsequent TiO 2 loading formed a heterojunction that narrows the band gap, suppresses charge recombination, and extends visible-light absorption. Compared to AC COF, the adsorption performance of the TiO 2 /AC COF@UiO-66 increased by 7.4 times, reaching 432.9 mg/g. The active species that play a main part in the photocatalytic degradation process are h + and ·OH. Experimental results demonstrate that tetracycline (TC) can be entirely degraded within 40 min. In this work, the functional design of adsorption and photocatalysis was carried out on UiO-66 framework material, which overcame the limitations of individual component in the treatment of tetracycline wastewater and provided a new strategy for the design of ternary composite photocatalytic materials.
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Journal of Materials Chemistry A
·
2024
·Vol. 12
·期 26
·15803-15813
·
IF 10.7
Huiling Wang,Qiang Li,Jing Chen,Hongpeng Jia
Resource utilization of carbon dioxide (CO2) is an effective strategy to mitigate global warming and achieve carbon neutrality and peak carbon goals. It is well known that different preparation methods affect the catalytic performance of catalysts. Herein, we designed an efficient Ru–ZrO2/C catalyst for photothermal catalytic CO2 reduction by pretreating UiO-66 in a N2 atmosphere and then loading Ru species. Compared to the reference sample of Ru/ZrO2 obtained by calcining UiO-66 in an air atmosphere, Ru–ZrO2/C exhibits much superior catalytic activity under full-spectrum light irradiation with a methane yield of 504.1 mmol g−1 h−1 and selectivity of 98.9%, respectively. In addition, the catalytic performance of Ru–ZrO2/C for photothermal CO2 methanation remains stable without obvious reduction in a 24 hour continuous test. The physicochemical characterization studies of Ru–ZrO2/C determine that the remarkable heat resistance, effective light-heat conversion ability, abundant oxygen vacancies, low-valence Ru, and good CO2 adsorption properties are responsible for the enhanced performance of photothermal CO2 hydrogenation. This work expands the application of MOFs as precursors and provides an effective guide for designing highly efficient photothermal catalysts for solar fuel production.
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