JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
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IF 8.128
Ahmed Mahmoud Idris,Xinyan Jiang,Jun Tan,Zhenzhi Cai,Xiaodan Lou,Jin Wang,Zhengquan Li
Dye-sensitized system holds great potential for the development of visible-light-responsive photocatalysts not only because it can enhance the light absorption and charge separation efficiency of the systems but also because it can tune the band structure of catalysts. Herein, two-dimensional (2D) Fe-MOF nanosheets (Fe-MNS) with a LUMO potential of 0.11 V ( vs. RHE) was prepared. Interestingly, it has been found that when the 2D Fe-MNS catalyst was functionalized with visible-light-responsive [Ru(bpy)] 3 2+ as a dye-sensitizer, the electrons from the [Ru(bpy)] 3 2+ can effectively inject into the 2D Fe-MNS, which resulted in a negative shift of the LUMO potential of the 2D Fe-MNS to −0.15 V ( vs. RHE). Consequently, the [Ru(bpy)] 3 2+ /Fe-MNS catalytic system exhibits a sound photocatalytic CO 2 -to-CO activity of 1120 μmol g -1 h −1 under visible-light-irradiation. The photocatalytic CO production was further ameliorated by regulating the electronic structure of the 2D Fe-MNS by doping Co ions , achieving a remarkable photocatalytic activity of 1637 μmol g -1 h −1 . This work further supports that the dye-sensitized system is an auspicious strategy worth exploring with different catalysts for the development of visible-light-responsive photocatalytic systems.
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高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
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2021
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IF 3.498
Wei Shuang,Hui Huang,Ming Liu,Tianyu Bai,Jijie Zhang,Danhong Wang
Copper sulfides are proved to be good candidates as anode materials for sodium ion batteries due to their abundant resources, moderate cost, and relatively high electrical conductivity . However, poor rate performance and cycling life still hinder their development as anode materials for sodium-ion batteries. Herein, we synthesized carbon-coated copper sulfide nanorod assembled into octahedron composites (CuS x @C) by sulfuration of a Cu-based metal-organic framework (Cu-MOF) under different temperatures. These composites with hierarchical structure exhibited superstable cycling performance as anodes of sodium-ion batteries. The CuS x @C sample obtained under 500 °C showed discharge capacity of 208 mA h g - 1 at 2 A g - 1 over 6300 cycles. Porosity and hierarchical stucture facilitate the storage of sodium ion, and carbon-coated structure buffers volume change of anode materials during the electrochemical reaction .
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APPLIED SURFACE SCIENCE
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2021
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IF 6.707
Yuan Wang,Zhaoxian Yang,Lei Liu,Yingbo Chen
In this study, hydrophobic nanofillers (ODA-h-NCs) were firstly synthesized through surface modification of MOF-derived nanocages by octadecylamine (ODA). ODA-h-NCs were then incorporated into poly(piperazine-amide) (PA) active layer to fabricate thin-film nanocomposite (TFN) nanofiltration membranes. The effects of ODA-h-NCs dosage on PA’s properties were characterized and the membrane performances on salt rejections were evaluated. Finally, the TFN nanofiltration membrane with the optimal nanoparticle doping amount was chosen. The experimental results show that the water permeance of the constructed TFN nanofiltration membrane reaches 8.97 L/(m 2 ·h·bar) with 95.8% Na 2 SO 4 rejection when ODA-h-NCs concentration is 0.0075 wt%, which is 1.7 times that of pristine membrane. It is also testified that the prepared TFN nanofiltration membrane possesses good stability through 50-h filtration test. Although the introduction of hydrophobic ODA-h-NCs increases the PA layer thickness, ODA-h-NCs decrease the crosslinking degree of PA layer by inhibiting the piperazine diffusion rate and pathway, their unique porous nanocage structure and large surface area provide additional transport path for water molecules, which equips TFN nanofiltration membrane with higher water flux.
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
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2021
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IF 8.742
Wenbo Chen,Zhenguo Zhang,Cancan Yang,Jing Liu,Hongcheng Shen,Kai Yang,Zhe Wang
In this work, we fabricated PIM-based mixed matrix membranes (MMMs) containing MOF-801/ionic liquid nanocomposites to enhance CO 2 separation performance of pure polymer membranes. All membranes and MOF-801/ionic liquid nanocomposites were prepared by solution casting method and wet impregnation, respectively. The samples were analyzed by SEM, XRD , FTIR, TGA and Nitrogen adsorption-desorption measurements. The nanocomposites are composed of metal-organic framework (MOF) MOF-801 and ionic liquid (IL) adsorption capacity. MOF-801 can well control the dispersion of IL in the polymer matrix , which is conducive to exposing more active sites in the nanocomposites to improve the CO 2 adsorption selectivity of MOF-801/ionic liquid nanocomposites. At the same time, the porous structure of nanocomposites also enhances the gas adsorption and diffusion, thereby improving the gas separation performance. Compared with pure PIM-1 membranes, the CO 2 permeability and CO 2 /N 2 selectivity of IL@MOF/PIM-5% MMMs was increased by 129% and 45% (CO 2 = 9420 Barrer, CO 2 /N 2 = 29）, respectively. Compared with MOF-801/PIM-1 MMMs, the permeability of CO 2 decreased slightly but the selectivity of CO 2 /N 2 increased from 27 to 29. The aging test showed that the CO 2 permeability of MMMs could remain above 70% after 90 days. The anti-plasticization performance of MMMs has also been significantly improved. The CO 2 separation performance of IL@MOF/PIM-5% MMMs significantly exceeded the 2008 Robeson upper bound, showing excellent gas separation performance and working stability.
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高影响因子
CHINESE JOURNAL OF CATALYSIS
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2019
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IF 4.914
Ruowen Liang,Zhiyu Liang,Feng Chen,Danhua Xie,Yanling Wu,Xuxu Wang,Guiyang Yan,Ling Wu
Magnetically recyclable porous sodium dodecyl sulfate (SDS)/Fe 2 O 3 hybrids, which combine the porous structure of Fe 2 O 3 and hydrophobicity of SDS, have been successfully synthesized for the first time. Porous Fe 2 O 3 has been first pyrolyzed from MIL-100(Fe) using a simple two-step calcination route. Then, the obtained porous Fe 2 O 3 nanoparticles have been self-assembled with SDS molecules and yielded hydrophobic SDS/Fe 2 O 3 hybrids. The porous SDS/Fe 2 O 3 hybrids have been demonstrated to be highly efficient for the denitrification of pyridine under visible light irradiation. The pyridine removal ratio has reached values as high as 100% after irradiation for 240 min. Combining the results of a series of experimental measurements, it was concluded that the superior photocatalytic performance of SDS/Fe 2 O 3 hybrids could be attributed to (i) the fast electron transport owing to the unique porous structure of Fe 2 O 3 , (ii) the superior visible light absorption of Fe 2 O 3 nanoparticles, and (iii) the “bridge molecule” role of SDS efficiently improving the separation and transfer across the interfacial domain of SDS/Fe 2 O 3 of photogenerated electron-hole pairs. More significantly, after the catalytic reaction , the SDS/Fe 2 O 3 hybrids could be easily recovered using magnets and reused during subsequent cycles, which indicated their stability and recyclability.
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Journal of Materials Chemistry C
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2019
·Vol. 7
·期 40
·12674-12681
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IF 6.641
Ming Gong,Jian Yang,Yongsheng Li,Qixin Zhuang,Jinlou Gu
The development of an effective strategy for the accurate detection of cholesterol in human serum is of great significance. Herein, a novel luminescent metal–organic framework (LMOF) probe was successfully constructed for the specific detection of cholesterol in blood. Owing to the large size of the mesopores in NU-1000, carboxymethyl β-cyclodextrin (β-CMCD) was grafted onto the LMOF with a high density and designed as an energy-transfer bridge and an inclusion site for cholesterol recognition. Upon adding a blood sample into the sensing system, the free cholesterol inside the serum competes with Rh6G to form a more stable inclusion complex with β-CMCD, and induces the fluorescence restoration of the ligand in LMOF proportionally, which was quenched in advance by Rh6G due to the fluorescent resonance energy transfer (FRET) effect. The specificity of the employed sensing probe for cholesterol recognition was scarcely affected by other possibly coexisting interfering substances. Furthermore, the LOD value was determined to be as low as 0.4 μM, which is far lower than the normal cholesterol level in human serum. This indicates the practical application of the current developed LMOF sensor for the accurate and rapid detection of cholesterol in disease diagnosis.
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高影响因子
CERAMICS INTERNATIONAL
·
2019
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IF 3.45
Runjiang Guo,Hongdong Wang,Ran Tian,Dongliang Shi,Hua Li,Yao Li,Hezhou Liu
In this report, a novel hollow boxes shape ZnSnO 3 is synthesized via a one-pot surfactant-free method. We synthesize CNT@ZnSnO 3 hollow boxes via hydrothermal reaction by using the Zn-MOF(ZIF-8) as the Zn source at the first time. Several characterization techniques are used to investigate the structure, morphology, composition and specific surface area of CNT@ZnSnO 3 . CNT@ZnSnO 3 hollow boxes demonstrated large specific surface area (up to 45.73 m 2 /g), which is favorable for the strong gas sensor response. The ethanol sensor based on CNT@ZnSnO 3 hollow boxes exhibited high response of ethanol up to 166 at 240 °C at the concentration of 100 ppm, which is about 8 times higher than the sensing response of ZnSnO 3 nanocubes. Moreover, CNT@ZnSnO 3 hollow boxes based ethanol sensor also shows the excellent selectivity and stability. As a novel green gas sensor, CNT@ZnSnO 3 hollow boxes show the great potential in the gas sensing field.
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高影响因子
DALTON TRANSACTIONS
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2019
·Vol. 48
·期 8
·2715-2721
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IF 4.052
Lin Lin,Siyu Huang,Yuxin Zhu,Biao Du,Zhihua Zhang,Chao Chen,Xuewen Wang,Ning Zhang
A new synthetic method was used to develop a CdS/MoS2 heterojunction. Cd-MOF was coated onto the surface of MoS2 flowers to construct a core–shell MoS2@Cd-MOF. Thioacetamide was used as a sulfur source to sulfurize the MoS2@Cd-MOF to form a CdS/MoS2 heterojunction. Since the Cd2+ ions were highly ordered and separated by the organic ligands of the Cd-MOF shell, the as-synthesized CdS/MoS2 heterojunction possessed a large surface area and intimate contact at the heterogeneous interface with a uniform loading of CdS nanoparticles on the MoS2 flowers. Consequently, the CdS/MoS2 heterojunction exhibited a significantly enhanced photocatalytic H2 evolution rate of average 5587 μmol h−1 g−1 under UV-visible light irradiation.
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高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2019
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IF 3.375
Junjie Zhu,Linbo Wu,Zhiyang Bu,Suyun Jie,Bo-Geng Li
Searching for highly efficient and robust CO2 adsorbents is very important for CO2 capture, utilization, and storage. In this study, new polyethylenimine-grafted metal–organic framework (MOF)–polymer composites, abbreviated as PEI@PGD-H, were synthesized via high internal phase emulsion (HIPE) template polymerization of divinylbenzene and glycidyl methacrylate, followed by in situ generation of HKUST-type MOF in the presence of hydrophobic-modified CuO nanoparticles via the reaction of CuO with 1,3,5-benzenetricarboxylic acid and then polyethylenimine (PEI) functionalization via epoxy–amine reaction and amine–metal sites interaction. The coexistence of the hierarchical interconnected porous skeleton of poly(glycidyl methacrylate–divinylbenzene) (PGD), high specific surface area of MOF, and chemical CO2 adsorption of PEI endows PEI@PGD-H with high CO2 adsorption capacity, rate, and selectivity. PEI70@PGD-H shows a CO2/N2 separation factor as high as 76 and CO2 adsorption capacities of 4.3, 3.0, and 1.8 mmol of CO2/g from pure CO2, simulated flue gas, and air, respectively. After 20 CO2 adsorption–desorption cycles, the adsorbent still retained a high and stable CO2 capture capacity over 2.8 mmol of CO2/g for simulated flue gas. The adsorbent also displays reasonably good thermal stability, excellent water endurance, low desorption energy, and easy shaping. The desorption heat is as low as 48 kJ/mol of CO2. These features make PEI@PGD-H highly efficient, robust, and low-energy CO2 adsorbents for practical application in CO2 capture.
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CATALYSIS TODAY
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2019
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IF 4.888
Le Yang,Rui Ma,Hui Zeng,Zebao Rui,Yongdan Li
This work provides a facile strategy to prepare core-shell structured catalysts with MOF-templated metal active species embedded carbon matrix core and a functional metal oxide shell in a controllable way. The procedure features with the facile introduction of functional shell metal oxide and delivery of MOF morphology. Co(II/Ⅲ)@ZnO hexagonal prisms are fabricated with this procedure and ZIF-67 as the template. When being used in the selective oxidation of vanillyl alcohol to produce vanillin, ZnO shell plays an important role by faciliating redox of Co 3+ /Co 2+ for promoting vanillyl alcohol oxidation to vanillin and protecting the Co species against leaching into the reaction system. Co(II/Ⅲ)@ZnO exhibits a conversion of 20% with a selectivity of 80% after a 2 h reaction and shows stability after 3 catalytic cycles.
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高影响因子
BIOSENSORS & BIOELECTRONICS
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2019
·
IF 9.518
Xiaoxue Fu,Junlin He,Chengli Zhang,Jun Chen,Yilin Wen,Jia li,Weiran Mao,Hangtian Zhong,Jiahao Wu,Xingduo Ji,Chao Yu
In this work, an aptamer was used as the target capturing agent and a trimetallic signal amplification strategy based on [email protected] and AuPtRu NPs was demonstrated for the sensitive detection of TSP-1. Herein, the synthesized AuPtRu nanocomposite (AuPtRu NPs) not only acts as the catalyst for catalyzing hydrogen peroxide but also acts as a nanocarrier for capturing the -NH 2 termination single strand DNA (S1) to obtain the signal probe (SP, AuPtRu nanocomposite/S1). Then, SP was efficiently linked into TSP-1 aptamers with the addition of complementary linking strands to form M1 (SP/aptamer). The [email protected] nanocomposites were obtained by in situ reduction and used as GCE electrode modification materials. The -NH 2 -modified capture probe (CP) DNA was immobilized on the surface of [email protected] nanocomposites for hybridizing SP. In the presence of the target TSP-1, the aptamer recognizes the target and binds strongly so that SP is released from the prepared M1 and then hybridized with CP. When the detection solution contains an electrochemical matrix of H 2 O 2 , AuPtRu NPs can oxidize H 2 O 2 to obtain an enhanced signal. Furthermore, the proposed aptasensor has a very low LOD of 0.13 fg mL −1 TSP-1 in the detection range of 1 fg mL −1 to 10 ng mL −1 . Moreover, the proposed platform also has application implications for other potential targets.
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高影响因子
CATALYSIS LETTERS
·
2019
·Vol. 150
·期 2
·322-331
·
IF 2.372
Wang Kaifeng,Liu Ya,Wu Wufeng,Chen Yu,Fang Lina,Li Wanbin,Ji Hongbing
Abstract In this study, Zr-MOF material (UiO-66) was modified with different metal oxides (CeO 2 , Ga 2 O 3 , and CoO) and employed in the conversion of cellulose to levulinic acid (LA) in aqueous medium. The research results showed that the introduction of the metal oxides increased the acid content of the catalysts, especially in medium-strong acid. The selectivity of LA was related to the type of metal oxide and the content of medium-strong acid. Due to the activity of Ga 2 O 3 and more medium-strong acid, the yield of LA reaches a maximum yield of 32.0 mol% at 513 K for 360 min when Ga 2 O 3 -UiO-66 was employed as the catalysts. The combination of metal oxide and UiO-66 enables the reaction to proceed, providing a new direction for the conversion of cellulose to LA in the aqueous phase. Graphic Abstract In this study, Zr-MOFs material (UiO-66) was modified with different metal oxides (CeO 2 , Ga 2 O 3 , and CoO) and employed in the conversion of cellulose to levulinic acid in aqueous medium. The results indicated that the addition of metal oxides changes the acidity of UiO-66, which improves the catalytic activity. The selectivity of LA was related to the type of metal oxide and the content of medium-strong acid.
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