RSC Advances
·
2017
·Vol. 7
·期 5
·2943-2952
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IF 3.108
Jia Yang,Xiaojun Niu,Shaorong An,Weiyi Chen,Jie Wang,Wei Liu
A novel Bi2MoO6–MIL-100(Fe) heterostructure photocatalyst was synthesized by a facile solvothermal method for the first time, and characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectra, transmission electron microscopy, and photoluminescence spectra. The as-prepared Bi2MoO6–MIL-100(Fe) composites exhibited excellent photocatalytic activity and stability towards the degradation of Rhodamine B (RhB) under visible light irradiation. The introduction of MIL-100(Fe) into semiconductor Bi2MoO6 improved the photocatalytic performance remarkably, and the optimal composite with 9% MIL-100(Fe) content showed the highest photocatalytic activity. According to the active radical trapping experiments, the h+ and ˙O2− radicals were the two main active species in the photocatalytic reaction. The enhanced photocatalytic performance is mainly attributed to the formation of the Bi2MoO6–MIL-100(Fe) heterostructure, which is beneficial to the transfer and separation of photo-generated electron–hole pairs. The possible mechanism of the enhanced photocatalytic performance of the Bi2MoO6–MIL-100(Fe) composites was discussed.
研究领域:
材料科学
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环境科学
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DOI
高影响因子
Materials
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2025
·Vol. 18
·期 6
·1343
·
IF 3.2
Hangmin Xu,Hao Song,Xiaozhi Wang,Xingwang Zhu
The substantial release of industrial carbon dioxide has been identified as a key factor in the development of various environmental issues. In addressing these concerns, the utilization of photocatalytic technology for carbon reduction has garnered significant attention. The disadvantage of CO2photoreduction is the problem of product yield and selectivity. It is known that MIL-125(Ti) with a high specific surface area (SBET) possesses more active sites using Ti as a node. The calcination of MIL-125(Ti) in a reducing atmosphere has been shown to introduce oxygen vacancies (OV), thereby enhancing the material’s surface and internal pores. This process has been demonstrated to result in a significant increase in the SBETand an enhancement of the Ti3+/Ti4+ratio. The increased Ti3+centers have been found to improve the material’s reducing properties. The results demonstrate that the OV-rich MIL-125-2H material exhibits the high-performance and highly selective photoreduction in CO2.
研究领域:
环境科学
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材料科学
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化学工程
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产品关联
DOI
PubMed
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2017
·
IF 3.615
Bo Xu,Xuejiao Li,Zhiming Chen,Tao Zhang,Cuncheng Li
Pd@MIL-100(Fe) composite nanoparticles were synthesized and characterized by high-resolution transmission electron microscopy (HRTEM), powder X-ray diffraction analysis, nitrogen adsorption-desorption analysis, X-ray photoelectron spectroscopic (XPS) analysis, energy-dispersive X-ray spectroscopy (EDS) and element mapping. Due to the local restriction or confinement effect of the unique pore/surface structure within the MIL-100(Fe) nanospheres , small Pd nanoparticle (4–6 nm) were obtained with high stability without using any surfactant as stabilizer . The as-synthesized Pd@MIL-100(Fe) composite nanoparticles were then employed for the catalytic reduction of 2/3/4-nitrophenol, which exhibiting high catalytic activity and recyclability attributed to the synergistic effect between Pd nanoparticles and MIL-100(Fe) nanospheres.
研究领域:
材料科学
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环境化学
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产品关联
DOI
高影响因子
DESALINATION
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2025
·
IF 9.8
Huiqun Ju,Xue Jiang,Chengyu Huangfu,Jiafei Lyu,Xianghai Guo
Metal-organic framework (MOF) materials exhibit excellent boron adsorption and isotope separation abilities, but their mechanisms are still unclear and require additional research. In this study, MIL-100(Fe), which has excellent comprehensive performance in boron adsorption and isotope separation among MOF materials, was selected to systematically investigate its boron adsorption and isotope separation performance. Based on this material, five MIL-100 (Fe 3+ , X 2+ ) bimetallic materials were prepared by doping different divalent metal ions, and the changes in the adsorption and separation capacities before and after doping were compared. The influence of different metal doping on adsorption was investigated. It was found that doping metal ions effectively increased the coordination of unsaturated metal sites in the materials, which improved the adsorption process and caused positive and effective isotopic separation. The isotopic separation factor of doping the alkali earth metal ion Ca 2+ was increased significantly from 1.033 to 1.092.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Shiyong Wei,Aijia Cao,Siyuan Huang,Yao Shen,Ting Lei,Songmei Luo,Mingjun Cai,Wenjun Xiang,Anying Chen,Rui Wang
Although MIL-100(Fe) was regarded as an ideal material for the environmental remediation, it could not be applied in practical because of the potential eco-environmental risk and cost. In this work, a novelty strategy of liquidizing crystal MIL-100(Fe) was posted for the first time through inhibiting the crystallization process and forming physical MIL-100(Fe) gel. Due to this MIL-100(Fe) sol–gel, MIL-100(Fe) could easy cover on the surface of silica powder (SiO 2 ) through simple soaking operation. MIL-100(Fe) covering on SiO 2 (MIL-100(Fe)@SiO 2 ) could be quickly separated from wastewater spontaneously owing to the carrier of SiO 2 , even in a tank of 2.0 m, which made it possible for purifying wastewater in practical. MIL-100(Fe)@SiO 2 could remove phosphate with a removing ratio of closing 100 % at an initial concentration of 10 mg/L, while more than 95 % towards methyl orange (MO). The removing ratio of MO by MIL-100(Fe)@SiO 2 did not obviously decrease when the concentration of MO increased to 100 mg/L. And the adsorption performance of phosphate did not affect by pH among 3.0–9.0. The adsorption amount exceeded 50 % of maximum adsorption capacity for phosphate within 30 min, while 90 % for MO. Monodentate mononuclear coordination could explain the adsorption of phosphate by MIL-100(Fe)@SiO 2 . The N atom in MO might be acted as Lewis acid to coordinate with MIL-100(Fe)@SiO 2 . After adsorption, the P-saturated and MO-saturated MIL-100(Fe)@SiO 2 could be effectively regenerated by the dilute HCl and NaOH solution, respectively. The recovery ratio of adsorption capacity for phosphate and MO were up to 97.7 % and 71.6 %.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
Nanoscience and Nanotechnology Letters
·
2019
·Vol. 11
·期 2
·229-233
·
IF 0
Zhao Tian,Yu Jun,He Ziyu,He Nongyue,Dong Ming,Chen Zhu,Chen Hong
The well investigated chromium-benzenedicarboxylate metal-organic framework (MOF), nano-sized MIL-101(Cr), was synthesized in this study by using tetramethylammonium hydroxide (TMAOH) or acetic acid (HAc) as modulator. The addition of TMAOH/HAc played a crucial role on particle size
and morphology of MIL-101(Cr). The obtained MIL-101(Cr) had average diameter of about ∼90 nm in selected condition, and possessed relatively high porosity (the BET surface area can up to 3500 m2/g). Furthermore, compared to bulk phase MIL-101(Cr), the nano-MIL-101(Cr) presented
significant improvement of catalytic activity in oxidation of indene.
研究领域:
化学
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材料科学
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DOI
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2025
·
IF 5.4
Zhicong Yuan,Xuelian Chen,Xiqiang Pan,Guojuan Hai
The development of efficient electrocatalysts through heterostructure engineering is crucial for boosting the oxygen evolution reaction (OER) kinetics. Herein, we demonstrate a hierarchical MIL-53/NiCu-LDH(12) heterostructure in-situ grown on nickel foam (NF), where the MIL-53 component is controllably constructed on NiCu-LDH/NF to establish robust interfacial contact and electronic coupling. This multi-level architecture synergistically endows the catalyst with enlarged electrochemical active surface area, abundant accessible active sites, accelerated electron transfer kinetics, and reduced band gap. Remarkably, operando characterization reveals that the heterojunction undergoes partial structural reconstruction during OER to generate γ-FeOOH/γ-NiOOH active phases. The formed Fe-O-Ni bridging bonds facilitate interfacial charge redistribution, which effectively modulates the electronic configuration and optimizes reaction intermediates adsorption. Benefiting from these merits, the MIL-53/NiCu-LDH(12)/NF electrode delivers exceptional alkaline OER performance, requiring ultralow overpotentials of 160 and 226 mV to achieve current densities of 10 and 100 mA cm −2 , respectively, along with a small Tafel slope of 42 mV dec −1 . This work proposes an innovative strategy integrating hierarchical architecture design with interfacial electronic modulation for developing advanced transition metal-based OER electrocatalysts.
研究领域:
材料科学
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电化学
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产品关联
DOI
高影响因子
CHEMOSPHERE
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2022
·
IF 8.943
Cheng Cheng,Dongyun Chen,Najun Li,Hua Li,Qingfeng Xu,Jinhui He,Jianmei Lu
This paper reports the application of NH 2 -MIL-125(Ti) modified carbon nitride C v -C 3 N 4 with carbon vacancies in the removal of NO. We performed a series of characterizations of the complex and compared various ratios with the individual components. The results of UV spectrum analysis show that the composite's range of light absorption expanded due to the modification of Ti metal–organic framework. Furthermore, the results of photocurrent and electrical impedance indicate the compound has a better ability to generate and transfer electrons . The increase in the compound's NO removal efficiency (up to 63%) indicates that MOF has a positive effect on C v -C 3 N 4 modification—a good method for photocatalysis . Moreover, the compound can promote photocatalysis in a favorable direction.
研究领域:
材料科学
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环境科学
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DOI
高影响因子
POLYHEDRON
·
2019
·
IF 2.284
Ning Tian,Yifang Dai,Qing Liu,Wei Dai
A general synthetic strategy for HS-Fe 3 O 4 @MIL-53(Al) adsorbent has been developed in this work. The composite material exhibits an efficient capture performance for rubidium ion due to sulfhydryl group and magnetic Fe 3 O 4 doped in its porous cavity. The results of X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and N 2 adsorption–desorption proved that the HS-Fe 3 O 4 was immobilized in the composite material. High Rb + uptake capacity over the HS-Fe 3 O 4 @MIL-53(Al) is attributed to the exchange of acidic protons between the sulfhydryl group and the Rb + . The pseudo-second-order and Freundlich model could make a good description of the adsorption process. The Rb + sorption selectivity was moderately influenced by any co-ions effect (K + , Na + and Cs + ) due to HS-Fe 3 O 4 doped. These results reveal that our novel composite material might be a promising industrial adsorbent for Rb + capture.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2015
·
IF 4.321
Tongtong Han,Yuanlong Xiao,Minman Tong,Hongliang Huang,Dahuan Liu,Luyan Wang,Chongli Zhong
A series of CNT@MIL-68(Al) composites with different carbon nanotubes (CNTs) loadings have been synthesized and characterized by SEM, TEM, PXRD, FT-IR, TGA, and N 2 adsorption. As evidenced from SEM and TEM images, the incorporation of CNTs can result in better dispersity of MIL-68(Al) in composites and smaller particle size than pure MIL-68(Al). Adding appropriate amounts of CNTs increases both the BET surface areas and the total volume of small micorpores (<16 Å), leading to largely improved performance of adsorptive removal of phenol from aqueous solution. In the industrial concentration range of phenol, the adsorption capacity of 0.75% CNT@MIL-68(Al) was improved up to 188.7% compared with the pristine MIL-68(Al), possibly due to the increase of small micropores introduced by the incorporation of CNTs. Regeneration experiments demonstrated that the composites are stable with good regenerability for at least five cycles. This work shows that the composites formed by the combination of CNTs and MOFs may find promising applications in liquid phase adsorption.
研究领域:
材料科学
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环境科学
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化学工程
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2021
·Vol. 32
·期 2
·1778-1786
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IF 2.478
Ding Ling,Zeng Min,Wang Huan,Jiang XiaoBing
In the present study, to broaden the application of metal–organic framework (MOF) materials in electronic functional materials, a simple solvothermal method was adopted to introduce bimetals, and metal–organic framework compounds (MIL-101 (Fe), MIL-101 (Fe, Co), MIL-101 (Fe, Cu)) acted as the templates. The hollow structures of Fe 2 O 3 , CoFe 2 O 4 , and CuFe 2 O 4 were formed through the simple calcinations at 600 °C for 3 h in Ar atmosphere. When the mentioned materials exhibiting hollow structures were tested as the negative electrode of a lithium-ion battery, introducing bimetals was reported to be able to improve their electrochemical performance. For instance, CoFe 2 O 4 and CuFe 2 O 4 were cycled 300 times under a high current density of 1000 mA/g, and the reversible capacity remained to be 978 mAh/g and 774 mAh/g. When 200 cycles were performed under a current density of 200 mA/g, these materials exhibited high specific capacities of 1118 mAh/g and 1155 mAh/g.
研究领域:
材料科学
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电化学
·
能源存储
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DOI
高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Hui Chen,Wengao Zeng,Yutang Liu,Wanyue Dong,Tao Cai,Lin Tang,Juan Li,Wenlu Li
It is important to find an effective way to enhance the photocatalytic efficiency of metal–organic frameworks. In this work, an organic supermolecule perylene diimide (PDI) semiconductor with a carboxyl terminal was added into the synthesis process of MIL-53(Fe) crystals. The PDI/MIL-53(Fe) (PM) composite photocatalyst was first obtained. The TC-H photodegradation rate of the most efficient 5PM was nearly 94.08% within 30 min, whose apparent reaction rate constant (k) is 4 times that of PDI and 33 times that of MIL-53(Fe), respectively. By investigation and characterization, it has been found that PDI nanofibers were dispersed and fixed in MIL-53(Fe) and bonded to each other by covalent bonds. The radical trap experiments and electron spin resonance analysis illustrated that hydroxyl radical (·OH), superoxide radical (·O2–), and photogenerated holes (h+) were active species. Combined with the band structure of PDI and MIL-53(Fe), it is proposed that the PM photocatalyst was a Z-scheme heterojunction mechanism. Therefore, PM photocatalysts showed excellent charge separation and transfer ability. The performance improvement of 5PM is due to enhanced visible light absorption, efficient charge separation, and excellent redox potential. Five cyclic photocatalytic tests and experiments further demonstrate that the 5PM photocatalyst has a promising future for pollutant removal.
研究领域:
材料科学
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环境科学
·
化学
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DOI
PubMed
高影响因子
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