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Mil-100(Fe)
CATALYSIS COMMUNICATIONS · 2017 · IF 3.33

Sandwich-like MIL-100(Fe)@Pt@MIL-100(Fe) nanoparticles for catalytic hydrogenation of 4-nitrophenol

Zhiming Chen,Bo Xu,Xiaomei Wang,Li Zhang,Xiaoqing Yang,Cuncheng Li

Separation and recycling of noble metal nanoparticles after catalytic reaction is critical to promote its application efficiency and cut down the cost. This work presents a facile synthesis strategy for the fabrication of sandwich-like MIL-100(Fe)@Pt@MIL-100(Fe) (denoted as S-Pt) nanoparticles with high stability and improved catalytic activity for hydrogenation of nitrophenol. MIL-100(Fe) acts as both carrier to make the catalyst easily separated and shield to protect the tiny Pt nanoparticles from leaching or aggregation during reaction. Moreover, mass transfer effect of the porous MIL-100(Fe) with its pore structure serving as nano-reactor is also benefit for promoting the catalytic efficiency.

CAS / MDL: 10060-10-3 554-95-0
研究领域: 材料科学 · 催化化学
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ANALYTICAL CHEMISTRY · 2025 · IF 6.7

Enhanced Chemiluminescence Induced by Natural Light-Driven MIL-100(Fe)/TiO2 for Dopamine Detection

Chengzhuo Yu,Jin Xu,Li Xiong,Yarui Wang,Silong Wang,Fanglan Geng,Zesen Shang,Huasheng Wu,Lixia Zhao,Yawei Wang

Luminol-based chemiluminescence (CL) systems, as a powerful tool for bioanalysis, are limited owing to their weak CL intensity and self-decomposition of the classic oxidant H2O2. Herein, we introduced a new luminol CL enhancer, the natural light-driven photocatalyst MIL-100(Fe)/TiO2, for the selective determination of dopamine (DA). By employing MIL-100(Fe)/TiO2 for the first time as an efficient enhancer, the MIL-100(Fe)/TiO2-luminol CL intensity was 100 times higher than that of the classical H2O2-luminol system. The CL spectrum, UV–vis absorption spectroscopy, radical scavenger experiments, and electron spin resonance spectroscopy were utilized to investigate the possible CL mechanism of the MIL-100(Fe)/TiO2-luminol system. All of the results indicated that MIL-100(Fe)/TiO2 can generate reactive oxygen species under mild natural light, which could react rapidly with the luminol anion radical and result in direct CL emission. The sensitive plate for DA was developed based on its inhibiting effect on CL intensity, and the linear range between CL intensity and DA concentration was 100 nM–1000 μM with a detection limit of 16.7 μM (S/N = 3). This study successfully achieved a stable reactant that can directly trigger the CL of luminol without the need for additional oxidizing agents under mild natural light and offers new possibilities for photoinduced amplification technology.

CAS / MDL: 98-00-0 144-55-8 51-61-6
研究领域: 分析化学 · 生物医学工程
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CATALYSIS COMMUNICATIONS · 2017 · IF 3.33

Glycol assisted synthesis of MIL-100(Fe) nanospheres for photocatalytic oxidation of benzene to phenol

Bo Xu,Zhiming Chen,Bing Han,Cuncheng Li

This work presents MIL-100(Fe) nanoparticles synthesized using glycol with uniform size and morphology. This is the first report of nanoscale MOFs material synthesized using glycol. The MIL-100(Fe) particles have been characterized by SEM, TEM, XRD and the results indicate that the MOFs particles show monodispersed nanospherical morphology. Photocatalytic study reveals that the MIL-100(Fe) nanospheres exhibit good oxidation ability of benzene to phenol under visible light irradiation with high selectivity.

CAS / MDL: 10060-10-3 554-95-0
研究领域: 材料科学 · 环境科学 · 化学工程
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Delignified wood supported MIL-100 (Fe) for fast adsorption removal of tetracycline

Xiuying Zhu,Mengjie Li,Xiong-Fei Zhang,Jianfeng Yao

Iron-based metal-organic framework (MIL-100) with intrinsic high surface area and low cost is extremely attractive in the field of organic pollutant remediation. Herein, delignified balsa wood is utilized as substrate/support for the in situ growth and dispersion of MIL-100 particles. Results demonstrate that the MIL-100 particles adhere tightly to the support and a hierarchal architecture is constructed. The MIL-100@Wood composite can be used as adsorbent and filter for the alleviation of organic contamination. With 25.4 wt% of MIL-100 loading, the MIL-100 decorated delignified wood (MD-Wood) exhibits a tetracycline (TC) adsorption capacity of 109.9 mg/g. The composite MD-Wood can be easily fabricated into an all-in-one filter and this filter presents an effective treatable volume of 1100 mL of TC solution (20 mg/L). The MD-Wood is further deposited with Ag particles and the Ag@MD-Wood can be directly applied for the flow catalytic reduction of 4-nitrophenol. Moreover, the composite woods are facile to regenerate and possess superior reusability and stability.

研究领域: 环境科学 · 材料科学
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DALTON TRANSACTIONS · 2025 ·Vol. 54 ·期 8 ·3467-3477 · IF 3.3

TiO2/CoOx heterostructure decorated MIL-100(Fe) by atomic layer deposition for enhanced photocatalytic oxygen production

Wenhui Hu,Zhongxin Song,Lingna Sun,Lei Zhang,Qianling Zhang,Xiangzhong Ren,Yongliang Li

Efficient separation of photogenerated charge carriers is essential for maximizing the photocatalytic efficiency of semiconductor materials in oxygen evolution reactions (OER). This study presents a novel trimetallic photocatalyst, MIL-100(Fe)/TiO2/CoOx, synthesized through a facile microwave-assisted hydrothermal method followed by atomic layer deposition (ALD). The porous MIL-100(Fe) serves as a support for the sequential deposition of TiO2 and CoOx layers via ALD, which enhances electron–hole pair separation and minimizes their recombination. Characterization using transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) confirms the uniform deposition of TiO2 and CoOx layers on the MIL-100(Fe) surface. The optimized photocatalyst, processed with 20 deposition cycles of Co, exhibits exceptional photocatalytic OER performance, with an oxygen evolution rate of 558.3 μmol g−1 h−1. This enhancement in activity is attributed to the synergistic interaction between the spatially separated TiO2 and CoOx cocatalysts, which facilitates efficient charge transfer and increases the number of active sites. These findings highlight the potential of ALD-fabricated heterostructures in the development of advanced photocatalysts for sustainable energy production.

CAS / MDL: 7439-89-6
研究领域: 材料科学 · 能源化学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Efficient photocatalytic degradation of phenolic pollutants using MIL-100(Fe)@Zn3In2S6 Z-scheme heterojunction

Shuyu Chen,Zhengkai Wu,Xueying Cheng,Lu Chen,Yunning Chen,Yingna Guo,Changhua Wang,Qingkun Shang

In this work, we used a simple hydrothermal method to in-situ grow Zn 3 In 2 S 6 on MIL-100(Fe) octahedra, and obtained a MIL-100(Fe)@Zn 3 In 2 S 6 Z-scheme heterojunction photocatalyst. We systematically studied its performance in degrading phenol and p-nitrophenol (PNP) under visible light. MIL-ZIS 6 -2 can remove 89.1 % of phenol within 120 min and nearly 100 % of PNP within 60 min. Its photocatalytic activity to the degradation of phenol is 30.7 times and 1.7 times higher than that of MIL-100(Fe) and Zn 3 In 2 S 6 , respectively. And the photocatalytic activity to degrade PNP is 18.2 times and 1.4 times higher than MIL-100(Fe) and Zn 3 In 2 S 6 . Further research was conducted on its band structure and photocatalytic response mechanism through photoelectric performance, ultraviolet photo-electron spectroscopy, and electron spin resonance spectrometer testing. The results showed that the formation of Z-scheme heterojunction not only increased the specific surface area of the composite photocatalyst, enabling it to provide more reaction sites, but also effectively suppressed the recombination of photogenerated holes and electrons, improving the redox ability of the photocatalyst. This work provides a new perspective for constructing efficient Zn 3 In 2 S 6 -based composite photocatalysts and addressing environmental issues.

研究领域: 材料科学 · 环境科学
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RSC Advances · 2017 ·Vol. 7 ·期 5 ·2943-2952 · IF 3.108

Facile synthesis of Bi2MoO6–MIL-100(Fe) metal–organic framework composites with enhanced photocatalytic performance

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 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Liquidizing crystal MIL-100(Fe) to coating silica powder for purifying wastewater

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 %.

CAS / MDL: 7631-86-9
研究领域: 环境科学 · 材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2017 · IF 3.615

Pd@MIL-100(Fe) composite nanoparticles as efficient catalyst for reduction of 2/3/4-nitrophenol: Synergistic effect between Pd and MIL-100(Fe)

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.

CAS / MDL: 7705-08-0 554-95-0
研究领域: 材料科学 · 环境化学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Design and Component Contribution Study of MIL-100(Fe)-Derived Materials for Adsorption Removal of Antipyrine from Water

Bolun Yu,Jun Chen,Quanzhang Liu,Shuoyang Li,Xiaohang Zhang,Bowen Liang,Zuhong Lin,Haipu Li,Jingjing Yao

The use of metal–organic framework-derived materials for removing micropollutants from water is increasing, but precise composition control remains a challenge. In this study, 14 MIL-100(Fe)-derived materials were synthesized to adsorb and remove antipyrine (ANT) from water by optimizing the heating rate, pyrolysis temperature, and activation methods. The adsorbents demonstrated excellent ANT removal performance across a pH range of 3 to 11, as well as in complex water bodies. They also exhibited easy recovery and outstanding regeneration capabilities. Under the optimized conditions (i.e., ANT content: 10 mg/L, M-600–2 dosage: 0.1 g/L, and pH: 7), M-600-10 displayed the highest adsorption capacity (23.10 mg/g for ANT) while MIL-100(Fe) had limited adsorption capability (2.56 mg/g for ANT). The adsorption process was exothermic and spontaneous, influenced by both membrane diffusion and intraparticle diffusion, and followed the Freundlich and pseudo-second-order models. Despite variations in surface areas (75.70–261.91 m2/g), total pore volumes (0.2019–0.5984 cm3/g), and average pore sizes (7.47–13.99 nm), there was no strong linear relationship with adsorption capacity (7.47–15.99 mg/g). The major components, including Fe/pyrrolic N-doped graphene (PING), Fe3C/PING, Fe3O4/PING, and PING, had calculated adsorption energies of −0.94, −2.16, −0.79, and −2.24 eV, respectively, which correlated positively with Bader charge transfer numbers. The adsorbents relied on van der Waals forces for ANT adsorption, with PING exhibiting the strongest interactions and Fe3O4/PING exhibiting the weakest. These findings enhance the theoretical understanding of derived materials and expand their application in water purification.

CAS / MDL: 1415-93-6 554-95-0
研究领域: 环境科学 · 材料科学
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FIBERS AND POLYMERS · 2021 ·Vol. 22 ·期 2 ·345-353 · IF 2.153

Highly Uniform Core/Shell Structured CoFe2O4/MIL-100(Fe) Nanofibers for Efficient Visible Light Photocatalysis

Liu Jun,Sun Meng,Chang Meng-Jie,Fan Si-Meng,Hui Qian,Ni Fu-Rong,Yuan Bin

Novel CoFe 2 O 4 /MIL-100(Fe) (CFO/MIL-100(Fe)) core/shell nanofibers were prepared by successive ionic layer adsorption and reaction (SILAR) assembly of MIL-100(Fe) on electrospun CoFe 2 O 4 nanofibers. The MIL-100(Fe) shells were constructed on the dispersed CoFe 2 O 4 fiber surface with high uniformity, homogeneous thickness and high stability. Due to the inherent porosity of MIL-100(Fe), a higher specific surface area of 225.77 m 2 /g is achieved for the CFO/MIL-100(Fe)-10 sample. The formed CFO/MIL-100(Fe) catalysts exhibit high catalytic activity towards degradation of rhodamine B (RhB) under visible light irradiation. The photocatalytic activity remains above 77 % within 60 min illumination after four cycles. Due to the simple synthetic method, highly uniform structure, strong magnetic recoverable, as well as good photocatalytic performance, the obtained CFO/MIL-100(Fe) core/shell nanofibers could be promising photocatalysts for practical application.

研究领域: 材料科学 · 环境科学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2020 · IF 3.573

Low-Temperature Rapid Synthesis and Performance of the MIL-100(Fe) Monolithic Adsorbent for Dehumidification

Yanshu Luo,Bingqiong Tan,Xianghui Liang,Shuangfeng Wang,Xuenong Gao,Zhengguo Zhang,Yutang Fang

MIL-100(Fe) has been proven to have good hydrothermal stability and high vapor uptake and is considered as a promising dehumidification material. However, reduction of the production cost and assembly of the adsorbent and glass fiber paper substrate into the MIL-100(Fe) monolith are challenging. This work presented a dry gel conversion strategy for the rapid synthesis of the MIL-100(Fe) monolith at low temperatures. The porosity and crystalline phase of the products obtained under different crystallization temperatures and times were carefully studied. XRD and SEM characterization indicated that the MIL-100(Fe) crystal could be conveniently synthesized on the substrate at a low temperature of 50–70 °C and in a short time of 2–6 h. The spherical particles assembled from crystals dispersed evenly and tightly on the glass fiber paper. The synthesized MIL-100(Fe) monolith had a thickness of about 270 μm and a MIL-100(Fe) loading of 77.7%. Dynamic and static water vapor adsorption tests revealed that the monolithic adsorbent obtained at 50 °C for 6 h had the largest vapor saturation adsorption capacity (0.581 g/g) and the fastest adsorption rate. Moreover, the monolith owned a low regeneration temperature (below 80 °C) and a satisfactory cycle stability. Convenient equipment, mild synthetic conditions, low renewable energy consumption, and good performance will promote its application in the rotary dehumidification system.

研究领域: 材料科学 · 化学工程
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