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MIL-125
SENSORS AND ACTUATORS B-CHEMICAL · 2014 · IF 3.84

Humidity sensing properties of FeCl3-NH2-MIL-125(Ti) composites

Ying Zhang,Bo Fu,Kuixue Liu,Yupeng Zhang,Xu Li,Shanpeng Wen,Yu Chen,Shengping Ruan

FeCl 3 -NH 2 -MIL-125(Ti) with different FeCl 3 content was prepared and characterized by XRD , SEM and XPS . The humidity sensing properties of FeCl 3 -NH 2 -MIL-125(Ti) have been investigated. Compared with NH 2 -MIL-125(Ti), FeCl 3 -NH 2 -MIL-125(Ti) was more effective in the humidity sensing. The optimal mixing ratio was FeCl 3 -NH 2 -MIL-125(Ti) (8   wt%), which exhibited the best linearity. The impedance of FeCl 3 -NH 2 -MIL-125(Ti) (8   wt%) decreases by almost three orders of magnitude in the range of 11%-95% RH. The response time and recovery time of the humidity sensor by FeCl 3 -NH 2 -MIL-125(Ti) (8   wt%) are 11   s and 86   s respectively. These results indicate the potential application of FeCl 3 -NH 2 -MIL-125(Ti) in humidity sensors.

研究领域: 材料科学 · 传感器技术 · 纳米材料 · 功能材料
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Materials · 2025 ·Vol. 18 ·期 6 ·1343 · IF 3.2

Oxygen Vacancy Modification MIL-125(Ti) Promotes CO2 Photoreduction to CO with Near 100% Selectivity

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.

CAS / MDL: 100-21-0
研究领域: 环境科学 · 材料科学 · 化学工程
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CHEMOSPHERE · 2022 · IF 8.943

NH2-MIL-125(Ti) modified graphitic carbon nitride with carbon vacancy for efficient photocatalytic NO removal

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 · 环境科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Induce (101) plane exposure boosting photocatalytic CO2 reduction in aerobic environment for NH2-MIL-125

Meidan Que,Peihong Ma,Yabo Wang,Yanbo Sun,Xiangwei Bai,Lili Gao,Jin Chen,Jian Wei,Hui Li

NH 2 -MIL-125 with abundant porosity and specific interactions with CO 2 molecules, has been demonstrate great potential in the field of photocatalytic CO 2 reduction. However, conventional NH 2 -MIL-125 and their composites much lower CO 2 photoreduction efficiency in aerobic environments because of the O 2 competition. To circumvent the issue, this study modifies NH 2 -MIL-125 through crystal facet engineering to enhance its selective CO 2 adsorption and photocatalytic efficiency in the environment of impurity CO 2 . The results indicate that NH 2 -MIL-125 featuring (101) crystal planes can sustain elevated catalytic activity in low-concentration CO 2 environments. In a pure CO 2 atmosphere, NM-5 achieves a CO production rate of 159.66 μmol·g −1 after 4 h, 1.85 times greater than the unmodified NH 2 -MIL-125. Under conditions simulating flue gas (5 % CO 2 ) and ultra-low CO 2 concentrations (0.15 % CO 2 ), NM-5 maintains CO production rates of 3.18 μmol·g −1 and 0.95 μmol·g −1 , respectively, representing 1.63 and 1.73 times the production rates of NM. Furthermore, theoretical calculations indicate that CO 2 exhibits a higher adsorption energy (−1.34 eV) compared to N 2 and O 2 (−0.67 eV and −0.15 eV) on the (101) crystal plane, which reveals the preferential adsorption of CO 2 on the (101) crystal planes. This study involves a novel strategy for optimizing MOFs crystal planes and provides significant insights into achieving efficient photocatalytic CO 2 reduction under aerobic conditions.

研究领域: 材料科学 · 环境科学
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POLYHEDRON · 2020 · IF 2.343

Synthesis of uniform-sized and microporous MIL-125(Ti) to boost arsenic removal by chemical adsorption

Zhongmin Liu,Cong Wang,Yongchuan Wu,Longlong Geng,Xiuling Zhang,Dashuai Zhang,Hui Hu,Yongzheng Zhang,Xin Li,Wei Liu,Ping Na

The adsorption behavior of arsenic on adsorbent have been researched widely, but chemical adsorption of arsenic is uncommon. In this work, a kind of microporous metal-organic framework (MIL-125(Ti)) with columnar morphology and uniform size was solvothermally synthesized, and its chemical adsorption behavior and mechanism of arsenic were firstly investigated by experimental and simulation study. Remarkably, ultra-fast adsorption behavior and excellent arsenic removal capability was achieved. It takes only 20 min to rapidly remove 5 mg L −1 arsenic with 0.2 g L −1 MIL-125(Ti), which is far superior to the previously reported materials. Both experimental and simulation study results show that the adsorption of arsenic obeys a new chemical adsorption mechanism. Both As(III) and As(V) can easily replace the terephthalic acid ligand via competitive coordination and bind to the Ti active site of MIL-125(Ti). In addition, the reaction energy barriers for ligand substitution by H 2 O, As(III) and As(V) are 0.46, 0.33 and 0.15 eV, respectively, which further confirming that structure reforming of MIL-125(Ti) plays a key role for chemical adsorption. The study solves the difficulty of removing low concentration of arsenic and provides molecular-level understanding of the chemical adsorption mechanism of arsenic on MIL-125(Ti).

CAS / MDL: 68-12-2 5593-70-4
研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Controlled thermal treatment of NH2-MIL-125(Ti) for drastically enhanced photocatalytic reduction of Cr(VI)

Guanglai Mo,Linxi Wang,Jianhong Luo

It is a challenge to achieve efficient photocatalytic activity of pure MOFs. Herein, the defective NH 2 -MIL-125(Ti) with adjustable linker vacancy level was successfully created by thermal treatment. The band gaps of samples decreased and the more Ti-O clusters on the surface of the samples can be achieved as the time of thermal treatment increased from 0 to 500 min, both of which facilitated the photocatalytic activity for the reduction of Cr(VI). Moreover, the ligands from the surface to the inside of the samples were successively decarboxylated, resulting in the declined specific surface area and the increased proportion of mesoporous and the defect level. The moderate defect level in NH 2 -MIL-125(Ti) can be obtained as the time of thermal treatment was 300 min, which facilitated the separation of photogenerated charges, contributing to the highest photocatalytic activity for reduction of Cr(VI), which was 9.2 times than that of the initial MOFs. However, the excessive linker vacancy defect level in NH 2 -MIL-125(Ti) may result in the seriously affected crystal structure and the retarded separation of photogenerated charges.

研究领域: 材料科学 · 环境科学
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JOURNAL OF COORDINATION CHEMISTRY · 2023 · IF 1.9

Synthesis, characterization and ethylene oligomerization of MIL-125(Ti)-NH2 grafted salicylaldehyde nickel complexes

Jinyan Tan,Na Zhang,Ling Wang,Liduo Chen,Cuiqin Li,Jun Wang

Metal-organic framework MIL-125(Ti)-NH2 was prepared and coordinated with salicylaldehyde and NiCl2·6H2O to create a heterogeneous catalyst for ethylene polymerization. The structure of the products was characterized by a variety of physical methods, such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma mass spectrometry (ICP-MS), and nitrogen adsorption-desorption. The catalytic performance of MIL-125(Ti)-NH2-Sal-Ni was also investigated. The results showed that the reaction temperature, Al/Ni molar ratio, and ethylene pressure influenced on the catalytic activity and product selectivity. Under optimal reaction conditions, the catalytic activity of MIL-125(Ti)-NH2-Sal-Ni for ethylene oligomerization could reach 5.90 × 104 g·(mol Ni·h)−1 using cyclohexane as the solvent and MAO as the co-catalyst; the main products were C4 and C6. In addition, MIL-125(Ti)-NH2-Sal-Ni had good catalytic stability and recycling, which could be reused at least twice without significant loss of activity. Moreover, based on the evaluation of catalytic performance, the catalytic ethylene oligomerization mechanism of MIL-125(Ti)-NH2-Sal-Ni was also deduced.

研究领域: 材料化学 · 催化化学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2025 · IF 8.3

Carbon dots as electron acceptors modified NH2-MIL-125 (Ti)/Cu2O heterojunction for highly efficient photocatalytic H2 production

Jun-Qing Ye,Bin Cheng,Yunfei Bu,Jun-Feng Qian,Qian Liang,Ming-Yang He,Qun Chen

The development of high-efficiency photocatalysts for water splitting to hydrogen (H 2 ) is crucial for alleviating energy crisis and environmental problems. In this study, a novel type-II ternary heterojunction photocatalyst, CDs/NH 2 -MIL-125 (Ti)/Cu 2 O, was fabricated through the integration of NH 2 -MIL-125 (Ti) with Cu 2 O and carbon dots (CDs), exhibited excellent photocatalytic H 2 production rate of 12817.1 μmol/g/h with apparent quantum efficiency (AQE) of 17.13 % under visible light irradiation. Characterization revealed a uniform and dense structural integration with a high Brunauer-Emmett-Teller (BET) surface area of 275.9 m 2  g −1 and a suitable energy band gap of 2.18 eV. Furthermore, the heterostructures promoted efficient photo-generated carrier separation and enhanced reduction capabilities . Notably, CDs, serving as cocatalysts or electron acceptors, improved visible light utilization and electron migration, significantly boosting H 2 production. Insights from electron spin resonance (ESR) and density functional theory (DFT) calculations supported the migration mechanisms of electrons. This work presents a significant advance in photocatalytic technology for sustainable energy by designing high-performance CDs-modified heterojunction photocatalysts.

CAS / MDL: 10312-55-7 50-81-7
研究领域: 材料科学 · 能源科学
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DALTON TRANSACTIONS · 2023 ·Vol. 52 ·期 11 ·3517-3525 · IF 4

Amino-functionalized MIL-125(Ti) for photodenitrification of pyridine in fuels via coordination activation by unsaturated Ti4+ centers

Shihui Wang,Zhoujun He,Ling Wu,Deling Wang,Ruiru Si,Xiyao Liu,Ruowen Liang

Due to their explicit structure, metal–organic frameworks (MOFs) have been supposed to be credible platforms to research the micro-mechanism of heterogeneous photocatalysis. In this study, amino-functionalized MOFs (MIL-125(Ti)–NH2 (denoted as MTi), UiO-66(Zr)–NH2 (denoted as UZr) and MIL-68(In)–NH2 (denoted as MIn)) with three different metal centers were synthesized and applied for the denitrification of simulated fuels under visible light irradiation, during which pyridine was used as a typical nitrogen-containing compound. The results showed that MTi had the best activity among the above three MOFs, and the denitrogenation rate increased to 80% after 4 h of visible light irradiation. On the grounds of the theoretical calculation of pyridine adsorption and actual activity experiments, it can be presumed that the unsaturated Ti4+ metal centers should be the key active sites. Meanwhile, the XPS and in situ infrared results verified that the coordinatively unsaturated Ti4+ sites facilitate the activation of pyridine molecules through the surface –N⋯Ti– coordination species. The coordination–photocatalysis synergism promotes the efficiency of photocatalytic performance and the corresponding mechanism is proposed.

CAS / MDL: 5593-70-4 9022-96-2
研究领域: 材料科学 · 环境科学 · 化学工程
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Journal of Water Process Engineering · 2022 · IF 7.34

Prepare of sunlight response NH2-MIL-125/PES composites ultrafiltration membrane for flux incrementation and fouling alleviation

JongNam Choe,JongMin Ji,MyongBok Kim,JuHyon Yu,JongYol Ri,KyongSu Ri,HyonIl Kim

In this paper, a novel hydrophilic composite polyethersulfone (PES) ultrafiltration membrane was prepared by blending sunlight response photocatalyst NH 2 -MIL-125 via the phase inversion method. The physical-chemistry performance of membrane was carried out by XRD, FTIR, UV-VIS/DRS, contact angle, and cross-section SEM images. The separation ability, anti-fouling ability, and self-cleaning efficiency of ultrafiltration membrane were analyzed by ultrafiltration experiment using the congo red solution. The results indicate that fouling resistance and the flux recovery ratio of ultrafiltration membrane is significantly improved, and it has higher solar response energy. There was no significant change in the rejection ratio of pollutants before and after illumination. For the pristine PES membrane and the 0.5% NH 2 -MIL-125/PES nanocomposite membrane, the water flux recovery ratio (FRR) could increase from 37.84% to 77.09%, and the R r could increase from 22.22% to 44.09%, and the R ir could decrease from 67.11% to 47.09%. In a conclusion, the addition of NH 2 -MIL-125 at a low concentration could result in membranes with more pure water flux, better rejection, and good fouling resistance compared to the unfilled PES membrane.

CAS / MDL: 25249-54-1 9003-39-8
研究领域: 材料科学 · 环境工程
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Materials Advances · 2023 ·Vol. 4 ·期 3 ·940-947 · IF 5

Construction of a La-ZnIn2S4/MIL-125(Ti) heterojunction for highly efficient photocatalytic degradation of aflatoxin B1

Xiaobing Yang,Junjie Pan,Bingcong Xing,Wenjie Lei,Yingchun Fu,Kejun Cheng

Nowadays, aflatoxin B1 (AFB1) contamination is considered as one of the most common food safety issues for humans and animals. As one of the most advanced oxidation techniques, photocatalytic degradation can break down organic contaminants into nontoxic and harmless materials efficiently. In this paper, we explored the degradation efficiency of AFB1 by ZnIn2S4. To promote the photocatalytic degradation efficiency of AFB1, ZnIn2S4 was coupled with MIL-125(Ti) and then doped with La [this hybrid is denoted as La-ZnIn2S4/MIL-125(Ti)] to effectively convert it via photocatalytic generation of superoxide radicals (˙O2− and ˙OH) and achieve much enhanced photocatalytic performance, which is demonstrated by degrading 97.6% of AFB1. According to the transient photocurrent responses, the doping of La and coupling with MIL-125(Ti) can highly improve the efficient separation of the photoinduced electron–hole pairs on ZnIn2S4, leading to the effective conversion of OH− and O2 into ˙O2− and ˙OH, respectively, during the photodegradation process. This strategy of coupling with MOFs and doping with rare earth elements provides a facile and efficient method for degrading food pollutants produced by aflatoxins.

CAS / MDL: 62-55-5 1162-65-8
研究领域: 食品安全 · 环境科学 · 材料科学
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Catalysis Science & Technology · 2018 ·Vol. 8 ·期 7 ·1936-1944 · IF 5.365

Effective elimination of As(III) via simultaneous photocatalytic oxidation and adsorption by a bifunctional cake-like TiO2 derived from MIL-125(Ti)

Zhongmin Liu,Yongchuan Wu,Jitao Chen,Yaru Li,Jingyu Zhao,Kaihua Gao,Ping Na

A bifunctional cake-like TiO2 was successfully synthesized via calcination of MIL-125(Ti) at a suitable temperature by a one-step method and was applied for As(III) removal by simultaneous photocatalytic oxidation and adsorption. The as-synthesized samples were characterized by XRD, TGA/DSC, SEM, TEM, N2 adsorption–desorption isotherms, PL spectra, photocurrent, FTIR and XPS. The effects of calcination temperature on the specific surface areas of the samples, transformation of the TiO2 crystal phase and properties of As(III) removal were investigated. The results showed that higher calcination temperature resulting in a lower specific surface area and more transformations of the TiO2 crystal phase from anatase to rutile. The TiO2 calcined at 380 °C (MIL-125(Ti)-380 °C) exhibited excellent properties for As(III) removal, including photocatalytic oxidation of As(III) and simultaneous adsorption of the generated As(V). In addition, MIL-125(Ti)-380 °C could be reused at least four times without significant reduction in the photocatalytic oxidation and adsorption performances. The excellent photocatalytic oxidation and adsorption abilities of MIL-125(Ti)-380 °C can be attributed to the synergistic effects of strong photogenerated electron–hole separation and high specific surface area. The bifunctional cake-like TiO2 provides a wonderful strategy to remove As(III) completely from contaminated water using a single step.

研究领域: 环境科学 · 材料科学
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