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MIL-125
APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

Defect-rich and electron-rich mesoporous Ti-MOFs based NH2-MIL-125(Ti)@ZnIn2S4/CdS hierarchical tandem heterojunctions with improved charge separation and enhanced solar-driven photocatalytic performance

Shiyu Zhang,Meng Du,Zipeng Xing,Zhenzi Li,Kai Pan,Wei Zhou

Defective-rich and electron-rich mesoporous NH 2 -MIL-125(Ti)@ZnIn 2 S 4 /CdS hierarchical tandem heterojunctions were fabricated through two-step solvothermal and one-step hydrothermal strategies. The interface with electron enrichment can cause active interface reaction, fast transfer and separation of charge carriers and restrain the photocorrosion of CdS. ZnIn 2 S 4 , as a bridge to connect Ti-MOFs and CdS, favors the separation of charge carriers and forms tandem heterojunctions. The as-prepared photocatalyst has a relative large surface area of ∼877.0 m 2 g −1 and a narrow band gap of ∼1.84 eV, which could absorb visible light efficiently. Furthermore, it exhibits a high photocatalytic hydrogen generation rate which was increased to 2.367 mmol g −1 h −1 and the high photocatalytic degradation efficiency for 2,6-dichlorophen and 2,4,5-trichlorophenol which were 98.6% and 97.5%, respectively. Additionally, recycling text for several cycles indicates the high stability. This novel Ti-MOFs based core@shell hierarchical tandem heterojunctions may offer a new insight for fabricating high-performance heterojunctions for multi-channel charges transfer.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2023 ·Vol. 30 ·期 26 ·68691-68700 · IF 5.8

Graphite oxide as an electronic conductor modified ZIF-8/NH2-MIL-125(Ti) hybrid material used as a photocatalyst for removal of organic dyes under visible light irradiation

Liu Yuhao,Wang Jieqi,Wang Xuyi,Chen Jiayue,Zhang Beibo,Chen Liping,Zheng Dan,Cheng Ming

It is a great challenge to develop photocatalysts for the degradation of organic pollutants in the aqueous environment, especially those with excellent catalytic performance under visible light conditions. In this work, using graphene oxide (GO) as an electron shuttle agent and carrier, a hybrid of ZIF-8/NH 2 -MIL-125(Ti) and GO (ZIF-8/NH 2 -MIL-125(Ti)/GO) was prepared by a simple two-step solvothermal method. The morphology, structure, and combination of the synthesized catalysts were studied. The results showed that graphene oxide and ZIF-8 formed an in situ load on NH 2 -MIL-125(Ti). The construction of hybrid materials significantly improved the catalytic activity of NH 2 -MIL-125(Ti) in the visible light range. The degradation activity of the synthesized catalyst was further tested with reactive red dye. The results showed that the catalyst exhibited excellent catalytic removal efficiency for active red, with a degradation rate of 99.8% within 2 h. The prepared hybrid materials have good application prospects in the field of organic pollutant treatment in water. Graphical Abstract

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Construction of a novel BiOCl/Bi2MoO6/MIL-125(Ti) with Z-scheme and II-type dual-functional heterojunctions for enhancing photocatalytic degradation of tetracycline under visible light irradiation

Xingping Fu,Qianqian Chen,Ye Zhang,Feng Yu,Junjie Pan,Xiaobing Yang

The overuse of antibiotics, coupled with inadequate wastewater treatment, has led to widespread environmental contamination, posing significant risks to ecosystems and public health. In this study, a novel BiOCl/Bi 2 MoO 6 /MIL-125(Ti) heterojunction catalyst featuring a Z -scheme and II-type dual-functional junctions was prepared via a two-step solvothermal method and employed for the degradation of tetracycline (TC). The synthesized samples were thoroughly characterized by XRD, SEM, BET, TEM, and UV–vis spectroscopy. The results indicate that the incorporation of BiOCl and Bi 2 MoO 6 effectively tunes the band structure of MIL-125(Ti), enhancing its visible-light absorption. Moreover, the formation of the heterojunction interfaces significantly suppresses recombination of photogenerated charge carriers, thereby improving photocatalytic performance. Under visible-light irradiation, the BiOCl/Bi 2 MoO 6 /MIL-125(Ti) catalyst generates reactive radicals (·OH and ·O₂ − ), enabling efficient degradation of TC with a removal efficiency of 95.71 %. The synergistic effect of the Z -scheme and II-type heterojunctions plays a crucial role in the efficient photocatalytic degradation of TC. This study provides new insights into the degradation mechanisms of bifunctional heterojunctions and presents a promising strategy for designing high-performance photocatalysts for tetracycline degradation.

CAS / MDL: 60-54-8
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Protonated NH2-MIL-125 via HCl vapor to introduce the moiety with charge and ample hydrogen as a novel bifunctional photocatalyst: Enhanced photocatalytic H2 production and NO purification

Shuang Luo,Chenghua Zhang,Xingyan Liu,Yue Li,Lei Tang,Min Fu,Song Wang,Jie Wu,Mengmeng Xu,Xiaoping Wang,Youzhou He

A novel protonated NH 2 -MIL-125 was fabricated to introduce the moiety with charge and ample hydrogen (–NH 3 + Cl - group) into NH 2 -MIL-125 using HCl vapor obtained by natural volatilization of hydrochloric acid as a protonating reagent, which could exhibit excellent photocatalytic activity in both hydrogen production and NO purification under visible light irradiation. The hydrogen production and NO purification rate of the best protonated NH 2 -MIL-125 were 6762.80 μmol g −1 and 49.17%, respectively, which were 20.53 and 1.84 times as that of the original NH 2 -MIL-125. A series of characterizations, such as Mott-Schottky, PL, FT-IR and in situ DRIFTS , etc. were used to characterize the photoelectrochemical properties of the optimal catalyst, which demonstrated the protonation effect can not only enhance the electron migration rate, but also effectively accelerate photo-generated electron-hole pairs separation in the photocatalytic reaction process. This research believed that using HCl vapor as a facile protonation reagent to introduce the moiety with charge and ample hydrogen (–NH 3 + Cl - ) was a very effective method to decorate MOFs for hydrogen evolution and NO removal.

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Journal of Materials Chemistry B · 2021 ·Vol. 9 ·期 30 ·5998-6005 · IF 6.331

Fabricating a wettable microwells array onto a nitrogen plasma-treated ITO substrate: high-throughput fluorimetric platform for selective sensing of ammonia in blood using polymer-stabilized NH2-MIL-125

Pan Li,Lixiang Zhang,Sheng Zhang,Chenchen Xu,Yinuo Li,Juan Qu,Shuai Li,Guojiang Mao,Hua Wang

A high-throughput and selective fluorimetric platform has been constructed for the analysis of ammonia in blood by using a polymer-stabilized metal–organic framework (MOF) of porous NH2-MIL-125, which was coated onto a wettable microwells array constructed on an indium tin oxide (ITO) substrate. It was found that the nitrogen plasma treatment for the ITO substrate could create a super-hydrophilic interface that combined with the hydrophobic pattern yielded a wettable microwells array, enabling the condensation-based enrichment of targets from the sample droplets. Moreover, the NH2-MIL-125 MOF encapsulated using polymers could be firmly coated onto the microwells to act as fluorescent probes for sensing NH3 with enhanced responses. In addition, the use of the polymer polyvinyl pyrrolidone could protect and stabilize the crystals of NH2-MIL-125 probe in aqueous media, revealing the improved hydrophilicity and significantly depressed signal background. The as-developed fluorimetric platform, containing a MOF-coated microwells array, can enable the detection of ammonia in blood, with concentrations ranging linearly from 0.10 to 300 μM. More importantly, this plasma treatment-based fabrication route may hold promise for designing different wettable microwells arrays for the high-throughput detection of multiple targets in the fields of biomedical analysis and environmental monitoring.

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JOURNAL OF CHROMATOGRAPHY A · 2026 · IF 4

Fabrication of NH2-MIL-125(Ti)@TpBD(SO3H)2 selective adsorption material for dispersive solid-phase extraction of quinolone antibiotics in fish and shrimp combined with liquid chromatography-tandem mass spectrometric analysis

Shijie Xing,Zhikun Li,Jiaxiang Liu,Wei Zhang,Fuqiang Sun,Shu-Xuan Liang

To address the ongoing issue of quinolones (QNs) residues in aquatic products, accurate and sensitive detection of trace QNs has always been necessary and urgent. In this work, a composite material of NH 2 −MIL-125(Ti)@TpBD(SO 3 H) 2 consisting of metal organic frameworks and based on bisulfonic acid-based covalent organic frameworks was synthesized and applied as a dispersive solid-phase extraction (dSPE) adsorbent. Combining with liquid chromatography-tandem mass spectrometry, a simple and effective method for simultaneous detection of 18 QNs in aquatic products was established. Meanwhile, the selective adsorption mechanism was thoroughly investigated through material characterization combined with density functional theory calculations. The results showed that the method had a good linear relationship ( r ≥ 0.9981), low limits of detection of 0.0019–0.0641 μg kg⁻¹, along with high recovery rates in the range of 80.6–113.2 %, and good precision with relative standard deviations less than 8.8 %. The selective adsorption mechanism revealed the synergistic adsorption mechanism of electrostatic interactions, hydrogen bonding, and π-π interactions. The material had good reusability and excellent stability. In summary, the dSPE method based on NH 2 −MIL-125(Ti)@TpBD(SO 3 H) 2 composites provided a practical sample pretreatment solution for the determination of trace QNs in complex matrixes.

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