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MIL-68 (In)
SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Tightly contacted heterojunction of ZnS/ZIS/In2S3: In situ construction from ZIF-8@MIL-68(In) and visible-light induced photocatalytic hydrogen generation

Boyi Yan,Zhongqiao Sun,Yide Han,Hao Meng,Xia Zhang

The construction of a tightly contacted heterojunction consisting of multi-components is proven to be one of the effective strategies to promote the photogenerated charges separation and to develop high-efficient photocatalysts in hydrogen evolution . Herein, a ternary hollow heterostructure of ZnS/ZIS/In 2 S 3 has been fabricated by using a binary MOF@MOF (ZIF-8@MIL-68(In)) as the precursor, and an in-situ sulfurization of ZIF-8@MIL-68(In) is controlled to optimize the photocatalytic performances. The resulting samples are signed as Z@M- t , where the t is pointed to the sulfurization time being varied from 4 h to 48 h. It’s shown that the hierarchical and hollow architecture is formed for Z@M- t , and with the reinforced light harvest ability in both UV and visible light regions. In the subsequent visible-light-induced photocatalytic hydrogen generation, the optimized Z@M-24 manifests significantly improved hydrogen evolution rate of 607.34 μmol g -1 h −1 , which values are evidently higher than that by the single MOF and binary ZIF-8@MIL-68(In) heterostructure. The electrochemical analyses and the electron paramagnetic resonance (EPR) spectrum were analyzed to clarify the charge transfer routes and the enhanced photocatalytic mechanism, in which the contribution of each metal sulfide is also discussed. Finally, the good photocatalytic stability and reusability of Z@M-24 heterostructure are also represented, which define the structure superior brought by the effective heterojunction based on the in-situ sulfurization strategy of binary ZIF-8@MIL-68(In), and determine their prospect applications in the efficient H 2 production under visible light irradiation.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

In2O3 porous microtubes derived from orientedly assembled MIL-68-In tubes via facile water etching for enhanced NO2 sensing performance at low temperature

Yan Jiang,Ping Wang,Ji Li,Xianfa Zhang,Yingming Xu,Hui Zhao,Xiaoli Cheng,Shan Gao,Lihua Huo

The porous and tubular structure is conducive to improving performance of sensing materials. At present, how to obtain sensitive materials with unique porosity and high surface activity by green, low-cost and simple synthesis methods is still a challenge. In this work, novel In 2 O 3 porous microtubes were obtained by water etching of MIL-68-In and calcination methods for the first time. The as-prepared microtubes exhibit excellent NO 2 sensitivity at 50 ℃ (S=156–3 ppm NO 2 ), and the limit of detection is 50 ppb. The sensor also has good NO 2 detection ability in the actual environment. The excellent NO 2 sensing performance at low temperature is closely related to high surface activity of In 2 O 3 porous microtubes. Combined with TPD, in-stiu DRIFT and XPS technologies, the NO 2 sensing mechanism was detailed analyzed. This work provides useful guidance for constructing high performance NO 2 sensor. The excellent NO 2 sensing performance at low temperature makes a positive contribution to promoting the application of metal oxide sensors in environmental detection.

CAS / MDL: 207398-97-8 100-21-0
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CELLULOSE · 2022 ·Vol. 29 ·期 2 ·1017-1034 · IF 6.123

Transparent and highly efficient full-band UV-shielding bioplastic designed by in-situ embedded metal-organic frameworks (MIL-68(In)-NH2) in cellulose matrix

Sun Lijian,Qian Xueren,An Xianhui

Cellulose-based bioplastics with degradability and remarkable mechanical performance have recently attracted increasing attention. As a high-performance material, cellulose-based bioplastics have a strong potential to replace synthetic plastic substrates in many applications. However, its poor shielding performance to UV light limit its application. In this work, transparent and UV-blocking MIL-68(In)-NH 2 @cellulose bioplastic (M(In)CBP) sheets are fabricated via a featured processing method, i.e., cellulose liquefaction, rapid solidification, in-situ synthesis and hot-press drying. The as-obtained functional bioplastic sheet (M(In)CBP1) exhibits high visible-light transparence (74.7% a 600 nm) and the existence of MIL-68(In)-NH 2 allows superior UV-blocking ability (below 400 nm, transmittance was under 4%). The M(In)CBP sheets show high photostability even after continuous UV irradiation (365 nm) for over 12 h. The superior UV-shielding performance is attributed to the uniform distribution and the high UV absorbance of MIL-68(In)-NH 2 in M(In)CBP sheets. High resistance to penetration by aqueous/nonaqueous liquids was proved. Moreover, the M(In)CBP sheets also show excellent mechanical properties and thermal stability. The present work designed a UV-blocking bioplastic constructed from cellulose and MIL-68(In)-NH 2 , which is potential candidates to replace synthetic plastics in many advanced applications such as a UV protection layer for electronic products, or useful as packaging materials to prevent food spoilage. Graphical abstract

CAS / MDL: 207398-97-8
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Metal-organic framework MIL-68(In)-NH2-derived carbon-covered cobalt-doped bi-crystalline In2O3 tubular structures for efficient photocatalytic degradation of tetracycline hydrochloride

Lijun Gao,Dongmei Han,Zhihua Wang,Fubo Gu

Tubular carbon-covered cobalt-doped bi-crystalline phase In 2 O 3 (denoted as CoInO-x) was synthesized by one-step calcination of the metal-organic framework cobalt-doped MIL-68(In)-NH 2 precursor. The photocatalytic activity of CoInO-x was investigated using tetracycline hydrochloride (TCH) degradation. The removal of TCH by CoInO-500 obtained by calcination at 500 °C under visible light irradiation was 90.1% after 70 min, which was significantly higher than that of In 2 O 3 . The reaction rate constant of CoInO-500 was 11.02 times higher than that of In 2 O 3 and could maintain a better photocatalytic performance after four cycles. The effects of photocatalyst dosing, pH, and inorganic anions on photocatalytic degradation were studied. The mechanism of photocatalytic degradation was analyzed in detail by reactive radical trapping experiments, Mott-Schottky measurements, and electron paramagnetic resonance (EPR) signal characterization. Enhanced photocatalytic performance is mostly attributed to the cobalt doping creating impurity energy levels and narrowing the forbidden bandwidth of In 2 O 3 , enhancing the visible light utilization and the photogenerated charge separation efficiency. Carbon covering can serve as a bridge for charge transport, accelerating the rapid transport of photogenerated charges.

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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Construction of Fe(III) doping modified AgI/NH2-MIL-68(In/Fe) Z-scheme heterojunction photocatalysts through unique internal and interfacial charge transmission and separation efficiency

Jiamin Wei,Qing Wang,Mian He,Shuai Li,Yunan Zhang,Yang Yang,Shipeng Luo,Lianshe Fu,Xin Wang,Tinghai Yang

The development of highly efficient strategy to facilitate comprehensive charge transmission and effective spatial charge separation is expected as a promising approach to improve photocatalytic performance. Herein, the Fe(III) doping modified AgI/NH 2 -MIL-68(In/Fe) Z-scheme heterojunction (ANM-x composite) with unique internal and interfacial charge transmission performance was fabricated by a facile ion exchange precipitation method. The optimized ANM-50 composite exhibits the maximum photocatalytic activity for the degradation of tetracycline, which is about 9.54, 2.61 and 1.86 times higher than that of pure NH 2 -MIL-68In, NH 2 -MIL-68(In/Fe) and AgI, respectively. The characterization results displayed that Ag nanoparticles (NPs) were generated during the photocatalytic procedure, which not only served as a charge transfer-highway, but also reduced the charge flow energy barrier, thereby accelerating charge transfer efficiency and consolidating the stability of the Z-scheme heterojunction. Mechanism exploration reflected that the superior photocatalytic performance was associated with synergetic effect among the introduced Fe(III), constructed ANM Z-scheme heterojunction and the generated Ag NPs, which significantly expands visible light response range and promotes more effective internal and interfacial charge separation. This research not only designs an efficient photocatalyst for decomposing tetracycline, but also opens a new perspective for rational developing Z-scheme heterojunction with unique internal and interfacial charge flow steering.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Enriched surface oxygen vacancies of Bi2WO6/NH2-MIL-68(In) Z-scheme heterojunction with boosted visible-light photocatalytic degradation for levofloxacin: Performance, degradation pathway and mechanism insight

Qing Wang,Xingyue Qian,Hui Xu,Guangyu He,Haiqun Chen

Exploring effective approach to promote more comprehensive charge transfer and efficient spatial charge separation is considered to be a prospective strategy to reinforce photocatalytic degradation activity. Herein, the oxygen vacancy modified Bi 2 WO 6 /NH 2 -MIL-68(In) Z-scheme heterojunction photocatalyst was successfully fabricated via a facile solvothermal method. The chemical structure, morphology, and optical properties of the photocatalyst were characterized in detail. The optimized Bi 2 WO 6 /NH 2 -MIL-68(In) Z-scheme heterojunction displayed the maximum photocatalytic efficiency (84.3 %) for the degradation of levofloxacin (LEV), which was significantly higher than that of pure Bi 2 WO 6 (45.1 %), oxygen vacancy modified Bi 2 WO 6 (69.4 %), and NH 2 -MIL-68(In) (49.3 %). Importantly, the high-resolution mass spectrometry (HRMS), three-dimensional excitation-emission matrix (3D EEMs) fluorescence spectra, the photo-electrochemical and photo-luminescence measurement, radical trapping test, and electron spin resonance (ESR) technique were carried out to illuminate the probable degradation pathway and mechanism of the LEV. The improved photocatalytic efficiency can be ascribed to the synergetic effect between oxygen vacancy and the Z-scheme heterojunction, which can serve as trapping centers to enhance the generation of photoexcited electrons and accelerate the charge transfer. Meanwhile, the effects of pH, photocatalyst dose, LEV concentration and different kinds of harmful organic pollutants were systematically explored from the practical application. This study offers a novel perspective for the integration of defect engineering and Z-scheme heterojunction in efficient organic pollutants degradation.

研究领域: 环境科学 · 材料化学 · 光催化 · 纳米技术 · 污染物降解
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RSC Advances · 2021 ·Vol. 11 ·期 33 ·20439-20445 · IF 3.361

Fabrication and application of a MIL-68(In)–NH2 incorporated high internal phase emulsion polymeric monolith as a solid phase extraction adsorbent in triazine herbicide residue analysis

Jinhua Luo,Liping Jiang,Guihua Ruan,Chengyong Li,Fuyou Du

In this work, a metal–organic framework MIL-68(In)–NH2 incorporated high internal phase emulsion polymeric monolith (MIL-68(In)–NH2/polyHIPE) was prepared and applied as a solid phase extraction adsorbent for the extraction and detection of trace triazine herbicides in environmental water samples by coupling with HPLC-UV detection. The fabricated material showed good adsorption for simazine, prometryn, and prometon in water samples because of π–π interactions and hydrogen bonding interactions. Under optimal conditions, the maximum adsorption capacity of simazine, prometon and prometryn was 800 μg g−1, 800 μg g−1 and 6.01 mg g−1, respectively. The linearities were 10–800 ng mL−1 for simazine, prometon and prometryn. The limits of detection were 31–97 ng L−1, and the recoveries were 85.6–118.2% at four spiked levels with relative standard deviations lower than 5.0%. The method has a high sensitivity for the determination of three triazine herbicides in environmental water samples.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Built-in electric field mediated S-scheme charge migration and Co-N4(II) sites in cobalt phthalocyanine/MIL-68(In)-NH2 heterojunction for boosting photocatalytic nitric oxide oxidation

Guojun Li,Zheng Lian,Qiuqiu Lyu,Chenyu Zhu,Zhinian Liu,Shule Zhang,Qin Zhong

The efficiency of photocatalytic Nitric Oxide(NO) oxidation is limited by the lack of oxygen(O 2 ) active sites and poor charge carrier separation. To address this challenge, we developed a molecular Cobalt Phthalocyanine modified MIL-68(In)–NH 2 photocatalyst with a robust Built-in electric field(BIEF). In the 2 % CoPc-MIN sample, the BIEF strength is increased by 3.54 times and 5.83 times compared to pristine CoPc and MIL-68(In)–NH 2 , respectively. This BIEF facilitates the efficient S-scheme charge transfer, thereby enhancing photogenerated carrier separation. Additionally, the Co-N4(II) sites in CoPc can effectively trap the separated photoexcited electrons in the S-scheme system. In addition, the Co-N4(II) sites can also serve as active sites for O 2 adsorption and activation, promoting the generation of superoxide radical ( O 2 – ), thereby driving the direct conversion of NO to nitrate(NO 3 – ). Consequently, the 2 % CoPc-MIN sample exhibits a remarkable photocatalytic NO removal efficiency of 79.37 % while effectively suppressing the formation of harmful by-product nitrogen dioxide(NO 2 ) to below 3.5 ppb. This study provides a feasible strategy for designing high-efficiency O 2 activation photocatalysts for NO oxidation.

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