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UIO-66
CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Three-Dimensional g-C3N4/NH2-UiO-66 graphitic aerogel hybrids with recyclable property for enhanced photocatalytic elimination of nitric oxide

Zhou Zhou,Dongyun Chen,Najun Li,Qingfeng Xu,Hua Li,Jinghui He,Jianmei Lu

In order to fix the photocatalyst and enhance the efficiency of NO degradation, a three-dimensional (3D) g-C 3 N 4 /NH 2 -UiO-66-rGO (CN/NU6-rGO) aerogel was devised and fabricated via solvothermal reaction and boiling-water bath. Herein, a type-II heterojunction was formed at CN/NU6 composite, and then, the composite was coupled with rGO. The resulting material significantly enhanced the nitric oxide (NO, 600 ppb) removal efficiency under visible-light irradiation. Optimizing the content of CN and rGO to a suitable mass ratio can increase the removal efficiency by 65.4%, which is 2.34 times that of pure NU6. This result is attributed to the construction of type-II heterojunction and the charge transport properties of rGO. The involvement of rGO not only provided extra pathways for charge transfer to prevent electron–hole pairs from recombining, but also fixed the catalyst. Moreover, the hybrid aerogel excellently reduced the harmful by-product NO 2 . Cycling experiments, along with transient photocurrent response measurements, verified that CN/NU6-rGO had excellent potential for recyclable and sustainable. This work might shed light on the construction of suitable photocatalytic systems with significant improvement of NO removal and convenient storage of catalyst.

CAS / MDL: 10026-11-6
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Intensification of water/ethanol separation by PVA hybrid membrane with different functional ligand UiO-66-X nanochannels in pervaporation process

Haoji Jiang,Wenxiong Shi,Qiang Liu,Heyun Wang,Jialu Li,Chunlin Wu,Yingchun Li,Zhong Wei

In order to investigate the effects of MOFs by altering ligands with various functional groups on separation selection in pervaporation dehydration, three hydrophilic UiO-66-X nanoparticles were respectively synthesized and blended into poly (vinyl alcohol) matrix to fabricate water-selective membrane for ethanol dehydration via PV technology. Both the experimental and molecular simulation results confirmed the UiO-66-X counterbalancing factors of enhanced polarity and suitable pore size gave rise to the optimal performance in ethanol dehydration. The PV performances could be tuned by the type and quantity of functional groups carried by UiO-66-X nanoparticles. As a result, the pore aperture of UiO-66-(COOH) 2 nanoparticles provided continuous channel for water diffusion, and water molecules could also be activated attributed to the strong interaction between the UiO-66-(COOH) 2 nanoparticles and water molecules which enhanced the penetration and diffusion of water molecular in hybrid membrane to increase the water flux. The optimized hybrid membranes with UiO-66-(COOH) 2 loading of 8 wt% exhibited the total flux of 979 ± 7 g/(m 2 ·h) and a separation factor of 2084 ± 21.

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FUEL PROCESSING TECHNOLOGY · 2020 · IF 4.982

Phosphomolybdic acid niched in the metal-organic framework UiO-66 with defects: An efficient and stable catalyst for oxidative desulfurization

Cheng Wang,Ai-Rong Li,Yu-Ling Ma

The synthesis of highly efficient and stable catalysts for oxidative desulfurization is still a challenging task. Herein, a composite material (HPMo@UiO-66) of phosphomolybdic acid (HPMo) encapsulated in the metal-organic framework UiO-66 with missing-linker defects was prepared via a one-pot hydrothermal method . A series of as-synthesized catalysts were systematically characterized by XRD , FT-IR, SEM , BET, TGA , XPS , UV–vis and PL . Through oxidative desulfurization experimental evaluations, the catalyst 0.5-HPMo@UiO-66-D with defects shows the superior catalytic oxidative desulfurization performance and high reusability . 0.5-HPMo@UiO-66-D is able to completely remove DBT in the model fuel in 60 min, and the reaction system can be recycled 10 times with a high activity. In addition, the kinetics and the activation energy of the oxidative desulfurization were studied.

CAS / MDL: 10026-11-6
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Robust super-hydrophobic/super-oleophilic sandwich-like UIO-66-F4@rGO composites for efficient and multitasking oil/water separation applications

Yingqing Zhan,Shuangjiang He,Jiaxin Hu,Shumei Zhao,Guangyong Zeng,Mi Zhou,Guiyuan Zhang,Arijit Sengupta

Super-wetting MOFs@graphene hybrid has shown promising application for oil/water separation, due to high porosity, low density, and controllable wettability, however, achieving excellent stability and recyclability are found to be still challenging. In this study, sandwich-like UIO-66-F 4 @rGO hybrid was synthesized by immobilization of UIO-66-F 4 nanoparticles on rGO matrix, which featured the unique micro/nano hierarchy with hydrophobic characteristics. In order to realize the oil/water separation, as-prepared sandwich-like UIO-66-F 4 @rGO hybrid was applied as a potential candidate for constructing robust super-hydrophobic/super-oleophilic interfaces by using filter paper (FP) and melamine sponge (MS) as substrates. Typically, the surface modification of substrates can be easily achieved by simple dip-coating method, and interfacial adhesion between substrates and UIO-66-F 4 @rGO was enhanced by cross-linking of hydroxyl-fluoropolysiloxane (FPSO). Consequently, the super-hydrophobic/oleophilic UIO-66-F 4 @rGO/FP exhibited high contact angle of 169.3 ± 0.6° and was capable of separating various water-in-oil emulsions effectively. The flux and separation efficiency were 990.45 ± 36.28 Lm −2 h −1 and 99.73 ± 0.19 % driven by gravity, respectively. The super-hydrophobic/super-oleophilic UIO-66-F 4 @rGO/MS possessed selective oil absorption with absorption capacity of 26∼61 g/g depending on the viscosity of oils and continuous cleaning of oil spill. Furthermore, the UIO-66-F 4 @rGO composite could tolerate high/low temperature, corrosive solutions, and physical damage, displaying robust and stable super-hydrophobic/super-oleophilic interfaces for treating oily wastewater in harsh environments.

CAS / MDL: 77-58-7 78-10-4
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2023 · IF 7.2

An enhanced proton conductivity of proton exchange membranes by constructing proton-conducting nanopores using PVP-UiO-66-NH-SO3H nanoparticles

Pengfei Li,Yingbo Chen,Fan Xiao,Ming Cao,Jingyu Pan,Jingfeng Zheng,Ke Zhao,Hao Li,Xianglin Zhang,Yuanyuan Zhang

The performance of proton exchange membranes (PEMs) can be enhanced by creating continuous proton conduction channels. In this work, PVP-UiO-66-NH-SO 3 H nanoparticles (PUNSNPs) were prepared and filled into sulfonated poly (ether ether ketone) (SPEEK) to fabricate PUNSNPs/SPEEK composite PEMs. To further improve the performance of the PEMs, phosphoric acid (PA) was doped and a continuous nanopore network was formed in PA/PUNSNPs/SPEEK porous PEMs due to the dissolution of PUNSNPs. The PA/PUNSNPs/SPEEK porous PEMs have high PA uptake ratio (96%–117 %) and dimensional stability thanks to the anchoring effect of the nitrogen-containing heterocyclic ring on the PVP chains. The acid-base pairing interaction between the chains (residual ligands from PUNSNPs) inside the unique continuous nanopore structure allows PA/PUNSNPs/SPEEK = 20 % porous PEMs to have the highest proton conductivity of 0.350 S cm −1 (80 °C/100 % RH). Furthermore, the PA/PUNSNPs/SPEEK porous PEMs retained PA up to more than 80 % (80 °C, 40 % RH, 7 days). Similarly, PA/PUNSNPs/SPEEK = 20 % porous PEMs immersed in deionized water for 45 days were able to maintain a proton conductivity of more than 83 %. Finally, PA/PUNSNPs/SPEEK porous PEMs have low methanol permeability . Thus, this study provides a new method for the preparation of porous PEMs with a continuous nanopore network structure and excellent performance.

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International Journal of Minerals Metallurgy and Materials · 2023 ·Vol. 30 ·期 10 ·1897-1905 · IF 4.8

A gel polymer electrolyte with IL@UiO-66-NH2 as fillers for high-performance all-solid-state lithium metal batteries

Wei Tao,Zhang Qi,Wang Sijia,Wang Mengting,Liu Ye,Sun Cheng,Zhou Yanyan,Huang Qing,Qiu Xiangyun,Tian Fang

All solid-state electrolytes have the advantages of good mechanical and thermal properties for safer energy storage, but their energy density has been limited by low ionic conductivity and large interfacial resistance caused by the poor Li + transport kinetics due to the solid–solid contacts between the electrodes and the solid-state electrolytes. Herein, a novel gel polymer electrolyte (UPP-5) composed of ionic liquid incorporated metal-organic frameworks nanoparticles (IL@MOFs) is designed, it exhibits satisfying electrochemical performances, consisting of an excellent electrochemical stability window (5.5 V) and an improved Li + transference number of 0.52. Moreover, the Li/UPP-5/LiFePO 4 full cells present an ultra-stable cycling performance at 0.2C for over 100 cycles almost without any decay in capacities. This study might provide new insight to create an effective Li + conductive network for the development of all-solid-state lithium-ion batteries.

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Small · 2023 ·Vol. 20 ·期 7 ·2306820 · IF 13.3

Enhanced Charge Transfer via S-Scheme Heterojunction Interface Engineering of Supramolecular SubPc–Br/UiO-66 Arrays for Efficient Photocatalytic Oxidation

Zheng Zheng,Bing Wang,Zhuo Li,Hong Hao,ChaoYang Wei,WenYu Luo,LinYu Jiao,Sheng Zhang,Bo Zhou,XiaoXun Ma

Constructing heterojunction of supramolecular arrays self-assembled on metal–organic frameworks (MOFs) with elaborate charge transfer mechanisms is a promising strategy for the photocatalytic oxidation of organic pollutants. Herein, H 12 SubPcB–Br (SubPc–Br) and UiO-66 are used to obtain the step-scheme (S-scheme) heterojunction SubPc–Br/UiO-66 for the first time, which is then applied in the photocatalytic oxidation of minocycline. Atomic-level B–O–Zr charge-transfer channels and van der Waals force connections synergistically accelerated the charge transfer at the interface of the SubPc–Br/UiO-66 heterojunction, while the establishment of the B–O–Zr bonds also led to the directional transfer of charge from SubPc–Br to UiO-66. The synergy is the key to improving the photocatalytic activity and stability of SubPc–Br/UiO-66, which is also verified by various characterization methods and theoretical calculations. The minocycline degradation efficiency of supramolecular SubPc–Br/UiO-66 arrays reach 90.9% within 30 min under visible light irradiation. The molecular dynamics simulations indicate that B–O–Zr bonds and van der Waals force contribute significantly to the stability of the SubPc–Br/UiO-66 heterojunction. This work reveals an approach for the rational design of semiconducting MOF-based heterojunctions with improved properties.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Heating-induced adsorption promoting the efficient removal of toluene by the metal-organic framework UiO-66 (Zr) under visible light

Jiajun Yu,Xiao Wang,Yan Wang,Xiaofeng Xie,Haijiao Xie,Nat Vorayos,Jing Sun

The removal of indoor/outdoor toluene by photocatalysis has drawn much attention due to its low energy consumption and easy availability. However, light inevitably generates heat, and pollutants desorb from catalysts as the temperature rises, which is not beneficial to degradation. Contrast to the frequently occurred phenomena, we firstly found that the adsorption capacity of UiO-66 (Zr) on toluene increased with increasing temperature as adsorption isotherms and in-situ Fourier transform infrared spectra (in-situ FTIR) showed. The optimum temperature was 30 °C. This stage in which adsorption capacity was positively correlated with temperature was called heating-induced adsorption, which achieved a toluene removal efficiency of 69.6 %. By density functional theory (DFT) calculations and changing the metal centers and organic ligands of UiO-66 (Zr) respectively, we disclosed that the heating-induced adsorption was mainly related to the π-π stacking interaction of MOF ligands and toluene. The analysis of samples before and after adsorption showed that the interaction between UiO-66 (Zr) and adsorbed toluene facilitated the charge transfer and prolonged the carrier lifetime, leading to the increase of hydroxyl radicals (•OH) in photocatalysis. Therefore, a synergistic effect between heating-induced adsorption and photocatalysis was proposed by analyzing the adsorption of toluene on UiO-66 (Zr) in detail. This work provided new viewpoint to understand the role of concomitant heat contributed to the adsorption and degradation of toluene during photocatalysis.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Efficient photocatalysis-Fenton for degradation of rhodamine B and inhibition of bacteria by core-shell Fe3O4 @UiO-66-NH2 nanospheres

Zhitong Xu,Ye Qi,Yueguang Fang,Peng Tian,Guiling Ning,Junwei Ye

Core-shell Fe 3 O 4 @UiO-66-NH 2 nanospheres with superior photocatalytic activity and photo-Fenton performance were synthesized using a layer-by-layer growth strategy. The synthesis involved the use of FeCl 3 , trisodium citrate, sodium acetate, ZrCl 4 , and 2-aminoterephthalic acid as raw materials, with mercaptoacetic acid serving as a modifier. Fe 3 O 4 @UiO-66-NH 2 demonstrated improved visible-light-driven photocatalytic performance in the oxidation degradation of Rhodamine B (RhB) in the presence of trace amounts of H 2 O 2 under visible light irradiation. The Fe(II)/Fe(III) cycle was accelerated by the transfer of the photogenerated electrons (e-) from UiO-66-NH 2 to Fe 3 O 4 , which in turn encouraged the Fenton reaction to produce hydroxyl radicals (•OH). With only 10 mmol/L H 2 O 2 , the removal rate of RhB approached 94% in 120 min. Furthermore, when exposed to visible light, Fe 3 O 4 @UiO-66-NH 2 exhibited 99% efficacious antibacterial activity against Escherichia coli and Staphylococcus aureus . Overall, the as-prepared Fe 3 O 4 @UiO-66-NH 2 core-shell nanospheres show promise for practical applications as photocatalysts for the degradation of organic pollutants and the inactivation of bacteria in wastewater.

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FOOD CHEMISTRY · 2023 · IF 8.8

Fluorescent and smartphone imaging detection of tetracycline residues based on luminescent europium ion-functionalized the regular octahedral UiO-66-NH2

Xiaoyue Yue,Long Fu,Jingwen Zhou,Yan Li,Min Li,Yawen Wang,Yanhong Bai

Antibiotic residues cause extensive damage to food security, thus arousing serious concerns. Hence, rapid and sensitive detection of antibiotic residues is crucial to food safety. This study aimed to propose a portable, visual, intelligent and rapid method for tetracycline detection. We developed a ratiometric fluorescent sensor based on the Eu 3+ -functionalized regular octahedral UiO-66-NH 2 material. The developed sensor could quantify tetracycline in the concentration range of 0.5–200 μM with a detection limit as low as 0.2 μM under the optimum conditions. Furthermore, the analytical results obtained using the designed sensor in the actual samples were basically consistent with those obtained using high-performance liquid chromatography. Based on these achievements, a smartphone application-integrated fluorescent testing paper was designed for facile, intelligent, and visual detection of tetracycline. The integrated portable sensor not only saved cost and time for testing but also provided a forward-looking approach to fast, sensitive detection of antibiotic residues.

CAS / MDL: 10312-55-7 10026-11-6
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Nitrogen activation and surface charge regulation for enhancing the visible-light-driven N2 fixation over MoS2/UiO-66(SH)2

Qingqing Li,Yingzhang Shi,Zhiwen Wang,Cheng Liu,Jinhong Bi,Jimmy C. Yu,Ling Wu

A series of dehydrated MoS 2 /UiO-66(SH) 2 (MS/UiS) composites has been prepared as photocatalysts for N 2 fixation. Typically, 10% MS/UiS exhibits the best performance with an NH 4 + yield rate of 54.08 μmol∙g −1 ∙h −1 . 15 N isotope test confirmed that the sample 10% MS/UiS was most effective for reducing N 2 to ammonia. Such enhanced activity was due to the presence of abundant unsaturated Zr and Mo sites which would synergistically promote the adsorption and activation of N 2 . The photogenerated electrons would transfer to the unsaturated Zr-O clusters while part of photogenerated electrons at the interface migrate to MS via Mo VI -O interactions between MS and UiS. These two electron transfer pathways effectively promote the separation of photogenerated carriers. The activated N 2 is reduced to ammonia by the synergistic effect of protonated hydrogen and photogenerated electrons. Finally, a possible N 2 fixation mechanism is proposed which emphasizes the significant roles of nitrogen activation and interface interaction in composites photocatalyst for improving photocatalytic performance.

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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2023 ·Vol. 34 ·期 24 ·1-17 · IF 2.8

The efficient removal towards tetracycline via photocatalytic persulfate activation using the heterostructured UiO-66-NH2-CA-Cu/g-C3N4 composite

Fan Yan,Wang Lei,Sun Xueqin,Li Cuili,Liu Jiacheng

A series of UiO-66-NH 2 -CA-Cu/g-C 3 N 4 (UCC 1 /CN x ) heterogeneous photocatalysts were constructed via a facile physical mixing treatment of the covalently post-modified MOF (UiO-66-NH 2 -CA-Cu) and functional materials g-C 3 N 4 . The tetracycline removal by the photocatalysis coupled with persulfate activation were studied under white light irradiation. The optimal UCC 1 /CN 20 photocatalyst showed the best photocatalytic performance, in which 94.0% TC could be efficiently eliminated ( k  = 0.08669 min −1 ) within 30 min. The satisfactory degradation performance could be ascribed to the effective separation of photogenerated electron-hole pairs over the heterogeneous binary structure, which were demonstrated by several characteristic technologies including photoluminescence spectra, electrochemical impedance spectroscopy, transient photocurrent response and Bader charge analysis based on density functional theory calculations. Moreover, a possible mechanism behind the photocatalytic degradation was proposed and further affirmed by the quenching experiments and electron spin resonance measurements. Our work may supply a feasible idea for treating wastewater contained organic pollutants based on the heterogeneous photocatalyst.

CAS / MDL: 10026-11-6
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