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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Bimetallic NiCu catalyst derived from spent MOF adsorbent for efficient photocatalytic CO2 reduction

Longyun Zhang,Ganghua Zhou,Gaoran Chen,Heming Wang,Qian Zhao,Weiqin Yin,Jianjian Yi,Xingwang Zhu,Xiaozhi Wang,Xin Ning

The metal–organic frameworks (MOFs) rich in porous structures and their derivatives have been widely developed and applied to heavy metal adsorption. However, little attention has been paid to the subsequent treatment and reutilization of spent MOFs adsorbents. A potential feasible strategy is to develop MOFs-derived bimetallic catalysts for energy conversion. Herein, a bimetallic Ni-Cu 2 O-Cu/C nanocomposite (Ni-Cu/C) derived from spent Cu-based MOFs (CuBTC) adsorbents was fabricated and applied to improve the performance of photocatalytic CO 2 reduction. The results demonstrate that Ni doping could improve the charge transfer dynamics. The synthesized Ni-Cu/C catalyst exhibits a high CO yield (12.45 μmol g −1 h −1 ) in the pure water system in the absence of other photosensitizers and sacrificial agents, which is 2.05 folds higher compared to Cu/C. The CO 2 conversion selectivity of the synthesized Ni-Cu/C catalyst reaches up to 99.0%. The mechanism of photocatalytic CO 2 reduction reaction was further investigated by in-situ experiments and density functional theory calculation. The in-situ FT-IR characterization show that photogenerated electrons could effectively adsorb CO 2 to produce CO 2 − and optimize *CO immediate. This work not only emphasizes the unique design of bimetallic catalyst derived from spent MOFs adsorbent, but also contributes a feasible solution to its reutilization for enhanced CO 2 conversion.

CAS / MDL: 6018-89-9 554-95-0
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

All-in-one electrochromic device from viologen-based Cu-MOF and photocurable eutectogel

Le Huy Thai,Le Thi Thanh Nhi,Nguyen Minh Hiep,Dinh Thanh Khan,Trinh Ngoc Dat,Le Vu Truong Son,Truong Quang Trung,Le Hoang Sinh

A novel all-in-one electrochromic device from viologen-based Cu-MOF was demonstrated successfully for the first time. The viologen-based Cu-MOF was dispersed in a photochemical eutectic solvent and directly used as an electrochromic material with the outstanding advantage of good modulation ability in a wide range of visible light. The electrochromic device's (ECD) color changed from transparent and light lime green to blue during the change of potential from 0 V to −3.5 V. The bistability of the ECD was demonstrated by the transmittance degradation of less than 10 % over 1.79 h when the power was turned off. This showed that the ECD could maintain its optical state long without a continuous power supply.

CAS / MDL: 207121-39-9 26570-48-9
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Journal of Saudi Chemical Society · 2024 · IF 5.8

Aluminium-based MOF CAU-1 facilitates effective removal of florfenicol via hydrogen bonding

Zhengjie Li,Miao Liu,Chunxia Fang,Huanshu Zhang,Tianyi Liu,Yixian Liu,Heli Tian,Jilong Han,Zhikun Zhang

The widespread use and subsequent accumulation of florfenicol (FFC), a common antibiotic, through the food chain poses significant risks to aquatic ecosystems and human health, necessitating effective strategies for its removal from water bodies. To solve the challenge, herein, we developed a novel aluminum-based metal–organic framework CAU-1, engineered for the efficient adsorption of FFC. CAU-1 contains the plentiful –NH 2 and μ-OH groups with the positively charged on the surface. In the adsorption process, CAU-1 perform hydrogen bonding interactions with FFC’s functional groups (−F, –OH, −Cl, –NH–, and −SO 2 –). Furthermore, the positively charged surface of CAU-1 enhances FFC adsorption via electrostatic attraction together. FFC adsorption equilibrium on CAU-1 is attained within 180 min with a monolayer adsorption capacity of 386 mg/g at 303 K, surpassing most of the reported adsorbents. The exothermic FFC adsorption process on CAU-1 remains largely unaffected by coexisting ions. Additionally, CAU-1 can be efficiently regenerated using a mixed solution of 0.1 M HCl and ethanol–water as an eluent. This work highlights CAU-1’s potential as an effective adsorbent for FFC removal, emphasizing the importance of tuning or designing surface functional groups on adsorbents to boost their adsorption capabilities.

CAS / MDL: 7784-13-6 10312-55-7
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

A strategy to obtain highly luminescent MOF-76 based on hydrothermal annealing treatment

Weijun Gui,Mingzhe Du,Xianmin Zhang,Miroslav Almáši,Lijia Wan,Lu Gan,Zhenxi Wang,Suhang Wu

The limited luminescence efficiency and poor stability of lanthanide-based metal-organic frameworks (Ln-MOFs) are the key factors restricting their practical applications. It is well known that high-temperature annealing can significantly enhance the photoelectric properties of inorganic materials, but it seems unfeasible for Ln-MOFs due to the existence of organic components. To overcome this dilemma, MOF-76 was synthesized by hydrothermal method and then hydrothermally annealed at 140 °C for 4 h. As a result, the annealing not only significantly improves the crystallinity of MOFs but also promotes their transition from the original tetragonal phase to the monoclinic phase. The annealed MOFs ( a MOF) exhibit about 3-fold emission enhancement and show better stability, especially under alkaline conditions or in water or saturated alkanes, such as cyclohexane, and dichloromethane. The total emission intensity of the as-prepared (AP) MOF is reduced to less than 1/10 compared to the a MOF due to the influence of water molecules. When the material was immersed in a mixture of ammonia and water, the a MOF emission remained stable, while the AP MOF emission rapidly decreased to approximately 12 % with an increasing volume ratio. Additionally, a notably enhanced 5 D 0 → 7 F 1 transition of Eu 3+ ions in MOF-76 has been observed for the first time. It was found that after hydrothermal annealing, the photoluminescence quantum yield of the MOF increases from 10.86 % to 61.48 %, and its synthesis yield can reach 73.8 %. The properties described above remarkably enhance the application values of the a MOFs. Interestingly, MOFs can also be solvothermal annealed, thus the schemes presented in this context open up novel approaches to significantly improve/modify the performance of other MOF materials. Finally, the obtained green and red emitting a MOFs combined with the N-CDs@starch were applied to warm white LED with the colour coordinates (CIE) of (0.3662, 0.3544), colour rendering index (CRI) of 88.5 and correlated colour temperature (CCT) of 4261 K.

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IONICS · 2025 · IF 2.6

Anthraquinone doped CoNi-MOF-74 composites as electrocatalysts for enhanced oxygen evolution reaction

Du Jia,Chen Lixuan,Wu Yiming,Wei Xin,Jia Jingyuan,Sun Kenan,Li Bingke

Nowadays, the advancement of eco-friendly, clean, sustainable and renewable new energy has emerged as a research priority for scientists worldwide. Electrolytic water technology is founded on the principle of electrochemical or photoelectric decomposition of water, is deemed as one of the most promising and most feasible approaches to reach industrial production. Traditional OER (oxygen evolution reaction) electrocatalysts like IrO 2 and RuO 2 are beset by high costs and vulnerability to poisoning. Hence, it is essential to develop more economical, more stable and more efficient materials for the application of OER reactions. In this study, a series of AQ-doped (AQ = anthraquinone) MOF-74 materials were fabricated through a one-step solvothermal approach. The surface loading of the conjugated organic small molecule AQ on CoNi-MOF-74 is capable of effectively boosting the inadequate electrical conductivity of the bulk MOF material, thus significantly enhancing the performance of OER. The optimized ratio of material composition of AQ20@MOF-74 displayed significantly enhanced OER activity. with a lower overpotential of 272 mV at 10 mA cm −2 and a smaller Tafel slope of 78 mV dec −1 . The research findings presented in this thesis provide a novel approach for the design and optimization of highly efficient OER electrocatalysts based on MOFs.

CAS / MDL: 6147-53-1
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

A hybrid linker-MOF fibrous composite for efficient diclofenac removal and self-cleaning

Yanxin Gao,Ting Cheng,Fankang Zhao,Guocheng Huang,Jinhong Bi

The treatment of emerging contaminants is essential but challenging. Herein, a novel MOF/PAN fibrous composite (TCPP@UiO-66/PAN) was synthesized and used as a self-cleaning membrane for the efficient removal of a typical emerging contaminant, diclofenac sodium (DF). The introduction of the secondary linker tetra(4-carboxyphenyl)porphyrin (TCPP) served to expand the pores and enhance its photocatalytic activity. TCPP@UiO-66/PAN shows higher adsorption capacity and initial adsorption rate than UiO-66/PAN. The maximum adsorption capacity of DF on TCPP@UiO-66/PAN reached 202 mg/g by Langmuir model. The DF adsorption mechanism involves the π-π/anion-π interaction, Lewis acid-base interaction, and hydrogen bonding. Based on the dynamic filtration experiment, TCPP@UiO-66/PAN exhibited a remarkable treatment capacity for DF-contaminated water, measuring 3.75 × 10 4   kg/kg. Given its fibrous membrane structure, TCPP@UiO-66/PAN could be easily separated from water and reused. In-situ photo-regeneration emerged as a highly effective method for regenerating TCPP@UiO-66/PAN after reaching adsorption saturation, with over 95 % DF degradation achieved under sunlight irradiation. The decomposition of DF primarily resulted from the generation of h +   and   1 O 2 . Additionally, TCPP@UiO-66/PAN exhibited notable antibacterial properties when exposed to visible light.   In vitro   cytotoxicity assessments further confirmed the safety of these MOF/PAN composites. Combining the advantages of hybrid-linker strategy and fibrous composite, this work provided new insight into constructing MOF-based functional material for wastewater purification.

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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2024 · IF 4.1

The flower-like Ni-MOF modified BiOBr nanosheets with enhancing photocatalytic degradation performance

Ting Lu,Xinyan Xiao,Fei Wang,Xia Cheng,Yu Zhang

A novel BiOBr/Ni-MOF composite was fabricated by in-situ growth of BiOBr nanosheets on Ni-MOF through a convenient precipitation process. The optimal photocatalytic performance was achieved with a Ni-MOF mass content of 45 wt% in the BiOBr/Ni-MOF composite. This composite exhibited remarkable efficiency, degrading 98.33 % of Rhodamine B in 90 min, surpassing the degradation rate constants of pristine BiOBr and Ni-MOF by 4.2 and 160 times, respectively. The superior performance was primarily ascribed to the efficient separation of photogenerated carriers facilitated by the formation of heterojunctions. Additionally, the increased specific surface area and pore structure provided numerous adsorption and active sites. Radical scavenger experiments and electron spin resonance experiments further revealed that O 2 − and h + played crucial roles in the degradation process. Furthermore, the structural properties of the prepared photocatalysts and the effects of different photocatalytic conditions on the degradation of RhB were investigated. This work offers an alternative perspective on the design and fabrication of BiOBr-based composite photocatalysts.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Porphyrin-based-MOF nanocomposite hydrogels for synergistic sonodynamic and gas therapy against tumor

Yunqi Kuang,Ziwen Zhang,Kai Zhu,Yangang Sun,Kaiyang Wang,Chunping Yuan,Jie Lu,Yu Luo,Xijian Liu,Jian Wan

The glioma is one of the most aggressive tumors in humans, which is difficult to eradicate clinically. Therefore, we devised a porphyrin-based metal-organic frameworks (MOFs) crosslinking hyaluronic acid (HA) hydrogel nanocomposite through double-network (Cu-MOF-S-S-HA-Gel, CSSH-Gel), which is tumor responsive for enhanced gas therapy and sonodynamic therapy (SDT). Firstly, the hydrogels show extraordinary injectability and biocompatibility, which enables intratumor administration to circumvent the danger associated with surgery. The Cu-MOF-Cys and HA-Cys are interconnected through ether and disulfide bonds to establish a dual-network gel structure. The overexpressed glutathione (GSH) in tumor microenvironment (TME) reacts with disulfide bonds to release of the nanosensitizer (Cu-MOF). Subsequently, Cu-MOF generates reactive oxygen species (ROS) upon ultrasound irradiation for SDT, and releases L-cysteine(L-Cys) catalyzed by 3-mercapto pyruvate sulfotransferase (3-MST) to generate H 2 S for gas therapy. The CSSH-Gel obtained excellent synergistic anti-tumor effects (82.34 % inhibition ratio in vivo), which holds tremendous promise for the advancement of minimally invasive glioma therapies.

CAS / MDL: 65-85-0 68-12-2
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JOURNAL OF HAZARDOUS MATERIALS · 2024 · IF 12.2

Superhydrophobic Co-MOF-based sponge for efficient oil-water separation utilizing photothermal effect

Xuanting He,Jihan Lu,Jiaxiang Liu,Zixuan Wu,Boyu Li,Zhong Chen,Wenquan Tao,Zhuo Li

Effectively addressing crude oil spills remains a global challenge due to its high viscosity and limited flow characteristics. In this study, we successfully prepared a modified sponge (PCP@MS) by embedding the photothermal material of Co-HHTP and coating the melamine sponge (MS) with low-surface-energy polydimethylsiloxane (PDMS). The PCP@MS exhibited outstanding hydrophobicity with WCA of 160.2° and high oil absorption capacity of 59–107 g/g. The PCP@MS showed high separation efficiency of 99.2% for various oil-water mixtures, along with notable self-cleaning properties and mechanical stability. The internal micro-nano hierarchical structure on the sponge surface significantly enhanced light absorption, synergizing with the photo-thermal conversion properties of Co-HHTP, enabled PCP@MS to achieve a surface temperature of 109.2 °C under 1.0 solar light within 300 s. With the aid of solar radiation, PCP@MS is able to heat up quickly and successfully lowering the viscosity of the surrounding crude oil, resulting in an oil recovery rate of 8.76 g/min. Density functional theory (DFT) calculation results revealed that Co-HHTP featured a zero-gap band structure, rendering advantageous electronic properties for full-wavelength light absorption. This in situ solar-heated absorbent design is poised to advance the practical application of viscous oil spill cleanup and recovery.

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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 20 ·9358-9365 · IF 2.7

Synthesis and characterization of hollow dual-tube MOF hybrid nanocomposites for electroanalytical applications

Junfeng Wang,Shuyue Tian,Sihua Pan,Yujuan Zhang,Wang Sun,Yang Wang

The effective assembly of hollow nanomaterials is of great importance for the rapid advancement of electroanalytical platforms. Herein, the hollow tubular zeolite imidazolium framework-8 (HTZIF-8) was carefully constructed via the precursor conversion pathway. Subsequently, the predictable assembly of HTZIF-8 with carbon nanotubes (CNTs) occurred to form a unique hollow dual-tube MOF hybrid material (HTZIF-8@CNTs). Meanwhile, the HTZIF-8@CNTs electroanalytical platform was established with dopamine (DA) as the objective biomolecule. In the electrochemical evaluation, the linear intervals of 0.06–600 μmol L−1 and detection limit of 0.02 μmol L−1 (S/N = 3) were determined, which were mainly ascribed to nano-synergistic engineering of HTZIF-8 and CNTs. The HTZIF-8@CNTs hybrid material exhibited superior electrocatalytic performance for DA compared to the solid rod-like MOF composite (SRZIF-8@CNTs), which was majorly based on the faster mass transfer characteristics of hollow MOFs. Additionally, the HTZIF-8@CNTs electrochemical sensor presented outstanding anti-interference capabilities as well as stability and could be utilized for the detection of DA in real samples. The employment of F and t statistics were employed to ensure the reliability of the results. This study will offer novel thoughts toward the application of hollow MOF composites in the area of electroanalytical platforms.

CAS / MDL: 308068-56-6 693-98-1
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2024 · IF 4.3

Robust and sensitive colorimetric detection of glutathione with double-triggering MOF-Fe(DTNB)

Kaining Zhang,Hao Sun,Long Wei,Rui Hu,Hao Liu,Yongchao Lai,Xun Li

Glutathione (GSH) levels have been well validated to correlate with a variety of physiological and pathological conditions, such as malignancy, cardiovascular disease and aging, making the development of accurate, robust and sensitive GSH detection methods highly desirable. In this study, a novel metal–organic framework (MOF-Fe(DTNB))-based colorimetric method with a favorable dual-triggering function was proposed. MOF-Fe(DTNB) exhibits high peroxidase activity, which can catalyze the oxidation of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue ox-TMB by hydrogen peroxide (H 2 O 2 ). This oxidation process of TMB can be inhibited not only by the reducing action of GSH, but also by the thiol exchange reaction between DTNB and GSH, in which the disulfide bond of DTNB in MOF-Fe(DTNB) is cleaved. Thus, with this dual triggering mechanism, the GSH concentration can be robustly measured in the MOF-Fe(DTNB)-derived colorimetric strategy. Significantly, this method is accurate (RSD < 6 %), selective and sensitive in biological plasma samples, with satisfactory recovery rates (96.7–103.3 %). It requires less instrumentation and has less interference from other substances. The linear range of the method is 0–80 µM, and the detection limit is as low as 0.28 µM. This dual-triggering MOF-Fe(DTNB)-derived colorimetric strategy has greatly simplified the GSH detection processes with improved accuracy, in both acidic and basic environments, which has potent applications in biochemical analysis and point-of-care testing.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Tetraaniline-modified Co-MOF-PDA for anti-corrosive reinforcement of waterborne epoxy coating

Dan Sun,Qilong Chen,Yi He,Yang Bai,Changhua Li,Rui Gou,Chuanfang Zhang,Xinbo Xu,Haichao Zhang

The main aim of this study was to exploit the advantages of dopamine and tetraaniline (TA) to enhance the physical barrier properties and active anti-corrosion performance of composite coatings ; in this study, the growth of polydopamine on the surface of Co-MOF enhanced its compatibility with waterborne epoxy, and Co-MOF-PDA-TA (MP-TA) was successfully synthesised by adding dopamine and tetraaniline via Michael addition , confirmed through characterisation methods such as Fourier-transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy. MP-TA can be added as a nanofiller additive to water-based epoxy coatings, and a detailed study on the corrosion resistance of the prepared composite coatings showed that the composite coating containing 0.50wt% MP-TA/WEC exhibits good anti-corrosion performance with an impedance modulus at low frequency (0.01 Hz) of 7.253 × 10 9 Ω cm 2 because TA not only prolongs the time required for corrosion ions to reach the interface but also forms a passivation film on the steel surface. Moreover, the reduced TA can be oxidised to EB or even LEB by releasing two electrons, which further promotes the formation of a passivation film, providing a good pathway for the application of MP-TA as a multifunctional additive.

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