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MICROCHIMICA ACTA · 2025 ·Vol. 192 ·期 7 ·1-10 · IF 5.3

Gold-graphdiyne linked [Ru(NH3)6]3+-UiO-66-NH2 with peptide for sensitive electrochemical detection of matrix metalloproteinase-7

Chen Fei,Wang Xiang,Yan Lei,Lin Zhixiong,Zheng Weijun,Wu Dianming,Qiu Bin,Fang Yifan,Liu Mingkun

By preparing gold nanoparticles-graphdiyne (Au-GDY) as sensing substrate and [Ru(NH 3 ) 6 ] 3+ -UiO-66-NH 2 MOFs (Ru-UiO-66) as signaling probe as well as linking the as-prepared Au-GDY and Ru-UiO-66 with the specific peptide (PT) of MMP-7 to form Ru-UiO-66/PT/Au-GDY, a cost-effective and sensitive electrochemical sensor was designed for the detection of matrix metalloproteinase-7 (MMP-7) which is an important biomarker for tumor and biliary atresia. The superior electrical properties, easy preparation, large surface area, and high stability of Au-GDY make it be a desirable substrate to immobilize PT. The unique structure of UiO-66-NH 2 is beneficial to assemble [Ru(NH 3 ) 6 ] 3+ probe and link PT. In the absence of MMP-7, the Ru-UiO-66/PT/Au-GDY modified electrode exhibited a prominent peak current of [Ru(NH 3 ) 6 ] 3+ , which is decreased after the addition of target MMP-7 since it can specifically recognize and cleave PT to induce the Ru-UiO-66 leave the electrode. The experimental results showed that the decrease of the [Ru(NH 3 ) 6 ] 3+ signal has a linear relation with the concentrations of MMP-7 in the range 0.01 pg mL −1 –10.0 ng mL −1 . By optimizing experimental conditions, the achieved detection limit (LOD) for MMP-7 is 5.0 fg mL −1 . The analysis of real serum samples has excellent accuracy. The simplicity of preparation and sensitivity make the Ru-UiO-66/PT/Au-GDY sensor a considerable promising analysis tool for MMP-7 detection. Graphical abstract

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JOURNAL OF MATERIALS RESEARCH · 2025 · IF 2.9

In situ construction of S-type core–shell NH2-MIL-125/TiO2 heterojunctions and mechanism for visible photodynamic antibacterial systems

Yang Wen,Wang Yujia,Gao Na,Zhu Zhengfa,Chen Yuanyuan,Wang Hao,Tang Xiaoning

Designing efficient visible light-driven photocatalytic antimicrobial agents presents significant challenges. In this study, S-shaped core–shell NH 2 -MIL-125/TiO 2 (NT-x) heterojunctions were constructed by simple in situ solvothermal method, as photocatalytic antimicrobial agents for efficient bactericidal use under visible light. Notably, 99.99% inhibition was achieved for both Escherichia coli and Staphylococcus aureus at low concentrations (0.02 and 0.035 mg mL −1 , respectively) after exposure to simulated sunlight for 20 min. Reasonable energy band configuration and built-in electric field of this structure provided improved photogenerated carrier transfer paths as well as enhanced separation and transport efficiency. Moreover, the core–shell structure enhanced the interaction between NH 2 -MIL-125 and TiO 2 , increased the total number of reactive sites, and promoted the efficient generation of reactive oxygen species. Finally, possible mechanisms for the inactivation of bacteria were discussed. This research offers new perspectives for the advancement of advanced metal–organic framework-based photocatalysts with antibacterial activity under visible light. Graphical abstract

CAS / MDL: 64-17-5 67-56-1 68-12-2
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ANALYTICA CHIMICA ACTA · 2025 · IF 6

AuNPs@UiO-66-(COOH)2–NH2/Eu for ratiometric fluorescent and colorimetric sensing of trace inorganic mercury in water samples

Zifei Wu,Hao Ding,Kailai Xu,Chenghui Li,Xiandeng Hou

Background due to the toxicity and widespread distribution of inorganic mercury ions (Hg 2+ ), it is a crucial task for researchers to develop simple methods for field analysis of water samples for trace Hg 2+ . Result a colorimetric and ratiometric fluorescent dual-mode assay based on bifunctional UiO–(COOH) 2 –NH 2 /Eu and gold nanocomplexes (AuNPs@UiO–(COOH) 2 –NH 2 /Eu) was constructed for the sensitive, selective and potentially on-site determination of Hg 2+ . The incorporation of Hg 2+ resulted in the formation of gold amalgam, which enhanced peroxidase-like activity of AuNPs@UiO–(COOH) 2 –NH 2 /Eu, accelerating the oxidization of zymolyte 3,3′,5,5′-tetramethylbenzidine (TMB). Concurrently, the color of the reaction solution turned blue, and the RGB (red, green, and blue) of the solution color changed accordingly. The fluorescence at 618 nm was almost unchanged with the increase of Hg 2+ concentration, whereas the fluorescence at 460 nm was obviously quenched due to the inner filter effect (IFE). Under UV irradiation, the fluorescence emission of the sensing system changed from blue to red, enabling easy visual detection. The probe showed great linearity over a wide range of 20–1200 nM (colorimetric) and 50–4000 nM (fluorescent), with limits of detection (LODs) of 8 nM and 3 nM, respectively. Significance the proposed method was successfully applied to the determination of trace Hg 2+ in tap water and groundwater, while the use of a smartphone enables its simplicity and portability. The results show that the colorimetric and ratiometric fluorescent dual-mode method based on AuNPs@UiO–(COOH) 2 –NH 2 /Eu can achieve rapid visual determination of Hg 2+ potentially useful for on-site analysis.

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Highly Selective Oxidation of 5-Hydroxymethylfurfural to 2,5-Formylfuran Mediated by Surface Superoxo and Peroxo on Mo3Cu1/NH2-SBA-15

Qian-Wen Lu,Qing He,Qing-Shuai Zhang,Da Sheng,Song-Hai Wu,Yong Liu,Xu Han

Although thermocatalytic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-formylfuran (DFF) by O2 is an important reaction, achieving a high yield of DFF is still challenging. In this study, a series of MoxCuy/NH2-SBA-15 are prepared, and Mo3Cu1/NH2-SBA-15 exhibits the desirable catalytic reactivity with a complete conversion of HMF and high selectivity of 94.4% toward DFF. XPS and EPR analyses indicate that the abundant oxygen vacancies (Ov) and Cu(I) are the reactive sites for O2 activation. Quenching experiments and various characterizations reveal that superoxo (≡Cu(II)/Ov-OO•) on the surface of catalyst, instead of •OH and O2•–, are the primary oxidizing species to abstract H from HMF to RCH2-O•, accompanied by the formation of ≡Cu(II)/Ov-OOH peroxo. Meanwhile, the doped Mo(V/VI) further activates ≡Cu(II)/Ov-OOH peroxo to form ≡Mo-(η2-O2) peroxo, which significantly promotes the oxidation selectivity of RCH2-O• toward DFF via the H-abstraction pathway. This study provides new insight on selective thermal-oxidation of biomass-derived compounds to high-value-added chemicals via regulating reactive oxidizing species on the surface of catalysts.

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ACS Omega · 2025 · IF 4.3

A Study on the Filtration Performance of NH2-MIL-53/Chitosan-Modified Paper-Based Functional Materials against Airborne Particulate Matter

Dandan Hao,Bing Yu,Tong Zhao,Meisi Chen

In response to the pollution of airborne inhalable particulate matter (PM) and the demand for high-efficiency, low-resistance filtration materials, this study prepared a CS/NP-2.5 paper-based filter by incorporating NH2-MIL-53 into pulp fibers and introducing chitosan (CS) as a carrier. Characterization results show that the composite material forms a complex three-dimensional network structure, significantly enhancing PM capture efficiency. The removal rates for PM2.5 and PM10 reached 98.41% and 99.05%, respectively, with a pressure drop of only 24.10 Pa, which is an improvement of approximately 7% compared to the directly doped NP-2.5 (PM2.5 removal rate of 91.57%). CS enhanced the loading stability of the MOFs on the fibers; after 10 cycle tests, the filtration efficiency was still maintained above 94%, demonstrating excellent reusability. This study, through green synthesis and functional synergy, provides a new approach for the design of high-efficiency paper-based filtration materials.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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ACS Applied Optical Materials · 2025 · IF 3.8

[C(NH2)3]2PO3(OH): A Deep-Ultraviolet Birefringent Crystal Enabled by Synergy of π-Conjugated Cations and Heteroleptic Tetrahedra

Huan Zhou,Meng Cheng,Zhihua Yang,Shilie Pan

Birefringent materials are crucial optical materials that enable the control of polarized light in optical technologies, yet achieving high birefringence in systems dominated by non-π-conjugated units in the deep-ultraviolet (UV) region remains a significant challenge. Herein, a birefringent material, [C(NH2)3]2PO3(OH), was successfully synthesized by integrating π-conjugated [C(NH2)3] units and heteroleptic tetrahedra [PO3(OH)]. The short UV cutoff edge (<200 nm) and large birefringence (0.086 @ 546 nm) make [C(NH2)3]2PO3(OH) a potential deep-UV birefringent crystal. This study provides the experience for the design of deep-UV optical crystals.

CAS / MDL: 7664-38-2 7758-11-4
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Platinum catalysts supported on mixed-phase TiO2 coated by nitrogen-doped carbon derived from NH2-MIL-125 for methanol oxidation

Junyan Liu,Liting Xu,Xingwei Li

Supports play a key role in the performance of platinum-based catalysts. In this work, using NH 2 -MIL-125 as the precursor, mixed-phase TiO 2 coated by nitrogen-doped carbon (TiO 2 @NC) is successfully prepared, and used to support platinum (Pt/TiO 2 @NC) for methanol oxidation reaction. In 0.5 M H 2 SO 4 solution containing 0.5 M CH 3 OH, the area specific activity of Pt/TiO 2 @NC catalyst (1.186 mA cm -2 Pt) is 4.4 times that of commercial Pt/C (0.272 mA cm -2 Pt). At a fixed potential of 0.15 V (vs. Hg/Hg 2 SO 4 ), the current density of Pt/TiO 2 @NC is still 3.6 times that of Pt/C after 3600 s of polarization. Meanwhile, Pt/TiO 2 @NC has also a low tafel slope, a large exchange current density and a high charge transfer coefficient. A large number of Ti-OH groups can alleviate poisoning effect caused by the produced "CO ads " intermediate during methanol oxidation reaction. Nitrogen-doped carbon not only improves the conductivity of TiO 2 support, but provides strong anchor sites for the nucleation of Pt nanoparticles , resulting in an enhanced catalytic activity of Pt/TiO 2 @NC.

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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Highly efficient and selective recovery of Au(III) from aqueous solution by bisthiourea immobilized UiO-66-NH2: Performance and mechanisms

Junkang Guo,Xiaohu Fan,Jiayuan Wang,Shenghui Yu,Minwang Laipan,Xinhao Ren,Chao Zhang,Lei Zhang,Yongtao Li

The design and synthesis of efficient adsorbents for recovery of precious metal from secondary resources are of great environmental and economic significance. In present study, an efficient and redox-active adsorbent (UiO-66-BTU) was fabricated by modifying Zr-MOF (Zirconium-based Metal Organic Framework) with bisthiourea for gold recovery in aqueous solution. It is indicated that Au(III) adsorbing onto UiO-66-BTU is an irreversible, favorable chemisorption process conformed to D-R model and pseudo-second-order model. The UiO-66-BTU showed significant adsorption ability (680.20 mg/g at pH 2.0) and high selectivity towards Au(III) in presence of various mixed ions in actual wastewater, which were mainly attributed to the Lewis soft–soft interaction, ion-exchange/electrostatic interactions, and redox reaction between Au(III) and S-containing functional groups. Notably, we demonstrated that the reduction of Au(III) to metallic gold as a dominant recovery mechanism involving the in situ confined nucleation, fusion and growth of AuNPs to branched Au precipitation, with Au(0) accounted for approximately 80% for the recycling products. Furthermore, the UiO-66-BTU membrane achieved similar high adsorption capacity and the membrane surface remains active to efficiently recovered metallic particles with an excellent repeatability at eight cycles of adsorption. The reduced Au particles formed isolated clusters with bigger size and regular hexagonal shape. Consequently, UiO-66-BTU has great potential for gold recycling in industrial practice.

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Frontiers of Chemical Science and Engineering · 2022 ·Vol. 16 ·期 9 ·1387-1398 · IF 4.803

Integrating of metal-organic framework UiO-66-NH2 and cellulose nanofibers mat for high-performance adsorption of dye rose bengal

Han Yuyao,Xia Lei,Zhuang Xupin,Liang Yuxia

UiO-66-NH 2 is an efficient material for removing pollutants from wastewater due to its high specific surface area, high porosity and water stability. However, recycling them from wastewater is difficult. In this study, the cellulose nanofibers mat deacetylated from cellulose acetate nanofibers were used to combine with UiO-66-NH 2 by the method of in-situ growth to remove the toxic dye, rose bengal. Compared to previous work, the prepared composite could not only provide ease of separation of UiO-66-NH 2 from the water after adsorption but also demonstrate better adsorption capacity (683 mg·g −1 ( T = 25 °C, pH = 3)) than that of the simple UiO-66-NH 2 (309.6 mg·g −1 ( T = 25 °C, pH = 3)). Through the analysis of adsorption kinetics and isotherms, the adsorption for rose bengal is mainly suitable for the pseudo-second-order kinetic model and Freundlich model. Furthermore, the relevant research revealed that the main adsorption mechanism of the composite was electrostatic interaction, hydrogen bonding and π — π interaction. Overall, the approach depicts an efficient model for integrating metal-organic frameworks on cellulose nanofibers to improve metal-organic framework recovery performance with potentially broad applications.

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Nano Research · 2023 ·Vol. 17 ·期 5 ·3752-3760 · IF 9.9

Nanoconfinement-induced water molecules and hydrogen molecules transport behaviors in ball-in-ball structure photocatalysts to improve hydrogen evolution

Chong Ben,Xu Baorong,Li He,Ou Honghui,Yang Guidong

The diffusion, adsorption/desorption behaviors of water molecules and hydrogen molecules are of great importance in heterogeneous photocatalytic hydrogen production. In the study of structure–property–performance relationships, nanoconfined space provides an ideal platform to promote mass diffusion and transfer due to their extraordinary properties that are different from the bulk systems. Herein, we designed and prepared a nanoconfined CdS@SiO 2 -NH 2 nanoreactor, whose shell is composed of amino-functionalized silica nanochannels, and encapsulates spherical CdS as a photocatalyst inside. Experimental and simulated results reveal that the amino-functionalized nanochannels promote water molecules’ and hydrogen molecules’ directional diffusion and transport. Water molecules are enriched in the nanocavity between the core and the shell, and promote the interfacial photocatalytic reaction. As a result, the maximized water enrichment and minimized hydrogen-occupied active sites enable photocatalyst with optimized mass transfer kinetics and localization electron distribution on the CdS surface, leading to superior hydrogen production performance with activity as high as 37.1 mmol·g −1 ·h −1 .

研究领域: 纳米技术 · 光催化 · 材料科学 · 化学工程
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2025 · IF 4.6

Construction of MWCNT-Bridged ternary S-scheme BiVO4/NH2-UiO-66 (Zr) heterojunction for enhanced visible-light photocatalytic degradation of tetracycline

Mingming Dong,Shuyong Yang,Peng Zhou,Yue Gao,Anshun Wang,Shenghui Tu

The accumulation of antibiotics in aquatic ecosystems poses a serious threat to the environment and to human health. Tetracyclines (TC) account for a significant proportion of antibiotic residues worldwide. In order to overcome the limitations of conventional degradation methods, we created a three-component S-scheme heterojunction consisting of BiVO 4 /MWCNTs@NH 2 -UiO-66 (Zr) using a two-step solvothermal process. This synergistic integration utilises: (i) MWCNTs as electron transport bridges; (ii) NH 2 -UiO-66 (Zr) for high TC adsorption (surface area of 931.86 m 2  g −1 ); and (iii) BiVO 4 for visible light harvesting. This architecture broadens light absorption, reduces charge recombination and enables dual-pathway Reactive Oxygen Species (ROS) generation. Under visible light, the optimised catalyst achieves 95.2 % TC degradation within 90 min–7.73 times faster than pristine BiVO 4 (k = 0.02721 vs. 0.00352 L mg −1 ·min −1 ). Radical trapping and EPR analyses confirm ·O 2 − and h + as the dominant species, while LC-MS reveals three degradation pathways. With 85.3 % activity retention after five cycles, this work provides a blueprint for the design of efficient, antibiotic-mineralising photocatalysts.

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COMPOSITES PART B-ENGINEERING · 2026 · IF 14

Rigid-flexible UiO66-NH2/carboxymethyl cellulose hierarchical interface for enhanced load-bearing capacity and adaptive wear resistance of carbon fabric composites

Xinyi Chen,Jie Fei,Xinyu Ke,Zhaoxi Gou,Lehua Qi,Hejun Li

Carbon fabric (CF)-reinforced polymer composites show great potential in wet friction applications, but their performance is severely limited by poor interfacial adhesion and susceptibility to abrasive wear. Herein, we propose a “rigid-flexible” hierarchical interface strategy utilizing a conformal defect-filling carboxymethyl cellulose (CMC) layer and an in-situ grown rigid UiO66-NH 2 octahedral array to enhance the mechanical and tribological properties of CF/phenolic composites. The CMC/UiO66-NH2 hierarchical modification reduced surface defects and increased the apparent single-fiber tensile strength by 89.3%. Meanwhile, the UiO66-NH 2 array increased the surface roughness and promoted mechanical interlocking with the resin matrix. The combined CMC/UiO66-NH 2 interface improved interfacial load transfer and reduced premature debonding, leading to a 75.1% increase in tensile strength. Furthermore, under alternating friction shear, the hierarchical interface promotes the formation of a protective tribofilm, promoting the in-situ formation of a continuous solid tribofilm. This transitions the wear mechanism from severe abrasive wear to mild sliding wear, resulting in an 81.1% reduction in the specific wear rate. This study provides an interfacial design strategy for designing high-load-bearing and highly durable fabric composites for demanding tribological applications.

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