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Covalent organic frameworks (COFs) are widely used due to their high structural order, tunable pore size, and large specific surface area. However, COFs are typically bulk solid microcrystalline powders that are insoluble and challenging to process, which significantly impacts their application prospects. We report a method for the in situ growth of COF-COOH on the surface of polyacrylonitrile (PAN) fibers by using electrospinning. COFs were synthesized via a solvothermal method suitable for most COF materials. Nitrogen atoms in the nitrile groups of the PAN macromolecular chain form hydrogen bonds with the hydrogen atoms of the monomer 2,5-diamino-terephthalic acid (DABDA). This interaction facilitates the effective mixing of PAN and DABDA, resulting in the uniform growth of COF-COOH, which adheres firmly to the fiber surface. The resulting PAN@COF-COOH fiber membrane exhibits remarkable structural stability. It has obvious adsorbability to chromium(VI) (Cr(VI)) in aqueous solution under acidic conditions and also for cationic dyes such as Rhodamine B and methylene blue. It is revealed that COF materials exhibit selective adsorption due to pore size limitations. The integration of the electrospinning method with COF materials allows for the large-scale production of COF fiber membranes, which holds significant importance and offers broad application prospects in this field.
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http://dx.doi.org/10.1021/acsami.5c02896 | DOI Listing |
Food Chem
August 2025
Department of Chemistry & IMO-IMOMEC, Hasselt University, 3590 Diepenbeek, Belgium.
Caffeic acid is a key indicator of wine quality, but its sensitive and accurate detection remains challenging due to the lack of high-performance sensing materials. Metal/N-doped porous carbon (M/NPC) electrocatalysts with abundant catalytic sites are promising to address this issue. Herein, a FeCo nanoalloy encapsulated in NPC (FeCo@NPC) was designed and synthesized via a "covalent organic framework (COF) adsorption-pyrolysis" strategy.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, PR China; Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt. Electronic address:
Post-synthetic modification (PSM) offers a promising approach for tailoring the compositional, structural, and electronic properties of covalent organic frameworks (COFs), thereby enhancing their exciton dissociation ability and facilitating charge transfer. The effectiveness of these approaches is largely compromised by the harsh conditions, complexity, and alteration of the original structure. Therefore, developing a facile yet effective PSM for modulating COFs' properties without altering the original geometry and/or structure is a challenge.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Key Laboratory of Precision and Intelligent Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China.
Solar-driven hydrogen peroxide (HO) production offers a green and sustainable alternative to the energy-intensive anthraquinone process, utilizing water and oxygen as feedstock and solar energy as the sole input. Covalent organic frameworks (COFs), owing to their well-defined crystalline structures and tunable electronic properties, have emerged as a compelling platform for photocatalytic HO synthesis. However, the efficiency of HO photosynthesis remains limited by sluggish charge separation and rapid carrier recombination.
View Article and Find Full Text PDFChem Sci
August 2025
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Science, Zhejiang Normal University Jinhua Zhejiang 321004 P. R. China
Selective photoreduction of CO with HO to hydrocarbons is challenged by inadequate and uncontrollable electron and proton feeding. Herein, this limitation is overcome by integrating HO dissociation, CO reduction, and O evolution catalysts into a dual S-scheme heterojunction and regulating exposed facets of the heterojunction supports. In this design, H and OH species generated by HO dissociation on the NH-MIL-125 support transfer to the T-COF shell and FeO insert for CO reduction and O evolution, respectively.
View Article and Find Full Text PDFAnal Chem
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. China.
Rational design of both mechanistic pathways and material compositions is essential to advance COF-based electrochemiluminescence (ECL) systems. In this study, aggregation-induced emission covalent organic framework (AIE-COF) nanoprobes with excellent ECL performance were developed based on Tb-functionalized covalent organic framework (Tb@A-COF). The Tb@A-COF system demonstrates enhanced ECL performance through synergistic integration of three complementary mechanisms: (1) (4',4',4',4'-(1,2-ethenediylidene)tetrakis [1,1'-biphenyl]-4-carboxaldehyde (ETBC) ligands function as antenna-like sensitizers that amplify luminescence intensity by 14.
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