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Covalent organic frameworks (COFs) have emerged as one of the hottest research topics in various applications due to their designed structures, adjustable pore sizes, and abundant active sites. However, the high electron-hole recombination rate and short carrier lifetime in non-donor-acceptor type COFs are inevitable issues. The electron donor-acceptor (D-A) type COFs, which are synthesized by introducing donor and acceptor units into the COF skeleton, combined with effective carrier separation, adjustable bandgap, and sensitive photoelectric response, are considered an effective strategy for improving exciton dissociation and optimizing carrier transport. In recent years, D-A type COFs have witnessed exponential expansion in applications spanning photocatalysis, energy storage, and photothermal therapy. Consequently, there exists an imperative necessity to comprehensively summarize and expound upon the challenges and prospects pertaining to the development of D-A type COFs. In this review, we first summarize the common connecting bonds as well as the building blocks for the synthesis of D-A type COFs. Several strategies for optimizing D-A type COFs and their recent progress in photocatalysis, photothermal therapy, and energy storage are then presented. Finally, we delineate the current challenges and impediments of D-A type COFs and offer a forward-looking perspective on the future development of D-A type COFs. This review is poised to encourage researchers with a more profound comprehension of the design strategies and applications of D-A type COFs, thereby inspiring them to conduct more incisive research into the challenges and developmental prospects of D-A type COFs.
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http://dx.doi.org/10.1039/d5sc01267h | DOI Listing |
Nanoscale
August 2025
Hybrid Porous Materials Lab, Department of Chemistry, Indian Institute of Technology Jammu, Jammu & Kashmir, 181221, India.
Among various pollutants, nitrogen oxides (NO) stand out as particularly harmful irritant gases, known to cause airway inflammation at elevated concentrations. Chemiresistive gas sensing (CGS) has revolutionized gas detection with its low power consumption, cost-effectiveness, high sensitivity, fast response, and long-term stability. Traditional materials such as metal oxides, conducting polymers, and carbon-based materials used for NO detection often suffer from poor selectivity and require high operating temperatures, leading to high noise levels.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Tissue Engineering, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran; Tabriz USERN Office, Universal Scientific Education and Research Network (USERN), Tabriz, Iran.
Calcitonin receptor-like receptor (CLR) and receptor activity-modifying protein type 1 (RAMP1) are key components of the calcitonin gene-related peptide (CGRP) receptor, which is upregulated during migraine attacks, contributing to enhanced CGRP signaling. This study aimed to investigate the binding of covalent organic framework (COFs) models to CLR/RAMP1 at the molecular level using molecular dynamics (MD) and docking simulations. To assess the efficacy and inhibitory effects of COF structures on the CLR/RAMP1 complex, two antimigraine drugs, ubrogepant and rimegepant, were used as controls.
View Article and Find Full Text PDFChem Sci
August 2025
Department of Materials Science and Engineering, City University of Hong Kong Hong Kong SAR 999077 P. R. China
Covalent Organic Frameworks (COFs) with diverse conjugated structures are extensively utilized as promising photocatalysts for hydrogen peroxide (HO) production. However, the current applications are constrained by the rapid recombination of photogenerated carriers and the slow reaction kinetics. To address these issues, in this study, we design and prepare four COF photocatalysts with a distinct donor-π-acceptor (D-π-A) structure to regulate the photogenerated charge carrier transportation.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Achieving both crystallinity and stability is challenging for covalent organic frameworks (COFs) as the reversible reaction required for enhancing crystallinity compromises stability. Amide linkages, a type of chemically stable bond for COF construction, are predominantly synthesized via postmodifications. This work presents a direct and convenient method for synthesizing highly crystalline amide-linked COFs via the ester-amine exchange reaction.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering & Technology, Tianjin University, Tianjin 300354, China. Electronic address:
The ecofriendly conversion of captured CO is crucial for global sustainable development. However, direct conversion of CO into value-added chemical feedstocks at atmospheric pressure remains challenging due to its thermodynamic stability and kinetic inertness. Herein, we report a new type of catalyst with low catalytic energy barrier, synthesized by post-modifying supercritical CO-activated imine-linked triazine-based covalent organic framework (TAPT-COF) through the covalent attachment of ionic liquid (IL) and coordination of Zn ion within its pores.
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