Synthesis of micrometre-thick oriented 2D covalent organic framework films by a kinetic polymerization pathway
Year: 2025
Type: article
Abstract: Despite advances in the field of 2D polymerization, the synthesis of high-quality, micrometre-thick films of oriented 2D covalent organic frameworks (COFs) remains challenging. Conventional approaches focusing on thermodynamic control of the polymerization pathway face a detrimental trade-off between orientation and thickness. Here we describe a straightforward method for preparing imine-linked 2D COF films with a near-perfect face-on orientation by leveraging kinetically trapped amorphous 3D covalent adaptable network (CAN) intermediates. These off-pathway intermediates are generated as coatings through solution casting, during which the CANs spontaneously align to relax tensile stresses induced by solvent evaporation. A subsequent lift-off process, followed by an amorphous-to-crystalline transformation under solvothermal conditions, converts the 3D-oriented polymer networks into thermodynamically stable, porous and free-standing 2D COF films. This versatile kinetic trapping strategy is suitable for a range of building blocks and network topologies, constituting a convenient synthetic tool for accessing high-quality, robust, large-area 2D COF films with a strongly aligned polycrystalline structure.
Source: Nature Synthesis
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $12,690
Awards: EXC 2089: econversion, G1489577826, G1537796, Par-delà les frontières, l'Université de Strasbourg, Light-Addressable 2D Covalent-Organic Framework Semiconductors, G258225891, G3764765484, G4613448559, G471331628, G5862656150, SFB 1333: Molekulare heterogene Katalyse in definierten, dirigierenden Geometrien, G7240651115, Bottom-Up generation of atomicalLy precise syntheTIc 2D MATerials for high performance in energy and Electronic applications – A multi-site innovative training action
OpenAlex ID: W4407789397
