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      Highly Conductive Covalent–Organic Framework Films

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          Abstract

          Chemically inert organic networks exhibiting electrical conductivity comparable to metals can advance organic electronics, catalysis, and energy storage systems. Covalent–organic frameworks (COFs) have emerged as promising materials for those applications due to their high crystallinity, porosity, and tunable functionality. However, their low conductivity has limited their practical utilization. In this study, copper‐coordinated‐fluorinated‐phthalocyanine and 2,3,6,7‐tetrahydroxy‐9,10‐anthraquinone‐based COF (CuPc‐AQ‐COF) films with ultrahigh conductivity are developed. The COF films exhibit an electrical conductivity of 1.53 × 10 3 S m −1 and a Hall mobility of 6.02 × 10 2 cm 2 V −1 s −1 at 298 K, reaching the level of metals. The films are constructed by linking phthalocyanines and anthraquinones through vapor‐assisted synthesis. The high conductivity properties of the films are attributed to the molecular design of the CuPc‐AQ‐COFs and the generation of high‐quality crystals via the vapor‐assisted method. Density functional theory analysis reveals that an efficient donor–acceptor system between the copper‐coordinated phthalocyanines and anthraquinones significantly promotes charge transfer. Overall, the CuPc‐AQ‐COF films set new records of COF conductivity and mobility and represent a significant step forward in the development of COFs for electronic, catalytic, and electrochemical applications.

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          First principles methods using CASTEP

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            Oxidation energies of transition metal oxides within theGGA+Uframework

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              Two-dimensional sp2 carbon-conjugated covalent organic frameworks.

              We synthesized a two-dimensional (2D) crystalline covalent organic framework (sp2c-COF) that was designed to be fully π-conjugated and constructed from all sp2 carbons by C=C condensation reactions of tetrakis(4-formylphenyl)pyrene and 1,4-phenylenediacetonitrile. The C=C linkages topologically connect pyrene knots at regular intervals into a 2D lattice with π conjugations extended along both x and y directions and develop an eclipsed layer framework rather than the more conventionally obtained disordered structures. The sp2c-COF is a semiconductor with a discrete band gap of 1.9 electron volts and can be chemically oxidized to enhance conductivity by 12 orders of magnitude. The generated radicals are confined on the pyrene knots, enabling the formation of a paramagnetic carbon structure with high spin density. The sp2 carbon framework induces ferromagnetic phase transition to develop spin-spin coherence and align spins unidirectionally across the material.
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                Author and article information

                Contributors
                Journal
                Small
                Small
                Wiley
                1613-6810
                1613-6829
                January 2024
                September 13 2023
                January 2024
                : 20
                : 4
                Affiliations
                [1 ] Department of Chemical and Biological Engineering The Hong Kong University of Science and Technology Hong Kong SAR 999077 China
                [2 ] Department of Chemistry The Hong Kong University of Science and Technology Hong Kong SAR 999077 China
                Article
                10.1002/smll.202306634
                91a0fabd-0c5a-4047-ac30-25af81cae538
                © 2024

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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