Electronic Structure of a Semiconducting Imine‐Covalent Organic Framework

Abstract Imine COF (covalent organic framework) based on the Schiff base reaction between p ‐phenylenediamine (PDA) and benzene‐1,3,5‐tricarboxaldehyde (TCA) was prepared on the HOPG‐air (air=humid N 2 ) interface and characterized using different probe microscopies. The role of the molar ratio of TCA and PDA has been explored, and smooth domains of imine COF up to a few μm are formed for a high TCA ratio (>2) compared to PDA. It is also observed that the microscopic roughness of imine COF is strongly influenced by the presence of water (in the reaction chamber) during the Schiff base reaction. The electronic property of imine COF obtained by tunneling spectroscopy and dispersion corrected density functional theory (DFT) calculation are comparable and show semiconducting nature with a band gap of ≈1.8 eV. Further, we show that the frontier orbitals are delocalized entirely over the framework of imine COF. The calculated cohesive energy shows that the stability of imine COF is comparable to that of graphene.