The peculiar electronic and optical properties of covalent organic frameworks (COFs) are largely determined by protonation, a ubiquitous phenomenon in the solution environment in which they are synthesized. The resulting effects are nontrivial and appear to be crucial for the intriguing functionalities of these materials. In the quantum-mechanical framework of time-dependent density-functional theory, we investigate from first principles the impact of protonation of triazine and amino groups in molecular building blocks of COFs in water solution. In all considered cases, we find that proton uptake leads to a gap reduction and to a reorganization of the electronic structure, driven by the presence of the proton and by the electrostatic attraction between the positively charged protonated species and the negative counterion in its vicinity. Structural distortions induced by protonation are found to play only a minor role. The interplay between band gap renormalization and exciton binding strength determines the energy of the absorption onsets: when the former prevails over the latter, a red shift is observed. Furthermore, the spatial and energetic rearrangement of the molecular orbitals upon protonation induces a splitting of the lowest-energy peaks and a decrease of their oscillator strength in comparison with the pristine counterparts. Our results offer quantitative and microscopic insight into the role of protonation in the electronic and optical properties of triazine derivatives as building blocks of COFs. As such, they contribute to rationalize the relationships between structure, property, and functionality of these materials.
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