Quantum-chemical calculations on graphitic carbon nitride (g-C3N4) single-layer nanostructures: polymeric slab vs. quantum dot

Abstract

Graphitic carbon nitride (g-C3N4) has been the focus of enormous attention in recent years for its fantastic in-plane and surface properties. Several periodic and cluster models of g-C3N4 including a quantum dot have been investigated using density functional theory (DFT) at the HSE06/Def2-TZVP level. The quantum dot with side triazine rings in nearly perpendicular alignment to the central ring was (by 98.40 kcal/mol) more stable than any other cluster, including its planar analogue—a metastable phase of carbon nitride. The g-C3N4 quantum dot showed the largest deviation (3.27 eV, 7.9%) from the bandgap of the polymeric material. On the other hand, the unrelaxed symmetrical cluster had the smallest deviation (+ 0.03 eV, 1.0%) from the reference bandgap (and also in terms of global hardness), indicating that it could be taken as a replacement cluster for modeling of a polymeric surface in such explorations. The plots of the density of states (DOS) revealed the inherent instabilities of the planar models compared to the quantum dot. Furthermore, the g-C3N4 quantum dot showed the highest chemical hardness among the models investigated. The electronic band structures of the g-C3N4 quantum dot implied its relatively better photoabsorption ability referenced to the polymeric surface. However, the structural changes had significant effects on the orbital and charge distributions in the C3N4 models.