C3N2: the missing part of highly stable porous graphitic carbon nitride semiconductors

Abstract

Two-dimensional (2D) porous graphitic carbon nitrides (PGCNs) with semiconducting features have attracted wide attention because of built-in pores with various active sites, large surface area, and high physicochemical stability. However, only a few PGCNs have been synthesized, covering a 1.23–3.18 eV band gap. We systematically investigate two new 2D PGCN monolayers, T-C₃N₂ and H-C₃N₂, including possible pathways for their experimental synthesis. Based on first-principles calculations, the mechanical, electronic, and optical properties of T-C₃N₂ and H-C₃N₂ have been systematically investigated. These two architectural frameworks exhibit contrasting mechanical characteristics owing to their structural differences. Both T-C₃N₂ and H-C₃N₂ monolayers are predicted to be intrinsic semiconductors. Exceptionally, the stacking bilayers of T-C₃N₂ can transform into a rare 2D nodal-line semimetal structure. The narrow bandgap (0.35 eV) of the T-C₃N₂ monolayer and its extraordinary transformation in the bilayer electronic structure fill the vacancy of PGCNs as electronic devices in the middle/long wave infrared region. C₃N₂ structures possess ultrahigh anisotropic carrier mobilities (×10⁴ cm² V⁻¹ s⁻¹) and exceptional absorption coefficients (×10⁵ cm⁻¹) in the near-infrared and visible light regions, suggesting its possible optoelectronic applications. The findings expand the scope of 2D PGCNs and offer guides for their experimental realization.