Research PaperOxygen-doped nanoporous carbon nitride via water-based homogeneous supramolecular assembly for photocatalytic hydrogen evolution

- O-doped porous C3N4via water-based homogeneous supramolecular assembly.
- g-C3N4 possess high surface area and well-defined 3D morphology.
- Oxygen atom doping in the lattice of g-C3N4 enhance its electronic properties.
- It Exhibits 11.3 times higher H2 evolution rate than bulk g-C3N4 under visible light.

Graphitic carbon nitride (g-C3N4) has emerged as a promising photocatalyst, but poor charge separation and low surface area limit its activity. Here, we report a hydrothermal method to generate hydrogen bonded supramolecular complex via water-based homogeneous supramolecular assembly, which is a promising precursor to fabricate porous and oxygen-doped g-C3N4. The hydrothermal treatment provides a homogeneous environment for hydrolysis of melamine to produce cyanuric acid and reaction of cyanuric acid with remained melamine to create the in-plane ordering and hydrogen bonded supramolecular complex. The complex can template uniform nanoporous structure and also provide an opportunity for O-doping in the g-C3N4 network upon calcination in air. The resulted g-C3N4(GCN-4) possesses high surface area, well-defined 3D morphology and oxygen-dopant in the lattice. Subsequently, the visible light absorption, charge separation, and wettability are considerably enhanced. This catalyst exhibits higher hydrogen evolution rate by 11.3 times than the bulk g-C3N4 under visible light irradiation, with apparent quantum efficiency of 10.3% at 420 nm.

194