Multiple Doped Carbon Nitrides with Accelerated Interfacial Charge/Mass Transportation for Boosting Photocatalytic Hydrogen Evolution.

The interaction of water molecule with catalysts is crucial to photocatalysis, but the surface property manipulation still remains a great challenge. In this study, we report an in situ multiple heteroelement (sodium, oxygen, and iodide) doping strategy based on a molten salt-assisted route to prepare a green-colored carbon nitride (GCN). The as-prepared GCN yields 25.5 times higher H2 evolution rate than that of bulk polymeric carbon nitride under visible light. Experimental characterization data demonstrate that the GCN delivers upshift of the conduction band and increased specific surface area and hydrophilicity. As confirmed by time-resolved PL spectra, DMPO spin-trapping EPR analysis, and so on, the excellent activity is dominantly ascribed to the greatly enhanced hydrophilicity and, subsequently, efficient interfacial charge transfer and hydrogen liberation. Moreover, through surface charge modification, the GCN also shows an increased degradation activity of rhodamine B. This work highlights the importance of surface modulation through multiple earth-abundant element incorporation for designing of advanced and practical photocatalysts.