Metal-free four-in-one modification of g-C3N4 for superior photocatalytic CO2 reduction and H2 evolution

Utilization of g-C3N4 as a single photocatalyst material without combination with other semiconductor remains challenging. Herein, we report a facile green method for synthesizing a metal free modified g-C3N4 photocatalyst. The modification process combines four different strategies in a one-pot thermal reaction: non-metal doping, porosity generation, functionalization with amino groups, and thermal oxidation etching. The as-prepared amino-functionalized ultrathin nanoporous boron-doped g-C3N4 exhibited a high specific surface area of 143.2 m2 g-1 which resulted in abundant adsorption sites for CO2 and water molecules. The surface amino groups act as Lewis basic sites to adsorb acidic CO2 molecules, which can also serve as active sites to facilitate hydrogen generation. Besides, the simultaneous use of ammonium chloride as a dynamic gas bubble template along with thermal oxidation etching efficiently boosts the delamination of the g-C3N4 layers to produce ultrathin sheets; this leads to stronger light-matter interactions and efficient charge generation. Consequently, the newly modified g-C3N4 achieved selective gas-phase CO2 reduction into CO with a production yield of 21.95 mu mol g-1, in the absence of any cocatalyst. Moreover, a high hydrogen generation rate of 3800 mu mol g-1h-1 and prominent apparent quantum yield of 10.6% were recorded. This work opens up a new avenue to explore different rational modifications of g-C3N4 nanosheets for the efficient production of clean energy.

Automated summary

This study presents a green method for synthesizing a metal free modified g-C3N4 photocatalyst, achieving high efficiency in gas-phase CO2 reduction and hydrogen generation without the need for any cocatalyst. This work provides a new avenue for exploring rational modifications of g-C3N4 nanosheets for efficient clean energy production.