This study investigates the mechanism behind the enhanced
photocatalytic
performance of carbon quantum dot (CQD)-induced photocatalysts. Red
luminescent CQDs (R-CQDs) were synthesized using a microwave ultrafast
synthesis strategy, exhibiting similar optical and structural properties
but varying in surface functional group sites. Model photocatalysts
were synthesized by combining R-CQDs with graphitic carbon nitride
(CN) using a facile coupling technique, and the effects of different
functionalized R-CQDs on CO2 reduction were investigated.
This coupling technique narrowed the band gap of R1-CQDs/CN, made
the conduction band potentials more negative, and made photogenerated
electrons and holes less likely to recombine. These improvements greatly
enhanced the deoxygenation ability of the photoinduced carriers, increased
light absorption of solar energy, and raised the carrier concentration,
resulting in excellent stability and remarkable CO production. R1-CQDs/CN
demonstrated the highest photocatalytic activity, with CO production
up to 77 μmol g–1 within 4 h, which is approximately
5.26 times higher than that of pure CN. Our results suggest that the
superior photocatalytic performance of R1-CQDs/CN arises from its
strong internal electric field and high Lewis acidity and alkalinity,
attributed to the abundant pyrrolic-N and oxygen-containing surface
groups, respectively. These findings offer a promising strategy for
producing efficient and sustainable CQD-based photocatalysts to address
global energy and environmental problems.