Abstract
Carbon quantum dots (CQDs), known for their exceptional optical properties, hold the potential to enhance light absorption, charges separation and transfer in semiconductor materials. However, using cheap medicinal materials as precursors in the field of photocatalysis to obtain CQDs has seldom concerned. In this study, we utilized biomass-derived CQDs from carbon-rich licorice powder to improve photocatalytic CO2 and Cr(VI) reduction in polymer carbon nitride (PCN). The CQDs/g-C3N4 heterojunctions were synthesized via a hydrothermal method, and the successful fabrication and integration of CQDs on g-C3N4 surfaces were confirmed through detailed characterization. The optimal sample with a licorice powder to PCN mass ratio of 0.05:1 ((50CQDs/CN) demonstrates a tripling in CO2 conversion efficiency under simulated sunlight compared to the reference PCN. Under visible light irradiation, the 50CQDs/CN also performs superior photocatalytic Cr (VI) removal efficiency, which is 2.48 times of that of the reference PCN. This significant boost is attributable to the successful construction of the CQDs/CN heterojunction and the abundance of functional groups on the CQDs surface, which provide more active sites, improve light absorption and increase charges migration rates. The stability of these new photocatalysts was confirmed through repeated photocatalytic cycles, indicating their potential for practical applications. Mechanistic studies reveal insights into the enhanced photocatalytic pathways and intermediate conversion processes. Our findings present a novel, efficient and sustainable route to fabricate g-C3N4-based photocatalysts, offering a promising strategy for further mitigate the greenhouse gas crisis and environmental pollution.
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