Abstract
Azo dye molecules represented by methyl orange (MO), widely exist in industrial wastewater, and their efficient degradation requires hydroxyl groups with high oxidation activity. g-C3N4/MoS2 heterojunctions are widely used in many photocatalytic applications. However, typical type-II narrow bandgap heterojunctions have holes that cannot be directly oxidized to hydroxyl groups, which is an important barrier to MO degradation. In this work, g-C3N4 nanosheets were modified with carbon quantum dots (CQDs) and combined with spherical MoS2 nanoparticles to form CCN/MS composite photocatalysts. CQDs can be used as electronic reservoir to efficiently separate photogenerated carriers and facilitate the indirect generation of hydroxyl radicals. The results showed that the CCN/MS (10:1) sample had the most excellent degradation performance, with 93 % MO degradation in 120 min, while the control sample of CN/MS (10:1) without introducing CQDs had a degradation rate of only 24 % within the same time interval. In the mixed MO/MB degradation experiments, the degradation of MO was preferred to that of MB, suggesting the existence of a competitive mechanism between the two molecules. Our work proposes a possible pathway for the generation of hydroxyl groups using narrow bandgap semiconductor heterojunction catalysts, which provides a new perspective for understanding the degradation mechanism of pollutant molecules in real industrial wastewater.
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