Nitrogen-doped carbon quantum dot as electron acceptor anchored on graphitic carbon nitride nanosheet for improving rhodamine B degradation

罗丹明B 光催化 石墨氮化碳 氮化碳 降级(电信) 纳米片 碳纤维 材料科学 化学工程 氮气 量子点 光化学 纳米技术 化学 催化作用 有机化学 复合材料 计算机科学 工程类 电信 复合数
作者
Milad Jourshabani,Nguyen Van Duc Long,Mahdieh Razi Asrami,Quoc Hue Pho,Byeong–Kyu Lee,Volker Hessel
出处
期刊:Materials Science And Engineering: B [Elsevier]
卷期号:305: 117417-117417 被引量:3
标识
DOI:10.1016/j.mseb.2024.117417
摘要

Carbon quantum dots (CQDs) hold significant promise for wastewater treatment because of their remarkable attributes, including robust stability, outstanding biocompatibility, minimal toxicity, superior water dispersibility, cost-effective production, and exceptional photo-stability. In this study, CQDs were synthesized using microplasma and tested for the degradation of rhodamine B (RhB) (5 mg/L) under different conditions, with a Solar simulator and UVA illumination. Specifically, graphitic carbon nitride nanosheets (NCN) in conjugation with carbon quantum dots (NCN@CQD) were prepared with different amounts of CQD. The synthesized CQD, NCN, and NCN@CQD underwent characterization using various compositional and structural analytical techniques. The results show that nitrogen species were effectively incorporated into the CQDs framework and CQDs are anchored on NCN forming NCN@CQD successfully. Subsequently, all samples were then investigated in degrading Rhodamin B, RhB, to assess the photocatalytic activity. The results reveal that the presence of CQDs substantially improved the photocatalytic efficiency of NCN. Specifically, the CQDs anchored on NCN exhibited a substantial enhancement in the photoactivity for RhB decomposition under a solar light simulator, surpassing that of pure NCN. The amount of CQD in the NCN@CQD sample exerted a strong influence on the photocatalytic activity. All NCN@CQD samples exhibited remarkable enhancements in both adsorption and photocatalytic performance compared to pure CQD and NCN samples. In an optimization study, a best NCN@CQ photocatalyst was identified, showing a 40 % enhancement of photocatalytic efficiency compared to the use of NCN alone. A visible light photocatalytic activity of 91 % can be attained within 150 min, exhibiting a reaction rate constant of 0.0135 min−1 toward RhB decomposition, which was double as for the individual NCN (0.0067 min−1). The boosted photocatalytic activity resulting from the synergistic effect between NCNs and CQDs can be attributed to the efficient function of CQD as an electron acceptor. The proposed mechanism of photocatalytic degradation of RhB is illustrated in detail.

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