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在可见光照射下通过在碳点异质结构上原位外延生长石墨相氮化碳(g-CN)实现磺胺嘧啶的高效降解:合成、机制和毒性评估。

Efficient sulfadiazine degradation via in-situ epitaxial grow of Graphitic Carbon Nitride (g-CN) on carbon dots heterostructures under visible light irradiation: Synthesis, mechanisms and toxicity evaluation.

机构信息

Key Laboratory of Building Safety and Energy Efficiency, Ministry of Education, Department of Water Engineering and Science, College of Civil Engineering, Hunan University, Changsha 410082, PR China.

Key Laboratory of Building Safety and Energy Efficiency, Ministry of Education, Department of Water Engineering and Science, College of Civil Engineering, Hunan University, Changsha 410082, PR China; Brook Byers Institute for Sustainable Systems and School of Civil and Environmental Engineering, Georgia Institute of Technology, 828 West Peachtree Street, Atlanta, GA 30332, United States.

出版信息

J Colloid Interface Sci. 2020 Mar 1;561:696-707. doi: 10.1016/j.jcis.2019.11.046. Epub 2019 Nov 18.

DOI:10.1016/j.jcis.2019.11.046
PMID:31767396
Abstract

The synthesis of environmental-friendly metal-free photocatalysts has great significance in photocatalytic technology. In this work, we firstly report the successful synthesis of in situ epitaxial growth of g-CN on carbon dots through a facile thermal polymerization technique. Characterization and density functional theory (DFT) calculations were conducted to clarify the structure engineering and the electronic/chemical properties of the in-plane interconnected carbon dots/g-CN (C-CN) heterostructures. With the optimal carbon dots content, the C-CN exhibited 3.2 times higher degradation rate for sulfadiazine (SDZ) than that of g-CN. Besides, the C-CN heterostructures displayed excellent stability and reusability in five consecutive cycles. The enhanced photocatalytic activity was related to the narrowed band gap and the local electronic density of valance band and conduction band orbitals of the unique plane heterostructures, corroborated by the spectroscopic characterizations and theoretical calculations. Photogenerated holes dominated the degradation of SDZ, while OH showed a negligible contribution. Moreover, DFT calculation succeeded to predict that the atoms with high Fukin index (f) on SDZ molecule were more vulnerable to radicals attack. SDZ degradation pathway mainly included smiles-type rearrangement, SO extrusion, ring hydroxylation and SN bond cleavage processes. The eco-toxicity assessment revealed the generation of less toxic intermediates after photocatalysis. Our findings not only afford a new technique for constructing g-CN-based in-plane heterostructures with high and stable photocatalytic efficiency, but also highlight the feasible application of metal-free photocatalysts in environmental remediation.

摘要

环保型无金属光催化剂的合成在光催化技术中具有重要意义。在本工作中,我们首次通过简便的热聚合技术成功地合成了 g-CN 在碳点上的原位外延生长。通过特征化和密度泛函理论(DFT)计算,阐明了面内互连的碳点/g-CN(C-CN)异质结构的结构工程和电子/化学性质。在最佳的碳点含量下,C-CN 对磺胺嘧啶(SDZ)的降解速率比 g-CN 提高了 3.2 倍。此外,C-CN 异质结构在五个连续循环中表现出优异的稳定性和可重复使用性。增强的光催化活性与独特的面异质结构的缩小带隙和价带和导带轨道的局部电子密度有关,这得到了光谱特性和理论计算的证实。光生空穴主导 SDZ 的降解,而 OH 几乎没有贡献。此外,DFT 计算成功预测了 SDZ 分子上具有高 Fukui 指数(f)的原子更容易受到自由基的攻击。SDZ 降解途径主要包括 Smiles 型重排、SO 挤出、环羟化和 SN 键断裂过程。生态毒性评估表明光催化后会产生毒性较小的中间产物。我们的发现不仅为构建具有高效和稳定光催化性能的 g-CN 基面内异质结构提供了一种新的技术,而且还强调了无金属光催化剂在环境修复中的可行应用。

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