Biowaste‐Derived Nitrogen‐Doped Carbon Dots for Real‐Time Detection of Fe 3+ and DFT Mechanistic Study

荧光 碳纤维 猝灭(荧光) 量子点 量子产额 材料科学 激发态 发光 电子转移 纳米技术 检出限 光化学 纳米颗粒 热液循环 碳量子点 光诱导电子转移 粒子(生态学) 金属有机骨架 化学 密度泛函理论 光致发光 荧光光谱法
作者
Hui Wang,Weixi Fan,Yan Gao,Li Han,Wen He,Chaoyue Shan,Ruixin Zhang,Yuanyuan Du,Xing Gao,Hongcui Li,Wenya Bao,Meng Gao
出处
期刊:Luminescence [Wiley]
卷期号:41 (2): e70455-e70455
标识
DOI:10.1002/bio.70455
摘要

Nitrogen-doped carbon dots (N-CDs) are emerging as materials for advancing technologies in fields such as environmental analysis, biosensing, and fluorescent probes due to their outstanding fluorescence and excellent biofriendliness. The synthesis of N-CDs involved a facile hydrothermal treatment of agricultural waste bagasse and urea, which acted as the carbon and nitrogen source, respectively. The as-synthesized dots were thoroughly characterized to elucidate the structure and properties, demonstrating that the N-CDs possessed well-defined particle sizes, rich surface functional groups, and promising luminescent characteristics. Specifically, the measured quantum yield was 27.8%. N-CDs exhibit an immediate fluorescence quenching response toward Fe3+, and based on this property, a novel sensing platform for real-time Fe3+ detection was constructed, achieving a limit of detection (LOD) of 0.17 μM. Mechanistic investigations, including fluorescence lifetime decay analysis, temperature-dependent Stern-Volmer studies, and DFT simulations, collectively reveal that the quenching process is primarily governed by dynamic electron transfer from the excited state of N-CDs to the 3d orbital of Fe3+. This work not only presents a sustainable and effective fluorescent sensor for Fe3+ detection but also provides deeper insight into the photophysical interactions between heteroatom-doped carbon dots and metal ions.
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