铀
电子转移
选择性
铀酰
检出限
碳化
材料科学
纳米点
碳纤维
光诱导电子转移
化学工程
离子
化学
荧光
二乙醇胺
纳米技术
无机化学
离子交换
比表面积
聚合
三乙醇胺
化学状态
石墨烯
氮气
光化学
作者
Qun Wang,Hengyang Zhang,Dongmei Yu,Qin Wei,Xiaohong Wu
出处
期刊:Carbon
[Elsevier BV]
日期:2022-07-15
卷期号:198: 162-170
被引量:47
标识
DOI:10.1016/j.carbon.2022.07.036
摘要
Unintended leakage of toxic and radioactive uranyl ion (UO 2 2+ ) ions poses high harmful to human health and environment, hence its monitoring and detection is of utmost significance. Here, we developed a mild synthetic route to prepare stable N-doped carbon nanodots (CDs) with special hydrophilicity functional groups and graphitic N by polymerization and carbonization of novel norfloxacin precursor with nitrogen heterocyclic structure. The morphology, chemical structure, fluorescent properties, sensing competition and selectivity behaviors of CDs-UO 2 2+ were systematically analyzed. Controllable experiments including low and high concentration CDs-UO 2 2+ and another type of carbon dots (TEA-CDs) with low graphitic N amount using triethanolamine (TEA) precursor without nitrogen heterocyclic structure were designed, which further confirmed the effective coordination and interaction mechanism between CDs and UO 2 2+ that graphitic N in CDs induced the formation UO 2 + (V) by electron transfer. It is very suitable for on-site and real-time monitoring of UO 2 2+ with an ultra-fast response time (∼20 s) and low detection limit of 20.38 nM (4.7 μg L −1 ), which is lower than the permissible limits (30 μg L −1 ) defined by the United States Environmental Protection Agency (EPA). More importantly, different form the liquid sensor, solid sensors (printed test strip and hydrogel) were also successfully employed to monitor UO 2 2+ targets quickly, broadening the potential application for the advanced image encryptions. Carbon nanodots (CDs) derived from norfloxacin precursor with nitrogen heterocyclic structure exhibited excellent selectivity and sensitivity for UO 2 2+ detection because graphitic N in CDs induced the formation UO 2 + (V) by electron transfer.
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