Highly selective detection of p-nitrophenol using fluorescence assay based on boron, nitrogen co-doped carbon dots

化学 荧光 检出限 X射线光电子能谱 吸收光谱法 分析化学(期刊) 硝基苯酚 荧光光谱法 傅里叶变换红外光谱 光谱学 选择性 拉曼光谱 吸收(声学) 光化学 色谱法 化学工程 有机化学 材料科学 工程类 光学 催化作用 复合材料 量子力学 物理
作者
Na Xiao,Shi Gang Liu,Shi Mo,Na Li,Yan Jun Ju,Ling Yu,Nian Bing Li,Hong Qun Luo
出处
期刊:Talanta [Elsevier]
卷期号:184: 184-192 被引量:122
标识
DOI:10.1016/j.talanta.2018.02.114
摘要

p-Nitrophenol (p-NP) contaminants seriously endanger environmental and living beings health, hence to establish a sensitive and selective method is of great importance for the determination of p-NP. In this work, boron and nitrogen co-doped carbon dots (B,N-CDs) were synthesized by one-step hydrothermal method using 3-aminophenylboronic acid as the sole precursor. The product was characterized through high-resolution transmission electron microscopy, fluorescence spectroscopy, UV-visible absorption spectroscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. Without any functionalized modification, B,N-CDs can be directly applied as a 'turn-off' fluorescent probe for rapid, highly selective, and sensitive detection of p-NP. The fluorescent sensor based on the B,N-CDs exhibited a broad linear response to the concentration of p-NP in the range of 0.5 - 60 μM and 60 - 200 μM, respectively, and provided a detection limit of 0.2 μM. It was found that only the absorption spectrum of p-NP has a wide overlap with the fluorescence excitation and emission spectra of B,N-CDs compared to those of other representative analogues. The response mechanism was due to the inner filter effect and the formation of dynamic covalent B-O bonds between B,N-CDs and p-NP, which endowed the sensing platform with the rapid response and high selectivity to p-NP. Finally, the sensor showed the practicability of p-NP determination in environmental water samples.
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