Enzyme-free carbon dots@MgO nanocomposite as an efficient sensor for on-site detection and degradation of paraoxon toxins

对氧磷 纳米复合材料 检出限 降级(电信) 荧光 材料科学 核化学 纳米技术 化学 分析化学(期刊) 色谱法 有机化学 乙酰胆碱酯酶 电信 物理 量子力学 计算机科学
作者
Bo Liu,Meijie Cai,Xiangling Feng,Siyu Lu,Song Lin,Feng Tian
出处
期刊:Carbon [Elsevier BV]
卷期号:209: 118003-118003 被引量:5
标识
DOI:10.1016/j.carbon.2023.118003
摘要

Serial nanocomposites consisting of blue fluorescent carbon dots (B-CDs) and MgO nanoparticles were facilely prepared. Then on-site detection and degradation of ethyl-paraoxon were achieved and evaluated. It was revealed that ethyl-paraoxon was firstly decomposed into p-nitrophenol by MgO. Then, p-nitrophenol could significantly quench the fluorescence of decorated B-CDs due to an inner filter effect (IFE). The [email protected] showed excellent comprehensive performance among the serial [email protected] samples due to its relatively high degradation ability towards ethyl-paraoxon and potent initial fluorescence emission intensity at an excitation wavelength of 360 nm between pH 4 and 10. Finally, based on the IFE, on-site paper sensors via color recognition app on a smartphone were explored compared with a conventional fluorescence spectrometer. Both the quantitative fluorescence intensities and G/B values showed the multi-piecewise linear correlations to ethyl-paraoxon concentration up to 3000 μg/mL in river water with a limit of detection to 0.06 μg/mL and 3.48 μg/mL as well as high recovery rates between 99%-102% and 95%–116%, respectively. The in vitro cytotoxicity and phytotoxicity assessment of the [email protected] revealed dose-dependent effects. Such portable and integrated fluorescent [email protected] nanocomposites on paper arrays show excellent potential in shortening the detection time and reducing the detection cost as a new strategy for the on-site quantitative detection and degradation of ethyl-paraoxon in actual river water.
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