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双官能化氮氟共掺杂碳点用于实际水样中铜离子和硫化物离子的选择性检测

Bifunctional Nitrogen and Fluorine Co-Doped Carbon Dots for Selective Detection of Copper and Sulfide Ions in Real Water Samples.

机构信息

Center for Biomedical Optics and Photonics (CBOP) & College of Physics and Optoelectronic Engineering, Key Laboratory of Optoelectronics Devices and Systems of Ministry of Education/Guangdong Province, Shenzhen University, Shenzhen 518060, China.

出版信息

Molecules. 2022 Aug 12;27(16):5149. doi: 10.3390/molecules27165149.

Abstract

Copper ions (Cu) and sulfur ions (S) are important elements widely used in industry. However, these ions have the risk of polluting the water environment. Therefore, rapid and quantitative detection methods for Cu and S are urgently required. Using 2,4-difluorobenzoic acid and L-lysine as precursors, nitrogen and fluorine co-doped dots (N, F-CDs) were synthesized in this study via a hydrothermal method. The aqueous N, F-CDs showed excellent stability, exhibited satisfactory selectivity and excellent anti-interference ability for Cu detection. The N, F-CDs, based on the redox reactions for selective and quantitative detection of Cu, showed a wide linear range (0-200 μM) with a detection limit (215 nM). By forming the N, F-CDs@Cu sensing platform and based on the high affinity of S to Cu, the N, F-CDs@Cu can specifically detect S over a linear range of 0-200 μM with a detection limit of 347 nM. In addition, these fluorescent probes achieved good results when used for Cu and S detection in environmental water samples, implying the good potential for applications.

摘要

铜离子(Cu)和硫离子(S)是工业中广泛应用的重要元素。然而,这些离子有污染水环境的风险。因此,急需快速定量检测 Cu 和 S 的方法。本研究以 2,4-二氟苯甲酸和 L-赖氨酸为前体,通过水热法合成了氮氟共掺杂点(N,F-CDs)。水相 N,F-CDs 表现出优异的稳定性,对 Cu 的检测具有令人满意的选择性和优异的抗干扰能力。基于 N,F-CDs 对 Cu 的氧化还原反应,实现了选择性和定量检测 Cu,检测限为 215 nM,线性范围为 0-200 μM。通过形成 N,F-CDs@Cu 传感平台,并基于 S 与 Cu 的高亲和力,N,F-CDs@Cu 可以在 0-200 μM 的线性范围内特异性检测 S,检测限为 347 nM。此外,这些荧光探针在环境水样中的 Cu 和 S 检测中取得了良好的效果,表明其具有良好的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b237/9416385/77c6d94aef9a/molecules-27-05149-g001.jpg

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