School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
College of Environmental Science and Engineering, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Ministry of Education Key Laboratory of Pollution Processes and Environmental Criteria, Nankai University, Wei Jin Road 94, Tianjin, 300071, China.
Mikrochim Acta. 2017 Dec 6;185(1):31. doi: 10.1007/s00604-017-2545-0.
The authors describe a fluorometric and colorimetric nanoprobe for HO. The detection scheme is based on the in-situ formation of silver(I) ions from a composite consisting of nitrogen-doped carbon quantum dots (N-CQDs) and silver nanoparticles (AgNPs). A drastic change occurs both in fluorescence and color of the solution of the N-CQD/AgNPs composite. The fluorescence of composite (with excitation/emission peaking at 320/384 nm) is enhanced on increasing the concentration of HO due to the oxidation of silver metal in the N-CQD/AgNPs to form Ag(I) ions. The latter undergo strong coordination with the nitrogen atoms of the N-CQDs. In-situ formation of Ag(I) ions further results in a change in color of the solution from pale yellow (with a peak at 408 nm) to colorless. Under optimized conditions, the probe gives a fluorometric and colorimetric response in the 10 to 50 μM HO concentration range with a 4.7 μM limit of detection. The probe is highly selective over several potentially interfering ions and agents. It was successfully applied to the determination of HO in spiked samples without prior treatment. Graphical abstract Graphical presentation for specific detection of HO based on the in-situ formation of Ag(I) ions from a composite consisting of silver nanoparticles and nitrogen-doped carbon quantum dots.
作者描述了一种用于检测 HO 的荧光和比色纳米探针。该检测方案基于由氮掺杂碳量子点 (N-CQDs) 和银纳米颗粒 (AgNPs) 组成的复合材料中银 (I) 离子的原位形成。由于氮掺杂碳量子点/银纳米颗粒复合材料中的银金属被氧化为 Ag(I) 离子,溶液的荧光和颜色都发生了剧烈变化。复合材料的荧光(激发/发射峰在 320/384nm 处)随着 HO 浓度的增加而增强,这是由于 AgNPs 中银金属的氧化形成 Ag(I) 离子所致。后者与 N-CQDs 的氮原子发生强烈配位。Ag(I) 离子的原位形成进一步导致溶液颜色从浅黄色(在 408nm 处有一个峰值)变为无色。在优化条件下,探针在 10 至 50μM HO 浓度范围内具有荧光和比色响应,检测限为 4.7μM。该探针对几种潜在干扰离子和试剂具有高度选择性。它无需预处理即可成功应用于加标样品中 HO 的测定。
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