Deciphering the mechanism of undoped and heteroatom doped-carbon dots for detection of lead ions at nanomolar level

杂原子 碳纤维 X射线光电子能谱 荧光 材料科学 分析化学(期刊) 量子产额 离子 量子点 兴奋剂 检出限 硫黄 水溶液中的金属离子 发光 猝灭(荧光) 化学 纳米技术 化学工程 有机化学 光电子学 色谱法 物理 复合材料 工程类 复合数 冶金 量子力学 戒指(化学)
作者
Neeraj Sohal,Soumen Basu,Banibrata Maity
出处
期刊:Microchemical Journal [Elsevier BV]
卷期号:185: 108287-108287 被引量:22
标识
DOI:10.1016/j.microc.2022.108287
摘要

Herein, two types of facile, simple, and eco-friendly nanosensors were developed for the sensing of Pb2+ ions follow the aggregation-induced emission enhancement (AIEE) and dynamic quenching mechanism. Two types of carbon dots i.e., undoped carbon dots (u-Cdots) and nitrogen, sulfur co-doped carbon dots (N, S-Cdots) were developed by a rapid single-step approach under high-temperature treatment without any solvent. Both the prepared carbon dots showed high water solubility and excellent stability. The particle size of u-Cdots and N, S-Cdots were determined to be 7.5 nm and N, S-Cdots 1.8 nm, respectively which was examined through transmission electron microscope (TEM). The incorporation of heteroatom doping into the N, S-Cdots was examined through X-ray photoelectron spectroscopy (XPS). The u-Cdots shows excitation-dependent PL behaviour whereas, N, S-Cdots shows excitation-independent PL behaviour. Further, both the carbon dots act as sensitive and selective sensing platforms for Pb2+ ions in nanomolar range. Different photophysical investigations (fluorescence quantum yield, average lifetime, and radiative and non-radiative deactivation channels) were thoroughly studied to support the different PL mechanisms. Both the prepared sensing platforms exhibited a good limit of detection (LOD) i.e., 30 nM and 7 nM for u-Cdots and N, S-Cdots, respectively. The developed sensing platforms were also used in real sample analysis for the detection of Pb2+ ions.
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