摘要
Heavy metal detection has become very important for the protection of water resource. In this work, a novel controllable probe is presented for the sensitive detection of Pb2+ in aqueous solutions. The probe was synthesized via the immobilization of surface functionalized carbon dots (named as CAEA-Hs) into the shell of the spherical polyelectrolyte brushes (SPB). The fluorescence of CAEA-H was firstly "turned off" via electrostatic interaction induced quenching. Based on the aggregation induced emission enhancement (AIEE), the fluorescence of the immobilized CAEA-H could be specifically turned on via the aggregation of the SPB particles. This fluorescence "turn on" sensor could selectively detect Pb2+ among five different metal ions with a relatively wide detecting range (0-1.67 mM) and good linear relationship (R2 = 0.9958). Moreover, the aggregating behavior and nano-structure of CAEA-H loaded SPB have been systematically analyzed via small angle X-ray scattering, turbidity titration, and Zeta-potential measurement. Based on a series of control experiments, we finally gain an insight into the sensing mechanism of this novel sensing probe. This contributed a proof of concept demonstration that sensitive and selective chemical detection can be achieved via a C-dot/SPB synergistic platform.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 470 |
| 期刊 | Frontiers in Chemistry |
| 卷 | 6 |
| 期 | SEP |
| DOI | |
| 出版状态 | 已出版 - 1 9月 2018 |
| 已对外发布 | 是 |
指纹
探究 'Facile fluorescence "turn on" sensing of lead ions in water via carbon nanodots immobilized in spherical polyelectrolyte brushes' 的科研主题。它们共同构成独一无二的指纹。引用此
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