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Design and Synthesis of Vanadate-Based Ratiometric Fluorescence Probe for Sequential Recognition of Cu2+ and Biothiol

Abstract

A novel YVO4:Eu3+@CDs core-shell nanomaterial with two main emission peaks at 405 and 617 nm was synthesized through a simple mixing method, in which the carbon quantum dots (CDs) self-assembled with the YVO4:Eu3+ nanoparticle, due to the high affinity of oxygen-containing groups such as –COOH or –OH of CDs to the metal ions on the surface of YVO4:Eu3+. The red fluorescence of YVO4:Eu3+@CDs located on 617 nm can be quenched by Cu2+ ions efficiently, while the blue emission remains invariable, based on this, we construct a ratio fluorescence probe YVO4:Eu3+@CDs for Cu2+ ions detection, in which the blue-emission of CDs is selected as the reference signal, and the red-emission of YVO4:Eu3+ acts as output signal. Furthermore, the addition of biothiol recovers the quenched red fluorescence quickly, which can be completed in 18 minutes. Thus, YVO4:Eu3+@CDs can also be used as a ‘turn on’ ratio fluorescence probe for biothiol rapid detection. Taking L-cysteine (L-Cys) as model, the fluorescence intensity of 617 nm peak increases with increasing Cys, and the ratio of F617/F405 is linear to the concentration of Cys in arange of 0.1 μM to 10 μM with a detection limit of 41 nM. Compared with those single wavelength emission biothiol fluorescence probes, an obvious change of the fluorescence color from blue to pink can be conveniently observed by the naked eye under a UV lamp. Meanwhile, this ratiometric probe has also been demonstrated to be used for visual identification of biothiol in real blood serum samples.

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Supplementary files

Publication details

The article was received on 08 Aug 2019, accepted on 09 Oct 2019 and first published on 10 Oct 2019


Article type: Paper
DOI: 10.1039/C9AN01518C
Analyst, 2019, Accepted Manuscript

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    Design and Synthesis of Vanadate-Based Ratiometric Fluorescence Probe for Sequential Recognition of Cu2+ and Biothiol

    H. Zeng, Z. Zhi-Ying , L. Fang , D. Jie , H. Shu-Yun , L. Guo-Ping, P. Lai, Y. Xie and X. Wei , Analyst, 2019, Accepted Manuscript , DOI: 10.1039/C9AN01518C

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