4.7 Article

Electrochemical synthesis of carbon dots with a Stokes shift of 309 nm for sensing of Fe3+ and ascorbic acid

期刊

DYES AND PIGMENTS
卷 185, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2020.108878

关键词

Carbon dot; Ratiometric sensing; Fe3+; Ascorbic acid; Stokes shift

资金

  1. National Natural Science Foundation of China [21505162, 21605003, 31571874]
  2. GrainOil Process and Quality Control 2011 Collaborative and Innovative Grant from Hunan province, Training Program for Excellent Young Innovators of Changsha [kq1905061]
  3. China Scholarship Council

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The study discusses the preparation of carbon dots with strong emission at long wavelengths using o-phenylenediamine for detection of Fe3+ and ascorbic acid. The electrochemically synthesized C dots demonstrate good fluorescence properties, allowing for highly selective detection of Fe3+ and quantification of ascorbic acid.
Preparation of carbon dots (C dots) with strong emission at long wavelengths is an ongoing goal to their advanced applications, especially in bioanalysis. For sensing Fe3+ and ascorbic acid (AA), we prepared C dots with a large Stokes shift using o-phenylenediamine (OPD) as the carbon source through an electrochemical method. During the electrolysis, OPD undergoes polymerization, carbonization, and passivation at the platinum anode to form C dots. These C dots were characterized by UV-Vis spectroscopy, transmission electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and FT-IR spectroscopy. They are composed of C, N, O, H elements, having a maximum of emission at 570 nm and a supreme excitation at 261 nm, with a Stokes shift of 309 nm. A new emission at 350 nm emerged with their exposure to Fe3+ and the intensity rises upon increasing Fe3+, while the emission intensity at 570 nm decreases. Thus, dissimilar to the usual quenching strategy, a novel ratiometric fluorescent sensor based on the fluorescence intensity ratio (F-350/F-570) of the C dots at 350 nm and 570 nm has been developed for quantitation of Fe3+ with a limit of detection (LOD) of 0.16 mu M and high selectivity toward Fe3+ against K+, Cu2+, and Fe2+. With evidence of decreased C-N=C and C-O/N-O in XPS and increased content of C=O/N=O and N-H, we suggested the complexation of Fe3+ with the surface groups led to the changes in chemical bonds accounting for their optical property variation. Furthermore, AA can quench the fluorescence of C dots at 570 nm and Fe3+-treated C dots (incubated with 50 mu M Fe3+) at 350 nm by a static mechanism. Accordingly, two assays toward AA were developed with LODs of 0.12 mu M and 0.32 mu M by using C dots and Fe3+-treated C dots, respectively. Especially, both AA assays exhibited excellent selectivity under various substances including those with strong reducing ability such as pyrogallic acid, sodium citrate, tea polyphenol, and dithiothreitol. The applications of the assays were validated with the quantitation of Fe3+ in urine and AA in beverages. Electrochemical method is a significant approach to develop novel C dots even using the same carbon sources as in other methods.

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