4.7 Article

Hydrothermal synthetic mercaptopropionic acid stabled CdTe quantum dots as fluorescent probes for detection of Ag+

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2012.09.005

Keywords

CdTe QDs; Hydrothermal synthesis; Fluorescence quenching; Detection; Ag+

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Funding

  1. National 863 Program of China [2009AA063005]
  2. Excellent Youth Foundation of Anhui Scientific Committee [1108085J19]
  3. Anhui Provincial Natural Science Foundation [11040606M26]
  4. Foundation of Director of Anhui Institute of Optics and Fine Mechanics [Y03AG31144]

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Mercaptopropionic acid (MPA) capped CdTe quantum dots (QDs) with particle size 3 nm have been successfully synthesized in aqueous medium by hydrothermal synthesis method. And the effects of different metal ions on MPA capped CdTe QDs fluorescence were studied using fluorescence spectrometry. The results demonstrated that at the same concentration level. Ag+ could strongly quench CdTe QDs fluorescence, and the other metal ions had little effect on CdTe QDs fluorescence except Cu2+. On the basis of this fact, a rapid, simple, highly sensitive and selective method based on fluorescence quenching principle for Ag+ detection in aqueous solution was proposed. Under optimal conditions, the quenched fluorescence intensity (F-0-F) increased linearly with the concentration of Ag+ ranging from 4 x 10(-7) to 32 x 10(-7) - mol L-1. The limit of detection for Ag+ was 4.106 x 10(-8) mol L-1. The obtained plot of F-0/F versus [Ag+] was an upward curvature, concave towards the y-axis, rather than a straight line. The modified form of the Stern-Volmer equation was third order in Ag+ concentration. According to the modified Stern-Volmer equation, it can be inferred that dynamic quenching and static quenching simultaneously occurred when Ag+ interacted with MPA capped CdTe QDs. At the same time other factors might also influence the quenching process. Based on this study, hydrothermal synthesized MPA capped CdTe QDs with particle size 3 nm may be used as a novel fluorescence probe to quantificationally and selectively detect Ag+. (C) 2012 Elsevier B.V. All rights reserved.

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