4.7 Article

Label-free Hg(II) electrochemiluminescence sensor based on silica nanoparticles doped with a self-enhanced Ru(bpy)32+-carbon nitride quantum dot luminophore

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 608, 期 -, 页码 1151-1161

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.10.106

关键词

Label-free; Self-enhanced ECL; SiO2 nanoparticles; Ru(bpy)(3)(2+); CNQDs; Hg(II)

资金

  1. National Natural Science Foundation of China [22074055, 61801195]
  2. Innovation/Entrepreneurship Program of Jiangsu Province
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions [PAPD-2018-87]
  4. Project of Shandong Province Higher Educational Science and Technology Program [KJ2018BZC043]
  5. Natural Science Foundation of Shandong Province [ZR2019MB068]

向作者/读者索取更多资源

A label-free, self-enhanced electrochemiluminescence (ECL) sensing strategy for divalent mercury (Hg(II)) detection was developed in this study. By utilizing a novel self-enhanced ECL luminophore and encapsulating it in silica nanoparticles, a highly efficient ECL system was established. The detection of Hg(II) was achieved by differentiating the affinity of Ru-QDs@SiO2 nanoparticles for ssDNA and Hg(II)-triggered dsDNA, leading to a sensitive and practical biosensor for Hg(II) detection.
Herein, a label-free, self-enhanced electrochemiluminescence (ECL) sensing strategy for divalent mercury (Hg(II)) detection was presented. First, a novel self-enhanced ECL luminophore was prepared by combining the ECL reagent tris(2, 2'-bipyridyl) dichlororuthenium(II) hexahydrate (Ru(bpy)(3)(2+)) and its coreactant carbon nitride quantum dots (CNQDs) via electrostatic interactions. In contrast to traditional ECL systems where the emitter and its co-reactant underwent an intermolecular reaction, the self-enhanced ECL system exhibited a shortened electron-transfer distance and enhanced luminous efficiency because the electrons transferred from CNQDs to oxidized Ru(bpy)(3)(2+) via an intramolecular pathway. Furthermore, the as-prepared self-enhanced ECL material was encapsulated in silica (SiO2) nanoparticles to generate a Ru-QDs@SiO2 luminophore. Based on the different affinity of Ru-QDs@SiO2 nanoparticles for single-stranded DNA (ssDNA) and Hg(II)-triggered double-stranded DNA (dsDNA), a label-free ECL biosensor for Hg(II) detection was developed as follows: in the absence of Hg(II), ssDNA was adsorbed on Ru-QDs@SiO2 surface via hydrogen bond, electrostatic, and hydrophobic interaction. Thus, quenched ECL signal was observed. On the contrary, in the presence of Hg(II), stable dsDNA was formed and carried the ssDNA separating from Ru-QDs@SiO2 surface, resulting in most of Ru-QDs@SiO2 existing in their free state. Therefore, a recovered ECL intensity was obtained. On this basis, Hg(II) was measured by the proposed method in the range of 0.1 nM-10 mu M, with a detection limit of 33 pM. Finally, Hg(II) spiked in water samples was measured to evaluate the practicality of the fabricated biosensor. (C) 2021 Published by Elsevier Inc.

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