Sensitive quantification of mercury ions in real water systems based on an aggregation-collision electrochemical detection.

Anal Chim Acta

Institute of Chemical Biology and Nanomedicine, State Key Laboratory of Chemical/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, China; Greater Bay Area Institute for Innovation, Hunan University, Guangzhou, 511300, Guangdong Province, China. Electronic address:

Published: October 2023

AI Article Synopsis

  • Nanoparticle impact electrochemistry (NIE) is a new technique for detecting biological species, but its use for trace ion detection has been limited due to weak signal amplification.
  • Researchers developed a sensing platform using NIE that detects mercury (Hg) in water by utilizing T-Hg-T coordination to cause aggregation of silver nanoparticles (AgNPs).
  • The method offers high sensitivity and accuracy through dual-mode analysis, making it suitable for practical environmental monitoring and point-of-care testing.

Article Abstract

Nanoparticle impact electrochemistry (NIE) is an emerging electroanalytical technique that has been utilized to the sensitive detection of a wide range of biological species. So far, the NIE based trace ion detection is largely unexplored due to the lack of effective signal amplification strategies. We herein develop an NIE-based electrochemical sensing platform that utilizes T-Hg-T coordination induced AgNP aggregation to detect Hg in aqueous solution. The proposed aggregation-collision strategy enables highly sensitive and selective detection. A dual-mode analysis based on the change in impact frequency and oxidative charge of the anodic oxidation of the AgNPs in NIE allows for more accurate self-validated quantification. Furthermore, the current NIE-based sensor demonstrates reliable analysis of Hg of real water samples, showing great potential for practical environmental monitoring and point-of-care testing (POCT) applications.

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Source
http://dx.doi.org/10.1016/j.aca.2023.341638DOI Listing

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