4.7 Article

Ultrasensitive optical detection of trinitrotoluene by ethylenediamine-capped gold nanoparticles

Journal

ANALYTICA CHIMICA ACTA
Volume 744, Issue -, Pages 92-98

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2012.07.029

Keywords

Ethylenediamine; Trinitrotoluene; Gold nanoparticles; Colorimetric; Dynamic light scattering

Funding

  1. National Basic Research Program of China [2011CB933700]
  2. National Instrumentation Program of China [2011YQ0301241001, 2011YQ0301241101]
  3. China Postdoctoral Science Foundation funded project [20100480706]

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This study found that 1,2-ethylenediamine (EDA) as a primary amine could be modified onto the surface of citrate-stabilized gold nanoparticles (Au NPs), and the EDA-capped Au NPs were successfully used as an ultrasensitive optical probe for TNT detection. The strong donor-acceptor (D-A) interactions between EDA and trinitrotoluene (TNT) at the Au NP/solution interface induced significant aggregation of the EDA-capped Au NPs, and enabled to easily realize the direct colorimetric detection of ultratrace TNT. The results showed that such a color change was readily seen by the naked eye. and the colorimetric detection could be down to 400 pM level of TNT with excellent discrimination against other nitro compounds. UV-vis absorption spectroscopy was used to examine the TNT-induced changes in local surface plasmon resonance (LSPR) of EDA-capped Au NPs, and a new LSPR band at ca. 630 nm arose along with the addition of TNT, which produced a detection limit of TNT down to ca. 40 pM. Furthermore, dynamic light scattering measurements evidenced the ultratrace TNT-induced small changes in the size of the EDA-capped Au NPs, and realized the quick and accurate detection of TNT in 0.4 pM level. These results demonstrated the ultrahigh sensitivity of this optical probe for TNT detection. Moreover, this optical probe is sample, stable, low-cost, and these excellent properties make it quite promising for infield and rapid detection of TNT. (c) 2012 Elsevier B.V. All rights reserved.

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