Issue 28, 2018

Synthesis of dual-functional Ag/Au nanoparticles based on the decreased cavitating rate under alkaline conditions and the colorimetric detection of mercury(ii) and lead(ii)

Abstract

By increasing the pH value of the reaction solution and introducing a small amount of ascorbic acid, Ag/Au nanoparticles with small tips and two surface plasmon resonance (SPR) modes have been prepared. The formation of the two SPR modes results from the different shell and core Au/Ag ratios, which relies on the enhanced dealloying rate of the shell and the weakened cavitating rate of the core under high pH conditions. Then, these Ag/Au nanoparticles have been used in the ultrasensitive detection of Hg2+ and Pb2+ based on the resultant absorption intensity decrease of peaks I and II, which originates from the specific dissolution of Ag and the accelerated speed of the reaction between Na2S2O3 and Au, respectively. The results showed an excellent limit of detection (LOD) of 5 nM for Hg2+ and 1.4 nM for Pb2+, and linear ranges from 30 to 400 nM and from 3 to 180 nM, respectively. Meanwhile, we believe that these bimetallic nanoparticles have widespread applications in sensing and modulating pH based on the dealloying rate of the shell and the cavitating rate of the core which can be extended to the synthesis of other dual-functional metallic nanoprobes.

Graphical abstract: Synthesis of dual-functional Ag/Au nanoparticles based on the decreased cavitating rate under alkaline conditions and the colorimetric detection of mercury(ii) and lead(ii)

Supplementary files

Article information

Article type
Paper
Submitted
19 Apr 2018
Accepted
20 Jun 2018
First published
25 Jun 2018

J. Mater. Chem. C, 2018,6, 7557-7567

Synthesis of dual-functional Ag/Au nanoparticles based on the decreased cavitating rate under alkaline conditions and the colorimetric detection of mercury(II) and lead(II)

T. Xing, J. Zhao, G. Weng, J. Li, J. Zhu and J. Zhao, J. Mater. Chem. C, 2018, 6, 7557 DOI: 10.1039/C8TC01867G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements