TY - JOUR
T1 - Colorimetric Dual Sensors of Metal Ions Based on 1,2,3-Triazole-4,5-Dicarboxylic Acid-Functionalized Gold Nanoparticles
AU - Mondal, Palash
AU - Yarger, Jeffery L.
N1 - Funding Information:
P.M. acknowledges UGC, New Delhi, India, for providing financial support in the form of “Raman Fellowship” [Sanctioned No. 5-103/2016(IC), Dated-10-02-2016] and Vivekananda Mahavidyalaya, Burdwan, West Bengal, India, for granting study leave. Professor J.L.Y.acknowledges funding from U.S. Army Research Office under Grant No. W911NF-11-1-0263 and U.S. Department of Defence Air Force Office of Scientific Research (FA9550-17-1-0282).
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/8/22
Y1 - 2019/8/22
N2 - A simple, rapid, selective, and cost-effective colorimetric assay for Cr3+ and Eu3+ ion detection has been developed using functionalized gold nanoparticles. Gold nanoparticles (AuNPs) were prepared using HAuCl4, where sodium citrate is a reducing agent as well as a capping agent, and then functionalized with 1,2,3-triazole-4,5-dicarboxylic acid (TADA). Fourier transform infrared (FTIR) and Raman spectroscopies suggested that TADA was functionalized on the surface of AuNPs through the N atom of triazole. The TADA-functionalized gold nanoparticles (TADA@AuNPs) simultaneously detect Cr3+ and Eu3+ ions from aqueous solution and showed different responses to the two metal ions (Cr3+ and Eu3+) based on an aggregation-induced color change of AuNPs. They showed a color change from wine red to blue, which was easily detected by the naked eye, as well as by UV-visible and FTIR spectroscopies. The surface plasmon resonance absorbances of Cr3+ and Eu3+ are 633 and 671 nm, respectively, when Cr3+ and Eu3+ react with TADA@AuNPs and showed good linearity with Cr3+ and Eu3+ concentrations with detection limits 5.89 nM and 4.30 μM, respectively (S/N = 3). The TADA@AuNPs showed excellent selectivity toward Cr3+ and Eu3+ compared to those of the 16 different metal ions. We had also tested the selectivity of TADA@AuNPs toward Eu3+ compared to that of the other 10 lanthanide systems. Optimal detection was achieved toward Cr3+ and Eu3+ ions in the pH range 4-10. In addition, TADA@AuNPs were applied to detect Cr3+ and Eu3+ ions from lake water showing low interference.
AB - A simple, rapid, selective, and cost-effective colorimetric assay for Cr3+ and Eu3+ ion detection has been developed using functionalized gold nanoparticles. Gold nanoparticles (AuNPs) were prepared using HAuCl4, where sodium citrate is a reducing agent as well as a capping agent, and then functionalized with 1,2,3-triazole-4,5-dicarboxylic acid (TADA). Fourier transform infrared (FTIR) and Raman spectroscopies suggested that TADA was functionalized on the surface of AuNPs through the N atom of triazole. The TADA-functionalized gold nanoparticles (TADA@AuNPs) simultaneously detect Cr3+ and Eu3+ ions from aqueous solution and showed different responses to the two metal ions (Cr3+ and Eu3+) based on an aggregation-induced color change of AuNPs. They showed a color change from wine red to blue, which was easily detected by the naked eye, as well as by UV-visible and FTIR spectroscopies. The surface plasmon resonance absorbances of Cr3+ and Eu3+ are 633 and 671 nm, respectively, when Cr3+ and Eu3+ react with TADA@AuNPs and showed good linearity with Cr3+ and Eu3+ concentrations with detection limits 5.89 nM and 4.30 μM, respectively (S/N = 3). The TADA@AuNPs showed excellent selectivity toward Cr3+ and Eu3+ compared to those of the 16 different metal ions. We had also tested the selectivity of TADA@AuNPs toward Eu3+ compared to that of the other 10 lanthanide systems. Optimal detection was achieved toward Cr3+ and Eu3+ ions in the pH range 4-10. In addition, TADA@AuNPs were applied to detect Cr3+ and Eu3+ ions from lake water showing low interference.
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U2 - 10.1021/acs.jpcc.9b03721
DO - 10.1021/acs.jpcc.9b03721
M3 - Article
AN - SCOPUS:85070898713
SN - 1932-7447
VL - 123
SP - 20459
EP - 20467
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 33
ER -