TY - JOUR
T1 - Fine-tunable fluorescence quenching properties of core-satellite assemblies of gold nanorod-nanosphere
T2 - Application in sensitive detection of Hg2+
AU - Yang, Ying
AU - Zhao, Jing
AU - Weng, Guo jun
AU - Li, Jian jun
AU - Zhu, Jian
AU - Zhao, Jun wu
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2020/3/5
Y1 - 2020/3/5
N2 - In this work, we developed a simple, effective fluorescence method to detect Hg2+ by inhibiting core-satellite assemblies of gold nanorods (AuNRs) and gold nanospheres (AuNPs). The fluorescence of Rhodamine 6G (Rh6G), which was simply mixed with the nanoassemblies, was efficiently quenched by the inner filter effect (IFE). When the heterogenous core-satellite nanostructures were assembled, the corresponding local surface plasmon resonance (LSPR) absorption shifts and broadens which results in the increase of the spectral overlap between the emission peak and the absorption band and more efficient energy transfer from Rh6G to nanoparticles. Fluorescence quenching efficiency is related to the size and number density of satellite nanoparticles. It is interesting that the AuNR-AuNP assemblies with the moderate size and high density of AuNPs have the best fluorescence quenching efficiency. In the presence of Hg2+, p-aminothiophenol (p-ATP) breaks away from the surface of AuNRs and competitively bounds to Hg2+, resulting in a low yield of the AuNR-AuNP assemblies, which further leads to the decrease of fluorescence quenching efficiency. Under the optimum conditions, the limit of detection (LOD) for Hg2+ was 0.18 nM, with an excellent linear response from 0.6 to 800 nM. Interference experiment and real samples detection indicate that these nanosensors endowed with higher sensitivity and selectivity for the detection of Hg2+ in the real samples. Compared with the conventional Hg2+ detection techniques, this method based on Hg2+ induced inhibition of core-satellite AuNR-AuNP assemblies has better performance and is suitable for the detection of Hg2+.
AB - In this work, we developed a simple, effective fluorescence method to detect Hg2+ by inhibiting core-satellite assemblies of gold nanorods (AuNRs) and gold nanospheres (AuNPs). The fluorescence of Rhodamine 6G (Rh6G), which was simply mixed with the nanoassemblies, was efficiently quenched by the inner filter effect (IFE). When the heterogenous core-satellite nanostructures were assembled, the corresponding local surface plasmon resonance (LSPR) absorption shifts and broadens which results in the increase of the spectral overlap between the emission peak and the absorption band and more efficient energy transfer from Rh6G to nanoparticles. Fluorescence quenching efficiency is related to the size and number density of satellite nanoparticles. It is interesting that the AuNR-AuNP assemblies with the moderate size and high density of AuNPs have the best fluorescence quenching efficiency. In the presence of Hg2+, p-aminothiophenol (p-ATP) breaks away from the surface of AuNRs and competitively bounds to Hg2+, resulting in a low yield of the AuNR-AuNP assemblies, which further leads to the decrease of fluorescence quenching efficiency. Under the optimum conditions, the limit of detection (LOD) for Hg2+ was 0.18 nM, with an excellent linear response from 0.6 to 800 nM. Interference experiment and real samples detection indicate that these nanosensors endowed with higher sensitivity and selectivity for the detection of Hg2+ in the real samples. Compared with the conventional Hg2+ detection techniques, this method based on Hg2+ induced inhibition of core-satellite AuNR-AuNP assemblies has better performance and is suitable for the detection of Hg2+.
KW - AuNPs
KW - AuNRs
KW - Core-satellite assemblies
KW - Fluorescence quenching
KW - Hg
UR - https://www.scopus.com/pages/publications/85075470224
U2 - 10.1016/j.saa.2019.117776
DO - 10.1016/j.saa.2019.117776
M3 - 文章
C2 - 31727522
AN - SCOPUS:85075470224
SN - 1386-1425
VL - 228
JO - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
JF - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
M1 - 117776
ER -