Halogen bond triggered aggregation induced emission in an iodinated cyanine dye for ultra sensitive detection of Ag nanoparticles in tap water and agricultural wastewater

被引:59
作者
Abdelbar, Mostafa F. [1 ]
El-Sheshtawy, Hamdy S. [1 ,2 ]
Shoueir, Kamel R. [1 ]
El-Mehasseb, Ibrahim [2 ]
Ebeid, El-Zeiny M. [3 ,4 ]
El-Kemary, Maged [1 ,2 ]
机构
[1] Kafrelsheikh Univ, Inst Nanosci & Nanotechnol, Kafrelsheikh 33516, Egypt
[2] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh, Egypt
[3] Tanta Univ, Fac Sci, Chem Dept, Tanta, Egypt
[4] MUST, 6th of October City, Egypt
关键词
CLOUD POINT EXTRACTION; LUMINESCENT POLYMERIC NANOPARTICLES; SILVER NANOPARTICLES; GOLD; FLUORESCENCE; PROBE; ENHANCEMENT; FABRICATION; IONS;
D O I
10.1039/c8ra04186e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aggregation induced emission (AIE) has emerged as a powerful method for sensing applications. Based on AIE triggered by halogen bond (XB) formation, an ultrasensitive and selective sensor for picomolar detection of Ag nanoparticles (Ag NPs) is reported. The dye (CyI) has an iodine atom in its skeleton which functions as a halogen bond acceptor, and aggregates on the Ag NP plasmonic surfaces as a halogen bond donor or forms halogen bonds with the vacant pi orbitals of silver ions (Ag+). Formation of XB leads to fluorescence enhancement, which forms the basis of the Ag NPs or Ag+ sensor. The sensor response is linearly dependent on the Ag NP concentration over the range 1.0-8.2 pM with an LOD of 6.21 pM (sigma = 3), while for Ag+ it was linear over the 1.0-10 mu M range (LOD = 2.36 mu M). The sensor shows a remarkable sensitivity for Ag NPs (pM), compared to that for Ag+ (mu M). The sensor did not show any interference from different metal ions with 10-fold higher concentrations. This result indicates that the proposed sensor is inexpensive, simple, sensitive, and selective for the detection of Ag NPs in both tap and wastewater samples.
引用
收藏
页码:24617 / 24626
页数:10
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