| Literature DB >> 24209363 |
Jia-Ming Liu1, Li Jiao, Li-Ping Lin, Ma-Lin Cui, Xin-Xing Wang, Li-Hong Zhang, Zhi-Yong Zheng, Shu-Lian Jiang.
Abstract
A label-free non-aggregation colorimetric sensor has been designed for the detection of Cu(2+), based on Cu(2+) catalyzing etching of gold nanorods (AuNRs) along longitudinal axis induced by dissolve oxygen in the presence of S2O3(2-), which caused the aspect ratio (length/width) of AuNRs to decrease and the color of the solution to distinctly change. The linear range and the detection limit (LD, calculated by 10 Sb/k, n=11) of this sensor were 0.080-4.8 µM Cu(2+) and 0.22 µM Cu(2+), respectively. This sensor has been utilized to detect Cu(2+) in tap water and human serum samples with the results agreeing well with those of inductively coupled plasma-mass spectroscopy (ICP-MS), showing its remarkable practicality. In order to prove the possibility of catalyzing AuNRs non-aggregation colorimetric sensor for the detection of Cu(2+), the morphological structures of AuNRs were characterized by high resolution transmission electron microscopy (HRTEM) and the sensing mechanism of colorimetric sensor for the detection of Cu(2+) was also discussed.Entities:
Keywords: Catalytic etching; Cu(2+); Gold nanorods; Non-aggregation colorimetric sensor
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Year: 2013 PMID: 24209363 DOI: 10.1016/j.talanta.2013.09.004
Source DB: PubMed Journal: Talanta ISSN: 0039-9140 Impact factor: 6.057