Ultrasensitive Copper(II) Detection Using Plasmon-Enhanced and Photo-Brightened Luminescence of CdSe Quantum Dots

被引:268
作者
Chan, Yang-Hsiang [1 ]
Chen, Jixin [1 ]
Liu, Qingsheng [1 ]
Wark, Stacey E. [1 ]
Son, Dong Hee [1 ]
Batteas, James D. [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
基金
美国国家科学基金会;
关键词
TIME-DEPENDENT PHOTOLUMINESCENCE; CORE/SHELL NANOCRYSTALS; GOLD NANOPARTICLES; METAL IONS; PROBE; RECOGNITION; MONOLAYERS; SULFIDE; HEAVY; STATE;
D O I
10.1021/ac902985p
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here, we present a simple platform for the use of the enhanced emission of 16-mercaptohexadecanoic acid (16-MHA) capped CdSe quantum dots (QDs) as a probe for ultrasensitive copper(II) detection. In this study, the photoluminescence (PL) of the QDs was first enhanced by Ag nanoprisms which were self-assembled on Si surfaces and then further increased by photobrightening. Using this approach, the control and different analytes could be readily probed all on a single platform using fluorescence microscopy. The enhanced PL intensity of CdSe QDs was selectively quenched in the presence of Cu2+, accompanied by the emergence of a new red-shifted luminescence band. The quenching mechanism was found to be due to a cation exchange mechanism as confirmed by X-ray photoelectron spectroscopy (XPS) measurements. Herein, we have demonstrated that this simple methodology can offer a rapid and reliable detection of Cu2+ with a detection limit as low as 5 nM and a dynamic range up to 100, mu M in a fixed fast reaction time of 5 min. The potential applications of this technique were tested in two ways, for mixed-ion solutions and in physiological fluids, and both experiments exhibited good selectivity toward Cu2+.
引用
收藏
页码:3671 / 3678
页数:8
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