A novel fluorescent array for mercury (II) ion in aqueous solution with functionalized cadmium selenide nanoclusters

被引:209
作者
Chen, Jinlong
Gao, YingChun
Xu, ZhiBing
Wu, GenHua
Chen, YouCun
Zhu, ChangQing [1 ]
机构
[1] Anqing Normal Coll, Sch Chem & Environm Sci, Anqing 246003, Peoples R China
[2] Anhui Normal Univ, Anhui Key Lab Funct Mol Solids, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
基金
中国国家自然科学基金;
关键词
cadmium selenide nanoclusters; fluorescence; Mercury (II);
D O I
10.1016/j.aca.2006.06.039
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Mono-disperse CdSe nanoclusters have been prepared facilely and functionalized with L-cysteine through two steps by using safe and low cost substances. They are water-soluble and biocompatible. Especially these functionalized quantum dots can be stably soluble in water more than for 30 days, and the intensity of fluorescence and absorbance was decreased less than 15% of fresh prepared CdSe colloids. These functionalized CdSe QDs exhibited strong specific affinity for mercury (11) through QDs interface functional groups. Based on the quenching of fluorescence signals of functionalized CdSe QDs at 530 nm and no obvious wavelength shift or no new emission band in present of Hg (II) at pH 7.75 of phosphate buffer solution, a simple, rapid and specific array for Hg (II) was proposed. In comparison with conventional organic fluorophores, these nanoparticles are brighter, more stable against photobleaching, and do not suffer from blinking. Under optimum conditions, the response of linearly proportional to the concentration of Hg (II) between 0 and 2.0 x 10(-6) mol L-1, and the limit of detection is 6.0 x 10(-9) mol L-1. The relative standard deviation of six replicate measurements is 1.8% for 1.0 x 10(-7) mol L-1 Hg (II). The mechanism of reaction is also discussed. The proposed method was successfully applied for Hg (11) detection in four real samples with a satisfactory result that was obtained by cold vapor atomic fluorescence spectrometry (CV-AFS). (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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