Visual and ratiometric fluorescence detection of Hg2+ based on a dual-emission carbon dots-gold nanoclusters nanohybrid

被引:67
|
作者
Xie, Huizhi [1 ]
Dong, Jing [1 ]
Duan, Junling [1 ]
Waterhouse, Geoffrey I. N. [1 ,2 ]
Hou, Juying [1 ]
Ai, Shiyun [1 ]
机构
[1] Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China
[2] Univ Auckland, Sch Chem Sci, Auckland 1142, New Zealand
基金
中国国家自然科学基金;
关键词
CDs-AuNCs nanohybrid; Ratiometric fluorescent detection; Mercury (II) ions; Hg2+-Au+ interaction; Boronic acid-diol specific binding; ASCORBIC-ACID; QUANTUM DOTS; OPTICAL-PROPERTIES; IN-VITRO; PROBE; GRAPHENE; MERCURY; ASSAY; WATER; NANOPARTICLES;
D O I
10.1016/j.snb.2017.12.149
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel dual-emission carbon dots-gold nanoclusters (CDs-AuNCs) nanohybrid was fabricated and successfully used in the visual and ratiometric fluorescent detection of mercury (II) ions. Boronic acid functionalized carbon dots (B-CDs) were synthesized by a one-pot hydrothermal method. Bovine serum albumin functionalized carbon dots (BSA-CDs) were then obtained by simply mixing the B-CDs with bovine serum albumin, aided by specific binding between the glycoprotein and boronic acid groups. Finally, the dual-emission nanohybrid was obtained by attaching AuNCs to the BSA-CDs template. The nanohybrid exhibited two well-resolved emission peaks at 440 nm and 655 nm under 360 nm excitation. The fluorescence of the BSA-CDs at 440 nm was insensitive to the presence of aqueous Hg2+, whereas the fluorescence of AuNCs at 655 nm could be completely quenched in the presence of Hg2+ through Hg2+-Au+ interactions. The fluorescence emission of the nanohybrid allowed sensitive and selective sensing of Hg2+ in the range of 2-15 nM, with a detection limit of 0.73 nM. Importantly, the emission color of the nanohybrid changed from red to blue with increasing Hg2+ concentration (due to corresponding changes in the I-440nm and I-655nm ratio), which could be clearly discerned by the naked eye. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1082 / 1089
页数:8
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