Synthesis of hemicellulose/deep eutectic solvent based carbon quantum dots for ultrasensitive detection of Ag+ and L-cysteine with "off-on" pattern

被引:68
|
作者
Jiang, Xueqin [1 ]
Huang, Jianbo [1 ]
Chen, Tianying [1 ]
Zhao, Qiang [1 ]
Xu, Feng [1 ]
Zhang, Xueming [1 ]
机构
[1] Beijing Forestry Univ, Beijing Key Lab Lignocellulos Chem, Beijing 100083, Peoples R China
关键词
Hemicellulose; Carbon quantum dots; DES; Silver ion; L-Cysteine; HIGHLY SENSITIVE DETECTION; FLUORESCENT-PROBE; SELECTIVE DETECTION; AQUEOUS-SOLUTION; SENSOR; SILVER; IONS; PHOTOLUMINESCENCE; NANOPARTICLES; HG2+;
D O I
10.1016/j.ijbiomac.2020.03.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hypersensitive detection of metal ions and amino acid becomes more important for environmental and human physical conditions monitor but remains still a great challenge. In this work, we have reported a green and straight forward procedure (solvothermal treatment) for the synthesis of N-doped hemicellulose-based carbon quantum dots (N-H-CQDs) used as an "off-on" fluorescence sensor for ultrasensitive detecting Ag+ ion and L-Cysteine (L-Cys). During this process, hemicellulose used as carbon source and nitrogen-rich deep eutectic solvent (DES) of choline chloride/urea acted as both solvent and doping agent. The prepared N-H-CQDs displayed narrow diameter ranging from 2 to 8 nm with relatively higher quantum yield (QY) of 23.45%. This probe was able to selectively detect Ag+ ion on account of the formation of N-H-CQDs-Ag(+)complex and possessed extremely low detection limit of 21 nM. Additionally, the fluorescence of N-H-CQDs-Ag+ complex was restored by the addition of L-Cysteine as Ag - ion would assemble a more stable Ag+-L-Cysteine complex through Ag+-thiol bonds. Accordingly, the N-H-CQDs-Ag+ solution behaved as secondary fluorescent probe to detect L-Cys in the dynamic range of 0-100 mu M with a LOD of 242 nM. The prepared N-H-CQDs are promising probes for hypersensitive detection of Ag+ and L-Cys. (C) 2020 Elsevier B.V. All tights reserved.
引用
收藏
页码:412 / 420
页数:9
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