Graphene quantum dots and Nafion composite as an ultrasensitive electrochemical sensor for the detection of dopamine

被引:56
|
作者
Pang, Pengfei [1 ]
Yan, Fuqing [1 ]
Li, Haizhen [1 ]
Li, Haiyan [1 ]
Zhang, Yanli [1 ]
Wang, Hongbin [1 ]
Wu, Zhan [2 ]
Yang, Wenrong [1 ,3 ]
机构
[1] Yunnan Minzu Univ, Key Lab Comprehens Utilizat Mineral Resources Eth, Kunming 650031, Peoples R China
[2] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[3] Deakin Univ, Sch Life & Environm Sci, Geelong, Vic 3217, Australia
基金
中国国家自然科学基金;
关键词
NITROGEN-DOPED GRAPHENE; ASCORBIC-ACID; URIC-ACID; SELECTIVE DETECTION; MODIFIED ELECTRODE; CARBON ELECTRODE; OXIDE; NANOSHEETS; PLATFORM; ADENINE;
D O I
10.1039/c6ay01254j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel electrochemical sensor for highly sensitive and selective detection of dopamine (DA) was developed based on a graphene quantum dots (GQDs) and Nafion composite modified glassy carbon electrode (GCE). GQDs were synthesized by a hydrothermal approach for cutting graphene sheets into GQDs and characterized by TEM, UV-vis, photoluminescence, and FT-IR spectra. The GQDs had carboxyl groups with a negative charge, which not only provided good stability, but also enabled interaction with amine functional groups in DA through electrostatic interaction to enhance the specificity of DA. The interaction and electron communication between GQDs and DA can be further strengthened via p-p stacking force. Nafion was used as an anchoring agent to increase the robustness of GQDs on the electrode surface and sensor stability and reproducibility. The GQDs-Nafion composite exhibits a good linear range of 5 nM to 100 mM and a limit of detection as low as 0.45 nM in the detection of DA. The proposed electrochemical sensor also displays good selectivity and high stability and could be used for the determination of DA in real samples with satisfactory results. The present study provides a powerful avenue for the design of an ultrasensitive detection method for clinical application.
引用
收藏
页码:4912 / 4918
页数:7
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