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Electrochemical sensor based on Cu2-xS/graphene heterostructures for sub-picomolar dopamine detection.

Authors :
Ai, Ding
Yu, Hao
Han, Yuting
Chang, Yuan
Ma, Yanhao
Wu, Chenglong
Liu, Mengning
Zhu, Yongsheng
Li, Shengbin
Dong, Chengye
Cheng, Yonghong
Source :
Microchimica Acta. Oct2024, Vol. 191 Issue 10, p1-11. 11p.
Publication Year :
2024

Abstract

Detecting dopamine (DA) in biological samples is vital to understand its crucial role in numerous physiological processes, such as motion, cognition, and reward stimulus. In this work, p-type graphene on sapphire, synthesized via chemical vapor deposition, serves as substrate for the preparation of p-type Cu2-xS films through solid-phase sulfurization. The optimized Cu2-xS/graphene heterostructure, prepared at 250 °C using a 15-nm copper film sulfurized for 2 h, exhibits superior electron transfer performance, ideal for electrochemical sensing. It is confirmed that the spontaneous charge transfer from graphene to Cu2-xS, higher Cu(II)/Cu(I) ratio (~ 0.8), and the presence of well-defined nanocrystalline structures with an average size of ~ 35 nm in Cu2-xS significantly contribute to the improved electron transfer of the heterostructure. The electrochemical sensor based on Cu2-xS/graphene heterostructure demonstrates remarkable sensitivity towards DA, with a detection limit as low as 100 fM and a dynamic range greater than 109 from 100 fM to 100 μM. Additionally, it exhibits excellent selectivity even in the presence of uric acid and ascorbic acid 100 times higher, alongside notable storage and measurement stability and repeatability. Impressively, the sensor also proves capable of detecting DA concentrations as low as 100 pM in rat serum, showcasing its potential for clinically relevant analytes and promising applications in sensitive, selective, reliable, and efficient point-of-care diagnostics. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00263672
Volume :
191
Issue :
10
Database :
Academic Search Index
Journal :
Microchimica Acta
Publication Type :
Academic Journal
Accession number :
180303331
Full Text :
https://doi.org/10.1007/s00604-024-06651-3