Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43332
Title: Laser-induced graphene decorated with Ni-Pt alloy nanoparticles for non-enzymatic electrochemical quantification of glucose
Authors: Liu, Peng
Zhang , Yuanyuan
Ye, Lei
Huang, Man
Zeng, Ting
Yang , Juan
Tian , Fan
Wu, Zhen
Zhang , Xiuhua
Hu, Chengguo
YANG, Nianjun 
Issue Date: 2024
Publisher: ELSEVIER SCIENCE SA
Source: DIAMOND AND RELATED MATERIALS, 146 (Art N° 111205)
Abstract: Enzyme-free electrochemical glucose (Glu) sensors, adopting electrochemically active catalysts, are of vital significance to effectively monitoring and analyzing the blood Glu level in diabetes diagnosis. Meanwhile, developing novel electrode substrates have been the hot research pot to meet the demand for constructing flexible sensors. In this work, porous laser-induced graphene (LIG) was prepared through a facile one-step laserengraving technique on a polyimide thin film, and then used directly as the electrode. Furthermore, NiPt alloyed nanoparticles (NPs) were electrodeposited on the LIG electrode surface to gain the NiPt/LIG composite electrode, which was applied to construct the nonenzymatic electrochemical Glu sensor. The morphology, element and electrochemical performance of NiPt/LIG composite was characterized through various techniques. NiPt alloyed NPs were homogeneously distributed on the LIG scaffolds, which possess plenty of porous structure, high surface area and many active sites. The cooperative effect between the outstanding electrocatalytic capacity of NiPt alloyed NPs, the extraordinary electroconductibility of LIG and the numerous exposed active sites endow the NiPt/LIG sensor outstanding electrocatalytic performance for electrochemical oxidation of Glu. Under the most appropriate conditions, the obtained NiPt/LIG sensor was adopted to detect Glu, showing a broad detection concentration range of 0.5 mu M to 2.1 mM and 2.1 mM to 5.6 mM, good sensitivities of 1.824 and 0.467 mu A mu M-1 cm-2, a low detection limit of 0.03 mu M. The as-fabricated nonenzymatic Glu sensor also displays high selectivity, stability considering ageing effects under different environment conditions and prominent reproducibility. Additionally, this novel NiPt/LIG nonenzymatic Glu sensor was applied to quantify Glu successfully in blood serum and food samples and the results were in good agreement with that by UV-vis spectrophotometer, demonstrating high precision and accuracy as well as excellent recovery, showing good application prospects in Glu monitoring. This research confirmed the potential of exploiting NiPt/LIG as a highly sensitive Glu nonenzymatic electrochemical sensor and provided a practicable and suitable approach for construction of novel electrochemical sensors.
Notes: Zhang, YY (corresponding author), Wuhan Inst Technol, Sch Chem & Environm Engn, Sch Mat Sci & Engn, Key Lab Green Chem Engn Proc,Minist Educ,Hubei Key, Wuhan 430205, Peoples R China.; Hu, CG (corresponding author), Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China.
yyzhang@wit.edu.cn; cghu@whu.edu.cn
Keywords: Electrochemical sensor;Laser-induced graphene (LIG);Nonenzymatic sensor;NiPt alloyed nanoparticles;Glucose
Document URI: http://hdl.handle.net/1942/43332
ISSN: 0925-9635
e-ISSN: 1879-0062
DOI: 10.1016/j.diamond.2024.111205
ISI #: 001246537800001
Rights: 2024 Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

Files in This Item:
File Description SizeFormat 
Laser-induced graphene decorated with Ni[sbnd]Pt alloy nanoparticles for non-enzymatic electrochemical quantification of glucose.pdf
  Restricted Access
Published version7.33 MBAdobe PDFView/Open    Request a copy
xx.pdf
  Until 2024-12-01
Peer-reviewed author version13.45 MBAdobe PDFView/Open    Request a copy
Show full item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.