Copper nanoparticles/polyaniline/graphene composite as a highly sensitive electrochemical glucose sensor
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Zheng, Weiran
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机构:Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
Zheng, Weiran
Hu, Liangsheng
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机构:Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
Hu, Liangsheng
Lee, Lawrence Yoon Suk
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
Lee, Lawrence Yoon Suk
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Wong, Kwok-Yin
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
Wong, Kwok-Yin
[1
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机构:
[1] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
A highly sensitive non-enzymatic glucose sensor based on Cu nanoparticles (CuNPs)/polyaniline (PANT)/graphene nanocomposite was fabricated via simple in-situ reduction of Cu precursor in polyaniline nanofibers under mild conditions followed by mechanical mixing with graphene suspension to form the composites with different graphene contents (0.5%, 1%, and 2%). The properties of nanocomposites were characterized by SEM, TEM, XRD, UV-Vis, and XPS. The CuNPs (d = 2-4 nm) only slightly altered the ordered structure of PANI. It was found that CuNPs have direct electronic interaction with PANI via the N atoms on the polymer backbone, which enabled fast electrons transfer from electrode to CuNPs through graphene and PANI. The CuNPs/PANI/graphene nanocomposites were coated on a glassy carbon electrode for the investigation of their electrochemical properties. Both CuNPs/PANI and CuNPs/PANI/graphene showed high sensitivity towards glucose oxidation which occurred at similar to 0.5 V vs. SCE. The best performance was achieved by the CuNPs/PANI/1% graphene-modified electrode which showed sensitivity of similar to 150 mA cm(-2) M-1, detection limit of 0.27 mu M (S/N = 3), and response time of about 3 s. This system was also highly selective towards glucose oxidation that almost no signal was detected from interferents such as ascorbic acid and dopamine, demonstrating its great potential as a non-enzymatic glucose sensor. (C) 2016 Elsevier B.V. All rights reserved.
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Iran Univ Sci & Technol, Electroanalyt Chem Res Ctr, Res Lab Real Samples Anal, Fac Chem, Tehran 1684613114, IranIran Univ Sci & Technol, Electroanalyt Chem Res Ctr, Res Lab Real Samples Anal, Fac Chem, Tehran 1684613114, Iran
Salahandish, Razieh
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Ghaffarinejad, Ali
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Naghib, Seyed Morteza
Majidzadeh-A, Keivan
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Acad Ctr Educ Culture & Res, Motamed Canc Inst, Genet Dept, Breast Canc Res Ctr, Tehran 141554364, IranIran Univ Sci & Technol, Electroanalyt Chem Res Ctr, Res Lab Real Samples Anal, Fac Chem, Tehran 1684613114, Iran
Majidzadeh-A, Keivan
Sanati-Nezhad, Amir
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Univ Calgary, BioMEMS & Bioinspired Microfluid Lab, Dept Mech & Mfg Engn, Calgary, AB T2N 1N4, CanadaIran Univ Sci & Technol, Electroanalyt Chem Res Ctr, Res Lab Real Samples Anal, Fac Chem, Tehran 1684613114, Iran