TY - JOUR
T1 - Magnetic-field-induced acicular nickel immobilized on carbon nanofibers as electrodes for electrochemical glucose sensing
AU - Chai, Ai Wen
AU - Wang, Cheng Chien
AU - Chen, Chuh Yung
N1 - Funding Information:
Special thanks to senior Chih-Wei Chen at the Department of Chemical Engineering, National Cheng Kung University, for his technical assistance and providing experimental materials. This work was supported by the Ministry of Science and Technology of the Republic of China [Grant No MOST 108–2221-E-218–030- ].
Funding Information:
Special thanks to senior Chih-Wei Chen at the Department of Chemical Engineering, National Cheng Kung University, for his technical assistance and providing experimental materials. This work was supported by the Ministry of Science and Technology of the Republic of China [Grant No MOST 108–2221-E-218–030-].
Publisher Copyright:
© 2021 Taiwan Institute of Chemical Engineers
PY - 2021/12
Y1 - 2021/12
N2 - Background: Effective high-throughput strategies to prepare nanostructured electrodes for glucose sensing remain significant interest for many applications. In this study, acicular nickel was immobilized on carbon nanofibers (CNFs) via electroless plating under a magnetic field to form CNFs-Ni, and its application as an electrode in amperometric non-enzymatic glucose sensing was investigated. Methods: Polyacrylonitrile (PAN) nanofibers (NFs) were fabricated by centrifuged-electrospinning, in which the combination of electrostatic and centrifugal forces produces a strong stretching force. PAN polymer chains were aligned parallel to the axis of the NFs, thereby stretching the dispersed PAN droplets into thin and molecularly orientated NFs. The PAN NFs were then subjected to stabilization followed by carbonization at 1200, 1300, 1400, or 1500 °C to produce PAN CNFs. The characteristics of the CNFs were confirmed by scanning electron microscopy (SEM), electron spectroscopy for chemical analysis, Raman spectroscopy, and four-point probe analysis. Additionally, the CNFs coated with acicular nickel (CNFs-Ni) were analyzed by SEM, X-ray diffraction, and high-resolution transmission electron microscopy. Significant Findings: Under the optimal conditions (CNFs1400-Ni), the glucose sensor showed a high sensitivity (7404 μA mM−1 cm−2) with a linear range from 2.1 × 10−2 to 6.0 × 10−1 mM (R2 = 0.993) and fast response (10 s).
AB - Background: Effective high-throughput strategies to prepare nanostructured electrodes for glucose sensing remain significant interest for many applications. In this study, acicular nickel was immobilized on carbon nanofibers (CNFs) via electroless plating under a magnetic field to form CNFs-Ni, and its application as an electrode in amperometric non-enzymatic glucose sensing was investigated. Methods: Polyacrylonitrile (PAN) nanofibers (NFs) were fabricated by centrifuged-electrospinning, in which the combination of electrostatic and centrifugal forces produces a strong stretching force. PAN polymer chains were aligned parallel to the axis of the NFs, thereby stretching the dispersed PAN droplets into thin and molecularly orientated NFs. The PAN NFs were then subjected to stabilization followed by carbonization at 1200, 1300, 1400, or 1500 °C to produce PAN CNFs. The characteristics of the CNFs were confirmed by scanning electron microscopy (SEM), electron spectroscopy for chemical analysis, Raman spectroscopy, and four-point probe analysis. Additionally, the CNFs coated with acicular nickel (CNFs-Ni) were analyzed by SEM, X-ray diffraction, and high-resolution transmission electron microscopy. Significant Findings: Under the optimal conditions (CNFs1400-Ni), the glucose sensor showed a high sensitivity (7404 μA mM−1 cm−2) with a linear range from 2.1 × 10−2 to 6.0 × 10−1 mM (R2 = 0.993) and fast response (10 s).
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U2 - 10.1016/j.jtice.2021.10.008
DO - 10.1016/j.jtice.2021.10.008
M3 - Article
AN - SCOPUS:85117127975
SN - 1876-1070
VL - 129
SP - 237
EP - 245
JO - Journal of the Taiwan Institute of Chemical Engineers
JF - Journal of the Taiwan Institute of Chemical Engineers
ER -