We created a glucose oxidase (GOx) working electrode on a silicon-on-insulator (SOI) wafer for glucose sensing. The SOI wafer was electrically connected to a copper wire, and the GOx was immobilized onto the hydrophilized SOI surface via silanization with aminopropyltriethoxysilane and glutaraldehyde. Electrochemical analysis (i.e., cyclic voltammetry) was employed to identify the sensing mechanism and to evaluate the performance of these SOI-GOx glucose sensors. The response of the SOI-GOx working electrode was significantly higher in the presence of oxygen than that without oxygen, indicating that a hydrogen peroxide pathway dominated in our SOI-GOx electrode. The height of cathodic peaks increased linearly with the increase of glucose concentrations up to 15 mM. The SOI-GOx working electrode displayed good stability after more than 30 cycles. On the 133 day after the electrode was made, although the response of the SOI-GOx electrode dropped to about one-half of its original response, it was still capable of distinguishing different glucose concentrations. This work suggests that the SOI-GOx working electrode that we developed might be a promising candidate for implantable glucose sensors.
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http://dx.doi.org/10.1021/acsomega.9b02384 | DOI Listing |
MethodsX
June 2025
Department of Materials Science and Engineering, Norwegian University of Science and Technology (NTNU), NO-7491, Trondheim, Norway.
Construction and experimental validation of electrochemical cells with multiple electrodes in a microfluidic channel is described. Details of the fabrication of the electrodes and polydimethylsiloxane channel using soft lithography methods are given. Calibration of the collection efficiencies and transit times between electrodes validate the use of these cells for fast electrochemical detection of soluble species.
View Article and Find Full Text PDFGreen Chem
January 2025
Van't Hoff Institute for Molecular Sciences, University of Amsterdam Science Park 904 1098 XH Amsterdam The Netherlands
The development of sustainable synthetic methods for converting alcohols to amines is of great interest due to their widespread use in pharmaceuticals and fine chemicals. In this work, we present an electrochemical approach by using green electrons for the selective oxidation of benzyl alcohol to benzaldehyde using a NiOOH catalyst, followed by its reductive amination to form benzyl--butylamine. The number of Ni monolayer equivalents on the catalyst was found to significantly influence selectivity, with 2 monolayers achieving up to 90% faradaic efficiency (FE) for benzaldehyde in NaOH, while 10 monolayers performed best in a -butylamine solution (pH 11), yielding 100% FE for benzaldehyde.
View Article and Find Full Text PDFACS Mater Au
January 2025
Solid State and Structural Chemistry Unit, IISc, Bengaluru 560012, Karnataka, India.
LiNiMnO (LNMO), with its high operating voltage, is a favorable cathode material for lithium-ion batteries. However, Ni and Mn dissolution and the associated low cycle life limit their widespread adoption. In this work, we investigate titanium doping as a strategy to mitigate Mn and Ni dissolution from LNMO electrodes.
View Article and Find Full Text PDFMed Devices (Auckl)
January 2025
Faculty of Geological Engineering, Universitas Padjadjaran, Jatinangor, Jawa Barat, 45363, Indonesia.
Background: Biomarkers are essential tools for diagnosing diseases. Saliva, as a human fluid, effectively reflects the body's condition due to its rich composition. Analyzing saliva components allows for noninvasive, cost-effective, and time-efficient screening and diagnosis.
View Article and Find Full Text PDFInorg Chem
January 2025
MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.
A novel antimonotungstate (AT)-based heterometallic framework {[Er(HO)][Fe(Hpdc)(B-β-SbWO)]}·50HO (, Hpdc = pyridine-2,5-dicarboxylic acid) was obtained through a synergistic strategy of in situ-generated transition-metal-encapsulated polyoxometalate (POM) building units and the substitution reaction. Its structural unit is composed of a tetra-Fe-substituted Krebs-type [Fe(Hpdc)(B-β-SbWO)] subunit and two [Er(HO)] cations. This subunit can be regarded as a product of carboxylic oxygen atoms of Hpdc ligands replacing active water ligands in the [Fe(HO)(B-β-SbWO)] species.
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