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Updated: Jan 10, 2026

Bridging the Bio-Electronic Interface with Biofabrication
Published on: June 6, 2012
Structural, optical, and electrochemical characterization of TiO2-x thin films for non-enzymatic amperometric glucose
J K Olarte Villamizar1, M Zapata Torres1, N Cruz González1
1Instituto Politécnico Nacional, CICATA Unidad Legaria, Legaria 694. Col. Irrigación, C.P. 11500, Ciudad de México, Mexico.
Abstract:
This work presents a novel approach to non-enzymatic glucose sensing based on oxygen-deficient titanium dioxide (TiO2-x) thin films deposited on metallic titanium substrates. The TiO2-x films were fabricated via RF magnetron reactive sputtering using a titanium target, and their structural, morphological, optical, and electrochemical properties were comprehensively characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis spectroscopy, and electrochemical techniques. The electrochemical performance was evaluated using cyclic voltammetry (CV) and chronoamperometry. The CV results revealed that the oxidation in phosphate buffer solution occurs at an applied potential of -0.54 V, increasing with a glucose concentration. Chronoamperometric analysis demonstrated a high sensitivity of 27.55 μA cm-2 mM-1 and a low detection limit of 0.11 mM. The sensor also exhibited a linear dynamic range from 0.2 mM to 2.4 mM and excellent selectivity against common interfering species, including histidine (His), cysteine (Cys), uric acid (UA), ascorbic acid (AA), and sucrose. These findings highlight the potential of Ti/TiO2-x electrodes as efficient, stable, and selective platforms for developing non-enzymatic glucose sensors suitable for biomedical and wearable applications, with possible use in detecting glucose concentrations in sweat (0.27 mM-1 mM) and saliva (0.23 mM-1.78 mM).
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