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Electrocatalytic Reduction and Determination of Dissolved Oxygen at a Preanodized Screen‐Printed Carbon Electrode Modified with Palladium Nanoparticles
36
Citations
30
References
2005
Year
Materials ScienceDissolved OxygenChemical EngineeringElectrode SurfacePalladium NanoparticlesElectrocatalytic ReductionEngineeringOxygen Reduction ReactionSurface ElectrochemistryCarbon InkCatalysisChemistryElectrochemical ProcessElectrode Reaction MechanismElectrochemistryElectrochemical Surface Science
Abstract Efficient and stable electrocatalytic activity for the reduction of O 2 at activated screen‐printed carbon electrodes modified with palladium nanoparticles (SPE*‐Pd) was demonstrated in this study. X‐ray photoelectron spectroscopy confirmed the formation of >CO functional group on electrode surface during the preanodization procedure at 2.0 V (vs. Ag/AgCl). The existence of chloride moieties was also identified possibly from the organic binder of carbon ink used in SPE fabrication. Both >CO and chloride functional groups were essential for the excellent stability of the SPE*‐Pd. Electrochemical impedance spectroscopy verified the enhanced kinetic rate of oxygen reduction reaction at the as‐prepared Pd nanoparticles. The SPE*‐Pd showed ca. 250 mV positive shift in peak potential together with twice increase in peak current compared to those observed at a SPE‐Pt. The calibration plot was linear up to 8 ppm of DO with sensitivity and regression coefficient of 4.49 μA/ppm and 0.9936, respectively. The variation coefficient of i pc for 7 DO determinations with O 2 ‐saturated pH 7.4 PBS was 2.1%. Real sample assays for ground and tap waters gave consistent values to those measured by a commercial dissolved oxygen meter.
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