Electrochemical Oxidation of Sodium Metabisulfite for Sensing Zinc Oxide Nanoparticles Deposited on Graphite Electrode

Abstract

A novel concept was successfully evaluated for the electrochemical quantitative analysis of zinc oxide nanoparticles originally in aqueous suspension. An aliquot of the suspension was first placed on the working area of a graphite screen-printed electrode and the water was evaporated to form a dry deposit of ZnO nanoparticles. Deposition of ZnO nanoparticles on the electrode was confirmed by energy-dispersive X-ray spectroscopy. A probe solution containing KCl and sodium metabisulfite was added on top of the deposit for electrochemical analysis by cyclic voltammetry. The anodic peak current (Ipa) for metabisulfite, measured at +1.2 V vs. Ag/AgCl, afforded a lower detection limit of 3 µg and exhibited a linear dependence on the mass of deposited ZnO nanoparticles up to 15 µg. Further, the current increased nonlinearly until it reached a saturation level beyond 60 µg of ZnO nanoparticles. The diffusion coefficient of metabisulfite anions through the electrical double layer was determined to be 4.16 × 10−5 cm2/s. Apparently the surface reactivity of ZnO originated from the oxide anion rather than the superoxide anion or the hydroxyl radical. Enhancement of the metabisulfite oxidation peak current can be developed into a sensitive method for the quantitation of ZnO nanoparticles.