Electrocatalytic reduction of hydrogen peroxide at nanostructured copper modified electrode

The electrocatalytic reduction of hydrogen peroxide (H2O2) has been studied at nanostructured copper (Cu-nano) modified glassy carbon (GC/Cu-nano) electrode in phosphate buffer (pH 7.2). The electrical properties of GC/Cu-nano modified electrodes were studied by electrochemical impedance spectroscopy (EIS). Surface and electrochemical characterization were carried out by using atomic force microscopy (AFM) and cyclic voltammetry. A well-defined H2O2 reduction signal, which is due to mediation of a surface active site redox transition exhibits at the GC/Cu-nano electrode. The Cu-nano is acting as a bridge without the aid of any other electron mediator, which enables the direct electron transfer between the modified electrode and the substrate. The results are compared with bulk copper macroelectrode and emphasized the efficiency of the Cu-nano modified electrode. Systematic investigations were made to optimize the experimental parameter, such as applied potential (E-app) for copper electrodeposition. The calibration curve obtained from chronoamperometric studies was found to be linear in the range 0.5 to 8.0 mu M H2O2 with a detection limit of ca.10 nM (S/N = 3) at the GC/Cu-nano electrode. The modified electrode is stable for 1 week in phosphate buffer after repetitive measurements.