Pulsed Electrodeposition of Co3 O4 Nanocrystals on One-Dimensional ZnO Scaffolds for Enhanced Electrochemical Water Oxidation.

Abstract

Pulsed electrodeposition has been introduced to deposit ultrathin flakes of Co3 O4 nanocrystals on ZnO nanorods. By fixing the seeding process, the scaffolding function of ZnO nanorods was studied by varying deposition times (30 s, 60 s, and 90 s) of Co3 O4 at a nucleation current of -1.0 mA cm-2 . The amount of deposited Co3 O4 has a strong influence on the oxygen evolution performance with ZnO scaffolds. To deliver a current density of 10.0 mA cm-2 in neutral solutions (0.5 M K2 SO4 ), the presence of ZnO scaffold electrodes negatively shifted the overpotential by ∼200 mV. In particular, the Co3 O4 /ZnO hybrid nanostructured electrode (60 s) exhibits the lowest onset potential of 1.5 V (vs. reversible hydrogen electrode, RHE). Electrochemical impedance spectra and double layer capacitance showed that the enhanced oxygen evolution activities originated from the improved charge transfer capability and the increased electrochemically active interface between Co3 O4 and ZnO.