Abstract
The electrocatalytic evolution of oxygen gas is investigated at manganese oxide nanorods (nano-MnO x ) modified Au, Pt and GC electrodes in a wide range of pH values, ranging from highly acidic to highly basic. Morphological investigation has been carried out by a scanning electron microscopy (SEM), which revealed the deposition of nano-MnO x in a nanorod morphology. A significant enhancement of the electrocatalytic activity of the Au, Pt and GC electrodes towards the oxygen evolution reaction (OER) was observed upon the electrodeposition of nano-MnO x onto the aforementioned electrodes. The effect of the surface coverage of the manganese oxide and the pH of the electrolyte was investigated to seek an optimization. The highest cathodic shift in the onset potential of the OER was obtained in 0.5 M KOH irrespective of the substrate whereas the optimum loading (surface coverage) was about ca. 52%. The origin of the enhancement of the OER is addressed with the assistance of an X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) techniques. The preferential electrodeposition of crystallographically oriented nano-MnOx (in the manganite phase, γ-MnOOH) is thought to play the primary role in the observed enhancement.
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