Affiliations 

  • 1 Institute of Nanotechnology &Catalysis (NanoCat), University Malaya, 50603 Kuala Lumpur, Malaysia
  • 2 Department of Chemistry, University Malaya, Kuala Lumpur 50603, Malaysia
  • 3 Center of Foundation Studies, Faculty of Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia
  • 4 Department of Chemistry, Shahid Sherafat, University of Farhangian, 15916, Tehran, Iran
  • 5 Department of Chemistry, Faculty of Sciences, Islamic Azad University, Gorgan, 49147-39975 Iran
  • 6 Department of Physics, Masjed-Soleiman Branch, Islamic Azad University, Masjed-Soleiman, Iran
Sci Rep, 2015;5:9108.
PMID: 25765731 DOI: 10.1038/srep09108

Abstract

Graphene oxide (GO) was deposited on the surface of a MnO2 air cathode by thermal evaporation at 50°C from a GO colloidal suspension. Fourier transformed infrared spectroscopy and field emission scanning electron microscopy confirmed the presence of GO on the MnO2 air cathode (GO-MnO2). Voltammetry and chrono-amperometry showed increased currents for the oxygen reduction reaction (ORR) in 6 M KOH solution for GO-MnO2 compared to the MnO2 cathode. The GO-MnO2 was used as an air cathode in an alkaline tin-air cell and produced a maximum power density of 13 mW cm(-2), in contrast to MnO2, which produced a maximum power density of 9.2 mW cm(-2). The electrochemical impedance spectroscopy results suggest that the chemical step for the ORR is the rate determining step, as proposed earlier by different researchers. It is suggested that the presence of GO and electrochemically reduced graphene oxide (ERGO) on the MnO2 surface are responsible for the increased rate of this step, whereby GO and ERGO accelerate the process of electron donation to the MnO2 and to adsorbed oxygen atoms.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.