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The electrochemical reduction of oxygen on Pd nanoparticle-decorated nitrogen-doped graphene (Pd/NG) catalyst has been investigated in acid and alkaline solutions using the rotating disk electrode (RDE) method. The Pd/NG nanocomposites were prepared by NaBH4reduction. The surface characterisation of Pd/NG composites was performed by transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The TEM images showed the uniform distribution of Pd nanoparticles over the N-doped graphene nanosheets. The RDE results indicated that Pd/NG catalysts possess a high electrocatalytic activity towards the oxygen reduction reaction (ORR). The prepared materials catalyse a 4-electron reduction of oxygen. The Tafel behaviour of O2reduction on Pd/NG catalysts was similar to that of bare Pd. The Pd/NG composite showed excellent ORR performance in alkaline media and is a promising material to be used as a cathode catalyst for alkaline membrane fuel cells. [ABSTRACT FROM AUTHOR]

Nitrogen-doped graphene oxide supported silver nanoparticles (Ag/NGO) have been synthesised using three different methods. The prepared catalysts were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemically tested for oxygen reduction reaction (ORR) in alkaline solution. The Ag/NGO catalysts prepared by borohydride reduction showed the least degree of nanoparticle agglomeration and the material which was prepared using ascorbic acid yielded the biggest Ag particles. XPS revealed that the nitrogen to carbon atomic ratio was about 0.07 and EDS mapping showed that nitrogen was uniformly distributed over the graphene. The ORR on all the Ag/NGO catalysts proceeded via 4-electron pathway yielding water while on the support material, N-doped graphene oxide, the number of electrons transferred per O 2 molecule was lower than four. The mass activity of all Ag/NGO catalysts was determined to be at least twice higher than that of NGO. [ABSTRACT FROM AUTHOR]

Abstract: The oxygen reduction reaction has been investigated on acid-treated single-walled (SWCNT) and multi-walled carbon nanotubes (MWCNT) modified glassy carbon (GC) electrodes in acid media using the rotating disk electrode (RDE) method. Different acids were used for the carbon nanotube (CNT) purification. A systematic study was carried out to elucidate whether the metal catalyst impurities of CNTs play a role in the electroreduction of oxygen on the CNT modified GC electrodes. The surface morphology of the carbon nanotube samples was examined by transmission electron microscopy and the concentration of metal catalysts in the CNT materials was determined by energy dispersive X-ray spectroscopy. The acid-treated MWCNTs were also characterised by Raman and X-ray photoelectron spectroscopies. Aqueous suspensions of SWCNTs and MWCNTs used for GC surface modification were prepared in the presence of Nafion. The RDE results indicated that the acid-treated CNT modified GC electrodes are less active catalysts for oxygen reduction than as-received CNTs which could be explained by the absence of metal catalysts on the surface of purified CNTs. [Copyright &y& Elsevier]

Abstract: The electrochemical reduction of oxygen was studied on vacuum evaporated thin Pt films (0.25–20nm thick) on polycrystalline Au substrate (Pt/Au) in 0.1M HClO4 and 0.05M H2SO4 solutions using the rotating disk electrode (RDE) method. The surface morphology of Pt films was examined by scanning tunnelling microscopy (STM). The O2 reduction specific activity of Pt films increased with increasing the film thickness in HClO4, but was lower than that of bulk Pt even for the thickest films. In H2SO4, the specific activity showed no significant dependence on the platinum loading and was lower than in HClO4. The Tafel slope values characteristic to polycrystalline Pt (−120mVdec−1 and −60mVdec−1) were found for all electrodes. The RRDE studies of 0.5nm Pt/Au electrode revealed that O2 reduction predominantly proceeds through 4e− pathway and H2O2 is produced in low quantities. [Copyright &y& Elsevier]