Graphene /TiO 2 Composite Electrode: Synthesis and Application towards the Oxygen Reduction Reaction

A graphene oxide (GO) was prepared from a commercial graphite nano-crystals using Hummers’ method. Later, GO powder was reduced either by placing it under a H 2 gas flow in a controlled gas reactor at 450 o C or using a hydrazine hydrate solution (HH) in a 1000-Watt microwave oven. X-ray photoelectr...

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Veröffentlicht in:ECS transactions 2014-10, Vol.61 (39), p.13-26
Hauptverfasser: Al-Kandari, Halema Ali, Abdullah, Aboubakr Moustafa, Mohamed, Ahmed meslam, Al-Kandari, Shikah Ali
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Sprache:eng
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Zusammenfassung:A graphene oxide (GO) was prepared from a commercial graphite nano-crystals using Hummers’ method. Later, GO powder was reduced either by placing it under a H 2 gas flow in a controlled gas reactor at 450 o C or using a hydrazine hydrate solution (HH) in a 1000-Watt microwave oven. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction patterns (XRD) confirmed that both of the oxidation and reduction processes of graphite and GO powders, respectively, were incomplete. Also, the surface area of the H 2 gas - reduced GO powder was found to be higher than the case where HH was used to reduce the same powder. Fourier transform infrared spectroscopy (FT-IR) and XPS have revealed that GO surface consists mainly of hydroxyl, epoxy, carbonyl and carboxylic groups. The electrocatalytic properties of (i) glassy carbon (GC), (ii) commercial TiO 2 (P25-TiO 2 /GC), (iii) TiO 2 -supported GO (GO/TiO 2 /GC), (iv) TiO 2 – supported HH – reduced GO (HHRGO/TiO 2 /GC) and (v) TiO 2 – supported H 2 gas – reduced GO (H 2 RGO/TiO 2 /GC) electrodes towards the oxygen reduction reaction (ORR) in acidic solution in presence and absence of UV radiation were examined. The results have shown that the H 2 RGO/TiO 2 /GC electrode has the best electrocatalytic activity in terms of current at a certain potential but glassy carbon electrode (GC) was found to be the best in terms of the onset potential of the ORR.
ISSN:1938-5862
1938-6737
DOI:10.1149/06139.0013ecst