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AuthorAl-Kandari, Halema Ali
AuthorAbdullah, Aboubakr Moustafa
AuthorMohamed, Ahmed meslam
AuthorAl-Kandari, Shikah Ali
Available date2025-07-21T04:19:02Z
Publication Date2014
Publication NameECS Transactions
ResourceScopus
Identifierhttp://dx.doi.org/10.1149/06139.0013ecst
ISSN1938-6737
URIhttp://hdl.handle.net/10576/66511
AbstractA 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 H2 gas flow in a controlled gas reactor at 450 oC 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 H2 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 TiO2 (P25-TiO2/GC), (iii) TiO2-supported GO (GO/TiO2/GC), (iv) TiO2 – supported HH – reduced GO (HHRGO/TiO2/GC) and (v) TiO2 – supported H2 gas – reduced GO (H2RGO/TiO2/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 H2RGO/TiO2/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.
Languageen
PublisherElectrochemical Society Inc.
SubjectGraphene oxide synthesis
Reduction methods of graphene oxide
Electrocatalytic oxygen reduction reaction
TiO2-supported graphene electrodes
Surface characterization of graphene oxide
TitleGraphene/TiO2 composite electrode: Synthesis and application towards the oxygen reduction reaction
TypeConference
Pagination13-26
Issue Number39
Volume Number61
dc.accessType Abstract Only


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