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dc.contributor.authorLiu, Shizhen
dc.contributor.authorSun, Hongqi
dc.contributor.authorSuvorova, A.
dc.contributor.authorWang, Shaobin
dc.date.accessioned2017-01-30T13:58:27Z
dc.date.available2017-01-30T13:58:27Z
dc.date.created2014-01-12T20:01:11Z
dc.date.issued2013
dc.identifier.citationLiu, Shizhen. and Sun, Hongqi and Suvorova, Alexandra and Wang, Shaobin. 2013. One-pot hydrothermal synthesis of ZnO-reduced graphene oxide composites using Zn powders for enhanced photocatalysis. Chemical Engineering Journal. 229: pp. 533-539.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/36917
dc.identifier.doi10.1016/j.cej.2013.06.063
dc.description.abstract

Zn powder was successfully utilized as a reducing agent and a precursor of ZnO for one-pot synthesis of reduced graphene oxide (rGO)–ZnO photocatalysts. Two rGO–ZnO composites were synthesized with or without a surfactant, cetyltrimethyl ammonium bromide (CTAB). The structural, morphological, and photochemical properties of the samples were thoroughly investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), N2 adsorption/desorption, UV–vis diffuse reflectance (UV–vis DRS), thermogravimetric-differential thermal analysis (TG-DTA), and Raman spectroscopy. Zn powder could effectively reduce GO to graphene and be transformed to ZnO with the assistance of the surfactant.The surfactant was found to influence the properties of rGO–ZnO. rGO–ZnO photocatalysts could decompose methylene blue under UV–vis illumination and exhibited higher activities than pristine ZnO. The coexistence of GO–rGO would be more favorable to photocatalysis.

dc.publisherElsevier BV
dc.subjectPhotocatalysis
dc.subjectMethylene blue
dc.subjectZno
dc.subjectReduced graphene oxide
dc.titleOne-pot hydrothermal synthesis of ZnO-reduced graphene oxide composites using Zn powders for enhanced photocatalysis
dc.typeJournal Article
dcterms.source.volume229
dcterms.source.startPage533
dcterms.source.endPage539
dcterms.source.issn1385-8947
dcterms.source.titleChemical Engineering Journal
curtin.note

NOTICE: This is the author’s version of a work that was accepted for publication in Chemical Engineering Journal. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published Chemical Engineering Journal, Volume 229, 1 August 2013, Pages 533–539. http://dx.doi.org/10.1016/j.cej.2013.06.063

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curtin.accessStatusOpen access


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