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dc.contributor.authorPlayford, Helen. Y.
dc.contributor.authorHannon, Alex C.
dc.contributor.authorTucker, Matthew G.
dc.contributor.authorDawson, Daniel M.
dc.contributor.authorAshbrook, Sharon E.
dc.contributor.authorKastiban, Reza J.
dc.contributor.authorSloan, Jeremy
dc.contributor.authorWalton, Richard I.
dc.date.accessioned2015-06-29T23:10:50Z
dc.date.available2015-06-29T23:10:50Z
dc.date.issued2014-07-24
dc.identifier156622644
dc.identifiera5e8bde9-d6f6-4f68-b19c-736082d28a1b
dc.identifier000339540700071
dc.identifier84904975692
dc.identifier.citationPlayford , H Y , Hannon , A C , Tucker , M G , Dawson , D M , Ashbrook , S E , Kastiban , R J , Sloan , J & Walton , R I 2014 , ' Characterization of Structural Disorder in γ-Ga 2 O 3 ' , Journal of Physical Chemistry C , vol. 118 , no. 29 , pp. 16188-16198 . https://doi.org/10.1021/jp5033806en
dc.identifier.issn1932-7447
dc.identifier.otherORCID: /0000-0002-4538-6782/work/56638946
dc.identifier.otherORCID: /0000-0002-8110-4535/work/34029120
dc.identifier.urihttps://hdl.handle.net/10023/6874
dc.descriptionThe authors thank the STFC for provision of beam time at ISIS and for part-funding a studentship for H.Y.P. through its Centre for Materials Physics and Chemistry (Grant CMPC08104). H.Y.P. also thanks the EPSRC for providing a Postdoctoral Prize Award (Grant EP/P50578X/1).en
dc.description.abstractSolvothermal oxidation of metallic gallium in monoethanolamine for 72 h at 240 degrees C yields a crystalline sample of gamma-Ga2O3 (similar to 30 nm crystallites). While Rietveld refinement (cubic spinel structure, Fd (3) over barm; a = 8.23760(9) angstrom) reveals that Ga occupies two pairs of octahedral and tetrahedral sites (ideal spinel and nonspinel), it provides no information about their local distribution, which cannot be statistical owing to the short Ga-Ga contacts produced if neighboring ideal spinel and nonspinel sites are simultaneously occupied. To create an atomistic model to reconcile this situation, a 6 x 6 x 6 supercell of the crystal structure is constructed and refined against neutron total scattering data using a reverse Monte Carlo (RMC) approach. This accounts well for the local as well as long-range structure and reveals significant local distortion in the octahedral sites that resembles the structure of thermodynamically stable beta-Ga2O3. Ga-71 solid-state NMR results reveal a octahedral:tetrahedral Ga ratio that is consistent with the model obtained from RMC. Nanocrystalline samples of gamma-Ga2O3 are produced by either a short solvotherrnal reaction (240 degrees C for 11 h in diethanolamine; similar to 15 nm crystallites) or by precipitation from an ethanolic solution of gallium nitrate (similar to 5 nm crystallites). For these samples, the Bragg scattering profile is broadened by their smaller crystallite size, consistent with transmission electron microscopy results, and analysis of the relative Bragg peak intensities provides evidence that a greater proportion of tetrahedral versus octahedral sites are filled. In contrast, neutron total scattering shows the same average Ga-O distance with decreasing particle size, consistent with Ga-71 solid-state NMR results that indicate that all samples contain the same overall proportion of octahedral:tetrahedral Ga. It is postulated that increased occupation of tetrahedral sites within the smaller crystallites is balanced by an increased proportion of octahedral surface Ga sites, owing to termination by bound solvent or hydroxide.
dc.format.extent11
dc.format.extent3266211
dc.language.isoeng
dc.relation.ispartofJournal of Physical Chemistry Cen
dc.subjectGeneral materials diffractometeren
dc.subjectGallium oxide catalystsen
dc.subjectGamma-aluminaen
dc.subjectNeutron-diffractionen
dc.subjectSurface-chemistryen
dc.subjectPolymorphsen
dc.subjectDehydrogenationen
dc.subjectAdsorptionen
dc.subjectCrystalen
dc.subjectPropaneen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleCharacterization of Structural Disorder in γ-Ga2O3en
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1021/jp5033806
dc.description.statusPeer revieweden
dc.date.embargoedUntil2015-06-30
dc.identifier.grantnumberEP/F018096/1en
dc.identifier.grantnumberEP/K039210/1en
dc.identifier.grantnumberEP/K031252/1en


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