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dc.contributor.authorAqeel, Tariq
dc.contributor.authorGreer, Heather F.
dc.contributor.authorZhou, Wuzong
dc.contributor.authorBruce, Duncan W.
dc.contributor.authorBumajdad, Ali
dc.date.accessioned2016-04-19T09:30:10Z
dc.date.available2016-04-19T09:30:10Z
dc.date.issued2016-03
dc.identifier241630821
dc.identifier380dfee2-dcdc-429e-809e-4990f1212e3b
dc.identifier84961237637
dc.identifier000377198800008
dc.identifier.citationAqeel , T , Greer , H F , Zhou , W , Bruce , D W & Bumajdad , A 2016 , ' Novel direct synthesis of mesoporous tin dioxide network intact up to 500°C ' , Journal of Nano Research , vol. 40 , pp. 79-89 . https://doi.org/10.4028/www.scientific.net/JNanoR.40.79en
dc.identifier.issn1662-5250
dc.identifier.otherORCID: /0000-0001-9752-7076/work/58055028
dc.identifier.urihttps://hdl.handle.net/10023/8632
dc.descriptionThis project is supported by PAAET project no. BE-­‐13-­‐08 in collaboration with Kuwait University and the University of York. The support of the research administration of Kuwait University to the XPS instrument (Project No. GS02/08) is acknowledged.en
dc.description.abstractWe present a direct soft templating method to synthesise mesoporous tin dioxide network that maintains a porous structure after calcination at 400 °C and 500 °C and has a relatively high BET surface area of 220 and 100 m2 g-1, respectively. TEM, BET and XRD results confirm that both crystal and pore sizes increase as a result of increasing the temperatures during the calcination step. This method is highly reproducible.
dc.format.extent11
dc.format.extent3101461
dc.language.isoeng
dc.relation.ispartofJournal of Nano Researchen
dc.subjectMesoporous tin dioxideen
dc.subjectTEMen
dc.subjectBETen
dc.subjectXRDen
dc.subjectXPSen
dc.subjectPore and crystal sizesen
dc.subjectCalcinationsen
dc.subjectQD Chemistryen
dc.subjectMaterials Science(all)en
dc.subjectPhysics and Astronomy(all)en
dc.subjectNDASen
dc.subject.lccQDen
dc.titleNovel direct synthesis of mesoporous tin dioxide network intact up to 500°Cen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.4028/www.scientific.net/JNanoR.40.79
dc.description.statusPeer revieweden
dc.identifier.grantnumberEP/F019580/1en
dc.identifier.grantnumberEP/K015540/1en


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