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dc.contributor.authorDalod, Antoine Robert Marie
dc.contributor.authorGrendal, Ola Gjønnes
dc.contributor.authorSkjærvø, Susanne Linn
dc.contributor.authorInzani, Katherine
dc.contributor.authorSelbach, Sverre Magnus
dc.contributor.authorHenriksen, Lars
dc.contributor.authorvan Beek, Wouter
dc.contributor.authorGrande, Tor
dc.contributor.authorEinarsrud, Mari-Ann
dc.date.accessioned2017-09-26T07:20:13Z
dc.date.available2017-09-26T07:20:13Z
dc.date.created2017-06-01T09:24:25Z
dc.date.issued2017
dc.identifier.citationJournal of Physical Chemistry C. 2017, 121 (21), 11897-11906.nb_NO
dc.identifier.issn1932-7447
dc.identifier.urihttp://hdl.handle.net/11250/2456643
dc.description.abstractUnderstanding growth mechanisms and the role of surface functionalization is of key importance to control shape and morphology of nanoparticles and their properties. Here, we describe the growth mechanism and the effect of hydrothermal synthesis parameters (pH, time, and precursor/functionalization agent ratio) during in situ functionalization of anatase TiO2 nanoparticles with 3-aminopropyltriethoxysilane. Elongated crystallographically oriented TiO2 nanoparticles were formed by oriented attachment mechanism in addition to spherical nanoparticles. The growth mechanism is determined by a combination of ex situ techniques such as high-resolution transmission electron microscopy combined with in situ synchrotron X-ray diffraction and density functional theory calculations. Oriented attachment induced by the functionalization agent is shown to be the origin of the elongation of the nanoparticles, as only spherical nanoparticles were formed in the absence of surface functionalization. Finally, it was shown that the amount and the size of the elongated nanoparticles can be tuned by adjusting pH.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleControlling Oriented Attachment and in Situ Functionalization of TiO2 Nanoparticles During Hydrothermal Synthesis with APTESnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber11897-11906nb_NO
dc.source.volume121nb_NO
dc.source.journalJournal of Physical Chemistry Cnb_NO
dc.source.issue21nb_NO
dc.identifier.doi10.1021/acs.jpcc.7b02604
dc.identifier.cristin1473385
dc.relation.projectNorges forskningsråd: 235210nb_NO
dc.relation.projectNotur/NorStore: NN9264Knb_NO
dc.description.localcodeThis is the authors' accepted and refereed manuscript to the article. Locked until 2 May 2018 due to copyright restrictionsnb_NO
cristin.unitcode194,66,35,0
cristin.unitnameInstitutt for materialteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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