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dc.contributor.authorHsieh, Ting-Huanen_US
dc.contributor.authorChen, Jui-Yuanen_US
dc.contributor.authorHuang, Chun-Weien_US
dc.contributor.authorWu, Wen-Weien_US
dc.date.accessioned2017-04-21T06:56:37Z-
dc.date.available2017-04-21T06:56:37Z-
dc.date.issued2016-06-28en_US
dc.identifier.issn0897-4756en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.chemmater.6b02040en_US
dc.identifier.urihttp://hdl.handle.net/11536/133916-
dc.description.abstractHydrothermal synthesis is commonly used to produce a large area of ZnO nanowires because of its simple and inexpensive process. However, the mechanism of hydrothermal synthesis remains unknown. In this work, zinc acetate and HMTA dissolved in deionized water as a precursor solution were sealed in a liquid cell for observation by in situ transmission electron microscopy. The growth of ZnO nanowires was classified into two steps. The first step was the nucleation and growth of ZnO nanoparticles. The ZnO nanoparticles grew as a result of either isotropic monomer attachment on the {2 (11) over bar0} and {0 (1) over bar 10} surfaces or coalescence of nanoparticles in the same crystal arrangement. The second step was the anisotropic growth of ZnO nanoparticles into nanowires on the (0001) surface. Because the (0001) surface is Zn-terminated with positive charges that can attract the negatively charged monomers, i.e., [Zn(OH)(4)](2-),the monomers tended to deposit on the (0001) surface, resulting in ZnO nanowires growing along the [0001] direction. Moreover, the growth of ZnO nanowires was identified to be a reaction controlled system. The direct observation of the dynamic process sheds light on the hydrothermal synthesis method.en_US
dc.language.isoen_USen_US
dc.titleObserving Growth of Nanostructured ZnO in Liquiden_US
dc.identifier.doi10.1021/acs.chemmater.6b02040en_US
dc.identifier.journalCHEMISTRY OF MATERIALSen_US
dc.citation.volume28en_US
dc.citation.issue12en_US
dc.citation.spage4507en_US
dc.citation.epage4511en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000378973100049en_US
Appears in Collections:Articles