完整後設資料紀錄
DC 欄位語言
dc.contributor.authorLiang, Wen-Ien_US
dc.contributor.authorZhang, Xiaoweien_US
dc.contributor.authorZan, Yunlongen_US
dc.contributor.authorPan, Mingen_US
dc.contributor.authorCzarnik, Coryen_US
dc.contributor.authorBustillo, Karenen_US
dc.contributor.authorXu, Junen_US
dc.contributor.authorChu, Ying-Haoen_US
dc.contributor.authorZheng, Haimeien_US
dc.date.accessioned2016-03-28T00:04:07Z-
dc.date.available2016-03-28T00:04:07Z-
dc.date.issued2015-12-02en_US
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jacs.5610076en_US
dc.identifier.urihttp://hdl.handle.net/11536/129340-
dc.description.abstractWe report an in situ study of Fe3Pt-Fe2O3 coreshell nanoparticle growth using liquid cell transmission electron microscopy. By controlling the Fe-to-Pt ratio in the precursor solution, we achieved the growth of nanoparticles with the formation of an ironplatinum alloy core followed by an iron oxide shell in the electron beam-induced reactions. There was no substantial change in the growth kinetics of the iron oxide shell after the FePt alloy core stopped growing. The core growth was arrested by depletion of the Pt precursor. Heteroepitaxy of Fe3Pt [101] (core)||alpha-Fe2O3 [111] (shell) was observed in most of the nanoparticles, while a polycrystalline iron oxide shell is developed eventually for strain relaxation. Our studies suggest that Pt atoms catalyze the reduction of Fe ions to form the Fe3Pt alloy core, and when Pt is depleted, a direct precipitation of iron oxide results in the core-shell nanostructure formation.en_US
dc.language.isoen_USen_US
dc.titleIn Situ Study of Fe3Pt-Fe2O3 Core-Shell Nanoparticle Formationen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jacs.5610076en_US
dc.identifier.journalJOURNAL OF THE AMERICAN CHEMICAL SOCIETYen_US
dc.citation.volume137en_US
dc.citation.issue47en_US
dc.citation.spage14850en_US
dc.citation.epage14853en_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:000365930600006en_US
dc.citation.woscount0en_US
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