完整後設資料紀錄
DC 欄位語言
dc.contributor.authorDong, Ji-Yaoen_US
dc.contributor.authorLin, Wei-Haoen_US
dc.contributor.authorHsu, Yung-Jungen_US
dc.contributor.authorWong, David Shan-Hillen_US
dc.contributor.authorLu, Shih-Yuanen_US
dc.date.accessioned2014-12-08T15:20:51Z-
dc.date.available2014-12-08T15:20:51Z-
dc.date.issued2011en_US
dc.identifier.issn1466-8033en_US
dc.identifier.urihttp://hdl.handle.net/11536/14831-
dc.identifier.urihttp://dx.doi.org/10.1039/c1ce05503hen_US
dc.description.abstractUltrafast formation of ZnO mesocrystals was achieved with a facile, green, Tris-assisted, room temperature ionic liquid based antisolvent process. A deep eutectic solvent, formed by simply mixing and heating urea and choline chloride at 70 degrees C, served as the solvent for ZnO, whereas Tris-containing de-ionized water acted as the anti-solvent to trigger the ultrafast formation of ZnO mesocrystals at 70 degrees C. The product mesocrystals were mesoporous and near-single-crystalline with high specific surface areas, showing excellent photocatalytic activities toward photodegradation of methylene blue, comparable to that of a commercial photocatalyst, P-25 TiO(2), which is rarely achieved for pristine ZnO. The present approach is a general one and can be readily extended to production of mesocrystals of other functional metal oxides.en_US
dc.language.isoen_USen_US
dc.titleUltrafast formation of ZnO mesocrystals with excellent photocatalytic activities by a facile Tris-assisted antisolvent processen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c1ce05503hen_US
dc.identifier.journalCRYSTENGCOMMen_US
dc.citation.volume13en_US
dc.citation.issue20en_US
dc.citation.spage6218en_US
dc.citation.epage6222en_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:000295810300040-
dc.citation.woscount10-
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