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dc.contributor.authorYang, Min-Hanen_US
dc.contributor.authorChen, Po-Chinen_US
dc.contributor.authorTsai, Min-Chiaoen_US
dc.contributor.authorChen, Ting-Tingen_US
dc.contributor.authorChang, I-Chunen_US
dc.contributor.authorChiu, Hsin-Tienen_US
dc.contributor.authorLee, Chi-Youngen_US
dc.date.accessioned2014-12-08T15:33:57Z-
dc.date.available2014-12-08T15:33:57Z-
dc.date.issued2014en_US
dc.identifier.issn1466-8033en_US
dc.identifier.urihttp://hdl.handle.net/11536/23396-
dc.identifier.urihttp://dx.doi.org/10.1039/c3ce41750fen_US
dc.description.abstractIn this work, brookite TiO2 has been synthesized by a simple hydrothermal approach using sodium titanate as a precursor in the presence of a sodium fluoride aqueous solution. The ratio of brookite and anatase TiO2 can be tailored by the NaF concentration. In a concentrated NaF solution, high quality brookite TiO2 was acquired. Pure anatase nanoparticles were obtained in only deionized water. Moreover, the morphology and size of brookite TiO2 can be tailored by using various acid treated titanates which influence the stability of the building blocks and nucleation points of TiO2. Micro-sized flower-like brookite, submicro-sized urchin-like brookite and brookite nanorods with anatase nanoparticles were obtained. The micro-sized flower-like brookite remains the same shape and phase even at 800 degrees C, whereas obvious grains were formed on the matrix with brookite, rutile and anatase mixture phases at 900 degrees C. On the other hand, as the submicro-sized urchin-like brookite was heated, a rutile phase appeared at 750 degrees C and 100% grain-like rutile was obtained at 900 degrees C.en_US
dc.language.isoen_USen_US
dc.titleAnatase and brookite TiO2 with various morphologies and their proposed building blocken_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3ce41750fen_US
dc.identifier.journalCRYSTENGCOMMen_US
dc.citation.volume16en_US
dc.citation.issue3en_US
dc.citation.spage441en_US
dc.citation.epage447en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000328549700017-
dc.citation.woscount2-
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