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Preparation and characterization of garnet phosphor nanoparticles derived from oxalate coprecipitation

dc.citation.epage441en_US
dc.citation.issue2en_US
dc.citation.spage437en_US
dc.citation.volume144en_US
dc.citation.woscount38
dc.contributor.authorChen, TMen_US
dc.contributor.authorChen, SCen_US
dc.contributor.authorYu, CJen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:46:39Z
dc.date.available2014-12-08T15:46:39Z
dc.date.issued1999-05-01en_US
dc.description.abstractTerbium-activated Y3Al5O12 (YAG:Tb) phosphor nanoparticles with homogeneous grain size and crystallinity have been prepared at 1000 degrees C by heat treatment of a metal oxalate precursor derived from an alkaline coprecipitation route, The diffraction profile of as-prepared YAG:Tb nanoparticles can be indexed as a garnet structure and exhibits peak broadening phenonmenon, as revealed by X-ray diffraction (XRD) data. Grains of YAG:Tb nanoparticles appear to be irregularly spherical or elliptical and their sizes range from 60 to 70 nm, as indicated by morphological studies from bright-field transmission electron microscopy (TEM) imaging. Furthermore, the photoluminescence (PL) spectra of the (Y2.9Tb0.1)Al5O12 phase were investigated to determine the energy level of electron transition related to luminescence processes and the possible blue shift in the excitation or emission PL spectra, (C) 1999 Academic Press.en_US
dc.identifier.doi10.1006/jssc.1999.8202en_US
dc.identifier.issn0022-4596en_US
dc.identifier.journalJOURNAL OF SOLID STATE CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1006/jssc.1999.8202en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/31368
dc.identifier.wosnumberWOS:000080181300029
dc.language.isoen_USen_US
dc.subject(Y,Tb)(3)Al5O12en_US
dc.subjectphosphor nanoparticlesen_US
dc.subjectoxalate coprecipitationen_US
dc.subjectphotoluminescenceen_US
dc.titlePreparation and characterization of garnet phosphor nanoparticles derived from oxalate coprecipitationen_US
dc.typeArticleen_US

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