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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMALO, Robin
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGLORIEUX, Benoit
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMORNET, Stéphane
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMUTELET, Brice
hal.structure.identifierLaboratoire de l'intégration, du matériau au système [IMS]
dc.contributor.authorVIGNAU, Laurence
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGARCIA, Alain
dc.date.issued2019
dc.identifier.issn0250-4707
dc.description.abstractEnY2.91Ce0.09Al5O12 is obtained by self-combustion, grinding and sol–gel coating. X-ray diffraction, transmission electron microscopy, photoluminescence and absorption measurements were used to identify the structural and optical properties of each step of the process. The process is composed of a combination of chemical and physico-chemical processesincluding combustion and thermal steps, followed by grinding, powder dispersion by acidic passivation, stabilization of particle dispersions with citrate ligands and embedding of yttrium aluminium garnet (YAG) particles into SiO2 shells usinga seeded growth process before drying. The initial state of the obtained powder is composed of 35 nm crystallites, sintered and agglomerated. The grinding step breaks the sintered bridge, while the passivation and citrate adsorption steps separate the particles by electrostatic repulsion before the silica coating. The optical characterizations are performed and compared separately for the powdered samples that represent the initial and final states of our process, and the dispersion sample represents the intermediate state of our process. The optical measurement revealed an important amount of optical defectsat the surface of the particles, compared with micrometric commercial particles. The grinding, nitric acid and citrate steps remove some of these defects. The final state of the sample still possesses lower quantum efficiency than that of a micrometric sample, but the SiO2 coating allows for a perfect separation of the particle, suitable for implementation in small devices.
dc.language.isoen
dc.publisherIndian Academy of Sciences
dc.subject.enSelf-combustion
dc.subject.enYAG
dc.subject.encore–shell
dc.subject.enSiO2 coating
dc.title.enSilica-coating of nano-Y3Al5O12:Ce3+ synthesized by self-combustion
dc.typeArticle de revue
dc.identifier.doi10.1007/s12034-018-1701-4
dc.subject.halChimie/Matériaux
bordeaux.journalBulletin of Materials Science
bordeaux.page6 (7 p.)
bordeaux.volume42
bordeaux.issue1
bordeaux.peerReviewedoui
hal.identifierhal-02048749
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02048749v1
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