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dc.contributor.authorPan, Ko-Yingen_US
dc.contributor.authorLiang, Yi-Fanen_US
dc.contributor.authorPu, Ying-Chihen_US
dc.contributor.authorHsu, Yung-Jungen_US
dc.contributor.authorYeh, Jien-Weien_US
dc.contributor.authorShih, Han C.en_US
dc.date.accessioned2019-04-02T06:00:46Z-
dc.date.available2019-04-02T06:00:46Z-
dc.date.issued2014-08-30en_US
dc.identifier.issn0169-4332en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apsusc.2014.05.074en_US
dc.identifier.urihttp://hdl.handle.net/11536/147741-
dc.description.abstractAbundant core-shelled silica-silver nanospheres with uniform diameter and morphology were successfully synthesized by Stober and seed-mediated method, in sequence. By the different additions of glucose, the silver nanoparticles were deposited on silica spheres by redox reaction, which well controlled in the range from 10 to 50 nm. The surface plasmon resonance absorption band shifted toward infra-red region and became broader gradually during the dimensions of silver nanoparticles were increased in the growth range. The amazing data imply that using core-shelled silica-silver nanospheres efficiently enhances the degradation of the organic pollutants under solar energy, which means the core-shelled silica-silver nanospheres is not only a cost-effective route but an energy-saving way to our planet. (C) 2014 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectCore-shelled silica silver nanospheres (SiO2@Ag NSs)en_US
dc.subjectSeed-mediated methoden_US
dc.subjectSurface plasmon resonance (SPR)en_US
dc.subjectInfra-red regionen_US
dc.subjectRed shiften_US
dc.titleStudies on the photocatalysis of core-shelled SiO2-Ag nanospheres by controlled surface plasmon resonance under visible lighten_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apsusc.2014.05.074en_US
dc.identifier.journalAPPLIED SURFACE SCIENCEen_US
dc.citation.volume311en_US
dc.citation.spage399en_US
dc.citation.epage404en_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:000339037200057en_US
dc.citation.woscount18en_US
Appears in Collections:Articles