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dc.contributor.authorChoi, Hyunbongen_US
dc.contributor.authorChen, Wei Taen_US
dc.contributor.authorKamat, Prashant V.en_US
dc.date.accessioned2014-12-08T15:23:15Z-
dc.date.available2014-12-08T15:23:15Z-
dc.date.issued2012-05-01en_US
dc.identifier.issn1936-0851en_US
dc.identifier.urihttp://hdl.handle.net/11536/16322-
dc.description.abstractNeighboring metal nanoparticles influence photovoltaic and photocatalytic behavior of semiconductor nanostructures either through Fermi level equilibration by accepting electrons or inducing localized surface plasmon effects. By employing SiO2- and TiO2-capped Au nanoparticles we have identified the mechanism with which the performance of dye-sensitized solar cells (DSSC) is Influenced by the neighboring metal nanoparticles. The efficiency of an N719 dye-sensitized solar cell (9.3%) increased to 10.2% upon incorporation of 0.7% Au@SiO2 and to 9.8% upon loading of 0.7% Au@TiO2 nanoparticles. The plasmonic effect as monitored by introducing Au@SiO2 in DSSC produces higher photocurrent. However, Au nanoparticles undergo charge equilibration with TiO2 nanoparticles and shift the apparent Fermi level of the composite to more negative potentials. As a result, Au@TiO2 nanoparticle-embedded DSSC exhibit higher photovoltage. A better understanding of these two effects is crucial in exploiting the beneficial aspects of metal nanoparticles in photovoltaics.en_US
dc.language.isoen_USen_US
dc.subjectsemiconductor-metal compositeen_US
dc.subjectphotocatalystsen_US
dc.subjectTiO2en_US
dc.subjectcore-shell nanoparticlesen_US
dc.subjectlocalized surface plasmonen_US
dc.subjectsolar energy conversionen_US
dc.subjectelectron storageen_US
dc.subjectFermi level equilibrationen_US
dc.titleKnow Thy Nano Neighbor. Plasmonic versus Electron Charging Effects of Metal Nanoparticles in Dye-Sensitized Solar Cellsen_US
dc.typeArticleen_US
dc.identifier.journalACS NANOen_US
dc.citation.volume6en_US
dc.citation.issue5en_US
dc.citation.epage4418en_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:000304231700085-
dc.citation.woscount100-
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