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dc.contributor.authorWu, Jyh-Lihen_US
dc.contributor.authorChen, Fang-Chungen_US
dc.contributor.authorHsiao, Yu-Shengen_US
dc.contributor.authorChien, Fan-Chingen_US
dc.contributor.authorChen, Peilinen_US
dc.contributor.authorKuo, Chun-Hongen_US
dc.contributor.authorHuang, Michael H.en_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.date.accessioned2014-12-08T15:37:30Z-
dc.date.available2014-12-08T15:37:30Z-
dc.date.issued2011-02-01en_US
dc.identifier.issn1936-0851en_US
dc.identifier.urihttp://dx.doi.org/10.1021/nn102295pen_US
dc.identifier.urihttp://hdl.handle.net/11536/25812-
dc.description.abstractWe have systematically explored how plasmonic effects influence the characteristics of polymer photovoltaic devices (OPVs) incorporating a blend of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM). We blended gold nanoparticles (Au NPs) into the anodic buffer layer to trigger localized surface plasmon resonance (LSPR), which enhanced the performance of the OPVs without dramatically sacrificing their electrical properties. Steady state photoluminescence (PL) measurements revealed a significant increase in fluorescence intensity, which we attribute to the increased light absorption in P3HT Induced by the LSPR. As a result, the rate of generation of excitons was enhanced significantly. Furthermore, dynamic PL measurements revealed that the LSPR notably reduced the lifetime of photogenerated excitons In the active blend, suggesting that interplay between the surface plasmons and excitons facilitated the charge transfer process. This phenomenon reduced the recombination level of geminate excitons and, thereby, Increased the probability of exciton dissociation. Accordingly, both the photocurrents and fill factors of the OPV devices were enhanced significantly. The primary origin of this improved performance was local enhancement of the electromagnetic field surrounding the Au NPs. The power conversion efficiency of the OPV device incorporating the Au NPs improved to 4.24% from a value of 3.57% for the device fabricated without Au NPs.en_US
dc.language.isoen_USen_US
dc.subjectpolymer photovoltaicsen_US
dc.subjectgold nanoparticlesen_US
dc.subjectsurface plasmonen_US
dc.subjectphotoluminescenceen_US
dc.subjectexciton lifetimeen_US
dc.titleSurface Plasmonic Effects of Metallic Nanoparticles on the Performance of Polymer Bulk Heterojunction Solar Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/nn102295pen_US
dc.identifier.journalACS NANOen_US
dc.citation.volume5en_US
dc.citation.issue2en_US
dc.citation.spage959en_US
dc.citation.epage967en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department光電工程學系zh_TW
dc.contributor.department顯示科技研究所zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentDepartment of Photonicsen_US
dc.contributor.departmentInstitute of Displayen_US
dc.identifier.wosnumberWOS:000287553800031-
dc.citation.woscount270-
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