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dc.contributor.authorUeno, Koseien_US
dc.contributor.authorOshikiri, Tomoyaen_US
dc.contributor.authorSun, Quanen_US
dc.contributor.authorShi, Xuen_US
dc.contributor.authorMisawa, Hiroakien_US
dc.date.accessioned2018-08-21T05:53:30Z-
dc.date.available2018-08-21T05:53:30Z-
dc.date.issued2018-03-28en_US
dc.identifier.issn0009-2665en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.chemrev.7b00235en_US
dc.identifier.urihttp://hdl.handle.net/11536/144781-
dc.description.abstractMetallic nanoparticles such as silver and gold show localized surface plasmon resonances (LSPRs), which are associated with near-field enhancement effects in the vicinity of nanoparticles. Therefore, strong light-matter interaction is induced by the near-field enhancement effects of LSPRs. Because the resonant wavelength of LSPRs can be easily controlled by the size and shape of the metallic nanoparticles in the visible and near-infrared wavelength range, LSPRs have received considerable attention as optical antennae for light energy conversion systems such as solar cells. LSPRs decay very quickly as a result of light scattering and excitation of electron-hole pairs in the metal itself. However, in addition to the near-field enhancement effect, this light scattering and electron-hole pair excitation, which are known to cause loss of LSPRs, can be utilized as a solar cell enhancement mechanism. Here, we focus on plasmonic solid-state solar cells. The mechanisms of the light scattering by LSPRs, near-field enhancement, and plasmon-induced charge separation based on electron-hole pair excitations can be clarified. We review the related studies from the viewpoint of these mechanisms rather than material science.en_US
dc.language.isoen_USen_US
dc.titleSolid-State Plasmonic Solar Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.chemrev.7b00235en_US
dc.identifier.journalCHEMICAL REVIEWSen_US
dc.citation.volume118en_US
dc.citation.spage2955en_US
dc.citation.epage2993en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000428972300005en_US
Appears in Collections:Articles