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dc.contributor.authorAbate, Seid Yimeren_US
dc.contributor.authorWu, Wen-Tien_US
dc.contributor.authorPola, Someshwaren_US
dc.contributor.authorTao, Yu-Taien_US
dc.date.accessioned2018-08-21T05:53:20Z-
dc.date.available2018-08-21T05:53:20Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7ra13744cen_US
dc.identifier.urihttp://hdl.handle.net/11536/144560-
dc.description.abstractFabrication of perovskite solar cells (PSCs) in a simple way with high efficiency and stability remains a challenge. In this study, silver nanoparticles (Ag NPs) were sandwiched between two compact TiO2 layers through a facile process of spin-coating an ethanolic AgNO3 solution, followed by thermal annealing. The presence of Ag NPs in the electron-transporting layer of TiO2 improved the light input to the device, the morphology of the perovskite film prepared on top, and eliminated leakage current. Photoluminescence and electron mobility studies revealed that the incorporation of Ag NPs in the ETL of the planar PSC device facilitated the electron-hole separation and promoted charge extraction and transport from perovskite to ETL. Hysteresis-free devices with incorporated Ag NPs gave a high average short-circuit current density (J(sc)) of 22.91 +/- 0.39 mA cm(-2) and maximum power conversion efficiency of 17.25%. The devices also showed enhanced stability versus a control device without embedded Ag NPs. The possible reasons for the improvement are analyzed and discussed.en_US
dc.language.isoen_USen_US
dc.titleCompact TiO2 films with sandwiched Ag nanoparticles as electron-collecting layer in planar type perovskite solar cells: improvement in efficiency and stabilityen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7ra13744cen_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume8en_US
dc.citation.spage7847en_US
dc.citation.epage7854en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000425647000060en_US
Appears in Collections:Articles