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dc.contributor.authorShahbazi, Saeeden_US
dc.contributor.authorTsai, Cheng-Minen_US
dc.contributor.authorNarra, Sudhakaren_US
dc.contributor.authorWang, Chi-Yungen_US
dc.contributor.authorShiu, Hau-Shiangen_US
dc.contributor.authorAfshar, Shahraraen_US
dc.contributor.authorTaghavinia, Nimaen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.date.accessioned2017-04-21T06:56:38Z-
dc.date.available2017-04-21T06:56:38Z-
dc.date.issued2017-02-23en_US
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpcc.6b09722en_US
dc.identifier.urihttp://hdl.handle.net/11536/133158-
dc.description.abstractWe report a simple synthetic approach to grow uniform CH3NH3PbI3 perovskite (PSK) layers free of pinholes via ciE varied portions of silver iodide (AgI) added to the precursor solution. XRD/EDS elemental mapping experiments demonstrated nearly uniform Ag distribution inside the perovskite film. When the 1% AgI- assisted perovskite films were fabricated into a p-i-n planar device, the a) photovoltaic performance was enhanced by similar to 30% (PCE increased from 9.5% to 12.0%) relative to the standard cell without added AgI. . Measurement of electronic properties using a hall setup indicated that perovskite films show p-type character after Ag doping, whereas the film is n-type without Ag. Transients of photoluminescence of perovskite films with and without AgI additive deposited on glass, p-type (PEDOT:PSS), and n-type (TiO2) contact layers were recorded with a time-correlated single-photon counting (TCSPC) technique. The TCSPC results indicate that addition of AgI inside perovskite in contact with PEDOT:PSS accelerated the hole-extraction motion whereas that in contact with TiO2 led to a decelerated electron extraction, in agreement with the trend observed from the photovoltaic results. The silver cationic dopant inside the perovskite films had hence an effect of controlling the morphology to improve photovoltaic performance for devices with p-i-n configuration.en_US
dc.language.isoen_USen_US
dc.titleAg Doping of Organometal Lead Halide Perovskites: Morphology Modification and p-Type Characteren_US
dc.identifier.doi10.1021/acs.jpcc.6b09722en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Cen_US
dc.citation.volume121en_US
dc.citation.issue7en_US
dc.citation.spage3673en_US
dc.citation.epage3679en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000394924800001en_US
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