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dc.contributor.authorNarra, Sudhakaren_US
dc.contributor.authorChung, Chih-Chunen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.contributor.authorShigeto, Shinsukeen_US
dc.date.accessioned2017-04-21T06:56:36Z-
dc.date.available2017-04-21T06:56:36Z-
dc.date.issued2016-07-07en_US
dc.identifier.issn1948-7185en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpclett.6b01111en_US
dc.identifier.urihttp://hdl.handle.net/11536/133882-
dc.description.abstractSolar cells based on organometal-halide perovskites such as CH3NH3PbI3 have emerged as a promising next generation photovoltaic system, but the underlying photo physics and photochemistry remain to be established because of the limited availability of methods to implement the simultaneous and direct measurement of various charge carriers and ions that play a crucial role in the operating device. We used nanosecond time-resolved infrared (IR) spectroscopy to investigate, with high molecular specificity, distinct transient species that are formed in perovskite solar cells after photoexcitation. In CH3NH3PbI3 planar-heterojuction solar cells, we simultaneously observed infrared spectral signatures that are associated with an intraband transition of conduction-band electrons, Fano resonance, and the spiro-OMeTAD cation having an exceptionally short lifetime of 1.0 mu s (at similar to 4485 cm(-1)). The present results show that the time resolved IR method offers a unique capability to elucidate these important transients in perovskite solar cells and their dynamic interplay in a comprehensive manner.en_US
dc.language.isoen_USen_US
dc.titleSimultaneous Observation of an Intraband Transition and Distinct Transient Species in the Infrared Region for Perovskite Solar Cellsen_US
dc.identifier.doi10.1021/acs.jpclett.6b01111en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY LETTERSen_US
dc.citation.volume7en_US
dc.citation.issue13en_US
dc.citation.spage2450en_US
dc.citation.epage2455en_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:000379457400027en_US
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