完整後設資料紀錄
DC 欄位語言
dc.contributor.authorJokar, Efaten_US
dc.contributor.authorChien, Cheng-Hsunen_US
dc.contributor.authorFathi, Amiren_US
dc.contributor.authorRameez, Mohammaden_US
dc.contributor.authorChang, Yu-Haoen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.date.accessioned2019-04-02T06:00:45Z-
dc.date.available2019-04-02T06:00:45Z-
dc.date.issued2018-09-01en_US
dc.identifier.issn1754-5692en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c8ee00956ben_US
dc.identifier.urihttp://hdl.handle.net/11536/148185-
dc.description.abstractWe investigated the doping effect of bulky organic cations with ethylenediammonium diiodide (EDAI(2)) and butylammonium iodide (BAI) as additives to passivate surface defects, to control the film morphology and to improve the crystallinity for inverted planar FASnI(3) perovskite solar cells. The addition of BAI altered significantly the orientation of crystal growth and improved the connectivity of the crystal grains, but the existence of pinholes in the surface of the pristine FASnI(3) films was unavoidable; this effect impeded further improvement of the device performance (PCE 5.5%), which is nevertheless superior to that of a pristine FASnI(3) film (PCE 4.0%). The addition of EDAI(2) had the effect of curing the pinhole problem, passivating the surface defect states, preventing Sn2+/Sn4+ oxidation and inducing slow relaxation of the crystal structure. In the presence of the EDAI(2) additive (1%), the FASnI(3) device attained the best initial efficiency, 7.4%, and the device performance continuously increased as a function of duration of storage; the maximum PCE, 8.9%, was obtained for a device stored in a glove box for over 1400 h with only slight degradation for storage beyond 2000 h. The observed slow passivation of surface defects and relaxation of crystal strain were verified with X-ray diffraction, X-ray photoelectron spectroscopy and photoluminescence decay techniques.en_US
dc.language.isoen_USen_US
dc.titleSlow surface passivation and crystal relaxation with additives to improve device performance and durability for tin-based perovskite solar cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c8ee00956ben_US
dc.identifier.journalENERGY & ENVIRONMENTAL SCIENCEen_US
dc.citation.volume11en_US
dc.citation.spage2353en_US
dc.citation.epage2362en_US
dc.contributor.department交大名義發表zh_TW
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.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000445215400005en_US
dc.citation.woscount8en_US
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