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dc.contributor.authorChung, Chih-Chunen_US
dc.contributor.authorTsai, Ting -Weien_US
dc.contributor.authorWu, Hui -Pingen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.date.accessioned2018-08-21T05:54:30Z-
dc.date.available2018-08-21T05:54:30Z-
dc.date.issued2017-08-31en_US
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpcc.7b07958en_US
dc.identifier.urihttp://hdl.handle.net/11536/146036-
dc.description.abstract1-Decyl phosphonic acid (DPA) proved an effective p-doping additive to oxidize spiro-OMeTAD as a hole-transporting material (HTM) for nanostructured Sb2S3 extremely thin absorber (ETA) solar cells. DPA had the effect of enhancing the hole conductivities of spiro-OMeTAD in the presence of lithium bis(trifluoromethyl- sulfonyl)-imide (LiTFSI) to significantly improve the device performance. Transient photoelectric measurements and electrochemical impedance spectra of devices fabricated with varied additive conditions provided information about the charge- transport and recombination kinetics and hole conductivities for Sb2S3 devices with additives DPA and LiTFSI that exhibited superior performance. Thirty-five identical devices were fabricated to show the excellent reproducibility and long-term stability in air; the best Sb2S3 ETA device attained efficiency of power conversion 6.0%, which is twice that of a device using other typical additives (LiTFSI and 4-tert-butyl-pyridine) for spiro-OMeTAD serving as HTM.en_US
dc.language.isoen_USen_US
dc.titlePhosphonic Acid and Lithium Salt as Effective p-Dopants to Oxidize Spiro-OMeTAD for Mesoscopic Sb2S3 Solar Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.jpcc.7b07958en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Cen_US
dc.citation.volume121en_US
dc.citation.spage18472en_US
dc.citation.epage18479en_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:000409395700017en_US
Appears in Collections:Articles