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dc.contributor.authorHuang, Jen-Hsienen_US
dc.contributor.authorIbrahem, Mohammed Azizen_US
dc.contributor.authorChu, Chih-Weien_US
dc.date.accessioned2015-12-02T02:59:18Z-
dc.date.available2015-12-02T02:59:18Z-
dc.date.issued2015-08-01en_US
dc.identifier.issn1062-7995en_US
dc.identifier.urihttp://dx.doi.org/10.1002/pip.2522en_US
dc.identifier.urihttp://hdl.handle.net/11536/128019-
dc.description.abstractIn this study, an air-stable bulk heterojunction organic solar cell demonstrated by utilization of titanium oxide (TiO2) nanoparticles as a hole blocking layer was prepared through high-energy grinding method. The large clumps of the anatase TiO2 underwent deaggregation to form a stable dispersed solution during the grinding process. The resultant suspension can form a uniform and smooth TiO2 film through spin coating on various substrates. Because of substantial oxygen and water protection effect of TiO2 thin film, the bulk heterojunction solar cells exhibit a significant long-term stability. It is also found that the cell performance can be promoted dramatically after ultraviolet activation. The mechanism responsible for the enhanced cell efficiency was also investigated. This solution-based method does not require surfactants, thus preserving the intrinsic electronic and optical properties of TiO2 that makes these proposed buffer layers quite attractive for next-generation flexible devices appealing high conductivity and transparency. Copyright (c) 2014 John Wiley & Sons, Ltd.en_US
dc.language.isoen_USen_US
dc.subjectsolar cellsen_US
dc.subjectsolution processen_US
dc.subjectTiO2en_US
dc.subjectelectronen_US
dc.subjectbuffer layeren_US
dc.subjectstabilityen_US
dc.titleWet-milled anatase titanium oxide nanoparticles as a buffer layer for air-stable bulk heterojunction solar cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/pip.2522en_US
dc.identifier.journalPROGRESS IN PHOTOVOLTAICSen_US
dc.citation.volume23en_US
dc.citation.spage1017en_US
dc.citation.epage1024en_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000357792700008en_US
dc.citation.woscount0en_US
Appears in Collections:Articles