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dc.contributor.authorChien, Shang-Chiehen_US
dc.contributor.authorChen, Fang-Chungen_US
dc.contributor.authorChung, Ming-Kaien_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.date.accessioned2014-12-08T15:21:29Z-
dc.date.available2014-12-08T15:21:29Z-
dc.date.issued2012-01-12en_US
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp211089nen_US
dc.identifier.urihttp://hdl.handle.net/11536/15260-
dc.description.abstractIn this study, we have systematically investigated the mechanism behind the formation of nanoscale self-assembled polymer buffer layers at the cathode interfaces of polymer solar cells. Poly(ethylene glycol) (PEG) molecules in a polymer blend, comprising poly(3-hexylthiophene) and [6,6]-phenyl-C-61-butyric acid methyl ester, spontaneously migrated to the surface where they reacted with the Al cathode to form ohmic contacts. In terms of thermodynamics, the surface energy of the substrates played an important role in triggering the vertical-type morphology. From a kinetics point of view, PEG polymers having lower molecular weights readily underwent vertical phase separation prior to solidification of the polymer films, due to their higher mobilities, whereas PEG polymers of higher molecular weights tended to become trapped in the active layer. Employing this knowledge, we prepared organic photovoltaic cells exhibiting both high efficiency and appreciable improvement in stability.en_US
dc.language.isoen_USen_US
dc.titleSelf-Assembled Poly(ethylene glycol) Buffer Layers in Polymer Solar Cells: Toward Superior Stability and Efficiencyen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp211089nen_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Cen_US
dc.citation.volume116en_US
dc.citation.issue1en_US
dc.citation.spage1354en_US
dc.citation.epage1360en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department光電工程學系zh_TW
dc.contributor.department顯示科技研究所zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentDepartment of Photonicsen_US
dc.contributor.departmentInstitute of Displayen_US
dc.identifier.wosnumberWOS:000298978700171-
dc.citation.woscount14-
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