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Facile synthesis of a 56 pi-electron 1,2-dihydromethano-[60]PCBM and its application for thermally stable polymer solar cells

dc.citation.epage10084en_US
dc.citation.issue36en_US
dc.citation.spage10082en_US
dc.citation.volume47en_US
dc.citation.woscount45
dc.contributor.authorLi, Chang-Zhien_US
dc.contributor.authorChien, Shang-Chiehen_US
dc.contributor.authorYip, Hin-Lapen_US
dc.contributor.authorChueh, Chu-Chenen_US
dc.contributor.authorChen, Fang-Chungen_US
dc.contributor.authorMatsuo, Yutakaen_US
dc.contributor.authorNakamura, Eiichien_US
dc.contributor.authorJen, Alex K. -Y.en_US
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 Photonicsen_US
dc.contributor.departmentInstitute of Displayen_US
dc.date.accessioned2014-12-08T15:37:41Z
dc.date.available2014-12-08T15:37:41Z
dc.date.issued2011en_US
dc.description.abstractA facile synthesis was employed to make a 56 pi-electron methano-PC(61)BM with a very small 1,2-dihydromethano (CH(2)) group. This new fullerene derivative possesses high electron mobility (0.014 cm(2) V(-1) s(-1)) and higher LUMO energy level (0.15 eV) than PC(61)BM. Bulk hetero-junction devices based on using poly(3-hexylthiophene) and methano-PC(61)BM as active layer exhibited better performance and thermal stability than those using the PC(61)BM analogue.en_US
dc.identifier.doi10.1039/c1cc14446den_US
dc.identifier.issn1359-7345en_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c1cc14446den_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/25923
dc.identifier.wosnumberWOS:000294433900036
dc.language.isoen_USen_US
dc.titleFacile synthesis of a 56 pi-electron 1,2-dihydromethano-[60]PCBM and its application for thermally stable polymer solar cellsen_US
dc.typeArticleen_US

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