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dc.contributor.authorLu, Chi-Kenen_US
dc.contributor.authorPi, Shu-Tingen_US
dc.contributor.authorMeng, Hsin-Feien_US
dc.date.accessioned2019-04-03T06:44:46Z-
dc.date.available2019-04-03T06:44:46Z-
dc.date.issued2007-05-01en_US
dc.identifier.issn1098-0121en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.75.195206en_US
dc.identifier.urihttp://hdl.handle.net/11536/10818-
dc.description.abstractThe generally observed higher hole mobility relative to electron mobility in conjugated polymers is explained with the defects and adsorbed molecular oxygen. Adsorption of the extrinsic molecular oxygen leads to that electrons are bound more tightly than holes by the traps in the originally symmetric electronic system. Hence, the mobility imbalance emerges from the asymmetric binding energies. Besides, the defects are the favored adsorption sites because the intermolecular attraction is enhanced due to stronger induced dipole-dipole interaction when gap defect levels appear.en_US
dc.language.isoen_USen_US
dc.titleEffect of defect-enhanced molecular oxygen adsorption on the imbalance of hole versus electron mobility in conjugated polymersen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.75.195206en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume75en_US
dc.citation.issue19en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department物理研究所zh_TW
dc.contributor.departmentInstitute of Physicsen_US
dc.identifier.wosnumberWOS:000246890800066en_US
dc.citation.woscount8en_US
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