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dc.contributor.authorTse, SCen_US
dc.contributor.authorSo, SKen_US
dc.contributor.authorYeung, MYen_US
dc.contributor.authorLo, CFen_US
dc.contributor.authorWen, SWen_US
dc.contributor.authorChen, CHen_US
dc.date.accessioned2014-12-08T15:16:35Z-
dc.date.available2014-12-08T15:16:35Z-
dc.date.issued2006-05-10en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2006.02.079en_US
dc.identifier.urihttp://hdl.handle.net/11536/12254-
dc.description.abstractThe charge transporting properties of t-butylated 9,10-di(2-naphthyl)anthracene (ADN) compounds have been investigated experimentally and computationally in relation to their molecular structures. The ADN compounds are found to be ambipolar with both electron and hole mobilities in the range of 1-4 x 10(-7) cm(2) V-1 s(-1) (electric field 0.5-0.8 MV/cm). As the degree of t-butylation increases, the carrier mobility decreases progressively. The mobility reduction was examined by Marcus theory of reorganization energies. All ADN compounds possess similar reorganization energies of similar to 0.3 eV. The reduction of carrier mobilities with increasing t-butylation can be attributed to a decrease in the charge-transfer integral or the wavefunction overlap. (c) 2006 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleThe role of charge-transfer integral in determining and engineering the carrier mobilities of 9,10-di(2-naphthyl)anthracene compoundsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2006.02.079en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume422en_US
dc.citation.issue4-6en_US
dc.citation.spage354en_US
dc.citation.epage357en_US
dc.contributor.department友訊交大聯合研發中心zh_TW
dc.contributor.departmentD Link NCTU Joint Res Ctren_US
dc.identifier.wosnumberWOS:000237840200012-
dc.citation.woscount28-
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