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dc.contributor.authorChou, Shu-Huaen_US
dc.contributor.authorKang, Hao-Weien_US
dc.contributor.authorChang, Shu-Tingen_US
dc.contributor.authorWu, Kuan-Yien_US
dc.contributor.authorBazan, Guillermo C.en_US
dc.contributor.authorWang, Chien-Lungen_US
dc.contributor.authorLin, Hong-Linen_US
dc.contributor.authorChang, Jung-Haoen_US
dc.contributor.authorLin, Hao-Wuen_US
dc.contributor.authorHuang, Yu-Chingen_US
dc.contributor.authorTsao, Cheng-Sien_US
dc.contributor.authorWong, Ken-Tsungen_US
dc.date.accessioned2017-04-21T06:56:22Z-
dc.date.available2017-04-21T06:56:22Z-
dc.date.issued2016-07-20en_US
dc.identifier.issn1944-8244en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acsami.6b03371en_US
dc.identifier.urihttp://hdl.handle.net/11536/132696-
dc.description.abstractTwo D-pi-A-A molecules (MIDTP and TIDTP) composed of an electron-rich ditolylamino group (D) and an electron-deficient 5-dicyanovinylenylpyrimidine (A-A) fragment bridged together with indeno[1,2-b]thiophene (IDT) were synthesized. These molecules provide an opportunity to examine in-depth the impact of side-chain variations (methyl vs p-tolyl) on the crystallization behaviors, solid-state morphology, physical properties, and optoelectronic characteristics relevant for practical applications. X-ray analyses on single-crystal structures indicate that methyl-substituted MIDTP forms coplanar antiparallel dimers via C-H center dot center dot center dot S interactions and organizes into an ordered slip-staircase arrays. In contrast, p-tolyl-bearing TIDTP shows cofacial centrosymmetric dimers via pi-pi interactions and packs into a less-ordered layered structures. The X-ray diffraction analyses upon thermal treatment are consistent with a superior crystallinity of MIDTP, as compared to that of TIDTP. This difference indicates a greater propensity to organization by introduction of the smaller methyl group versus the bulkier p-tolyl group. The increased propensity for order by MIDTP facilitates the crystallization of MIDTP in both solution-processed and vacuum-deposited thin films. MIDTP forms solution-processed single-crystal arrays that deliver OFET hole mobility of 6.56 x 10(-4) cm(2) V-1 s(-1), whereas TIDTP only forms amorhpous films that gave lower hole mobility of 1.34 x 10(-5) cm(2) V-1 s(-1). MIDTP and TIDTP were utilized to serve as donors together with C-70 as acceptor in the fabrication of small-molecule organic solar cells (SMOSCs) with planar heterojunction (PHJ) or planar-mixed heterojunction (PMHJ) device architectures. OPV devices based on higher crystalline MIDTP delivered power conversion efficiencies (PCEs) of 2.5% and 4.3% for PHJ and PMHJ device, respectively, which are higher than those of TIDTP-based cells. The improved PCEs of MIDTP-based devices are attributed to better hole-transport character.en_US
dc.language.isoen_USen_US
dc.subjectorganic solar cellen_US
dc.subjectplanar-mixed heterojunctionen_US
dc.subjectorganic field effect transistorsen_US
dc.subjectpush-pull moleculesen_US
dc.subjectsubstitution effecten_US
dc.subjectcrystallinityen_US
dc.titleCofacial Versus Coplanar Arrangement in Centrosymmetric Packing Dimers of Dipolar Small Molecules: Structural Effects on the Crystallization Behaviors and Optoelectronic Characteristicsen_US
dc.identifier.doi10.1021/acsami.6b03371en_US
dc.identifier.journalACS APPLIED MATERIALS & INTERFACESen_US
dc.citation.volume8en_US
dc.citation.issue28en_US
dc.citation.spage18266en_US
dc.citation.epage18276en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000380298400058en_US
Appears in Collections:Articles