Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Chou, Shu-Hua | en_US |
dc.contributor.author | Kang, Hao-Wei | en_US |
dc.contributor.author | Chang, Shu-Ting | en_US |
dc.contributor.author | Wu, Kuan-Yi | en_US |
dc.contributor.author | Bazan, Guillermo C. | en_US |
dc.contributor.author | Wang, Chien-Lung | en_US |
dc.contributor.author | Lin, Hong-Lin | en_US |
dc.contributor.author | Chang, Jung-Hao | en_US |
dc.contributor.author | Lin, Hao-Wu | en_US |
dc.contributor.author | Huang, Yu-Ching | en_US |
dc.contributor.author | Tsao, Cheng-Si | en_US |
dc.contributor.author | Wong, Ken-Tsung | en_US |
dc.date.accessioned | 2017-04-21T06:56:22Z | - |
dc.date.available | 2017-04-21T06:56:22Z | - |
dc.date.issued | 2016-07-20 | en_US |
dc.identifier.issn | 1944-8244 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/acsami.6b03371 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/132696 | - |
dc.description.abstract | Two 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.iso | en_US | en_US |
dc.subject | organic solar cell | en_US |
dc.subject | planar-mixed heterojunction | en_US |
dc.subject | organic field effect transistors | en_US |
dc.subject | push-pull molecules | en_US |
dc.subject | substitution effect | en_US |
dc.subject | crystallinity | en_US |
dc.title | Cofacial Versus Coplanar Arrangement in Centrosymmetric Packing Dimers of Dipolar Small Molecules: Structural Effects on the Crystallization Behaviors and Optoelectronic Characteristics | en_US |
dc.identifier.doi | 10.1021/acsami.6b03371 | en_US |
dc.identifier.journal | ACS APPLIED MATERIALS & INTERFACES | en_US |
dc.citation.volume | 8 | en_US |
dc.citation.issue | 28 | en_US |
dc.citation.spage | 18266 | en_US |
dc.citation.epage | 18276 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000380298400058 | en_US |
Appears in Collections: | Articles |