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dc.contributor.authorLiang, Wei-Weien_US
dc.contributor.authorHuang, Chi-Fengen_US
dc.contributor.authorWu, Kuan-Yien_US
dc.contributor.authorWu, San-Lienen_US
dc.contributor.authorChang, Shu-Tingen_US
dc.contributor.authorCheng, Yen-Juen_US
dc.contributor.authorWang, Chien-Lungen_US
dc.date.accessioned2019-04-03T06:42:17Z-
dc.date.available2019-04-03T06:42:17Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn2041-6520en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5sc04242aen_US
dc.identifier.urihttp://hdl.handle.net/11536/133563-
dc.description.abstractA giant amphiphile, which is constructed with an amorphous nano-pyramid (triphenylamine, TPA) and a crystalline nano-sphere (C-60), was synthesized. Structural characterization indicates that this pyramid-sphere-shaped amphiphile (TPA-C-60) forms a solvent-induced ordered phase, in which the two constituent units self-assemble into alternating stacks of two-dimensional (2D) TPA and C-60 nanosheets. Due to the complexity of the molecular structure and the amorphous nature of the nano-pyramid, phase formation was driven by intermolecular C-60-C-60 interactions and the ordered phase could not be reformed from the TPA-C-60 melt. Oriented crystal arrays of TPA-C-60, which contain flaton TPA/C-60 nano-stacks, can be obtained via a PDMS-assisted crystallization (PAC) technique. The flaton dual-channel supramolecular structure of TPA-C-60 delivered ambipolar and balanced charge-transport characteristics with an average me of 2.11 x 10(-4) cm(2) V-1 s(-1) and mh of 3.37 x 10(-4) cm(2) V-1 s(-1). The anisotropic charge-transport ability of the pyramid-sphere-shaped amphiphile was further understood based on the lattice structure and the lattice orientation of TPA-C-60 revealed from electron diffraction analyses.en_US
dc.language.isoen_USen_US
dc.titleFlat-on ambipolar triphenylamine/C-60 nano-stacks formed from the self-organization of a pyramid-sphere-shaped amphiphileen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5sc04242aen_US
dc.identifier.journalCHEMICAL SCIENCEen_US
dc.citation.volume7en_US
dc.citation.issue4en_US
dc.citation.spage2768en_US
dc.citation.epage2774en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000372614800041en_US
dc.citation.woscount12en_US
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