Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4089
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGhosh, S-
dc.contributor.authorPrasanthkumar, S-
dc.contributor.authorDas, S-
dc.contributor.authorSaeki, S-
dc.contributor.authorAjayaghosh, A-
dc.date.accessioned2022-10-13T04:46:14Z-
dc.date.available2022-10-13T04:46:14Z-
dc.date.issued2022-
dc.identifier.citationChemical Communications;58(48):6837-6840en_US
dc.identifier.urihttps://doi.org/10.1039/d2cc02111k-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4089-
dc.description.abstractHigh charge carrier mobility is a prerequisite for organic electronics for which molecular arrangement and morphology play a vital role. Herein, we report how the self-assembly of thienylenevinylenes T1 and T2 can achieve morphologically distinct nanostructures with improved charge carrier mobility. Morphological analysis revealed that T1 forms 2D nanosheets that further extend to an array of hierarchical pseudo-1D assemblies, whereas T2 results in 1D nanofibers. Flash photolysis – time resolved microwave conductivity and transient absorption spectroscopy (FP-TRMC and TAS) revealed that 1D fibers of T2 show 1.75 fold higher charge carrier mobility (9.2 × 10−2 cm2 V−1 s−1) when compared to the array of 2D sheets obtained from T1 (5.0 × 10−2 cm2 V−1 s−1). This simple approach can be extended to design self-assembled organic photoconducting materials for optoelectronic applications.en_US
dc.language.isoenen_US
dc.publisherRoyal society of chemistryen_US
dc.subjectthienylenevinylene,en_US
dc.subject2D sheets,en_US
dc.subject1D fibersen_US
dc.titleStructurally Directed Thienylenevinylene Self-assembly for Improved Charge Carrier Mobility: 2D Sheets vs. 1D Fibersen_US
dc.typeArticleen_US
Appears in Collections:2022



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.