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Solution phase epitaxial self-assembly and high charge-carrier mobility nanofibers of semiconducting molecular gelators

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dc.contributor.author Prasanthkumar, S
dc.contributor.author Saeki, A
dc.contributor.author Seki, S
dc.contributor.author Ajayaghosh, A
dc.date.accessioned 2014-03-31T08:19:31Z
dc.date.available 2014-03-31T08:19:31Z
dc.date.issued 2010
dc.identifier.citation Journal of the American Chemical Society 132(26):8866-8867;7Jul 2010 en_US
dc.identifier.issn 0002-7863
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1250
dc.description.abstract Trithienylenevinylenes having amide end functional groups form supramolecular gels in nonpolar solvents, comprised of self-assembled nanowires. These gels exhibit the unique property of solution phase epitaxy leading to the alignment of fibers on mica surface. FP-TRMC studies revealed high charge carrier mobility for xerogels from decane-chloroform whereas films obtained from chloroform solutions showed less mobility, highlighting the role of self-assembly and gelation on the electronic properties of semiconducting molecular gelators. This study opens the window for a new class of conducting gelators which may find wide application in organic electronic devices. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject PI-conjugated systems en_US
dc.subject Thienylenevinylene oligomers en_US
dc.subject Quaterthiophene en_US
dc.subject Nanowires en_US
dc.subject Organogels en_US
dc.title Solution phase epitaxial self-assembly and high charge-carrier mobility nanofibers of semiconducting molecular gelators en_US
dc.type Article en_US


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