| Literature DB >> 30605617 |
Yoonkyung Park1, Jin Won Jung1, Hungu Kang1, Jhumur Seth1, Youngjong Kang1, Myung Mo Sung1.
Abstract
We fabricated single-crystal poly[4-(4,4-dihexadecyl-4H-cyclopenta[1,2-b:5,4-b']-dithiophen-2-yl)- alt-[1,2,5]thiadiazolo-[3,4- c]pyridine] (PCDTPT) nanowires with ultrahigh mobility using a liquid-bridge-mediated nanotransfer molding method. The structural analysis of the single-crystal PCDTPT nanowires reveals that PCDTPT crystals have a triclinic structure, and the nanowires grow parallel to PCDTPT backbone chains, which provide important insights into its intrinsic charge transport. The single-crystal PCDTPT nanowire exhibits a superior charge carrier mobility of 72.94 ± 18.02 cm2 V-1 s-1 (maximum mobility up to 92.64 cm2 V-1 s-1), which is a record high value among conjugated polymers to date. In the single-crystal PCDTPT nanowire, the backbone chains in the linear structure along the nanowire growth axis lead to strong backbone delocalization, resulting in highly conductive polymer backbones and a drastic increase in charge carrier mobility. In addition, the single-crystal PCDTPT nanowire shows good environmental stability under air conditions compared to small-molecule organic semiconductors.Entities:
Keywords: PCDTPT; donor−acceptor-conjugated copolymers; liquid-bridge-mediated nanotransfer molding; single-crystal polymer nanowire
Year: 2019 PMID: 30605617 DOI: 10.1021/acs.nanolett.8b04302
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189