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Simultaneous enhancement of charge density and molecular stacking order of polymer semiconductors by viologen dopants for high performance organic field-effect transistors

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Abstract
Simultaneous enhancement of both charge density and favourable molecular stacking order is demonstrated by the incorporation of a molecular dopant into -conjugated polymer semiconductors. Neutral-state benzyl viologen has a high reduction potential, which can induce direct intermolecular charge transfer to N-type semiconductors for increased mobile electrons in organic field-effect transistors (OFETs). This viologen dopant remarkably improves OFET performance, increasing the charge carrier mobility by an order of magnitude with a simultaneous decrease in activation energy for charge transport. This improvement in OFET performance is attributed to the filling of deep trap sites in the semiconductor band-gaps by induced excess charge carriers. Moreover, this benzyl viologen dopant also helps to rearrange polymeric semiconductors into more favourable molecular stacking orders that promote charge transport in staggered OFETs. Blending with benzyl viologen changed the initial amorphous and face-on' predominant molecular orientation in pristine P(NDI2OD-T2) films to a more crystalline and bimodal stacking order, which consists of face-on' and edge-on' orientations with respect to the substrate. Therefore, this single molecule could play important roles both as a molecular dopant and an additive to modify the solid structures of similar active semiconducting materials in order to significantly improve the charge transport properties for organic/soft electronic applications.
Author(s)
Lee, Dong-HyeonKang, MinjiLim, Dae-HeeKim, YunseulLee, JiyoulKim, Dong-YuBaeg, Kang-Jun
Issued Date
2018-05
Type
Article
DOI
10.1039/c8tc01076e
URI
https://scholar.gist.ac.kr/handle/local/13274
Publisher
ROYAL SOC CHEMISTRY
Citation
Journal of Materials Chemistry c, v.6, no.20, pp.5497 - 5505
ISSN
2050-7526
Appears in Collections:
Department of Materials Science and Engineering > 1. Journal Articles
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