4.8 Article

Quinoline-Flanked Diketopyrrolopyrrole Copolymers Breaking through Electron Mobility over 6 cm(2) V-1 s(-1) in Flexible Thin Film Devices

期刊

ADVANCED MATERIALS
卷 30, 期 10, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201704843

关键词

charge transport; conjugated copolymers; electron mobility; flexible devices

资金

  1. Ministry of Science and Technology of China [2016YFB0401100, 2017YFA0204503, 2013CB933403, 2013CB933504]
  2. National Natural Science Foundation of China [51633006, 51733004, 91433115, 91222203, 91233205, 51303185, 21473222]
  3. Chinese Academy of Sciences [XDB12030300]

向作者/读者索取更多资源

Herein, the design and synthesis of novel pi-extended quinoline-flanked diketopyrrolopyrrole (DPP) [abbreviated as QDPP] motifs and corresponding copolymers named PQDPP-T and PQDPP-2FT for high performing n-type organic field-effect transistors (OFETs) in flexible organic thin film devices are reported. Serving as DPP-flankers in backbones, quinoline is found to effectively tune copolymer optoelectric properties. Compared with TDPP and pyridine-flanked DPP (PyDPP) analogs, widened bandgaps and strengthened electron deficiency are achieved. Moreover, both hole and electron mobility are improved two orders of magnitude compared to those of PyDPP analogs (PPyDPP-T and PPyDPP-2FT). Notably, featuring an all-acceptor-incorporated backbone, PQDPP-2FT exhibits electron mobility of 6.04 cm(2) V-1 s(-1), among the highest value in OFETs fabricated on flexible substrates to date. Moreover, due to the widened bandgap and strengthened electron deficiency of PQDPP, n-channel on/off ratio over 10(5) with suppressed hole transport is first realized in the ambipolar DPP-based copolymers.

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