4.8 Article

Boosting the Ambipolar Performance of Solution-Processable Polymer Semiconductors via Hybrid Side-Chain Engineering

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 25, 页码 9540-9547

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja403949g

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资金

  1. National Research Foundation of Korea (NRF)
  2. Korean Government (MEST) [2010-0019408, 2010-0026916, 2010-0025292, 2011-0017174, 2013R1A1A1A05004475]
  3. Global Frontier Research Center for Advanced Soft Electronics [2011-0031628]
  4. International Cooperation of the Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  5. Korea government Ministry of Knowledge Economy [2012T100100740]
  6. Korea Evaluation Institute of Industrial Technology (KEIT) [20128520010010] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [2010-0026916, 2011-0031628, 2010-0019408, 2011-0017174, 2013R1A1A1A05004475, 2010-0025292] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Ambipolar polymer semiconductors are highly suited for use in flexible, printable, and large-area electronics as they exhibit both n-type (electron-transporting) and p-type (hole-transporting) operations within a single layer. This allows for cost-effective fabrication of complementary circuits with high noise immunity and operational stability. Currently, the performance of ambipolar polymer semiconductors lags behind that of their unipolar counterparts. Here, we report on the side-chain engineering of conjugated, alternating electron donoracceptor (D-A) polymers using diketopyrrolopyrrole-selenophene copolymers with hybrid siloxane-solubilizing groups (PTDPPSe-Si) to enhance ambipolar performance. The alkyl spacer length of the hybrid side chains was systematically tuned to boost ambipolar performance. The optimized three-dimensional (3-D) charge transport of PTDPPSe-Si with pentyl spacers yielded unprecedentedly high hole and electron mobilities of 8.84 and 4.34 cm(2) V-1 s(-1), respectively. These results provide guidelines for the molecular design of semiconducting polymers with hybrid side chains.

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