4.8 Article

Solution-Processable Ambipolar Diketopyrrolopyrrole-Selenophene Polymer with Unprecedentedly High Hole and Electron Mobilities

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 51, Pages 20713-20721

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja308927g

Keywords

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Funding

  1. National Research Foundation of Korea (NRF)
  2. Korean Government (MEST) [2010-0002494, 2010-0019408, 2010-0026916, 2011-0026424, 2011-0017174]
  3. Global Frontier Research Center for Advanced Soft Electronics [2011-0031628]
  4. National Research Foundation of Korea [2010-0002494, 2010-0019408, 2010-0026916] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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There is a fast-growing demand for polymer-based ambipolar thin-film transistors (TFTs), in which both n-type and p-type transistor operations are realized in a single layer, while maintaining simplicity in processing. Research progress toward this end is essentially fueled by molecular engineering of the conjugated backbones of the polymers and the development of process architectures for device fabrication, which has recently led to hole and electron mobilities of more than 1.0 cm(2) V-1 s(-1). However, ambipolar polymers with even higher performance are still required. By taking into account both the conjugated backbone and side chains of the polymer component, we have developed a dithienyi-diketopyrrolo-pyrrole (TDPP) and selenophene containing polymer with hybrid silmane-solubilizing groups (PTDPPSe-Si). A synergistic combination of rational polymer backbone design, side-chain dynamics, and solution processing affords an enormous boost in ambipolar TFT performance, resulting in unprecedentedly high hole and electron mobilities of 3.97 and 2.20 cm(2) V-1 s(-1), respectively.

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