4.6 Article

Two-dimensional benzodithiophene and benzothiadiazole based solution-processed small molecular organic field-effect transistors & solar cells

期刊

JOURNAL OF MATERIALS CHEMISTRY C
卷 2, 期 20, 页码 3921-3927

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4tc00086b

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资金

  1. National Natural Science Foundation of China [21274134, 51173199, 61107090]
  2. Ministry of Science and Technology of China [2010DFA52310]
  3. New Century Excellent Talents in University [NCET-11-0473]
  4. Shandong Provincial Natural Science Foundation [ZR2011BZ007]
  5. Hong Kong Scholar Program
  6. Shenzhen Municipal Science and Technology Program [JCYJ20130401145617279]
  7. Qingdao Municipal Science and Technology Program [13-1-4-200-jch, 11-2-4-22-hz]
  8. Postdoctoral Science Foundation of China [XJ2012042, 2012T50630, 2013M530329]

向作者/读者索取更多资源

Benzodithiophene (BDT) and benzothiadiazole (BT) based small molecules have been synthesized through palladium-catalyzed Stille coupling reactions. The molecules with and without the conjugated thiophene side-chain were named as DRTBTTBDTT (2D) and DRTBTTBDT (1D), respectively. These molecules exhibited an optical band gap of around 1.8 eV. Solution-processed thin films of 1D and 2D showed that the conjugated thiophene side-chain oriented to produce a uniform 2D structure, which led to a relatively high hole mobility of 0.016 cm(2) V-1 s(-1), and this was one of the highest values for solutionprocessed small-molecule donors in organic solar cells (OSCs). With proper engineering of energy levels, the organic solar cells based on DRTBTTBDTT (2D) as donors exhibited a high Voc of around 0.9 V.

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