Two-dimensional benzodithiophene and benzothiadiazole based solution-processed small molecular organic field-effect transistors & solar cells
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
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Detail(s)
Original language | English |
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Pages (from-to) | 3921-3927 |
Journal / Publication | Journal of Materials Chemistry C |
Volume | 2 |
Issue number | 20 |
Publication status | Published - 28 May 2014 |
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Abstract
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 cm2 V-1 s-1, and this was one of the highest values for solution-processed 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. © 2014 the Partner Organisations.
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Two-dimensional benzodithiophene and benzothiadiazole based solution-processed small molecular organic field-effect transistors & solar cells. / Chen, Yanhua; Yan, Yan; Du, Zhengkun et al.
In: Journal of Materials Chemistry C, Vol. 2, No. 20, 28.05.2014, p. 3921-3927.
In: Journal of Materials Chemistry C, Vol. 2, No. 20, 28.05.2014, p. 3921-3927.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review