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New Angular-Shaped and Isomerically Pure Anthradithiophene with Lateral Aliphatic Side Chains for Conjugated Polymers: Synthesis, Characterization, and Implications for Solution-Prossessed Organic Field-Effect Transistors and Photovoltaics
| Content Provider | Semantic Scholar |
|---|---|
| Author | Wu, Jhong-Sian Lin, Chung-Te Wang, Chien-Lung Cheng, Yen-Ju Hsu, Chain-Shu |
| Copyright Year | 2012 |
| Abstract | An isomerically pure anti-anthradithiophene (aADT) arranged in an angular shape is developed. Formation of the framework of aADT incorporating four lateral alkyl substituents was accomplished by a one-pot benzannulation via multiple Suzuki coupling. This newly designed 2,8-stannylated aADT monomer was copolymerized with a ditheniodiketopyrrolopyrrole (DPP) unit and a bithiophene unit, respectively, to furnish an alternating donor–acceptor copolymer poly(anthradithiophene-alt-dithienyldiketopyrrolopyrrole) (PaADTDPP) and a thiophene-rich poly(anthradithiophene-alt-bithiophene) (PaADTT). PaADTT with crystalline nature achieved a high FET mobility of 7.9 × 10–2 cm2 V–1 s–1 with an on–off ratio of 1.1 × 107. The photovoltaic device based on the PaADTDPP:PC71BM (1:2.5, w/w) blend exhibited a Voc of 0.66 V, a Jsc of 9.49 mA/cm2, and a FF of 58.4%, delivering a power conversion efficiency (PCE) of 3.66%. By adding 1.5 vol % 1-chloronaphthalene (CN) as a processing additive, the PCE can be improved to 4.24%. We d... |
| Starting Page | 2391 |
| Ending Page | 2399 |
| Page Count | 9 |
| File Format | PDF HTM / HTML |
| DOI | 10.1021/cm301176s |
| Volume Number | 24 |
| Alternate Webpage(s) | https://7f6633fd-e2f3-465b-a389-cbefb50bb994.filesusr.com/ugd/ddee22_13d7f6fe5d234306b33a88caf54a5c87.pdf |
| Alternate Webpage(s) | https://ir.nctu.edu.tw/bitstream/11536/16466/1/000305662000020.pdf |
| Alternate Webpage(s) | https://doi.org/10.1021/cm301176s |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |