An Asymmetric Furan/Thieno[3, 2‐b]Thiophene Diketopyrrolopyrrole Building Block for Annealing‐Free Green‐Solvent Processable Organic Thin‐Film Transistors. Issue 15 (21st June 2018)
- Record Type:
- Journal Article
- Title:
- An Asymmetric Furan/Thieno[3, 2‐b]Thiophene Diketopyrrolopyrrole Building Block for Annealing‐Free Green‐Solvent Processable Organic Thin‐Film Transistors. Issue 15 (21st June 2018)
- Main Title:
- An Asymmetric Furan/Thieno[3, 2‐b]Thiophene Diketopyrrolopyrrole Building Block for Annealing‐Free Green‐Solvent Processable Organic Thin‐Film Transistors
- Authors:
- Ding, Shang
Ni, Zhenjie
Hu, Mengxiao
Qiu, Gege
Li, Jie
Ye, Jun
Zhang, Xiaotao
Liu, Feng
Dong, Huanli
Hu, Wenping - Abstract:
- Abstract: A new asymmetric furan and thieno[3, 2‐ b ]thiophene flanked diketopyrrolopyrrole (TTFDPP ) building block for conjugated polymers is designed and used to generate a donor–acceptor semiconducting polymer, poly[3‐(furan‐2‐yl)‐2, 5‐bis(2‐octyldodecyl)‐6‐(thieno[3, 2‐ b ]thiophen‐2‐yl)pyrrolo[3, 4‐ c ]pyrrole‐1, 4(2 H, 5 H )‐dione‐ alt ‐thieno[3, 2‐ b ]thiophene] (abbreviated to PTTFDPP‐TT), consisting of TTFDPP unit copolymerized with thieno[3, 2‐ b ]thiophene comonomer (TT ), which is further synthesized. Results demonstrate that PTTFDPP‐TT‐ based thin‐film transistors in a bottom‐gate bottom‐contact device configuration exhibit typical hole‐transporting property, with weak temperature dependence for charge carrier mobility from room temperature to 200 °C. In addition, the good solubility of PTTFDPP‐TT due to the incorporation of a polar furan unit and an asymmetric conjugated structure makes it able to be solution processed with a less toxic nonchlorinated solvent such as toluene, demonstrating comparable performance with that prepared from chlorinated solution. These results suggest PTTFDPP‐TT as a promising organic semiconductor candidate for annealing‐free, environmentally benign, and less energy‐consuming applications in large‐area flexible organic electronic devices. Abstract : A new copolymer, poly[3‐(furan‐2‐yl)‐2, 5‐bis(2‐octyldodecyl)‐6‐(thieno[3, 2‐ b ]thiophen‐2‐yl)pyrrolo[3, 4‐ c ]pyrrole‐1, 4(2 H, 5 H )‐dione‐ alt ‐thieno[3, 2‐ bAbstract: A new asymmetric furan and thieno[3, 2‐ b ]thiophene flanked diketopyrrolopyrrole (TTFDPP ) building block for conjugated polymers is designed and used to generate a donor–acceptor semiconducting polymer, poly[3‐(furan‐2‐yl)‐2, 5‐bis(2‐octyldodecyl)‐6‐(thieno[3, 2‐ b ]thiophen‐2‐yl)pyrrolo[3, 4‐ c ]pyrrole‐1, 4(2 H, 5 H )‐dione‐ alt ‐thieno[3, 2‐ b ]thiophene] (abbreviated to PTTFDPP‐TT), consisting of TTFDPP unit copolymerized with thieno[3, 2‐ b ]thiophene comonomer (TT ), which is further synthesized. Results demonstrate that PTTFDPP‐TT‐ based thin‐film transistors in a bottom‐gate bottom‐contact device configuration exhibit typical hole‐transporting property, with weak temperature dependence for charge carrier mobility from room temperature to 200 °C. In addition, the good solubility of PTTFDPP‐TT due to the incorporation of a polar furan unit and an asymmetric conjugated structure makes it able to be solution processed with a less toxic nonchlorinated solvent such as toluene, demonstrating comparable performance with that prepared from chlorinated solution. These results suggest PTTFDPP‐TT as a promising organic semiconductor candidate for annealing‐free, environmentally benign, and less energy‐consuming applications in large‐area flexible organic electronic devices. Abstract : A new copolymer, poly[3‐(furan‐2‐yl)‐2, 5‐bis(2‐octyldodecyl)‐6‐(thieno[3, 2‐ b ]thiophen‐2‐yl)pyrrolo[3, 4‐ c ]pyrrole‐1, 4(2 H, 5 H )‐dione‐ alt ‐thieno[3, 2‐ b ]thiophene](PTTFDPP‐TT), comprising of an asymmetric furan and thieno[3, 2‐ b ]thiophene flanked diketopyrrolopyrrole building block is designed and synthesized. As expected this copolymer exhibits good capacity for annealing‐free green‐solvent processable organic thin‐film transistors, giving thermal‐stable hole carrier mobility of 0.12 cm 2 V −1 s −1 . This result suggests PTTFDPP‐TT is a potential promising candidate for environmentally benign and less‐energy‐consuming electronic applications. … (more)
- Is Part Of:
- Macromolecular rapid communications. Volume 39:Issue 15(2018)
- Journal:
- Macromolecular rapid communications
- Issue:
- Volume 39:Issue 15(2018)
- Issue Display:
- Volume 39, Issue 15 (2018)
- Year:
- 2018
- Volume:
- 39
- Issue:
- 15
- Issue Sort Value:
- 2018-0039-0015-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-06-21
- Subjects:
- annealing free -- field‐effect transistors -- green solvents -- polymer semiconductors
Macromolecules -- Periodicals
Polymers -- Periodicals
Chemistry -- Periodicals
547.705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/marc.201800225 ↗
- Languages:
- English
- ISSNs:
- 1022-1336
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.400000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14523.xml