High-performance ambipolar benzodifurandione-based donor-acceptor copolymer with balanced hole and electron mobility. (March 2019)
- Record Type:
- Journal Article
- Title:
- High-performance ambipolar benzodifurandione-based donor-acceptor copolymer with balanced hole and electron mobility. (March 2019)
- Main Title:
- High-performance ambipolar benzodifurandione-based donor-acceptor copolymer with balanced hole and electron mobility
- Authors:
- Cheng, Sun
Yu, Seong Hoon
Kwon, Soon-Ki
Chung, Dae Sung
Kim, Yun-Hi - Abstract:
- Abstract: Well-balanced ambipolar benzodifurandione (BDO) donor–acceptor copolymers were synthesized by tuning its intramolecular charge transfer nature by expanding the volumetric portion of the donor moiety, i.e., by using thiophene copolymerized with thiophene vinylene thiophene (TVT) or selenophene vinylene selenophene (SVS). Photophysical analyses revealed that BDO-SVS formed highly aggregated states in the solution state compared with BDO-TVT, facilitating a well-ordered self-assembled crystalline structure in the solid state. Using two-dimensional grazing incident X-ray diffraction and quantitative pole figure analyses, we established that the molecular orientation and degree of crystallinity was higher in BDO-SVS than in BDO-TVT. The morphological features identified by atomic force microscopy also showed a higher crystalline nature of SVS derivative, implying that SVS can strengthen intermolecular charge transport. This improved environment for charge transport, was revealed by the performance of organic field-effect transistors: BDO-SVS had superior performance than that of BDO-TVT for both hole and electron mobilities. This research shows that BDO, with a strong acceptor moiety, renders high-performance ambipolar characteristics when copolymerized with an expanded and aggregating donor moiety, such as SVS. Highlights: New benzodifurandione-based donor-acceptor copolymers. Well balanced ambipolar benzodifurandione. BDO-SVS had superior performance than that ofAbstract: Well-balanced ambipolar benzodifurandione (BDO) donor–acceptor copolymers were synthesized by tuning its intramolecular charge transfer nature by expanding the volumetric portion of the donor moiety, i.e., by using thiophene copolymerized with thiophene vinylene thiophene (TVT) or selenophene vinylene selenophene (SVS). Photophysical analyses revealed that BDO-SVS formed highly aggregated states in the solution state compared with BDO-TVT, facilitating a well-ordered self-assembled crystalline structure in the solid state. Using two-dimensional grazing incident X-ray diffraction and quantitative pole figure analyses, we established that the molecular orientation and degree of crystallinity was higher in BDO-SVS than in BDO-TVT. The morphological features identified by atomic force microscopy also showed a higher crystalline nature of SVS derivative, implying that SVS can strengthen intermolecular charge transport. This improved environment for charge transport, was revealed by the performance of organic field-effect transistors: BDO-SVS had superior performance than that of BDO-TVT for both hole and electron mobilities. This research shows that BDO, with a strong acceptor moiety, renders high-performance ambipolar characteristics when copolymerized with an expanded and aggregating donor moiety, such as SVS. Highlights: New benzodifurandione-based donor-acceptor copolymers. Well balanced ambipolar benzodifurandione. BDO-SVS had superior performance than that of BDO-TVT for OTFT. … (more)
- Is Part Of:
- Dyes and pigments. Volume 162(2019)
- Journal:
- Dyes and pigments
- Issue:
- Volume 162(2019)
- Issue Display:
- Volume 162, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 162
- Issue:
- 2019
- Issue Sort Value:
- 2019-0162-2019-0000
- Page Start:
- 481
- Page End:
- 486
- Publication Date:
- 2019-03
- Subjects:
- Benzodifurandione -- Ambipolar -- Molecular orientation -- Crystallinity -- Organic field-effect transistor
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2018.10.038 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9062.xml