All-acceptor polymers with noncovalent interactions for efficient ambipolar transistors. Issue 6 (10th January 2020)
- Record Type:
- Journal Article
- Title:
- All-acceptor polymers with noncovalent interactions for efficient ambipolar transistors. Issue 6 (10th January 2020)
- Main Title:
- All-acceptor polymers with noncovalent interactions for efficient ambipolar transistors
- Authors:
- Chen, Zhicai
Li, Mingguang
Hu, Mengxiao
Wang, Shuang
Miao, Zhagen
Xu, Shen
Chen, Cailin
Dong, Huanli
Huang, Wei
Chen, Runfeng - Abstract:
- Abstract : By invoking intrachain noncovalent interactions (NCIs) in diazine-based mA-wA polymers, high and balanced hole and electron mobilities were achieved. Abstract : Exciting progress has been made recently regarding organic field-effect transistors (OFETs) owing to significant efforts devoted to the material design of semiconducting conjugated small molecules and polymers. However, the development of ambipolar or n-type OFETs lags behind that of p-type devices. Here, we propose a new strategy for the design of ambipolar polymers based on acceptors (A) of diazines (pyridazine or pyrazine) in a "moderate A-weak A (mA-wA)" architecture by integrating intrachain noncovalent interactions to rationally engineer the electronic structure, molecular planarity and backbone curvature of the conjugated copolymers. Thus designed mA-wA polymers with intrachain N⋯S interactions exhibit both high-lying HOMO and low-lying LUMO energy levels for ambipolar charge transport and good planarity with a linear backbone for high and balanced hole and electron mobilities up to 0.39 and 0.30 cm 2 V −1 s −1, respectively. Furthermore, the flexible OFETs fabricated on polyethylene terephthalate substrates show high mobilities of 0.26 and 0.32 cm 2 V −1 s −1 for holes and electrons, respectively. This design strategy with the newly discovered diazine acceptors to invoke both mA-wA and NCI effects in conjugated polymers for backbone engineering may be applicable to other systems, representing anAbstract : By invoking intrachain noncovalent interactions (NCIs) in diazine-based mA-wA polymers, high and balanced hole and electron mobilities were achieved. Abstract : Exciting progress has been made recently regarding organic field-effect transistors (OFETs) owing to significant efforts devoted to the material design of semiconducting conjugated small molecules and polymers. However, the development of ambipolar or n-type OFETs lags behind that of p-type devices. Here, we propose a new strategy for the design of ambipolar polymers based on acceptors (A) of diazines (pyridazine or pyrazine) in a "moderate A-weak A (mA-wA)" architecture by integrating intrachain noncovalent interactions to rationally engineer the electronic structure, molecular planarity and backbone curvature of the conjugated copolymers. Thus designed mA-wA polymers with intrachain N⋯S interactions exhibit both high-lying HOMO and low-lying LUMO energy levels for ambipolar charge transport and good planarity with a linear backbone for high and balanced hole and electron mobilities up to 0.39 and 0.30 cm 2 V −1 s −1, respectively. Furthermore, the flexible OFETs fabricated on polyethylene terephthalate substrates show high mobilities of 0.26 and 0.32 cm 2 V −1 s −1 for holes and electrons, respectively. This design strategy with the newly discovered diazine acceptors to invoke both mA-wA and NCI effects in conjugated polymers for backbone engineering may be applicable to other systems, representing an advanced concept for the construction of high-performance ambipolar polymers. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 8:Issue 6(2020)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 8:Issue 6(2020)
- Issue Display:
- Volume 8, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 6
- Issue Sort Value:
- 2020-0008-0006-0000
- Page Start:
- 2094
- Page End:
- 2101
- Publication Date:
- 2020-01-10
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9tc05944j ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12901.xml