Boosting the Charge Transport Property of Indeno[1, 2‐b]fluorene‐6, 12‐dione though Incorporation of Sulfur‐ or Nitrogen‐Linked Side Chains. (9th October 2017)
- Record Type:
- Journal Article
- Title:
- Boosting the Charge Transport Property of Indeno[1, 2‐b]fluorene‐6, 12‐dione though Incorporation of Sulfur‐ or Nitrogen‐Linked Side Chains. (9th October 2017)
- Main Title:
- Boosting the Charge Transport Property of Indeno[1, 2‐b]fluorene‐6, 12‐dione though Incorporation of Sulfur‐ or Nitrogen‐Linked Side Chains
- Authors:
- Fan, Zhi‐Ping
Li, Xiang‐Yang
Luo, Xiao‐E.
Fei, Xian
Sun, Bing
Chen, Li‐Chuan
Shi, Zi‐Fa
Sun, Chun‐Lin
Shao, Xiangfeng
Zhang, Hao‐Li - Abstract:
- Abstract: Alkyl chains are basic units in the design of organic semiconductors for purposes of enhancing solubility, tuning electronic energy levels, and tailoring molecular packing. This work demonstrates that the carrier mobilities of indeno[1, 2‐ b ]fluorene‐6, 12‐dione (IFD )‐based semiconductors can be dramatically enhanced by the incorporation of sulfur‐ or nitrogen‐linked side chains. ThreeIFD derivatives possessing butyl, butylthio, and dibutylamino substituents are synthesized, and their organic field‐effect transistors (OFET) are fabricated and characterized. TheIFD possessing butyl substituents exhibits a very poor charge transport property with mobility lower than 10 −7 cm 2 V −1 s −1 . In contrast, the hole mobility is dramatically increased to 1.03 cm 2 V −1 s −1 by replacing the butyl units with dibutylamino groups (DBA‐IFD ), while the butylthio‐modifiedIFD (BT‐IFD ) derivative exhibits a high and balanced ambipolar charge transport property with the maximum hole and electron mobilities up to 0.71 and 0.65 cm 2 V −1 s −1, respectively. Moreover, the complementary metal–oxide–semiconductor‐like inverters incorporated with the ambipolar OFETs shows sharp inversions with a maximum gain value up to 173. This work reveals that modification of the aromatic core with heteroatom‐linked side chains, such as alkylthio or dialkylamino, can be an efficient strategy for the design of high‐performance organic semiconductors. Abstract : Dramatic improvement of hole andAbstract: Alkyl chains are basic units in the design of organic semiconductors for purposes of enhancing solubility, tuning electronic energy levels, and tailoring molecular packing. This work demonstrates that the carrier mobilities of indeno[1, 2‐ b ]fluorene‐6, 12‐dione (IFD )‐based semiconductors can be dramatically enhanced by the incorporation of sulfur‐ or nitrogen‐linked side chains. ThreeIFD derivatives possessing butyl, butylthio, and dibutylamino substituents are synthesized, and their organic field‐effect transistors (OFET) are fabricated and characterized. TheIFD possessing butyl substituents exhibits a very poor charge transport property with mobility lower than 10 −7 cm 2 V −1 s −1 . In contrast, the hole mobility is dramatically increased to 1.03 cm 2 V −1 s −1 by replacing the butyl units with dibutylamino groups (DBA‐IFD ), while the butylthio‐modifiedIFD (BT‐IFD ) derivative exhibits a high and balanced ambipolar charge transport property with the maximum hole and electron mobilities up to 0.71 and 0.65 cm 2 V −1 s −1, respectively. Moreover, the complementary metal–oxide–semiconductor‐like inverters incorporated with the ambipolar OFETs shows sharp inversions with a maximum gain value up to 173. This work reveals that modification of the aromatic core with heteroatom‐linked side chains, such as alkylthio or dialkylamino, can be an efficient strategy for the design of high‐performance organic semiconductors. Abstract : Dramatic improvement of hole and electron transport properties of indeno[1, 2‐b]fluorene‐6, 12‐dione is achieved through incorporation of sulfur‐ or nitrogen‐linked side chains. Materials containing sulfur linkage give ambipolar organic field‐effect transistors (OFETs) with high and balanced hole and electron mobilities. Complementary metal–oxide–semiconductor‐like inverters based on the ambipolar OFETs exhibit high gain value up to 173. … (more)
- Is Part Of:
- Advanced functional materials. Volume 27:Number 45(2017)
- Journal:
- Advanced functional materials
- Issue:
- Volume 27:Number 45(2017)
- Issue Display:
- Volume 27, Issue 45 (2017)
- Year:
- 2017
- Volume:
- 27
- Issue:
- 45
- Issue Sort Value:
- 2017-0027-0045-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2017-10-09
- Subjects:
- ambipolar materials -- inverters -- organic field‐effect transistors -- side‐chain engineering
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.201702318 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5427.xml