Precise Control of Noncovalent Interactions in Semiconducting Polymers for High-Performance Organic Field-Effect Transistors
Abstract
Performed through side-chain engineering or by incorporating intramolecular locking units, the directionality and dynamic nature of noncovalent interactions are particularly attractive for the design of novel semiconducting materials in a wide variety of applications. This work investigates the nature and position of hydrogen bonding (intra- versus intermolecular), with the objective of developing a rational approach to the design of new semiconducting materials with improved properties in the solid state. To control the polymer chains’ self-assembly, a π-conjugated polymer incorporating a moiety capable of generating intramolecular hydrogen bonding is evaluated against a polymer that allows for intermolecular hydrogen bonding. Characterization through various techniques, optical spectroscopies, grazing incidence wide-angle x-ray scattering, and solution small-angle neutron scattering showed that intramolecular hydrogen bonds resulted in materials with improved crystallinity and higher effective conjugation in the solid state. Additionally, the effect of the noncovalent interaction configuration on the optoelectronic properties was analyzed in organic field-effect transistor fabrication. Devices prepared from the materials with intramolecular hydrogen bonds showed significantly higher performance, with three orders of magnitude higher charge mobility than their counterparts fabricated from polymers with intermolecular hydrogen bonds. These results confirm the importance of chemical design on polymer structures and offer a novel route formore »
- Authors:
-
- Univ. of Windsor, ON (Canada)
- National Taiwan University of Science and Technology, Taipei City (Taiwan)
- Univ. of Southern Mississippi, Hattiesburg, MS (United States)
- Publication Date:
- Research Org.:
- Univ. of Southern Mississippi, Hattiesburg, MS (United States); University of Southern Mississippi, Hattiesburg, MS (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); Natural Sciences and Engineering Research Council of Canada (NSERC); Canadian Foundation for Innovation; Ministry of Science and Technology, Taiwan
- OSTI Identifier:
- 1865521
- Alternate Identifier(s):
- OSTI ID: 1985410
- Grant/Contract Number:
- SC0019361; RGPIN-2017-06611; 110-2221-E-011-009
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Chemistry of Materials
- Additional Journal Information:
- Journal Volume: 33; Journal Issue: 21; Journal ID: ISSN 0897-4756
- Publisher:
- American Chemical Society (ACS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE
Citation Formats
Ocheje, Michael U., Goodman, Renée B., Lu, Kuan-Ting, Wang, Yunfei, Galuska, Luke A., Soullard, Lénaïc, Cao, Zhiqiang, Zhang, Song, Yadiki, Madhumitha, Gu, Xiaodan, Chiu, Yu-Cheng, and Rondeau-Gagné, Simon. Precise Control of Noncovalent Interactions in Semiconducting Polymers for High-Performance Organic Field-Effect Transistors. United States: N. p., 2021.
Web. doi:10.1021/acs.chemmater.1c02426.
Ocheje, Michael U., Goodman, Renée B., Lu, Kuan-Ting, Wang, Yunfei, Galuska, Luke A., Soullard, Lénaïc, Cao, Zhiqiang, Zhang, Song, Yadiki, Madhumitha, Gu, Xiaodan, Chiu, Yu-Cheng, & Rondeau-Gagné, Simon. Precise Control of Noncovalent Interactions in Semiconducting Polymers for High-Performance Organic Field-Effect Transistors. United States. https://doi.org/10.1021/acs.chemmater.1c02426
Ocheje, Michael U., Goodman, Renée B., Lu, Kuan-Ting, Wang, Yunfei, Galuska, Luke A., Soullard, Lénaïc, Cao, Zhiqiang, Zhang, Song, Yadiki, Madhumitha, Gu, Xiaodan, Chiu, Yu-Cheng, and Rondeau-Gagné, Simon. Fri .
"Precise Control of Noncovalent Interactions in Semiconducting Polymers for High-Performance Organic Field-Effect Transistors". United States. https://doi.org/10.1021/acs.chemmater.1c02426. https://www.osti.gov/servlets/purl/1865521.
@article{osti_1865521,
title = {Precise Control of Noncovalent Interactions in Semiconducting Polymers for High-Performance Organic Field-Effect Transistors},
author = {Ocheje, Michael U. and Goodman, Renée B. and Lu, Kuan-Ting and Wang, Yunfei and Galuska, Luke A. and Soullard, Lénaïc and Cao, Zhiqiang and Zhang, Song and Yadiki, Madhumitha and Gu, Xiaodan and Chiu, Yu-Cheng and Rondeau-Gagné, Simon},
abstractNote = {Performed through side-chain engineering or by incorporating intramolecular locking units, the directionality and dynamic nature of noncovalent interactions are particularly attractive for the design of novel semiconducting materials in a wide variety of applications. This work investigates the nature and position of hydrogen bonding (intra- versus intermolecular), with the objective of developing a rational approach to the design of new semiconducting materials with improved properties in the solid state. To control the polymer chains’ self-assembly, a π-conjugated polymer incorporating a moiety capable of generating intramolecular hydrogen bonding is evaluated against a polymer that allows for intermolecular hydrogen bonding. Characterization through various techniques, optical spectroscopies, grazing incidence wide-angle x-ray scattering, and solution small-angle neutron scattering showed that intramolecular hydrogen bonds resulted in materials with improved crystallinity and higher effective conjugation in the solid state. Additionally, the effect of the noncovalent interaction configuration on the optoelectronic properties was analyzed in organic field-effect transistor fabrication. Devices prepared from the materials with intramolecular hydrogen bonds showed significantly higher performance, with three orders of magnitude higher charge mobility than their counterparts fabricated from polymers with intermolecular hydrogen bonds. These results confirm the importance of chemical design on polymer structures and offer a novel route for the design of high-efficiency semiconducting polymers for next-generation electronics.},
doi = {10.1021/acs.chemmater.1c02426},
journal = {Chemistry of Materials},
number = 21,
volume = 33,
place = {United States},
year = {Fri Oct 01 00:00:00 EDT 2021},
month = {Fri Oct 01 00:00:00 EDT 2021}
}
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