The Effects of Side Chains on the Charge Mobilities and Functionalities of Semiconducting Conjugated Polymers beyond Solubilities

Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant efforts have been made to develop various conjugated frameworks and linkers. However, studies are increasingly demonstrating that the side ch...

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Published inAdvanced materials (Weinheim) Vol. 31; no. 46; pp. e1903104 - n/a
Main Authors Yang, Yizhou, Liu, Zitong, Zhang, Guanxin, Zhang, Xisha, Zhang, Deqing
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.11.2019
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Abstract Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant efforts have been made to develop various conjugated frameworks and linkers. However, studies are increasingly demonstrating that the side chains of semiconducting polymers can significantly affect interchain packing, thin film crystallinity, and thus semiconducting performance. Ways to modify the side alkyl chains to improve the interchain packing order and charge mobilities for conjugated polymers are first discussed. It is shown that modifying the branching chains by moving the branching points away from the backbones can boost the charge mobilities, which can also be improved through partially replacing branching chains with linear ones. Second, the effects of side chains with heteroatoms and functional groups are discussed. The siloxane‐terminated side chains are utilized to enhance the semiconducting properties. The fluorinated alkyl chains are beneficial for improving both charge mobility and air stability. Incorporating H bonding group side chains can improve thin film crystallinities and boost charge mobilities. Notably, incorporating functional groups (e.g., glycol, tetrathiafulvalene, and thymine) into side chains can improve the selectivity of field‐effect transistor (FET)‐based sensors, while photochromic group containing side chains in conjugated polymers result in photoresponsive semiconductors and optically tunable FETs. Recent developments in side chain modifications of conjugated polymers, including alkyl side chains, heteroatom, and functional group containing side chains, are reviewed for field‐effect transistor studies. The review shows that side chain modification can not only improve the charge transport properties, but also endow the conjugated polymers with new functions (malleability, sensing, stimuli‐responsiveness, etc.).
AbstractList Abstract Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant efforts have been made to develop various conjugated frameworks and linkers. However, studies are increasingly demonstrating that the side chains of semiconducting polymers can significantly affect interchain packing, thin film crystallinity, and thus semiconducting performance. Ways to modify the side alkyl chains to improve the interchain packing order and charge mobilities for conjugated polymers are first discussed. It is shown that modifying the branching chains by moving the branching points away from the backbones can boost the charge mobilities, which can also be improved through partially replacing branching chains with linear ones. Second, the effects of side chains with heteroatoms and functional groups are discussed. The siloxane‐terminated side chains are utilized to enhance the semiconducting properties. The fluorinated alkyl chains are beneficial for improving both charge mobility and air stability. Incorporating H bonding group side chains can improve thin film crystallinities and boost charge mobilities. Notably, incorporating functional groups (e.g., glycol, tetrathiafulvalene, and thymine) into side chains can improve the selectivity of field‐effect transistor (FET)‐based sensors, while photochromic group containing side chains in conjugated polymers result in photoresponsive semiconductors and optically tunable FETs.
Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant efforts have been made to develop various conjugated frameworks and linkers. However, studies are increasingly demonstrating that the side chains of semiconducting polymers can significantly affect interchain packing, thin film crystallinity, and thus semiconducting performance. Ways to modify the side alkyl chains to improve the interchain packing order and charge mobilities for conjugated polymers are first discussed. It is shown that modifying the branching chains by moving the branching points away from the backbones can boost the charge mobilities, which can also be improved through partially replacing branching chains with linear ones. Second, the effects of side chains with heteroatoms and functional groups are discussed. The siloxane‐terminated side chains are utilized to enhance the semiconducting properties. The fluorinated alkyl chains are beneficial for improving both charge mobility and air stability. Incorporating H bonding group side chains can improve thin film crystallinities and boost charge mobilities. Notably, incorporating functional groups (e.g., glycol, tetrathiafulvalene, and thymine) into side chains can improve the selectivity of field‐effect transistor (FET)‐based sensors, while photochromic group containing side chains in conjugated polymers result in photoresponsive semiconductors and optically tunable FETs. Recent developments in side chain modifications of conjugated polymers, including alkyl side chains, heteroatom, and functional group containing side chains, are reviewed for field‐effect transistor studies. The review shows that side chain modification can not only improve the charge transport properties, but also endow the conjugated polymers with new functions (malleability, sensing, stimuli‐responsiveness, etc.).
Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant efforts have been made to develop various conjugated frameworks and linkers. However, studies are increasingly demonstrating that the side chains of semiconducting polymers can significantly affect interchain packing, thin film crystallinity, and thus semiconducting performance. Ways to modify the side alkyl chains to improve the interchain packing order and charge mobilities for conjugated polymers are first discussed. It is shown that modifying the branching chains by moving the branching points away from the backbones can boost the charge mobilities, which can also be improved through partially replacing branching chains with linear ones. Second, the effects of side chains with heteroatoms and functional groups are discussed. The siloxane‐terminated side chains are utilized to enhance the semiconducting properties. The fluorinated alkyl chains are beneficial for improving both charge mobility and air stability. Incorporating H bonding group side chains can improve thin film crystallinities and boost charge mobilities. Notably, incorporating functional groups (e.g., glycol, tetrathiafulvalene, and thymine) into side chains can improve the selectivity of field‐effect transistor (FET)‐based sensors, while photochromic group containing side chains in conjugated polymers result in photoresponsive semiconductors and optically tunable FETs.
Author Zhang, Deqing
Zhang, Xisha
Zhang, Guanxin
Yang, Yizhou
Liu, Zitong
Author_xml – sequence: 1
  givenname: Yizhou
  surname: Yang
  fullname: Yang, Yizhou
  organization: University of Chinese Academy of Sciences
– sequence: 2
  givenname: Zitong
  orcidid: 0000-0003-1185-9219
  surname: Liu
  fullname: Liu, Zitong
  email: dqzhang@iccas.ac.cn
  organization: Chinese Academy of Sciences
– sequence: 3
  givenname: Guanxin
  orcidid: 0000-0002-8422-3126
  surname: Zhang
  fullname: Zhang, Guanxin
  organization: Chinese Academy of Sciences
– sequence: 4
  givenname: Xisha
  orcidid: 0000-0003-0794-2159
  surname: Zhang
  fullname: Zhang, Xisha
  organization: University of Chinese Academy of Sciences
– sequence: 5
  givenname: Deqing
  orcidid: 0000-0002-5709-6088
  surname: Zhang
  fullname: Zhang, Deqing
  email: zitong_@iccas.ac.cn
  organization: University of Chinese Academy of Sciences
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31483542$$D View this record in MEDLINE/PubMed
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Issue 46
Keywords field-effect transistors-based sensors
side chains with functional groups
semiconducting conjugated polymers
modifications of side chains
charge mobility
Language English
License 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Snippet Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors. Significant...
Abstract Recent decades have witnessed the rapid development of semiconducting polymers in terms of high charge mobilities and applications in transistors....
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SubjectTerms Chain branching
Chains (polymeric)
charge mobility
Crystal structure
Crystallinity
Field effect transistors
field‐effect transistors‐based sensors
Functional groups
Materials science
modifications of side chains
Polymers
Selectivity
semiconducting conjugated polymers
Semiconductor devices
side chains with functional groups
Thin films
Thymine
Title The Effects of Side Chains on the Charge Mobilities and Functionalities of Semiconducting Conjugated Polymers beyond Solubilities
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadma.201903104
https://www.ncbi.nlm.nih.gov/pubmed/31483542
https://www.proquest.com/docview/2313498190/abstract/
https://search.proquest.com/docview/2284562293
Volume 31
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