Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability
Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobilit...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Xiaobo Yu [verfasserIn] Cheng Li [verfasserIn] Chenying Gao [verfasserIn] Xisha Zhang [verfasserIn] Guanxin Zhang [verfasserIn] Deqing Zhang [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2021 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
In: SmartMat - Wiley, 2021, 2(2021), 3, Seite 347-366 |
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| Übergeordnetes Werk: |
volume:2 ; year:2021 ; number:3 ; pages:347-366 |
| Links: |
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| DOI / URN: |
10.1002/smm2.1062 |
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| Katalog-ID: |
DOAJ058343539 |
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| 520 | |a Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. | ||
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| 700 | 0 | |a Deqing Zhang |e verfasserin |4 aut | |
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10.1002/smm2.1062 doi (DE-627)DOAJ058343539 (DE-599)DOAJbf3f8020ae5643919570d0a9ac52a1cf DE-627 ger DE-627 rakwb eng TA401-492 Xiaobo Yu verfasserin aut Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. conjugated polymers field‐effect transistors flexible and stretchable electronics hydrogen‐bonding self‐healable and wearable electronics Materials of engineering and construction. Mechanics of materials Cheng Li verfasserin aut Chenying Gao verfasserin aut Xisha Zhang verfasserin aut Guanxin Zhang verfasserin aut Deqing Zhang verfasserin aut In SmartMat Wiley, 2021 2(2021), 3, Seite 347-366 (DE-627)1754879101 (DE-600)3060484-9 2688819X nnns volume:2 year:2021 number:3 pages:347-366 https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/article/bf3f8020ae5643919570d0a9ac52a1cf kostenfrei https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/toc/2688-819X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2021 3 347-366 |
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10.1002/smm2.1062 doi (DE-627)DOAJ058343539 (DE-599)DOAJbf3f8020ae5643919570d0a9ac52a1cf DE-627 ger DE-627 rakwb eng TA401-492 Xiaobo Yu verfasserin aut Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. conjugated polymers field‐effect transistors flexible and stretchable electronics hydrogen‐bonding self‐healable and wearable electronics Materials of engineering and construction. Mechanics of materials Cheng Li verfasserin aut Chenying Gao verfasserin aut Xisha Zhang verfasserin aut Guanxin Zhang verfasserin aut Deqing Zhang verfasserin aut In SmartMat Wiley, 2021 2(2021), 3, Seite 347-366 (DE-627)1754879101 (DE-600)3060484-9 2688819X nnns volume:2 year:2021 number:3 pages:347-366 https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/article/bf3f8020ae5643919570d0a9ac52a1cf kostenfrei https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/toc/2688-819X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2021 3 347-366 |
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10.1002/smm2.1062 doi (DE-627)DOAJ058343539 (DE-599)DOAJbf3f8020ae5643919570d0a9ac52a1cf DE-627 ger DE-627 rakwb eng TA401-492 Xiaobo Yu verfasserin aut Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. conjugated polymers field‐effect transistors flexible and stretchable electronics hydrogen‐bonding self‐healable and wearable electronics Materials of engineering and construction. Mechanics of materials Cheng Li verfasserin aut Chenying Gao verfasserin aut Xisha Zhang verfasserin aut Guanxin Zhang verfasserin aut Deqing Zhang verfasserin aut In SmartMat Wiley, 2021 2(2021), 3, Seite 347-366 (DE-627)1754879101 (DE-600)3060484-9 2688819X nnns volume:2 year:2021 number:3 pages:347-366 https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/article/bf3f8020ae5643919570d0a9ac52a1cf kostenfrei https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/toc/2688-819X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2021 3 347-366 |
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10.1002/smm2.1062 doi (DE-627)DOAJ058343539 (DE-599)DOAJbf3f8020ae5643919570d0a9ac52a1cf DE-627 ger DE-627 rakwb eng TA401-492 Xiaobo Yu verfasserin aut Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. conjugated polymers field‐effect transistors flexible and stretchable electronics hydrogen‐bonding self‐healable and wearable electronics Materials of engineering and construction. Mechanics of materials Cheng Li verfasserin aut Chenying Gao verfasserin aut Xisha Zhang verfasserin aut Guanxin Zhang verfasserin aut Deqing Zhang verfasserin aut In SmartMat Wiley, 2021 2(2021), 3, Seite 347-366 (DE-627)1754879101 (DE-600)3060484-9 2688819X nnns volume:2 year:2021 number:3 pages:347-366 https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/article/bf3f8020ae5643919570d0a9ac52a1cf kostenfrei https://doi.org/10.1002/smm2.1062 kostenfrei https://doaj.org/toc/2688-819X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 2021 3 347-366 |
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TA401-492 Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability conjugated polymers field‐effect transistors flexible and stretchable electronics hydrogen‐bonding self‐healable and wearable electronics |
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Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability |
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Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. |
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Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. |
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Abstract The soft nature has endowed conjugated polymers with promising applications in a wide range of field‐effect transistor (FET) based flexible electronics. With unremitting efforts on revealing the molecular structure–property relationships, numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades. Incorporating hydrogen‐bonding (H‐bonding) units into semiconducting polymers is one of the most successful strategies for designing high‐performance semiconducting materials. In this review, we aim to highlight the roles of H‐bonding units in the performances of polymeric FETs from three aspects. These include (i) charge mobility enhancement for semiconducting polymers after incorporation of H‐bonding units into the side chains, (ii) the effects of H‐bonding units on the stretchability of conjugated polymers, and (iii) the improvement of self‐healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H‐bonding units in the side chains or conjugated backbones. |
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