Bis(2-oxo-7-azaindolin-3-ylidene)benzodifuran-dione-based donor–acceptor polymers for high-performance n-type field-effect transistors

Two donor–acceptor (D–A) conjugated polymers were synthesized using a strongly electron-deficient unit as the acceptor, and dithiophene and (E)-2-(2-(thiophen-2-yl)vinyl)thiophene as the donor units.

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Biaxially extended thiophene–isoindigo donor–acceptor conjugated polymers for high-performance flexible field-effect transistors

Polymer Chemistry ◽

10.1039/c6py00726k ◽

2016 ◽

Vol 7 (26) ◽

pp. 4378-4392 ◽

Cited By ~ 8

Author(s):

Hung-Chin Wu ◽

Chian-Wen Hong ◽

Wen-Chang Chen

Keyword(s):

Electrical Properties ◽

Conjugated Polymers ◽

Field Effect ◽

High Performance ◽

Carrier Mobility ◽

Field Effect Transistors ◽

Charge Carrier Mobility ◽

Ambient Atmosphere ◽

Donor Acceptor ◽

A Charge

Biaxially-extended thiophene–isoindigo donor–acceptor conjugated polymers were explored for high-performance flexible field-effect transistors. A charge carrier mobility of 1.0 cm2 V−1 s−1 was achieved under ambient atmosphere with stable electrical properties.

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Cyclopentadithiophene–Benzothiadiazole Donor–Acceptor Polymers as Prototypical Semiconductors for High-Performance Field-Effect Transistors

Accounts of Chemical Research ◽

10.1021/acs.accounts.8b00025 ◽

2018 ◽

Vol 51 (5) ◽

pp. 1196-1205 ◽

Cited By ~ 41

Author(s):

Mengmeng Li ◽

Cunbin An ◽

Wojciech Pisula ◽

Klaus Müllen

Keyword(s):

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Donor Acceptor

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Methoxylation of quinoidal bithiophene as a single regioisomer building block for narrow-bandgap conjugated polymers and high-performance organic field-effect transistors

Journal of Materials Chemistry C ◽

10.1039/d0tc02199g ◽

2020 ◽

Vol 8 (43) ◽

pp. 15168-15174 ◽

Cited By ~ 1

Author(s):

Yunlong Sun ◽

Yunpeng Zhang ◽

Yang Ran ◽

Longxian Shi ◽

Qingsong Zhang ◽

...

Keyword(s):

Conjugated Polymers ◽

Building Block ◽

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Hole Mobility ◽

Methoxyl Group ◽

Organic Field Effect Transistors ◽

Narrow Bandgap

Methoxyl group was introduced to obtain isomer-free methoxylation quinoidal bithiophene building block. Four polymers displayed narrow bandgap (<1.20 eV) and hole mobility of up to 2.70 cm2 V−1 s−1.

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Structure–property relationship of D–A type copolymers based on phenanthrene and naphthalene units for organic electronics

Journal of Materials Chemistry C ◽

10.1039/c7tc02925j ◽

2017 ◽

Vol 5 (39) ◽

pp. 10332-10342 ◽

Cited By ~ 4

Author(s):

Yeong-A Kim ◽

Minji Kang ◽

Ye-Jin Jeon ◽

Kyeongil Hwang ◽

Yeon-Ju Kim ◽

...

Keyword(s):

Conjugated Polymers ◽

Organic Electronics ◽

Organic Photovoltaics ◽

Field Effect ◽

Field Effect Transistors ◽

Organic Field Effect Transistors ◽

Structure Property ◽

Structure Property Relationship ◽

Donor Acceptor ◽

Relationship Of

Four donor–acceptor (D–A) type conjugated polymers were synthesized for organic photovoltaics and organic field effect transistors.

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Rational Design of Highly Soluble and Crystalline Conjugated Polymers for High‐Performance Field‐Effect Transistors

Advanced Electronic Materials ◽

10.1002/aelm.202101105 ◽

2021 ◽

pp. 2101105

Author(s):

Kyumin Lee ◽

Moon‐Ki Jeong ◽

Eui Hyun Suh ◽

WonJo Jeong ◽

Jong Gyu Oh ◽

...

Keyword(s):

Conjugated Polymers ◽

Field Effect ◽

High Performance ◽

Rational Design ◽

Field Effect Transistors

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Naphtho[1,2b;5,6b′]difuran-based donor–acceptor polymers for high performance organic field-effect transistors

RSC Advances ◽

10.1039/c5ra14721b ◽

2015 ◽

Vol 5 (86) ◽

pp. 70319-70322 ◽

Cited By ~ 7

Author(s):

Shaowei Shi ◽

Keli Shi ◽

Gui Yu ◽

Xiaoyu Li ◽

Haiqiao Wang

Keyword(s):

Field Effect ◽

High Performance ◽

Annealing Temperature ◽

Main Chain ◽

Field Effect Transistors ◽

Side Chain ◽

Organic Field Effect Transistors ◽

Π Stacking ◽

Donor Acceptor

Two naphthodifuran-based donor–acceptor copolymers are presented. Via reasonable main-chain modification and side-chain engineering, remarkably dense π–π stacking spacings (2 V−1 s−1 are achieved at a moderate annealing temperature of 120 °C.

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