Acceptor–donor–acceptor molecule processed using polar non-halogenated solvents for organic field-effect transistors

We reported a one-step synthesis of a high-performance acceptor–donor–acceptor small molecule based on indacenodithieno[3,2-b]thiophene (IDTT) as the donor unit and benzothiadiazole (BT) as the acceptor unit.

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Controllable microstructure of polymer-small molecule blend thin films for high-performance organic field-effect transistors

Applied Surface Science ◽

10.1016/j.apsusc.2019.143822 ◽

2019 ◽

Vol 498 ◽

pp. 143822 ◽

Cited By ~ 4

Author(s):

Tao Shen ◽

Hui Zhou ◽

Juan Xin ◽

Qin Fan ◽

Zilu Yang ◽

...

Keyword(s):

Thin Films ◽

Small Molecule ◽

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Organic 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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Controlling Conjugation and Solubility of Donor–Acceptor Semiconducting Copolymers for High-Performance Organic Field-Effect Transistors

ACS Applied Materials & Interfaces ◽

10.1021/acsami.5b01746 ◽

2015 ◽

Vol 7 (23) ◽

pp. 12781-12788 ◽

Cited By ~ 16

Author(s):

Mi Jang ◽

Ji-Hoon Kim ◽

Do-Hoon Hwang ◽

Hoichang Yang

Keyword(s):

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Organic Field Effect Transistors ◽

Donor Acceptor

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Highly soluble small-molecule organic semiconductor with trihexylsilyloxy side chain for high-performance organic field-effect transistors with mobility of up to 3.10 cm 2 V −1 s −1

Dyes and Pigments ◽

10.1016/j.dyepig.2017.03.025 ◽

2017 ◽

Vol 142 ◽

pp. 17-23 ◽

Cited By ~ 17

Author(s):

Bogyu Lim ◽

Huabin Sun ◽

Yong-Young Noh

Keyword(s):

Small Molecule ◽

Organic Semiconductor ◽

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Side Chain ◽

Organic Field Effect Transistors

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Poly(pentacyclic lactam-alt-diketopyrrolopyrrole) for field-effect transistors and polymer solar cells processed from non-chlorinated solvents

Polymer Chemistry ◽

10.1039/c5py01406a ◽

2016 ◽

Vol 7 (1) ◽

pp. 164-170 ◽

Cited By ~ 8

Author(s):

Guitao Feng ◽

Yunhua Xu ◽

Chengyi Xiao ◽

Jianqi Zhang ◽

Xiaotao Zhang ◽

...

Keyword(s):

Solar Cells ◽

Conjugated Polymer ◽

Field Effect ◽

High Performance ◽

Field Effect Transistors ◽

Polymer Solar Cells ◽

Chlorinated Solvents ◽

Organic Field Effect Transistors

A highly crystalline conjugated polymer incorporating two electron-deficient units was applied in high performance organic field-effect transistors and polymer solar cells.

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