Asymmetric organic semiconductors for high performance single crystalline field-effect transistors with low activation energy

2020 ◽  
Vol 8 (18) ◽  
pp. 6006-6012 ◽  
Author(s):  
Fei Qiu ◽  
Yicai Dong ◽  
Jie Liu ◽  
Yanan Sun ◽  
Hua Geng ◽  
...  
Keyword(s):  
Activation Energy ◽  
Organic Semiconductors ◽  
Field Effect ◽  
High Field ◽  
High Performance ◽  
Field Effect Transistors ◽  
Field Effect Mobility ◽  
Crystalline Field ◽  
Asymmetric Structures ◽  
Anthracene Derivatives

We synthesized three asymmetric anthracene derivatives, in which 2-phvA shows a high field-effect mobility of 10 cm2 V−1 s−1. This work demonstrates the potential advantages of asymmetric structures for high-performance organic semiconductors.

Tailoring crystal polymorphs of organic semiconductors towards high-performance field-effect transistors

2016 ◽  
Vol 27 (8) ◽  
pp. 1330-1338 ◽  
Author(s):  
Yong-Gang Zhen ◽  
Huan-Li Dong ◽  
Lang Jiang ◽  
Wen-Ping Hu
Keyword(s):  
Organic Semiconductors ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors

scholarly journals 2,2'-(Arylenedivinylene)bis-8-hydroxyquinolines exhibiting aromatic π-π stacking interactions as solution-processable p-type organic semiconductors for high-performance organic field effect transistors

2021 ◽  
Author(s):  
Suman Yadav ◽  
Shivani Sharma ◽  
Satinder K Sharma ◽  
Chullikkattil P. Pradeep
Keyword(s):  
Organic Semiconductors ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistor ◽  
Field Effect Transistors ◽  
Organic Field Effect Transistors ◽  
Organic Thin Film ◽  
Effect Transistor ◽  
Solution Processable ◽  
P Type

Solution-processable organic semiconductors capable of functioning at low operating voltages (~5 V) are in demand for organic field-effect transistor (OFET) applications. Exploration of new classes of compounds as organic thin-film...

scholarly journals Correction: Naphthalene flanked diketopyrrolopyrrole based organic semiconductors for high performance organic field effect transistors

2018 ◽  
Vol 42 (19) ◽  
pp. 16384-16384
Author(s):  
Qian Liu ◽  
Huabin Sun ◽  
Chula Blaikie ◽  
Chiara Caporale ◽  
Sergei Manzhos ◽  
...  
Keyword(s):  
Organic Semiconductors ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Organic Field Effect Transistors

Correction for ‘Naphthalene flanked diketopyrrolopyrrole based organic semiconductors for high performance organic field effect transistors’ by Qian Liu et al., New J. Chem., 2018, 42, 12374–12385.

Naphtho[2,1-b:3,4-b′]bisthieno[3,2-b][1]benzothiophene-based semiconductors for organic field-effect transistors

2015 ◽  
Vol 3 (31) ◽  
pp. 8024-8029 ◽  
Author(s):  
Zhaoguang Li ◽  
Ji Zhang ◽  
Kai Zhang ◽  
Weifeng Zhang ◽  
Lei Guo ◽  
...  
Keyword(s):  
Organic Semiconductors ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Hole Mobility ◽  
Building Blocks ◽  
Organic Field Effect Transistors ◽  
Next Generation

Naphtho[2,1-b:3,4-b′]bisthieno[3,2-b][1]benzothiophene derivatives exhibiting a hole mobility of up to 0.25 cm2 V−1 s−1 show promise as useful building blocks to construct next-generation high performance organic semiconductors.

Molecular Requirements for Printable Organic Semiconductors in 7-Alkyl-2-phenyl[1]benzothieno[3,2-b][1]benzothiophenes (Ph-BTBT-Cn’s)

MRS Advances ◽  
2016 ◽  
Vol 1 (38) ◽  
pp. 2653-2658
Author(s):  
S. Inoue ◽  
H. Minemawari ◽  
J. Tsutsumi ◽  
T. Hamai ◽  
S. Arai ◽  
...  
Keyword(s):  
Chain Length ◽  
Organic Semiconductors ◽  
Field Effect ◽  
High Performance ◽  
Carrier Transport ◽  
Alkyl Chain ◽  
Field Effect Transistors ◽  
Systematic Investigation ◽  
Alkyl Chain Length

ABSTRACTHere we discuss requirements for high performance and solution processable organic semiconductors, by presenting a systematic investigation of 7-alkyl-2-phenyl[1]benzothieno[3,2-b][1]benzothiophenes (Ph-BTBT-Cn’s). We found that the solubility and thermal properties of Ph-BTBT-Cn’s depend systematically on the substituted alkyl-chain length n. The observed features are well understood in terms of the change of molecular packing motif with n: The compounds with n ≤ 4 do not form independent alkyl chain layers, whereas those with n ≥ 5 form isolated alkyl chain layers. The latter compounds afford a series of isomorphous bilayer-type crystal structures that form two-dimensional carrier transport layers within the crystals. We also show that the Ph-BTBT-C10 afford high performance single-crystalline field-effect transistors the mobility of which reaches as high as 15.9 cm2/Vs. These results demonstrate a crucial role of the substituted alkyl chain length for obtaining high performance organic semiconductors and field-effect transistors.

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