Maximizing Field-Effect Mobility and Solid-State Luminescence in Organic Semiconductors

2012 ◽  
Vol 51 (16) ◽  
pp. 3837-3841 ◽  
Author(s):  
Afshin Dadvand ◽  
Andrey G. Moiseev ◽  
Kosuke Sawabe ◽  
Wei-Hsin Sun ◽  
Brandon Djukic ◽  
...  
Keyword(s):  
Solid State ◽  
Organic Semiconductors ◽  
Field Effect ◽  
Field Effect Mobility ◽  
State Luminescence

Maximizing Field-Effect Mobility and Solid-State Luminescence in Organic Semiconductors

2012 ◽  
Vol 124 (16) ◽  
pp. 3903-3907 ◽  
Author(s):  
Afshin Dadvand ◽  
Andrey G. Moiseev ◽  
Kosuke Sawabe ◽  
Wei-Hsin Sun ◽  
Brandon Djukic ◽  
...  
Keyword(s):  
Solid State ◽  
Organic Semiconductors ◽  
Field Effect ◽  
Field Effect Mobility ◽  
State Luminescence

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.

scholarly journals 2,3-Thienoimide-ended oligothiophenes as ambipolar semiconductors for multifunctional single-layer light-emitting transistors

2020 ◽  
Vol 8 (43) ◽  
pp. 15048-15066
Author(s):  
Mario Prosa ◽  
Salvatore Moschetto ◽  
Emilia Benvenuti ◽  
Massimo Zambianchi ◽  
Michele Muccini ◽  
...  
Keyword(s):  
Solid State ◽  
Self Assembly ◽  
Field Effect ◽  
Single Layer ◽  
Field Effect Mobility ◽  
Light Emitting ◽  
Light Emitting Transistors

In view of developing multifunctional OLETs, 2,3-thienoimide-ended oligothiophenes are proposed as ideal candidates to effectively ensure good ambipolar field-effect mobility, self-assembly capability and high luminescence in solid state.

Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b′]diquinoxalines

2015 ◽  
Vol 51 (20) ◽  
pp. 4275-4278 ◽  
Author(s):  
Shuaijun Yang ◽  
Danqing Liu ◽  
Xiaomin Xu ◽  
Qian Miao
Keyword(s):  
Thin Film ◽  
Organic Semiconductors ◽  
Thin Film Transistors ◽  
Field Effect ◽  
Molecular Packing ◽  
Field Effect Mobility

Introduction of chlorine substituents into cyclobuta[1,2-b:3,4-b′]diquinoxaline leads to tunable molecular packing motifs and n-type organic semiconductors with a field effect mobility of up to 0.42 cm2 V−1 s−1 in thin film transistors.

Enhancing field-effect mobility and maintaining solid-state emission by incorporating 2,6-diphenyl substitution to 9,10-bis(phenylethynyl)anthracene

2017 ◽  
Vol 5 (10) ◽  
pp. 2519-2523 ◽  
Author(s):  
Jie Liu ◽  
Jinyu Liu ◽  
Zichao Zhang ◽  
Chunhui Xu ◽  
Qingyuan Li ◽  
...  
Keyword(s):  
Solid State ◽  
Organic Semiconductor ◽  
Field Effect ◽  
Field Effect Mobility

2,6-Diphenyl-9,10-bis(phenylethynyl)anthracene demonstrates improved mobility and comparable solid-state emission compared with 9,10-bis(phenylethynyl)anthracene, suggesting it could be a new and better integrated optoelectronic organic semiconductor.

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