Synthesis and characterization of carbazolo[2,1-a]carbazole in thin film and single crystal field-effect transistors

2017 ◽  
Vol 5 (28) ◽  
pp. 7020-7027 ◽  
Author(s):  
Miriam Más-Montoya ◽  
José Pedro Cerón-Carrasco ◽  
Shino Hamao ◽  
Ritsuko Eguchi ◽  
Yoshihiro Kubozono ◽  
...  
Keyword(s):  
Thin Film ◽  
Single Crystal ◽  
Crystal Field ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Synthesis And Characterization ◽  
Organic Field Effect Transistors ◽  
Crystal Field Effect

Carbazole-based azaphenacene with high performance in organic field-effect transistors.

Thin film field-effect transistors of 2,6-diphenyl anthracene (DPA)

2015 ◽  
Vol 51 (59) ◽  
pp. 11777-11779 ◽  
Author(s):  
Jie Liu ◽  
Huanli Dong ◽  
Zongrui Wang ◽  
Deyang Ji ◽  
Changli Cheng ◽  
...  
Keyword(s):  
Thin Film ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Synthesis And Characterization ◽  
Design Synthesis

The present work showed the design, synthesis and characterization of a high performance anthracene-based semiconductor.

High-performance dinaphtho-thieno-thiophene single crystal field-effect transistors

2009 ◽  
Vol 95 (2) ◽  
pp. 022111 ◽  
Author(s):  
Simon Haas ◽  
Yukihiro Takahashi ◽  
Kazuo Takimiya ◽  
Tatsuo Hasegawa
Keyword(s):  
Single Crystal ◽  
Crystal Field ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Crystal Field Effect

Single-crystal field-effect transistors based on a fused-ring electron acceptor with high ambipolar mobilities

2020 ◽  
Vol 8 (16) ◽  
pp. 5370-5374 ◽  
Author(s):  
Chengyi Xiao ◽  
Cheng Li ◽  
Feng Liu ◽  
Lei Zhang ◽  
Weiwei Li
Keyword(s):  
Single Crystal ◽  
Crystal Field ◽  
Electron Acceptor ◽  
Field Effect ◽  
Field Effect Transistors ◽  
Organic Field Effect Transistors ◽  
Crystal Field Effect ◽  
Fused Ring

A fused-ring electron acceptor Y6 was used to fabricate single-crystal organic field-effect transistors, providing high ambipolar mobilities.

A bowl-shaped sumanene derivative with dense convex–concave columnar packing for high-performance organic field-effect transistors

2017 ◽  
Vol 53 (83) ◽  
pp. 11407-11409 ◽  
Author(s):  
Beibei Fu ◽  
Xueqing Hou ◽  
Cong Wang ◽  
Yu Wang ◽  
Xiaotao Zhang ◽  
...  
Keyword(s):  
Charge Carrier ◽  
Single Crystal ◽  
Field Effect ◽  
High Performance ◽  
Carrier Mobility ◽  
Field Effect Transistors ◽  
Charge Carrier Mobility ◽  
Organic Field Effect Transistors ◽  
Crystal Field Effect ◽  
First Time

The charge carrier mobility of a sumanene derivative was probed using single-crystal field-effect transistors for the first time.

Correction to Large Scale Pattern Graphene Electrode for High Performance in Transparent Organic Single Crystal Field-Effect Transistors

ACS Nano ◽  
2011 ◽  
Vol 5 (3) ◽  
pp. 2412-2412 ◽  
Author(s):  
Wei Liu ◽  
Biyun Li Jackson ◽  
Jing Zhu ◽  
Cong-Qin Miao ◽  
Choong-Heui Chung ◽  
...  
Keyword(s):  
Single Crystal ◽  
Crystal Field ◽  
Field Effect ◽  
High Performance ◽  
Large Scale ◽  
Field Effect Transistors ◽  
Graphene Electrode ◽  
Crystal Field Effect ◽  
Organic Single Crystal

Large Scale Pattern Graphene Electrode for High Performance in Transparent Organic Single Crystal Field-Effect Transistors

ACS Nano ◽  
2010 ◽  
Vol 4 (7) ◽  
pp. 3927-3932 ◽  
Author(s):  
Wei Liu ◽  
Biyun Li Jackson ◽  
Jing Zhu ◽  
Cong-Qin Miao ◽  
Choon-Heui, Chung ◽  
...  
Keyword(s):  
Single Crystal ◽  
Crystal Field ◽  
Field Effect ◽  
High Performance ◽  
Large Scale ◽  
Field Effect Transistors ◽  
Graphene Electrode ◽  
Crystal Field Effect ◽  
Organic Single Crystal

Organic field-effect transistors based on tetrathiafulvalene derivatives

2008 ◽  
Vol 80 (11) ◽  
pp. 2405-2423 ◽  
Author(s):  
Xike Gao ◽  
Wenfeng Qiu ◽  
Yunqi Liu ◽  
Gui Yu ◽  
Daoben Zhu
Keyword(s):  
Thin Film ◽  
Single Crystal ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Low Cost ◽  
Device Fabrication ◽  
Organic Field Effect Transistors ◽  
Large Area ◽  
Solution Processed

In recent years, tetrathiafulvalene (TTF) and its derivatives have been used as semiconducting materials for organic field-effect transistors (OFETs). In this review, we summarize the recent progress in the field of TTF-based OFETs. We introduce the structure and operation of OFETs, and focus on TTF derivatives used in OFETs. TTF derivatives used in OFETs can be divided into three parts by the semiconductor's morphology and the device fabrication technique: (1) TTF derivatives used for single-crystal OFETs, (2) TTF derivatives used for vacuum-deposited thin-film OFETs, and (3) TTF derivatives used for solution-processed thin-film OFETs. The single-crystal OFETs based on TTF derivatives were fabricated by drop-casting method and showed high performance, with the mobility up to 1.4 cm2/Vs. The vacuum-deposited thin-film OFETs based on TTF derivatives were well developed, some of which have shown high performance comparable to that of amorphous silicon, with good air-stability. Although the mobilities of most solution-processed OFETs based on TTF derivatives are limited at 10-2 cm2/Vs, the study on solution-processable TTF derivatives and their devices are promising, because of their low-cost, large-area-coverage virtues. The use of organic charge-transfer (OCT) compounds containing TTF or its derivatives in OFETs is also included in this review.

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