Correlating crystalline structure with charge mobility in conjugated statistical copolymers for field-effect transistors

Polymer ◽  
2021 ◽  
pp. 123854
Author(s):  
Dongqi Huang ◽  
Juan Peng
Keyword(s):  
Crystalline Structure ◽  
Field Effect ◽  
Field Effect Transistors ◽  
Charge Mobility

Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processing

2014 ◽  
Vol 2 (47) ◽  
pp. 10110-10115 ◽  
Author(s):  
Jessica Wade ◽  
Florian Steiner ◽  
Dorota Niedzialek ◽  
David T. James ◽  
Youngsuk Jung ◽  
...  
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Solution Processing ◽  
Organic Field Effect Transistors ◽  
Charge Mobility

Unravelling the Correlation between Charge Mobility and Cocrystallization in Rod-Rod Block Copolymers for High-Performance Field-Effect Transistors

2018 ◽  
Vol 130 (28) ◽  
pp. 8780-8784 ◽  
Author(s):  
Mingjing Zhu ◽  
Shuang Pan ◽  
Yue Wang ◽  
Ping Tang ◽  
Feng Qiu ◽  
...  
Keyword(s):  
Block Copolymers ◽  
Field Effect ◽  
High Performance ◽  
Field Effect Transistors ◽  
Charge Mobility

scholarly journals Control of roughness at interfaces and the impact on charge mobility in all-polymer field-effect transistors

Soft Matter ◽  
2008 ◽  
Vol 4 (11) ◽  
pp. 2220 ◽  
Author(s):  
Shion Seng Chang ◽  
Ana B. Rodríguez ◽  
Anthony M. Higgins ◽  
Chuan Liu ◽  
Mark Geoghegan ◽  
...  
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Charge Mobility ◽  
The Impact

Cocrystallization-Promoted Charge Mobility in All-Conjugated Diblock Copolymers for High-Performance Field-Effect Transistors

2020 ◽  
Vol 12 (52) ◽  
pp. 58094-58104
Author(s):  
Shuwen Chen ◽  
Lixin Li ◽  
Dalong Zhai ◽  
Yue Yin ◽  
Xin Shang ◽  
...  
Keyword(s):  
Field Effect ◽  
High Performance ◽  
Diblock Copolymers ◽  
Field Effect Transistors ◽  
Charge Mobility

Charge Density and Film Morphology Dependence of Charge Mobility in Polymer Field-Effect Transistors

2003 ◽  
Vol 15 (11) ◽  
pp. 913-916 ◽  
Author(s):  
S. Shaked ◽  
S. Tal ◽  
Y. Roichman ◽  
A. Razin ◽  
S. Xiao ◽  
...  
Keyword(s):  
Charge Density ◽  
Field Effect ◽  
Field Effect Transistors ◽  
Film Morphology ◽  
Charge Mobility

Thionating iso-diketopyrrolopyrrole-based polymers: from p-type to ambipolar field effect transistors with enhanced charge mobility

2018 ◽  
Vol 9 (14) ◽  
pp. 1807-1814 ◽  
Author(s):  
Haichang Zhang ◽  
Kun Yang ◽  
Kai Zhang ◽  
Zhenzhen Zhang ◽  
Qikun Sun ◽  
...  
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Charge Mobility ◽  
P Type

Two polymers based on isoDPP and isoDTPP were designed and synthesized. Thionation reactions could transform p-type polymers into ambipolar polymers for field effect transistors with enhanced charge mobility.

scholarly journals Tuning polymorphism in 2,3-thienoimide capped oligothiophene based field-effect transistors by implementing vacuum and solution deposition methods

2018 ◽  
Vol 6 (21) ◽  
pp. 5601-5608 ◽  
Author(s):  
Emilia Benvenuti ◽  
Denis Gentili ◽  
Fabio Chiarella ◽  
Alberto Portone ◽  
Mario Barra ◽  
...  
Keyword(s):  
Field Effect ◽  
Field Effect Transistors ◽  
Processing Method ◽  
Solution Deposition ◽  
Charge Mobility ◽  
The Impact

The impact of the processing method in controlling the polymorphism and field-effect charge mobility of 2,3-thienoimide-based oligothiophenes semiconductors was investigated.

First Synthesis of Diindeno[1,2-g:1',2'-s]rubicene Derivatives and their Evaluation as Semiconductors

2012 ◽  
Vol 65 (2) ◽  
pp. 145 ◽  
Author(s):  
Mark Bown ◽  
Christopher J. Dunn ◽  
Craig M. Forsyth ◽  
Peter Kemppinen ◽  
Th. Birendra Singh ◽  
...  
Keyword(s):  
Field Effect ◽  
Crystalline State ◽  
Field Effect Transistors ◽  
Poor Performance ◽  
Ring System ◽  
Electronic Coupling ◽  
The Novel ◽  
Charge Mobility ◽  
High Charge ◽  
X Ray

Solution-processable derivatives 4a–d of the novel diindeno[1,2-g:1′,2′-s]rubicene ring system have been prepared in three steps from 1,5-dichloroanthraquinone. Charge extraction by linearly increasing voltage measurements indicates that 4a–d have bulk mobilities <10–7 cm2 V–1 s–1. Consistent with these low mobility values, field-effect transistors fabricated from 4a–d show poor performance. X-ray crystallographic analyses indicate that in the crystalline state, molecules of compounds 4b–d pack in a manner that hinders π–π stacking, thus preventing strong electronic coupling between molecules that is essential for high charge mobility semiconductor performance.

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