Bisperfluorophenyl-Substituted Thiophene Oligomers. Organic Semiconductors with Complementary-Type Carrier Mobility

2002 ◽  
Vol 736 ◽  
Author(s):  
Antonio Facchetti ◽  
Howard E. Katz ◽  
Tobin J. Marks
Keyword(s):  
Thin Films ◽  
Cyclic Voltammetry ◽  
Molecular Characterization ◽  
Organic Semiconductors ◽  
Field Effect ◽  
Carrier Mobility ◽  
Field Effect Transistor ◽  
Photoluminescence Spectroscopy ◽  
Design Synthesis ◽  
Effect Transistor

ABSTRACTThe design, synthesis, and properties of two mixed perfluorophenyl-thiophene oligomers 5,5″′-diperfluorophenyl-2,2′:5′,2″:5″,2″′:5″′,2″″:5″″,2″″′-quaterthiophene (2) and 5,5′-bis{1-[4-(thien-2-yl)-2,3,5,6-tetrafluorophenyl)] }-2,2′-dithiophene (3) are presented. Molecular characterization included the following techniques: multinuclear NMR, DSC and TGA, optical UV-Vis and photoluminescence spectroscopy, and cyclic voltammetry. Thin films can be easily grown by vacuum evaporation and have been characterized by optical UV-Vis and photoluminescence, XRD, and field-effect transistor measurements. Electron and hole mobilities of 0.06–0.08 cm2/(V s) and 0.001–0.003 cm2/(V s) were found for 2 and 3, respectively.

Patterning rubrene crystalline thin films for sub-micrometer channel length field-effect transistor arrays

2014 ◽  
Vol 2 (44) ◽  
pp. 9359-9363 ◽  
Author(s):  
Juan Zhu ◽  
Wenchong Wang ◽  
Qigang Zhong ◽  
Liqiang Li ◽  
Chuan Du ◽  
...  
Keyword(s):  
Thin Films ◽  
Field Effect ◽  
Carrier Mobility ◽  
Field Effect Transistor ◽  
Channel Length ◽  
Organic Films ◽  
Porous Structures ◽  
Patterned Growth ◽  
Effect Transistor ◽  
Magnitude Difference

The patterned growth of crystalline rubrene films directly on electrodes is demonstrated. In addition, organic films with close packed and porous structures are locally achieved by controlling the electrode spaces, resulting in a two orders of magnitude difference in carrier mobility.

scholarly journals Dithienylbenzothiadiazole-Based Donor-Acceptor Organic Semiconductors and Effect of End Capping Groups on Organic Field Effect Transistor Performance

2013 ◽  
Vol 66 (3) ◽  
pp. 370
Author(s):  
Prashant Sonar ◽  
Samarendra P. Singh ◽  
Ting Ting Lin ◽  
Ananth Dodabalapur
Keyword(s):  
Molecular Orbital ◽  
Organic Semiconductors ◽  
Field Effect ◽  
Carrier Mobility ◽  
Field Effect Transistor ◽  
Energy Levels ◽  
Lumo Energy ◽  
Donor Acceptor ◽  
Effect Transistor ◽  
End Capping

Donor-Acceptor-Donor (D-A-D) based conjugated molecules 4,7-bis(5-(4-butoxyphenyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole (BOP-TBT) and 4,7-bis(5-(4-trifluoromethyl)phenyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole (TFP-TBT) using thiophene-benzothiadiazole-thiophene central core with trifluoromethyl phenyl and butoxyphenyl end capping groups were designed and synthesised via Suzuki coupling. Optical, electrochemical, thermal, and organic field effect transistor (OFET) device properties of BOP-TBT and TFP-TBT were investigated. Both small molecules possess two absorption bands. Optical band gaps were calculated from the absorption cut off to be in the range of 2.06–2.25 eV. Cyclic voltammetry indicated reversible oxidation and reduction processes and the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels were calculated to be in the range of 5.15–5.40 eV and 3.25–3.62 eV, respectively. Upon testing both materials for OFET, trifluoromethylphenyl end capped material (TFP-TBT) shows n-channel behaviour whereas butoxyphenyl end capped material (BOP-TBT) shows p-channel behaviour. Density functional theory calculations correlated with shifting of HOMO-LUMO energy levels with respect to end capping groups. Vacuum processed OFET of these materials have shown highest hole carrier mobility of 0.02 cm2/Vs and electron carrier mobility of 0.004 cm2/Vs, respectively using Si/SiO2 substrate. By keeping the central D-A-D segment and just by tuning end capping groups gives both p- and n-channel organic semiconductors which can be prepared in a single step using straightforward synthesis.

Electron-Transporting Thiophene-Based Semiconductors Exhibiting Very High Field Effect Mobilities

2004 ◽  
Vol 814 ◽  
Author(s):  
Antonio Facchetti ◽  
Myung-Han Yoon ◽  
Tobin J. Marks
Keyword(s):  
Organic Semiconductors ◽  
Field Effect ◽  
Carrier Mobility ◽  
Field Effect Transistor ◽  
Thin Film Transistor ◽  
Structural Features ◽  
Improve Performance ◽  
Plastic Electronics ◽  
Effect Transistor ◽  
Very High

AbstractOrganic semiconductors exhibiting complementary n-type carrier mobility are the key components for the development of the field of “plastic electronics”. We present here a novel series of oligothiophenes designed to improve performance and stability under electron- transporting conditions. Furthermore, the key structural features of these compounds allows additional modifications of the n-type conducting core to achieve material solubility and processability. Thin film transistor (TFT) devices were fabricated employing both vacuum- and solution-deposited semiconducting layers. Field-effect transistor measurements indicate that all the members of this new series are n-type semiconductors with mobilities and Ion:Ioff ratios approaching 1 cm2/(Vs) and 107, respectively. This family represents a key milestone in the design, understanding, and development of the next generation of highly efficient n-type OTFT components.

High Carrier Mobility and Environmentally stable Microporous Zeolite Imidazolate Framework (ZIF-67): A Field-Effect Transistor (FET) Approach

2021 ◽  
pp. 138690
Author(s):  
Pasha W. Sayyad ◽  
Aafiya A. Farooqui ◽  
Nikesh N. Ingle ◽  
Theeazen Al-Gahouari ◽  
Gajanan A. Bodkhe ◽  
...  
Keyword(s):  
Field Effect ◽  
Carrier Mobility ◽  
Field Effect Transistor ◽  
High Carrier Mobility ◽  
High Carrier ◽  
Effect Transistor ◽  
Microporous Zeolite

On Razors Edge: Influence of the Source Insulator Edge on the Charge Transport of Vertical Organic Field Effect Transistors

MRS Advances ◽  
2017 ◽  
Vol 2 (23) ◽  
pp. 1249-1257 ◽  
Author(s):  
F. Michael Sawatzki ◽  
Alrun A. Hauke ◽  
Duy Hai Doan ◽  
Peter Formanek ◽  
Daniel Kasemann ◽  
...  
Keyword(s):  
Charge Transport ◽  
Organic Semiconductors ◽  
Organic Solar Cells ◽  
Field Effect ◽  
Field Effect Transistor ◽  
Field Effect Transistors ◽  
Electrical Power ◽  
Strong Impact ◽  
Organic Field Effect Transistor ◽  
Effect Transistor

ABSTRACTTo benefit from the many advantages of organic semiconductors like flexibility, transparency, and small thickness, electronic devices should be entirely made from organic materials. This means, additionally to organic LEDs, organic solar cells, and organic sensors, we need organic transistors to amplify, process, and control signals and electrical power. The standard lateral organic field effect transistor (OFET) does not offer the necessary performance for many of these applications. One promising candidate for solving this problem is the vertical organic field effect transistor (VOFET). In addition to the altered structure of the electrodes, the VOFET has one additional part compared to the OFET – the source-insulator. However, the influence of the used material, the size, and geometry of this insulator on the behavior of the transistor has not yet been examined. We investigate key-parameters of the VOFET with different source insulator materials and geometries. We also present transmission electron microscopy (TEM) images of the edge area. Additionally, we investigate the charge transport in such devices using drift-diffusion simulations and the concept of a vertical organic light emitting transistor (VOLET). The VOLET is a VOFET with an embedded OLED. It allows the tracking of the local current density by measuring the light intensity distribution.We show that the insulator material and thickness only have a small influence on the performance, while there is a strong impact by the insulator geometry – mainly the overlap of the insulator into the channel. By tuning this overlap, on/off-ratios of 9x105 without contact doping are possible.

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 Diacenopentalene dicarboximides as new n-type organic semiconductors for field-effect transistors

2016 ◽  
Vol 4 (37) ◽  
pp. 8758-8764 ◽  
Author(s):  
Gaole Dai ◽  
Jingjing Chang ◽  
Linzhi Jing ◽  
Chunyan Chi
Keyword(s):  
Organic Semiconductors ◽  
Electron Mobility ◽  
Field Effect ◽  
Field Effect Transistor ◽  
Field Effect Transistors ◽  
Processing Technique ◽  
Solution Processing ◽  
Effect Transistor

Two diacenopentalene dicarboximides were synthesized, and their devices made with solution-processing technique exhibited n-type field-effect transistor behavior with electron mobility of up to 0.06 cm2 V−1 s−1.

scholarly journals Morphology and Field-Effect-Transistor Mobility in Tetracene Thin Films

2005 ◽  
Vol 15 (3) ◽  
pp. 375-380 ◽  
Author(s):  
F. Cicoira ◽  
C. Santato ◽  
F. Dinelli ◽  
M. Murgia ◽  
M. A. Loi ◽  
...  
Keyword(s):  
Thin Films ◽  
Field Effect ◽  
Field Effect Transistor ◽  
Effect Transistor
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