Effects of Intercalation on the Hole Mobility of Amorphous Semiconducting Polymer Blends

2010 ◽  
Vol 22 (11) ◽  
pp. 3543-3548 ◽  
Author(s):  
Nichole C. Cates ◽  
Roman Gysel ◽  
Jeremy E. P. Dahl ◽  
Alan Sellinger ◽  
Michael D. McGehee
Science ◽  
2018 ◽  
Vol 362 (6419) ◽  
pp. 1131-1134 ◽  
Author(s):  
Aristide Gumyusenge ◽  
Dung T. Tran ◽  
Xuyi Luo ◽  
Gregory M. Pitch ◽  
Yan Zhao ◽  
...  

Although high-temperature operation (i.e., beyond 150°C) is of great interest for many electronics applications, achieving stable carrier mobilities for organic semiconductors at elevated temperatures is fundamentally challenging. We report a general strategy to make thermally stable high-temperature semiconducting polymer blends, composed of interpenetrating semicrystalline conjugated polymers and high glass-transition temperature insulating matrices. When properly engineered, such polymer blends display a temperature-insensitive charge transport behavior with hole mobility exceeding 2.0 cm2/V·s across a wide temperature range from room temperature up to 220°C in thin-film transistors.


2020 ◽  
Author(s):  
Micaela Matta ◽  
Ruiheng Wu ◽  
Bryan D. Paulsen ◽  
Anthony Petty ◽  
Rajendar Sheelamanthula ◽  
...  

<p>Organic electrochemical transistors (OECTs) are based on the doping of a semiconducting polymer by an electrolyte. Due to their ability to conjugate volumetric ion penetration with high hole mobility and charge density, polythiophenes bearing glycolated side chains have rapidly surged as the highest performing materials for OECTs; amongst them, p(g2T-TT) is amongst those with the highest figure of merit. While recent studies have shown how different doping anions tend to affect the polymer microstructure, only a handful of electrolytes have been tested in mixed conduction devices. Our work provides an atomistic picture of the p(g2T-TT) -electrolyte interface in the ‘off’ state of an OECT, expected to be dominated by cation-polymer interactions. Using a combination of molecular dynamics simulations and X-ray fluorescence, we show how different anions effectively tune the coordination and chelation of cations by glycolated polymers. At the same time, softer and hydrophobic anions such as TFSI and ClO<sub>4</sub> are found to preferentially interact with the p(g2T-TT) phase, further enhancing polymer-cation coordination. Besides opening the way for a full study of electrolyte doping mechanisms in operating devices, our results suggest that tailoring the electrolyte for different applications and materials might be a viable strategy to tune the performance of mixed conducting devices.</p>


2004 ◽  
Author(s):  
Xiong Gong ◽  
Daniel Moses ◽  
Alan J. Heeger

2004 ◽  
Vol 16 (7) ◽  
pp. 615-619 ◽  
Author(s):  
X. Gong ◽  
W. Ma ◽  
J. C. Ostrowski ◽  
G. C. Bazan ◽  
D. Moses ◽  
...  

2016 ◽  
Vol 2 (10) ◽  
pp. 1600267 ◽  
Author(s):  
Guanghao Lu ◽  
Riccardo Di Pietro ◽  
Lisa Sophie Kölln ◽  
Iyad Nasrallah ◽  
Ling Zhou ◽  
...  

2011 ◽  
Vol 24 (5) ◽  
pp. 669-674 ◽  
Author(s):  
Xueliang Liu ◽  
Sven Huettner ◽  
Zhuxia Rong ◽  
Michael Sommer ◽  
Richard H. Friend

2015 ◽  
Vol 27 (20) ◽  
pp. 7164-7170 ◽  
Author(s):  
Yan Zhao ◽  
Xikang Zhao ◽  
Michael Roders ◽  
Ge Qu ◽  
Ying Diao ◽  
...  

2020 ◽  
Author(s):  
Micaela Matta ◽  
Ruiheng Wu ◽  
Bryan D. Paulsen ◽  
Anthony Petty ◽  
Rajendar Sheelamanthula ◽  
...  

<p>Organic electrochemical transistors (OECTs) are based on the doping of a semiconducting polymer by an electrolyte. Due to their ability to conjugate volumetric ion penetration with high hole mobility and charge density, polythiophenes bearing glycolated side chains have rapidly surged as the highest performing materials for OECTs; amongst them, p(g2T-TT) is amongst those with the highest figure of merit. While recent studies have shown how different doping anions tend to affect the polymer microstructure, only a handful of electrolytes have been tested in mixed conduction devices. Our work provides an atomistic picture of the p(g2T-TT) -electrolyte interface in the ‘off’ state of an OECT, expected to be dominated by cation-polymer interactions. Using a combination of molecular dynamics simulations and X-ray fluorescence, we show how different anions effectively tune the coordination and chelation of cations by glycolated polymers. At the same time, softer and hydrophobic anions such as TFSI and ClO<sub>4</sub> are found to preferentially interact with the p(g2T-TT) phase, further enhancing polymer-cation coordination. Besides opening the way for a full study of electrolyte doping mechanisms in operating devices, our results suggest that tailoring the electrolyte for different applications and materials might be a viable strategy to tune the performance of mixed conducting devices.</p>


2018 ◽  
Vol 10 (5) ◽  
pp. 4904-4909 ◽  
Author(s):  
Aristide Gumyusenge ◽  
Xikang Zhao ◽  
Yan Zhao ◽  
Jianguo Mei

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