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Fluorinated benzothiadiazole (BT) groups as a powerful unit for high-performance electron-transporting polymers
Junghoon Lee1, Moonjeong Jang, Sang Myeon Lee
1School of Energy and Chemical Engineering, KIER-UNIST Advanced Center for Energy, Low Dimensional Carbon Materials Center, Ulsan National Institute of Science and Technology (UNIST) , Ulsan 689-798, South Korea.
Fluorinated benzothiadiazole (BT) units in polymers enhance electron transport for organic field-effect transistors (OFETs). This molecular design strategy improves electron mobility without compromising hole mobility in polymer solar cells (PSCs).
Area of Science:
- Materials Science
- Organic Electronics
- Polymer Chemistry
Background:
- Polymer solar cells (PSCs) have seen significant advances with fluorinated 2,1,3-benzothiadiazole (BT)-based polymers.
- These materials offer improved power conversion efficiency, but their charge-transport characteristics require further investigation.
Purpose of the Study:
- To synthesize and investigate new diketopyrrolopyrrole (DPP)-based polymers with single- and double-fluorinated BT units.
- To assess the influence of fluorinated BT units on charge-transport properties in organic field-effect transistors (OFETs).
Main Methods:
- Synthesis of PDPP-FBT and PDPP-2FBT polymers incorporating DPP and fluorinated BT units.
- Characterization using UV-Vis spectroscopy, cyclic voltammetry, and grazing incidence X-ray diffraction (GIXD).
- Charge-transport measurements in organic field-effect transistors (OFETs).
Main Results:
- The introduction of double-fluorinated BT (PDPP-2FBT) altered optical profiles and energy levels, resulting in a wider bandgap and deeper HOMO compared to PDPP-FBT and PDPP-BT.
- Both fluorinated polymers exhibited semicrystalline lamellar structures with edge-on orientations.
- Electron mobilities reached up to 0.42 cm² V⁻¹ s⁻¹ (PDPP-FBT) and 0.30 cm² V⁻¹ s⁻¹ (PDPP-2FBT), while hole mobilities remained above 0.1 cm² V⁻¹ s⁻¹.
Conclusions:
- Fluorinated BT blocks are a promising strategy for enhancing electron transport in polymers.
- This approach improves electron mobility in OFETs without negatively impacting hole mobility.
- The findings contribute to the molecular design of high-performance organic electronic materials.
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