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Published on: April 19, 2019
Making Nonconjugated Small-Molecule Organic Radicals Conduct
Ilhwan Yu1, Yerin Jo1,2, Jaehyoung Ko1
1Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST), 92 Chudong-ro, Bongdong-eup, Wanju-gun, Jeonbuk 55324, Republic of Korea.
Charge neutral organic radicals, like 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (h-TEMPO), show potential for electronic applications. Thermal annealing of h-TEMPO single crystals significantly boosts electrical conductivity through enhanced charge transfer.
Area of Science:
- Materials Science
- Organic Electronics
- Solid-State Physics
Background:
- Organic radicals are promising active materials for solid-state electronics.
- Fundamental understanding of charge transport in radical molecules remains limited.
- Previous work highlighted potential of radical-based macromolecules in devices.
Purpose of the Study:
- To investigate charge transport in a nonconjugated organic radical, specifically 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (h-TEMPO).
- To explore the impact of crystal structure and thermal annealing on the electrical properties of h-TEMPO.
Main Methods:
- Formation of single crystals of h-TEMPO using physical vapor deposition (PVD).
- Characterization of charge transport properties in the single crystal.
- Thermal annealing of the single crystal to study changes in electrical conductivity.
Main Results:
- Single crystals of h-TEMPO were successfully formed via PVD.
- Initial charge transport in the macroscopic single crystal was relatively low.
- Thermal annealing led to a rapid charge transfer reaction, increasing electrical conductivity to over 0.05 S m-1.
- This was attributed to enhanced electronic communication between open-shell sites.
Conclusions:
- Nonconjugated organic radicals, exemplified by h-TEMPO, offer a novel pathway for developing next-generation conductors.
- Thermal annealing is an effective strategy to enhance charge transport in organic radical single crystals.
- This work presents an alternative model to conjugated systems for organic electronic materials.
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