Exploring transport properties of stable rubrene derivatives

Crystalline organic semiconductors, such as rubrene, are crucial for addressing the low mobility of organic materials, with rubrene offering high hole mobility of up to 10 cm<sup>2</sup>/Vs, even in thin films. Thin films are particularly beneficial for scalable device fabrication, having shown success in photodetectors and bipolar transistors, where rubrene supports both n- and p-type doping. However, rubrene's susceptibility to oxygen under UV light limits its stability. To tackle this, novel fluorinated rubrene derivatives were synthesized to reduce oxidation while preserving mobility. Stability under UV light and ambient conditions was studied, alongside device-relevant evaluations, such as HOMO level measurements (via UPS) and conductivity under doping. Crystallization studies compared single and thin-film crystals, analyzing them using XRD and GIWAXS. The acquired data is compared to simulated crystal structures. Thin-film morphology was further characterized using PLM and AFM, providing insights into their structural properties. The compounds with varying degrees of low fluorination pave the way for advanced device engineering and facilitate heteroepitaxial growth on rubrene.

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Publication Details

Published
2025-09-15
DOI
https://doi.org/10.1117/12.3063787
Primary Topic
Synthesis and properties of polymers
Type
article
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article

Exploring transport properties of stable rubrene derivatives

Anna‐Lena Hofmann, Johannes Benduhn, Karl Leo, Mike Hambsch et al.
Synthesis and properties of polymers
article

Exploring transport properties of stable rubrene derivatives

Anna‐Lena Hofmann, Johannes Benduhn, Karl Leo, Mike Hambsch, Stephanie Buchholtz, Bhoomika Chelur Shivakumar, Stefan C. B. Mannsfeld, Frank Ortmann, S. P. S. Dutta, Jonas Schröder, Nora Engelmann, Fritz Henke, Anna Marie Fichtl, Alexander Turchanin, Adrian Kishonti
article en

Abstract

Crystalline organic semiconductors, such as rubrene, are crucial for addressing the low mobility of organic materials, with rubrene offering high hole mobility of up to 10 cm<sup>2</sup>/Vs, even in thin films. Thin films are particularly beneficial for scalable device fabrication, having shown success in photodetectors and bipolar transistors, where rubrene supports both n- and p-type doping. However, rubrene's susceptibility to oxygen under UV light limits its stability. To tackle this, novel fluorinated rubrene derivatives were synthesized to reduce oxidation while preserving mobility. Stability under UV light and ambient conditions was studied, alongside device-relevant evaluations, such as HOMO level measurements (via UPS) and conductivity under doping. Crystallization studies compared single and thin-film crystals, analyzing them using XRD and GIWAXS. The acquired data is compared to simulated crystal structures. Thin-film morphology was further characterized using PLM and AFM, providing insights into their structural properties. The compounds with varying degrees of low fluorination pave the way for advanced device engineering and facilitate heteroepitaxial growth on rubrene.

Technische Universität Dresden (DE)
Openalex Percentile: Top 78%
Synthesis and properties of polymers
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