Exploring the Potential of Nucleic Acid Bases in Organic Light Emitting Diodes
Source abstract
Abstract
Naturally occurring biomolecules have increasingly found applications in organic electronics as a low cost, performance‐enhancing, environmentally safe alternative. Previous devices, which incorporated DNA in organic light emitting diodes (OLEDs), resulted in significant improvements in performance. In this work, nucleobases (NBs), constituents of DNA and RNA polymers, are investigated for integration into OLEDs. NB small molecules form excellent thin films by low‐temperature evaporation, enabling seamless integration into vacuum deposited OLED fabrication. Thin film properties of adenine (A), guanine (G), cytosine (C), thymine (T), and uracil (U) are investigated. Next, their incorporation as electron‐blocking (EBL) and hole‐blocking layers (HBL) in phosphorescent OLEDs is explored. NBs affect OLED performance through charge transport control, following their electron affinity trend: G < A < C < T < U. G and A have lower electron affinity (1.8–2.2 eV), blocking electrons but allowing hole transport. C, T, and U have higher electron affinities (2.6–3.0 eV), transporting electrons and blocking hole transport. A‐EBL‐based OLEDs achieve current and external quantum efficiencies of 52 cd A−1 and 14.3%, a ca. 50% performance increase over the baseline device with conventional EBL. The combination of enhanced performance, wide diversity of material properties, simplicity of use, and reduced cost indicate the promise of nucleobases for future OLED development.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Conducting polymers and applications · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nanoelectronics Laboratory University of Cincinnati Cincinnati OH 45221–0030 USA
Air Force Research Laboratory Wright‐Patterson Air Force Base OH 45433–7707 USA
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