Fluorene Oligomers Featuring a Central 2,1,3-Benzothiadiazole Unit with High Photoluminescence Quantum Yield and Amplified Spontaneous Emission

This is the authors' abstract. We don't add key points for this paper.

High Resolution Image Download MS PowerPoint Slide Fluorene-based conjugated materials are pivotal to optoelectronic applications due to their tunable optical properties and high photoluminescence quantum yields. While conjugated polymers like poly(fluorene- co -benzothiadiazole) have been extensively studied, their performance is often limited by product inhomogeneity and morphological constraints. Oligofluorenes, with their well-defined structures and controlled morphologies, offer a promising alternative but have been underexplored in substoichiometric fluorene-benzothiadiazole systems. Here, we report the synthesis and characterization of a novel series of substoichiometric fluorene-BT oligomers featuring a central BT unit flanked by dioctylfluorene arms of varying repeat lengths, ranging from trimers to heptamers. These oligomers exhibit superior optical properties compared to conventional F8BT polymers, including enhanced quantum yields and amplified spontaneous emission thresholds of down to 1.5 μJ cm –2 . The optical performance is analyzed in relation to oligomer length and fluorene-to-BT ratio, providing insights into the relationship between molecular design and photophysical behavior. Our findings highlight the potential of these defect-free, tunable green-emitting oligomers for next-generation light-emitting diodes and low-threshold lasers, paving the way for further advancements in photonic and optoelectronic materials.