Reveals deep-red emission and switchable polarization in chiral OLEDs, indicating new optoelectronic potentials.
Stable organic radicals with unique luminescence have demonstrated great importance in photoelectromagnetic materials and have found broad applicability in the field of organic light-emitting diode (OLEDs). Aiming to further extend their application into chiral optoelectronic devices, by employing topologically chiral [2]catenane as the key chiral skeleton, this work presents the first successful construction of circularly polarized OLEDs (CP-OLEDs) based on donor–acceptor (D–A•) type neutral tris(2,4,6-trichlorophenyl)methyl (TTM) radicals. Remarkably, the topologically chiral skeleton, in combination with its controllable dynamic features, enables the system to exhibit a luminescence dissymmetry factor (|gPL|) value as high as 7.1 × 10-3, as well as reversible circularly polarized luminescence (CPL) on/off switching in film state. Importantly, the resulting CP-OLEDs exhibit deep red emission, a maximum external quantum efficiency (EQEmax) of 3.92%, and a |gEL| value of 7.2 × 10-3. These findings demonstrate the successful development of not only luminescent radicals with unique switchable CPL performances, but also the first CP-OLEDs with promising device performance based on topologically chiral radical emitter, providing a distinctive design principle and a versatile platform for the creation of next-generation smart CP-OLEDs. Organic radicals can emit light but extending them to chiral optoelectronics with controllable circular polarization remains challenging. Wang et al. build topologically chiral catenane-based radical emitters and demonstrate efficient deep-red devices with switchable circularly polarized emission.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: