Abstract

Solution-processed polymer light emitting devices (PLEDs) using high-quality thermally activated delayed fluorescence (TADF) polymers as the emitting layers are attractive, however, high-efficiency white-light TADF polymers are very rare because of the complicated radiative transition channels. In this study, a series of hyperbranched TADF conjugated polymers were designed and synthesized which adopted the linear D-A-type TADF emitter of 1,8-naphthalimide-acridine as red chromophores, conjugated poly(fluorene-carbazole) as the blue backbone and triphenylamine as the hyperbranched cores. By adjusting the appropriate feed ratios of monomers, energy transfer process from the blue backbone to the red chromophores could be regulated and HR0.8 film had the highest photoluminescent quantum yield of 24%. Consequently, its doped electroluminescent device showed the cold-white emission with the CIE color coordinates of (0.35, 0.23) and the maximum EQE of 6.82%. By simply raising the concentration of the red chromophore in the polymers, the rapid reverse intersystem crossing (RISC) process and the enlarged energy gap between S1 and T1 were achievable.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.