PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
I will present a new iodine functionalized light emitting tris(2,4,6-trichlorophenyl) methyl (TTM) radical, which allows coupling of virtually any organic electron donor as well as acceptor moiety. We present a series of around 30 N-coupled donors and acceptors to TTM and explain why a medium strength donor gives the highest photoluminescence quantum yield. Moreover, I will elucidate the limits for tuning of the emission wavelength within the class of these N-donor coupled TTM emitters. These results will enable new design strategies for more stable and performant light emitting radicals and potentially allow us to expand the range of emission wavelength and overcome the current boundaries beyond the red spectrum.
Alexander J. C. Kuehne
"Design strategies for high performance light-emitting triarylmethyl radicals", Proc. SPIE PC12659, Organic and Hybrid Light Emitting Materials and Devices XXVII, PC1265907 (1 October 2023); https://doi.org/10.1117/12.2676278
ACCESS THE FULL ARTICLE
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Alexander J. C. Kuehne, "Design strategies for high performance light-emitting triarylmethyl radicals," Proc. SPIE PC12659, Organic and Hybrid Light Emitting Materials and Devices XXVII, PC1265907 (1 October 2023); https://doi.org/10.1117/12.2676278