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. 2020 May 1;11:2131. doi: 10.1038/s41467-020-15998-z

Fig. 1. Temperature-activated delayed fluorescence: system and processes.

Fig. 1

a [Cu4(PCP)3]+ (PCP = 2,6-(PPh2)2C6H3) complex. b Scheme of light emission from Cu-based OLEDs due to temperature-activated delayed fluorescence (TADF) under electroluminescence conditions. After electron-hole recombination, the singlet and triplet excited states are occupied in a 1:3 ratio due to one possible momentum projection in the singlet and three possible projections in the triplet state. If the energy of the triplet state T1 is close to the energy of the singlet S1, temperature-activated reverse intersystem crossing (T1 → S1) occurs which is followed by light emission from the singlet state. c Structure of [Cu4(PCP)3]+ derived from single crystal X-ray diffraction. Cu atoms are brown, P atoms are magenta, C atoms are gray, H atoms are not shown. d Schematic illustration showing that non-radiative relaxation paths in Cu OLED materials are more probable if equilibrium excited and ground state structures are displaced along some vibrational coordinates. e Green emission from an OLED prototype with [Cu4(PCP)3]+ as a luminophore.