Dual Emission through Thermally Activated Delayed Fluorescence and Room-Temperature Phosphorescence, and Their Thermal Enhancement via Solid-State Structural Change in a Carbazole-Quinoline Conjugate.

The emergence of single-component organic dual light emitters holds great promise for white light-emitting diodes (WLEDs) and biological detection due to the involvement of broad emission covering visible spectrum. Here we show experimental studies on dual emission of carbazole-quinoline conjugate (CQ) that exhibits both thermally activated delayed fluorescence (TADF) via reverse intersystem crossing (r ISC) from the higher-lying triplet state ( T2 ) to the singlet state ( S1 ) and room-temperature phosphorescence (RTP) from the lowest triplet state ( T1 ) due to low energy gap between T2 and S1 , and energetic proximity of T1 with T2 . We found in thermal effect that the intensity of the dual features is enhanced with increasing temperatures up to 100 °C, which can be explained by a thermal-induced structural change (TISC) mechanism that compensates the emission losses due to nonradiative transitions at elevated temperatures. This property, in addition to its enhanced TADF and phosphorescence decay rates (∼107 s-1 and 101 s-1 ) at 100 °C, would have great promise for high-efficiency LEDs.