Gaining New Insights into Trace Guest Doping Role in Manipulating Organic Crystal Phosphorescence

Trace guest doping systems often show better room temperature phosphorescence (RTP), but trace guest doping role and mechanism are not recognized well. Here we cocrystallize commercial (CCZ) and self-made (LCZ) carbazole derivatives and verify that 0.2‰ isomer doping can afford the deserved crystal RTP, but further increasing the isomer amount hardly improves RTP. Isomer doping does not affect crystal stacking modes and intermolecular interactions and is inefficient in monomolecular and amorphous states. LCZ derivatives are intrinsically phosphorescent, but crystallization itself cannot effectively inhibit thermal deactivation, and isomer doping restricts nonradiative relaxation and reduces the energy level of the triplet emissive state via space action at a distance rather than currently described adjacent intermolecular interactions. This work has updated some existing views and represented an important conceptual advance in a fresh understanding of trace guest doping RTP systems.