Abstract
Organic long afterglow materials can be incorporated into commercial polar polymer in very small amount to significantly reduce cost for application, while gaining excellent mechanical deformability attractively. Their luminescence can be usually enhanced, as the polar polymer can block oxygen diffusion and inhibit inclusion aggregation. However, due to thermal instability of most afterglow materials at high temperature, it is still a great challenge when they are applied for widely used polymer melt in material industry. Herein we report a new afterglow material of doped polymer system by blending a new luminescent, two-dimensional polyamide sheet (TIB-3CPBA-TAPA) with a high-temperature polyamide 6 (?PA6) melt. The excellent thermal stability of TIB-3CPBA-TAPA results from the amide bond-linked, imidazolium salted and conjugated structure. Interestingly, TIB-3CPBA-TAPA/?PA6 is found to emit greenish afterglow luminescence that can last for 4 s at room temperature, only under a loading of 0.1 wt% that harvests the UV exposure efficiently. Different from converting non-afterglow ? crystal (?PA) into afterglow a crystal (aPA), our facile strategy achieves longer afterglow with a higher melting point (220 degrees C) and a tripled quantum yield (1.8%). In addition, the viscoelasticity of the polymer melt is improved by TIB-3CPBA-TAPA with a mechanical toughening effect.