材料科学
磷光
无定形固体
发光
聚乙烯醇
纳米技术
平面的
聚合物
堆积
分子
光电子学
结晶学
荧光
有机化学
复合材料
化学
光学
物理
计算机图形学(图像)
计算机科学
作者
Hongwei Wu,Weijie Chi,Zhao Chen,Guofeng Liu,Long Gu,Anivind Kaur Bindra,Guangbao Yang,Xiaogang Liu,Yanli Zhao
标识
DOI:10.1002/adfm.201807243
摘要
Abstract Development of novel strategies for achieving amorphous ultralong organic phosphorescence (UOP) at room temperature is highly desired. Herein, a simple approach is reported by coassembling small organic molecules with polyvinyl alcohol (PVA) to afford amorphous UOP. These small organic molecules with planar conformation present quenched triplet state emission in an excessive stacking solid state. When coassembling these molecules with PVA, their planar structures are well confined in coassembly films. Such a confined environment leads to restricted molecular rotation and vibration, permitting these molecules to show stable triplet state and generate UOP. In control studies, corresponding structurally distorted molecules are also coassembled with PVA. However, they exhibit very weak or quenched UOP, since distorted structures with molecular rotation and vibration could easily dissipate the excitation energy in dilute film state. By employing this polymer confinement strategy, multicomponent luminescence dyes are further coassembled with PVA for multicolor luminescence displays, providing multicolor, uniform, and flexible luminescence films. This work demonstrates a general strategy of employing small organic molecules to coassemble with PVA to obtain amorphous UOP, which greatly expands the scope of organic molecules for developing simple but useful UOP films.
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