磷光
系统间交叉
余辉
材料科学
纤维素
发光
制作
光化学
光电子学
纳米技术
单重态
化学物理
光学
化学
原子物理学
有机化学
激发态
物理
天文
伽马射线暴
医学
荧光
病理
替代医学
作者
Peng Fang,Changjing Qiu,Pingping Wu,Songnan Hu,Pan Chen,Xingxing Li,Mengke Li,Zijian Chen,Shi‐Jian Su,Haisong Qi
标识
DOI:10.1002/adom.202401419
摘要
Abstract The large‐scale fabrication of long‐lived and sustainable room‐temperature phosphorescence (RTP) materials with color‐tunable afterglow is of considerable practical importance in diverse optoelectronic applications but remains challenging. Herein, based on a process for the mass production of cellulose acetoacetate filaments, large‐scale RTP filaments are synthesized by introducing amino‐bearing luminophores via a mild enamine reaction. Attributed to efficient intersystem crossing facilitated by acetoacetyl and benzoyloxy groups alongside a rigid environment provided by multiple hydrogen bonding, the resulting filaments exhibit impressive RTP with a lifetime of 772 ms and a phosphorescence quantum yield of 45.06%. Furthermore, the afterglow color of RTP filaments is rationally modulated from blue to greenish‐yellow to rosy‐red through triplet‐to‐singlet Förster resonance energy transfer. Meanwhile, the formation of diverse clusters with comparable but different lifetimes leads to interesting excitation‐dependent afterglows. This work not only provides an effective strategy to construct long‐lived, color‐tunable, sustainable afterglows but also establishes large‐scale and continuous preparation routes for functional cellulose filaments.
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