磷光
材料科学
共价键
纤维素
罗丹明B
两亲性
发色团
荧光
水溶液
光化学
猝灭(荧光)
锚固
罗丹明
纳米技术
生物结合
衍生工具(金融)
费斯特共振能量转移
氧化纤维素
纳米颗粒
化学工程
聚合物
共价有机骨架
发光
共聚物
超分子化学
组合化学
作者
Xinyan Fan,Ying Wang,Ying Wang,Yixuan Jiao,Xiaoqian Zhou,Xiangyu Tang,Cunshi Zhao,Wuming Fan,Yunfeng Guo,Dong Wang,Qingbo Wang,Zefang Xiao,Yanjun Xie,Yonggui Wang,Yonggui Wang
标识
DOI:10.1002/adma.202520138
摘要
Developing organic room-temperature phosphorescence (RTP) materials stable in aqueous environments remains highly challenging due to the facile quenching of triplet excitons. Inspired by the protective β-barrel architecture of the green fluorescent protein (Aequorea victoria), the study presented a covalent anchoring strategy based on an amphiphilic cellulose derivative (cellulose acetate) to construct water-resistant and scalable RTP materials. Covalent immobilization of chromophores within the rigid framework yields dynamic photoactivated afterglow, extending the lifetime from 2.1 to 946.4 ms. The resulting films retain bright RTP even under water while exhibiting water-mediated tunable mechanical properties. Furthermore, Förster resonance energy transfer with Rhodamine B enables full-color RTP spanning blue to orange. Benefiting from the inherent thermoplasticity and hydroplasticity of cellulose acetate, the RTP cellulose derivatives are readily processed into diverse 1D/2D/3D architectures and applied in multilevel information encryption. This covalent anchoring strategy offers a sustainable and commercially viable pathway to robust polysaccharide-based RTP, opening new opportunities for optoelectronics, security, and eco-friendly photonic technologies.
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