Color-Tunable, Excitation-Dependent, and Time-Dependent Afterglows from Pure Organic Amorphous Polymers

被引:265
作者
Dou, Xueyu [1 ,2 ]
Zhu, Tianwen [2 ]
Wang, Zhengshuo [1 ,2 ]
Sun, Wei [3 ]
Lai, Yueying [2 ]
Sui, Kunyan [1 ]
Tan, Yeqiang [1 ]
Zhang, Yongming [2 ]
Yuan, Wang Zhang [2 ]
机构
[1] Qingdao Univ, Coll Mat Sci & Engn, State Key Lab Biofibers & Ecotext, Collaborat Innovat Ctr Marine Biobased Fiber & Ec, 308 Ningxia Rd, Qingdao 266071, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Frontiers Sci Ctr Transformat Mol, Shanghai Key Lab Elect Insulat & Thermal Aging, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Orthopaed, Shanghai 200240, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
amorphous polymers; excitation-dependent afterglows; film-forming ability; persistent room-temperature phosphorescence; time-dependent afterglows; ROOM-TEMPERATURE PHOSPHORESCENCE; ACHIEVING PERSISTENT; EMISSION; DESIGN;
D O I
10.1002/adma.202004768
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Achieving persistent room-temperature phosphorescence (p-RTP), particularly those of tunable full-colors, from pure organic amorphous polymers is attractive but challenging. Particularly, those with tunable multicolorp-RTP in response to excitation wavelength and time are highly important but both fundamentally and technically underexplored. Here, a facile and general strategy toward color-tunablep-RTP from blue to orange-red based on amidation grafting of luminophores onto sodium alginate (SA) chains, resulting in amorphous polymers with distinctp-RTP and even impressively excitation-dependent and time-dependent afterglows is reported.p-RTP is associated with the unique semi-rigidified SA chains, effective hydrogen bonding network, and oxygen barrier properties of SA, whereas excitation-dependent and time-dependent afterglows should stem from the formation of diversifiedp-RTP emissive species with comparable but different lifetimes. These results outline a rational strategy toward amorphous smart luminophores with colorful, excitation-dependent, and time-dependentp-RTP, excellent solution processability, and film-forming ability for versatile applications.
引用
收藏
页数:8
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