磷光
激子
材料科学
激发态
猝灭(荧光)
光化学
化学
荧光
物理
原子物理学
光学
凝聚态物理
作者
Qing Cao,Kai-Kai Liu,Ya‐Chuan Liang,Shiyu Song,Yuan Deng,Xin Mao,Yong Wang,Wenbo Zhao,Qing Lou,Chongxin Shan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-05-10
卷期号:22 (10): 4097-4105
被引量:61
标识
DOI:10.1021/acs.nanolett.2c00788
摘要
Triplet excitons usually do not emit light under ambient conditions due to the spin-forbidden transition rule, thus they are called dark excitons. Herein, triplet excitons in carbon nanodots (CNDs) are brightened by embedding the CNDs into poly(vinyl alcohol) (PVA) films; flexible multicolor phosphorescence films are thus demonstrated. PVA chains can isolate the CNDs, and excited state electron or energy transfer induced triplet exciton quenching is thus reduced; while the formed hydrogen bonds between the CNDs and PVA can restrict vibration/rotation of the CNDs, thus further protecting the triplet excitons from nonradiative recombination. The lifetimes of the flexible multicolor phosphorescence films can reach 567, 1387, 726, and 311 ms, and the longest-lasting phosphorescence film can be observed by naked eyes for nearly 15 s even after bending 5000 times. The phosphorescence films can be processed into various patterns, and a dynamic optical signature concept has been proposed and demonstrated based on the phosphorescence films.
科研通智能强力驱动
Strongly Powered by AbleSci AI