In Situ Confining Citric Acid-Derived Carbon Dots for Full-Color Room-Temperature Phosphorescence

被引:54
作者
Ding, Zhong-Zheng [1 ]
Shen, Cheng-Long [1 ]
Han, Jiang-Fan [1 ]
Zheng, Guang-Song [1 ]
Ni, Qing-Chao [1 ]
Song, Run-Wei [1 ]
Liu, Kai-Kai [1 ]
Zang, Jin-Hao [1 ]
Dong, Lin [1 ]
Lou, Qing [1 ]
Shan, Chong-Xin [1 ]
机构
[1] Zhengzhou Univ, Sch Phys & Microelect, Henan Key Lab Diamond Optoelect Mat & Devices, Key Lab Mat Phys,Minist Educ, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
carbon dots; confining aggregation; encryption; full-color; room-temperature phosphorescence; ORGANIC PHOSPHORESCENCE; FLUORESCENCE; EMISSION;
D O I
10.1002/smll.202205916
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Room-temperature phosphorescence has received much attention owing to its potential applications in information encryption and bioelectronics. However, the preparation of full-color single-component-derived phosphorescent materials remains a challenge. Herein, a facile in situ confining strategy is proposed to achieve full-color phosphorescent carbon dots (CDs) through rapid microwave-assisted carbonization of citric acid in NaOH. By tuning the mass ratio of citric acid and NaOH, the obtained CDs exhibit tunable phosphorescence wavelengths ranging from 483 to 635 nm and alterable lifetimes from 58 to 389 ms with a synthesis yield of up to 83.7% (>30 g per synthesis). Theoretical calculations and experimental results confirm that the formation of high-density ionic bonds between cations and CDs leads to efficient afterglow emission via the dissociation of CD arrangement, and the evolution of the aggregation state of CDs results in redshifted phosphorescence. These findings provide a strategy for the synthesis of new insights into achieving and manipulating room-temperature phosphorescent CDs, and prospect their applications in labeling and information encryption.
引用
收藏
页数:10
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