author:
Luo, Wuzhen
(Luo, Wuzhen.)
[1]
|
Chen, Liming
(Chen, Liming.)
[2]
|
Yin, Guangqiang
(Yin, Guangqiang.)
[3]
|
Yue, Chaojun
(Yue, Chaojun.)
[4]
|
Xie, Shiye
(Xie, Shiye.)
[5]
|
Zhou, Jiayin
(Zhou, Jiayin.)
[6]
|
Feng, Weihao
(Feng, Weihao.)
[7]
|
Nie, Yujing
(Nie, Yujing.)
[8]
|
Qiu, Huakai
(Qiu, Huakai.)
[9]
|
Li, Feiming
(Li, Feiming.)
[10]
|
Cai, Shunyou
(Cai, Shunyou.)
[11]
|
Li, Yijiang
(Li, Yijiang.)
[12]
|
Cai, Zhixiong
(Cai, Zhixiong.)
[13]
|
Chen, Tao
(Chen, Tao.)
[14]
Unfold
Abstract:
High-temperature phosphorescence (HTP) materials have attracted considerable attention owing to their expanded application prospects, whereas they still suffer from severe deactivation in polar media, limiting their reliability and utility. Here, we present an efficient multivalent assembly strategy to achieve high-temperature liquid-phase phosphorescence (HTLP). The supramolecular assembly of multivalent modules leads to extremely robust hydrogen-bonding networks, which firmly immobilize the organic phosphors and protect triplet excitons from annihilation in high-temperature polar media, resulting in excellent HTLP emission. Moreover, the photophysical properties of HTLP are significantly enhanced by boosting multivalent interactions using multitopic phosphors, demonstrating a visible afterglow of 5 s in boiling water, more than 2 s in dimethylsulfoxide at 460 K (187 °C), and a long lifetime of 70.3 ms in N-methylpyrrolidone at 476 K (203 °C). Based on their fluidity and robust HTLP emission, in situ microcracks detection of high-temperature operating instruments and spatial-time-temperature-resolved anticounterfeiting are demonstrated. © 2025 Wiley-VCH GmbH.
Keyword:
Phosphorescence
Phosphors
Prisms
Classification
741.1 Light/Optics - 741.3 Optical Devices and Systems - 804 Chemical Products
Type
This project was financially supported by the National Natural Science Foundation of China (21904055 and 22205249), the Natural Science Foundation of Fujian province (Grant 2024J01806 and 2023J011815), Zhejiang Provincial Natural Science Foundation of China (LQ23B040002), Sino-German Mobility Program (M-0424), Ningbo International Cooperation Project (2023H019), Ningbo Yongjiang Talent Programme (2024Z212). The authors also thanked Dr. Lijun Mao from Taizhou University for supporting theoretical simulations.This project was financially supported by the National Natural Science Foundation of China (21904055 and 22205249), the Natural Science Foundation of Fujian province (Grant 2024J01806 and 2023J011815), Zhejiang Provincial Natural Science Foundation of China (LQ23B040002), Sino‐German Mobility Program (M‐0424), Ningbo International Cooperation Project (2023H019), Ningbo Yongjiang Talent Programme (2024Z212). The authors also thanked Dr. Lijun Mao from Taizhou University for supporting theoretical simulations.
Access Number
EI:20250317687992
Corresponding s email
czx1816@mnnu.edu.cnyinguangqiang@nimte.ac.cntao.chen@nimte.ac.cn