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1.School of Electronics and Information, Zhengzhou University of Light Industry, 450002 Zhengzhou, China
2.Academy for Quantum Science and Technology, Zhengzhou University of Light Industry, 450002 Zhengzhou, China
3.Henan Key Laboratory of Diamond Optoelectronic Material and Devices, School of Physics and Laboratory of Zhongyuan Light, Zhengzhou University, 450001 Zhengzhou, China
4.College of Electrical and Information Engineering, Zhengzhou University of Light Industry, 450002 Zhengzhou, China
5.Key Laboratory of Low-Dimensional Quantum Structures and Quantum Control of Ministry of Education, Department of Physics and Synergetic Innovation Center for Quantum Effects and Applications, Hunan Normal University, 410081 Changsha, China
Kaikai Liu (liukaikai@zzu.edu.cn)
Liying Jiang (jiangliying@zzuli.edu.cn)
Hui Jing (jinghui@hunnu.edu.cn)
Received:01 April 2025,
Revised:2025-07-10,
Accepted:14 July 2025,
Published Online:11 September 2025,
Published:30 November 2025
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Liang, Y. C. et al. Ultrasound-responsive phosphorescence in aqueous solution enabled by microscale rigid framework engineering of carbon nanodots. Light: Science & Applications, 14, 3441-3453 (2025).
Liang, Y. C. et al. Ultrasound-responsive phosphorescence in aqueous solution enabled by microscale rigid framework engineering of carbon nanodots. Light: Science & Applications, 14, 3441-3453 (2025). DOI: 10.1038/s41377-025-01965-0.
Solid-state phosphorescent materials with stimulus-responsive properties have been widely developed for diverse applications. However
the task of generating excited states with long lifetimes in aqueous solution remains challenging due to the ultrafast deactivation of the triplet excitons and the difficulty in regulating stimulation sites in an aqueous environment. Additionally
most existing materials are primarily responsive to limited stimuli
such as light
oxygen
or temperature. Here
we present a microscale rigid framework engineering strategy that can be used to modulate the phosphorescence properties of carbon nanodots (CNDs)
by brightening triplet excitons through ultrasound-enhanced rigidity in CNDs. Ultrasound-responsive phosphorescent CNDs with a lifetime of 1.25 seconds in an aqueous solution were achieved. The CNDs exhibit high sensitivity to surrounding ultrasound
showing a linear response to ultrasound exposure during the treatment period. The ultrasound-responsive phosphorescent CNDs demonstrate potential applications as sensing units in ultrasound radar detection and in vivo afterglow imaging.
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