磷光
材料科学
水溶液
余辉
激子
微尺度化学
纳米点
纳米颗粒
纳米囊
激发态
纳米技术
光电子学
超短脉冲
光化学
化学物理
纳米材料
作者
Ya‐Chuan Liang,Hao‐Chun Shao,Kai-Kai Liu,Qing Cao,Sifan Zhang,Haiyan Wang,Liying Jiang,Chongxin Shan,Le‐Man Kuang,Hui Jing
标识
DOI:10.1038/s41377-025-01965-0
摘要
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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